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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Combined Small-Angle Neutron Scattering, Diffusion NMR, and Molecular Dynamics Study of a Eutectogel: Illuminating the Dynamical Behavior of Glyceline Confined in Bacterial Cellulose Gels
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Combined Small-Angle Neutron Scattering, Diffusion NMR, and Molecular Dynamics Study of a Eutectogel: Illuminating the Dynamical Behavior of Glyceline Confined in Bacterial Cellulose Gels

机译:结合小角中子散射,扩散NMR和Eutectogel的分子动力学研究:照亮细菌纤维素凝胶中限局限的血型曲线的动力学行为

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摘要

A deep eutectic solvent (DES) entrapped in a bacterial cellulose (BC) network gives rise to a gelatin-like, self-supported material termed a bacterial cellulose eutectogel (BCEG). Although this novel material holds potential for numerous industrial, environmental, energy, or medical applications, little is known about the structural features or dynamical behavior within a eutectogel. In this work, we employ X-ray diffraction (XRD), nuclear magnetic resonance (NMR), and small-angle neutron scattering (SANS) to probe the structural and diffusive behavior of the prevailing DES glyceline (1:2 molar ratio of choline chloride:glycerol) confined within bacterial cellulose. XRD investigations demonstrate that the bacterial cellulose maintains its crystallinity even as the glyceline content approaches 95 wt % in the BCEG, an outcome corroborated by molecular dynamics (MD) simulations, which suggest minimal changes in the structural features of the cellulose chains due to the presence of glyceline. SANS measurements reveal a significant reduction in the radius of gyration (R-g) for BC in a BCEG compared to its hydrogel analogue, indicating a collapse in the microfibrillar structure that we attribute to removal of waters from the interfibrillar space due to a higher affinity of DES for water than for cellulose. Furthermore, SANS experiments suggest that the vast majority of DES is hosted within large micropores in the BCEG (i.e., mesoscopic confinement). Interestingly, proton NMR experiments disclose faster diffusional rates for choline and glycerol entrapped in a BCEG compared to neat glyceline. MD simulations offer the possible explanation that this diffusional acceleration results from significant migration of chloride from the bulk to cellulose microfibrillar surfaces, thereby reducing hydrogen bonding with choline and glycerol partners. This study provides the first comprehensive investigation into the structure and diffusional dynamics of glyceline within a eutectogel, offering insights into mass transport that should be useful for tailoring these novel materials to potential applications.
机译:在细菌纤维素(BC)网络中捕获的深度共晶溶剂(DES)产生了类似明胶的自支撑材料称为细菌纤维素eutectogel(BCEG)。虽然这种新材料具有众多工业,环境,能源或医学应用的潜力,但对于Eutectogel内的结构特征或动态行为知之甚少。在这项工作中,我们采用X射线衍射(XRD),核磁共振(NMR)和小角度中子散射(SAN)来探测普遍的DES血糖(1:2摩尔比的胆碱比例)的结构和扩散行为氯化物:甘油)限制在细菌纤维素内。 XRD调查表明,细菌纤维素均匀地保持其结晶度,甚至在BCEG中接近95wt%,通过分子动力学(MD)模拟的结果,这表明由于存在而显着的纤维素链的结构特征的变化。血晶线。与其水凝胶类似物相比,SAN测量揭示了BCEG中BC的循环(RG)的显着降低,表明我们归因于DES的较高亲和力,从而归因于微纤维结构中的塌陷。对于水而不是纤维素。此外,SANS实验表明,绝大多数DES在BCEG中的大型微孔中托管(即,介观监禁)。有趣的是,与整齐的甘油线相比,质子NMR实验公开了捕获在BCEG中的胆碱和甘油的更快的扩散速率。 MD仿真提供了可能的解释,即该扩散加速度从大量迁移到纤维素微生物表面的显着迁移,从而减少了与胆碱和甘油合作伙伴的氢键。本研究提供了对Eutectogel内综合线结构和扩散动态的第一次综合调查,提供了对大规模运输的见解,这应该有助于将这些新颖的材料定制到潜在的应用。

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