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层层自组装聚电解质嵌段共聚物蠕虫在平面衬底上。

Layer-By-Layer Self-Assembly of Polyelectrolytic Block Copolymer Worms on a Planar Substrate.

机构信息

Department of Chemistry, The University of Sheffield, Dainton Building , Brook Hill, Sheffield S3 7HF, U.K.

Department of Physics & Astronomy, The University of Sheffield, Hicks Building , Hounsfield Road, Sheffield S3 7RH, U.K.

出版信息

Langmuir. 2017 Dec 19;33(50):14425-14436. doi: 10.1021/acs.langmuir.7b03571. Epub 2017 Dec 8.

Abstract

Cationic and anionic block copolymer worms are prepared by polymerization-induced self-assembly via reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion copolymerization of 2-hydroxypropyl methacrylate and glycidyl methacrylate (GlyMA), using a binary mixture of a nonionic poly(ethylene oxide) macromolecular RAFT agent and either a cationic poly([2-(methacryloyloxy)ethyl]trimethylammonium chloride) or an anionic poly(potassium 3-sulfopropyl methacrylate) macromolecular RAFT agent. In each case, covalent stabilization of the worm cores was achieved via reaction of the epoxide groups on the GlyMA repeat units with 3-mercaptopropyltriethoxysilane. Aqueous electrophoresis studies indicated a pH-independent mean zeta potential of +40 mV and -39 mV for the cationic and anionic copolymer worms, respectively. These worms are expected to mimic the rigid rod behavior of water-soluble polyelectrolyte chains in the absence of added salt. The kinetics of adsorption of the cationic worms onto a planar anionic silicon wafer was examined at pH 5 and was found to be extremely fast at 1.0 w/w % copolymer concentration in the absence of added salt. Scanning electron microscopy (SEM) analysis indicated that a relatively constant worm surface coverage of 16% was achieved at 20 °C for adsorption times ranging from just 2 s up to 2 min. Furthermore, the successive layer-by-layer deposition of cationic and anionic copolymer worms onto planar surfaces was investigated using SEM, ellipsometry, and surface zeta potential measurements. These techniques confirmed that the deposition of oppositely charged worms resulted in a monotonic increase in the mean layer thickness, with a concomitant surface charge reversal occurring on addition of each new worm layer. Unexpectedly, two distinct linear regimes were observed when plotting the mean layer thickness against the total number of adsorbed worm layers, with a steeper gradient (corresponding to thicker layers) being observed after the deposition of six worm layers.

摘要

阳离子和阴离子嵌段共聚物蠕虫是通过可逆加成-断裂链转移(RAFT)水溶液聚合 2-羟丙基甲基丙烯酸酯和甲基丙烯酸缩水甘油酯(GlyMA),使用非离子聚(氧化乙烯)大分子 RAFT 剂和阳离子聚(2-(甲基丙烯酰氧乙基)三甲基氯化铵)或阴离子聚( 3-磺丙基甲基丙烯酸钾)大分子 RAFT 剂的二元混合物制备的。在每种情况下,通过 GlyMA 重复单元上的环氧基团与 3-巯丙基三乙氧基硅烷的反应实现了蠕虫核的共价稳定化。水电泳研究表明,阳离子和阴离子共聚物蠕虫的平均 zeta 电位分别为+40 mV 和-39 mV,与 pH 无关。这些蠕虫有望在没有添加盐的情况下模拟水溶性聚电解质链的刚性棒行为。在 pH 5 下研究了阳离子蠕虫在平面阴离子硅片上的吸附动力学,发现在没有添加盐的情况下,在 1.0 w/w %共聚物浓度下,吸附非常快。扫描电子显微镜(SEM)分析表明,在 20°C 下,对于吸附时间从 2 秒到 2 分钟的吸附时间,相对恒定的蠕虫表面覆盖率为 16%。此外,使用 SEM、椭圆测量法和表面 zeta 电位测量研究了阳离子和阴离子共聚物蠕虫在平面表面上的逐层沉积。这些技术证实,相反电荷的蠕虫的沉积导致平均层厚度单调增加,并且在添加每个新的蠕虫层时会发生表面电荷反转。出乎意料的是,当将平均层厚度与吸附的蠕虫层总数作图时,观察到两个明显的线性区域,在沉积六个蠕虫层后观察到更陡的梯度(对应于较厚的层)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8e3/5789390/8cf4fc4aa45b/la-2017-03571a_0008.jpg

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