Cyclic tetravinylsiloxanetetraols as hybrid inorganic-organic thiol-ene networks

被引:22
|
作者
Sparks, Bradley J. [1 ]
Kuchera, Timothy J. [1 ]
Jungman, Matthew J. [1 ]
Richardson, Adam D. [1 ]
Savin, Daniel A. [1 ]
Hait, Sukhendu [2 ]
Lichtenhan, Joseph [2 ]
Striegel, Mary F. [3 ]
Patton, Derek L. [1 ]
机构
[1] Univ So Mississippi, Sch Polymers & High Performance Mat, Hattiesburg, MS 39406 USA
[2] Hybrid Plast Inc, Hattiesburg, MS 39401 USA
[3] Natl Ctr Preservat Technol & Training, Natchitoches, LA 71457 USA
基金
美国国家科学基金会;
关键词
PHOTOPOLYMERIZATIONS; POLYMERIZATION; KINETICS; COMPOSITES; CHEMISTRY; MECHANISM;
D O I
10.1039/c2jm15484f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, organic-inorganic hybrid materials containing stable silanol functionalities were designed by incorporating cyclic tetravinylsiloxanetetraols into photopolymerized polymer networks via the thiol-ene reaction, with the intent of tailoring the thermal and mechanical properties of the resulting materials. The effects of the cyclic tetravinylsiloxanetetraols concentration on the thermomechanical properties and thermal stability of pentaerythritol triallyl ether/pentaerythritol tetra(3-mercaptopropionate) (APE-PETMP) and allyl isocyanurate/pentaerythritol tetra(3-mercaptopropionate) (TTT-PETMP) ternary networks were evaluated using dynamic thermomechanical analysis and thermogravimetric analysis, respectively. Photopolymerization kinetics were monitored using real-time FTIR. Interestingly, an increase in glass transition temperature was observed with the APE-PETMP networks while a decrease in glass transition temperature was observed for the TTT-PETMP networks with increasing concentration of [Vi(OH)SiO](4). These observations are discussed in terms of cross-link density and monomer rigidity.
引用
收藏
页码:3817 / 3824
页数:8
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