期刊
CHEMOSPHERE
卷 289, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.133073
关键词
CoBi-LDH; Carbon nanotubes; Nanocomposite; Adsorption; Dyes
资金
- Department of Chemistry DST (FIST and PURSE)
- University Sophisticated Instrument Facility (USIF)
The CoBi-LDH/Cr@CNT composite was successfully synthesized and showed significant adsorption efficiency for lead and organic dyes, with a removal efficiency of up to 100%. It can be utilized as an effective adsorbent for pollutant removal in wastewater treatment.
Transition metal-doped carbon-coated layered double hydroxides for the removal of lead (II) and hazardous organic dyes have attracted increasing attention for wastewater treatment in recent years. In this work, nanostructured CoBi-LDH/Cr@CNT composites were successfully synthesized by hydrothermal route. The CoBi-LDH/ Cr@CNT was characterized by instrumental techniques such as XRD, FTIR, TEM, SEM, XPS and TGA/DTA. Adsorption of Pb2+ and organic dyes, i.e.,Rose Bengal (RB) and Congo red (CR) by CoBi-LDH/Cr@CNT was performed by batch experiment.The effect of several parameters including contact time, adsorbent dose, pH, temperature, and concentration was also investigated. Under optimum conditions, the adsorption capacity of CoBi-LDH/Cr@CNT for RB, CR and Pb2+ pollutants were (278.4 mg g(-1)), (164.6 mg g(-1)) and (503.2 mg g(-1)) and the removal efficiency achieved is 98.2%, 95.0% and 100% respectively. The selectivity of CoBi-LDH/Cr@CNT nanocomposite towards Pb2+ has been studied using ICP-AES.The isothermal results were analyzed using Freundlich and Langmuir models. Adsorption isotherm for Pb2+ (R-2 = 0.975), RB (R-2 = 0.997) and CR (R-2 = 0.992) agrees with the Langmuir model indicating monolayer adsorption. The sorption kinetics data well fitted pseudo-first-order model for Pb2+ (R-2 = 0.975), RB (R-2 = 0.996), and CR (R-2 = 0.995).The results demonstrated that the synthesized CoBi-LDH/Cr@CNT nanocomposite can be used as an effective sorbent for the removal of pollutants from wastewater.
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