CO green technologies in CO capture and direct utilization processes: methanation, reverse water-gas shift, and dry reforming of methane

CO 2 green technologies, such as methanation, reverse water-gas shift (rWGS), and dry reforming of methane (DRM), in CO 2 capture and direct utilization processes are proposed to reduce the total thermal energy by effectively combining CO 2 capture and conversion using Ni/CaO catal-sorbents. Compare...

Full description

Saved in:
Bibliographic Details
Published inSustainable energy & fuels Vol. 4; no. 11; pp. 5543 - 5549
Main Authors Jo, Seong Bin, Woo, Jin Hyeok, Lee, Jong Heon, Kim, Tae Young, Kang, Hu In, Lee, Soo Chool, Kim, Jae Chang
Format Journal Article
LanguageEnglish
Published 27.10.2020
Online AccessGet full text

Cover

Loading…
More Information
Summary:CO 2 green technologies, such as methanation, reverse water-gas shift (rWGS), and dry reforming of methane (DRM), in CO 2 capture and direct utilization processes are proposed to reduce the total thermal energy by effectively combining CO 2 capture and conversion using Ni/CaO catal-sorbents. Compared to conventional calcium looping using CaO-based sorbents, carbonated Ni/CaO catal-sorbents are completely regenerated at lower temperatures by simultaneously converting the captured CO 2 into chemicals via methanation, rWGS, or DRM. At optimum temperatures and concentrations of the feed gas (H 2 or CH 4 ), the Ni/CaO catal-sorbents show excellent CO 2 capture capacity and productivity. In addition, the structural variation of the Ni/CaO catal-sorbents is elucidated. Based on these theoretical and experimental studies, the novel integrated CO 2 capture and direct utilization processes can be a promising technology to produce chemicals as well as mitigate CO 2 levels from large-scale sources. CO 2 green technologies, such as methanation, reverse water-gas shift (rWGS), and dry reforming of methane (DRM) in CO 2 capture and direct utilization process are developed using Ni/CaO catal-sorbents.
Bibliography:10.1039/d0se00951b
Electronic supplementary information (ESI) available. See DOI
ISSN:2398-4902
DOI:10.1039/d0se00951b