Reactivity of Polysilazanes Allows Catalyst‐Free Curing of Silicones

التفاصيل البيبلوغرافية
العنوان: Reactivity of Polysilazanes Allows Catalyst‐Free Curing of Silicones
المؤلفون: René Sønderbæk‐Jørgensen, Sebastian Meier, Kim Dam‐Johansen, Anne L. Skov, Anders E. Daugaard
المصدر: Sønderbæk-Jørgensen, R, Meier, S, Dam-Johansen, K, Skov, A L & Daugaard, A E 2022, ' Reactivity of Polysilazanes Allows Catalyst free Curing of Silicones ', Macromolecular Materials and Engineering, vol. 307, 2200157 . https://doi.org/10.1002/mame.202200157
بيانات النشر: Wiley, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Polymers and Plastics, General Chemical Engineering, Organic Chemistry, Materials Chemistry
الوصف: Silicones are typically cured at room temperature by means of metal catalyst such as tin or platinum. When networks are formed the catalyst become unrecoverable, which is of economic as well as environmental concern. Very few methods for producing metal catalyst-free room-temperature vulcanised (RTV) silicones exist and require conditions unavailable in industrial settings. Through the study of organic polysilazane (PSz) reactivity with simple alcohols by NMR, we discovered an unexpected fragmentation preference for breaking the Si-N bond rather than the Si-H; thereby, casting a new light on the fragmentation mechanism of polysilazanes. Utilising the polysilazane fragmentation as a silyl ether coupling agent for multifunctional carbinol silicones, we present a method of producing catalyst free RTV silicone networks at ambient conditions. These silicone networks were proven chemically similar to a standard condensation cured silicone and stoichiometric variations of PSz content demonstrated adjustable network properties.
وصف الملف: application/pdf
تدمد: 1439-2054
1438-7492
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925bfb6015f132a1bfd5041ae027d4c3
https://doi.org/10.1002/mame.202200157
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....925bfb6015f132a1bfd5041ae027d4c3
قاعدة البيانات: OpenAIRE