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首页> 外文期刊>Kinetics and catalysis >The role of para-meta isomerization in the selective synthesis of para-tert-butylphenol in the presence of modern macroporous sulfonic cation-exchange resins
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The role of para-meta isomerization in the selective synthesis of para-tert-butylphenol in the presence of modern macroporous sulfonic cation-exchange resins

机译:在现代大孔磺酸阳离子交换树脂存在下对位异构化在对叔丁基苯酚选择性合成中的作用

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摘要

The formation of meta-tert-butylphenol (m-TBP), which decreasing the quality of the commercial product, is shown to be possible in the target synthesis of para-tert-butylphenol (p-TBP) in the presence of sulfonic cation-exchange resins using macroporous Amberlyst 36 Dry as an example. The equilibrium concentration of m-TBP in the liquid phase (the maximum value at 409 K is 47 wt %) is calculated from experimental and published data. Up to 10 wt % m-TBP (on the reaction mixture basis) is formed at the maximum values of temperature (409 K) and contact time (450 min). Kinetic characteristics are determined for the + phenol reaction, which supplements the kinetic model for the production of p-TBP. The rate constants of this reaction are several orders of magnitude smaller than those for the main (ortho-para) transformations. The temperature range (353-383 K) and contact time at which the formation of m-TBP is minimum and exerts no effect on the qualitative characteristics of the target p-isomer are determined.
机译:研究表明,在存在磺酸阳离子的条件下,对叔丁基苯酚(p-TBP)的目标合成中可能形成降低商业产品质量的间叔丁基苯酚(m-TBP)。以大孔Amberlyst 36 Dry为例交换树脂。根据实验数据和公开数据计算出液相中m-TBP的平衡浓度(409 K处的最大值为47 wt%)。在温度(409 K)和接触时间(450分钟)的最大值下形成高达10 wt%的m-TBP(基于反应混合物)。确定了+苯酚反应的动力学特征,这补充了生产p-TBP的动力学模型。该反应的速率常数比主(邻位)转换的速率常数小几个数量级。确定了温度范围(353-383 K)和接触时间,在该温度范围内m-TBP的形成最小,并且对目标p-异构体的定性特性没有影响。

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