| 1. |
- Barrientos, Javier, et al.
(författare)
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Fischer-Tropsch Synthesis Over Zr-Promoted Co/gamma-Al2O3 Catalysts
- 2017
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Ingår i: Topics in catalysis. - : SPRINGER/PLENUM PUBLISHERS. - 1022-5528 .- 1572-9028. ; 60:17-18, s. 1285-1298
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Tidskriftsartikel (refereegranskat)abstract
- Two Zr-modified alumina supports were synthetized containing the same amount of Zr but a different distribution of this modifier over the alumina surface. These supports, together with the unmodified alumina carrier, were used to prepare three cobalt-based catalysts which were characterized and tested under relevant Fischer-Tropsch conditions. The three catalysts presented very similar porosity and cobalt dispersion. The addition of Zr nor its distribution enhanced the catalyst reducibility. The catalyst activity was superior when using a carrier consisting of large ZrO2 islands over the alumina surface. The use of a carrier with a homogeneous Zr distribution had however, a detrimental effect. Moreover, a faster initial deactivation rate was observed for the Zr-promoted catalysts, fact that may explain this contradictory effect of Zr on activity. Finally, the addition of Zr showed a clear enhancement of the selectivity to long chain hydrocarbons and ethylene, especially when Zr was well dispersed.
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| 2. |
- Behravesh, Erfan, et al.
(författare)
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Synthesis and characterization of Au nano particles supported catalysts for partial oxidation of ethanol : Influence of solution pH, Au nanoparticle size, support structure and acidity
- 2017
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Ingår i: Journal of Catalysis. - : Elsevier. - 0021-9517 .- 1090-2694. ; 353, s. 223-238
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Tidskriftsartikel (refereegranskat)abstract
- Partial oxidation of ethanol to acetaldehyde was carried out over gold catalysts supported on various oxides and zeolites by deposition precipitation. The special focus of this work was on the influence of H-Y zeolite surface charge on Au cluster size and loading linking it to activity and selectivity in ethanol oxidation and comparing with other studied catalysts. The catalysts were characterized by nitrogen physisorption, transmission electron microscopy (TEM), scanning electron microscopy/energy dispersive X-ray analysis (SEM/EDXA), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and zeta potential measurements. pH of the solution governed the Au NPs size within the range of 5.8–13.2 nm with less negatively charged surfaces leading to formation of smaller clusters. Au loading on H-Y zeolite with silica to alumina ratio of 80 was increased by raising the pH. In fact, H-Y-12 and H-Beta-25 were selective towards diethyl ether while acetaldehyde was the prevalent product on less acidic H-Y-80. The results demonstrated strong dependency of the catalytic activity on the Au cluster size. Namely turn over frequency (TOF) decreased with an increase in metal size from 6.3 to 9.3 nm on H-Y-80. Selectivity towards acetaldehyde and ethyl acetate did not change significantly on H-Y-80 within 6.3–9.3 nm Au particle size range. On Al2O3 support, however, selectivity towards acetaldehyde increased considerably upon diminishing Au average particle size from 3.7 to 2.1 nm.
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| 3. |
- Kumar, Narendra, et al.
(författare)
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Synthesis and characterization of solid base mesoporous and microporous catalysts: Influence of the support, structure and type of base metal
- 2012
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Ingår i: Microporous and Mesoporous Materials. - : Elsevier. - 1387-1811 .- 1873-3093. ; 152, s. 71-77
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Tidskriftsartikel (refereegranskat)abstract
- Synthesis of solid base Ce–H-MCM-41, Ce–Si-MCM-41, Cs-MCM-41, K-MCM-41 mesoporous materials and Na-ZSM-12, Cs-ZSM-12 microporous zeolites were carried out by means of evaporation impregnation and ion-exchange methods. The solid basecatalysts were characterized using X-ray powder diffraction, scanning electron microscope, nitrogen adsorption, FTIR of pyridine and temperature programmed desorption of CO2. The H-ZSM-12, Cs-ZSM-12 zeolite, H-MCM-41, Ce–H-MCM-41 and Ce–Si-MCM-41 mesoporous catalysts were studied for the synthesis of diethyl carbonate starting from ethanol and carbon dioxide, using butylene oxide as the dehydrating agent. Catalyst testing for the synthesis of diethyl carbonate was carried out at 170 °C and 4.5 MPa of initial CO2 pressure. 16 wt.% Ce–H-MCM-41 mesoporous material exhibited higher amount of weak, medium and strong basic sites than that of 32 wt.% Ce–Si-MCM-41. The presence of weak and strong basic sites was observed in the microporous 2 wt.% Cs-ZSM-12 catalyst. Diethyl carbonate formation was observed over Ce–H-MCM-41 and Ce–Si-MCM-41 mesoporous materials. Amount of basic sites and its strength influenced the synthesis of diethyl carbonate over the mesoporous materials.
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| 4. |
- Leino, Ewelina, et al.
(författare)
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Influence of the synthesis parameters on the physico-chemical and catalytic properties of cerium oxide for application in the synthesis of diethyl carbonate
- 2013
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Ingår i: Materials Chemistry and Physics. - : Elsevier. - 0254-0584 .- 1879-3312. ; 143:1, s. 65-75
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Tidskriftsartikel (refereegranskat)abstract
- Synthesis of cerium (IV) oxide by means of room temperature precipitation method was carried out. The effect of preparation variables such as synthesis time, calcination temperature and pH of the solution on resulting CeO2 properties was discussed. Moreover, the comparison of CeO2 samples prepared in a static and rotation mode of synthesis is presented. The solid catalysts were characterized by means of X-ray powder diffraction, scanning electron microscopy, transmission electron microscope, nitrogen physisorption, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy using pyridine as a probe molecule and temperature programmed desorption of CO2. Significant variations in physicochemical properties of CeO2 by varying the preparation conditions were observed. Furthermore, the catalytic performances of CeO2 catalysts were compared in the synthesis of diethyl carbonate starting from ethanol and CeO2 using butylene oxide as a dehydrating agent. The dependence of CeO2 properties on its catalytic activity is evaluated in detail. (C) 2013 Elsevier B.V. All rights reserved.
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| 5. |
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| 6. |
- Murzin, Dmitry Yu., et al.
(författare)
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Hemicellulose arabinogalactan hydrolytic hydrogenation over Ru-modified H-USY zeolites
- 2015
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Ingår i: Journal of Catalysis. - : Elsevier BV. - 0021-9517 .- 1090-2694. ; 330, s. 93-105
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Tidskriftsartikel (refereegranskat)abstract
- The hydrolytic hydrogenation of hemicellulose arabinogalactan was investigated in the presence of protonic and Ru (1-5 wt.%)-modified USY zeolites (Si/Al ratio = 15 and 30). The use of the purely acidic materials was effective in depolymerizing the macromolecule into free sugars. While the latter partly dehydrated into 5-hydroxymethylfurfural and furfural, the generation of high molecular-weight compounds (aggregates of sugars and humins) was not favored, in contrast to previous evidences over beta zeolites. Application of the bifunctional Ru/USY catalyst, comprising well-dispersed metallic nanopartides on the aluminosilicate support, resulted in the formation of galactitol and arabitol, in the suppression of dehydration side products, and further inhibition of polymerization reactions, which only yielded low molecular-weight oligomers. Detailed analysis of the reaction pathways as well as kinetic modeling of hydrolytic hydrogenation was performed with an advanced reaction mechanism.
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| 7. |
- Regali, Francesco, 1971-, et al.
(författare)
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Deactivation of a Pt/Silica–Alumina Catalyst and Effecton Selectivity in the Hydrocracking of n-Hexadecane
- 2013
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Ingår i: Topics in catalysis. - : Springer Science and Business Media LLC. - 1022-5528 .- 1572-9028. ; 56:9-10, s. 594-601
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Tidskriftsartikel (refereegranskat)abstract
- The deactivation behavior of a bifunctionalcatalyst consisting of platinum on amorphous silica–aluminawas studied in the hydrocracking of n-hexadecane.The initial decline in activity and the change in selectivitywere monitored at the following reaction conditions:pressure = 30 bar; temperature = 310 C; hydrogen-tohexadecanefeed molar ratio = 10. Initially, hexadecaneconversion and selectivity to cracking products decreasedrapidly with time-on-stream, and stabilized after 40 h onstream. This could be related to an initial loss of metalsurface area, which decreased the activity of monofunctionalhydrogenolysis generating cracking products. Theacidic function seemed to be unaffected under these reactionconditions. The stable catalyst was exposed to a lowerhydrogen-to-hexadecane ratio to accelerate deactivation bycoking. A decline in the activity of both functions wasobserved. The activity of the acidic function could bealmost completely recovered by oxidative regeneration,while the metal activity was only partially recovered.
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| 8. |
- Rozmyslowicz, Bartosz, et al.
(författare)
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Selective hydrogenation of fatty acids to alcohols over highly dispersed ReOx/TiO2 catalyst
- 2015
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Ingår i: Journal of Catalysis. - : Elsevier BV. - 0021-9517 .- 1090-2694. ; 328, s. 197-207
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Tidskriftsartikel (refereegranskat)abstract
- Production of fatty alcohols through selective hydrogenation of fatty acids was studied over a 4% ReOx/TiO2 catalyst. Stearic acid was hydrogenated to octadecanol at temperatures and pressures between 180-200 degrees C and 2-4 MPa, with selectivity reaching 93%. A high yield of octadecanol was attributed to a strong adsorption of the acid compared to alcohol on the catalyst, which inhibits further alcohol transformation to alkanes. Low amounts (<7%) of alkanes (mainly octadecane) were formed during the conversion of stearic acid. However, it was found that the catalyst could be tuned for the production of alkanes. The reaction intermediates were octadecanal and stearyl stearate. Based on the reaction products analysis and catalyst characterization, a reaction mechanism and possible pathways were proposed.
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| 9. |
- Saeid, Soudabeh, et al.
(författare)
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Advanced Oxidation Process for Degradation of Carbamazepine from Aqueous Solution : Influence of Metal Modified Microporous, Mesoporous Catalysts on the Ozonation Process
- 2020
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Ingår i: Catalysts. - : MDPI. - 2073-4344. ; 10:1
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Tidskriftsartikel (refereegranskat)abstract
- Carbamazepine (CBZ), a widely used pharmaceutical compound, is one of the most detected drugs in surface waters. The purpose of this work was to identify an active and durable catalyst, which, in combination with an ozonation process, could be used to remove CBZ and its degradation products. It was found that the CBZ was completely transformed after ozonation within the first minutes of the treatment. However, the resulting degradation products, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM) and 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD), were more resistant during the ozonation process. The formation and degradation of these products were studied in more detail and a thorough catalytic screening was conducted to reveal the reaction kinetics of both the CBZ and its degradation products. The work was performed by non-catalytic ozonation and with six different heterogeneous catalysts (Pt-MCM-41-IS, Ru-MCM-41-IS, Pd-H-Y-12-EIM, Pt-H-Y-12-EIM, Pd-H-Beta-300-EIM and Cu-MCM-41-A-EIM) operating at two temperatures 20 °C and 50 °C. The influence of temperature on degradation kinetics of CBZ, BQM and BQD was studied. The results exhibited a notable difference in the catalytic behavior by varying temperature. The higher reactor temperature (50 °C) showed a higher activity of the catalysts but a lower concentration of dissolved ozone. Most of the catalysts exhibited higher removal rate for BQM and BQD compared to non-catalytic experiments in both temperatures. The Pd-H-Y-12-EIM catalyst illustrated a higher degradation rate of by-products at 50 °C compared to other catalysts.
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| 10. |
- Saeid, Soudabeh, et al.
(författare)
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Pt Modified Heterogeneous Catalysts Combined with Ozonation for the Removal of Diclofenac from Aqueous Solutions and the Fate of by-Products
- 2020
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Ingår i: Catalysts. - : MDPI. - 2073-4344. ; 10:3
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Tidskriftsartikel (refereegranskat)abstract
- The degradation of the pharmaceutical compound diclofenac in an aqueous solution was studied with an advanced oxidation method, catalytic ozonation. Diclofenac was destroyed in a few minutes by ozonation but several long-lasting degradation by-products were formed. For this reason, the combination of heterogeneous catalysts and ozonation was applied to eliminate them completely. The kinetics of the diclofenac degradation and the formation of by-products were thoroughly investigated. Loading of Pt on the catalysts resulted in an improvement of the activity. The Mesoporous Molecular Sieves (MCM) were one of the promising catalysts for the degradation of organic pollutants. In this study, six heterogeneous catalysts were screened, primarily MCM-22-100 catalysts with different Pt concentrations loaded via the evaporation-impregnation (EIM) method, and they were applied on the degradation of diclofenac. It was found that the presence of Pt improved the degradation of diclofenac and gave lower concentrations of by-products. The 2 wt % Pt-H-MCM-22-100-EIM demonstrated the highest degradation rate compared to the proton form, 1% or 5 wt % Pt concentration, i.e., an optimum was found in between. Pt-H-Y-12-IE and Pt-γ-Al2O3 (UOP)-IMP catalysts were applied and compared with the MCM-22 structure. Upon use of both of these catalysts, an improvement in the degradation of diclofenac and by-products was observed, and the 2 wt % Pt-H-MCM-22-100-EIM illustrated the maximum activity. All important characterization methods were applied to understand the behavior of the catalysts (X-ray powder diffraction, transmission electron microscopy, nitrogen physisorption, scanning electron microscopy, energy dispersive X-ray micro-analyses, pyridine adsorption-desorption with FTIR spectroscopy, X-ray photoelectron spectroscopy). Finally, leaching of Pt and Al were analyzed by inductively coupled optical emission spectrometry.
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