首页> 外文学位 >Magnetic and dielectric properties of sulfonated (S) poly[(styrene)-(ethylene-co-butylene)]-styrene (SEBS) block copolymer/magnetic metal oxide nanocomposites synthesized via an in-situ precipitation method.
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Magnetic and dielectric properties of sulfonated (S) poly[(styrene)-(ethylene-co-butylene)]-styrene (SEBS) block copolymer/magnetic metal oxide nanocomposites synthesized via an in-situ precipitation method.

机译:通过原位沉淀法合成的磺化(S)聚[(苯乙烯)-(乙烯-丁烯)]-苯乙烯(SEBS)嵌段共聚物/磁性金属氧化物纳米复合材料的磁性和介电性能。

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Block copolymer/magnetic metal oxide nanocomposites were synthesized by growing metal oxide nanoparticles (cobalt ferrite, CoFe2O 4 and iron oxide, alpha-Fe2O3) in sulfonated (s) poly (styrene) (PS) block domains of sulfonated poly [(styrene)-(ethylene-co-butylene)-(styrene)] (SEBS) BCP preformed films via an in-situ precipitation method by dissolving the salts of respective metal chloride (s) in a suitable solvent that selectively swells the sPS regions. Inorganic uptake was determined using thermogravimetric analysis (TGA), and it was observed that none of the samples incorporated more than 5 wt % of the inorganic component. Dynamical mechanical analysis was used to observe the changes in the glass transition temperatures (T g) in both blocks of the BCP by plotting tan delta vs. temperature responses in tensile mode on all samples. The results showed that the T g of the sPS block domains increased with sulfonation level and further increased with the incorporation of both nanoparticles in the same blocks, indicating that growth of nanoparticles takes place only in sPS blocks. The crystalline structure of the nanoparticles was observed using wide angle X-ray diffractometry (WAXD), and it was determined that cobalt iron oxide nanoparticles in 20 mole % sulfonated SEBS exhibited an inverse spinel structure confirming the structure to be CoFe2O4. And with iron oxide nanoparticles in 10 mole % sulfonated SEBS exhibiting a hematite (alpha-Fe2O 3) phase. Transmission electron microscopy (TEM) was used to investigate the particle size and distribution of nanoparticles in sBCP matrices at all sulfonation levels. Select area electron diffraction in TEM was used to determine crystalline structures of individual nanoparticles to compare with the structure observed from WAXD.;The changes in thickness of interfaces between the individual PS and EB block domains with increase in sulfonation of PS blocks were investigated semi-quantitatively using tapping mode atomic force microscopy. The interfacial thickness decreased with the increase in sulfonation level up to 16 mole % and then increased from there onwards until 20 mole % sulfonation.;Magnetometric measurements were conducted on samples incorporated with inorganic metal oxide nanoparticles using an alternating gradient magnetometer at room temperature; and the samples showed superparamagnetism. Magnetic properties at temperatures near absolute zero and above were measured using a superconducting quantum interference device magnetometer and samples exhibited some magnetic hysteresis; hence they are ferrimagnetic. Zero field cooled and field cooled measurements were conducted on samples to determine the transition temperature at which the inorganic metal oxide transitions from being ferri- to superparamagnetic. Dielectric spectroscopy measurements were conducted on iron oxide nanoparticles in sSEBS matrices to observe the presence of nanoparticles in the PS blocks; the effect of nanoparticles on relaxation times and glass transition temperatures was investigated.
机译:嵌段共聚物/磁性金属氧化物纳米复合材料是通过在磺化聚[(苯乙烯)-)的磺化(s)聚(苯乙烯)(PS)嵌段域中生长金属氧化物纳米颗粒(钴铁氧体,CoFe2O 4和氧化铁,α-Fe2O3)合成的。 (乙烯-共-丁烯)-(苯乙烯)](SEBS)BCP通过原位沉淀法将相应的一种或多种金属氯化物的盐溶解在合适的溶剂中而选择性溶胀sPS区域的预制膜。使用热重分析(TGA)确定无机吸收,并且观察到没有样品掺入超过5wt%的无机组分。通过绘制所有样品在拉伸模式下的正切增量与温度响应的曲线图,使用动态力学分析来观察BCP两个模块中玻璃化转变温度(T g)的变化。结果表明,sPS嵌段结构域的T g随着磺化水平的增加而增加,并且随着两个纳米颗粒在同一嵌段中的掺入而进一步增加,表明纳米颗粒的生长仅在sPS嵌段中发生。使用广角X射线衍射法(WAXD)观察纳米颗粒的晶体结构,并且确定20摩尔%磺化的SEBS中的钴铁氧化物纳米颗粒表现出反尖晶石结构,证实该结构为CoFe 2 O 4。并且在10摩尔%的磺化SEBS中,氧化铁纳米粒子表现出赤铁矿(α-Fe2O3)相。透射电子显微镜(TEM)用于研究所有磺化水平下sBCP基质中纳米颗粒的粒径和分布。用透射电子显微镜中的选择区域电子衍射确定单个纳米颗粒的晶体结构,以与从WAXD观察到的结构进行比较。研究了各个PS和EB嵌段结构域之间界面厚度随PS嵌段磺化程度的增加而发生的变化。使用攻丝模式原子力显微镜进行定量分析。界面厚度随着磺化水平的增加而降低,直至达到16摩尔%,然后从那里开始增加直至20摩尔%的磺化。在室温下,使用交替梯度磁力计对掺入无机金属氧化物纳米粒子的样品进行磁力测量。并且样品显示出超顺磁性。使用超导量子干涉仪磁力计测量了在绝对零附近和更高温度下的磁性能,样品表现出一些磁滞现象;因此它们是亚铁磁性的。对样品进行零场冷却和场冷却测量,以确定无机金属氧化物从亚铁磁性转变为超顺磁性的转变温度。在sSEBS矩阵中对氧化铁纳米颗粒进行了介电谱测量,以观察PS嵌段中纳米颗粒的存在。研究了纳米粒子对弛豫时间和玻璃化转变温度的影响。

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