TY  - JOUR
AU  - Obradović, Nina
AU  - Filipović, Suzana
AU  - Marković, Smilja
AU  - Mitrić, Miodrag
AU  - Rusmirović, Jelena
AU  - Marinković, Aleksandar
AU  - Antić, Vesna
AU  - Pavlović, Vladimir B.
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3755
AB  - In this study, porous macro- and micro-cellular wollastonite-based ceramics was synthesized. A ceramic precursor, methylhydrocyclosiloxane, together with micro-sized CaCO3, was used as a starting material. After 20 min of ultrasound treatment, and calcination at 250 degrees C for 30 min, different pore-forming agents were added to the as-obtained powders. Differential thermal analysis was used to determine characteristic temperatures of processes occurring within powders during heating. Based on the obtained results, the sintering regime was set up. The prepared mixtures were pressed into pallets and sintered at 900 degrees C. During the sintering regime, porous wollastonite-based ceramics was obtained. The phase composition of the sintered samples, as well as the microstructures, were analyzed by using X-ray diffraction and SEM. A two-phase system was detected in all samples, CaSiO3 wollastonite and Ca2SiO4 larnite, and their ratio varied with each pore-forming agent. It was observed that the addition of different pore-forming agents resulted in significantly different microstructures. In a batch test, the influence of pH, the contact time and the initial ion concentration on the adsorption efficiency of As+5, Cr(+6)and phosphate ions on the synthesized adsorbents were studied. Time-dependent adsorption is best described by the pseudo-second-order kinetic model and the Weber-Morris model, which predict intra-particle diffusion as a rate-controlling step of the overall process. High adsorption capacities, 21.93, 23.88, and 27.29 mg g(-1), were obtained for the CaCO3-siloxane-nanocellulose sorbent, and similar/lower capacities were obtained for the CaCO3-siloxane-PMMA and CaCO3-siloxane-cotton wool adsorbents.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - Influence of different pore-forming agents on wollastonite microstructures and adsorption capacities
EP  - 7468
IS  - 10
SP  - 7461
VL  - 43
DO  - 10.1016/j.ceramint.2017.03.021
ER  - 

@article{
author = "Obradović, Nina and Filipović, Suzana and Marković, Smilja and Mitrić, Miodrag and Rusmirović, Jelena and Marinković, Aleksandar and Antić, Vesna and Pavlović, Vladimir B.",
year = "2017",
abstract = "In this study, porous macro- and micro-cellular wollastonite-based ceramics was synthesized. A ceramic precursor, methylhydrocyclosiloxane, together with micro-sized CaCO3, was used as a starting material. After 20 min of ultrasound treatment, and calcination at 250 degrees C for 30 min, different pore-forming agents were added to the as-obtained powders. Differential thermal analysis was used to determine characteristic temperatures of processes occurring within powders during heating. Based on the obtained results, the sintering regime was set up. The prepared mixtures were pressed into pallets and sintered at 900 degrees C. During the sintering regime, porous wollastonite-based ceramics was obtained. The phase composition of the sintered samples, as well as the microstructures, were analyzed by using X-ray diffraction and SEM. A two-phase system was detected in all samples, CaSiO3 wollastonite and Ca2SiO4 larnite, and their ratio varied with each pore-forming agent. It was observed that the addition of different pore-forming agents resulted in significantly different microstructures. In a batch test, the influence of pH, the contact time and the initial ion concentration on the adsorption efficiency of As+5, Cr(+6)and phosphate ions on the synthesized adsorbents were studied. Time-dependent adsorption is best described by the pseudo-second-order kinetic model and the Weber-Morris model, which predict intra-particle diffusion as a rate-controlling step of the overall process. High adsorption capacities, 21.93, 23.88, and 27.29 mg g(-1), were obtained for the CaCO3-siloxane-nanocellulose sorbent, and similar/lower capacities were obtained for the CaCO3-siloxane-PMMA and CaCO3-siloxane-cotton wool adsorbents.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "Influence of different pore-forming agents on wollastonite microstructures and adsorption capacities",
pages = "7468-7461",
number = "10",
volume = "43",
doi = "10.1016/j.ceramint.2017.03.021"
}

Obradović, N., Filipović, S., Marković, S., Mitrić, M., Rusmirović, J., Marinković, A., Antić, V.,& Pavlović, V. B.. (2017). Influence of different pore-forming agents on wollastonite microstructures and adsorption capacities. in Ceramics International
Elsevier Sci Ltd, Oxford., 43(10), 7461-7468.
https://doi.org/10.1016/j.ceramint.2017.03.021

Obradović N, Filipović S, Marković S, Mitrić M, Rusmirović J, Marinković A, Antić V, Pavlović VB. Influence of different pore-forming agents on wollastonite microstructures and adsorption capacities. in Ceramics International. 2017;43(10):7461-7468.
doi:10.1016/j.ceramint.2017.03.021 .

Obradović, Nina, Filipović, Suzana, Marković, Smilja, Mitrić, Miodrag, Rusmirović, Jelena, Marinković, Aleksandar, Antić, Vesna, Pavlović, Vladimir B., "Influence of different pore-forming agents on wollastonite microstructures and adsorption capacities" in Ceramics International, 43, no. 10 (2017):7461-7468,
https://doi.org/10.1016/j.ceramint.2017.03.021 . .

TY  - JOUR
AU  - Stefanović, Ivan S.
AU  - Djonlagić, Jasna
AU  - Tovilović, Gordana
AU  - Nestorov, Jelena
AU  - Antić, Vesna
AU  - Ostojić, Sanja
AU  - Pergal, Marija V.
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5794
AB  - Polyurethane copolymers based on ,-dihydroxypropyl poly(dimethylsiloxane) (PDMS) with a range of soft segment contents were prepared by two-stage polymerization, and their microstructures, thermal, thermomechanical, and surface properties, as well as in vitro hemo- and cytocompatibility were evaluated. All utilized characterization methods confirmed the existence of moderately microphase separated structures with the appearance of some microphase mixing between segments as the PDMS (i.e., soft segment) content increased. Copolymers showed higher crystallinity, storage moduli, surface roughness, and surface free energy, but less hydrophobicity with decreasing PDMS content. Biocompatibility of copolymers was evaluated using an endothelial EA.hy926 cell line by direct contact, an extraction method and after pretreatment of copolymers with multicomponent protein mixture, as well as by a competitive protein adsorption assay. Copolymers showed no toxic effect to endothelial cells and all copolymers, except that with the lowest PDMS content, exhibited resistance to endothelial cell adhesion, suggesting their unsuitability for long-term biomedical devices which particularly require re-endothelialization. All copolymers exhibited excellent resistance to fibrinogen adsorption and adsorbed more albumin than fibrinogen in the competitive adsorption assay, suggesting their good hemocompatibility. The noncytotoxic chemistry of these synthesized materials, combined with their nonadherent properties which are inhospitable to cell attachment and growth, underlie the need for further investigations to clarify their potential for use in short-term biomedical devices.
PB  - Wiley-Blackwell, Hoboken
T2  - Journal of Biomedical Materials Research Part A
T1  - Poly(urethane-dimethylsiloxane) copolymers displaying a range of soft segment contents, noncytotoxic chemistry, and nonadherent properties toward endothelial cells
EP  - 1475
IS  - 4
SP  - 1459
VL  - 103
DO  - 10.1002/jbm.a.35285
ER  - 

@article{
author = "Stefanović, Ivan S. and Djonlagić, Jasna and Tovilović, Gordana and Nestorov, Jelena and Antić, Vesna and Ostojić, Sanja and Pergal, Marija V.",
year = "2015",
abstract = "Polyurethane copolymers based on ,-dihydroxypropyl poly(dimethylsiloxane) (PDMS) with a range of soft segment contents were prepared by two-stage polymerization, and their microstructures, thermal, thermomechanical, and surface properties, as well as in vitro hemo- and cytocompatibility were evaluated. All utilized characterization methods confirmed the existence of moderately microphase separated structures with the appearance of some microphase mixing between segments as the PDMS (i.e., soft segment) content increased. Copolymers showed higher crystallinity, storage moduli, surface roughness, and surface free energy, but less hydrophobicity with decreasing PDMS content. Biocompatibility of copolymers was evaluated using an endothelial EA.hy926 cell line by direct contact, an extraction method and after pretreatment of copolymers with multicomponent protein mixture, as well as by a competitive protein adsorption assay. Copolymers showed no toxic effect to endothelial cells and all copolymers, except that with the lowest PDMS content, exhibited resistance to endothelial cell adhesion, suggesting their unsuitability for long-term biomedical devices which particularly require re-endothelialization. All copolymers exhibited excellent resistance to fibrinogen adsorption and adsorbed more albumin than fibrinogen in the competitive adsorption assay, suggesting their good hemocompatibility. The noncytotoxic chemistry of these synthesized materials, combined with their nonadherent properties which are inhospitable to cell attachment and growth, underlie the need for further investigations to clarify their potential for use in short-term biomedical devices.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Journal of Biomedical Materials Research Part A",
title = "Poly(urethane-dimethylsiloxane) copolymers displaying a range of soft segment contents, noncytotoxic chemistry, and nonadherent properties toward endothelial cells",
pages = "1475-1459",
number = "4",
volume = "103",
doi = "10.1002/jbm.a.35285"
}

Stefanović, I. S., Djonlagić, J., Tovilović, G., Nestorov, J., Antić, V., Ostojić, S.,& Pergal, M. V.. (2015). Poly(urethane-dimethylsiloxane) copolymers displaying a range of soft segment contents, noncytotoxic chemistry, and nonadherent properties toward endothelial cells. in Journal of Biomedical Materials Research Part A
Wiley-Blackwell, Hoboken., 103(4), 1459-1475.
https://doi.org/10.1002/jbm.a.35285

Stefanović IS, Djonlagić J, Tovilović G, Nestorov J, Antić V, Ostojić S, Pergal MV. Poly(urethane-dimethylsiloxane) copolymers displaying a range of soft segment contents, noncytotoxic chemistry, and nonadherent properties toward endothelial cells. in Journal of Biomedical Materials Research Part A. 2015;103(4):1459-1475.
doi:10.1002/jbm.a.35285 .

Stefanović, Ivan S., Djonlagić, Jasna, Tovilović, Gordana, Nestorov, Jelena, Antić, Vesna, Ostojić, Sanja, Pergal, Marija V., "Poly(urethane-dimethylsiloxane) copolymers displaying a range of soft segment contents, noncytotoxic chemistry, and nonadherent properties toward endothelial cells" in Journal of Biomedical Materials Research Part A, 103, no. 4 (2015):1459-1475,
https://doi.org/10.1002/jbm.a.35285 . .

TY  - JOUR
AU  - Pergal, Marija
AU  - Stefanović, Ivan
AU  - Gođevac, Dejan
AU  - Antić, Vesna
AU  - Milačić, Vesna
AU  - Ostojić, Sanja
AU  - Rogan, Jelena
AU  - Đonlagić, Jasna
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2692
AB  - In this study, the synthesis, structure and physical properties of two series of thermoplastic polyurethanes based on hydroxypropyl-terminated poly(dimethylsiloxane) (HP-PDMS) or hydroxyethoxypropyl-terminated poly(dimethylsiloxane) (EO-PDMS) as soft segments, and 4,4'-methylenediphenyl diisocyanate and 1,4-butanediol as hard segments were investigated. The polyurethanes were synthesized by two-step polyaddition in solution. The effects of the type and content of PDMS segments on the structure, thermal and surface properties of copolymers were studied by H-1-, C-13-nuclear magnetic resonance (NMR) spectroscopy and two-dimensional NMR spectroscopies (heteronuclear multiple bond correlation (HMBC) and rotating-frame nuclear Overhauser effect (ROESY)), gel permeation chromatography (GPC), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), wide-angle X-ray scattering (WAXS), scanning electron microscopy (SEM) and water contact angle and water absorption measurements. Thermal properties investigated by DSC indicated that the presence of soft PDMS segments lowers the glass transition and melting temperatures of the hard phase as well as the degree of crystallinity. SEM analysis of the copolymers with a lower soft segment content confirmed the presence of spherulite superstructures, which arise from the crystallization of the hard segments. When compared with polyurethanes prepared from HP-PDMS, the copolymers synthesized from EO-PDMS with the same content of the soft segments had a higher degree of crystallinity, better thermal stability and a less hydrophobic surface. The obtained results showed that the synthesized polyurethanes had good thermal and surface properties, which could be further modified by changing the type or content of the soft segments.
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Structural, thermal and surface characterization of thermoplastic polyurethanes based on poly(dimethylsiloxane)
EP  - +
IS  - 7
SP  - 843
VL  - 79
DO  - 10.2298/JSC130819149P
ER  - 

@article{
author = "Pergal, Marija and Stefanović, Ivan and Gođevac, Dejan and Antić, Vesna and Milačić, Vesna and Ostojić, Sanja and Rogan, Jelena and Đonlagić, Jasna",
year = "2014",
abstract = "In this study, the synthesis, structure and physical properties of two series of thermoplastic polyurethanes based on hydroxypropyl-terminated poly(dimethylsiloxane) (HP-PDMS) or hydroxyethoxypropyl-terminated poly(dimethylsiloxane) (EO-PDMS) as soft segments, and 4,4'-methylenediphenyl diisocyanate and 1,4-butanediol as hard segments were investigated. The polyurethanes were synthesized by two-step polyaddition in solution. The effects of the type and content of PDMS segments on the structure, thermal and surface properties of copolymers were studied by H-1-, C-13-nuclear magnetic resonance (NMR) spectroscopy and two-dimensional NMR spectroscopies (heteronuclear multiple bond correlation (HMBC) and rotating-frame nuclear Overhauser effect (ROESY)), gel permeation chromatography (GPC), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), wide-angle X-ray scattering (WAXS), scanning electron microscopy (SEM) and water contact angle and water absorption measurements. Thermal properties investigated by DSC indicated that the presence of soft PDMS segments lowers the glass transition and melting temperatures of the hard phase as well as the degree of crystallinity. SEM analysis of the copolymers with a lower soft segment content confirmed the presence of spherulite superstructures, which arise from the crystallization of the hard segments. When compared with polyurethanes prepared from HP-PDMS, the copolymers synthesized from EO-PDMS with the same content of the soft segments had a higher degree of crystallinity, better thermal stability and a less hydrophobic surface. The obtained results showed that the synthesized polyurethanes had good thermal and surface properties, which could be further modified by changing the type or content of the soft segments.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Structural, thermal and surface characterization of thermoplastic polyurethanes based on poly(dimethylsiloxane)",
pages = "+-843",
number = "7",
volume = "79",
doi = "10.2298/JSC130819149P"
}

Pergal, M., Stefanović, I., Gođevac, D., Antić, V., Milačić, V., Ostojić, S., Rogan, J.,& Đonlagić, J.. (2014). Structural, thermal and surface characterization of thermoplastic polyurethanes based on poly(dimethylsiloxane). in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 79(7), 843-+.
https://doi.org/10.2298/JSC130819149P

Pergal M, Stefanović I, Gođevac D, Antić V, Milačić V, Ostojić S, Rogan J, Đonlagić J. Structural, thermal and surface characterization of thermoplastic polyurethanes based on poly(dimethylsiloxane). in Journal of the Serbian Chemical Society. 2014;79(7):843-+.
doi:10.2298/JSC130819149P .

Pergal, Marija, Stefanović, Ivan, Gođevac, Dejan, Antić, Vesna, Milačić, Vesna, Ostojić, Sanja, Rogan, Jelena, Đonlagić, Jasna, "Structural, thermal and surface characterization of thermoplastic polyurethanes based on poly(dimethylsiloxane)" in Journal of the Serbian Chemical Society, 79, no. 7 (2014):843-+,
https://doi.org/10.2298/JSC130819149P . .

TY  - JOUR
AU  - Balaban, Milica
AU  - Antić, Vesna
AU  - Pergal, Marija
AU  - Gođevac, Dejan
AU  - Francolini, Iolanda
AU  - Martinelli, Andrea
AU  - Rogan, Jelena
AU  - Đonlagić, Jasna
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2500
AB  - Segmented poly(urethane-urea-siloxane)s (PUUS) were synthesized using 4,4'-methylenediphenyl diisocyanate (MDI) and ethylene diamine (ED) as the hard segment components and hydroxypropyl-terminated poly(dimethylsiloxane) (PDMS) as the soft segment component, where the hard segment content ranged from 38 to 65 wt%. Segmented PUUSs were prepared by a two-step polymerization procedure in tetrahydrofuran/N-methylpyrrolidone (THF/NMP) mixture with a large proportion of polar solvent. The structure, composition and hard segment length were determined by C-13 NMR and two-dimensional correlation spectroscopy. Thermal, mechanical, small-angle X-ray scattering and hydrogen bonding analyses indicated the formation of the microphase-separated copolymers with high tensile strength. Globular superstructures observed in the copolymer films by scanning electron microscopy (SEM) and atomic force microscopy (AFM) were probably arisen from the microstructural organization of the MDI-ED segments, depending on their content and length. The PUUS copolymers showed high water resistance and became more hydrophobic with increasing weight fraction of PDMS.
PB  - Springer, New York
T2  - Polymer Bulletin
T1  - Influence of the chemical structure of poly(urea-urethane-siloxane)s on their morphological, surface and thermal properties
EP  - 2518
IS  - 9
SP  - 2493
VL  - 70
DO  - 10.1007/s00289-013-0968-2
ER  - 

@article{
author = "Balaban, Milica and Antić, Vesna and Pergal, Marija and Gođevac, Dejan and Francolini, Iolanda and Martinelli, Andrea and Rogan, Jelena and Đonlagić, Jasna",
year = "2013",
abstract = "Segmented poly(urethane-urea-siloxane)s (PUUS) were synthesized using 4,4'-methylenediphenyl diisocyanate (MDI) and ethylene diamine (ED) as the hard segment components and hydroxypropyl-terminated poly(dimethylsiloxane) (PDMS) as the soft segment component, where the hard segment content ranged from 38 to 65 wt%. Segmented PUUSs were prepared by a two-step polymerization procedure in tetrahydrofuran/N-methylpyrrolidone (THF/NMP) mixture with a large proportion of polar solvent. The structure, composition and hard segment length were determined by C-13 NMR and two-dimensional correlation spectroscopy. Thermal, mechanical, small-angle X-ray scattering and hydrogen bonding analyses indicated the formation of the microphase-separated copolymers with high tensile strength. Globular superstructures observed in the copolymer films by scanning electron microscopy (SEM) and atomic force microscopy (AFM) were probably arisen from the microstructural organization of the MDI-ED segments, depending on their content and length. The PUUS copolymers showed high water resistance and became more hydrophobic with increasing weight fraction of PDMS.",
publisher = "Springer, New York",
journal = "Polymer Bulletin",
title = "Influence of the chemical structure of poly(urea-urethane-siloxane)s on their morphological, surface and thermal properties",
pages = "2518-2493",
number = "9",
volume = "70",
doi = "10.1007/s00289-013-0968-2"
}

Balaban, M., Antić, V., Pergal, M., Gođevac, D., Francolini, I., Martinelli, A., Rogan, J.,& Đonlagić, J.. (2013). Influence of the chemical structure of poly(urea-urethane-siloxane)s on their morphological, surface and thermal properties. in Polymer Bulletin
Springer, New York., 70(9), 2493-2518.
https://doi.org/10.1007/s00289-013-0968-2

Balaban M, Antić V, Pergal M, Gođevac D, Francolini I, Martinelli A, Rogan J, Đonlagić J. Influence of the chemical structure of poly(urea-urethane-siloxane)s on their morphological, surface and thermal properties. in Polymer Bulletin. 2013;70(9):2493-2518.
doi:10.1007/s00289-013-0968-2 .

Balaban, Milica, Antić, Vesna, Pergal, Marija, Gođevac, Dejan, Francolini, Iolanda, Martinelli, Andrea, Rogan, Jelena, Đonlagić, Jasna, "Influence of the chemical structure of poly(urea-urethane-siloxane)s on their morphological, surface and thermal properties" in Polymer Bulletin, 70, no. 9 (2013):2493-2518,
https://doi.org/10.1007/s00289-013-0968-2 . .

TY  - JOUR
AU  - Balaban, Milica
AU  - Antić, Vesna
AU  - Pergal, Marija
AU  - Francolini, Iolanda
AU  - Martinelli, Andrea
AU  - Đonlagić, Jasna
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5743
AB  - Segmented poly(urethane-urea-siloxanes) (PUUS) based on 4,4'- methylene diphenyl diisocyanate-ethylene diamine (MDI-ED) hard segments and hydroxypropyl-terminated poly(dimethylsiloxane) (PDMS, Mn = 1000 g mol-1) soft segments were prepared under various experimental conditions. The copolymers with constant molar ratio of hard and soft segments (PDMS:MDI:ED = 1:2:1; 20 wt. % of the hard segments) were synthesized in two different solvent mixtures, by a two-step polyaddition procedure. The first one was tetrahydrofuran/N,N-dimethylacetamide (THF/DMAc) with different co-solvent ratios (1/1, 1/2 and 1/9, v/v), whereas the second one was tetrahydrofuran/N-methylpyrrolidone (THF/NMP, 1/9, v/v). The reaction conditions were optimized by varying the co-solvents ratio, the concentration of the catalyst, the initial monomer concentration, as well as the time of the first and the second step of the reaction. The effects of the experimental conditions on the size of the PUUS were investigated by gel permeation chromatography (GPC) and dilute solution viscometry. The copolymers with the highest molecular weights were obtained in the THF/NMP mixture (1/9, v/v). The structure and composition of the copolymers were determined by 1H-NMR and FTIR spectroscopy. The morphology of the synthesized copolymers was investigated by atomic force microscopy (AFM), while the thermal properties were studied by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The surface properties were evaluated by measuring the water contact angle (WCA). The copolymers exhibited phase-separated microstructure and were stable up to 200°C in nitrogen.
AB  - Segmentirani poli(uretan-urea-siloksani) (PUUS), sa tvrdim segmentima na bazi 4,4'-metilendifenildiizocijanata i etilendiamina (MDI-ED) i mekim segmentima na bazi hidroksipropil-terminiranog poli(dimetilsiloksana) (PDMS, Mn = 1000 g mol-1), sintetisani su pod različitim eksperimentalnim uslovima. Kopolimeri sa konstantnim molskim odnosom tvrdih i mekih segmenata (PDMS:MDI:ED = 1:2:1; 20 mas. % tvrdih segmenata), sintetisani su u dve različite smeše rastvarača kao reakcionog medijuma, metodom dvostepene poliadicije. Prva kombinacija rastvarača je bila smeša tetrahidrofurana (THF) i N,N-dimetilacetamida (DMAc), dok je u drugom slučaju korišćena smeša THF-a i N-metilpirolidona (NMP). Reakcioni uslovi su optimizovani u pogledu odnosa ko-rastvarača, koncentracije katalizatora, početne koncentracije monomera i vremena odigravanja prve i druge faze reakcije. Ispitan je uticaj primenjenih eksperimentalnih uslova na veličinu PUUS primenom gel-propusne hromatografije (GPC) i viskozimetrije razblaženih rastvora [η]. Kopolimeri najvećih molarnih masa su dobijeni u smeši THF/NMP (1/9, v/v). Struktura i sastav kopolimera su okarakterisani 1H-NMR i FTIR spektroskopijom. Morfologija sintetisanih kopolimera je ispitana mikroskopijom atomskih sila (AFM), dok su termička svojstva ispitana diferencijalnom skenirajućom kalorimetrijom (DSC) i termogravimetrijskom analizom (TGA). Površinska svojstva kopolimera su ispitana određivanjem kontaktnih uglova sa vodom (WCA). Kopolimeri su pokazali dvofaznu mikrostrukturu i bili su stabilni do 200°C u atmosteri azota.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - The effect of polar solvents on the synthesis of poly(urethane-urea-siloxane)s
T1  - Uticaj polarnih rastvarača na sintezu poli(uretan-urea-siloksana)
EP  - 1481
IS  - 10
SP  - 1457
VL  - 77
DO  - 10.2298/JSC111025056B
ER  - 

@article{
author = "Balaban, Milica and Antić, Vesna and Pergal, Marija and Francolini, Iolanda and Martinelli, Andrea and Đonlagić, Jasna",
year = "2012",
abstract = "Segmented poly(urethane-urea-siloxanes) (PUUS) based on 4,4'- methylene diphenyl diisocyanate-ethylene diamine (MDI-ED) hard segments and hydroxypropyl-terminated poly(dimethylsiloxane) (PDMS, Mn = 1000 g mol-1) soft segments were prepared under various experimental conditions. The copolymers with constant molar ratio of hard and soft segments (PDMS:MDI:ED = 1:2:1; 20 wt. % of the hard segments) were synthesized in two different solvent mixtures, by a two-step polyaddition procedure. The first one was tetrahydrofuran/N,N-dimethylacetamide (THF/DMAc) with different co-solvent ratios (1/1, 1/2 and 1/9, v/v), whereas the second one was tetrahydrofuran/N-methylpyrrolidone (THF/NMP, 1/9, v/v). The reaction conditions were optimized by varying the co-solvents ratio, the concentration of the catalyst, the initial monomer concentration, as well as the time of the first and the second step of the reaction. The effects of the experimental conditions on the size of the PUUS were investigated by gel permeation chromatography (GPC) and dilute solution viscometry. The copolymers with the highest molecular weights were obtained in the THF/NMP mixture (1/9, v/v). The structure and composition of the copolymers were determined by 1H-NMR and FTIR spectroscopy. The morphology of the synthesized copolymers was investigated by atomic force microscopy (AFM), while the thermal properties were studied by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The surface properties were evaluated by measuring the water contact angle (WCA). The copolymers exhibited phase-separated microstructure and were stable up to 200°C in nitrogen., Segmentirani poli(uretan-urea-siloksani) (PUUS), sa tvrdim segmentima na bazi 4,4'-metilendifenildiizocijanata i etilendiamina (MDI-ED) i mekim segmentima na bazi hidroksipropil-terminiranog poli(dimetilsiloksana) (PDMS, Mn = 1000 g mol-1), sintetisani su pod različitim eksperimentalnim uslovima. Kopolimeri sa konstantnim molskim odnosom tvrdih i mekih segmenata (PDMS:MDI:ED = 1:2:1; 20 mas. % tvrdih segmenata), sintetisani su u dve različite smeše rastvarača kao reakcionog medijuma, metodom dvostepene poliadicije. Prva kombinacija rastvarača je bila smeša tetrahidrofurana (THF) i N,N-dimetilacetamida (DMAc), dok je u drugom slučaju korišćena smeša THF-a i N-metilpirolidona (NMP). Reakcioni uslovi su optimizovani u pogledu odnosa ko-rastvarača, koncentracije katalizatora, početne koncentracije monomera i vremena odigravanja prve i druge faze reakcije. Ispitan je uticaj primenjenih eksperimentalnih uslova na veličinu PUUS primenom gel-propusne hromatografije (GPC) i viskozimetrije razblaženih rastvora [η]. Kopolimeri najvećih molarnih masa su dobijeni u smeši THF/NMP (1/9, v/v). Struktura i sastav kopolimera su okarakterisani 1H-NMR i FTIR spektroskopijom. Morfologija sintetisanih kopolimera je ispitana mikroskopijom atomskih sila (AFM), dok su termička svojstva ispitana diferencijalnom skenirajućom kalorimetrijom (DSC) i termogravimetrijskom analizom (TGA). Površinska svojstva kopolimera su ispitana određivanjem kontaktnih uglova sa vodom (WCA). Kopolimeri su pokazali dvofaznu mikrostrukturu i bili su stabilni do 200°C u atmosteri azota.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "The effect of polar solvents on the synthesis of poly(urethane-urea-siloxane)s, Uticaj polarnih rastvarača na sintezu poli(uretan-urea-siloksana)",
pages = "1481-1457",
number = "10",
volume = "77",
doi = "10.2298/JSC111025056B"
}

Balaban, M., Antić, V., Pergal, M., Francolini, I., Martinelli, A.,& Đonlagić, J.. (2012). The effect of polar solvents on the synthesis of poly(urethane-urea-siloxane)s. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 77(10), 1457-1481.
https://doi.org/10.2298/JSC111025056B

Balaban M, Antić V, Pergal M, Francolini I, Martinelli A, Đonlagić J. The effect of polar solvents on the synthesis of poly(urethane-urea-siloxane)s. in Journal of the Serbian Chemical Society. 2012;77(10):1457-1481.
doi:10.2298/JSC111025056B .

Balaban, Milica, Antić, Vesna, Pergal, Marija, Francolini, Iolanda, Martinelli, Andrea, Đonlagić, Jasna, "The effect of polar solvents on the synthesis of poly(urethane-urea-siloxane)s" in Journal of the Serbian Chemical Society, 77, no. 10 (2012):1457-1481,
https://doi.org/10.2298/JSC111025056B . .

TY  - JOUR
AU  - Pergal, Marija
AU  - Antić, Vesna
AU  - Govedarica, Milutin
AU  - Gođevac, Dejan
AU  - Ostojić, Sanja
AU  - Đonlagić, Jasna
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5658
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, Malden
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 and Antić, Vesna and Govedarica, Milutin and Gođevac, Dejan and Ostojić, Sanja and Đonlagić, 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, Malden",
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., Antić, V., Govedarica, M., Gođevac, D., Ostojić, S.,& Đonlagić, 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, Malden., 122(4), 2715-2730.
https://doi.org/10.1002/app.33926

Pergal M, Antić V, Govedarica M, Gođevac D, Ostojić S, Đonlagić 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, Antić, Vesna, Govedarica, Milutin, Gođevac, Dejan, Ostojić, Sanja, Đonlagić, 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 . .

TY  - JOUR
AU  - Pergal, Marija
AU  - Antić, Vesna
AU  - Ostojić, Sanja
AU  - Marinović-Cincović, Milena
AU  - Đonlagić, Jasna
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5644
AB  - A series of novel thermoplastic urethane-siloxane copolymers (TPUSs) based on a α,ω-dihydroxy-[poly(ε-caprolactone)-b-poly(dimethylsiloxane)-b- -poly(ε-caprolactone)] (α,ω-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 1H- and quantitative 13C-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.
AB  - U ovom radu prikazana je struktura i neka svojstva serije novih termoplastičnih uretan-siloksanskih kopolimera (TPUSs) na bazi α,ω-dihidroksi-[poli(ε-kaprolakton)-b-poli(dimetilsiloksan)-b-poli(ε-kaprolakton)] triblok kopolimera (α,ω-dihidroksi-PCL-PDMS-PCL), 4,4'-metilendifenildiizocijanata (MDI) i 1,4-butandiola (BD). Ispitan je uticaj sadržaja uretanskog tvrdog segmenta (9-63 mas. %) i njegove dužine, tj. stepena polimerizacije, izražene preko broja MDI-BD ostataka, na svojstva segmentiranih TPUSs. Struktura, sastav i stepen polimerizacije tvrdog segmenta su ispitani pomoću 1H- i kvantitativne 13C-NMR spektroskopije. Stepen kristaliničnosti kopolimera je određen metodom difrakcije X-zraka na velikim uglovima (WAXS). Površinska svojstva kopolimera su ispitana određivanjem kontaktnih uglova sa vodom i merenjem apsorpcije vode. U seriji kopolimera dužina tvrdog segmenta izražena preko broja ponavljajućih MDI-BD jedinica je varirana od 1,2 do 14,4. Utvrđeno je da tvrdi segmenti sa 3,8 do 14,4 ponavljajućih MDI-BD jedinica efikasno kristališu, što je rezultovalo u povećanju stepena mikrofazne separacije kopolimera. SEM analiza je pokazala prisustvo sferulitne strukture u kopolimernim filmovima, koja najverovatnije potiče od kristalizacije tvrdih i/ili PCL segmenata, zavisno od sadržaja tvrdih segmenata. Hidrofobnost površine kopolimera je rasla sa povećanjem masenog udela PDMS-a u odgovarajućem uzorku. Sintetisani poliuretani na bazi PCL-PDMS-PCL pokazuju povećanje termičke stabilnosti sa povećanjem sadržaja mekih PDMS segmenata, što je potvrđeno porastom početne temperature degradacije, određene TG analizom.
PB  - Serbian Chemical Society
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(ε-caprolactone)-b-poly(dimethylsiloxane)-b-poly(ε-caprolactone) triblock copolymer
T1  - Uticaj sadržaja tvrdog segmenta na svojstva novih uretan-siloksanskih kopolimera na bazi poli(e-kaprolakton)-b-poli(dimetilsiloksan)-b-poli(e-kaprolaktona)
EP  - 1723
IS  - 12
SP  - 1703
VL  - 76
DO  - 10.2298/JSC110307146P
ER  - 

@article{
author = "Pergal, Marija and Antić, Vesna and Ostojić, Sanja and Marinović-Cincović, Milena and Đonlagić, Jasna",
year = "2011",
abstract = "A series of novel thermoplastic urethane-siloxane copolymers (TPUSs) based on a α,ω-dihydroxy-[poly(ε-caprolactone)-b-poly(dimethylsiloxane)-b- -poly(ε-caprolactone)] (α,ω-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 1H- and quantitative 13C-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., U ovom radu prikazana je struktura i neka svojstva serije novih termoplastičnih uretan-siloksanskih kopolimera (TPUSs) na bazi α,ω-dihidroksi-[poli(ε-kaprolakton)-b-poli(dimetilsiloksan)-b-poli(ε-kaprolakton)] triblok kopolimera (α,ω-dihidroksi-PCL-PDMS-PCL), 4,4'-metilendifenildiizocijanata (MDI) i 1,4-butandiola (BD). Ispitan je uticaj sadržaja uretanskog tvrdog segmenta (9-63 mas. %) i njegove dužine, tj. stepena polimerizacije, izražene preko broja MDI-BD ostataka, na svojstva segmentiranih TPUSs. Struktura, sastav i stepen polimerizacije tvrdog segmenta su ispitani pomoću 1H- i kvantitativne 13C-NMR spektroskopije. Stepen kristaliničnosti kopolimera je određen metodom difrakcije X-zraka na velikim uglovima (WAXS). Površinska svojstva kopolimera su ispitana određivanjem kontaktnih uglova sa vodom i merenjem apsorpcije vode. U seriji kopolimera dužina tvrdog segmenta izražena preko broja ponavljajućih MDI-BD jedinica je varirana od 1,2 do 14,4. Utvrđeno je da tvrdi segmenti sa 3,8 do 14,4 ponavljajućih MDI-BD jedinica efikasno kristališu, što je rezultovalo u povećanju stepena mikrofazne separacije kopolimera. SEM analiza je pokazala prisustvo sferulitne strukture u kopolimernim filmovima, koja najverovatnije potiče od kristalizacije tvrdih i/ili PCL segmenata, zavisno od sadržaja tvrdih segmenata. Hidrofobnost površine kopolimera je rasla sa povećanjem masenog udela PDMS-a u odgovarajućem uzorku. Sintetisani poliuretani na bazi PCL-PDMS-PCL pokazuju povećanje termičke stabilnosti sa povećanjem sadržaja mekih PDMS segmenata, što je potvrđeno porastom početne temperature degradacije, određene TG analizom.",
publisher = "Serbian Chemical Society",
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(ε-caprolactone)-b-poly(dimethylsiloxane)-b-poly(ε-caprolactone) triblock copolymer, Uticaj sadržaja tvrdog segmenta na svojstva novih uretan-siloksanskih kopolimera na bazi poli(e-kaprolakton)-b-poli(dimetilsiloksan)-b-poli(e-kaprolaktona)",
pages = "1723-1703",
number = "12",
volume = "76",
doi = "10.2298/JSC110307146P"
}

Pergal, M., Antić, V., Ostojić, S., Marinović-Cincović, M.,& Đonlagić, J.. (2011). Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(ε-caprolactone)-b-poly(dimethylsiloxane)-b-poly(ε-caprolactone) triblock copolymer. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 76(12), 1703-1723.
https://doi.org/10.2298/JSC110307146P

Pergal M, Antić V, Ostojić S, Marinović-Cincović M, Đonlagić J. Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(ε-caprolactone)-b-poly(dimethylsiloxane)-b-poly(ε-caprolactone) triblock copolymer. in Journal of the Serbian Chemical Society. 2011;76(12):1703-1723.
doi:10.2298/JSC110307146P .

Pergal, Marija, Antić, Vesna, Ostojić, Sanja, Marinović-Cincović, Milena, Đonlagić, Jasna, "Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(ε-caprolactone)-b-poly(dimethylsiloxane)-b-poly(ε-caprolactone) triblock copolymer" in Journal of the Serbian Chemical Society, 76, no. 12 (2011):1703-1723,
https://doi.org/10.2298/JSC110307146P . .

TY  - JOUR
AU  - Vučković, Marija V.
AU  - Antić, Vesna
AU  - Govedarica, Milutin
AU  - Đonlagić, Jasna
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5615
AB  - A series of thermoplastic elastomers based on ethylene oxide- poly(dimethylsiloxane)-ethylene oxide (EO-PDMS-EO), as the soft segment, and poly(butylene terephthalate) (PBT), as the hard segment, were synthesized by catalyzed two-step, melt transesterification reaction of dimethyl terephthalate (DMT) with 1, 4-butanediol (BD) and α, ω-dihydroxy-(EO-PDMS-EO). Copolymers with a content of hard PBT segments between 40 and 90 mass % and a constant length of the soft EO-PDMS-EO segments were prepared. The siloxane prepolymer with hydrophilic terminal EO units was used to improve the miscibility between the polar comonomers, DMT and BD, and the nonpolar PDMS. The molecular structure and composition of the copolymers were determined by 1HNMR spectroscopy, whereas the effectiveness of the incorporation of α, ω-dihydroxy-(EO-PDMS-EO) into the copolymer chains was verified by chloroform extraction. The effects of the structure and composition of the copolymers on the melting temperatures and the degree of crystallinity, as well as on the thermal degradation stability and some rheological properties, were studied. It was demonstrated that the degree of crystallinity, the melting and crystallization temperatures of the copolymers increased with increasing mass fraction of the PBT segments. The thermal stability of the copolymers was lower than that of PBT homopolymer, because of the presence of thermoliable ether bonds in the soft segments.
PB  - Wiley
T2  - Journal of Applied Polymer Science
T1  - Synthesis and characterization of copolymers based on poly(butylene terephthalate) and ethylene oxide-poly(dimethylsiloxane)-ethylene oxide
EP  - 3216
IS  - 6
SP  - 3205
VL  - 115
DO  - 10.1002/app.31416
ER  - 

@article{
author = "Vučković, Marija V. and Antić, Vesna and Govedarica, Milutin and Đonlagić, Jasna",
year = "2010",
abstract = "A series of thermoplastic elastomers based on ethylene oxide- poly(dimethylsiloxane)-ethylene oxide (EO-PDMS-EO), as the soft segment, and poly(butylene terephthalate) (PBT), as the hard segment, were synthesized by catalyzed two-step, melt transesterification reaction of dimethyl terephthalate (DMT) with 1, 4-butanediol (BD) and α, ω-dihydroxy-(EO-PDMS-EO). Copolymers with a content of hard PBT segments between 40 and 90 mass % and a constant length of the soft EO-PDMS-EO segments were prepared. The siloxane prepolymer with hydrophilic terminal EO units was used to improve the miscibility between the polar comonomers, DMT and BD, and the nonpolar PDMS. The molecular structure and composition of the copolymers were determined by 1HNMR spectroscopy, whereas the effectiveness of the incorporation of α, ω-dihydroxy-(EO-PDMS-EO) into the copolymer chains was verified by chloroform extraction. The effects of the structure and composition of the copolymers on the melting temperatures and the degree of crystallinity, as well as on the thermal degradation stability and some rheological properties, were studied. It was demonstrated that the degree of crystallinity, the melting and crystallization temperatures of the copolymers increased with increasing mass fraction of the PBT segments. The thermal stability of the copolymers was lower than that of PBT homopolymer, because of the presence of thermoliable ether bonds in the soft segments.",
publisher = "Wiley",
journal = "Journal of Applied Polymer Science",
title = "Synthesis and characterization of copolymers based on poly(butylene terephthalate) and ethylene oxide-poly(dimethylsiloxane)-ethylene oxide",
pages = "3216-3205",
number = "6",
volume = "115",
doi = "10.1002/app.31416"
}

Vučković, M. V., Antić, V., Govedarica, M.,& Đonlagić, J.. (2010). Synthesis and characterization of copolymers based on poly(butylene terephthalate) and ethylene oxide-poly(dimethylsiloxane)-ethylene oxide. in Journal of Applied Polymer Science
Wiley., 115(6), 3205-3216.
https://doi.org/10.1002/app.31416

Vučković MV, Antić V, Govedarica M, Đonlagić J. Synthesis and characterization of copolymers based on poly(butylene terephthalate) and ethylene oxide-poly(dimethylsiloxane)-ethylene oxide. in Journal of Applied Polymer Science. 2010;115(6):3205-3216.
doi:10.1002/app.31416 .

Vučković, Marija V., Antić, Vesna, Govedarica, Milutin, Đonlagić, Jasna, "Synthesis and characterization of copolymers based on poly(butylene terephthalate) and ethylene oxide-poly(dimethylsiloxane)-ethylene oxide" in Journal of Applied Polymer Science, 115, no. 6 (2010):3205-3216,
https://doi.org/10.1002/app.31416 . .

TY  - JOUR
AU  - Antić, Vesna
AU  - Pergal, Marija
AU  - Antić, Mališa
AU  - Đonlagić, Jasna
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5613
AB  - Two series of thermoplastic elastomers (TPES), based on poly(dimethylsiloxane) (PDMS) as the soft segment and poly(butylene terephthalate) (PBT) as the hard segment, were analyzed by dynamic mechanical spectroscopy. In the first TPES series the lengths of both hard and soft segments were varied while the mass ratio of the hard to soft segments was nearly constant (about 60 mass%). In the second series, the mass ratio of hard and soft segments was varied in the range from 60/40 to 40/60, with a constant length of soft PDMS segments. The influence of the structure and composition of TPESs on the rheological properties, such as complex dynamic viscosity, μ*, the storage, G', and loss, G', shear modulus as well as the microphase separation transition temperature, TMST, was examined. The obtained results showed that the storage modulus of the TPESs increased in a rubbery plateau region with increase in degree of crystallinity. The rheological measurements of TPESs also showed that a microphase reorganization occurred during the melting process. The microphase separation transition temperatures were in the range from 220 to 234°C. In the isotropic molten state, the complex dynamic viscosity increased with increasing both the content and length of hard PBT segments.
AB  - Dve serije termoplastičnih elastomera (TPES) na bazi poli(dimetilsiloksana) kao mekog segmenta i poli(butilentereftalata) kao tvrdog segmenta su analizirane dinamičko-mehaničkom spektroskopijom. U prvoj TPES seriji varirane su dužine tvrdih i mekih segmenata dok je njihov maseni odnos bio skoro konstantan (oko 60 mas%). U drugoj seriji, odnos tvrdih i mekih segmenata je variran u opsegu od 60/40 do 40/60, dok je dužina mekih PDMS segmenata bila konstantna. Ispitan je uticaj strukture i sastava TPES kopolimera na reološka svojstva, kao što su kompleksni dinamički viskozitet, μ*, moduli sačuvane, G', i izgubljene energije, G', i temperatura mikrofaznog razdvajanja, TMST. Dobijeni rezultati su pokazali da su uzorci sa većim stepenom kristaliničnosti imali i veće module sačuvane energije u gumolikom platou. Reološka merenja su takođe pokazala da svi TPES uzorci ispoljavaju mikrofaznu reorganizaciju u procesu topljenja. Temperature mikrofaznog razdvajanja su bile u opsegu od 220 do 234°C. U izotropskom rastopu, kompleksni dinamički viskoziteti su rasli sa povećanjem sadržaja i dužine PBT segmenata.
PB  - Association of Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Rheological behaviour of thermoplastic poly(ester-siloxane)s
T1  - Reološko ponašanje termoplastičnih poli(estar-siloksana)
EP  - 545
IS  - 6
SP  - 537
VL  - 64
DO  - 10.2298/HEMIND101015067A
ER  - 

@article{
author = "Antić, Vesna and Pergal, Marija and Antić, Mališa and Đonlagić, Jasna",
year = "2010",
abstract = "Two series of thermoplastic elastomers (TPES), based on poly(dimethylsiloxane) (PDMS) as the soft segment and poly(butylene terephthalate) (PBT) as the hard segment, were analyzed by dynamic mechanical spectroscopy. In the first TPES series the lengths of both hard and soft segments were varied while the mass ratio of the hard to soft segments was nearly constant (about 60 mass%). In the second series, the mass ratio of hard and soft segments was varied in the range from 60/40 to 40/60, with a constant length of soft PDMS segments. The influence of the structure and composition of TPESs on the rheological properties, such as complex dynamic viscosity, μ*, the storage, G', and loss, G', shear modulus as well as the microphase separation transition temperature, TMST, was examined. The obtained results showed that the storage modulus of the TPESs increased in a rubbery plateau region with increase in degree of crystallinity. The rheological measurements of TPESs also showed that a microphase reorganization occurred during the melting process. The microphase separation transition temperatures were in the range from 220 to 234°C. In the isotropic molten state, the complex dynamic viscosity increased with increasing both the content and length of hard PBT segments., Dve serije termoplastičnih elastomera (TPES) na bazi poli(dimetilsiloksana) kao mekog segmenta i poli(butilentereftalata) kao tvrdog segmenta su analizirane dinamičko-mehaničkom spektroskopijom. U prvoj TPES seriji varirane su dužine tvrdih i mekih segmenata dok je njihov maseni odnos bio skoro konstantan (oko 60 mas%). U drugoj seriji, odnos tvrdih i mekih segmenata je variran u opsegu od 60/40 do 40/60, dok je dužina mekih PDMS segmenata bila konstantna. Ispitan je uticaj strukture i sastava TPES kopolimera na reološka svojstva, kao što su kompleksni dinamički viskozitet, μ*, moduli sačuvane, G', i izgubljene energije, G', i temperatura mikrofaznog razdvajanja, TMST. Dobijeni rezultati su pokazali da su uzorci sa većim stepenom kristaliničnosti imali i veće module sačuvane energije u gumolikom platou. Reološka merenja su takođe pokazala da svi TPES uzorci ispoljavaju mikrofaznu reorganizaciju u procesu topljenja. Temperature mikrofaznog razdvajanja su bile u opsegu od 220 do 234°C. U izotropskom rastopu, kompleksni dinamički viskoziteti su rasli sa povećanjem sadržaja i dužine PBT segmenata.",
publisher = "Association of Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Rheological behaviour of thermoplastic poly(ester-siloxane)s, Reološko ponašanje termoplastičnih poli(estar-siloksana)",
pages = "545-537",
number = "6",
volume = "64",
doi = "10.2298/HEMIND101015067A"
}

Antić, V., Pergal, M., Antić, M.,& Đonlagić, J.. (2010). Rheological behaviour of thermoplastic poly(ester-siloxane)s. in Hemijska industrija
Association of Chemical Engineers of Serbia., 64(6), 537-545.
https://doi.org/10.2298/HEMIND101015067A

Antić V, Pergal M, Antić M, Đonlagić J. Rheological behaviour of thermoplastic poly(ester-siloxane)s. in Hemijska industrija. 2010;64(6):537-545.
doi:10.2298/HEMIND101015067A .

Antić, Vesna, Pergal, Marija, Antić, Mališa, Đonlagić, Jasna, "Rheological behaviour of thermoplastic poly(ester-siloxane)s" in Hemijska industrija, 64, no. 6 (2010):537-545,
https://doi.org/10.2298/HEMIND101015067A . .

TY  - JOUR
AU  - Dojčinović, Biljana
AU  - Antić, Vesna
AU  - Vučković, Marija V.
AU  - Đonlagić, Jasna
PY  - 2005
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5489
AB  - Two series of thermoplastic elastomers, based on poly(dimethylsiloxane) PDMS, as the soft segment and poly(butylene terephthalate), PBT, as the hard segment, were synthesized by catalyzed transesterification, from dimethyl terephthalate, DMT, silanol-terminated poly(dimethylsiloxane), PDMS-OH Mn=1750g/mol, and 1,4-butanediol, BD. The mole ratio of the starting comonomers was selected to result in a constant hard to soft weight ratio of 55:45. The first series was synthesized in order to determine the optimal mole ratio of BD and DMT for the synthesis of high molecular weight thermoplastic poly(ester-siloxane)s, TPESs. The second series was performed in the presence of the high-boiling solvent, 1,2,4-trichlorbenzene in order to increase the mixing between the extremely non-polar siloxane prepolymer and the polar reactants, DMT and BD, and, therefore, avoid phase separation during synthesis. The structure and composition of the synthesized poly(ester-siloxane)s were verified by 1H-NMR spectroscopy, while the melting temperatures and degree of crystallinity were determined by differential scanning calorimetry (DSC). The effectiveness of the incorporation of the silanol-terminated poly( dimethylsiloxane) into the polyester chains was verified by chloroform extraction. The rheological properties of the poly(ester-siloxane)s were investigated by dynamic mechanical spectroscopy (DMA).
AB  - Dve serije termoplastičnih elastomera na bazi poli(dimetilsiloksana) kao mekog segmenta i poli(butilentereftalata) kao tvrdog segmenta sintetisane su katalizovanom transesterifikacijom polazeći od dimetiltereftalata, DMT silanol-terminarnog poli(dimetil-siloksana), PDMS-OH, Mn=1750g/mol i 1,4-butandiola, BD. Molski odnos početnih komonomera odabran je tako da je rezultovao u konstantnom masenom odnosu tvrdih i mekih segmenata od 55:45. Prva serija je sintetisana sa ciljem da se odredi optimalan molski odnos komonomera BD i DMT za dobijanje termoplastičnih elastomera velikih molarnih masa. U drugoj seriji sinteze su izvođene u prisustvu teško isparljivog rastvarača 1,2,4-trihlorbenzena sa ciljem da se poveća mešljivost izuzetno nepolarnog poli(dimetilsiloksanskog)pretpolimera i polarnih reaktanata, kao što su DMT i BD i samim tim da se izbegne fazna separacija u reakcionoj smeši tokom sinteze. Struktura i sastav sintetisanih poli(estar-siloksana) potvrđeni su 1H-NMR spektroskopijom, dok su temperatura topljenja i stepen kristaliničnosti određeni diferencijalnom skenirajućom kalometrijom (DSC). Efikasnost ugradnje silanol-terminiranog poli(dimetilsiloksana) u poliestarske lance utvrđena je na osnovu ekstrakcije hloroformom. Reološka svojstva poli(estara-siloksana) ispitana su dinamičko-mehaničkom spektroskopijom.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis of thermoplastic poly(ester-siloxane)s in the melt and in solution
T1  - Sinteza termoplastičnih poli(estar-siloksana) u rastopu i rastvoru
EP  - 1485
IS  - 12
SP  - 1469
VL  - 70
DO  - 10.2298/JSC0512469D
ER  - 

@article{
author = "Dojčinović, Biljana and Antić, Vesna and Vučković, Marija V. and Đonlagić, Jasna",
year = "2005",
abstract = "Two series of thermoplastic elastomers, based on poly(dimethylsiloxane) PDMS, as the soft segment and poly(butylene terephthalate), PBT, as the hard segment, were synthesized by catalyzed transesterification, from dimethyl terephthalate, DMT, silanol-terminated poly(dimethylsiloxane), PDMS-OH Mn=1750g/mol, and 1,4-butanediol, BD. The mole ratio of the starting comonomers was selected to result in a constant hard to soft weight ratio of 55:45. The first series was synthesized in order to determine the optimal mole ratio of BD and DMT for the synthesis of high molecular weight thermoplastic poly(ester-siloxane)s, TPESs. The second series was performed in the presence of the high-boiling solvent, 1,2,4-trichlorbenzene in order to increase the mixing between the extremely non-polar siloxane prepolymer and the polar reactants, DMT and BD, and, therefore, avoid phase separation during synthesis. The structure and composition of the synthesized poly(ester-siloxane)s were verified by 1H-NMR spectroscopy, while the melting temperatures and degree of crystallinity were determined by differential scanning calorimetry (DSC). The effectiveness of the incorporation of the silanol-terminated poly( dimethylsiloxane) into the polyester chains was verified by chloroform extraction. The rheological properties of the poly(ester-siloxane)s were investigated by dynamic mechanical spectroscopy (DMA)., Dve serije termoplastičnih elastomera na bazi poli(dimetilsiloksana) kao mekog segmenta i poli(butilentereftalata) kao tvrdog segmenta sintetisane su katalizovanom transesterifikacijom polazeći od dimetiltereftalata, DMT silanol-terminarnog poli(dimetil-siloksana), PDMS-OH, Mn=1750g/mol i 1,4-butandiola, BD. Molski odnos početnih komonomera odabran je tako da je rezultovao u konstantnom masenom odnosu tvrdih i mekih segmenata od 55:45. Prva serija je sintetisana sa ciljem da se odredi optimalan molski odnos komonomera BD i DMT za dobijanje termoplastičnih elastomera velikih molarnih masa. U drugoj seriji sinteze su izvođene u prisustvu teško isparljivog rastvarača 1,2,4-trihlorbenzena sa ciljem da se poveća mešljivost izuzetno nepolarnog poli(dimetilsiloksanskog)pretpolimera i polarnih reaktanata, kao što su DMT i BD i samim tim da se izbegne fazna separacija u reakcionoj smeši tokom sinteze. Struktura i sastav sintetisanih poli(estar-siloksana) potvrđeni su 1H-NMR spektroskopijom, dok su temperatura topljenja i stepen kristaliničnosti određeni diferencijalnom skenirajućom kalometrijom (DSC). Efikasnost ugradnje silanol-terminiranog poli(dimetilsiloksana) u poliestarske lance utvrđena je na osnovu ekstrakcije hloroformom. Reološka svojstva poli(estara-siloksana) ispitana su dinamičko-mehaničkom spektroskopijom.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis of thermoplastic poly(ester-siloxane)s in the melt and in solution, Sinteza termoplastičnih poli(estar-siloksana) u rastopu i rastvoru",
pages = "1485-1469",
number = "12",
volume = "70",
doi = "10.2298/JSC0512469D"
}

Dojčinović, B., Antić, V., Vučković, M. V.,& Đonlagić, J.. (2005). Synthesis of thermoplastic poly(ester-siloxane)s in the melt and in solution. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 70(12), 1469-1485.
https://doi.org/10.2298/JSC0512469D

Dojčinović B, Antić V, Vučković MV, Đonlagić J. Synthesis of thermoplastic poly(ester-siloxane)s in the melt and in solution. in Journal of the Serbian Chemical Society. 2005;70(12):1469-1485.
doi:10.2298/JSC0512469D .

Dojčinović, Biljana, Antić, Vesna, Vučković, Marija V., Đonlagić, Jasna, "Synthesis of thermoplastic poly(ester-siloxane)s in the melt and in solution" in Journal of the Serbian Chemical Society, 70, no. 12 (2005):1469-1485,
https://doi.org/10.2298/JSC0512469D . .