Encapsulating uniform Pd nanoparticles in TS-1 zeolite as efficient catalyst for catalytic abatement of indoor formaldehyde at room temperature

被引:68
作者
Chen, Hongxia [1 ]
Zhang, Runduo [1 ]
Wang, Hao [1 ]
Bao, Wenjing [1 ]
Wei, Ying [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing Key Lab Energy Environm Catalysis, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
TS-1; zeolite; Encapsulated Pd catalyst; Complete oxidation of HCHO; Room temperature; High dispersion; COMPLETE OXIDATION; HCHO OXIDATION; PALLADIUM NANOPARTICLES; BETA-ZEOLITE; PERFORMANCE; TITANIUM; METHANE; EPOXIDATION; REMOVAL; SILICA;
D O I
10.1016/j.apcatb.2020.119311
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
One-pot hydrothermal method was adopted to synthesize Pd catalysts encapsulated by TS-1 zeolites [Pd@TS1(x)]. The strategy could effectively improve Pd dispersion and reduce the sizes of Pd nanoparticles (NPs). These Pd NPs with an average size of 2.2-3.5 nm were well encapsulated inside the TS-1 matrix. The Pd@TS-1(x) catalysts with Si/Ti molar ratio of 50 exhibited the best catalytic activity for HCHO oxidation [the temperature for complete oxidation of HCHO was 25 degrees C under the reaction conditions of space velocity (SV) = 100,000 mL/(g x h) and relative humidity (RH) = 35 %]. In combination with CO chemisorption, H-2-TPR, and HCHO-TPSR, the excellent catalytic performance of Pd@TS-1(50) was ascribed to small size of Pd domain, high Pd dispersion, and prompt surface reaction. Benefit from the core-shell like structure exposing a hydrophobic silicon-rich surface, the Pd@TS-1(50) catalyst also possessed satisfactory stability for a long-term test.
引用
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页数:14
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