TY  - JOUR
AU  - Pergal, Marija V.
AU  - Antić, Vesna V.
AU  - Ostojić, Sanja
AU  - Marinović-Cincović, Milena
AU  - Đonlagić, Jasna A.
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5638
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
EP  - 1723
IS  - 12
SP  - 1703
VL  - 76
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",
pages = "1723-1703",
number = "12",
volume = "76",
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 . .

TY  - JOUR
AU  - Vučković, Marija V.
AU  - Antić, Vesna V.
AU  - Dojčinović, Biljana P.
AU  - Govedarica, Milutin N.
AU  - Đonlagić, Jasna
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5472
AB  - A series of novel thermoplastic elastomers based on ABA-type triblock prepolymers, poly[(propylene oxide)-(dimethylsiloxane)-(propylene oxide)] (PPO-PDMS-PPO), as the soft segments, and poly(butylene terephthalate) (PBT), as the hard segments, was synthesized by catalyzed two-step melt transesterification of dimethyl terephthalate (DMT) with 1,4-butanediol (BD) and α,ω-dihydroxy-(PPO-PDMS-PPO) (M̄ n = 2930 g mol -1 ). Several copolymers with a content of hard PBT segments between 40 and 60 mass% and a constant length of the soft PPO-PDMS-PPO segments were prepared. The siloxane-containing triblock prepolymer with hydrophilic terminal PPO blocks was used to improve the compatibility between the polar comonomers, i.e. DMT and BD, and the non-polar PDMS segments. The structure and composition of the copolymers were examined using 1 H NMR spectroscopy, while the effectiveness of the incorporation of α,ω-dihydroxy-(PPO-PDMS-PPO) prepolymer into the copolyester chains was controlled by chloroform extraction. The effect of the structure and composition of the copolymers on the transition temperatures (T m and T g ) and the thermal and thermo-oxidative degradation stability, as well as on the degree of crystallinity, and some rheological properties, were studied.
PB  - John Wiley and Sons Ltd
T2  - Polymer International
T1  - Synthesis and characterization of poly(ester ether siloxane)s
EP  - 1314
IS  - 11
SP  - 1304
VL  - 55
DO  - 10.1002/pi.2085
ER  - 

@article{
author = "Vučković, Marija V. and Antić, Vesna V. and Dojčinović, Biljana P. and Govedarica, Milutin N. and Đonlagić, Jasna",
year = "2006",
abstract = "A series of novel thermoplastic elastomers based on ABA-type triblock prepolymers, poly[(propylene oxide)-(dimethylsiloxane)-(propylene oxide)] (PPO-PDMS-PPO), as the soft segments, and poly(butylene terephthalate) (PBT), as the hard segments, was synthesized by catalyzed two-step melt transesterification of dimethyl terephthalate (DMT) with 1,4-butanediol (BD) and α,ω-dihydroxy-(PPO-PDMS-PPO) (M̄ n = 2930 g mol -1 ). Several copolymers with a content of hard PBT segments between 40 and 60 mass% and a constant length of the soft PPO-PDMS-PPO segments were prepared. The siloxane-containing triblock prepolymer with hydrophilic terminal PPO blocks was used to improve the compatibility between the polar comonomers, i.e. DMT and BD, and the non-polar PDMS segments. The structure and composition of the copolymers were examined using 1 H NMR spectroscopy, while the effectiveness of the incorporation of α,ω-dihydroxy-(PPO-PDMS-PPO) prepolymer into the copolyester chains was controlled by chloroform extraction. The effect of the structure and composition of the copolymers on the transition temperatures (T m and T g ) and the thermal and thermo-oxidative degradation stability, as well as on the degree of crystallinity, and some rheological properties, were studied.",
publisher = "John Wiley and Sons Ltd",
journal = "Polymer International",
title = "Synthesis and characterization of poly(ester ether siloxane)s",
pages = "1314-1304",
number = "11",
volume = "55",
doi = "10.1002/pi.2085"
}

Vučković, M. V., Antić, V. V., Dojčinović, B. P., Govedarica, M. N.,& Đonlagić, J.. (2006). Synthesis and characterization of poly(ester ether siloxane)s. in Polymer International
John Wiley and Sons Ltd., 55(11), 1304-1314.
https://doi.org/10.1002/pi.2085

Vučković MV, Antić VV, Dojčinović BP, Govedarica MN, Đonlagić J. Synthesis and characterization of poly(ester ether siloxane)s. in Polymer International. 2006;55(11):1304-1314.
doi:10.1002/pi.2085 .

Vučković, Marija V., Antić, Vesna V., Dojčinović, Biljana P., Govedarica, Milutin N., Đonlagić, Jasna, "Synthesis and characterization of poly(ester ether siloxane)s" in Polymer International, 55, no. 11 (2006):1304-1314,
https://doi.org/10.1002/pi.2085 . .

TY  - JOUR
AU  - Antić, Vesna V.
AU  - Đonlagić, Jasna
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5471
AB  - Two series of thermoplastic poly(ester-siloxane) elastomers (TPES), with hard segments based on poly(butylene terephthalate) (PBT) and soft segments based on poly(dimethylsiloxane) (PDMS), were synthesized by high-temperature, two-step transesterification reaction in the melt. In series I, the mass ratio of hard and soft segments was kept constant (57:43), while the length of the segments was varied, whereas in series II, the mass ratio of hard and soft segments was varied in range from 70:30 to 40:60, with a constant length of the soft segments. The segmented structure of the poly(ester-siloxane) copolymers was verified by 1H-NMR spectroscopy of the soluble and insoluble fractions, obtained after extraction of the samples with chloroform. The influence of the structure and composition of the TPES on the melting temperatures and degrees of crystallinity was investigated by differential scanning calorimetry (DSC). The rheological properties were investigated by dynamic mechanical analysis (DMA).
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis, structure and properties of thermoplastic poly(ester-siloxane) elastomers
EP  - 842
IS  - 7
SP  - 839
VL  - 71
DO  - 10.2298/JSC0607839A
ER  - 

@article{
author = "Antić, Vesna V. and Đonlagić, Jasna",
year = "2006",
abstract = "Two series of thermoplastic poly(ester-siloxane) elastomers (TPES), with hard segments based on poly(butylene terephthalate) (PBT) and soft segments based on poly(dimethylsiloxane) (PDMS), were synthesized by high-temperature, two-step transesterification reaction in the melt. In series I, the mass ratio of hard and soft segments was kept constant (57:43), while the length of the segments was varied, whereas in series II, the mass ratio of hard and soft segments was varied in range from 70:30 to 40:60, with a constant length of the soft segments. The segmented structure of the poly(ester-siloxane) copolymers was verified by 1H-NMR spectroscopy of the soluble and insoluble fractions, obtained after extraction of the samples with chloroform. The influence of the structure and composition of the TPES on the melting temperatures and degrees of crystallinity was investigated by differential scanning calorimetry (DSC). The rheological properties were investigated by dynamic mechanical analysis (DMA).",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis, structure and properties of thermoplastic poly(ester-siloxane) elastomers",
pages = "842-839",
number = "7",
volume = "71",
doi = "10.2298/JSC0607839A"
}

Antić, V. V.,& Đonlagić, J.. (2006). Synthesis, structure and properties of thermoplastic poly(ester-siloxane) elastomers. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 71(7), 839-842.
https://doi.org/10.2298/JSC0607839A

Antić VV, Đonlagić J. Synthesis, structure and properties of thermoplastic poly(ester-siloxane) elastomers. in Journal of the Serbian Chemical Society. 2006;71(7):839-842.
doi:10.2298/JSC0607839A .

Antić, Vesna V., Đonlagić, Jasna, "Synthesis, structure and properties of thermoplastic poly(ester-siloxane) elastomers" in Journal of the Serbian Chemical Society, 71, no. 7 (2006):839-842,
https://doi.org/10.2298/JSC0607839A . .

TY  - JOUR
AU  - Antić, Vesna V.
AU  - Govedarica, Milutin N.
AU  - Đonlagić, Jasna
PY  - 2004
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5405
AB  - A series of thermoplastic elastomers based on soft polydimethylsiloxane (PDMS) and hard poly(butylene terephthalate) (PBT) segments was synthesized using a two-step transesterification reaction in the melt. The molar mass of the soft PDMS component was constant (M̄ n P DMS = 1056 g mol -1 ) while the starting reaction mixture compositions were varied to obtained copolymers with a mass ratio of hard to soft segments in the range from 70/30 to 40/60. The structure and composition of the copolymers was verified by 1 H NMR spectroscopy. It appeared that there was a pronounced molar mass maximum when the PBT content of the copolymers was approximately 60 mass%, whereas all samples were considerably inhomogeneous with respect to the distribution of the lengths of the hard segments. Differential scanning calorimetry-(DSC) thermograms showed that the melting and crystallization temperature increased with increasing PBT content, as did the total degree of crystallinity, which was confirmed by wide-angle X-ray scattering (WAXS) analysis. Thermogravimetric analysis (TGA) performed in nitrogen gave subtle differences for samples of different composition, including that of the PBT homopolymer, whereas in oxygen these differences were more pronounced in the way the thermo-oxidative stability of the obtained copolymers decreased with decreasing PBT content. Finally, it was shown that the hardness depended directly on the PBT content, ie the higher the PBT content, the greater the hardness of the corresponding copolymer.
PB  - John Wiley and Sons Ltd
T2  - Polymer International
T1  - The effect of the mass ratio of hard and soft segments on some properties of thermoplastic poly(ester-siloxane)s
EP  - 1794
IS  - 11
SP  - 1786
VL  - 53
DO  - 10.1002/pi.1582
ER  - 

@article{
author = "Antić, Vesna V. and Govedarica, Milutin N. and Đonlagić, Jasna",
year = "2004",
abstract = "A series of thermoplastic elastomers based on soft polydimethylsiloxane (PDMS) and hard poly(butylene terephthalate) (PBT) segments was synthesized using a two-step transesterification reaction in the melt. The molar mass of the soft PDMS component was constant (M̄ n P DMS = 1056 g mol -1 ) while the starting reaction mixture compositions were varied to obtained copolymers with a mass ratio of hard to soft segments in the range from 70/30 to 40/60. The structure and composition of the copolymers was verified by 1 H NMR spectroscopy. It appeared that there was a pronounced molar mass maximum when the PBT content of the copolymers was approximately 60 mass%, whereas all samples were considerably inhomogeneous with respect to the distribution of the lengths of the hard segments. Differential scanning calorimetry-(DSC) thermograms showed that the melting and crystallization temperature increased with increasing PBT content, as did the total degree of crystallinity, which was confirmed by wide-angle X-ray scattering (WAXS) analysis. Thermogravimetric analysis (TGA) performed in nitrogen gave subtle differences for samples of different composition, including that of the PBT homopolymer, whereas in oxygen these differences were more pronounced in the way the thermo-oxidative stability of the obtained copolymers decreased with decreasing PBT content. Finally, it was shown that the hardness depended directly on the PBT content, ie the higher the PBT content, the greater the hardness of the corresponding copolymer.",
publisher = "John Wiley and Sons Ltd",
journal = "Polymer International",
title = "The effect of the mass ratio of hard and soft segments on some properties of thermoplastic poly(ester-siloxane)s",
pages = "1794-1786",
number = "11",
volume = "53",
doi = "10.1002/pi.1582"
}

Antić, V. V., Govedarica, M. N.,& Đonlagić, J.. (2004). The effect of the mass ratio of hard and soft segments on some properties of thermoplastic poly(ester-siloxane)s. in Polymer International
John Wiley and Sons Ltd., 53(11), 1786-1794.
https://doi.org/10.1002/pi.1582

Antić VV, Govedarica MN, Đonlagić J. The effect of the mass ratio of hard and soft segments on some properties of thermoplastic poly(ester-siloxane)s. in Polymer International. 2004;53(11):1786-1794.
doi:10.1002/pi.1582 .

Antić, Vesna V., Govedarica, Milutin N., Đonlagić, Jasna, "The effect of the mass ratio of hard and soft segments on some properties of thermoplastic poly(ester-siloxane)s" in Polymer International, 53, no. 11 (2004):1786-1794,
https://doi.org/10.1002/pi.1582 . .

TY  - JOUR
AU  - Antić, Vesna V.
AU  - Govedarica, Milutin N.
AU  - Đonlagić, Jasna
PY  - 2003
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5400
AB  - A series of novel thermoplastic elastomers, based on poly(dimethylsiloxane) (PDMS) as the soft segment and poly(butylene terephthalate) (PBT) as the hard segment, were synthesized by catalyzed two-step, melt transesterification reactions of dimethyl terephthalate and methyl esters of carboxypropyl-terminated poly(dimethylsiloxane)s (M̄ n = 550-2170 g mol -1 ) with 1,4-butanediol. The lengths of both the hard and soft segments were varied while the weight ratio of the hard to soft segments in the reaction mixture was maintained constant (57/43). The molecular structure, composition and molecular weights of the poly(ester-siloxane)s were examined by 1 H NMR spectroscopy. The effectiveness of the incorporation of the methyl-ester-terminated poly(dimethylsiloxane)s into the copolymer chains was verified by chloroform extraction. The effect of the segment length on the transition temperatures (T m and T g ) and the thermal and thermo-oxidative degradation stability, as well as the degree of crystallinity and hardness properties of the synthesized TPESs, were studied.
PB  - John Wiley and Sons Ltd
T2  - Polymer International
T1  - The effect of segment length on some properties of thermoplastic poly(ester-siloxane)s
EP  - 1197
IS  - 7
SP  - 1188
VL  - 52
DO  - 10.1002/pi.1241
ER  - 

@article{
author = "Antić, Vesna V. and Govedarica, Milutin N. and Đonlagić, Jasna",
year = "2003",
abstract = "A series of novel thermoplastic elastomers, based on poly(dimethylsiloxane) (PDMS) as the soft segment and poly(butylene terephthalate) (PBT) as the hard segment, were synthesized by catalyzed two-step, melt transesterification reactions of dimethyl terephthalate and methyl esters of carboxypropyl-terminated poly(dimethylsiloxane)s (M̄ n = 550-2170 g mol -1 ) with 1,4-butanediol. The lengths of both the hard and soft segments were varied while the weight ratio of the hard to soft segments in the reaction mixture was maintained constant (57/43). The molecular structure, composition and molecular weights of the poly(ester-siloxane)s were examined by 1 H NMR spectroscopy. The effectiveness of the incorporation of the methyl-ester-terminated poly(dimethylsiloxane)s into the copolymer chains was verified by chloroform extraction. The effect of the segment length on the transition temperatures (T m and T g ) and the thermal and thermo-oxidative degradation stability, as well as the degree of crystallinity and hardness properties of the synthesized TPESs, were studied.",
publisher = "John Wiley and Sons Ltd",
journal = "Polymer International",
title = "The effect of segment length on some properties of thermoplastic poly(ester-siloxane)s",
pages = "1197-1188",
number = "7",
volume = "52",
doi = "10.1002/pi.1241"
}

Antić, V. V., Govedarica, M. N.,& Đonlagić, J.. (2003). The effect of segment length on some properties of thermoplastic poly(ester-siloxane)s. in Polymer International
John Wiley and Sons Ltd., 52(7), 1188-1197.
https://doi.org/10.1002/pi.1241

Antić VV, Govedarica MN, Đonlagić J. The effect of segment length on some properties of thermoplastic poly(ester-siloxane)s. in Polymer International. 2003;52(7):1188-1197.
doi:10.1002/pi.1241 .

Antić, Vesna V., Govedarica, Milutin N., Đonlagić, Jasna, "The effect of segment length on some properties of thermoplastic poly(ester-siloxane)s" in Polymer International, 52, no. 7 (2003):1188-1197,
https://doi.org/10.1002/pi.1241 . .

TY  - JOUR
AU  - Antić, Vesna V.
AU  - Balaban, Milica R.
AU  - Đonlagić, Jasna
PY  - 2001
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5349
AB  - Two series of thermoplastic poly (ester-siloxane)s, based on poly(dimethylsiloxane) (PDMS) as the soft segment and poly(butylene terephthalate) as the hard segment, were synthesized by two-step catalyzed transesterification reactions in the melt. Incorporation of soft poly(dimethylsiloxane) segments into the copolyester backbone was accomplished in two different ways. The first series was prepared based on dimethyl terephthalate, 1,4-butanediol and silanol-terminated poly(dimethylsiloxane) (PDMS-OH). For the second series, the PDMS-OH was replaced by methyl diesters of carboxypropyl-terminated poly(dimethylsiloxane)s. The syntheses were optimized in terms of both the concentration of catalyst, tetra-n-butyl-titanate (Ti(OBu)4), and stabilizer, N,N′-diphenyl-p-phenylene-diamine, as well as the reaction time. The reactions were followed by measuring the inherent viscosities of the reaction mixture. The molecular structures of the synthesized poly(ester-siloxane)s were verified by 1H NMR spectroscopy, while their thermal properties were investigated using differential scanning calorimetry.
PB  - Wiley-Blackwell
T2  - Polymer International
T1  - Synthesis and characterization of thermoplastic poly(ester-siloxane)s
EP  - 1208
IS  - 11
SP  - 1201
VL  - 50
DO  - 10.1002/pi.764
ER  - 

@article{
author = "Antić, Vesna V. and Balaban, Milica R. and Đonlagić, Jasna",
year = "2001",
abstract = "Two series of thermoplastic poly (ester-siloxane)s, based on poly(dimethylsiloxane) (PDMS) as the soft segment and poly(butylene terephthalate) as the hard segment, were synthesized by two-step catalyzed transesterification reactions in the melt. Incorporation of soft poly(dimethylsiloxane) segments into the copolyester backbone was accomplished in two different ways. The first series was prepared based on dimethyl terephthalate, 1,4-butanediol and silanol-terminated poly(dimethylsiloxane) (PDMS-OH). For the second series, the PDMS-OH was replaced by methyl diesters of carboxypropyl-terminated poly(dimethylsiloxane)s. The syntheses were optimized in terms of both the concentration of catalyst, tetra-n-butyl-titanate (Ti(OBu)4), and stabilizer, N,N′-diphenyl-p-phenylene-diamine, as well as the reaction time. The reactions were followed by measuring the inherent viscosities of the reaction mixture. The molecular structures of the synthesized poly(ester-siloxane)s were verified by 1H NMR spectroscopy, while their thermal properties were investigated using differential scanning calorimetry.",
publisher = "Wiley-Blackwell",
journal = "Polymer International",
title = "Synthesis and characterization of thermoplastic poly(ester-siloxane)s",
pages = "1208-1201",
number = "11",
volume = "50",
doi = "10.1002/pi.764"
}

Antić, V. V., Balaban, M. R.,& Đonlagić, J.. (2001). Synthesis and characterization of thermoplastic poly(ester-siloxane)s. in Polymer International
Wiley-Blackwell., 50(11), 1201-1208.
https://doi.org/10.1002/pi.764

Antić VV, Balaban MR, Đonlagić J. Synthesis and characterization of thermoplastic poly(ester-siloxane)s. in Polymer International. 2001;50(11):1201-1208.
doi:10.1002/pi.764 .

Antić, Vesna V., Balaban, Milica R., Đonlagić, Jasna, "Synthesis and characterization of thermoplastic poly(ester-siloxane)s" in Polymer International, 50, no. 11 (2001):1201-1208,
https://doi.org/10.1002/pi.764 . .