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用于将生物质升级为汽车用酯基生物润滑剂的催化剂配合物的开发:综述

Development of catalyst complexes for upgrading biomass into ester-based biolubricants for automotive applications: a review.

作者信息

Hossain Md Anwar, Mohamed Iqbal Mohammad Anwar, Julkapli Nurhidayatullaili Muhd, San Kong Pei, Ching Juan Joon, Lee Hwei Voon

机构信息

Nanotechnology & Catalysis Research Centre (NANOCAT), Institute of Postgraduate Studies, Universiti Malaya 50603 Kuala Lumpur Malaysia

Department of Chemistry, Rajshahi University of Engineering & Technology Rajshahi 6204 Bangladesh.

出版信息

RSC Adv. 2018 Feb 1;8(10):5559-5577. doi: 10.1039/c7ra11824d. eCollection 2018 Jan 29.

Abstract

Biomass-derived oils are recognised as the most promising renewable resources for the production of ester-based biolubricants due to their biodegradable, non-toxic and metal adhering properties. Homogeneous acid catalysts have been conventionally used in catalytic esterification and transesterification for the synthesis of ester-based biolubricants. Although homogeneous acid catalysts encounter difficulty during phase separation, they exhibit superior selectivity and good stereochemistry and regiochemistry control in the reaction. Consequently, transition metal complex catalysts (also known as homogeneous organometallic catalysts) are proposed for biolubricant synthesis in order to achieve a higher selectivity and conversion. Herein, the potential of both homogeneous transition metal complexes and heterogeneous supported metal complexes towards the synthesis of biolubricants, particularly, in esterification and transesterification, as well as the upgrading process, including hydrogenation and hydrogenation-esterification, is critically reviewed.

摘要

生物质衍生油因其可生物降解、无毒和金属附着特性,被认为是生产酯基生物润滑剂最有前景的可再生资源。传统上,均相酸催化剂已用于催化酯化和酯交换反应以合成酯基生物润滑剂。尽管均相酸催化剂在相分离过程中遇到困难,但它们在反应中表现出优异的选择性以及良好的立体化学和区域化学控制。因此,人们提出使用过渡金属络合物催化剂(也称为均相有机金属催化剂)来合成生物润滑剂,以实现更高的选择性和转化率。本文对均相过渡金属络合物和非均相负载金属络合物在生物润滑剂合成方面的潜力进行了批判性综述,特别是在酯化和酯交换反应以及包括氢化和氢化酯化在内的升级过程中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee76/9078193/c6f69b5ce4e5/c7ra11824d-f1.jpg

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