Runxia He

Effects of alkali-oxygen oxidation temperature on the structures and combustion properties of Shengli lignite

Spontaneous combustion has become a critical limiting factor for the safe and efficient utilization of low rank coals. In this work, the alkali-oxygen oxidation (AOO) of Chinese Shengli lignite was conducted to inhibit the spontaneous combustion tendency, and the influences of AOO on the structures and combustion properties were investigated. The structures of AOO treated lignite under different conditions were characterized by XRD, Raman, XPS and FTIR. The combustion characteristics of the samples were investigated by thermogravimetric analysis and fixed bed combustion. The results revealed that the temperature of AOO treatment had significant influence on the crystallite structures and combustion characteristics of Shengli lignite. After the AOO pretreatment, the benzene ring skeleton structures in lignite had no obvious changes, but the amounts of aliphatic side chains on the aromatic nucleus decreased. Compared with raw lignite, the degree of order and ignition temperature increased after AOO treatment, especially when the AOO temperature was 150–200 °C. The ignition temperatures moved from 310 °C for raw lignite to 740–760 °C for the samples treated by AOO at 150–200 °C. On further increasing the AOO temperatures to 250–300 °C, the ignition temperature of the samples decreased to 410–440 °C. In conclusion, AOO pretreatment under suitable conditions is an efficient way to inhibit the spontaneous combustion tendency of low rank lignite, and it is believed that the results in this work are meaningful for the safe transportation and efficient utilization process of lignite in industry.

Direct use of humic acid mixtures to construct efficient Zr-containing catalysts for Meerwein–Ponndorf–Verley reactions

With the increasing demands for energy and carbon resources, exploration of novel utilization approaches of fossil resources and promotion of the conversion of sustainable resources become critical issues facing human society. In this study, we used humic acids (HAs), which are important derivatives from the low-rank coal, and the transition metal zirconium (Zr) to construct novel Zr-containing catalysts (Zr-HAs) for Meerwein–Ponndorf–Verley (MPV) reactions of biomass-derived platforms. Both commercial HAs and HAs extracted directly from lignite without any purification were used as raw materials to prepare the catalysts. The results showed that Zr-HAs catalysts were highly efficient for the conversion of furfural, with a high furfuryl alcohol yield of up to 97%, and also effective for the conversion of other carbonyl compounds with different structures under mild conditions. This novel strategy to construct catalysts using HAs as raw materials may be beneficial for both value-added utilization of low-rank coal and the conversion of biomass resources.

Effect of anions on the structure and catalytic properties of a La-doped Cu-Mn catalyst in the water-gas shift reaction

Effects of the anion type on the structure, thermal stability, and catalytic performance of La-doped Cu-Mn catalysts prepared by co-precipitation were characterized by X-ray diffraction, Brunauer-Emmett-Teller, temperature-programmed reduction, temperature-programmed reduction of oxidized surfaces, and temperature-programmed desorption. The Cu-Mn catalyst was tested for the water-gas shift (WGS) reaction. The main crystalline phase of samples prepared with sulfate, acetate, chloride, and nitrate as the starting materials was a Cu1.5Mn1.5O4 spinel structure, following the WGS reaction, the main crystalline phases were transformed into Cu and MnO. The sample prepared with acetate as the starting material showed the most obvious MnCO3 characteristic diffraction peaks, with better synergistic effects of Cu and MnO, increased adsorption of CO2 and improved dispersion of Cu on the catalyst surface; also, the best thermal stability and the highest low temperature catalytic activity were observed. The sample prepared with nitrate as the starting material maintained high thermal stability and catalytic performance in the range of 400°C to 450°C, but CO conversion decreased below 350°C. Catalytic performance of the sample prepared with sulfate and chloride as the starting materials was poor, ranging from 200°C to 450°C.

The catalytic effect of calcium and potassium on CO2 gasification of Shengli lignite: the role of carboxyl

The CO2 gasification of Chinese Shengli lignite (SL) catalysed by K+ and Ca2+ was studied. The results showed that calcium could greatly decrease the gasification reaction temperature of SL, and the gasification reaction rates of acid-treated SL catalysed by calcium were significantly higher than that catalysed by potassium. Kinetic analysis showed that the activation energy of the reaction catalysed by calcium was much lower than that catalysed by potassium, which was the reason for the higher catalytic activity of calcium. Fourier transform infrared characterization showed that, compared with acid-treated SL, the addition of K+/Ca2+ resulted in the significant weakening of C=O bond, and new peaks attributed to carboxylate species appeared. X-ray photoelectron spectroscopy results indicated that the numbers of C=O decreased after the metal ions were added, indicating the formation of metal–carboxylate complexes. Raman characterization showed that the ID1/IG values increased, suggesting more structural defects, which indicated that the reactivity of coal samples had a close relation with amorphous carbon structures. Ca2+ could interact with the carboxyl structure in lignite by both ionic forces and polycarboxylic coordination, while K+ interacted with carboxyl structure mainly via ionic forces.