2010
DOI: 10.1002/pen.21781
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Amphiphile polydimethylsiloxane‐based networks reinforced with in situ generated silica

Abstract: Polydimethylsiloxanes, side functionalized in different degrees with chloromethyl groups, were reacted with 4,4′‐bipyridyl and crosslinking occurred by the formation of ionic (bipyridinium) groups. The reactions were carried out in a silica sol–gel system, and thus, two networks were generated simultaneously: amphiphile siloxane‐organic and silica networks. The samples, processed as films, were characterized by Fourier transform infrared spectroscopy to verify the occurrence of the crosslinking reactions. Diff… Show more

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Cited by 9 publications
(6 citation statements)
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“… except the used equilibration catalyst, trifluoromethanesulfonic acid, which in our case was replaced with an ion exchanger with sulfonic acid groups. We still have used this procedure previously …”
Section: Methodsmentioning
confidence: 99%
“… except the used equilibration catalyst, trifluoromethanesulfonic acid, which in our case was replaced with an ion exchanger with sulfonic acid groups. We still have used this procedure previously …”
Section: Methodsmentioning
confidence: 99%
“…Unfortunately, the synthesis of the homopolymer is limited to low molar mass products, as the high polarity of the chloromethyl‐modified siloxane impairs the conversion and, thus, the degree of polymerization. [ 33,34 ] A sufficient molar mass of the vinyl‐terminated polymer is necessary to achieve suitable mechanical properties, especially high strain at break. Therefore, we selected the polymer with 70% polar groups and permittivity of 6.4 for further investigation.…”
Section: Synthesis Of Chloromethyl‐functional High‐permittivity Polys...mentioning
confidence: 99%
“…18 Mercapto-functionalized polymethyltrifluoropropylsilicone with low-molecular weight was prepared according to the controlled acid-catalyzed ring opening polymerization of 1,3,5-tris[(3,3,3-trifluoropropyl)methyl]cyclotrisiloxane (D 3 F) and 1,3-bis(mercaptomethyl)tetramethyldisiloxane. [19][20][21] The mixture of D 3 F (70.2 g, 1.5 mol), 1,3-bis(mercaptomethyl)tetramethyldisiloxane (3.39 g, 0.15 mol), and purolite CT-175 (2.5 g, 3 wt %) were stirred at 908C for 8 h. The catalyst was then removed by filtration. The reaction mixture was devolatilized by heating at 1608C/5 mmHg.…”
Section: Materials Preparationmentioning
confidence: 99%