Pt/UiO-66 Nanocomposites as Catalysts for CO2 Methanation Process

被引:28
作者
Mihet, Maria [1 ]
Blanita, Gabriela [1 ]
Dan, Monica [1 ]
Barbu-Tudoran, Lucian [1 ]
Lazar, Mihaela D. [1 ]
机构
[1] Natl Inst R&D Isotop & Mol Technol INCDTIM, 67-103 Donat St, Cluj Napoca 400293, Romania
基金
美国国家卫生研究院;
关键词
Pt/UiO-66; Catalysts; CO2; Hydrogenation; H-2-TPD; CO2-TPD; METAL-ORGANIC FRAMEWORKS; SELECTIVE OXIDATION; NANOPARTICLES; HYDROGENATION; UIO-66; CHALLENGES; PORES;
D O I
10.1166/jnn.2019.16607
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pt/UiO-66 nanocomposites with platinum target concentration of 3 wt.% were prepared by 3 preparation methods, characterized and tested in the CO2 methanation process. Choice of the microporous UiO-66 metal-organic framework (Zr6O4(OH)(4) with 1,4-benzene-dicarboxylate ligand) as catalytic support was motivated by the CO2 chemisorption capacity (proven by CO2-TPD profiles), large specific surface area (1477 m(2)/g) which favors a high dispersion of metal nanoparticles and good thermal stability. The preparation methods for the Pt/UiO-66 nanocomposites are: (1) wet-impregnation followed by reduction in H-2 at 200 degrees C for 2 h; (2) wet-impregnation followed by reduction with an aqueous solution of NaBH4; and (3) "double-solvent" method, followed by reduction with NaBH4. The UiO-66 based nanocomposites were characterized by N-2 adsorption-desorption (BET method), XRD, and SEM/TEM. The Pt/UiO-66 catalyst prepared by method 3 was chosen for catalytic testing due to its highest surface area, smallest platinum nanoparticles (PtNPs) size, the localization of PtNPs both on the grain's internal and external surface and best thermal stability in the desired temperature range. Its capacity to adsorb and activate CO2 and H-2 was evaluated in thermo-programmed desorption experiments (H-2-TPD and CO2-TPD). Hydrogen is molecularly adsorbed, while CO2 is adsorbed both molecularly and dissociatively. The catalytic performance in the CO2 methanation process was evaluated by Temperature Programmed Reactions (TPRea, 2 degrees C/min, 30-350 degrees C), at atmospheric pressure. The best results were obtained at 350 degrees C, CO2:H-2 molar ratio of 1:5.2 and GHSV = 1650 h(-1). In these conditions CO2 conversion is almost 50% and CH4 selectivity is 36%, the rest of the converted CO2 being transformed in CO.
引用
收藏
页码:3187 / 3196
页数:10
相关论文
共 31 条
[1]   Immobilizing Highly Catalytically Active Pt Nanoparticles inside the Pores of Metal-Organic Framework: A Double Solvents Approach [J].
Aijaz, Arshad ;
Karkamkar, Abhi ;
Choi, Young Joon ;
Tsumori, Nobuko ;
Roennebro, Ewa ;
Autrey, Tom ;
Shioyama, Hiroshi ;
Xu, Qiang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (34) :13926-13929
[2]   Challenges in the Greener Production of Formates/Formic Acid, Methanol, and DME by Heterogeneously Catalyzed CO2 Hydrogenation Processes [J].
Alvarez, Andrea ;
Bansode, Atul ;
Urakawa, Atsushi ;
Bavykina, Anastasiya V. ;
Wezendonk, Tim A. ;
Makkee, Michiel ;
Gascon, Jorge ;
Kapteijn, Freek .
CHEMICAL REVIEWS, 2017, 117 (14) :9804-9838
[3]   State of the art and perspectives in catalytic processes for CO2 conversion into chemicals and fuels: The distinctive contribution of chemical catalysis and biotechnology [J].
Aresta, Michele ;
Dibenedetto, Angela ;
Quaranta, Eugenio .
JOURNAL OF CATALYSIS, 2016, 343 :2-45
[4]   Sustainable Conversion of Carbon Dioxide: An Integrated Review of Catalysis and Life Cycle Assessment [J].
Artz, Jens ;
Mueller, Thomas E. ;
Thenert, Katharina ;
Kleinekorte, Johanna ;
Meys, Raoul ;
Sternberg, Andre ;
Bardow, Andre ;
Leitner, Walter .
CHEMICAL REVIEWS, 2018, 118 (02) :434-504
[5]   CO2 methanation over heterogeneous catalysts: recent progress and future prospects [J].
Aziz, M. A. A. ;
Jalil, A. A. ;
Triwahyono, S. ;
Ahmad, A. .
GREEN CHEMISTRY, 2015, 17 (05) :2647-2663
[6]   High Pressure Adsorption of CO2 and CH4 on Zr-MOFs [J].
Cavka, Jasmina H. ;
Grande, Carlos A. ;
Mondino, Giorgia ;
Blom, Richard .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2014, 53 (40) :15500-15507
[7]   Opportunities and prospects in the chemical recycling of carbon dioxide to fuels [J].
Centi, Gabriele ;
Perathoner, Siglinda .
CATALYSIS TODAY, 2009, 148 (3-4) :191-205
[8]   Pd@UiO-66: An Efficient Catalyst for Suzuki-Miyaura Coupling Reaction at Mild Condition [J].
Dong, Wenhuan ;
Feng, Cheng ;
Zhang, Li ;
Shang, Ningzhao ;
Gao, Shutao ;
Wang, Chun ;
Wang, Zhi .
CATALYSIS LETTERS, 2016, 146 (01) :117-125
[9]   Comparison of Pd-UiO-66 and Pd-UiO-66-NH2 catalysts performance for phenol hydrogenation in aqueous medium [J].
Guan, Qingqing ;
Wang, Bin ;
Chai, Xinsheng ;
Liu, Jing ;
Gu, Junjie ;
Ning, Ping .
FUEL, 2017, 205 :130-141
[10]   A dye-sensitized Pt@UiO-66(Zr) metal-organic framework for visible-light photocatalytic hydrogen production [J].
He, Jiao ;
Wang, Jiaqiang ;
Chen, Yongjuan ;
Zhang, Jinping ;
Duan, Deliang ;
Wang, Yao ;
Yan, Zhiying .
CHEMICAL COMMUNICATIONS, 2014, 50 (53) :7063-7066