journal article·2010-06-08

Hydrophobic Polymer-Coated Metal Oxide Catalysts for Effective Low-Temperature Oxidation of CO under Moisture-Rich Conditions

Chun-Hu Chen, Eric C. Njagi, Shih-Po Sun, Homer Genuino, Boxun Hu, Steven L. Suib

Chemistry of Materials· Volume 22· Issue 11
Publisher page

Abstract

The first example of a highly water-tolerant, hydrophobic polymer coated metal oxide catalyst systems is reported for CO oxidation. Studies show that protected catalysts have 5.3 times longer lifetimes than unprotected catalysts under highly humid conditions. This idea is simple and general for many different metal oxide catalyst systems.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Catalytic Processes in Materials Science · Catalysis and Oxidation Reactions · Mesoporous Materials and Catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry

Polymer Program, Institute of Materials Science

Institute of Materials Science

References (26)

Show source-provided references
1. Lamb A. B. · J. Ind. Eng. Chem. · 1920 · 13 · 21310.1021/ie50123a007 ↗
2. Corti C. W. · Top. Catal. · 2007 · 44 · 33110.1007/s11244-007-0307-7 ↗
3. Hoflund G. B. · Langmuir · 1995 · 11 · 343110.1021/la00009a026 ↗
4. Faur Ghenciu A. · Curr. Opin. Solid State Mater. Sci. · 2002 · 6 · 38910.1016/S1359-0286(02)00108-0 ↗
5. Gamarra D. · J. Am. Chem. Soc. · 2007 · 129 · 1206410.1021/ja073926g ↗
6. Over H. · Science · 2000 · 287 · 147410.1126/science.287.5457.1474 ↗
7. Yan W. · J. Am. Chem. Soc. · 2005 · 127 · 1048010.1021/ja053191k ↗
8. Von Oertzen A. · J. Phys. Chem. B · 2000 · 104 · 315510.1021/jp9927799 ↗
9. Oh S.-H. · J. Catal. · 2006 · 245 · 35
10. Lin H.-Y. · Ind. Eng. Chem. Res. · 2005 · 44 · 456910.1021/ie0491488 ↗
11. Xia G. G. · J. Catal. · 1999 · 185 · 9110.1006/jcat.1999.2484 ↗
12. Saalfrank J. W. · Angew. Chem., Int. Ed. · 2004 · 43 · 202810.1002/anie.200351935 ↗
13. Gulari E. · Appl. Catal., A · 1999 · 182 · 14710.1016/S0926-860X(99)00002-2 ↗
14. Guo Q. · Chem. Lett. · 2008 · 37 · 127410.1246/cl.2008.1274 ↗
15. Liu W. · J. Catal. · 1995 · 153 · 30410.1006/jcat.1995.1132 ↗
16. Xie X. · Nature · 2009 · 458 · 74610.1038/nature07877 ↗
17. Grillo F. · Appl. Catal., B · 2004 · 48 · 26710.1016/j.apcatb.2003.11.003 ↗
18. Hou X.-D. · Catal. Lett. · 2008 · 123 · 32110.1007/s10562-008-9426-4 ↗
19. Wolfson A. · Chem. Commun. · 2002 · 38810.1039/b109234k ↗
20. Bonchio M. · Adv. Synth. Catal. · 2003 · 345 · 111910.1002/adsc.200303076 ↗
21. Parton R. F. · Nature · 1994 · 370 · 54110.1038/370541a0 ↗
22. Mwangi M. T. · J. Am. Chem. Soc. · 2006 · 128 · 1443410.1021/ja0642212 ↗
23. Yuan J. · Nat. Nanotechnol. · 2008 · 3 · 33210.1038/nnano.2008.136 ↗
24. Kraemer M. · Appl. Catal., A · 2006 · 302 · 25710.1016/j.apcata.2006.01.018 ↗
25. Mizutani F. · Sens. Actuators, B · 2001 · 76 · 48910.1016/S0925-4005(01)00596-2 ↗
26. Khorasani M. T. · Appl. Surf. Sci. · 2005 · 242 · 33910.1016/j.apsusc.2004.08.035 ↗