2006
DOI: 10.1007/s00396-006-1596-2
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Kinetics of the acid hydrolysis of isoproturon in the absence and presence of sodium lauryl sulfate micelles

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Cited by 8 publications
(4 citation statements)
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“…These observations indicate that the same mechanism is being followed in both aqueous medium and micellar medium. The increased rate of reaction in the presence of CTAB and SDS may be explained on the basis of pseudophase model of micelles in which reactions are considered to occur both in aqueous and micellar pseudophases with varying rate constants [18][19][20][21][22]. Scheme 2 has been proposed for reactions occurring in aqueous and micellar media as follows.…”
Section: Barrett and Mcbridementioning
confidence: 99%
“…These observations indicate that the same mechanism is being followed in both aqueous medium and micellar medium. The increased rate of reaction in the presence of CTAB and SDS may be explained on the basis of pseudophase model of micelles in which reactions are considered to occur both in aqueous and micellar pseudophases with varying rate constants [18][19][20][21][22]. Scheme 2 has been proposed for reactions occurring in aqueous and micellar media as follows.…”
Section: Barrett and Mcbridementioning
confidence: 99%
“…Gangwar and Rafiquee studied acid hydrolysis of a urea function in isoproturon in the presence of anionic micelles. 54 The results, treated using the pseudophase model, suggested that the reaction is catalysed by micelles. The likely explanation is that the binding of anionic surfactants to the positively charged urea intermediate lowers its energy thus facilitating hydrolysis.…”
Section: Interface Effectmentioning
confidence: 99%
“…The mechanisms of hydrolysis of phenylureas, carboxylic acid, esters, and amide have been subject of investigation by many workers [3][4][5][6][7][8][9][10][11][12]. The hydrolysis of phenylureas pesticides proceeds through an addition-elimination mechanism in both acidic and basic media.…”
Section: Introductionmentioning
confidence: 99%