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Kinetics of oxidation of rosalinine hydrochloride by potassium peroxydisulphate in mixed micelles of binary surfactant system

机译:过氧二硫酸钾在二元表面活性剂体系混合胶束中氧化玫瑰红碱的动力学

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The kinetics of oxidation of rosaniline hydrochloride (R-HCl) has been studied in binary combinations of cationiconionic and anioniconionic surfactant systems at 30 deg C. The pre-micellar environment of single C_(16)TA Br catalyses the reactions whereas single sodium dodecyl sulphate (SDS) and nonionic surfactants, viz,Triton X-100, Triton X-102, Tween-20 and Tween-80 strongly inhibit the reaction rate of R-HCl. The values of rate constant in mixed micellar solutions (C_(16)TABr + Tween-20, C_(16)TABr + Tween-80) are less than the single cationic surfactant but are higher than the single nonionic surfactant; while the value of rate constant in mixed micellar solutions (SDS + Triton X-100, SDS + Triton X - 102) is less than that in single anionic as well as in nonionic surfactant.
机译:已在30°C下以阳离子/非离子和阴离子/非离子表面活性剂体系的二元组合形式研究了盐酸罗莎胺盐酸盐(R-HCl)的氧化动力学。单个C_(16)TA Br的胶束前环境可催化反应,而单十二烷基硫酸钠(SDS)和非离子表面活性剂,即Triton X-100,Triton X-102,Tween-20和Tween-80强烈抑制R-HCl的反应速率。混合胶束溶液(C_(16)TABr + Tween-20,C_(16)TABr + Tween-80)中的速率常数值小于单一阳离子表面活性剂,但高于单一非离子表面活性剂;而混合胶束溶液(SDS + Triton X-100,SDS + Triton X-102)中速率常数的值小于单阴离子和非离子表面活性剂中的速率常数。

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