Radiation-induced dry reforming: A negative emission process

被引:4
作者
Ramirez-Corredores, M. M. [1 ]
Rollins, Harry W. [1 ]
Morco, Ryan P. [1 ]
Zarzana, Christopher A. [1 ]
Diaz, Luis A. [1 ]
机构
[1] Idaho Natl Lab, Idaho Falls, ID 83415 USA
关键词
CO2; utilization; Integrated energy systems; Radiolysis; Catalysis; Nuclear energy integration; Radiation integration; Gamma-induced reactions; METHANE; CATALYSTS; COKING; CO2; REDUCTION;
D O I
10.1016/j.jclepro.2023.139539
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The reaction between the most abundant greenhouse gases (GHG) to produce hydrogen might represent the most powerful and effective decarbonizing opportunity, if a low-carbon energy source is used to drive it. This is the case of methane (CH4) dry reforming (MDR) where its reaction with carbon dioxide (CO2) produces synthesis gas (syngas, a mixture of carbon monoxide and hydrogen). This study explores the feasibility of using ionizing ra-diation to induce the MDR reaction, at low temperatures and/or less energy demanding conditions. Additionally, the ionizing radiation is proposed to be supplied by nuclear power plants (NPPs), which are low-carbon reliable energy generation sources. Thus, the radiolysis of CO2, CH4 and their mixtures, under gamma-irradiation was evaluated in the absence and presence of nickel catalysts. The radiation-induced MDR reaction and radiation-induced catalytic promotion were proven to take place at temperatures close to ambient though at low conversion, with yields below 1%. Since irradiation and heat can be provided by a nuclear power plant, this radiation-induced reaction establishes a connection between nuclear energy to renewable resources and enables a pathway for a decarbonized cleaner chemical industry, for producing green chemicals.
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页数:13
相关论文
共 33 条
[11]   NUMERICAL-MODEL OF CARBON-DIOXIDE RADIOLYSIS [J].
KUMMLER, R ;
LEFFERT, C ;
IM, K ;
PICCIRELLI, R ;
KEVAN, L ;
WILLIS, C .
JOURNAL OF PHYSICAL CHEMISTRY, 1977, 81 (25) :2451-2463
[12]  
Latourrette T., 2010, RAND Corporation Monograph Series, P95
[13]  
Lercher JA, 1996, STUD SURF SCI CATAL, V101, P463
[14]   TEMPERATURE-PROGRAMMED-REDUCTION STUDIES OF NICKEL-OXIDE ALUMINA CATALYSTS - EFFECTS OF THE PREPARATION METHOD [J].
LI, CP ;
CHEN, YW .
THERMOCHIMICA ACTA, 1995, 256 (02) :457-465
[15]   Coke-Resistant Ni-Co/ZrO2-CaO-Based Microwave Catalyst for Highly Effective Dry Reforming of Methane by Microwave Catalysis [J].
Li, Ran ;
Xu, Wentao ;
Deng, Jie ;
Zhou, Jicheng .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2021, 60 (48) :17458-17468
[16]   Carbon dioxide reforming of methane to synthesis gas over Ni-MCM-41 catalysts [J].
Liu, Dapeng ;
Lau, Raymond ;
Borgna, Armando ;
Yang, Yanhui .
APPLIED CATALYSIS A-GENERAL, 2009, 358 (02) :110-118
[17]  
Livingston P., 2020, J. Earth Sci. Climatic Change, V11
[18]  
Mccullum R., 2009, P NUC WAST TECHN REV, P15
[19]   Dry reforming of methane to syngas: a potential alternative process for value added chemicals-a techno-economic perspective [J].
Mondal, Kartick ;
Sasmal, Sankar ;
Badgandi, Srikant ;
Chowdhury, Dipabali Roy ;
Nair, Vinod .
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2016, 23 (22) :22267-22273
[20]   Methane reforming with CO2 over Ni/ZrO2-CeO2 catalysts prepared by sol-gel [J].
Montoya, JA ;
Romero-Pascual, E ;
Gimon, C ;
Del Angel, P ;
Monzón, A .
CATALYSIS TODAY, 2000, 63 (01) :71-85