Phenol decomposition under sunlight using a sonochemically synthesized CdSe/TiO2 nanocatalyst

被引:33
作者
Ghodrati, Mohammad Saleh [1 ,2 ,3 ]
Haghighi, Mohammad [1 ,2 ]
Mohamdzadeh, Jafar Sadegh Soltan [1 ,2 ,4 ]
Pourabas, Behzad [3 ]
Pipelzadeh, Ehsan [1 ,2 ,3 ]
机构
[1] Sahand Univ Technol, Chem Engn Fac, Tabriz, Iran
[2] Sahand Univ Technol, RCRC, Tabriz, Iran
[3] Sahand Univ Technol, NMRC, Tabriz, Iran
[4] Univ Saskatchewan, Dept Chem Engn, Saskatoon, SK S7N 5A9, Canada
关键词
Phenol decomposition; Titanium dioxide; Cadmium selenide; Nanocatalyst; Sonochemistry; Photocatalytic; Sunlight; PHOTOCATALYTIC DEGRADATION; TITANIUM-DIOXIDE; AQUEOUS-SOLUTION; TIO2; 4-CHLOROPHENOL; IRRADIATION; PERFORMANCE; SUSPENSIONS; OXIDATION; KINETICS;
D O I
10.1007/s11144-011-0338-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ultrasound energy has been successfully employed to synthesize CdSe/TiO2 nanocatalysts for the photocatalytic degradation of phenol under solar light irradiation. The photocatalytic performance test was carried out using TiO2 as well as synthesized CdSe/TiO2 nanocatalysts. Nanocatalyst characterization was accomplished using XRD, SEM, FTIR, BET and UV-vis spectroscopy. It was shown that the synthesized nanocatalysts have crystal characteristics and are in nano-scale size range. The coupled nanocatalyst has shown a shift in the absorption spectrum from the UV range to the visible range. The results of photocatalytic tests showed that the CdSe/TiO2 coupled nanocatalyst could remove phenol from wastewater under solar light irradiation, while TiO2 did not have enough activity in this process. It is also shown that the CdSe nanoparticles act as photosensitizers, not only extending the spectral response of TiO2 to the visible region but also reducing the electron-hole recombination. Furthermore, the CdSe/TiO2 synthesized samples provided more photomineralization efficiency than that of TiO2 in terms of total organic carbon analysis.
引用
收藏
页码:49 / 60
页数:12
相关论文
共 20 条
[1]   Effect of rutile phase on the photocatalytic properties of nanocrystalline titania during the degradation of p-coumaric acid [J].
Bacsa, RR ;
Kiwi, J .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 16 (01) :19-29
[2]   Poly(tetraethylene glycol malonate) titanium oxide hybrid materials by sol-gel methods [J].
Deng, C ;
James, PF ;
Wright, PV .
JOURNAL OF MATERIALS CHEMISTRY, 1998, 8 (01) :153-159
[3]   Role of the crystallite phase of TiO2 in heterogeneous photocatalysis for phenol oxidation in water [J].
Ding, Z ;
Lu, GQ ;
Greenfield, PF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (19) :4815-4820
[4]   Degradation of phenol by nanomaterial TiO2 in wastewater [J].
Guo, Zhifeng ;
Ma, Ruixin ;
Li, Guojun .
CHEMICAL ENGINEERING JOURNAL, 2006, 119 (01) :55-59
[5]   Photocatalytic degradation of phenols in aqueous solution under irradiation of 254 and 185 nm UV light [J].
Han, WY ;
Zhu, WP ;
Zhang, PY ;
Zhang, Y ;
Li, LS .
CATALYSIS TODAY, 2004, 90 (3-4) :319-324
[6]   Sonochemical synthesis and visible light photocatalytic behavior of CdSe and CdSe/TiO2 nanoparticles [J].
Ho, WK ;
Yu, JC .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2006, 247 (1-2) :268-274
[7]   Photocatalytic degradation of 2-phenylphenol on TiO2 and ZnO in aqueous suspensions [J].
Khodja, AA ;
Sehili, T ;
Pilichowski, JF ;
Boule, P .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2001, 141 (2-3) :231-239
[8]   Photocatalytic activity of sol-gel derived titania converted into nanocrystalline powders by supercritical drying [J].
Kolen'ko, YV ;
Garshev, AV ;
Churagulov, BR ;
Boujday, S ;
Portes, P ;
Colbeau-Justin, C .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2005, 172 (01) :19-26
[9]   Photocatalytic degradability of substituted phenols over UV irradiated TiO2 [J].
Ksibi, M ;
Zemzemi, A ;
Boukchina, R .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2003, 159 (01) :61-70
[10]   Decomposition of 2-chlorophenol in aqueous solution by UV irradiation with the presence of titanium dioxide [J].
Ku, Y ;
Leu, RM ;
Lee, KC .
WATER RESEARCH, 1996, 30 (11) :2569-2578