In this work, we refer to the fraction of hydrides and vinyl groups consumed in cross‐linking reaction as a variation of the properties of poly(dimethylsiloxane) (PDMS) with varying the formulation of a curing agent from 3.2 wt % to 50 wt %. Youn...
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https://www.riss.kr/link?id=O107884078
2021년
eng
0253-2964
1229-5949
KCI등재;SCOPUS;SCIE
학술저널
Bulletin of the Korean Chemical Society
1225-1231 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
In this work, we refer to the fraction of hydrides and vinyl groups consumed in cross‐linking reaction as a variation of the properties of poly(dimethylsiloxane) (PDMS) with varying the formulation of a curing agent from 3.2 wt % to 50 wt %. Youn...
In this work, we refer to the fraction of hydrides and vinyl groups consumed in cross‐linking reaction as a variation of the properties of poly(dimethylsiloxane) (PDMS) with varying the formulation of a curing agent from 3.2 wt % to 50 wt %. Young's modulus, density, and refractive indices of PDMS were observed to have a maxima at a formulation of about 10 wt % of cross linker. The intensity of the Raman band for the SiH stretching mode in cross‐linker is almost zero if the cross‐linking agent is less than 10 wt %, but it is linearly increasing with increasing the content of cross‐linker. The dependence of the elastic modulus on the formulation could be explained in terms of the fraction of cross‐linked network. The analytical framework proposed in this work could be used for optimizing the formulation of PDMS and hence its properties can be tailored for specific applications.
In this work, we have propose a framework to correlate the dependence of the properties of PDMS on its formulation with the fraction of SiH as well as CC bond, which consumed by cross‐linking reaction. The effect of the formulation on the mechanical, physical, optical, and wetting properties was investigated by measuring the Young's modulus, density, refractive index, and contact angle of the resultant solid PDMS substrate. These properties showed extrema at the formulation of around 10 wt % curing agent. We have further tried to study the content of SiH and CC groups in quantitatively by utilizing Raman spectroscopy and UV absorption spectrophotometry, respectively. We successfully explained the dependence of the above properties of the PDMS on the formulation in terms of the fraction of the cross‐linked network. Finally, we confidently propose that the analytical framework developed in this work can be useful to predict a formulation to optimize the properties of PDMS for future applications in the biomedical and industrial fields.
Sharp Phase Transition by the Enhanced Lattice Stability of Low‐Temperature Phase of Cr‐Doped VO2