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Co embedded within biomass-derived mesoporous N-doped carbon as an acid-resistant and chemoselective catalyst for transfer hydrodeoxygenation of biomass with formic acid

机译:CO嵌入生物质衍生的中孔N掺杂碳中,作为耐酸和化学选择性催化剂,用于用甲酸转移生物质的加氢氢胺

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摘要

An N-doped Co@C catalyst (Co@NC) is synthesized by a one-pot carbonization of biomass-derived glucose and harmless melamine with CoCl2 as the catalyst, where C and N resources could be transformed into highly graphitic N-doped carbon, while the coordinated Co2+ ions are reduced to uniform Co nanoparticles (NPs), which are embedded in N-doped graphitic structures. Under base-free conditions with formic acid (FA) as a hydrogen donor, the optimized Co@NC-700 (pyrolyzed at 700 degrees C) shows a highly efficient H-2 generation from FA and the best activity for vanillin hydrodeoxygenation (HDO) with FA. For example, Co@NC-700 exhibits 15.4 times higher activity in comparison with uncovered Co on AC (Co/AC), and affords 95% vanillin conversion with 2-methoxy-4-methylphenol (MMP) as the sole product at 180 degrees C for 4 degrees.Compared with molecular hydrogen, Co@NC-700 gives a much higher activity and MMP selectivity for vanillin HDO with FA. The Co@NC-700 demonstrates enhanced acid resistance in acidic medium and adsorption of vanillin, and is recyclable and versatile for hydrogenating various unsaturated compounds. The superior performance of Co@NC-700 could be ascribed to N-derived defective sites on Co@NC, which could play multiple roles as base additives in FA dehydrogenation and as a metallike active center in vanillin HDO.
机译:通过将生物量衍生的葡萄糖和无害的三聚氰胺的单罐碳化为催化剂,将N掺杂的CO催化剂(CO @ NC)合成,其中C和N资源可以转化为高石墨N-掺杂碳,而协调的CO 2 +离子被降低到均匀的Co纳米颗粒(NPS),其嵌入N掺杂的石墨结构中。在无甲酸(FA)作为氢供体的无基条件下,优化的CO @ NC-700(700℃热解)显示出来自FA的高效H-2和Vanillin加氢脱氧(HDO)的最佳活性。与fa。例如,与AC(CO / AC)的未染成的CO相比,CO @ NC-700表现出15.4倍的活性,并提供& 95%香草蛋白转化用2-甲氧基-4-甲基苯酚(MMP),作为180℃的唯一产物4度。与分子氢,CO @ NC-700对Vanillin HDO具有更高的活性和MMP选择性,具有FA 。 CO @ NC-700表明酸性介质中的增强耐酸性和香草蛋白的吸附,是可回收和多功能用于氢化各种不饱和化合物。 CO @ NC-700的优异性能可以归因于CO @ NC的N衍生的缺陷位点,这可能在FA脱氢中的基础添加剂发挥多种作用,并作为香草蛋白HDO的金属锂活性中心。

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  • 来源
    《Green chemistry》 |2017年第23期|共9页
  • 作者单位

    Hubei Univ Hubei Collaborat Innovat Ctr Adv Organ Chem Mat Sch Chem &

    Chem Engn Wuhan 430062 Hubei Peoples R China;

    Hubei Univ Hubei Collaborat Innovat Ctr Adv Organ Chem Mat Sch Chem &

    Chem Engn Wuhan 430062 Hubei Peoples R China;

    Hubei Univ Hubei Collaborat Innovat Ctr Adv Organ Chem Mat Sch Chem &

    Chem Engn Wuhan 430062 Hubei Peoples R China;

    Hubei Univ Hubei Collaborat Innovat Ctr Adv Organ Chem Mat Sch Chem &

    Chem Engn Wuhan 430062 Hubei Peoples R China;

    China Jiliang Univ Coll Mat Sci &

    Engn Hangzhou 310018 Zhejiang Peoples R China;

    Hubei Univ Hubei Collaborat Innovat Ctr Adv Organ Chem Mat Sch Chem &

    Chem Engn Wuhan 430062 Hubei Peoples R China;

    Hubei Univ Hubei Collaborat Innovat Ctr Adv Organ Chem Mat Sch Chem &

    Chem Engn Wuhan 430062 Hubei Peoples R China;

    Hubei Univ Hubei Collaborat Innovat Ctr Adv Organ Chem Mat Sch Chem &

    Chem Engn Wuhan 430062 Hubei Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境化学;数理科学和化学;化学工业废物处理与综合利用;
  • 关键词

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