2000
DOI: 10.1016/s0032-3861(99)00245-1
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Comparison of hydrogen bonding in polydimethylsiloxane and polyether based urethane and urea copolymers

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Cited by 237 publications
(206 citation statements)
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“…Single chain and double chain urea-based anionic surfactants (-alanine derivatives) [14] and anionic gemini surfactants derived from cysteine [15] showed better tendency to adsorb at the air/water interface than to form micelles. Urea-based gemini surfactants with octyl chains displayed cmc values comparable to other carboxylate surfactants of higher hydrocarbon chain length (decyl and dodecyl chains) [15] which is attributed to the hydrogen bonding ability of urea group [16]. Increase of micelle ionization degree and decrease in anion selectivity of cetyltrimethylammonium bromide and cetyltrimethylammonium chloride micelles in presence of urea indicates a preferential headgroup solvation by urea squeezing the counterions out of the Stern layer [17].…”
Section: Introductionmentioning
confidence: 82%
“…Single chain and double chain urea-based anionic surfactants (-alanine derivatives) [14] and anionic gemini surfactants derived from cysteine [15] showed better tendency to adsorb at the air/water interface than to form micelles. Urea-based gemini surfactants with octyl chains displayed cmc values comparable to other carboxylate surfactants of higher hydrocarbon chain length (decyl and dodecyl chains) [15] which is attributed to the hydrogen bonding ability of urea group [16]. Increase of micelle ionization degree and decrease in anion selectivity of cetyltrimethylammonium bromide and cetyltrimethylammonium chloride micelles in presence of urea indicates a preferential headgroup solvation by urea squeezing the counterions out of the Stern layer [17].…”
Section: Introductionmentioning
confidence: 82%
“…Dther peak at 1075 cm -1 is attributed to the stretching of C−D−C groups. The peak at 2269 cm -1 corresponding to the N=C=D residual groups and it only appears for CAPU, indicating that the reaction is not still complete or that the proportions are not for TPU) are attributed to the C=D free and H-bond (C=D) urethane respectively 11,30 and that at 3345 cm -1 N-H group stretch.…”
Section: Infrared Spectroscopymentioning
confidence: 99%
“…The PAni incorporation increases the T g from 3 °C to 18 °C for CAPU/SPAN 2.0 membranes and from 3 °C to 25 °C for the CAPU/PAni TSA membranes. The increase on T g due to the PAni incorporation can be explained considering the formation of H-bonds 30,32 between PAni amine groups and PU urethane groups as shown in Figure 6. The difference between CAPU/SPAN 2.0 and CAPU/PAni TSA temperatures can be explained by the stronger steric effect in the SPAN 2.0 than in the PAni TSA due to sulphonic group linked chemically to the aromatic ring, which would disfavor the formation of the H-bonds.…”
Section: Thermal Analysismentioning
confidence: 99%
“…Besides a crystalline or at least highly ordered phase, soft and hard segments form corresponding phases which are partially soluble in each other [16][17][18][19][20][21]. Solubility depends very much on the interaction of the components, the urethane groups are capable of forming specific interactions, H-bonds with each other, but also with the soft segments [22,23]. Depending on preparation conditions, the final structure of the product is determined by kinetic effects, but a very large extent by interactions [24].…”
Section: Introductionmentioning
confidence: 99%