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  2. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Organic peroxides are often sold as formulations that include one or more phlegmatizing agents. That is, for safety sake or performance benefits the properties of an organic peroxide formulation are commonly modified by the use of additives to phlegmatize (desensitize), stabilize, or otherwise enhance the organic peroxide for commercial use.

  3. HAZMAT Class 5 Oxidizing agents and organic peroxides

    en.wikipedia.org/wiki/HAZMAT_Class_5_Oxidizing...

    An organic peroxide is any organic compound containing oxygen (O) in the bivalent -O-O- structure and which may be considered a derivative of hydrogen peroxide, where one or more of the hydrogen atoms have been replaced by organic radicals, unless any of the following paragraphs applies:

  4. Peroxide - Wikipedia

    en.wikipedia.org/wiki/Peroxide

    The peroxide group is marked in blue. R, R 1 and R 2 mark hydrocarbon moieties. The most common peroxide is hydrogen peroxide (H 2 O 2), colloquially known simply as "peroxide". It is marketed as solutions in water at various concentrations. Many organic peroxides are known as well. In addition to hydrogen peroxide, some other major classes of ...

  5. Hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxide

    When R is organic, the compounds are called organic hydroperoxides. Such compounds are a subset of organic peroxides , which have the formula ROOR. Organic hydroperoxides can either intentionally or unintentionally initiate explosive polymerisation in materials with unsaturated chemical bonds .

  6. Benzoyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_peroxide

    Benzoyl peroxide is a chemical compound (specifically, an organic peroxide) with structural formula (C 6 H 5 −C(=O)O−) 2, often abbreviated as (BzO) 2.In terms of its structure, the molecule can be described as two benzoyl (C 6 H 5 −C(=O)−, Bz) groups connected by a peroxide (−O−O−).

  7. Self accelerating decomposition temperature - Wikipedia

    en.wikipedia.org/wiki/Self_Accelerating...

    Organic peroxides do not usually produce oxygen as part of the decomposition process, so there is little risk of enhanced burning rates due to oxygen enrichment. This is unlike the decomposition of hydrogen peroxide and solid oxidizers that can liberate oxygen.

  8. Peroxy acid - Wikipedia

    en.wikipedia.org/wiki/Peroxy_acid

    Several organic peroxyacids are commercially useful. [5] They can be prepared in several ways. Most commonly, peracids are generated by treating the corresponding carboxylic acid with hydrogen peroxide: [6] RCO 2 H + H 2 O 2 ⇌ RCO 3 H + H 2 O. A related reaction involves treatment of the carboxylic anhydride: (RCO) 2 O + H 2 O 2 → RCO 3 H ...

  9. Fenton's reagent - Wikipedia

    en.wikipedia.org/wiki/Fenton's_reagent

    Fenton's reagent is a solution of hydrogen peroxide (H 2 O 2) and an iron catalyst (typically iron(II) sulfate, FeSO 4). [1] It is used to oxidize contaminants or waste water as part of an advanced oxidation process. Fenton's reagent can be used to destroy organic compounds such as trichloroethylene and tetrachloroethylene (perchloroethylene