Gas potentiometric

The minimum concentration is often related to the minimum amount of electroactive substance that can be measured with the electrochemical probe. Generally, with ISE or gas potentiometric probes the limit of concentration measurable is 10 moll The calibration graphs are therefore often S-shaped, leveling off at high concentration due to the or fCm-related maximum concentration measurable and at low values by the performances of the potentiometric base probe (Figure 1). 

Lorenz H, Tittmann K, Sitzki L, Trippler S, Rau H (1996) Gas-potentiometric method with solid electrolyte oxygen sensors for the investigation of combustion. Fresenius J Anal Chem 356 215-220... 

HarheckW, Guth U (1990) Determination of bum-off of gas flames by means of gas potentiometric method (in German). Gas-Warme-Intemational (Essen) 39 10-24... 

Mobius H-H (1965) Basic principles of gas-potentiometric determination of oxygen. Z physik Chem [Leipzig] 230 396-412, Published in German Grundlagen der gaspotentiometrischen Sauerstoffbestimmung... 

Potcntiomctric Biosensors Potentiometric electrodes for the analysis of molecules of biochemical importance can be constructed in a fashion similar to that used for gas-sensing electrodes. The most common class of potentiometric biosensors are the so-called enzyme electrodes, in which an enzyme is trapped or immobilized at the surface of an ion-selective electrode. Reaction of the analyte with the enzyme produces a product whose concentration is monitored by the ion-selective electrode. Potentiometric biosensors have also been designed around other biologically active species, including antibodies, bacterial particles, tissue, and hormone receptors. 

Few potentiometric biosensors are commercially available. As shown in Figures 11.16 and 11.17, however, available ion-selective and gas-sensing electrodes may be easily converted into biosensors. Several representative examples are described in Table 11.5, and additional examples can be found in several reviews listed in the suggested readings at the end of the chapter. 

One important application of amperometry is in the construction of chemical sensors. One of the first amperometric sensors to be developed was for dissolved O2 in blood, which was developed in 1956 by L. C. Clark. The design of the amperometric sensor is shown in Figure 11.38 and is similar to potentiometric membrane electrodes. A gas-permeable membrane is stretched across the end of the sensor and is separated from the working and counter electrodes by a thin solution of KCl. The working electrode is a Pt disk cathode, and an Ag ring anode is the... 

Potentiometric electrodes also can be designed to respond to molecules by incorporating a reaction producing an ion whose concentration can be determined using a traditional ion-selective electrode. Gas-sensing electrodes, for example, include a gas-permeable membrane that isolates the ion-selective electrode from the solution containing the analyte. Diffusion of a dissolved gas across the membrane alters the composition of the inner solution in a manner that can be followed with an ion-selective electrode. Enzyme electrodes operate in the same way. 

The routine compositional and functional testing done on the adhesives includes gas chromatographic testing for purity, potentiometric titrations for acid stabilizer concentrations, accelerated thermal stabiUty tests for shelf life, fixture time cure speed tests, and assorted ASTM tests for tensile shear strengths, peel and impact strengths, and hot strengths. 

The crystalline mineral silicates have been well characterized and their diversity of stmcture thoroughly presented (2). The stmctures of siHcate glasses and solutions can be investigated through potentiometric and dye adsorption studies, chemical derivatization and gas chromatography, and laser Raman, infrared (ftir), and Si Fourier transform nuclear magnetic resonance ( Si ft-nmr) spectroscopy. References 3—6 contain reviews of the general chemical and physical properties of siHcate materials. 

There are a variety of analytical methods commonly used for the characterization of neat soap and bar soaps. Many of these methods have been pubUshed as official methods by the American Oil Chemists Society (29). Additionally, many analysts choose United States Pharmacopoeia (USP), British Pharmacopoeia (BP), or Pood Chemical Codex (FCC) methods. These methods tend to be colorimetric, potentiometric, or titrametric procedures. However, a variety of instmmental techniques are also frequendy utilized, eg, gas chromatography, high performance Hquid chromatography, nuclear magnetic resonance spectroscopy, infrared spectroscopy, and mass spectrometry. 

Ga.s Eeeders. Chlorine gas is usually fed from a chlorine cylinder equipped with a pressure gauge, reducing valve, regulating valve, feed-rate indicator, and aspirator-type injector for dissolving the chlorine gas in water. The feeder can be manually, or more desirably automatically, controlled utili2ing continuous amperometric or potentiometric measurement of the free chlorine residual. The chlorine solution is normally introduced into the return line to the filter. 

Sta.bilizers. Cyanuric acid is used to stabilize available chlorine derived from chlorine gas, hypochlorites or chloroisocyanurates against decomposition by sunlight. Cyanuric acid and its chlorinated derivatives form a complex ionic and hydrolytic equilibrium system consisting of ten isocyanurate species. The 12 isocyanurate equilibrium constants have been determined by potentiometric and spectrophotometric techniques (30). Other measurements of two of the equilibrium constants important in swimming-pool water report significantly different and/or less precise results than the above study (41—43). A critical review of these measurements is given in Reference 44. 

Other usefiil gas sensors include the potentiometric ammonia (64) or hydrogen cyanide probes (65), and amperometric carbon monoxide (66) and nitrogen dioxide (67) devices. The hydrogen cyanide probe is an example of a modem device that relies on changes in the conductivity of electropolymerized film (polyanihne) in the presence of a given gas. 

Neither the usual membrane ISEs nor the gas-sensing electrodes, in which their internal indicator electrode functions as a zero-current potentiometric half-cell, are under consideration here. 

The methods most commonly used to detect hydrogen sulfide in environmental samples include GC/FPD, gas chromatography with electrochemical detection (GC/ECD), iodometric methods, the methylene blue colorimetric or spectrophotometric method, the spot method using paper or tiles impregnated with lead acetate or mercuric chloride, ion chromatography with conductivity, and potentiometric titration with a sulfide ion-selective electrode. Details of commonly used analytical methods for several types of environmental samples are presented in Table 6-2. 

After passing through the column, the separated solutes are sensed by an in-line detector. The output of the detector is an electrical signal, the variation of which is displayed on a potentiometric recorder, a computing integrator or a vdu screen. Most of the popular detectors in hplc are selective devices, which means that they may not respond to all of the solutes that are present in a mixture. At present there is no universal detector for hplc that can compare with the sensitivity and performance of the flame ionisation detector used in gas chromatography. Some solutes are not easy to detect in hplc, and have to be converted into a detectable form after they emerge from the column. This approach is called post-column derivatisation. 

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