Effect of initial solution apparent pH on nano-sized nickel catalysts in p-nitrophenol hydrogenation

被引:45
作者
Chen, Rizhi [1 ]
Wang, Qinqin [1 ]
Du, Yan [2 ]
Xing, Weihong [1 ]
Xu, Nanping [1 ]
机构
[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Coll Chem & Chem Engn, Nanjing 210009, Peoples R China
[2] Nanjing Univ Technol, Coll Environm Sci, Nanjing 210009, Peoples R China
关键词
Apparent pH effect; Nano-sized nickel; p-Nitrophenol; Catalytic hydrogenation; AMINOPHENOL; NITROBENZENE; OXIDATION; KINETICS;
D O I
10.1016/j.cej.2008.07.042
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
The effect of initial solution apparent pH (pH.) on nano-sized nickel in the catalytic hydrogenation of p-nitrophenol to p-aminophenol was investigated in detail. Experimental results show that the catalytic activity of the nano-sized nickel shows a strong dependence on the initial Solution pH., and is the highest at the initial solution pH(a) 4.8. At lower or higher pH(a) values the nano-sized nickel will obviously deactivate, but the deactivation mechanisms are fully different. With respect to the former, the nickel dissolution and the strong adsorption of the complex compound of nickel ion and p-nitrophenol on the surface of nano-sized nickel are the main reasons. The severe agglomeration of nickel particles also causes the deactivation of nickel used at the initial solution pH(a) 1.6. For the latter the main reasons are the formation of nickel hydroxide surface species and the decrease of p-nitrophenol adsorption on the hydrogenation sites. (c) 2008 Published by Elsevier B.V.
引用
收藏
页码:371 / 376
页数:6
相关论文
共 15 条
[1]
Theoretical infrared spectrum and revised assignment for para-nitrophenol.: Density functional theory studies [J].
Abkowicz-Bienko, AJ ;
Latajka, Z ;
Bienko, DC ;
Michalska, D .
CHEMICAL PHYSICS, 1999, 250 (02) :123-129
[2]
The photodegradation kinetics of aqueous sodium oxalate solution using TiO2 catalyst [J].
Bangun, J ;
Adesina, AA .
APPLIED CATALYSIS A-GENERAL, 1998, 175 (1-2) :221-235
[3]
Deactivation of metal catalysts in liquid phase organic reactions [J].
Besson, M ;
Gallezot, P .
CATALYSIS TODAY, 2003, 81 (04) :547-559
[4]
Selective oxidation of D-glucose on gold catalyst [J].
Biella, S ;
Prati, L ;
Rossi, M .
JOURNAL OF CATALYSIS, 2002, 206 (02) :242-247
[5]
The effect of titania structure on Ni/TiO2 catalysts for p-nitrophenol hydrogenation [J].
Chen, Rizhi ;
Du Yan ;
Xing Weihong ;
Xu Nanping .
CHINESE JOURNAL OF CHEMICAL ENGINEERING, 2006, 14 (05) :665-669
[6]
Synthesis of p-aminophenol from p-nitrophenol over nano-sized nickel catalysts [J].
Du, Y ;
Chen, HL ;
Chen, RZ ;
Xu, NP .
APPLIED CATALYSIS A-GENERAL, 2004, 277 (1-2) :259-264
[7]
Poisoning effect of some nitrogen compounds on nano-sized nickel catalysts in p-nitrophenol hydrogenation [J].
Du, Yan ;
Chen, Hongling ;
Chen, Rizhi ;
Xu, Nanping .
CHEMICAL ENGINEERING JOURNAL, 2006, 125 (01) :9-14
[8]
Effect of initial solution pH on the degradation of Orange II using clay-based Fe nanocomposites as heterogeneous photo-Fenton catalyst [J].
Feng, JY ;
Hu, XJ ;
Yue, PL .
WATER RESEARCH, 2006, 40 (04) :641-646
[9]
Surface behavior of nickel powders in aqueous suspensions [J].
Hernández, N ;
Moreno, R ;
Sánchez-Herencia, AJ ;
Fierro, JLG .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (10) :4470-4474
[10]
Catalytic wet air oxidation of aqueous solution of 2-chlorophenol over Ru/zirconia catalysts [J].
Li, Ning ;
Descorme, Claude ;
Besson, Michele .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 71 (3-4) :262-270