{"title":"木质素催化解聚制备富烃生物油:Ni掺杂对LaCoO3催化剂和氢源的影响","authors":"Yanfang Zhu, Xu Jiang, Xiaoyuan Jin, Wenqi Song, Yuzhen Zhao","doi":"10.1016/j.joei.2024.101869","DOIUrl":null,"url":null,"abstract":"<div><div>The catalytic properties of metals and metal oxides are vital for lignin depolymerization into phenolic and cyclohexane compounds production. This study investigated the lignin depolymerization of with different Ni content LaCoO<sub>3</sub> perovskite catalysts at different reaction conditions such as reaction temperature, time, catalysts amount. Furthermore, various hydrogen sources, including formic acid, ethanol, and pure hydrogen were tested. The highest bio-oil yield (75.3 wt%) was achieved with hydrogen under ethanol solvent, but selectivity for cyclohexane and phenolic monomers compound was low. Using formic acid (FA) with 7 % Ni-LaCoO<sub>3</sub> catalysts at 280 °C, a bio-oil yield of 72.4 wt% was obtained, with higher selectivity for 2,6-dimethoxyphenol (19.5 %), cyclohexane (18.5 %), and methylcyclohexane (14.2 %). This suggests that Ni with presence of FA facilitates the cleavage of lignin's β-O (C-O) and β-β (C-C) bonds efficiently. The reaction using FA, resulted in the lowest O/C ratio (0.06), highest H/C ratio (0.14), and the highest HHV (36.6 MJ/kg). The catalyst exhibited the highest reaction rate and hydrogenation activity, attributed to the presence of highly dispersed surface Co and Ni species. Notably, after three recycling test, the Ni-LaCoO<sub>3</sub> catalyst maintained very good catalytic activity. These results suggest that catalysts with this composite support have the potential to convert lignin-derived phenolic compounds into higher-grade hydrocarbon liquid fuels.</div></div>","PeriodicalId":17287,"journal":{"name":"Journal of The Energy Institute","volume":"118 ","pages":"Article 101869"},"PeriodicalIF":5.6000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Catalytic depolymerization of lignin for hydrocarbon rich bio-oil production: Influence of Ni doped on LaCoO3 catalysts and hydrogen sources\",\"authors\":\"Yanfang Zhu, Xu Jiang, Xiaoyuan Jin, Wenqi Song, Yuzhen Zhao\",\"doi\":\"10.1016/j.joei.2024.101869\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The catalytic properties of metals and metal oxides are vital for lignin depolymerization into phenolic and cyclohexane compounds production. This study investigated the lignin depolymerization of with different Ni content LaCoO<sub>3</sub> perovskite catalysts at different reaction conditions such as reaction temperature, time, catalysts amount. Furthermore, various hydrogen sources, including formic acid, ethanol, and pure hydrogen were tested. The highest bio-oil yield (75.3 wt%) was achieved with hydrogen under ethanol solvent, but selectivity for cyclohexane and phenolic monomers compound was low. Using formic acid (FA) with 7 % Ni-LaCoO<sub>3</sub> catalysts at 280 °C, a bio-oil yield of 72.4 wt% was obtained, with higher selectivity for 2,6-dimethoxyphenol (19.5 %), cyclohexane (18.5 %), and methylcyclohexane (14.2 %). This suggests that Ni with presence of FA facilitates the cleavage of lignin's β-O (C-O) and β-β (C-C) bonds efficiently. The reaction using FA, resulted in the lowest O/C ratio (0.06), highest H/C ratio (0.14), and the highest HHV (36.6 MJ/kg). The catalyst exhibited the highest reaction rate and hydrogenation activity, attributed to the presence of highly dispersed surface Co and Ni species. Notably, after three recycling test, the Ni-LaCoO<sub>3</sub> catalyst maintained very good catalytic activity. These results suggest that catalysts with this composite support have the potential to convert lignin-derived phenolic compounds into higher-grade hydrocarbon liquid fuels.</div></div>\",\"PeriodicalId\":17287,\"journal\":{\"name\":\"Journal of The Energy Institute\",\"volume\":\"118 \",\"pages\":\"Article 101869\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Energy Institute\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1743967124003477\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Energy Institute","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1743967124003477","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
摘要
金属和金属氧化物的催化性能对木质素解聚生产酚类和环己烷类化合物至关重要。本研究考察了不同Ni含量LaCoO3钙钛矿催化剂在不同反应温度、时间、催化剂用量等条件下对木质素解聚的影响。此外,还测试了各种氢源,包括甲酸、乙醇和纯氢。在乙醇溶剂下,以氢为溶剂的生物油收率最高(75.3 wt%),但对环己烷和酚类单体化合物的选择性较低。采用甲酸(FA)和7% Ni-LaCoO3催化剂,在280℃条件下,生物油收率为72.4 wt%,对2,6-二甲氧基苯酚(19.5%)、环己烷(18.5%)和甲基环己烷(14.2%)具有较高的选择性。这表明在FA的存在下,Ni能有效地促进木质素β- o (C-O)和β-β (C-C)键的断裂。结果表明,FA反应的0 /C比最低(0.06),H/C比最高(0.14),HHV最高(36.6 MJ/kg)。该催化剂表现出最高的反应速率和加氢活性,这是由于其表面高度分散的Co和Ni的存在。值得注意的是,经过三次回收测试,Ni-LaCoO3催化剂保持了很好的催化活性。这些结果表明,具有这种复合载体的催化剂具有将木质素衍生的酚类化合物转化为更高品位的碳氢化合物液体燃料的潜力。
Catalytic depolymerization of lignin for hydrocarbon rich bio-oil production: Influence of Ni doped on LaCoO3 catalysts and hydrogen sources
The catalytic properties of metals and metal oxides are vital for lignin depolymerization into phenolic and cyclohexane compounds production. This study investigated the lignin depolymerization of with different Ni content LaCoO3 perovskite catalysts at different reaction conditions such as reaction temperature, time, catalysts amount. Furthermore, various hydrogen sources, including formic acid, ethanol, and pure hydrogen were tested. The highest bio-oil yield (75.3 wt%) was achieved with hydrogen under ethanol solvent, but selectivity for cyclohexane and phenolic monomers compound was low. Using formic acid (FA) with 7 % Ni-LaCoO3 catalysts at 280 °C, a bio-oil yield of 72.4 wt% was obtained, with higher selectivity for 2,6-dimethoxyphenol (19.5 %), cyclohexane (18.5 %), and methylcyclohexane (14.2 %). This suggests that Ni with presence of FA facilitates the cleavage of lignin's β-O (C-O) and β-β (C-C) bonds efficiently. The reaction using FA, resulted in the lowest O/C ratio (0.06), highest H/C ratio (0.14), and the highest HHV (36.6 MJ/kg). The catalyst exhibited the highest reaction rate and hydrogenation activity, attributed to the presence of highly dispersed surface Co and Ni species. Notably, after three recycling test, the Ni-LaCoO3 catalyst maintained very good catalytic activity. These results suggest that catalysts with this composite support have the potential to convert lignin-derived phenolic compounds into higher-grade hydrocarbon liquid fuels.
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