Crosslinked chitosan embedded TiO2 NPs and carbon dots-based nanocomposite: An excellent photocatalyst under sunlight irradiation

被引:26
作者
Midya, Lipi [1 ]
Sarkar, Abanindra Nath [1 ]
Das, Raghunath [2 ]
Maity, Arjun [2 ,3 ]
Pal, Sagar [1 ]
机构
[1] Indian Inst Technol ISM Dhanbad, Dept Chem, Jharkhand 826004, India
[2] Univ Johannesburg, Dept Chem Sci, Johannesburg, South Africa
[3] Council Sci & Ind Res CSIR, Ctr Nanostruct & Adv Mat CeNAM, DST CSIR, ZA-0001 Pretoria, South Africa
关键词
Chitosan; Microwave; Nanocomposite; Photocatalyst; QUANTUM DOTS; NANOPARTICLES; DEGRADATION; METAL; NANOSTRUCTURES; POLYMERIZATION; PARTICLES; REMOVAL; ANATASE; HYBRID;
D O I
10.1016/j.ijbiomac.2020.08.230
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Herein, a new hybrid nanocomposite, comprising of titania nanoparticles (TiO2 NPs) and carbon dots (CDs) deposited polyvinyl imidazole crosslinked chitosan [cl-Ch-p(VI)/TiO(2)NPs-CDs] has been developed. The nanocomposite has been synthesised by in-situ deposition of TiO2 NPs and CDs onto the surface of the copolymer under microwave irradiation. To the best of our knowledge, this in-situ approach has effectively been applied for the first time to fabricate green fluorescent CDs from sugar cane juice at moderate temperature (75 degrees C) under microwave irradiation. The developed nanocomposite has been characterized using UV-Vis spectroscopy, C-13 NMR, XRD, HR-TEM, STEM and XPS analyses. The results suggest that the successful deposition of TiO2 NPs and CDs onto the surface of crosslinked chitosan is achieved. The experimental studies indicate that the NPs/CDs-impregnated nanocomposite allows efficient photocatalytic degradation of toxic organic compounds (similar to 98.6% degradation of 2,4-dicholorophenol, similar to 95.8% degradation of Reactive Blue 4, similar to 98.2% degradation of Reactive Red 15) in the presence of sunlight. Finally, LC-MS analysis of the resultant degraded materials reveals the formation of organic molecules with lower molecular mass. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:3676 / 3686
页数:11
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