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Poly(N-isopropylacrylamide) Brushes Grafted from Cellulose Nanocrystals via Surface-Initiated Single-Electron Transfer Living Radical Polymerization

机译:通过表面引发的单电子转移活性自由基聚合从纤维素纳米晶体接枝的聚(N-异丙基丙烯酰胺)刷子

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摘要

Cellulose nanocrystals (CNCs) or nanowhiskers produced from sulfuric acid hydrolysis of ramie fibers were used as substrates for surface chemical functionalization with thermoresponsive macromolecules. The CNCs were grafted with poly(AMsopropylacrylamide) brushes via surface-initiated single-electron transfer living radical polymerization (SI-SET-LRP) under various conditions at room temperature. The grafting process was confirmed via Fourier transform IR spectroscopy and X-ray photoelectron spectroscopy and the different molecular masses of the grafts were quantified and found to depend on the initiator and monomer concentrations used. No observable damage occurred to the CNCs after grafting, as determined by X-ray diffraction. Size exclusion chromatography analyses of polymer chains cleaved from the cellulose nanocrystals indicated that a higher degree of polymerization was achieved by increasing initiator or monomer loading, most likely caused by local heterogeneities yielding higher rates of polymerization. It is expected that suspension stability, interfacial interactions, friction, and other properties of grafted CNCs can be controlled by changes in temperature and provide a unique platform for further development of stimuli-responsive nanomaterials.
机译:由麻纤维经硫酸水解制得的纤维素纳米晶体(CNC)或纳米晶须用作热响应大分子进行表面化学功能化的底物。在室温下,在各种条件下,通过表面引发的单电子转移活性自由基聚合(SI-SET-LRP),用聚(AMso丙基丙烯酰胺)刷将CNC接枝。通过傅里叶变换红外光谱和X射线光电子能谱确认了接枝过程,并对接枝物的不同分子量进行了定量,发现其取决于引发剂和单体浓度。通过X射线衍射确定,嫁接后的CNC部件未发生可观察到的损坏。从纤维素纳米晶体裂解的聚合物链的尺寸排阻色谱分析表明,通过增加引发剂或单体的负载量可以实现更高的聚合度,这很可能是由于局部异质性导致了更高的聚合率。预期通过温度变化可以控制接枝CNC的悬浮液稳定性,界面相互作用,摩擦和其他特性,并为刺激响应性纳米材料的进一步开发提供了独特的平台。

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