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在一个集成系统中,通过酶促(漆酶)和过渡金属(MnO和Co-Mn/AC)催化将5-羟甲基糠醛选择性绿色转化为2,5-呋喃二甲酸。

Selective and green conversion of 5-HMF to FDCA enzymatic (laccase) and transition metal (MnO and Co-Mn/AC) catalysis in an integrated system.

作者信息

Gujar Rakesh J, Thombe Raju T, Dhindale Pratibha

机构信息

Department of Chemical Engineering and Bioprocess Technology, Institute of Chemical Technology (ICT) Mumbai Maharashtra 400019 India

Department of Chemical Engineering and Green Technology, Institute of Chemical Technology (ICT) Mumbai Maharashtra 400019 India

出版信息

RSC Adv. 2025 Sep 8;15(39):32337-32360. doi: 10.1039/d5ra04438c. eCollection 2025 Sep 5.

Abstract

The sustainable synthesis of bio-based monomers from renewable biomass intermediates is a central goal in green chemistry and biorefinery innovation. This study introduces a synergistic catalytic-enzymatic strategy for the efficient and eco-friendly oxidation of 5-hydroxymethylfurfural (5-HMF) into 2,5-furandicarboxylic acid (FDCA), a key monomer for next-generation biodegradable plastics. The catalytic phase employed non-noble metal catalysts, MnO and Co-Mn supported on activated carbon (Co-Mn/AC), under mild batch reaction conditions at 90 °C. Through systematic optimization, a metal-modified catalyst composition was developed to enhance both conversion and selectivity. Complementing this, the enzymatic oxidation step utilized laccase, a sustainable biocatalyst, immobilized in a packed-bed column reactor operating under continuous flow. Preliminary batch studies were conducted to understand the conversion kinetics and establish optimal parameters. Maximum FDCA yield was achieved with an enzyme concentration of 1 mg mL at 40 °C and pH 5. Additionally, the influence of substrate concentration, residence time, and reaction temperature was assessed for process intensification. This dual-step process exemplifies a green and scalable pathway, merging heterogeneous catalysis and biocatalysis for the valorization of biomass into high-value bio-based chemicals. The approach provides a forward-looking model for industrial adoption of sustainable oxidation technologies in the development of environmentally friendly polymers.

摘要

从可再生生物质中间体可持续合成生物基单体是绿色化学和生物炼制创新的核心目标。本研究介绍了一种协同催化-酶促策略,用于将5-羟甲基糠醛(5-HMF)高效且环保地氧化为2,5-呋喃二甲酸(FDCA),FDCA是下一代可生物降解塑料的关键单体。催化阶段采用非贵金属催化剂,即负载在活性炭上的MnO和Co-Mn(Co-Mn/AC),在90℃的温和间歇反应条件下进行。通过系统优化,开发了一种金属改性的催化剂组合物以提高转化率和选择性。与此相辅相成的是,酶促氧化步骤利用漆酶,一种可持续的生物催化剂,固定在连续流动操作的填充床柱反应器中。进行了初步的间歇研究以了解转化动力学并确定最佳参数。在40℃和pH 5条件下,酶浓度为1 mg/mL时可实现FDCA的最大产率。此外,还评估了底物浓度、停留时间和反应温度对过程强化的影响。这种两步法工艺体现了一条绿色且可扩展的途径,将多相催化和生物催化相结合,将生物质转化为高价值的生物基化学品。该方法为可持续氧化技术在环保聚合物开发中的工业应用提供了一个前瞻性模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd3/12415952/7ffe281e6419/d5ra04438c-f1.jpg

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