Laboratory investigation of flux reduction from dense non-aqueous phase liquid (DNAPL) partial source zone remediation by enhanced dissolution

This study investigated the benefits of partial removal of dense nonaqueous phase liquid (DNAPL) source zones using enhanced dissolution in eight laboratory scale experiments. The benefits were assessed by characterizing the relationship between reductions in DNAPL mass and the corresponding reduction in contaminant mass flux. Four flushing agents were evaluated in eight controlled laboratory experiments to examine the effects of displacement fluid property contrasts and associated override and underride on contaminant flux reduction (R(j)) vs. mass reduction (R(m)) relationships (R(j)(R(m))): 1) 50% ethanol/50% water (less dense than water), 2) 40% ethyl-lactate/60% water (more dense than water), 3) 18% ethanol/26% ethyl-lactate/56% water (neutrally buoyant), and 4) 2% Tween-80 surfactant (also neutrally buoyant). For each DNAPL architecture evaluated, replicate experiments were conducted where source zone dissolution was conducted with a single flushing event to remove most of the DNAPL from the system, and with multiple shorter-duration floods to determine the path of the R(j)(R(m)) relationship. All of the single-flushing experiments exhibited similar R(j)(R(m)) relationships indicating that override and underride effects associated with cosolvents did not significantly affect the remediation performance of the agents. The R(j)(R(m)) relationship of the multiple injection experiments for the cosolvents with a density contrast with water tended to be less desirable in the sense that there was less R(j) for a given R(m). UTCHEM simulations supported the observations from the laboratory experiments and demonstrated the capability of this model to predict R(j)(R(m)) relationships for non-uniformly distributed NAPL sources.     

Comparison of nickel adsorption on biochars produced from mixed softwood and Miscanthus straw

Environmental Science and Pollution Research - In order to understand the influence of feedstock type on biochar adsorption of heavy metals, the adsorption characteristics of nickel (Ni2+), copper...     

Devising indicators of sustainable development for the mining and minerals industry: An analysis of critical background issues

The exact application of sustainable development in the mining and minerals industry has precipitated considerable debate in recent years. Since the publication of the Brundtland Commission's Report, Our Common Future, numerous explanations have been put forth in an attempt to define sustainable development in the mining and minerals context. Specifically, the inability of the Brundtland Report to outline an effective sustainability framework, combined with its contention that no single blueprint for sustainable development exists, has prompted a number of academics and practitioners to provide personal viewpoints on the application of sustainable development in the mining and minerals industry. This paper focuses on one aspect of the mining and minerals-sustainable development debate: the corporate perspective. It first uses the burgeoning body of literature to define sustainable development in the corporate mining context. Second, it addresses, against the background of this interpretation, many of the salient issues associated with developing a series of plausible Sustainable Development Indicators (SDIs) for use in the mining and minerals extraction industry. The paper clearly illustrates the difficulty in both arriving at a suitable working definition of sustainable development for an industry, and developing an acceptable set of universal standards for measuring environmental and socioeconomic performance.     

Turbulent Prandtl number and characteristic length scales in stably stratified flows: steady-state analytical solutions

Environmental Fluid Mechanics - In this study, the stability dependence of turbulent Prandtl number ( $$Pr_t$$ ) is quantified via a novel and simple analytical approach. Based on the variance and...     

Groundwater characterization and potential impacts of agricultural activities in the Sers El Kef plain

Tunisia has very limited potential of surface and groundwater resources which are subject to different quantitative and qualitative forms of degradation. The risk of groundwater pollution results from the interaction between the vulnerability of aquifers to pollution and anthropogenic activities. Our research focuses on the study of the Sers water table water quality (northwest Tunisia) following the inputs used for agricultural activities in the region. Water samples were extracted from 40 wells to analyze the main physicochemical parameter indicators of the groundwater quality. The results obtained show that these waters have two major facies: Na-Cl and Ca-Mg-SO₄. The nitrate contents are relatively high suggesting that the agricultural activities are probably the most important anthropogenic source of water contamination. The results of the Standardized Principal Component Analysis (SPCA) confirm the geochemical methods and results and provide further information about the water quality of the Sers El Kef aquifer. In addition, the pollution degree differs from one site to another depending on the spreading rate of nitrogen fertilizers and the distance from the pollution source.     

Two-dimensional modeling of torrefaction of a large biomass particle

A two-dimensional (2-D) model is developed to predict the torrefaction behavior of a large wet biomass particle. Although one-dimensional (1-D) model is found to be adequate for L/D ≥ 6, the necessity of using 2-D model at lower L/D ratios and higher torrefaction temperature is established. Errors up to 18% are observed in predicted mass fractions between 1-D and 2-D models. The center temperatures differed more, up to 96%, between z = 0 and z = L/2 in 2-D model which is not captured by the 1-D model. The model predictions agree well with the experimental results of the present authors and others. The evolution of the temperature profile is found to govern the mass fraction profile. At higher reactor temperature, three distinct zones are visible in the contour plots: peripheral fully torrefied zone, intermediate torrefying zone, and core with unreacted virgin biomass zone. Simulation studies show the formation of two symmetric annular hot spots at the ends, which move inward axially and subsequently merge at the center, the rate being faster for smaller L/D ratio. However, 1-D model does not provide such insight. The effects of reactor temperature, particle size, the residence time, and the initial moisture content on the torrefaction behavior are investigated.     

Electrochemical oxidation of polyethylene glycol in electroplating solution using paraffin composite copper hexacyanoferrate modified (PCCHM) anode

Electrochemical oxidation of polyethylene glycol (PEG) in an acidic(pH 0.18 to 0.42) and high ionic strength electroplating solution was investigated. The electroplating solution is a major source of wastewater in the printing wiring board industry. A paraffin composite copper hexacyanoferrate modified(PCCHM) electrode was used as the anode and a bare graphite electrode was used as the cathode. The changes in PEG and total organic carbon (TOC) concentrations during the course of the reaction were monitored. The efficiency of the PCCHM anode was compared with bare graphite anode and it was found that the former showed significant electrocatalytic property for PEG and TOC removal. Chlorides present in the solution were found to contribute significantly in the overall organic removal process. Short chain organic compounds like acetic acid, oxalic acid, formic acid and ethylene glycol formed during electrolysis were identified by HPLC method. Anode surface area and applied current density were found to influence the electro-oxidation process, in which the former was found to be dominating. Investigations of the kinetics for the present electrochemical reaction suggested that the two stage first-order kinetic model provides a much better representation of the overall mechanism of the process if compared to the generalized kinetic model.