Peroxygen

Dialkyl peroxides have the stmctural formula R—OO—R/ where R and R are the same or different primary, secondary, or tertiary alkyl, cycloalkyl, and aralkyl hydrocarbon or hetero-substituted hydrocarbon radicals. Organomineral peroxides have the formulas R Q(OOR) and R QOOQR, where at least one of the peroxygens is bonded directly to the organo-substituted metal or metalloid, Q. Dialkyl peroxides include cyclic and bicycflc peroxides where the R and R groups are linked, eg, endoperoxides and derivatives of 1,2-dioxane. Also included are polymeric peroxides, which usually are called poly(alkylene peroxides) or alkylene—oxygen copolymers, and poly(organomineral peroxides) (44), where Q = As or Sb. 

Solid Peroxygen Compounds. Hydrogen peroxide reacts with many compounds, such as borates, carbonates, pyrophosphates, sulfates, sihcates, and a variety of organic carboxyHc acids, esters, and anhydrides to give peroxy compounds or peroxyhydrates. A number of these compounds are stable sohds that hydrolyze readily to give hydrogen peroxide in solution. 

Perbora.tes, Sodium perborate [7632-04-4] is the most widely used soHd peroxygen compound. Commercially it is available as a tetrahydrate [10486-00-7] and a monohydrate [10322-33-9]. The tetrahydrate is produced by treating a borax solution with hydrogen peroxide and sodium hydroxide ... 

J. Parker and O. Raney, "The Use of Peroxygen Compounds as a Means of Improving Detergent Performance," in C. Bapa, ed., Hew Hori ns 19S9A.nA.OCS CSMA Tdetergent Industry Conference Hershey, Pa., 1989. 

Carbon tetrachloride forms telomers with ethylene and certain other olefins (14—16). The mixture of Hquid products derived from ethylene telomerization may be represented CCl2(CH2CH2) Cl ia which nis 2l small number. Reaction of ethylene and carbon tetrachloride takes place under pressure and is induced by the presence of a peroxygen compound, eg, ben2oyl peroxide (17—19) or metal carbonyls (14,15). 

A. P. James, "Chemistry of Peroxygen Bleaching," paper presented at 83rdAmerican Oil Chemists Society Toronto, Canada, May 1992, Interox America Reprints, Houston, Tex., 1992. 

Tetraacetylethylenediarnine [10543-57-4] (T A ED) has been widely adopted for use in home laundry products as an activator for peroxygen bleaches. 

Macroinitiators are macromolecules having peroxygen and/or azo groups that can thermally initiate a vinyl polymerization to obtain block copolymers in one step. They can be classified as macroperoxyinitiators (MPl), macroazoinitiators (MAI), and macroazo-peroxyiniti-ators. 

Bacterial spores are the most resistant of all microbial forms to chemical treatment. The majority of antimicrobial agents have no useful sporicidal action, with the exception of the aldehydes, halogens and peroxygen compounds. Such chemicals are sometimes used as an alternative to physical methods for sterilization ofheat sensitive equipment. In these circumstances, correct usage of the agent is of paramount importance since safety margins are lower in comparison with physical methods of sterilization (Chapter 20). 

Of the other peroxygen compounds with antimicrobial activity, potassium monoperoxysulphate is the main product marketed for disinfectant use. It is used for body fluid spillages and equipment contaminated with body fluids, but its activity against mycobacteria and some viruses is limited. 

Heaney, H. Novel Organic Peroxygen Reagents for Use in Organic Synthesis. 164, 1-19... 

Duplex (2) A process for making sodium perborate from both sodium peroxide and hydrogen peroxide. Developed in the United States from the 1920s and used until the development of the present process, which uses hydrogen peroxide as the only source of the peroxygen. See also Acid. 

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