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脱铝分子筛固体酸催化葡萄糖制备5-羟甲基糠醛

何世坤 张荣花 李昊阳 潘晖 冯君锋

化工进展2024,Vol.43Issue(z1):374-381,8.
化工进展2024,Vol.43Issue(z1):374-381,8.DOI:10.16085/j.issn.1000-6613.2024-0836

脱铝分子筛固体酸催化葡萄糖制备5-羟甲基糠醛

Preparation of 5-hydroxymethylfurfural from glucose catalyzed by dealuminized molecular sieve solid acids

何世坤 1张荣花 1李昊阳 1潘晖 2冯君锋2

作者信息

  • 1. 南京林业大学化学工程学院,江苏南京 210037
  • 2. 南京林业大学化学工程学院,江苏南京 210037||南京林业大学江苏省林业资源高效加工利用协同创新中心||江苏省高校农林生物质化学与利用国家重点实验室培育建设点,江苏南京 210037
  • 折叠

摘要

Abstract

HY molecular sieves were dealuminized with nitric acid of different concentrations.The dealuminized HY molecular sieves had different specific surface areas and pore sizes.The Sn-doped bifunctional catalyst for the conversion of glucose to 5-HMF was prepared by impregnation method using the dealuminized molecular sieve as the carrier.The catalysts were characterized by X-ray diffraction(XRD),scanning electron microscopy(SEM),N2 adsorption/desorption,X-ray photoelectron spectroscopy(XPS)and acid-base titration.The results showed that the synthesized 0.5mol/L-10%Sn-HY had mesoporous structure,octahedral morphology and suitable B/L acid site ratio.In the reaction system of methyl isobutyl ketone(MIBK)and NaCl-H2O,the yield of 5-hydroxymethylfurfural was 67.3%under the optimized conditions of 0.2g catalyst,165℃ and 60min.After five cycles,the 5-HMF yield could still reach 49%,indicating that the catalyst had good stability.Meanwhile,the reaction mechanism for the conversion of glucose to 5-HMF was preliminarily investigated.Overall,this work established an efficient multiphase catalytic system that demonstrated the great potential of converting biomass into platform compounds.

关键词

催化剂/分子筛/生物质/双相体系/5-羟甲基糠醛

Key words

catalyst/molecular sieves/biomass/biphasic system/5-hydroxymethylfurfural

分类

化学化工

引用本文复制引用

何世坤,张荣花,李昊阳,潘晖,冯君锋..脱铝分子筛固体酸催化葡萄糖制备5-羟甲基糠醛[J].化工进展,2024,43(z1):374-381,8.

基金项目

国家自然科学基金(32101469) (32101469)

广西林产化学与工程重点实验室(国家民委重点实验室)开放基金(GXFK2204) (国家民委重点实验室)

江苏省生物质能源与材料重点实验室自主科研项目(JSBEN-S-202202). (JSBEN-S-202202)

化工进展

OA北大核心CSTPCD

1000-6613

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