2012
DOI: 10.1016/j.cej.2012.01.092
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Hydrothermal decomposition of alkali lignin in sub- and supercritical water

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Cited by 158 publications
(81 citation statements)
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“…For example, Yong and Matsumura (2012) studied decomposition of lignin in a flow reactor over the temperature range of 390 to 480°C and at residence times from 0.5 to 40 s, claiming complete decomposition within 5 s. Pińkowska et al (2012) studied hydrothermal treatment of alkali lignin over the temperature range of 280 to 390°C. The authors found the greatest yields of stable phenol and cresol products at 280°C Barbier et al (2012) performed a detailed analysis of the products of lignin decomposition in sub-and supercritical water (370-390°C) and concluded that the mechanism consisted of a complex network of parallel and sequential fragmentation and re-condensation reactions.…”
Section: Subcritical and Supercritical Water Hydrolysis Technologymentioning
confidence: 99%
“…For example, Yong and Matsumura (2012) studied decomposition of lignin in a flow reactor over the temperature range of 390 to 480°C and at residence times from 0.5 to 40 s, claiming complete decomposition within 5 s. Pińkowska et al (2012) studied hydrothermal treatment of alkali lignin over the temperature range of 280 to 390°C. The authors found the greatest yields of stable phenol and cresol products at 280°C Barbier et al (2012) performed a detailed analysis of the products of lignin decomposition in sub-and supercritical water (370-390°C) and concluded that the mechanism consisted of a complex network of parallel and sequential fragmentation and re-condensation reactions.…”
Section: Subcritical and Supercritical Water Hydrolysis Technologymentioning
confidence: 99%
“…The authors found that changes in water density affected the yields and composition of the phenolic compounds with increasing reaction times in a batch reactor. Pinkowska et al [6] reported a maximum combined yield of 11.23 wt% for guaiacol, catechol, phenol and cresol isomers at 280 °C (zero holding time) in the absence of any catalysts. Zakzeski et al [16] obtained 17 wt% yield of monomeric aromatic oxygenates such as guaiacols during liquid-phase reforming of Organosolv lignin in a water/ethanol mixture at 225 °C, 58bar with Pt/Al 2 O 3 catalyst.…”
Section: A Introductionmentioning
confidence: 99%
“…Besides, based on the structure of lignin, it is potentially a likely renewable source of aromatic chemicals. This is probably driving the increasing research on the valorization of lignin for chemical and liquid fuel production around the world in recent years [1][2][3][4][5][6][7][8]. In this regard, different thermochemical methods of depolymerizing lignin into high-value aromatic chemicals are being investigated, including fast pyrolysis, wet oxidation and hydrothermal processing.…”
Section: A Introductionmentioning
confidence: 99%
“…This indicated that a lengthy reaction time was not conducive to the depolymerization of alkali lignin in sub-and super-critical ethanol. A longer reaction time could lead to the mass of char was due to carbonization and recondensation between lignin-degraded products (Yuan et al 2010;Pińkowska et al 2012).…”
Section: Effect Of Reaction Conditions On the Yields Of Depolymerizatmentioning
confidence: 99%