Catalytic Conversion of Biomass to Monofunctional Hydrocarbons and Targeted Liquid-Fuel Classes

Kunkes, Edward L.; Simonetti, Dante A.; West, Ryan; Serrano‐Ruiz, Juan Carlos; Gärtner, Christian; Dumesic, James A.

doi:10.1126/science.1159210

Cited by 868 publications

(593 citation statements)

References 23 publications

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“…[77] This material showed desirable catalytic properties for ketonization of carbohydrate-derived carboxylic acids in the presence of other monofunctional oxygenated species, such as alcohols or ketones. [78] Under these conditions two different reactions take place, esterification and ketonization.…”

Section: Acid Condensationmentioning

confidence: 99%

Ceria‐Based Solid Catalysts for Organic Chemistry

Vivier¹,

Duprez²

2010

ChemSusChem

362

244

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Ceria has been the subject of thorough investigations, mainly because of its use as an active component of catalytic converters for the treatment of exhaust gases. However, ceria‐based catalysts have also been developed for different applications in organic chemistry. The redox and acid–base properties of ceria, either alone or in the presence of transition metals, are important parameters that allow to activate complex organic molecules and to selectively orient their transformation. Pure ceria is used in several organic reactions, such as the dehydration of alcohols, the alkylation of aromatic compounds, ketone formation, and aldolization, and in redox reactions. Ceria‐supported metal catalysts allow the hydrogenation of many unsaturated compounds. They can also be used for coupling or ring‐opening reactions. Cerium atoms can be added as dopants to catalytic system or impregnated onto zeolites and mesoporous catalyst materials to improve their performances. This Review demonstrates that the exceptional surface (and sometimes bulk) properties of ceria make cerium‐based catalysts very effective for a broad range of organic reactions.

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Section: Acid Condensationmentioning

confidence: 99%

Ceria‐Based Solid Catalysts for Organic Chemistry

Vivier¹,

Duprez²

2010

ChemSusChem

362

244

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“…1 Among six-carboned carbohydrates, hexoses are the most abundant monosaccharides existing in nature. 2,3 Of these, fructose and glucose are suitable for the use as an economical chemical feedstock for producing heterocyclic furan chemicals such as 5-hydroxymethylfurfural (5-HMF), 4 furfuryl alcohol (FFA), 5 2,5-diformylfuran (2,5-DFF) 6 and 2,5-dimethylfuran (2,5-DMF).…”

Section: Introductionmentioning

confidence: 99%

One-flow syntheses of diverse heterocyclic furan chemicals directly from fructose via tandem transformation platform

et al. 2015

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The sustainable green chemistry associated with lignocellulosic biomass is of current interest for producing various chemical feedstocks via multi-step transformation processes. Here we introduce a chemical platform system for the multicomponent cascade transformation of natural lignocellulosic biomass resources. We demonstrate the concept by developing an integrated continuous two-step microfluidic system as a tandem transformation platform for direct conversion of fructose to diverse furan chemicals with excellent yields up to 99% via decarbonylation, etherification, oxidation and hydrogenolysis of a 5-hydroxymethylfurfural (HMF) intermediate. A sequential two-step process is utilized to complete the dehydration of fructose in the surface acid catalyst at 150°C for 6 min, which is followed by the four types of HMF conversion in a binary or ternary phase to produce furfuryl alcohol (94% yield), 5-ethoxymethylfurfural (99%), 2,5-diformylfuran (82%) and 2,5-dimethylfuran (90%) with magnetic-based heterogeneous catalysts at 70-150°C for 6-60 min. This innovative tandem microfluidic platform enables precise control of the reaction temperature and time for each individual biomass conversion step in a one-flow manner with no separation and purification steps for intermediates and catalysts.

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“…It can serve as a precursor to numerous products and chemical intermediates relevant to the fuel, polymer, and pharmaceutical industries [4][5][6][7][8][9]. Selective hydrogenation gives a fuel additive with combustion properties similar to ethanol, and superior diesel miscibility [10].…”

Section: Introductionmentioning

confidence: 99%

Bifunctional Solid Catalysts for the Selective Conversion of Fructose to 5-Hydroxymethylfurfural

et al. 2010

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Solid catalysts based on SBA-15 silica were designed for the conversion of fructose to 5-hydroxymethylfurfural (HMF). The catalysts incorporate thioether groups that may promote the tautomerization of fructose to its furanose form, as well as sulfonic acid groups to catalyze its dehydration. The materials were characterized by elemental analysis, X-ray diffraction, N 2 adsorption/ desorption, and solid-state 13 C and 29 Si CP/MAS NMR spectroscopy. Functional groups incorporated into mesoporous silica by co-condensation are more robust under the reaction conditions (water at 180°C) than those grafted onto a non-porous silica. The bifunctional mesoporous catalyst achieved a selectivity for HMF of 74% at 66% fructose conversion.

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Catalytic Conversion of Biomass to Monofunctional Hydrocarbons and Targeted Liquid-Fuel Classes

Cited by 868 publications

References 23 publications

Ceria‐Based Solid Catalysts for Organic Chemistry

Ceria‐Based Solid Catalysts for Organic Chemistry

One-flow syntheses of diverse heterocyclic furan chemicals directly from fructose via tandem transformation platform

Bifunctional Solid Catalysts for the Selective Conversion of Fructose to 5-Hydroxymethylfurfural

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