Photocatalytic efficiency of TiO2/poly[acrylamide-co-(acrylic acid)] composite for textile dye degradation

被引:98
作者
Kangwansupamonkon, Wiyong [2 ]
Jitbunpot, Walasinee [3 ]
Kiatkamjornwong, Suda [1 ]
机构
[1] Chulalongkorn Univ, Fac Sci, Dept Imaging & Printing Technol, Bangkok 10330, Thailand
[2] Natl Sci & Technol Dev Agcy, Natl Nanotechnol Ctr, Klongluang 12120, Pathumthani, Thailand
[3] Chulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
关键词
TiO2; Hydrogel; Photocatalytic degradation; Dye removal; METHYLENE-BLUE; WASTE-WATER; TITANIUM-DIOXIDE; PHASE-TRANSITION; AQUEOUS-SOLUTION; CATIONIC DYES; METAL-IONS; REMOVAL; TIO2; ADSORPTION;
D O I
10.1016/j.polymdegradstab.2010.04.019
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
A novel photocatalytically degradable TiO2/poly[acrylamide-co-(acrylic acid)) composite hydrogel (TiO2/poly[AAm-co-AAc]) was synthesized by polymerization in an aqueous solution with N,N'-methyl-enebisacrylamide as the crosslinker and ammonium persulphate and TEMED as the initiator pair. The combined and separate effects of photodegradation and adsorption processes for dye removal were evaluated using methylene blue (MB) as the model dye for a photodegradation target, and compared with those of the neat poly[AAm-co-AAc], and a commercially available TiO2 photocatalyst (Degussa P-25). Without photodegradation (i.e. in the dark), the TiO2/poly[AAm-co-AAc] composite adsorbed up to 85% of the MB from a 5 mg L-1 MB solution in 15 min compared to only 10% for the pristine TiO2. The reproducibility in photodegradation of the reused poly[AAm-co-AAc] composite was also investigated, where poly[AAm-co-AAc] was found to be photocatalytically degraded under UV irradiation. Therefore, the TiO2/poly[AAm-co-AAc] composite hydrogel is a good dye adsorber with self-photodegradability and it also can easily be separated from the reaction by simple filtration. With these properties, the TiO2/poly[AAm-co-AAc] hydrogel can be called a green polymer for use in the photodegradation adsorption process for the abatement of various pollutants. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1894 / 1902
页数:9
相关论文
共 37 条
[1]
Sonochemical degradation of Basic Blue 41 dye assisted by nano TiO2 and H2O2 [J].
Abbasi, Mahmood ;
Asl, Nima Razzaghi .
JOURNAL OF HAZARDOUS MATERIALS, 2008, 153 (03) :942-947
[2]
Potential of immobilized bitter gourd (Momordica charantia) peroxidases in the decolorization and removal of textile dyes from polluted wastewater and dyeing effluent [J].
Akhtar, S ;
Khan, AA ;
Husain, Q .
CHEMOSPHERE, 2005, 60 (03) :291-301
[3]
Removal of toxic metal ions from wastewater by semiconductor photocatalysis [J].
Chen, D ;
Ray, AK .
CHEMICAL ENGINEERING SCIENCE, 2001, 56 (04) :1561-1570
[4]
Recent developments in polysaccharide-based materials used as adsorbents in wastewater treatment [J].
Crini, G .
PROGRESS IN POLYMER SCIENCE, 2005, 30 (01) :38-70
[5]
Solar detoxification of fuel-contaminated groundwater using fixed-bed photocatalysts [J].
Crittenden, JC ;
Zhang, Y ;
Hand, DW ;
Perram, DL ;
Marchand, EG .
WATER ENVIRONMENT RESEARCH, 1996, 68 (03) :270-278
[6]
Removal of anionic dyes from aqueous solution using poly [N-vinyl pyrrolidone/2-(methacryloyloxyethyl) trimethyl ammonium chloride] superswelling hydrogels [J].
Dadhaniya, Pratish V. ;
Patel, Manish P. ;
Patel, Ranjan G. .
POLYMER BULLETIN, 2007, 58 (02) :359-369
[7]
Photocatalytic efficiency of titanium dioxide immobilized on PVP/AAc hydrogel membranes: A comparative study for safe disposal of wastewater of Remazol Red RB-133 textile dye [J].
Hafez, HS ;
Ali, AEH ;
Abdel-Mottaleb, MSA .
INTERNATIONAL JOURNAL OF PHOTOENERGY, 2005, 7 (04) :181-185
[8]
Bi-functional starch composites prepared by γ-irradiation for removal of anionic and cationic dyes from aqueous solutions [J].
Hashem, A. ;
Abdel-Halim, E. S. ;
Sokker, H. H. .
POLYMER-PLASTICS TECHNOLOGY AND ENGINEERING, 2007, 46 (01) :71-77
[9]
The kinetics of sorption of basic dyes from aqueous solution by sphagnum moss peat [J].
Ho, YS ;
McKay, G .
CANADIAN JOURNAL OF CHEMICAL ENGINEERING, 1998, 76 (04) :822-827
[10]
HOU H, 2007, P INT C INT COMM MIC, P89