Defining Reactivity of Solid Sorbents: What Is the Most Appropriate Metric?
Source abstract
Abstract
A series of solid sorbent materials, including alumina (Al 2 O 3 ), magnesia (MgO), titania (TiO 2 ), silica (SiO 2 ), and carbon, of widely varying physical properties, have been studied as sorbents for two toxic substances: sulfur dioxide gas (SO 2 ) and chemical warfare surrogate 2-chloroethyl ethyl sulfide (2-CEES, ClCH 2 CH 2 SCH 2 CH 3 ). Sorbent surface areas, average pore sizes, pore volumes, surface hydroxyl groups, and nitrogen adsorption−desorption isotherms were measured. Surface areas varied from 18 m 2 /g to over 1000 m 2 /g, pore volumes from 0.04 to 1.2 cm 3 /g, and pore diameters from 1.7 to 4.9 nm. Breakthrough studies of SO 2 and 2-CEES sorption yielded information about the effectiveness of each sorbent. Carbon samples worked well for 2-CEES but not SO 2, while silica samples were poor for both. The best MgO and TiO 2 samples were good for both SO 2 and 2-CEES, and overall, the highest surface area (459 m 2 /g) TiO 2 sample was the superior sorbent. The important features for an effective sorbent under the conditions employed are high surface area and high pore volume, possessing isolated surface −OH groups, mesoporous nature, and a polar surface (Lewis base and Lewis acid sites).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Zeolite Catalysis and Synthesis · Mesoporous Materials and Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, and NanoScale Corporation, 1310 Research Park Drive, Manhattan, Kansas 66502
References (25)
Show source-provided references
1. Zhao X. S. · J. Mater. Chem. · 2006 · 16 · 63710.1039/B513060C ↗
2. Zhang H. · Soft Matter · 2005 · 1 · 10710.1039/b502551f ↗
3. Wakayama H. · Phys. Chem. Chem. Phys. · 2003 · 5 · 378410.1039/b305653h ↗
4. Zub Y. L. · Mendeleev Commun. · 2001 · 11 · 20810.1070/MC2001v011n06ABEH001486 ↗
5. Tanaka S. · Chem. Commun. · 2005 · 212510.1039/B501259G ↗
6. Guizard C. G. · J. Mater. Chem. · 1999 · 9 · 5510.1039/a805867i ↗
7. Fernández-García M. · Chem. Rev. · 2004 · 104 · 406310.1021/cr030032f ↗
8. Soler-Illia G. J. A. A. · Chem. Rev. · 2002 · 102 · 409310.1021/cr0200062 ↗
9. Barton T. J. · Chem. Mater. · 1999 · 11 · 263310.1021/cm9805929 ↗
10. Beck J. S. · J. Am. Chem. Soc. · 1992 · 114 · 1083410.1021/ja00053a020 ↗
11. Kresge C. T. · Nature · 1992 · 359 · 71010.1038/359710a0 ↗
12. Zhao D. Y. · Science · 1998 · 279 · 54810.1126/science.279.5350.548 ↗
13. Zhao D. Y. · J. Am. Chem. Soc. · 1998 · 120 · 602410.1021/ja974025i ↗
14. Branauer S. · J. Am. Chem. Soc. · 1938 · 60 · 30910.1021/ja01269a023 ↗
15. Barrett E. P. · J. Am. Chem. Soc. · 1951 · 73 · 37310.1021/ja01145a126 ↗
16. Rajagopalan S. · Chem.—Eur. J. · 2002 · 8 · 260210.1002/1521-3765(20020603)8:11<2602::AID-CHEM2602>3.0.CO;2-3 ↗
17. Klabunde K. J. · 200110.1002/0471220620 ↗
18. cKlabunde, K. J.Introduction to Nanotechnology, Chapter 1, pp1−13.
19. dKlabunde, K. J.; Mulukutla, R.Chemical and Catalytic Aspects of Nanocrystals, Chapter 7, pp223−261.10.1002/0471220620.ch7 ↗
20. Wagner G. W. · J. Phys. Chem. B · 2000 · 104 · 511810.1021/jp000101j ↗
21. Wagner G. W. · J. Phys. Chem. B · 1999 · 103 · 322510.1021/jp984689u ↗
22. Klabunde K. J. · J. Phys. Chem. · 1996 · 100 · 1214210.1021/jp960224x ↗
23. Koper O. B. · Chem. Mater. · 1997 · 9 · 246810.1021/cm970357a ↗
24. iKlabunde, K. J.Nanometer Sized Metal Oxide Particles for Ambient Temperature Adsorption of Toxic Chemicals. U.S. Patent 5,990,373, November 23, 1999.
25. jKoper, O; Klabunde, K. J.Nanoparticles for the Destructive Sorption of Biological and Chemical Contaminants. U.S. Patent 6,057,488; May 2, 2000.