том 74 страницы 230-257

Recent advances in catalytic transformation of biomass-derived 5-hydroxymethylfurfural into the innovative fuels and chemicals

Тип публикацииJournal Article
Дата публикации2017-07-01
scimago Q1
wos Q1
БС1
SJR3.901
CiteScore38
Impact factor16.3
ISSN13640321, 18790690
Renewable Energy, Sustainability and the Environment
Краткое описание
In contrast to the nonrenewable fossil resources, biomass, the only renewable resource of organic carbon in the nature, is considered as a special kind of inexhaustible feedstocks, which can be used for the synthesis of numerous valuable products in a sustainable manner. Among many biomass-derived products, 5-hydroxymethylfurfural (HMF) is identified to be a crucially important versatile compound due to its marvelous structure that is composed of an aldehyde group, a hydroxyl group and a furan ring. Hence, HMF possesses a very strong chemical reactivity, and it can be further transformed into a wide variety of value-added derivatives. In recent years, the synthetic methods, physicochemical properties and commercial prospects of HMF-based conventional derivatives such as 2,5-dimethylfuran (DMF), 5-ethoxymethylfurfural (EMF), ethyl levulinate (EL), long chain alkane (LLA), levulinic acid (LA), 2,5-diformylfuran (DFF) and 2,5-furandicarboxylic acid (FDCA) have been intensively reviewed by many researchers. However, up to now, the preparation of HMF-based innovative derivatives such as 2,5-dihydroxymethylfuran (DHMF), 2,5-dihydroxymethyltetrahydrofuran (DHMTHF), 1,2,6-hexanetriol (HTO), 1,6-hexanediol (HDO), 1-hydroxyhexane-2,5-dione (HHD), 3-hydroxymethylcyclopetanone (HMCPN), furan-2,5-dimethylcarboxylate (FDMC), maleic anhydride (MA), 5-hydroxy-5-(hydroxymethyl)furan-2(5H)-one (HHMFO), 5-alkoxymethylfurfural (AMF), 5,5-oxy-(bismethylene)-2-furaldehyde (OBMF), 5-arylaminomethyl-2-furanmethanol (AAMFM), 2,5-furandiamidine dihydrochloride (FDADHC), 1-alkyl-5-hydroxy-2-(hydroxymethyl)pyridinium (AHHMP), 5,5-bis(hydroxymethyl)furoin (BHMF), 5-(dialkyloxymethyl)-2-furanmethanol (DAMFM), 5-chloromethylfurfural (CMF), 5-alkanoyloxymethylfurfural (AOOMF) and furfuryl alcohol (FFA) has not yet been comprehensively summarized. In order to fill this gap, the latest studies and advancements on the preparation of HMF-based innovative derivatives via various catalytic approaches such as hydrogenation, oxidation, etherification, amination, condensation, halogenation, esterification and decarbonylation are systematically outlined and discussed in this review. Furthermore, a few potential research trends in the future studies are also proposed to provide some useful ideas for the further preparation of HMF-based innovative derivatives in a much more green, simple, efficient and economical way.
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ГОСТ |
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Hu L. et al. Recent advances in catalytic transformation of biomass-derived 5-hydroxymethylfurfural into the innovative fuels and chemicals // Renewable and Sustainable Energy Reviews. 2017. Vol. 74. pp. 230-257.
ГОСТ со всеми авторами (до 50) Скопировать
Hu L., Lin L., Wu Z., Zhou S., Liu S. Recent advances in catalytic transformation of biomass-derived 5-hydroxymethylfurfural into the innovative fuels and chemicals // Renewable and Sustainable Energy Reviews. 2017. Vol. 74. pp. 230-257.
RIS |
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TY - JOUR
DO - 10.1016/j.rser.2017.02.042
UR - https://doi.org/10.1016/j.rser.2017.02.042
TI - Recent advances in catalytic transformation of biomass-derived 5-hydroxymethylfurfural into the innovative fuels and chemicals
T2 - Renewable and Sustainable Energy Reviews
AU - Hu, Lei
AU - Lin, Lu
AU - Wu, Zhen
AU - Zhou, S
AU - Liu, Shijie
PY - 2017
DA - 2017/07/01
PB - Elsevier
SP - 230-257
VL - 74
SN - 1364-0321
SN - 1879-0690
ER -
BibTex
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BibTex (до 50 авторов) Скопировать
@article{2017_Hu,
author = {Lei Hu and Lu Lin and Zhen Wu and S Zhou and Shijie Liu},
title = {Recent advances in catalytic transformation of biomass-derived 5-hydroxymethylfurfural into the innovative fuels and chemicals},
journal = {Renewable and Sustainable Energy Reviews},
year = {2017},
volume = {74},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/j.rser.2017.02.042},
pages = {230--257},
doi = {10.1016/j.rser.2017.02.042}
}