Investigation of reducing particulate matter (PM) and heavy metals pollutions by adding a novel additive from metallurgical dust (MD) during coal combustion.

In this study, a novel additive from metallurgical dust(MD)was applied to reduce particulate matter (PM) emissions and heavy metals pollutions during coal combustion. PM samples were collected and divided into 13 stages from 0.03 µm to 10 µm. Results showed that the irregular morphology of fine particles with equal to/less than 2.5 µm (PM2.5), fine particles with equal to/less than 4 µm (PM4) and fine particles with equal to/less than10 µm (PM10) gradually became dense with increasing of MD content. The PM10 concentration with 10% MD dosage was about 3 times higher than that of raw coal. Zn, Ti, Cu and Cr were the most abundant elements in all particulate matters (PMs), meanwhile, heavy metals accumulated into large particles with increasing MD content. The mechanism of reducing PM emissions indicated that MD reacted with nucleation elements (Pb, Cd, etc.) and trapped a large amount of alkali metal (Na/K), which aggregated into large particles. The study highlights the potential of adding MD into coal to prevent the attachment of heavy metals onto ultrafine particles, thereby reducing the heavy metals emissions.

Study of Catalytic Combustion of Dioxins on Ce-V-Ti Catalysts Modified by Graphene Oxide in Simulating Iron Ore Sintering Flue Gas.

Ce-V-Ti and Ce-V-Ti/GO catalysts synthesized by the sol-gel method were used for the catalytic combustion of dioxins at a low temperature under simulating sintering flue gas in this paper. The catalytic mechanism of Ce-V-Ti catalysts modified with graphene oxides (GO) at a low temperature was revealed through X-ray diffractometer (XRD), Brunauer-Emmett-Teller (BET), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), H2-temperature-programmed reduction (H2-TPR) and Fourier transform infrared (FTIR). During the tests, chlorobenzene (CB) was used as a model reagent since the dioxins are poisonous. The results showed that introducing GO to Ce-V-Ti catalysts can improve the specific surface area and promote the CB adsorption on the surface of catalysts. Simultaneously, the Ce-V-Ti with 0.7 wt % GO support showed the high activity with the conversion of 60% at 100 °C and 80% at 150 °C. The adsorb ability of catalysts is strengthened by the electron interaction between GO and CB through π-π bond. In the case of Ce-V-Ti catalysts, Ce played a major catalytic role and V acted as a co-catalytic composition. After GO modification, the concentration of Ce3+ and V4+ were enlarged. The synergy between Ce3+ and V3+ played the critical role on the low-temperature performance of catalysts under sintering flue gas.