Issue 47, 2016

Concurrent electrochemical CO2 reduction to HCOOH and methylene blue removal on metal electrodes

Abstract

Experimental studies were done for simultaneous CO2 reduction and methylene blue (MB) dye removal using Sn and Zn as cathode and Co3O4 as anode electrocatalysts. The extent of CO2 reduction and dye removal were observed in NaHCO3 and KHCO3 electrolytes separately. The electrodes (cathode and anode) were prepared by coating the respective electrocatalyst on the graphite plate surface. A mixture of 0.5 M salt and 10 mg l−1 of MB was considered as a base solution to conduct the reduction and dye removal studies at different applied voltages of 2 to 3.8 V. The reacted samples were collected for different time intervals of 5, 10, 15, 20 and 25 min to obtain the product formation using ultra-fast liquid chromatography (UFLC) and dye analysis by an UV visible spectrophotometer. The results confirm the formation of HCOOH for both cases with simultaneous CO2 and MB removal. A maximum faradaic efficiency of 57.9% (KHCO3) was observed using Sn as an electrocatalyst for a reaction time of 15 min and 31.7% (KHCO3) in 5 min using Zn as an electrocatalyst. With increasing applied voltages the faradaic efficiencies were gradually decreased whereas dye removal is increased. However, the present studies were able to give a new topic for both simultaneous dye removal and CO2 reduction in order to reduce atmospheric CO2 concentrations and water purification. The selected electrocatalyst combinations were able to be used effectively for reduction studies which gives a new application for both CO2 reduction and dye removal.

Graphical abstract: Concurrent electrochemical CO2 reduction to HCOOH and methylene blue removal on metal electrodes

Article information

Article type
Paper
Submitted
20 Feb 2016
Accepted
18 Apr 2016
First published
20 Apr 2016

RSC Adv., 2016,6, 40916-40922

Concurrent electrochemical CO2 reduction to HCOOH and methylene blue removal on metal electrodes

V. S. K. Yadav and M. K. Purkait, RSC Adv., 2016, 6, 40916 DOI: 10.1039/C6RA04549A

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