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PES/SiO2 Nanocomposite by In Situ Polymerization: Synthesis, Structure, Properties, and New Applications

机译:原位聚合制备PES / SiO2纳米复合材料:合成,结构,性能及新应用

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SiO2 nanoparticles of a quantum size (15 nm or less) were prepared via sol-gel method using tetraethylor-thosilicate as a precursor. SiO2 nanoparticles were characterized by X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM) analyses. Polyethersulfone/silica (PES/SiOJ crystal structure nanocomposite was prepared by in situ polymerization using silica nanoparticles as reinforcement filler. The polymerization reaction was done at 160 C in paraffin bath in the presence of diphenolic monomers. XRD and FESEM analyses were used to study the morphology of the synthesized nanocomposite. The purity and thermal property of the PES/SiO2 nanocomposite were studied by energy dispersion of X-ray analysis and differential scanning calorimetry, respectively. The effect of silica particles on the hydrophilicity of PES/SiO2 nanocomposite was also investigated. It was showed that the PES/SiO2 nanocomposite had a higher swelling degree when compared with the pure PES. The synthesized PES/SiOz powder was used to remove Cu(ll) ions from its aqueous solution. The effect of experimental conditions such as pH, shaking time, and sorbent mass on adsorption capacity of PES/SiO2 nanocomposite were investigated. It was found that incorporation of a low amount of silica (2 wt%) into the polymer matrix caused the increase of the Cu(ll) ions adsorption capacity of PES.
机译:使用四乙基原硅酸盐作为前体,通过溶胶-凝胶法制备了量子尺寸(15nm以下)的SiO 2纳米粒子。 SiO2纳米粒子通过X射线衍射(XRD)和场发射扫描电子显微镜(FESEM)分析进行了表征。以二氧化硅纳米粒子为增强填料,通过原位聚合制备聚醚砜/二氧化硅(PES / SiOJ晶体结构纳米复合材料),在160℃,双酚单体存在的条件下,在石蜡浴中进行聚合反应,并利用XRD和FESEM进行了研究。通过X射线能谱分析和差示扫描量热法研究了PES / SiO2纳米复合材料的纯度和热性能,并研究了二氧化硅颗粒对PES / SiO2纳米复合材料亲水性的影响。结果表明,与纯PES相比,PES / SiO2纳米复合材料的溶胀度更高,合成的PES / SiOz粉末可用于去除水溶液中的Cu(II)离子,对pH等实验条件的影响对PES / SiO2纳米复合材料的吸附性能,振摇时间和吸附剂质量进行了研究,结果发现,如果少量的二氧化硅(2 wt%)进入聚合物基质,则会导致PES的Cu(II)离子吸附能力提高。

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