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Wyszukujesz frazę "Wroblewska, P." wg kryterium: Autor


Wyświetlanie 1-5 z 5
Tytuł:
The oxidation of limonene at raised pressure and over the various titanium-silicate catalysts
Autorzy:
Wróblewska, A.
Makuch, E.
Miądlicki, P.
Powiązania:
https://bibliotekanauki.pl/articles/779024.pdf
Data publikacji:
2015
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
limonene oxidation
hydrogen peroxide
TBHP
Opis:
This work presents the studies on the oxidation of limonene with hydrogen peroxide and tert-butyl hydroperoxide (TBHP) in the presence of : TS-2, Ti-Beta, Ti-MCM-41 and Ti-MWW catalysts, at the autogenic pressure and atmospheric pressure. The examination were performed at the following conditions: the temperature of 140°C (studies in the autoclave) and 80°C (studies in glass reactor), the molar ratio of limonene/oxidant (H2O2 or WNTB) = 1:1, the methanol concentration 80 wt%, the catalyst content 3 wt%, the reaction time 3 h and the intensity of stirring 500 rpm. The analysis of the results showed that in process not only 1,2-epoxylimonene was formed but also: 1,2-epoxylimonene diol, carveol, carvone and perillyl alcohol but for 1,2-epoxylimonene obtaining the better method was the method at the autogenic pressure and in the presence of TBHP.
Źródło:
Polish Journal of Chemical Technology; 2015, 17, 4; 82-87
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Epoxidation of natural limonene extracted from orange peels with hydrogen peroxide over Ti-MCM-41 catalyst
Autorzy:
Wróblewska, A.
Miądlicki, P.
Makuch, E.
Benedyczak, N.
Powiązania:
https://bibliotekanauki.pl/articles/777909.pdf
Data publikacji:
2018
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Opis:
The paper presents the oxidation of natural limonene (extracted from waste orange peels) by 60 wt% hydrogen peroxide, in the presence of Ti-MCM-41 catalyst and in methanol as the solvent. The aim of the research was to develop the most favorable technological parameters for the process of limonene oxidation (temperature, molar ratio of limonene to hydrogen peroxide, methanol concentration, Ti-MCM-41 catalyst content and reaction time) by analyzing changes in the main functions describing this process: the conversion of limonene, selectivities of appropriate products, the conversion of hydrogen peroxide and the effective conversion of hydrogen peroxide. The process is environmentally friendly process and it uses renewable raw material - limonene and a safe oxidant -hydrogen peroxide. During the study, very valuable oxygenated derivatives of limonene were obtained: 1,2-epoxylimonene, its diol, carvone, carveol, and perillyl alcohol. These compounds are used in medicine, cosmetics, perfumery, food and polymers industries.
Źródło:
Polish Journal of Chemical Technology; 2018, 20, 1; 1-6
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The utilization of the mesoporous Ti-SBA-15 catalyst in the epoxidation of allyl alcohol to glycidol and diglycidyl ether in the water medium
Autorzy:
Wróblewska, A.
Makuch, E.
Dzięcioł, M.
Jędrzejewski, R.
Kochmański, P.
Kochmańska, A.
Kucharski, Ł.
Powiązania:
https://bibliotekanauki.pl/articles/777977.pdf
Data publikacji:
2015
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
glycidol
diglycidyl ether
Ti-SBA-15 catalyst
allyl alcohol epoxidation
hydrogen peroxide
Opis:
This work presents the studies on the optimization the process of allyl alcohol epoxidation over the Ti-SBA-15 catalyst. The optimization was carried out in an aqueous medium, wherein water was introduced into the reaction medium with an oxidizing agent (30 wt% aqueous solution of hydrogen peroxide) and it was formed in the reaction medium during the processes. The main investigated technological parameters were: the temperature, the molar ratio of allyl alcohol/hydrogen peroxide, the catalyst content and the reaction time. The main functions the process were: the selectivity of transformation to glycidol in relation to allyl alcohol consumed, the selectivity of transformation to diglycidyl ether in relation to allyl alcohol consumed, the conversion of allyl alcohol and the selectivity of transformation to organic compounds in relation to hydrogen peroxide consumed. The analysis of the layer drawings showed that in water solution it is best to conduct allyl alcohol epoxidation in direction of glycidol (selectivity of glycidol 54 mol%) at: the temperature of 10–17°C, the molar ratio of reactants 0.5–1.9, the catalyst content 2.9–4.0 wt%, the reaction time 2.7–3.0 h and in direction of diglycidyl ether (selectivity of diglycidyl ether 16 mol%) at: the temperature of 18–33°C, the molar ratio of reactants 0.9–1.65, the catalyst content 2.0–3.4 wt%, the reaction time 1.7–2.6 h. The presented method allows to obtain two very valuable intermediates for the organic industry.
Źródło:
Polish Journal of Chemical Technology; 2015, 17, 4; 23-31
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Preparation, properties and potential applications of a photocurable varnish with pleasant limonene smell
Autorzy:
Bednarczyk, P.
Wróblewska, A.
Czech, Z.
Malko, M.W.
Rozwadowski, Z.
Markowska-Szczupak, A.
Powiązania:
https://bibliotekanauki.pl/articles/778106.pdf
Data publikacji:
2016
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
varnishes with limonene
smelling varnishes
urethane acrylate
UV-curing coating
Opis:
Photocurable materials which are obtained on the basis of urethane acrylate resins are often used in the industry for the production varnishes or protective coatings. The main disadvantage which is connected with the utilization of these varnishes is their unpleasant smell during the process of production and curing. This work presents the photocurable varnish which was obtained on the basis of aliphatic urethane acrylate and R-(+)-limonene. The utilization of this raw materials allows to obtain the smelling coatings. The aim of this work were the studies on the influence of limonene molecules on the mechanical properties of the UV-cured coatings. These studies showed that the coatings with limonene molecules retain their properties, and are characterized by the very good adhesion, cohesion and high gloss. These kinds of varnishes can be applied for preparation of appropriate protective coatings on the surface of wood, metals, and nail plates. These protective coatings have not only pleasure smell but also can have the bactericidal and fungicidal properties. The studies performed with Escherichia coli ATCC29425 and Candida albicans confirmed these properties.
Źródło:
Polish Journal of Chemical Technology; 2016, 18, 2; 13-19
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Montmorillonite as the catalyst in oxidation of limonene with hydrogen peroxide and in isomerization of limonene
Autorzy:
Malko, M.
Antosik, A. K.
Wróblewska, A.
Czech, Z.
Wilpiszewska, K.
Miądlicki, P.
Michalkiewicz, B.
Powiązania:
https://bibliotekanauki.pl/articles/779496.pdf
Data publikacji:
2017
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
montmorillonite
R-(+)-limonene
oxidation
isomerization
hydrogen peroxide
heterogeneous catalysis
Opis:
In our studies montmorillonite (MMT) was used as the heterogeneous, natural catalyst. This material was previously prepared by bentonite purification with help of the sedimentation method. The obtained catalyst was characterized by: XRD, SEM, BET and EDX. Catalytic tests with montmorillonite as the catalyst were performed with the natural terpene – R-(+)-limonene. This compound was oxidized with hydrogen peroxide and, moreover, in the separate process it was also isomerized. As the main products of limonene oxidation were detected: (1,2-8,9)-diepoxide, perillyl alcohol, carvone, carveol, 1,2-epoxylimonene and 1,2-epoxylimonene diol. In the isomerization of R-(+)-limonene were formed: terpinenes, terpinolene and p-cymene. Conversions of limonene in these processes reached 70–80%. The application of montmorillonite (the natural of origin) in the studied processes (oxidation and isomerization) is environmentally friendly, it allows to reduce the cost of the studied processes. The resulting products of the processes of oxidation and isomerization of R-(+)-limonene have many applications.
Źródło:
Polish Journal of Chemical Technology; 2017, 19, 4; 50-58
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-5 z 5

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