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首页> 外文期刊>Journal of Colloid and Interface Science >Tunable Pickering emulsions with polymer-grafted lignin nanoparticles (PGLNs)
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Tunable Pickering emulsions with polymer-grafted lignin nanoparticles (PGLNs)

机译:具有聚合物接枝的木质素纳米颗粒(PGLN)的可调Pickering乳液

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摘要

Lignin is an abundant biopolymer that has native interfacial functions but aggregates strongly in aqueous media. Polyacrylamide was grafted onto kraft lignin nanoparticles using reversible addition-fragmentation chain transfer (RAFT) chemistry to form polymer-grafted lignin nanoparticles (PGLNs) that tune aggregation strength while retaining interfacial activities in forming Pickering emulsions. Polymer graft density on the particle surface, ionic strength, and initial water and cyclohexane volume fractions were varied and found to have profound effects on emulsion characteristics, including emulsion volume fraction, droplet size, and particle interfacial concentration that were attributed to changes in lignin aggregation and hydrophobic interactions. In particular, salt concentration was found to have a significant effect on aggregation, zeta potential, and interfacial tension, which was attributed to changes in solubility of both the kraft lignin and the polyacrylamide grafts. Dynamic light scattering, UV-vis spectroscopy, optical microscopy, and tensiometry were used to quantify emulsion properties and nanoparticle behavior. Under all conditions, the emulsions exhibited relatively fast creaming but were stable against coalescence and Ostwald ripening for a period of months. All emulsions were also oil-in-water (o/w) emulsions, as predicted by the Bancroft rule, and no catastrophic phase inversions were observed for any nanoparticle compositions. We conclude that lower grafting density of polyacrylamide on a lignin core resulted in high levels of interfacial activity, as characterized by higher concentration at the water-cyclohexane interface with a corresponding decrease in interfacial tension. These results indicate that the interfacial properties of polymer-grafted lignin nanoparticles are primarily due to the native hydrophobic interactions of the lignin core. These results suggest that the forces that drive aggregation are also correlated with interfacial activities, and polymer-nanoparticle interactions are critical for optimizing interfacial activities. Controlled radical polymerization is a powerful tool for polymer grafting that can leverage the intrinsic interfacial functions of lignin for the formation of Pickering emulsions. (C) 2015 Elsevier Inc. All rights reserved.
机译:木质素是具有天然界面功能但在水性介质中强烈聚集的丰富生物聚合物。使用可逆的加成-断裂链转移(RAFT)化学方法将聚丙烯酰胺接枝到牛皮纸木质素纳米颗粒上,以形成聚合物接枝的木质素纳米颗粒(PGLN),该纳米颗粒可调节聚集强度,同时保留形成Pickering乳液时的界面活性。改变了聚合物在颗粒表面的接枝密度,离子强度以及初始水和环己烷的体积分数,发现它们对乳液特性产生了深远的影响,其中包括乳液体积分数,液滴尺寸和颗粒界面浓度,这归因于木质素聚集的变化和疏水相互作用。特别地,发现盐浓度对聚集,ζ电位和界面张力具有显着影响,这归因于硫酸盐木质素和聚丙烯酰胺接枝物的溶解度变化。动态光散射,紫外-可见光谱,光学显微镜和张力测定法用于量化乳液性能和纳米粒子行为。在所有条件下,乳液均表现出相对较快的乳霜状,但在几个月内对聚结和奥斯特瓦尔德熟化稳定。如Bancroft法则所预测的,所有乳液也是水包油(o / w)乳液,并且对于任何纳米颗粒组合物均未观察到灾难性的相转化。我们得出的结论是,木质素核心上聚丙烯酰胺的较低接枝密度导致较高的界面活性,其特征在于水-环己烷界面处的浓度较高,界面张力相应降低。这些结果表明,聚合物接枝的木质素纳米颗粒的界面性质主要归因于木质素核心的天然疏水相互作用。这些结果表明驱动聚集的力也与界面活性相关,并且聚合物-纳米颗粒的相互作用对于优化界面活性至关重要。受控的自由基聚合是聚合物接枝的有力工具,可以利用木质素的固有界面功能来形成Pickering乳液。 (C)2015 Elsevier Inc.保留所有权利。

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