Coal-mine gas disaster is one of the most serious coal-mine disasters in China. The main component of coal-mine gas, methane is chemically stable and very difficult to be degraded by conventional methods. Hydroxyl radical (OH), due to strong oxidizing ability and high electro-negativity, is the primary degradation source of atmospheric methane. In the present study, methane degradation using hydroxyl radicals generated by Fenton’s reagent, Fe2+/H2O2, has been carried out in the self-designed bubbling reactor. The effects of H2O2 concentration, dosage of FeSO4·7H2O and initial pH value on methane removal efficiency were investigated respectively. It has been found that the optimal reaction conditions were 100 mM of hydrogen peroxide, 2.00 mM of ferrous ion and initial pH value of 2.5. Under optimal conditions, the removal efficiency of methane reached 25% after 30 min. The preliminary experimental results unambiguously demonstrate that the degradation of methane using hydroxyl radicals generated by Fenton’s reagent is feasible. 相似文献
Combustion-generated hydrogen chloride (HCl) is considered to be a very hazardous acid gaseous pollutant. This paper presents a laboratory study on the dry adsorption of HCl. The experiments were conducted in a dual-layer granular bed filter, at gas temperatures of 500℃-700℃ and n(Ca)/n(Cl)molar ratios of 1.0-5.0 using the silver nitrate titration method by dry adsorbent powders Ca(OH)2. Mainly, the adsorption efficiency of HCI and utilization efficiency of Calcium were studied, by varying relevant factors including n(Ca)/n(Cl), tempera- ture, feeding method, water vapor and CO2. With a relatively higher HCl concentration of 1000ppm, the experimental results revealed that 600℃ may be the optimum temperature for HCl adsorption when optimum n (Ca)/n(Cl) was 2.5 in our tests. The results also demonstrated that the feeding at a constant pressure was more effective, and the HCl adsorption efficiency could rapidly reach over 90% with n(Ca)/n(Cl) = 2.5 at 600℃. Furthermore, the HCl adsorption efficiency was found to be slightly promoted by water vapor, while could be impeded by CO2, and the utilization efficiency of calcium could be up to 74.4% without CO2, while was only 36.8% with CO2 when n(Ca)/n(Cl) was 2.5 at 600℃. 相似文献
Nansi Lake is composed of four sub-lakes from north to south: Nanyang Lake, Dushan Lake, Zhaoyang Lake and Weishan Lake. An environmental pollution investigation was carried out to determine the fractionation, and pollution assessments of mercury (Hg) in surficial sediments from Nansi Lake. Results showed that the mean concentration of Hg was 3.1 times higher than its background value (0.015 mg kg?1), and the high concentration of Hg which even reached up to five times than the background value in the part of Dushan Lake and Weishan Lake, which indicated that there are obvious spatial differences. The content of Hg was positively correlated with that of total organic carbon, and negatively correlated with that of pH and SiO2 in surface sediments. An improved Tessier sequential extraction procedure was used to study the fractions of Hg in sediments. The results indicated that Hg existed primarily in the fraction of residual, which accounts for 58.4% of total mercury (THg), and the percentage of extractable Hg was only 1.93% of total mercury. High concentrations of mercury of non-residual phase were found in part lake area from the Nanyang Lake and the Weishan Lake, which indicating a higher potential ecological risk relative to the other lake areas. Based on the values of enrichment factor and geo-accumulation index, most part of Dushan Lake and Nanyang Lake and Weishan Lake were in a moderate pollution. And based on the fractionation of mercury, risk assessment code of Hg exhibited low risks to the environment in Nansi Lake. 相似文献
The novel microwave catalyst MgFe2O4-SiC was synthesized via sol-gel method, to remove azo dye Direct Black BN (DB BN) through adsorption and microwave-induced catalytic reaction. Microwave-induced catalytic degradation of DB BN, including adsorption behavior and its influencing factors of DB BN on MgFe2O4-SiC were investigated. According to the obtained results, it indicated that the pseudo-second-order kinetics model was suitable for the adsorption of DB BN onto MgFe2O4-SiC. Besides, the consequence of adsorption isotherm depicted that the adsorption of DB BN was in accordance with the Langmuir isotherm, which verified that the singer layer adsorption of MgFe2O4-SiC was dominant than the multi-layer one. The excellent adsorption capacities of MgFe2O4-SiC were kept in the range of initial pH from 3 to 7. In addition, it could be concluded that the degradation rate of DB BN decreased over ten percent after the adsorption equilibrium had been attained, and the results from the result of comparative experiments manifested that the adsorption process was not conducive to the process of microwave-induced catalytic degradation. The degradation intermediates and products of DB BN were identified and determined by GC-MS and LC-MS. Furthermore, combined with the catalytic mechanism of MgFe2O4-SiC, the proposed degradation pathways of DB BN were the involution of microwave-induced $OH and holes in this catalytic system the breakage of azo bond, hydroxyl substitution, hydroxyl addition, nitration reaction, deamination reaction, desorbate reaction, dehydroxy group and ring-opening reaction.