Effects of pore volume-transmissivity correlation on transport phenomena

The relevant velocity that describes transport phenomena in a porous medium is the pore velocity. For this reason, one needs not only to describe the variability of transmissivity, which fully determines the Darcy velocity field for given source terms and boundary conditions, but also any variability of the pore volume. We demonstrate that hydraulically equivalent media with exactly the same transmissivity field can produce dramatic differences in the displacement of a solute if they have different pore volume distributions. In particular, we demonstrate that correlation between pore volume and transmissivity leads to a much smoother and more homogeneous solute distribution. This was observed in a laboratory experiment performed in artificial fractures made of two plexiglass plates into which a space-dependent aperture distribution was milled. Using visualization by a light transmission technique, we observe that the solute behaviour is much smoother and more regular after the fractures are filled with glass powder, which plays the role of a homogeneous fault gouge material. This is due to a perfect correlation between pore volume and transmissivity that causes pore velocity to be not directly dependent on the transmissivity, but only indirectly through the hydraulic gradient, which is a much smoother function due to the diffusive behaviour of the flow equation acting as a filter. This smoothing property of the pore volume-transmissivity correlation is also supported by numerical simulations of tracer tests in a dipole flow field. Three different conceptual models are used: an empty fracture, a rough-walled fracture filled with a homogeneous material and a parallel-plate fracture with a heterogeneous fault gouge. All three models are hydraulically equivalent, yet they have a different pore volume distribution. Even if piezometric heads and specific flow rates are exactly the same at any point of the domain, the transport process differs dramatically. These differences make it important to discriminate in situ among different conceptual models in order to simulate correctly the transport phenomena. For this reason, we study the solute breakthrough and recovery curves at the extraction wells. Our numerical case studies show that discrimination on the basis of such data might be impossible except under very favourable conditions, i.e. the integral scale of the transmissivity field has to be known and small compared to the dipole size. If the latter conditions are satisfied, discrimination between the rough-walled fracture filled with a homogeneous material and the other two models becomes possible, whereas the parallel-plate fracture with a heterogeneous fault gouge and the empty fracture still show identifiability problems. The latter may be solved by inspection of aperture and pressure testing.     

化学发光测定示踪剂罗丹明B的新方法

天然河流水质模型的扩散系数通常采用罗丹明Ｂ作示踪剂来测定。囚此，河水中罗丹明Ｂ测定的准确度对水质模型的建立和精度至关重要。本文建立了化学发光分析罗丹明Ｂ的新方法，从而消除了河水浊度的影响。     

Incomplete mixing in a small, urban stream

Conservative solute tracer experiments were conducted in Indian Creek, a small urban stream located in Philadelphia, Pennsylvania, USA. Estimated flow rates were between 46 Ls(-1) and 81 Ls(-1), average stream width was 5.5m and average stream depth was 0.2m. Given these dimensions, most researchers would think it reasonable to assume that the stream is completely mixed vertically and horizontally. However, we found that the stream was not vertically completely mixed in a 1.0m deep, 30 m long pool. The limited mixing was demonstrated by the vertical stratification of a tracer cloud which was completely mixed both laterally and vertically across the stream prior to entering the pool. We suggest that the cause of limited mixing is due to a balance between groundwater inflow and transverse dispersion at the cross-section. We show that the unsupported assumption of complete mixing may result in a wide range, and thus increased uncertainty, of the values of stream flow and longitudinal dispersion coefficient estimated from these data. We conclude that the assumption of complete mixing and one-dimensional modeling must be checked against actual field conditions, even in small streams.     

Calibration and Validation of Far Field Dilution Models for Outfall at Worli, Mumbai

The city of Mumbai, India with a population of 15 million discharges about 2225 MLD of domestic wastewater after partial treatment to adjoining marine water body. Under the Mumbai Sewage Disposal Project Scheme, sewage is being disposed to the west coast at Worli and Bandra through 3.4 kms long submarine outfalls. A field study was conducted at recently commissioned outfall diffuser location at Worli, at the onset of neap flood tide to study the dispersion patterns and measure the far field dilutions using radio and dye tracers. Estimated dilutions using different tracers were compared with outputs from an empirical model (Brooks) and a 2D numerical model (DIVAST). Validation using parameters such as BOD and FC, indicated a good match for BOD in near field compared to FC. The radiotracer ⁸²Br and Rhodamine WT generally gave good correlation with Brooks' and DIVAST models for nearfield, however at further distances predictions were not accurate.     

Perfluorocarbon background concentrations in Europe

Five studies of the background level of several perfluorocarbon compounds in Europe are here presented together with measurements from the European Tracer Experiment (ETEX). The tracers used during the two ETEX tracer releases were the perfluorocarbons (PFCs); perfluoromethylcyclohexane (C₇F₁₄, PMCH) and perfluoromethylcyclopentane (C₆F₁₂, PMCP). Their background concentrations were detected by using both passive and active sampling techniques, to define the spatial and temporal variation of the PFCs over Europe. Also the background variations of four isomers of the PFC compound perfluorodimethylcyclohexane (C₈F₁₆, PDCH) were studied. The results were compared to other PFC tracer studies in the U.S.A. and Europe. The mean and median values of the measured PFCs were found to vary slightly and randomly in space and time. They were found to be higher and to have a larger standard deviation than the measurements from the American studies. The background concentrations were still found to be low and stable enough for PFCs to be highly suitable for use in tracer studies. The following concentrations were found: PMCP; 4.6±0.3 fl ℓ^-1, PMCH: 4.6±0.8 fl ℓ^-1, ocPDCH: 0.96±0.33 fl ℓ^-1, mtPDCH: 9.3±0.8 fl ℓ^-1, mcPDCH: 8.8±0.8 fl ℓ^-1, ptPDCH: 6.1±0.8 fl ℓ^-1. A study of the correlation between the measured PFC compounds showed a significant correlation between most of the compounds, which indicate that there are no major PFC sources in Europe.     

Evaluation of the effect of meteorological data resolution on Lagrangian particle dispersion simulations using the ETEX experiment

This paper presents results from a series of numerical experiments designed to evaluate operational long-range dispersion model simulations, and to investigate the effect of different temporal and spatial resolution of meteorological data from numerical weather prediction models on these simulations. Results of Lagrangian particle dispersion simulations of the first tracer release of the European Tracer Experiment (ETEX) are presented and compared with measured tracer concentrations. The use of analyzed data of higher resolution from the European Center for Medium-Range Weather Forecasts (ECMWF) model produced significantly better agreement between the concentrations predicted with the dispersion model and the ETEX measurements than the use of lower resolution Navy Operational Global Atmospheric Prediction System (NOGAPS) forecast data. Numerical experiments were performed in which the ECMWF model data with lower vertical resolution (4 instead of 7 levels below 500 mb), lower temporal resolution (12 h instead of 6 h intervals), and lower horizontal resolution (2.5° instead of 0.5°) were used. Degrading the horizontal or temporal resolution of the ECMWF data resulted in decreased accuracy of the dispersion simulations. These results indicate that flow features resolved by the numerical weather prediction model data at approximately 45 km horizontal grid spacing and 6 h time intervals, but not resolved at 225 km spacing and 12 h intervals, made an important contribution to the long-range dispersion.     

核素示踪法研究农耕地土壤侵蚀的定量模型及其评价

应用137Cs示踪技术估算农耕地土壤侵蚀量的定量模型主要有两类径流小区上建立的经验关系式及各种理论模型.文章主要对各种主要模型作了简要介绍,并对各种模型的优点、局限性进行了比较和评价;指出今后在模型的建立和应用中注意的问题.     

污染物总量控制中载体水流量的测定

示踪剂法测定河水流量是较为准确的办法 ,利用河流动力模型计算出示踪剂投放点 ,利用示踪剂投放量与测定浓度之间的关系可方便地获得河水流量结果     

直接进样-热脱附-GC-MS快速测定大气细颗粒物中有机示踪物

建立了直接进样-热脱附-GC-MS快速测定细颗粒物中甾烷类和藿烷类有机示踪物的方法。经实验条件优化,13种目标化合物的线性回归方程的相关系数均在0.990以上,空白加标回收率为81.4%~102.3%,实际样品加标回收率为79.1%~112.9%,相对标准偏差小于13.2%。当采样体积为24 m~3时,各目标化合物的检出限为0.008~0.084 ng/m~3,方法灵敏度高。利用该方法测定了北京城区采暖季和非采暖季PM2.5实际样品,结果表明:各目标物均有检出,且采暖季的甾烷类和藿烷类化合物的总量均明显高于非采暖季。该方法无需复杂的前处理和有机溶剂,操作简便快捷,在颗粒物中非极性化合物的快速检测方面具有很大的应用价值。     

Occurrence of monoethylmercury in the Florida Everglades: Identification and verification

A few studies have reported the occurrence of monoethylmercury (CH₃CH₂Hg⁺) in the natural environment, but further verification is needed due to the lack of direct evidence and/or uncertainty in analytical procedures. Various analytical techniques were employed to verify the occurrence of CH₃CH₂Hg⁺ in soil of the Florida Everglades. The identity of CH₃CH₂Hg⁺ in Everglades soil was clarified, for the first time, by GC/MS. The employment of the recently developed aqueous phenylation-purge-and-trap-GC coupled with ICPMS confirmed that the detected CH₃CH₂Hg⁺ was not a misidentification of CH₃SHg⁺. Stable isotope-tracer experiments further indicated that the detected CH₃CH₂Hg⁺ indeed originated from Everglades soil and was not an analytical artifact. All these evidence clearly confirmed the occurrence of CH₃CH₂Hg⁺ in Everglades soil, presumably as a consequence of ethylation occurring in this wetland. The prevalence of CH₃CH₂Hg⁺ in Everglades soil suggests that ethylation could play an important role in the biogeochemical cycling of Hg.