Marinović-Cincović, Milena

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  • Marinović-Cincović, Milena (4)

Author's Bibliography

Simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) nanocomposite films with enhanced electrical conductivity and hydrophobicity

Kepić, Dejan P.; Ristić, Ivan S.; Marinović-Cincović, Milena; Perusko, Davor; Spitalsky, Zdenko; Pavlović, Vladimir; Budimir, Milica D.; Siffalović, Peter; Dramicanin, Miroslav D.; Micusik, Matej; Kleinova, Angela; Janigova, Ivica; Marković, Zoran M.; Todorović-Marković, Biljana

(Wiley, Hoboken, 2018)

TY  - JOUR
AU  - Kepić, Dejan P.
AU  - Ristić, Ivan S.
AU  - Marinović-Cincović, Milena
AU  - Perusko, Davor
AU  - Spitalsky, Zdenko
AU  - Pavlović, Vladimir
AU  - Budimir, Milica D.
AU  - Siffalović, Peter
AU  - Dramicanin, Miroslav D.
AU  - Micusik, Matej
AU  - Kleinova, Angela
AU  - Janigova, Ivica
AU  - Marković, Zoran M.
AU  - Todorović-Marković, Biljana
PY  - 2018
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/4778
AB  - This paper reports a simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) (SBS) nanocomposite films employing a vacuum filtration method. Graphene is exfoliated well by an electrochemical procedure and homogeneously dispersed in the polymer matrix. The prepared nanocomposite films were characterized by XRD, Fourier transform IR (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, AFM and SEM. Morphological studies showed that graphene formed a smooth coating over the surface of SBS. The increase in graphene concentration induces the wrinkling of graphene sheets at the composite surface which causes a further increase in surface roughness. The FTIR, Raman and XPS spectra of graphene/SBS nanocomposite films indicate the strong interactions between graphene and the polymer matrix. According to the XRD patterns, introducing SBS into graphene did not modify the graphene structure additionally, i.e. the crystal lattice parameters do not depend on SBS content in graphene/SBS nanocomposite films. The graphene/SBS nanocomposite films also exhibited better hydrophobicity due to the increased surface roughness and lower sheet resistivity (reduced 10 times) compared to exfoliated graphene.
PB  - Wiley, Hoboken
T2  - Polymer International
T1  - Simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) nanocomposite films with enhanced electrical conductivity and hydrophobicity
EP  - 1127
IS  - 8
SP  - 1118
VL  - 67
DO  - 10.1002/pi.5620
ER  - 
@article{
author = "Kepić, Dejan P. and Ristić, Ivan S. and Marinović-Cincović, Milena and Perusko, Davor and Spitalsky, Zdenko and Pavlović, Vladimir and Budimir, Milica D. and Siffalović, Peter and Dramicanin, Miroslav D. and Micusik, Matej and Kleinova, Angela and Janigova, Ivica and Marković, Zoran M. and Todorović-Marković, Biljana",
year = "2018",
abstract = "This paper reports a simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) (SBS) nanocomposite films employing a vacuum filtration method. Graphene is exfoliated well by an electrochemical procedure and homogeneously dispersed in the polymer matrix. The prepared nanocomposite films were characterized by XRD, Fourier transform IR (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, AFM and SEM. Morphological studies showed that graphene formed a smooth coating over the surface of SBS. The increase in graphene concentration induces the wrinkling of graphene sheets at the composite surface which causes a further increase in surface roughness. The FTIR, Raman and XPS spectra of graphene/SBS nanocomposite films indicate the strong interactions between graphene and the polymer matrix. According to the XRD patterns, introducing SBS into graphene did not modify the graphene structure additionally, i.e. the crystal lattice parameters do not depend on SBS content in graphene/SBS nanocomposite films. The graphene/SBS nanocomposite films also exhibited better hydrophobicity due to the increased surface roughness and lower sheet resistivity (reduced 10 times) compared to exfoliated graphene.",
publisher = "Wiley, Hoboken",
journal = "Polymer International",
title = "Simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) nanocomposite films with enhanced electrical conductivity and hydrophobicity",
pages = "1127-1118",
number = "8",
volume = "67",
doi = "10.1002/pi.5620"
}
Kepić, D. P., Ristić, I. S., Marinović-Cincović, M., Perusko, D., Spitalsky, Z., Pavlović, V., Budimir, M. D., Siffalović, P., Dramicanin, M. D., Micusik, M., Kleinova, A., Janigova, I., Marković, Z. M.,& Todorović-Marković, B.. (2018). Simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) nanocomposite films with enhanced electrical conductivity and hydrophobicity. in Polymer International
Wiley, Hoboken., 67(8), 1118-1127.
https://doi.org/10.1002/pi.5620
Kepić DP, Ristić IS, Marinović-Cincović M, Perusko D, Spitalsky Z, Pavlović V, Budimir MD, Siffalović P, Dramicanin MD, Micusik M, Kleinova A, Janigova I, Marković ZM, Todorović-Marković B. Simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) nanocomposite films with enhanced electrical conductivity and hydrophobicity. in Polymer International. 2018;67(8):1118-1127.
doi:10.1002/pi.5620 .
Kepić, Dejan P., Ristić, Ivan S., Marinović-Cincović, Milena, Perusko, Davor, Spitalsky, Zdenko, Pavlović, Vladimir, Budimir, Milica D., Siffalović, Peter, Dramicanin, Miroslav D., Micusik, Matej, Kleinova, Angela, Janigova, Ivica, Marković, Zoran M., Todorović-Marković, Biljana, "Simple route for the preparation of graphene/poly(styrene-b-butadiene-b-styrene) nanocomposite films with enhanced electrical conductivity and hydrophobicity" in Polymer International, 67, no. 8 (2018):1118-1127,
https://doi.org/10.1002/pi.5620 . .
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Semi-transparent, conductive thin films of electrochemical exfoliated graphene

Marković, Z.M.; Budimir, Milica D.; Kepić, Dejan P.; Holclajtner-Antunović, Ivanka; Marinović-Cincović, Milena; Dramicanin, Miroslav D.; Spasojević, V.D.; Perusko, Davor; Spitalsky, Z.; Micusik, M.; Pavlović, Vladimir; Todorović-Marković, Biljana

(Royal Soc Chemistry, Cambridge, 2016)

TY  - JOUR
AU  - Marković, Z.M.
AU  - Budimir, Milica D.
AU  - Kepić, Dejan P.
AU  - Holclajtner-Antunović, Ivanka
AU  - Marinović-Cincović, Milena
AU  - Dramicanin, Miroslav D.
AU  - Spasojević, V.D.
AU  - Perusko, Davor
AU  - Spitalsky, Z.
AU  - Micusik, M.
AU  - Pavlović, Vladimir
AU  - Todorović-Marković, Biljana
PY  - 2016
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/4203
AB  - The electrochemical exfoliation of graphite to give one-atom-thick graphene with desirable properties is a green, cost-effective method for high-yield graphene production. This paper presents the results of electrochemical exfoliation of two different graphite precursors under an applied direct current voltage of +12 V. The used characterization techniques (elemental analysis, Fourier transform infrared spectroscopy, X-ray diffraction, X-photoelectron spectroscopy, Raman spectroscopy, field emission scanning electron microscopy and atomic force microscopy) showed that the exfoliated powder is highly functionalized with a low carbon/oxygen content that is similar to graphene oxide. The exfoliated graphene sheets dispersed in N,N'-dimethylformamide were deposited on ano-discs by vacuum filtration and transferred to glass ceramic substrates. The thermal annealing of the as-deposited films at 600 degrees C for 30 minutes resulted in an increase in the carbon/oxygen ratio by more than 3 fold and a decrease in the sheet resistance by 25%. The lowest values for the sheet resistance of the annealed graphene thin films were in the range of 0.32 +/- 0.04 to 0.84 +/- 0.1 kohm sq(-1) depending on the graphite source that was used.
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Semi-transparent, conductive thin films of electrochemical exfoliated graphene
EP  - 39283
IS  - 45
SP  - 39275
VL  - 6
DO  - 10.1039/c6ra04250c
ER  - 
@article{
author = "Marković, Z.M. and Budimir, Milica D. and Kepić, Dejan P. and Holclajtner-Antunović, Ivanka and Marinović-Cincović, Milena and Dramicanin, Miroslav D. and Spasojević, V.D. and Perusko, Davor and Spitalsky, Z. and Micusik, M. and Pavlović, Vladimir and Todorović-Marković, Biljana",
year = "2016",
abstract = "The electrochemical exfoliation of graphite to give one-atom-thick graphene with desirable properties is a green, cost-effective method for high-yield graphene production. This paper presents the results of electrochemical exfoliation of two different graphite precursors under an applied direct current voltage of +12 V. The used characterization techniques (elemental analysis, Fourier transform infrared spectroscopy, X-ray diffraction, X-photoelectron spectroscopy, Raman spectroscopy, field emission scanning electron microscopy and atomic force microscopy) showed that the exfoliated powder is highly functionalized with a low carbon/oxygen content that is similar to graphene oxide. The exfoliated graphene sheets dispersed in N,N'-dimethylformamide were deposited on ano-discs by vacuum filtration and transferred to glass ceramic substrates. The thermal annealing of the as-deposited films at 600 degrees C for 30 minutes resulted in an increase in the carbon/oxygen ratio by more than 3 fold and a decrease in the sheet resistance by 25%. The lowest values for the sheet resistance of the annealed graphene thin films were in the range of 0.32 +/- 0.04 to 0.84 +/- 0.1 kohm sq(-1) depending on the graphite source that was used.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Semi-transparent, conductive thin films of electrochemical exfoliated graphene",
pages = "39283-39275",
number = "45",
volume = "6",
doi = "10.1039/c6ra04250c"
}
Marković, Z.M., Budimir, M. D., Kepić, D. P., Holclajtner-Antunović, I., Marinović-Cincović, M., Dramicanin, M. D., Spasojević, V.D., Perusko, D., Spitalsky, Z., Micusik, M., Pavlović, V.,& Todorović-Marković, B.. (2016). Semi-transparent, conductive thin films of electrochemical exfoliated graphene. in RSC Advances
Royal Soc Chemistry, Cambridge., 6(45), 39275-39283.
https://doi.org/10.1039/c6ra04250c
Marković Z, Budimir MD, Kepić DP, Holclajtner-Antunović I, Marinović-Cincović M, Dramicanin MD, Spasojević V, Perusko D, Spitalsky Z, Micusik M, Pavlović V, Todorović-Marković B. Semi-transparent, conductive thin films of electrochemical exfoliated graphene. in RSC Advances. 2016;6(45):39275-39283.
doi:10.1039/c6ra04250c .
Marković, Z.M., Budimir, Milica D., Kepić, Dejan P., Holclajtner-Antunović, Ivanka, Marinović-Cincović, Milena, Dramicanin, Miroslav D., Spasojević, V.D., Perusko, Davor, Spitalsky, Z., Micusik, M., Pavlović, Vladimir, Todorović-Marković, Biljana, "Semi-transparent, conductive thin films of electrochemical exfoliated graphene" in RSC Advances, 6, no. 45 (2016):39275-39283,
https://doi.org/10.1039/c6ra04250c . .
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Comparison of structural properties of pristine and gamma irradiated single-wall carbon nanotubes: Effects of medium and irradiation dose

Kleut, D.; Jovanović, S.; Marković, Z.; Kepić, Dejan P.; Tosić, D.; Romcević, N.; Marinović-Cincović, Milena; Dramicanin, Miroslav D.; Holclajtner-Antunović, Ivanka; Pavlović, Vladimir; Drazić, G.; Milosavljević, M.; Todorović-Marković, Biljana

(Elsevier Science Inc, New York, 2012)

TY  - JOUR
AU  - Kleut, D.
AU  - Jovanović, S.
AU  - Marković, Z.
AU  - Kepić, Dejan P.
AU  - Tosić, D.
AU  - Romcević, N.
AU  - Marinović-Cincović, Milena
AU  - Dramicanin, Miroslav D.
AU  - Holclajtner-Antunović, Ivanka
AU  - Pavlović, Vladimir
AU  - Drazić, G.
AU  - Milosavljević, M.
AU  - Todorović-Marković, Biljana
PY  - 2012
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/2980
AB  - A systematic study of the gamma irradiation effects on single wall carbon nanotube (SWCNT) structure was conducted. Nanotubes were exposed to different doses of gamma irradiation in three media. Irradiation was carried out in air, water and aqueous ammonia. Thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), elemental analysis (EA) and Raman spectroscopy confirmed the changes in the SWCNT structure. TGA measurements showed the highest percentage of introduced groups for the SWCNTs irradiated with 100 kGy. FTIR spectroscopy provided evidence for the attachment of hydroxyl, carboxyl and nitrile functional groups to the SWCNT sidewalls. Those groups were confirmed by EA. All irradiated SWCNTs had hydroxyl and carboxyl groups irrelevant to media used for irradiation, but nitrile functional groups were only identified in SWCNTs irradiated in aqueous ammonia. Raman spectroscopy indicated that the degree of disorder in the carbon nanotube structure correlates with the irradiation dose. For the nanotubes irradiated with the dose of 100 kGy, the Raman I-D/I-G ratio was three times higher than for the pristine ones. Atomic force microscopy showed a 50% decrease in nanotube length at a radiation dose of 100 kGy. Scanning and transmission electron microscopies showed significant changes in the morphology and structure of gamma irradiated SWCNTs.
PB  - Elsevier Science Inc, New York
T2  - Materials Characterization
T1  - Comparison of structural properties of pristine and gamma irradiated single-wall carbon nanotubes: Effects of medium and irradiation dose
EP  - 45
SP  - 37
VL  - 72
DO  - 10.1016/j.matchar.2012.07.002
ER  - 
@article{
author = "Kleut, D. and Jovanović, S. and Marković, Z. and Kepić, Dejan P. and Tosić, D. and Romcević, N. and Marinović-Cincović, Milena and Dramicanin, Miroslav D. and Holclajtner-Antunović, Ivanka and Pavlović, Vladimir and Drazić, G. and Milosavljević, M. and Todorović-Marković, Biljana",
year = "2012",
abstract = "A systematic study of the gamma irradiation effects on single wall carbon nanotube (SWCNT) structure was conducted. Nanotubes were exposed to different doses of gamma irradiation in three media. Irradiation was carried out in air, water and aqueous ammonia. Thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), elemental analysis (EA) and Raman spectroscopy confirmed the changes in the SWCNT structure. TGA measurements showed the highest percentage of introduced groups for the SWCNTs irradiated with 100 kGy. FTIR spectroscopy provided evidence for the attachment of hydroxyl, carboxyl and nitrile functional groups to the SWCNT sidewalls. Those groups were confirmed by EA. All irradiated SWCNTs had hydroxyl and carboxyl groups irrelevant to media used for irradiation, but nitrile functional groups were only identified in SWCNTs irradiated in aqueous ammonia. Raman spectroscopy indicated that the degree of disorder in the carbon nanotube structure correlates with the irradiation dose. For the nanotubes irradiated with the dose of 100 kGy, the Raman I-D/I-G ratio was three times higher than for the pristine ones. Atomic force microscopy showed a 50% decrease in nanotube length at a radiation dose of 100 kGy. Scanning and transmission electron microscopies showed significant changes in the morphology and structure of gamma irradiated SWCNTs.",
publisher = "Elsevier Science Inc, New York",
journal = "Materials Characterization",
title = "Comparison of structural properties of pristine and gamma irradiated single-wall carbon nanotubes: Effects of medium and irradiation dose",
pages = "45-37",
volume = "72",
doi = "10.1016/j.matchar.2012.07.002"
}
Kleut, D., Jovanović, S., Marković, Z., Kepić, D. P., Tosić, D., Romcević, N., Marinović-Cincović, M., Dramicanin, M. D., Holclajtner-Antunović, I., Pavlović, V., Drazić, G., Milosavljević, M.,& Todorović-Marković, B.. (2012). Comparison of structural properties of pristine and gamma irradiated single-wall carbon nanotubes: Effects of medium and irradiation dose. in Materials Characterization
Elsevier Science Inc, New York., 72, 37-45.
https://doi.org/10.1016/j.matchar.2012.07.002
Kleut D, Jovanović S, Marković Z, Kepić DP, Tosić D, Romcević N, Marinović-Cincović M, Dramicanin MD, Holclajtner-Antunović I, Pavlović V, Drazić G, Milosavljević M, Todorović-Marković B. Comparison of structural properties of pristine and gamma irradiated single-wall carbon nanotubes: Effects of medium and irradiation dose. in Materials Characterization. 2012;72:37-45.
doi:10.1016/j.matchar.2012.07.002 .
Kleut, D., Jovanović, S., Marković, Z., Kepić, Dejan P., Tosić, D., Romcević, N., Marinović-Cincović, Milena, Dramicanin, Miroslav D., Holclajtner-Antunović, Ivanka, Pavlović, Vladimir, Drazić, G., Milosavljević, M., Todorović-Marković, Biljana, "Comparison of structural properties of pristine and gamma irradiated single-wall carbon nanotubes: Effects of medium and irradiation dose" in Materials Characterization, 72 (2012):37-45,
https://doi.org/10.1016/j.matchar.2012.07.002 . .
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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 V.; Antić, Vesna; Ostojić, Sanja; Marinović-Cincović, Milena; Djonlagić, Jasna

(Srpsko hemijsko društvo, Beograd, 2011)

TY  - JOUR
AU  - Pergal, Marija V.
AU  - Antić, Vesna
AU  - Ostojić, Sanja
AU  - Marinović-Cincović, Milena
AU  - Djonlagić, Jasna
PY  - 2011
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/2697
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  - Srpsko hemijsko društvo, Beograd
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 V. and Antić, Vesna and Ostojić, Sanja and Marinović-Cincović, Milena and Djonlagić, 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 = "Srpsko hemijsko društvo, Beograd",
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. V., Antić, V., Ostojić, S., Marinović-Cincović, M.,& Djonlagić, 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
Srpsko hemijsko društvo, Beograd., 76(12), 1703-1723.
https://doi.org/10.2298/JSC110307146P
Pergal MV, Antić V, Ostojić S, Marinović-Cincović M, Djonlagić 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 V., Antić, Vesna, Ostojić, Sanja, Marinović-Cincović, Milena, Djonlagić, 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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