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Redefining conventional biomass hydrolysis models by including mass transfer effects. Kinetic model of cellulose hydrolysis in supercritical water

机译:通过包括传质效应重新定义常规生物质水解模型。 超临界水中纤维素水解的动力学模型

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Conventional kinetic models of cellulose hydrolysis in supercritical water do not accurately represent the operation with concentrated suspensions since they neglect the mass transfer effects. This work proposes a kinetic model which is able to reproduce cellulose hydrolysis at high concentrations providing the optimum reaction conditions to obtain nanocellulose particles and oligomers of controlled size. The basic idea of the model, which is applicable to other lignocellulosic materials, is that the hydrolysis of the cellulose particles generates an oligosaccharides layer which creates a mass transfer resistance. Therefore, it considers both the diffusion of the water molecules from the bulk phase to the surfaces of the cellulose particles and the superficial hydrolysis kinetics. Experimental points were obtained working with two different cellulose types (Dp = 75 mu m and Dp = 50 mu m) at 390 degrees C and 25 MPa, residence times between 50 ms and 250 ms and initial cellulose suspension concentration from 3% to 7% w/w (1% to 2.3% w/w at the inlet of the reactor). The average deviation between the experimental points and the theoretical values is lower than 10% proving the applicability of the kinetic model. The experimental and theoretical results demonstrated that increasing the total number of cellulose particles, either increasing the initial concentration or decreasing the average particle diameter, reduces the hydrolysis rate.
机译:超临界水中的纤维素水解的常规动力学模型不能精确地代表浓缩悬浮液的操作,因为它们忽略了传质效应。该工作提出了一种动力学模型,其能够在高浓度下再现纤维素水解,提供最佳的反应条件,以获得受控尺寸的纳米纤维素颗粒和低聚物。适用于其他木质纤维素材料的模型的基本思想是纤维素颗粒的水解产生寡糖层,其产生传质抗性。因此,它考虑了水分子的扩散与批量相到纤维素颗粒的表面和表面水解动力学的表面。获得实验点在390℃和25MPa的390℃和25MPa下使用两种不同的纤维素类型(DP =75μm和dp =50μm),在50ms和250ms之间的停留时间和初始纤维素悬浮浓度为3%至7% W / W(在反应器的入口处为1%至2.3%w / w)。实验点和理论值之间的平均偏差低于10%,证明了动力学模型的适用性。实验和理论结果表明,增加纤维素颗粒的总数,即增加初始浓度或降低平均粒径,降低了水解速率。

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