Anionic co-contaminants and the biogeochemical evolution of aquifer heterogeneity. Final technical report

PDF Version Also Available for Download.

Description

Adsorption heterogeneity of subsoils may depend on the sorbate and its concentration. Ligands in natural and contaminated subsoils may dissolve substantial metal oxides thereby altering the subsoil heterogeneity. We investigated these hypotheses on sands artificially and naturally coated with various amounts of metal oxides. The adsorbates Cu, oxalate, and mixtures of Cu and oxalate (Cu-Oxalate) were used as probes of the surface. For the concentration range studied, Binding Strength Analysis revealed that the naturally coated samples were heterogeneous at the microscale and the macroscale when oxalate was used as the probe of the surface. Cu revealed a smaller heterogeneity while ... continued below

Physical Description

208 p.

Creation Information

Fish, W. July 1, 1997.

Context

This report is part of the collection entitled: Office of Scientific & Technical Information Technical Reports and was provided by UNT Libraries Government Documents Department to Digital Library, a digital repository hosted by the UNT Libraries. More information about this report can be viewed below.

Who

People and organizations associated with either the creation of this report or its content.

Provided By

UNT Libraries Government Documents Department

Serving as both a federal and a state depository library, the UNT Libraries Government Documents Department maintains millions of items in a variety of formats. The department is a member of the FDLP Content Partnerships Program and an Affiliated Archive of the National Archives.

Contact Us

What

Descriptive information to help identify this report. Follow the links below to find similar items on the Digital Library.

Description

Adsorption heterogeneity of subsoils may depend on the sorbate and its concentration. Ligands in natural and contaminated subsoils may dissolve substantial metal oxides thereby altering the subsoil heterogeneity. We investigated these hypotheses on sands artificially and naturally coated with various amounts of metal oxides. The adsorbates Cu, oxalate, and mixtures of Cu and oxalate (Cu-Oxalate) were used as probes of the surface. For the concentration range studied, Binding Strength Analysis revealed that the naturally coated samples were heterogeneous at the microscale and the macroscale when oxalate was used as the probe of the surface. Cu revealed a smaller heterogeneity while Cu-Oxalate indicated an intermediate heterogeneity. Various elaborations of homogeneous-site Surface Complexation Models (SCM), calibrated to the surface protonation properties of goethite, modeled accurately the edges of oxalate, Cu, and mixtures of Cu and oxalate. The poorer fits for large concentrations was probably because of the site heterogeneity. The accuracy of SCMs was insensitive to the choice of surface protonation constants (pK{sub a}) and moderately sensitive to the choice of site density. The effective surface complexation constants (K{sup eff}) obtained from individual edges were somewhat different because of the concentration dependent heterogeneity. It was not always possible to use K{sup eff} values for one sorbate concentration to reproduce adsorption of other concentrations of the same sorbate. A modified version of the discrete pK{sub a} spectrum model closely reproduced the acid-base titration curve with two adsorption sites (four pK{sub a}`s). The adsorption of all concentrations of Cu, oxalate, and Cu-Oxalate was often reproduced with only one of those sites. The competition between the dissolved Al and the surface for the oxalate in solution was accurately reproduced with both sites. The dissolution of the oxide coating was often influenced by the pore velocity.

Physical Description

208 p.

Notes

OSTI as DE97008500

Source

  • Other Information: PBD: Jul 1997

Language

Item Type

Identifier

Unique identifying numbers for this report in the Digital Library or other systems.

  • Other: DE97008500
  • Report No.: DOE/ER/60845--5
  • Grant Number: FG06-89ER60845
  • DOI: 10.2172/519154 | External Link
  • Office of Scientific & Technical Information Report Number: 519154
  • Archival Resource Key: ark:/67531/metadc693428

Collections

This report is part of the following collection of related materials.

Office of Scientific & Technical Information Technical Reports

Reports, articles and other documents harvested from the Office of Scientific and Technical Information.

Office of Scientific and Technical Information (OSTI) is the Department of Energy (DOE) office that collects, preserves, and disseminates DOE-sponsored research and development (R&D) results that are the outcomes of R&D projects or other funded activities at DOE labs and facilities nationwide and grantees at universities and other institutions.

What responsibilities do I have when using this report?

When

Dates and time periods associated with this report.

Creation Date

  • July 1, 1997

Added to The UNT Digital Library

  • Aug. 14, 2015, 8:43 a.m.

Description Last Updated

  • Nov. 4, 2015, 3:07 p.m.

Usage Statistics

When was this report last used?

Yesterday: 0
Past 30 days: 0
Total Uses: 3

Interact With This Report

Here are some suggestions for what to do next.

Start Reading

PDF Version Also Available for Download.

International Image Interoperability Framework

IIF Logo

We support the IIIF Presentation API

Fish, W. Anionic co-contaminants and the biogeochemical evolution of aquifer heterogeneity. Final technical report, report, July 1, 1997; United States. (digital.library.unt.edu/ark:/67531/metadc693428/: accessed October 17, 2018), University of North Texas Libraries, Digital Library, digital.library.unt.edu; crediting UNT Libraries Government Documents Department.