TY - JOUR
T1 - Redox and Nonredox CO2Utilization
T2 - Dry Reforming of Methane and Catalytic Cyclic Carbonate Formation
AU - Subramanian, Saravanan
AU - Song, Youngdong
AU - Kim, Doyun
AU - Yavuz, Cafer T.
N1 - Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (No. NRF-2016R1A2B4011027, NRF-2017M3A7B4042140, and NRF-2017M3A7B4042235). S.S. thanks DST, India for the INSPIRE Faculty award (DST/INSPIRE/04-I/2017/000003).
Publisher Copyright:
Copyright © 2020 American Chemical Society.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2020/5/8
Y1 - 2020/5/8
N2 - CO2 emissions are too large to tackle with a single process, but a combination of avoidance with chemical utilization may be able to slow global warming. In this Focus Review, we identify two large-scale CO2 conversion processes based on their viability and opposite energy requirements. In the high-energy, stationary path, CO2 reforming of methane could provide gigatons of CO2 utilization through synthesis gas. The main problem is the lack of a durable, effective, low-cost dry reforming catalyst. The exothermic cyclic carbonate formation from CO2 and organic epoxides offers a low-energy, mobile, nonredox route. The catalysts, however, must be metal-free and robust, have a high surface area, and be low-cost while being easily scalable. These two processes could potentially address at least a quarter of all current CO2 emissions.
AB - CO2 emissions are too large to tackle with a single process, but a combination of avoidance with chemical utilization may be able to slow global warming. In this Focus Review, we identify two large-scale CO2 conversion processes based on their viability and opposite energy requirements. In the high-energy, stationary path, CO2 reforming of methane could provide gigatons of CO2 utilization through synthesis gas. The main problem is the lack of a durable, effective, low-cost dry reforming catalyst. The exothermic cyclic carbonate formation from CO2 and organic epoxides offers a low-energy, mobile, nonredox route. The catalysts, however, must be metal-free and robust, have a high surface area, and be low-cost while being easily scalable. These two processes could potentially address at least a quarter of all current CO2 emissions.
UR - http://www.scopus.com/inward/record.url?scp=85120951235&partnerID=8YFLogxK
U2 - 10.1021/acsenergylett.0c00406
DO - 10.1021/acsenergylett.0c00406
M3 - Review article
AN - SCOPUS:85120951235
SN - 2380-8195
VL - 5
SP - 1689
EP - 1700
JO - ACS Energy Letters
JF - ACS Energy Letters
IS - 5
ER -