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利用嵌段共聚物中间相作为模板的具有可调机械性能的热可逆水凝胶。

Thermoreversible hydroferrogels with tunable mechanical properties utilizing block copolymer mesophases as template.

机构信息

Makromolekulare Chemie II, Universität Bayreuth, D-95440 Bayreuth, Germany.

出版信息

Langmuir. 2010 Dec 21;26(24):19181-90. doi: 10.1021/la1040823. Epub 2010 Nov 24.

DOI:10.1021/la1040823
PMID:21090823
Abstract

Thermoreversible hydroferrogels (FGs) have been prepared via gelation of aqueous maghemite ferrofluids (FFs) using the triblock copolymer Pluronic P123 as gelator. In the investigated concentration range of 28-42 wt % P123, long-term stable homogeneous FGs can be prepared from FFs with a maximum maghemite content of 14 wt %. For higher FF concentrations up to 29 wt %, however, homogeneous FGs were formed only for gelator contents up to ca. 33 wt %. A combination of rheology and μ-DSC was applied as an alternative method to construct the P123 phase diagram, without the need for visual methods or scattering techniques. Using this procedure, we could show that maghemite nanoparticles can be effectively templated by the cubic and hexagonal P123 mesophases in a concentration range of 33-38 wt % P123 and FF concentrations up to 14 wt %, respectively. Most importantly, the phase behavior and the corresponding phase-transition temperatures of P123 were not significantly altered. As a result, the FGs show a reversible temperature-triggered transition from a cubic hard gel to a hexagonal gel, which is linked with a softening of the gel. Furthermore, this concept can be applied to template cobalt ferrite nanoparticle effectively, too. Magnetization experiments revealed that the superparamagnetic behavior of the maghemite nanoparticles, which show a Néel type relaxation, is not altered in the corresponding FGs. In contrast, FGs based on blocked cobalt ferrite nanoparticles show a hysteretic behavior, which indicates a strong mechanical coupling between the P123 mesophase and the magnetic nanoparticles.

摘要

水热磁凝胶(FGs)是通过使用三嵌段共聚物 Pluronic P123 作为凝胶剂使磁赤铁矿铁磁流体(FF)凝胶化而制备的。在所研究的 28-42wt%P123 浓度范围内,可以从最大磁赤铁矿含量为 14wt%的 FF 制备出长期稳定的均相 FGs。然而,对于更高的 FF 浓度高达 29wt%,仅对于凝胶剂含量高达约 33wt%,才能形成均相 FGs。流变学和μ-DSC 的组合被用作替代方法来构建 P123 相图,而无需视觉方法或散射技术。使用该程序,我们可以证明在 33-38wt%P123 和 FF 浓度高达 14wt%的浓度范围内,磁赤铁矿纳米颗粒可以有效地被立方和六方 P123 介孔模板化。最重要的是,P123 的相行为和相应的相转变温度没有明显改变。结果,FGs 表现出从立方硬凝胶到六方凝胶的可逆温度触发转变,这与凝胶的软化有关。此外,该概念也可以有效地应用于模板化钴铁氧体纳米颗粒。磁化实验表明,具有奈耳型弛豫的磁赤铁矿纳米颗粒的超顺磁性行为在相应的 FGs 中没有改变。相比之下,基于受阻钴铁氧体纳米颗粒的 FGs 表现出滞后行为,这表明 P123 介孔相与磁性纳米颗粒之间存在强烈的机械耦合。

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