journal article·2013-05

Polyacrylamide gel synthesis and photocatalytic properties of TiO2 nanoparticles

T. Xian, H. Yang, L. J. Di, X. F. Chen, J. F. Dai

Publisher page

Abstract

In this study, a polyacrylamide gel route was introduced to synthesize TiO2 nanoparticles. The influence of synthesis conditions on the properties of products was investigated. It is found that the samples prepared at the calcination temperature of 400 °C crystallize majorly in the anatase phase with a minor rutile phase. The second rutile phase has a dependence on the chelating agent, which is formed more readily when using acetic acid as the chelating agent. The introduction of acrylamide and glucose to the precursor solution shows the capability of improving the particle morphology, and the resulted particles are uniformly shaped like spheres. The photocatalytic activity of the prepared TiO2 samples was evaluated by the degradation of acid orange 7 under 254 nm ultraviolet irradiation, revealing that they exhibit a good photocatalytic activity. Ethanol was used as a ·OH scavenger to investigate its effect on the photocatalytic efficiency as well as the ·OH radical yields. Based on the experimental results, ·OH radical is suggested to be the dominant active species responsible for the dye degradation.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Nanomaterials for catalytic reactions

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

References (21)

Show source-provided references
1. Carey JH (1976) Bull Environ Contam Toxicol 16:69710.1007/BF01685575 ↗
2. Bahnemannt DW, Kholuiskaya SN, Dillert R, Kulak AI, Kokorin AI (2002) Appl Catal B 36:16110.1016/S0926-3373(01)00301-0 ↗
3. Ruan SP, Wu FQ, Zhang T, Gao W, Xu BK, Zhao MY (2001) Mater Chem Phys 69:710.1016/S0254-0584(00)00301-1 ↗
4. Shen L, Bao N, Zheng Y, Gupta A, An T, Yanagisawa K (2008) J Phys Chem C 112:880910.1021/jp711369e ↗
5. Zhang Z, Wang C-C, Zakaria R, Ying JY (1998) J Phys Chem B 102:1087110.1021/jp982948+ ↗
6. Scepanovic M, Abramovic B, Golubovic A, Kler S, Grujic-Brojcin M, Dohcevic-Mitrovic Z, Babic B, Matovic B, Popovic ZV (2012) J Sol–Gel Sci Technol 61:39010.1007/s10971-011-2639-9 ↗
7. Karthick SN, Prabakar K, Subramania A, Hong J-T, Jang J-J, Kim H-J (2011) Powder Technol 205:3610.1016/j.powtec.2010.08.061 ↗
8. Behnajady MA, Eskandarloo H, Modirshahla N, Shokri M (2011) Desalination 278:1010.1016/j.desal.2011.04.019 ↗
9. Hussain M, Ceccarelli R, Marchisio DL, Fino D, Russo N, Geobaldo F (2010) Chem Eng J 157:4510.1016/j.cej.2009.10.043 ↗
10. Yan X, Pan D, Li Z, Liu Y, Zhang J, Xu G, Wu M (2010) Mater Lett 64:183310.1016/j.matlet.2010.05.051 ↗
11. Xie H, Gao G, Tian Z, Bing N, Wang L (2009) Particuology 7:20410.1016/j.partic.2009.03.003 ↗
12. Viana MM, Soares VF, Mohallem NDS (2010) Ceram Int 36:204710.1016/j.ceramint.2010.04.006 ↗
13. Shao Z, Chen Y, Luan W, Chen X (2005) Chin J Mater Res 19:213
14. Daneshvar N, Salari D, Khataee AR (2003) J Photochem Photobiol A 157:11110.1016/S1010-6030(03)00015-7 ↗
15. Czili H, Horvath A (2008) Appl Catal B 81:29510.1016/j.apcatb.2008.01.001 ↗
16. Spurr RA, Myers H (1957) Anal Chem 29:76010.1021/ac60125a006 ↗
17. Chang JA, Vithal M, Baek IC, Seok SI (2009) J Solid State Chem 182:74910.1016/j.jssc.2008.12.024 ↗
18. Wu SQ, Liu YY, He LN, Wang FP (2004) Mater Lett 58:277210.1016/j.matlet.2004.04.017 ↗
19. Komornickoi S, Radecka M, Sobas P (2004) Mater Res Bull 39:200710.1016/j.materresbull.2004.07.017 ↗
20. Konstantinou IK, Albanis TA (2004) Appl Catal B 49:110.1016/j.apcatb.2003.11.010 ↗
21. Bansal P, Singh D, Sud D (2010) Sep Purif Technol 72:35710.1016/j.seppur.2010.03.005 ↗