TweetElectrical conductivity indicates solution concentration and ionization of the dissolved material. Since temperature greatly affects ionization, conductivity measurements are temperature dependent and are normally corrected to read what they would be at 25°C. A. How It’s Done Once the effect of temperature is removed, the compensated conductivity is a function of the concentration (TDS). Temperature […]
Electrical conductivity indicates solution concentration and ionization of the dissolved material. Since temperature greatly affects ionization, conductivity measurements are temperature dependent and are normally corrected to read what they would be at 25°C.
A. How It’s Done
Once the effect of temperature is removed, the compensated conductivity is a function of the concentration (TDS). Temperature compensation of the conductivity of a solution is performed automatically by the internal processor with data derived from chemical tables. Any dissolved salt at a known temperature has a known ratio of conductivity to concentration. Tables of conversion ratios referenced to 25°C have been published by chemists for decades.
B. Solution Characteristics
Real world applications have to measure a wide range of materials and mixtures of electrolyte solutions. To address this problem, industrial users commonly use the characteristics of a standard material as a model for their solution, such as KCl, which is favored by chemists for its stability.
Users dealing with sea water, etc., use NaCl as the model for their concentration calculations. Users dealing with freshwater work with mixtures including sulfates, carbonates and chlorides, the three predominant components (anions) in freshwater that Myron L calls “Natural Water”. These are modeled in a mixture called “442™” which Myron L uses as a calibration standard, as it does standard KCl and NaCl solutions.
The Ultrameter II contains algorithms for these 3 most commonly referenced compounds. The solution type in use is displayed on the left. Besides KCl, NaCl, and 442, there is the User choice. The benefit of the User solution type is that one may enter the temperature compensation and TDS ratio by hand, greatly increasing accuracy of readings for a specific solution. That value remains a constant for all measurements and should be reset for different dilutions or temperatures.
C. When does it make a lot of difference?
First, the accuracy of temperature compensation to 25°C determines the accuracy of any TDS conversion. Assume we have industrial process water to be pretreated by RO. Assume it is 45°C and reads 1500 µS uncompensated.
1. If NaCl compensation is used, an instrument would report 1035 µS compensated, which corresponds to 510 ppm NaCl.
2. If 442 compensation is used, an instrument would report 1024 µS compensated, which corresponds to 713 ppm 442.
The difference in values is 40%.
In spite of such large error, some users will continue to take data in the NaCl mode because their previous data gathering and process monitoring was done with an older NaCl referenced device.
Selecting the correct Solution Type on the Ultrameter II will allow the user to attain true TDS readings that correspond to evaporated weight.
If none of the 3 standard solutions apply, the User mode must be used.
TEMPERATURE COMPENSATION (Tempco) and TDS DERIVATION
The Ultrameter II contains internal algorithms for characteristics of the 3 most commonly referenced compounds. The solution type in use is displayed on the left. Besides KCl, NaCl, and 442, there is the User choice. The benefit of User mode is that one may enter the tempco and TDS conversion values of a unique solution via the keypad.
A. Conductivity Characteristics
When taking conductivity measurements, the Solution Selection determines the characteristic assumed as the instrument reports what a measured conductivity would be if it were at 25°C. The characteristic is represented by the tempco, expressed in %/°C. If a solution of 100 µS at 25°C increases to 122 µS at 35°C, then a 22% increase has occurred over this change of 10°C. The solution is then said to have a tempco of 2.2 %/°C. Tempco always varies among solutions because it is dependent on their individual ionization activity, temperature and concentration. This is why the Ultrameter II features mathematically generated models for known salt characteristics that also vary with concentration and temperature.
B. Finding the Tempco of an Unknown Solution
One may need to measure compensated conductivity of some solution unlike any of the 3 standard salts. In order to enter a custom fixed tempco for a limited measurement range, enter a specific value through the User function. The tempco can be determined by 2 different methods:
1. Heat or cool a sample of the solution to 25°C, and measure its conductivity. Heat or cool the solution to a typical temperature where it is normally measured. After selecting User function, set the tempco to 0 %/°C as in Disabling Temperature Compensation, pg. 15 (No compensation). Measure the new conductivity and the new temperature. Divide the % decrease or increase by the 25°C value. Divide that difference by the temperature difference.
2. Heat or cool a sample of the solution to 25°C, and measure its conductivity. Change the temperature to a typical measuring temperature. Set the tempco to an expected value as in User Programmable Temperature Compensation, pg. 15. See if the compensated value is the same as the 25°C value. If not, raise or lower the tempco and measure again until the 25°C value is read.
C. Finding the TDS Ratio of an Unknown Solution
Once the effect of temperature is removed, the compensated conductivity is a function of the concentration (TDS).
There is a ratio of TDS to compensated conductivity for any solution, which varies with concentration. The ratio is set during calibration in User mode as in User Programmable Conductivity to TDS Ratio, pg. 16.
A truly unknown solution has to have its TDS determined by evaporation and weighing. Then the solution whose TDS is now known can be measured for conductivity and the ratio calculated. Next time the same solution is to be measured, the ratio is known.
ph and ORP (6PFCE)
1. pH as an Indicator (6PFCE)
pH is the measurement of Acidity or Alkalinity of an aqueous solution. It is also stated as the Hydrogen Ion activity of a solution. pH measures the effective, not the total, acidity of a solution.
A 4% solution of acetic acid (pH 4, vinegar) can be quite palatable, but a 4% solution of sulfuric acid (pH 0) is a violent poison. pH provides the needed quantitative information by expressing the degree of activity of an acid or base. In a solution of one known component, pH will indicate concentration indirectly. However, very dilute solutions may be very slow reading, just because the very few ions take time to accumulate.
2. pH Units (6PFCE)
The acidity or alkalinity of a solution is a measurement of the relative availabilities of hydrogen (H+) and hydroxide (OH-) ions. An increase in (H+) ions increases acidity, while an increase in (OH-) ions increases alkalinity. The total concentration of ions is fixed as a characteristic of water, and balance would be 10-7 mol/liter (H+) and (OH-) ions in a neutral solution (where pH sensors give 0 voltage).
pH is defined as the negative logarithm of hydrogen ion concentration. Where (H+) concentration falls below 10-7, solutions are less acidic than neutral, and therefore are alkaline. A concentration of 10-9 mol/liter of (H+) would have 100 times less (H+) ions than (OH-) ions and be called an alkaline solution of pH 9.
3. The pH Sensor (6PFCE)
The active part of the pH sensor is a thin glass surface that is selectively receptive to hydrogen ions. Available hydrogen ions in a solution will accumulate on this surface and a charge will build up across the glass interface. The voltage can be measured with a very high impedance voltmeter circuit; the dilemma is how to connect the voltmeter to solution on each side.
The glass surface encloses a captured solution of potassium chloride holding an electrode of silver wire coated with silver chloride. This is the most inert connection possible from a metal to an electrolyte. It can
still produce an offset voltage, but using the same materials to connect to the solution on the other side of the membrane causes the 2 equal offsets to cancel.
The problem is, on the other side of the membrane is an unknown test solution, not potassium chloride. The outside electrode, also called the Reference Junction, is of the same construction with a porous plug in place of a glass barrier to allow the junction fluid to contact the test solution without significant migration of liquids through the plug material. Figure 33 shows a typical 2 component pair. Migration does occur, and this limits the lifetime of a pH junction from depletion of solution inside the reference junction or from contamination. The junction may be damaged if dried out because insoluble crystals may form in a layer, obstructing contact with test solutions.
4. The Myron L Integral pH Sensor (6PFCE)
The sensor in the Ultrameter II (see Figure 34) is a single construction in an easily replaceable package. The sensor body holds an oversize solution supply for long life. The reference junction “wick” is porous to provide a very stable, low permeable interface, and is located under the glass pH sensing electrode. This construction combines all the best features of any pH sensor known.
5. Sources of Error (6PFCE)
The most common sensor problem will be a clogged junction because a sensor was allowed to dry out. The symptom is a drift in the “zero” setting at 7 pH. This is why the Ultrameter II 6PFCE does not allow more than 1 pH unit of offset during calibration. At that point the junction is unreliable.
b. Sensitivity Problems
Sensitivity is the receptiveness of the glass surface. A film on the surface can diminish sensitivity and cause a long response time.
c. Temperature Compensation
pH sensor glass changes its sensitivity slightly with temperature, so the further from pH 7 one is, the more effect will be seen. A pH of 11 at 40°C would be off by 0.2 units. The Ultrameter II 6PFCE senses the sensor well temperature and compensates the reading.
B. ORP/Oxidation-Reduction Potential/REDOX (6PFCE)
1. ORP as an Indicator (6PFCE)
ORP is the measurement of the ratio of oxidizing activity to reducing activity in a solution. It is the potential of a solution to give up electrons (oxidize other things) or gain electrons (reduce).
Like acidity and alkalinity, the increase of one is at the expense of the other, so a single voltage is called the Oxidation-Reduction Potential, with a positive voltage showing, a solution wants to steal electrons (oxidizing agent). For instance, chlorinated water will show a positive ORP value.
2. ORP Units (6PFCE)
ORP is measured in millivolts, with no correction for solution temperature. Like pH, it is not a measurement of concentration directly, but of activity level. In a solution of only one active component, ORP indicates concentration. Also, as with pH, a very dilute solution will take time to accumulate a readable charge.
3. The ORP Sensor (6PFCE)
An ORP sensor uses a small platinum surface to accumulate charge without reacting chemically. That charge is measured relative to the solution, so the solution “ground” voltage comes from a reference junction – same as the pH sensor uses.
4. The Myron L ORP Sensor (6PFCE)
Figure 34, pg. 45, shows the platinum button in a glass sleeve. The same reference is used for both the pH and the ORP sensors. Both pH and ORP will indicate 0 for a neutral solution. Calibration at zero compensates for error in the reference junction. A zero calibration solution for ORP is not practical, so the Ultrameter II 6PFCE uses the offset value determined during calibration to 7 in pH calibration (pH 7 = 0 mV). Sensitivity of the ORP surface is fixed, so there is no gain adjustment either.
5. Sources of Error (6PFCE)
The basics are presented in pH and ORP, pg. 44, because sources of error are much the same as for pH. The junction side is the same, and though the platinum surface will not break like the glass pH surface, its protective glass sleeve can be broken. A surface film will slow the response time and diminish sensitivity. It can be cleaned off with detergent or acid, as with the pH glass.
C. Free Chlorine
1. Free Chlorine as an Indicator of Sanitizing Strength Chlorine, which kills bacteria by way of its power as an oxidizing agent, is the most popular germicide used in water treatment. Chlorine is not only used as a primary disinfectant, but also to establish a sufficient residual level of Free Available Chlorine (FAC) for ongoing disinfection.
FAC is the chlorine that remains after a certain amount is consumed by killing bacteria or reacting with other organic (ammonia, fecal matter) or inorganic (metals, dissolved CO2, Carbonates, etc) chemicals in solution. Measuring the amount of residual free chlorine in treated water is a well accepted method for determining its effectiveness in microbial control.
The Myron L FCE method for measuring residual disinfecting power is based on ORP, the specific chemical attribute of chlorine (and other oxidizing germicides) that kills bacteria and microbes.
2. FCE Free Chlorine Units
The 6PIIFCE is the first handheld device to detect free chlorine directly, by measuring ORP. The ORP value is converted to a concentration reading (ppm) using a conversion table developed by Myron L Company through a series of experiments that precisely controlled chlorine levels and excluded interferants.
Other test methods typically rely on the user visually or digitally interpreting a color change resulting from an added reagent-dye. The reagent used radically alters the sample’s pH and converts the various chlorine species present into a single, easily measured species. This ignores the effect of changing pH on free chlorine effectiveness and disregards the fact that some chlorine species are better or worse sanitizers than others.
The Myron L 6PIIFCE avoids these pitfalls. The chemistry of the test sample is left unchanged from the source water. It accounts for the effect of pH on chlorine effectiveness by including pH in its calculation. For these reasons, the Ultrameter II’s FCE feature provides the best reading-to-reading picture of the rise and fall in sanitizing effectivity of free available chlorine.
The 6PIIFCE also avoids a common undesirable characteristic of other ORP-based methods by including a unique Predictive ORP value in its FCE calculation. This feature, based on a proprietary model for ORP sensor behavior, calculates a final stabilized ORP value in 1 to 2 minutes rather than the 10 to 15 minutes or more that is typically required for an ORP measurement.
The Myron L Ultrameter II 6PFCe is available at MyronLMeters.com, the premier internet retailer of Myron L products. Save 10% on the Myron L Ultrameter II6 PFCe when you order online here: http://www.myronlmeters.com/Myron-L-6P-Ultrameter-II-Multiparameter-Meter-p/dh-umii-6pii.htm
TweetWHAT IS ORP? Oxidation Reduction Potential or Redox is the activity or strength of oxidizers and reducers in relation to their concentration. Oxidizers accept electrons, reducers lose electrons. Examples of oxidizers are: chlorine, hydrogen peroxide, bromine, ozone, and chlorine dioxide. Examples of reducers are sodium sulfite, sodium bisulfate and hydrogen sulfide. Like acidity and alkalinity, […]
WHAT IS ORP?
Oxidation Reduction Potential or Redox is the activity or strength of oxidizers and reducers in relation to their concentration. Oxidizers accept electrons, reducers lose electrons. Examples of oxidizers are: chlorine, hydrogen peroxide, bromine, ozone, and chlorine dioxide. Examples of reducers are sodium sulfite, sodium bisulfate and hydrogen sulfide. Like acidity and alkalinity, the increase of one is at the expense of the other.
A single voltage is called the Oxidation-Reduction Potential, where a positive voltage shows a solution attracting electrons (oxidizing agent). For instance, chlorinated water will show a positive ORP value whereas sodium sulfite (a reducing agent) loses electrons and will show a negative ORP value.
ORP is measured in millivolts (mV), with no correction for solution temperature. Like pH, it is not a measurement of concentration directly, but of activity level. In a solution of only one active component, ORP indicates concentration. As with pH, a very dilute solution will take time to accumulate a measurable charge.
An ORP sensor uses a small platinum surface to accumulate charge without reacting chemically. That charge is measured relative to the solution, so the solution “ground” voltage comes from the reference junction – the same type used by a pH sensor.
HISTORY OF ORP
ORP electrodes were first studied at Harvard University in 1936. These studies showed a strong correlation of ORP and bacterial activity. These tests were confirmed by studies on drinking water and swimming pools in other areas of the world. In 1971 ORP (700 mV) was adopted by the World Health Organization (WHO) as a standard for drinking water. In 1982 the German Standards Agency adopted the ORP (750 mV) for public pools and in 1988 the National Swimming Pool Institute adopted ORP (650 mV) for public spas.
WHERE IS ORP USED?
As you can tell by the previous paragraphs, ORP is used for drinking water, swimming pools and spas. However, ORP is also used for cooling tower disinfection, groundwater remediation, bleaching, cyanide destruction, chrome reductions, metal etching, fruit and vegetable disinfection and dechlorination.
In test after test on poliovirus, E. coli, and other organisms, a direct correlation between ORP and the rate of inactivation was determined. It is, therefore, possible to select an individual ORP value, expressed in millivolts, at which a predictable level of disinfection will be achieved and sustained regardless of variations in either oxidant demand or oxidant concentration. Thus, individual ORP targets, expressed in millivolts, can be determined for each application, which will result in completely reliable disinfection of pathogens, oxidation of organics, etc. Any level of oxidation for any purpose can be related to a single ORP number which, if maintained, will provide utterly consistent results at the lowest possible dosage.
WHY USE ORP?
ORP is a convenient measure of the oxidizer’s or reducer’s ability to perform a chemical task. ORP is not only valid over a wide pH range, but it is also a rugged electrochemical test, which can easily be accomplished using in-line and handheld instrumentation. It is by far a more consistent and reliable measurement than say chlorine alone.
LIMITATIONS FOR ORP
As with all testing, ORP has certain limitations. The speed of response is directly related to the exchange current density which is derived from concentration, the oxidation reduction system, and the electrode. If the ORP of a sample is similar to the ORP of the electrode, the speed will be diminished.
Carryover is also a possible problem when checking strong oxidizers or reducers, and rinsing well will help greatly.
Although a better indicator of bactericidal activity, ORP cannot be used as a direct indicator of the residual of an oxidizer due to the effect of pH and temperature on the reading. ORP can be correlated to a system by checking the oxidizer or reducer in a steady state system with a wet test, and measuring pH. If the system stays within the confines of this steady state parameter (usually maintained by in- line or continuous control), a good correlation can be made. The best recommendation for ORP is to use wet tests, and over three test periods correlate the ORP values to those test parameters.
FREE CHLORINE CONVERSION USING ORP
The most ubiquitous and cost-effective sanitizing agent used in disinfection systems is chlorine. When chlorine is used as the sanitizer, free chlorine measurements are required to ensure residual levels high enough for ongoing bactericidal activity. Myron L meters accurately convert ORP measurements to free chlorine based on the understanding of the concentrations of the forms of free chlorine at a given pH and temperature. The conversion is accurate when chlorine is the only oxidizing/reducing agent in solution and pH is stable between 5 and 9. This pH range fits most applications because pH is usually maintained such that the most effective form of free chlorine, hypochlorous acid, exists in the greatest concentration with respect to other variables such as human tolerance.
MYRON L METERS
Myron L offers a variety of handheld instruments and in-line Monitor/controllers that may be used to measure, monitor and/or control ORP. The latest is the Ultrapen PT3, ORP/Redox and Temperature Pen. The Ultrameter III™ 9PTKA, Ultrameter II™ 6PFCE, PoolPro™ PS6FCE and PS9TK, and D-6 Digital Dialysate Meter™ are multi-parameter handheld instruments with ORP and FCE free chlorine measuring capabilities. These instruments also have the capability to measure conductivity, TDS, resistivity, pH, mineral/salt concentration and temperature, making them the preferred instruments for all water treatment professionals. The 720 Series II Monitor/controllers are an excellent choice for continuous in-line measurements.
For additional information, visit us at MyronLMeters.com.
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TweetWhat is the ORP of water? ORP stands for Oxidation Reduction Potential, also known as Redox. It is a measure of the tendency of a chemical species to acquire electrons and thereby be reduced. The ORP measurement is displayed in millivolts (mV) and the usual range for ORP meters is (+1000 mV) to (-1000 mV) […]
What is the ORP of water?
ORP stands for Oxidation Reduction Potential, also known as Redox. It is a measure of the tendency of a chemical species to acquire electrons and thereby be reduced. The ORP measurement is displayed in millivolts (mV) and the usual range for ORP meters is (+1000 mV) to (-1000 mV) with no temperature compensation. It is not a direct measurement of concentration, but rather an indicator of the activity level or strength of an oxidizer or reducer.
An oxidizer gains electrons, while a reducer loses electrons. Examples of oxidizers are: chlorine, hydrogen peroxide, bromine, ozone, and chlorine dioxide. Examples of reducers are sodium sulfite, sodium bisulfate and hydrogen sulfide. Like acidity and alkalinity, the increase of one is at the expense of the other.
When measuring with an ORP meter, a positive voltage shows a solution gaining electrons (oxidizing) and a negative voltage shows a solution losing electrons (reducing). For instance, chlorinated water will show a positive ORP value and a solution with sodium sulfite will have a negative ORP value.
ORP meters are used for swimming pools and spas, drinking water, cooling tower disinfection, and groundwater remediation. ORP meters are also crucial for bleaching applications, cyanide destruction, chrome reductions, metal etching, fruit and vegetable disinfection and dechlorination.
Many organizations around the world have accepted ORP as a standard for disinfection. An ORP of 750 mV was adopted by the German Standards Agency in 1982 for public pools. The National Swimming Pool Institute also adopted an ORP of 650 mV for public spas. The World Health Organization (WHO) adopted an ORP of 700 mV as a standard for drinking water.
How to use ORP?
Oxidation Reduction Potential is a convenient measure of the oxidizer’s or reducer’s ability to perform a chemical task. It is a more consistent and reliable measurement than chlorine alone. You can establish an ORP measurement at which acceptable sanitation is achieved and maintained for your application by testing the rate of inactivation of various microorganisms. There are published standards for many applications or a lab water analysis should be able to provide these results if necessary. For example, the above paragraph mentions the 750 mV standard for public swimming pools. Once that has been determined you can use an ORP controller to maintain that level of sanitation.
Similar to pH, high purity solutions will take extra time to stabilize a reading due to the low ionic strength. Also, if the ORP measurement of a sample solution is similar to the mV of the ORP probe, it will take slightly longer for a reading to respond and stabilize. Rinsing the probe with a strong oxidizer will help to increase the reaction time and give accurate readings quickly. Ensure that there is not residual solution in the ORP probe by rinsing thoroughly with the solution to be tested.
ORP meters like the 728II are used to monitor the sanitizer level. A pH controller, such as the 723II, is also used to monitor pH. The controllers automatically turn the appropriate chemical feeders on and off, as required to maintain the proper sanitizer and pH levels. This results in good water quality and elimination of chloramines and other unpleasant contaminants, as well as in savings in chemical and labor.
Generally, ORP meters without pH control should not be used with alkaline sanitizers such as sodium hypochlorite or calcium hypochlorite. If the pH remains fairly constant, these inexpensive controllers provide a very cost effective solution to the problem of chemical control in small commercial applications.
Other handheld instruments like the POOLPRO PS6 have been designed to test ORP reliably for swimming pools and other applications. If you are in the medical dialysis industry, you will definitely be interested in the Digital Dialysate Meter D-6 that test ORP, among other parameters.