Published March 2017 | Version v1
Journal article

Corrosion of copper and authigenic sulfide mineral growth in hydrothermal bentonite experiments

  • 1. Los Alamos National Laboratory, Earth and Environmental Sciences, MS J966, Los Alamos, NM 87545 (United States)
  • 2. University of California, Los Angeles, CA 90095 (United States)
  • 3. Sandia National Laboratory, Albuquerque, NM 87185 (United States)

Description

The focus of this experimental work is to characterize interaction of bentonite with possible used-fuel waste container materials. Experiments were performed up to 300 °C at 150–160 bars for five to six weeks. Bentonite was saturated with a 1900 ppm K-Ca-Na-Cl-bearing water with Cu-foils. Copper rapidly degrades into chalcocite (CuS2) and minor covellite (CuS) in the presence of H2S. Chalcocite growth and corrosion pit depths were measured for four different experimental runs yielding corrosion rates between 8.8 and 116 μm/yr depending on duration of experiment, brine composition, and clay type (bentonite vs. Opalinus Clay). Results of this research show that although pit-corrosion is demonstrated on Cu substrates, experiments show that the reactions that ensue, and the formation of minerals that develop, are extraordinarily slow. This supports the use of Cu in nuclide-containment systems as a possible engineered barrier system material. - Highlights: • Experiments run at 300 °C and 150 bars for up to six weeks. • Copper degrades to chalcocite (CuS2) and minor covellite (CuS) in presence of H2S. • Corrosion rates between 8.8 and 116 μm/yr. • Rate dependent on experiment duration, brine composition, and clay type. • Sulfide corrosion products may inhibit further corrosion of copper.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jnucmat.2016.12.036

Additional details

Identifiers

DOI
10.1016/j.jnucmat.2016.12.036;
PII
S0022-3115(16)30615-8;

Publishing Information

Journal Title
Journal of Nuclear Materials
Journal Volume
485
Journal Page Range
p. 137-146
ISSN
0022-3115
CODEN
JNUMAM

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.