Photocatalysis, microstructure, and surface characterization of TiO2‐loaded wooden‐activated carbon fibers
Source abstract
Abstract
In this study, TiO2‐loaded wooden‐activated carbon fibers (TiO2/WACFs) were prepared by sol–gel method. TiO2/WACFs were detected by scanning electron microscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, and X‐ray photoelectron spectroscopy. The results showed that TiO2 was deposited on almost each WCAF with a coating thickness. All the TiO2 films on the surface of WACFs were composed of anatase with high photocatalytic property. The characteristic adsorption peaks of nano‐TiO2 emerged at 1,402 and 471 cm−1 on the infrared spectrum of TiO2/WACFs. It was also found that Ti was in the binding state of Ti4+ (TiO2) in the TiO2/WACFs. As the calcination temperature increased, the content of elements Ti and TiO bond of lattice oxygen on the surface of TiO2/WACFs increased and then decreased, but the loaded nano‐TiO2 did not affect the formation of graphite structure of WACFs. It is suggested that TiO2/WACFs obtained at 450°C have the best photocatalytic property. POLYM. COMPOS., 36:62–68, 2015. © 2014 Society of Plastics Engineers
Source: crossref · Quality: baseline
Research context
OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Microplastics and Plastic Pollution
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Wood Science and Technology Tianjin University of Science & Technology Tianjin 300222 People's Republic of China
Funding
National Natural Science Foundation of People's Republic of China · Tianjin Outstanding Postdoctoral Internationalization Training Plan
References (40)
Show source-provided references
1. 10.1021/j100078a02310.1021/j100078a023 ↗
2. 10.1021/es950483k10.1021/es950483k ↗
3. 10.1016/S0920-5861(01)00298-X10.1016/S0920-5861(01)00298-X ↗
4. 10.1016/S1389-5567(03)00002-910.1016/S1389-5567(03)00002-9 ↗
5. 10.1007/s10086030001310.1007/s100860300013 ↗
6. 10.1016/S0926-3373(03)00214-510.1016/S0926-3373(03)00214-5 ↗
7. 10.1016/j.jphotochem.2003.12.01310.1016/j.jphotochem.2003.12.013 ↗
8. 10.1007/s12034-007-0007-810.1007/s12034-007-0007-8 ↗
9. 10.1016/j.apsusc.2008.10.08310.1016/j.apsusc.2008.10.083 ↗
10. 10.1016/j.carbon.2010.10.01010.1016/j.carbon.2010.10.010 ↗
11. 10.1007/BF0076789910.1007/BF00767899 ↗
12. 10.1016/S1672-2515(07)60027-X10.1016/S1672-2515(07)60027-X ↗
13. 10.1016/S1001-0742(06)60025-910.1016/S1001-0742(06)60025-9 ↗
14. 10.1016/j.surfcoat.2008.10.00710.1016/j.surfcoat.2008.10.007 ↗
15. 10.1016/j.partic.2010.03.01310.1016/j.partic.2010.03.013 ↗
16. 10.1023/B:JMSC.0000007745.62879.7410.1023/B:JMSC.0000007745.62879.74 ↗
17. 10.1007/s10853-005-2561-z10.1007/s10853-005-2561-z ↗
18. 10.1016/j.jcis.2004.09.02710.1016/j.jcis.2004.09.027 ↗
19. 10.1016/j.carbon.2006.05.04810.1016/j.carbon.2006.05.048 ↗
20. 10.1016/j.cej.2006.09.01010.1016/j.cej.2006.09.010 ↗
21. 10.1016/j.jcis.2010.03.06410.1016/j.jcis.2010.03.064 ↗
22. 10.1016/j.apsusc.2009.12.06210.1016/j.apsusc.2009.12.062 ↗
23. 10.1515/hfsg.1996.50.1.8510.1515/hfsg.1996.50.1.85 ↗
24. 10.1007/BF0070289710.1007/BF00702897 ↗
25. 10.1007/s00226-009-0264-310.1007/s00226-009-0264-3 ↗
26. 10.1002/app.3414210.1002/app.34142 ↗
27. 10.1016/j.biortech.2012.01.14110.1016/j.biortech.2012.01.141 ↗
28. Teruhisa O. · J. Phys. Chem. B · 1997 · 101 · 6415
29. 10.1016/S0008-6223(02)00105-710.1016/S0008-6223(02)00105-7 ↗
30. 10.1007/s10570-007-9148-610.1007/s10570-007-9148-6 ↗
31. 10.1016/j.jcis.2008.01.01210.1016/j.jcis.2008.01.012 ↗
32. 10.1021/ie901212m10.1021/ie901212m ↗
33. 10.1016/S0008-6223(03)00340-310.1016/S0008-6223(03)00340-3 ↗
34. 10.1016/j.carbon.2005.02.01310.1016/j.carbon.2005.02.013 ↗
35. 10.1007/s10570-009-9352-710.1007/s10570-009-9352-7 ↗
36. 10.1016/j.apcatb.2006.05.01810.1016/j.apcatb.2006.05.018 ↗
37. 10.1021/jp061802510.1021/jp0618025 ↗
38. 10.1016/j.carbon.2005.12.04710.1016/j.carbon.2005.12.047 ↗
39. 10.1016/j.biortech.2010.06.04610.1016/j.biortech.2010.06.046 ↗
40. 10.1016/0039-6028(95)00022-410.1016/0039-6028(95)00022-4 ↗