Efficient valorization of biomass to biofuels with bifunctional solid catalytic materials. (July 2016)
- Record Type:
- Journal Article
- Title:
- Efficient valorization of biomass to biofuels with bifunctional solid catalytic materials. (July 2016)
- Main Title:
- Efficient valorization of biomass to biofuels with bifunctional solid catalytic materials
- Authors:
- Li, Hu
Fang, Zhen
Smith, Richard L.
Yang, Song - Abstract:
- Graphical Abstract: Abstract: Mono-functional catalytic materials are used for many types of chemical transformations, but are tedious for delivering products from multiple-step reactions required for the valorization of biomass. An emerging trend is to integrate catalytic transformations, reaction engineering and product separation into a single operation, wherein catalyst design is considered as the key approach to develop efficient, low energy and environmentally-friendly reaction systems. Bifunctional solid catalysts open a door for carrying out domino/cascade- and tandem/sequential-type reactions in a single pot, for which the number of isolation or purification steps can be lessened or eliminated so that removal of unwanted by-products becomes unnecessary. This review introduces bifunctional materials used in one-pot multiple transformations of biomass into biofuels and related chemicals. Emphasis is placed on the assessment of the bifunctionality of catalytic materials, including Bronsted–Lewis acid, acid–base, and metal particles–acid or base bifunctional catalysts with some discussion being on combined catalytic systems with electrochemical, chemo-enzymatic and photochemical methods. Plausible reaction mechanisms for key pathways are shown. Relevant auxiliaries to boost catalytic activity and product selectivity, such as reaction media, heating modes and morphological properties of the catalytic materials are analyzed. Use of appropriate bifunctional catalyticGraphical Abstract: Abstract: Mono-functional catalytic materials are used for many types of chemical transformations, but are tedious for delivering products from multiple-step reactions required for the valorization of biomass. An emerging trend is to integrate catalytic transformations, reaction engineering and product separation into a single operation, wherein catalyst design is considered as the key approach to develop efficient, low energy and environmentally-friendly reaction systems. Bifunctional solid catalysts open a door for carrying out domino/cascade- and tandem/sequential-type reactions in a single pot, for which the number of isolation or purification steps can be lessened or eliminated so that removal of unwanted by-products becomes unnecessary. This review introduces bifunctional materials used in one-pot multiple transformations of biomass into biofuels and related chemicals. Emphasis is placed on the assessment of the bifunctionality of catalytic materials, including Bronsted–Lewis acid, acid–base, and metal particles–acid or base bifunctional catalysts with some discussion being on combined catalytic systems with electrochemical, chemo-enzymatic and photochemical methods. Plausible reaction mechanisms for key pathways are shown. Relevant auxiliaries to boost catalytic activity and product selectivity, such as reaction media, heating modes and morphological properties of the catalytic materials are analyzed. Use of appropriate bifunctional catalytic materials provides many opportunities for design of highly efficient reaction systems and simplified processing for producing biofuels and chemicals from lignocellulosic biomass. … (more)
- Is Part Of:
- Progress in energy and combustion science. Volume 55(2016:Aug.)
- Journal:
- Progress in energy and combustion science
- Issue:
- Volume 55(2016:Aug.)
- Issue Display:
- Volume 55 (2016)
- Year:
- 2016
- Volume:
- 55
- Issue Sort Value:
- 2016-0055-0000-0000
- Page Start:
- 98
- Page End:
- 194
- Publication Date:
- 2016-07
- Subjects:
- Lignocellulose -- Catalyst design -- Catalysis -- One-pot reaction -- Platform chemicals -- Nanotechnology
AC activated carbon -- AgSTA silver exchanged silicotungstic acid -- APPO aqueous phase partial oxidation -- ATP attapulgite -- 1, 4-BDO 1, 4-butanediol -- BG 1, 4-butylene glycol -- BHMF 2, 5-bis(hydroxymethyl)furan -- BHMTF 2, 5-bis(hydroxymethyl)tetrahydrofuran -- BMF 5-bromomethylfurfural -- [BMIM]Cl 1-butyl-3-methylimidazolium chloride -- BS benzene sulfonate -- BV Baeyer–Villiger -- CFP catalytic fast pyrolysis -- CMF 5-chloromethylfurfural -- CNFs carbon nanofibers -- CNT carbon nanotube -- Coni α-conidendrin -- ConiA α-conidendric acid -- CP chloromethyl polystyrene -- Cu-BTC copper benzene-1, 3, 5-tricarboxylate -- CVD catalytic vapor deposition -- DBU 1, 8-diazabicyclo[5.4.0]undec-7-ene -- DFF 2, 5-diformylfuran -- DFT density functional theory -- DHA dihydroxyacetone -- DHH 2, 5-dihydroxyhexane -- DMA N, N-dimethylacetamide -- DMF 2, 5-dimethylfuran -- DMSO dimethylsulfoxide -- DMTHF 2, 5-dimethyltetrahydrofuran -- DS dodecyl sulfate -- DVB divinylbenzene -- EDX energy-dispersive X-ray spectroscopy -- EG ethylene glycol -- EL ethyl levulinate -- EMF 5-ethoxymethylfurfural -- [EMIM]Cl 1-ethyl-3-methylimidazolium chloride -- F2Ac 1, 4-pentandien-3-on-1, 5-di-2-furanyl -- FAc 4-(2-furyl)-3-buten-2-on -- FAMEs fatty acid methyl esters -- FDCA 2, 5-furandicarboxylic acid -- FDMC 2, 5-dimethylfuroate -- Fe3+-POP-1 Fe3+-porous organic polymer -- Fe-BTC iron benzene-1, 3, 5-tricarboxylate -- FfA furfuryl alcohol -- FFAs free fatty acids -- FFCA 5-formyl-2-furancarboxylic acid -- FT-IR Fourier transform infrared spectroscopy -- GC-MS gas chromatography–mass spectrometry -- GLY glyceraldehyde -- GO graphene oxide -- GVL γ-valerolactone -- HAA hydroalkylation/alkylation -- HAP hydroxylapatite -- HDO hydrodeoxygenation -- HHD 5-hydroxy-2, 5-hexanedione -- HMF 5-hydroxymethylfurfural -- HMFCA 5-hydroxymethyl-2-furancarboxylic acid -- HMMF 5-hydroxymethyl methylfuroate -- HMR hydroxymatairesinol -- HNTs halloysite nanotubes -- HOAc acetic acid -- HPAs heteropoly acids -- HPLC high-performance liquid chromatography -- HT hydrotalcite -- HTFA trifluoroacetic acid -- ICP-AES inductively coupled plasma-atomic emission spectroscopy -- ILs ionic liquids -- LA levulinic acid -- LAS-OH Lewis acid site-OH -- MA maleic anhydride -- MC mesoporous carbon) -- MF 2-methylfuran -- MFA methyl furoate -- MFFA 5-methylfurfuryl alcohol -- MFF methyl 5-formyl-2-furoate -- MFf 5-methylfurfural -- MIBK methyl isobutyl ketone -- [MIMPS]3PW12O40 1-(3-sulfonic acid)propyl-3-methyl imidazolium phosphotungstate -- ML methyl levulinate -- MOF metal organic framework -- MSNs mesoporous silica nanoparticles -- MTHF 2-methyltetrahydrahydrofuran -- NA-p niobium hydroxide treated with 1 M phosphoric acid -- NHC N-heterocyclic carbene -- oxoMAT oxomatairesinol -- P[BVIM]Cl poly(3-butyl-1-vinylimidazolium chloride) -- PAL pyruvic aldehyde -- PBF poly(butylene 2, 5-furandicarboxylate) -- PMIM propyl-3-methylimidazolium -- POM polyoxometalate -- PON1 paraoxonase I -- PVP polyvinyl pyrrolidone -- ROP ring opening products -- SA succinic acid -- SAPO silicoaluminophosphate -- SC supercritical -- SZ sulfated zirconia -- TA-p tantalum hydroxide treated with 1 M phosphoric acid -- TBAC tetrabutylammonium chloride -- TEAB tetraethylammonium bromide -- TEMPO 2, 2, 6, 6-tetramethyl-piperidin-1-oxyl -- TEOS tetraethoxysilane -- TGA thermogravimetric -- THF tetrahydrofuran -- THFA tetrahydrofurfuryl alcohol -- TiZ titania zirconia -- TRS total reducing sugar -- TS TiO2SiO2 -- VPO vanadium phosphate -- WCx tungsten carbide -- WP tungsten phosphide -- WZ tungstated zirconia -- XPS X-ray photoelectron spectroscopy -- XRD X-ray diffraction -- ZrC zirconium carbonate
Combustion -- Periodicals
Power (Mechanics) -- Periodicals
Combustion engineering -- Periodicals
621.4023 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03601285 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.pecs.2016.04.004 ↗
- Languages:
- English
- ISSNs:
- 0360-1285
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6868.330000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2071.xml