摘要:
A bidentate free radical crosslinking initiator binds chemically to silica and silica rich surfaces and enables the free radical based polymerization of various materials such as styrene, divinylbenzene and methylmethacrylate onto silica and silica rich surfaces. When used in connection with aerogels, the resultant crosslinked aerogels exhibit greatly increased strength with only nominal increase in density.
摘要:
Porous three-dimensional networks of polyurea and porous three-dimensional networks of carbon and methods of their manufacture are described. In an example, polyurea aerogels are prepared by mixing an triisocyanate with water and a triethylamine to form a sol-gel material and supercritically drying the sol-gel material to form the polyurea aerogel. Subjecting the polyurea aerogel to a step of pyrolysis may result in a three dimensional network having a carbon skeleton, yielding a carbon aerogel. The density and morphology of polyurea aerogels can be controlled by varying the amount of isocyanate monomer in the initial reaction mixture. A lower density in the aerogel gives rise to a fibrous morphology, whereas a greater density in the aerogel results in a particulate morphology. Polyurea aerogels described herein may also exhibit a reduced flammability.
摘要:
Porous three-dimensional networks of polyurea and porous three-dimensional networks of carbon and methods of their manufacture are described. In an example, polyurea aerogels are prepared by mixing an triisocyanate with water and a triethylamine to form a sol-gel material and supercritically drying the sol-gel material to form the polyurea aerogel. Subjecting the polyurea aerogel to a step of pyrolysis may result in a three dimensional network having a carbon skeleton, yielding a carbon aerogel. The density and morphology of polyurea aerogels can be controlled by varying the amount of isocyanate monomer in the initial reaction mixture. A lower density in the aerogel gives rise to a fibrous morphology, whereas a greater density in the aerogel results in a particulate morphology. Polyurea aerogels described herein may also exhibit a reduced flammability.
摘要:
Macroporous monolithic silica aerogels having mesoporous walls are produced via an acid-catalyzed sol-gel process from tetramethoxysilane (TMOS) using a triblock co-polymer (Pluronic P123) as a structure-directing agent and 1,3,5-trimethylbenzene (TMB) as a micelle-swelling reagent. Pluronic P 123 was removed by solvent extraction, and monoliths were obtained by removing the pore-filling solvent with liquid CO2, which was removed under supercritical conditions. The resulting materials are more robust compared to base-catalyzed silica aerogels of similar density. Mechanical properties can be further improved by reacting a di-isocyanate with the silanol groups on the macro and mesoporous surfaces. The polymer forms a conformal coat on the macropores and blocks access to the mesopores of templated samples, so that BET surface areas decrease dramatically.