Loss of volatile hydrocarbons from an LNAPL oil source

The light nonaqueous phase liquid (LNAPL) oil pool in an aquifer that resulted from a pipeline spill near Bemidji, Minnesota, was analyzed for volatile hydrocarbons (VHCs) to determine if the composition of the oil remains constant over time. Oil samples were obtained from wells at five locations in the oil pool in an anaerobic part of the glacial outwash aquifer. Samples covering a 21-year period were analyzed for 25 VHCs. Compared to the composition of oil from the pipeline source, VHCs identified in oil from wells sampled in 2008 were 13 to 64% depleted. The magnitude of loss for the VHCs analyzed was toluene?o-xylene, benzene, C(6) and C(10-12)n-alkanes>C(7)-C(9)n-alkanes>m-xylene, cyclohexane, and 1- and 2-methylnaphthalene>1,2,4-trimethylbenzene and ethylbenzene. Other VHCs including p-xylene, 1,3,5- and 1,2,3-trimethylbenzenes, the tetramethylbenzenes, methyl- and ethyl-cyclohexane, and naphthalene were not depleted during the time of the study. Water-oil and air-water batch equilibration simulations indicate that volatilization and biodegradation is most important for the C(6)-C(9)n-alkanes and cyclohexanes; dissolution and biodegradation is important for most of the other hydrocarbons. Depletion of the hydrocarbons in the oil pool is controlled by: the lack of oxygen and nutrients, differing rates of recharge, and the spatial distribution of oil in the aquifer. The mass loss of these VHCs in the 5 wells is between 1.6 and 7.4% in 29years or an average annual loss of 0.06-0.26%/year. The present study shows that the composition of LNAPL changes over time and that these changes are spatially variable. This highlights the importance of characterizing the temporal and spatial variabilities of the source term in solute-transport models.     

Methane oxidation in a crude oil contaminated aquifer: Delineation of aerobic reactions at the plume fringes

High resolution direct-push profiling over short vertical distances was used to investigate CH(4) attenuation in a petroleum contaminated aquifer near Bemidji, Minnesota. The contaminant plume was delineated using dissolved gases, redox sensitive components, major ions, carbon isotope ratios in CH(4) and CO(2), and the presence of methanotrophic bacteria. Sharp redox gradients were observed near the water table. Shifts in δ(13)C(CH4) from an average of -57.6‰ (±1.7‰) in the methanogenic zone to -39.6‰ (±8.7‰) at 105m downgradient, strongly suggest CH(4) attenuation through microbially mediated degradation. In the downgradient zone the aerobic/anaerobic transition is up to 0.5m below the water table suggesting that transport of O(2) across the water table is leading to aerobic degradation of CH(4) at this interface. Dissolved N(2) concentrations that exceeded those expected for water in equilibrium with the atmosphere indicated bubble entrapment followed by preferential stripping of O(2) through aerobic degradation of CH(4) or other hydrocarbons. Multivariate and cluster analysis were used to distinguish between areas of significant bubble entrapment and areas where other processes such as the infiltration of O(2) rich recharge water were important O(2) transport mechanisms.     

高声能密度超声波破碎污泥细胞效能的研究

采用超声波在较高声能密度下处理SBR的剩余污泥,主要考察了含固率、声能密度和作用时间对污泥细胞破碎效果的影响。结果表明,在声能密度0.5～3 W/mL内,含固率1%～1.5%的剩余污泥经超声波作用后,上清液SCOD随作用时间呈线性升高;在声能密度1～3 W/mL内,含固率0.25%～0.5%的剩余污泥经超声波作用后,上清液SCOD随作用时间呈平缓缓慢升高。高声能密度超声波更适合对较高含固率污泥的细胞破碎;此情况下,上清液SCOD增幅、NH4＋-N、TN及TP升幅均与声能密度正相关。经超声波作用6 min后,污泥形态结构已破坏。     

Influence of aeration on CH4, N2O and NH3 emissions during aerobic composting of a chicken manure and high C/N waste mixture

Co-composting of chicken manure, straw and dry grasses was investigated in a forced aeration system to estimate the effect of aeration rates on NH₃, CH₄ and N₂O emissions and compost quality. Continuous measurements of gas emissions were carried out and detailed gas emission patterns were obtained using an intermittent-aeration of 30 min on/30 min off at rates of 0.01 (A1), 0.1 (A2) and 0.2 (A3) m³ min⁻¹ m⁻³. Concentrations of CH₄ and N₂O at the low aeration rate (A1) were significantly greater than those at the other two rates, but there was no significant difference between the A2 and A3 treatments. CH₄ and N₂O emissions for this mixture could be controlled when the composting process was aerobic and ammonia emissions were reduced at a lower aeration rate. Comparison of CH₄, N₂O, NH₃ emissions and compost quality showed that the aeration rate of the A2 treatment was superior to the other two aeration rates.     

停止退税对废钢铁市场的影响

论述了我国现行"再生资源增值税政策"的法规主体及其演变过程;分析了现行税收政策的施法效果及良好预期,以及停止退税对废钢铁市场的正面和负面影响;对2011年我国废钢铁供需市场进行预测,并提出政策层面的立法建议.     

国内废钢铁市场触底上扬动态浅析

2010年7月中旬至8月中旬,中国废钢铁市场连续五周持续上扬。进口矿石的上扬、国际废钢市场的全面涨价、国际钢材市场的普遍回升及我国钢铁工业低利润格局的变化等,都是支撑我国废钢铁市场回升的内在动力。     

过氧化氢及次氯酸钠的同步电合成及其原位氨氮去除效果

利用电解法在离子隔膜电解槽反应器的阴阳极室以较高的电流效率分别合成了过氧化氢和次氯酸钠。对原位合成的次氯酸钠等含氯氧化剂的氨氮去除效果进行了考察,在初始ρ(NH_4~+-N)为1 000 mg/L和电极间距为5 mm的条件下,阴极合成过氧化氢的电流效率和TN去除率均高达100%。     

Remediation of DDT‐contaminated soil using optimized mixtures of surfactants and a mixing system

Soil contaminated with persistent pesticides, such as DDT, poses a serious risk to humans and to wildlife. A surfactant‐aided soil‐washing technique was studied as an alternative method for remediation of DDT‐contaminated soil. An ex situ soil washing method was investigated using nonionic and anionic surfactants due to the clayey structure of the contaminated soil. A mixture of 1 percent nonionic surfactant (Brij 35) and 1 percent anionic surfactant (SDBS) removed more than 50 percent of DDT from soil in a flow‐through system, whereas individual surfactants or other combinations of the surfactants had a lower removal efficiency. The soil‐washing technique was improved using a mixing system. The mixture of surfactants was optimized in the mixing system, and the combination of 2 percent Brij 35 and 0.1 percent SDBS was found to be optimum, removing 70 to 80 percent of DDT. Prewashing of the soil with tap water decreased the adsorption of surfactants to soil particles by 30 to 40 percent, and postwashing recovered 90 percent of the surfactants. © 2010 Wiley Periodicals, Inc.     

浅析含油污泥处理中石油烃控制指标

石油烃含量是含油污泥处理中必不可少的重要控制指标。文章分析了含油污泥中石油烃组成及主要污染控制要求,介绍了国内外含油污泥处置对石油烃含量的控制现状;依据危险废物鉴别标准的相关规定,以及对原油中芳香族化合物及其多环芳烃含量的研究成果,对采用石油烃指标进行危险废物鉴别做了推论计算。结果认为:含油污泥等固体废物及其处理残余物的石油烃含量≤0.25%,不属于危险废物;石油烃含量介于0.25%～1.7%时,其是否属于危险废物,最终需要进行危险废物鉴别而确定;石油烃含量1.7%,则属于危险废物。     

Seasonal variations of nitrogen and phosphorus retention in an agricultural drainage river in East China

Background, aim, and scope  

Riverine retention decreases loads of nitrogen (N) and phosphorus (P) in running water. It is an important process in nutrient cycling in watersheds. However, temporal riverine nutrient retention capacity varies due to changes in hydrological, ecological, and nutrient inputs into the watershed. Quantitative information of seasonal riverine N and P retention is critical for developing strategies to combat diffuse source pollution and eutrophication in riverine and coastal systems. This study examined seasonal variation of riverine total N (TN) and total P (TP) retention in the ChangLe River, an agricultural drainage river in east China.