Antić, Vesna V.

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  • Antić, Vesna V. (1)
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Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer

Pergal, Marija V.; Antić, Vesna V.; Ostojić, Sanja ; Marinović-Cincović, Milena; Đonlagić, Jasna A.

(2011)

TY  - JOUR
AU  - Pergal, Marija V.
AU  - Antić, Vesna V.
AU  - Ostojić, Sanja 
AU  - Marinović-Cincović, Milena
AU  - Đonlagić, Jasna A.
PY  - 2011
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4638
AB  - A series of novel thermoplastic urethane-siloxane copolymers (TPUSs) based on a alpha,omega-dihydroxy-[poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone)] (alpha,omega-dihydroxy-PCL-PDMS-PCL) triblock. copolymer, 4,4-methylenediphenyl diisocyanate (MDI) and 1,4-butanediol (BD) was synthesized. The effects of the content (9-63 mass %) of hard urethane segments and their degree of polymerization on the properties of the segmented TPUSs were investigated. The structure, composition and hard segment degree of polymerization of the hard segments were examined using (1)H- and quantitative (13)C-NMR spectroscopy. The degree of crystallinity of the synthesized copolymers was determined using wide-angle X-ray scattering (WAXS). The surface properties were evaluated by measuring the water contact angle and water absorption. In the series of the TPUSs, the average degree of polymerization of the hard segments was varied from 1.2 to 14.4 MDI-BD units. It was found that average values from 3.8 to 14.4 MDI-BD units were effective segment lengths for crystallization of hard segments, which resulted in an increase in the degree of microphase separation of the copolymers. Spherulite-like superstructures were observed in copolymer films by scanning electron microscopy (SEM), which are believed to arise from the crystallization of the hard segments and/or PCL segments, depending on the content of the hard segments. The surface of the copolymers became more hydrophobic with increasing weight fraction of PDMS. The synthesized copolymers based on a PCL-PDMS-PCL segment showed good thermal stability, which increased with increasing content of soft PDMS segments, as was confirmed by the value of the starting temperature of thermal degradation.
T2  - Journal of the Serbian Chemical Society
T1  - Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer
VL  - 76
IS  - 12
SP  - 1703
EP  - 1723
DO  - 10.2298/JSC110307146P
ER  - 
@article{
author = "Pergal, Marija V. and Antić, Vesna V. and Ostojić, Sanja  and Marinović-Cincović, Milena and Đonlagić, Jasna A.",
year = "2011",
abstract = "A series of novel thermoplastic urethane-siloxane copolymers (TPUSs) based on a alpha,omega-dihydroxy-[poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone)] (alpha,omega-dihydroxy-PCL-PDMS-PCL) triblock. copolymer, 4,4-methylenediphenyl diisocyanate (MDI) and 1,4-butanediol (BD) was synthesized. The effects of the content (9-63 mass %) of hard urethane segments and their degree of polymerization on the properties of the segmented TPUSs were investigated. The structure, composition and hard segment degree of polymerization of the hard segments were examined using (1)H- and quantitative (13)C-NMR spectroscopy. The degree of crystallinity of the synthesized copolymers was determined using wide-angle X-ray scattering (WAXS). The surface properties were evaluated by measuring the water contact angle and water absorption. In the series of the TPUSs, the average degree of polymerization of the hard segments was varied from 1.2 to 14.4 MDI-BD units. It was found that average values from 3.8 to 14.4 MDI-BD units were effective segment lengths for crystallization of hard segments, which resulted in an increase in the degree of microphase separation of the copolymers. Spherulite-like superstructures were observed in copolymer films by scanning electron microscopy (SEM), which are believed to arise from the crystallization of the hard segments and/or PCL segments, depending on the content of the hard segments. The surface of the copolymers became more hydrophobic with increasing weight fraction of PDMS. The synthesized copolymers based on a PCL-PDMS-PCL segment showed good thermal stability, which increased with increasing content of soft PDMS segments, as was confirmed by the value of the starting temperature of thermal degradation.",
journal = "Journal of the Serbian Chemical Society",
title = "Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer",
volume = "76",
number = "12",
pages = "1703-1723",
doi = "10.2298/JSC110307146P"
}
Pergal, M. V., Antić, V. V., Ostojić, S., Marinović-Cincović, M.,& Đonlagić, J. A.. (2011). Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer. in Journal of the Serbian Chemical Society, 76(12), 1703-1723.
https://doi.org/10.2298/JSC110307146P
Pergal MV, Antić VV, Ostojić S, Marinović-Cincović M, Đonlagić JA. Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer. in Journal of the Serbian Chemical Society. 2011;76(12):1703-1723.
doi:10.2298/JSC110307146P .
Pergal, Marija V., Antić, Vesna V., Ostojić, Sanja , Marinović-Cincović, Milena, Đonlagić, Jasna A., "Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer" in Journal of the Serbian Chemical Society, 76, no. 12 (2011):1703-1723,
https://doi.org/10.2298/JSC110307146P . .
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