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Tytuł:
The influence of the chain length and the functional group steric accessibility of thiols on the phase transfer efficiency of gold nanoparticles from water to toluene
Autorzy:
Soliwoda, K.
Tomaszewska, E.
Tkacz-Szczesna, B.
Rosowski, M.
Celichowski, G.
Grobelny, J.
Powiązania:
https://bibliotekanauki.pl/articles/779168.pdf
Data publikacji:
2014
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
gold nanoparticles
phase transfer
thiols
1-decanethiol
1,1-dimethyldecanethiol
1-dodecanethiol
1-oktadecanethiol
1-tetradecanethiol
Opis:
This paper describes the influence of the chain length and the functional group steric accessibility of thiols modifiers on the phase transfer process efficiency of water synthesized gold nanoparticles (AuNPs) to toluene. The following thiols were tested: 1-decanethiol, 1,1-dimethyldecanethiol, 1-dodecanethiol, 1-tetradecanethiol and 1-oktadecanethiol. Nanoparticles (NPs) synthesized in water were precisely characterized before the phase transfer process using Atomic Force Microscopy (AFM) and Transmission Electron Microscopy (TEM). The optical properties of AuNPs before and after the phase transfer were studied by the UV-Vis spectroscopy. Additionally, the particle size and size distribution before and after the phase transfer of nanoparticles were investigated using Dynamic Light Scattering (DLS). It turned out that the modification of NPs surface was not effective in the case of 1,1-dimethyldecanethiol, probably because of the difficult steric accessibility of the thiol functional group to NPs surface. Consequently, the effective phase transfer of AuNPs from water to toluene did not occur. In toluene the most stable were nanoparticles modified with 1-decanethiol, 1-dodecanethiol and 1-tetradecanethiol.
Źródło:
Polish Journal of Chemical Technology; 2014, 16, 1; 86-91
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Influence of reduction time of copper based catalysts: Cu/Al2O3 and CuCr2O4 on hydrogenolysis of glycerol
Autorzy:
Wołosiak-Hnat, A.
Milchert, E.
Lewandowski, G.
Grzmil, B.
Powiązania:
https://bibliotekanauki.pl/articles/779823.pdf
Data publikacji:
2011
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
hydrogenoliza
1,3-propanodiol
glicerol
hydrogenolysis
1,2-propanediol
1,3-propanediol
glycerol
Opis:
High activity of copper based catalysts for C-O bond hydro-dehydrogenation and their poor activity for C-C bond cleavage1 have prompted an attempt to apply such catalysts in the hydrogenolysis of glycerol to 1,2- and 1,3-propanediol. In the present study the infl uence of hydrogen reduction time of the Cu/ Al2O3 and CuCr2O4 copper catalysts on glycerol conversion and selectivity of transformation to propanediols and by-products was studied. At fi rst a general comparison was made between the commercial catalysts and those prepared by the co-precipitation method. As better results were obtained in the presence of catalysts prepared by co-precipitation, they were selected for further detailed studies of the influence of reduction time. For both prepared catalysts Cu/Al2O3 and CuCr2O4 the reduction time of 8 h was optimal. In the presence of Cu/Al2O3 catalyst the conversion of glycerol was 59.0%, selectivity of transformation to 1,2-propanediol 77.4% and selectivity to 1,3-propanediol 1.9%. In the presence of CuCr2O4 the glycerol conversion was 30.3% and selectivity to 1,2-propanediol 67.3%.
Źródło:
Polish Journal of Chemical Technology; 2011, 13, 4; 71-76
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Lewis acids immobilized in ionic liquid – application for the acetal synthesis
Autorzy:
Janus, E.
Powiązania:
https://bibliotekanauki.pl/articles/778768.pdf
Data publikacji:
2013
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
acetal formation
ionic liquid
Lewis acid
1,1-diethoxycyclohexane
Opis:
Catalytic systems composed of metal chloride (InCl3, ScCl3, YCl3, YbCl3, LaCl3, BiCl3, ZnCl3 and CuCl3) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)-imide, [C1C4Pyrr][NTf2] as ionic liquid were prepared. Catalytic activity of all the systems were compared in acetalization reaction between cyclohexanone and triethyl orthoformate. 1,1-Diethoxycyclohexane were formed with high yield and the selectivity at 0°C within 5 minutes. Selected metal chlorides immobilized in ionic liquid were recycled 5 times without a decrease in their activities.
Źródło:
Polish Journal of Chemical Technology; 2013, 15, 3; 78-80
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Application of catalysts in the treatment of selected waste chloroorganic compounds
Autorzy:
Żarczyński, A.
Zaborowski, M.
Paryjczak, T.
Gorzka, Z.
Kaźmierczak, M.
Powiązania:
https://bibliotekanauki.pl/articles/779801.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
utlenianie termokatalityczne
tetrachlorometan
1,1,2,2-tetrachloroetan
odpady chloroorganiczne
emisja dioksyn
thermocatalytic oxidation
tetrachloromethane
1,1,2,2-tetrachloroethane
chloroorganic wastes
dioxins emission
Opis:
Tetrachloromethane (TCM) and 1,1,2,2-tetrachloroethane (TChE) were oxidized in the temperature range from 300 to 600°C and at contact time of 0.36 s. The following catalysts were applied during the process: the granular one - platinum (0.12%) at the TiO2-SiO2 carrier, platinum ZChO-80 (0.15%) at γ-Al2O3 carrier, palladium (1%) at γ-Al2O3 carrier and monolithic platinum-rhodium catalyst (Pt - 0.09% and Rh - 0.04%) at the cordierite carrier. The substrates were oxidized in the presence of the above mentioned catalysts with various efficiencies depending on the molecular structure and the type of the catalyst. Palladium contact appeared to be the most active among the others. In the presence of this catalyst, total oxidation of TCM and TChE proceeded at the temperature of 425 and 500°C, respectively. The content of PCDD/Fs in gaseous products obtained during the oxidation of both substrates, was significantly lower than the admissible value of the toxicity equivalent (0.1 ng TEQ/m3).
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 2; 61-64
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solvent-free synthesis of 1-amidoalkyl-2-naphthol and 3-amino-1-phenyl-1H benzo[f]chromene-2-carbonitrile derivatives by Fe3O4@enamine-B(OSO3H)2 as an efficient and novel heterogeneous magnetic nanostructure catalyst
Autorzy:
Li, Fangping
Zhang, Jun
Wang, Longjiang
Liu, Weijian
Yousif, Qahtan A.
Powiązania:
https://bibliotekanauki.pl/articles/778863.pdf
Data publikacji:
2020
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
1-amidoalkyl-2-naphthol
3-amino-1-phenyl-1H benzo[f]chromene-2-carbonitrile
solvent-free conditions
magnetic
catalyst
Opis:
A green procedure for the one-pot three-component synthesis of 1-amidoalkyl-2-naphthol and 3-amino-1-phenyl-1H benzo[f]chromene-2-carbonitrile derivatives from the reaction of 2-naphtol, aldehydes, and malononitrile/acetamide in the presence of a catalytic amount of Fe3O4@enamine-B(OSO3H)2 as an efficient and novel heterogeneous magnetic nanostructure catalyst is described. The catalyst was characterized using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), energy dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD). These strategies possess some merits such as simple work-up method, easy preparation of the catalyst, short reaction times, good-to-high yields, and non-use of hazardous solvents during all steps of the reactions. Moreover, due to the magnetic nature of the catalyst, it was readily recovered by magnetic decantation and can be recycled at least six runs with no considerable decrease in catalytic activity.
Źródło:
Polish Journal of Chemical Technology; 2020, 22, 2; 9-19
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:
Evaluation on Curing Properties and Kinetics of Isophthalonitrile Oxide
Autorzy:
Fan, Y.
Tang, C.
Hu, Q.
Lei, Y.
Huo, J.
Powiązania:
https://bibliotekanauki.pl/articles/780045.pdf
Data publikacji:
2018
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
N,N-dihydroxybenzene-1,3-dicarboximidoyl dichloride
kinetics
elastomer
synthesis
1,3-dipolar cycloaddition
Opis:
N,N-dihydroxybenzene-1,3-dicarboximidoyl dichloride was synthesized from benzene-1,3-dicarboxaldehyde and characterized by fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance  1H and 13C NMR). The elastomer was prepared through the 1,3-dipolar cycloaddition of reaction between liquid polybutadiene (LPB) and isophthalonitrile oxide in this work. The tensile strength of different elastomer was enhanced from 0.14 MPa to 0.33 MPa as the elongation at break decreased from 145% to 73%, and the modulus increased from 0.09 kPa to 0.47 kPa. The parameters of kinetic indicated that the curing reaction was first order reaction and the apparent activation energy of each curing system was less than 10.10 kJ/mol when the content of N,N-dihydroxybenzene-1,3- dicarboximidoyl dichloride was increased from 7% to 12%. These results suggested that nitrile oxides achieved curing of polymer binders at room temperature and this work had definite guiding significance for the application of nitrile oxides in polymer binders.
Źródło:
Polish Journal of Chemical Technology; 2018, 20, 3; 37-46
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Modelling of a batch anaerobic digest
Autorzy:
Szewczyk, K.W.
Bukowski, J.
Powiązania:
https://bibliotekanauki.pl/articles/778247.pdf
Data publikacji:
2008
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
fermentacja beztlenowa
model ADM1
fermentacja okresowa
anaerobic digestion
ADM1 model
batch fermentation
Opis:
The Anaerobic Digestion Model no 1 (ADM1) has been implemented to simulate batch fermentation. The pH changes and inhibition of the fermentation have been studied. The model has been used to investigate the effects of substrate composition and concentration as well as the composition of the microorganism population on the course of fermentation. The overload of a reactor has been discussed.
Źródło:
Polish Journal of Chemical Technology; 2008, 10, 1; 45-48
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Study on safe disposal of cephalosporins based on kinetic pyrolysis mechanism
Autorzy:
Fan, Jiangxue
Zhang, Meng
Hou, Xiaofei
Wang, Fang
Bai, Mengyuan
Jiao, Ruoxi
Yang, Zhongyu
Duan, Erhong
Cheng, Fengfei
Zhou, Wen
Powiązania:
https://bibliotekanauki.pl/articles/27315672.pdf
Data publikacji:
2023
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
Distillation residues
Thermal analysis kinetics
Template “3-2-2”
Template “1+1”
Pyrolysis mechanism
Opis:
Based on the global goals for cleaner production and sustainable development, the pyrolysis behavior of cephalosporin residues was studied by TG-MS method. The influence of full temperature window on the safe disposal of residues was analyzed based on the “3-2-2” and “1+1” of thermal analysis kinetics, and the gas by-products of thermal degradation were monitored. Results showed that the pyrolysis of distillation residues were divided into low and high-temperature zones, including six stages. Maximum error rate (8.55%) by multiple scan rate was presented based on “3-2-2” pattern and maximum total fluctuation (33.7) by single scan rate was presented based on “1+1” pattern, which implied that the comprehensive multi-level comparison method was very reliable. The E value “E” of six stages showed an increasing trend ranging 166.8 to 872.8 kJ/mol. LgA(mean) was 27.28. Most mechanism function of stage 1, 2 were Z-L-T equation (3D), stage 3, 4, 6 were Avrami-Erofeev equation (AE3, AE4, AE2/3) and stage 5 was Reaction Order (O2). In addition, various small molecular micromolecule substances were detected such as C2H4O, C2H6, NH3, CH4, CO2 under full temperature windows and a possible pyrolysis path of residues was provided.
Źródło:
Polish Journal of Chemical Technology; 2023, 25, 4; 52--60
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Optimization of the epoxidation process of (1Z,5E,9E)-1,5,9-cyclododecatriene to 1,2-epoxy-(5Z,9E)-5,9-cyclododecadiene with tert-buthyl hydroperoxide — the influence of technological parameters on the hydroperoxide conversion
Autorzy:
Lewandowski, G.
Rytwińska, E.
Milchert, E.
Powiązania:
https://bibliotekanauki.pl/articles/778202.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
epoksydowanie
wodoronadtlenek tert-butylu
(1Z,5E,9E)-1,5,9-cyklododekatrien
1,2-epoksy-(Z,E)-5,9-cyklododekadien
planowanie doświadczeń
optymalizacja
epoxidation
tert-butyl hydroperoxide
(1Z,5E,9E)-1,5,9-cyclododecatriene
1,2-epoxy-(5Z,9E)-5,9-cyclododecadiene
design of experiments
optimization
Opis:
The optimization studies of the epoxidation process of (1Z,5E,9E)-1,5,9-cyclododecatriene (CDT) with tert-buthyl hydroperoxide (TBHP) over the molybdenum catalyst Mo(CO)6 were performed. The reaction was examined in terms of a uniform-rotatable design. Three factors were analyzed: the reaction time, CDT:TBHP molar ratio, and the molar concentration of the catalyst (Mo(CO)6). According to the design 20 experiments were performed at the constant temperature of 70°C.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 3; 105-107
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:
Cu(II), Co(II), Ni(II), Mn(II) and Zn(II) Schiff base complexes of 3-hydroxy-4-[N-(2-hydroxynaphthylidene)-amino]-naphthalene-1-sulfonic acid: Synthesis, Spectroscopic, thermal, and antimicrobial studies
Autorzy:
Bakare, Safyah B.
Powiązania:
https://bibliotekanauki.pl/articles/778830.pdf
Data publikacji:
2019
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
Schiff base
hydroxynaphthalene-1-sulfonic acid
hydroxy-1-naphthaldehyde
transition metal ions
morphology
antimicrobial activity
Opis:
Five divalent transition metals Cu(II), Co(II), Ni(II), Mn(II) and Zn(II) complexes have been synthesized using 3-hydroxy-4-[N-(2-hydroxynaphthylidene)-amino]-naphthalene-1-sulfonic acid (H3L) Schiff base as a ligand derived from the condensation reaction between 4-amino-3-hydroxynaphthalene-1-sulfonic acid and 2-hydroxy-1-naphthalde-hyde. The synthesized complexes were characterized using microanalytical, conductivity, FTIR, electronic, magnetic, ESR, thermal, and SEM studies. The microanalytical values revealed that the metal-to-ligand stoichiometry is 1:1 with molecular formula [M2+(NaL)(H2O)x].nH2O (where x = 3 for all metal ions except of Zn(II) equal x = 1; n = 4, 10, 7, 4, and 6 for Cu(II), Co(II), Ni(II), Mn(II) and Zn(II), respectively). The molar conductivity result indicates that all these complexes are neutral in nature with non-electrolytic behavior. Dependently on the magnetic, electronic, and ESR spectral data, octahedral geometry is proposed for all the complexes except to zinc(II) complex is tetrahedral. Thermal assignments of the synthesized complexes indicates the coordinated and lattice water molecules are present in the complexes. SEM micrographs of the synthesized complexes have a different surface morphologies. The antimicrobial activity data show that metal complexes are more potent than the parent ligand.
Źródło:
Polish Journal of Chemical Technology; 2019, 21, 3; 26-34
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Mass transfer in the bath reactor of the adsorption process of 1,2-dichloropropane from aqueous solution onto the activated carbon
Autorzy:
Pełech, R.
Powiązania:
https://bibliotekanauki.pl/articles/779985.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
1,2-dichloropropan
węgiel aktywny
adsorpcja
kinetyka
ścieki
1,2-dichloropropane
activated carbon
adsorption
kinetic
waste
Opis:
A pseudo-second order rate equation describing the kinetics of the adsorption of 1,2-dichloropropane from aqueous solution onto the activated carbon at different initial concentrations, adsorbent dose, temperature, particle diameter and the rate of stirring have been developed. The rate constant was calculated. The rate constant correlation in a good mixing conditions was described as a function of the temperature.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 2; 30-33
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Application of the design of experiments in the epoxidation process of 1,5,9-cyclododecatriene
Autorzy:
Lewandowski, G.
Ćwirko, J.
Powiązania:
https://bibliotekanauki.pl/articles/778595.pdf
Data publikacji:
2007
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
epoksydowanie
planowanie doświadczeń
1,5,9-cyklododekatrien
optymalizacja
epoxidation
design of experiments
1,5,9-cyclododecatriene
optimization
Opis:
An influence of the molar ratio of cis, trans, trans-1,5,9-cyclododecatriene to tert-butyl hydroperoxide, the concentration of the catalyst and the reaction time on the performance of the epoxidation process of cis, trans, trans-1,5,9-cyclodecatriene with tert-butyl hydroperoxide at the presence of molybdenum hexacarbonyl Mo(CO)6 was examined. Examinations were performed using statistical methods of the design of experiments. A mathematical model describing the influence of the parameters on conversion cis, trans, trans-1,5,9-cyclododecatriene was obtained. An analysis of the data and rests was performed and an optimal value of conversion of cis, trans, trans-1,5,9-cyclododecatriene was established.
Źródło:
Polish Journal of Chemical Technology; 2007, 9, 4; 68-71
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Studies of polypropylene membrane fouling during microfiltration of broth with Citrobacter freundii bacteria
Autorzy:
Gryta, M.
Waszak, M.
Tomaszewska, M.
Powiązania:
https://bibliotekanauki.pl/articles/779770.pdf
Data publikacji:
2015
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
microfiltration
fouling
glycerol fermentation
1,3-propanediol
Opis:
In this work a fouling study of polypropylene membranes used for microfiltration of glycerol solutions fermented by Citrobacter freundii bacteria was presented. The permeate free of C. freundii bacteria and having a turbidity in the range of 0.72–1.46 NTU was obtained. However, the initial permeate flux (100–110 L/m2h at 30 kPa of transmembrane pressure) was decreased 3–5 fold during 2–3 h of process duration. The performed scanning electron microscope observations confirmed that the filtered bacteria and suspensions present in the broth formed a cake layer on the membrane surface. A method of periodical module rinsing was used for restriction of the fouling influence on a flux decline. Rinsing with water removed most of the bacteria from the membrane surface, but did not permit to restore the initial permeate flux. It was confirmed that the irreversible fouling was dominated during broth filtration. The formed deposit was removed using a 1 wt% solution of sodium hydroxide as a rinsing solution.
Źródło:
Polish Journal of Chemical Technology; 2015, 17, 4; 56-64
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
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