油污土壤中微生物数量变化与原油降解速率关系的实验研究

微生物法治理油污土壤具有成本低、效果好的特点 ,其原理是微生物利用油烃作为碳源合成自身物质 ,进行生长繁殖 ,从而使油烃的含量得到减少。而与此同时 ,微生物的数量也会发生相应的变化。目前油污土壤微生物的研究主要局限于对污染土壤中分离提纯的单一菌种的降解效能的研究。本文对土著油污土壤微生物在适宜条件下的数量和种类变化进行了实验分析 ,并对油烃的化学组成作了初步探讨。分离出 4株对石油具有耐受性和降解能力的微生物。结果表明 ,在 4株微生物数量都增加的时候 ,石油烃的降解速度最快。     

电化学法消毒处理医院污水的试验研究

采用电化学法消毒处理医院污水,通过选用不同阳极材料构建的电化学体系,探讨电化学法的消毒机理.试验表明,以涂有贵金属(钌、铂和铱)氧化物的钛板作阳极,不锈钢板作阴极,在电流密度为8 mA/cm2、水力停留时间为15 min、空气流量为40L/h、极水比为1.0的试验条件下,消毒后污水中总大肠菌群数＜500 cfu/L,达到国家一级排放标准(GB8978-1996).     

扩散荷电作用下线板式ESP中PM2.5捕集效率的数值模拟

为考察线板式静电除尘器中PM2.5颗粒的除尘性能,建立电场、颗粒动力场和流场多场耦合下的数学理论模型。采用GAMBIT软件构造ESP实体结构,将用户自定义程序UDF导入到FLUENT软件中进行数值仿真,并应用Deutsch-Anderson公式计算粉尘在不同荷电机理和2种不同除尘操作参数下的除尘效率。数值结果表明,扩散荷电效应对PM2.5分级除尘效率贡献率随粒径增大非线性减小;外加工作电压越低或烟道气流速越高,扩散荷电效应对PM2.5粉尘颗粒的影响越大;在较高外加电压工况下,扩散荷电对综合效率的影响与降低一定量的烟道气流速相当。     

Fe2O3/TiO2/γ-Al2O3催化剂同时脱硫脱硝性能

以溶胶凝胶法制备的15%TiO2/γ-Al2O3为载体,通过浸渍法制备12%Fe2O3/15%TiO2/γ-Al2O3催化剂,采用XRD和TPR对催化剂结构和性质进行表征,并考察不同焙烧温度、焙烧时间和载体对催化剂脱硫脱硝性能的影响。结果显示,最佳焙烧条件为500℃下焙烧3 h,12%Fe2O3/15%TiO2/γ-Al2O3催化剂达到的最高脱硝脱硫率分别为98.2%和95.4%。     

半干法烧结烟气脱硫灰的氧化改性

半干法烧结烟气脱硫灰中含有大量CaSO3,而CaSO3对于脱硫灰的稳定性具有重要影响,限制了脱硫灰的处理和综合利用。为了解决该问题,采用低温静态氧化改性实验和高温动态焙烧改性实验,在掺加和不掺加催化剂条件下,对含CaSO3的脱硫灰进行了氧化改性研究,并结合热重实验考察了半干法烧结烟气脱硫灰中CaSO3的高温动态氧化改性效果。结果表明,在低温为45、75和90℃时,掺入不同催化剂对半干法烧结烟气脱硫灰中CaSO3进行氧化改性2 h,效果依次为:MnO2 > Fe2O3 > 不掺催化剂 > V2O5,且CaSO3的氧化率均低于2.2%;在不掺催化剂的条件下,在350℃以上焙烧30~60 min,CaSO3的氧化率均可达到85%以上。结合热重分析结果发现,选择合适的焙烧温度和时间对提高CaSO3的氧化率有重要作用。     

Influence of H2SO4 and ferric iron on Cd bioleaching from spent Ni–Cd batteries

The paper is concerned with biohydrometallurgical methods of cadmium recovery from spent Ni–Cd batteries. Cd leaching efficiency from electrode material in different media (H₂SO₄ and Fe₂(SO₄)₃ solutions), at different Fe(III) concentrations and using the bacteria Acidithiobacillus ferrooxidans were investigated. The main aim of this study was to understand which from the bioleaching products (sulphuric acid or ferric sulphate) play a main role in the bioleaching process of Cd recovery. The influence of Fe ions on Cd leachability was confirmed. The best leaching efficiency of Cd (100%) was reached by bioleaching and also by leaching in Fe₂(SO₄)₃ solution. The results of X-ray diffraction confirmed that no cadmium was present in solid residuum obtained after the Cd bioleaching as well as Cd leaching using solely ferric iron. The use of H₂SO₄ solution resulted in the lowest efficiency of Cd leachability, the presence of hydroxides in electrode materials caused neutralization of the leaching solution and inhibition of Cd leaching.     

Kinetics of base-catalyzed dehydrochlorination of hexachlorocyclohexanes: I. Homogeneous systems

Base-catalyzed dehydrochlorination of alpha-, beta-, and gamma-hexachlorocyclohexane (HCH) was examined at different pH and temperature conditions. No reaction was observed for beta-HCH under all tested conditions likely due to the fact that all chlorines are at the equatorial positions. Highly pH- and temperature-dependent reaction rates were observed for alpha- and gamma-HCH, and pentachlorocyclohexenes (PCCHs) and 1,2,4- and 1,2,3-trichlorobenzene (TCB) were detected as the intermediates and final products of the transformation of both alpha- and gamma-HCH. The pseudo-first-order rate constants of each step of the reactions were calculated at different T and pH conditions. For the first step, the rate constants were at approximately 0.0005 d-1 in solutions below pH 7.0, and increased by about an order of magnitude per pH unit from pH 7.01 to pH 12.02. The second-order reaction rate constants (kb) of this step were 3.57+/-0.03 and 3.19+/-0.19 M-1 d-1, respectively, and the associated activation energies (Ea) at pH 9.26 were 60.4+/-7.8 and 67.7+/-8.7 kJ mol-1, respectively, for alpha- and gamma-HCH. The rate constants for the formation of 1,2,3-TCB (k21) and 1,2,4-TCB (k22) were 0.0032+/-0.0001 d-1 and 0.051+/-0.003 d-1 from alpha-HCH, and 0.0017+/-0.0001 d-1 and 0.0041+/-0.0002 d-1 from gamma-HCH at pH 8.28 and 25 degrees C. Both k21 and k22 also showed an increase by about one order of magnitude per pH unit from pH 8.28 to pH 12.02. The Ea values were 64.4+/-6.8 and 88.8+/-5.2 kJ mol-1, respectively, for the formation of 1,2,4-TCB and 1,2,3-TCB from alpha-HCH, and 70.6+/-8.7 and 92.0+/-4.9 kJ mol-1, respectively, for the formation of 1,2,4- and 1,2,3-TCB from gamma-HCH at pH 9.26. Data provided by this study may be used for calculation of the percentages of the TCBs formed at different environmental conditions.     

影响津河水生生态环境的主要因素及保护对策

论述了津河改造后整体水生生态环境的改善成效，对影响津河生态环境的城市径流、工业废水、生活垃圾、海河水质、津河底质等因素进行分析，并提出了相关的防护措施和建议。     

新标准促进安全鞋“走出去”——GB 21148-2020《足部防护安全鞋》解读

1 标准任务的来源 根据2016年强制性标准整合精简结论,对GB21148-2007《个体防护装备安全鞋》、GB 21147-2007《个体防护装备防护鞋》、GB 21146-2007《个体防护装备职业鞋》、GB 12011-2009《足部防护电绝缘鞋》4项标准提出整合修订,并继续作为强制性标准执行. 2017年12月...     

Dechlorane plus (DP) in indoor and outdoor air of an urban city in South China: Implications for sources and human inhalation exposure

Dechlorane Plus (DP) is a chemical of emerging concern due to the restrictions on brominated flame retardant formulations. However, very little information is known about the occurrence of DP in indoor and outdoor air and its associated health risk to the exposed human population. In this study, we examined the concentrations and isomer profiles of DP in archived air samples collected from 14 homes, 6 offices, and 10 public microenvironments in Guangzhou, China in 2004–2005. The average (median) value of atmospheric ΣDP (sum of anti-DP and syn-DP) concentration in the three indoor air was 5.73 ± 5.33 (3.62) for offices, 8.08 ± 5.17 (6.87) for homes, and 57.27 ± 83.08 (32.58) pg/m³ for public microenvironments, respectively. ΣDP concentration was significantly higher in the public microenvironments than those in homes and offices. The arithmetic mean and median concentrations of ΣDP in outdoor air were 36.00 and 28.76 pg/m³, respectively. Spatially and temporally consistent indoor and outdoor samples comparison suggested that outdoor air might be a relevant source of DP for indoor air. Average anti-DP fractional abundance (f_anti = 0.65 ± 0.04) in all outdoor samples was similar to those reported in other studies and indistinguishable from that of the commercial mixture (f_anti = 0.65). In contrast, a relatively large variation of f_anti values was found in the indoor samples, suggesting a complex degradation process of DP existing in these microenvironments. The calculated average daily doses of ΣDP were in the range of 0.38–2.21 ng/day for people intake through air inhalation, which was in the same order of magnitude compared with other exposure pathways for the general publics.