石油化工高等学校学报

石油化工高等学校学报 ›› 2012, Vol. 25 ›› Issue (4): 10-13.DOI: 10.3969/j.issn.1006-396X.2012.04.003

• 石油化工 • 上一篇    下一篇

NiB/C催化剂的制备及其在合成对氨基苯酚中的应用

王利,宋威,张宇,秦玉才,王旺银,宋丽娟*   

  1. (辽宁石油化工大学辽宁省石油化工重点实验室,辽宁抚顺113001)
  • 收稿日期:2012-04-09 出版日期:2012-08-25 发布日期:2012-08-25
  • 作者简介:王利(1984-),女,河北石家庄市,在读硕士
  • 基金资助:
    辽宁省教育厅科学技术研究项目(20060501)

Preparation of NiB/C Catalyst and Its Application in the Synthesis of p-Aminophenol

  1. (Liaoning Key Laboratory of Petrochemical Engineering, Liaoning Shihua University, Fushun Liaoning 113001, P.R.China)
  • Received:2012-04-09 Published:2012-08-25 Online:2012-08-25

摘要: 采用化学还原法制备了NiB/C催化剂,利用电感耦合等离子直读光谱(ICP)、X-射线衍射(XRD)、扫描电镜(SEM)和差示扫描量热分析(DSC)等表征手段对其组成、结构、形貌及最高晶化温度进行了分析,对硫酸锌水溶液中硝基苯催化加氢制备对氨基苯酚(PAP)的反应及其催化性能进行了研究。表征结果显示,NiB/C催化剂中非晶态NiB合金的组成为Ni79.4B20.6,最高晶化温度为643K,合金颗粒粒度约为30nm。实验结果表明,硫酸锌溶液中硝基苯催化加氢反应硝基苯转化率为80.23%,对氨基苯酚选择性为11.21%,NiB/C催化剂具有较高的催化加氢活性。

关键词: NiB/C催化剂 , 硝基苯 , 催化加氢 , 对氨基苯酚 , 硫酸锌

Abstract: A NiB/C catalyst was prepared by a chemical reduction method, and characterized by inductively coupled plasma direct-reading spectrometer (ICP), X-ray diffraction (XRD), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) techniques. Its catalytic properties were investigated by the reaction of catalytic hydrogenation of nitrobenzene to p-aminophenol (PAP). The characterization result suggests the composition of the amorphous NiB alloy is Ni79.4B20.6, the highest crystallization temperature is 643 K and the alloy particle size is about 30 nm. Nitrobenzene conversion of 80.23%, PAP yield of 11.21% was obtained. The results show that NiB/C catalyst had high catalytic activity on the reaction of catalytic hydrogenation of nitrobenzene.

Key words: NiB/C catalyst, Nitrobenzene, Catalytic hydrogenation, p-Aminophenol, Zinc sulfate

引用本文

王利,宋威,张宇,秦玉才,王旺银,宋丽娟. NiB/C催化剂的制备及其在合成对氨基苯酚中的应用[J]. 石油化工高等学校学报, 2012, 25(4): 10-13.

WANG Li, SONG Wei, ZHANG Yu, et al. Preparation of NiB/C Catalyst and Its Application in the Synthesis of p-Aminophenol[J]. Journal of Petrochemical Universities, 2012, 25(4): 10-13.

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