Milovanović, Miloš

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  • Milovanović, Miloš (3)
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Author's Bibliography

The thermal stability of poly(methyl methacrylate) prepared by RAFT polymerisation

Katsikas, Lynne; Avramović, Milena; Cortés, Betancourt Darío Rubén; Milovanović, Miloš; Kalagasidis Krušić, Melina; Popović, Ivanka

(Serbian Chemical Society, Belgrade, 2008)

TY  - JOUR
AU  - Katsikas, Lynne
AU  - Avramović, Milena
AU  - Cortés, Betancourt Darío Rubén
AU  - Milovanović, Miloš
AU  - Kalagasidis Krušić, Melina
AU  - Popović, Ivanka
PY  - 2008
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1326
AB  - Poly(methyl methacrylate), PMMA, was prepared by reversible addition-fragmentation chain transfer, RAFT, polymerisation using 2-(2-cyanopropyl)-dithiobenzoate, CPDB, as the RAFT agent. The thermal stability of the resulting polymer approached that of anionically prepared PMMA, as determined by thermogravimetry. This was the consequence of the RAFT prepared polymer having no head-to-head links and no chain end double bonds, which are responsible for the relatively low thermal stability of radically prepared PMMA.
AB  - Poli(metil metakrilat), PMMA, je sintetisan kontrolisanom radikalnom RAFT polimerizacijom, odnosno reverzibilnom adiciono-fragmentacionom transfer polimerizacijom, u prisustvu 2-(2-cijanopropil)-ditiobenzoata, CPDB, kao RAFT agensa. Termička stabilnost PMMA sintetisanog RAFT polimerizacijom je slična polimeru dobijenom anjonskom polimerizacijom, što je pokazala termogravimetrijska analiza. PMMA sintetisan RAFT polimerizacijom pokazuje znatno bolju termičku stabilnost u odnosu na PMMA sintetisan polimerizacijom preko slobodnih radikala, zbog odsustva termički labilnih veza glava-glava ostataka monomera u polimernom lancu, kao i dvostrukih veza na krajevima lanaca.
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - The thermal stability of poly(methyl methacrylate) prepared by RAFT polymerisation
T1  - Termička stabilnost poli(metil metakrilata) sintetisanog RAFT polimerizacijom
EP  - 921
IS  - 8-9
SP  - 915
VL  - 73
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1326
ER  - 
@article{
author = "Katsikas, Lynne and Avramović, Milena and Cortés, Betancourt Darío Rubén and Milovanović, Miloš and Kalagasidis Krušić, Melina and Popović, Ivanka",
year = "2008",
abstract = "Poly(methyl methacrylate), PMMA, was prepared by reversible addition-fragmentation chain transfer, RAFT, polymerisation using 2-(2-cyanopropyl)-dithiobenzoate, CPDB, as the RAFT agent. The thermal stability of the resulting polymer approached that of anionically prepared PMMA, as determined by thermogravimetry. This was the consequence of the RAFT prepared polymer having no head-to-head links and no chain end double bonds, which are responsible for the relatively low thermal stability of radically prepared PMMA., Poli(metil metakrilat), PMMA, je sintetisan kontrolisanom radikalnom RAFT polimerizacijom, odnosno reverzibilnom adiciono-fragmentacionom transfer polimerizacijom, u prisustvu 2-(2-cijanopropil)-ditiobenzoata, CPDB, kao RAFT agensa. Termička stabilnost PMMA sintetisanog RAFT polimerizacijom je slična polimeru dobijenom anjonskom polimerizacijom, što je pokazala termogravimetrijska analiza. PMMA sintetisan RAFT polimerizacijom pokazuje znatno bolju termičku stabilnost u odnosu na PMMA sintetisan polimerizacijom preko slobodnih radikala, zbog odsustva termički labilnih veza glava-glava ostataka monomera u polimernom lancu, kao i dvostrukih veza na krajevima lanaca.",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "The thermal stability of poly(methyl methacrylate) prepared by RAFT polymerisation, Termička stabilnost poli(metil metakrilata) sintetisanog RAFT polimerizacijom",
pages = "921-915",
number = "8-9",
volume = "73",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1326"
}
Katsikas, L., Avramović, M., Cortés, B. D. R., Milovanović, M., Kalagasidis Krušić, M.,& Popović, I.. (2008). The thermal stability of poly(methyl methacrylate) prepared by RAFT polymerisation. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 73(8-9), 915-921.
https://hdl.handle.net/21.15107/rcub_technorep_1326
Katsikas L, Avramović M, Cortés BDR, Milovanović M, Kalagasidis Krušić M, Popović I. The thermal stability of poly(methyl methacrylate) prepared by RAFT polymerisation. in Journal of the Serbian Chemical Society. 2008;73(8-9):915-921.
https://hdl.handle.net/21.15107/rcub_technorep_1326 .
Katsikas, Lynne, Avramović, Milena, Cortés, Betancourt Darío Rubén, Milovanović, Miloš, Kalagasidis Krušić, Melina, Popović, Ivanka, "The thermal stability of poly(methyl methacrylate) prepared by RAFT polymerisation" in Journal of the Serbian Chemical Society, 73, no. 8-9 (2008):915-921,
https://hdl.handle.net/21.15107/rcub_technorep_1326 .
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Hindered, 1,1-disubstituted monomers. Chain transfer to benzene in the radical polymerisation of di-n-butylitaconate

Katsikas, Lynne; Milovanović, Miloš; Popović, Ivanka

(Pergamon-Elsevier Science Ltd, Oxford, 2008)

TY  - JOUR
AU  - Katsikas, Lynne
AU  - Milovanović, Miloš
AU  - Popović, Ivanka
PY  - 2008
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1232
AB  - The transfer constant to benzene in the radical polymerisation of di-n-butyl itaconate, DBI, was measured at 60 degrees C and found to have the value of 2.2 x 10(-3). This value is surprisingly high considering that benzene has no readily extractable hydrogen atoms and is usually considered to be a relatively inert solvent in radical polymerisations. The high values of transfer constants in the radical polymerisation of itaconates must be taken into consideration when planning the tailored polymerisation of these monomers.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - European Polymer Journal
T1  - Hindered, 1,1-disubstituted monomers. Chain transfer to benzene in the radical polymerisation of di-n-butylitaconate
EP  - 3031
IS  - 9
SP  - 3028
VL  - 44
DO  - 10.1016/j.eurpolymj.2008.06.039
ER  - 
@article{
author = "Katsikas, Lynne and Milovanović, Miloš and Popović, Ivanka",
year = "2008",
abstract = "The transfer constant to benzene in the radical polymerisation of di-n-butyl itaconate, DBI, was measured at 60 degrees C and found to have the value of 2.2 x 10(-3). This value is surprisingly high considering that benzene has no readily extractable hydrogen atoms and is usually considered to be a relatively inert solvent in radical polymerisations. The high values of transfer constants in the radical polymerisation of itaconates must be taken into consideration when planning the tailored polymerisation of these monomers.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "European Polymer Journal",
title = "Hindered, 1,1-disubstituted monomers. Chain transfer to benzene in the radical polymerisation of di-n-butylitaconate",
pages = "3031-3028",
number = "9",
volume = "44",
doi = "10.1016/j.eurpolymj.2008.06.039"
}
Katsikas, L., Milovanović, M.,& Popović, I.. (2008). Hindered, 1,1-disubstituted monomers. Chain transfer to benzene in the radical polymerisation of di-n-butylitaconate. in European Polymer Journal
Pergamon-Elsevier Science Ltd, Oxford., 44(9), 3028-3031.
https://doi.org/10.1016/j.eurpolymj.2008.06.039
Katsikas L, Milovanović M, Popović I. Hindered, 1,1-disubstituted monomers. Chain transfer to benzene in the radical polymerisation of di-n-butylitaconate. in European Polymer Journal. 2008;44(9):3028-3031.
doi:10.1016/j.eurpolymj.2008.06.039 .
Katsikas, Lynne, Milovanović, Miloš, Popović, Ivanka, "Hindered, 1,1-disubstituted monomers. Chain transfer to benzene in the radical polymerisation of di-n-butylitaconate" in European Polymer Journal, 44, no. 9 (2008):3028-3031,
https://doi.org/10.1016/j.eurpolymj.2008.06.039 . .
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The thermal degradation of poly(diethyl fumarate)

Milovanović, Miloš; Bošković, Radomir; Tosić, Tomica; Katsikas, Lynne; Popović, Ivanka

(Elsevier Sci Ltd, Oxford, 2006)

TY  - JOUR
AU  - Milovanović, Miloš
AU  - Bošković, Radomir
AU  - Tosić, Tomica
AU  - Katsikas, Lynne
AU  - Popović, Ivanka
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/993
AB  - The kinetics and mechanism of the thermal degradation of poly(diethyl fumarate) (PDEF) were studied by thermogravimetry, as well as by analysis of the thermolysis volatiles and polymer residue. The characteristic mass loss temperatures were determined, as were the overall thermal degradation activation energies of three PDEF samples of varying molar mass. Ethylene and ethanol were present in the thermolysis volatiles at degradation temperatures below 300 degrees C, while diethyl fumarate was also evidenced at higher degradation temperatures. The amount of monomer increased with increasing degradation temperature. The dependence of the molar mass of the residual polymer on the degradation time and temperature was established and the number of main-chain scissions per monomer unit, s/P-0, calculated. A thermal degradation mechanism including de-esterification and random main-chain scission is proposed. The thermal degradation of PDEF was compared to the thermolysis of poly(ethyl methacrylate) (PEMA), poly(diethyl itaconate) (PDEI) and poly(ethyl acrylate) (PEA).
PB  - Elsevier Sci Ltd, Oxford
T2  - Polymer Degradation and Stability
T1  - The thermal degradation of poly(diethyl fumarate)
EP  - 3229
IS  - 12
SP  - 3221
VL  - 91
DO  - 10.1016/j.polymdegradstab.2006.07.007
ER  - 
@article{
author = "Milovanović, Miloš and Bošković, Radomir and Tosić, Tomica and Katsikas, Lynne and Popović, Ivanka",
year = "2006",
abstract = "The kinetics and mechanism of the thermal degradation of poly(diethyl fumarate) (PDEF) were studied by thermogravimetry, as well as by analysis of the thermolysis volatiles and polymer residue. The characteristic mass loss temperatures were determined, as were the overall thermal degradation activation energies of three PDEF samples of varying molar mass. Ethylene and ethanol were present in the thermolysis volatiles at degradation temperatures below 300 degrees C, while diethyl fumarate was also evidenced at higher degradation temperatures. The amount of monomer increased with increasing degradation temperature. The dependence of the molar mass of the residual polymer on the degradation time and temperature was established and the number of main-chain scissions per monomer unit, s/P-0, calculated. A thermal degradation mechanism including de-esterification and random main-chain scission is proposed. The thermal degradation of PDEF was compared to the thermolysis of poly(ethyl methacrylate) (PEMA), poly(diethyl itaconate) (PDEI) and poly(ethyl acrylate) (PEA).",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Polymer Degradation and Stability",
title = "The thermal degradation of poly(diethyl fumarate)",
pages = "3229-3221",
number = "12",
volume = "91",
doi = "10.1016/j.polymdegradstab.2006.07.007"
}
Milovanović, M., Bošković, R., Tosić, T., Katsikas, L.,& Popović, I.. (2006). The thermal degradation of poly(diethyl fumarate). in Polymer Degradation and Stability
Elsevier Sci Ltd, Oxford., 91(12), 3221-3229.
https://doi.org/10.1016/j.polymdegradstab.2006.07.007
Milovanović M, Bošković R, Tosić T, Katsikas L, Popović I. The thermal degradation of poly(diethyl fumarate). in Polymer Degradation and Stability. 2006;91(12):3221-3229.
doi:10.1016/j.polymdegradstab.2006.07.007 .
Milovanović, Miloš, Bošković, Radomir, Tosić, Tomica, Katsikas, Lynne, Popović, Ivanka, "The thermal degradation of poly(diethyl fumarate)" in Polymer Degradation and Stability, 91, no. 12 (2006):3221-3229,
https://doi.org/10.1016/j.polymdegradstab.2006.07.007 . .
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