Melamine-Formaldehyde Polymer-Based Nanocomposite for Sunlight-Driven Photodegradation of Multiple Dyes and Their Mixture

被引:9
|
作者
Garg, Anjali Kumari [1 ]
Singh, Buta [1 ]
Naskar, Sourenjit [2 ]
Prajapati, Rajneesh Kumar [3 ]
Dalal, Chumki [4 ,5 ]
Sonkar, Sumit Kumar [1 ]
机构
[1] Malaviya Natl Inst Technol, Dept Chem, Jaipur 302017, Rajasthan, India
[2] Indian Oil Corp Ltd, Qual Control Dept MD, Jaipur 303904, Rajasthan, India
[3] Indian Inst Technol Kanpur, Ctr Nanosci, Kanpur 208016, Uttar Pradesh, India
[4] JECRC Univ, Dept Chem, Jaipur 303905, Rajasthan, India
[5] Natl Inst Technol, Dept Appl Sci, New Delhi 110040, Delhi, India
关键词
PHOTOCATALYTIC DEGRADATION; METHYLENE-BLUE; GRAPHENE NANOSHEETS; CADMIUM-SULFIDE; POLLUTANT SOOT; CARBON; NANOPARTICLES; REMOVAL; RESIN; HETEROJUNCTION;
D O I
10.1021/acs.langmuir.3c01349
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cadmiumsulfide (CdS)-decorated, cross-linked melamine-formaldehydepolymer-based nanocomposite (MFP-CdS) has been synthesized. MFP-CdSis utilized here as a photoactive material for the photodegradationof six model organic dyes and their mixture in an aqueous medium inthe presence of sunlight. The half-life values from the kinetic studyof multiple dyes strongly support the importance of sunlight on thefast degradation of all six dyes compared to bulb light and control(dark) conditions. A comparative H-1 NMR analysis of thedyes and their degraded products has been performed to support thebreakdown of the aromatic framework of organic dyes using MFP-CdSin sunlight. The mechanisms involved in the photodegradation of dyeshave been investigated based on radical trapping studies that supportthe significant involvement of superoxide radicals along with holes.Moreover, the dye removal efficiency using MFP-CdS from real industrialwastewater samples is evaluated via the external spiking of organicdyes and their mixture in unknown industrial effluents where theyshowed similar photodegradation results. Based on the high recyclabilityof MFP-CdS, these are used for multiple cycles.
引用
收藏
页码:11036 / 11047
页数:12
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