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Epoxidation of castor oil with peracetic acid formed in situ in the presence of an ion exchange resin

机译:在离子交换树脂的存在下,蓖麻油被原位形成的过乙酸环氧化

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The influence of reaction variables on the epoxidation of castor oil (CO) in benzene with peracetic acid (P) generated in situ from acetic acid (A) and hydrogen peroxide (H) in the presence of an ion exchange resin as catalyst was examined. The highest relative epoxy yield (REY) of 78.32% was achieved at 323 K after 8 h when 0.5 mol of acetic acid and 1.5 mol of 30 wt% aqueous hydrogen peroxide per mol of double bond in oil were used in the presence of 15 wt% of Amberlite IR-120. The experimental data were fitted by proposed pseudo-homogeneous kinetic model which considers the side reaction of epoxy ring cleavage involving the formation of hydroxy acetate in addition to reactions of the peracetic acid and epoxy compound formation. Temperature dependency of the kinetic parameters is expressed by a repa-rameterized Arrhenius equation. The constants of the Arrhenius equation were determined by fitting experimental data using the Marquardt method. An increase of all rate coefficients for considered reactions with temperature and good agreement of the calculated reactant and product concentrations with experimental data, indicate the correctness of the proposed kinetic model. The model was compared with pseudo-homogeneous models reported in the literature.
机译:在离子交换树脂作为催化剂的存在下,研究了反应变量对蓖麻油(CO)在苯中被乙酸(A)和过氧化氢(H)原位生成的过氧乙酸(P)环氧化的影响。当在15 wt%的油中使用每摩尔双键油中使用0.5 mol的乙酸和1.5 mol的30 wt%的过氧化氢水溶液时,在8小时后的323 K下,最高相对环氧收率(REY)为78.32%。 Amberlite IR-120的百分比。通过提出的拟均相动力学模型拟合了实验数据,该模型考虑了过氧乙酸和环氧化合物形成的反应,还涉及环氧环裂解的副反应,该反应涉及羟基乙酸的形成。动力学参数的温度依赖性通过重新设定参数的Arrhenius方程表示。通过使用Marquardt方法拟合实验数据来确定Arrhenius方程的常数。考虑到的反应的所有速率系数随温度的增加以及所计算出的反应物和产物浓度与实验数据的良好一致性表明所提出的动力学模型的正确性。该模型与文献报道的伪均质模型进行了比较。

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