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SAXS studies of the thermally-induced fusion of diblock copolymer spheres formation of hybrid nanoparticles of intermediate size and shape

机译:SAXS研究的二嵌段共聚物球体的热诱导融合的中间尺寸和形状的杂化纳米粒子的形成

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Dilute dispersions of poly(lauryl methacrylate)–poly(benzyl methacrylate) (PLMA–PBzMA) diblock copolymer spheres (a.k.a. micelles) of differing mean particle diameter were mixed and thermally annealed at 150 °C to produce spherical nanoparticles of intermediate size. The two initial dispersions were prepared via reversible addition–fragmentation chain transfer (RAFT) dispersion polymerization of benzyl methacrylate in n -dodecane at 90 °C. Systematic variation of the mean degree of polymerization of the core-forming PBzMA block enabled control over the mean particle diameter: small-angle X-ray scattering (SAXS) analysis indicated that PLMA _(39) –PBzMA _(97) and PLMA _(39) –PBzMA _(294) formed well-defined, non-interacting spheres at 25 °C with core diameters of 21 ± 2 nm and 48 ± 5 nm, respectively. When heated separately, both types of nanoparticles regained their original dimensions during a 25–150–25 °C thermal cycle. However, the cores of the smaller nanoparticles became appreciably solvated when annealed at 150 °C, whereas the larger nanoparticles remained virtually non-solvated at this temperature. Moreover, heating caused a significant reduction in mean aggregation number for the PLMA _(39) –PBzMA _(97) nanoparticles, suggesting their partial dissociation at 150 °C. Binary mixtures of PLMA _(39) –PBzMA _(97) and PLMA _(39) –PBzMA _(294) nanoparticles were then studied over a wide range of compositions. For example, annealing a 1.0% w/w equivolume binary mixture led to the formation of a single population of spheres of intermediate mean diameter (36 ± 4 nm). Thus we hypothesize that the individual PLMA _(39) –PBzMA _(97) chains interact with the larger PLMA _(39) –PBzMA _(294) nanoparticles to form the hybrid nanoparticles. Time-resolved SAXS studies confirm that the evolution in copolymer morphology occurs on relatively short time scales (within 20 min at 150 °C) and involves weakly anisotropic intermediate species. Moreover, weakly anisotropic nanoparticles can be obtained as a final copolymer morphology over a restricted range of compositions ( e.g. for PLMA _(39) –PBzMA _(97) volume fractions of 0.20–0.35) when heating dilute dispersions of such binary nanoparticle mixtures up to 150 °C. A mechanism involving both chain expulsion/insertion and micelle fusion/fission is proposed to account for these unexpected observations.
机译:在150℃下混合不同平均粒径的聚(甲基丙烯酸甲酯)(PLMA-PBZMA)(PLMA-PBZMA)二嵌段共聚物(A.K.A.胶束)的稀释分散体。在150℃下热退火。通过在90℃下通过N-DodeCane的苄基甲基丙烯酸苄酯的甲基丙烯酸苄酯的可逆添加 - 碎片链转移(筏)分散聚合来制备两个初始分散体。系统变化的核心形成PBZMA块的平均聚合度使能控制在平均粒径上:小角度X射线散射(SAX)分析表明PLMA _(39)-PBZMA _(97)和PLMA _ (39)-PBZMA _(294)在25℃下形成明确定义的非相互作用的球体,核心直径分别为21±2nm和48±5nm。当分开加热时,两种类型的纳米颗粒在25-150-25℃的热循环中恢复了原始尺寸。然而,当在150℃下退火时,较小纳米颗粒的核心变得明显溶剂化,而较大的纳米颗粒在该温度下基本上不溶剂。此外,加热导致PLMA _(39)-PBZMA _(97)纳米颗粒的平均聚集数显着降低,表明其在150℃下部分解离。然后在各种组合物上研究了PLMA _(39)-PBZMA _(97)和PLMA _(394)纳米颗粒的二元混合物。例如,退火1.0%w / w等离模糊二元混合物导致形成中等平均直径(36±4nm)的单个球体。因此,我们假设单个PLMA _(39)-PBZMA _(97)链与较大的PLMA _(39)-PBZMA _(294)纳米颗粒相互作用以形成杂化纳米颗粒。时间分辨的萨克斯研究证实,共聚物形态的进化发生在相对短的时间尺度(在150°C时在20分钟内),并且涉及弱各向异性的中间物种。此外,当在加热这种二元纳米粒子混合物的稀释分散时间时,可以在限制的组合物(例如,用于PLMA _(39)-PBZMA _(97)的体积分数的限制的组合物的最终共聚物形态(例如,0.20-0.35)中的最终各向异性纳米颗粒。到150°C。提出了一种涉及链条驱逐/插入和胶束融合/裂变的机制,以考虑这些意想不到的观察结果。

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