拉曼光谱
衰减全反射
硅氢加成
原位
红外光谱学
红外线的
傅里叶变换红外光谱
光谱学
硅酮
分析化学(期刊)
化学
材料科学
光学
催化作用
有机化学
物理
量子力学
作者
Xiaoyun Chen,Yang Cheng,Masashi Matsuba,Xianghuai Wang,Sangyoon J. Han,Mowbray Jordan,Qing Zhu
标识
DOI:10.1177/0003702819858916
摘要
Heterogeneous reaction systems are prevalent in the chemical industry. In situ monitoring of heterogeneous reaction systems by vibrational spectroscopy techniques offers real-time composition and conversion information without sampling and with minimal perturbation. The multiphase nature introduces new challenges which are not typically encountered in the monitoring of homogeneous systems. We investigated the kinetics of the Pt catalyzed hydrosilylation reactions between allyl polyether and SiH containing silicone using both infrared (IR) and Raman spectroscopy. The reaction mixture remains biphasic for the majority of the reaction time due to the low miscibility of polyether and silicone. The results demonstrated that by normalization with appropriate internal standards (phase-specific normalization), more accurate quantitation of the SiH and allyl functional groups can be achieved based on in situ Raman results than that based on in situ attenuated total reflection Fourier transform infrared (ATR FT-IR) results. This is believed to be due to the wavelength-dependent penetration depth of the ATR mode. Raman results were obtained using two immersion optics with different focal lengths. The advantages and disadvantages of these two immersion optics are clearly illustrated in this study.
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