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881.
Abstract

The traditional technologies for odor removal of thiol usually create either secondary pollution for scrubbing, adsorption, and absorption processes, or sulfur (S) poisoning for catalytic incineration. This study applied a laboratory-scale radio-frequency plasma reactor to destructive percentage-grade concentrations of odorous dimethyl sulfide (CH3SCH3, or DMS). Odor was diminished effectively via reforming DMS into mainly carbon disulfide (CS2) or sulfur dioxide (SO2). The removal efficiencies of DMS elevated significantly with a lower feeding concentration of DMS or a higher applied rf power. A greater inlet oxygen (O2)/DMS molar ratio slightly improved the removal efficiency. In an O2-free environment, DMS was converted primarily to CS2, methane (CH4), acetylene (C2H2), ethylene (C2H4), and hydrogen (H2), with traces of hydrogen sulfide (H2S), methyl mercaptan (CH3SH), and dimethyl disulfide. In an O2-containing environment, the species detected were SO2, CS2, carbonyl sulfide, carbon dioxide (CO2), CH4, C2H4, C2H2, H2, formal-dehyde, and methanol. Differences in yield of products were functions of the amounts of added O2 and the applied power. This study provided useful information for gaining insight into the reaction pathways for the DMS dissociation and the formation of products in the plasmolysis and conversion processes.  相似文献   
882.
稻壳基活性炭的制备及其对亚甲基蓝吸附的研究   总被引:8,自引:3,他引:5  
以稻壳为原料,采用K2CO3活化法和H3P04活化法制备了比表面积为1312m^2/g和682m^2/g的活性炭,通过扫描电子显微镜(SEM)、X-射线衍射仪(XRD)对样品进行了表征,并将孔隙发达的活性炭样品用于对亚甲基蓝的吸附,结果表明,K2CO3活化法制备的活性炭样品具有更多的微孔结构;随着亚甲基蓝溶液初始浓度的增加、活性炭吸附时间的延长,亚甲基蓝的去除率呈现逐渐降低和逐渐增大的变化规律,当pH值为6时,活性炭对亚甲基蓝的吸附效果最佳;稻壳基活性炭对亚甲基蓝的吸附等温线符合Langmuir模型,Qm最高可达476.2mg/g;热力学参数△G^0△H^0和△S^0均为负值,表明稻壳基活性炭对亚甲基蓝的吸附是一个自发的放热反应。  相似文献   
883.
Drinking highly arsenic-contaminated groundwater is a likely cause of blackfoot disease in Taiwan, but microorganisms that potentially control arsenic mobility in the subsurface remain unstudied. The objective of this study was to investigate the relevant arsenite-oxidizing and arsenate-reducing microbial community that exists in highly arsenic-contaminated groundwater in Taiwan. We cultured and identified arsenic-transforming bacteria, analyzed arsenic resistance and transformation, and determined the presence of genetic markers for arsenic transformation. In total, 11 arsenic-transforming bacterial strains with different colony morphologies and varying arsenic transformation abilities were isolated, including 10 facultative anaerobic arsenate-reducing bacteria and one strictly aerobic arsenite-oxidizing bacterium. All of the isolates exhibited high levels of arsenic resistance with minimum inhibitory concentrations of arsenic ranging from 2 to 200 mM. Strain AR-11 was able to rapidly oxidize arsenite to arsenate at concentrations relevant to environmental groundwater samples without the addition of any electron donors or acceptors. We provide evidence that arsenic-reduction activity may be conferred by the ars operon(s) that were not amplified by the designed primers currently in use. The 16S rRNA sequence analysis grouped the isolates into the following genera: Pseudomonas, Bacillus, Psychrobacter, Vibrio, Citrobacter, Enterobacter, and Bosea. Among these genera, we present the first report of the genus Psychrobacter being involved in arsenic reduction. Our results further support the hypothesis that bacteria capable of either oxidizing arsenite or reducing arsenate coexist and are ubiquitous in arsenic-contaminated groundwater.  相似文献   
884.
This report demonstrates that organic matter was an important factor in lake sediment 210Pbex dating. Sediment cores from lakes in central and western China with different-trophic levels were collected, and the 210Pbex activity and total organic carbon (TOC) were measured. The Rock-Eval pyrolysis technique was used to deconvolute TOC into free hydrocarbons (S1), thermally less-stable macromolecular organic matter (S2a), kerogen (S2b), and residual carbon (RC). The results show significant correlations between TOC and 210Pbex, particularly between S2a and 210Pbex, in all the sediment cores. This indicated that the algal-derived organic component S2a may play the most important role in controlling the distribution of 210Pbex. Scavenging by algal-derived organic matter may be the main mechanism. As chronology is the key to the understanding of pollution reconstruction and early diagenesis in sediments, more attention should be paid to the influence of organic matter on 210Pbex.  相似文献   
885.
In present study, atmospheric particles from Shanghai, the biggest city and the most important industrial base in China, were analyzed for polybrominated diphenyl ethers (PBDEs) and Dechlorane Plus (DP). Concentrations of ∑(20)PBDEs and DP both exhibited the changing trend of industrial area > urban areas. Jiading District had the highest levels of particulate PBDEs and DP with values of 744 ± 152 pg/m(3) and 5.48 ± 1.28 pg/m(3), respectively. Compared with similar data in other areas of the world, PBDEs in Shanghai were at medium pollution level, while DP was at lower level, which reflected their different production and use in Shanghai. The results from multiple linear regression analysis suggested that deca-BDE mixture was the most important contributor of particulate PBDEs in Shanghai. The fractions of anti-DP showed no significant differences to those of the technical mixtures (p > 0.05), which suggested that no obviously stereoselective process occurred in ambient air around Shanghai.  相似文献   
886.
Yuan SY  Liu C  Liao CS  Chang BV 《Chemosphere》2002,49(10):1295-1299
Concentrations and microbial degradation rates were measured for eight phthalate esters (PAEs) found in 14 surface water and six sediment samples taken from rivers in Taiwan. The tested PAEs were diethyl phthalate (DEP), dipropyl phthalate (DPP), di-n-butyl phthalate (DBP), diphenyl phthalate (DPhP), benzylbutyl phthalate (BBP), dihexyl phthalate (DHP), dicyclohexyl phthalate (DCP), and di-(2-ethylhexyl) phthalate (DEHP). In all samples, concentrations of DEHP and DBP were found to be higher than the other six PAEs. DEHP concentrations in the water and sediment samples ranged from ND to 18.5 μg/l and 0.5 to 23.9 μg/g, respectively; for DBP the concentration ranges were 1.0–13.5 μg/l and 0.3–30.3 μg/g, respectively. Concentrations of DHP, BBP, DCP and DPhP were below detection limits. Under aerobic conditions, average degradation half-lives for DEP, DPP, DBP, DPhP, BBP, DHP, DCP and DEHP were measured as 2.5, 2.8, 2.9, 2.6, 3.1, 9.7, 11.1 and 14.8 days, respectively; under anaerobic conditions, respective average half-lives were measured as 33.6, 25.7, 14.4, 14.6, 19.3, 24.1, 26.4 and 34.7 days. In other words, under aerobic conditions we found that DEP, DPP, DBP, DPhP and BBP were easily degraded, but DEHP was difficult to degrade; under anaerobic conditions, DBP, DPhP and BBP were easily degraded, but DEP and DEHP were difficult to degrade. Aerobic degradation rates were up to 10 times faster than anaerobic degradation rates.  相似文献   
887.
Series sludge straw–based activated carbons were prepared by sewage sludge and corn straw with potassium hydroxide (KOH) activation, and the desulfurization performance of activated carbons was studied. To obtain the best desulfurization performance, the optimum ratio between the raw materials and the activator was investigated. The results showed that when the mass ratio of sewage sludge, corn straw, and KOH was 3:7:2, the activated carbon obtained the best breakthrough and saturation sulfur sorption capacities, which were 12.38 and 5.74 times, respectively, those of samples prepared by the nonactivated raw materials. The appropriate KOH could improve the microporosity and alkaline groups, meanwhile reducing the lactone groups, which were all beneficial to desulfurization performance. The chemical adsorption process of desulfurization can be simplified to four main steps, and the main desulfurization products are elemental sulfur and sulfate.

Implications: Sewage sludge (SS) and corn straw (CS) both have great production and wide distribution and are readily available in China. Much attention has been paid on how to deal with them effectively. Based on the environment protection idea of waste treatment with waste and resource recycling, low-cost adsorbents were prepared by these processes. The proposed method can be expanded to the municipal solid waste recycling programs and renewable energy plan. Thus, proceeding with the study of preparing activated carbon by SS and straw as a carbon-based dry desulfurization agent could obtain huge social, economic, and environmental benefits.  相似文献   

888.

Identification of different pollution sources in groundwater is challenging, especially in areas with diverse land uses and receiving multiple inputs. In this study, principal component analysis (PCA) was combined with geographic information system (GIS) to explore the spatial and temporal variation of groundwater quality and to identify the sources of pollution and main factors governing the quality of groundwater in a multiple land-use area in southwestern China. Groundwater samples collected from 26 wells in 2012 and 38 wells in 2018 were analyzed for 13 water quality parameters. The PCA results showed that the hydro-geochemical process was the predominant factor determining groundwater quality, followed by agricultural activities, domestic sewage discharges, and industrial sewage discharges. Agriculture expansion from 2012 to 2018 resulted in increased apportionment of agricultural pollution. In contrast, economic restructure and infrastructure improvement reduced the contributions of domestic sewage and industrial pollution. Anthropogenic activities were found the major causes of elevated nitrogen concentrations (NO3?, NO2?, NH4+) in groundwater, highlighting the necessity of controlling N sources through effective fertilizer managements in agricultural areas and reducing sewage discharges in urban areas. The applications of GIS and PCA successfully identified the sources of pollutants and major factors driving the variations of groundwater quality in tested years.

  相似文献   
889.
选取云南的砂岩作为试验岩样,研究砂岩经过化学溶蚀及冻融循环作用下的力学特性。通过对砂岩在3种水化环境(PH=3的HCl溶液、PH=7的水溶液、PH=12的NaOH溶液)作用后分别进行循环冻融试验,并在不同冻融循环温度 (-20 ℃、-30 ℃、-40 ℃、-50 ℃)作用下对试样进行单轴压缩试验和三点弯曲试验。结果表明:砂岩经过化学溶蚀和冻融循环作用下的劣化损伤模式主要受冻融循环温度及不同水溶液影响,在不同的水溶液中,单轴抗压强度、弹性模量、应力峰值和断裂韧度均随着冻融循环温度的降低而逐渐降低;HCl溶液浸泡后的砂岩损伤变量最大,而在对砂岩有修补作用的NaOH溶液中出现了负损伤的变化。  相似文献   
890.
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