Ostojić, Sanja

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1d6f3bc7-9992-4364-892c-7bdadba13637
  • Ostojić, Sanja (5)
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Author's Bibliography

Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays

Mirković, Ilinka; Nikolić, Marija; Ostojić, Sanja; Maletaškić, Jelena; Petrović, Zoran; Đonlagić, Jasna

(Srpsko hemijsko društvo, Beograd, 2020)

TY  - JOUR
AU  - Mirković, Ilinka
AU  - Nikolić, Marija
AU  - Ostojić, Sanja
AU  - Maletaškić, Jelena
AU  - Petrović, Zoran
AU  - Đonlagić, Jasna
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4365
AB  - Semi-interpenetrating polymer networks (SIPN) based on thermo-responsive poly(N-isopropylacrylamide) (PNIPA) and water-soluble sodium salts of linear hyaluronic acid (Na-HA) were physically cross-linked with synthetic nanoclay (laponite XLG). PNIPA hydrogels with different cross-linking densities and Na-HA concentrations were synthesized by in situ free-radical redox polymerization. The structure and heterogeneity of the semi-IPN hydrogels were examined by SEM and XRD. The content of clay incorporated in the gel was determined by TGA. DSC measurements showed that volume phase transition temperature and its enthalpy varied with the clay and hyaluronic acid content. SIPN hydrogels containing negatively charged polyelectrolyte, Na-HA, exhibited higher Q(e) and faster deswelling rates than the corresponding PNIPA NC hydrogels. The presence of the anionic Na-HA polymer reduced the storage modulus, indicating a weakening of the hydrogel network structure, especially at lower clay contents. The nanocomposite hydrogels exhibited high tan delta values, which increased with increasing Na-HA content.
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays
EP  - 1221
IS  - 9
SP  - 1197
VL  - 85
DO  - 10.2298/JSC200109023M
ER  - 
@article{
author = "Mirković, Ilinka and Nikolić, Marija and Ostojić, Sanja and Maletaškić, Jelena and Petrović, Zoran and Đonlagić, Jasna",
year = "2020",
abstract = "Semi-interpenetrating polymer networks (SIPN) based on thermo-responsive poly(N-isopropylacrylamide) (PNIPA) and water-soluble sodium salts of linear hyaluronic acid (Na-HA) were physically cross-linked with synthetic nanoclay (laponite XLG). PNIPA hydrogels with different cross-linking densities and Na-HA concentrations were synthesized by in situ free-radical redox polymerization. The structure and heterogeneity of the semi-IPN hydrogels were examined by SEM and XRD. The content of clay incorporated in the gel was determined by TGA. DSC measurements showed that volume phase transition temperature and its enthalpy varied with the clay and hyaluronic acid content. SIPN hydrogels containing negatively charged polyelectrolyte, Na-HA, exhibited higher Q(e) and faster deswelling rates than the corresponding PNIPA NC hydrogels. The presence of the anionic Na-HA polymer reduced the storage modulus, indicating a weakening of the hydrogel network structure, especially at lower clay contents. The nanocomposite hydrogels exhibited high tan delta values, which increased with increasing Na-HA content.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays",
pages = "1221-1197",
number = "9",
volume = "85",
doi = "10.2298/JSC200109023M"
}
Mirković, I., Nikolić, M., Ostojić, S., Maletaškić, J., Petrović, Z.,& Đonlagić, J.. (2020). Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays. in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 85(9), 1197-1221.
https://doi.org/10.2298/JSC200109023M
Mirković I, Nikolić M, Ostojić S, Maletaškić J, Petrović Z, Đonlagić J. Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays. in Journal of the Serbian Chemical Society. 2020;85(9):1197-1221.
doi:10.2298/JSC200109023M .
Mirković, Ilinka, Nikolić, Marija, Ostojić, Sanja, Maletaškić, Jelena, Petrović, Zoran, Đonlagić, Jasna, "Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays" in Journal of the Serbian Chemical Society, 85, no. 9 (2020):1197-1221,
https://doi.org/10.2298/JSC200109023M . .
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Biocomposite membranes of highly methylated pectin and mesoporous silica SBA-15

Nešić, Aleksandra; Kokunešoski, Maja; Ilić, Svetlana M.; Gordić, Milan V.; Ostojić, Sanja; Micić, Darko M.; Veličković, Sava J.

(Elsevier Ltd., 2014)

TY  - JOUR
AU  - Nešić, Aleksandra
AU  - Kokunešoski, Maja
AU  - Ilić, Svetlana M.
AU  - Gordić, Milan V.
AU  - Ostojić, Sanja
AU  - Micić, Darko M.
AU  - Veličković, Sava J.
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5757
AB  - Manufacturing of synthetic composites consumes huge energy and their disposal at the end of the life cycle is very difficult since there is virtually no recycling option. Therefore, biocomposite materials have recently received considerable attention in academic research and industrial application compared to the synthetic composite materials due biodegradability, nontoxicity and economical point of view. Biocomposite membranes of highly methylated pectin and SBA-15, a form of mesoporous silica, were prepared by membrane casting. The amount of SBA-15 was 10%, 20% and 30% by membrane mass. These membranes were characterized by optical microscopy, FTIR, XRD, thermogravimetry, mechanical analysis and swelling in water, HCl, NaOH and methanol. The incorporation of SBA-15 in pectin matrix enhanced the stability of these membranes in all tested solutions, compared to the pure pectin membranes. The pectin/SBA photomicrographs contain rod-like domains which indicate the presence of SBA-15 in membrane. Mechanical analysis proves that incorporation of SBA-15 enhances the elasticity and tensile strength of pectin membranes. Thermogravimety in nitrogen has shown that the presence of SBA-15 in the membranes increased the onset temperatures of pectin degradation. The novel composite material represents promising way for practical membrane application. (C) 2014 Elsevier Ltd. All rights reserved.
PB  - Elsevier Ltd.
T2  - Composites: Part B: Engineering
T1  - Biocomposite membranes of highly methylated pectin and mesoporous silica SBA-15
EP  - 167
SP  - 162
VL  - 64
DO  - 10.1016/j.compositesb.2014.04.019
ER  - 
@article{
author = "Nešić, Aleksandra and Kokunešoski, Maja and Ilić, Svetlana M. and Gordić, Milan V. and Ostojić, Sanja and Micić, Darko M. and Veličković, Sava J.",
year = "2014",
abstract = "Manufacturing of synthetic composites consumes huge energy and their disposal at the end of the life cycle is very difficult since there is virtually no recycling option. Therefore, biocomposite materials have recently received considerable attention in academic research and industrial application compared to the synthetic composite materials due biodegradability, nontoxicity and economical point of view. Biocomposite membranes of highly methylated pectin and SBA-15, a form of mesoporous silica, were prepared by membrane casting. The amount of SBA-15 was 10%, 20% and 30% by membrane mass. These membranes were characterized by optical microscopy, FTIR, XRD, thermogravimetry, mechanical analysis and swelling in water, HCl, NaOH and methanol. The incorporation of SBA-15 in pectin matrix enhanced the stability of these membranes in all tested solutions, compared to the pure pectin membranes. The pectin/SBA photomicrographs contain rod-like domains which indicate the presence of SBA-15 in membrane. Mechanical analysis proves that incorporation of SBA-15 enhances the elasticity and tensile strength of pectin membranes. Thermogravimety in nitrogen has shown that the presence of SBA-15 in the membranes increased the onset temperatures of pectin degradation. The novel composite material represents promising way for practical membrane application. (C) 2014 Elsevier Ltd. All rights reserved.",
publisher = "Elsevier Ltd.",
journal = "Composites: Part B: Engineering",
title = "Biocomposite membranes of highly methylated pectin and mesoporous silica SBA-15",
pages = "167-162",
volume = "64",
doi = "10.1016/j.compositesb.2014.04.019"
}
Nešić, A., Kokunešoski, M., Ilić, S. M., Gordić, M. V., Ostojić, S., Micić, D. M.,& Veličković, S. J.. (2014). Biocomposite membranes of highly methylated pectin and mesoporous silica SBA-15. in Composites: Part B: Engineering
Elsevier Ltd.., 64, 162-167.
https://doi.org/10.1016/j.compositesb.2014.04.019
Nešić A, Kokunešoski M, Ilić SM, Gordić MV, Ostojić S, Micić DM, Veličković SJ. Biocomposite membranes of highly methylated pectin and mesoporous silica SBA-15. in Composites: Part B: Engineering. 2014;64:162-167.
doi:10.1016/j.compositesb.2014.04.019 .
Nešić, Aleksandra, Kokunešoski, Maja, Ilić, Svetlana M., Gordić, Milan V., Ostojić, Sanja, Micić, Darko M., Veličković, Sava J., "Biocomposite membranes of highly methylated pectin and mesoporous silica SBA-15" in Composites: Part B: Engineering, 64 (2014):162-167,
https://doi.org/10.1016/j.compositesb.2014.04.019 . .
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Poly(urethane-siloxane)s based on hyperbranched polyester as crosslinking agent: Synthesis and characterization

Pergal, Marija; Džunuzović, Jasna; Ostojić, Sanja; Pergal, Miodrag M.; Radulović, Aleksandra; Jovanovic, Slobodan

(Serbian Chemical Society, 2012)

TY  - JOUR
AU  - Pergal, Marija
AU  - Džunuzović, Jasna
AU  - Ostojić, Sanja
AU  - Pergal, Miodrag M.
AU  - Radulović, Aleksandra
AU  - Jovanovic, Slobodan
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5732
AB  - A series of novel polyurethane crosslinked structures (PUs) was prepared from α,ω-dihydroxy-(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS-EO), 4,4'-methylenediphenyl diisocyanate and Boltorn ® hyperbranched polyester of the third pseudo generation. The hydroxyfunctional hyperbranched aliphatic polyester with 26 end groups was used as a crosslinking agent. In order to improve the compatibility of all the reactants during the synthesis, the PU samples were prepared by two-stage, step-growth polymerization in solution. The content of the soft EO-PDMS-EO segments was varied in the range from 15 to 40 wt. %. The influence of the EO-PDMS-EO content on the swelling behavior, crosslink density, hardness, and the thermal and surface properties of the synthesized PUs was investigated. The structure of the synthesized polyurethanes was confirmed by the presence of specific bands in the Fourier transform infrared spectra. Swelling studies were performed to determine the crosslink density and polyurethane networks with lower EO-PDMS-EO contents had higher crosslink densities. The glass transition temperature of the synthesized PUs, determined by differential scanning calorimetry, slightly increased from 50 to 58°C on decreasing the EO-PDMS-EO content because of the higher crosslink density of the samples. Increasing the EO-PDMS-EO content led to better thermal stability, as was evidenced by the onset temperature of weight loss. The surface of the polyurethane networks became more hydrophobic with increasing EO-PDMS-EO content. The surface morphology of synthesized polyurethanes was analyzed by scanning electron microscopy.
AB  - U ovom radu prikazana je sinteza, struktura i neka svojstva novih umreženih poliuretana pripremljenih polazeći od α,ω-dihidroksi-(etilenoksid-poli(dimetilsiloksan)-etilenoksid) pretpolimera (EO-PDMS-EO), 4,4'-metilendifenildiizocijanata i Boltorn® hiperrazgranatog poliestra treće pseudo-generacije. Hiperrazgranati hidroksi funkcionalni alifatski poliestar sa 26 krajnjih grupa služio je kao umrežavajući agens pri sintezi poliuretana. U cilju poboljšanja kompatibilnosti reaktanata tokom sinteze, poliuretani su sintetisani dvostepenom polimerizacijom u rastvoru. Sadržaj mekog EO-PDMS-EO segmenta variran je u opsegu od 15 do 40 mas. %. Ispitan je uticaj EO-PDMS-EO sadržaja na ponašanje pri bubrenju, gustinu umrežavanja, tvrdoću, termička i površinska svojstva sintetisanih poliuretana. Struktura sintetisanih poliuretana potvrđena je FTIR spektroskopijom. Ponašanje pri bubrenju je ispitivano kako bi se odredila gustina umrežavanja i pokazano je da poliuretanske mreže sa nižim EO-PDMS-EO sadržajem imaju veću gustinu umrežavanja. Rezultati diferencijalne skenirajuće kalorimetrije pokazali su povećanje temperature ostakljivanja poliuretana od 50 do 58°C sa smanjenjem EO-PDMS-EO sadržaja kao posledicu veće gustine umreženosti uzoraka. Sintetisani poliuretani sa većim sadržajem EO-PDMS-EO segmenata pokazuju bolju termičku stabilnost, što je potvrđeno porastom početne temperature degradacije, određene TG analizom. Hidrofobnost površine poliuretana je rasla sa povećanjem sadržaja EO-PDMS-EO u odgovarajućem uzorku. Površinska morfologija sintetisanih poliuretana je analizirana skenirajućom elektronskom mikroskopijom.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Poly(urethane-siloxane)s based on hyperbranched polyester as crosslinking agent: Synthesis and characterization
T1  - Poli(uretan-siloksani) na bazi hiperrazgranatog poliestra kao umreživača - sinteza i karakterizacija
EP  - 935
IS  - 7
SP  - 919
VL  - 77
DO  - 10.2298/JSC111013006P
ER  - 
@article{
author = "Pergal, Marija and Džunuzović, Jasna and Ostojić, Sanja and Pergal, Miodrag M. and Radulović, Aleksandra and Jovanovic, Slobodan",
year = "2012",
abstract = "A series of novel polyurethane crosslinked structures (PUs) was prepared from α,ω-dihydroxy-(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS-EO), 4,4'-methylenediphenyl diisocyanate and Boltorn ® hyperbranched polyester of the third pseudo generation. The hydroxyfunctional hyperbranched aliphatic polyester with 26 end groups was used as a crosslinking agent. In order to improve the compatibility of all the reactants during the synthesis, the PU samples were prepared by two-stage, step-growth polymerization in solution. The content of the soft EO-PDMS-EO segments was varied in the range from 15 to 40 wt. %. The influence of the EO-PDMS-EO content on the swelling behavior, crosslink density, hardness, and the thermal and surface properties of the synthesized PUs was investigated. The structure of the synthesized polyurethanes was confirmed by the presence of specific bands in the Fourier transform infrared spectra. Swelling studies were performed to determine the crosslink density and polyurethane networks with lower EO-PDMS-EO contents had higher crosslink densities. The glass transition temperature of the synthesized PUs, determined by differential scanning calorimetry, slightly increased from 50 to 58°C on decreasing the EO-PDMS-EO content because of the higher crosslink density of the samples. Increasing the EO-PDMS-EO content led to better thermal stability, as was evidenced by the onset temperature of weight loss. The surface of the polyurethane networks became more hydrophobic with increasing EO-PDMS-EO content. The surface morphology of synthesized polyurethanes was analyzed by scanning electron microscopy., U ovom radu prikazana je sinteza, struktura i neka svojstva novih umreženih poliuretana pripremljenih polazeći od α,ω-dihidroksi-(etilenoksid-poli(dimetilsiloksan)-etilenoksid) pretpolimera (EO-PDMS-EO), 4,4'-metilendifenildiizocijanata i Boltorn® hiperrazgranatog poliestra treće pseudo-generacije. Hiperrazgranati hidroksi funkcionalni alifatski poliestar sa 26 krajnjih grupa služio je kao umrežavajući agens pri sintezi poliuretana. U cilju poboljšanja kompatibilnosti reaktanata tokom sinteze, poliuretani su sintetisani dvostepenom polimerizacijom u rastvoru. Sadržaj mekog EO-PDMS-EO segmenta variran je u opsegu od 15 do 40 mas. %. Ispitan je uticaj EO-PDMS-EO sadržaja na ponašanje pri bubrenju, gustinu umrežavanja, tvrdoću, termička i površinska svojstva sintetisanih poliuretana. Struktura sintetisanih poliuretana potvrđena je FTIR spektroskopijom. Ponašanje pri bubrenju je ispitivano kako bi se odredila gustina umrežavanja i pokazano je da poliuretanske mreže sa nižim EO-PDMS-EO sadržajem imaju veću gustinu umrežavanja. Rezultati diferencijalne skenirajuće kalorimetrije pokazali su povećanje temperature ostakljivanja poliuretana od 50 do 58°C sa smanjenjem EO-PDMS-EO sadržaja kao posledicu veće gustine umreženosti uzoraka. Sintetisani poliuretani sa većim sadržajem EO-PDMS-EO segmenata pokazuju bolju termičku stabilnost, što je potvrđeno porastom početne temperature degradacije, određene TG analizom. Hidrofobnost površine poliuretana je rasla sa povećanjem sadržaja EO-PDMS-EO u odgovarajućem uzorku. Površinska morfologija sintetisanih poliuretana je analizirana skenirajućom elektronskom mikroskopijom.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Poly(urethane-siloxane)s based on hyperbranched polyester as crosslinking agent: Synthesis and characterization, Poli(uretan-siloksani) na bazi hiperrazgranatog poliestra kao umreživača - sinteza i karakterizacija",
pages = "935-919",
number = "7",
volume = "77",
doi = "10.2298/JSC111013006P"
}
Pergal, M., Džunuzović, J., Ostojić, S., Pergal, M. M., Radulović, A.,& Jovanovic, S.. (2012). Poly(urethane-siloxane)s based on hyperbranched polyester as crosslinking agent: Synthesis and characterization. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 77(7), 919-935.
https://doi.org/10.2298/JSC111013006P
Pergal M, Džunuzović J, Ostojić S, Pergal MM, Radulović A, Jovanovic S. Poly(urethane-siloxane)s based on hyperbranched polyester as crosslinking agent: Synthesis and characterization. in Journal of the Serbian Chemical Society. 2012;77(7):919-935.
doi:10.2298/JSC111013006P .
Pergal, Marija, Džunuzović, Jasna, Ostojić, Sanja, Pergal, Miodrag M., Radulović, Aleksandra, Jovanovic, Slobodan, "Poly(urethane-siloxane)s based on hyperbranched polyester as crosslinking agent: Synthesis and characterization" in Journal of the Serbian Chemical Society, 77, no. 7 (2012):919-935,
https://doi.org/10.2298/JSC111013006P . .
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Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer

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

(2011)

TY  - JOUR
AU  - Pergal, Marija V.
AU  - Antić, Vesna V.
AU  - Ostojić, Sanja
AU  - Marinović-Cincović, Milena
AU  - Đonlagić, Jasna A.
PY  - 2011
UR  - 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 . .
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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

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

(Serbian Chemical Society, 2011)

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 . .
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