Tuning selectivity in the gas phase hydrogenation of phenylacetylene over the platinum-mesoporous carbon nitride composites using organic modifiers

被引:2
作者
Akhmedov, V. M. [1 ]
Melnikova, N. E. [1 ]
Akhmedov, Vs M. [1 ]
Tagiyev, D. B. [1 ]
机构
[1] Natl Acad Sci Azerbaijan, M Nagiev Inst Catalysis & Inorgan Chem, 113 Prosp H Javid, AZ-1143 Baku, Azerbaijan
关键词
mesoporous carbon nitride; platinum complexes; heterogeneous catalysis; phenylacetylene; styrene; hydrogenation; CATALYTIC ACTIVITY; PD; PALLADIUM; ACETYLENE; NANOPARTICLES; KINETICS; SUPPORTS; STYRENE; DESIGN;
D O I
10.1007/s11172-022-3408-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The platinum nanocomposites with mesoporous carbon nitride (Pt/mpg-C3N4) were synthesized by in situ reduction of H2PtCl6 center dot 6H(2)O with aqueous methanol and studied as catalysts in phenylacetylene hydrogenation in the gas phase at 150 degrees C and atmospheric pressure in the flow process. The efficiency of hydrogenation can be enhanced by using available organic modifiers. The addition of pyridine, piperidine, or morpholine to the starting solution of phenylacetylene in hexane provides 95-100% conversion and 90-92% selectivity to styrene on the Pt/mpg-C3N4 catalyst. A sharp increase in the selectivity to styrene without substantial changes in conversion is observed when THF, ethanol, triethylamine, dioxane, or chloroform are used as diluents. No loss of activity or selectivity was observed during 10-h tests of the catalyst in the flow process.
引用
收藏
页码:276 / 282
页数:7
相关论文
共 42 条
[31]   Single-atom Catalysis Using Pt/Graphene Achieved through Atomic Layer Deposition [J].
Sun, Shuhui ;
Zhang, Gaixia ;
Gauquelin, Nicolas ;
Chen, Ning ;
Zhou, Jigang ;
Yang, Songlan ;
Chen, Weifeng ;
Meng, Xiangbo ;
Geng, Dongsheng ;
Banis, Mohammad N. ;
Li, Ruying ;
Ye, Siyu ;
Knights, Shanna ;
Botton, Gianluigi A. ;
Sham, Tsun-Kong ;
Sun, Xueliang .
SCIENTIFIC REPORTS, 2013, 3
[32]   Graphitic carbon nitride materials: variation of structure and morphology and their use as metal-free catalysts [J].
Thomas, Arne ;
Fischer, Anna ;
Goettmann, Frederic ;
Antonietti, Markus ;
Mueller, Jens-Oliver ;
Schloegl, Robert ;
Carlsson, Johan M. .
JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (41) :4893-4908
[33]   Catalytic Reactions of Acetylene: A Feedstock for the Chemical Industry Revisited [J].
Trotus, Ioan-Teodor ;
Zimmermann, Tobias ;
Schueth, Ferdi .
CHEMICAL REVIEWS, 2014, 114 (03) :1761-1782
[34]   A Metal-Free Carbon-Based Catalyst: An Overview and Directions for Future Research [J].
Veerakumar, Pitchaimani ;
Thanasekaran, Pounraj ;
Subburaj, Thiruvengadam ;
Lin, King-Chuen .
C-JOURNAL OF CARBON RESEARCH, 2018, 4 (04)
[35]   Advances in the Design of Nanostructured Catalysts for Selective Hydrogenation [J].
Vile, Gianvito ;
Albani, Davide ;
Almora-Barrios, Neyvis ;
Lopez, Nuria ;
Perez-Ramirez, Javier .
CHEMCATCHEM, 2016, 8 (01) :21-33
[36]   A Stable Single-Site Palladium Catalyst for Hydrogenations [J].
Vile, Gianvito ;
Albani, Davide ;
Nachtegaal, Maarten ;
Chen, Zupeng ;
Dontsova, Dariya ;
Antonietti, Markus ;
Lopez, Nuria ;
Perez-Ramirez, Javier .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (38) :11265-11269
[37]   Gas phase selective hydrogenation of phenylacetylene to styrene over Au/Al2O3 [J].
Wang, Xiaodong ;
Keane, Mark A. .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2019, 94 (12) :3772-3779
[38]   Selective hydrogenation of phenylacetylene over bimetallic Pd-Cu/Al2O3 and Pd-Zn/Al2O3 catalysts [J].
Wang, Zhanqi ;
Yang, Lei ;
Zhang, Rui ;
Li, Li ;
Cheng, Zhenmin ;
Zhou, Zhiming .
CATALYSIS TODAY, 2016, 264 :37-43
[39]   Kinetics of phenylacetylene hydrogenation over Pt/γ-Al2O3 catalyst [J].
Wilhite, BA ;
McCready, MJ ;
Varma, A .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2002, 41 (14) :3345-3350
[40]   BASF NanoSelect™ Technology: Innovative Supported Pd- and Pt-based Catalysts for Selective Hydrogenation Reactions [J].
Witte, Peter T. ;
Berben, Peter H. ;
Boland, Susan ;
Boymans, Evert H. ;
Vogt, Dieter ;
Geus, John W. ;
Donkervoort, Johannes G. .
TOPICS IN CATALYSIS, 2012, 55 (7-10) :505-511