共查询到19条相似文献,搜索用时 109 毫秒
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以强酸性阳离子交换树脂为催化剂合成氯乙酸甲酯,研究催化反应的动力学,研究确定为表观正、逆向二级反应,求得其表观活化能为Ea+=34.201KJ/mol,Ea=48.305KJ/mol。 相似文献
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磺酸型阳离子交换树脂催化合成肉桂酸甲酯 总被引:11,自引:0,他引:11
以磺酸型阳离子交换树脂为催化剂,由肉桂酸和甲醇合成了肉桂酸甲酯。考察了反应条件对酯化反应的影响和树脂的催化稳定性。结果表明,肉桂酸的转化率可达95.5%,且催化剂的性能稳定。 相似文献
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使用阳离子交换树脂D61、D72为催化剂,合成了七种巯基乙酸酯。文中对影响反应的诸因素进行了讨论。酯收率为90%左右。 相似文献
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以丙烯酸和甲醇为原料,强酸性阳离子交换树脂Amberlyst-15为催化剂,对苯二酚为阻聚剂,合成丙烯酸甲酯。考察了醇酸摩尔比、催化剂用量和温度对反应过程的影响,在实验范围内,随着温度或者催化剂用量的增加,反应速率加快,丙烯酸的转化率也不断提高。醇酸摩尔比的增加能提高丙烯酸的转化率,反应速率出现先增加后减缓的现象。与此同时,建立该催化酯化反应的Pseudo-Homogeneous(PH)的理想和非理想以及Langmuir-Hinshelwood(LH)反应动力学模型,辨识得到相应反应动力学方程。经比较,采用活度替代物质的量浓度的LH模型的平均相对偏差(MRD)最小,计算值为1.466%,最适合实际反应。 相似文献
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以丙烯酸和甲醇为原料,强酸性阳离子交换树脂Amberlyst-15为催化剂,对苯二酚为阻聚剂,合成丙烯酸甲酯。 考察了醇酸摩尔比、催化剂用量和温度对反应过程的影响,在实验范围内,随着温度或者催化剂用量的增加,反应速率加快,丙烯酸的转化率也不断提高。 醇酸摩尔比的增加能提高丙烯酸的转化率,反应速率出现先增加后减缓的现象。 与此同时,建立该催化酯化反应的Pseudo-Homogeneous(PH)的理想和非理想以及Langmuir-Hinshelwood(LH)反应动力学模型,辨识得到相应反应动力学方程。 经比较,采用活度替代物质的量浓度的LH模型的平均相对偏差(MRD)最小,计算值为1.466%,最适合实际反应。 相似文献
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强酸阳离子交换树脂催化性能的研究 总被引:1,自引:1,他引:1
通过叔丁醇脱水生成异丁烯的反应研究对比了国内外常见种类的凝胶型和大孔型强酸阳离子交换树脂的催化性能,并对树脂的性质,预处理方法,以及其用量和再生程度等因素对树脂催化活性的影响进行了研究。在此基础上,合成了具有较高催化活性的新型大孔强酸阳离子交换树脂。 相似文献
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G. S. Dmitriev A. V. Terekhov S. N. Khadzhiev L. N. Zanaveskin 《Russian Journal of Applied Chemistry》2016,89(1):45-50
Technological specific features of the solketal synthesis on a KU-2-8 cation-exchange resin were improved. Data are presented on the mutual solubility of the components in the glycerol–acetone–water and glycerol–acetone–water–ethanol systems. It is shown that use of ethanol for homogenization of the starting reagents is more than twice more efficient than performing the process with delivery of an emulsion of the reagents or reaching a full solubility of glycerol in acetone due to the 20-fold excess of the latter at 35°C. It is shown that the delivery of a glycerol emulsion in acetone to an immobile bed of a heterogeneous catalyst working in the falling-film mode leads to flooding of the reactor at spraying densities exceeding 0.15 m3 m–2 h–1. 相似文献
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The type of bonding of Cr(III) on the surface of cation-exchange resins has been studied. The complexes of Cr(III) with ethylenediamine were obtained by direct synthesis on the surface. Coordination to nitrogen bases increases the catalytic activity of Cr(III) ions in hydrogen peroxide decomposition.
Cr(III) . Cr(III) . Cr(III) .相似文献
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Cylindrical pellets were made by mixing ion-exchange resin particles with binding powders and heating to 140°C. To compare catalytic activities of these resin pellets with those of resin particles and sulfuric acid, the esterification of palmitic acid with isobutyl alcohol was carried out in a batch reactor. The rate equation for sulfuric acid could be applied to ion-exchange resins although the values of parameters were different. 相似文献
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Takao Fujimori Kousuke KurisakiTadashi Okobira Kazuya UezuKazuhisa Yoshimura 《Polymer Degradation and Stability》2011,96(8):1516-1521
This paper deals with the desulfonation properties of some strong acid cation-exchange resins. The sulfate concentration in solution is continuously increased when a strong acid cation-exchange resin is mixed with water. The leaching of sulfate results from the desulfonation of the fixed group, and the amount of leached sulfate depends on the counter ion charge, the crosslinking degree and the exchanger matrix. The effects of the counter ion charge on the desulfonation rate suggested that the counter ion induces the nucleophilic attack of a water molecule on the sulfo group. This interpretation was supported by semiempirical molecular orbital calculations for the C6H5SO3−Mm+ (Mm+ = Na+, Mg2+ and Al3+) systems, and the transition state of the Na+ system was successfully predicted by DFT calculations. The crosslinking degree influenced the desulfonation rate, which can be related to the decreasing hydration number of each counter ion in the resin phase with the increasing crosslinking degree. Furthermore, different exchanger matrices produced the differences in the rates, which may be derived from the electron-density donation from the exchanger matrix to the sulfo group. The desulfonation is governed by the electron-density of the sulfur atom and the water activity in the solid phase. 相似文献
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The kinetics of esterification of bisphenol‐A based epoxy resin with acrylic acid in presence of triphenylphosphine has been studied. The reaction exhibits a first‐order rate dependence with respect to [Epoxy] and [Catalyst]. A first‐order dependence of rate with respect to [Acid] has been observed during a particular kinetic run. However, a retarding effect of [Acid] on the rate has been observed by increasing the initial concentration of acid. A suitable mechanism consistent with the kinetic data is proposed and discussed. © 2004 Wiley Periodicals, Inc. Int J Chem Kinet 36: 280–285, 2004 相似文献
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