化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2015年
3期
1007-1011
,共5页
王艳涛%李坤兰%马英冲%魏立纲%王俊梅%王鑫
王豔濤%李坤蘭%馬英遲%魏立綱%王俊梅%王鑫
왕염도%리곤란%마영충%위립강%왕준매%왕흠
催化%无酸无溶剂法%脂肪酸甲酯%环氧化%合成%催化剂
催化%無痠無溶劑法%脂肪痠甲酯%環氧化%閤成%催化劑
최화%무산무용제법%지방산갑지%배양화%합성%최화제
catalysis%acid-free non-solvent%fatty acid methyl esters%epoxidation%synthesis%catalyst
在无酸、无溶剂条件下,以[C16H33N(CH3)3]3[PO4(WO3)4]为反应控制相转移催化剂,研究各因素对脂肪酸甲酯(FAME)环氧化反应的影响。结果表明,水相pH对环氧化反应的影响最大,反应适宜pH为4;适宜反应条件为过氧化氢与脂肪酸甲酯中双键摩尔比为1.05:1,反应温度50~60℃,反应时间5 h。在此反应条件下催化剂循环5次不失活,产品环氧值大于4.0%,碘值小于5 g I·(100 g)?1。并通过元素分析与红外光谱,研究了催化剂在反应过程中的变化,认为磷钨杂多阴离子的分解是导致催化剂失活的关键原因。
在無痠、無溶劑條件下,以[C16H33N(CH3)3]3[PO4(WO3)4]為反應控製相轉移催化劑,研究各因素對脂肪痠甲酯(FAME)環氧化反應的影響。結果錶明,水相pH對環氧化反應的影響最大,反應適宜pH為4;適宜反應條件為過氧化氫與脂肪痠甲酯中雙鍵摩爾比為1.05:1,反應溫度50~60℃,反應時間5 h。在此反應條件下催化劑循環5次不失活,產品環氧值大于4.0%,碘值小于5 g I·(100 g)?1。併通過元素分析與紅外光譜,研究瞭催化劑在反應過程中的變化,認為燐鎢雜多陰離子的分解是導緻催化劑失活的關鍵原因。
재무산、무용제조건하,이[C16H33N(CH3)3]3[PO4(WO3)4]위반응공제상전이최화제,연구각인소대지방산갑지(FAME)배양화반응적영향。결과표명,수상pH대배양화반응적영향최대,반응괄의pH위4;괄의반응조건위과양화경여지방산갑지중쌍건마이비위1.05:1,반응온도50~60℃,반응시간5 h。재차반응조건하최화제순배5차불실활,산품배양치대우4.0%,전치소우5 g I·(100 g)?1。병통과원소분석여홍외광보,연구료최화제재반응과정중적변화,인위린오잡다음리자적분해시도치최화제실활적관건원인。
The influence of reaction conditions on epoxidation of unsaturated fatty acid methyl ester (FAME) under acid and solvent free conditions with [C16H33N(CH3)3]3[PO4(WO3)4] as a reaction controlled phase transfer catalyst was investigated. The results indicated that pH of the aqueous phase was the most important factor and the proper pH value of solution was 4. With molar ratio of hydrogen peroxide to double bond in FAME is 1.05:1, reaction at 50—60℃ for 5 h, the catalyst could be recycled 5 times without deactivation, and epoxy value of the product was more than 4.0%, while iodine value was less than 5 g I·(100 g)?1. Change of catalyst during the epoxidation process was investigated with IR spectroscopy and elemental analysis, and the result indicated that decomposition of heteropolyphosphatotungstate anion was the key reason for catalyst deactivation.