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Modelling of laboratory high-pressure infiltration experiments

Abstract

This report describes the modelling of break-through curves from a series of two-tracer dynamic infiltration experiments, which are intended to complement larger scale experiments at the Nagra Grimsel Test Site. The tracers are {sup 82}Br, which is expected to be non-sorbing, and {sup 24}Na, which is weakly sorbing. The {sup 24}Na concentration is well below the natural Na concentration in the infiltration fluid, so that sorption on the rock is governed by isotopic exchange, exhibiting a linear isotherm. The rock specimens are sub-samples (cores) of granodiorite from the Grimsel Test Site, each containing a distinct shear zone. Best-fits to the break-through curves using single-porosity and dual-porosity transport models are compared and several physical parameters are extracted. It is shown that the dual-porosity model is required in order to reproduce the tailing part of the break-through curves for the non-sorbing tracer. The single-porosity model is sufficient to reproduce the break-through curves for the sorbing tracer within the estimated experimental errors. Extracted K{sub d} values are shown to agree well with a field rock-water interaction experiment and in situ migration experiments. Static, laboratory batch-sorption experiments give a larger K{sub d}, but this difference could be explained by the larger surface area available  More>>
Authors:
Smith, P A [1] 
  1. Paul Scherrer Inst. (PSI), Villigen (Switzerland)
Publication Date:
Feb 01, 1992
Product Type:
Technical Report
Report Number:
PSI-116
Reference Number:
SCA: 540211; PA: AIX-23:052971; SN: 92000774641
Resource Relation:
Other Information: PBD: Feb 1992
Subject:
54 ENVIRONMENTAL SCIENCES; GRANODIORITES; DRILL CORES; WATER INFLUX; ADSORPTION; BROMINE 82; COMPUTERIZED SIMULATION; DISTRIBUTION FUNCTIONS; EXPERIMENTAL DATA; POROSITY; SODIUM 24; THEORETICAL DATA; TRACER TECHNIQUES; 540211; RADIOMETRIC TECHNIQUES
OSTI ID:
10157662
Research Organizations:
Paul Scherrer Inst. (PSI), Villigen (Switzerland)
Country of Origin:
Switzerland
Language:
English
Other Identifying Numbers:
Other: ON: DE92636242; TRN: CH9200388052971
Availability:
OSTI; NTIS; INIS
Submitting Site:
CHN
Size:
37 p.
Announcement Date:
Jul 06, 2005

Citation Formats

Smith, P A. Modelling of laboratory high-pressure infiltration experiments. Switzerland: N. p., 1992. Web.
Smith, P A. Modelling of laboratory high-pressure infiltration experiments. Switzerland.
Smith, P A. 1992. "Modelling of laboratory high-pressure infiltration experiments." Switzerland.
@misc{etde_10157662,
title = {Modelling of laboratory high-pressure infiltration experiments}
author = {Smith, P A}
abstractNote = {This report describes the modelling of break-through curves from a series of two-tracer dynamic infiltration experiments, which are intended to complement larger scale experiments at the Nagra Grimsel Test Site. The tracers are {sup 82}Br, which is expected to be non-sorbing, and {sup 24}Na, which is weakly sorbing. The {sup 24}Na concentration is well below the natural Na concentration in the infiltration fluid, so that sorption on the rock is governed by isotopic exchange, exhibiting a linear isotherm. The rock specimens are sub-samples (cores) of granodiorite from the Grimsel Test Site, each containing a distinct shear zone. Best-fits to the break-through curves using single-porosity and dual-porosity transport models are compared and several physical parameters are extracted. It is shown that the dual-porosity model is required in order to reproduce the tailing part of the break-through curves for the non-sorbing tracer. The single-porosity model is sufficient to reproduce the break-through curves for the sorbing tracer within the estimated experimental errors. Extracted K{sub d} values are shown to agree well with a field rock-water interaction experiment and in situ migration experiments. Static, laboratory batch-sorption experiments give a larger K{sub d}, but this difference could be explained by the larger surface area available for sorption in the artificially crushed samples used in the laboratory and by a slightly different water chemistry. (author) 13 figs., tabs., 19 refs.}
place = {Switzerland}
year = {1992}
month = {Feb}
}