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Integrated Fractionation-Hydrolysis Process using Sub- and Supercritical Water for Lignocellulosic Biomass Valorization

机译:使用亚临界水和超临界水的分馏-水解综合工艺,用于木质纤维素生物质的平衡

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摘要

A novel process coupling the fractionation and hydrolysis reactors is presented. Holm oak was used as real lignocellulosic biomass to be treated. In the fractionation reactor, hemicellulose and cellulose were solubilized and partially hydrolyzed in different stages with the aim of feeding the hydrolysis reactor with high C5 concentrations or C6 concentrations. The fractionation was performed in two stages: at 180°C optimizing the hemicellulose extraction and at 260°C extracting cellulose and hard hemicellulose remaining in the biomass structure. Three water flows were tested: 11, 17 and 26 cm³/min. Sugar yields from 71 to 75% were reached, mainly composed of xylose and glucose oligomers and lower amounts of other chemicals, like retro-aldol products, acetic acid or 5-HMF. The outlet stream from the fractionation reactor was directly mixed with sub or supercritical water at the inlet mixer of a SHR where the reaction time was precisely controlled. The temperature, pressure and reaction time were modified to get an insight of their effect on the yield of retro-aldol condensation products. Yields of 24% for glycolaldehyde, and pyruvaldehyde were found at 8.3 s, 350°C and 162 bar (hydrolysis reactor conditions). On other hand, 25% of lactic acid was found at 0.23 s, 396°C and 245 bar. A discussion based on a known reaction pathway is proposed. Moreover, a kinetic model for the hydrolysis reactor was proposed, being able to reproduce the experimental data with deviations lower than 10% for sugars and other products extracted. This combined process performs a selective valorization of real lignocellulosic biomass, avoiding the costly process of extreme grinding needed for the fluidization in a continuous hydrothermal process.
机译:提出了一种将分馏和水解反应器耦合的新方法。霍尔姆橡木被用作待处理的真正的木质纤维素生物质。在分馏反应器中,半纤维素和纤维素在不同的阶段被溶解并部分水解,目的是向水解反应器中供给高的C5浓度或C6浓度。分馏分两个阶段进行:在180°C下优化半纤维素提取,在260°C下提取残留在生物质结构中的纤维素和硬半纤维素。测试了三种水流量:11、17和26cm³/ min。糖的收率从71%增至75%,主要由木糖和葡萄糖低聚物以及少量其他化学物质(如逆醛醇产品,乙酸或5-HMF)组成。来自分馏反应器的出口物流在SHR的入口混合器中直接与亚临界或超临界水混合,在该反应器中精确控制反应时间。修改了温度,压力和反应时间,以了解它们对逆醛醇缩合产物产率的影响。在8.3 s,350°C和162 bar(水解反应器条件)下,发现乙醇醛和丙酮醛的产率为24%。另一方面,在0.23s,396℃和245bar下发现25%的乳酸。提出了基于已知反应途径的讨论。此外,提出了水解反应器的动力学模型,该模型能够再现糖和其他提取产物的偏差小于10%的实验数据。该组合过程对真实的木质纤维素生物质进行选择性增值,从而避免了连续水热过程中流态化所需的昂贵的极端研磨过程。

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