scholarly journals Effect of Secondary Additives on the Properties of Vanadium-Aluminum Mixed Oxide Catalysts Used in the Oxidation of Propane

Author(s):  
Víctor Gabriel Baldovino Medrano ◽  
Benjamin Farin ◽  
Eric M. Gaigneaux

<div>We investigated how secondary additives for tableting vanadium-aluminum</div><div>mixed-oxides affect the mechanical resistance, surface chemistry, and catalytic performance in</div><div>propane oxidation of tablets based on this material. The secondary additives were magnesium </div><div>oxide, silica, boron nitride, sepiolite, and zinc oxide while graphite was used as the primary</div><div>shaping agent. Our results showed that the changes in mechanical strength and porosity were</div><div>directly related to the softness and ductility of the secondary additive. Overall, we learned that</div><div>when manufacturing catalyst tablets, there is a compromise between mechanical strength and</div><div>loss in mesoporosity and surface area. On the other hand, the components of the formulated</div><div>tablets did not show signs of establishing a chemical interaction with the vanadium-aluminum</div><div>mixed oxide. Therefore, the effects of the additives that we found on the catalytic performance</div><div>were ascribed to the fact that the selected secondary additives may act as co-catalysts during</div><div>propane oxidation. In this sense, boron nitride and sepiolite were best for promoting both the</div><div>reactivity of the catalytic formulations while showing a better productivity of propene. The data</div><div>was interpreted suggesting that the promotion effect may be due to the combination of a redox</div><div>mechanism over the vanadium-aluminum mixed oxide phase and to a surface radical mechanism</div><div>occurring over the active moieties of these secondary additives.</div>

2020 ◽  
Author(s):  
Víctor Gabriel Baldovino Medrano ◽  
Benjamin Farin ◽  
Eric M. Gaigneaux

<div>We investigated how secondary additives for tableting vanadium-aluminum</div><div>mixed-oxides affect the mechanical resistance, surface chemistry, and catalytic performance in</div><div>propane oxidation of tablets based on this material. The secondary additives were magnesium </div><div>oxide, silica, boron nitride, sepiolite, and zinc oxide while graphite was used as the primary</div><div>shaping agent. Our results showed that the changes in mechanical strength and porosity were</div><div>directly related to the softness and ductility of the secondary additive. Overall, we learned that</div><div>when manufacturing catalyst tablets, there is a compromise between mechanical strength and</div><div>loss in mesoporosity and surface area. On the other hand, the components of the formulated</div><div>tablets did not show signs of establishing a chemical interaction with the vanadium-aluminum</div><div>mixed oxide. Therefore, the effects of the additives that we found on the catalytic performance</div><div>were ascribed to the fact that the selected secondary additives may act as co-catalysts during</div><div>propane oxidation. In this sense, boron nitride and sepiolite were best for promoting both the</div><div>reactivity of the catalytic formulations while showing a better productivity of propene. The data</div><div>was interpreted suggesting that the promotion effect may be due to the combination of a redox</div><div>mechanism over the vanadium-aluminum mixed oxide phase and to a surface radical mechanism</div><div>occurring over the active moieties of these secondary additives.</div>


Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 231
Author(s):  
Maximilian Sennerich ◽  
Peter G. Weidler ◽  
Stefan Heißler ◽  
Bettina Kraushaar-Czarnetzki

The present study investigates modified Mo/V/W mixed oxides as a possible alternative for state of the art heteropoly acid catalysts (HPA) in the partial oxidation of methacrolein (MAC) to methacrylic acid (MAA). Even though HPAs show an excellent activity and MAA selectivity, their long-term stability is unsatisfying, rendering the catalyst inoperable after runtimes of roughly 6 months. Mo/V/W mixed oxides consisting of M1 and a hexagonal (Mo,V,W)Ox-phase (h-phase) in varying proportions were modified by impregnation with aqueous solutions containing cesium and phosphate ions. All samples were characterized with respect to specific surface area, crystallinity, elemental and phase composition. The catalytic performance in the oxidation of MAC to MAA was investigated using a continuously operated reaction unit with tubular fixed bed reactor. Impregnation with cesium and phosphate ions and subsequent heating triggers the transformation of the mixed oxide into a Keggin-type HPA, whereby the h-phase is more reactive than M1. The transformation into HPA is accompanied by a change in the catalytic properties, i.e., the selectivity to MAA is considerably improved. Compared to HPA synthesized directly, however, the HPA samples obtained by transformation of mixed oxides exhibit no advantages, be it with respect to activity, MAA selectivity or stability.


Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 370
Author(s):  
Juan Jimenez ◽  
Kathleen Mingle ◽  
Teeraya Bureerug ◽  
Cun Wen ◽  
Jochen Lauterbach

The catalytic performance of Mo8V2Nb1-based mixed-oxide catalysts for ethane partial oxidation is highly sensitive to the doping of elements with redox and acid functionality. Specifically, control over product distributions to ethylene and acetic acid can be afforded via the specific pairing of redox elements (Pd, Ni, Ti) and acid elements (K, Cs, Te) and the levels at which these elements are doped. The redox element, acid element, redox/acid ratio, and dopant/host ratio were investigated using a three-level, four-factor factorial screening design to establish relationships between catalyst composition, structure, and product distribution for ethane partial oxidation. Results show that the balance between redox and acid functionality and overall dopant level is important for maximizing the formation of each product while maintaining the structural integrity of the host metal oxide. Overall, ethylene yield was maximized for a Mo8V2Nb1Ni0.0025Te0.5 composition, while acetic acid yield was maximized for a Mo8V2Nb1Ti0.005Te1 catalyst.


Catalysts ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 593 ◽  
Author(s):  
Pacultová ◽  
Bílková ◽  
Klegova ◽  
Karásková ◽  
Fridrichová ◽  
...  

Fundamental research on direct NO decomposition is still needed for the design of a sufficiently active, stable and selective catalyst. Co-based mixed oxides promoted by alkali metals are promising catalysts for direct NO decomposition, but which parameters play the key role in NO decomposition over mixed oxide catalysts? How do applied preparation conditions affect the obtained catalyst’s properties?


Materials ◽  
2019 ◽  
Vol 12 (20) ◽  
pp. 3436 ◽  
Author(s):  
Amar Bendieb Aberkane ◽  
María Pilar Yeste ◽  
Djazi Fayçal ◽  
Daniel Goma ◽  
Miguel Ángel Cauqui

A series of NiO–CeO2 mixed oxide catalysts have been synthesized by a modified coprecipitation method at three different pH values (pH = 8, 9, and 10). The NiO–CeO2 mixed oxide samples were characterized by TGA, XRD, inductively coupled plasma atomic emission spectroscopy (ICP-AES), FTIR, Brunauer–Emmett–Teller (BET) surface area, H2 temperature-programmed reduction (H2-TPR), and electron microscopy (high-angle annular dark-field transmission electron microscopy/energy-dispersive X-ray spectroscopy (HAADF-TEM/EDS)). The catalytic activities of the samples for soot oxidation were investigated under loose and tight contact conditions. The catalysts exhibited a high BET surface area with average crystal sizes that varied with the pH values. Electron microscopy results showed the formation of small crystallites (~5 nm) of CeO2 supported on large plate-shaped particles of NiO (~20 nm thick). XRD showed that a proportion of the Ni2+ was incorporated into the ceria network, and it appeared that the amount on Ni2+ that replaced Ce4+ was higher when the synthesis of the mixed oxides was carried out at a lower pH. Among the synthesized catalysts, Ni-Ce-8 (pH = 8) exhibited the best catalytic performance.


Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 613
Author(s):  
Hussein Mahdi S. Al-Aani ◽  
Mihaela M. Trandafir ◽  
Ioana Fechete ◽  
Lucia N. Leonat ◽  
Mihaela Badea ◽  
...  

To improve the catalytic performance of an active layered double hydroxide (LDH)-derived CuCeMgAlO mixed oxide catalyst in the total oxidation of methane, it was promoted with different transition-metal cations. Thus, two series of multicationic mixed oxides were prepared by the thermal decomposition at 750 °C of their corresponding LDH precursors synthesized by coprecipitation at constant pH of 10 under ambient atmosphere. The first series of catalysts consisted of four M(3)CuCeMgAlO mixed oxides containing 3 at.% M (M = Mn, Fe, Co, Ni), 15 at.% Cu, 10 at.% Ce (at.% with respect to cations), and with Mg/Al atomic ratio fixed to 3. The second series consisted of four Co(x)CuCeMgAlO mixed oxides with x = 1, 3, 6, and 9 at.% Co, while keeping constant the Cu and Ce contents and the Mg/Al atomic ratio. All the mixed oxides were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) coupled with X-ray energy dispersion analysis (EDX), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption-desorption at −196 °C, temperature-programmed reduction under hydrogen (H2-TPR), and diffuse reflectance UV-VIS spectroscopy (DR UV-VIS), while thermogravimetric and differential thermal analyses (TG-DTG-DTA) together with XRD were used for the LDH precursors. The catalysts were evaluated in the total oxidation of methane, a test reaction for volatile organic compounds (VOC) abatement. Their catalytic performance was explained in correlation with their physicochemical properties and was compared with that of a reference Pd/Al2O3 catalyst. Among the mixed oxides studied, Co(3)CuCeMgAlO was found to be the most active catalyst, with a temperature corresponding to 50% methane conversion (T50) of 438 °C, which was only 19 °C higher than that of a reference Pd/Al2O3 catalyst. On the other hand, this T50 value was ca. 25 °C lower than that observed for the unpromoted CuCeMgAlO system, accounting for the improved performance of the Co-promoted catalyst, which also showed a good stability on stream.


Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 505 ◽  
Author(s):  
Xiaoli Wang ◽  
Gongde Wu ◽  
Tongfa Jin ◽  
Jie Xu ◽  
Shihao Song

A series of transition metal oxides or mixed oxides supported nano-Au catalysts were prepared for the selective oxidation of glycerol to glyceric acid using 3% H2O2. It was found that the composition and structure of supports significantly influenced the catalytic performance of catalysts. The mesoporous trimetal mixed oxide (CuNiAlO) supported nano-Au catalysts were more active in comparison with the others. In the present catalytic system, the highest glycerol conversion was 90.5%, while the selectivity of glyceric acid could reach 72%. Moreover, the catalytic performance remained after 11 times of reaction.


2017 ◽  
Vol 7 (4) ◽  
pp. 797-801 ◽  
Author(s):  
Xianyuan Wu ◽  
Zheng Fang ◽  
Hui Pan ◽  
Yifan Zheng ◽  
Dahao Jiang ◽  
...  

Mg–La mixed oxide catalysts with a strong interaction between Mg and La oxides had higher amounts of oxygen vacancies and surface adsorbed oxygen species, resulting in a better performance in H2 oxidation and CH4 oxidative reactions.


2014 ◽  
Vol 4 (10) ◽  
pp. 3713-3722 ◽  
Author(s):  
Hisahiro Einaga ◽  
Akihiro Kiya ◽  
Satoru Yoshioka ◽  
Yasutake Teraoka

Copper–manganese (Cu–Mn) mixed oxide catalysts were prepared by a coprecipitation technique from metal nitrates in aqueous solution using tetramethylammonium hydroxide (TMAH) as a pH regulator.


2015 ◽  
Vol 5 (12) ◽  
pp. 5062-5076 ◽  
Author(s):  
Itika Kainthla ◽  
Jayesh T. Bhanushali ◽  
Rangappa S. Keri ◽  
Bhari Mallanna Nagaraja

The activity of V, Fe and carbon based catalysts depends on V5+, Fe3+and active carbon sites. The mixed oxide catalysts show superior activity than individual oxides.


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