Geology topics

Sheng-Fu J. Chou

Publications and source records attributed to Sheng-Fu J. Chou.

6 recordsLinked to original sources

USGS2010

Chemical fate and transport of atrazine in soil gravel materials at agrichemical distribution facilities

The gravel commonly used to cover parking lots and roadways at retail agrichemical facilities may contain relatively large concentrations of pesticides that resulted from past management problems. These pesticides may threaten groundwater quality. Previous studies, however, suggested that the pesticides had not moved from the gravel in several sample profiles. Excavations at a closed facility revealed tremendous variability in pesticide distribution within the site. Pesticides were present below the gravel in two profiles, but the mechanism(s) for their movement were not clear. The objectives of this study were to investigate how the physical and chemical properties of the gravel influence the environmental fate of atrazine. All of the gravel samples collected and characterized contained atrazine and sufficient organic C to adsorb significant amounts of atrazine, thus retarding its movement through the gravel. Laboratory column leaching experiments, however, suggested that much of the atrazine should leach from the gravel within a year or two. A field-scale test plot was constructed to study how atrazine moves through the gravel under controlled conditions. Atrazine was “spilled” in the test plot. Atrazine moved from the gravel both vertically and horizontally. It appears that formulated product spilled on gravel will leach. A single discrete spill can give rise to phantom spills whose occurrence and distribution is not related to any specific pesticide-management practice. The apparent lack of atrazine leaching from gravel appeared to be a transient phenomenon and/or the result of sampling limitations in previous studies. The contaminated gravel clearly poses a risk to groundwater quality.

Soil and Sediment Contamination↗

USGS2009

Producing fired bricks using coal slag from a gasification plant in indiana

Integrated gasification combined cycle (IGCC) is a promising power generation technology which increases the efficiency of coal-to-power conversion and enhances carbon dioxide concentration in exhaust emissions for better greenhouse gas capture. Two major byproducts from IGCC plants are bottom slag and sulfur. The sulfur can be processed into commercially viable products, but high value applications need to be developed for the slag material in order to improve economics of the process. The purpose of this study was to evaluate the technical feasibility of incorporating coal slag generated by the Wabash River IGCC plant in Indiana as a raw material for the production of fired bricks. Full-size bricks containing up to 20 wt% of the coal slag were successfully produced at a bench-scale facility. These bricks have color and texture similar to those of regular fired bricks and their water absorption properties met the ASTM specifications for a severe weathering grade. Other engineering properties tests, including compressive strength tests, are in progress.

Conference Paper↗

USGS2005

Producing ammonium sulfate from flue gas desulfurization by-products

Emission control technologies using flue gas desulfurization (FGD) have been widely adopted by utilities burning high-sulfur fuels. However, these technologies require additional equipment, greater operating expenses, and increased costs for landfill disposal of the solid by-products produced. The financial burdens would be reduced if successful high-volume commercial applications of the FGD solid by-products were developed. In this study, the technical feasibility of producing ammonium sulfate from FGD residues by allowing it to react with ammonium carbonate in an aqueous solution was preliminarily assessed. Reaction temperatures of 60, 70, and 80??C and residence times of 4 and 6 hours were tested to determine the optimal conversion condition and final product evaluations. High yields (up to 83%) of ammonium sulfate with up to 99% purity were achieved under relatively mild conditions. The optimal conversion condition was observed at 60??C and a 4-hour residence time. The results of this study indicate the technical feasibility of producing ammonium sulfate fertilizer from an FGD by-product. Copyright ?? Taylor & Francis Inc.

Energy Sources↗

USGS2001

Pesticide storage and release in unsaturated soil in Illinois, USA

The chemical fate and movement of pesticides may be subject to transient storage in unsaturated soils during periods of light rainfall, and subsequent release into shallow groundwater by increased rainfall. The objective of this study was to conduct field-scale experiments to determine the relative importance of transient storage and subsequent release of agrichemicals from the vadose zone into potential aquifers. Two field-scale experiments were conducted under a rain exclusion shelter. In the 1 x experiment, atrazine and chlorpyrifos were applied at application-rate equivalents (1.6 kg ha-1 and 1.3 kg ha-1, respectively). In the 4x experiment, atrazine was applied in an amount that was four times greater than that usually applied to fields (6.7 kg ha-1). Water was either applied to simulate rain or withheld to simulate dry periods. In the 1 x experiment, atrazine was detected in the water samples whereas chlorpyrifos was not detected in the majority of the samples. The dry period imposed on the treatment plot did not appear to result in storage of the chemicals, whereas the wet period resulted in greater leaching of atrazine, although the concentrations remained less than the Maximum Contaminant Level of 3 ?? L-1. Both chemicals were detected in soil samples collected from a 20- to 30-cm depth, but it appeared that both chemicals dissipated before the field experiment was concluded. It appeared that the one-time application of atrazine and chlorpyrifos at the label rates did not result in a sufficient mass to be stored and flushed in significant concentrations to the saturated zone. When atrazine was applied at 4x and a longer drought period was imposed on the treatment plot, the resulting concentrations of dissolved atrazine were still less than 3 ??g L-1. Atrazine was detected in only the near-surface (0 to 15 cm) soil samples and the herbicide dissipated before the onset of the dry period in the treatment plot. The results of this field study demonstrated that atrazine and chlorpyrifos were not sufficiently persistent to be stored and then released in significantly large concentrations to the saturated zone. The dissipation half-life of atrazine in the 4x application was about 44 days. This study, in addition to others, suggested that atrazine may be less persistent in surface soil than has been generally reported.

Journal of Environmental Science and Health - Part↗

USGS1995

Off-site movement of pesticide-contaminated fill from agrichemical facilities during the 1993 flooding in Illinois

Twenty retail agrichemical facilities were flooded. There was a concern that pesticide-contaminated road fill at these facilities had been transported into residential areas by the flooding. Forty fill and flood-related sediment samples were collected at six facilities. No significant accumulation of sediments was present at any of the six facilities. At five of the six facilities, it did not appear that road fill had been transported off-site. Pesticides were detected in sediment samples collected off-site adjacent to five of the facilities. Of the 21 samples collected off-site, atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazide) and metolachlor (2-chloro-6′-ethyl- N -(2-methoxy-1-methylethyl)acet- o -toluidine) were detected in 86 and 81% of the samples, respectively. When compared with on-site concentrations, off-site pesticide concentrations were either at similar levels, or were as much as three orders of magnitude less. The interpretation of the pesticide data was difficult and often inconclusive, because there were no background data on the occurrence and distribution of pesticides at each site before flooding.

Journal of Environmental Quality↗

USGS1987

Products of hexachlorocyclopentadiene (C-56) in aqueous solution

The photodegradation and degradation products of hexachlorocyclopentadiene (C-56) in aqueous solutions were studied in the laboratory. In each case, the half-life of C-56 was less than 4 min when exposed to sunlight. At least eight degradation products were positively or tentatively identified: 2,3,4,4,5-Pentachloro-2-cyclopentenone, hexachloro-2-cyclopentenone and hexachloro-3-cyclopentenone were the primary photodegradation products, and pentachloro- cis -2,4-pentadienoic acid, Z- and E-pentachlorobutadiene and tetrachlorobutyne were the secondary degradation products. Dissociation of the primary photolysis products may proceed through corresponding pentadienoic acids to form smaller molecular weight compounds such as pentachlorobutadiene isomers and tetrachlorobutyne. In addition, dimerization of 2,3,4,4,5-pentachloro-2-cyclopentenone to form higher molecular weight compounds such as hexachloroindenone may present a minor route of degradation. The results also indicate that C-56 is highly photoreactive and suggest a possible pathway for the compound's transformation in the environment when exposed to sunlight.

Environmental Toxicology and Chemistry↗