1964
DOI: 10.1021/jo01035a004
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Decompositions of Hydroperoxides in Oxidizing Olefins

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1965
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Cited by 15 publications
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“…Both chain initiation and peroxide disappearance are initially autocatalytic; the oxidation later becomes slower, but does not stop, as the original free hydroperoxide is exhausted. Formaldehyde forms addition compounds with hydroperoxides and complicates analytical problems and the interpretation of the results [21]. Equal weights of styrene and methyl esters of different acids such as stearic, oleic, linoleic, trans-10,12-octadecadienoic, conjugated linoleic, and linolenic were mixed and polymerized using benzoyl peroxide as the initiator by Tolberg and co-workers.…”
Section: Modification Of Oils and Alkyd Resins With Functional Monomersmentioning
confidence: 99%
“…Both chain initiation and peroxide disappearance are initially autocatalytic; the oxidation later becomes slower, but does not stop, as the original free hydroperoxide is exhausted. Formaldehyde forms addition compounds with hydroperoxides and complicates analytical problems and the interpretation of the results [21]. Equal weights of styrene and methyl esters of different acids such as stearic, oleic, linoleic, trans-10,12-octadecadienoic, conjugated linoleic, and linolenic were mixed and polymerized using benzoyl peroxide as the initiator by Tolberg and co-workers.…”
Section: Modification Of Oils and Alkyd Resins With Functional Monomersmentioning
confidence: 99%