Polyaniline - BiVO4 nanocomposite as an efficient adsorbent for the removal of methyl orange from aqueous solution

被引:31
作者
Vidya, J. [1 ]
Bosco, A. John [2 ]
Haribaaskar, K. [2 ]
Balamurugan, P. [1 ]
机构
[1] Govt Arts Coll Men Autonomous, PG & Res Dept Phys, Chennai 600035, Tamil Nadu, India
[2] SRM Inst Sci & Technol, Dept Chem, Kattankulathur 603203, India
关键词
Polyaniline; Bismuth vanadate; Methyl orange; Adsorption; Nanosheet; Nanocomposite; PHOTOCATALYTIC DEGRADATION; BISMUTH VANADATE; FACILE SYNTHESIS; DYE REMOVAL; ADSORPTION; BLUE; PERFORMANCE; OPTIMIZATION; NANOFIBERS; KINETICS;
D O I
10.1016/j.mssp.2019.104645
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Herein, we report the synthesis of Polyaniline - BiVO4 nanocomposites by in-situ oxidative polymerization using aniline monomer in the presence of hydrochloric acid and bismuth vanadate nanosheets. The physiochemical properties of the adsorbents were characterized by X-ray diffraction spectroscopy (XRD), field emission scanning electron microscopy, transmission electron microscopy (HR-TEM) and RAMAN spectroscopy. TEM images confirmed the formation of BiVO4 nanosheet on the PANi matrix. The surface area analysis showed that the PANi - BiVO4 nanocomposites have a high surface area (16.58 and 19.58 m(2)/g) than the PANi nanofiber (9.14 m(2)/g). The adsorption behavior of PANi and PANi - BiVO4 nanocomposites were evaluated by monitoring the adsorption of methyl orange dye within the time interval of 2 h. The PANi - BiVO4 nanocomposite shows 99% of adsorption efficiency which is higher than that of pure PANi (70%). The pseudo-first-order kinetics and Langmuir isotherm model represents the MO adsorption on PANi - BiVO4 was monolayer sorption and the adsorption sites were homogeneous. The reusability of the as-prepared nanocomposite was analyzed and it shows 78% of adsorption after five cycles.
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页数:9
相关论文
共 65 条
[1]   Recent advances in new generation dye removal technologies: novel search for approaches to reprocess wastewater [J].
Ahmad, Akil ;
Mohd-Setapar, Siti Hamidah ;
Chuong, Chuo Sing ;
Khatoon, Asma ;
Wani, Waseem A. ;
Kumar, Rajeev ;
Rafatullah, Mohd .
RSC ADVANCES, 2015, 5 (39) :30801-30818
[2]   Optical and electrical conducting properties of Polyaniline/Tin oxide nanocomposite [J].
Alam, Manawwer ;
Ansari, Anees A. ;
Shaik, Mohammed Rafi ;
Alandis, Naser M. .
ARABIAN JOURNAL OF CHEMISTRY, 2013, 6 (03) :341-345
[3]   An effective nanocomposite of polyaniline and ZnO: preparation, characterizations, and its photocatalytic activity [J].
Ameen, Sadia ;
Akhtar, M. Shaheer ;
Kim, Young Soon ;
Yang, O-Bong ;
Shin, Hyung-Shik .
COLLOID AND POLYMER SCIENCE, 2011, 289 (04) :415-421
[4]  
[Anonymous], 2016, POLYMERS, DOI DOI 10.3390/P0LYM8020027
[5]  
[Anonymous], DESALIN WATER TREAT
[6]   Efficient and stable photocatalytic reduction of aqueous hexavalent chromium ions by polyaniline surface-hybridized ZnO nanosheets [J].
Bao, Chongzhuo ;
Chen, Mingxin ;
Jin, Xin ;
Hu, Dongwen ;
Huang, Qiang .
JOURNAL OF MOLECULAR LIQUIDS, 2019, 279 :133-145
[7]   Estrogenic and anti-estrogenic activity of 23 commercial textile dyes [J].
Bazin, Ingrid ;
Hassine, Aziza Ibn Hadj ;
Hamouda, Yosra Haj ;
Mnif, Wissem ;
Bartegi, Ahgleb ;
Lopez-Ferber, Miguel ;
De Waard, Michel ;
Gonzalez, Catherine .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2012, 85 :131-136
[8]   An impressive emulsion polymerization route for the synthesis of highly soluble and conducting polyaniline salts [J].
Bilal, Salma ;
Gul, Salma ;
Holze, Rudolf ;
Shah, Anwar-ul-Haq Ali .
SYNTHETIC METALS, 2015, 206 :131-144
[9]   Assessment of water contamination caused by a mutagenic textile effluent/dyehouse effluent bearing disperse dyes [J].
Carneiro, Patricia A. ;
Umbuzeiro, Gisela A. ;
Oliveira, Danielle P. ;
Zanoni, Maria Valnice B. .
JOURNAL OF HAZARDOUS MATERIALS, 2010, 174 (1-3) :694-699
[10]   Sensitizer molecular structure-device efficiency relationship in dye sensitized solar cells [J].
Clifford, John N. ;
Martinez-Ferrero, Eugenia ;
Viterisi, Aurelien ;
Palomares, Emilio .
CHEMICAL SOCIETY REVIEWS, 2011, 40 (03) :1635-1646