Contribution of Deep Eutectic Solvents for Biomass Processing: Opportunities, Challenges, and Limitations
暂无分享,去创建一个
François Jérôme | F. Jérôme | K. D. O. Vigier | G. Châtel | Gregory Chatel | Karine De Oliveira Vigier | K. Vigier
[1] Juben Nemchand Chheda,et al. Katalytische Flüssigphasenumwandlung oxygenierter Kohlenwasserstoffe aus Biomasse zu Treibstoffen und Rohstoffen für die Chemiewirtschaft , 2007 .
[2] Lynn F. Gladden,et al. Glycerol eutectics as sustainable solvent systems , 2010 .
[3] Kati Vilonen,et al. Biorefining: heterogeneously catalyzed reactions of carbohydrates for the production of furfural and hydroxymethylfurfural. , 2011, ChemSusChem.
[4] Xiaohong Wang,et al. Conversion of highly concentrated fructose into 5-hydroxymethylfurfural by acid–base bifunctional HPA nanocatalysts induced by choline chloride , 2014 .
[5] Johnathan E. Holladay,et al. Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-Hydroxymethylfurfural , 2007, Science.
[6] Ronny Martínez,et al. Ionic liquid and deep eutectic solvent-activated CelA2 variants generated by directed evolution , 2014, Applied Microbiology and Biotechnology.
[7] R. Rogers,et al. Ionic liquid processing of cellulose. , 2012, Chemical Society reviews.
[8] B. Han,et al. Direct conversion of inulin to 5-hydroxymethylfurfural in biorenewable ionic liquids , 2009 .
[9] George W. Huber,et al. The critical role of heterogeneous catalysis in lignocellulosic biomass conversion , 2009 .
[10] Hongdeng Qiu,et al. Deep eutectic solvents as novel extraction media for phenolic compounds from model oil. , 2014, Chemical communications.
[11] M. Farah,et al. A facile acidic choline chloride–p-TSA DES-catalysed dehydration of fructose to 5-hydroxymethylfurfural , 2014 .
[12] T. Welton,et al. Ionic liquids: not always innocent solvents for cellulose , 2015 .
[13] Geert-Jan Witkamp,et al. Natural deep eutectic solvents as a new extraction media for phenolic metabolites in Carthamus tinctorius L. , 2013, Analytical chemistry.
[14] Ferdi Schüth,et al. Design of solid catalysts for the conversion of biomass , 2009 .
[15] J. Hallett,et al. Deconstruction of lignocellulosic biomass with ionic liquids , 2013 .
[16] Rui L. Reis,et al. Natural Deep Eutectic Solvents – Solvents for the 21st Century , 2014 .
[17] J. Yang,et al. Catalytic dehydration of carbohydrates suspended in organic solvents promoted by AlCl3 /SiO2 coated with choline chloride. , 2015, ChemSusChem.
[18] M. Coelho,et al. Extraction of saponins from sisal (Agave sisalana) and juá (Ziziphus joazeiro) with cholinium-based ionic liquids and deep eutectic solvents , 2013, European Food Research and Technology.
[19] François Jérôme,et al. Deep eutectic solvents: syntheses, properties and applications. , 2012, Chemical Society reviews.
[20] F. Mjalli,et al. A novel technique for separating glycerine from palm oil-based biodiesel using ionic liquids , 2010 .
[21] James A. Dumesic,et al. Solvent Effects on Fructose Dehydration to 5-Hydroxymethylfurfural in Biphasic Systems Saturated with Inorganic Salts , 2009 .
[22] Friedrich Srienc,et al. Hydrolase-catalyzed biotransformations in deep eutectic solvents. , 2008, Chemical communications.
[23] Mohd Ali Hashim,et al. Eutectic solvents for the removal of residual palm oil-based biodiesel catalyst , 2011 .
[24] Fei Liu,et al. Conversion of wheat straw to furfural and levulinic acid in a concentrated aqueous solution of betaïne hydrochloride , 2014 .
[25] Brent H. Shanks,et al. Catalytic dehydration of C6 carbohydrates for the production of hydroxymethylfurfural (HMF) as a versatile platform chemical , 2014 .
[26] K. Shimizu,et al. Toward a rational control of solid acid catalysis for green synthesis and biomass conversion , 2011 .
[27] C. Mukesh,et al. Dissolution of α-chitin in deep eutectic solvents , 2013 .
[28] Emma L. Smith,et al. Deep eutectic solvents (DESs) and their applications. , 2014, Chemical reviews.
[29] Roberto Rinaldi. Aufschluss pflanzlicher Biomasse trifft auf Katalyse , 2014 .
[30] Hua Zhao,et al. Ionic liquids and deep eutectic solvents for biodiesel synthesis: a review , 2013 .
[31] Ed de Jong,et al. Hydroxymethylfurfural, a versatile platform chemical made from renewable resources. , 2013, Chemical reviews.
[32] Gary A. Baker,et al. Deep eutectic solvents: sustainable media for nanoscale and functional materials. , 2014, Accounts of chemical research.
[33] R. Rogers,et al. Review: Oxidation of Lignin Using Ionic Liquids—An Innovative Strategy To Produce Renewable Chemicals , 2014 .
[34] Katalin Barta,et al. Homogeneous catalysis for the conversion of biomass and biomass-derived platform chemicals , 2014 .
[35] M. Gutiérrez,et al. Deep-eutectic solvents playing multiple roles in the synthesis of polymers and related materials. , 2012, Chemical Society reviews.
[36] J. Barrault,et al. Conversion of fructose and inulin to 5-hydroxymethylfurfural in sustainable betaine hydrochloride-based media , 2012 .
[37] R. Rinaldi. Plant biomass fractionation meets catalysis. , 2014, Angewandte Chemie.
[38] Emma Lloyd Raven,et al. Extraction of glycerol from biodiesel into a eutectic based ionic liquid , 2007 .
[39] P. Fatehi,et al. Recent advancements in the production of hydroxymethylfurfural , 2014 .
[40] Fei Liu,et al. Dehydration of highly concentrated solutions of fructose to 5-hydroxymethylfurfural in a cheap and sustainable choline chloride/carbon dioxide system. , 2012, ChemSusChem.
[41] Basudeb Saha,et al. Advances in 5-hydroxymethylfurfural production from biomass in biphasic solvents , 2014 .
[42] Zaira Maugeri,et al. Ionic liquids in biotransformations: from proof-of-concept to emerging deep-eutectic-solvents. , 2011, Current opinion in chemical biology.
[43] Hongbing Yu,et al. Conversion of Xylan and Xylose into Furfural in Biorenewable Deep Eutectic Solvent with Trivalent Metal Chloride Added , 2013 .
[44] R. Bogel-Łukasik,et al. Ionic liquid-mediated formation of 5-hydroxymethylfurfural-a promising biomass-derived building block. , 2011, Chemical reviews.
[45] Raymond K. Rasheed,et al. Deep eutectic solvents formed between choline chloride and carboxylic acids: versatile alternatives to ionic liquids. , 2004, Journal of the American Chemical Society.
[46] A. Pádua,et al. Selectivity enhancement in the aqueous acid-catalyzed conversion of glucose to 5-hydroxymethylfurfural induced by choline chloride , 2013 .
[47] G. Huber,et al. Liquid-phase catalytic processing of biomass-derived oxygenated hydrocarbons to fuels and chemicals. , 2007, Angewandte Chemie.
[48] Honglei Fan,et al. Conversion of fructose to 5-hydroxymethylfurfural using ionic liquids prepared from renewable materials , 2008 .
[49] P. Domínguez de María,et al. Lipase-catalyzed (trans)esterification of 5-hydroxy- methylfurfural and separation from HMF esters using deep-eutectic solvents. , 2013, ChemSusChem.
[50] A. Corma,et al. Chemical routes for the transformation of biomass into chemicals. , 2007, Chemical reviews.
[51] P. D. D. María. Recent trends in (ligno)cellulose dissolution using neoteric solvents: switchable, distillable and bio-based ionic liquids. , 2014 .
[52] Shiguo Zhang,et al. Recent advances in ionic liquid catalysis , 2011 .
[53] Mohd Ali Hashim,et al. Using Deep Eutectic Solvents Based on Methyl Triphenyl Phosphunium Bromide for the Removal of Glycerol from Palm-Oil-Based Biodiesel , 2011 .
[54] A. Corma,et al. Synthesis of transportation fuels from biomass: chemistry, catalysts, and engineering. , 2006, Chemical reviews.
[55] Suxiang Wu,et al. Effect of CO2 on conversion of inulin to 5-hydroxymethylfurfural and propylene oxide to 1,2-propanediol in water , 2010 .
[56] P. Gallezot,et al. Conversion of biomass to selected chemical products. , 2012, Chemical Society reviews.
[57] Maaike C. Kroon,et al. New natural and renewable low transition temperature mixtures (LTTMs): screening as solvents for lignocellulosic biomass processing , 2012 .
[58] D. Kralisch,et al. Conversion of carbohydrates into 5-hydroxymethylfurfural in highly concentrated low melting mixtures , 2009 .
[59] Pablo Domínguez de María,et al. Novel choline-chloride-based deep-eutectic-solvents with renewable hydrogen bond donors: levulinic acid and sugar-based polyols , 2012 .