Titration hydrogen peroxide determination

Oxidation indices, 656-72 peroxide determination, 762-3 peroxide value, 656, 657-64 colorimetry, 658-61 definition, 657 direct titration, 657 electrochemical methods, 663-4 IR spectrophotometry, 661-3 NIR spectrophotometry, 663 UV-visible spectrophotometry, 658-61 secondary oxidation products, 656, 665-72 tests for stability on storage, 664-5, 672 thermal analysis, 672 Oxidative amperometiy, hydroperoxide determination, 686 Oxidative cleavage alkenes, 1094-5 double bonds, 525-7 Oxidative couphng, hydrogen peroxide determination, 630, 635 Oxidative damage... 

Tetramethylammonium ozonide, 736 Tetramethyl-l,2-dioxetane (TMD) chemical titration, 1224 chemiluminescence, 1221, 1234 quantum yield standard, 1224, 1226 N,N, N, A -Tetramethyl-p-phenylenediamine hydrogen peroxide determination, 735, 631, 633... 

Analytical Methods. Peroxides were determined by iodometric titration. Hydrogen peroxide was determined from the difference between the titers before and after treatment with catalase that decomposes hydrogen peroxide selectively. It was ascertained by separate experiments that hydrogen peroxide could be decomposed quantitatively by catalase over the pH range 2.8-8.0. 

Analytical Methods. The official NIOSH recommended method for determining sulfur dioxide in air consists of drawing a known prefiltered volume of air through a bubbler containing hydrogen peroxide, thus oxidising the sulfur dioxide to sulfuric acid. Isopropyl alcohol is then added to the contents in the bubbler and the pH of the sample is adjusted with dilute perchloric acid. The resultant solution is then titrated for sulfate with 0.005 M. barium perchlorate, and Thorin is used as the indicator. 

Analytical Methods. A classical and stiU widely employed analytical method is iodimetric titration. This is suitable for determination of sodium sulfite, for example, in boiler water. Standard potassium iodate—potassium iodide solution is commonly used as the titrant with a starch or starch-substitute indicator. Sodium bisulfite occurring as an impurity in sodium sulfite can be determined by addition of hydrogen peroxide to oxidize the bisulfite to bisulfate, followed by titration with standard sodium hydroxide (279). 

This is typically accompHshed by cooling the titration solution with ice, determining the blank, and titrating rapidly. Another method utilizes deterrnination of the total peroxide and peracid content by use of a ceric sulfate titration to measure hydrogen peroxide followed by a iodide/thiosulfate titration to measure total active oxygen (60). 

Wet-Chemical Determinations. Both water-soluble and prepared insoluble samples must be treated to ensure that all the chromium is present as Cr(VI). For water-soluble Cr(III) compounds, the oxidation is easily accompHshed using dilute sodium hydroxide, dilute hydrogen peroxide, and heat. Any excess peroxide can be destroyed by adding a catalyst and boiling the alkaline solution for a short time (101). Appropriate ahquot portions of the samples are acidified and chromium is found by titration either using a standard ferrous solution or a standard thiosulfate solution after addition of potassium iodide to generate an iodine equivalent. The ferrous endpoint is found either potentiometricaHy or by visual indicators, such as ferroin, a complex of iron(II) and o-phenanthroline, and the thiosulfate endpoint is ascertained using starch as an indicator. 

Sulfur Dioxide EPA Method 6 is the reference method for determining emissions of sulfur dioxide (SO9) from stationary sources. As the gas goes through the sampling apparatus (see Fig. 25-33), the sulfuric acid mist and sulfur trioxide are removed, the SO9 is removed by a chemical reaction with a hydrogen peroxide solution, and, finally, the sample gas volume is measured. Upon completion of the rim, the sulfuric acid mist and sulfur trioxide are discarded, and the collected material containing the SO9 is recovered for analysis at the laboratory. The concentration of SO9 in the sample is determined by a titration method. 

It is possible to monitor the reaction and determine the end point by the absence of an a,/S-unsaturated ketone absorption in the UV or by the determination of the consumption of ca. one molar equivalent of hydrogen peroxide by permanganate titration. 

The methylene blue test can also be used to determine cation exchange capacity of clays and shales. In the test a weighed amount of clay is dispersed into water by a high-speed stirrer. Titration is carried out as for drilling muds, except that hydrogen peroxide is not added. The cation exchange capacity of clays is expressed as milliequivalents of methylene blue per 100 g of clay. 

Satisfactory 40% peracetic acid is obtainable from Buffalo Electrochemical Corporation, Food Machinery and Chemical Corporation, Buffalo, New York. The specifications given by the manufacturer for its composition are peracetic acid, 40% hydrogen peroxide, 5% acetic acid, 39% sulfuric acid, 1% water, 15%. Its density is 1.15 g./ml. The peracetic acid concentration should be determined by titration. A method for the analysis of peracid solutions is based on the use of ceric sulfate as a titrant for the hydrogen peroxide present, followed by an iodometric determination of the peracid present.3 The checkers found that peracetic acid of a lower concentration (27.5%) may also be used without a decrease in yield. The product was found to be sufficiently pure, after only one recrystallization from 60 ml. of petroleum ether (b.p. 40-60°) and cooling overnight to —18°, to be used in the next step. 

This is one source of acid rain, a serious environmental problem. The sulfur dioxide content of an air sample can be determined. A sample of air is bubbled through an aqueous solution of hydrogen peroxide to convert all of the SO2 to H2 SO4. H2 O2 + SO2 H2 SO4 Titration of the resulting solution completes the analysis (both H atoms of H2 SO4 are titrated). In one such case, the analysis of 1.55 X 10 Lof Los Angeles air gave a solution that required 5.70 mL of 5.96 X 10 M NaOH to complete the titration. Determine the number of grams of SO2 present in the air sample. 

It is worth mentioning that an attempt was made by Tsao and Willmarth to determine the acid dissociation constant of HO2. The reaction between hydrogen peroxide and peroxydisulphate was used for the generation of the HO2 radical. However, these experiments, like others where the HO2 radical is studied under steady-state conditions, could yield only a value of acidity constant multiplied by a coefficient consisting of a ratio of kinetic parameters. Unfortunately, in this case there are no independent data for the kinetic coefficient, and the value of cannot be evaluated. Considering the kinetic analogue of the titration curve it can be stated only that ionization of HO2 becomes important in the pH range from 4.5-6.5. The value of acidity constant of HO2 obtained by Czapski and Dorfman is (3.5 + 2.0)x 10 mole.l. . ... 

Determination of Additive Effects on the Decomposition of tert-Butyl Hydroperoxide and Hydrogen Peroxide. Solutions of tert-butyl hydroperoxide (1.0 mmol) and 30% aqueous hydrogen peroxide (1.32 mmol) in 5 mL of tert-butyl alcohol with the various additives (Tables 9 and 10) were held at 80°C for 24 hr. Peroxide analyses were obtained by sodium iodide/0.05N sodium thiosulfate titration. 

Determination of the level of total sulfur in a rubber can give information on the type of cure system used, for example, elemental sulfur plus accelerator or sulfur donor system, etc. The ISO 6528-1 1992 method — Rubber — Determination of total sulfur content — Part 1 Oxygen combustion flask method is often employed. The principle of the method is oxidation by ignition in an atmosphere of oxygen in the presence of hydrogen peroxide, conversion of sulfur to sulfuric acid and determination of the sulfate by titration with barium perchlorate. The method is... 

In cases like this, assay determination of hydrogen peroxide concentration would be the most sensitive metric. Titrametric determination will give a reliable measure of the specific ingredient that is most crucial to the polishing process. Assay by titration of low-concentration ingredients, such as hydrogen peroxide or ammonium hydroxide, both of which degrade over... 

The Reich test is used to estimate sulfur dioxide content of a gas by measuring the volume of gas required to decolorize a standard iodine solution (274). Equipment has been developed commercially for continuous monitoring of stack gas by measuring the near-ultraviolet absorption bands of sulfur dioxide (275—277). The determination of sulfur dioxide in food is conducted by distilling the sulfur dioxide from the acidulated sample into a solution of hydrogen peroxide, followed by acidimetric titration of the sulfuric acid thus produced (278). Analytical methods for sulfur dioxide have been reviewed (279). 

A rapid volumetric method for the determination of sulphur is as follows 2 The sulphur is dissolved in a known volume of hot standard sodium hydroxide solution and after cooling is oxidised to sulphate by the addition of hydrogen peroxide the excess of alkali is then titrated with standard acid.3 The method is applicable to gases containing any common sulphur compound except thiophen (e.g. coke oven gas).4... 

An alternative principle for the volumetric determination is to apply an acidimetric process. The thiosulphate may be oxidised with hydrogen peroxide in the presence of a known quantity of an alkali in excess and the excess of alkali measured by titration with standard add,8 or the oxidation may be effected with hydrogen peroxide alone and the resulting acidity directly titrated with a standard alkali 9... 

An attractive modification of this method is to treat the neutralised polythionate solution with neutral hydrogen peroxide and a known excess of standard sodium hydroxide solution on the water-bath and to determine the quantity of acid formed by the amount of standard alkali neutralised during the oxidation.3 All polythionates except the dithionates are completely oxidised to sulphate by heating in a closed tube for one hour with iodine and sodium bicarbonate by titrating the excess of iodine the total polythionate present may be estimated.4... 

Quantitative Determination. —Weigh off 1 gm. of hydrogen peroxide in a graduated flask of 100 cc. capacity, and fill with water to the mark. Dilute 20 cc. of this liquid with 50 cc. of water, add 40 cc. of 16 per cent sulphuric acid, and titrate with decinormal potassium permanganate. At least 35 cc. should be required to produce the end-point. 

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