摘要
以氯钯酸为前驱体,采用浸渍共沉淀还原法制备Pd/纳米碳管(CNTs)和Pd/活性炭(AC)催化剂。在493 K,3.5 MPa下,考察催化剂在"苯酚+甲醇+水"原位加氢反应中的催化活性。实验结果表明,Pd/CNTs对苯酚原位加氢制环己酮有更高的选择性。通过COTPD,TEM表征结果表明,这主要是由于Pd/CNTs催化剂独特的中孔结构和内腔孔道。
Carbon nanotube(CNT) and activated carbon(AC)-supported Pd catalysts have been prepared by impregnation and reduction-precipitation method using chloropalladate acid as metal precursor.The catalytic performance for "phenol+methanol+water" in-situ hydrogenation was evaluated under 493 K,3.5 MPa. The results show that Pd/CNTs catalyst has higher selective for phenol in-situ hydrogenation to cyclohexanone. The catalysts have been characterised by CO-TPD and TEM. The mesoporosity structure and inner hollow cavities of Pd/CNTs catalyst are responsible for the distinguished properties.
作者
徐雷金
孔令鸟
赵瑞强
XU Lei-jin;KONG Ling-niao;ZHAO Rui-qiang(Zhejiang Qicai ECO Technology Co.,Ltd.,Shaoxing,Zhejiang 312000,China)
出处
《浙江化工》
CAS
2018年第6期25-28,共4页
Zhejiang Chemical Industry
关键词
PD催化剂
纳米碳管
苯酚
原位加氢
Pd catalyst
carbon nanotube
phenol
in-situ hydrogenation