Loos, Katja

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orcid::0000-0002-4613-1159
  • Loos, Katja (3)
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Author's Bibliography

Recommendations for replacing PET on packaging, fiber, and film materials with biobased counterparts

Sousa, Andreia F.; Patricio, Rafael; Terzopoulou, Zoi; Bikiaris, Dimitrios N.; Stern, Tobias; Wenger, Julia; Loos, Katja; Lotti, Nadia; Siracusa, Valentina; Szymczyk, Anna; Paszkiewicz, Sandra; Triantafyllidis, Konstantinos S.; Zamboulis, Alexandra; Nikolić, Marija S.; Spasojević, Pavle; Thiyagarajan, Shanmugam; van Es, Daan S.; Guigo, Nathanael

(2021)

TY  - JOUR
AU  - Sousa, Andreia F.
AU  - Patricio, Rafael
AU  - Terzopoulou, Zoi
AU  - Bikiaris, Dimitrios N.
AU  - Stern, Tobias
AU  - Wenger, Julia
AU  - Loos, Katja
AU  - Lotti, Nadia
AU  - Siracusa, Valentina
AU  - Szymczyk, Anna
AU  - Paszkiewicz, Sandra
AU  - Triantafyllidis, Konstantinos S.
AU  - Zamboulis, Alexandra
AU  - Nikolić, Marija S.
AU  - Spasojević, Pavle
AU  - Thiyagarajan, Shanmugam
AU  - van Es, Daan S.
AU  - Guigo, Nathanael
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4837
AB  - This review sheds light on urgent questions that arise from the need to replace a polymer resin,-poly(ethylene terephthalate), which represents 7.7% market-share in the global plastic demand (Plastics-the Facts 2019), by renewable alternatives. The main question that this review will address is: what are the most promising PET replacements made from biomass? Currently, under debate is naturally its biobased counterpart bio-PET (or even recycle rPET), as well as other aromatic key-players with comparable thermo-mechanical performance and enhanced barrier properties, such as poly(ethylene 2,5-furandicarboxylate) (PEF) and poly(trimethylene 2,5-furandicarboxylate) (PTF). They are most adequate for packaging, but not restricted to. Additional alternatives are the miscellaneous of lignin-based thermoplastic polymers, although the technology involved in this latter case is still premature. (Bio)degradable aliphatic polyesters, despite their typical inferior thermo-mechanical properties, can also play a role e.g., among PET fiber industry applications. Poly(lactic acid) (PLA) is the most developed renewable polyester, already a commercial reality. All biobased polymers reviewed face a major hindrance for their wider deployment their cost-competitiveness. A pertinent question arises then: Are these alternatives, or will they be, economically feasible? Social, political and legal frameworks together with supportive financial schemes are boosting rapid changes. In the future, most probably more than one polymer will come to the market and will be used in some of the panoply of PET applications. This evaluation overviews sustainability issues, including perspectives on their green synthesis. Moreover, this review does also not neglect the accumulation of plastics waste in the environment and the inherent challenges of polymers' end-of-life. Approximately 8 M tons of polymers waste leaks into the environment each year, a fact not disconnected to PET's non-biodegradability and still insufficient collection and recycling rates.
T2  - Green Chemistry
T1  - Recommendations for replacing PET on packaging, fiber, and film materials with biobased counterparts
EP  - 8820
IS  - 22
SP  - 8795
VL  - 23
DO  - 10.1039/d1gc02082j
ER  - 
@article{
author = "Sousa, Andreia F. and Patricio, Rafael and Terzopoulou, Zoi and Bikiaris, Dimitrios N. and Stern, Tobias and Wenger, Julia and Loos, Katja and Lotti, Nadia and Siracusa, Valentina and Szymczyk, Anna and Paszkiewicz, Sandra and Triantafyllidis, Konstantinos S. and Zamboulis, Alexandra and Nikolić, Marija S. and Spasojević, Pavle and Thiyagarajan, Shanmugam and van Es, Daan S. and Guigo, Nathanael",
year = "2021",
abstract = "This review sheds light on urgent questions that arise from the need to replace a polymer resin,-poly(ethylene terephthalate), which represents 7.7% market-share in the global plastic demand (Plastics-the Facts 2019), by renewable alternatives. The main question that this review will address is: what are the most promising PET replacements made from biomass? Currently, under debate is naturally its biobased counterpart bio-PET (or even recycle rPET), as well as other aromatic key-players with comparable thermo-mechanical performance and enhanced barrier properties, such as poly(ethylene 2,5-furandicarboxylate) (PEF) and poly(trimethylene 2,5-furandicarboxylate) (PTF). They are most adequate for packaging, but not restricted to. Additional alternatives are the miscellaneous of lignin-based thermoplastic polymers, although the technology involved in this latter case is still premature. (Bio)degradable aliphatic polyesters, despite their typical inferior thermo-mechanical properties, can also play a role e.g., among PET fiber industry applications. Poly(lactic acid) (PLA) is the most developed renewable polyester, already a commercial reality. All biobased polymers reviewed face a major hindrance for their wider deployment their cost-competitiveness. A pertinent question arises then: Are these alternatives, or will they be, economically feasible? Social, political and legal frameworks together with supportive financial schemes are boosting rapid changes. In the future, most probably more than one polymer will come to the market and will be used in some of the panoply of PET applications. This evaluation overviews sustainability issues, including perspectives on their green synthesis. Moreover, this review does also not neglect the accumulation of plastics waste in the environment and the inherent challenges of polymers' end-of-life. Approximately 8 M tons of polymers waste leaks into the environment each year, a fact not disconnected to PET's non-biodegradability and still insufficient collection and recycling rates.",
journal = "Green Chemistry",
title = "Recommendations for replacing PET on packaging, fiber, and film materials with biobased counterparts",
pages = "8820-8795",
number = "22",
volume = "23",
doi = "10.1039/d1gc02082j"
}
Sousa, A. F., Patricio, R., Terzopoulou, Z., Bikiaris, D. N., Stern, T., Wenger, J., Loos, K., Lotti, N., Siracusa, V., Szymczyk, A., Paszkiewicz, S., Triantafyllidis, K. S., Zamboulis, A., Nikolić, M. S., Spasojević, P., Thiyagarajan, S., van Es, D. S.,& Guigo, N.. (2021). Recommendations for replacing PET on packaging, fiber, and film materials with biobased counterparts. in Green Chemistry, 23(22), 8795-8820.
https://doi.org/10.1039/d1gc02082j
Sousa AF, Patricio R, Terzopoulou Z, Bikiaris DN, Stern T, Wenger J, Loos K, Lotti N, Siracusa V, Szymczyk A, Paszkiewicz S, Triantafyllidis KS, Zamboulis A, Nikolić MS, Spasojević P, Thiyagarajan S, van Es DS, Guigo N. Recommendations for replacing PET on packaging, fiber, and film materials with biobased counterparts. in Green Chemistry. 2021;23(22):8795-8820.
doi:10.1039/d1gc02082j .
Sousa, Andreia F., Patricio, Rafael, Terzopoulou, Zoi, Bikiaris, Dimitrios N., Stern, Tobias, Wenger, Julia, Loos, Katja, Lotti, Nadia, Siracusa, Valentina, Szymczyk, Anna, Paszkiewicz, Sandra, Triantafyllidis, Konstantinos S., Zamboulis, Alexandra, Nikolić, Marija S., Spasojević, Pavle, Thiyagarajan, Shanmugam, van Es, Daan S., Guigo, Nathanael, "Recommendations for replacing PET on packaging, fiber, and film materials with biobased counterparts" in Green Chemistry, 23, no. 22 (2021):8795-8820,
https://doi.org/10.1039/d1gc02082j . .
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Cu(II) immobilization onto a one-step synthesized poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) resin: Kinetics and XPS analysis

Maksin, Danijela; Nastasović, Aleksandra; Maksin, Tatjana N.; Sandić, Zvjezdana P.; Loos, Katja; Ekmeščić, Bojana; Onjia, Antonije

(Savez hemijskih inženjera, Beograd, 2016)

TY  - JOUR
AU  - Maksin, Danijela
AU  - Nastasović, Aleksandra
AU  - Maksin, Tatjana N.
AU  - Sandić, Zvjezdana P.
AU  - Loos, Katja
AU  - Ekmeščić, Bojana
AU  - Onjia, Antonije
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3470
AB  - Synthesis of an unconventional resin based on 4-vinylpyridine (4-VP) and its Cu(II) sorption behavior were studied. Three samples of macroporous crosslinked poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) (P4VPE) with different porosity parameters were prepared by suspension copolymerization by varying the n-heptane amount in the inert component. The samples were characterized by mercury porosimetry, elemental analysis and X-ray photoelectron spectroscopy (XPS). The sorption of P4VPE for Cu(II) ions, determined under non-competitive conditions, was relatively rapid, i.e., the maximum capacity was reached within 30 min. The maximum experimental sorption capacity for the sample with the highest values of pore diameter and specific pore volume (sample 3, Q(eq) = 89 mg g(-1)) was 17.5 times higher than for the sample with the lowest values of pore diameter and specific pore volume (sample 1, Q(eq) = 5.1 mg g(-1)). Since the values for pyridine content in all P4VPE samples were almost the same, it was concluded that the porosity parameters have predominant influence on Cu(II) sorption rates on P4VPE. The sorption behavior and the rate-controlling mechanisms were analyzed using six kinetic models (pseudo-first order, pseudo-second order, Elovich, intraparticle diffusion, Bangham and Boyd models). XPS study clarified the nature of the formed P4VPE-Cu(II) species.
PB  - Savez hemijskih inženjera, Beograd
T2  - Hemijska industrija
T1  - Cu(II) immobilization onto a one-step synthesized poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) resin: Kinetics and XPS analysis
EP  - 19
IS  - 1
SP  - 9
VL  - 70
DO  - 10.2298/HEMIND141203007M
ER  - 
@article{
author = "Maksin, Danijela and Nastasović, Aleksandra and Maksin, Tatjana N. and Sandić, Zvjezdana P. and Loos, Katja and Ekmeščić, Bojana and Onjia, Antonije",
year = "2016",
abstract = "Synthesis of an unconventional resin based on 4-vinylpyridine (4-VP) and its Cu(II) sorption behavior were studied. Three samples of macroporous crosslinked poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) (P4VPE) with different porosity parameters were prepared by suspension copolymerization by varying the n-heptane amount in the inert component. The samples were characterized by mercury porosimetry, elemental analysis and X-ray photoelectron spectroscopy (XPS). The sorption of P4VPE for Cu(II) ions, determined under non-competitive conditions, was relatively rapid, i.e., the maximum capacity was reached within 30 min. The maximum experimental sorption capacity for the sample with the highest values of pore diameter and specific pore volume (sample 3, Q(eq) = 89 mg g(-1)) was 17.5 times higher than for the sample with the lowest values of pore diameter and specific pore volume (sample 1, Q(eq) = 5.1 mg g(-1)). Since the values for pyridine content in all P4VPE samples were almost the same, it was concluded that the porosity parameters have predominant influence on Cu(II) sorption rates on P4VPE. The sorption behavior and the rate-controlling mechanisms were analyzed using six kinetic models (pseudo-first order, pseudo-second order, Elovich, intraparticle diffusion, Bangham and Boyd models). XPS study clarified the nature of the formed P4VPE-Cu(II) species.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Hemijska industrija",
title = "Cu(II) immobilization onto a one-step synthesized poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) resin: Kinetics and XPS analysis",
pages = "19-9",
number = "1",
volume = "70",
doi = "10.2298/HEMIND141203007M"
}
Maksin, D., Nastasović, A., Maksin, T. N., Sandić, Z. P., Loos, K., Ekmeščić, B.,& Onjia, A.. (2016). Cu(II) immobilization onto a one-step synthesized poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) resin: Kinetics and XPS analysis. in Hemijska industrija
Savez hemijskih inženjera, Beograd., 70(1), 9-19.
https://doi.org/10.2298/HEMIND141203007M
Maksin D, Nastasović A, Maksin TN, Sandić ZP, Loos K, Ekmeščić B, Onjia A. Cu(II) immobilization onto a one-step synthesized poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) resin: Kinetics and XPS analysis. in Hemijska industrija. 2016;70(1):9-19.
doi:10.2298/HEMIND141203007M .
Maksin, Danijela, Nastasović, Aleksandra, Maksin, Tatjana N., Sandić, Zvjezdana P., Loos, Katja, Ekmeščić, Bojana, Onjia, Antonije, "Cu(II) immobilization onto a one-step synthesized poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) resin: Kinetics and XPS analysis" in Hemijska industrija, 70, no. 1 (2016):9-19,
https://doi.org/10.2298/HEMIND141203007M . .

High performance alkyd resins synthesized from postconsumer PET bottles

Spasojević, Pavle; Panić, Vesna; Džunuzović, Jasna; Marinković, Aleksandar; Woortman, A J J; Loos, Katja; Popović, Ivanka

(Royal Soc Chemistry, Cambridge, 2015)

TY  - JOUR
AU  - Spasojević, Pavle
AU  - Panić, Vesna
AU  - Džunuzović, Jasna
AU  - Marinković, Aleksandar
AU  - Woortman, A J J
AU  - Loos, Katja
AU  - Popović, Ivanka
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3119
AB  - The glycolytic recycling of waste PET presents a challenge for the production of secondary value-added products, such as alkyd resins. A way to overcome the unsatisfactory mechanical, drying and chemical resistance properties of alkyds obtained from difunctional glycolyzates was proposed. Waste PET was glycolyzed using multifunctional alcohols: glycerol (G), trimethylolethane (TME), trimethylolpropane (TMP) and pentaerythritol (PE), giving tetra-and hexa-functional glycolyzates and, for comparison, using diethylene glycol (DEG), propylene glycol (PG) and dipropylene glycol (DPG) giving di-functional glycolyzates. The obtained glycolyzates were examined by H-1 and C-13 NMR, FTIR spectroscopy and elemental analysis and further used in the synthesis of alkyd resins. The properties of the prepared alkyd resins (acid, hydroxyl and iodine values, color, average molar masses and molar mass distributions, viscosity, drying time, hardness, flexibility, gloss, adhesion and chemical resistance) were investigated with respect to the functionality and the structure of the used glycolyzates. Alkyd resins derived from multifunctional glycolyzates (TME and TMP) showed considerably enhanced properties compared to those produced from difunctional glycolyzates and also to conventional general purpose resins.
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - High performance alkyd resins synthesized from postconsumer PET bottles
EP  - 62283
IS  - 76
SP  - 62273
VL  - 5
DO  - 10.1039/c5ra11777a
ER  - 
@article{
author = "Spasojević, Pavle and Panić, Vesna and Džunuzović, Jasna and Marinković, Aleksandar and Woortman, A J J and Loos, Katja and Popović, Ivanka",
year = "2015",
abstract = "The glycolytic recycling of waste PET presents a challenge for the production of secondary value-added products, such as alkyd resins. A way to overcome the unsatisfactory mechanical, drying and chemical resistance properties of alkyds obtained from difunctional glycolyzates was proposed. Waste PET was glycolyzed using multifunctional alcohols: glycerol (G), trimethylolethane (TME), trimethylolpropane (TMP) and pentaerythritol (PE), giving tetra-and hexa-functional glycolyzates and, for comparison, using diethylene glycol (DEG), propylene glycol (PG) and dipropylene glycol (DPG) giving di-functional glycolyzates. The obtained glycolyzates were examined by H-1 and C-13 NMR, FTIR spectroscopy and elemental analysis and further used in the synthesis of alkyd resins. The properties of the prepared alkyd resins (acid, hydroxyl and iodine values, color, average molar masses and molar mass distributions, viscosity, drying time, hardness, flexibility, gloss, adhesion and chemical resistance) were investigated with respect to the functionality and the structure of the used glycolyzates. Alkyd resins derived from multifunctional glycolyzates (TME and TMP) showed considerably enhanced properties compared to those produced from difunctional glycolyzates and also to conventional general purpose resins.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "High performance alkyd resins synthesized from postconsumer PET bottles",
pages = "62283-62273",
number = "76",
volume = "5",
doi = "10.1039/c5ra11777a"
}
Spasojević, P., Panić, V., Džunuzović, J., Marinković, A., Woortman, A. J. J., Loos, K.,& Popović, I.. (2015). High performance alkyd resins synthesized from postconsumer PET bottles. in RSC Advances
Royal Soc Chemistry, Cambridge., 5(76), 62273-62283.
https://doi.org/10.1039/c5ra11777a
Spasojević P, Panić V, Džunuzović J, Marinković A, Woortman AJJ, Loos K, Popović I. High performance alkyd resins synthesized from postconsumer PET bottles. in RSC Advances. 2015;5(76):62273-62283.
doi:10.1039/c5ra11777a .
Spasojević, Pavle, Panić, Vesna, Džunuzović, Jasna, Marinković, Aleksandar, Woortman, A J J, Loos, Katja, Popović, Ivanka, "High performance alkyd resins synthesized from postconsumer PET bottles" in RSC Advances, 5, no. 76 (2015):62273-62283,
https://doi.org/10.1039/c5ra11777a . .
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