%0 Journal Article %T 反应控制相转移催化液相丙烯环氧化工艺研究
Study on the Process of Epoxidation of Liquid Propylene by Reaction-Controlled Phase Transfer Catalyst %A 黄方方 %A 齐永红 %A 沈寒晰 %A 高爽 %A 史李刚 %A 景艳妮 %J Studies in Synthetic Chemistry %P 35-42 %@ 2332-7960 %D 2015 %I Hans Publishing %R 10.12677/SSC.2015.32006 %X
在含有反应控制相转移催化剂及H2O2的均相有机体系中,以H2O2为氧源,研究反应控制相转移催化液体丙烯(PP)环氧化制备环氧丙烷(PO)的反应过程,考察了反应温度、反应时间、原料配比、H2O2浓度对反应的影响;并进行了反应条件下H2O2的稳定性考察及反应过程中催化剂相变规律的探讨,在此基础上初步进行反应动力学探索。结果表明:反应速率随温度的升高而增加,但综合考虑H2O2的分解因素,以60℃为最佳,反应时间控制在100 min左右为宜,最佳原料配比( (摩尔比))为3:1,催化剂的催化性能与其相变状况密切相关,催化剂加量为0.3%时,H2O2浓度以1.8~2.2 mmol/g为宜;根据反应平衡建立了反应动力学速率方程,并通过matlab编程,确定了丙烯环氧化反应的反应级数及速率常数。
When using aqueous hydrogen peroxide as oxidant, the process of the reaction of the liquid pro-pylene epoxidation by reaction-controlled phase transfer catalyst was studied in the organic sol-vent including reaction-controlled phase transfer catalyst and H2O2; the effects of reaction tem-perature, the ratio of raw materials, reaction time and H2O2 concentration on the epoxidation were investigated. Under the reaction condition, the stability of H2O2 and the phase transforma-tion of the catalyst were also researched. On the basis, the reaction kinetics was explored preli-minarily. The results showed that the reaction rate increased with increasing temperature; the optimal reaction temperature was 60?C considering the factor of H2O2 decomposition; the reaction time can be controlled at about 100 min; the mole rate of raw material ( (mole)) was 3:1; the catalytic activity was closely related to its phase transition; when the dosage of catalyst was 0.3%, the concentration of H2O2 in 1.8 - 2.2 mmol/g was appropriate. The reaction rate equation was established according to the reaction equilibrium. The order and the rate constant of reaction of epoxy propane were calculated using the MATLAB program.
%K 反应控制相转移催化,丙烯,环氧化,环氧丙烷,反应动力学
Reaction-Controlled Phase-Transfer Catalysis %K Propylene %K Epoxidation %K Propylene Oxide %K Reaction Kinetics %U http://www.hanspub.org/journal/PaperInformation.aspx?PaperID=15874