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Magnetic poly(glycidyl methacrylate)-based microspheres prepared by suspension polymerization in the presence of modified La0.75Sr0.25MnO3 nanoparticles

机译:在改性的La0.75Sr0.25MnO3纳米粒子的存在下通过悬浮聚合制备的磁性聚甲基丙烯酸缩水甘油酯基微球

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摘要

With the aim of preparing new magnetic poly(glycidyl methacrylate) (PGMA) microspheres suitable for magnetic separation, La0.75Sr0.25MnO3 nanoparticles were selected as a core material. In order to improve their compatibility with PGMA, the surface of the nanoparticles was treated with penta(methylethylene glycol) phosphate methacrylate (PMGPMA) as a stabilizer. Subsequently, the nanoparticles were encapsulated by the suspension polymerization of glycidyl methacrylate (GMA) resulting in a relatively homogeneous distribution Of La0.75Sr0.25MnO3 nanoparticle aggregates inside the polymer microspheres. Microspheres in the size range of a hundred micrometers with a broad particle size distribution were obtained. PMGPMA can be considered to be an efficient compatibilizer between La0.75Sr0.25MnO3 nanoparticles and PGMA. Both PMGPMA-coated La0.75Sr0.25MnO3 nanoparticles and magnetic PGMA microspheres were characterized in terms of morphology, particle size, composition and magnetic properties by the appropriate methods, such as X-ray diffraction, FTIR spectroscopy, thermogravimetric analysis (TGA), transmission electron microscopy (TEM), light microscopy and SQUID magnetometry.
机译:为了制备适合磁性分离的新型磁性聚(甲基丙烯酸缩水甘油酯)(PGMA)微球,选择了La0.75Sr0.25MnO3纳米颗粒作为核心材料。为了改善其与PGMA的相容性,纳米颗粒的表面用作为稳定剂的五(甲基乙二醇)磷酸甲基丙烯酸甲酯(PMGPMA)处理。随后,通过甲基丙烯酸缩水甘油酯(GMA)的悬浮聚合来封装纳米颗粒,从而在聚合物微球内部形成相对均匀分布的La0.75Sr0.25MnO3纳米颗粒聚集体。获得了具有宽粒度分布的尺寸为一百微米的微球。可以将PMGPMA视为La0.75Sr0.25MnO3纳米颗粒与PGMA之间的有效相容剂。 PMGPMA包覆的La0.75Sr0.25MnO3纳米颗粒和磁性PGMA微球均通过适当的方法(如X射线衍射,FTIR光谱,热重分析(TGA),透射率)在形貌,粒径,组成和磁性能方面进行了表征。电子显微镜(TEM),光学显微镜和SQUID磁力计。

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