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Polymerizable oil synthesis by hydroxyhalogenation of soybean oil in dense CO2

机译:在浓二氧化碳中大豆油的羟基卤代反应可聚合油的合成

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The aim of this research is to hydroxybrominate and hydroxychlorinate the double bonds of methyl oleate and soybean oil in dense CO2. The hydroxychlorination reactions of vegetable oils in dense CO2 are the first such report in literature. Experiments were performed at the reaction conditions of 8, 25 and 40 degrees C and 60, 100, 120 and 150 bar. Effects of temperature, pressure, reaction time and the reactant amounts on the extent of reaction are studied. Hydroxybromination and hydroxychlorination reactions are conducted using sodium hypobromite (NaOBr) and sodium hypochlorite (NaOCl) solutions, respectively. The polymerization of the product is performed by urethane formation with toluenediisocyanate at 40 degrees C. The products were analyzed by NMR and IR spectrometry. Fifty percent consumption of the double bonds was observed in the hydroxybromination reaction of methyl oleate, but no -OH addition was determined. In hydroxychlorination reactions of methyl oleate the consumption of double bonds ranges from 40 to 95%, and the introduction of -OH groups ranges from 14 to 30%. Best yields were observed when the mole ratio of NaOCl to methyl oleate double bonds is 5 to 1. The consumption of soybean triglyceride double bonds, in the hydroxychlorination reactions, are observed to range from 18 to 75% and the formation of -OH groups ranges from 8 to 33%. The highest conversion for one-step hydroxychlorination of soybean is obtained at 25 degrees C and 120 bar for a reaction time of 6 h, with 10/l ratio of NaOCl to double bonds. Better results were obtained when the product of the reaction was reintroduced to the reactor and retreated with NaOCl and 75% consumption of double bonds and 33% formation of -OH groups were observed. (C) 2005 Elsevier B.V. All rights reserved.
机译:这项研究的目的是在浓密的二氧化碳中羟基溴化和羟基氯化油酸甲酯和大豆油的双键。植物油在浓二氧化碳中的羟基氯化反应是文献中的首次此类报道。实验是在8、25和40摄氏度以及60、100、120和150巴的反应条件下进行的。研究了温度,压力,反应时间和反应物用量对反应程度的影响。分别使用次溴酸钠(NaOBr)和次氯酸钠(NaOCl)溶液进行羟基溴化和羟基氯化反应。通过在40℃下与甲苯二异氰酸酯形成氨基甲酸酯来进行产物的聚合。通过NMR和IR光谱分析产物。在油酸甲酯的羟基溴化反应中观察到双键消耗了50%,但未确定添加-OH。在油酸甲酯的羟基氯化反应中,双键的消耗范围为40%至95%,-OH基的引入范围为14%至30%。当NaOCl与油酸甲酯双键的摩尔比为5:1时,观察到最佳收率。在羟基氯化反应中,大豆甘油三酸酯双键的消耗量为18-75%,-OH基团的形成范围为从8到33%。在25°C和120 bar下,反应时间为6 h,NaOCl与双键之比为10 / l时,大豆一步羟基氯化的转化率最高。当将反应产物重新引入反应器并用NaOCl再处理时,获得了更好的结果,观察到75%的双键消耗和33%的-OH基团形成。 (C)2005 Elsevier B.V.保留所有权利。

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