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Cenospheres were modified with iron, manganese and/or copper ions by the hydrotalcite method. The obtained catalysts were characterized by FTIR, XRD and low-temperature nitrogen sorption. The best catalyst at low temperature (200 °C) was CBFe-Mn while at the highest measured temperature of 500 °C both CBFe-Mn and CBMn-Cu showed similar performance.

Methane tri-reforming process is a combination of three reactions: steam methane reforming (SRM), dry methane reforming (DRM), and partial oxidation of methane (POM). The first two reactions have endothermic character, while the POM is the exothermic reaction, which allows to obtain the energy necessary for the other two processes in situ. CH4 reacts with H2O, CO2, O2, and synthesis gas is produced with desired H2/CO ratios (1.5 – 2.0). The presence of H2O and O2 in the reaction environment can positively influence the stability of the used catalyst, by the inhibition of coke formation. In this paper two scenarios for methane tri-reforming implementation are discussed: (i) Tri-reforming as a effective way for chemical CO2 utilization, without the separation of carbon dioxide from flue gases from fossil fuel-fired power stations, and (ii) dry reforming of methane improved by the addition of water and oxygen, which may be applied as a chemical energy storage process. The literature on the subject of trireforming is shortly reviewed, including thermodynamics of the process, the possible conversions of methane and carbon dioxide, and proposed catalysts, both studied in tri-reforming, and in single processes (SRM, DRM and POM).

The catalytic activity in dry methane reforming of hydrotalcite-derived catalysts with ceria and/or nickel species introduced into hydrotalcite interlayer spaces was examined. The prepared materials were characterized (XRF, XRD, FT-IR, H2-TPR and N2 sorption) and subsequently tested in CO2 methane reforming at 550 °C. The obtained results showed that the incorporation of nickel species between hydrotalcite layers resulted in active catalyst with no sign of carbon deposition. Additionally, a beneficial effect of ceria promotion was observed. Ceria-promoted sample exhibited higher activity, stability and selectivity towards DRM, which may be explained by the formation of small Ni crystallites and prevention of the formation of inactive NiAl2O4 spinel phase.

The aim of this work was to study the influence of the modification of montmorillonites by carbonaceous and Al species as well as copper deposition. Commercial acid-treated montmorillonites, K5 and K30 (Sigma-Aldrich GmBH), were modified and used as catalysts in Selective Catalytic Reduction process of nitrogen oxides by ammonia. The characterisation was carried out by low-temperature nitrogen sorption, Fourier-transform-infrared spectroscopy and X-ray diffraction. Catalytic performance in SCR-NH3 of so-modified montmorillonites was compared under the following conditions: mass of catalyst: 200 g, flow 100 cm3/min, reaction mixture: 800 ppm NO, 800 ppm NH3, 3 % O2, and He. The modification with copper and polyacrylamide led to the increase in NO conversion. The studied catalysts showed low N2O formation.

Natural layered clay, vermiculite, was modified and tested as catalyst for the selective catalytic reduction of NOx with ammonia (NH3-SCR). Its modification included the application of the blowing agent (azodicarbonamide), acid treatment and pillaring with Al2O3. Active phase (transition metals: Cu or Fe) was introduced via impregnation. The obtained materials were characterized by N2 sorption (texture), XRD (structure), DR-UV-Vis (oxidation state and aggregation of the active phase), H2-TPR (reducibility of the active phase), in situ DRIFTS (types of adsorbed species due to contact of the sample NH3) and NH3-TPD (type/strength of the acidic sites). The initial modification procedures (treatment with azodicarboamide) resulted in the increase of specific surface area of vermiculite. The introduction of transition metal ions provided a significant amount of acidic sites. The promoting impact of holmium was confirmed by the increased strength of the sites. The highest catalytic activity was exhibited by the sample Fe-containing vermiculite and doped with Ho. [ABSTRACT FROM AUTHOR]