Jie Ren, Hongliang Li, Hao Lou, Weili Zhou, Feng Zeng, Yu Wang, Xiaokang Liu, Chalachew Mebrahtu, Gang Pei, Jing-Pei Cao, Tao Yao, Zhandong Wang, Jie Zeng
{"title":"以催化 NH3 裂解和二氧化碳加氢为媒介的碳中性氨燃料发动机方案。","authors":"Jie Ren, Hongliang Li, Hao Lou, Weili Zhou, Feng Zeng, Yu Wang, Xiaokang Liu, Chalachew Mebrahtu, Gang Pei, Jing-Pei Cao, Tao Yao, Zhandong Wang, Jie Zeng","doi":"10.1002/anie.202420292","DOIUrl":null,"url":null,"abstract":"<p>Utilizing near zero-carbon NH<sub>3</sub> as fuel in engines is promising for carbon-neutrality. However, the application of NH<sub>3</sub> into the engine suffers from the intrinsic poor combustion characteristics of NH<sub>3</sub> and the emission of harmful NO<sub>x</sub> exhausts. Herein, we proposed and successfully confirmed a novel scenario for converting a conventional “CH<sub>4</sub>-fueled” engine to “NH<sub>3</sub>-fueled” engine. Specifically, CH<sub>4</sub> was used to power the internal combustion engine and release CO<sub>2</sub> as the exhaust. Afterwards, we put forward two routes to convert the exhaust and NH<sub>3</sub> into N<sub>2</sub> and CH<sub>4</sub> for enclosing the carbon cycle. The first “spatially decoupled” route splits the exhaust treatment into NH<sub>3</sub> cracking over Ru clusters on the calcined Mg−Al hydrotalcite (Ru/MAO) and CO<sub>2</sub> methanation over a commercial Ni/Al<sub>2</sub>O<sub>3</sub>. Both NH<sub>3</sub> and CO<sub>2</sub> were almost completely converted into the target products under their respective optimal conditions. The second “spatially coupled” route refers to an one-pot reaction of NH<sub>3</sub> and CO<sub>2</sub> into N<sub>2</sub>, CH<sub>4</sub>, and H<sub>2</sub>O. Due to the mismatch of reaction conditions and the competitive adsorption of reactants, the conversions of NH<sub>3</sub> and CO<sub>2</sub> were lowered to 80.1 % and 49.3 %, respectively, over Ru/MAO under 1 bar (CO<sub>2</sub>:NH<sub>3</sub>=3 : 8) at 550 °C.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"64 8","pages":""},"PeriodicalIF":16.9000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Scenario for a Carbon-Neutral Ammonia-Fueled Engine Mediated by Catalytic NH3 Cracking and CO2 Hydrogenation\",\"authors\":\"Jie Ren, Hongliang Li, Hao Lou, Weili Zhou, Feng Zeng, Yu Wang, Xiaokang Liu, Chalachew Mebrahtu, Gang Pei, Jing-Pei Cao, Tao Yao, Zhandong Wang, Jie Zeng\",\"doi\":\"10.1002/anie.202420292\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Utilizing near zero-carbon NH<sub>3</sub> as fuel in engines is promising for carbon-neutrality. However, the application of NH<sub>3</sub> into the engine suffers from the intrinsic poor combustion characteristics of NH<sub>3</sub> and the emission of harmful NO<sub>x</sub> exhausts. Herein, we proposed and successfully confirmed a novel scenario for converting a conventional “CH<sub>4</sub>-fueled” engine to “NH<sub>3</sub>-fueled” engine. Specifically, CH<sub>4</sub> was used to power the internal combustion engine and release CO<sub>2</sub> as the exhaust. Afterwards, we put forward two routes to convert the exhaust and NH<sub>3</sub> into N<sub>2</sub> and CH<sub>4</sub> for enclosing the carbon cycle. The first “spatially decoupled” route splits the exhaust treatment into NH<sub>3</sub> cracking over Ru clusters on the calcined Mg−Al hydrotalcite (Ru/MAO) and CO<sub>2</sub> methanation over a commercial Ni/Al<sub>2</sub>O<sub>3</sub>. Both NH<sub>3</sub> and CO<sub>2</sub> were almost completely converted into the target products under their respective optimal conditions. The second “spatially coupled” route refers to an one-pot reaction of NH<sub>3</sub> and CO<sub>2</sub> into N<sub>2</sub>, CH<sub>4</sub>, and H<sub>2</sub>O. 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A Scenario for a Carbon-Neutral Ammonia-Fueled Engine Mediated by Catalytic NH3 Cracking and CO2 Hydrogenation
Utilizing near zero-carbon NH3 as fuel in engines is promising for carbon-neutrality. However, the application of NH3 into the engine suffers from the intrinsic poor combustion characteristics of NH3 and the emission of harmful NOx exhausts. Herein, we proposed and successfully confirmed a novel scenario for converting a conventional “CH4-fueled” engine to “NH3-fueled” engine. Specifically, CH4 was used to power the internal combustion engine and release CO2 as the exhaust. Afterwards, we put forward two routes to convert the exhaust and NH3 into N2 and CH4 for enclosing the carbon cycle. The first “spatially decoupled” route splits the exhaust treatment into NH3 cracking over Ru clusters on the calcined Mg−Al hydrotalcite (Ru/MAO) and CO2 methanation over a commercial Ni/Al2O3. Both NH3 and CO2 were almost completely converted into the target products under their respective optimal conditions. The second “spatially coupled” route refers to an one-pot reaction of NH3 and CO2 into N2, CH4, and H2O. Due to the mismatch of reaction conditions and the competitive adsorption of reactants, the conversions of NH3 and CO2 were lowered to 80.1 % and 49.3 %, respectively, over Ru/MAO under 1 bar (CO2:NH3=3 : 8) at 550 °C.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.