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Representative temperature profiles for a triplicate experiment at a nominal temperature of 180 °C.

Representative temperature profiles for a triplicate experiment at a nominal temperature of 180 °C.

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Xylose-based oligosaccharides produced from xylan-rich hemicelluloses (xylo-oligomers) are carbohydrates with potential food and pharmaceutical uses. Autohydrolysis of lignocellulosic biomass is an efficient way to produce xylo-oligomers in a reasonable yield and a wide variety of compositions (anhydroarabinose/anhydroxylose and acetyl/anhydroxylos...

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... the end of the desired reaction time, the reactor was extracted from the oil bath and immediately immersed in cold water to quench the reaction. Figure 1 shows the excellent reproducibility of the temperature profiles obtained for a triplicate experiment at 179 °C. The experiments were nonisothermal because of the length of the heating period at the beginning of the reaction (around 8 min), which was as long as the quasi-isothermal period for some of the experiments at the higher temperatures. ...

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... The portion of lignin in the residues from the 200 and the 220 • C treatments were 31.7 and 39.4 %. Small amounts of cellulose-degraded compounds (up to 3 %) were identified in the liquid resulting from the treatment at 180 • C. HWE of corncob conducted by Nabarlatz et al. and Makishima et al. [133,134] showed that the higher yields of hemicellulose-products in the liquid fraction after the HWE process occurs in the 190-200 • C range of temperatures. The extracts, as in other materials, are constituted mainly by xylan. ...
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... Hemicellulose also may be responsible for thermal and photochemical discoloration of paper (Lee and Feller 1986). Under more severe conditions of heating, aqueous suspensions of cellulose have been found to decrease in pH, which can be attributed to the same reaction; such acidity contributes to autohydrolysis during certain treatments of biomass for the production of monomeric sugars and various biofuels (Garrote et al. 2001;Nabarlatz et al. 2004;Liu et al. 2015a;Surek and Buyukkileci 2017). ...
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... Adding more acids beyond those released naturally from the biomass may enhance Xylan breakdown into XOS. Also, [19] were reported to have produced XOS in good yield by autohydrolysis of corncob biomass at 150°C [15]. Another team of researchers also synthesized XOS via hydrothermal processing of wood chips of Eucalyptus nitens. ...
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... The above studies have been performed for various LCMs, including: (a) woods and woody legumes [16,19,[21][22][23][24]27,[32][33][34]39,42,44,49,50]; (b) seeds, straws, shells, hulls, and various agricultural byproducts or wastes [13,14,21,25,26,28,37,40,41,43,[45][46][47][48][52][53][54][55]; (c) industrial byproducts [30,35,45,51]; (d) herbs and grasses, including dedicated energy crops [15,17,20,21,26,29,36]. ...
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... After an incubation at 180 • C for 10 min, the XOS-H present in the rice straw liquor mainly contained X 2 at 15.2%, followed by 14.3% X 3 , 11.1% X 4 , 8.8% X 5 , 7.9% arabinose, 6.8% X 6 , 2.1% A 2 XX, 1.4% XA 3 XX and 1.1% A 3 X (Fig. 3B). Nabarlatz, Farriol, and Montane (2004) used autohydrolysis at 150 • C for 50.8 min to treat arabinoxylan from corn cobs, and the largest molar mass of XOS had an average DP of 7. In this study, rice husk and rice straw liquors treated at 170 • C for 10 min released XOS with a DP of 2-6 and some AXOS. Notably, AXOS were inconsistently detected after increasing the treatment time and temperature (Supplementary Tables S1 and S2). ...
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... It has biphasic pattern in hydrolytic process comprising fast-rate and slow-rate hydrolysis portions. A comprehensive model of hemicellulose hydrolysis has been proposed on the basis of pseudo-homogeneous assumption following a first-order reaction ( Fig. 4.1) [26][27][28]. The kinetic model can be developed described as Eqs. ...
Chapter
Liquid hot water (LHW) technology has been thought as a green process which hardly pollutes the environment due to no addition of chemical reagents. It is usually employed as a pretreatment method for producing ethanol, butanol, lactic acid, biogas, and other biochemicals from lignocellulose. It is also used as a technology to directly obtain products from lignocellulose such as xylooligosaccharide, microcrystalline cellulose, hydrochar, and so on. This chapter describes the technological characteristics and development of LHW process, summarizes the way of LHW treatment to influence the physicochemical features of lignocellulose and the biorefinery efficiency, and depicts the application of LHW technology for bioproduct production. It concludes that LHW treatment is a versatile biorefinery technology and outlooks the promising way for the practical application of LHW technology.
... Pubescens was heated to 200 • C in water without addition of catalyst, and more than 95% of hemicellulose could be dissolved (hydrolyzed), while cellulose and lignin structure were hardly destroyed. Nabarlatz et al. built an autocatalytic hydrolysis model for xylan based on the experimental results at 150-190 • C [202]. According to the model, high temperature could promote the conversion of polymers to oligomers. ...
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Furan energy platform compounds including furfural and 5-hydroxymethylfurfural (HMF), can be produced by hydrothermal conversion of biomass. After hydrodeoxygenation, these furans can be converted into value-added chemicals and liquid fuels. This will help achieve efficient utilization of biomass and alleviate the environment issues caused by the overuse of fossil fuels. This review introduces the recent progress in the production of furfural and HMF from biomass and its derived sugars in homogeneous catalytic systems. The topics mainly include catalytic mechanisms, catalytic systems, and conversion processes. The synergistical catalytic effect of Lewis acid and Brønsted acid is crucial in furan production. Therefore, the development of metal salts and ionic liquids, which exhibit both kinds of acidity, has been the focus of recent attention. The type and composition of catalyst also play key roles in producing furan products. Thus, the design and improvement of the catalyst based on mechanism research will be helpful to the highly selective hydrothermal conversion of biomass. Reasonable selection of solvent system can improve the conversion efficiency significantly and avoid the occurrence of various side reactions. Especially, the online extraction of the biphasic solvent system can prevent some certain products from being consumed by the secondary reaction. Till now, the lab-scale homogeneous conversion process has been fully developed. Future research will focus on the magnification and commercialization of laboratory process. The key technical problems in the commercialization process is how to increase the recyclability, economy and eco-friendly property of the reaction system under the premise of satisfying product yield.