A Fe3O4@Nico@Ag nanocatalyst for the hydrogenation of nitroaromatics

doi:10.1016/S1872-2067(14)60316-8

摘要/Abstract

摘要：

We report the fabrication and characterization of a magnetically recyclable Fe₃O₄@Nico@Ag catalyst for reduction reactions in the liquid phase. Fe₃O₄ is a magnetic core and nicotinic acid was used as the linker for Ag. The characterization was done with X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, vibrating sample magnetometry (VSM), and ultraviolet-visible spectroscopy. VSM measurements proved the superparamagnetic property of the catalyst.

关键词: Magnetic recycable nanocatalyst, Nitro compound, Catalytic reduction, Magnetic nanomaterial, Hydrogenation

Abstract:

Key words: Magnetic recycable nanocatalyst, Nitro compound, Catalytic reduction, Magnetic nanomaterial, Hydrogenation

U. Kurtan, Md. Amir, A. Baykal. A Fe₃O₄@Nico@Ag nanocatalyst for the hydrogenation of nitroaromatics[J]. 催化学报, 2015, 36(5): 705-711.

U. Kurtan, Md. Amir, A. Baykal. A Fe₃O₄@Nico@Ag nanocatalyst for the hydrogenation of nitroaromatics[J]. Chinese Journal of Catalysis, 2015, 36(5): 705-711.

×
扫码分享

导出引用管理器 EndNote|Ris|BibTeX

链接本文: https://www.cjcatal.com/CN/10.1016/S1872-2067(14)60316-8

https://www.cjcatal.com/CN/Y2015/V36/I5/705

参考文献

[1] Booth G. Nitro Compounds, Aromatic. In: Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH, 2005
[2] Wu X Q, Wu X W, Huang Q, Shen J S, Zhang H W. Appl Sur Sci, 2015, 331: 210
[3] Arora P K, Sasikala C, Ramana C V. Appl Microbiol Biotechnol, 2012, 93: 2265
[4] Luan F B, Xie L, Li J, Zhou Q. Chemosphere, 2013, 91: 1035
[5] Chang Y C, Chen D H. J Hazard Mater, 2009, 165: 664
[6] Feng J, Su L, Ma Y H, Ren C L, Guo Q, Chen X G. Chem Eng J, 2013, 221: 16
[7] Sun J H, Sun S P, Fan M H, Guo H Q, Qiao L P, Sun R X. J Hazard Mater, 2007, 148: 172
[8] Zok S, Goerge G, Kalsch W, Nagel R. Sci Total Environ, 1991, 109-110: 411
[9] Nair R S, Auletta C S, Schroeder R E, Johannsen F R. Fundam Appl Toxicol, 1990, 15: 607
[10] Wang G X, Zhang X Y, Yao C Z, Tian M Z. Drug Chem Toxicol, 2010, 33: 238
[11] Wu K L, Wei X W, Zhou X M, Wu D H, Liu X M, Ye Y, Wang Q. J Phys Chem C, 2011, 115: 16268
[12] Chen R Z, Wang Q Q, Du Y, Xing W L, Xu N P. Chem Eng J, 2009, 145: 371
[13] Singh R, Rao R S S. J Mol Struct, 1981, 71: 23
[14] Huh H S, Lee S W. J Mol Struct, 2007, 829: 44
[15] Yeh C W, Suen M C, Hu H L, Chen J D, Wang J C. Polyhedron, 2004, 23: 1947
[16] Laurent S, Forge D, Port M, Roch A, Robic C, Vander Elst L, Muller R N. Chem Rev, 2008, 108: 2064
[17] Zhang S X, Zhao X L, Niu H Y, Shi Y L, Cai Y Q, Jiang G B. J Hazard Mater, 2009, 167: 560
[18] Wang N, Zhu L H, Wang M Q, Wang D L, Tang H Q. Ultrason Sonochem, 2010, 17: 78
[19] Wang N, Zhu L H, Wang D L, Wang M Q, Lin Z F, Tang H Q. Ultrason Sonochem, 2010, 17: 526
[20] Ernest V, Shiny P J, Mukherjee A, Chandrasekaran N. Carbohydrate Res, 2012, 352: 60
[21] Junejo Y, Karaoğlu E, Baykal A, Sirajuddin. J Inorg Organomet Polym, 2013, 23: 970
[22] Junejo Y, Sirajuddin, Baykal A, Safdar M, Balouch A. Appl Surf Sci, 2014, 290: 499
[23] Junejo Y, Baykal A, Sirajuddin. J Inorg Organomet Polym, 2014, 24: 401
[24] Junejo Y, Baykal A. Turk J Chem, 2014, 38: 765
[25] Junejo Y, Güner A, Baykal A. Appl Surf Sci, 2014, 317: 914
[26] Sheldon R A, Wallau M, Arends I W C E, Schuchardt U. Acc Chem Res, 1998, 31: 485
[27] McMorn P, Hutchings G J. Chem Soc Rev, 2004, 33: 108
[28] Thomas J M, Raja R, Lewis D W. Angew Chem Int Ed, 2005, 44: 6456
[29] Tada M, Iwasawa Y. Chem Commun, 2006: 2833
[30] Copéret C, Basset J M. Adv Synth Catal, 2007, 349: 78
[31] Astruc D, Lu F, Aranzaes J R. Angew Chem Int Ed, 2005, 44: 7852
[32] Shahwan T, Abu Sirriah S, Nairat M, Boyaci E, Eroglu A E, Scott T B, Hallam K R. Chem Eng J, 2011, 172: 258
[33] Koga H, Kitaoka T. Chem Eng J, 2011, 168: 420
[34] Wang J, Zhang X B, Wang Z L, Wang L M, Xing W, Liu X. Nanoscale, 2012, 4: 1549
[35] Ye Y J, Chen J, Ding Q Q, Lin D Y, Dong R L, Yang L B, Liu J H. Nanoscale, 2013, 5: 5887
[36] Chang S W, Chung W J, Yu S H, Lee S J. Desalin Water Treat, 2014, DOI: 10.1080/19443994.2014.923207
[37] Zhang Y X, Yu X Y, Jia Y, Jin Z, Liu J H, Huang X J. Eur J Inorg Chem, 2011, 2011: 5096
[38] Lin F, Doong R. J Phys Chem C, 2011, 115: 6591
[39] Demir M, Şenel M, Baykal A. Appl Surf Sci, 2014, 314: 697
[40] Mottaghi N, Ranjbar M, Farrokhpour H, Khoshouei M, Khoshouei A, Kameli P, Salamati H, Tabrizchi M, Jalilian-Nosrati M. Appl Surf Sci, 2014, 292: 892
[41] Tao Y T. J Am Chem Soc, 1993, 115: 4350
[42] Ahn S J, Son D H, Kim K. J Mol Struct, 1994, 324: 223
[43] Shafi K V P M, Ulman A, Yan X Z, Yang N L, Estournes C, White H, Rafailovich M. Langmuir, 2001, 17: 5093
[44] Xuan S H, Hao L Y, Jiang W Q, Gong X L, Hu Y, Chen Z Y. J Magn Magn Mater, 2007, 308: 210
[45] Unal B, Toprak M S, Durmus Z, Sözeri H, Baykal A. J Nanopart Res, 2010, 12: 3039
[46] Suksrichavalit T, Prachayasittikul S, Piacham T, Isarankura-Na-Ayudhya C, Nantasenamat C, Prachayasittikul V. Molecules, 2008, 13: 3040
[47] Unal B, Durmus Z, Kavas H, Baykal A, Toprak M S. Mater Chem Phys, 2010, 123: 184
[48] Tang M Y, Zhang S, Li X X, Pang X B, Qiu H X. Mater Chem Phys, 2014, 148: 639
[49] Le X D, Dong Z P, Zhang W, Li X L, Ma J T. J Mol Catal A, 2014, 395: 58
[50] Kurtan U, Baykal A. Mater Res Bull, 2014, 60: 79
[51] Demirelli M, Karaoğlu E, Baykal A, Sözeri H, Uysal E. J Alloy Compd, 2014, 582: 201
[52] Karaoğlu E, Özel U, Caner C, Baykal A, Summak M M, Sözeri H. Mater Res Bull, 2012, 47: 4316
[53] Karaoglu E, Summak M M, Baykal A, Sözeri H, Toprak M S. J Inorg Organomet Polym, 2013, 23: 409
[54] Kurtan U, Baykal A. J Inorg Organomet Polym, 2015, DOI: 10.1007/s10904-014-0138-5
[55] Demirelli M, Karaoğlu E, Baykal A, Sözeri H, Uysal E, Duygulu O. J Inorg Organomet Polym, 2013, 23: 937
[56] Demirelli M, Karaoglu E, Baykal A, Sozeri H. J Inorg Organomet Polym, 2013, 23: 1274
[57] Amir M, Kurtan U, Baykal A. J Ind Eng Chem, 2015, DOI: 10.1016/j.jiec.2015.01.013
[58] Rauf M A, Meetani M A, Khaleel A, Ahmed A. Chem Eng J, 2010, 157: 373
[59] Gupta A K, Naregalkar R R, Vaidya V D, Gupta M. Nanomedicine, 2007, 2: 23

A Fe₃O₄@Nico@Ag nanocatalyst for the hydrogenation of nitroaromatics

A Fe₃O₄@Nico@Ag nanocatalyst for the hydrogenation of nitroaromatics

PDF

可视化

摘要/Abstract

引用本文

使用本文

扫码分享

参考文献

相关文章 15

编辑推荐

Metrics

[1]	Md. Amir, U. Kurtan, A. Baykal. Synthesis and application of magnetically recyclable nanocatalyst Fe₃O₄@Nico@Cu in the reduction of azo dyes[J]. 催化学报, 2015, 36(8): 1280-1286.
[2]	Dana Bílková, Petr Jansa, Iva Paterová, Libor Červený. Hydrogenation of coumarin to octahydrocoumarin over a Ru/Ccatalyst[J]. 催化学报, 2015, 36(7): 957-960.
[3]	Sanjay Srivastava, Pravakar Mohanty, Jigisha K. Parikh, Ajay K. Dalai, S. S. Amritphale, Anup K. Khare. Cr-free Co-Cu/SBA-15 catalysts for hydrogenation of biomass-derived α-, β-unsaturated aldehyde to alcohol[J]. 催化学报, 2015, 36(7): 933-942.
[4]	Susmit Basu. High enantioselectivity in the asymmetric hydrogenation of ketones by a supported Pt nanocatalyst on a mesoporous modified MCM-41 support[J]. 催化学报, 2015, 36(4): 634-638.
[5]	Anne Giroir-Fendler, Sonia Gil, Alexandre Baylet. (La_0.8A_0.2)MnO₃ (A = Sr, K) perovskite catalysts for NO and C₁₀H₂₂ oxidation and selective reduction of NO by C₁₀H₂₂[J]. 催化学报, 2014, 35(8): 1299-1304.
[6]	Cuong Duong-Viet, Housseinou Ba, Yuefeng Liu, Lai Truong-Phuoc, Jean-Mario Nhut, Cuong Pham-Huu. Nitrogen-doped carbon nanotubes on silicon carbide as a metal-free catalyst[J]. 催化学报, 2014, 35(6): 906-913.
[7]	De Chen, Anders Holmen, Zhijun Sui, Xinggui Zhou. Carbon mediated catalysis：A review on oxidative dehydrogenation[J]. 催化学报, 2014, 35(6): 824-841.
[8]	Jerrik Mielby, Raju Poreddy, Christian Engelbrekt, Søren Kegnæs. Highly selective formation of imines catalyzed by silver nanoparticles supported on alumina[J]. 催化学报, 2014, 35(5): 670-676.
[9]	Hossein Khoshro, Hamid R. Zare, Rasoul Vafazadeh. Electrocatalytic measurement of H₂O₂ concentration using bis(N-2-methylphenyl-salicyldenaminato)copper(Ⅱ) spiked in a carbon paste electrode[J]. 催化学报, 2014, 35(2): 247-254.
[10]	Lucie Smoláková, Šárka Botková, Libor Čapek, Peter Priecel, Agnieszka Sołtysek, Martin Kout, Lenka Matějová. Precursors of active Ni species in Ni/Al₂O₃ catalysts for oxidative dehydrogenation of ethane[J]. 催化学报, 2013, 34(10): 1905-1913.
[11]	Sachin U. NANDANWAR, Mousumi CHAKRABORTY. Synthesis of Colloidal CuO/γ-Al₂O₃ by Microemulsion and Its Catalytic Reduction of Aromatic Nitro Compounds[J]. 催化学报, 2012, 33(9): 1532-1541.
[12]	K. Joseph Antony RAJ, M. G. PRAKASH, R. MAHALAKSHMY, T. ELANGOVAN, B. VISWANATHAN. Liquid Phase Hydrogenation of Nitrobenzene over Nickel Supported on Titania[J]. 催化学报, 2012, 33(8): 1299-1305.
[13]	Achim STOLLE, Christine SCHMOGER, Bernd ONDRUSCHKA, Werner BONRATH. Liquid Phase Hydrogenation of Benzalacetophenone: Effect of Solvent, Catalyst Support, Catalytic Metal and Reaction Conditions[J]. 催化学报, 2011, 32(8): 1312-1322.
[14]	Yan ZHU, Huifeng QIAN, Anindita DAS, Rongchao JIN. Comparison of the Catalytic Properties of 25-Atom Gold Nanospheres and Nanorods[J]. 催化学报, 2011, 32(7): 1149-1155.
[15]	Mouna AOUN, Aicha BENAMAR, Mohamed CHATER. Rh/ZnO-Al2O3 Catalysts for Selective Hydrogenation of Crotonaldehyde[J]. 催化学报, 2011, 32(7): 1185-1190.