Govedarica, Milutin N.

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  • Govedarica, Milutin N. (2)
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Author's Bibliography

Synthesis and Characterization of Novel Urethane-Siloxane Copolymers with a High Content of PCL-PDMS-PCL Segments

Pergal, Marija V.; Antić, Vesna; Govedarica, Milutin N.; Godjevac, Dejan; Ostojić, Sanja; Djonlagić, Jasna

(Wiley-Blackwell, Hoboken, 2011)

TY  - JOUR
AU  - Pergal, Marija V.
AU  - Antić, Vesna
AU  - Govedarica, Milutin N.
AU  - Godjevac, Dejan
AU  - Ostojić, Sanja
AU  - Djonlagić, Jasna
PY  - 2011
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/2675
AB  - Novel polyurethane copolymers derived from 4,4'-methylenediphenyl diisocyanate (MDI), 1,4-butanediol (BD) and alpha, omega-dihydroxy-[poly(caprolactone)-poly (dimethylsiloxane)-poly(caprolactone)] (a, x-dihydroxy( PCL-PDMS-PCL); (M) over bar (n) 6100 g mol(-1)) were synthesized by a two-step polyaddition reaction in solution. In the synthesis of the polyurethanes, the PCL blocks served as a compatibilizer between the nonpolar PDMS blocks and the polar comonomers, MDI and BD. The synthesis of thermoplastic polyurethanes (TPU) with high soft segment contents was optimized in terms of the concentrations of the reactants, the molar ratio of the NCO/OH groups, and the time and temperature of the polyaddition reaction. The structure, composition, and hard MDI/BD segment length of the synthesized polyurethane copolymers were determined by H-1, C-13-NMR, and two-dimensional correlation (COSY, HSQC, and HMBC) spectroscopy, while the hydrogen bonding interactions in the copolymers were analyzed by FT-IR spectroscopy. The influence of the reaction conditions on the structure, molecular weight, thermal, and some physical properties was studied at constant composition of the reaction mixture. A change in the molar ratio of the NCO/OH groups and the reaction conditions modified not only the molecular weight of the synthesized polyurethanes, but also the microstructure and therefore the thermal and physical properties of the copolymers. It was demonstrated that only PCL segments with high soft segment contents crystallize, thereby showing spherulitic morphology.
PB  - Wiley-Blackwell, Hoboken
T2  - Journal of Applied Polymer Science
T1  - Synthesis and Characterization of Novel Urethane-Siloxane Copolymers with a High Content of PCL-PDMS-PCL Segments
EP  - 2730
IS  - 4
SP  - 2715
VL  - 122
DO  - 10.1002/app.33926
ER  - 
@article{
author = "Pergal, Marija V. and Antić, Vesna and Govedarica, Milutin N. and Godjevac, Dejan and Ostojić, Sanja and Djonlagić, Jasna",
year = "2011",
abstract = "Novel polyurethane copolymers derived from 4,4'-methylenediphenyl diisocyanate (MDI), 1,4-butanediol (BD) and alpha, omega-dihydroxy-[poly(caprolactone)-poly (dimethylsiloxane)-poly(caprolactone)] (a, x-dihydroxy( PCL-PDMS-PCL); (M) over bar (n) 6100 g mol(-1)) were synthesized by a two-step polyaddition reaction in solution. In the synthesis of the polyurethanes, the PCL blocks served as a compatibilizer between the nonpolar PDMS blocks and the polar comonomers, MDI and BD. The synthesis of thermoplastic polyurethanes (TPU) with high soft segment contents was optimized in terms of the concentrations of the reactants, the molar ratio of the NCO/OH groups, and the time and temperature of the polyaddition reaction. The structure, composition, and hard MDI/BD segment length of the synthesized polyurethane copolymers were determined by H-1, C-13-NMR, and two-dimensional correlation (COSY, HSQC, and HMBC) spectroscopy, while the hydrogen bonding interactions in the copolymers were analyzed by FT-IR spectroscopy. The influence of the reaction conditions on the structure, molecular weight, thermal, and some physical properties was studied at constant composition of the reaction mixture. A change in the molar ratio of the NCO/OH groups and the reaction conditions modified not only the molecular weight of the synthesized polyurethanes, but also the microstructure and therefore the thermal and physical properties of the copolymers. It was demonstrated that only PCL segments with high soft segment contents crystallize, thereby showing spherulitic morphology.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Journal of Applied Polymer Science",
title = "Synthesis and Characterization of Novel Urethane-Siloxane Copolymers with a High Content of PCL-PDMS-PCL Segments",
pages = "2730-2715",
number = "4",
volume = "122",
doi = "10.1002/app.33926"
}
Pergal, M. V., Antić, V., Govedarica, M. N., Godjevac, D., Ostojić, S.,& Djonlagić, J.. (2011). Synthesis and Characterization of Novel Urethane-Siloxane Copolymers with a High Content of PCL-PDMS-PCL Segments. in Journal of Applied Polymer Science
Wiley-Blackwell, Hoboken., 122(4), 2715-2730.
https://doi.org/10.1002/app.33926
Pergal MV, Antić V, Govedarica MN, Godjevac D, Ostojić S, Djonlagić J. Synthesis and Characterization of Novel Urethane-Siloxane Copolymers with a High Content of PCL-PDMS-PCL Segments. in Journal of Applied Polymer Science. 2011;122(4):2715-2730.
doi:10.1002/app.33926 .
Pergal, Marija V., Antić, Vesna, Govedarica, Milutin N., Godjevac, Dejan, Ostojić, Sanja, Djonlagić, Jasna, "Synthesis and Characterization of Novel Urethane-Siloxane Copolymers with a High Content of PCL-PDMS-PCL Segments" in Journal of Applied Polymer Science, 122, no. 4 (2011):2715-2730,
https://doi.org/10.1002/app.33926 . .
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About the mode of incorporation of silanol-terminated polysiloxanes into butylene terephthalate-b-dimethylsiloxane copolymers

Antić, Vesna; Vucković, Marija V.; Dojčinović, Biljana; Antić, Mališa; Barać, Miroljub; Govedarica, Milutin N.

(Elsevier, Amsterdam, 2008)

TY  - JOUR
AU  - Antić, Vesna
AU  - Vucković, Marija V.
AU  - Dojčinović, Biljana
AU  - Antić, Mališa
AU  - Barać, Miroljub
AU  - Govedarica, Milutin N.
PY  - 2008
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/1801
AB  - The modality of the incorporation of silanol-terminated siloxanes into copolymers with butylene terephthalate were investigated and determined. Besides siloxanes, the other participants in this well-known copolymerization, called the catalyzed two-step transesterification/polycondensation reaction, are dimethyl terephthalate and 1,4-butanediol. The employed approach to this problem was to exactly examine all the possibilities of the reactions between particular pairs of reactants, as well as of single reactants. The final results were, firstly, that reactions between siloxanes and dimethyl terephthalate did not occur and, secondly, that the only possibility for silanol-terminated siloxanes to be incorporated into the copolymers was by means of their condensation with 1,4-butanediol. This means that siloxanes are incorporated into the copolymer by ether and not by ester linkages.
PB  - Elsevier, Amsterdam
T2  - Reactive & Functional Polymers
T1  - About the mode of incorporation of silanol-terminated polysiloxanes into butylene terephthalate-b-dimethylsiloxane copolymers
EP  - 860
IS  - 4
SP  - 851
VL  - 68
DO  - 10.1016/j.reactfunctpolym.2007.12.004
ER  - 
@article{
author = "Antić, Vesna and Vucković, Marija V. and Dojčinović, Biljana and Antić, Mališa and Barać, Miroljub and Govedarica, Milutin N.",
year = "2008",
abstract = "The modality of the incorporation of silanol-terminated siloxanes into copolymers with butylene terephthalate were investigated and determined. Besides siloxanes, the other participants in this well-known copolymerization, called the catalyzed two-step transesterification/polycondensation reaction, are dimethyl terephthalate and 1,4-butanediol. The employed approach to this problem was to exactly examine all the possibilities of the reactions between particular pairs of reactants, as well as of single reactants. The final results were, firstly, that reactions between siloxanes and dimethyl terephthalate did not occur and, secondly, that the only possibility for silanol-terminated siloxanes to be incorporated into the copolymers was by means of their condensation with 1,4-butanediol. This means that siloxanes are incorporated into the copolymer by ether and not by ester linkages.",
publisher = "Elsevier, Amsterdam",
journal = "Reactive & Functional Polymers",
title = "About the mode of incorporation of silanol-terminated polysiloxanes into butylene terephthalate-b-dimethylsiloxane copolymers",
pages = "860-851",
number = "4",
volume = "68",
doi = "10.1016/j.reactfunctpolym.2007.12.004"
}
Antić, V., Vucković, M. V., Dojčinović, B., Antić, M., Barać, M.,& Govedarica, M. N.. (2008). About the mode of incorporation of silanol-terminated polysiloxanes into butylene terephthalate-b-dimethylsiloxane copolymers. in Reactive & Functional Polymers
Elsevier, Amsterdam., 68(4), 851-860.
https://doi.org/10.1016/j.reactfunctpolym.2007.12.004
Antić V, Vucković MV, Dojčinović B, Antić M, Barać M, Govedarica MN. About the mode of incorporation of silanol-terminated polysiloxanes into butylene terephthalate-b-dimethylsiloxane copolymers. in Reactive & Functional Polymers. 2008;68(4):851-860.
doi:10.1016/j.reactfunctpolym.2007.12.004 .
Antić, Vesna, Vucković, Marija V., Dojčinović, Biljana, Antić, Mališa, Barać, Miroljub, Govedarica, Milutin N., "About the mode of incorporation of silanol-terminated polysiloxanes into butylene terephthalate-b-dimethylsiloxane copolymers" in Reactive & Functional Polymers, 68, no. 4 (2008):851-860,
https://doi.org/10.1016/j.reactfunctpolym.2007.12.004 . .
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