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Modification of microcrystalline cellulose structural properties by ball-milling and ionic liquid treatments and their correlation to enzymatic hydrolysis rate and yield

机译:球磨和离子液体处理的微晶纤维素结构性能及其与酶水解率的相关性及产率

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摘要

This study investigated the characteristics of cellulose Avicel PH-101 (NPA) and Avicel samples treated by either ball milling (BMA) or ionic liquid 1-ethyl-3-methylimidazolium acetate (ILA), which alter cellulose structural properties specifically and, consequently, affect the enzymatic hydrolysis of these materials differently. All materials were submitted to 48h hydrolysis using the commercial enzymatic preparations Celluclast 1.5 L and Novozymes N188. For ILA hydrolysis, a high yield of 96.8% was observed, which was related to its high specific surface area, low cellulose crystallinity, and high cellulose II content rather than to the particle size. The hydrolysis yields of BMA and NPA were 74.4% and 41.6%, respectively. BMA crystallinity was higher in comparison to ILA and lower in comparison to NPA, whereas the BMA surface area was lower in comparison to ILA and NPA. X-ray diffraction (XRD) analysis suggested the formation of cellulose II by both pretreatments on Avicel, which was reinforced by the samples' diffractograms and an additional characterization by XRD/crystallinity index of the partial hydrolyzed BMA insoluble residue. In the presence of amorphous cellulose, cellulose II allomorph presented higher hydrolysis recalcitrance. The set of results showed that crystallinity and surface area provided a straightforward correlation with the hydrolysis rate and yield of Avicel cellulose. In addition, the understanding of the effects that can be caused by pretreatments of cellulosic materials was improved and these findings contribute with the interpretation of the kinetics and yields of enzymatic hydrolysis.
机译:本研究研究了通过球磨(BMA)或离子液体1-乙基-3-甲基咪唑鎓(ILA)处理的纤维素二肌蛋白pH-101(NPA)和抗肌醇样品的特性,其特异性地改变纤维素结构特性,影响这些材料的酶水解不同。使用商业酶促制剂Celluclast 1.5L和Novozymes N188,将所有材料提交至48h水解。对于ILA水解,观察到高产96.8%,其与其高比表面积,低纤维素结晶度和高纤维素II含量有关而不是颗粒尺寸。 BMA和NPA的水解产率分别为74.4%和41.6%。与NPA相比,Bma结晶度与ILA相比较高,而与ILA和NPA相比,BMA表面积较低。 X射线衍射(XRD)分析表明,通过对样品的衍生图和部分水解BMA不溶性残基的XRD /结晶度指数进行了加固的预处理,形成纤维素II的形成。在非晶纤维素的存在下,纤维素II丙莫罗莫族族呈较高的水解重批量。该一组结果表明,结晶度和表面积与培养纤维素的水解速率和产率提供了直接的相关性。此外,改善了对纤维素材料预处理引起的效果的理解,这些发现有助于解释动力学和酶水解产量。

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