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Water-soluble temperature-responsive polyelectrolytes and hydrogels have been synthesized by ␥-radiation copolymerization of [2-(methacryloyloxy)-ethyl]trimethylammonium chloride with N-isopropylacrylamide. Complex formation of soluble copolymers with potassium hexacyanoferrates (II, III) was studied in aqueous solutions. It was shown that, depending on the concentration and temperature, the formation of soluble or insoluble polycomplexes is observed. The hydrogels show good ability to absorb potassium hexacyanoferrates (II, III) from aqueous solutions. Sorption ability of hydrogels depends on the content of cationic monomer in copolymer and the nature of coordination ion.
Several bimetallic Ni−Co catalysts supported on θ‐Al2O3 together with 10 wt % Ni and 10 wt % Co on θ‐Al2O3 were prepared via the incipient wetness method, characterized by X‐ray diffraction (XRD), nitrogen adsorption, transmission electron microscopy, temperature programmed reduction, temperature programmed CO2 desorption, Fourier Transformed Infrared Spectroscopy (FTIR) with pyridine adsorption‐desorption and tested in dry methane reforming at 700 °C in a fixed bed reactor. According to XRD the metal oxide crystallite sizes decreased from 20 nm for 10 wt % Co/θ‐Al2O3 to 13 nm for 5 wt % Ni‐5 wt % Co/θ‐Al2O3, which also showed formation of a mixed oxide alloy. The unit cell parameters for spinel in the fresh catalyst and fcc metal formed during the reaction followed the Vegard's rule. Although monometallic 10 wt % Co/θ‐Al2O3 exhibited high hydrogen consumption, desorption temperature was also high resulting in a rather low activity of 10 wt % Co/θ‐Al2O3 in comparison to bimetallic 5 wt % Ni‐5 wt % Co/θ‐Al2O3. The latter exhibited the highest initial activity for hydrogen formation due to its relatively small metal particle size. This catalyst suffered, however, from extensive coking. The most stable catalyst was 10 wt % Ni/θ‐Al2O3 for which the hydrogen yield decreased form 56 % to 45 % during 100 h time‐on‐stream. For this catalyst no sintering occurred, opposite to 10 wt % Co/θ‐Al2O3.
Dry reforming of methane (DRM) is a promising method to utilize two greenhouse gases, such as CH4 and CO2, to produce synthesis gas. In the current work, both monometallic Ni and bimetallic Ni–Fe catalysts with different Fe/Ni molar ratios, synthesized by solution combustion synthesis (SCS) in DRM, were investigated using a feed ratio of CH4/CO2/Ar of 1:1:1 at 600–900 °C. The catalysts were characterized by several physicochemical techniques such as X-ray diffraction (XRD), scanning electron microscopy energy-dispersive X-ray (SEM-EDX) spectroscopy, transmission electron microscopy (TEM), CHNS, N2 physisorption, H2-TPR, O2-TPO, NH3-TPD, and thermogravimetric analysis (TGA). One of the highest hydrogen yields of 81% was obtained at 93% conversion of CH4 and 94% conversion of CO2 for the bimetallic 15Ni–5Fe–30Al catalyst, which contained, according to XRD, NiAl2O4 spinel and metallic Ni phases. The spinel phase was decomposed during the reaction, while the Ni3Fe alloy was formed. Catalysts with a higher Fe/Ni ratio exhibited lower conversion and contained an inactive FeAl2O4 spinel. Rather stable yields of CO and H2 were obtained in an experiment with 20 h time-on-stream.
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