journal article·2001-11-01

Microporous Decatungstates: Synthesis and Photochemical Behavior

Yihang Guo, Changwen Hu, Xinlong Wang, Yonghui Wang, Enbo Wang, Yongcun Zou, Hong Ding, Shouhua Feng

Chemistry of Materials· Volume 13· Issue 11
Publisher page

Abstract

Photoreactive decatungstates Na 4 W 10 O 32 and (nBu 4 N) 4 W 10 O 32 were heterogenized inside the silica network via a sol−gel technique, resulting in the Na 4 W 10 O 32 /SiO 2 (Na 1 ) and (nBu 4 N) 4 W 10 O 32 /SiO 2 (Q 1 ) composites. The physicochemical properties of as-synthesized composites were measured by UV diffuse reflectance spectrum, Fourier transform infrared, thermogravimetric analysis and differential thermal analysis, inductively coupled plasma-atomic emission spectroscopy, and scanning electron microgragh, suggesting that the structural integrity of the decatungstates has been preserved after incorporation into the silica network. The microporous structures of the Na 1 and Q 1 were confirmed by the nitrogen adsorption measurements. The photocatalytic behaviors of the composites were studied via degradation and mineralization of organophosphorus pesticide, trichorofon (TCF), under near-UV irradiation and in media where they are insoluble. The photocatalytic behaviors of the Na 1 and Q 1 were also compared with two silica-supported decatungstates, Na 4 W 10 O 32 −SiO 2 (Na 2 ) and (nBu 4 N) 4 W 10 O 32 −SiO 2 (Q 2 ). It indicated that the Na 1 had the highest photocatalytic efficiency among four insoluble decatungstates, and the leakage of the catalyst from the support was hardly observed for Na 1 . Studies on the reaction mechanism indicate that OH • radical attack may be responsible for the degradation and final mineralization of TCF.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Polyoxometalates: Synthesis and Applications · Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications

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

References (46)

Show source-provided references
1. Okuhara T. · Adv. Catal. · 1996 · 41 · 11310.1016/S0360-0564(08)60041-3 ↗
2. Yamase T. · J. Chem. Soc., Dalton Trans. · 1984 · 79310.1039/dt9840000793 ↗
3. Chemseddine A. · Inorg. Chem. · 1984 · 23 · 260910.1021/ic00185a014 ↗
4. Renneke R. F. · J. Am. Chem. Soc. · 1988 · 110 · 546110.1021/ja00224a034 ↗
5. Papaconstantinou E. · Chem. Soc. Rev. · 1989 · 18 · 110.1039/cs9891800001 ↗
6. Stattari D. · J. Chem. Soc., Chem. Commun. · 1990 · 63410.1039/c39900000634 ↗
7. Stattari D. · J. Am. Chem. Soc. · 1993 · 115 · 464910.1021/ja00064a028 ↗
8. Tanielian C. · Coord. Chem. Rev. · 1998 · 178 · 116510.1016/S0010-8545(98)00160-X ↗
9. Duncan D. C. · Inorg. Chem. · 1995 · 464010.1021/ic00122a021 ↗
10. Okuhara T. · Chem. Mater. · 2000 · 12 · 223010.1021/cm9907561 ↗
11. Okuhara T. · Stud. Surf. Sci. Catal. · 1994 · 90 · 41910.1016/S0167-2991(08)61853-4 ↗
12. Lee K. Y. · J. Am. Chem. Soc. · 1992 · 114 · 2863
13. Izumi Y. · Microporous Mater. · 1995 · 5 · 25510.1016/0927-6513(95)00059-3 ↗
14. Einaga H. · Bull. Chem. Soc. Jpn. · 1997 · 70 · 155110.1246/bcsj.70.1551 ↗
15. Hou Y. · New J. Chem. · 1992 · 16 · 909
16. Yamase T. · J. Chem. Soc., Dalton Trans. · 1998 · 183
17. Mylonas A. · J. Photochem. Photobiol. A · 1996 · 94 · 7710.1016/1010-6030(95)04207-5 ↗
18. Ozer R. R. · J. Phys. Chem. B · 2000 · 104 · 944410.1021/jp000783a ↗
19. Hu C. · Appl. Catal. A · 2000 · 194 · 9910.1016/S0926-860X(99)00358-0 ↗
20. Molinari A. · J. Chem. Soc., Dalton Trans. · 1999 · 120310.1039/a901051c ↗
21. Molinari A. · Eur. J. Inorg. Chem. · 2000 · 9110.1002/(SICI)1099-0682(200001)2000:1<91::AID-EJIC91>3.0.CO;2-J ↗
22. Guo Y. · Chem. Mater. · 2000 · 12 · 350110.1021/cm000074+ ↗
23. Guo Y. · Appl. Catal. B · 2001 · 3 · 33710.1016/S0926-3373(00)00246-0 ↗
24. Friesen D. A. · J. Photochem. Photobiol. A · 2000 · 133 · 21310.1016/S1010-6030(00)00237-9 ↗
25. Friesen D. A. · Environ. Sci. Technol. · 1999 · 33 · 319310.1021/es980912p ↗
26. Friesen D. A. · J. Chem. Soc., Chem. Commun. · 1998 · 54310.1039/a800381e ↗
27. Cavani F. · Catal. Today · 1998 · 7310.1016/S0920-5861(98)00039-X ↗
28. Okuhara, T.; Nishimura, T.; Misono, M.11th International Congresson Catalysis40th Anniversary; Elsevier Science B.V. Amsterdam, 1996; p 581.10.1016/S0167-2991(96)80269-2 ↗
29. Texier I. · Catal. Today · 1999 · 54 · 29710.1016/S0920-5861(99)00191-1 ↗
30. Herrmann J. M. · Catal. Today · 1999 · 54 · 35310.1016/S0920-5861(99)00196-0 ↗
31. Assabane A. · Appl. Catal. B · 2000 · 24 · 7110.1016/S0926-3373(99)00094-6 ↗
32. Zaleska A. · J. Photochem. Photobiol. A · 2000 · 135 · 21310.1016/S1010-6030(00)00296-3 ↗
33. Wang K. · Appl. Catal. B · 1999 · 21 · 110.1016/S0926-3373(98)00116-7 ↗
34. Doong R. · J. Photochem. Photobiol. A · 1997 · 107 · 23910.1016/S1010-6030(96)04579-0 ↗
35. Tanaka K. · J. Mol. Catal. A · 1999 · 144 · 42510.1016/S1381-1169(99)00112-0 ↗
36. D'ollveira J.-C. · Environ. Sci. Technol. · 1990 · 24 · 99010.1021/es00077a007 ↗
37. Herrmann J.-M. · Catal. Today · 1999 · 53 · 11510.1016/S0920-5861(99)00107-8 ↗
38. Malato S. · Appl. Catal. B · 2000 · 25 · 3110.1016/S0926-3373(99)00114-9 ↗
39. O'Shea K. E. · J. Photochem. Photobiol. A · 1997 · 107 · 22110.1016/S1010-6030(96)04420-6 ↗
40. Hoffmann M. R. · Chem. Rev. · 1995 · 95 · 6910.1021/cr00033a004 ↗
41. Torimoto T. · Environ. Sci. Technol. · 1996 · 30 · 127510.1021/es950483k ↗
42. Ollis D. F. · Environ. Sci. Technol. · 1991 · 25 · 152210.1021/es00021a001 ↗
43. Legrini O. · Chem. Rev. · 1993 · 93 · 67110.1021/cr00018a003 ↗
44. Pramaur E. · Environ. Sci. Technol. · 1993 · 27 · 170910.1021/es00046a613 ↗
45. Hastings J. J. · J. Chem. Soc., Dalton Trans. · 1992 · 20910.1039/dt9920000209 ↗
46. Schwarz H. A. · J. Phys. Chem. · 1989 · 93 · 40910.1021/j100338a079 ↗