Mineralogical study and leaching behavior of a stabilized harbor sediment with hydraulic binder

The environmental assessment of potential effects of contaminated harbor sediments stabilized with hydraulic binders and the determination of remediation endpoints require the determination of pollutants leaching potentials. Moreover, little information about the speciation and mobility of inorganic contaminants in these specific solid matrices is available in the literature. The objective of this paper is to investigate the relationship between mineralogy and leachability of contaminants (copper, lead, and zinc) present in a French harbor sediment stabilized with quicklime and Portland cement. Batch equilibrium leaching tests at various pH, chemical analysis of leachates, and mineralogical studies (X-ray diffraction, scanning electron microscopy–energy dispersive spectroscopy, and diffuse reflectance infrared Fourier transform) have been combined in the present investigation. The acid neutralization capacity of the stabilized matrix studied is first controlled by the dissolution of portlandite (pH?~12), followed by the dissolution of C–S–H (pH?~11) and the dissolution of ettringite (pH?~10). Finally, a very high buffering capacity of this stabilized sediment is observed for pH values around 6. This equilibrium is mainly controlled by the dissolution of iron sulfides and carbonate minerals. Consequently, the mobilization of inorganic contaminants as a function of pH remains very low (<0.1 wt%) for pH values above 6 and significantly increases for pH below these values. This research confirms the importance of a combined methodology for the intrinsic characterization of potential mobilization of contaminants in a stabilized sediment and for a better understanding of geochemical processes that affect contaminant fate, transformation, and transport in the subsurface environment.     

A Laboratory Assessment of an Innovative Technology for the Detection of DNAPLs

A promising new technology for the detection of dense nonaqueous phase liquids, or DNAPLs, is cosolvent injection/extraction. Cosolvents, such as alcohols, are injected into the subsurface and interact with DNAPLs to increase their aqueous solubility, which increases recovery of the chemicals. A laboratory assessment was performed to determine if incorporating this technology with cone penetrometers could provide a useful sampling tool for DNAPL detection. A cone penetrometer was modeled in the laboratory by injecting and extracting small quantities of ethanol and propylene glycol at low concentrations into a homogeneous sand reactor contaminated with a residual saturation of tetrachloroethene (PCE). Experimental test results show that this technology is extremely sensitive to the vertical placement of the sampler, but is capable of enhancing PCE solubility while recovering most of the alcohol injected. Field testing of this technology will provide the next step in determining the feasibility of this technology for DNAPL detection.     

Agricultural pesticide residues of farm runoff in the Okanagan Valley,British Columbia,Canada

The objectives of this study were to determine environmental occurrence and concentrations of selected currently-used-pesticides and some transformation products in agricultural farms in the Okanagan Valley (OKV), and to conduct a simple risk assessment of environmental pesticides levels detected in OKV on non-target aquatic organisms. The OKV is the tree fruit country of the Province of British Columbia where considerable amount of pesticides are applied annually. Water, sediment and soil samples were collected at eleven sites in early June and late September following rainfall events and/or extended periods of irrigation from drainage ditches and/or from small streams. Undisturbed reference sites were also sampled. Study results showed that forty of the eighty chemicals analyzed, including organochlorine, nitrogen-containing and organophosphate pesticides commonly used for OKV crops, were detected in runoff and small stream water samples. Among which, endosulfan-sulfate was the most frequently detected chemical. Also, azinophos-methyl (0.699–25.5 ng/L), diazinon (0.088–214 ng/L) exceeded, and α-, β- endosulfan, endosulfan sulphate approached the guidelines for the protection of aquatic life.