Furfural residue (FR), composed mainly of cellulose and lignin, is an industrial waste produced during furfural manufacture. In this study, dioxane, alkali, ethanol, alkali-ethanol, and alkaline hydrogen peroxide (AHP) were used to extract lignins from FR. The structural features of these lignins obtained were characterized by sugar analysis, GPC, UV, FT-IR, and HSQC spectra. As compared to dioxane lignin (DL), other lignins showed lower molecular weights (M w ) owing to the partial cleavage of the linkages between lignin units. Results from HSQC spectra revealed that β-O-4' and β-5' were still the major linkages of the FR lignin. Moreover, p-coumaric and ferulic acids were released and coprecipitated in the lignin preparations extracted with alkali and AHP, whereas part of the esters in DL were preserved during the dioxane extraction. Antioxidant activity investigation indicated that the antioxidant property of the alkali and alkali-ethanol lignins was higher than that of the commercial antioxidant, butylated hydroxytoluene.
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INTRODUCTIONFurfural residue (FR), an industrial waste, is produced during the manufacture of furfural from corncob, during which hemicelluloses are hydrolyzed to produce the furfural by acid catalysis, while the residue (mainly cellulose and lignin) is usually burnt. It has been estimated that the annual production of FR is about 23 million tons . With the rapidly increasing demand for energy and the declining supply of fossil resources, bioconversion of FR into biofuels, such as bioethanol, has received much attention. Ethanol production from FR would not only reduce environmental pollution, but also efficiently use the corncob material. It has been reported that the furfural production process decreases the degree of polymerization of cellulose, which is beneficial for the enzymatic hydrolysis (Zhang et al. 2009). However, lignin plays a vital role as an inter-and intra-molecular glue, strengthening plant cell walls, which leads to its inability to undergo rapid biotransformation into useful biofuels (Elumalai et al. 2012). Therefore, pretreatment of FR before its biotransformation is needed. The treatment approach is achieved by fractionation of FR into cellulose and lignin with good selectivity and high yield. Thus FR can be fully exploited for the subsequent conversion into biofuels, commodities (i.e., alkali lignin, organosolv lignin, etc.), and other high value-added products.PEER-REVIEWED ARTICLE bioresources.com Sun et al. (2014). "Lignins from furfural residue," BioResources 9(1), 772-785. 773Lignin is an amorphous polymer consisting of phenylpropane units, and their precursors are three monolignols, namely p-coumaryl, coniferyl, and sinapyl alcohols (Terashima and Fukushima 1989). The respective aromatic constituents of these alcohols in the polymers are called p-hydroxyphenyl (H), guaiacyl (G), and syringyl (S) units (Buranov and Mazza 2008). During the lignification process, these monolignols form various interunit bonds, such as β- O-4′, α-O-4′, 4-O-5′, β-5′, β-1′...