Direct Catalytic Hydroxylation of Benzene to Phenol Catalyzed by FeCl3 Supported on Exfoliated Graphitic Carbon Nitride

被引:9
作者
Yu, Zhou-Hong [1 ]
Gan, Yu-Lin [1 ]
Xu, Jie [1 ]
Xue, Bing [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Gehu Middle Rd 21, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphitic carbon nitride (g-C3N4); FeCl3; Benzene; Hydroxylation; Phenol; HETEROGENEOUS CATALYST; MESOPOROUS SILICA; HYDROGEN-PEROXIDE; SELECTIVE HYDROXYLATION; EFFICIENT CATALYST; HIGHLY EFFICIENT; FACILE SYNTHESIS; NANOSHEETS; OXIDATION; G-C3N4;
D O I
10.1007/s10562-019-03003-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Direct hydroxylation of benzene in the presence of H2O2 is a promising approach for the production of phenol. Most of transition-metal compound catalysts have high activity yet suffer from difficulty in catalyst recycling and product purification. In this work, graphitic carbon nitride (g-C3N4) material was exfoliated, and then applied as a catalyst support to load FeCl3. The physical and chemical properties of the synthesized materials were characterized by N-2 adsorption-desorption, XRD, FT-IR, UV-Vis, XPS, and benzene-TPD. The results exhibited that the exfoliation improved the surface area and pore volume of g-C3N4, and FeCl3 was stably anchored on the surface of eg-C3N4. As a heterogeneous catalyst, FeCl3/eg-C3N4 showed good catalytic activity and selectivity in hydroxylation of benzene under H2O2 affording a maximum yield of phenol as 22% at 60 degrees C. [GRAPHICS] .
引用
收藏
页码:301 / 311
页数:11
相关论文
共 52 条
[1]   Eclectic Hydroxylation of Benzene to Phenol Using Ferrites of Fe and Zn as Durable and Magnetically Retrievable Catalysts [J].
Al-Sabagh, A. M. ;
Yehia, F. Z. ;
Eshaq, Gh. ;
ElMetwally, A. E. .
ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2017, 5 (06) :4811-4819
[2]   Ionothermal Synthesis of Crystalline, Condensed, Graphitic Carbon Nitride [J].
Bojdys, Michael J. ;
Mueller, Jens-Oliver ;
Antonietti, Markus ;
Thomas, Arne .
CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (27) :8177-8182
[3]   VOPO4•2H2O encapsulated in graphene oxide as a heterogeneous catalyst for selective hydroxylation of benzene to phenol [J].
Borah, Parijat ;
Datta, Arunabha ;
Kim Truc Nguyen ;
Zhao, Yanli .
GREEN CHEMISTRY, 2016, 18 (02) :397-401
[4]   A Vanadyl Complex Grafted to Periodic Mesoporous Organosilica: A Green Catalyst for Selective Hydroxylation of Benzene to Phenol [J].
Borah, Parijat ;
Ma, Xing ;
Kim Truc Nguyen ;
Zhao, Yanli .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (31) :7756-7761
[5]   Selective direct hydroxylation of benzene to phenol with hydrogen peroxide by iron and vanadyl based homogeneous and heterogeneous catalysts [J].
Carneiro, Liliana ;
Silva, Ana Rosa .
CATALYSIS SCIENCE & TECHNOLOGY, 2016, 6 (22) :8166-8176
[6]   Fe-g-C3N4-Catalyzed Oxidation of Benzene to Phenol Using Hydrogen Peroxide and Visible Light [J].
Chen, Xiufang ;
Zhang, Jinshui ;
Fu, Xianzhi ;
Antonietti, Markus ;
Wang, Xinchen .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (33) :11658-+
[7]   The texture evolution of g-C3N4 nanosheets supported Fe catalyst during Fischer-Tropsch synthesis [J].
Chen, Zheng ;
Zhang, Juan ;
Zheng, Shenke ;
Ding, Jian ;
Sun, Jiaqiang ;
Dong, Mei ;
Abbas, Mohamed ;
Chen, Yilong ;
Jiang, Zheng ;
Chen, Jiangang .
MOLECULAR CATALYSIS, 2018, 444 :90-99
[8]   Gold Nanoparticles Embedded in a Mesoporous Carbon Nitride Stabilizer for Highly Efficient Three-Component Coupling Reaction [J].
Datta, K. K. R. ;
Reddy, B. V. Subba ;
Ariga, Katsuhiko ;
Vinu, Ajayan .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (34) :5961-5965
[9]   Highly Selective Synthesis of Phenol from Benzene over a Vanadium-Doped Graphitic Carbon Nitride Catalyst [J].
Ding, Guodong ;
Wang, Weitao ;
Jiang, Tao ;
Han, Buxing ;
Fan, Honglei ;
Yang, Guanying .
CHEMCATCHEM, 2013, 5 (01) :192-200
[10]   Hydrothermal Glucose Modified C/V-SiO2 as a Reusable Heterogeneous Catalyst for Benzene Oxidation to Phenol by O2 [J].
Gao, Ya ;
Gao, Yuan ;
Shi, Lei ;
Sun, Qi .
CATALYSIS LETTERS, 2017, 147 (11) :2799-2806