CO Oxidation Efficiency and Hysteresis Behavior over Mesoporous Pd/SiO2 Catalyst

被引:18
作者
Al Soubaihi, Rola Mohammad [1 ]
Saoud, Khaled Mohammad [2 ]
Myint, Myo Tay Zar [3 ]
Gothelid, Mats A. [4 ]
Dutta, Joydeep [1 ]
机构
[1] KTH Royal Inst Technol, Sch Engn Sci, Dept Appl Phys, Funct Mat,AlbaNova Univ Ctr, S-10691 Stockholm, Sweden
[2] Virginia Commonwealth Univ Qatar, Liberal Arts & Sci Program, Doha, Qatar
[3] Sultan Qaboos Univ, Coll Sci, Dept Phys, POB 36, Muscat 123, Oman
[4] KTH Royal Inst Technol, Mat Fys, SCI, Hannes Alfvens Vag 12, S-11419 Stockholm, Sweden
关键词
CO oxidation; hysteresis; thermal stability; pretreatment; structure-activity;
D O I
10.3390/catal11010131
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
Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (T-ig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the catalysts continue to exhibit high catalytic activity (CO conversion remains at 100%) during the extinction even at temperatures lower than T-ig. The catalyst was characterized using BET, TEM, XPS, TGA-DSC, and FTIR. In this work, the influence of pretreatment conditions and stability of the active sites on the catalytic activity and hysteresis is presented. The CO oxidation on the Pd/SiO2 catalyst has been attributed to the dissociative adsorption of molecular oxygen and the activation of the C-O bond, followed by diffusion of adsorbates at T-ig to form CO2. Whereas, the hysteresis has been explained by the enhanced stability of the active site caused by thermal effects, pretreatment conditions, Pd-SiO2 support interaction, and PdO formation and decomposition.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 50 条
[1]   Inverse Hysteresis Phenomena During CO and C3H6 Oxidation over a Pt/Al2O3 Catalyst [J].
Abedi, Ali ;
Hayes, Robert ;
Votsmeier, Martin ;
Epling, William S. .
CATALYSIS LETTERS, 2012, 142 (08) :930-935
[2]   Synthesis of hierarchically porous silica aerogel supported Palladium catalyst for low-temperature CO oxidation under ignition/extinction conditions [J].
Al Soubaihi, Rola Mohammad ;
Saoud, Khaled Mohammad ;
Ye, Fei ;
Myint, Myo Tay Zar ;
Saeed, Shaukat ;
Dutta, Joydeep .
MICROPOROUS AND MESOPOROUS MATERIALS, 2020, 292
[3]   Critical Review of Low-Temperature CO Oxidation and Hysteresis Phenomenon on Heterogeneous Catalysts [J].
Al Soubaihi, Rola Mohammad ;
Saoud, Khaled Mohammad ;
Dutta, Joydeep .
CATALYSTS, 2018, 8 (12)
[4]  
An W, 2016, PHYS CHEM CHEM PHYS, V18, P30899, DOI 10.1039/c6cp04734c
[5]   Ignition, extinction, and thermal hysteresis of a heterogeneous exothermic reaction [J].
Assovskii, IG .
COMBUSTION EXPLOSION AND SHOCK WAVES, 1998, 34 (02) :163-169
[6]   Thermal behavior of Pd@SiO2 nanostructures in various gas environments: a combined 3D and in situ TEM approach [J].
Baaziz, Walid ;
Bahri, Mounib ;
Gay, Anne Sophie ;
Chaumonnot, Alexandra ;
Uzio, Denis ;
Valette, Sebastien ;
Hirlimann, Charles ;
Ersen, Ovidiu .
NANOSCALE, 2018, 10 (43) :20178-20188
[7]   DETERMINATION OF NITROGEN ADSORPTION-DESORPTION ISOTHERMS - ESTIMATION OF TOTAL PORE VOLUMES OF POROUS SOLIDS [J].
BARRETT, EP ;
JOYNER, LG .
ANALYTICAL CHEMISTRY, 1951, 23 (05) :791-792
[8]   KINETICS OF CO OXIDATION ON SINGLE-CRYSTAL PD, PT, AND IR [J].
BERLOWITZ, PJ ;
PEDEN, CHF ;
GOODMAN, DW .
JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (18) :5213-5221
[9]   RAMAN AND INFRARED-SPECTRA ON SILICA-GEL EVOLVING TOWARD GLASS [J].
BERTOLUZZA, A ;
FAGNANO, C ;
MORELLI, MA ;
GOTTARDI, V ;
GUGLIELMI, M .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 1982, 48 (01) :117-128
[10]  
Briggs D., 1990, Auger and X-ray Photoelectron Spectroscopy, V1, P657, DOI [DOI 10.1002/JCTB.280530219, 10.1002/jctb.280530219]