Promotional effect of Pd addition on the catalytic activity of composite Pt-Pd/AlSBA-15–β\beta catalyst for enhanced n-heptane hydroisomerization

Hierarchical AlSBA-15–zeolite materials were utilized as a supports for preparing hydroisomerization catalysts. Detailed consideration was given to: (i) the effect of the zeolite type introduced into AlSBA-15–zeolite composites (where zeolite is β, mordenite or ZSM-5) as well as (ii) the promotion effect of Pd addition. The composites showed higher activity in isomerization as compared to Pt/AlSBA-15. The enhanced isomerization efficiency were explained by the appropriate metallic and acidic function as well as suitable transport properties. The modification of the hydrogenating function by Pd incorporation increases the hydroisomerization efficiency of Pt-Pd/AlSBA-15–β catalyst. Over bimetallic Pt-Pd/AlSBA-15–β, the high yields of isomers (68 wt%) with respect to 50 wt% for a control catalyst. The most promising Pt-Pd/AlSBA-15–β catalyst allows to improve research octane number from 0 to the 74 value

The Impact of Synthesis Method on the Properties and CO2 Sorption Capacity of UiO-66(Ce)

A series of cerium-based UiO-66 was obtained via hydrothermal and sonochemical methods, using the same quantities of reagents (cerium ammonium nitrate (CAN), terephthalic acid (H2BDC)) and solvents) in each synthesis. The impact of synthesis method and metal to linker ratio on the structural and textural properties of obtained UiO-66(Ce), as well as their composition in terms of Ce4+/Ce3+ ratio, structure defects resulting from missing linker, and CO2 adsorption capacity was discussed. By using typical characterization techniques and methods, such as XRD, N2 and CO2 sorption, TGA, XPS, and SEM, it was shown that the agitation of reacting mixture during synthesis (caused by stirring or ultrasounds) allows to obtain structures that have more developed surfaces and fewer linker defects than when MOF was obtained in static conditions. The specific surface area was found to be of minor importance in the context of CO2 adsorption than the contribution of Ce3+ ions that were associated with the concentration of linker defects.This work was financed by a statutory activity subsidy from the Polish Ministry of Science and Higher Education for the Faculty of Chemistry of Wrocław University of Technology and Project No 0402/0100/17

Structure-sensitive behavior of supported vanadia-based catalysts for combustion of soot

Catalytic performance of 3 and 5 wt.% of vanadia, supported on zirconia, zirconia-ceria, and zirconia-yttria, tested in the combustion of soot without and in the presence of NO was described. The catalysts were characterized by structural (XRD, RS) and functional (EPR, TPR) methods. The effect of composition on the catalytic performance of the investigated systems in soot combustion was discussed in detail. Zirconia-supported vanadia was found to be the most active catalyst for soot oxidation characterized by the lowest combustion temperature (~375 °C) attributed to the maximal signal of conversion to the detected products. The relationship between the reducibility of surface oxovanadium species and their catalytic activity was established, revealing the involvement of the lattice oxygen in the combustion process. The importance of thermal treatment conditions and the nature of zirconia-based support determining the stability of specific oxovanadium entities on the catalyst surface was emphasized

Effect of a Support on the Properties of Zinc Oxide Based Sorbents

We present the comparative analysis of three Zn-based sorbents for the process of sulphur removal from hot coal gas. The sorbents were prepared by a slurry impregnation of TiO2, SiO2 and Al2O3, resulting in complex, multiphase materials, with the dominant phases of Zn2TiO4, Zn2SiO4 and ZnAl2O4, respectively. We have analyzed the effect of supports on the phase composition, texture, reducibility and H2S sorption. We have found that the phase composition significantly influences the susceptibility of the investigated materials to reduction by hydrogen. Zn2TiO4 have been found to be the easiest to reduce which correlates with its ability to adsorb the largest amount of hydrogen sulphide—up to 4.2 gS/100 g—compared to the other sorbents, which absorb up to 2.2 gS/100 g. In the case of Zn2SiO4 and ZnAl2O4, this effect also correlates with reducibility—these sorbents have been found to be highly resistant to reduction by hydrogen and to absorb much less hydrogen sulphide. In addition, the capacity of ZnAl2O4 for H2S adsorption decreases in the subsequent work cycles—from 2.2 gS/100 g in the first cycle to 0.8 gS/100 g in the third one. Computational analysis on the DFT level has shown that these materials show different thermodynamic stability of sulphur sites within the unit cells of the sorbents. For Zn2TiO4 and Zn2SiO4, the adsorption is favorable in both the first and second layers of the former and only the top layer of the latter, while for zinc aluminate it is not favorable, which is consistent with the experimental findings

HKUST-1-Supported Cerium Catalysts for CO Oxidation

The synthesis method of metal–organic frameworks (MOFs) has an important impact on their properties, including their performance in catalytic reactions. In this work we report on how the performance of [Cu3(TMA)2(H2O)3]n (HKUST-1) and Ce@HKUST-1 in the reaction of CO oxidation depends on the synthesis method of HKUST-1 and the way the cerium active phase is introduced to it. The HKUST-1 is synthesised in two ways: via the conventional solvothermal method and in the presence of a cationic surfactant (hexadecyltrimethylammonium bromide (CTAB)). Obtained MOFs are used as supports for cerium oxide, which is deposited on their surfaces by applying wet and incipient wetness impregnation methods. To determine textural properties, structure, morphology, and thermal stability, the HKUST-1 supports and Ce@HKUST-1 catalysts are characterised using X-ray diffraction (XRD), N2 sorption, scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), and thermogravimetric analysis (TGA). It is proven that the synthesis method of HKUST-1 has a significant impact on its morphology, surface area, and thermal stability. The synthesis method also influences the dispersion and the morphology of the deposited cerium oxide. Last but not least, the synthesis method affects the catalytic activity of the obtained material.This research was founded by a statutory activity subsidy from the Polish Ministry of Science and Higher Education for the Faculty of Chemistry of Wrocław University of Technology and the project number 0402/0029/18. The APC was founded by the Faculty of Chemistry of Wrocław University of Technology