我国大气中挥发性有机物的分布特征

大气中挥发性有机物(VOCs)是臭氧和二次有机气溶胶形成的关键前体物之一,研究表明烷烃、烯烃、芳香烃是我国大气VOCs的重要组分。在不同区域,城市地区烷烃含量最高,而偏远地区芳香烃为含量最丰富的VOCs。VOCs浓度日间变化多呈双峰分布趋势,峰值多出现在早晨与傍晚的上下班高峰期。目前对我国臭氧污染事件的研究均表明芳香烃和烯烃是对臭氧生成贡献最大的化合物。VOCs源解析中广泛运用的模型包括CMB、PMF和PCA/APCS,各模型均存在优点和局限性。比较各地VOCs源解析结果,发现交通排放源和工业排放源为我国VOCs的主要人为来源。VOCs的跨区域传输决定与周边地区的合作将是未来空气治理中的发展方向。     

西安市重污染与清洁天PM2.5组分及其活性氧物质对比

针对重霾污染,在西安市冬季重污染日(2015-11-30~2015-12-09)和清洁日(2016-01-13~2016-01-22)各进行了为期10d的PM_(2.5)采集,测量其中的有机碳、元素碳,及NH_4~+、NO_3~-、SO_4~(2-)等无机水溶性离子,探讨两种污染条件下的组分特征及其成因.结果表明:观测期,重霾日和清洁日PM_(2.5)质量浓度分别为(170±47.5)μg·m~(-3)和(48.6±17.9)μg·m~(-3),且重霾日伴随低能见度、高湿静风等多种不利气象条件;重霾日二次无机离子(NH_4~+、NO_3~-、SO_4~(2-))组分占PM_(2.5)质量浓度的49.8%±13.1%,而清洁日为19.4%±5.95%,并且重霾日硫氧化速率(sulfur oxidation ratio,SOR)和氮氧化速率(nitrogen oxidation ratio,NOR)分别为0.282±0.157和0.269±0.124,远高于清洁日(SOR和NOR分别为0.189±0.057和0.077±0.046),重霾日二次有机组分浓度[(6.22±3.87)μg·m~(-3)]是清洁日[(1.44±1.63)μg·m~(-3)]的5倍,表明二次污染及不利气象条件是造成重霾期间相关组分浓度升高的重要原因.最后,通过二氯荧光黄双乙酸盐(2',7'-DCFH)化学荧光分析法测定了其中活性氧物质(reactive oxygen species,ROS)的浓度,探讨其对于二次无机组分形成的影响,结果表明观测期ROS平均浓度(以H_2O_2计)分别为(4.99±1.54)nmol·m~(-3)(重霾期),(0.492±0.356)nmol·m~(-3)(清洁期),二次反应及积累效应可能是西安重霾条件下ROS浓度升高的主要原因.NO_3~-、SO_4~(2-)与ROS均呈现正相关(P0.05),表明ROS可能通过二次氧化过程参与到二次无机组分形成过程中.     

湖泊热结构和蒸发的模拟计算

应用一维涡扩散模型计算一年内不同时期的湖泊垂直温度分布和湖水蒸发率。主管方程是同一水平面内均温的一维非定常热传导方程。模型不要求特定的湖泊拟合参数。模型中涡扩散系数通过Ｒｉｃｈａｒｄｓｏｎｏ数计算,水面热交换用能量平衡法计算,湖底假定为绝热,主管方程用有限差分法求解。对Ｃｏｌｏｒａｄｏ Ｃｉｔｙ湖和Ｃａｌｈｏｕｎ湖的模拟计算表明：水面温度和温度剖面的计算值与实测值吻合很好,最大差值均在２℃范围内。     

The Impact of Scrubber Sludge on Ground Water Quality at an Abandoned Mine Site

A sulfate-rich flue gas desulfurization scrubber sludge was used as a substitute backfill material in reclamation of an abandoned coal strip mine. The site was surrounded by monitor wells and the material was characterized for leaching behavior using open column experiments. A drain was placed directly beneath the 45 000 ton fill to enable sampling before dilution or attenuation. The column studies indicated that the scrubber sludge would adsorb manganese, iron, aluminium, cobalt, nickel, thallium and zinc contaminants from the water. Changes in pH appear inadequate to explain the removal by precipitation. The groundwater cleaning phenomenon has been confirmed on a field scale by the drain samples. Boron and molybdenum leach from the fly ash was used to fix the scrubber sludge and serve as marker elements enabling calibration of the dispersivity in computer models of the groundwater system at the site. The leachate front appears to be diluted by a factor of 8 : 1 within the first 15 meters. Since boron and molybdenum release are associated only with the first flush, environmental impacts will be minimal. Columns appear to create a time compression effect on the duration of leaching phenomenon. The effect for this site appears to be at least 5 : 1. The columns were effective in predicting which elements would leach or adsorb in the field and in predicting the actual source concentrations. Other shake tests such as the TCLP and the ASTM shake test were found to be less effective at predicting which elements would leach and were not helpful in predicting field concentrations.     

H2O2/VisUV photo-oxidation process for treatment of waterborne hazardous substances—Reaction mechanism, rate model, and data for tubular flow and flow stirred tank reactors

This paper presents the chemical reaction engineering development of the H₂O₂/VisUV photo-oxidation process for treatment of hazardous waterborne substances, that occur in groundwater, leachates, and industrial wastewater. Reaction results, on benzene (BNZ), dichlorobenzene (DCB), trichloroethene (TCE), trichloroethane (TCA), and carbon tetrachloride (CTC), have been obtained, providing engineering data and models that can be used to size full-scale equipment. A photochemical flow stirred tank reactor (pcfSTR) and a photo-chemical tubular flow reactor (pcTFR) were used in the experimental work. Two experimental discoveries were made in the course of the work: (1) conventional thermal kinetics do not apply, the rate controlling variable is the photon flux, and (2) for the photo-chemical reactors used, the pcfSTR was more effective than the pcTFR. The following sub-topics are discussed: reaction mechanism, reactor hydrodynamics, photon flux effects, typical reaction data (on benzene and trichloroethane), and rate constants.     

Investigation of the Aerobic Biodegradability of Several Types of Cyclodextrins in a Laboratory-Controlled Composting Test

The biodegradation of several types of cyclodextrins (CDs) under laboratory-controlled composting conditions was investigated. CDs are used in a broad range of applications in food, pharmaceutical, medical, chemical, and textile industries because of their specific chemical characteristics related to their hydrophobic interior and hydrophilic exterior. The three naturally occurring cyclodextrins -CD, -CD, and -CD proved to be completely and readily biodegradable. Chemical modification of these basic compounds can have a major impact on the biodegradation rate and final biodegradation percentage. Fully acetylated -CD and -CD were found to be nonbiodegradable during 45 days of composting. Reducing the degree of acetylation had a positive effect on the biodegradation. Complete biodegradation was obtained for partially acetylated -CD with a degree of substitution (DS) of 7. The methylation (DS = 13) of -CD resulted in an undegradable compound during the 47 days composting, while (2-hydroxy)propyl--CD reached a plateau in biodegradation at a percentage of 20%. The incorporation of the antimicrobial agents imazalil and allyl-isothiocyanate into -CD had no negative impact on biodegradation, which makes these antimicrobial agents/CD complexes suitable for incorporation into biodegradable active packaging.