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In situ rheometry of concentrated cellulose fibre suspensions and relationships with enzymatic hydrolysis

机译:浓缩纤维素纤维悬浮液的原位流变学及其与酶促水解的关系

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摘要

This work combines physical and biochemical analyses to scrutinize liquefaction and saccharification of complex lignocellulose materials. A multilevel analysis (macroscopic: rheology, microscopic: particle size and morphology and molecular: sugar product) was conducted at the lab-scale with three matrices: microcrystalline cellulose (MCC), Whatman paper (WP) and extruded paper-pulp (PP). A methodology to determine on-line viscosity is proposed and validated using the concept of Metzner and Otto (1957) and Rieger and Novak’s (1973). The substrate suspensions exhibited a shear-thinning behaviour with respect to the power law. A structured rheological model was established to account for the suspension viscosity as a function of shear rate and substrate concentration. The critical volume fractions indicate the transition between diluted, semi-diluted and concentrated regimes. The enzymatic hydrolysis was performed with various solid contents: MCC 273.6 gdm/L, WP 56.0 gdm/L, PP 35.1 gdm/L. During hydrolysis, the suspension viscosity decreased rapidly. The fibre diameter decreased two fold within 2h of starting hydrolysis whereas limited bioconversion was obtained (10–15%).
机译:这项工作结合了物理和生化分析,以检查复杂的木质纤维素材料的液化和糖化作用。在实验室规模下使用三种基质进行了多级分析(宏观:流变学,微观:粒度和形态以及分子:糖产品):微晶纤维素(MCC),Whatman纸(WP)和挤压纸浆(PP) 。提出并通过Metzner和Otto(1957)以及Rieger和Novak(1973)的概念验证了确定在线粘度的方法。基材悬浮液相对于幂律表现出剪切稀化行为。建立了结构化的流变模型,以解释悬浮液粘度与剪切速率和底物浓度的关系。临界体积分数指示稀释,半稀释和浓缩方案之间的过渡。以各种固体含量进行酶促水解:MCC 273.6 gdm / L,WP 56.0 gdm / L,PP 35.1 gdm / L。在水解过程中,悬浮液粘度迅速降低。在开始水解后2小时内,纤维直径降低了两倍,而获得的生物转化率却有限(10-15%)。

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