Remediating Subsurface Arsenic Contamination with Monitored

Nov 15, 2005 - Janet G. Hering , Peggy A. O'Day , Robert G. Ford , Y. Thomas He , Azra Bilgin , H. James Reisinger , David R. Burris. Ground Water Mon...
0 downloads 0 Views 390KB Size
Remediating Subsurface ARSENIC Contamination with Monitored Natural Attenuation

I

For some sites, it may be an attractive and viable option.

state libr ary and archives of florida

FPO

H. Ja mes REISINGER Dav id R. BURRIS INTEGR ATED SCIENCE & TECHNOLOGY, INC. Ja net G. HERING CALIFORNI A INSTITUTE OF TECHNOLOGY 458A n Environmental Science & Technology / november 15, 2005

n January 2001, the U.S. EPA established a new standard of 10 µg/L for arsenic in drinking water (1). Even before this revision, arsenic was at the top of the Comprehensive Environmental Response, Compensation, and Liability Act (Superfund) Priority List of Hazardous Substances (2). Prepared by EPA and the Agency for Toxic Substances and Disease Registry, this list prioritizes substances that occur most commonly at Superfund sites and that, on the basis of their toxicity and potential for human exposure, pose the most significant risk to human health. Because the revision of the arsenic standard was driven by health concerns—specifically the risks of bladder and lung cancer—closer scrutiny will most likely be directed toward the potential threats at contaminated sites. At some sites, however, arsenic contamination poses no immediate hazard to human or ecosystem health. In such cases, the potential risks associated with arsenic migration and exposure may be mitigated by natural attenuation, which is defined as “physical, chemical, or biological processes that, under favorable conditions, act without human intervention to reduce the mass, toxicity, volume, or concentration of contaminants in soil or groundwater” (3). Here, we examine the processes that could affect the natural attenuation of arsenic and the feasibility of these natural processes as a remediation strategy for arsenic-contaminated sites.

Sources and active solutions Arsenic contamination in the environment stems from various human activities, most notably mining and smelting operations, manufacture and use of arsenical biocides, and disposal of ash from coaland oil-fired power plants (4). Industrial demand for arsenic is summarized in Table S1 (all figures and tables with an “S” can be found in Supporting Information online). These activities have contaminated soils, sediments, surface water, and groundwater. Naturally occurring arsenic is found in soils or aquifer sediments of the conterminous U.S. in © 2005 American Chemical Society

the range of