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首页> 外文期刊>Journal of the American Oil Chemists' Society >Synthesis of trimethylolpropane esters of oleic acid using a multi-SO3H-functionalized ionic liquid as an efficient catalyst.
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Synthesis of trimethylolpropane esters of oleic acid using a multi-SO3H-functionalized ionic liquid as an efficient catalyst.

机译:以多SO 3 H-官能化离子液体为有效催化剂,合成油酸三羟甲基丙烷酯。

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摘要

Biodegradable trimethylolpropane triesters of oleic acid were synthesized by esterification of trimethylolpropane and oleic acid over a multi-SO3H-functionalized strong Bronsted acidic ionic liquid as the catalyst. The results showed that the esterification can proceed satisfactorily over the catalyst at an ambient pressure even without simultaneous removal of water. Under the optimal reaction conditions temperature: 100 degrees C, reaction time: 3 h, reactant molar ratio: 3.6:1, and catalyst amount, high conversion rate of trimethylolpropane (99.0%) and selectivity of trimethylolpropane triester (92.1%) were obtained. The ionic liquid was reused six times after the removal of water and no obvious change in catalytic activity was detected. Operational simplicity, high yields along with good reusability makes the multi-SO3H-functionalized ionic liquid a promising catalyst for the esterification of trimethylolpropane with oleic acid.
机译:以三羟甲基丙烷和油酸在多SO 3 功能化的强布朗斯泰德酸性离子液体为催化剂上进行酯化反应,合成了可生物降解的油酸三羟甲基丙烷三酯。结果表明,即使不同时除去水,酯化反应也可以在环境压力下在催化剂上令人满意地进行。在最佳反应条件下,温度:100℃,反应时间:3h,反应物摩尔比:3.6:1,和催化剂量,三羟甲基丙烷的高转化率(99.0%)和三羟甲基丙烷三酯的选择性(92.1%)。除去水后,离子液体重复使用了六次,未发现催化活性有明显变化。操作简便,高收率以及良好的可重复使用性使多-SO 3 官能化的离子液体成为三羟甲基丙烷与油酸酯化的有前途的催化剂。

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