Measurement and Result of Soil Gas Radon and Soil Gas Mercury in the Exploration of Haihe Hidden Fault

In the exploration of the hidden Haihe fault,radon and mercury in soil gas were measured by using FG-3017 radon detector and XG-4 mercury analyzer.In this paper,based on the measurement results of 12 fault gas profiles,and integrating with the exploration results of artificial seismic prospecting,the relationship between anomalous site of fault gas and fault location is analyzed.Using the relationship between anomalous strength of fault gas and fault activity,the activity of Haihe fault is studied,thus the location and activity segmentation of the Haihe fault in Tianjin region are presented.This study shows that the method of fault gas detection can not only identify the preliminary location of fault,but also make preliminary segmentation of fault activity.The fault detected by the method of fault gas measurement is shown as a band.Through contrasting with exploration results of artificial seismic prospecting and analyzing,we find that the fault is located inside the band.According to the measurements of soil gas radon,the Haihe fault can be divided into east and west segments and the activity of the east segment of Haihe fault is stronger than that of the west segment.This is only a relative result,and it is difficult to judge whether the fault is active or not with this result.

Mercury removal from coal combustion flue gas by modified fly ash

Fly ash is a potential alternative to activated carbon for mercury adsorption. The effects of physicochemical properties on the mercury adsorption performance of three fly ash samples were investigated. X-ray fluorescence spectroscopy, X-ray photoelectron spectroscopy, and other methods were used to characterize the samples. Results indicate that mercury adsorption on fly ash is primarily physisorption and chemisorption. High specific surface areas and small pore diameters are beneficial to efficient mercury removal. Incompletely burned carbon is also an important factor for the improvement of mercury removal efficiency, in particular. The C-M bond, which is formed by the reaction of C and Ti, Si and other elements, may improve mercury oxidation. The samples modified with CuBr2 , CuCl 2 and FeCl3 showed excellent performance for Hg removal, because the chlorine in metal chlorides acts as an oxidant that promotes the conversion of elemental mercury （Hg0） into its oxidized form （Hg2＋）. Cu2＋ and Fe3＋ can also promote Hg 0 oxidation as catalysts. HCl and O2 promote the adsorption of Hg by modified fly ash, whereas SO2 inhibits the Hg adsorption because of competitive adsorption for active sites. Fly ash samples modified with CuBr2 , CuCl2 and FeCl3 are therefore promising materials for controlling mercury emissions.

Absorption characteristics of elemental mercury in mercury chloride solutions

Elemental mercury （Hg^0） in flue gases can be efficiently captured by mercury chloride （HgCl2） solution. However, the absorption behaviors and the influencing effects are still poorly understood. The mechanism of Hg^0 absorption by HgCl2 and the factors that control the removal were studied in this paper. It was found that when the mole ratio of Cl^- to HgCl2 is 10：1, the Hg^0 removal efficiency is the highest. Among the main mercury chloride species, HgCl3^- is the most efficient ion for Hg^0 removal in the HgCl2 absorption system when moderate concentrations of chloride ions exist. The Hg^0 absorption reactions in the aqueous phase were investigated computationaIIy using Moller-Plesset perturbation theory. The calculated Gibbs free energies and energy barriers are in excellent agreement with the results obtained from experiments. In the presence of SO3^2- and SO2, Hg^2＋ reduction occurred and Hg^0 removal efficiency decreased. The reduced Hg^0 removal can be controlled through increased chloride concentration to some degree. Low pH value in HgCla solution enhanced the Hg^0 removal efficiency, and the effect was more significant in dilute HgCl2 solutions. The presence of SO4^2- and NO3^- did not affect Hg^0 removal by HgCl2.

Enhancement of elemental mercury adsorption by silver supported material

Mercury, generally found in natural gas, is extremely hazardous. Although average mercury levels are relatively low, they are further reduced to comply with future mercury regulations,which are stringent in order to avoid releasing to the environment. Herein, vapor mercury adsorption was therefore investigated using two kinds of supports, granular activated carbon（GAC） and titanium dioxide（Ti O2）. Both supports were impregnated by silver（5 and 15 wt.%）,before testing against a commercial adsorbent（sulfur-impregnated activated carbon, SAC）. The adsorption isotherm, kinetics, and its thermodynamics of mercury adsorption were reported.The results revealed that Langmuir isotherm provided a better fit to the experimental data.Pseudo second-order was applicable to describe adsorption kinetics. The higher uniform Ag dispersion was a key factor for the higher mercury uptake. Ti O2 supported silver adsorbent showed higher mercury adsorption than the commercial one by approximately 2 times.Chemisorption of mercury onto silver active sites was confirmed by an amalgam formation found in the spent adsorbents.