TY  - JOUR
AU  - Godiya, Chirag B.
AU  - Marcantoni, Enrico
AU  - Dunjić, Branko
AU  - Tomić, Miloš
AU  - Nikolić, Marija
AU  - Maletaškić, Jelena
AU  - Đonlagić, Jasna
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/13115
AB  - Poly(methyl methacrylate) (PMMA)/clay nanocomposites (NCs) were prepared by suspension polymerization of methyl methacrylate in the presence of two different organoclays (Cloisite 30B, Cloisite 15A) with clay loading ranged from 0.5 to 5 wt%. Increase in molecular weight of the PMMA matrix with addition of the clay was revealed by gel permeation chromatography (GPC) and intrinsic viscosity measurements. As confirmed by X-ray diffraction (XRD), the NCs had an intercalated structure. The organoclays-MMA/PMMA compatibility was investigated by swelling tests and solubility parameter approach. Rheological behavior of PMMA NCs in molten state was analyzed through construction of master curves of complex viscosity, storage, and loss modulus by applying the time-temperature superposition procedure. Melt rheology, scanning electron microscopy (SEM), and UV/Vis spectroscopy results confirmed higher extent of clay dispersion in the NCs with Cloisite 30B. Compared to pure PMMA, all these NCs show increase of glass transition temperature as measured by DSC and improved thermal stability determined by thermogravimetric analysis (TGA). The results obtained by dynamic mechanical analysis showed that the storage modulus of the NCs was higher by incorporation of clay into the PMMA matrix, increasing as the amount of clay increased and that their mechanical performance was significantly enhanced.
T2  - Polymer Bulletin
T1  - Effect of organoclay modifier structure on the viscoelastic and thermal properties of poly(methyl methacrylate)/organoclay nanocomposites
VL  - 78
IS  - 6
SP  - 2911
EP  - 2932
DO  - 10.1007/s00289-020-03248-7
ER  - 

@article{
author = "Godiya, Chirag B. and Marcantoni, Enrico and Dunjić, Branko and Tomić, Miloš and Nikolić, Marija and Maletaškić, Jelena and Đonlagić, Jasna",
year = "2021",
abstract = "Poly(methyl methacrylate) (PMMA)/clay nanocomposites (NCs) were prepared by suspension polymerization of methyl methacrylate in the presence of two different organoclays (Cloisite 30B, Cloisite 15A) with clay loading ranged from 0.5 to 5 wt%. Increase in molecular weight of the PMMA matrix with addition of the clay was revealed by gel permeation chromatography (GPC) and intrinsic viscosity measurements. As confirmed by X-ray diffraction (XRD), the NCs had an intercalated structure. The organoclays-MMA/PMMA compatibility was investigated by swelling tests and solubility parameter approach. Rheological behavior of PMMA NCs in molten state was analyzed through construction of master curves of complex viscosity, storage, and loss modulus by applying the time-temperature superposition procedure. Melt rheology, scanning electron microscopy (SEM), and UV/Vis spectroscopy results confirmed higher extent of clay dispersion in the NCs with Cloisite 30B. Compared to pure PMMA, all these NCs show increase of glass transition temperature as measured by DSC and improved thermal stability determined by thermogravimetric analysis (TGA). The results obtained by dynamic mechanical analysis showed that the storage modulus of the NCs was higher by incorporation of clay into the PMMA matrix, increasing as the amount of clay increased and that their mechanical performance was significantly enhanced.",
journal = "Polymer Bulletin",
title = "Effect of organoclay modifier structure on the viscoelastic and thermal properties of poly(methyl methacrylate)/organoclay nanocomposites",
volume = "78",
number = "6",
pages = "2911-2932",
doi = "10.1007/s00289-020-03248-7"
}

Godiya, C. B., Marcantoni, E., Dunjić, B., Tomić, M., Nikolić, M., Maletaškić, J.,& Đonlagić, J.. (2021). Effect of organoclay modifier structure on the viscoelastic and thermal properties of poly(methyl methacrylate)/organoclay nanocomposites. in Polymer Bulletin, 78(6), 2911-2932.
https://doi.org/10.1007/s00289-020-03248-7

Godiya CB, Marcantoni E, Dunjić B, Tomić M, Nikolić M, Maletaškić J, Đonlagić J. Effect of organoclay modifier structure on the viscoelastic and thermal properties of poly(methyl methacrylate)/organoclay nanocomposites. in Polymer Bulletin. 2021;78(6):2911-2932.
doi:10.1007/s00289-020-03248-7 .

Godiya, Chirag B., Marcantoni, Enrico, Dunjić, Branko, Tomić, Miloš, Nikolić, Marija, Maletaškić, Jelena, Đonlagić, Jasna, "Effect of organoclay modifier structure on the viscoelastic and thermal properties of poly(methyl methacrylate)/organoclay nanocomposites" in Polymer Bulletin, 78, no. 6 (2021):2911-2932,
https://doi.org/10.1007/s00289-020-03248-7 . .

TY  - JOUR
AU  - Mirković, Ilinka
AU  - Nikolić, Marija
AU  - Ostojić, Sanja
AU  - Maletaškić, Jelena
AU  - Petrović, Zoran
AU  - Đonlagić, Jasna
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9718
AB  - Semi-interpenetrating polymer networks (SIPN) based on thermo-responsive poly(N-isopropylacrylamide) (PNIPA) and water-soluble sodium salts of linear hyaluronic acid (Na-HA) were physically cross-linked with synthetic nanoclay (laponite XLG). PNIPA hydrogels with different cross-linking densities and Na-HA concentrations were synthesized by in situ free-radical redox polymerization. The structure and heterogeneity of the semi-IPN hydrogels were examined by SEM and XRD. The content of clay incorporated in the gel was determined by TGA. DSC measurements showed that volume phase transition temperature and its enthalpy varied with the clay and hyaluronic acid content. SIPN hydrogels containing negatively charged polyelectrolyte, Na-HA, exhibited higher Q(e) and faster deswelling rates than the corresponding PNIPA NC hydrogels. The presence of the anionic Na-HA polymer reduced the storage modulus, indicating a weakening of the hydrogel network structure, especially at lower clay contents. The nanocomposite hydrogels exhibited high tan delta values, which increased with increasing Na-HA content.
T2  - Journal of the Serbian Chemical Society
T1  - Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays
VL  - 85
IS  - 9
SP  - 1197
EP  - 1221
DO  - 10.2298/JSC200109023M
ER  - 

@article{
author = "Mirković, Ilinka and Nikolić, Marija and Ostojić, Sanja and Maletaškić, Jelena and Petrović, Zoran and Đonlagić, Jasna",
year = "2020",
abstract = "Semi-interpenetrating polymer networks (SIPN) based on thermo-responsive poly(N-isopropylacrylamide) (PNIPA) and water-soluble sodium salts of linear hyaluronic acid (Na-HA) were physically cross-linked with synthetic nanoclay (laponite XLG). PNIPA hydrogels with different cross-linking densities and Na-HA concentrations were synthesized by in situ free-radical redox polymerization. The structure and heterogeneity of the semi-IPN hydrogels were examined by SEM and XRD. The content of clay incorporated in the gel was determined by TGA. DSC measurements showed that volume phase transition temperature and its enthalpy varied with the clay and hyaluronic acid content. SIPN hydrogels containing negatively charged polyelectrolyte, Na-HA, exhibited higher Q(e) and faster deswelling rates than the corresponding PNIPA NC hydrogels. The presence of the anionic Na-HA polymer reduced the storage modulus, indicating a weakening of the hydrogel network structure, especially at lower clay contents. The nanocomposite hydrogels exhibited high tan delta values, which increased with increasing Na-HA content.",
journal = "Journal of the Serbian Chemical Society",
title = "Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays",
volume = "85",
number = "9",
pages = "1197-1221",
doi = "10.2298/JSC200109023M"
}

Mirković, I., Nikolić, M., Ostojić, S., Maletaškić, J., Petrović, Z.,& Đonlagić, J.. (2020). Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays. in Journal of the Serbian Chemical Society, 85(9), 1197-1221.
https://doi.org/10.2298/JSC200109023M

Mirković I, Nikolić M, Ostojić S, Maletaškić J, Petrović Z, Đonlagić J. Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays. in Journal of the Serbian Chemical Society. 2020;85(9):1197-1221.
doi:10.2298/JSC200109023M .

Mirković, Ilinka, Nikolić, Marija, Ostojić, Sanja, Maletaškić, Jelena, Petrović, Zoran, Đonlagić, Jasna, "Thermo-responsive hydrogels based on poly(N-isopropyl- acrylamide) and hyaluronic acid cross-linked with nanoclays" in Journal of the Serbian Chemical Society, 85, no. 9 (2020):1197-1221,
https://doi.org/10.2298/JSC200109023M . .

TY  - JOUR
AU  - Tomić, Miloš
AU  - Dunjić, Branko
AU  - Nikolić, Marija S.
AU  - Trifković, Kata
AU  - Stanković, Nadežda
AU  - Pavlović, Vladimir B.
AU  - Bajat, Jelena B.
AU  - Đonlagić, Jasna A.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0300944018312487
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8076
AB  - In the present study the commercial multifunctional fatty acid polyamidoamine (PAA) was for the first time simultaneously applied as a curing agent and clay modifier for epoxy/clay nanocomposites (NC) based on diglycidyl ether of bisphenol A. The montmorillonite (Cloisite®Na + ) was modified with different quantities of partially and fully protonated polyamidoamine. The NCs with 0.5 wt% novel organoclay were prepared by solution intercalation method. The major aims of this paper are investigations of the effects of the composition of PAA modified clays on structure, mechanical, barrier properties and corrosion stability on steel substrates of NCs were studied. The thermogravimetric, flame photometry and X-ray diffraction analyses confirmed the efficient modification of clay surface with polyamidoamine, predominantly located within layers. The NCs exhibited an intercalated/exfoliated morphology and the presence of free amino groups and increased content of modifier facilitated dispersion of clay particles within the polymer matrix, as shown by electron microscopy techniques (SEM, TEM). Under an optimized loading of PAA (molar quantity of total amino groups per clay cation exchange capacity of 1.75), the layers in stacks were separated by 5.0 nm and high number of individual layers was present in NC. Clay modified by PAA with free amino groups showed increased storage modulus in the rubbery state, glass transition temperature of NCs, while dumping factor was decreased. The tensile test confirmed that introduction of flexible modifier on the epoxy/clay interface lead to increase in the ultimate tensile strenght and elongation at break by 31% and toughness up to 83%. The electrochemical impedance spectroscopy and permeability tests proved the pronounced barrier effect of clay particles against corrosive species and water vapor when high dispersion degree of clay in NC was achieved. © 2019 Elsevier B.V.
T2  - Progress in Organic Coatings
T1  - Polyamidoamine as a clay modifier and curing agent in preparation of epoxy nanocomposites
VL  - 131
SP  - 311
EP  - 321
DO  - 10.1016/j.porgcoat.2019.02.037
ER  - 

@article{
author = "Tomić, Miloš and Dunjić, Branko and Nikolić, Marija S. and Trifković, Kata and Stanković, Nadežda and Pavlović, Vladimir B. and Bajat, Jelena B. and Đonlagić, Jasna A.",
year = "2019",
abstract = "In the present study the commercial multifunctional fatty acid polyamidoamine (PAA) was for the first time simultaneously applied as a curing agent and clay modifier for epoxy/clay nanocomposites (NC) based on diglycidyl ether of bisphenol A. The montmorillonite (Cloisite®Na + ) was modified with different quantities of partially and fully protonated polyamidoamine. The NCs with 0.5 wt% novel organoclay were prepared by solution intercalation method. The major aims of this paper are investigations of the effects of the composition of PAA modified clays on structure, mechanical, barrier properties and corrosion stability on steel substrates of NCs were studied. The thermogravimetric, flame photometry and X-ray diffraction analyses confirmed the efficient modification of clay surface with polyamidoamine, predominantly located within layers. The NCs exhibited an intercalated/exfoliated morphology and the presence of free amino groups and increased content of modifier facilitated dispersion of clay particles within the polymer matrix, as shown by electron microscopy techniques (SEM, TEM). Under an optimized loading of PAA (molar quantity of total amino groups per clay cation exchange capacity of 1.75), the layers in stacks were separated by 5.0 nm and high number of individual layers was present in NC. Clay modified by PAA with free amino groups showed increased storage modulus in the rubbery state, glass transition temperature of NCs, while dumping factor was decreased. The tensile test confirmed that introduction of flexible modifier on the epoxy/clay interface lead to increase in the ultimate tensile strenght and elongation at break by 31% and toughness up to 83%. The electrochemical impedance spectroscopy and permeability tests proved the pronounced barrier effect of clay particles against corrosive species and water vapor when high dispersion degree of clay in NC was achieved. © 2019 Elsevier B.V.",
journal = "Progress in Organic Coatings",
title = "Polyamidoamine as a clay modifier and curing agent in preparation of epoxy nanocomposites",
volume = "131",
pages = "311-321",
doi = "10.1016/j.porgcoat.2019.02.037"
}

Tomić, M., Dunjić, B., Nikolić, M. S., Trifković, K., Stanković, N., Pavlović, V. B., Bajat, J. B.,& Đonlagić, J. A.. (2019). Polyamidoamine as a clay modifier and curing agent in preparation of epoxy nanocomposites. in Progress in Organic Coatings, 131, 311-321.
https://doi.org/10.1016/j.porgcoat.2019.02.037

Tomić M, Dunjić B, Nikolić MS, Trifković K, Stanković N, Pavlović VB, Bajat JB, Đonlagić JA. Polyamidoamine as a clay modifier and curing agent in preparation of epoxy nanocomposites. in Progress in Organic Coatings. 2019;131:311-321.
doi:10.1016/j.porgcoat.2019.02.037 .

Tomić, Miloš, Dunjić, Branko, Nikolić, Marija S., Trifković, Kata, Stanković, Nadežda, Pavlović, Vladimir B., Bajat, Jelena B., Đonlagić, Jasna A., "Polyamidoamine as a clay modifier and curing agent in preparation of epoxy nanocomposites" in Progress in Organic Coatings, 131 (2019):311-321,
https://doi.org/10.1016/j.porgcoat.2019.02.037 . .

TY  - JOUR
AU  - Tomić, Miloš
AU  - Dunjić, Branko
AU  - Nikolić, Marija S.
AU  - Maletaškić, Jelena
AU  - Pavlović, Vladimir B.
AU  - Bajat, Jelena B.
AU  - Đonlagić, Jasna A.
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1951
AB  - The major aims of this paper are the investigation of the effects of the mixing procedure and the montmorillonite (Mt) surface modification on the structure (optical microscopy, XRD, TEM, SEM), rheological, mechanical properties (DMA, tensile test) and corrosion stability (electrochemical impedance spectroscopy) of clay mineral/epoxy nanocomposite (CPN). Two series of CPN samples were prepared based on diglycidyl ether of bisphenol A (DGEBA) and polyamidoamine curing agent with three organophilic Mt and sodium-montmorillonite (1 wt%). Mt were mixed with DGEBA solution in the powder (direct mixing) and in the form of dispersions, preswollen in a commercial coating thinner (solution intercalation). The commercial Mt (Cloisite 30B) modified by quaternary alkylammonium ions bearing hydroxyl groups and especially Mt functionalized by primary (HDA(+)-Mt) alkylammonium ions, at loadings close to cation exchange capacity (CRC), were significantly swollen by thinner and further uniformly dispersed into CPN. Meanwhile, low gel volumes in thinner were found for more hydrophobic Mt (Cloisite 15A). The compatibility of Mt with solvents was well described by solubility and Flory-Huggins interaction parameters. In contrast to the direct incorporation of Mt powders in CPN, swelling enhanced intercalation of epoxy matrix into Mt, and for HDA(+)-Mt based CPN interlayer spacing reached 4.4 nm. The usage of HDA(+)-Mt organoclay and solution intercalation procedure provided the highest enhancement in rheological parameters (G, G, of Mt/epoxy dispersions and glassy storage modulus, Youngs modulus and barrier properties of cured CPN.
T2  - Applied Clay Science
T1  - Dispersion efficiency of montmorillonites in epoxy nanocomposites using solution intercalation and direct mixing methods
VL  - 154
SP  - 52
EP  - 63
DO  - 10.1016/j.clay.2017.12.047
ER  - 

@article{
author = "Tomić, Miloš and Dunjić, Branko and Nikolić, Marija S. and Maletaškić, Jelena and Pavlović, Vladimir B. and Bajat, Jelena B. and Đonlagić, Jasna A.",
year = "2018",
abstract = "The major aims of this paper are the investigation of the effects of the mixing procedure and the montmorillonite (Mt) surface modification on the structure (optical microscopy, XRD, TEM, SEM), rheological, mechanical properties (DMA, tensile test) and corrosion stability (electrochemical impedance spectroscopy) of clay mineral/epoxy nanocomposite (CPN). Two series of CPN samples were prepared based on diglycidyl ether of bisphenol A (DGEBA) and polyamidoamine curing agent with three organophilic Mt and sodium-montmorillonite (1 wt%). Mt were mixed with DGEBA solution in the powder (direct mixing) and in the form of dispersions, preswollen in a commercial coating thinner (solution intercalation). The commercial Mt (Cloisite 30B) modified by quaternary alkylammonium ions bearing hydroxyl groups and especially Mt functionalized by primary (HDA(+)-Mt) alkylammonium ions, at loadings close to cation exchange capacity (CRC), were significantly swollen by thinner and further uniformly dispersed into CPN. Meanwhile, low gel volumes in thinner were found for more hydrophobic Mt (Cloisite 15A). The compatibility of Mt with solvents was well described by solubility and Flory-Huggins interaction parameters. In contrast to the direct incorporation of Mt powders in CPN, swelling enhanced intercalation of epoxy matrix into Mt, and for HDA(+)-Mt based CPN interlayer spacing reached 4.4 nm. The usage of HDA(+)-Mt organoclay and solution intercalation procedure provided the highest enhancement in rheological parameters (G, G, of Mt/epoxy dispersions and glassy storage modulus, Youngs modulus and barrier properties of cured CPN.",
journal = "Applied Clay Science",
title = "Dispersion efficiency of montmorillonites in epoxy nanocomposites using solution intercalation and direct mixing methods",
volume = "154",
pages = "52-63",
doi = "10.1016/j.clay.2017.12.047"
}

Tomić, M., Dunjić, B., Nikolić, M. S., Maletaškić, J., Pavlović, V. B., Bajat, J. B.,& Đonlagić, J. A.. (2018). Dispersion efficiency of montmorillonites in epoxy nanocomposites using solution intercalation and direct mixing methods. in Applied Clay Science, 154, 52-63.
https://doi.org/10.1016/j.clay.2017.12.047

Tomić M, Dunjić B, Nikolić MS, Maletaškić J, Pavlović VB, Bajat JB, Đonlagić JA. Dispersion efficiency of montmorillonites in epoxy nanocomposites using solution intercalation and direct mixing methods. in Applied Clay Science. 2018;154:52-63.
doi:10.1016/j.clay.2017.12.047 .

Tomić, Miloš, Dunjić, Branko, Nikolić, Marija S., Maletaškić, Jelena, Pavlović, Vladimir B., Bajat, Jelena B., Đonlagić, Jasna A., "Dispersion efficiency of montmorillonites in epoxy nanocomposites using solution intercalation and direct mixing methods" in Applied Clay Science, 154 (2018):52-63,
https://doi.org/10.1016/j.clay.2017.12.047 . .

TY  - JOUR
AU  - Nikolić, Marija S.
AU  - Petrović, Rada
AU  - Veljović, Đorđe N.
AU  - Ćosović, Vladan
AU  - Stanković, Nadežda
AU  - Đonlagić, Jasna A.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1899
AB  - Poly(epsilon-caprolactone) (PCL) based nanocomposites with unmodified and organomodified sepiolites were prepared by solution casting method. The sepiolites were modified with short (3-mercaptopropyl)trimethoxysilane (SEP-SI) by using covalent grafting or with long hexadecylamine (SEP-HDA) by using ionic exchange. In order to reveal the influence of the organomodification on the nanoclay dispersion and the properties of the nano composites XRD, DSC, TG, SEM, TEM, optical microscopy, melt rheology and dynamic-mechanical analyses were performed. A better dispersion was achieved when organomodified sepiolites instead of native ones were used as fillers. As deduced from the melt rheology data, by analysis of the Cole-Cole plots, the best dispersion was obtained for SEP-SI nanoclay. The thermal stability was not improved, however in the initial stages of the thereto-oxidative degradation a delay in the weight loss was observed for nanocomposites with organomodified sepiolites. The mechanical properties of the nanocomposites were improved in comparison to PCL, particularly for those with modified sepiolites. In terms of mechanical properties the use of sepiolite modified with HDA gave the best results, as a consequence of better interaction between longer alkyl hydrophobic part of the organic modificator and the hydrophobic PCL matrix.
T2  - European Polymer Journal
T1  - Effect of sepiolite organomodification on the performance of PCL/sepiolite nanocomposites
VL  - 97
SP  - 198
EP  - 209
DO  - 10.1016/j.eurpolymj.2017.10.010
ER  - 

@article{
author = "Nikolić, Marija S. and Petrović, Rada and Veljović, Đorđe N. and Ćosović, Vladan and Stanković, Nadežda and Đonlagić, Jasna A.",
year = "2017",
abstract = "Poly(epsilon-caprolactone) (PCL) based nanocomposites with unmodified and organomodified sepiolites were prepared by solution casting method. The sepiolites were modified with short (3-mercaptopropyl)trimethoxysilane (SEP-SI) by using covalent grafting or with long hexadecylamine (SEP-HDA) by using ionic exchange. In order to reveal the influence of the organomodification on the nanoclay dispersion and the properties of the nano composites XRD, DSC, TG, SEM, TEM, optical microscopy, melt rheology and dynamic-mechanical analyses were performed. A better dispersion was achieved when organomodified sepiolites instead of native ones were used as fillers. As deduced from the melt rheology data, by analysis of the Cole-Cole plots, the best dispersion was obtained for SEP-SI nanoclay. The thermal stability was not improved, however in the initial stages of the thereto-oxidative degradation a delay in the weight loss was observed for nanocomposites with organomodified sepiolites. The mechanical properties of the nanocomposites were improved in comparison to PCL, particularly for those with modified sepiolites. In terms of mechanical properties the use of sepiolite modified with HDA gave the best results, as a consequence of better interaction between longer alkyl hydrophobic part of the organic modificator and the hydrophobic PCL matrix.",
journal = "European Polymer Journal",
title = "Effect of sepiolite organomodification on the performance of PCL/sepiolite nanocomposites",
volume = "97",
pages = "198-209",
doi = "10.1016/j.eurpolymj.2017.10.010"
}

Nikolić, M. S., Petrović, R., Veljović, Đ. N., Ćosović, V., Stanković, N.,& Đonlagić, J. A.. (2017). Effect of sepiolite organomodification on the performance of PCL/sepiolite nanocomposites. in European Polymer Journal, 97, 198-209.
https://doi.org/10.1016/j.eurpolymj.2017.10.010

Nikolić MS, Petrović R, Veljović ĐN, Ćosović V, Stanković N, Đonlagić JA. Effect of sepiolite organomodification on the performance of PCL/sepiolite nanocomposites. in European Polymer Journal. 2017;97:198-209.
doi:10.1016/j.eurpolymj.2017.10.010 .

Nikolić, Marija S., Petrović, Rada, Veljović, Đorđe N., Ćosović, Vladan, Stanković, Nadežda, Đonlagić, Jasna A., "Effect of sepiolite organomodification on the performance of PCL/sepiolite nanocomposites" in European Polymer Journal, 97 (2017):198-209,
https://doi.org/10.1016/j.eurpolymj.2017.10.010 . .

TY  - JOUR
AU  - Nikolić, Marija S.
AU  - Mitrić, Miodrag
AU  - Dapčević, Aleksandra
AU  - Đonlagić, Jasna A.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/790
AB  - Viscoelastic properties in solid and in melt state of poly(epsilon-caprolactone), PCL, nanocomposites with organomodified clays (Cloisite30B and Cloisite15A) are thoroughly investigated. Although WAXD is insensitive to the difference in the nanocomposites structure, the melt rheology reveals pronounced differences between the two series. Melt yield stress values, obtained from fittings by the Carreau-Yasuda model, are used as a measure of partial exfoliation of the clay. Temperature dependence of the shift factors, used for time-temperature superposition of the modulus curves, yields similar values of the flow activation energies for all the samples. Temperature dependences of the dynamic modulus and loss factor of solid nanocomposites were correlated to the structural differences deduced from the melt rheology. The increase in the storage modulus is compared to the theoretical predictions from the Hal-pin-Tsai model. The effective aspect ratio obtained from this comparison agrees reasonably with the value estimated from the melt rheology. (C) 2015 Wiley Periodicals, Inc.
T2  - Journal of Applied Polymer Science
T1  - Viscoelastic properties of poly(e-caprolactone)/clay nanocomposites in solid and in melt state
VL  - 133
IS  - 3
DO  - 10.1002/app.42896
ER  - 

@article{
author = "Nikolić, Marija S. and Mitrić, Miodrag and Dapčević, Aleksandra and Đonlagić, Jasna A.",
year = "2016",
abstract = "Viscoelastic properties in solid and in melt state of poly(epsilon-caprolactone), PCL, nanocomposites with organomodified clays (Cloisite30B and Cloisite15A) are thoroughly investigated. Although WAXD is insensitive to the difference in the nanocomposites structure, the melt rheology reveals pronounced differences between the two series. Melt yield stress values, obtained from fittings by the Carreau-Yasuda model, are used as a measure of partial exfoliation of the clay. Temperature dependence of the shift factors, used for time-temperature superposition of the modulus curves, yields similar values of the flow activation energies for all the samples. Temperature dependences of the dynamic modulus and loss factor of solid nanocomposites were correlated to the structural differences deduced from the melt rheology. The increase in the storage modulus is compared to the theoretical predictions from the Hal-pin-Tsai model. The effective aspect ratio obtained from this comparison agrees reasonably with the value estimated from the melt rheology. (C) 2015 Wiley Periodicals, Inc.",
journal = "Journal of Applied Polymer Science",
title = "Viscoelastic properties of poly(e-caprolactone)/clay nanocomposites in solid and in melt state",
volume = "133",
number = "3",
doi = "10.1002/app.42896"
}

Nikolić, M. S., Mitrić, M., Dapčević, A.,& Đonlagić, J. A.. (2016). Viscoelastic properties of poly(e-caprolactone)/clay nanocomposites in solid and in melt state. in Journal of Applied Polymer Science, 133(3).
https://doi.org/10.1002/app.42896

Nikolić MS, Mitrić M, Dapčević A, Đonlagić JA. Viscoelastic properties of poly(e-caprolactone)/clay nanocomposites in solid and in melt state. in Journal of Applied Polymer Science. 2016;133(3).
doi:10.1002/app.42896 .

Nikolić, Marija S., Mitrić, Miodrag, Dapčević, Aleksandra, Đonlagić, Jasna A., "Viscoelastic properties of poly(e-caprolactone)/clay nanocomposites in solid and in melt state" in Journal of Applied Polymer Science, 133, no. 3 (2016),
https://doi.org/10.1002/app.42896 . .

TY  - JOUR
AU  - Pergal, Marija V.
AU  - Antić, Vesna V.
AU  - Ostojić, Sanja 
AU  - Marinović-Cincović, Milena
AU  - Đonlagić, Jasna A.
PY  - 2011
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4638
AB  - A series of novel thermoplastic urethane-siloxane copolymers (TPUSs) based on a alpha,omega-dihydroxy-[poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone)] (alpha,omega-dihydroxy-PCL-PDMS-PCL) triblock. copolymer, 4,4-methylenediphenyl diisocyanate (MDI) and 1,4-butanediol (BD) was synthesized. The effects of the content (9-63 mass %) of hard urethane segments and their degree of polymerization on the properties of the segmented TPUSs were investigated. The structure, composition and hard segment degree of polymerization of the hard segments were examined using (1)H- and quantitative (13)C-NMR spectroscopy. The degree of crystallinity of the synthesized copolymers was determined using wide-angle X-ray scattering (WAXS). The surface properties were evaluated by measuring the water contact angle and water absorption. In the series of the TPUSs, the average degree of polymerization of the hard segments was varied from 1.2 to 14.4 MDI-BD units. It was found that average values from 3.8 to 14.4 MDI-BD units were effective segment lengths for crystallization of hard segments, which resulted in an increase in the degree of microphase separation of the copolymers. Spherulite-like superstructures were observed in copolymer films by scanning electron microscopy (SEM), which are believed to arise from the crystallization of the hard segments and/or PCL segments, depending on the content of the hard segments. The surface of the copolymers became more hydrophobic with increasing weight fraction of PDMS. The synthesized copolymers based on a PCL-PDMS-PCL segment showed good thermal stability, which increased with increasing content of soft PDMS segments, as was confirmed by the value of the starting temperature of thermal degradation.
T2  - Journal of the Serbian Chemical Society
T1  - Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer
VL  - 76
IS  - 12
SP  - 1703
EP  - 1723
DO  - 10.2298/JSC110307146P
ER  - 

@article{
author = "Pergal, Marija V. and Antić, Vesna V. and Ostojić, Sanja  and Marinović-Cincović, Milena and Đonlagić, Jasna A.",
year = "2011",
abstract = "A series of novel thermoplastic urethane-siloxane copolymers (TPUSs) based on a alpha,omega-dihydroxy-[poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone)] (alpha,omega-dihydroxy-PCL-PDMS-PCL) triblock. copolymer, 4,4-methylenediphenyl diisocyanate (MDI) and 1,4-butanediol (BD) was synthesized. The effects of the content (9-63 mass %) of hard urethane segments and their degree of polymerization on the properties of the segmented TPUSs were investigated. The structure, composition and hard segment degree of polymerization of the hard segments were examined using (1)H- and quantitative (13)C-NMR spectroscopy. The degree of crystallinity of the synthesized copolymers was determined using wide-angle X-ray scattering (WAXS). The surface properties were evaluated by measuring the water contact angle and water absorption. In the series of the TPUSs, the average degree of polymerization of the hard segments was varied from 1.2 to 14.4 MDI-BD units. It was found that average values from 3.8 to 14.4 MDI-BD units were effective segment lengths for crystallization of hard segments, which resulted in an increase in the degree of microphase separation of the copolymers. Spherulite-like superstructures were observed in copolymer films by scanning electron microscopy (SEM), which are believed to arise from the crystallization of the hard segments and/or PCL segments, depending on the content of the hard segments. The surface of the copolymers became more hydrophobic with increasing weight fraction of PDMS. The synthesized copolymers based on a PCL-PDMS-PCL segment showed good thermal stability, which increased with increasing content of soft PDMS segments, as was confirmed by the value of the starting temperature of thermal degradation.",
journal = "Journal of the Serbian Chemical Society",
title = "Influence of the content of hard segments on the properties of novel urethane-siloxane copolymers based on a poly(epsilon-caprolactone)-b-poly(dimethylsiloxane)-b-poly(epsilon-caprolactone) triblock copolymer",
volume = "76",
number = "12",
pages = "1703-1723",
doi = "10.2298/JSC110307146P"
}

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

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

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

TY  - JOUR
AU  - Pepić, Dragana
AU  - Radoičić, Marija
AU  - Nikolić, Marija
AU  - Đonlagić, Jasna
PY  - 2007
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12271
AB  - Novel poly(ester-ether)s based on poly(butylene succinate) (PBS) as the hard segments and 30 mass % of poly(propylene oxide) (PPO) as the soft segments were synthesized with varying amount of the antioxidant (N,N'-diphenyl-p-phenylenediamine, DPPD). The influences of the addition of DPPD and the impact of post-synthetic treatment by precipitation on the molecular structure, thermal and physical properties, as well as on the storage stability of the biodegradable aliphatic copolyesters, were investigated. The structure and composition of the copolymers were determined by means of 1H-NMR spectroscopy. The molecular weight and polydispersity of the poly(ester-ether)s were evaluated from solution viscosity and GPC measurements. The thermal properties and stability were evaluated, respecttively, by means of DSC and non-isothermal thermogravimetry in an inert nitrogen atmosphere. The biodegradability potential of the polymers was studied in hydrolytic and enzymatic degradation tests with Candida cylindracea lipase by monitoring the weight loss of polymer films after incubation. The weight losses of the samples increased with time and were in the range from 1 to 5 mass % after 4 weeks. GPC analysis confirmed that there were changes in the molecular weight of the copolyesters during both hydrolytic and enzymatic degradation tests, leading to the conclusion that the degradation mechanism of poly(butylene succinate)s modified with PPO occurred through surface erosion and bulk degradation.
T2  - Journal of the Serbian Chemical Society
T1  - The influence of antioxidant and post-synthetic treatment on the properties of biodegradable poly(butylene succinate)s modified with poly(propylene oxide)
T1  - Uticaj antioksiodansa i načina izdvajanja polimera na svojstva biodegradabilnih poli(butilen sukcinata) modifikovanih poli(propilenoksidom)
VL  - 72
IS  - 12
SP  - 1515
EP  - 1531
DO  - 10.2298/JSC0712515P
ER  - 

@article{
author = "Pepić, Dragana and Radoičić, Marija and Nikolić, Marija and Đonlagić, Jasna",
year = "2007",
abstract = "Novel poly(ester-ether)s based on poly(butylene succinate) (PBS) as the hard segments and 30 mass % of poly(propylene oxide) (PPO) as the soft segments were synthesized with varying amount of the antioxidant (N,N'-diphenyl-p-phenylenediamine, DPPD). The influences of the addition of DPPD and the impact of post-synthetic treatment by precipitation on the molecular structure, thermal and physical properties, as well as on the storage stability of the biodegradable aliphatic copolyesters, were investigated. The structure and composition of the copolymers were determined by means of 1H-NMR spectroscopy. The molecular weight and polydispersity of the poly(ester-ether)s were evaluated from solution viscosity and GPC measurements. The thermal properties and stability were evaluated, respecttively, by means of DSC and non-isothermal thermogravimetry in an inert nitrogen atmosphere. The biodegradability potential of the polymers was studied in hydrolytic and enzymatic degradation tests with Candida cylindracea lipase by monitoring the weight loss of polymer films after incubation. The weight losses of the samples increased with time and were in the range from 1 to 5 mass % after 4 weeks. GPC analysis confirmed that there were changes in the molecular weight of the copolyesters during both hydrolytic and enzymatic degradation tests, leading to the conclusion that the degradation mechanism of poly(butylene succinate)s modified with PPO occurred through surface erosion and bulk degradation.",
journal = "Journal of the Serbian Chemical Society",
title = "The influence of antioxidant and post-synthetic treatment on the properties of biodegradable poly(butylene succinate)s modified with poly(propylene oxide), Uticaj antioksiodansa i načina izdvajanja polimera na svojstva biodegradabilnih poli(butilen sukcinata) modifikovanih poli(propilenoksidom)",
volume = "72",
number = "12",
pages = "1515-1531",
doi = "10.2298/JSC0712515P"
}

Pepić, D., Radoičić, M., Nikolić, M.,& Đonlagić, J.. (2007). The influence of antioxidant and post-synthetic treatment on the properties of biodegradable poly(butylene succinate)s modified with poly(propylene oxide). in Journal of the Serbian Chemical Society, 72(12), 1515-1531.
https://doi.org/10.2298/JSC0712515P

Pepić D, Radoičić M, Nikolić M, Đonlagić J. The influence of antioxidant and post-synthetic treatment on the properties of biodegradable poly(butylene succinate)s modified with poly(propylene oxide). in Journal of the Serbian Chemical Society. 2007;72(12):1515-1531.
doi:10.2298/JSC0712515P .

Pepić, Dragana, Radoičić, Marija, Nikolić, Marija, Đonlagić, Jasna, "The influence of antioxidant and post-synthetic treatment on the properties of biodegradable poly(butylene succinate)s modified with poly(propylene oxide)" in Journal of the Serbian Chemical Society, 72, no. 12 (2007):1515-1531,
https://doi.org/10.2298/JSC0712515P . .