Hydrogen peroxide applications

Hydrogen peroxide applications include commercial bleaching dye oxidation, the manufacture of organic and peroxide chemicals. Hydrogen peroxide is also used in pulp and paper chemical synthesis, textiles, and environmental control, including municipal and industrial water treatment. 

Hydrogen peroxide applications to water, wastewater and hazardous waste treatment US Peroxide http //www.h2o2.com... 

Zhou M, Diwu Z, Panchuk-Voloshina N et al (1997) A stable nonfluorescent derivative of resorufin for the fluorometric determination of trace hydrogen peroxide applications in detecting the activity of phagocyte NADPH oxidase and other oxidases. Anal Biochem 253 162-168... 

Figure 9.1 Hydrogen peroxide applications (%). (a) Pulp and paper, (b) Chemicals, (c) Textiles, (d) Environment, (e) Other/miscellaneous.

Appleby, A. and Savy, M. (1978). Kinetics of Oxygen Reduction Reactions Involving Catalytic Decomposition of Hydrogen Peroxide Application to Porous and Rotating Ring-disk Electrodes, J. Electroanal. Chem., 92, pp. 15-30. 

The method is basically an application of the Wacker oxidation except that the catalyst used is palladium acetate ( Pd(AcO)2 or Pd(02CCH3)2). the solvent is acetic acid or tert-butyl alcohol and the oxygen source is the previously suggested hydrogen peroxide (H202)[17]. 

The earliest examples of analytical methods based on chemical kinetics, which date from the late nineteenth century, took advantage of the catalytic activity of enzymes. Typically, the enzyme was added to a solution containing a suitable substrate, and the reaction between the two was monitored for a fixed time. The enzyme s activity was determined by measuring the amount of substrate that had reacted. Enzymes also were used in procedures for the quantitative analysis of hydrogen peroxide and carbohydrates. The application of catalytic reactions continued in the first half of the twentieth century, and developments included the use of nonenzymatic catalysts, noncatalytic reactions, and differences in reaction rates when analyzing samples with several analytes. 

Hydrogen peroxide is used in many applications throughout a wide variety of industries. The principal use areas are shown in Table 9. Most ate based on the oxidizing properties of hydrogen peroxide. Some are derived from substitution, decomposition, or the formation of perhydrates. 

Environmental Applications. Hydrogen peroxide is an ecologically desirable poUution-control agent because it yields only water or oxygen on decomposition. It has been used in increasingly greater amounts to convert domestic and industrial effluents to an environmentally compatible state... 

Jones, C.W. (1999) Applications of Hydrogen Peroxide and Derivatives, Royal Society of Chemistry, London. 

Deuterioboration of 5a-cholest-2-ene (171), followed by oxidation of the alkylborane intermediate with hydrogen peroxide in the presence of sodium hydroxide, illustrates the application of this method for the preparation of c/5-deuterium labeled alcohols.(For the preparation of tra 5 -deuterium labeled alcohols see section VII-A.) The predominant reaction product is 2a-di-5a-cholestan-3a-ol (172, 1.03 D/mole) which is accompanied by 3a-di-5a-cholestan-2a-ol (173) and other minor products." ... 

The high degree of stereoselectivity associated with most syntheses and reactions of oxiranes accounts for the enormous utility of these systems in steroid syntheses. Individual selectivity at various positions in the steroid nucleus necessitates the discussion of a collection of uniquely specific reactions used in the synthesis of steroidal epoxides. The most convenient and generally applicable methods involve the peracid, the alkaline hydrogen peroxide and the halohydrin reactions. Several additional but more limited techniques are also available. 

This method is widely applicable to the unambiguous synthesis of quinoxalin-2-ones." It involves the intermediate preparation of a l,2,3,4-tetrahydro-2-oxoquinoxaline by the reductive ring closure of the o-nitrophenyl derivative of an a-aminoacid. These derivatives are formed readily from the aminoacid and an o-nitrohalogenobenzene. The final step of oxidation of the tetrahydro- to the dihydro-quinoxa-line is carried out with potassium permanganate or hydrogen peroxide. The preparation of 7-nitroquinoxalin-2-one illustrates the application of this synthesis ... 

The Payne epoxidation with benzonitrile/ hydrogen peroxide is also an efficient epoxidation process. It is often the method of choice for industrial batch-type applications, but on a small scale the need for continuous pH control is inconvenient. 

Applications of the oxalate-hydrogen peroxide chemiluminescence-based and fluorescence-based assays with NDA/CN derivatives to the analysis of amino acids and peptides are included. The sensitivity of the chemiluminescence and fluorescence methods is compared for several analytes. In general, peroxyoxalate chemiluminescence-based methods are 10 to 100 times more sensitive than their fluorescence-based counterparts. The chief limitation of chemiluminescence is that chemical excitation of the fluorophore apparently depends on its structure and oxidation potential. 

Though we and others (27-29) have demonstrated the utility and the improved sensitivity of the peroxyoxalate chemiluminescence method for analyte detection in RP-HPLC separations for appropriate substrates, a substantial area for Improvement and refinement of the technique remains. We have shown that the reactions of hydrogen peroxide and oxalate esters yield a very complex array of reactive intermediates, some of which activate the fluorophor to its fluorescent state. The mechanism for the ester reaction as well as the process for conversion of the chemical potential energy into electronic (excited state) energy remain to be detailed. Finally, the refinement of the technique for routine application of this sensitive method, including the optimization of the effi-ciencies for each of the contributing factors, is currently a major effort in the Center for Bioanalytical Research. 

Another consequence of application of organic solvents as a reaction medium is associated with the mechanism of enzyme-catalyzed transformations. According to the commonly accepted mechanism, the first product of the interaction of a hydrolytic (serine) enzyme with an ester is an O-acylenzyme (Scheme 5.4). When the reaction is performed in an aqueous solution, water acts as a nucleophile in the next step, to give acid B. If more nucleophilic hydrogen peroxide is present in the reaction mixture, peroxycarboxylic acids C are formed. However, in organic solvents the O-acylenzyme also reacts readily with other nucleophiles, such as... 

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