A retrospective comparison of model-based forecasted PM2.5 concentrations with measurements

This study presents an assessment of the performance of the Community Multiscale Air Quality (CMAQ) photochemical model in forecasting daily PM2.5 (particulate matter < or = 2.5 microm in aerodynamic diameter) mass concentrations over most of the eastern United States for a 2-yr period from June 14, 2006 to June 13, 2008. Model predictions were compared with filter-based and continuous measurements of PM2.5 mass and species on a seasonal and regional basis. Results indicate an underprediction of PM2.5 mass in spring and summer, resulting from under-predictions in sulfate and total carbon concentrations. During winter, the model overpredicted mass concentrations, mostly at the urban sites in the northeastern United States because of overpredictions in unspeciated PM2.5 (suggesting possible overestimation of primary emissions) and sulfate. A comparison of observed and predicted diurnal profiles of PM2.5 mass at five sites in the domain showed significant discrepancies. Sulfate diurnal profiles agreed in shape across three sites in the southern portion of the domain but differed at two sites in the northern portion of the domain. Predicted organic carbon (OC) profiles were similar in shape to mass, suggesting that discrepancies in mass profiles probably resulted from the underprediction in OC. The diurnal profiles at a highly urbanized site in New York City suggested that the overpredictions at that site might be resulting from overpredictions during the morning and evening hours, displayed as sharp peaks in predicted profiles. An examination of the predicted planetary boundary layer (PBL) heights also showed possible issues in the modeling of PBL.     

Determination of antibiotics in sewage from hospitals, nursery and slaughter house, wastewater treatment plant and source water in Chongqing region of Three Gorge Reservoir in China

Sewage samples from 4 hospitals, 1 nursery, 1 slaughter house, 1 wastewater treatment plant and 5 source water samples of Chongqing region of Three Gorge Reservoir were analyzed for macrolide, lincosamide, trimethoprim, fluorouinolone, sulfonamide and tetracycline antibiotics by online solid-phase extraction and liquid chromatography-tandem mass spectrometry. Results showed that the concentration of ofloxacin (OFX) in hospital was the highest among all water environments ranged from 1.660 μg/L to 4.240 μg/L and norfloxacin (NOR, 0.136-1.620 μg/L), ciproflaxacin (CIP, ranged from 0.011 μg/L to 0.136 μg/L), trimethoprim (TMP, 0.061-0.174 μg/L) were commonly detected. Removal range of antibiotics in the wastewater treatment plant was 18-100% and the removal ratio of tylosin, oxytetracycline and tetracycline were 100%. Relatively higher removal efficiencies were observed for tylosin (TYL), oxytetracycline (OXY) and tetracycline (TET)(100%), while lower removal efficiencies were observed for Trimethoprim (TMP, 1%), Epi-iso-chlorotetracycline (EICIC, 18%) and Erythromycin-H₂O (ERY-H₂O, 24%). Antibiotics were removed more efficiently in primary treatment compared with those in secondary treatment.     

高锰酸钾预氧化-缺氧/好氧生物铁法处理乙酰嘧啶废水工艺研究

采用高锰酸钾预氧化-缺氧/好氧生物铁法处理维生素B1厂乙酰嘧啶生产段实际废水,实验结果表明该组合工艺对嘧啶生产废水具有良好的处理效果:预氧化将嘧啶废水中大分子难降解乙酰嘧啶几乎全部转化为具有饱和碳氢键的小分子有机物,使乙酰嘧啶去除率达90%以上,且COD去除率在40%以上,BOD5/COD由0.17~0.23提高至0.35~0.44。通过与后续A/O生物铁工艺相结合,使COD、TN和氨氮总去除率分别达到93.3%、81.7%和78.6%,出水pH为6.6~7.5。     

高加速应力试验装置技术参数的测量

气锤驱动的高加速应力试验装置,能产生温度和非高斯随机振动应力,其中振动应力是由多个气锤作六自由度运动产生的。一般用来进行高温步进、低温步进、快速温度变化、振动、快速温变和振动复合试验。目前国家标准和校准规程中均无关于该试验装置的技术参数的校准方法。本文结合试验装置的技术特点,提出了几个关于温度和振动技术参数的测量方法,如:温度偏差、温度波动度、温度均匀度、温度过冲量、温度变化速率、均方根加速度、横向振动比、功率谱密度等。     

张家界溶洞旅游资源价值评价与开发研究

溶洞是重要的旅游资源,开发得当可获得良好经济效益,否则便会造成不可逆的资源破坏。以张家界溶洞资源为研究对象,在对溶洞资源基本情况进行调查的基础上,对溶洞的景观价值进行定量评价,并提出溶洞开发措施,为张家界市溶洞旅游的可持续开发利用提供理论依据。     

德国环境设备责任制度初探

德国《民法典》确定了一般环境侵权的规则——行为责任,再以《环境责任法》确立了特殊的环境侵权的规则——设备责任。设备侵权是危险责任的一种,其构成要件有两个:设备运营对环境产生不良影响进而导致损害;人身、财产受侵害。设备责任的承担不要求设备运营人的过错。设备责任归责采用因果关系推定原则。     

海洋酸化与重金属、有机污染物和人工纳米颗粒的联合毒性效应研究进展

由于大量人类活动的影响,大气CO_2浓度持续增加,其中约1/3被海洋吸收,导致表层海水pH值降低和碳酸盐平衡体系波动,即"海洋酸化"现象。污染物的海洋环境效应一直是全球环境科学领域研究的热点。在实际环境中,海洋酸化往往与污染物共同存在并作用于海洋生态系统,且海洋酸化极有可能改变污染物的海洋环境行为从而影响其毒性效应。但现有研究大多针对海洋酸化或者污染物单独作用下的毒性效应展开,对海洋酸化与污染物的联合毒性效应的研究不足、亟待加强。为此,综述了近年来海洋酸化与典型污染物(重金属、有机污染物)及新型污染物(人工纳米颗粒)的相关文献,重点阐述了海洋酸化对污染物环境行为的影响和海洋酸化与污染物对海洋生物的联合毒性效应,指出当前的研究不足,并对未来的研究方向进行了展望。     

Impacts of emissions and meteorological changes on China’s ozone pollution in the warm seasons of 2013 and 2017

O₃ increment is mainly caused by changes in meteorology rather than emissions. Emission reduction is effective to reduce O₃ nationwide, especially in summer. Strengthened NO_x controls are necessary to meet the ambient O₃ standard. We have quantified the impacts of anthropogenic emissions reductions caused by the Air Pollution Control Action Plan and changes in meteorological fields between 2013 and 2017 on the warm-season O₃ concentration in China using a regional 3D chemical transport model. We found that the impact on daily maximum eight-hour (MDA8) O₃ concentration by the meteorological variation that mostly increased O₃ was greater than that from emission reduction, which decreased O₃. Specifically, the control measures implemented since 2013 in China have reduced SO₂, NO_x, PM_2.5, and VOC emissions by 33%, 25%, 30%, and 4% in 2017, while NH₃ emissions have increased by 7%. The changes in anthropogenic emissions lowered MDA8 O₃ by 0.4–3.7 ppb (0.8%–7.6%, varying by region and month), although MDA8 O₃ was increased slightly in some urban areas (i.e. North China) at the beginning/end of warm seasons. Relative to 2013, the average 2 m temperature in 2017 shows increments in North, North-east, East, and South China (0.34℃–0.83℃) and decreases in Central China (0.24℃). The average solar radiation shows increments in North, North-east, and South China (7.0–9.7 w/m²) and decreases in Central, South-west, and North-west China (4.7–10.3 w/m²). The meteorological differences significantly change MDA8 O₃ by -3.5–8.5 ppb (-8.2%–18.8%) with large temporal variations. The average MDA8 O₃ was slightly increased in North, North-east, East, and South China. The response surface model suggests that the O₃ formation regime transfers from NO_x-saturated in April to NO_x-limited in July on average in China.     

Enhanced activation of peroxymonosulfate by CNT-TiO2 under UV-light assistance for efficient degradation of organic pollutants

CNT-TiO₂ composite is used to activate PMS under UV-light assistance. Superior performance is due to the enhanced electron-transfer ability of CNT. SO₄•⁻, •OH and ¹O₂ play key roles in the degradation of organic pollutants. In this work, a UV-light assisted peroxymonosulfate (PMS) activation system was constructed with the composite catalyst of multi-walled carbon nanotubes (CNT) - titanium dioxide (TiO₂). Under the UV light irradiation, the photoinduced electrons generated from TiO₂ could be continuously transferred to CNT for the activation of PMS to improve the catalytic performance of organic pollutant degradation. Meanwhile, the separation of photoinduced electron-hole pairs could enhance the photocatalysis efficiency. The electron spin resonance spectroscopy (EPR) and quenching experiments confirmed the generation of sulfate radical (SO₄•⁻), hydroxyl radical (•OH) and singlet oxygen (¹O₂) in the UV/PMS/20%CNT-TiO₂ system. Almost 100% phenol degradation was observed within 20 min UV-light irradiation. The kinetic reaction rate constant of the UV/PMS/20%CNT-TiO₂ system (0.18 min⁻¹) was 23.7 times higher than that of the PMS/Co₃O₄ system (0.0076 min⁻¹). This higher catalytic performance was ascribed to the introduction of photoinduced electrons, which could enhance the activation of PMS by the transfer of electrons in the UV/PMS/CNT-TiO₂ system.