A novel boron nitride supported Pt catalyst for VOC incineration

被引:65
作者
Wu, JCS [1 ]
Lin, ZA
Pan, JW
Rei, MH
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
[2] Chang Gung Univ, Dept Chem & Mat Engn, Tao Yuan 333, Taiwan
关键词
catalytic deep oxidation; Pt; hexagonal BN; gamma-alumina; VOC; gasoline;
D O I
10.1016/S0926-860X(01)00673-1
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
Low-crystalline hexagonal boron nitride (h-BN) and gamma -alumina supported Pt catalysts were employed to investigate the catalytic destruction of volatile organic compounds (VOC). The 0.3 wt.% Pt catalysts were prepared via incipient wetness method using H2PtCl6 as precursor. The oxidation of volatile gasoline was performed in a concentration of 2500 ppmv with volume hour space velocity (VHSV) near 20 000 h(-1) from 100 to 500 degreesC. Instead of deactivation, the activity of Pt/h-BN increased significantly in the second run of the oxidation reaction. The light-off temperature (50% conversion) decreased from 210 to 160-170 degreesC in the second run of oxidation. Furthermore, 95% conversion was achieved at less than 200 degreesC. Meanwhile, the Pt/gamma -Al2O3 became deactivated in the second run of oxidation. The activity of Pt/h-BN was maintained for three temperature cycles. Long-term oxidation proved that Pt/h-BN activity did not decline over up to 80 h. The positive binding energy shift from XPS revealed that a few boron oxide impurities contaminated on the h-BN surface, these provided the anchorage for the Pt clusters. Metallic Pt surface was oxidized to PtO during the initial oxidation, thus enhancing the oxidation activity. Based on irreversible H-2 chemisorption, the platinum dispersion of Pt/h-BN were near 20% and did not change after oxidation at 500 degreesC. Metal sintering was minimal, owing to the high thermal conductivity of h-BN, which prevented any hot spots of oxidation on Pt sites. In sum, experimental results demonstrated that Pt/h-BN was a promising catalyst for VOC destruction. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:117 / 124
页数:8
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