Comparison of different cyclic organic carbonates in the oxyalkylation of various types of lignin
Tài liệu tham khảo
Clements, 2003, Reactive applications of cyclic alkylene carbonates, Ind. Eng. Chem. Res., 42, 663, 10.1021/ie020678i
Liebert, 1987, Final report on the safety assessment of propylene carbonate, J. Am. Coll. Toxicol., 6, 23, 10.3109/10915818709095488
Schäffner, 2009, Organische carbonate. Grüne Lösungsmittel für Synthese und Katalyse, Chem. Unserer Zeit., 43, 12, 10.1002/ciuz.200900468
Schäffner, 2010, Organic carbonates as solvents in synthesis and catalysis, Chem. Rev., 110, 4554, 10.1021/cr900393d
Huntsman Corporation, 2001
Huntsman Corporation, 2010
Sonnati, 2013, Glycerol carbonate as a versatile building block for tomorrow: synthesis, reactivity, properties and applications, Green Chem., 15, 283, 10.1039/C2GC36525A
Parrish, 2000, Perspectives on alkyl carbonates in organic synthesis, Tetrahedron, 56, 8207, 10.1016/S0040-4020(00)00671-2
Over, 2016, Sustainable allylation of organosolv lignin with diallyl carbonate and detailed structural characterization of modified lignin, Green Chem., 18, 197, 10.1039/C5GC01882J
Llevot, 2016, Renewability is not enough: recent advances in the sustainable synthesis of biomass-derived monomers and polymers, Chem. Eur. J., 22, 11510, 10.1002/chem.201602068
Tomani, 2010, The lignoboost process, Cell. Chem. Technol., 44, 53
Nagy, 2010, Characterization of CO2 precipitated kraft lignin to promote its utilization, Green Chem., 12, 31, 10.1039/B913602A
Velez, 2013, Solvated liquid-lignin fractions from a kraft black liquor, Bioresour. Technol., 148, 586, 10.1016/j.biortech.2013.08.097
Kouisni, 2012, The Lignoforce System: A new process for the production of high-quality lignin from black liquor, J. Sci. Technol. For. Prod. Proc., 2, 6
Podschun, 2015, Structure–function relationships in the phenolation of lignins from different sources, ACS Sustain. Chem. Eng., 3, 2526, 10.1021/acssuschemeng.5b00705
Cateto, 2009, Optimization study of lignin oxypropylation in view of the preparation of polyurethane rigid foams, Ind. Eng. Chem. Res., 48, 2583, 10.1021/ie801251r
Cui, 2013, Toward thermoplastic lignin polymers; part II: thermal & polymer characteristics of kraft lignin & derivatives, BioResources, 8, 864, 10.15376/biores.8.1.864-886
Nadji, 2005, Oxypropylation of lignin and preparation of rigid polyurethane foams from ensuing polyols, Macromol. Mater. Eng., 290, 1009, 10.1002/mame.200500200
Wu, 1984, Engineering plastics from lignin. I. Synthesis of hydroxypropyl lignin, J. Appl. Polym. Sci., 29, 1111, 10.1002/app.1984.070290408
Saraf, 1985, Engineering plastics from lignin. VI. Structure property relationship of PEG-containing polyurethane networks, J. Appl. Polym. Sci., 30, 2207, 10.1002/app.1985.070300533
Rials, 1986, Engineering plastics from lignin. XIII. Effect of lignin structure on polyurethane network formation, Holzforschung, 40, 353, 10.1515/hfsg.1986.40.6.353
W.W. Carlson, Process of hydroxyethylation. US2448767 A, 1947.
L.T. Monson, W.J. Dickson, Oxyalkylated lignin sulfonic acid compounds and method of preparing same. US2854444 A, 1953.
Kühnel, 2015, Synthesis of lignin polyols via oxyalkylation with propylene carbonate, Holzforschung, 69, 531, 10.1515/hf-2014-0068
Kühnel, 2017, Oxyalkylation of lignin with propylene carbonate: Influence ofreaction parameters on the ensuing bio-based polyols, Ind. Crop. Prod., 101, 75, 10.1016/j.indcrop.2017.03.002
Zhang, 2015, Ring-opening graft polymerization of propylene carbonate onto xylan in an ionic liquid, Molecules, 20, 6033, 10.3390/molecules20046033
Akil, 2016, Safe and non-toxic hydroxyalkylation of xylan using propylene carbonate, Eur. Polym. J., 77, 88, 10.1016/j.eurpolymj.2016.02.010
Akil, 2016, Novel synthesis of hydroxyvinylethyl xylan using 4-vinyl-1,3-dioxolan-2-one, Tetrahedron Lett., 57, 4200, 10.1016/j.tetlet.2016.08.009
Duval, 2016, Oxyalkylation of condensed tannin with propylenecarbonate as alternative to propylene oxide, ACS Sustain. Chem. Eng., 4, 3103, 10.1021/acssuschemeng.6b00081
Duval, 2017, Cyclic carbonates as safe and versatile etherifying reagents for the functionalization of lignins and tannins, ACS Sustain. Chem. Eng., 5, 7334, 10.1021/acssuschemeng.7b01502
1971
El Mansouri, 2006, Structural characterization of technical lignins for the production of adhesives: application to lignosulfonate, kraft, soda-anthraquinone, organosolv and ethanol process lignins, Ind. Crop. Prod., 24, 8, 10.1016/j.indcrop.2005.10.002
Dehne, 2016, Influence of lignin source and esterification on properties of lignin-polyethylene blends, Ind. Crop. Prod., 86, 320, 10.1016/j.indcrop.2016.04.005
Gandini, 2002, Lignin as Macromonomers for polyester and polyurethanes, 57
Puls, 2009, Conversion of beech wood into platform chemicals after organosolv treatment
Vieböck, 1930, Eine neue Methode zur maßanalytischen Bestimmung der Methoxyl- und Äthoxylgruppe, Ber. Dtsch. Chem. Ges., 63, 2818, 10.1002/cber.19300631022
Capanema, 2004, A comprehensive approach for quantitative lignin characterization by NMR spectroscopy, J. Agric. Food Chem., 52, 1850, 10.1021/jf035282b
Granata, 1995, 2-Chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane, a reagent for the accurate determination of uncondensed and condensed phenolic moieties in lignins, J. Agric. Food Chem., 43, 1538, 10.1021/jf00054a023
Rokicki, 2000, Synthesis of oligocarbonate diols and their characterization by MALDI-TOF spectrometry, Polymer, 41, 9013, 10.1016/S0032-3861(00)00273-1
Tundo, 2007
Tomczyk, 2012, Intramolecular etherification of five-membered cyclic carbonates bearing hydroxyalkyl groups, Green Chem., 14, 1749, 10.1039/c2gc35265f
Ionescu, 2016
Tomita, 2001, Model reaction for the synthesis of polyhydroxyurethanes from cyclic carbonates with amines: Substituent effect on the reactivity and selectivity of ring-opening direction in the reaction of five-membered cyclic carbonates with amine, J. Polym. Sci. A Polym. Chem., 39, 162, 10.1002/1099-0518(20010101)39:1<162::AID-POLA180>3.0.CO;2-O
Glasser, 1984, Engineering plastics from lignin. II. Characterization of hydroxyalkyl lignin derivatives, J. Appl. Polym. Sci., 29, 1815, 10.1002/app.1984.070290533
Kéki, 2004, Mechanism of the anionic ring-opening oligomerization of propylene carbonate initiated by the tert-butylphenol/KHCO3 system, Macromol. Symp., 215, 141, 10.1002/masy.200451112