TY  - JOUR
AU  - Marković, Bojana M.
AU  - Stefanović, Ivan
AU  - Hercigonja, Radmila
AU  - Pergal, Marija
AU  - Marković, Jelena P.
AU  - Onjia, Antonije
AU  - Nastasović, Aleksandra
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3753
AB  - Macroporous copolymers of poly[(glycidyl methacrylate)-co-(ethylene glycol dimethacrylate)] (PGME) with various crosslinker (ethylene glycol dimethacrylate) concentrations and porosity parameters and additionally functionalized with hexamethylene diamine (PGME-HD) were tested as potential Cr(VI) oxyanion sorbents from aqueous solutions. Kinetics of Cr(VI) sorption was investigated in the temperature range 298-343 K and the results were fitted to chemical reaction and particle diffusion models. The Cr(VI) sorption obeys the pseudo-second-order model with definite influence of pore diffusion. A temperature rise promotes chromium removal, with a maximum experimental uptake capacity of 4.21 mmol g(-1) at 343 K for the sample with the highest amino group concentration. Equilibrium data were analysed with Langmuir, Freundlich and Temkin adsorption isotherm models. Thermodynamic parameters, i.e. Gibbs free energy (G(0)), enthalpy (H-0) and entropy change (S-0) and activation energy of sorption (E-a), were calculated. The Cr(VI) adsorption onto PGME-HD was found to be spontaneous and endothermic, with increased randomness in the system. Desorption experiments show that chromium anion sorption was reversible and the PGME-HD sample GMA 60 HD was easily regenerated with 0.1 mol L-1 NaOH up to 90% recovery in the fourth sorption/desorption cycle. In the fifth cycle, a substantial sorption loss of 37% was observed.
PB  - Wiley, Hoboken
T2  - Polymer International
T1  - Novel hexamethylene diamine-functionalized macroporous copolymer for chromium removal from aqueous solutions
EP  - 689
IS  - 5
SP  - 679
VL  - 66
DO  - 10.1002/pi.5306
ER  - 

@article{
author = "Marković, Bojana M. and Stefanović, Ivan and Hercigonja, Radmila and Pergal, Marija and Marković, Jelena P. and Onjia, Antonije and Nastasović, Aleksandra",
year = "2017",
abstract = "Macroporous copolymers of poly[(glycidyl methacrylate)-co-(ethylene glycol dimethacrylate)] (PGME) with various crosslinker (ethylene glycol dimethacrylate) concentrations and porosity parameters and additionally functionalized with hexamethylene diamine (PGME-HD) were tested as potential Cr(VI) oxyanion sorbents from aqueous solutions. Kinetics of Cr(VI) sorption was investigated in the temperature range 298-343 K and the results were fitted to chemical reaction and particle diffusion models. The Cr(VI) sorption obeys the pseudo-second-order model with definite influence of pore diffusion. A temperature rise promotes chromium removal, with a maximum experimental uptake capacity of 4.21 mmol g(-1) at 343 K for the sample with the highest amino group concentration. Equilibrium data were analysed with Langmuir, Freundlich and Temkin adsorption isotherm models. Thermodynamic parameters, i.e. Gibbs free energy (G(0)), enthalpy (H-0) and entropy change (S-0) and activation energy of sorption (E-a), were calculated. The Cr(VI) adsorption onto PGME-HD was found to be spontaneous and endothermic, with increased randomness in the system. Desorption experiments show that chromium anion sorption was reversible and the PGME-HD sample GMA 60 HD was easily regenerated with 0.1 mol L-1 NaOH up to 90% recovery in the fourth sorption/desorption cycle. In the fifth cycle, a substantial sorption loss of 37% was observed.",
publisher = "Wiley, Hoboken",
journal = "Polymer International",
title = "Novel hexamethylene diamine-functionalized macroporous copolymer for chromium removal from aqueous solutions",
pages = "689-679",
number = "5",
volume = "66",
doi = "10.1002/pi.5306"
}

Marković, B. M., Stefanović, I., Hercigonja, R., Pergal, M., Marković, J. P., Onjia, A.,& Nastasović, A.. (2017). Novel hexamethylene diamine-functionalized macroporous copolymer for chromium removal from aqueous solutions. in Polymer International
Wiley, Hoboken., 66(5), 679-689.
https://doi.org/10.1002/pi.5306

Marković BM, Stefanović I, Hercigonja R, Pergal M, Marković JP, Onjia A, Nastasović A. Novel hexamethylene diamine-functionalized macroporous copolymer for chromium removal from aqueous solutions. in Polymer International. 2017;66(5):679-689.
doi:10.1002/pi.5306 .

Marković, Bojana M., Stefanović, Ivan, Hercigonja, Radmila, Pergal, Marija, Marković, Jelena P., Onjia, Antonije, Nastasović, Aleksandra, "Novel hexamethylene diamine-functionalized macroporous copolymer for chromium removal from aqueous solutions" in Polymer International, 66, no. 5 (2017):679-689,
https://doi.org/10.1002/pi.5306 . .

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  - 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 . .

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  - Džunuzović, Jasna
AU  - Pergal, Marija
AU  - Vodnik, Vesna
AU  - Špírková, Milena
AU  - Poręba, Rafał
AU  - Jovanović, Slobodan
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5694
AB  - Two series of crosslinked poly(urethane-ester-siloxane)s were synthesized from α,ω-dihydroxy-(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS- -EO), 4,4'-methylenediphenyl diisocyanate and Boltorn® hyperbranched polyesters of the second and third pseudo generation, by two-step polymerization in solution. The effect of the EO-PDMS-EO content and functionality of the applied crosslinking agent on the morphology and surface properties of the prepared poly(urethane-ester-siloxane)s was investigated by FTIR spectroscopy, small-angle X-ray scattering (SAXS), atomic force microscopy (AFM), scanning electron microscopy (SEM) and water absorption measurement. Different techniques (FTIR peak deconvolution, SAXS and AFM) revealed that decrease of the crosslinking agent functionality and EO-PDMS-EO content promotes microphase separation in the synthesized poly(urethane-ester-siloxane)s. SEM analysis and water absorption experiments showed that, due to the hydrophobic character of EO-PDMS-EO and its ability to migrate to the surface of poly(urethane-ester-siloxane)s, samples synthesized with higher EO-PDMS-EO content and crosslinking agents of lower functionality had more hydrophobic surfaces and better waterproof performances. The obtained results indicate that the synthesis of poly(urethane-ester-siloxane)s based on EO-PDMS-EO and Boltorn® hyperbranched polyesters leads to the creation of networks with interesting morphological and surface properties, which can be easily tailored by changing the content of EO-PDMS-EO segment or functionality of hyperbranched polyester.
AB  - U ovom radu sintetisane su dve serije umreženih poli(uretan-estar-siloksana) (PUS) korišćenjem α,ω-dihidroksi-(etilenoksid-poli(dimetilsiloksan)-etilenoksida) (EO-PDMS-EO), 4,4'-diizocijanatodifenilmetana i dva Boltorn® hiperrazgranata poliestra (HRP) druge i treće pseudo generacije kao umreživača. Svaka serija se sastoji od uzoraka koji imaju različiti udeo mekog segmenta (EO-PDMS-EO). Uticaj funkcionalnosti korišćenog HRP i udela mekog segmenta na morfologiju i površinska svojstva PUS ispitan je primenom FTIR spektroskopije, SAXS, AFM i SEM analize i merenjem količine apsorbovane vode. Pokazano je da sa smanjenjem funkcionalnosti umreživača i udela EO-PDMS-EO dolazi do povećanja stepena mikrofaznog razdvajanja kod sintetisanih PUS. Pored toga, uzorci PUS sa većim udelom mekog segmenta i sintetisani primenom HRP niže funkcionalnosti pokazuju bolju otpornost na vodu.
PB  - Association of Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Investigation of the morphology and surface properties of crosslinked poly(urethane-ester-siloxane)s
T1  - Ispitivanje morfologije i površinskih svojstava umreženih poli(uretan-estar-siloksana)
EP  - 821
IS  - 6
SP  - 813
VL  - 66
DO  - 10.2298/HEMIND121004101D
ER  - 

@article{
author = "Džunuzović, Jasna and Pergal, Marija and Vodnik, Vesna and Špírková, Milena and Poręba, Rafał and Jovanović, Slobodan",
year = "2012",
abstract = "Two series of crosslinked poly(urethane-ester-siloxane)s were synthesized from α,ω-dihydroxy-(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS- -EO), 4,4'-methylenediphenyl diisocyanate and Boltorn® hyperbranched polyesters of the second and third pseudo generation, by two-step polymerization in solution. The effect of the EO-PDMS-EO content and functionality of the applied crosslinking agent on the morphology and surface properties of the prepared poly(urethane-ester-siloxane)s was investigated by FTIR spectroscopy, small-angle X-ray scattering (SAXS), atomic force microscopy (AFM), scanning electron microscopy (SEM) and water absorption measurement. Different techniques (FTIR peak deconvolution, SAXS and AFM) revealed that decrease of the crosslinking agent functionality and EO-PDMS-EO content promotes microphase separation in the synthesized poly(urethane-ester-siloxane)s. SEM analysis and water absorption experiments showed that, due to the hydrophobic character of EO-PDMS-EO and its ability to migrate to the surface of poly(urethane-ester-siloxane)s, samples synthesized with higher EO-PDMS-EO content and crosslinking agents of lower functionality had more hydrophobic surfaces and better waterproof performances. The obtained results indicate that the synthesis of poly(urethane-ester-siloxane)s based on EO-PDMS-EO and Boltorn® hyperbranched polyesters leads to the creation of networks with interesting morphological and surface properties, which can be easily tailored by changing the content of EO-PDMS-EO segment or functionality of hyperbranched polyester., U ovom radu sintetisane su dve serije umreženih poli(uretan-estar-siloksana) (PUS) korišćenjem α,ω-dihidroksi-(etilenoksid-poli(dimetilsiloksan)-etilenoksida) (EO-PDMS-EO), 4,4'-diizocijanatodifenilmetana i dva Boltorn® hiperrazgranata poliestra (HRP) druge i treće pseudo generacije kao umreživača. Svaka serija se sastoji od uzoraka koji imaju različiti udeo mekog segmenta (EO-PDMS-EO). Uticaj funkcionalnosti korišćenog HRP i udela mekog segmenta na morfologiju i površinska svojstva PUS ispitan je primenom FTIR spektroskopije, SAXS, AFM i SEM analize i merenjem količine apsorbovane vode. Pokazano je da sa smanjenjem funkcionalnosti umreživača i udela EO-PDMS-EO dolazi do povećanja stepena mikrofaznog razdvajanja kod sintetisanih PUS. Pored toga, uzorci PUS sa većim udelom mekog segmenta i sintetisani primenom HRP niže funkcionalnosti pokazuju bolju otpornost na vodu.",
publisher = "Association of Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Investigation of the morphology and surface properties of crosslinked poly(urethane-ester-siloxane)s, Ispitivanje morfologije i površinskih svojstava umreženih poli(uretan-estar-siloksana)",
pages = "821-813",
number = "6",
volume = "66",
doi = "10.2298/HEMIND121004101D"
}

Džunuzović, J., Pergal, M., Vodnik, V., Špírková, M., Poręba, R.,& Jovanović, S.. (2012). Investigation of the morphology and surface properties of crosslinked poly(urethane-ester-siloxane)s. in Hemijska industrija
Association of Chemical Engineers of Serbia., 66(6), 813-821.
https://doi.org/10.2298/HEMIND121004101D

Džunuzović J, Pergal M, Vodnik V, Špírková M, Poręba R, Jovanović S. Investigation of the morphology and surface properties of crosslinked poly(urethane-ester-siloxane)s. in Hemijska industrija. 2012;66(6):813-821.
doi:10.2298/HEMIND121004101D .

Džunuzović, Jasna, Pergal, Marija, Vodnik, Vesna, Špírková, Milena, Poręba, Rafał, Jovanović, Slobodan, "Investigation of the morphology and surface properties of crosslinked poly(urethane-ester-siloxane)s" in Hemijska industrija, 66, no. 6 (2012):813-821,
https://doi.org/10.2298/HEMIND121004101D . .

TY  - JOUR
AU  - Džunuzović, Jasna
AU  - Pergal, Marija
AU  - Poreba, Rafal
AU  - Ostojić, Sanja
AU  - Lazić, Nada
AU  - Spirkova, Milena
AU  - Jovanovic, Slobodan
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5740
AB  - Polyurethane networks based on Boltorn hyperbranched polyesters (HBPs) of different pseudogenerations as cross-linkers, alpha,omega-dihydroxy(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS-EO) and 4,4'-methylenediphenyl diisocyanate were synthesized using a two-step polymerization reaction in solution. The influence of the pseudogeneration number of Boltorn HBPs on the thermomechanical and thermal properties and morphologies of polyurethane networks was investigated using FTIR, DMTA, TGA, hardness measurements, SEM, and SAXS. Synthesized polyurethanes showed higher cross-linking density and hardness and lower thermal stability with increasing pseudogeneration number of HBP. Samples with lower EO-PDMS-EO content exhibited slightly better thermal stability and higher hardness. All utilized characterization methods yielded consistent results and confirmed the existence of microphase separated morphology with the appearance of certain microphase mixing between segments as the pseudogeneration number of HBP increased. The obtained results revealed that the synthesized polyurethanes have good thermal and thermomechanical properties, which can be tailored by changing the pseudogeneration number of the HBP or the EO-PDMS-EO content.
PB  - American Chemical Society (ACS)
T2  - Industrial and Engineering Chemistry Research
T1  - Studies of the Thermal and Mechanical Properties of Poly(urethane-siloxane)s Cross-Linked by Hyperbranched Polyesters
EP  - 10832
IS  - 33
SP  - 10824
VL  - 51
DO  - 10.1021/ie300927z
ER  - 

@article{
author = "Džunuzović, Jasna and Pergal, Marija and Poreba, Rafal and Ostojić, Sanja and Lazić, Nada and Spirkova, Milena and Jovanovic, Slobodan",
year = "2012",
abstract = "Polyurethane networks based on Boltorn hyperbranched polyesters (HBPs) of different pseudogenerations as cross-linkers, alpha,omega-dihydroxy(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS-EO) and 4,4'-methylenediphenyl diisocyanate were synthesized using a two-step polymerization reaction in solution. The influence of the pseudogeneration number of Boltorn HBPs on the thermomechanical and thermal properties and morphologies of polyurethane networks was investigated using FTIR, DMTA, TGA, hardness measurements, SEM, and SAXS. Synthesized polyurethanes showed higher cross-linking density and hardness and lower thermal stability with increasing pseudogeneration number of HBP. Samples with lower EO-PDMS-EO content exhibited slightly better thermal stability and higher hardness. All utilized characterization methods yielded consistent results and confirmed the existence of microphase separated morphology with the appearance of certain microphase mixing between segments as the pseudogeneration number of HBP increased. The obtained results revealed that the synthesized polyurethanes have good thermal and thermomechanical properties, which can be tailored by changing the pseudogeneration number of the HBP or the EO-PDMS-EO content.",
publisher = "American Chemical Society (ACS)",
journal = "Industrial and Engineering Chemistry Research",
title = "Studies of the Thermal and Mechanical Properties of Poly(urethane-siloxane)s Cross-Linked by Hyperbranched Polyesters",
pages = "10832-10824",
number = "33",
volume = "51",
doi = "10.1021/ie300927z"
}

Džunuzović, J., Pergal, M., Poreba, R., Ostojić, S., Lazić, N., Spirkova, M.,& Jovanovic, S.. (2012). Studies of the Thermal and Mechanical Properties of Poly(urethane-siloxane)s Cross-Linked by Hyperbranched Polyesters. in Industrial and Engineering Chemistry Research
American Chemical Society (ACS)., 51(33), 10824-10832.
https://doi.org/10.1021/ie300927z

Džunuzović J, Pergal M, Poreba R, Ostojić S, Lazić N, Spirkova M, Jovanovic S. Studies of the Thermal and Mechanical Properties of Poly(urethane-siloxane)s Cross-Linked by Hyperbranched Polyesters. in Industrial and Engineering Chemistry Research. 2012;51(33):10824-10832.
doi:10.1021/ie300927z .

Džunuzović, Jasna, Pergal, Marija, Poreba, Rafal, Ostojić, Sanja, Lazić, Nada, Spirkova, Milena, Jovanovic, Slobodan, "Studies of the Thermal and Mechanical Properties of Poly(urethane-siloxane)s Cross-Linked by Hyperbranched Polyesters" in Industrial and Engineering Chemistry Research, 51, no. 33 (2012):10824-10832,
https://doi.org/10.1021/ie300927z . .

TY  - JOUR
AU  - Džunuzović, Jasna
AU  - Pergal, Marija
AU  - Poreba, Rafal
AU  - Vodnik, Vesna
AU  - Simonović, Branislav
AU  - Spirkova, Milena
AU  - Jovanovic, Slobodan
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5666
AB  - Six polyurethane networks were synthesized from Boltorn (R) hyperbranched polyester of the second pseudo generation, alpha,omega-dihydroxy-(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS-EO) and 4,4'-methylenediphenyl diisocyanate. The effect of the EO-PDMS-EO content on the properties of prepared polyurethanes was investigated by dynamic mechanical thermal analysis (DMTA), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), swelling measurements, water contact angle and water absorption. Different techniques (FTIR peak deconvolution, DMTA and SEM) revealed that decrease of EO-PDMS-EO content promotes microphase separation in the synthesized polyurethanes. Samples synthesized with higher EO-PDMS-EO content have more hydrophobic surface and better waterproof performances, but lower crosslinking density. TGA results suggest that thermal stability of the synthesized polyurethane networks in nitrogen is significantly affected by the mutual influence of the crosslinking density and EO-PDMS-EO content. The results obtained in this work indicate that the synthesis of polyurethanes based on hyperbranched polyester and EO-PDMS-EO leads to the creation of networks with good thermal, thermomechanical and surface properties.
PB  - Elsevier
T2  - Journal of Non-Crystalline Solids
T1  - Analysis of dynamic mechanical, thermal and surface properties of poly(urethane-ester-siloxane) networks based on hyperbranched polyester
EP  - 3169
IS  - 23
SP  - 3161
VL  - 358
DO  - 10.1016/j.jnoncrysol.2012.09.013
ER  - 

@article{
author = "Džunuzović, Jasna and Pergal, Marija and Poreba, Rafal and Vodnik, Vesna and Simonović, Branislav and Spirkova, Milena and Jovanovic, Slobodan",
year = "2012",
abstract = "Six polyurethane networks were synthesized from Boltorn (R) hyperbranched polyester of the second pseudo generation, alpha,omega-dihydroxy-(ethylene oxide-poly(dimethylsiloxane)-ethylene oxide) (EO-PDMS-EO) and 4,4'-methylenediphenyl diisocyanate. The effect of the EO-PDMS-EO content on the properties of prepared polyurethanes was investigated by dynamic mechanical thermal analysis (DMTA), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), swelling measurements, water contact angle and water absorption. Different techniques (FTIR peak deconvolution, DMTA and SEM) revealed that decrease of EO-PDMS-EO content promotes microphase separation in the synthesized polyurethanes. Samples synthesized with higher EO-PDMS-EO content have more hydrophobic surface and better waterproof performances, but lower crosslinking density. TGA results suggest that thermal stability of the synthesized polyurethane networks in nitrogen is significantly affected by the mutual influence of the crosslinking density and EO-PDMS-EO content. The results obtained in this work indicate that the synthesis of polyurethanes based on hyperbranched polyester and EO-PDMS-EO leads to the creation of networks with good thermal, thermomechanical and surface properties.",
publisher = "Elsevier",
journal = "Journal of Non-Crystalline Solids",
title = "Analysis of dynamic mechanical, thermal and surface properties of poly(urethane-ester-siloxane) networks based on hyperbranched polyester",
pages = "3169-3161",
number = "23",
volume = "358",
doi = "10.1016/j.jnoncrysol.2012.09.013"
}

Džunuzović, J., Pergal, M., Poreba, R., Vodnik, V., Simonović, B., Spirkova, M.,& Jovanovic, S.. (2012). Analysis of dynamic mechanical, thermal and surface properties of poly(urethane-ester-siloxane) networks based on hyperbranched polyester. in Journal of Non-Crystalline Solids
Elsevier., 358(23), 3161-3169.
https://doi.org/10.1016/j.jnoncrysol.2012.09.013

Džunuzović J, Pergal M, Poreba R, Vodnik V, Simonović B, Spirkova M, Jovanovic S. Analysis of dynamic mechanical, thermal and surface properties of poly(urethane-ester-siloxane) networks based on hyperbranched polyester. in Journal of Non-Crystalline Solids. 2012;358(23):3161-3169.
doi:10.1016/j.jnoncrysol.2012.09.013 .

Džunuzović, Jasna, Pergal, Marija, Poreba, Rafal, Vodnik, Vesna, Simonović, Branislav, Spirkova, Milena, Jovanovic, Slobodan, "Analysis of dynamic mechanical, thermal and surface properties of poly(urethane-ester-siloxane) networks based on hyperbranched polyester" in Journal of Non-Crystalline Solids, 358, no. 23 (2012):3161-3169,
https://doi.org/10.1016/j.jnoncrysol.2012.09.013 . .

TY  - JOUR
AU  - Pergal, Marija
AU  - Džunuzović, Jasna
AU  - Kicanovic, M.
AU  - Vodnik, Vesna
AU  - Pergal, Miodrag M.
AU  - Jovanovic, S.
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5663
AB  - Novel polyurethanes (PUs) were synthesized using hydroxy-terminated hyperbranched polyester (BH-20) and 4,4'-methylenediphenyl diisocyanate (MDI) as hard segments and hydroxy-terminated ethylene oxide-poly(dimethylsiloxane)-ethylene oxide triblock copolymer (PDMS-EO) as soft segment, with soft segment content ranging from 30 to 60 wt %. The PUs were synthesized by two-step solution polymerization method. The influence of the soft segment content on the structure, swelling behavior and thermal properties of PUs was investigated. According to the results obtained by swelling measurements, the increase of the hard segment content resulted in the increase of the crosslinking density of synthesized samples. DSC results showed that the glass transition temperatures increase from 36 to 65A degrees C with increasing hard segment content. It was demonstrated using thermogravimetric analysis (TGA) that thermal stability of investigated PUs increases with increase of the soft PDMS-EO content. This was concluded from the temperatures corresponding to the 10 wt % loss, which represents the beginning of thermal degradation of samples.
PB  - Maik Nauka/Interperiodica/Springer, New York
T2  - Russian Journal of Physical Chemistry A
T1  - Thermal properties of poly(urethane-ester-siloxane)s based on hyperbranched polyester
EP  - 2256
IS  - 13
SP  - 2251
VL  - 85
DO  - 10.1134/S0036024411130243
ER  - 

@article{
author = "Pergal, Marija and Džunuzović, Jasna and Kicanovic, M. and Vodnik, Vesna and Pergal, Miodrag M. and Jovanovic, S.",
year = "2011",
abstract = "Novel polyurethanes (PUs) were synthesized using hydroxy-terminated hyperbranched polyester (BH-20) and 4,4'-methylenediphenyl diisocyanate (MDI) as hard segments and hydroxy-terminated ethylene oxide-poly(dimethylsiloxane)-ethylene oxide triblock copolymer (PDMS-EO) as soft segment, with soft segment content ranging from 30 to 60 wt %. The PUs were synthesized by two-step solution polymerization method. The influence of the soft segment content on the structure, swelling behavior and thermal properties of PUs was investigated. According to the results obtained by swelling measurements, the increase of the hard segment content resulted in the increase of the crosslinking density of synthesized samples. DSC results showed that the glass transition temperatures increase from 36 to 65A degrees C with increasing hard segment content. It was demonstrated using thermogravimetric analysis (TGA) that thermal stability of investigated PUs increases with increase of the soft PDMS-EO content. This was concluded from the temperatures corresponding to the 10 wt % loss, which represents the beginning of thermal degradation of samples.",
publisher = "Maik Nauka/Interperiodica/Springer, New York",
journal = "Russian Journal of Physical Chemistry A",
title = "Thermal properties of poly(urethane-ester-siloxane)s based on hyperbranched polyester",
pages = "2256-2251",
number = "13",
volume = "85",
doi = "10.1134/S0036024411130243"
}

Pergal, M., Džunuzović, J., Kicanovic, M., Vodnik, V., Pergal, M. M.,& Jovanovic, S.. (2011). Thermal properties of poly(urethane-ester-siloxane)s based on hyperbranched polyester. in Russian Journal of Physical Chemistry A
Maik Nauka/Interperiodica/Springer, New York., 85(13), 2251-2256.
https://doi.org/10.1134/S0036024411130243

Pergal M, Džunuzović J, Kicanovic M, Vodnik V, Pergal MM, Jovanovic S. Thermal properties of poly(urethane-ester-siloxane)s based on hyperbranched polyester. in Russian Journal of Physical Chemistry A. 2011;85(13):2251-2256.
doi:10.1134/S0036024411130243 .

Pergal, Marija, Džunuzović, Jasna, Kicanovic, M., Vodnik, Vesna, Pergal, Miodrag M., Jovanovic, S., "Thermal properties of poly(urethane-ester-siloxane)s based on hyperbranched polyester" in Russian Journal of Physical Chemistry A, 85, no. 13 (2011):2251-2256,
https://doi.org/10.1134/S0036024411130243 . .

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  - Popov-Pergal, Katarina M.
AU  - Poleti, Dejan
AU  - Rancic, Milica P.
AU  - Meden, Antun
AU  - Pergal, Marija
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5616
AB  - The derivatives of 5-substituted-2,4-thiazolidinedione have a broad spectrum of biological activities. In this article, new 5-(arylidene)-3-(4-methylbenzoyl)thiayolidine-2,4-diones 3a-k, with arylidene groups such as 4-phenylbenzylidene 3a, 3,4-dimethoxybenzylidene 3b, 2-hydroxybenzylidene 3c, 4-ethoxybenzylidene 3d, 5-methyl-2-furfurylidene 3e, 4-dimethylaminobenzylidene 3f, 1-naphthylidene 3g, 3,4-methylenedioxybenzylidene 3h, 4-benzyloxybenzylidene 3i, benzylidene 3j, and 4-methoxybenzylidene 3k, were synthesized by direct acylation of alkali metal salts of 5-arylidene-2,4-thiazolidinediones with 4-methylbenzoylchloride. Their structures were confirmed by elemental analysis, IR, (1)H NMR and MS spectroscopy. In addition, crystal structure of the compound 3d was determined using single-crystal X-ray diffraction data.
PB  - Wiley-Blackwell Publishing, Inc, Malden
T2  - Journal of Heterocyclic Chemistry
T1  - Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones
EP  - 228
IS  - 1
SP  - 224
VL  - 47
DO  - 10.1002/jhet.288
ER  - 

@article{
author = "Popov-Pergal, Katarina M. and Poleti, Dejan and Rancic, Milica P. and Meden, Antun and Pergal, Marija",
year = "2010",
abstract = "The derivatives of 5-substituted-2,4-thiazolidinedione have a broad spectrum of biological activities. In this article, new 5-(arylidene)-3-(4-methylbenzoyl)thiayolidine-2,4-diones 3a-k, with arylidene groups such as 4-phenylbenzylidene 3a, 3,4-dimethoxybenzylidene 3b, 2-hydroxybenzylidene 3c, 4-ethoxybenzylidene 3d, 5-methyl-2-furfurylidene 3e, 4-dimethylaminobenzylidene 3f, 1-naphthylidene 3g, 3,4-methylenedioxybenzylidene 3h, 4-benzyloxybenzylidene 3i, benzylidene 3j, and 4-methoxybenzylidene 3k, were synthesized by direct acylation of alkali metal salts of 5-arylidene-2,4-thiazolidinediones with 4-methylbenzoylchloride. Their structures were confirmed by elemental analysis, IR, (1)H NMR and MS spectroscopy. In addition, crystal structure of the compound 3d was determined using single-crystal X-ray diffraction data.",
publisher = "Wiley-Blackwell Publishing, Inc, Malden",
journal = "Journal of Heterocyclic Chemistry",
title = "Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones",
pages = "228-224",
number = "1",
volume = "47",
doi = "10.1002/jhet.288"
}

Popov-Pergal, K. M., Poleti, D., Rancic, M. P., Meden, A.,& Pergal, M.. (2010). Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones. in Journal of Heterocyclic Chemistry
Wiley-Blackwell Publishing, Inc, Malden., 47(1), 224-228.
https://doi.org/10.1002/jhet.288

Popov-Pergal KM, Poleti D, Rancic MP, Meden A, Pergal M. Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones. in Journal of Heterocyclic Chemistry. 2010;47(1):224-228.
doi:10.1002/jhet.288 .

Popov-Pergal, Katarina M., Poleti, Dejan, Rancic, Milica P., Meden, Antun, Pergal, Marija, "Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones" in Journal of Heterocyclic Chemistry, 47, no. 1 (2010):224-228,
https://doi.org/10.1002/jhet.288 . .

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  - Vuković, Jasna
AU  - Pergal, Marija
AU  - Jovanović, Slobodan
AU  - Vodnik, Vesna
PY  - 2008
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5515
AB  - In this paper, two samples of polyurethane (PU) crosslinked with hydroxy -functonal hyperbranched aliphatic polyester of the second pseudo generation were investigated. For the synthesis of these crosslinked PUs two different macrodiols were used: poly(tetramethyleneoxide) (PTMO) for PUPTMO and ethylene oxide-poly(dimethylsiloxane)-ethylene oxide (PDMS-EO) for PUPDMS-EO sample. Synthesized samples behave as elastomers and have yellow color. Obtained results show that swelling degree of the sample PUPDMS-EO in N-methyl-2-pyrrolidinon (NMP) determined at room temperature is higher than for the sample PUPTMO. It has been also observed that thermal properties of these polyurethane networks can be changed by incorporation of siloxane sequences in their structure.
AB  - U ovom radu su prikazani rezultati dobijeni ispitivanjem dva uzorka poliuretana (PU) umrežena hidroksi-funkcionalnim hiperrazgranatim alifatskim poliestrom druge pseudo generacije. Pri sintezi ovih umreženih PU korišćena su dva različita makrodiola: poli(tetrametilenoksid) (PTMO) za sintezu uzorka PUPTMO i etilenoksid-poli(dimetilsiloksan)- etilenoksid (PDMS-EO) za sintezu uzorka PUPDMS-EO. Sintetizovani uzorci se ponašaju kao elastomeri i imaju žuto obojenje. Određivanjem stepena bubrenja u N-metil-2-pirolidonu (NMP) pri sobnoj temperaturi pokazano je da uzorak PUPDMS-EO ima veći stepen bubrenja od uzorka PUPTMO. Primenom termogravimetrije konstatovano je da se uvođenjem siloksanskih sekvenci u korišćeni makrodiol može uticati na termička svojstva sintetizovanih umreženih poliuretana.
PB  - Association of Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Crosslinked polyurethanes based on hyperbranched polymers
T1  - Umreženi poliuretani na bazi hiperrazgranatih polimera
EP  - 359
IS  - 6
SP  - 353
VL  - 62
DO  - 10.2298/HEMIND0806353V
ER  - 

@article{
author = "Vuković, Jasna and Pergal, Marija and Jovanović, Slobodan and Vodnik, Vesna",
year = "2008",
abstract = "In this paper, two samples of polyurethane (PU) crosslinked with hydroxy -functonal hyperbranched aliphatic polyester of the second pseudo generation were investigated. For the synthesis of these crosslinked PUs two different macrodiols were used: poly(tetramethyleneoxide) (PTMO) for PUPTMO and ethylene oxide-poly(dimethylsiloxane)-ethylene oxide (PDMS-EO) for PUPDMS-EO sample. Synthesized samples behave as elastomers and have yellow color. Obtained results show that swelling degree of the sample PUPDMS-EO in N-methyl-2-pyrrolidinon (NMP) determined at room temperature is higher than for the sample PUPTMO. It has been also observed that thermal properties of these polyurethane networks can be changed by incorporation of siloxane sequences in their structure., U ovom radu su prikazani rezultati dobijeni ispitivanjem dva uzorka poliuretana (PU) umrežena hidroksi-funkcionalnim hiperrazgranatim alifatskim poliestrom druge pseudo generacije. Pri sintezi ovih umreženih PU korišćena su dva različita makrodiola: poli(tetrametilenoksid) (PTMO) za sintezu uzorka PUPTMO i etilenoksid-poli(dimetilsiloksan)- etilenoksid (PDMS-EO) za sintezu uzorka PUPDMS-EO. Sintetizovani uzorci se ponašaju kao elastomeri i imaju žuto obojenje. Određivanjem stepena bubrenja u N-metil-2-pirolidonu (NMP) pri sobnoj temperaturi pokazano je da uzorak PUPDMS-EO ima veći stepen bubrenja od uzorka PUPTMO. Primenom termogravimetrije konstatovano je da se uvođenjem siloksanskih sekvenci u korišćeni makrodiol može uticati na termička svojstva sintetizovanih umreženih poliuretana.",
publisher = "Association of Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Crosslinked polyurethanes based on hyperbranched polymers, Umreženi poliuretani na bazi hiperrazgranatih polimera",
pages = "359-353",
number = "6",
volume = "62",
doi = "10.2298/HEMIND0806353V"
}

Vuković, J., Pergal, M., Jovanović, S.,& Vodnik, V.. (2008). Crosslinked polyurethanes based on hyperbranched polymers. in Hemijska industrija
Association of Chemical Engineers of Serbia., 62(6), 353-359.
https://doi.org/10.2298/HEMIND0806353V

Vuković J, Pergal M, Jovanović S, Vodnik V. Crosslinked polyurethanes based on hyperbranched polymers. in Hemijska industrija. 2008;62(6):353-359.
doi:10.2298/HEMIND0806353V .

Vuković, Jasna, Pergal, Marija, Jovanović, Slobodan, Vodnik, Vesna, "Crosslinked polyurethanes based on hyperbranched polymers" in Hemijska industrija, 62, no. 6 (2008):353-359,
https://doi.org/10.2298/HEMIND0806353V . .