University of North Florida
Browse the Citations
-OR-

Contact Info

Stuart Chalk, Ph.D.
Department of Chemistry
University of North Florida
Phone: 1-904-620-1938
Fax: 1-904-620-3535
Email: schalk@unf.edu
Website: @unf

View Stuart Chalk's profile on LinkedIn

David A. Atwood

Abbrev:
Atwood, D.A.
Other Names:
Address:
Albert B. Chandler Medical Center, Department of Anatomy and Neurobiology, University of Kentucky, Lexington KY, USA
Phone:
+1-859-257-7304
Fax:
+1-859-323-1069

Citations 2

"Irreversible Precipitation Of Mercury And Lead"
J. Hazard. Mater. 2001 Volume 84, Issue 1 Pages 73-82
Matthew M. Matlock, Brock S. Howerton and David A. Atwood

Abstract: There are immediate concerns with current commercial reagents that are used for heavy metal precipitation; in particular the fact that the reagents are not specifically designed to bind the targeted metals. The current literature reveals that not only do commercial reagents lack sufficient ability to strongly bind the metals, but they also fail to provide long-term stability as ligand-metal complexes under a variety of moderate conditions. For this reason a new ligand was designed and synthesized: 1,3-benzenediamidoethanethiol (BDETH2). It offers multiple, concerted, bonding sites for heavy metals and forms a stable metal-ligand precipitate. In this study, the formation of compounds comprised of this ligand with the divalent metals, lead and mercury, was explored and the pH stability of the water insoluble precipitates was determined. The leaching properties of the metal-ligand precipitates were determined using inductively coupled plasma (ICP) spectroscopy and cold vapor atomic fluorescence spectroscopy (CVAFS). The results indicate that a 50.00 ppm lead solution at a pH of 4.0 may be reduced to a concentration of 0.05 ppm (99.9% lead removal) and to 0.13 ppm (99.7% lead removal) at a pH 6.0. A 50.00 ppm mercury solution at pH 4.0 may be reduced to a concentration of 0.02 ppm (99.97% mercury removal) and to 0.02 ppm (99.97% mercury removal) at a pH of 6.0.

"Advanced Mercury Removal From Gold Leachate Solutions Prior To Gold And Silver Extraction: A Field Study From An Active Gold Mine In Peru"
Environ. Sci. Technol. 2002 Volume 36, Issue 7 Pages 1636-1639
Matthew M. Matlock, Brock S. Howerton, Mike A. Van Aelstyn, Fredrik L. Nordstrom, and David A. Atwood

Abstract: Mercury contamination in the Gold-Cyanide Process (GCP) is a serious health and environmental problem. Following the heap leaching of gold and silver ores with NaCN solutions, portions of the mercury-cyano complexes often adhere to the activated carbon (AC) used to extract the gold. During the electrowinning and retorting steps, mercury can be (and often is) emitted to the air as a vapor. This poses a severe health hazard to plant workers and the local environment. Additional concerns relate to the safety of workers when handling the mercury-laden AC. Currently, mercury treatment from the heap leach solution is nonexistent. This is due to the fact that chelating ligands which can effectively work under the adverse pH conditions (as present in the heap leachate solutions) do not exist. In an effort to economically and effectively treat the leachate solution prior to passing over the AC, a dipotassium salt of 1;3-benzenediamidoethanethiol (BDET2-) has been developed to irreversibly bind and precipitate the mercury. The ligand has proven to be highly effective by selectively reducing mercury levels from average initial concentrations of 34.5 ppm (parts per million) to 0.014 ppm within 10 min and to 0.008 ppm within 15 min. X-ray powder diffraction (XRD), proton nuclear magnetic resonance (H-1 NMR), Roman, and infrared (IR) spectroscopy demonstrate the formation of a mercury-ligand compound, which remains insoluble over pH ranges of 0.0-14.0. Leachate samples from an active gold mine in Peru have been analyzed using cold vapor atomic fluorescence (CVAFS) and inductively coupled plasma optical emission spectroscopy (ICP-OES) for metal concentrations before and after treatment with the BDET2- ligand.