四丁基溴化铵催化合成环氧大豆油
Synthesis of epoxy soybean oil catalyzed by tetrabutylammonium bromide
  
DOI:
中文关键词:  无溶剂  四丁基溴化铵  叔丁基过氧化氢  环氧大豆油
英文关键词:solvent free  tetrabutylammonium bromide  tert-butyl hydroperoxide  epoxy soybean oil
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Author NameAffiliation
PU Jiyun, YANG Xiaojun, BAI Hang, etc  
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中文摘要:
      在无溶剂无羧酸条件下,以四丁基溴化铵为相转移催化剂,用65%的叔丁基过氧化氢(TBHP)为氧源直接合成环氧大豆油。考察了反应温度、反应时间、催化剂用量及TBHP与碳碳双键摩尔比对环氧化反应的影响,通过红外光谱对催化环氧化的机理进行了初步探究。结果表明:在反应温度65?℃、反应时间3 h、催化剂用量3.0 g(10.0 g大豆油)、TBHP与碳碳双键摩尔比 1.5∶?1条件下,催化环氧化效果最好,环氧值、转化率和选择性分别达到3.5%、53.9%和77.5%。此方法操作简单,催化剂价格低,简化了工艺流程,降低了工艺成本,同时克服了传统方法使用羧酸和溶剂等造成的弊端。
英文摘要:
      In the absence of solvent and carboxylic acid, epoxy soybean oil was synthesized with tetrabutylammonium bromide as phase transfer catalyst and TBHP (65%) as oxygen source. The effects of reaction time, reaction temperature, dosage of catalyst and molar ratio of TBHP to carbon-carbon double bond on the epoxy reaction were investigated, and the reaction mechanism was analyzed by FTIR. The results showed that the optimal reaction conditions were obtained as follows: reaction temperature 65?℃, reaction time 3 h, dosage of catalyst 3.0 g(soybean oil mass 10.0 g), molar ratio of TBHP to carbon-carbon double bond 1.5∶?1.Under the optimal conditions, the catalytic epoxy result was the best, and the epoxy value of the product, conversion and selectivity could reach 3.5%, 53.9% and 77.5%, respectively. The method had the items of simply process, easy operation and low cost, and it overcame the drawbacks of the traditional methods of using carboxylic acids and solvents.
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