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Indirect H2O2 synthesis without H2
被引:12
|作者:
Fink, Arthur G.
[1
]
Delima, Roxanna S.
[2
,3
]
Rousseau, Alexandra R.
[3
]
Hunt, Camden
[1
,2
]
Lesage, Natalie E.
[1
]
Huang, Aoxue
[1
]
Stolar, Monika
[1
]
Berlinguette, Curtis P.
[1
,2
,3
,4
]
机构:
[1] Univ British Columbia, Dept Chem, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
[2] Univ British Columbia, Stewart Blusson Quantum Matter Inst, 2355 East Mall, Vancouver, BC V6T 1Z4, Canada
[3] Univ British Columbia, Dept Chem & Biol Engn, 2360 East Mall, Vancouver, BC V6T 1Z3, Canada
[4] Canadian Inst Adv Res CIFAR, 661 Univ Ave, Toronto, ON M5G 1M1, Canada
关键词:
HYDROGEN-PEROXIDE;
2-ETHYL-9,10-ANTHRAQUINONE EAQ;
ELECTROCHEMICAL REDUCTION;
MEDIATED FORMATION;
2-PHASE MEDIUM;
ANTHRAQUINONE;
ELECTROSYNTHESIS;
ELECTRODE;
D O I:
10.1038/s41467-024-44741-1
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Industrial hydrogen peroxide (H2O2) is synthesized using carbon-intensive H-2 gas production and purification, anthraquinone hydrogenation, and anthrahydroquinone oxidation. Electrochemical hydrogenation (ECH) of anthraquinones offers a carbon-neutral alternative for generating H2O2 using renewable electricity and water instead of H-2 gas. However, the H2O2 formation rates associated with ECH are too low for commercialization. We report here that a membrane reactor enabled us to electrochemically hydrogenate anthraquinone (0.25 molar) with a current efficiency of 70% at current densities of 100 milliamperes per square centimeter. We also demonstrate continuous H2O2 synthesis from the hydrogenated anthraquinones over the course of 48 h. This study presents a fast rate of electrochemically-driven anthraquinone hydrogenation (1.32 +/- 0.14 millimoles per hour normalized per centimeter squared of geometric surface of electrode), and provides a pathway toward carbon-neutral H2O2 synthesis.
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页数:9
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