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Peroxidase-catalyzed polymerization ofp-cresol in supercritical CO2

机译:过氧化物酶催化的对甲酚在超临界CO2中的聚合反应

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The feasibility of the catalysis of horseradish peroxidase (HRP)in supercriticalCO2was studied for the polymerization ofp-cresol in the presence of H2O2. The reactions were performed at 40‡C and 74.8 aim (1 100 psia) above the critical conditions ofCO2. In the initial tests with 2 mM ofP-crcsol and 1 mM of H2O2, more oligomers ofp-cresol were produced as more HRP was added. This indicates that HRP is active in supercritical CO2. HRP was not completely inhibited by H2O2at concentrations up to 20 mM. Increasing the initial concentrations ofp-cresol and H2O2to 20 mM, respectively, resulted in the formation of precipitates which were undissolved either in water or in dimcthylforamide (DMF). The effects of adding water and/or methanol as cosolvents on the reactivity of HRP were studied subsequently. When more than 13.3 mL of water per liter of reaction volume was added, the formation of precipitates was not observed. The reactivity of HRP was sustained when up to 11.8 mL of methanol per liter of reaction volume was added. In most cases conversion ofP-cresol was less than 50 for 5 hours of reaction tim
机译:研究了辣根过氧化物酶(HRP)在H2O2存在下催化对甲酚聚合的可行性。反应在40‡C和74.8 a目标(1 100 psia)下进行,高于CO2的临界条件。在使用 2 mM 的 P-crcsol 和 1 mM 的 H 2 O 2 的初始测试中,随着 HRP 的增加,产生了更多的低聚物 ofp-甲酚。这表明HRP在超临界CO2中具有活性。 HRP没有被高达20 mM浓度的H 2 O 2 O 2 AT完全抑制。将p-甲酚和H2O2的初始浓度分别提高到20 mM,导致形成不溶于水或二甲酰基孔酰胺(DMF)的沉淀物。随后研究了添加水和/或甲醇作为助溶剂对HRP反应性的影响。当每升反应体积添加超过 13.3 mL 的水时,未观察到沉淀物的形成。当每升反应体积中加入高达 11.8 mL 的甲醇时,HRP 的反应性得以维持。在大多数情况下,P-甲酚的转化率在5小时的反应时间内低于50%

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