Validation of temporal and spatial consistency of facility- and speed-specific vehicle-specific power distributions for emission estimation: A case study in Beijing,China

Vehicle-specific power (VSP) has been found to be highly correlated with vehicle emissions. It is used in many studies on emission modeling such as the MOVES (Motor Vehicle Emissions Simulator) model. The existing studies develop specific VSP distributions (or OpMode distribution in MOVES) for different road types and various average speeds to represent the vehicle operating modes on road. However, it is still not clear if the facility- and speed-specific VSP distributions are consistent temporally and spatially. For instance, is it necessary to update periodically the database of the VSP distributions in the emission model? Are the VSP distributions developed in the city central business district (CBD) area applicable to its suburb area? In this context, this study examined the temporal and spatial consistency of the facility- and speed-specific VSP distributions in Beijing. The VSP distributions in different years and in different areas are developed, based on real-world vehicle activity data. The root mean square error (RMSE) is employed to quantify the difference between the VSP distributions. The maximum differences of the VSP distributions between different years and between different areas are approximately 20% of that between different road types. The analysis of the carbon dioxide (CO₂) emission factor indicates that the temporal and spatial differences of the VSP distributions have no significant impact on vehicle emission estimation, with relative error of less than 3%.

Implications: The temporal and spatial differences have no significant impact on the development of the facility- and speed-specific VSP distributions for the vehicle emission estimation. The database of the specific VSP distributions in the VSP-based emission models can maintain in terms of time. Thus, it is unnecessary to update the database regularly, and it is reliable to use the history vehicle activity data to forecast the emissions in the future. In one city, the areas with less data can still develop accurate VSP distributions based on better data from other areas.     

GIS罐体内部异物清理机器人的研发与应用

针对气体绝缘金属封闭开关设备( gas insulated switchgear, GIS)内部异物颗粒引起设备内部电场畸变,从而造成设备闪络故障问题,通过对异物颗粒的产生原因及影响因素进行分析,研制了一种GIS罐体内部异物颗粒清理机器人,实现了GIS设备内部可视化异物清理功能。应用结果表明:机器人检测不仅提高了750kV GIS内部缺陷检查的效率,而且保证了检测人员的安全,为GIS状态检修提供了有效技术支持。     

厌氧折流板反应器处理石化剩余污泥

研究了厌氧折流板反应器(ABR)在厌氧消化处理石化剩余污泥启动过程中的性能及相关参数。实验结果表明:污泥挥发性固体含量的去除率达43.7%;反应器内pH维持在6.4~7.4;从启动到稳定运行,第一隔室最大比产甲烷活性变化不大,在0.14 L/(g·d)以下,第二、第三、第四隔室的最大比产甲烷活性在0.29 L/(g·d)以上,污泥在反应器内部实现了分级分相处理。     

南京大气细粒子中重金属污染特征及来源解析

利用2011年1月、4月、7月和10月在南京市区和北郊采集的气溶胶样品,研究了南京大气细粒子中zn、Ph、Hg、As和cd5种重金属的污染水平,通过元素相关性分析和因子分析方法,对细粒子中这些重金属的污染来源进行了初步解析。结果表明,南京大气细粒子及其重金属污染严重,北郊普遍比市区严重;As严重超标,cd在南京北郊超标约5倍,zn在市区与北郊的质量浓度均高于其他重金属元素。每种重金属的浓度均随季节而变化。市区细粒子中,As和zn可能主要与燃煤、轮胎灰尘和建筑扬尘等有关,Pb、Hg和cd主要来自交通尘、城市垃圾焚烧等。北郊细粒子中,As、Hg和zn主要来源于燃煤、钢铁冶炼等工业,Pb和cd主要与农作物秸秆燃烧、汽车尾气、道路扬尘等影响有关。     

混凝-超滤短流程工艺处理北方水库原水简

采用混凝-超滤膜短流程工艺对大伙房水库原水进行处理,考察其除污染性能和膜污染情况,并对该短流程工艺参数进行优化。结果表明,当利用超滤膜直接过滤原水时,膜污染较重,并且对污染物质的去除率较低;而采用混凝-超滤短流程工艺时,膜污染得到一定程度上的缓解;当絮凝剂投加量为7 mg/L、膜清洗周期为30 min时,对浊度、COD_Mn和UV₂₅₄的去除率分别为95.61%、40.42%和37.12%,出水水质能够满足生活饮用水卫生标准。     

Comprehensive Environmental Investigation at Former Industrial/Petroleum Underground Storage Tank Sites in Long Beach,CA: A Forensic Perspective

Two industrial sites were investigated based on years of available hydrogeologic information and monitoring data for soil and groundwater. Collected data were forensically evaluated using age-dating and fingerprinting methods. The previous business uses of the project sites were as a gas station, laundry/dry-cleaning service, and car wash with petroleum underground storage tanks (USTs). As a result, these sites were exposed to a number of toxic contaminants at relatively high concentrations. Source control was necessary for successful remediation and the ultimate removal of the remaining compounds from these industrial sites. Although contaminated soil around the source was excavated during the remedial action and the high concentrations of contaminants were reduced, typical groundwater contaminants such as petroleum hydrocarbons as gasoline (TPH-G), benzene, toluene, ethylbenzene, xylenes (BTEX), and oxygenates including methyl tert-butyl ether (MTBE), diisopropyl ether (DIPE), ethyl tert-butyl ether (ETBE), tert-amyl methyl ether (TAME), and tert-butyl alcohol (TBA) were persistently found at the studied sites around the source points. The plume and concentration of contaminants had changed their shapes and strength for all monitoring periods. Thus, additional source control seems to be a requirement for the complete removal of source contamination, which must be ascertained with groundwater and soil monitoring on a regular time base. For the study sites, monitored natural attenuation was relatively feasible for the long-term plan; however, it did not offer a perfect remediation solution for an ultimate goal because of residual toxic compounds that might have affected the surrounding residential areas at higher concentrations than their health limits. Therefore, as a remediation strategy, the combination of clean-up technology and natural attenuation with monitoring activities are more highly recommended than either clean-up or natural attenuation used separately.     

阳宗海沉积物中磷的稳定性

絮凝剂(Fe Cl3)治理阳宗海砷污染的过程中,水体中的磷被大量沉积进入底泥,弄清其是否会在环境条件变化后发生反溶形成二次污染对湖泊富营养化防治具有重要意义。通过模拟实验模拟泥-水界面p H变化、物理扰动和微生物活动的变化,旨在分析这些环境因子变化对沉积物中磷溶出的影响。结果表明,阳宗海水体在目前这种磷浓度下,底泥的磷会随时间的增加而溶出再次造成水体磷污染,当暴露在清洁水条件下时磷的释放率会增加;这种由于絮凝剂吸附沉淀到湖底的磷,在上覆水p H增加0.5时底泥磷解吸附释放速率增加;每年秋季湖泊上下层水的交换活动会造成水体磷浓度的季节性升高,形成不可忽视的磷内源。而夏季水温分层导致湖泊底部厌氧,使厌氧微生物活性增强,这将进一步促进底泥中磷的释放。     

Photocatalytic degradation of acetaminophen in modified TiO2 under visible irradiation

This study investigated the photocatalytic degradation of acetaminophen (ACT) in synthetic titanium dioxide (TiO₂) solution under a visible light (λ >440 nm). The TiO₂ photocatalyst used in this study was synthesized via sol–gel method and doped with potassium aluminum sulfate (KAl(SO₄)₂) and sodium aluminate (NaAlO₂). The influence of some parameters on the degradation of acetaminophen was examined, such as initial pH, photocatalyst dosage, and initial ACT concentration. The optimal operational conditions were also determined. Results showed that synthetic TiO₂ catalysts presented mainly as anatase phase and no rutile phase was observed. The results of photocatalytic degradation showed that LED alone degraded negligible amount of ACT but with the presence of TiO₂/KAl(SO₄)₂, 95 % removal of 0.10-mM acetaminophen in 540-min irradiation time was achieved. The synthetic TiO₂/KAl(SO₄)₂ presented better photocatalytic degradation of acetaminophen than commercially available Degussa P-25. The weak crystallinity of synthesized TiO₂/NaAlO₂ photocatalyst showed low photocatalytic degradation than TiO₂/KAl(SO₄)₂. The optimal operational conditions were obtained in pH 6.9 with a dose of 1.0 g/L TiO₂/KAl(SO₄)₂ at 30 °C. Kinetic study illustrated that photocatalytic degradation of acetaminophen fits well in the pseudo-first order model. Competitive reactions from intermediates affected the degradation rate of ACT, and were more obvious as the initial ACT concentration increased.     

Effect of temperature and particle size on the thermal desorption of PCBs from contaminated soil

Thermal desorption is widely used for remediation of soil contaminated with volatiles, such as solvents and distillates. In this study, a soil contaminated with semivolatile polychlorinated biphenyls (PCBs) was sampled at an interim storage point for waste PCB transformers and heated to temperatures from 300 to 600 °C in a flow of nitrogen to investigate the effect of temperature and particle size on thermal desorption. Two size fractions were tested: coarse soil of 420–841 μm and fine soil with particles <250 μm. A PCB removal efficiency of 98.0 % was attained after 1 h of thermal treatment at 600 °C. The residual amount of PCBs in this soil decreased with rising thermal treatment temperature while the amount transferred to the gas phase increased up to 550 °C; at 600 °C, destruction of PCBs became more obvious. At low temperature, the thermally treated soil still had a similar PCB homologue distribution as raw soil, indicating thermal desorption as a main mechanism in removal. Dechlorination and decomposition increasingly occurred at high temperature, since shifts in average chlorination level were observed, from 3.34 in the raw soil to 2.75 in soil treated at 600 °C. Fine soil particles showed higher removal efficiency and destruction efficiency than coarse particles, suggesting that desorption from coarse particles is influenced by mass transfer.     

Probing the distribution and contamination levels of 10 trace metal/metalloids in soils near a Pb/Zn smelter in Middle China

The horizontal and vertical distribution patterns and contamination status of ten trace metal/metalloids (Ag, Bi, Co, Cr, Ge, In, Ni, Sb, Sn, Tl) in soils around one of the largest Chinese Pb–Zn smelter in Zhuzhou City, Central China, were revealed. Different soil samples were collected from 11 areas, including ten agricultural areas and one city park area, with a total of 83 surface soil samples and six soil cores obtained. Trace metal/metalloids were determined by inductively coupled plasma–mass spectrometry after digestion by an acid mixture of HF and HNO₃. The results showed that Ag, Bi, In, Sb, Sn, and Tl contents decreased both with the distance to the Pb–Zn smelter as well as the soil depth, hinting that these elements were mainly originated from the Pb–Zn smelting operations and were introduced into soils through atmospheric deposition. Soil Ge was influenced by the smelter at a less extent, while the distributions of Co, Cr, and Ni were roughly even among most sampling sites and soil depths, suggesting that they were primarily derived from natural sources. The contamination status, as revealed by the geo-accumulation index (I _geo), indicated that In and Ag were the most enriched elements, followed by Sb, Bi, and Sn. In general, Cr, Tl, Co, Ni, and Ge were of an uncontaminated status.