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首页> 外文期刊>Zeitschrift fur Physikalische Chemie: International Journal of Research in Physical Chemistry and Chemical Physics >Activators Regenerated by Electron Transfer for Atom Transfer Radical Polymerization of Styrene in the Presence of Hydrophobically Modified Silica Aerogel Nanoparticles
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Activators Regenerated by Electron Transfer for Atom Transfer Radical Polymerization of Styrene in the Presence of Hydrophobically Modified Silica Aerogel Nanoparticles

机译:在疏水改性的二氧化硅气凝胶纳米粒子的存在下,通过电子转移再生的苯乙烯原子转移自由基聚合活化剂

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Pristine hydrophilic silica aerogel nanoparticles surface was functionalized with hexamethyldisilazane (HMDS). Then, the resultant modified nanoparticles were used for in situ polymerization of styrene by activators regenerated by electron transfer for atom transfer radical polymerization (ARGET ATRP) to synthesize well-defined polystyrene nanocomposites. Success surface modification of hydrophilic silica aerogel nanoparticles with HMDS is demonstrated by FTIR spectroscopy and TGA. Nitrogen adsorption/desorption isotherm is applied to examine surface area and structural characteristics of the synthesized hydrophobic silica aerogel nanoparticles. Evaluation of size distribution and morphological studies were also performed by SEM and TEM. Conversion and molecular weight determinations were carried out using gas and size exclusion chromatography respectively. Adding of hydrophobic silica aerogel nanoparticles by 3 wt % results in a decrease of conversion from 89 to 64%. Molecular weight polystyrene chains decreases from 53 991 to 42 701 g . mol(-1) by addition of 3 wt % hydrophobic silica aerogel nanoparticles; however, polydispersity index values increases from 1.22 to 1.6. A peak around 4.15 ppm which originates from hydrogen atom of terminal units of polystyrene chains in proton nuclear magnetic resonance spectra can appropriately demonstrate the living nature of the polymerization. Increasing thermal stability of the nanocomposites is demonstrated by TGA. Differential scanning calorimetry shows a decrease in glass transition temperature from 80.3 to 68.9 degrees C by addition of 3 wt % hydrophobic silica aerogel nanoparticles.
机译:用六甲基二硅氮烷(HMDS)对原始的亲水性二氧化硅气凝胶纳米颗粒表面进行功能化。然后,将所得的改性纳米粒子用于通过电子转移再生的活化剂进行苯乙烯的原位聚合,以进行原子转移自由基聚合(ARGET ATRP),以合成定义明确的聚苯乙烯纳米复合材料。 FTIR光谱和TGA证明了用HMDS对亲水性二氧化硅气凝胶纳米颗粒进行成功的表面改性。应用氮吸附/解吸等温线检查合成的疏水性二氧化硅气凝胶纳米颗粒的表面积和结构特征。尺寸分布和形态研究的评价也通过SEM和TEM进行。分别使用气相色谱和尺寸排阻色谱法进行转化率和分子量的测定。疏水二氧化硅气凝胶纳米颗粒的添加量为3 wt%时,转化率将从89%降低至64%。聚苯乙烯链的分子量从53991降低至42701 g。通过添加3 wt%的疏水性二氧化硅气凝胶纳米颗粒获得mol(-1);但是,多分散指数值从1.22增加到1.6。来自质子核磁共振谱中的聚苯乙烯链末端单元的氢原子的约4.15ppm的峰可以适当地证明聚合的活性。 TGA证明了纳米复合材料的热稳定性提高。差示扫描量热法显示通过加入3wt%的疏水性二氧化硅气凝胶纳米颗粒,玻璃化转变温度从80.3℃降低到68.9℃。

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