Suppr超能文献

由氨基封端的聚二甲基硅氧烷和聚二甲基-甲基-苯基硅氧烷共聚物制备的聚硅氧烷基脲弹性体的合成及力学性能表征数据。

Data on the synthesis and mechanical characterization of polysiloxane-based urea-elastomers prepared from amino-terminated polydimethylsiloxanes and polydimethyl-methyl-phenyl-siloxane-copolymers.

作者信息

Riehle Natascha, Götz Tobias, Kandelbauer Andreas, Tovar Günter E M, Lorenz Günter

机构信息

Reutlingen Research Institute, Reutlingen University, Alteburgstr. 150, 72762 Reutlingen, Germany.

School of Applied Chemistry, Reutlingen University, Alteburgstr. 150, 72762 Reutlingen, Germany.

出版信息

Data Brief. 2018 Apr 30;18:1784-1794. doi: 10.1016/j.dib.2018.04.083. eCollection 2018 Jun.

Abstract

This article contains data on the synthesis and mechanical characterization of polysiloxane-based urea-elastomers (PSUs) and is related to the research article entitled "Influence of PDMS molecular weight on transparency and mechanical properties of soft polysiloxane-urea-elastomers for intraocular lens application" (Riehle et al., 2018) [1]. These elastomers were prepared by a two-step polyaddition using the aliphatic diisocyanate 4,4'-Methylenbis(cyclohexylisocyanate) (HMDI), a siloxane-based chain extender 1,3-Bis(3-aminopropyl)-1,1,3,3-tetramethyldisiloxane (APTMDS) and amino-terminated polydimethylsiloxanes (PDMS) or polydimethyl-methyl-phenyl-siloxane-copolymers (PDMS-Me,Ph), respectively. (More details about the synthesis procedure and the reaction scheme can be found in the related research article (Riehle et al., 2018) [1]). Amino-terminated polydimethylsiloxanes with varying molecular weights and PDMS-Me,Ph-copolymers were prepared prior by a base-catalyzed ring-chain equilibration of a cyclic siloxane and the endblocker APTMDS. This DiB article contains a procedure for the synthesis of the base catalyst tetramethylammonium-3-aminopropyl-dimethylsilanolate and a generic synthesis procedure for the preparation of a PDMS having a targeted number average molecular weight of 3000 g mol. Molecular weights and the amount of methyl-phenyl-siloxane within the polysiloxane-copolymers were determined by H NMR and Si NMR spectroscopy. The corresponding NMR spectra and data are described in this article. Additionally, this DiB article contains processed data on and FTIR-ATR spectroscopy, which was used to follow the reaction progress of the polyaddition by showing the conversion of the diisocyanate. All relevant IR band assignments of a polydimethylsiloxane-urea spectrum are described in this article. Finally, data on the tensile properties and the mechanical hysteresis-behaviour at 100% elongation of PDMS-based polyurea-elastomers are shown in dependence to the PDMS molecular weight.

摘要

本文包含基于聚硅氧烷的脲弹性体(PSU)的合成及力学表征数据,且与题为《聚二甲基硅氧烷分子量对用于人工晶状体的柔软聚硅氧烷 - 脲弹性体的透明度和力学性能的影响》(里尔等人,2018年)[1]的研究论文相关。这些弹性体通过两步聚加成反应制备,分别使用脂肪族二异氰酸酯4,4'-亚甲基双(环己基异氰酸酯)(HMDI)、基于硅氧烷的扩链剂1,3 - 双(3 - 氨丙基)- 1,1,3,3 - 四甲基二硅氧烷(APTMDS)以及端氨基聚二甲基硅氧烷(PDMS)或聚二甲基 - 甲基 - 苯基 - 硅氧烷共聚物(PDMS - Me,Ph)。(关于合成步骤和反应方案的更多细节可在相关研究论文(里尔等人,2018年)[1]中找到。)不同分子量的端氨基聚二甲基硅氧烷和PDMS - Me,Ph共聚物先前通过环状硅氧烷与封端剂APTMDS的碱催化环链平衡反应制备。这篇DiB文章包含碱催化剂四甲基铵 - 3 - 氨丙基 - 二甲基硅醇盐的合成步骤以及制备数均分子量为3000 g·mol的PDMS的通用合成步骤。聚硅氧烷共聚物中的分子量和甲基苯基硅氧烷的含量通过¹H NMR和²⁹Si NMR光谱测定。本文描述了相应的NMR光谱和数据。此外,这篇DiB文章包含关于FTIR - ATR光谱的处理数据,该光谱用于通过显示二异氰酸酯的转化率来跟踪聚加成反应的进程。本文描述了聚二甲基硅氧烷 - 脲光谱的所有相关红外谱带归属。最后,展示了基于PDMS的聚脲弹性体在100%伸长率下的拉伸性能和力学滞后行为与PDMS分子量的关系数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb91/5998215/7cae41aa4a68/gr1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验