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作 者:夏斌 马凤云[1] 张祎 刘景梅[1] 殷双杰 XIA Bin;MA Fengyun;ZHANG Yi;LIU Jingmei;YIN Shuangjie(College of Chemistry and Chemical Engineering,Xinjiang University,Urumqi 830046,China;School of Law and Humanities,China University of Mining and Technology,Beijing 100083,China;Xinjiang Dahua Fushan Chemical Company Limited,Shihezi 832000,China)
机构地区:[1]新疆大学化学化工学院,新疆乌鲁木齐830046 [2]中国矿业大学文法学院,北京100083 [3]新疆大化富山化工有限公司,新疆石河子832000
出 处:《大连工业大学学报》2024年第5期373-378,共6页Journal of Dalian Polytechnic University
基 金:中央引导地方科技发展专项资金项目(2021年度).
摘 要:基于文丘里型空化管的水力空化场强化,苯酚与过氧化氢在常温下进行氧化反应。采用气相色谱-质谱联用分析反应产物,考察反应条件对苯酚转化率的影响,并根据产物分布推测并验证了反应历程。在水力空化强化下,过氧化氢解离的羟基进攻苯酚形成对苯二酚,再由氢自由基的脱离形成半醌,最后成键形成苯醌。最佳反应条件:空化管入口压力0.4MPa,反应终温35.8℃,过氧化氢体积分数9%,溶剂水体积分数91%,初始苯酚加入量8g,反应时间10min。苯酚转化率和苯醌选择性分别为34.5%和80.5%。The oxidation reaction between phenol and H 2O_(2) at room temperature was strengthened in the field of hydrodynamic cavitation on the basis of a Venturi tube. The products were analyzed by gas chromatography-mass spectrometry. The effect of reaction conditions on the phenol conversion efficiency was investigated, and the reaction process was also deduced and verified according to the products distribution. With the enhancement of hydrodynamic cavitation field, the hydroxide radical dissociated by H 2O_(2) could attack the phenol and thus transferred into hydroquinone. Hemiquinone was formed by the dissociation of hydrogen radicals, and finally bonded to form benzoquinone. The optimum reaction conditions were with 0.4 MPa venturi tube inlet pressure, 9% volume fraction of oxidant H 2O_(2), 91% volume fraction of solvent water, 8 g initial dosage of phenol, at 35.8 ℃ for 10 min, the conversion rate of phenol and the selectivity of benzoquinone are 34.5% and 80.5%.
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