Photocatalytic degradation of Congo red using Carissa edulis extract capped zinc oxide nanoparticles

被引:178
作者
Fowsiya, J. [1 ]
Madhumitha, G. [1 ]
Al-Dhabi, Naif Abdullah [2 ]
Arasu, Mariadhas Valan [2 ]
机构
[1] VIT Univ, Sch Adv Sci, Dept Chem, Chem Heterocycles & Nat Prod Res Lab, Vellore 632014, Tamil Nadu, India
[2] King Saud Univ, Coll Sci, Addiriyah Chair Environm Studies, Dept Bot & Microbiol, POB 2455, Riyadh 11451, Saudi Arabia
关键词
Carissa edulis; Zinc oxide nanoparticles; Antioxidant; Antibacterial activity; COCOS-NUCIFERA; CATALYST; DYE; ZNO;
D O I
10.1016/j.jphotobiol.2016.07.011
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
The use of plant extract to synthesize nanoparticle has been considered as one of the eco-friendly method. Additionally, it is a strong alternate for conventional methods which includes chemical and physical approach. In this study, microwave assisted extraction of Carissa edulis (C edulis) at 70 degrees C and 400 W was used to extract the secondary metabolites. Further, the metabolites were used as capping agent and Zn (NO3)(2) as the metal precursor to synthesize ZnO nanoparticles (ZnO NPs). UV-Vis spectroscopy, FT-IR, XRD, SEM and HR-TEM were used for the characterization of nanoparticles. The Surface Plasmon Resonance around 358 nm from the UV-Vis spectroscopy result represents the ZnO NPs formation. The FT-IR confirms the presence of functional groups that acts as the capping agent for the synthesis of ZnO NPs. The crystalline structure of nanoparticles is revealed in the XRD result, morphology showed by SEM results and the size of the ZnO NPs were predicted by HR-TEM. We have carried out the photocatalytic degradation of Congo red at 365 nm in photo reactor using ZnO NPs. The result from the photocatalytic degradation Congo red showed rate constant is (-k) 0.4947 with 97% of degradation. This is our first attempt on the C edulis extract on ZnO NPs preparation and Congo red dye degradation revels that ZnO NPs exhibit good photocatalytic property. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:395 / 401
页数:7
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