Case Studies & Application Stories
Electrical Conductivity Testing Applied to the Assessment of Freshly Collected Kielmeyera coriacea Mart. Seeds: MyronLMeters.com
Tweet MyronLMeters.com brings you the latest in conductivity measurement research like the article below. Please click here for accurate, reliable, conductivity meters. Abstract Assessment of seed vigor has long been an important tool of seed quality control programs. The conductivity test is a promising method for assessment of seed vigor, but proper protocols for its […]
MyronLMeters.com brings you the latest in conductivity measurement research like the article below. Please click here for accurate, reliable, conductivity meters.
Assessment of seed vigor has long been an important tool of seed quality control programs. The conductivity test is a promising method for assessment of seed vigor, but proper protocols for its execution have yet to be established. The objective of this study was to assess the efficiency of electrical conductivity (EC) testing as a means of assessing the viability of freshly collected Kielmeyera Coriacea Mart. seeds. The test was performed on individual seeds rather than in a bulk configuration. Seeds were soaked for different periods (30 min, 90 min, 120 min., 180 min, and 240 min) at a constant temperature of 25°C. Conductivity was then measured with a benchtop EC meter.
Seeds are the primary factor of the seedling production process, despite their minor contribution to the end cost of each seedling. In order to estimate the success rate of seedling production, it is essential that seed characteristics such as vigor and germinability be known .
The importance of knowing the characteristics of Brazilian forest species to safer and more objective management of seedling production cannot be overstated. However, such studies are scarce, particularly in light of the vast number of species with this potential . Given the intensity of anthropogenic pressure and the importance of rehabilitating disrupted or degraded environments, in-depth research of forest species is warranted.
Routine methods used for determination of seed quality and viability include germination testing and the tetrazolium test. Methods such as measurement of soak solution pH, electrical conductivity, and potassium content of leachate, all based on the permeability of the cell membrane system, are increasingly being employed in the assessment of seed vigor, as they are reliable and fast and can thus speed the decision making process.
Electrical conductivity testing, as applied to forest seeds, has yet to be standardized. Studies conducted thus far have focused on assessment of seed soaking times, which may range from 4 to 48 hours. Even at 48 hours, the conductivity test is considered a rapid technique as compared to the germination test, which, despite its status as a widespread and firmly established method, can take anywhere from 30 to 360 days to yield results (depending on species), and is limited by factors such as dormant seeds.
The total concentration of electrolytes leached by seeds during soaking has long been assessed indirectly, mostly through the conductivity test, which takes advantage of the fact that inorganic ions make up a substantial portion of these electrolytes [3–5].
Rapid assessment of seed quality allows for preemptive decision-making during harvest, processing, sale and storage operations, thus optimizing use of financial resources throughout these processes.
K. coriacea Mart. is a species of the Clusiaceae (Guttiferae) family popularly known in Brazil as pau-santo (Portuguese for “holy wood”), due to its properties as a medicinal and melliferous plant and as a source of cork. In traditional Brazilian medicine, the leaves are used as an emollient and antitumor agent, and the resin as a tonic and in the treatment of toothache and various infections. The fruits are used in regional crafts and flower arrangements. Even if the dye is of the leaves and bark. The trunk provides cork .
K. coriaceae specimens grow to approximately 4 meters in height. The flowering period extends from January to April and the fruiting period from May to September, and seed collection can take place from September onwards. Leaves are alternate, simple, oval to elliptical, coriaceous, and clustered at the end of the branches, and feature highly visible, pink midribs. A white to off-white latex is secreted in small amounts upon removal of leaves. Flowers are white to pale pink in color, large, fragrant, with many yellow stamens and are borne in short clusters near the apex of the branches. Seedling production requires that seeds be sown shortly after collection.
In the fruit are found 60 to 80 seeds with anemochoric. The seed varies from round to oblong, winged at the ends, light brown color, has integument thin and fragile, with smooth texture, the sizes range from 4.3 to 5.6 cm long, 1.3 to 1.9 cm wide, and 0.2 to 0.5 centimeter thick. The individual weight of the seeds ranges from. 112 to.128 grams. Nursery radicle emission occurred at 7 days and the germination rate was 90%. Germination occurs within 7 to 10 days. The species is slow growing, both in the field and in a nursery setting .
The present study sought to assess the applicability of the conductivity test to freshly collected K. coriacea Mart. seeds by determining the optimal soak time for performance of the test and comparing results obtained with this method against those obtained by tetrazolium and germination testing of seeds from the same batch.
2. Materials and Methods
2.1. Seed Collection
Seeds were collected in the cerrado sensu stricto, in SCA (Clean Water Farm), area of study at the University of Brasília (UNB) in August 2010, matrixes marked with the aid of GPS, after the period of physiological maturation of the seeds. The collection of fruits was directly from the tree, with the help of trimmer, then the seeds were processed and stored in paper bags at room temperature in the laboratory.
2.2. Conductivity Test
The development of tests to evaluate the physiological quality of seeds, as well as the standardization of these is essential for the establishment of an efficient quality control . One of the main requirements for the seed vigor refers to obtain reliable results in a relatively short period of time, allowing the speed of decision making especially as regards the operations of collection, processing, and marketing . The literature indicates that rapid tests are most studied early events related to the deterioration of the sequence proposed by Delouche and Baskin  as the degradation of cell membranes and reduced activity, and biosynthetic respiratory . The measurement of electrical conductivity through the electrolyte amount released by soaking seeds in water has been applied by the individual method where each seed is a sample or more often, a sample of seed representative of a population (mass method). For this case, the results represent the average conductivity of a group of seeds, may a small amount of dead seeds affect the conductivity of a batch with many high-quality seed generating a read underestimated. To minimize this problem, we recommend choosing the seeds, excluding the damaged seeds.
The electrical conductivity is based on the principle that the deterioration process is the leaching of the cells of seeds soaked in water due to loss of integrity of cellular systems. Thus, low conductivity means a high-quality seed and high conductivity, that is, greater output seed leachate, suggests that less force .
The electrical conductivity is not yet widely used in Brazil, its use is restricted to activities related to research (Krzyzanowski et al., 1991). There are common jobs using this test to determine the physiological quality of tree seeds. However, it is a promising vigor test for possible standardization of the methodology, at least within a species. However, it is a promising vigor test for possible standardization of the methodology, at least within a species. However, there are factors which influence the conductivity values as the size, the initial water content, temperature and time of soaking, the number of seeds per sample, and genotype .
Five treatments were carried out to test the efficiency of the conductivity test as a means of evaluating the viability of freshly collected K. coriacea Mart. seeds.
Five runs of 20 seeds were tested for each treatment. Seeds were individually placed into containers holding 50 mL of distilled water and left to soak for 30, 90, 120, 180, and 240 minutes in a germination chamber set to a constant temperature of 25°C. The minimum time taken for the soaking of 30 minutes was adopted by the same authors and Amaral and peske , Fernandes et al. , and Matos  who concluded that the period of 30 minutes of soaking is more effective to estimate the germination of the seeds. After each period, the conductivity of the soak solution was immediately tested with a benchtop EC meter precise to +/−1% (Quimis). Readings were expressed as μS·cm−1/g−1 seed .
Data thus obtained were subjected to analysis of variance with partitioning into orthogonal polynomials for analysis of the effect of soaking times on electrical conductivity.
2.3. Tetrazolium Test
The tetrazolium test, also known as biochemical test for vitality, is a technique used to estimate the viability and seed germination. A fundamental condition for ensuring the efficiency of the test is the direct contact of the tetrazolium solution with the tissues of the seed to be tested. Due to the impermeability of the coats of most forest tree seeds, it is necessary to adopt a previous preparation of the seeds that were tested. This preparation is based on facilitating entry of the solution in the seed. Among the preparations that precede the test we have cutting the seed coat, seed coat removal, scarification by sandpaper scarification by soaking in hot water and water . In the previous preparation of the seeds, factors such as concentration of the solution or even the time of the staining solution can affect the efficiency of the test in the evaluation of seed quality. The time required for the development of appropriate color according to the Rules for Seed Analysis  varies depending on each species, can be between 30 and 240 minutes.
The tetrazolium test has been widely used in seeds of various species due to the speed and efficiency in the characterization of the viability and vigor, and the possibility of damage to the same distinction, assisting in the process of quality control from the steps of harvest storage (GRIS et al, 2007).
The tetrazolium test was also applied to freshly collected K. coriacea Mart. seeds, for a total of three runs and 20 seeds. Seeds were soaked in a 0.5% solution of 2,3,5-triphenyl-2H-tetrazolium for 24 hours in a germination chamber set to a constant temperature of 25°C. After each run, seeds were washed, bisected, and the half-containing the embryonic axis placed under a stereo viewer for examination of staining patterns .
2.4. Germination Test
The standard germination test is the official procedure to evaluate the ability of seeds to produce normal seedlings under favorable conditions in the field, but does not always reveal differences in quality and performance among seed lots, which can manifest in storage or in the field .
During the germination test optimum conditions are provided and controlled for seeds to encourage the resumption of metabolic activity which will result in the seedlings. The main objective of the germination test is the information about the quality of seeds, which is used in the identification of lots for storage and sowing .
Freshly collected K. coriacea Mart. seeds were placed in a germination chamber at a constant temperature of 25°C (Treatment 1) or an alternating temperature of 20–30°C (Treatment 2), on a standard cycle of 8 hours of light and 16 hours of dark. Each test consisted of five runs and was performed on 20 seeds.
Germination was defined as emergence of at least 2.0 mm of the primary root . Assessment was conducted daily, and emergence was observed between day 6 and day 7. At the end of the 14-day test period, the germination percentage was calculated on the basis of radicle emergence .
3.1. Conductivity Test
Different soaking times were not associated with any significant differences in conductivity results in K. coriacea Mart. seeds (Table 1).
Table 1: Conductivity ranges of freshly collected Kielmeyera coriacea Mart. seeds after soaking for different periods.
Seeds with a leachate conductivity range of 7–17.99 μS·cm·g were considered nonviable, confirming the hypothesis behind conductivity testing, which is the nonviable seeds that have higher soaking solution conductivity values (Table 2).
Table 2: Percentage of viable Kielmeyera coriacea Mart. seeds according to EC range.
Analysis of variance revealed a low coefficient of variation (20.26%), which suggests good experimental control (Table 3).
Table 3: Analysis of variance of various soaking times for electrical conductivity testing of Kielmeyera coriacea Mart. seeds.
After analysis of variance, the correlation between the soaking time and electrical conductivity variables was assessed. The cubic model yielded
which is indicative of a positive correlation between the study variables.
The following equation was obtained on the basis of the cubic model:
Analysis of a plot of the above function in the GeoGebra 2007 software package shows that variation in electrical conductivity as a function of soaking time is minor and approaches a constant, which is consistent with the study results, in which changes in soaking time had no influence on conductivity (Figure 1).
Matos  reported that a 30-minute soak was enough for assessment of Anadenanthera falcata, Copaifera langsdorffii, and Enterolobium contortisiliquum seeds by the soaking solution pH method—that is, the amount of matter leached after this period sufficed for measurement.
Although the principle of conductivity is the same used for the test pH of exudate, the soaking time needed to analyze the differential seeds through the conductivity may be explained by the fact that this technique is quantitative, while pH in the art exudate analyzes are qualitative. In other words to the technique of pH values of the exudate it is important to detect the acidity of imbibition while on the electrical conductivity we draw a comparison between the analyzed values to separate viable from nonviable samples. To determine a value of electrical conductivity as a reference to determine viable seeds are to be considered the values obtained for fresh seeds and seeds stored.
The thickness of the K. coriacea Mart. seed coat may also have affected the soaking procedure; this species has very thin seed coats, which makes soaking a very fast process.
These results are consistent with those reported by Rodrigues , who subjected stored K. coriaceaMart. seeds to the conductivity test and found that 90 minutes is an appropriate soaking time for analysis.
Therefore, it can be inferred that for seed Kielmeyera coriacea Mart. the soaking time of 90 minutes can be applied to obtain satisfactory results.
3.2. Tetrazolium Test
Table 4 shows the results of tetrazolium testing of K. coriacea Mart. seeds in our sample. The mean viability rate was 96.6%. The testing procedure was based on Brazilian Ministry of Agriculture recommendations .
The results of the tetrazolium test were quite similar to those obtained with the conductivity method, thus confirming the efficiency of the latter method as a means for assessing the viability of K. coriaceaMart. seeds.
3.3. Germination Test
The germination test results of freshly collected K. coriacea Mart. seeds are shown in Table 5. Regardless of temperature, both test batches exhibited good viability, and no seed dormancy was detected.
Radicle emergence was observed between day 7 and day 9 of the test, according to the analysis criteria proposed by Labouriau .
These findings are consistent with those of Melo et al.,  who reported high and relatively rapid germination rates for K. coriacea seeds kept at 25°C on paper towels, with emergence of a perfect radicle on the 7th day of assessment.
The electrical conductivity can be used as an indicator of seed viability and presents two advantages: to provide rapid and reliable results and the technique is not destructive and can use the seeds after the conductivity test, so they can be used to produce seedlings.
The present study showed that different soaking times had no effect on the results of conductivity testing of freshly collected K. coriacea Mart. seeds, suggesting that the amount of leached matter was never below the threshold required for adequate testing.
Electrical conductivity testing proved to be a feasible option for viability testing of K. coriacea Mart. seeds, as the results obtained with conductivity testing were confirmed by germination testing and by the tetrazolium test.
- J. M. M. Matos, Evaluation of pH test on exudate check feasibility of forest seeds, dissertation, University of Brasília, Brasília, Brazil, 2009.
- F. Poggiani, S. Bruni, and E. S. Q. Barbos, “Effect of shading on seedling growth of three species forest,” in National conference on native plants, vol. 2, pp. 564–569, Institute of Forestry, 1992.
- M. B. Mcdonald Jr. and D. O. Wilson, “ASA-610 ability to detect changes in soybean seed quality,” Journal of Seed Technology, vol. 5, no. 1, pp. 56–66, 1980.
- S. Matthews and A. Powell, “A eletrical conductivity test,” in Handbook of Vigor Test Methods, D. A. Perry, Ed., pp. 37–42, International Seed Testing Associaty, Zurich, Switzerland, 1981.
- J. Son Mark, W. R. Singh, A. D. C. Novembre, and H. M. C. P. Chamma, “Comparative studies to evaluate dem’etodos physiological quality of soybean seeds, with emphasis the electrical conductivity test,” Brazilian Journal of Agricultural Research, vol. 25, no. 12, pp. 1805–1815, 1990.
- S. R. Singh, A. P. Silva, C. B. Munhoz, et al., Guide of Cerrado Plants Used in the Chapada Veadeiros, WWF-Brazil, Brasilia, Brazil, 2001.
- J. M. Felfili, C. W. Fagg, J. C. S. Silva, et al., Plants of the APA Gama Cabeça de Veado: Species, ecosystems and recovery, University of Brasilia, Brasília, Department of Engineering Forest, Brasília, Brazil, 2002.
- M. F. B. Muniz, et al., “Comparison of methods for evaluating the physiological and health quality of melon seeds,” Journal of Seeds, Pellets, vol. 26, no. 2, pp. 144–149, 2004.
- D. C. F. S. Dias and J. Marcos Filho, “Electrical conductivity to assess seed vigor of soybean (Glycine max (L.) Merrill),” Scientia Agricola, vol. 53, no. 1, Article ID article id, pp. 31–42, 1996.View at Publisher · View at Google Scholar
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- R. D. Vieira and F. C. Krzyzanowski, “Electrical conductivity test,” in Seed Vigor: Concepts and Tests, F. C. Krzyzanowski, R. D. Vieira, and J. B. França Neto, Eds., pp. 4.1–4.26, Abrates, London, UK, 1999.
- R. D. Vieira, “Electrical conductivity test,” in Seed Vigor Tests, R. D. Vieira and N. M. Carvalho, Eds., p. 103, FUNEP, Jaboticabal, Brazil, 1994.
- A. S. Amaral and S. T. Peske, “Exudate pH to estimate, in 30 minutes seed viability of soybeans,”Journal of seeds, vol. 6, no. 3, pp. 85–92, 1984.
- E. J. Fernandes, R. Sader, and N. M. Carvalho, “seed viability beans (Phaseolus vulgaris L.) estimated by the pH of the exudate,” in Congress Brazil’s Seeds, Gramado, Brazil, 1987.
- F. C. Krzyzanowski and R. D. Vieira, “Electrical conductivity test,” in Seed Vigor: Concepts and Tests, F. C. Krzyzanowski, R. D. Vieira, and J. B. France Neto, Eds., pp. 4.1–4.26, Abrates, London, UK, 1999.
- Ministry of Agriculture, Livestock and Supply, Rule for seed testing, SNPA/DNPV/CLAV, Brasilia, Brazil, 1992.
- Ministry of Agriculture, Livestock and Supply, Rule for seed testing, SNPA/DNPV/CLAV, Brasilia, Brazil, 2009.
- N. M. Carvalho and J. Nakagawa, Seeds: Science, Technology and Production, FUNEP, Jaboticabal, Brazil, 2000.
- Pina-Rodrigues, et al., “Quality test,” in Germination from Basic to Applied, A. Ferreira and G. F. Borghetti, Eds., pp. 283–297, 2004.
- A. G. Ferreira and F. Borghetti, from basic to Germination applied, Artmed, Porto Alegre, Brazil, 2004.
- L. G. Labouriau, seed germination, OAS, Washington, DC, USA, 1983.
- L. L. Rodrigues, Study of imbibition time for application the method of electrical conductivity in the verification of the feasibility forest seeds stored, monograph, University of Brasília, Brasília, Brazil, 2010.
- J. T. Melo, J. F. Ribeiro, and V. L. G. F. Lima, “Germination of Seeds of some tree species native to the Cerrado,” Journal of Seeds, vol. 1, no. 2, pp. 8–12, 1979.
1Seed Technology Laboratory of Forestry, Department of Forestry, University of Brasilia, CP 04357, 70919970 Campus Asa Norte, DF, Brazil
2Department of Forestry, University of Brasilia, CP 04357, 70919970 Campus Asa Norte, DF, Brazil
Received 17 December 2011; Accepted 14 February 2012
Academic Editors: A. Berville, C. Gisbert, J. Hatfield, and Y. Ito
Copyright © 2012 Kennya Mara Oliveira Ramos et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
TweetHypothesis: Does the time of year affect the conductivity of stagnant water in a given location? Abstract: We decided to test the conductivity levels of the water at Flat Rock Brook. If the conductivity levels are higher, it might imply higher total dissolved solid levels. We would like to see if the conductivity level changes during seasons […]
Hypothesis: Does the time of year affect the conductivity of stagnant water in a given location? Abstract: We decided to test the conductivity levels of the water at Flat Rock Brook. If the conductivity levels are higher, it might imply higher total dissolved solid levels. We would like to see if the conductivity level changes during seasons with snowfall versus seasons without snowfall. Background:
- Independent Variable: Time of Year (Season)
- Independent Variable: Location
- Dependent Variable: Conductivity Level (mg/L TDS)
The purpose of the experiment is to test the change in conductivity level throughout the year (on a seasonal basis) in various locations. While doing this experiment, it is important to keep in mind these three things:
- How does conductivity vary at any of the given sites during a given season.(1)
- What human influence might have an impact on the conductivity of the water at any given part of the year.(1)
- Why might this change affect the ability of organisms to live in the given test sites.(1)
This is important to Flat Rock Brook because the data could be used to do several things. For example, the change in conductivity may change the organic life in the water, thus changing the ability to safely drink it. The change may impact the ability of organisms to grow in the water, and it may change the reactive nature of the water. Conductivity can be measured by the total dissolved solids in the water. Total Dissolves Solids include the number of mineral and salt impurities in the water. (1) Ultimately, the number of minerals and salts determines how many ions in mg/L. The impurities in the water can include runoff from roads, wastewater from industrial plants, and soils and rocks. (1) The amount of total dissolved solids in the water can have a physiological effect on plants and animals living in the ponds. (2) Conductivity can be used as a way of noting changes in water conditions over short periods of time. (2) Also, the level of total dissolved solvents in water can have an effect of the ability of habitat-forming plants to grow, thus disrupting the presence of certain species. (2) Materials:
- GPS Navigator by Magellan: We used the GPS as a way to mark off specific testing sites at McFadden’s Pond and Quarry Pond, in order to test in a precise and consistent location
- pH/Conductivity Probe: We used the pH/Conductivity Probe to test the level of conductivity in the various locations. The conductivity was measured in mg/L (TDS), and microsiemens (µS), but due to the difficult nature of working with microsiemens, we chose to work primarily with mg/L(TDS).
- Distilled Water: We used the distilled water to wash off the probe in between tests in order to maintain accurate readings without tainted results.
- Map of Flat Rock Brook: We used the map of Flat Rock Brook in order to find locations from which we could test conductivity levels of water.
- Vernier conductivity probe used with a Lab Pro interface: We used this for our May data in order to get a more accurate reading. By taking samples from Flat Rock Brook, we connected this probe to Logger Pro and recorded the conductivity which was also measured in TDS. NOTE: We used the conductivity data from these readings in our graphs and overall analysis because it provided a more accurate measurement
Methods: *Adapted from Electrical Conductivity Protocol Used by University Corporation for Atmospheric Research, Colorado State University, and NASA. (Water Temperature was not recorded.)
- Record water temperature
- Pour water sample into two containers (or measure in water body)
- Rinse electrodes with distilled water, blot dry
- Place meter in first container, 2-3 seconds
- Remove meter, shake gently, and place in second
container, 1 minute (Do not rinse with distilled water)
- Record value when stabilized
- Repeat measurement with new sample water, twice
- Average three measurements and check for accuracy
Original Protocol can be found at this link*: http://184.108.40.206/search?q=cache:tpTXJUjpiHgJ:globe.ucar.edu/trr-
Cleaning off the conductivity probe before testing the water. (Figure 2)
Testing the conductivity of the pond (Figure 3)
Results: Fall (November) : -Quarry Pond:
- .9 mg/L
-McFadden’s Pond (site A)*:
- 3.1 mg/L
-McFadden’s Pond (site B)*:
- 3.05 mg/L
Spring (May): (with ph/conductivity probe) -Quarry Pond:
- .83 mg/L
-McFadden’s Pond (Site A):
- 2.95 mg/L
-McFadden’s Pond (Site B):
- 2.02 mg/L
Spring (May): (LoggerPro Data) -Quarry Pond:
- .8 mg/L
-McFadden’s Pond (Site A):
- 3.1 mg/L
-McFadden’s Pond (Site B):
- 2.1 mg/L
Data Graph for Quarry Pond (Figure 4)
Data Graph for McFadden’s Pond Site A (Figure 5)
Data Graph for McFadden’s Pond Site B (Figure 6)
Data Graph for all three locations (Figure 7)
Discussion: Throughout our research, there was a general shift in the conductivity level in each site we tested. At Quarry Pond, the total dissolved solids reduced from .9 mg/L to .8 mg/L from November to May. This shift can be seen in the graph shown in Figure 4. McFadden’s Pond Site B also showed a substantial shift between the November and May readings, from 3.05 mg/L to 2.1 mg/L, as seen in Figure 6. Despite these significant changes, Site A at McFadden’s Pond did not change. This could potentially be due to its close proximity to moving water. A subtle, unnoticed under-current may have existed which may have caused the water to be mixed, and therefore diluted. The figures for this measurement can be seen in Figure 5.
The changes in conductivity at Quarry Pond may be the result of runoff from the parking lot and the roads in close proximity to it. Quarry Pond, unlike the other locations was close enough to a road that run-off affects the level of total dissolved solids. Although there was a significant change in conductivity between readings, the total dissolved solids were much lower than that of McFadden’s Pond. This may explain why the presence of algae was much higher in Quarry Pond than in McFadden’s Pond. McFadden’s Pond’s conductivity may have been higher due to a larger level of mineral deposits from soil runoff. One possible explanation for this shift in conductivity is the dilution of total dissolved solids in pond water due to rainfall and melting water from snow.
Conclusion: When comparing conductivity of water at a given point of time during the year, it is clear that there are noticeable differences. During the Fall and Winter, when there is more soil and road runoff, the conductivity level is higher. Conversely, during the spring, when there is more rainwater and melted snow and ice to dilute the ponds, the conductivity level drops. This would suggest that during fall and winter, the conditions of the pond are noticeably different. This suggests the possibility that there may be a shift in population from one group of organisms to another on a seasonal basis. Knowledge of these changes may help to explain why animals would migrate to a different habitat during different seasons. Because of the nature of soil runoff and road runoff, the level of Total Dissolved Solids in the water changes on a seasonal basis, and with that, the conductivity changes as well. In conclusion, conductivity does change over time of year in stagnant water, primarily because of external conditions such as runoff and wastewater.
(1)The GLOBE Program, “Electrical Conductivity Protocol.” Hydro-Electrical Conductivity. Ed. UCAR, Colorado State University, NASA.
We used the Power Point file linked to this page as our primary source of background information as well as a standard protocol for our field tests.
(2)Conductivity And Water Quality.
<[[http://kywater.org/ww/ramp/rmcond.htm%3C/span%3E%3Cspan|http://kywater.org/ww/ramp/rmcond.htm<span]] We used this website as our second source of data for finding out environmental impacts of change in conductivity and overall water quality. (Note: No Author, Publisher or Editor could be found for this web page.) __ *Site A is to the right of Mystery Bridge *Site B is to the left of Mystery Bridge *Note, this protocol was implemented both in the field and in a lab dependent on the time the data was collected *If the web page is difficult to view, a link to a .ppt file is available at the top of the page. The protocol can be found on slide #12.
Study authors: Margot Bennett and Rob Schwartz
Contributions to http://d-e-science11.wikispaces.com/ are licensed under a Creative Commons Attribution Share-Alike 3.0 License
Tweet Water quality testing is vital to the design of an efficient, cost-effective RO system, and is one of the best ways to preserve system life and performance. Using an accurate Total Dissolved Solids (TDS) measurement to assess the system load prevents costly mistakes up front. The TDS measurement gives users the information they need […]
Water quality testing is vital to the design of an efficient, cost-effective RO system, and is one of the best ways to preserve system life and performance.
Using an accurate Total Dissolved Solids (TDS) measurement to assess the system load prevents costly mistakes up front. The TDS measurement gives users the information they need to determine whether or not pretreatment is required and the type of membrane/s to select. Ultrameter™ and ULTRAPEN PT1™ Series TDS instruments feature the unique ability to select from 3 industry standard solution models: 442 Natural Water™ NaCl; and KCl. Choosing the model that most closely matches the characteristics of source water yields measurements accurate enough to check and calibrate TDS monitor/controllers that can help alert to system failures, reducing downtime and increasing productivity. The same instruments provide a fast and accurate test for permeate TDS quality control. Measuring concentrate values and analyzing quality trends lets users accurately determine membrane usage according to the manufacturer’s specifications so they can budget consumption correctly. These daily measurements are invaluable in detecting problems with system performance where changes in the ionic concentration of post-filtration streams can indicate scaling or fouling. System maintenance is generally indicated if there is either a 10-15% drop in performance or permeate quality as measured by TDS.
Thin-film composite membranes degrade when exposed to chlorine. In systems where chlorine is used for microbiological control, the chlorine is usually removed by carbon adsorption or sodium bisulfite addition before membrane filtration. The presence of any chlorine in such systems will at best reduce the life of the membrane, thus, a target of 0 ppm free chlorine in the feedwater is desirable.
ORP gives the operator the total picture of all chemicals in solution that have oxidizing or reducing potential including chlorine, bromine, chloramines, chlorine dioxide, peracetic acid, iodine, ozone, etc. However, ORP can be used to monitor and control free chlorine in systems where chlorine is the only sanitizer used. ORP over +300 mV is generally considered undesirable for membranes. Check manufacturer’s specifications for tolerable ORP levels.
An inline ORP monitor/controller placed ahead of the RO unit to automatically monitor for trends and breakthroughs coupled with spot checks by a portable instrument will prevent equipment damage and failure. Myron L 720 Series II™ ORP monitor/controllers can be configured with bleed and feed switches as well as visible and audible alarms.
Ultrameter and ULTRAPEN portable handhelds are designed for fast field testing and are accurate enough to calibrate monitor/controllers. Our measurement methods are objective and have superior accuracy and convenience when compared to colorimetric methods where determination of equivalence points is subjective and can be skewed by colored or turbid solutions.
Monitoring pH of the source water will allow users to make adjustments that optimize the performance of antiscalants, corrosion inhibitors and anti-foulants. Using a 720 II Series Monitor/controller to maintain pH along with an Ultrameter Series or ULTRAPEN PT2™ handheld to spot check pH values will reduce consumption of costly chemicals and ensure their efficacy.
Most antiscalants used in chemical system maintenance specify a Langelier Saturation Index maximum value. Some chemical manufacturers and control systems develop their own proprietary methods for determining a saturation index based on solubility constants in a defined system. However, LSI is still used as the predominant scaling indicator because calcium carbonate is present in most water. Using a portable Ultrameter III 9PTKA™ provides a simple method for determining LSI to ensure the chemical matches the application.
The Ultrameter III 9PTKA computes LSI from independent titrations of alkalinity and hardness along with electrometric measurements of pH and temperature. Using the 9PTKA LSI calculator, alterations to the water chemistry can be determined to achieve the desired LSI. Usually, pH is the most practical adjustment. If above 7, acid additions are made to achieve the pH value in the target LSI. Injections are made well ahead of the RO unit to ensure proper mixing and avoid pH hotspots. A Myron L 720 Series II pH Monitor/controller will automatically detect and divert solution with pH outside the range of tolerance for the RO unit. ULTRAPEN PT2, TechPro II and Ultrameter Series instruments can be used to spot check and calibrate the monitor/controller as part of routine maintenance and to ensure uniform mixing.
Water hardness values indicate whether or not ion exchange beds are required in pretreatment. Checking hardness values directly after the softening process with the Ultrameter III 9PTKA ensures proper functioning and anticipates the regeneration schedule.
Alkalinity is not only important in its effect on the scaling tendency of solution, but on pH maintenance. Additions of lime are used to buffer pH during acid injection. Use a 9PTKA to measure alkalinity values for fast field analysis where other instrumentation is too cumbersome to be practical.
Though testing and monitoring pressure is a good way to evaluate system requirements and performance over time, measuring other water quality parameters can help pinpoint problems when troubleshooting. For example, if the pressure differential increases over the second stage, the most likely cause is scaling by insoluble salts. This means that any degradation in performance is likely due to the dissolved solids in the feed. Using a 9PTKA to evaluate LSI and calculate parameter adjustments is a simple way to troubleshoot a costly problem.
Myron L Meters saves you 10% on all Ultrameters and Ultrapens when you order online at MyronLMeters.com, where you can find the complete selection of Myron L meters, including the Ultrameter III 9PTKA.
Original story from International Filtration News V 32, no. 2
TweetMyronLMeters.com has the most advanced lineup of pool analysis meters for the professional pool maintenance technician from the Ultrapen to the PoolPro PS9. Pool Draining Tips to Protect Water Quality With summer right around the corner, many swimming pool owners will be readying their swimming pools in anticipation of the season’s heat. As part of […]
Pool Draining Tips to Protect Water Quality
With summer right around the corner, many swimming pool owners will be readying their swimming pools in anticipation of the season’s heat. As part of this process, some pool owners like to drain old swimming pool water which has been sitting all winter. Though not a necessary task, the following tips are provided for you to properly drain pool water in order to protect the water resources in your community.
Whenever possible, it is best to drain your pool onto your landscape. This recycles your pool water, conserves irrigation water, and avoids the environmental risks associated with draining your pool to the street. Before draining your pool water to the street or to your landscape, be sure to follow the guidelines outlined below.
While draining pool water to the street is a common practice, it can prove harmful to the environment if the pool owner does not properly plan and prepare prior to draining. When pool water is drained to the street, it can carry other pollutants such as oil, grease, sediment, bacteria and trash down the storm drain and into the nearest creek, river, or the ocean. Swimming pool water also often contains harmful additives and chemicals. If the water is not properly treated to remove these pollutants prior to draining, they can cause further damage to the health of our waterways and to the plants and animals that live there.
Also, prior to draining to the street, residents are asked to sweep the curb and gutter between the discharge point from their yard to the storm drain down hill from their home. This will remove any pollutants from the gutter that may be carried up by the drained pool water to the storm drain.
For chlorine pools, chlorine levels must be lowered to less than 1 part per million prior to draining. This can be done naturally, by simply allowing the pool water to sit in the sun for a minimum of three days. Alternatively, de-chlorination kits can be purchased at home supply stores at a very reasonable cost. These kits have the tools you need to reach the appropriate chlorine levels before draining your pool to the curb and gutter.
Some people have salt water pool systems which may be preferred due to the lower amount of chemicals required for their operation. However, these pools must not be drained to the storm drain system due to their high salt content relative to the fresh water systems they drain into. Total dissolved solids (TDS) must be below 500 parts per million in order to drain into the street.
“Green pools,” which are pools in which algae is growing, also must not be drained to the street. In these instances, algae must first be killed and removed. This is usually done by chlorinating the swimming pool until the algae is gone, then lowering chlorine to the allowable discharge level. Cartridge filters or diatomaceous earth (DE) filters should be rinsed onto a pervious surface such as landscaped areas or grass. While DE is actually beneficial in your garden, it can build up in storm drains and clog them. DE residues can be scooped up and simply thrown in the trash or put to use fending off worms in your garden.
For more information on how to reach acceptable chemical and TDS levels, call your pool maintenance specialist.
If you are a pool maintenance specialist, consider the PoolPro PS9TKA from MyronLMeters.com – the most advanced and comprehensive pool water analysis meter on the market.
Pool Pro PS9TK
Measures 9 Parameters: Conductivity, Mineral/Salts, TDS, Alkalinity, Hardness, LSI, pH, ORP/Free Chlorine, Temperature
LSI Calculator for hypothetical water balance calculations
Wireless data transfer capability with bluDock option
Auto-ranging delivers increased resolution across diverse applications
Adjustable Temperature Compensation and Cond/TDS conversion ratios for user-defined solutions
Nonvolatile memory of up to 100 readings for stored data protection
Date & time stamp makes record-keeping easy
pH calibration prompts alert you when maintenance is required
Auto-off minimizes energy consumption
Low battery indicator
(Includes instrument with case and solutions)
Peat Water Treatment Using Combination of Cationic Surfactant Modified Zeolite, Granular Activated Carbon, and Limestone
Tweet MyronLMeters.com attempts to provide its customers with the latest in water quality research and industry updates. Find more at https://www.myronlmeters.com/. Abstract This research was conducted essentially to treat fresh peat water using a series of adsorbents. Initially, the characterization of peat water was determined and five parameters, including pH, colour, COD, turbidity, and iron ion […]
MyronLMeters.com attempts to provide its customers with the latest in water quality research and industry updates. Find more at https://www.myronlmeters.com/.
This research was conducted essentially to treat fresh peat water using a series of adsorbents. Initially, the characterization of peat water was determined and five parameters, including pH, colour, COD, turbidity, and iron ion exhibited values that exceeded the water standard limit. There were two factors influencing the adsorption capacity such as pH, and adsorbent dosages that were observed in the batch study. The results obtained indicated that the majority of the adsorbents were very efficient in removing colour, COD, turbidity at pH range 2-4 and Fe at pH range 6-8. The optimum dosage of cationic surfactant modified zeolite (CSMZ) was found around 2 g while granular activated carbon (GAC) was exhibited at 2.5 g. In column study, serial sequence of CSMZ, GAC, and limestone showed that the optimal reduction on the 48 hours treatment were found pH = 7.78, colour = 12 TCU, turbidity = 0.23 NTU, COD = 0 mg/L, and Fe= 0.11 mg/L. Freundlich isotherm model was obtained for the best description on the adsorption mechanisms of all adsorbents.
Keywords: cationic surfactant modified zeolite, granular activated carbon, limestone, peat water
Water is essential and fundamental to all living forms and is spread over 70.9% of the earth’s surface. However, only 3% of the earth’s water is found as freshwater, of which 97% is in ice caps, glaciers and ground water (Bhatmagar & Minocha, 2006). In Malaysia, more than 90% of fresh water supply comes from rivers and streams. The demand for residential and industrial water supply has grown rapidly coupled with an increase in population and urban growth (WWF Malaysia, 2004). Water demand in affected populations such as rural areas also demands that attention is paid to providing more sustainable solutions rather than transporting bottled water (Loo et al., 2012). For this reason, it is essential to ensure availability of local sources of water supply and even develop new potential sources of water such as from peat swamp forest to overcome future water shortages.
River water surrounded by peat swamp forest is defined as peat water and is commonly available as freshwater since it has a low concentration of salinity. The previous study shows that peat swamp forest has high levels of acidity and organic material depending on its region and vegetation types (Huling et al., 2001). Under natural conditions, tropical peat lands serve as reservoirs of fresh water, moderate water levels, reduce storm-flow and maintain river flows, even in the dry season, and they buffer against saltwater intrusion (Wosten et al., 2008).
Due to the acidity and high concentration of organic material, selective treatment of peat water must be conducted prior to its use as water supply. Recently, many methods have been designed and have proven their effectiveness in treating raw water such as coagulation and flocculation (Franceschi et al., 2002; Liu et al., 2011; Syafalni et al., 2012a), absorption (Ćurković et al., 1997), filtration (Paune et al., 1998) and combining (Hidaka et al., 2003). Careful consideration of the most suitable method is important to ensure that the adsorption process is the most beneficial, economically feasible method as well as easy to operate for producing high quality of water in a particular location.
Many researchers have shown that activated carbon is an effective adsorbent for treating water with high concentrations of organic compounds (Eltekova et al., 2000; Syafalni et al., 2012b). Its usefulness derives mainly from its large micropore and mesopore volumes and the resulting high surface area (Fu & Wang, 2011). However, its high initial cost makes it less economically viable as an adsorbent. Low cost adsorbent such as zeolite nowadays has been explored for its ability in many fields especially in water treatment. Natural zeolite has negative surface charge which gives advantages in absorbing unwanted positive ions in water such heavy metal. These ions and water molecules can move within the large cavities allowing ionic exchange and reversible rehydration (Jamil et al., 2010). The effectiveness of zeolite has been improvised by modified zeolite with surfactant in order to achieve higher performance in removing organic matter (Li & Bowman, 2001). Among tested cationic surfactants, hexa-decyl-tri-methyl ammonium (HDTMA) ions adsorbed onto adsorbent surfaces are particularly useful for altering the surface charge from negative to positive (Chao & Chen, 2012). Surfactant modified zeolite has been shown to be an effective adsorbent for multiple types of contaminants (Zhaohu et al., 1999).
Zeolite is modified to improve its capability of exchanging the anion by cationic surfactants, called CSMZ. CSMZ adsorbs all major classes of water contaminants (anions, cations, organics and pathogens), thus making it reliable for a variety of water treatment applications (Bowman, 2003). Nowadays, interest in the adsorption of anions and neutral molecules by surfactant modified zeolite has increased (Zhang et al., 2002). Modification of zeolite by surfactant is commonly done by cationic or amphoteric surfactants. By introducing surfactant to the zeolite, an organic layer is developed on the external surfaces and the charge is reversed to positive (Li et al., 1998). However, the present study used zeolite that had been modified using Uniquat (QAC-50) as cationic surfactant (CSMZ) and their performance towards the removal of color, COD, turbidity and iron ion from peat water were investigated.
Four adsorbents were used in these experiments which are natural zeolite, zeolite modified by cationic surfactant, activated carbon and limestone. All adsorbents were prepared with equivalent sizes of 1.18 mm – 2.00 mm. Hydrochloric acid (HCl) and sodium hydroxide (NaOH) were used for polishing zeolite during the preparation phase and for pH adjustment of the sample. Furthermore, potassium dichromate (K2CrO7), silver sulphate (Ag2SO4), sulphuric acid (H2SO4) and mercury (II) sulphate (HgSO4) were used as digestion solution reagents and acid reagents for COD analysis. Lastly, Uniquat (QAC-50) was used as cationic surfactant to modify the zeolite.
2.1 Preparation of Surfactant Modified Zeolite
In these studies, 100 g of prewashed natural zeolite was contacted with 5.6 ml/l Uniquat (QAC-50) as cationic surfactant (CSMZ). The mixture was then stirred at room temperature for 4 hours at 300 rpm (Karadag et al., 2007). The zeolite then was filtered and washed with distilled water several times. After that, the absorbent was dried in an oven at a temperature of 105 °C for 15 hours.
2.2 est Procedures
2.2.1 Batch Studies
Serial batch studies were conducted at room temperature (28 ± 1 °C) to investigate the influence of pH and dosage for removing colour, COD, turbidity and iron ion from peat water. Shaking speed of 200 rpm for 20 minutes were fixed and operated respectively. A working volume of 150ml peat water sample was set up in 250 ml conical flasks. Preceding the batch studies, initial concentration for those parameters was determined. The optimum pH and dosage of absorbent were determined. Subsequently, the percentage of removal was finally determined, plotted, and compared.
2.2.2 Batch Column Studies
Column studies were carried out using a plastic column with dimensions: 5.4 cm diameter and 48 cm length. Three adsorbents were filled inside the column at a specific depth with the supporting layers of marbles, cotton wool, and perforated net. Total volume of 2000 ml peat water was pumped in the up flow mode from the vessel into the column by using a Masterflex peristaltic pump at a minimum flow rate of (30, 60, 90) ml/min. In this study, however, column studies were performed un-continuously (batch) due to limitations of time. All parameters related to the column design are summarized in the following Table 1.
Table 1. Column studies parameters
|Horizontal Surface Area, A||cm2||
|Column volume, V||cm3||1099.3|
|Flowrate, Q||ml/min||30, 60, 90|
|Surface Loading Rate, SLR= Q/A||cm/min||1.31, 2.62, 3.93|
The serial sequence arrangements of adsorbents were conducted as shown in Figure 1 below. Effluent samples were collected at various time intervals, whilst maintaining room temperature, and analysed.
Figure 1. Schematic diagrams of lab-scale column studies
3. Results and Discussion
3.1 eat Water Characterization
Surface water originating from the peat swamp forest was taken from Beriah peat swamp river along the Kerian River on several occasions as the main sample. The characterization of peat water was carried out at the sampling point (in-situ measurement) using a multi-parameter probe as well as in the environmental laboratory of civil engineering, USM. Fundamentally, the characterization procedures were based on the Standard Methods for the Examination of Water and Wastewater (APHA, 1992). Table 2 represents the peat water characteristics in average value and the comparison to the standard drinking water quality in Malaysia.
Table 2. The characteristics of peat water sample from Beriah Peat Swamp Forest
|4.67 – 4.98|
Thirteen parameters were successfully determined where the first six parameters, including pH, temperature, TDS, DO, conductivity, and salinity were measured at the sampling point, whilst the rest of the parameters, including colour, turbidity, COD, iron ion, Ammoniacal Nitrogen, NH3-N, Ammonia (NH3), and Ammonium (NH4+) were examined from the sample brought to the environmental laboratory on the same day.
Acidic pH of the peat water was predicted due to the composition of the surrounding peat soil itself which had been formed by decaying material possessing humic substances (Rieley, 1992). Besides that, humic substances also lead to the high organic content as humic substances are comprised of numerous oxygen containing functional group and fractions (humic acid, fulvic acids and humin) with different molecular weights which mean yielding high concentration of turbidity and COD as well as coloured water (Torresday et al., 1996). Moreover, composition of peat soil may also have an impact on the iron ion concentration of peat water (Botero et al., 2010).
From the thirteen parameters, five parameters were indicated exceeding the standard limit. These parameters were pH, colour, turbidity, COD, and iron ion that showed values of 4.67 – 4.98, 224.7 TCU, 20.8 NTU, 33.3 mg/l, and
1.24 mg/l respectively while the standard limit of these parameters are 6.5 – 9.0, 15 TCU, 5 NTU, 10 mg/l, and 0.3 mg/l accordingly.
3.2 Effect of Initial pH on the Efficiency of Colour, COD, Turbidity, and Iron Ion (Fe) Removal
Influence of initial pH on the adsorption capacity for removing colour, COD, turbidity, and iron ion were investigated.
Figure 2(a) to Figure 2(d) below, displayed the percentage removal of colour, COD, turbidity, and iron ion against pH of adsorbents respectively.
Figure 2(a) shows the maximum removal percentage of colour that was removed by natural zeolite, CSMZ, and granular activated carbon (GAC) which were 79%, 90%, 82% respectively. This adsorption is depended on the characteristic of adsorbents itself. For zeolite and CSMZ were related to the amount of cationic ions (Al3+) increased, resulting in high reaction activity and GAC was related to the adsorption capacity. It was observed that the adsorption capacity was highly dependent on the pH of the solution, and indicated that the colour removal efficiencies decreased with the increase of solution pH.
The pH of the system exerts profound influence on the adsorptive uptake of adsorbate molecules presumably due to its influence on the surface properties of the adsorbent and ionization or dissociation of the adsorbate molecule. Figure 2(b) represents the percentage removal of natural zeolite and CSMZ where they reach optimum efficiency in removing organic compound (COD) at pH 2 with efficiency of 53% and 60% respectively. Meanwhile, the highest percentage removal of COD for GAC was achieved at pH 4 with efficiency obtained about 61%. Identical trends in colour removal were exhibited in percentage removal of COD for natural zeolite, CSMZ and GAC. In fact, this result also reveals that GAC has the highest percentage removal among natural zeolite and CSMZ yet optimum in difference pH solution. Neutralization mechanism occurs in low pH makes color removal, COD removal and Turbidity removals at pH 2 are higher for most of absorbents in this process.
In Figure 2(c), percentage turbidity removal against pH for each adsorbent revealed that optimal reduction of turbidity was obtained in an acidic environment with efficiency removal of 96%, 98%, 95% for natural zeolite, CSMZ, and GAC respectively. When the pH of the solution was adjusted above pH 6 to pH 12, the tendencies of all adsorption performances were gradually decreased. Moreover, it also showed that the lowest efficiency for the three adsorbents were identified at pH 12 with percentage values removal 55%, 61%, and 59% for natural zeolite, CSMZ, and GAC respectively.
Figure 2(d) demonstrates the removal efficiencies of iron ion as a function of the influent pH. The maximum removal of iron ion was observed at pH 8 for both natural zeolite and CSMZ whereas GAC had its optimum removal at pH 6. Natural zeolite and CSMZ only yielded 73% and 62% removal efficiency while GAC had more significant removal with removal efficiency of 80% to the iron ion concentration. Further, it is evident from the graph that gradual increment of removal efficiency for natural zeolite, CSMZ, and GAC occurred when the initial pH of the solution was increased to higher values. Somehow, at pH values greater than 6 the removal efficiency of GAC reduced slightly while for natural zeolite and CSMZ the reduction occurred from pH values above 8.
3.3 Effect of Adsorbent Dosage on the Efficiency of Colour, COD, Turbidity, and Iron Ion (Fe) Removal
The effect of adsorbent dosage was studied for all adsorbents employed on colour, COD, turbidity, and iron ion removal by varying the dosage of adsorbent and keeping all other experimental conditions constant. The pH was set to acidic conditions which were most favourable in obtaining the highest removal efficiency. In this study, to find optimal adsorbent dosage of natural zeolite and CSMZ, the appropriate experiments were carried out at adsorbent dosages in the range of 0.5 g to 5.0 g while for GAC, the adsorbent dosage was varied from 0.01 g to 4.0
- The experimental results for all the adsorbents are represented by Figure 3(a) to Figure 4(d).
Figure 3. Percentage of color (a), COD (b), turbidity (c), and Fe (d) removal against pH for NZ, and CSMZ
Figure 3(a) displays the relationship between the amount of adsorbent mass (dosage) and adsorption efficiency for natural zeolite and CSMZ in terms of removing colour. The colour removal of peat water increased from about 25% to 52% with increasing adsorbent dosage of natural zeolite from 0.5 g to 3.5 g whereas for CSMZ, removal percentage increased from 41% to 53% with increasing adsorbent dosage from 0.5 g to 2.0 g. However, further increase in adsorbent dosage to 5.0 g only led to slight degradation of removal efficiency to 50% and 41% for natural zeolite and CSMZ respectively. This degradation with further increases in adsorbent dosage was due to the unsaturated adsorption active sites during the adsorption process since the adsorbates in the vessel were only shaken for 20 minutes (insufficient time). Besides, modification of zeolite by cationic surfactant had proven to have better colour removal as presented in the graph.
Percentage removal of COD against the adsorbent dosage is shown in Figure 3(b). It was observed that the highest percentage removal for both natural zeolite and CSMZ to remove COD were 51% and 59%, achieved at adsorbent dosage 3.5 g and 2.0 g respectively.
The variations in removal of turbidity of peat water at various system pH are shown in Figure 3(c). The removal rate of turbidity was highest at the adsorbent dosage of 0.5 g with 70% and 93% removal efficiency for respective natural zeolite and CSMZ. The removal rate showed a smooth downward trend with the increase in adsorbent dosage. Concurrently, the adsorption capacity gradually decreased with the increasing adsorbent dosage. The least efficient removal of turbidity was noted at dosage 5.0 g with percentage removal recorded for natural zeolite and CSMZ only 57% and 70% respectively.
Figure 3(d) demonstrates the percentage iron ion removal of natural zeolite and CSMZ with respect to their dosage. The result shows that there was a significant difference trend in iron ion adsorption efficiencies between natural zeolite and CSMZ. For natural zeolite, it was shown that the removal percentage of iron ion had increased until it reached 1.0g of dosage with 72% of removal efficiency. On the other hands, CSMZ was only able to remove about 63% of iron ion when its dosage was increased to 2.5 g. The lowest percentage removals were 47% and 57% recognized at the adsorbent dosage 5.0 g for respective natural zeolite and CSMZ.
Figure 4. Percentage of color (a), COD (b), turbidity (c), and Fe (d) removal against dosage for GAC
The result illustrated in Figure 4(a) shows the maximum removal percentage of colour for GAC at 2.5 g dosage was 62%. Moderate increment in colour removal was identified along with the addition dosage of 2.5 g whilst abatement of removal efficiency began subsequently at adsorbent dosage of 3.0 g to 4.0 g.
The results from Figure 4(b) indicated that increasing the GAC dosage would increase the efficiency in removing COD respectively. The optimum dosage was recorded at 3.0 g with 72% of removal efficiency. Meanwhile, increasing the dosage above 3.0 g exhibited a slight decrease in removal efficiency with 67% to 61% for COD removal. A better result in removing COD was also shown by GAC compared to the natural zeolite and CSMZ.
The percentage of turbidity removed by GAC in different dosages is described in Figure 4(c). The highest removal was indicated at adsorbent dosage 2.5 g with removal efficiency of 70% while the minimum removal was 52% recorded at the adsorbent dosage 0.01 g. However, starting from adsorbent dosage of 3.0 to 4.0 g, removal efficiency began to decrease to 68%, 67%, and 69% respectively.
The result of percentage removal of iron ion by GAC in peat water is presented in Figure 4(d). It was found that the rate of removal was rapid in the initial dosage between 0.01 g to 3.0 g at which the removal efficiency increased from 28% to 71% accordingly. Subsequently, a few significant changes in the rate of removal were observed. Possibly, at the beginning, the solute molecules were absorbed by the exterior surface of adsorbent particles, so the adsorption rate was rapid. However, after the optimum dose was reached, the adsorption of the exterior surface becomes saturated and thereby the molecules will need to diffuse through the pores of the adsorbent into the interior surface of the particle (Ahmad & Hameed, 2009).
3.4 Batch Column Experiment
On the first running, the column was packed with natural zeolite (1st layer), limestone (2nd layer), and GAC (3rd layer) as shown in Figure 5(a). Removal efficiency for colour, COD, turbidity, and iron ion was recognized to be increased when the contact time was increased. At the time interval 1 hour to 6 hours, however, the increment was not so significant. The removal efficiency at 1 hour treatment was 39%, 21%, 54%, 36% while at 6 hours treatment was 77%, 65%, 73%, 60% recorded for respective colour, COD, turbidity, and iron ion. Poor removal efficiency at 1 hour treatment indicated that the required time to remove all parameters were insufficient. It is evident that if the adsorption process is allowed to run for 24 hours on the column, the removal efficiency shows notable removal. Percentage removals of colour, COD, turbidity, and iron ion at 24 hours were 83%, 72%, 76%, 65% respectively. Furthermore, the highest removal for respective colour, COD, turbidity, and iron ion were obtained at 48 hours treatment with 87%, 81%, 86%, and 79% of removal efficiency.
Figure 5. Percentage removal of color, COD, turbidity, and Fe for 1st run(a), 2nd run(b), and 3rd run (c) at flowrate 30 ml/min
On the second running, the column was packed with CSMZ (1st layer), limestone (2nd layer), and GAC (3rd layer) as presented in Figure 5(b). The removal percentages of colour, COD, turbidity, and iron ion were noticed after 1 hour to be 52%, 49%, 71%, and 30% respectively. The time of contact between adsorbate and adsorbent is proven to play an important role during the uptake of pollutants from peat water samples by adsorption process. In addition, the development of charge on the adsorbent surface was governed by contact time and hence the efficiency and feasibility of an adsorbent for its use in water pollution control can also be predicted by the time taken to attain its equilibrium (Sharma, 2003). Removal efficiency of 90% for colour, 81% for COD, 91% for turbidity, and 57% for iron ion were obtained at 24 hours of contact time.
On the third running, the column was packed with a difference sequence of CSMZ (1st layer), GAC (2nd layer), and limestone (3rd layer) demonstrated in Figure 5(c). It can be seen that the adsorption of these four parameters were slightly rapid at time interval 1 hour to 6 hours treatment. Further gradual increment with the prolongation of contact time form 24 hours to 48 hours has also occurred. Observation at 1 hour treatment recorded the removal efficiency of 62%, 58%, 87%, and 48% for respective colour, COD, turbidity, and iron ion. Whereby, 6 hours treatment had yielded higher removal percentage removal of 75%, 77%, 93%, and 58% respectively for colour, COD, turbidity, and iron ion. Further removal of colour, COD, turbidity, and iron ion was recorded when the treatment was run for 24 hours which exhibited 92%, 91%, 98%, 77% of removal efficiency respectively. Prolonged time to 48 hours indeed showed better removal of colour, COD, turbidity, iron ion with percentage removal of 95%, 100%, 99%, and 89% respectively. It can be seen that the arrangement of CSMZ, GAC, and limestone has the highest removal efficiency for all parameters at the flow rate influent of 30 ml/min.
Figure 6. Percentage removal of color, COD, turbidity, and Fe against contact time for 2nd run(a) at flow rate 60 mL/min and at flowrate 90 mL/min (b)
The experimental adsorption behaviour was further seen for its adsorption capacity during 60 ml/min and 90 ml/min flow rate. In addition, the flow rate adjustment had also resulted in differences in surface loading rate in which the sample going through the surface area of adsorbent bed (horizontal surface area, A= 22.9 cm2) for 30 ml/min equals to 1.31 cm/min while the flow rate of 60ml/min equals to 2.62 cm/min, and the flow rate of 90 ml/min equals to 3.93 cm/min. The percentage removal for both flow rate adjustments of CSMZ, GAC, and limestone arrangement were exhibited in Figure 6 (a) and Figure 6 (b). Based on these Figures, lower removal efficiencies were indicated at 1 hour time interval of 6 hours of contact time. The percentage removals for both 60 ml/min and 90 ml/min flow rate at 1 hour were 57%, 56%, 80%, 38% and 49%, 58%, 61%, 35% for colour, COD, turbidity, and iron ion respectively. Subsequently, when the contact time was at 6 hours, the removal percentage were 70%, 79%, 88%, 56%, and 60%, 77%, 70%, 47%. However, the maximum removal efficiency at 48 hours for both flow rates was not much different from the 30ml/min flow rate.
3.5 Adsorption Isotherm
In the present investigation, the experimental data were tested with respect to both Freundlich and Langmuir isotherms. Based on the linearized Freundlich isotherm models for natural zeolite, CSMZ, GAC in terms of adsorptive capacity to remove colour, COD, turbidity, and iron ion, the majority of them exhibited fits for all adsorbate with regression value (R2) above 0.6, except for iron ion and turbidity for respective CSMZ, and GAC. On the other hand, the linearized Langmuir isotherm models for natural zeolite, CSMZ, GAC in terms of adsorptive capacity to remove colour, COD, turbidity, and iron ion, had exhibited fits for all adsorbate with regression value (R2) was at range of 0.242 to 0.912. The Langmuir isotherm model for all adsorption mechanisms were identified to have smaller R2 values compared to the Freundlich isotherm model. Thereby, it can be concluded that the Freundlich isotherm model was more applicable in determining the adsorption mechanisms for this study.
3.6 Peat Water Quality Post Column Treatment
Peat water treatment in column with serial sequence of natural zeolite, CSMZ, and limestone had exhibited the highest removal with percentage removal at 48 hours at 95%, 100%, 99%, and 89% for colour, COD, turbidity, and iron ion respectively. Final readings at 48 hours treatment on pH, TDS, DO, conductivity, salinity, colour, turbidity, COD, and iron ion were 7.78, 74 mg/l, 4.03 mg/l, 137 uS/cm, 0.05 ppt, 12 TCU, 0.23 NTU, 0 mg/l, and 0.11 mg/l respectively (see Table 3). These findings, on the other hand, have indicated that peat water treatment had successfully produced water which satisfied the standard drinking water quality.
Table 3. The characteristics of results of peat water treatment from Beriah Peat Swamp Forest
Note: 1. *)Malaysian standard for drinking water quality;2. NA = Not analyzed.
From the results presented in this paper, the following conclusions can be drawn:
1) The optimum removal of colour, COD, and turbidity for all adsorbents were observed to occur during acidic conditions at pH range 2 – 4 whereas for iron ion, the maximum removal was noted at pH range 6 – 8.
2) At pH 2, CSMZ yielded the highest removal for colour and turbidity with removal efficiency of 90% and 98% respectively. Meanwhile, GAC has the highest percentage removal of COD at pH 4 with removal efficiency obtained about 61% while at pH 6, GAC exhibited the best removal of iron ion with percentage removal around 80%.
3) CSMZ revealed stronger adsorptive capacity for colour, COD, and turbidity compared to natural zeolite.
4) The optimal removal was achieved for the serial sequence of CSMZ (1st layer), GAC (2nd layer), and Limestone (3rd layer) with the adsorbent media at 30 ml/min of flow rate.
5) Freundlich isotherm was more reliable to describe the adsorption mechanisms of colour, COD, turbidity, and iron ion for natural zeolite, CSMZ, and GAC.
The authors wish to acknowledge the financial support from the School of Civil Engineering, Engineering Campus, Universiti Sains Malaysia and Universiti Sains Malaysia (Short Term Grant No. 304/PAWAM/60312015).
Ahmad, A. A., & Hameed, B. H. (2009). Reduction of COD and colour of dyeing effluent from a cotton textile mill by adsorption onto bamboo-based activated carbon. Journal of Hazardous Materials, 172, 1538-1543. http://dx.doi.org/10.1016/j.jhazmat.2009.08.025
American Public Health Association (APHA), AWWA, WPCF. (1992). Standard Methods for Examination of Water and Wastewater (16th ed.). Washington.
Bhatmagar, A., & Minocha, A. K. (2006). Conventional and non-conventional adsorbents for removal of pollutant from water – A review. In Indian Journal of Chemical Technology, 13, 203-217
Botero, W. G., Oliveira, L. C., Rocha, J. C., Rosa, H. R., & Santos, A. D. (2010). Peat humic substances enriched with nutrients for agricultural applications: competition between nutrients and non-essential meals present in tropical soils. Journal of Hazardous Materials, 177, 307-311.
Bowman, R. S. (2003). Applications of surfactant-modified zeolites to environmental remediation. Microporous Mesoporous Materials, 61, 43-56. http://dx.doi.org/10.1016/S1387-1811(03)00354-8
Chao, H. P., & Chen, S. H. (2012). Adsorption characteristics of both cationic and oxyanionic metal ions on hexadecyltrimethylammonium bromide-modified NaY zeolite. Chemical Engineering Journal, 193-194, 283-289. http://dx.doi.org/10.1016/j.cej.2012.04.059
Ćurković, L., Cerjan-Stefanović, Š., & Filipan, T. (1997). Metal ion exchange by natural and modified zeolites,
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Franceschi, M., Girou, A., Carro-Diaz, A. M., Maurette, M. T., & Puech-Coste, E. (2002), Optimisation of the coagulation–flocculation process of raw water by optimal design method. Water Research, 36(14), 3561-72.
Fu, F., & Wang, Q. (2011). Removal of heavy metal ions from wastewaters: A review. Journal of Environmental Management, 92, 407-418. http://dx.doi.org/10.1016/j.jenvman.2010.11.011
Hidaka, T., Hiroshi, T., & Kishimoto, N. (2003). Advanced treatment of sewage by pre-coagulation and biological filtration process. Water Research, 37(17), 4259-4269. http://dx.doi.org/10.1016/S0043-1354(03)00353-1
Huling, S. G., Robert, G. A., Raymond, A. S., & Matthew, R. M. (2001). Influence of Peat on Fenton Oxidation.
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Jamil, T. S., Ibrahim, H. S., Abd El-Maksoud, I. H., & El-Wakeel, S. T. (2010). Application of zeolite prepared from Egyptian kaolin for removal of heavy metals: I. Optimum conditions. Desalination, 258, 34-40. http://dx.doi.org/10.1016/j.desal.2010.03.052
Karadag, D., Akgul, E., Tok, S., Erturk, F., Arif Kaya, M., & Turan, M., (2007). Basic and reactive dye removal using natural and modified zeolite. Journal of Chemical Engineering Data, 52, 2436-2441. http://dx.doi.org/10.1021/je7003726
Liu, T., Chen, Zh. L., Yu, W. Z., Shen, J. M., & Gregory, J. (2011). Effect of two-stage coagulant addition on coagulation-ultrafiltration process for treatment of humic-rich water. Water Research, 45(14), 4260-4268. http://dx.doi.org/10.1016/j.watres.2011.05.037
Li, Zh. H., & Bowman, R. S. (2001). Regeneration of surfactant-modified zeolite after saturation with chromate and perchloroethylene. Water Research, 35(1), 322-326. http://dx.doi.org/10.1016/S0043-1354(00)00258-X
Li, Z. H., Jones, H. K., Robert, S., Bowman, & Helferich, H. (1999). Enhanced Reduction of Chromate and PCE by Pelletized Surfactant Modified Zeolite/Zerovalent Iron. Environmental Science and Technology, 33, 4326-4330. http://dx.doi.org/10.1021/es990334s
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Modern Applied Science; Vol. 7, No. 2; 2013
ISSN 1913-1844 E-ISSN 1913-1852
Published by Canadian Center of Science and Education
S. Syafalni1, Ismail Abustan1, Aderiza Brahmana1, Siti Nor Farhana Zakaria1 & Rohana Abdullah1
1 School of Civil Engineering, Engineering Campus, Universiti Sains Malaysia, Nibong Tebal, Penang, Malaysia. Correspondence: S. Syafalni, School of Civil Engineering, Engineering Campus, Universiti Sains Malaysia,
Nibong Tebal 14300, Penang, Malaysia. E-mail: email@example.com
Received: December 3, 2012 Accepted: January 14, 2013 Online Published: January 22, 2013 doi:10.5539/mas.v7n2p39 URL: http://dx.doi.org/10.5539/mas.v7n2p39
Shared via Creative Commons Attribution 3.0 Unported license
Tweet Myron L Meters Myron L Meters sells the most accurate, reliable conductivity instruments in the water treatment industry. You can find some of our most popular meters here: http://www.myronlmeters.com/SearchResults.asp?Search=conductivity&x=-1345&y=-145 Introduction Along with the development of more and more complex integrated models for urban water systems the need of sufficient data bases grows as well. […]
Myron L Meters
Myron L Meters sells the most accurate, reliable conductivity instruments in the water treatment industry. You can find some of our most popular meters here:
Along with the development of more and more complex integrated models for urban water systems the need of sufficient data bases grows as well. It is even complicated to measure relevant parameters,e.g. dissolved nitrogen or COD, for their use in Waste Water Treatment Plants and sewer models to describe the influence of catchments to the receiving water.
This poster presents a method regarding the possibility of substituting an online ammonia measurement by conductivity measurements in the inflow of a Waste Water Treatment Plant . The aim was the description of the dynamics in wet weather flow through storm water events for modelling purposes.
The conductivity of an aqueous solution is the measure of its ability to conduct electricity. Responsible for that phenomenon are ions of dissolved salts. In natural and drinking water these are mainly carbonates, chlorides and sulphates of calcium, magnesium, sodium and potassium. Conducted experiences and measurements in combined sewers showed a relation between conductivity in Waste Water Treatment Plant inflow and the concentration of dissolved components, e.g. ammonia, in case of rainfall events. The data for different 3 Waste Water Treatment Plant are shown in Figure 1. Rainwater has nearly no ions that cause conductivity to be measured. Therefore, diluted wastewater flowing into the Waste Water Treatment Plant can be detected by a conductivity probe. The measure and quality of linear regression between ammonia concentration and conductivity can be found in Table 1 for all data from Figure 1.
Material and Methods
With this knowledge a simple regression-based inflow model for use in activated sludge modelling of Waste Water Treatment Plant was defined to use conductivity beside available composite samples as a measure for dynamics in ammonia concentration as one of the most dynamic measure.
Results and Discussion
For one of the considered Waste Water Treatment Plants (WWTP) the resulting quality for the inflow model is shown in Figure 2 for a time series of a week.
Furthermore, the inflow model was used as a source for a retention tank model at the inlet of another Waste Water Treatment Plant to describe the impact of different management strategies (storage or flow through) on receiving water and Waste Water Treatment Plant (Figure 3).
A long-term modelling of 9 storm water events was used to show the predictive capacity of the model. The regression parameters were fitted by an optimisation routine to get best fit for all concentrations (also for COD, not presented here). Figure 3 shows the fit for all events. A good prediction of dynamics and absolute values for ammonia can be seen.
The results of different Goodness-of-fit measures are summarized in Table 2 for both presented WWTP inflows. Especially the values for the modified Coefficient of Efficiency, as a well-known and used measure for model quality in hydrological sciences, show the degree of predicting of the used method and the usability of conductivity for description of influent dynamics to Waste Water Treatment Plant in storm water cases.
This simple and easy-to-use method is well suited for implementation in Waste Water Treatment Plant models to describe the inflow dynamics regarding a more realistic behavior e.g. for optimization of process control.
by Markus Ahnert*, Norbert Günther*, Volker Kuehn*, University of Dresden
Ahnert, M., Blumensaat, F., Langergraber, G., Alex, J., Woerner, D., Frehmann, T., Halft, N., Hobus, I., Plattes, M., Spering, V. und Winkler, S. (2007), Goodness-of-fit measures for numerical modelling in urban water management – a summary to support practical applications., paper presented at 10th IWA Specialised Conference on “Design, Operation and Economics of Large Wastewater Treatment Plants”, 9-13 September 2007, Vienna, Austria, 9-13 September 2007.
Nash, J. E. und Sutcliffe, J. V. (1970), River flow forecasting through conceptual models part I – A discussion of principles, Journal of Hydrology, 10, 282.
TweetTDS meter Whether or not you’re a newcomer to hydroponic growing, keeping your hydroponic system’s nutrient solution properly balanced with a satisfactory nutrient concentration can be tough. Regular testing of one’s t solution is required if you want to keep the hydroponic system balanced and your plants healthy and growing. The simplest way to keep […]
Whether or not you’re a newcomer to hydroponic growing, keeping your hydroponic system’s nutrient solution properly balanced with a satisfactory nutrient concentration can be tough. Regular testing of one’s t solution is required if you want to keep the hydroponic system balanced and your plants healthy and growing. The simplest way to keep your nutrient solution balanced is via testing. You must check your solution’s pH level and nutrient concentration no less than every couple of days. To be able to try out your solution you need a few basic devices. You need to get a trusted pH tester and either an overall total Dissolved Solids (TDS) meter or perhaps a Conductivity (EC) meter.
It is generally agreed that the pH of one’s nutrient solution should be kept slightly acidic using a pH range of 5.5-6.0. You will find exceptions for this generalization. If you are unsure what are the best pH range is for the plants you might be growing, there are many resources open to guide you. You can find three basic means of testing pH. The least expensive technique is paper testing strips. They’re simple to use but could be difficult to learn. Typically the most popular testing way is liquid test kits. This method is extremely accurate and easier to see than paper testing strips but it is also more expensive. An electronic digital pH meter may be the last available option. Digital pH meters are available in various shapes, sizes, and price ranges. The benefit of an electronic pH meter is that it can be really user friendly, fast, and accurate. However, they are the most costly of the testing options, they can break easily, plus they has to be calibrated frequently if you’d like them to remain accurate.
Both conductivity meters and TDS meters are used to look at the strength, or concentration, of your hydroponic nutrient solution. Even though it is crucial that you know the concentration of your solution, this is because measurements ought to be used being a guideline only. EC meters will almost always be measured much the same way. Two sensors they fit within the solution being tested along with a little bit of electricity is emitted by one sensor and received by the other sensor. How well the electricity travels is then based on the EC meter. The harder electricity conducted, the greater the power of solids in the solution. A TDS meter uses the EC after which calculates the amount of solids inside the solution according to among three conversion factors. Considering that the TDS is dependant on a calculation, it really is only a quote of solids in the nutrient solution.
With this particular basic comprehension of the main difference between TDS and conductivity meters you can determine which measurement process is best for you. When you use a packaged nutrient solution, browse the product label to learn which kind of meter the maker recommends. In the event the manufacturer recommends a TDS, they’ll also inform you which conversion step to use as well as the recommended concentration range for his or her product. If you use a homemade nutrient solution plus a TDS meter, a great general guideline is to keep your TDS between 800 and 1200 ppm (ppm). If you work with an EC meter to test your homemade nutrient solution, a good range is 1.0 to 3.0 mS/cm (milisiemens per centimeter).
This information will help keep your hydroponics nutrient solution balanced and your plants healthy.
Myron L Meters has the perfect solution for hydroponics testing – the Ultrapen Combo.
ULTRACOMBO – ULTRAPEN PT1 Conductivity – TDS – Salinity pen & PT2 – pH – Temp Pen
List Price: $318.00
Exclusive Online Price: $280.50
Material Shared via Creative Commons Attribution-Share Alike 2.5 Croatia, original found here: http://blog.dnevnik.hr/nathanielwhite566668/2012/02/1629933596/tds-meter.html
Tweet WHY TEST FOUNTAIN SOLUTIONS? Accurate fountain (dampening) solution concentration control is essential for consistent, high-quality results in lithography. Low concentration can cause drying on the non-image area of the plate resulting in tinting, scumming, blanket piling, etc. High concentrations, on the other hand, bring about over-emulsification of the ink. This results in weakening of […]
WHY TEST FOUNTAIN SOLUTIONS?
Accurate fountain (dampening) solution concentration control is essential for consistent, high-quality results in lithography. Low concentration can cause drying on the non-image area of the plate resulting in tinting, scumming, blanket piling, etc. High concentrations, on the other hand, bring about over-emulsification of the ink. This results in weakening of color strength and changes in ink rheology (body and flow properties). Correct concentration will allow the non-image areas of the plate to be appropriately wetted.
WAYS TO TEST
Traditionally, pH was the test relied on to determine fountain solution concentration. Today, however, conductivity testing is recognized as a much more accurate method. Many modern dampening solutions are pH stabilized (or buffered), so only small changes in pH are seen even when dramatic changes occur in solution strength. Conductivity measurement is a fast and easy test which is more indicative of fountain solution concentration than pH. This is true for all neutral, alkaline, and many acid type solutions.
pH is still important, however, with unbuffered acid fountain solutions. Checking both conductivity and pH can provide valuable information. Acid fountain solution is a mixture of gum arabic, wetting agents, salts, acids, buffers, etc. Conductivity will tell you if the proper amount of most ingredients are present, but pH is necessary to check acid concentrations. pH will also determine how effective one ingredient, gum arabic, will be.
What is conductivity? Conductivity is the measurement of a solution’s ability to conduct an electrical current. It is usually expressed in microsiemens (micromhos). Absolutely pure water is actually a poor electrical conductor. It is the substances dissolved in water which determine how conductive the solution will be. Therefore, conductivity is an excellent indicator of solution strength.
To properly measure the conductivity of fountain solutions:
1. Test and write down the conductivity of the water used to prepare the solution.
- Mix the fountain solution concentrate with the water, using the manufacturer’s recommendations or as experience dictates.
- Measure the conductivity of the mixed solution.
- Subtract the water conductivity value obtained in step 1. This is necessary because tap water quality can change from day to day.
The resulting number is an accurate indicator of fountain solution strength. Caution: because alcohol will lower a solution’s conductivity, always test solution conductivity before and after the addition of alcohol.
Determining the best concentration of fountain solution is mostly “trial and error.” It can be very useful to make a graph, recording readings for every one-half or one ounce of concentrate added to a gallon of water. Record readings on a graph with the vertical axis representing conductivity values and the horizontal axis representing ounces/gallon. Such a graph will help “fine tune” your system during future press runs.
For “on the spot” fountain solution tests, Myron L handheld instruments are fast, accurate, and reliable. Measurements are made in seconds simply by pouring a small sample of solution into the instrument cell cup and pressing a button. Automatic temperature compensated accuracy and famous Myron L reliability have made our instruments popular in pressrooms worldwide.
Even though pH usually is not the best method to check the concentration of fountain solution, it is still very important and must be checked regularly. The pH of acid dampening solution affects sensitivity, plate-life, ink-drying, etc. Also, pH can change during a run if the paper has a high acid or alkaline content. pH, therefore, must be maintained at the proper level for good printing.
A convenient and accurate way to test pH (as well as temperature) is Myron L’s waterproof Ultrameter II™ Model 6PFCE or TechPro II™ TH1. The 6PFCE has a 100 reading memory and the TH1 has a 20 reading memory to store test results on site. The 6P also measures conductivity. All electrodes are contained in the cell cup for protection. Model M6/PH also measures pH and conductivity.
For continuous monitoring and/or control of fountain solution concentration, Myron L offers a complete series of in-line conductivity instruments. These economical, accurate, and reliable models use a remotely installed sensor and a panel/wall mount meter enclosure. Most contain an adjustable set point and heavy duty relay circuit which can be used to activate alarms, valves, feedpumps, etc. All models contain a 0-10 VDC output for a chart recorder or PLC (SCADA) input, if required, (4-20 mA output is also available).
The 750 Series II with dual set point option has become quite popular in pressrooms. The two set points allow a “safe zone” for controlling fountain solution concentration.
Ultrameter II 6PFCE, 512M5 and M6/PH are available with the useful LITHO-KIT™. This accessory includes a foam-lined, rugged all-plastic carry case with calibrating solutions and buffers. In addition, a syringe to simplify drawing samples and a thermometer for testing fountain solution temperature are also included.
|Improperly mixed fountain solution||Carefully follow manufacturer’s directions, checking both water and mixed solution with a conductivity instrument||Ultrameter 4PII, 6PIIFCE and 9PTK; ULTRAPEN PT1; and TechPro II TPH1 or TP1 all test 0-9999 ppm TDS or microsiemens conductivity, and temperature. 512M5 por- table DS Meter™ with a 0-5000 microsiemens conductivity range.|
|Halftones sharpen and highlight dots lost during run||Check pH of fountain solution to determine if it’s too acidic||Ultrameter 4PII, 6PIIFCE and 9PTK; ULTRAPEN PT2; and TechPro II TH1.M6/PH portable pDS Meter. Ranges: 0-5000 microsiemens and 2-12 pH.|
|Reverse osmosis water treatment system monitor indicates membrane failure||Test RO water quality and verify in-line instrument accuracy||Ultrameter 4PII, 6PIIFCE and 9PTK; ULTRAPEN PT1; and TechPro II TPH1 or TP1 all test 0-9999 ppm TDS or microsiemens conductivity, and temperature.|
|Scum streaks across plate after 10,000 – 20,000impressions||Check acid/gum levels infountain solution||Ultrameter 6PIIFCE and 9PTK; ULTRAPEN PT2; and TechPro II TH1.M6/PH portable pDS Meter. Ranges: 0-5000 microsiemens and 2-12 pH.|
|Personnel unable to test fountain solution concentration||Continuously control fountain solution with conductivity Monitor/controller||758II-123 (0-5000 µS) in-lineMonitor/controller.|
You can save 10% on any recommended meter at MyronLMeters.com.
TweetSustainability in Water Supply Sustainable water systems should provide adequate water quantity and appropriate water quality for a given need, without compromising the future ability to provide this capacity and quality. Water systems in the realm of sustainable development may not literally include the use of water, but include systems where the use of water […]
Sustainability in Water Supply
Sustainable water systems should provide adequate water quantity and appropriate water quality for a given need, without compromising the future ability to provide this capacity and quality. Water systems in the realm of sustainable development may not literally include the use of water, but include systems where the use of water has traditionally been required. Examples include waterless toilets and waterless car washes, whose use helps to alleviate water stress and secure a sustainable water supply.
Accessing the sustainability features in water supply, that is to say, the three-fold goals of economic feasibility, social responsibility and environmental integrity, is linked to the purpose of water use. Sometimes, these purposes compete when resources are limited; for example, water needed to meet the demands of an increasingly urban population and those needs of rural agriculture. Water is used (1) for drinking as a survival necessity, (2) in industrial operations (energy production, manufacturing of goods, etc.), (3) domestic applications (cooking, cleaning, bathing, sanitation), and (4) agriculture. Sustainable water supply is a component of integrated water resource management, the practice of bringing together multiple stakeholders with various viewpoints in order to determine how water should best be managed. In order to decide if a water system is sustainable, various economical, social and ecological considerations must be considered.
Surface freshwater is unfortunately limited and unequally distributed in the world. Almost 50% of the world’s lakes are located in Canada alone (UNEP, 2002). In addition, pollution from various activities leads to surface water that is not drinking quality. Therefore, treatment systems (either large scale or at the household level) must be put in place.
Structures such as dams may be used to impound water for consumption. Dams can be used for power generation, water supply, irrigation, flood prevention, water diversion, navigation, etc. If properly designed and constructed, dams can help provide a sustainable water supply. The design should consider peak flood flows (historical and projected for climate change), earthquake faults, soil permeability, slope stability and erosion, silting, wetlands, water table, human impacts, ecological impacts (including wildlife), compensation for resettlement, and other site characteristics. There are various challenges that large-scale dam projects may present to sustainability: negative environmental impacts on wildlife habitats, fish migration, water flow and quality, and socioeconomic impacts resulting from resettled local communities. A sustainability impact assessment should therefore be performed to determine the environmental, economic and social consequences of the construction.
Groundwater accounts for greater than 50% of global freshwater; thus, it is critical for potable water (Lozan et al, 2007). Groundwater can be a sustainable water supply source if the total amount of water entering, leaving, and being stored in the system is conserved. There are three main factors which determine the source and amount of water flowing through a groundwater system: precipitation, location of streams and other surface-water bodies, and evapotranspiration rate; it is thus not possible to generalize a sustainable withdrawal or pumping rate for groundwater (USGS, 1999). Unsustainable groundwater use results in water-level decline, reduced streamflow, and low water quality, jeopardizing the livelihood of effected communities. Various practices of sustainable groundwater supply include changing rates or spatial patterns of ground-water pumpage, increasing recharge to the ground-water system, decreasing discharge from the groundwater system, and changing the volume of groundwater in storage at different time scales (USGS, 1999). A long-term vision is necessary when extracting groundwater since the effects of its development can take years before becoming apparent. It is important to integrate groundwater supply within adequate land planning and sustainable urban drainage systems.
Collecting water from precipitation is one of the most sustainable sources of water supply since it has inherent barriers to the risk of over-exploitation found in surface and groundwater sources, and directly provides drinking water quality. However, rainwater harvesting systems must be properly designed and maintained in order to collect water efficiently, prevent contamination and use sustainable treatment systems in case the water is contaminated. A number of drinking water treatments exist at point-of-use, each with advantages and disadvantages. These include solar treatment, boiling, using filters, chlorination, combined methods such as filtration and chlorination, flocculation and chlorination. Although technically given the Earth’s surface and precipitation, rainwater harvesting can meet global water demand, the solution can most practically be a supplement to sustainable water supply systems given a level of uncertainty (especially with climate change), and competing land-use applications.
Reclaimed water, or water recycled from human use, can also be a sustainable source of water supply. It is an important solution to reduce stress on primary water resources such as surface and groundwater. There are both centralized and decentralized systems which include greywater recycling systems and the use of microporous membranes. Reclaimed water must be treated to provide the appropriate quality for a given application (irrigation, industry use, etc.). It is often most efficient to separate greywater from blackwater, thereby using the two water streams for different uses. Greywater comes from domestic activities such as washing, whereas blackwater contains human waste. The characteristics of the two wastestreams thus differ.
Desalinisation has the potential to provide an adequate water quantity to those regions that are freshwater poor, including small island states. However, the energy demands of reverse osmosis, a widely-used procedure used to remove salt from water, are a challenge to the adaptation of this technology as a sustainable one. The costs of desalination average around 0.81 USD per cubic meter compared to roughly 0.16 USD per cubic meter from other supply sources (USGS, 2010). If desalination can be provided with renewable energies and efficient technologies, the sustainable features of this supply source would increase. Currently, desalination increases operational costs because of the needed energy (and also carbon dioxide emissions); this in turn raises the cost of the final product. In addition, desalination plants can have negative impacts on marine life, and cause water pollution due to the chemicals used to treat water and the discharge of brine.
Bottled water is a 21st century phenomenon whereby mostly private companies provide potable water in a bottle for a cost. In some areas, bottled water is the only reliable source of safe drinking water. However, often in these same locations, the cost is prohibitively expensive for the local population to use in a sustainable manner. Bottled water is not considered an “improved drinking water source” when it is the only potable source available (UN, 2010). When sustainability metrics are used to access bottled water, it falls short in many situations of being a sustainable water supply. Economic costs, pollution associated with its manufacturing (plastic, energy, etc.) and transportation, as well as extra water use, makes bottled water an unsustainable water supply system for many regions and for many brands. It takes 3-4 liters of water to make less than 1 liter of bottled water (Pacific Institute, 2008).
Potable water requires some of the strictest standards of quality in terms of bacteriological and chemical pollutants. These standards are often governed by national governments; international recommendations can be found from the World Health Organization (http://www.who.int/water_sanitation_health/dwq/guidelines/en/index.html). Drinking water must be freshwater and should be free of pathogens and free of harmful chemicals.
Water in Industry
Water is used in just about every industry. Industrial water withdrawls represent 22% of total global water use (significant regional differences). Its use is notable for manufacturing, processing, washing, diluting, cooling, transporting substances, sanitation needs within a facility, incorporating water into a final product, etc. (USGS, 2010). The food, paper, chemicals, refined petroleum, and primary metal industries use large amounts of water (USGS, 2010). A sustainable water supply in industry involves limiting water use through efficient appliances and methods adapted to the particular industry. Rainwater harvesting on-site (including the creation of large pond-like structures), as well as recycling water in industrial processes, can provide a sustainable water supply for industry without straining municipal water supplies. Industry releases organic water pollutants, heavy metals, solvents, toxic sludge, and other wastes into water supply sources. Industry thus has a dual responsibility for internal sustainable water supply and the protection of external water supply sources.
Water in Agriculture
Agriculture uses the largest amount of freshwater on a global scale. It represents roughly 70% of all water withdrawal worldwide, with various regional differences. In the United States, for example, agriculture accounts for over 80% of water consumption (USDA, 2010). The productivity of irrigated land is approximately three times greater than that of rain-fed land (FAO, 2010). Thus, irrigation is an important factor for sustainable agriculture systems. In addition, global food production is expected to increase by 60% from 2000 to 2030, creating a 14% increase in water demand for irrigation (UN, 2005). Agriculture is also responsible for some of the surface and groundwater degradation because of run-off (chemical and erosion-based). It thus has a dual role in sustainable water supply: (1) using water efficiently for irrigation and (2) protecting surface and groundwater supply sources. Techniques for sustainable water supply in agriculture include organic farming practices which limit substances that would contaminate water, efficient water delivery, micro-irrigation systems, adapted water lifting technologies, zero tillage, rainwater harvesting, runoff farming, and drip irrigation (efficient method that allows water to drip slowly to plant roots by using pipes, valves, tubes and emitters).
Domestic Water Uses
The average household needs an estimated 20-50 liters of water per person per day, depending on various assumptions and practices (Gleick, 1996). Reducing water use through waterless toilets, water efficient appliances, and water quantity monitoring, is an important part of sustainability for domestic water supply. Efficient piping systems that are leak-free and well insulated provide a network that is reliable and help to limit water waste. The aforementioned potable water supply sources, with their sustainability features and sustainability challenges, are all relevant to other domestic uses. Since water quality standards are not as strict for household uses as for drinking, there is more flexibility when considering sustainable domestic water supply (including the potential for reclaimed water use).
A water supply system will be sustainable only if it promotes efficiencies in both the supply and the demand sides. Initiatives to meet demand for water supply will be sustainable if they prioritize measures to avoid water waste. Avoiding wastage will contribute to reducing water consumption and, consequently, to delaying the need for new resources.
On the supply side, it is fundamental to enhance operation and maintenance capabilities of water utilities, reducing non-revenue water (NRW), leakages, and energy use, as well as improving the capacity of the workforce to understand and operate the system. It is also necessary to ensure cost-recovery through a fair tariff system and “intelligent” investment planning. In addition, all alternatives to increase the water supply must be analysed considering the entire life cycle.
On the demand side, the adoption of water efficient technology can considerably reduce water consumption. Investments in less water intensive industrial processes and more efficient buildings lead to a more sustainable water supply. Concrete possibilities of economic savings, social benefits (such as the involvement of different sectors of society to reach a common objective, environmental awareness of the population, etc.) and a range of environmental gains make the adoption of water efficient technologies viable.
Sustainable water supply involves a sequence of combined actions and not isolated strategies. It depends on the individual’s willingness to save water, governmental regulations, changes in the building industry, industrial processes reformulation, land occupation, etc. The challenge is to create mechanisms of regulation, incentives and affordability to ensure the sustainability of the system.
Food and Agriculture Organization of the United Nations (FAO). (2010). Water Use in Agriculture. Retrieved from http://www.fao.org/ag/magazine/0511sp2.htm
Gleick, Peter H. (1996). Basic Water Requirements for Human Activities: Meeting Basic Needs.” Water International 21, 2: 83-92.
US Geological Survey. (2010). Industrial Water Use. Retrieved from http://ga.water.usgs.gov/edu/wuin.html
United States Department of Agriculture. (2010). Irrigation and Water Use. Retrieved from http://www.ers.usda.gov/Briefing/WaterUse/
Lozan, Grassl, et al. (2007). The water problem of our Earth: From climate and the water cycle to the human right for water.
UN Water for Life Decade. (2005). United Nations Department of Public Information (32948—DPI/2378—September 2005—10M).
UNEP. (2002). Vital Water Graphics: An Overview of the State of the World’s Fresh and Marine Waters. Retrieved from http://www.unep.org/dewa/assessments/ecosystems/water/vitalwater/.
Pacific Institute. Water Content of Things. The World’s Water 2008-2009.
United Nations (WHO and UNICEF). (2010). Progress on Sanitation and Drinking Water Update 2010. Retrieved from http://www.unicef.org/media/files/JMP-2010Final.pdf.
USGS. (2010). Thirsty? How ’bout a cool, refreshing cup of seawater? Retrieved from http://ga.water.usgs.gov/edu/drinkseawater.html.
USGS. (1999). Sustainability of Ground-Water Resources. Retrieved from http://pubs.usgs.gov/circ/circ1186/pdf/circ1186.pdf.
Waite, Marilyn. (2010). Sustainable Water Resources in the Built Environment. IWA Publishing: London.
Many of the issues in this article are covered in the book, Sustainable Water Resources in the Built Environment, published in 2010, written by Marilyn Waite.
Sustainable Water Resources in the Built Environment covers elements of water engineering and policy making in the sustainable construction of buildings with a focus on case studies from Panama and Kenya. It provides comprehensive information based on case studies, experimental data, interviews, and in-depth research.
The book focuses on the water aspects of sustainable construction in less economically developed environments. It covers the importance of sustainable construction in developing country contexts with particular reference to what is meant by the water and wastewater aspects of sustainable buildings, the layout, climate, and culture of sites, the water quality tests performed and results obtained, the design of rainwater harvesting systems and policy considerations.
The book is a useful resource for practitioners in the field working on the water aspects of sustainable construction (international aid agencies, engineering firms working in developing contexts, intergovernmental organizations and NGOs). It is also useful as a text for water and sanitation practices in developing countries.
Technology and Equipment for Water Loss Management – Malcolm Farley, Bambos Charalambous and Stuart Hamilton
Publication Date: Dec 2013 – ISBN – 9781843390862
Best Practice Guide on the Control of Arsenic in Drinking Water
Publication Date: Aug 2013 – ISBN – 9781843393856
Management of Change in Water Companies – Joaquim Pocas Martins
Publication Date: Jun 2013 – ISBN – 9781843391951
Arsenic in Groundwater: Poisoning and Risk Assessment – M. Manzurul Hassan, Peter J. Atkins
Publication Date: Apr 2013 – ISBN – 9781780400204
Microbial Growth in Drinking Water Distribution Systems – Dirk van der Kooij and Paul W.J.J. van der Wielen
Publication Date: Feb 2013 – ISBN – 9781780400402
Arsenic Contamination in the World – Susan Murcott
Publication Date: Oct 2012 – ISBN – 9781780400389
Internal Corrosion Control of Water Supply Systems – Colin Hayes
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Managing Climate Risk in Water Supply Systems – Casey Brown and M. Neil Ward
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TweetContent Table Recent Papers in Adsorption and Ion Exchange Processes Magnetic ion exchange resin treatment for drinking water production Removal of radiocobalt from EDTA-complexes using oxidation and selective ion exchange Ammonium removal from anaerobic digester effluent by ion exchange A hybrid ion exchange-nanofiltration (HIX-NF) process for energy efficient desalination of brackish/seawater Adsorption kinetics and isotherm […]
- Recent Papers in Adsorption and Ion Exchange Processes
- Magnetic ion exchange resin treatment for drinking water production
- Removal of radiocobalt from EDTA-complexes using oxidation and selective ion exchange
- Ammonium removal from anaerobic digester effluent by ion exchange
- A hybrid ion exchange-nanofiltration (HIX-NF) process for energy efficient desalination of brackish/seawater
- Adsorption kinetics and isotherm characteristics of selected endocrine disrupting compounds on activated carbon in natural waters
- Influence of hybrid coagulation-ultrafiltration pretreatment on trace organics adsorption in drinking water treatment
- Phosphorus adsorption on water treatment residual solids
- Influence of surface chemistry and structure of activated carbon on adsorption of fulvic acids from water solution
- Synthesis of carboxylated chitosan and its adsorption properties for cadmium (II), lead (II) and copper (II) from aqueous solutions
- Competitive adsorption of heavy metals in soil underlying an infiltration facility installed in an urban area
Magnetic ion exchange resin treatment for drinking water production
Journal of Water Supply: Research and Technology—AQUA Vol 58 No 1 pp 41–50 © IWA Publishing 2009 doi:10.2166/aqua.2009.081
B. Sani, E. Basile, L. Rossi and C. Lubello
Department of Civil and Environmental Engineering, University of Florence, Via S. Marta 3, I-50139, Florence, Italy Tel.: +39 55 479 6317 E-mail: firstname.lastname@example.org
Publiacqua SpA, Via Villamagna 39, I-50126, Florence, Italy
Italian drinking water treatment plants (DWTP) generally use chlorine-based chemicals to achieve the oxidation/disinfection phases of their treatment trains. The main problem related to the application of such disinfectants consists in the formation of disinfection by-products (DBPs) as a result of the reaction with organic substances in the water. Italian regulations set very strict limits for the maximum concentration of chlorine DBPs and, for many DWTPs, the compliance with such a regulation is difficult. Non-oxidative pre-treatments, able to remove organic substances from the water prior to chlorination, could be a suitable solution to overcome this problem. These treatments could increase the water quality, decrease the oxidant demand and, hence, reduce the formation of DBPs. This paper presents an experimental investigation of ion exchange processes for the dissolved organic carbon (DOC) removal by using MIEX® resin. The process was studied as a pre-treatment on raw river water. The DOC removal efficiency and the effects on downstream processes of the treatment train were evaluated.
Removal of radiocobalt from EDTA-complexes using oxidation and selective ion exchange
Water Science & Technology—WST Vol 60 No 4 pp 1097–1101 © IWA Publishing 2009 doi:10.2166/wst.2009.458
org.xwiki.gwt.dom.client.Element#placeholderhttp://www.iwaponline.com/wst/06004/wst060041097.htm“>Link to Summary Page
L. K. Malinen, R. Koivula and R. Harjula
Laboratory of Radiochemistry, Department of Chemistry, University of Helsinki, P.O. Box 55 (A. I. Virtasen aukio 1), FI-00014, Finland E-mail: email@example.com; firstname.lastname@example.org; email@example.com
Methods for the removal of radiocobalt from an ethylenediaminetetraacetic acid (EDTA) complex of Co(II) (aqueous solution containing 10 mM Co(II) and 10 mM or 50 mM EDTA traced with 57Co) are presented. The studies examined a combination of different oxidation methods and the sorption of 57Co on a selective inorganic ion exchange material, CoTreat. The oxidation methods used were ultraviolet (UV) irradiation with and without hydrogen peroxide (H2O2), as well as ozonation alone or in combination with UV irradiation. Also, the possible contribution of Degussa P25 TiO2 photocatalyst to degradation of EDTA was studied. The best results for the equimolar solution of Co(II) and EDTA were achieved by combining ozonation, UV irradiation, Degussa P25 TiO2 and CoTreat, with approximately 94% sorption of 57Co. High values for the 57Co sorption were also achieved by ozonation (~88%) and UV irradiation (~90%) in the presence of CoTreat and Degussa P25 TiO2. A surplus of EDTA over Co(II) was also tested using 10 mM Co(II) and 50mM EDTA. Only a slight decrease, to ~88% sorption of 57Co, was detected compared to the value (~90%) obtained with 10 mM EDTA.
Ammonium removal from anaerobic digester effluent by ion exchange
Water Science & Technology—WST Vol 60 No 1 pp 201–210 © IWA Publishing 2009 doi:10.2166/wst.2009.317
T. Wirthensohn, F. Waeger, L. Jelinek and W. Fuchs
Department of IFA-Tulln, Institute for Environmental Biotechnology, University of Natural Resources and Applied Life Sciences—Vienna, Konrad Lorenz Strasse 20, 3430 Tulln, Austria E-mail: firstname.lastname@example.org; email@example.com; firstname.lastname@example.org
Department of Power Engineering, Faculty of Environmental Technology, Institute of Chemical Technology, Technicka 5, 166 28 Prague 6, Czech Republic E-mail: Ludek.Jelinek@vscht.cz
The effluent of a 500 kW biogas plant is treated with a solid separation, a micro filtration and a reverse osmosis to achieve nutrient recovery and an effluent quality which should meet disposal quality into public water bodies. After the reverse osmosis, the ammonium concentration is still high (NH4-N = 467 mg/l), amongst other cations (K+=85 mg/l; Na+=67 mg/l; Mg2 + =0.74 mg/l; Ca2 + =1.79 mg/l). The aim of this study was to remove this ammonium by ion exchange. Acidic gel cation exchange resins and clinoptilolite were tested in column experiments to evaluate their capacity, flow rates and pH. Amberjet 1,500 H was the most efficient resin, 57 BV of the substrate could be treated, 1.97 mol NH4-N/l resin were removed. The ammonium removal was more than 99% and the quality of the effluent was very satisfactory (NH4-N < 2 mg/l). The breakthrough of the observed parameters happened suddenly, the order was sodium—pH—ammonium—potassium. The sharp increase of the pH facilitates the online control, while the change in conductivity is less significant. A regeneration with 3 bed volumes of 2 M HCl recovered 91.7% of the original cation exchange capacity.
A hybrid ion exchange-nanofiltration (HIX-NF) process for energy efficient desalination of brackish/seawater
Water Science & Technology: Water Supply—WSTWS Vol 9 No 4 pp 369–377 © IWA Publishing 2009 doi:10.2166/ws.2009.634
S. Sarkar and A. K. SenGupta
Department of Civil and Environmental Engineering, Lehigh University, Fritz Engineering Laboratory, 13 E Packer Avenue, Bethlehem PA, 18015, USA E-mail: email@example.com;firstname.lastname@example.org
This study reports a new hybrid ion exchange-nanofiltration (HIX-NF) process for desalination of sea and brackish water that can attain significant energy economy over the conventional membrane-based pressure driven processes. In this hybrid process, an ion exchange step converts monovalent chloride ions of saline water to divalent sulfate ions and the resulting solution, having a reduced osmotic pressure than the feed, is desalinated using a nanofiltration (NF) membrane. The sulfate rich reject stream from the NF process is used to regenerate the anion exchanger. Results validate that NF membranes can desalinate sodium sulfate solution at a much lower transmembrane pressure compared to RO membranes as well as yield a higher permeate flux. The sulfate-chloride selectivity of the anion exchangers plays important role in sustainability of the process. Laboratory studies have revealed that a single type of anion exchanger cannot sustain the process for saline water with different salt concentrations. However, anion exchangers with different sizes of amine functional groups (e.g. quaternary-, tertiary-, secondary- and primary amine) hold the promise that the process can be tailored to achieve sustainability. Laboratory studies have validated the basic premise of the hybrid process including greater than two times less energy requirement than RO process for the same feed water and same permeate recovery condition.
Adsorption kinetics and isotherm characteristics of selected endocrine disrupting compounds on activated carbon in natural waters
Water Science & Technology: Water Supply—WSTWS Vol 9 No 1 pp 51–58 © IWA Publishing 2009 doi:10.2166/ws.2009.063
A. Assoumani, L. Favier-Teodorescu and D. Wolbert
Ecole Nationale Supérieure de Chimie de Rennes,CNRS, UMR 6226, Avenue du Général Leclerc, CS 50837, 35700, Rennes Cedex 4, France E-mail: email@example.com
Bisphenol A (BPA) and ethynylestradiol (EE2), two representative endocrine disrupting compounds (EDCs), were tested for their adsorbabilities onto two powdered activated carbons (PACs). The main aim of the study was to create a prediction tool for the determination of the EDCs adsorbabilities at low ng.L-1 level. Single solute solution adsorption isotherms at high concentrations, for prediction purposes, and low concentrations, for verification of the prediction, were performed for one EDC/PAC couple. Over the whole range of concentration, results showed that the Langmuir-Freundlich model better suits the adsorption phenomenon than the Freundlich or Langmuir model. Kinetics experiments were carried out on the same EDC/PAC couple. HSDM modelling of single solute adsorption kinetics at high concentration allowed determining the kinetic coefficients kf and Ds; both were shown to dominate the mass transfer mechanism. Competitive adsorption isotherms at high and low concentrations showed that downward extrapolation of low concentration adsorption capacities from solely high concentration information results in acceptable error compared to the total range isotherm. The IAST-EBC approach combined with the Langmuir-Freundlich single solute model, for the target compound, and the Langmuir model, for the EBC, appears as an acceptable global model.
Influence of hybrid coagulation-ultrafiltration pretreatment on trace organics adsorption in drinking water treatment
Journal of Water Supply: Research and Technology—AQUA Vol 58 No 3 pp 170–180 © IWA Publishing 2009 doi:10.2166/aqua.2009.071
S. Müller and W. Uhl
Institute of Urban Water Management (ISI), Chair of Water Supply Engineering, Technische Universität Dresden, Dresden, 01062, Germany Tel.: +49-(0)351-46333126 Fax: +49-(0)351-46337204 E-mail: firstname.lastname@example.org
The treatment of raw water by hybrid coagulation-ultrafiltration was investigated. Coagulation-ultrafiltration removed high molecular weight organics, preferentially humics. Adsorption of the trace compound cis-1,2-dichloroethene, present in raw water, on granular activated carbon was improved considerably as compounds competing for adsorption space had been removed. This was shown in isotherms and breakthrough curves. Aeration during filtration did not affect membrane performance as expressed in permeability. However, aeration in the submerged membrane container resulted in a release of organic matter from the flocs, which resulted in higher concentrations of dissolved organic carbon in the filtrate.
Phosphorus adsorption on water treatment residual solids
Journal of Water Supply: Research and Technology—AQUA Vol 58 No 1 pp 1–10 © IWA Publishing 2009 doi:10.2166/aqua.2009.017
Meaghan K. Gibbons, Md. Maruf Mortula and Graham A. Gagnon
Department of Civil and Resource Engineering, Dalhousie University, Halifax, Nova Scotia, B3J 1X1, Canada Tel.: +1 902 494 3268 Fax:+1 902 494 3108 E-mail: email@example.com
Department of Civil Engineering, American University of Sharjah, Sharjah, PO Box, 26666, UAE
The treatment and disposal of water treatment plant residual solids has become an increasingly important environmental priority for drinking water utilities. This study examines water treatment residual solids (WTRSs) from four North American water treatment plants to determine the role that coagulant types play in phosphate adsorption by the residual solids. In total, two alum residual solids (one solid from a plant that has a raw water with low alkalinity and one solid from a plant that has a raw water with high alkalinity), one lime residual solid and one ferric residual solid were used in batch adsorption experiments with deionized water at a pH of 6.2±0.2 and secondary municipal wastewater effluent at a pH of 6.8. Langmuir isotherm modeling showed that ferric residuals had the highest adsorptive capacity for phosphate (Qmax=2,960 mg/kg), followed by lime (Qmax=1,390 mg/kg) and alum (Qmax=1,110 mg/kg and 1,030 mg/kg) for adsorption experiments with P-spiked deionized water. Of the two alum residuals, the residual with a higher weight percent of metal oxides had a higher adsorptive capacity. The ferric residuals were less affected by competing species in the wastewater effluent, while the lime and alum residuals had a higher rate of phosphate removal from the deionized water compared to the wastewater effluent. Overall, ferric water treatment residuals were the best adsorbent for phosphate adsorption, followed by lime and alum residuals.
Influence of surface chemistry and structure of activated carbon on adsorption of fulvic acids from water solution
Water Science & Technology—WST Vol 60 No 2 pp 441–447 © IWA Publishing 2009 doi:10.2166/wst.2009.344
L. A. Savchyna, I. P. Kozyatnyk, T. V. Poliakova and N. A. Klymenko
Institute of Colloid Chemistry and Chemistry of Water, Ukrainian National Academy of Sciences, 42 Vernadsky Avenue, Kiev 03680, Ukraine E-mail: firstname.lastname@example.org
The adsorption of fulvic acids (FA) from aqueous solutions on activated carbon (AC) with different characteristics of surface chemical state has been investigated. To characterize the adsorbability of FA with complex fractional composition, a method of estimation of modified Freundlich equation constants was employed, and “conventional component” was used to evaluate the change in Gibbs free adsorption energy. It has been shown that change in activated carbon surface energy in-homogeneity due to oxidation leads mainly to a decrease in the adsorption energy of fulvic acids and to an increase of the concentration range of the conventional portion of the low adsorbable fraction. Decrease in the adsorption energy of organic substrate may result in higher degree of spontaneous bioregeneration of activated carbon and hence in its longer life in the processes of FA solutions filtration.
Synthesis of carboxylated chitosan and its adsorption properties for cadmium (II), lead (II) and copper (II) from aqueous solutions
Water Science & Technology—WST Vol 60 No 2 pp 467–474 © IWA Publishing 2009 doi:10.2166/wst.2009.369
K. L. Lv, Y. L. Du and C. M. Wang
Department of Chemistry, Lanzhou University, Lanzhou 730000, China E-mail: email@example.com
Carboxylated chitosan (CKCTS) was prepared for the removal of Cd(II), Pb(II), and Cu(II) from aqueous solutions. The effects of experimental parameters such as pH value, initial concentration, contact time and temperature on the adsorption were studied. From the results we can see that the adsorption capacities of Cd(II), Pb(II), and Cu(II) increase with increasing pH of the solution. The kinetic rates were best fitted to the pseudo-second-order model. The adsorption equilibrium data were fitted well with the Langmuir isotherm, which revealed that the maximum adsorption capacities for monolayer saturation of Cd(II), Pb(II), and Cu(II) were 0.555, 0.733 and 0.827 mmol/g, respectively. The adsorption was an exothermic process.
Competitive adsorption of heavy metals in soil underlying an infiltration facility installed in an urban area
Water Science & Technology—WST Vol 59 No 2 pp 303–310 © IWA Publishing 2009 doi:10.2166/wst.2009.865
M. A. Hossain, H. Furumai and F. Nakajima
Institute of Water and Flood Management, Bangladesh University of Engineering and Technology, Dhaka, 1000, Bangladesh E-mail: firstname.lastname@example.org; email@example.com
Research Center for Water Environment Technology, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan E-mail: firstname.lastname@example.org
Environmental Science Center, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan E-mail- email@example.com
Accumulation of heavy metals at elevated concentration and potential of considerable amount of the accumulated heavy metals to reach the soil system was observed from earlier studies in soakaways sediments within an infiltration facility in Tokyo, Japan. In order to understand the competitive adsorption behaviour of heavy metals Zn, Ni and Cu in soil, competitive batch adsorption experiments were carried out using single metal and binary metal combinations on soil samples representative of underlying soil and surface soil at the site. Speciation analysis of the adsorbed metals was carried out through BCR sequential extraction method. Among the metals, Cu was not affected by competition while Zn and Ni were affected by competition of coexisting metals. The parameters of fitted ‘Freundlich’ and ‘Langmuir’ isotherms indicated more intense competition in underlying soil compared to surface soil for adsorption of Zn and Ni. The speciation of adsorbed metals revealed less selectivity of Zn and Ni to soil organic matter, while dominance of organic bound fraction was observed for Cu, especially in organic rich surface soil. Compared to underlying soil, the surface soil is expected to provide greater adsorption to heavy metals as well as provide greater stability to adsorbed metals, especially for Cu.