北京夏季大气主要含氮无机化合物的变化规律与相互作用

利用SJAC-MOBIC/FIA在2006年8月16日—9月9日在线测量了北京城市大气细颗粒物中主要水溶性含氮离子组分(NO₃^-和 NH₄⁺),与重要含氮气态污染物(HNO₃、HNO₂和 NH₃),以追踪细颗粒物中含氮二次无机组分和含氮气态污染物的变化规律及其相互作用。观测期间,NO₃^- 和 NH₄⁺的平均浓度分别为13.08和11.93 μg/m³,它们与SO₄^2-浓度之和在细颗粒物(PM_2.5)中的平均比例为55%,明显高于其他季节;污染过程中,积聚模态颗粒物体积浓度及其与爱根核模态颗粒物体积浓度比值逐渐增加,说明二次转化是北京夏季细颗粒物的重要来源。白天HONO迅速光解产生OH自由基,而OH自由基是生成HNO₃的重要物种,因此HONO和HNO₃具有相反的日变化规律。在温度较高的白天,大气环境不利于NH₄NO₃的生成与存在;夜间低温高湿的条件下硝酸铵理论平衡系数Ke与气态氨和硝酸的乘积Km相当或低于后者,较有利于NH₄NO₃的生成。北京夏季大气具有足量气态NH₃以中和硫酸盐;但在NO₃^-与阳离子的电荷平衡中,金属阳离子也非常重要。     

湘东北地区大气降水和地下水的氢氧稳定同位素研究

深入认识湘东北地区的水文循环过程,对规范该区水资源的有效利用和减缓该区生态环境问题具有重要意义。在2021年10月—2023年2月,对该区金井镇的大气降水和不同深度（~4.7 m和~61 m）井水每月开展样品采集和测试。该区大气降水稳定同位素值（δ¹⁸O、δD）呈现夏半年偏负、冬半年偏正,且氘盈余、水汽通量和HYSPLIT模型分析结果显示,在夏季,影响该区降水气团主要来自暖湿的海洋洋面,冬季主要来自稳定的南支西风和局地水汽输送。浅井水和深井水的δ¹⁸O和δD与该区大气降水δ¹⁸O和δD的均值接近,变幅较小且呈现夏季偏正冬季偏负的特征,说明地下水受到大气降水的补给,但可能滞后于大气降水的变化。然而,不同深度地下水对大气降水的响应机制和滞后时间,还需进一步研究。     

Ⅲ型储氢气瓶内胆6061-T6铝合金的氢致损伤研究进展

基于在多次循环充、放氢过程中,Ⅲ型储氢气瓶6061-T6铝合金内胆内部结构中渗入氢,从而导致性能衰减,影响气瓶服役安全可靠性,文中从氢渗透损伤、高压气体渗氢、溶液渗氢等几个方面综述了国内外开展包括6061铝在内的铝及铝合金中氢渗透行为及对铝合金拉伸力学性能、疲劳性能的影响的研究进展.简述了采用高压气体渗氢及溶液渗氢开展...     

基于FLACS的氢气检测器布置优化

采用某石化装置1∶1模型,以位于框架平台上的氢气分液罐泄漏为例,运用事故后果模拟软件FLACS构建计算流体力学模型并将氢气检测器设置为模型中的检测点,通过氢气泄漏及扩散过程数值模拟获得各检测点的氢气体积分数及响应时间,据此对氢气检测器的布置进行优化。主要研究成果有:1)提出氢气检测器探测效率的评价标准;2)明确工程中氢气检测器相对于潜在释放源的最优水平和竖向位置;3)给出花纹钢板和格栅板2种不同上层平台形式下氢气检测器的布置方案。     

Hydrogen Peroxide and Ultraviolet Irradiations in Water Treatment

Trihalomethanes (THMs) the by-products of chlorination in water treatment are recognised as a threat to public health due to their carcinogenicity. The photodegradation of THMs using hydrogen peroxide has been found to give increased removal efficiency and the outcome of the study may find, its application in designing a unit process for water treatment. Batch experiments were carried out using UV lamp of 83 W and 40% w/w Hydrogen peroxide (H₂O₂) in test waters between 2.5–10 pH range of chloroform, bromodichloromethane, dibromochloromethane and bromoform at 50–200 μg L⁻¹ initial concentration. 92–100% removal of chloroform, bromodichloromethane, dibromochloromethane and bromoform were found with 0.1% of H₂O₂ and 90 min of UV exposure.     

Nitrogenous and carbonaceous aerosols in PM2.5 and TSP during pre-monsoon: Characteristics and sources in the highly polluted mountain valley

This study reports for the first time a comprehensive analysis of nitrogenous and carbonaceous aerosols in simultaneously collected PM_2.5 and TSP during pre-monsoon (March–May 2018) from a highly polluted urban Kathmandu Valley (KV) of the Himalayan foothills. The mean mass concentration of PM_2.5 (129.8 µg/m³) was only ~25% of TSP mass (558.7 µg/ m³) indicating the dominance of coarser mode aerosols. However, the mean concentration as well as fractional contributions of water-soluble total nitrogen (WSTN) and carbonaceous species reveal their predominance in find-mode aerosols. The mean mass concentration of WSTN was 17.43±4.70 µg/m³ (14%) in PM_2.5 and 24.64±8.07 µg/m³ (5%) in TSP. Moreover, the fractional contribution of total carbonaceous aerosols (TCA) is much higher in PM_2.5 (~34%) than that in TSP (~20%). The relatively low OC/EC ratio in PM_2.5 (3.03 ± 1.47) and TSP (4.64 ± 1.73) suggests fossil fuel combustion as the major sources of carbonaceous aerosols with contributions from secondary organic aerosols. Five-day air mass back trajectories simulated with the HYSPLIT model, together with MODIS fire counts indicate the influence of local emissions as well as transported pollutants from the Indo-Gangetic Plain region to the south of the Himalayan foothills. Principal component analysis (PCA) also suggests a mixed contribution from other local anthropogenic, biomass burning, and crustal sources. Our results highlight that it is necessary to control local emissions as well as regional transport while designing mitigation measures to reduce the KV's air pollution.     

富氧空位MoO2强化Fe2+/过一硫酸盐体系降解四环素

采用NaBH₄超声还原法合成了富含氧空位的MoO₂,并通过多种表征方法证明了氧空位的存在.10-MoO₂作为助催化剂显著增强了Fe²⁺/过一硫酸盐体系催化性能,构建的10-MoO₂/Fe²⁺/PMS体系可快速降解四环素（TC）,10 min内对TC的降解率接近100%.系统研究了各种影响因素对TC降解效果的影响,探讨了助催化剂的稳定性及该体系的实用性.电化学、铁离子循环及自由基捕获实验的结果表明,由于氧空位（O_vacancy）的存在,降低了MoO₂的电阻,增强了电子转移能力,加速了Fe³⁺/Fe²⁺循环,提高了活性氧物种的产率,从而增强了Fe²⁺/PMS类芬顿体系的催化活性.本研究为类芬顿法处理抗生素废水提供了一种新的视角.     

受限空间瓦斯爆炸与氢气促进机理研究

为探索受限空间中瓦斯爆炸及氢气对爆炸过程的影响,采用GRI-Mech 3.0甲烷燃烧机理,建立受限空间中瓦斯爆炸的数学模型,应用CHEMKIN软件,对受限空间内瓦斯爆炸过程及氢气对反应物浓度、活化中心浓度、主要致灾性气体浓度的影响进行模拟分析。通过对反应机理的敏感性分析,找出影响瓦斯爆炸及爆炸后主要致灾性气体生成的关键反应步。结果表明:混合气中分别充入0.5%,2%,3.5%氢气时,爆炸时间分别提前0.005 7,0.010 5,0.011 1 s;爆炸后压力分别提高2.53,4.05,7.60 kPa;爆炸后温度分别提高20,60,100 K。由此可见,随着混合气中氢气含量的增加,瓦斯引爆时间越来越短,其爆炸强度也随之增大,且氢气在一定程度上对有害气体CO,CO2,NO,NO2的生成有很大影响。     

An experimental study on fermentative H2 production from food waste as affected by pH

Batch dark fermentation experiments were performed on food waste and mixtures of food waste and wastewater activated sludge to evaluate the influence of pH on biological H₂ production and compare the process performance with and without inoculum addition. The effect of a preliminary thermal shock treatment of the inoculum was also investigated as a means to harvest the hydrogenogenic biomass. The best performance in terms of both H₂ generation potential and process kinetics was observed at pH = 6.5 under all experimental conditions (no inoculum, and untreated or thermally treated inoculum added). H₂ production from food waste was found to be feasible even without inoculum addition, although thermal pre-treatment of the inoculum notably increased the maximum production and reduced the lag phase duration. The analysis of the fermentation products indicated that the biological hydrogen production could be mainly ascribed to a mixed acetate/butyrate-type fermentation. However, the presence of additional metabolites in the digestate, including propionate and ethanol, also indicated that other metabolic pathways were active during the process, reducing substrate conversion into hydrogen. The plateau in H₂ generation was found to mirror the condition at which soluble carbohydrates were depleted. Beyond this condition, homoacetogenesis probably started to play a role in the degradation process.     

Migration of inorganic ions from the leachate of the Rio das Ostras landfill: A comparison of three different configurations of protective barriers

Batch tests and diffusion tests were performed to analyze the efficiency of a protective barrier in a landfill consisting of compacted soil with 10% bentonite compared to the results obtained for only compacted soil and for compacted soil covered with a 1-mm-thick HDPE geomembrane; the soil and leachate were collected from the Rio das Ostras Landfill in Rio de Janeiro, Brazil. The diffusion tests were performed for periods of 3, 10 and 60 days. After the test period, the soil pore water was analyzed and the profiles for chloride, potassium and ammonium were determined along a 6-cm soil depth. The results of the batch tests performed to define sorption parameters were used to adjust the profiles obtained in the diffusion cell experiment by applying an ion transfer model between the interstitial solution and the soil particles. The MPHMTP model (Multi Phase Heat and Mass Transfer Program), which is based upon the solution of the transport equations of the ionic contaminants, was used to solve the inverse problem of simultaneously determining the effective diffusion coefficients. The results of the experimental tests and of the model simulation confirmed that the compacted soil with 10% bentonite was moderately efficient in the retention of chloride, potassium and ammonium ions compared to the configurations of compacted soil with a geomembrane and compacted soil alone, representing a solution that is technically feasible and requires potentially lower costs for implementation in landfills.