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二氧化硅负载磷钨酸催化合成蒽醌
引用本文:王桂荣,栾艳勤,郝苏霞,赵新强,王延吉. 二氧化硅负载磷钨酸催化合成蒽醌[J]. 石油化工, 2011, 40(1): 69-74
作者姓名:王桂荣  栾艳勤  郝苏霞  赵新强  王延吉
作者单位:河北工业大学化工学院,天津,300130
基金项目:河北省自然科学基金资助项目,河北省教育厅博士基金资助项目
摘    要:采用等体积浸渍法制备了负载型磷钨酸(HPW)催化剂,将其用于催化邻苯甲酰苯甲酸(BBA)脱水合成蒽醌;采用XRD,FTIR,TG-DTG等手段对SiO_2负载的磷钨酸(HPW/SiO_2)催化剂进行表征;考察了载体种类、焙烧温度、HPW负载量对其催化性能的影响。实验结果表明,制备负载型HPW催化剂的适宜条件为:以SiO_2为载体、焙烧温度250℃、焙烧时间3 h、HPW负载量为30%。HPW/SiO_2催化剂催化合成蒽醌的适宜反应条件为:催化剂与BBA的质量比为1.60、反应温度220℃、反应时间2.0 h,在此条件下,蒽醌收率可达99.6%。HPW/SiO_2催化剂的稳定性较差,BET,UV-Vis,Py-IR表征结果显示,积碳结焦使催化剂B酸酸量减小是催化剂失活的原因。

关 键 词:邻苯甲酰苯甲酸  脱水  蒽醌  磷钨酸催化剂  二氧化硅

Synthesis of Anthraquinone over HPW/SiO2 Catalyst
Wang Guirong,Luan Yanqin,Hao Suxia,Zhao Xinqiang,Wang Yanji. Synthesis of Anthraquinone over HPW/SiO2 Catalyst[J]. Petrochemical Technology, 2011, 40(1): 69-74
Authors:Wang Guirong  Luan Yanqin  Hao Suxia  Zhao Xinqiang  Wang Yanji
Affiliation:Wang Guirong,Luan Yanqin,Hao Suxia,Zhao Xinqiang,Wang Yanji (School of Chemical Engineering and Technology,Hebei University of Technology,Tianjin 300130,China)
Abstract:A series of the supported phosphotungstic acid(HPW) catalysts were prepared through an isochoric impregnation method and were used in synthesis of anthraquinone(AQ) through dehydration of o-benzoylbenzoic acid(BBA),with SiO2,activated carbon,bentonite orγ-Al2O3 as supports.The supported catalyst HPW/SiO2 was characterized by means of TG-DTG,XRD and FTIR.Effects of the support type,calcination temperature and HPW loading on the catalyst activity were investigated and the catalytic performance of HPW/SiO2 catalyst in the anthraquinone synthesis was evaluated.The results indicated that under the optimal conditions for the catalyst preparation:SiO2 as support, calcination temperature 250℃,calcination time 3 h and HPW loading 30%(mass fraction),and the optimal conditions for the synthesis:m(catalyst):m(BBA) 1.60,reaction temperature 220℃and reaction time 2 h,the AQ yield could reach 99.6%.But the HPW/SiO2 catalyst stability in the AQ synthesis was not good.It was found by means of BET,UV-Vis and Py-IR that the catalyst deactivation was due to decrease of the Br(o|¨)nsted acid sites,which was caused by coking on the catalyst surface.
Keywords:o-benzoylbenzoic acid  dehydration  anthraquinone  phosphotungstic acid catalyst  silicon dioxide  
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