Ambient Aerosol and its Carbon Content in Gainesville, a Mid-Scale City in Florida

Ambient aerosols were collected during 2000–2001 in Gainesville, Florida, using a micro-orifice uniform deposit impactor (MOUDI) to study mass size distribution and carbon composition. A bimodal mass distribution was found in every sample with major peaks for aerosols ranging from 0.32 to 0.56 μm, and 3.2 to 5.6 μm in diameter. The two distributions represent the fine mode (<2.5 μm) and the coarse mode (>2.5 μm) of particle size. Averaged over all sites and seasons, coarse particles consisted of 15% carbon while fine particles consisted of 22% carbon. Considerable variation was noted between winter and summer seasons. Smoke from fireplaces in winter appeared to be an important factor for the carbon, especially the elemental carbon contribution. In summer, organic carbon was more abundant. The maximum secondary organic carbon was also found in this season (7.0 μg m⁻³), and the concentration is between those observed in urban areas (15–20 μg m⁻³) and in rural areas (4–5 μg m⁻³). However, unlike in large cities where photochemical activity of anthropogenic emissions are determinants of carbon composition, biogenic sources were likely the key factor in Gainesville. Other critical factors that affect the distribution, shape and concentration were precipitation, brushfire and wind.     

Results of An Indoor Size Fractionated PM School Sampling Program in Libby, Montana

Libby, Montana is the only PM_2.5 nonattainment area in the western United States with the exceptions of parts of southern California. During January through March 2005, a particulate matter (PM) sampling program was conducted within Libby’s elementary and middle schools to establish baseline indoor PM concentrations before a wood stove change-out program is implemented over the next several years. As part of this program, indoor concentrations of PM mass, organic carbon (OC), and elemental carbon (EC) in five different size fractions (>2.5, 1.0–2.5, 0.5–1.0, 0.25–0.5, and <0.25 μm) were measured. Total measured PM mass concentrations were much higher inside the elementary school, with particle size fraction (>2.5, 0.5–1.0, 0.25–0.5, and <0.25 μm) concentrations between 2 and 5 times higher when compared to the middle school. The 1.0–2.5 μm fraction had the largest difference between the two sites, with elementary school concentrations nearly 10 times higher than the middle school values. The carbon component for the schools’ indoor PM was found to be predominantly composed of OC. Measured total OC and EC concentrations, as well as concentrations within individual size fractions, were an average of two to five times higher at the elementary school when compared to the middle school. For the ultrafine fraction (<0.25), EC concentrations were similar between each of the schools. Despite the differences in concentrations between the schools at the various fraction levels, the OC/EC ratio was determined to be similar.     

Influence of natural dissolved organic carbon on the bioavailability of mercury to a freshwater alga

Bioavailability of mercury (Hg) to Selenastrum capricornutum was assessed in bioassays containing field-collected freshwater of varying dissolved organic carbon (DOC) concentrations. Bioconcentration factor (BCF) was measured using stable isotopes of methylmercury (MeHg) and inorganic Hg(II). BCFs for MeHg in low-DOC lake water were significantly larger than those in mixtures of lake water and high-DOC river water. The BCF for MeHg in rainwater (lowest DOC) was the largest of any treatment. Rainwater and lake water also had larger BCFs for Hg(II) than river water. Moreover, in freshwater collected from several US and Canadian field sites, BCFs for Hg(II) and MeHg were low when DOC concentrations were >5mg L(-1). These results suggest high concentrations of DOC inhibit bioavailability, while low concentrations may provide optimal conditions for algal uptake of Hg. However, variability of BCFs at low DOC indicates that DOC composition or other ligands may determine site-specific bioavailability of Hg.     

Sorption of polar and nonpolar aromatic compounds to four surface soils of eastern China

Improved predictions on the fate of organic pollutants in surface environments require a better understanding of the underlying sorption mechanisms that control their uptake by soils. In this study, we monitored sorption of nine aromatic compounds with varying physicochemical properties (hydrophobicity, electron-donor/acceptor ability and polarity), including two polycyclic aromatic hydrocarbons, two chlorobenzenes, two nitroaromatic compounds, dichlobenil, carbaryl and 2,4-dichlorophenol in aqueous suspension of four surface soils of eastern China. The tested soils were characterized with respect to organic carbon (OC) content, black carbon content, mineralogy, morphology and size fraction to assess the role of the diverse soil characteristics in sorption. The results of this study show that not only the solute hydrophobicity and the OC content of soil are important to the retention of organic pollutants, but also the solute molecular structure and the soil nature.     

Relationships between organic matter, black carbon and persistent organic pollutants in European background soils: Implications for sources and environmental fate

Black carbon (BC) and total organic carbon (TOC) contents of UK and Norwegian background soils were determined and their relationships with persistent organic pollutants (HCB, PAHs, PCBs, co-planar PCBs, PBDEs and PCDD/Fs) investigated by correlation and regression analyses, to assess their roles in influencing compound partitioning/retention in soils. The 52 soils used were high in TOC (range 54-460 mg/g (mean 256)), while BC only constituted 0.24-1.8% (0.88%) of the TOC. TOC was strongly correlated (p < 0.001) with HCB, PCBs, co-PCBs and PBDEs, but less so with PCDD/Fs (p < 0.05) and PAHs. TOC explained variability in soil content, as follows: HCB, 80%; PCBs, 44%; co-PCBs, 40%; PBDEs, 27%. BC also gave statistically significant correlations with PBDEs (p < 0.001), co-PCBs (p < 0.01) and PCBs, HCB, PCDD/F (p < 0.05); TOC and BC were correlated with each other (p < 0.01). Inferences are made about possible combustion-derived sources, atmospheric transport and air-surface exchange processes for these compounds.     

川中丘陵区村级景观土壤有机碳密度和储量分析

本文综合运用了地理信息系统(GIS)、遥感(RS)和全球卫星定位系统(GPS)等技术手段,分析了人口密集的川中丘陵乡村区域土壤有机碳密度(SOCD)和储量(SOCS)的空间分布及影响因素。结果表明,区域内SOCD和SOCS平均值分别为5.58kg/m2和75.77×105g,SOCD随丘体高度的降低向四周逐渐增大,SOCS主要分布于旱地、水田等土地利用类型中。0~30cm土层和土体深度内,SOCD以冬水田最高,裸岩最低;SOCS则以丘脚旱地和轮作水田最高,裸岩最低。地形、土地利用和土地覆盖对SOCD、SOCS影响明显。     

活性炭纤维复合材料的脱硫性能

本实验以粘胶基活性炭纤维和酚醛树脂复合,制备出了一种可用于烟气脱硫的活性炭纤维复合材料（ACFM）,考察了制备工艺条件对脱硫性能和比表面积的影响,测试其在填充床的压降。结果表明：粘结剂用量、炭化及活化条件对样品的脱硫性能和比表面积有较大的影响;与其他活性炭材料相比ACFM压降相对较低,只有活性炭纤维的1／20。     

Predicting Water Quality Impaired Stream Segments using Landscape-Scale Data and a Regional Geostatistical Model: A Case Study in Maryland

In the United States, probability-based water quality surveys are typically used to meet the requirements of Section 305(b) of the Clean Water Act. The survey design allows an inference to be generated concerning regional stream condition, but it cannot be used to identify water quality impaired stream segments. Therefore, a rapid and cost-efficient method is needed to locate potentially impaired stream segments throughout large areas. We fit a set of geostatistical models to 312 samples of dissolved organic carbon (DOC) collected in 1996 for the Maryland Biological Stream Survey using coarse-scale watershed characteristics. The models were developed using two distance measures, straight-line distance (SLD) and weighted asymmetric hydrologic distance (WAHD). We used the Corrected Spatial Akaike Information Criterion and the mean square prediction error to compare models. The SLD models predicted more variability in DOC than models based on WAHD for every autocovariance model except the spherical model. The SLD model based on the Mariah autocovariance model showed the best fit (r² = 0.72). DOC demonstrated a positive relationship with the watershed attributes percent water, percent wetlands, and mean minimum temperature, but was negatively correlated to percent felsic rock type. We used universal kriging to generate predictions and prediction variances for 3083 stream segments throughout Maryland. The model predicted that 90.2% of stream kilometers had DOC values less than 5 mg/l, 6.7% were between 5 and 8 mg/l, and 3.1% of streams produced values greater than 8 mg/l. The geostatistical model generated more accurate DOC predictions than previous models, but did not fit the data equally well throughout the state. Consequently, it may be necessary to develop more than one geostatistical model to predict stream DOC throughout Maryland. Our methodology is an improvement over previous methods because additional field sampling is not necessary, inferences about regional stream condition can be made, and it can be used to locate potentially impaired stream segments. Further, the model results can be displayed visually, which allows results to be presented to a wide variety of audiences easily.     

生物活性炭法深度处理印染废水及其生物毒性的表征

采用负载经驯化后微生物的活性炭深度处理实际印染废水,研究生物活性炭系统中存在的生物相及其降解有机污染物的作用,并表征了处理后印染废水的生物毒性.结果表明,生物相中含有草履虫、轮虫及钟虫等原生动物.随着运行次数的增加,活性炭反应器在运行5次后出水的COD、NH3-N及色度去除率骤降,但是生物活性炭处理后出水的COD、NH3-N及色度去除率缓慢下降.生物活性炭能很好地降解印染废水中的苯酚类和稠环芳烃污染物.本研究中生物活性炭反应器对氨氮和COD的去除符合一级动力学方程,去除动力学常数分别为1.02和0.96.经过生物活性炭的处理可以将印染废水的生物毒性降到适于小球藻生长的水平.     

超声前处理强化活性炭吸附活性艳红X-3B染料废水

探究了超声前处理活性艳红X-3B染料废水强化活性炭吸附降解性能及不同超声参数的影响规律,包括超声功率和超声时间。研究结果表明,超声前处理活性艳红X-3B染料废水可通过空化效应使有机大分子裂解为小分子易于被活性炭吸附,同时可强化其到活性炭微孔中传输,提高了活性炭吸附降解性能,最佳超声功率为320 W。浓度越高,所需超声时间越长,当超声达到一定时间后,继续超声不会影响染料分子的吸附。超声前处理虽然不会改变吸附平衡时间,但可有效增加活性炭处理活性艳红X-3B染料废水的饱和吸附量。