Development of new alcohol synthesis process from CO2 by combined thermochemical and electrochemical reactions
| Project/Area Number |
26249115
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Metal making/Resorce production engineering
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| Research Institution | The University of Tokyo |
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Principal Investigator |
YAMAGUCHI Shu 東京大学, 大学院工学系研究科(工学部), 教授 (10182437)
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| Co-Investigator(Kenkyū-buntansha) |
三好 正悟 東京大学, 大学院工学系研究科(工学部), 講師 (30398094)
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| Project Period (FY) |
2014-04-01 – 2017-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥41,990,000 (Direct Cost: ¥32,300,000、Indirect Cost: ¥9,690,000)
Fiscal Year 2016: ¥9,490,000 (Direct Cost: ¥7,300,000、Indirect Cost: ¥2,190,000)
Fiscal Year 2015: ¥9,490,000 (Direct Cost: ¥7,300,000、Indirect Cost: ¥2,190,000)
Fiscal Year 2014: ¥23,010,000 (Direct Cost: ¥17,700,000、Indirect Cost: ¥5,310,000)
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| Keywords | エコマテリアル化 / 省エネルギープロセス |
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| Outline of Final Research Achievements |
In this project, we investigated a method to realize a selective and efficient CO2 protonation reaction by taking into account both acid-base and oxidation-reduction reactions on hydrated oxide surfaces. We employed both experiment and theoretical approaches: The former revealed electrochemical reaction characteristics using single cell experiments on the preferential adsorption of CO2 utilizing surface proton activity and electrochemical reduction via protonation. The latter revealed the origin of proton activities on the hydrated surface that the difference in acid constant between two acid-base sites and the mechanism of proton migration. From the single cell experiments, we examined catalytic electrodes with a controlled dimensionality of reaction sites and the preferential reduction reaction of CO2 but end up with the predominant hydrogen gas formation owing to its low overpotential.
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Report
(4 results)
Research Products
(25 results)
