Ultrafine Pt particles directed by polyvinylpyrrolidone on zeolite beta as an efficient low-temperature H2-SCR catalyst

被引:23
作者
Cao, Limei [1 ,2 ]
Wang, Qian [1 ]
Yang, Ji [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Sch Resources & Environm Engn, State Environm Protect Key Lab Environm Risk Asse, Shanghai 200237, Peoples R China
[2] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
来源
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING | 2020年 / 8卷 / 01期
基金
中国国家自然科学基金;
关键词
H-2-SCR; Low temperature; Ultrafine; Pt/Beta; Sulfur resistance; REDUCTION; NOX; PLATINUM; NANOPARTICLES; HYDROGEN; DISPERSION; CHROMIUM; STATE;
D O I
10.1016/j.jece.2019.103631
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel ultrafine Pt/Beta catalyst supported on carbon paper was prepared and applied to selective catalytic reduction of NOx by H-2 at a low temperature below 90 degrees C. Here, 0.8 wt.% Pt/Beta reached approximately 100 % NO conversion at 90 degrees C under oxygen-rich conditions (1000 ppm NO, 1 % H-2, and 4 % O-2). The influence of the dispersion and particle size of Pt on the catalytic performance was investigated using Polyvinylpyrrolidone (PVP) as a structure directing agent to regulate the Pt particles. The feeding amount of PVP significantly influenced the catalytic activity of the catalysts. When the feeding amount was less than 50 mg, the Pt particle size was smaller, and the dispersion was higher, providing a higher NO conversion. However, when the feeding amount exceeded 50 mg, the dispersion no longer increased, and the activity slightly decreased. N-2 physisorption (BET) confirmed that excessive PVP decreased the specific surface area, which suppressed the catalytic activity of Pt/Beta. Moreover, the NO conversion efficiency was dependent on the dispersion and particle size of Pt and was minimally affected by the surface area of the catalysts. The Pt/Beta catalyst system was deactivated, and an irreversible poisoning phenomenon for SO2 was observed. Zr, Ce, and V were introduced into the catalyst system as metal auxiliaries. The Ce-modified Pt-Ce/Beta catalyst prepared in this study showed resistance to SO2.
引用
收藏
页数:9
相关论文
共 37 条
[1]   LIQUID-PHASE ALKYLATION OF BENZENE WITH LIGHT OLEFINS CATALYZED BY BETA-ZEOLITES [J].
BELLUSSI, G ;
PAZZUCONI, G ;
PEREGO, C ;
GIROTTI, G ;
TERZONI, G .
JOURNAL OF CATALYSIS, 1995, 157 (01) :227-234
[2]   Vapour phase hydrogenation of phenol over Pd/C catalysts: A relationship between dispersion, metal area and hydrogenation activity [J].
Chary, Komandur V. R. ;
Naresh, Dhachapally ;
Vishwanathan, V. ;
Sadakane, Masahiro ;
Ueda, Wataru .
CATALYSIS COMMUNICATIONS, 2007, 8 (03) :471-477
[3]  
Choo ST, 2000, APPL CATAL A-GEN, V200, P177, DOI 10.1016/S0926-860X(00)00636-0
[4]   Transient isotopic kinetic study of the NO/H2/O2 (lean de-NOx) reaction on Pt/SiO2 and Pt/La-Ce-Mn-O catalysts [J].
Costa, CN ;
Efstathiou, AM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (08) :2620-2630
[5]   An investigation of the NO/H2/O2 (lean-deNOx) reaction on a highly active and selective Pt/La0.5Ce0.5MnO3 catalyst [J].
Costa, CN ;
Stathopoulos, VN ;
Belessi, VC ;
Efstathiou, AM .
JOURNAL OF CATALYSIS, 2001, 197 (02) :350-364
[6]   Industrial H2-SCR of NO on a novel Pt/MgO-CeO2 catalyst [J].
Costa, Costas N. ;
Savva, Petros G. ;
Fierro, Jose Luis G. ;
Efstathiou, Angelos M. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 75 (3-4) :147-156
[7]   Interface-Confined Ferrous Centers for Catalytic Oxidation [J].
Fu, Qiang ;
Li, Wei-Xue ;
Yao, Yunxi ;
Liu, Hongyang ;
Su, Hai-Yan ;
Ma, Ding ;
Gu, Xiang-Kui ;
Chen, Limin ;
Wang, Zhen ;
Zhang, Hui ;
Wang, Bing ;
Bao, Xinhe .
SCIENCE, 2010, 328 (5982) :1141-1144
[8]  
GUTBERLET H, 1993, CATAL TODAY, V16, P207
[9]   PREPARATION OF COLLOIDAL RHODIUM IN POLYVINYL-ALCOHOL) BY REDUCTION WITH METHANOL [J].
HIRAI, H ;
NAKAO, Y ;
TOSHIMA, N .
JOURNAL OF MACROMOLECULAR SCIENCE-CHEMISTRY, 1978, A12 (08) :1117-1141
[10]   Physicochemical Characterization of Highly Dispersed Platinum and Chromium on Zeolite Beta [J].
Izutsu, Yoshiyuki ;
Oku, Yuki ;
Hidaka, Yusuke ;
Kanaya, Naoki ;
Nakajima, Yoshiki ;
Fukuroi, Jun ;
Yoshida, Kaname ;
Sasaki, Yukichi ;
Sekine, Yasushi ;
Matsukata, Masahiko .
JOURNAL OF PHYSICAL CHEMISTRY C, 2014, 118 (20) :10746-10753