Milošević, Milena

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orcid::0000-0002-4949-5062
  • Milošević, Milena (5)
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Author's Bibliography

Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties

Gavrilović-Grmuša, Ivana; Rančić, Milica; Tesić, Tamara; Stupar, Stevan; Milošević, Milena; Gržetić, Jelena

(2024)

TY  - JOUR
AU  - Gavrilović-Grmuša, Ivana
AU  - Rančić, Milica
AU  - Tesić, Tamara
AU  - Stupar, Stevan
AU  - Milošević, Milena
AU  - Gržetić, Jelena
PY  - 2024
UR  - https://omorika.sfb.bg.ac.rs/handle/123456789/1508
AB  - The possibility of producing and designing bio-epoxides based on the natural polyphenol lignin/epoxidized lignin and tannic acids for application as wood adhesives is presented in this work. Lignin and tannic acids contain numerous reactive hydroxyl phenolic moieties capable of being efficiently involved in the reaction with commercial epoxy resins as a substitute for commercial, non-environmentally friendly, toxic amine-based hardeners. Furthermore, lignin was epoxidized in order to obtain an epoxy lignin that can be a replacement for diglycidyl ether bisphenol A (DGEBA). Cross-linking of bio-epoxy epoxides was investigated via FTIR spectroscopy and their prospects for wood adhesive application were evaluated. This study determined that the curing reaction of epoxy resin can be conducted using lignin/epoxy lignin or tannic acid. Tensile shear strength testing results showed that lignin and tannic acid can effectively replace amine hardeners in epoxy resins. Examination of the failure of the samples showed that all samples had a 100% fracture through the wood. All samples of bio-epoxy adhesives displayed significant tensile shear strength in the range of 5.84-10.87 MPa. This study presents an innovative approach to creating novel cross-linked networks of eco-friendly and high-performance wood bio-adhesives.
T2  - Polymers
T1  - Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties
IS  - 18
VL  - 16
DO  - 10.3390/polym16182602
UR  - conv_1824
ER  - 
@article{
author = "Gavrilović-Grmuša, Ivana and Rančić, Milica and Tesić, Tamara and Stupar, Stevan and Milošević, Milena and Gržetić, Jelena",
year = "2024",
abstract = "The possibility of producing and designing bio-epoxides based on the natural polyphenol lignin/epoxidized lignin and tannic acids for application as wood adhesives is presented in this work. Lignin and tannic acids contain numerous reactive hydroxyl phenolic moieties capable of being efficiently involved in the reaction with commercial epoxy resins as a substitute for commercial, non-environmentally friendly, toxic amine-based hardeners. Furthermore, lignin was epoxidized in order to obtain an epoxy lignin that can be a replacement for diglycidyl ether bisphenol A (DGEBA). Cross-linking of bio-epoxy epoxides was investigated via FTIR spectroscopy and their prospects for wood adhesive application were evaluated. This study determined that the curing reaction of epoxy resin can be conducted using lignin/epoxy lignin or tannic acid. Tensile shear strength testing results showed that lignin and tannic acid can effectively replace amine hardeners in epoxy resins. Examination of the failure of the samples showed that all samples had a 100% fracture through the wood. All samples of bio-epoxy adhesives displayed significant tensile shear strength in the range of 5.84-10.87 MPa. This study presents an innovative approach to creating novel cross-linked networks of eco-friendly and high-performance wood bio-adhesives.",
journal = "Polymers",
title = "Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties",
number = "18",
volume = "16",
doi = "10.3390/polym16182602",
url = "conv_1824"
}
Gavrilović-Grmuša, I., Rančić, M., Tesić, T., Stupar, S., Milošević, M.,& Gržetić, J.. (2024). Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties. in Polymers, 16(18).
https://doi.org/10.3390/polym16182602
conv_1824
Gavrilović-Grmuša I, Rančić M, Tesić T, Stupar S, Milošević M, Gržetić J. Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties. in Polymers. 2024;16(18).
doi:10.3390/polym16182602
conv_1824 .
Gavrilović-Grmuša, Ivana, Rančić, Milica, Tesić, Tamara, Stupar, Stevan, Milošević, Milena, Gržetić, Jelena, "Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties" in Polymers, 16, no. 18 (2024),
https://doi.org/10.3390/polym16182602 .,
conv_1824 .

One-Pot Syntheses of PET-Based Plasticizer and Tetramethyl Thiuram Monosulfide (TMTS) as Vulcanization Accelerator for Rubber Production

Milentijević, Goran; Milošević, Milena; Milojević, Svetomir; Marković, Smiljana; Rančić, Milica; Marinković, Aleksandar; Milosavljević, Milutin

(2023)

TY  - JOUR
AU  - Milentijević, Goran
AU  - Milošević, Milena
AU  - Milojević, Svetomir
AU  - Marković, Smiljana
AU  - Rančić, Milica
AU  - Marinković, Aleksandar
AU  - Milosavljević, Milutin
PY  - 2023
UR  - https://omorika.sfb.bg.ac.rs/handle/123456789/1427
AB  - Styrene-butadiene (SBR) and acrylonitrile-butadiene (NBR) rubber blends with tetramethyl thiuram disulfide (TMTD) and tetramethyl thiuram monosulfide (TMTS) accelerators and environmentally friendly plasticizers, obtained from PET recycling and biobased resources (LA/PG/PET/EG/LA), were prepared. The mechanical properties of the obtained rubber products were tested and compared with those of commercial dioctyl terephthalate (DOTP). TMTS was prepared by simple and efficient one-pot synthesis from dimethylamine, carbon disulfide, potassium cyanide, and ammonium chloride as catalysts in recycled isopropanol/water azeotrope as solvent. In a comparative study, methoxide, ethoxide, iodide, and amide ions were also used. The two-step reaction mechanism of TMTS synthesis involves the oxidation of the amine salt of dimethyldithiocarbamic acid to TMTD by hydrogen peroxide and sulfur elimination from the TMTD disulfide bond. Potassium cyanide appears to be the most efficient nucleophile. The simplicity of operation, mild reaction conditions, solvent recycling, high yields, and applicability to the industrial level are the advantages of this process. Shore hardness, tensile strength, and compression test results of vulcanized blends before and after aging showed similar properties for both accelerators, while somewhat better results were obtained with LA/PG/PET/EG/LA plasticizer.
T2  - Processes
T1  - One-Pot Syntheses of PET-Based Plasticizer and Tetramethyl Thiuram Monosulfide (TMTS) as Vulcanization Accelerator for Rubber Production
IS  - 4
VL  - 11
DO  - 10.3390/pr11041033
UR  - conv_1699
ER  - 
@article{
author = "Milentijević, Goran and Milošević, Milena and Milojević, Svetomir and Marković, Smiljana and Rančić, Milica and Marinković, Aleksandar and Milosavljević, Milutin",
year = "2023",
abstract = "Styrene-butadiene (SBR) and acrylonitrile-butadiene (NBR) rubber blends with tetramethyl thiuram disulfide (TMTD) and tetramethyl thiuram monosulfide (TMTS) accelerators and environmentally friendly plasticizers, obtained from PET recycling and biobased resources (LA/PG/PET/EG/LA), were prepared. The mechanical properties of the obtained rubber products were tested and compared with those of commercial dioctyl terephthalate (DOTP). TMTS was prepared by simple and efficient one-pot synthesis from dimethylamine, carbon disulfide, potassium cyanide, and ammonium chloride as catalysts in recycled isopropanol/water azeotrope as solvent. In a comparative study, methoxide, ethoxide, iodide, and amide ions were also used. The two-step reaction mechanism of TMTS synthesis involves the oxidation of the amine salt of dimethyldithiocarbamic acid to TMTD by hydrogen peroxide and sulfur elimination from the TMTD disulfide bond. Potassium cyanide appears to be the most efficient nucleophile. The simplicity of operation, mild reaction conditions, solvent recycling, high yields, and applicability to the industrial level are the advantages of this process. Shore hardness, tensile strength, and compression test results of vulcanized blends before and after aging showed similar properties for both accelerators, while somewhat better results were obtained with LA/PG/PET/EG/LA plasticizer.",
journal = "Processes",
title = "One-Pot Syntheses of PET-Based Plasticizer and Tetramethyl Thiuram Monosulfide (TMTS) as Vulcanization Accelerator for Rubber Production",
number = "4",
volume = "11",
doi = "10.3390/pr11041033",
url = "conv_1699"
}
Milentijević, G., Milošević, M., Milojević, S., Marković, S., Rančić, M., Marinković, A.,& Milosavljević, M.. (2023). One-Pot Syntheses of PET-Based Plasticizer and Tetramethyl Thiuram Monosulfide (TMTS) as Vulcanization Accelerator for Rubber Production. in Processes, 11(4).
https://doi.org/10.3390/pr11041033
conv_1699
Milentijević G, Milošević M, Milojević S, Marković S, Rančić M, Marinković A, Milosavljević M. One-Pot Syntheses of PET-Based Plasticizer and Tetramethyl Thiuram Monosulfide (TMTS) as Vulcanization Accelerator for Rubber Production. in Processes. 2023;11(4).
doi:10.3390/pr11041033
conv_1699 .
Milentijević, Goran, Milošević, Milena, Milojević, Svetomir, Marković, Smiljana, Rančić, Milica, Marinković, Aleksandar, Milosavljević, Milutin, "One-Pot Syntheses of PET-Based Plasticizer and Tetramethyl Thiuram Monosulfide (TMTS) as Vulcanization Accelerator for Rubber Production" in Processes, 11, no. 4 (2023),
https://doi.org/10.3390/pr11041033 .,
conv_1699 .
1
1
1

Vatrootporni kompoziti na bazi akril-funkcionalizovanog lignina i poliesterske smole dobijene od otpadnog poli(etilen tereftalata)

Knežević, Nataša; Jovanović, Aleksandar; Bošnjaković, Jovan; Milošević, Milena; Rančić, Milica; Marinković, Aleksandar; Gržetić, Jelena; Gamoudi, Houda

(Vojnotehnički institut, Beograd, 2022)

TY  - JOUR
AU  - Knežević, Nataša
AU  - Jovanović, Aleksandar
AU  - Bošnjaković, Jovan
AU  - Milošević, Milena
AU  - Rančić, Milica
AU  - Marinković, Aleksandar
AU  - Gržetić, Jelena
AU  - Gamoudi, Houda
PY  - 2022
UR  - https://omorika.sfb.bg.ac.rs/handle/123456789/1356
AB  - U ovom radu ispitivan je potencijal korišćenja akril-funkcionalizovanog kraft lignina (AKL) u smanjenju zapaljivosti polimernih kompozita na bazi recikliranih nezasićenih poliesterskih smola (NZPS). Akrilna funkcionalizacija kraft lignina je izvedena direktnom esterifikacijom slobodnih polifenolnih grupa sa akriloil hloridom, nakon čega je AKL umešan u NZP smolu sintetizovanu od poliola dobijenih katalitičkom depolimerizacijom otpadnog poli(etilen tereftalata). AKL je homogenizovan sa NZPS pri različitim masenim udelima: 2,5, 5,0, 7,5 i 12,5 mas.%. Strukturne i dinamičko-mehaničke karakteristike akril-funkcionalizovanog kraft lignina i kompozita određene su primenom FTIR spektroskopije, dinamičkomehaničke analize (DMA) i testova jednoosnog zatezanja. Proučavan je uticaj funkcionalizacije i masenog udela AKL na zatezna i termička svojstva NZPS. Vatrootporna svojstva kompozita su ispitivana prema standardnoj UL-94V metodi, na osnovu koje je kompozit sa 12,5 tež. % akril-funkcionalizovanog lignina dostigao najvišu kategorija toplotno otpornih materijala.
AB  - This paper investigates the using potential of acryl-functionalized kraft lignin (AKL) in reducing the flammability of polymer composites based on recycled unsaturated polyester resins (UPR). Acryl functionalization of kraft lignin was performed by direct esterification of free polyphenolic groups with acryloyl chloride, after what, the AKL was blended in UPR resin synthesized from the polyols obtained by catalytic depolymerization of waste poly(ethylene terephthalate). The AKL was homogenized in UPR resin in different weight ratios: 2.5, 5.0, 7.5, and 12.5 wt.%. Structural and dynamic-mechanical characteristics of acryl-functionalized kraft lignin and composites were determined using FTIR spectroscopy, dynamicmechanical analysis (DMA), and tensile tests. The influence of functionalization and mass fraction of AKL on tensile and thermal properties of UPR resin was studied. The thermal properties of the composite were tested according to the standard UL-94 method, based on which the highest category of heat-resistant materials is a composite with 12.5 wt.% acylfunctionalized lignin.
PB  - Vojnotehnički institut, Beograd
T2  - Scientific Technical Review
T1  - Vatrootporni kompoziti na bazi akril-funkcionalizovanog lignina i poliesterske smole dobijene od otpadnog poli(etilen tereftalata)
T1  - Fire-resistant composites based on acrylic-functionalized lignin and polyester resin obtained from waste poly(ethylene terephthalate)
EP  - 37
IS  - 2
SP  - 32
VL  - 72
DO  - 10.5937/str2202032K
UR  - conv_736
ER  - 
@article{
author = "Knežević, Nataša and Jovanović, Aleksandar and Bošnjaković, Jovan and Milošević, Milena and Rančić, Milica and Marinković, Aleksandar and Gržetić, Jelena and Gamoudi, Houda",
year = "2022",
abstract = "U ovom radu ispitivan je potencijal korišćenja akril-funkcionalizovanog kraft lignina (AKL) u smanjenju zapaljivosti polimernih kompozita na bazi recikliranih nezasićenih poliesterskih smola (NZPS). Akrilna funkcionalizacija kraft lignina je izvedena direktnom esterifikacijom slobodnih polifenolnih grupa sa akriloil hloridom, nakon čega je AKL umešan u NZP smolu sintetizovanu od poliola dobijenih katalitičkom depolimerizacijom otpadnog poli(etilen tereftalata). AKL je homogenizovan sa NZPS pri različitim masenim udelima: 2,5, 5,0, 7,5 i 12,5 mas.%. Strukturne i dinamičko-mehaničke karakteristike akril-funkcionalizovanog kraft lignina i kompozita određene su primenom FTIR spektroskopije, dinamičkomehaničke analize (DMA) i testova jednoosnog zatezanja. Proučavan je uticaj funkcionalizacije i masenog udela AKL na zatezna i termička svojstva NZPS. Vatrootporna svojstva kompozita su ispitivana prema standardnoj UL-94V metodi, na osnovu koje je kompozit sa 12,5 tež. % akril-funkcionalizovanog lignina dostigao najvišu kategorija toplotno otpornih materijala., This paper investigates the using potential of acryl-functionalized kraft lignin (AKL) in reducing the flammability of polymer composites based on recycled unsaturated polyester resins (UPR). Acryl functionalization of kraft lignin was performed by direct esterification of free polyphenolic groups with acryloyl chloride, after what, the AKL was blended in UPR resin synthesized from the polyols obtained by catalytic depolymerization of waste poly(ethylene terephthalate). The AKL was homogenized in UPR resin in different weight ratios: 2.5, 5.0, 7.5, and 12.5 wt.%. Structural and dynamic-mechanical characteristics of acryl-functionalized kraft lignin and composites were determined using FTIR spectroscopy, dynamicmechanical analysis (DMA), and tensile tests. The influence of functionalization and mass fraction of AKL on tensile and thermal properties of UPR resin was studied. The thermal properties of the composite were tested according to the standard UL-94 method, based on which the highest category of heat-resistant materials is a composite with 12.5 wt.% acylfunctionalized lignin.",
publisher = "Vojnotehnički institut, Beograd",
journal = "Scientific Technical Review",
title = "Vatrootporni kompoziti na bazi akril-funkcionalizovanog lignina i poliesterske smole dobijene od otpadnog poli(etilen tereftalata), Fire-resistant composites based on acrylic-functionalized lignin and polyester resin obtained from waste poly(ethylene terephthalate)",
pages = "37-32",
number = "2",
volume = "72",
doi = "10.5937/str2202032K",
url = "conv_736"
}
Knežević, N., Jovanović, A., Bošnjaković, J., Milošević, M., Rančić, M., Marinković, A., Gržetić, J.,& Gamoudi, H.. (2022). Vatrootporni kompoziti na bazi akril-funkcionalizovanog lignina i poliesterske smole dobijene od otpadnog poli(etilen tereftalata). in Scientific Technical Review
Vojnotehnički institut, Beograd., 72(2), 32-37.
https://doi.org/10.5937/str2202032K
conv_736
Knežević N, Jovanović A, Bošnjaković J, Milošević M, Rančić M, Marinković A, Gržetić J, Gamoudi H. Vatrootporni kompoziti na bazi akril-funkcionalizovanog lignina i poliesterske smole dobijene od otpadnog poli(etilen tereftalata). in Scientific Technical Review. 2022;72(2):32-37.
doi:10.5937/str2202032K
conv_736 .
Knežević, Nataša, Jovanović, Aleksandar, Bošnjaković, Jovan, Milošević, Milena, Rančić, Milica, Marinković, Aleksandar, Gržetić, Jelena, Gamoudi, Houda, "Vatrootporni kompoziti na bazi akril-funkcionalizovanog lignina i poliesterske smole dobijene od otpadnog poli(etilen tereftalata)" in Scientific Technical Review, 72, no. 2 (2022):32-37,
https://doi.org/10.5937/str2202032K .,
conv_736 .
2

Solvent and substituent effect on intramolecular charge transfer in 5-arylidene-3-substituted-2,4-thiazolidinediones: Experimental and theoretical study

Rančić, Milica; Stojiljković, Ivana; Milošević, Milena; Prlainović, Nevena; Jovanović, Maja; Milcić, Miloš K.; Marinković, Aleksandar D.

(Elsevier, 2019)

TY  - JOUR
AU  - Rančić, Milica
AU  - Stojiljković, Ivana
AU  - Milošević, Milena
AU  - Prlainović, Nevena
AU  - Jovanović, Maja
AU  - Milcić, Miloš K.
AU  - Marinković, Aleksandar D.
PY  - 2019
UR  - https://omorika.sfb.bg.ac.rs/handle/123456789/1002
AB  - The substituent and solvent effect on intramolecular charge transfer (ICT) in 5-aryli dene-3-methyl-2,4-thiazolidinediones (series 1) and 5-arylidene-3-phenyl-2,4-thiazolidinediones (series 2) was studied by using experimental and theoretical methodology. The effect of specific and non-specific solvent-solute interactions on the UV-vis absorption maxima shifts was evaluated by using the Kamlet-Taft and Catalan solvent parameter sets. Linear free energy relationships (LFERs) have been applied to the UV-vis and C-13 NMR data by using SSP (single substituent parameter) and DSP (dual substituent parameters). Comparative LFER analysis of 10 styrenic series was performed in order to distinguish contribution of structural and electronic substituent effect on extent of p-polarization in a side chain (vinyl) group. Furthermore, the experimental findings were interpreted with the aid of ab initio MP2 and time-dependent density functional (TD-DFT) methods. TD-DFT calculations are performed to quantify the efficiency of intramolecular charge transfer (ICT) allowing us to define the charge-transfer distance (DCT), amount of transferred charge (QCT), and difference of dipole moments between the ground and excited states (mu CT). It was found that both substituents and solvents influence electron density shift, i.e. extent of conjugation, and affect intramolecular charge transfer character in the course of excitation.
PB  - Elsevier
T2  - Arabian Journal of Chemistry
T1  - Solvent and substituent effect on intramolecular charge transfer in 5-arylidene-3-substituted-2,4-thiazolidinediones: Experimental and theoretical study
EP  - 5161
IS  - 8
SP  - 5142
VL  - 12
UR  - conv_2358
ER  - 
@article{
author = "Rančić, Milica and Stojiljković, Ivana and Milošević, Milena and Prlainović, Nevena and Jovanović, Maja and Milcić, Miloš K. and Marinković, Aleksandar D.",
year = "2019",
abstract = "The substituent and solvent effect on intramolecular charge transfer (ICT) in 5-aryli dene-3-methyl-2,4-thiazolidinediones (series 1) and 5-arylidene-3-phenyl-2,4-thiazolidinediones (series 2) was studied by using experimental and theoretical methodology. The effect of specific and non-specific solvent-solute interactions on the UV-vis absorption maxima shifts was evaluated by using the Kamlet-Taft and Catalan solvent parameter sets. Linear free energy relationships (LFERs) have been applied to the UV-vis and C-13 NMR data by using SSP (single substituent parameter) and DSP (dual substituent parameters). Comparative LFER analysis of 10 styrenic series was performed in order to distinguish contribution of structural and electronic substituent effect on extent of p-polarization in a side chain (vinyl) group. Furthermore, the experimental findings were interpreted with the aid of ab initio MP2 and time-dependent density functional (TD-DFT) methods. TD-DFT calculations are performed to quantify the efficiency of intramolecular charge transfer (ICT) allowing us to define the charge-transfer distance (DCT), amount of transferred charge (QCT), and difference of dipole moments between the ground and excited states (mu CT). It was found that both substituents and solvents influence electron density shift, i.e. extent of conjugation, and affect intramolecular charge transfer character in the course of excitation.",
publisher = "Elsevier",
journal = "Arabian Journal of Chemistry",
title = "Solvent and substituent effect on intramolecular charge transfer in 5-arylidene-3-substituted-2,4-thiazolidinediones: Experimental and theoretical study",
pages = "5161-5142",
number = "8",
volume = "12",
url = "conv_2358"
}
Rančić, M., Stojiljković, I., Milošević, M., Prlainović, N., Jovanović, M., Milcić, M. K.,& Marinković, A. D.. (2019). Solvent and substituent effect on intramolecular charge transfer in 5-arylidene-3-substituted-2,4-thiazolidinediones: Experimental and theoretical study. in Arabian Journal of Chemistry
Elsevier., 12(8), 5142-5161.
conv_2358
Rančić M, Stojiljković I, Milošević M, Prlainović N, Jovanović M, Milcić MK, Marinković AD. Solvent and substituent effect on intramolecular charge transfer in 5-arylidene-3-substituted-2,4-thiazolidinediones: Experimental and theoretical study. in Arabian Journal of Chemistry. 2019;12(8):5142-5161.
conv_2358 .
Rančić, Milica, Stojiljković, Ivana, Milošević, Milena, Prlainović, Nevena, Jovanović, Maja, Milcić, Miloš K., Marinković, Aleksandar D., "Solvent and substituent effect on intramolecular charge transfer in 5-arylidene-3-substituted-2,4-thiazolidinediones: Experimental and theoretical study" in Arabian Journal of Chemistry, 12, no. 8 (2019):5142-5161,
conv_2358 .
7
8

Tehno-ekonomska analiza proizvodnje nezasićenih poliestara iz otpadnog PET-a

Drah, Abdusalam; Rusmirović, Jelena D.; Milošević, Milena; Kalifa, Mustafa; Stojiljković, Ivana; Rančić, Milica; Marinković, Aleksandar D.

(Inženjersko društvo za koroziju, Beograd, 2016)

TY  - JOUR
AU  - Drah, Abdusalam
AU  - Rusmirović, Jelena D.
AU  - Milošević, Milena
AU  - Kalifa, Mustafa
AU  - Stojiljković, Ivana
AU  - Rančić, Milica
AU  - Marinković, Aleksandar D.
PY  - 2016
UR  - https://omorika.sfb.bg.ac.rs/handle/123456789/774
AB  - Nezasićene poliestarske smole (UPe) su sintetisane iz anhidrida maleinske kiseline i proizvoda glikolize, dobijenih depolimerizacijom poli(etilen tereftalata) (PET-a) sa dipropilen-glikolom (DPG) u prisustvu tetrabutil-titanata kao katalizatora. Proizvod glikolize otpadnog PET-a i UPe smole su okarakterisani pomoću FTIR i NMR spektroskopije, elementalne analize, kiselinskog (AV), hidroksilnog (HV) i jodnog broja. Nanokompoziti, bazirani na nezasićenim poliestarskim smolama i nanočesticama silicijum-dioksida modifikovanim heksametildisilazanom, pripremljene su sa namerom da se prikaže jedna od značajnih komercijalnih primena UPe smola. U cilju određivanja mogućnosti mogućih implementacija razvijenih novih tehnologija proizvodnje UPe smola, urađena je neki tehno-ekonomska analiza. Ekonomska korist i profitabilnost procesa prikazane tehnologije su zasnovani na primeni reciklaže sirovog materijala, otpadnog PET-a, što predstavlja jedan od najefektivnijih načina da se očuvaju prirodni resursi, zaštiti životna sredina i uštedi novac. Principi zelene ekonomije su ugrađeni u razvijenoj tehnologiji proizvodnje UPe smola, što se odnosi i na zaštitu životne sredine i dostizanje profitabilnosti bez dodatnih negativnih uticaja na životnu sredinu, odnosno na smanjenje zagađenja bez negativnog uticaja na implementiranu tehnologiju.
AB  - Unsaturated polyester resins (UPe) were synthesized from maleic anhydride and products of glycolysis, obtained by polyethylene terephthalate (PET) depolymerization with dipropylene glycol (DPG) in the presence of tetrabutyl titanate catalyst. Waste PET glycolyzed product and UPes were characterized by FTIR and NMR spectroscopy, elemental analysis, acid value (AV), hydroxyl value (HV) and iodine value. Nanocomposites, based on unsaturated polyester resins and hexamethyldisilazane modified silica nanoparticles, were prepared with intention to show one of valuable applicative commercialization of UPe resin. In order to determine potential of the possible implementation of developed new technology for UPe production some aspect of techno- economic analysis was analyzed. Economic potential/benefit and process profitability of the presented technology was based on the use of recycled raw input materials, i.e. waste PET, which is one of the most effective ways to save natural resources, protect the environment, and save money. Principles of green economy was incorporated in the results of developed UPe production technology which is related to both environmental protection and profitability achievement with no additional negative impact to environment, i.e. pollution decrease without negative effect of implemented technology.
PB  - Inženjersko društvo za koroziju, Beograd
T2  - Zaštita materijala
T1  - Tehno-ekonomska analiza proizvodnje nezasićenih poliestara iz otpadnog PET-a
T1  - Techno-economic analysis of unsaturated polyester production from waste PET
EP  - 612
IS  - 4
SP  - 605
VL  - 57
DO  - 10.5937/ZasMat1604605D
UR  - conv_61
ER  - 
@article{
author = "Drah, Abdusalam and Rusmirović, Jelena D. and Milošević, Milena and Kalifa, Mustafa and Stojiljković, Ivana and Rančić, Milica and Marinković, Aleksandar D.",
year = "2016",
abstract = "Nezasićene poliestarske smole (UPe) su sintetisane iz anhidrida maleinske kiseline i proizvoda glikolize, dobijenih depolimerizacijom poli(etilen tereftalata) (PET-a) sa dipropilen-glikolom (DPG) u prisustvu tetrabutil-titanata kao katalizatora. Proizvod glikolize otpadnog PET-a i UPe smole su okarakterisani pomoću FTIR i NMR spektroskopije, elementalne analize, kiselinskog (AV), hidroksilnog (HV) i jodnog broja. Nanokompoziti, bazirani na nezasićenim poliestarskim smolama i nanočesticama silicijum-dioksida modifikovanim heksametildisilazanom, pripremljene su sa namerom da se prikaže jedna od značajnih komercijalnih primena UPe smola. U cilju određivanja mogućnosti mogućih implementacija razvijenih novih tehnologija proizvodnje UPe smola, urađena je neki tehno-ekonomska analiza. Ekonomska korist i profitabilnost procesa prikazane tehnologije su zasnovani na primeni reciklaže sirovog materijala, otpadnog PET-a, što predstavlja jedan od najefektivnijih načina da se očuvaju prirodni resursi, zaštiti životna sredina i uštedi novac. Principi zelene ekonomije su ugrađeni u razvijenoj tehnologiji proizvodnje UPe smola, što se odnosi i na zaštitu životne sredine i dostizanje profitabilnosti bez dodatnih negativnih uticaja na životnu sredinu, odnosno na smanjenje zagađenja bez negativnog uticaja na implementiranu tehnologiju., Unsaturated polyester resins (UPe) were synthesized from maleic anhydride and products of glycolysis, obtained by polyethylene terephthalate (PET) depolymerization with dipropylene glycol (DPG) in the presence of tetrabutyl titanate catalyst. Waste PET glycolyzed product and UPes were characterized by FTIR and NMR spectroscopy, elemental analysis, acid value (AV), hydroxyl value (HV) and iodine value. Nanocomposites, based on unsaturated polyester resins and hexamethyldisilazane modified silica nanoparticles, were prepared with intention to show one of valuable applicative commercialization of UPe resin. In order to determine potential of the possible implementation of developed new technology for UPe production some aspect of techno- economic analysis was analyzed. Economic potential/benefit and process profitability of the presented technology was based on the use of recycled raw input materials, i.e. waste PET, which is one of the most effective ways to save natural resources, protect the environment, and save money. Principles of green economy was incorporated in the results of developed UPe production technology which is related to both environmental protection and profitability achievement with no additional negative impact to environment, i.e. pollution decrease without negative effect of implemented technology.",
publisher = "Inženjersko društvo za koroziju, Beograd",
journal = "Zaštita materijala",
title = "Tehno-ekonomska analiza proizvodnje nezasićenih poliestara iz otpadnog PET-a, Techno-economic analysis of unsaturated polyester production from waste PET",
pages = "612-605",
number = "4",
volume = "57",
doi = "10.5937/ZasMat1604605D",
url = "conv_61"
}
Drah, A., Rusmirović, J. D., Milošević, M., Kalifa, M., Stojiljković, I., Rančić, M.,& Marinković, A. D.. (2016). Tehno-ekonomska analiza proizvodnje nezasićenih poliestara iz otpadnog PET-a. in Zaštita materijala
Inženjersko društvo za koroziju, Beograd., 57(4), 605-612.
https://doi.org/10.5937/ZasMat1604605D
conv_61
Drah A, Rusmirović JD, Milošević M, Kalifa M, Stojiljković I, Rančić M, Marinković AD. Tehno-ekonomska analiza proizvodnje nezasićenih poliestara iz otpadnog PET-a. in Zaštita materijala. 2016;57(4):605-612.
doi:10.5937/ZasMat1604605D
conv_61 .
Drah, Abdusalam, Rusmirović, Jelena D., Milošević, Milena, Kalifa, Mustafa, Stojiljković, Ivana, Rančić, Milica, Marinković, Aleksandar D., "Tehno-ekonomska analiza proizvodnje nezasićenih poliestara iz otpadnog PET-a" in Zaštita materijala, 57, no. 4 (2016):605-612,
https://doi.org/10.5937/ZasMat1604605D .,
conv_61 .
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