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Wyszukujesz frazę "Wróblewska, A." wg kryterium: Wszystkie pola


Tytuł:
Oxidation of hexafluoropropylene with molecular oxygen
Autorzy:
Meissner, E.
Wróblewska, A.
Powiązania:
https://bibliotekanauki.pl/articles/778427.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
heksafluoropropylen
tlenek heksafluoropropylenu
epoksydacja
oligomeryzacja
Opis:
The results of the oxidation of hexafluoropropylene (HFP) to hexafluoropropylene oxide (HFPO) have been presented. The oxidation was carried out in an autoclave within the range of temperatures of 120 - 170°C and in the presence of an organic solvent (carbon tetrachloride). Molecular oxygen was used here as an oxidizing agent. The influence of: the molar ratio of HFP/O from 13.4 to 4.09:1, the process temperature, the addition of inert gas (nitrogen) from 4 to 18 atm and the periodical dosing of oxygen were investigated. The functions describing the process were: the conversion of HFP and the yield of HFPO in relation to HFP consumed. The presented process is very interesting owing to a wide application of HFPO.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 1; 20-22
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Oligomerization of hexafluoropropylene oxide in the presence of alkali metal halides
Autorzy:
Meissner, E.
Wróblewska, A.
Powiązania:
https://bibliotekanauki.pl/articles/777879.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
tlenek heksafluoropropylenu
oligomeryzacja
oligomery tlenku heksafluoropropylenu
heksafluoropropylene oxide
oligomers of hexafluoropropylene oxide
Opis:
Oligomers of hexafluoropropylene oxide are raw materials for the synthesis of compounds having unique properties such as high chemical and thermal resistance. Two basic parameters have influence on the process of hexafluoropropylene oxide oligomerization: the kind of the catalyst and the solvent. The temperature and pressure influence this process to a lesser extent. The influence of halide ions, the solvent and the temperature on the oligomerization of hexafluoropropylene oxide has been studied.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 3; 95-97
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Epoxidation of allyl-glycidyl ether with hydrogen peroxide over Ti-SBA-15 catalyst and in methanol medium
Autorzy:
Walasek, M.
Wróblewska, A.
Powiązania:
https://bibliotekanauki.pl/articles/778347.pdf
Data publikacji:
2016
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
diglycidyl ether
allyl-glycidyl ether
Ti-SBA-15
epoxidation
Opis:
This work presents the studies on the epoxidation of allyl-glycidyl ether (AGE) over the Ti-SBA-15 catalyst. In these studies an aqueous hydrogen peroxide was used as an oxidizing agent and as a solvent methanol was applied. The studies on the influence the following parameters: temperature (20–80°C), molar ratio of AGE/H2O2  (1:1.5–5:1), methanol concentration (10–90 wt%), catalyst content (1–9 wt%) and reaction time (15–240 min.) were carried out and the most favourable values of these parameters were chosen (temperature 80°C, molar ratio of AGE/H2O2 = 5:1, methanol concentration 30 wt%, catalyst content 3 wt% and the reaction time 240 min.). At these conditions the functions describing the process reached the following values: the selectivity of diglycidyl ether (DGE) 9.2 mol%, the conversion of AGE 13.9 mol% and the efficiency of H2O2  conversion 89.9 mol%.
Źródło:
Polish Journal of Chemical Technology; 2016, 18, 4; 9-14
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Research on the influence of parameters on hexafluoropropylene oxide oligomerization in the presence of complex amines
Autorzy:
Meissner, E.
Wróblewska, A.
Powiązania:
https://bibliotekanauki.pl/articles/777883.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
tlenek heksafluoropropylenu
oligomery tlenku heksafluoropropylenu
hexafluoropropylene oxide
oligomers of hexafluoropropylene oxide
Opis:
Oligomers of hexafluoropropylene oxide were tested as potential materials for obtaining various compounds with unique properties, of which most important are chemical and thermal resistance. Two basic parameters influence the oligomerization process of hexafluoropropylene oxide: the type of the catalyst and the type of the solvent. Other parameters such as temperature and pressure have significantly less influence. The influence of tertiary amines as catalyst, the type of the solvent, temperature, pressure and catalyst concentration were tested in the process of hexafluoropropylene oxide oligomerization.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 3; 98-100
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The new method of 1,2-epoxy-3-butanol production over titanium silicalite catalysts
Autorzy:
Wajzberg, J.
Wróblewska, A.
Powiązania:
https://bibliotekanauki.pl/articles/779811.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
1,2-epoksy-3-butanol
epoksydacja w fazie ciekłej
TS-1
Ti-Beta
Ti-MCM-41
1,2-epoxy-3-butanol
liquid phase epoxidation
Opis:
The results of 1-butene-3-ol (1B3O) epoxidation over the titanium silicalite catalysts: TS-1, Ti-Beta, Ti-MCM-41 has been presented. The optimal parameters obtained for the individual catalyst were compared. The main functions describing the process were: the selectivity of transformation to 1,2-epoxy-3-butanol (1,2E3B) in relation to 1B3O consumed, the conversions of 1B3O and hydrogen peroxide and the selectivity of the transformation to organic compounds in relation to the H2O2 consumed. The main product of the epoxidation process was 1,2-epoksy-3-butanol, the chemical compounds having a lot of applications.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 2; 49-52
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Studies on the deactivation of Ti-MCM-41 catalyst in the process of allyl alcohol epoxidation
Autorzy:
Wróblewska, A.
Makuch, E.
Powiązania:
https://bibliotekanauki.pl/articles/778158.pdf
Data publikacji:
2013
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
titanium silicate Ti-MCM-41 catalyst
deactivation of Ti-MCM-41catalyst
regeneration of Ti-MCM-41catalyst
Opis:
The synthesis of Ti-MCM-41 catalyst was performed. The obtained catalyst was characterized by the following instrumental methods: UV-vis, IR spectroscopy, XRD, and X-ray microanalysis. The activity of the obtained catalyst was tested in the process of allyl alcohol epoxidation with 30 wt.% hydrogen peroxide in methanol as a solvent and under atmospheric pressure. In the next stage, recovery of Ti-MCM-41 catalyst from the post-reaction mixture and its regeneration by washing with appropriate solvents and drying were conducted. In the case of total loss of the activity of the catalyst, calcination of the catalyst was also carried out. The loss of titanium from the structure of Ti-MCM-41 catalyst and a partial collapsing of the structure of this catalyst can be the main reason of the decrease the activity of the catalyst what was manly visible in the decrease of the values of two functions of this process: the allyl alcohol conversion and conversion of hydrogen peroxide to organic compounds.
Źródło:
Polish Journal of Chemical Technology; 2013, 15, 4; 111-115
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Epoxidation of 1-buten-3-ol under atmospheric pressure over the Ti-Beta catalyst
Autorzy:
Wróblewska, A.
Wajzberg, J.
Powiązania:
https://bibliotekanauki.pl/articles/779898.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
epoksydacja w fazie ciekłej
1,2-epoksy-3-butanol
katalizator Ti-Beta
liquid phase epoxidation
1,2-epoxy-3-butanol
Ti-Beta catalyst
Opis:
The results of 1-buten-3-ol (1B3O) epoxidation with 30% hydrogen peroxide over the Ti-Beta catalyst were presented. The studies were performed under the atmospheric pressure and at the presence of methanol as a solvent. There was examined the influence of the following parameters: the temperature (0 - 60°C), the molar ratio of 1B3O/H2O2 (1:1 - 5:1), methanol concentration (5 - 90 wt%), the Ti-Beta catalyst concentration (0.1 - 5.0 wt%) and the reaction time (0.5 - 5.0 h). The optimal parameters were determined by using the following functions: the selectivity of the transformation to 1,2-epoxy-3-butanol (1,2E3B) in relation to 1B3O consumed, the selectivity of the transformation to organic compounds in relation to hydrogen peroxide consumed, the conversions of 1B3O and hydrogen peroxide. The main product of epoxidation was 1,2-epoxy-3-butanol, epoxide having several applications.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 2; 110-113
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bis(3-methyl-1-propene) ether and 3-(3-methyl-1-propene)-3-methyl-1,2-epoxypropane ether synthesis during the epoxidation of 1-butene-3-ol with hydrogen peroxide over the TS-2 catalyst
Autorzy:
Wróblewska, A.
Wójtowicz, G.
Powiązania:
https://bibliotekanauki.pl/articles/779202.pdf
Data publikacji:
2010
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
bis(3-methyl-1-propen) eter
3-(3-metylo-1-propen) eter-3-metylo-1 ,2-epoksypropan
TS-2
nadtlenek wodoru
epoksydowanie w fazie ciekłej
bis(3-methyl-1-propene) ether
3-(3-methyl-1-propene)-3-methyl-1,2-epoxypropane ether
hydrogen peroxide
epoxidation in liquid phase
Opis:
The influence of technological parameters on the transformation of 1-butene-3-ol (1B3O) to bis(3-methyl- 1-propene) ether (2x1B3O ether) and 3-(3-methyl-1-propene)-3-methyl-1,2-epoxypropane ether (1B3Ox1,2EB3O ether) over the TS-2 catalyst was presented. The reaction was performed in a glass reactor at atmospheric pressure and in methanol medium (protic solvent). The optimum conditions of 2x1B3O ether and 1B3Ox1,2EB3O ether obtaining were established by the mathematical method of experiments design (rotatable-uniform design) and after the analyses of the layer drawings.
Źródło:
Polish Journal of Chemical Technology; 2010, 12, 3; 66-71
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and characteristics of titanium silicalite TS-1, Ti-Beta and Ti-MWW catalysts
Autorzy:
Wróblewska, A.
Fajdek, A.
Milchert, E.
Powiązania:
https://bibliotekanauki.pl/articles/779396.pdf
Data publikacji:
2009
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
TS-1
Ti-Beta
Ti-MWW
titanium-silicalite catalysts
Opis:
The synthesis methods of the following titanium-silicalite catalysts: TS-1, Ti-Beta and Ti-MWW were presented. The results of the analyses of the catalysts by XRD, SEM and IR, UV-vis methods were also shown. A brief description of the catalytic performances of these catalysts in the oxidation process of olefins, alkenes, alcohols and aromatic compounds was presented.
Źródło:
Polish Journal of Chemical Technology; 2009, 11, 1; 64-71
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Epoxidation of crotyl alcohol in the presence of titanium silicalite Ti-MWW catalyst – the new and friendly method of 2,3-epoxybutane-1-ol synthesis
Autorzy:
Wróblewska, A.
Fajdek, A.
Milchert, E.
Powiązania:
https://bibliotekanauki.pl/articles/779457.pdf
Data publikacji:
2010
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
Ti-MWW
krotyl epoksydacji alkoholu
2,3-epoksybutan-1-ol
crotyl alcohol epoxidation
2,3-epoxybutane-1-ol
Opis:
Epoxidation of crotyl alcohol (CA) with 30 wt% hydrogen peroxide over Ti-MWW catalyst has been studied with methanol as a solvent and at autogenic pressure. The influence of temperature in the range of 20 – 120oC, the molar ratio of CA/H2O21:1-5:1, methanol concentration 5 – 90 wt%, Ti-MWW catalyst concentration 0.0 – 5.0 wt% and the reaction time 5 – 300 min have been studied. The main product of CA epoxidation is 2,3-epoxybutane-1-ol (2,3EB1O), a compound with many applications.
Źródło:
Polish Journal of Chemical Technology; 2010, 12, 2; 57-61
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Epoxidation of 2-buten-1-ol over Ti-MCM-41 and Ti-MCM-48 titanium silicalite catalysts
Autorzy:
Wróblewska, A.
Ławro, E.
Milchert, E.
Powiązania:
https://bibliotekanauki.pl/articles/777986.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
epoksydacja
2,3-epoksybutan-1-ol
Ti-MCM-41
Ti-MCM-48
epoxidation
2,3-epoxybutan-1-ol
Opis:
The results of the epoxidation of 2-buten-1-ol with 30 wt% hydrogen peroxide have been presented. As a solvent methanol was used. The process was carried out over the titanium silicalite catalysts: Ti-MCM-41 and Ti-MCM-48. The influence of temperature (20 - 120°C). the molar ratio of CRA/H2O2 (5:1 - 5:1), methanol concentration (5 - 90 wt%), catalyst concentration (0.1 - 5.0 wt%) and the reaction time (30 -300 min) was investigated. The obtained results were used for the determination of optimum conditions of running the epoxidation process of 2-buten-1-ol.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 3; 1-4
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Environmental friendly method of the epoxidation of limonene with hydrogen peroxide over the Ti-SBA-15 catalyst
Autorzy:
Wróblewska, A.
Malko, M.
Walasek, M.
Powiązania:
https://bibliotekanauki.pl/articles/779494.pdf
Data publikacji:
2018
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
Limonene epoxidation
1,2-epoxylimonene
1,2-epoxylimonene diol
perillyl alcohol
Ti-SBA-15 catalyst
titanium-silicate catalysts
hydrogen peroxide
Opis:
This work presents the studies on the epoxidation of limonene to 1,2-epoxylimonene with hydrogen peroxide and over the titanium-silicate Ti-SBA-15 catalyst. The main object of the research was a solvent effect on the epoxidation process. The influence of solvents, such as: methanol, toluene, propan-2-ol (isopropyl alcohol), acetonitrile and ethanol has been studied. Furthermore, the influence of temperature in the range of 0-120°C and the reaction time in the range of 0.25-48 h have been investigated. Gas chromatography and iodometric titration methods were used to establish the products of this process and amount of the unreacted hydrogen peroxide. 1,2-Epoxylimonene, 1,2-epoxylimonene diol, perillyl alcohol, carvone and carveol have been determined as the main products of this process. All these compounds are very valuable raw materials for organic syntheses, medicine or cosmetic and food industry.
Źródło:
Polish Journal of Chemical Technology; 2018, 20, 4; 6-12
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
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 Ti-MWW catalyst - its characteristic and catalytic properties in the epoxidation of allyl alcohol by hydrogen peroxide
Autorzy:
Wróblewska, A.
Fajdek, A.
Milchert, E.
Grzmil, B.
Powiązania:
https://bibliotekanauki.pl/articles/778365.pdf
Data publikacji:
2010
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
Ti-MWW
katalizatory tytanowo-silikalitowe
glicydol
epoksydacja w fazie ciekłej
nadtlenek wodoru
titanium-silicalites
glycidol
liquid phase epoxidation
hydrogen peroxide
Opis:
Ti-MWW, one of the latest titanium-silicalite catalysts, has been prepared by direct hydrothermal synthesis using hexamethyleneimine as a structure-directing agent. The characteristic of the catalyst was performed by means of the following methods: XRD, SEM, IR, UV-vis and X'Ray microanalysis. The catalytic properties of Ti-MWW have been compared with those of the conventional titanium-silicalites TS-1 and TS-2 in the epoxidation of allyl alcohol with hydrogen peroxide. The process has been described by the following main functions: the selectivity of the transformation to glycidol in relation to allyl alcohol consumed, the conversions of the substrates (allyl alcohol and hydrogen peroxide) and the selectivity of the transformation to organic compounds in relation to hydrogen peroxide consumed.
Źródło:
Polish Journal of Chemical Technology; 2010, 12, 1; 29-34
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł

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