Abstract
Several experiments of arsenic (As) adsorption by aquifer material of the San Antonio-El Triunfo (SA-ET) mining area were conducted to test the feasibility of this material acting as a natural control for As concentrations in groundwater. This aquifer material is mineralogically complex, composed of quartz, feldspar, calcite, chlorite, illite, and magnetite/hematite. The total iron content (Fe2O3) in the fine fraction is ∼12%, whereas Fe2O3 in the coarse fraction is <10 wt%. The experimental percent total As adsorbed vs. pH curves obtained match the topology of total As adsorbed onto iron oxi-hydroxides surface (arsenate + arsenite; high adsorption at low pH, low adsorption at high pH). A maximum of about 80% adsorbed in the experiments suggests the presence of arsenite in the experimental solutions. The experimental adsorption isotherm at pH 7 indicates saturation of surface sites at high solute concentrations. Surface titration of the aquifer material indicates a point of zero charge (PZC) for the adsorbent of about 8 to 8.5 (PZC for iron oxyhydroxides =7.9–8.2). Comparison between experimental and modeled results (using the MICROQL and MINTEQA2 geochemical modeling and speciation computer programs) suggests that As is being adsorbed mostly by oxyhydroxides surfaces in the natural environment. Based on an estimated retardation factor (R), the travel time of the As plume from the SA-ET area to La Paz and Los Planes is about 700 to 5000 years.
Article PDF
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Avoid common mistakes on your manuscript.
Author information
Authors and Affiliations
Additional information
Received: 17 March 1997 · Accepted: 8 September 1997
Rights and permissions
About this article
Cite this article
Carrillo, A., Drever, J. Adsorption of arsenic by natural aquifer material in the San Antonio-El Triunfo mining area, Baja California, Mexico. Environmental Geology 35, 251–257 (1998). https://doi.org/10.1007/s002540050311
Issue Date:
DOI: https://doi.org/10.1007/s002540050311