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Aluminum(Ⅲ) triflate-catalyzed selective oxidation of glycerol to formic acid with hydrogen peroxide 被引量:1
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作者 Kang Kong Difan Li +3 位作者 Wenbao Ma Qingqing Zhou Guoping Tang Zhenshan Hou 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第4期534-542,M0003,共10页
Glycerol is a by-product of biodiesel production and is an important readily available platform chemical.Valorization of glycerol into value-added chemicals has gained immense attention.Herein,we carried out the conve... Glycerol is a by-product of biodiesel production and is an important readily available platform chemical.Valorization of glycerol into value-added chemicals has gained immense attention.Herein,we carried out the conversion of glycerol to formic acid and glycolic acid using H2O2 as an oxidant and metal(Ⅲ)triflate-based catalytic systems.Aluminum(Ⅲ)triflate was found to be the most efficient catalyst for the selective oxidation of glycerol to formic acid.A correlation between the catalytic activity of the metal cations and their hydrolysis constants(Kh)and water exchange rate constants was observed.At 70 ℃,a formic acid yield of up to 72% could be attained within 12 h.The catalyst could be recycled at least five times with a high conversion rate,and hence can also be used for the selective oxidation of other biomass platform molecules.Reaction kinetics and 1H NMR studies showed that the oxidation of glycerol(to formic acid)involved glycerol hydrolysis pathways with glyceric acid and glycolic acid as the main intermediate products.Both the [Al(OH)x]^n+ Lewis acid species and CF3SO3H Brosted acid,which were generated by the in-situ hydrolysis of Al(OTf)3,were responsible for glycerol conversion.The easy availability,high efficiency,and good recyclability of Al(OTf)3 render it suitable for the selective oxidation of glycerol to high value-added products. 展开更多
关键词 aluminum(Ⅲ)triflate GLYCEROL Hydrogen peroxide Selective oxidation Formic acid
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非氧化还原金属离子加速Pd(Ⅱ)催化丁香酚双键异构化反应的研究 被引量:1
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作者 何金义 李红静 朱凯 《应用化工》 CAS CSCD 北大核心 2018年第3期474-477,共4页
以Pd(OAc)_2和Al(OTf)_3为催化剂,研究非氧化还原金属离子加速Pd(Ⅱ)催化丁香酚双键异构化的反应。对不同的非氧化还原金属离子进行筛选,确定选用Al(OTf)_3为非氧化还原金属离子催化剂,采用单因素结合正交实验的方法对丁香酚的双键异构... 以Pd(OAc)_2和Al(OTf)_3为催化剂,研究非氧化还原金属离子加速Pd(Ⅱ)催化丁香酚双键异构化的反应。对不同的非氧化还原金属离子进行筛选,确定选用Al(OTf)_3为非氧化还原金属离子催化剂,采用单因素结合正交实验的方法对丁香酚的双键异构化工艺进行优化。结果表明,最佳工艺条件为:反应温度50℃,反应时间6 h,n[Al(OTf)_3]∶n[Pd(OAc)_2]=2∶1,Pd(OAc)_2和Al(OTf)_3的总用量为3.45%(以丁香酚的质量分数计)。在此条件下,反应稳定性较好,产物得率可达96.3%,其中反式异丁香酚的选择性为89.5%,产品香气较为纯正。采用IR、GC-MS、和~1H NMR等对产物进行了分析与表征。 展开更多
关键词 丁香酚 PD(OAC)2 al(otf)3 异构
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