Annual Meeting Preliminary Program - Full Brochure (PDF) - SME
Annual Meeting Preliminary Program - Full Brochure (PDF) - SME
Annual Meeting Preliminary Program - Full Brochure (PDF) - SME
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TECHNICAL PROGRAM<br />
3:25 PM<br />
Microbial Ecology of Iron Cycling in Mined Environments<br />
L. Kirk, L. Bozeman and M. Kozubal; Enviromin, Inc.,<br />
Bozeman, MT<br />
Biogeochemical cycling of iron is critically important to effective management of<br />
acid rock drainage, trace element attenuation, and carbon cycling in mined environments,<br />
but its control requires better understanding of microbial community<br />
structure and metabolism. A data mining approach has been employed to compile<br />
and characterize the geomicrobiology of iron cycling in mining environments<br />
worldwide where geochemistry, microbial populations and metabolic data<br />
have been published. Results show important differences in microbial ecology depending<br />
on mineralogy, aqueous chemistry, pH, and temperature, and suggest<br />
that conceptual geochemical models of iron cycling can be significantly expanded<br />
through inclusion of microbiological data. Analysis of isolate and environmental<br />
genomes is especially valuable in characterizing the metabolic potential<br />
of in situ microbial communities. This work also indicates important gaps in<br />
understanding of geomicrobiology in mining environments, and offers insight<br />
into methods need to address gaps in knowledge about biogeochemical processes<br />
of critical importance to the mining industry.<br />
chair:<br />
2:00 PM<br />
Introductions<br />
environmental:<br />
Mine Water treatment I<br />
2:00 PM • Tuesday, February 26<br />
M. Mierzejewski, CH2MHill, Richmond, VA<br />
2:05 PM<br />
Thermodynamic Constraints on Arsenic and Heavy Metals<br />
Removal from Water with Limestone-Based Material<br />
A. Davis 1 , C. Webb 2 , J. Sorensen 3 and D. Dixon 4 ; 1 Geological<br />
Engineering, South Dakota School of Mines and Technology,<br />
Rapid City, SD; 2 Chemistry Dept., Western Kentucky University,<br />
Bowling Green, KY; 3 RESPEC, Rapid City, SD and 4 Chemical and<br />
Biological Engineering, South Dakota School of Mines and<br />
Technology, Rapid City, SD<br />
Limestone-based material is effective for reducing arsenic concentrations below<br />
the current limit of 10 parts per billion for drinking water, typically resulting in<br />
final concentrations of about 4 to 6 ppb. However, in laboratory and field testing,<br />
further reductions to the 1 ppb range are difficult to achieve with limestone. The<br />
removal mechanism appears to be the formation of a low-solubility precipitate of<br />
hydrated calcium arsenate. Likely reactions and thermodynamic data indicate a<br />
theoretical removal limit of about 2 to 4 ppb for arsenic. Limestone also can reduce<br />
concentrations of cadmium and lead below 1 ppb, resulting in >99% removal<br />
efficiency. Thermodynamic constraints appear to be favorable for reactions<br />
involving the formation of hydrocerussite during lead removal and the formation<br />
of otavite during cadmium removal.<br />
2:25 PM<br />
Targeted Removal of Molybdenum, Radium, Uranium and<br />
Selenium from a Mining<br />
H. Liang and J. Tamburini; Tetra Tech, Denver, CO<br />
Although uranium, radium, molybdenum, and selenium occur naturally and can<br />
be found in waters throughout many parts of the world, ingesting water containing<br />
these substances above established concentrations is considered harmful to<br />
human health and can also harm aquatic life. Therefore, successful treatment and<br />
removal of these toxicants is crucial to protecting human and environmental<br />
health. This presentation will highlight research conducted at a water treatment<br />
plant where optimization of conventional treatment processes such as lime softening<br />
and ferric coagulation led to the successful treatment of all four inorganic<br />
contaminants to their target levels. Because uranium, molybdenum, and selenium<br />
all undergo complex speciation chemistry in aqueous solution, much of the<br />
presentation will focus on details of the water chemistry and speciation considerations<br />
for optimizing the removal of these contaminants. Both bench scale tests<br />
and full scale water treatment plant data and analyses will be presented, and the<br />
rationales for the refinement of the inorganic contaminants removal treatment<br />
processes will be discussed.<br />
2:45 PM<br />
Design and Construction of Twin-PRBs to Intercept Arsenic in a<br />
Former Arroyo<br />
J. Horst 1 , G. Leone 2 and A. Griffin 3 ; 1 ARCADIS, Newtown, PA;<br />
2<br />
ARCADIS, Denver, CO and 3 ARCADIS, Seattle, WA<br />
The 100+ year history of operation at a former lead and copper smelter has resulted<br />
in groundwater across most of the site footprint being impacted primarily<br />
with arsenic. The highest concentrations of arsenic and the majority of groundwater<br />
flow are both focused along former (now buried) arroyos. These features<br />
represent the greatest contribution of contaminant mass flux toward off- site receptors,<br />
and are the key to an integrated strategy for groundwater restoration.<br />
With groundwater seepage velocities ranging between approximately 4 and 10<br />
feet per day, one part of that strategy involved the use of sequential permeable reactive<br />
barriers to reduce contaminant flux toward off-site receptors. This presentation<br />
will review the pre-design, design, and final configuration of a pair of test<br />
barriers. It will also review the construction of the barriers and present some<br />
post-construction performance data.<br />
3:05 PM<br />
Successful Negotiation of Natural Attenuation for Arsenic Using<br />
the EPA Framework<br />
J. Horst 1 and M. Gentile 2 ; 1 ARCADIS, Newtown, PA and<br />
2<br />
ARCADIS, San Francisco, CA<br />
EPA recently released a new framework for supporting natural attenuation<br />
demonstrations associated with metals and other inorganics. This framework<br />
was applied for a site with an arsenic plume in groundwater, sourced by the flushing<br />
of residual organics from beneath a former waste repository. Natural<br />
biodegradation of these organics resulted in an anaerobic environment and<br />
caused naturally occurring arsenic in the aquifer matrix to dissolve into groundwater<br />
via reductive dissolution. This presentation will review the details of a<br />
phased biogeochemical evaluation that included geochemical analysis of aquifer<br />
solids and identification of precedents at other EPA-lead sites, and summarize<br />
the demonstration that supported EPA approval of a change in remedy from<br />
pump and treat to MNA.<br />
3:25 PM<br />
Constructed Wetland Treatment Systems for Mine Drainage Can<br />
They Really Provide Green and Sustainable Solutions?<br />
P. Eger 1 and C. KairiesBeatty 2 ; 1 Global Minerals Engineering,<br />
Hibbing, MN and 2 Winona State University, Winona, MN<br />
The use of wetlands to treat mine drainage has become increasingly common.<br />
They offer the promise of a green and sustainable solution, but how long will<br />
they really work? Treatment lifetime is a function of the metal removal processes.<br />
In surface flow wetlands, trace metals can be removed from neutral mine<br />
drainage by reactions with the organic substrate. Over 90% of the copper and<br />
nickel have been removed in these systems in Minnesota. The primary removal<br />
processes include adsorption, ion exchange and complexation. These processes<br />
are finite since they depend on the existence of suitable removal sites. Removal<br />
will cease unless new removal sites are generated. Two wetlands in northeastern<br />
Minnesota have been treating mine drainage for almost 20 years and are believed<br />
to be the oldest wetlands treating metal mine drainage in the United States.<br />
Treatment lifetime has been estimated to exceed a hundred years. At one of the<br />
wetlands, the annual production of new removal sites has been estimated to be<br />
equal to the annual metal input. As a result, metal removal should theoretically<br />
continue indefinitely resulting in a green and sustainable solution.<br />
This is the Technical <strong>Program</strong> as of September 1, 2012. IT IS SUBJECT TO CHANGE.<br />
83<br />
Please see the Onsite <strong>Program</strong> for final details.