Miladinović, Marija R.

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  • Miladinović, Marija R. (5)
  • Miladinović, Marija (1)
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Author's Bibliography

Recovery of bioactive molecules from Hypericum perforatum L. dust using microwave-assisted extraction

Milutinović, Milica; Miladinović, Marija; Gašić, Uroš; Dimitrijević-Branković, Suzana; Rajilić‑Stojanović, Mirjana

(Springer Science and Business Media Deutschland GmbH, 2022)

TY  - JOUR
AU  - Milutinović, Milica
AU  - Miladinović, Marija
AU  - Gašić, Uroš
AU  - Dimitrijević-Branković, Suzana
AU  - Rajilić‑Stojanović, Mirjana
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5137
AB  - Microwave-assisted extraction (MAE) conditions were optimized to improve extract quality of medicinal herb — Hypericum perforatum L. (St. John’s wort) dust. Response surface methodology was applied initially to obtain the highest concentration of total polyphenols in extract solids (MAE-e). St. John’s wort was mixed with 30% ethanol in 50 mL/g solvent to solid ratio, and treated with 170 W microwave power for 40 s to yield an extract with 411.26 ± 6.21 mg GAE/g of polyphenols. This extract contained a significantly higher content of polyphenols (42.50%) and had significantly higher antioxidant activity than the macerate obtained by using European Medicines Agency (EMA) recommended procedure. The advantage of the EMA procedure was the higher yield of extract per gram of plant material. Therefore, another set of MAE conditions was defined to maximize the yield of polyphenols per gram of plant material (MAE-p). The MAE-p extract was produced by using 30% ethanol, 10 mL/g solvent to solid ratio, and 170 W microwave power for 100 s, which was, again, a markedly shorter period than 72 h of maceration. The MAE-p extract had a slightly, but significantly higher yield (5.2%), more polyphenols (8.8%), and improved antioxidant activity compared to the EMA macerate. Antimicrobial activity against several pathogens was stronger for the MAE extracts. The chemical composition of extracts was slightly different and MAE favored extraction of glycosides, in particular, rutin (quercetin-3-O-rutinoside), while the EMA macerate contained quercetin aglycon in the highest concentration. Our study demonstrates that statistically planned experiments allow for significant improvement of the extraction process, which application could facilitate better use of natural resources and deliver more potent extracts than those obtained by currently recommended procedures.
PB  - Springer Science and Business Media Deutschland GmbH
T2  - Biomass Conversion and Biorefinery
T1  - Recovery of bioactive molecules from Hypericum perforatum L. dust using microwave-assisted extraction
DO  - 10.1007/s13399-022-02717-5
ER  - 
@article{
author = "Milutinović, Milica and Miladinović, Marija and Gašić, Uroš and Dimitrijević-Branković, Suzana and Rajilić‑Stojanović, Mirjana",
year = "2022",
abstract = "Microwave-assisted extraction (MAE) conditions were optimized to improve extract quality of medicinal herb — Hypericum perforatum L. (St. John’s wort) dust. Response surface methodology was applied initially to obtain the highest concentration of total polyphenols in extract solids (MAE-e). St. John’s wort was mixed with 30% ethanol in 50 mL/g solvent to solid ratio, and treated with 170 W microwave power for 40 s to yield an extract with 411.26 ± 6.21 mg GAE/g of polyphenols. This extract contained a significantly higher content of polyphenols (42.50%) and had significantly higher antioxidant activity than the macerate obtained by using European Medicines Agency (EMA) recommended procedure. The advantage of the EMA procedure was the higher yield of extract per gram of plant material. Therefore, another set of MAE conditions was defined to maximize the yield of polyphenols per gram of plant material (MAE-p). The MAE-p extract was produced by using 30% ethanol, 10 mL/g solvent to solid ratio, and 170 W microwave power for 100 s, which was, again, a markedly shorter period than 72 h of maceration. The MAE-p extract had a slightly, but significantly higher yield (5.2%), more polyphenols (8.8%), and improved antioxidant activity compared to the EMA macerate. Antimicrobial activity against several pathogens was stronger for the MAE extracts. The chemical composition of extracts was slightly different and MAE favored extraction of glycosides, in particular, rutin (quercetin-3-O-rutinoside), while the EMA macerate contained quercetin aglycon in the highest concentration. Our study demonstrates that statistically planned experiments allow for significant improvement of the extraction process, which application could facilitate better use of natural resources and deliver more potent extracts than those obtained by currently recommended procedures.",
publisher = "Springer Science and Business Media Deutschland GmbH",
journal = "Biomass Conversion and Biorefinery",
title = "Recovery of bioactive molecules from Hypericum perforatum L. dust using microwave-assisted extraction",
doi = "10.1007/s13399-022-02717-5"
}
Milutinović, M., Miladinović, M., Gašić, U., Dimitrijević-Branković, S.,& Rajilić‑Stojanović, M.. (2022). Recovery of bioactive molecules from Hypericum perforatum L. dust using microwave-assisted extraction. in Biomass Conversion and Biorefinery
Springer Science and Business Media Deutschland GmbH..
https://doi.org/10.1007/s13399-022-02717-5
Milutinović M, Miladinović M, Gašić U, Dimitrijević-Branković S, Rajilić‑Stojanović M. Recovery of bioactive molecules from Hypericum perforatum L. dust using microwave-assisted extraction. in Biomass Conversion and Biorefinery. 2022;.
doi:10.1007/s13399-022-02717-5 .
Milutinović, Milica, Miladinović, Marija, Gašić, Uroš, Dimitrijević-Branković, Suzana, Rajilić‑Stojanović, Mirjana, "Recovery of bioactive molecules from Hypericum perforatum L. dust using microwave-assisted extraction" in Biomass Conversion and Biorefinery (2022),
https://doi.org/10.1007/s13399-022-02717-5 . .
4
3

Valorization of walnut shell ash as a catalyst for biodiesel production

Miladinović, Marija R.; Zdujić, Miodrag; Veljović, Đorđe; Krstić, Jugoslav; Banković-Ilić, Ivana B.; Veljković, Vlada B.; Stamenković, Olivera S.

(Pergamon-Elsevier Science Ltd, Oxford, 2020)

TY  - JOUR
AU  - Miladinović, Marija R.
AU  - Zdujić, Miodrag
AU  - Veljović, Đorđe
AU  - Krstić, Jugoslav
AU  - Banković-Ilić, Ivana B.
AU  - Veljković, Vlada B.
AU  - Stamenković, Olivera S.
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4350
AB  - The catalytic activity of the walnut shell ash was investigated in the biodiesel production by the sunflower oil methanolysis. The catalyst was characterized by the TG-DTA, XRD, Hg porosimetry, Ny physisorption, SEM, and Hammett method. In addition, the effects of the catalyst loading and the methanolto-oil molar ratio on the methyl esters synthesis were tested at the reaction temperature of 60 degrees C. The walnut shell ash provided a very fast reaction and a high FAME content (over 98%). As the reaction occurred in the absence of triacylglycerols mass transfer limitation, the pseudo-first-order model was employed for describing the kinetics of the reaction. The catalyst was successfully reused four times after the regeneration of the catalytic activity by recalcination at 800 degrees C.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Renewable Energy
T1  - Valorization of walnut shell ash as a catalyst for biodiesel production
EP  - 1043
SP  - 1033
VL  - 147
DO  - 10.1016/j.renene.2019.09.056
ER  - 
@article{
author = "Miladinović, Marija R. and Zdujić, Miodrag and Veljović, Đorđe and Krstić, Jugoslav and Banković-Ilić, Ivana B. and Veljković, Vlada B. and Stamenković, Olivera S.",
year = "2020",
abstract = "The catalytic activity of the walnut shell ash was investigated in the biodiesel production by the sunflower oil methanolysis. The catalyst was characterized by the TG-DTA, XRD, Hg porosimetry, Ny physisorption, SEM, and Hammett method. In addition, the effects of the catalyst loading and the methanolto-oil molar ratio on the methyl esters synthesis were tested at the reaction temperature of 60 degrees C. The walnut shell ash provided a very fast reaction and a high FAME content (over 98%). As the reaction occurred in the absence of triacylglycerols mass transfer limitation, the pseudo-first-order model was employed for describing the kinetics of the reaction. The catalyst was successfully reused four times after the regeneration of the catalytic activity by recalcination at 800 degrees C.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Renewable Energy",
title = "Valorization of walnut shell ash as a catalyst for biodiesel production",
pages = "1043-1033",
volume = "147",
doi = "10.1016/j.renene.2019.09.056"
}
Miladinović, M. R., Zdujić, M., Veljović, Đ., Krstić, J., Banković-Ilić, I. B., Veljković, V. B.,& Stamenković, O. S.. (2020). Valorization of walnut shell ash as a catalyst for biodiesel production. in Renewable Energy
Pergamon-Elsevier Science Ltd, Oxford., 147, 1033-1043.
https://doi.org/10.1016/j.renene.2019.09.056
Miladinović MR, Zdujić M, Veljović Đ, Krstić J, Banković-Ilić IB, Veljković VB, Stamenković OS. Valorization of walnut shell ash as a catalyst for biodiesel production. in Renewable Energy. 2020;147:1033-1043.
doi:10.1016/j.renene.2019.09.056 .
Miladinović, Marija R., Zdujić, Miodrag, Veljović, Đorđe, Krstić, Jugoslav, Banković-Ilić, Ivana B., Veljković, Vlada B., Stamenković, Olivera S., "Valorization of walnut shell ash as a catalyst for biodiesel production" in Renewable Energy, 147 (2020):1033-1043,
https://doi.org/10.1016/j.renene.2019.09.056 . .
89
31
83

Optimization and kinetic modeling of waste lard methanolysis in a continuous reciprocating plate reactor

Miladinović, Marija R.; Stojković, Ivan; Velicković, Ana V.; Stamenković, Olivera S.; Banković-Ilić, Ivana B.; Veljković, Vlada B.

(Chemical Industry Press Co Ltd, Beijing, 2019)

TY  - JOUR
AU  - Miladinović, Marija R.
AU  - Stojković, Ivan
AU  - Velicković, Ana V.
AU  - Stamenković, Olivera S.
AU  - Banković-Ilić, Ivana B.
AU  - Veljković, Vlada B.
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4067
AB  - Continuous biodiesel production from a waste pig-roasting lard, methanol and KOH was carried out in a reciprocating plate reactor (RPR) using a factorial design containing three process factors, namely methanol/lard molar ratio, catalyst loading, and normalized height of the reactor. The main goals were to optimize the influential process factors with respect to biodiesel purity using the response surface methodology and to model the kinetics of the transesterification reaction in order to describe the change of triacylglycerols (TAG) and fatty acid methyl esters (FAME) concentrations along the RPR height. The first-order rate law was proved for both the reaction and the mass transfer. The model of the changing reaction mechanism and mass transfer of TAG was also applicable. Both kinetic models agreed with the experimental concentrations of TAG and FAME determined along the RPR height.
PB  - Chemical Industry Press Co Ltd, Beijing
T2  - Chinese Journal of Chemical Engineering
T1  - Optimization and kinetic modeling of waste lard methanolysis in a continuous reciprocating plate reactor
EP  - 2490
IS  - 10
SP  - 2481
VL  - 27
DO  - 10.1016/j.cjche.2019.02.019
ER  - 
@article{
author = "Miladinović, Marija R. and Stojković, Ivan and Velicković, Ana V. and Stamenković, Olivera S. and Banković-Ilić, Ivana B. and Veljković, Vlada B.",
year = "2019",
abstract = "Continuous biodiesel production from a waste pig-roasting lard, methanol and KOH was carried out in a reciprocating plate reactor (RPR) using a factorial design containing three process factors, namely methanol/lard molar ratio, catalyst loading, and normalized height of the reactor. The main goals were to optimize the influential process factors with respect to biodiesel purity using the response surface methodology and to model the kinetics of the transesterification reaction in order to describe the change of triacylglycerols (TAG) and fatty acid methyl esters (FAME) concentrations along the RPR height. The first-order rate law was proved for both the reaction and the mass transfer. The model of the changing reaction mechanism and mass transfer of TAG was also applicable. Both kinetic models agreed with the experimental concentrations of TAG and FAME determined along the RPR height.",
publisher = "Chemical Industry Press Co Ltd, Beijing",
journal = "Chinese Journal of Chemical Engineering",
title = "Optimization and kinetic modeling of waste lard methanolysis in a continuous reciprocating plate reactor",
pages = "2490-2481",
number = "10",
volume = "27",
doi = "10.1016/j.cjche.2019.02.019"
}
Miladinović, M. R., Stojković, I., Velicković, A. V., Stamenković, O. S., Banković-Ilić, I. B.,& Veljković, V. B.. (2019). Optimization and kinetic modeling of waste lard methanolysis in a continuous reciprocating plate reactor. in Chinese Journal of Chemical Engineering
Chemical Industry Press Co Ltd, Beijing., 27(10), 2481-2490.
https://doi.org/10.1016/j.cjche.2019.02.019
Miladinović MR, Stojković I, Velicković AV, Stamenković OS, Banković-Ilić IB, Veljković VB. Optimization and kinetic modeling of waste lard methanolysis in a continuous reciprocating plate reactor. in Chinese Journal of Chemical Engineering. 2019;27(10):2481-2490.
doi:10.1016/j.cjche.2019.02.019 .
Miladinović, Marija R., Stojković, Ivan, Velicković, Ana V., Stamenković, Olivera S., Banković-Ilić, Ivana B., Veljković, Vlada B., "Optimization and kinetic modeling of waste lard methanolysis in a continuous reciprocating plate reactor" in Chinese Journal of Chemical Engineering, 27, no. 10 (2019):2481-2490,
https://doi.org/10.1016/j.cjche.2019.02.019 . .
8
5
6

Continuous biodiesel production under subcritical condition of methanol - Design of pilot plant and packed bed reactor with MnCO3/Na-silicate catalyst

Liu, Hui; Lukić, Ivana; Miladinović, Marija R.; Veljković, Vlada B.; Zdujić, Miodrag; Zhu, Xiaosun; Zhang, Yanan; Skala, Dejan

(Pergamon-Elsevier Science Ltd, Oxford, 2018)

TY  - JOUR
AU  - Liu, Hui
AU  - Lukić, Ivana
AU  - Miladinović, Marija R.
AU  - Veljković, Vlada B.
AU  - Zdujić, Miodrag
AU  - Zhu, Xiaosun
AU  - Zhang, Yanan
AU  - Skala, Dejan
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4016
AB  - The continuous biodiesel production from soybean oil was carried out under the subcritical condition of methanol with MnCO3/Na-silicate as a heterogeneous catalyst. The transesterification rate was first investigated in a set of experiments performed in a batch autoclave at 448 K using methanol-to-oil molar ratio of 18:1 and various catalyst loadings (5, 10 and 20 wt% based on the oil mass). The results from these experiments, as well as the experimental data and the appropriate kinetic model recently reported in the literature were used for designing a packed bed tubular reactor (PBTR), a main unit of the pilot plant with the capacity of 100 L of biodiesel per day. The pilot plant was constructed and tested under various operating conditions. The first 11 h of the pilot-plant operation was realized in the tubular reactor packed with inert glass beads (i.e. without the catalyst) in order to analyze the effect of the non-catalyzed subcritical biodiesel (fatty acid methyl esters, FAME) production. Then, glass beads were replaced with a mix of MnCO3/Na-silicate catalyst particles and glass beads, and the catalytic biodiesel production was continuously run under the subcritical methanol condition for 85 h. Two mass balance tests during the continuous pilot plant operation were performed.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Energy Conversion and Management
T1  - Continuous biodiesel production under subcritical condition of methanol - Design of pilot plant and packed bed reactor with MnCO3/Na-silicate catalyst
EP  - 504
SP  - 494
VL  - 168
DO  - 10.1016/j.enconman.2018.05.028
ER  - 
@article{
author = "Liu, Hui and Lukić, Ivana and Miladinović, Marija R. and Veljković, Vlada B. and Zdujić, Miodrag and Zhu, Xiaosun and Zhang, Yanan and Skala, Dejan",
year = "2018",
abstract = "The continuous biodiesel production from soybean oil was carried out under the subcritical condition of methanol with MnCO3/Na-silicate as a heterogeneous catalyst. The transesterification rate was first investigated in a set of experiments performed in a batch autoclave at 448 K using methanol-to-oil molar ratio of 18:1 and various catalyst loadings (5, 10 and 20 wt% based on the oil mass). The results from these experiments, as well as the experimental data and the appropriate kinetic model recently reported in the literature were used for designing a packed bed tubular reactor (PBTR), a main unit of the pilot plant with the capacity of 100 L of biodiesel per day. The pilot plant was constructed and tested under various operating conditions. The first 11 h of the pilot-plant operation was realized in the tubular reactor packed with inert glass beads (i.e. without the catalyst) in order to analyze the effect of the non-catalyzed subcritical biodiesel (fatty acid methyl esters, FAME) production. Then, glass beads were replaced with a mix of MnCO3/Na-silicate catalyst particles and glass beads, and the catalytic biodiesel production was continuously run under the subcritical methanol condition for 85 h. Two mass balance tests during the continuous pilot plant operation were performed.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Energy Conversion and Management",
title = "Continuous biodiesel production under subcritical condition of methanol - Design of pilot plant and packed bed reactor with MnCO3/Na-silicate catalyst",
pages = "504-494",
volume = "168",
doi = "10.1016/j.enconman.2018.05.028"
}
Liu, H., Lukić, I., Miladinović, M. R., Veljković, V. B., Zdujić, M., Zhu, X., Zhang, Y.,& Skala, D.. (2018). Continuous biodiesel production under subcritical condition of methanol - Design of pilot plant and packed bed reactor with MnCO3/Na-silicate catalyst. in Energy Conversion and Management
Pergamon-Elsevier Science Ltd, Oxford., 168, 494-504.
https://doi.org/10.1016/j.enconman.2018.05.028
Liu H, Lukić I, Miladinović MR, Veljković VB, Zdujić M, Zhu X, Zhang Y, Skala D. Continuous biodiesel production under subcritical condition of methanol - Design of pilot plant and packed bed reactor with MnCO3/Na-silicate catalyst. in Energy Conversion and Management. 2018;168:494-504.
doi:10.1016/j.enconman.2018.05.028 .
Liu, Hui, Lukić, Ivana, Miladinović, Marija R., Veljković, Vlada B., Zdujić, Miodrag, Zhu, Xiaosun, Zhang, Yanan, Skala, Dejan, "Continuous biodiesel production under subcritical condition of methanol - Design of pilot plant and packed bed reactor with MnCO3/Na-silicate catalyst" in Energy Conversion and Management, 168 (2018):494-504,
https://doi.org/10.1016/j.enconman.2018.05.028 . .
9
4
8

Biodiesel production by methanolysis of waste lard from piglet roasting over quicklime

Stojković, Ivan; Miladinović, Marija R.; Stamenković, Olivera S.; Banković-Ilić, Ivana B.; Povrenović, Dragan; Veljković, Vlada B.

(Elsevier Sci Ltd, Oxford, 2016)

TY  - JOUR
AU  - Stojković, Ivan
AU  - Miladinović, Marija R.
AU  - Stamenković, Olivera S.
AU  - Banković-Ilić, Ivana B.
AU  - Povrenović, Dragan
AU  - Veljković, Vlada B.
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3289
AB  - Waste lard from piglet roasting and quicklime (basically CaO) as a priceless fatty feedstock and a cheap solid catalyst, respectively were tested for the biodiesel production by methanolysis in a batch stirred reactor at moderate reaction temperatures (40-60 degrees C) for the kinetic study. For comparison, unheated and heated pork lards, as well as pure CaO, were also included in this study. The mass transfer limitation was observed in the initial period of all methanolysis reactions. The kinetic model combining the changing-and first-order reaction rate laws with respect to triacylglycerols and fatty acid methyl esters (FAMEs), respectively was verified for all three lardy feedstocks and both catalysts. The catalytic activity of quicklime was the same as that of pure CaO. The activation energy was demonstrated to be independent of the feedstock and the catalyst (59.1 +/- 0.6 kJ/mol) but the waste lard reacted faster than the unheated and heated pork lards. At the methanol-to-lard molar ratio of 6:1, the catalyst amount of 5% (based on the lard weight) and the reaction temperature of 60 degrees C, a high FAME concentration in the final ester products (97.5%) within 60 min were achieved with the waste lard and quicklime in two consecutive batches. The same kinetic model was applicable in a continuous packed-bed tubular reactor filled with quicklime bits (2.0-3.15 mm) at the methanol-to-waste lard molar ratio of 6:1, the reaction temperature of 60 degrees C and the residence time of 1 h. Under these conditions, the biodiesel yield was 97.6%, while the FAME concentration in the biodiesel product was 96.5%.
PB  - Elsevier Sci Ltd, Oxford
T2  - Fuel
T1  - Biodiesel production by methanolysis of waste lard from piglet roasting over quicklime
EP  - 466
SP  - 454
VL  - 182
DO  - 10.1016/j.fuel.2016.06.014
ER  - 
@article{
author = "Stojković, Ivan and Miladinović, Marija R. and Stamenković, Olivera S. and Banković-Ilić, Ivana B. and Povrenović, Dragan and Veljković, Vlada B.",
year = "2016",
abstract = "Waste lard from piglet roasting and quicklime (basically CaO) as a priceless fatty feedstock and a cheap solid catalyst, respectively were tested for the biodiesel production by methanolysis in a batch stirred reactor at moderate reaction temperatures (40-60 degrees C) for the kinetic study. For comparison, unheated and heated pork lards, as well as pure CaO, were also included in this study. The mass transfer limitation was observed in the initial period of all methanolysis reactions. The kinetic model combining the changing-and first-order reaction rate laws with respect to triacylglycerols and fatty acid methyl esters (FAMEs), respectively was verified for all three lardy feedstocks and both catalysts. The catalytic activity of quicklime was the same as that of pure CaO. The activation energy was demonstrated to be independent of the feedstock and the catalyst (59.1 +/- 0.6 kJ/mol) but the waste lard reacted faster than the unheated and heated pork lards. At the methanol-to-lard molar ratio of 6:1, the catalyst amount of 5% (based on the lard weight) and the reaction temperature of 60 degrees C, a high FAME concentration in the final ester products (97.5%) within 60 min were achieved with the waste lard and quicklime in two consecutive batches. The same kinetic model was applicable in a continuous packed-bed tubular reactor filled with quicklime bits (2.0-3.15 mm) at the methanol-to-waste lard molar ratio of 6:1, the reaction temperature of 60 degrees C and the residence time of 1 h. Under these conditions, the biodiesel yield was 97.6%, while the FAME concentration in the biodiesel product was 96.5%.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Fuel",
title = "Biodiesel production by methanolysis of waste lard from piglet roasting over quicklime",
pages = "466-454",
volume = "182",
doi = "10.1016/j.fuel.2016.06.014"
}
Stojković, I., Miladinović, M. R., Stamenković, O. S., Banković-Ilić, I. B., Povrenović, D.,& Veljković, V. B.. (2016). Biodiesel production by methanolysis of waste lard from piglet roasting over quicklime. in Fuel
Elsevier Sci Ltd, Oxford., 182, 454-466.
https://doi.org/10.1016/j.fuel.2016.06.014
Stojković I, Miladinović MR, Stamenković OS, Banković-Ilić IB, Povrenović D, Veljković VB. Biodiesel production by methanolysis of waste lard from piglet roasting over quicklime. in Fuel. 2016;182:454-466.
doi:10.1016/j.fuel.2016.06.014 .
Stojković, Ivan, Miladinović, Marija R., Stamenković, Olivera S., Banković-Ilić, Ivana B., Povrenović, Dragan, Veljković, Vlada B., "Biodiesel production by methanolysis of waste lard from piglet roasting over quicklime" in Fuel, 182 (2016):454-466,
https://doi.org/10.1016/j.fuel.2016.06.014 . .
29
17
25

Heterogeneous base-catalyzed methanolysis of vegetable oils: State of art

Miladinović, Marija R.; Lukić, Ivana; Stamenković, Olivera S.; Veljković, Vlada B.; Skala, Dejan

(Association of Chemical Engineers of Serbia, 2010)

TY  - JOUR
AU  - Miladinović, Marija R.
AU  - Lukić, Ivana
AU  - Stamenković, Olivera S.
AU  - Veljković, Vlada B.
AU  - Skala, Dejan
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1626
AB  - Today, homogeneous base-catalyzed methanolysis is the most frequently used method for industrial biodiesel production. High requirements for the quality of the feedstocks and the problems related to the huge amount of wastewaters have led to the development of novel biodiesel production technologies. Among them, the most important is heterogeneous base-catalyzed methanolysis, which has been intensively investigated over the last decade in order to develop new catalytic systems, optimize the reaction conditions and to recycle catalysts. These studies are a basis for continuous development of biodiesel production on an industrial scale in the near future. The presented work summarize up-to-date studies on biodiesel production by heterogeneous base-catalyzed methanolysis. The main goals were to point out the application of different base compounds as catalysts, the methods of catalyst preparation, impregnation on carriers and recycling as well as the possibilities to improve existing base-catalyzed biodiesel production processes and to develop novel ones.
AB  - Homogena bazno katalizovana metanoliza je najčešće primenjivan postupak dobijanja biodizela u industrijskim uslovima. Visoki zahtevi u pogledu kvaliteta uljnih sirovina i ekološki problemi otpadnih voda doprineli su razvoju novih postupaka sinteze biodizela. Među njima značajno mesto zauzima heterogena bazno katalizovana metanoliza ulja, koja je u poslednjoj deceniji intenzivno proučavana sa aspekta razvoja novih katalitičkih sistema, optimizacije reakcionih uslova metanolize i mogućnosti reciklovanja katalizatora. Ispitivanja ovakvih sistema čine osnovu za razvoj kontinualnih postupaka heterogene bazno katalizovane metanolize, na kojima će se u bliskoj budućnosti bazirati industrijska proizvodnja biodizela. U ovom radu analizirana su dosadašnja ispitivanja postupaka dobijanja biodizela heterogenom bazno katalizovanom metanolizom. Cilj rada je da se ukaže na primenu različitih baznih jedinjenja kao katalizatora, načine njihove pripreme, nanošenja na nosače i recikliranja, kao i na mogućnosti unapređenja postojećih i razvoja novih procesa dobijanja biodizela baznom katalizom.
PB  - Association of Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Heterogeneous base-catalyzed methanolysis of vegetable oils: State of art
T1  - Heterogena bazno katalizovana metanoliza biljnih ulja - presek stanja
EP  - 80
IS  - 2
SP  - 63
VL  - 64
DO  - 10.2298/HEMIND100304012M
ER  - 
@article{
author = "Miladinović, Marija R. and Lukić, Ivana and Stamenković, Olivera S. and Veljković, Vlada B. and Skala, Dejan",
year = "2010",
abstract = "Today, homogeneous base-catalyzed methanolysis is the most frequently used method for industrial biodiesel production. High requirements for the quality of the feedstocks and the problems related to the huge amount of wastewaters have led to the development of novel biodiesel production technologies. Among them, the most important is heterogeneous base-catalyzed methanolysis, which has been intensively investigated over the last decade in order to develop new catalytic systems, optimize the reaction conditions and to recycle catalysts. These studies are a basis for continuous development of biodiesel production on an industrial scale in the near future. The presented work summarize up-to-date studies on biodiesel production by heterogeneous base-catalyzed methanolysis. The main goals were to point out the application of different base compounds as catalysts, the methods of catalyst preparation, impregnation on carriers and recycling as well as the possibilities to improve existing base-catalyzed biodiesel production processes and to develop novel ones., Homogena bazno katalizovana metanoliza je najčešće primenjivan postupak dobijanja biodizela u industrijskim uslovima. Visoki zahtevi u pogledu kvaliteta uljnih sirovina i ekološki problemi otpadnih voda doprineli su razvoju novih postupaka sinteze biodizela. Među njima značajno mesto zauzima heterogena bazno katalizovana metanoliza ulja, koja je u poslednjoj deceniji intenzivno proučavana sa aspekta razvoja novih katalitičkih sistema, optimizacije reakcionih uslova metanolize i mogućnosti reciklovanja katalizatora. Ispitivanja ovakvih sistema čine osnovu za razvoj kontinualnih postupaka heterogene bazno katalizovane metanolize, na kojima će se u bliskoj budućnosti bazirati industrijska proizvodnja biodizela. U ovom radu analizirana su dosadašnja ispitivanja postupaka dobijanja biodizela heterogenom bazno katalizovanom metanolizom. Cilj rada je da se ukaže na primenu različitih baznih jedinjenja kao katalizatora, načine njihove pripreme, nanošenja na nosače i recikliranja, kao i na mogućnosti unapređenja postojećih i razvoja novih procesa dobijanja biodizela baznom katalizom.",
publisher = "Association of Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Heterogeneous base-catalyzed methanolysis of vegetable oils: State of art, Heterogena bazno katalizovana metanoliza biljnih ulja - presek stanja",
pages = "80-63",
number = "2",
volume = "64",
doi = "10.2298/HEMIND100304012M"
}
Miladinović, M. R., Lukić, I., Stamenković, O. S., Veljković, V. B.,& Skala, D.. (2010). Heterogeneous base-catalyzed methanolysis of vegetable oils: State of art. in Hemijska industrija
Association of Chemical Engineers of Serbia., 64(2), 63-80.
https://doi.org/10.2298/HEMIND100304012M
Miladinović MR, Lukić I, Stamenković OS, Veljković VB, Skala D. Heterogeneous base-catalyzed methanolysis of vegetable oils: State of art. in Hemijska industrija. 2010;64(2):63-80.
doi:10.2298/HEMIND100304012M .
Miladinović, Marija R., Lukić, Ivana, Stamenković, Olivera S., Veljković, Vlada B., Skala, Dejan, "Heterogeneous base-catalyzed methanolysis of vegetable oils: State of art" in Hemijska industrija, 64, no. 2 (2010):63-80,
https://doi.org/10.2298/HEMIND100304012M . .
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