Study of S poisoning mechanism on LaMnO3 perovskite catalyst surface based on DFT method.

The sulfur poisoning mechanism of low-temperature SCR de-NOx catalyst has always been one of the hot spots in academic circles. By studying the surface sulfur poisoning mechanism, low-temperature catalysts can be developed pertinently. In this paper, the mechanism of sulfur poisoning on the surface of LaMnO3 catalyst was studied by DFT method, and the adsorption process of sulfur oxides on the surface and its influence on SCR reaction process, as well as the morphology and decomposition process of ammonium sulfate on the surface were calculated. The results show that sulfur oxides will be adsorbed on the surface and occupy the adsorption site, which will adversely affect the subsequent SCR reaction. At the same time, ammonium sulfate will accumulate on the catalyst surface, which will lead to sulfur poisoning.

The co-pyrolysis of waste urea-formaldehyde resin with pine sawdust: co-pyrolysis behavior, pyrocarbon and its adsorption performance for Cr (VI).

Urea-formaldehyde (UF) resin is difficult to degrade and classified as hazardous organic waste. To address this concern, the co-pyrolysis behavior of UF resin with pine sawdust (PS) was studied, and the adsorption properties of pyrocarbon were evaluated with Cr (VI). Thermogravimetric analysis revealed that adding a small amount of PS can improve the pyrolysis behavior of UF resin. Based on the Flynn Wall Ozawa (FWO) method, the kinetics and activation energy values were estimated. It was observed that when the amount of UF resin exceeded twice that of PS, the activation energy of the reaction decreased, and they acted synergistically. The characterization of pyrocarbon samples showed that the specific surface area increased with the increase of temperature, while the content of functional groups showed the opposite trend. Intermittent adsorption experiments showed that 5UF + PS400 achieved 95% removal of 50 mg/L Cr (VI) at 0.6 g/L dosage and at pH 2. The adsorption process was consistent with the Langmuir isotherm and pseudo-second-order kinetics, and the maximum adsorption was 143.66 mg/g at 30 ℃. Furthermore, the adsorption process consisted of electrostatic adsorption, chelation, and redox reaction. Overall, this study provides a useful reference for the co-pyrolysis of UF resin and the adsorption capacity of pyrocarbon.

Combustion Characteristics of Low Calorific Value Biogas and Reaction Path of NOx Based on Sensitivity Analysis.

The combustion mechanism of biogas mixture is unclear, which leads to the lack of basis for the control of operating parameters. Combustion characteristics and reaction path of typical low calorific value biogas with variation of preheating temperature and air equivalence ratio (Φ) are discussed in this paper. Preheating can not only improve the flame propagation speed and flame temperature, but also increase the proportion of NO in the product at the end of combustion flame. To some extent, improving combustion efficiency and NOx control are contradictory operating parameters. The amount of NO increases with the increase in flame distance. The maximum value of NO appears when Φ is 1.1. NO formation rate is improved by preheating the biogas. The paths of N2 → N2O →NO, N2 → NNH →NO, and N2 →NO are all enhanced. When the equivalence ratio changes from 1.0 to 0.8, NO formation rates decrease.

Direct reduction of copper slag-carbon composite pellets by coal and biochar.

As a renewable resource of reducer, biochar prepared by pine sawdust is proposed for direct reduction of copper slag in this paper. Combined with thermodynamic analysis, effects of reduction time, temperature and CaO addition ratio on solid copper slag reduction characteristics are discussed. The oxides of iron in copper slag are Fe3O4 and 2FeO·SiO2. The reduction processes were carried out step by step for Fe3O4 and 2FeO·SiO2, respectively: Fe3O4 → FeO → Fe and 2FeO·SiO2 → Fe. The porous structure of biochar exhibits higher reduction reactivity and reaction rate than that of coal. CaO reduced the Gibbs free energy of reduction reactions and facilitated the reduction of 2FeO·SiO2 with C and CO. When CaO was added, separation reaction of FeO and SiO2 took place and α-SiO2 and ß-SiO2 were produced. When the addition ratio of CaO is above 0.3, CaO·SiO2 and 2CaO·SiO2 are produced. The reduction process of copper slag was established as follows: (a) dehydration and fast pyrolysis; (b) reduction of iron oxides by C and CO; and (c) sweating metallic iron outflows from cracks in pellet. Besides, direct reduction reaction mechanism and transport process of Cu are established based on reduction experiments, XRD and SEM-EDS analysis.