Karaca Nurcan
Central Research Laboratory Research and Application Center, Yalova University, Yalova Turkey.
Turk J Chem. 2021 Jun 30;45(3):761-774. doi: 10.3906/kim-2012-48. eCollection 2021.
This article describes the synthesis of modified silica nanoparticles (SiO-MPTMS) via the condensation reaction carried out between silanol moieties of silica nanoparticles and the trialkoxy silyl groups of (3-mercaptopropyl) trimethoxysilane (MPTMS). Then, SiO-MPTMS nanoparticles in certain amounts (0.5 wt %, 1 wt %, 2.5 wt % and 5 wt %) were incorporated into thiol-ene resins consisting of bisphenol A glycerolate dimethacrylate and trimethylolpropane tris(3-mercaptopropionate) to prepare nanocomposite films via the photoinitiated thiol-ene polymerization in presence of 2,2-Dimethoxy-2-phenylacetophenone 99% as a photoinitiator. Fourier transform infrared spectroscopy, dynamic light scattering, scanning transmission electron microscopy, thermal gravimetric analyzer, and X-ray photoelectron spectrometer were employed to characterize SiO-MPTMS nanoparticles. It was revealed that the nanosilica surface was successfully grafted by MPTMS with the grafting ratio of 22.9%. Properties of the nanocomposite films such as decomposition temperature, thermal glass transition temperature, tensile strength, hardness, and particle distribution were investigated and the results were compared with each other and neat film. The addition of MPTMS-modified silica particles did not improve the thermal stability of the films. In scanning electron microscopy study, it was seen that 2.5 wt % of these nanoparticles used as additives were about 200 nm in size and dispersed homogeneously in the polymer matrix. The increase in tensile strength of nanocomposite films compared to the neat film was measured as 77.3% maximum.
本文描述了通过二氧化硅纳米颗粒的硅醇部分与(3-巯基丙基)三甲氧基硅烷(MPTMS)的三烷氧基甲硅烷基之间进行的缩合反应合成改性二氧化硅纳米颗粒(SiO-MPTMS)。然后,将一定量(0.5 wt%、1 wt%、2.5 wt%和5 wt%)的SiO-MPTMS纳米颗粒加入到由双酚A甘油酸酯二甲基丙烯酸酯和三羟甲基丙烷三(3-巯基丙酸酯)组成的硫醇-烯树脂中,在作为光引发剂的99% 2,2-二甲氧基-2-苯基苯乙酮存在下,通过光引发硫醇-烯聚合制备纳米复合薄膜。采用傅里叶变换红外光谱、动态光散射、扫描透射电子显微镜、热重分析仪和X射线光电子能谱对SiO-MPTMS纳米颗粒进行表征。结果表明,MPTMS成功地接枝到纳米二氧化硅表面,接枝率为22.9%。研究了纳米复合薄膜的分解温度、热玻璃化转变温度、拉伸强度、硬度和颗粒分布等性能,并将结果相互比较以及与纯薄膜进行比较。添加MPTMS改性的二氧化硅颗粒并未提高薄膜的热稳定性。在扫描电子显微镜研究中可以看到,用作添加剂的这些纳米颗粒中2.5 wt%的尺寸约为200 nm,并且均匀地分散在聚合物基体中。与纯薄膜相比,纳米复合薄膜的拉伸强度最大提高了77.3%。