Glen R. Longhurst

Hydrogen isotope retention in beryllium for tokamak plasma-facing applications

Beryllium has been used as a plasma-facing material to effect substantial improvements in plasma performance in the Joint European Torus (JET), and it is planned as a plasma-facing material for the first wall (FW) and other components of the International Thermonuclear Experimental Reactor (ITER). The interaction of hydrogenic ions, and charge-exchange neutral atoms from plasmas, with beryllium has been studied in recent years with widely varying interpretations of results. In this paper we review experimental data regarding hydrogenic atom inventories in experiments pertinent to tokamak applications and show that with some very plausible assumptions, the experimental data appear to exhibit rather predictable trends. A phenomenon observed in high ion-flux experiments is the saturation of the beryllium surface such that inventories of implanted particles become insensitive to increased flux and to continued implantation fluence. Methods for modeling retention and release of implanted hydrogen in beryllium are reviewed and an adaptation is suggested for modeling the saturation effects. The TMAP4 code used with these modifications has succeeded in simulating experimental data taken under saturation conditions where codes without this feature have not. That implementation also works well under more routine conditions where the conventional recombination-limited release model is applicable. Calculations of tritium inventory and permeation in the ITER FW during the basic performance phase (BPP) using both the conventional recombination model and the saturation effects assumptions show a difference of several orders of magnitude in both inventory and permeation rate to the coolant.

Hydrogen transport behavior of beryllium

Beryllium is being evaluated for use as a plasma-facing material in the International Thermonuclear Experimental Reactor (ITER). One concern in the evaluation is the retention and permeation of tritium implanted into the plasma-facing surface. We performed laboratory-scale studies to investigate mechanisms that influence hydrogen transport and retention in beryllium foil specimens of rolled powder metallurgy product and rolled ingot cast beryllium. Specimen characterization was accomplished using scanning electron microscopy, Auger electron spectroscopy, and Rutherford backscattering spectrometry (RBS) techniques. Hydrogen transport was investigated using ion-beam permeation experiments and nuclear reaction analysis (NRA). Results indicate that trapping plays a significant role in permeation, re-emission, and retention, and that surface processes at both upstream and downstream surfaces are also important.

Tritium retention in S-65 beryllium after 100 eV plasma exposure

Abstract The tritium plasma experiment (TPE) has been used to measure the retention of tritium in S-65 beryllium under conditions similar to that expected for the international thermonuclear experimental reactor (ITER). Beryllium samples 2 mm thick and 50 mm in diameter were exposed to a plasma of tritium and deuterium. The particle flux striking the samples was varied from approximately 1 × 1017 (D + T)/cm2s up to about 3 × 1018 (D + T)/cm2s. The beryllium samples were negatively biased to elevate the energy of the impinging ions to 100 eV. The temperature of the samples was varied from 373 K to 973 K. Exposure times of 1 h were used. Subsequent to the plasma exposure, the samples were outgassed in a separate system where 99% He and 1% H2 gas was swept over the samples during heating. The sweep gas along with the released tritium was sent through an ionization chamber, through a copper oxide catalyst bed, and into a series of glycol bubblers. The amount of released tritium was determined both by the ionization chamber and by liquid scintillation counting of the glycol. Tritium retention in the beryllium disks varied from a high of 2.4 × 1017 (D + T)/cm2 at 373 K to a low of 1 × 1016 (D + T)/cm2 at 573 K. For almost every case, the tritium retention in the beryllium was less than that calculated using the C = 0 boundary condition at the plasma facing surface. It is believed that this lower than expected retention is due to rapid release of tritium from the large specific surface area created in the implant zone due to the production of voids, bubbles, and blisters.

Hydrogen permeation properties of plasma-sprayed tungsten☆

Abstract Tungsten has been proposed as a plasma-facing component material for advanced fusion facilities. This paper reports on laboratory-scale studies that were done to assess the hydrogen permeation properties of plasma-sprayed tungsten for such applications. The work entailed deuterium permeation measurements for plasma-sprayed (PS) tungsten coatings, sputter-deposited (SP) tungsten coatings, and steel substrate material using a mass-analyzed, 3 keV D3+ ion beam with fluxes of ∼6.5 × 1019 D/m2 s. Extensive characterization analyses for the plasma-sprayed tungsten coatings were made using Auger spectrometry and scanning electron microscopy (SEM). Observed permeation rates through composite PS-tungsten/steel specimens were several orders of magnitude below the permeation levels observed for SP-tungsten/steel composite specimens and pure steel specimens. Characterization analyses indicated that the plasma-sprayed tungsten coating had a nonhomogeneous microstructure that consisted of splats with columnar solidification, partially-melted particles with grain boundaries, and void regions. Reduced permeation levels can be attributed to the complex microstructure and a substantial surface-connected porosity.

The soret effect and its implications for fusion reactors

Abstract Tritium permeation through and retention in fusion reactor structures may be strongly influenced by the heat load carried by the structures through the Soret effect. After a short discussion suggestive of a heuristic model for predicting the associated energy and the heat of transport, data from several experiments are analyzed to show that the simplistic model works reasonably well with endothermic materials such as Fe and Ni, but is less successful with hydride formers. The implications of the model for tritium permeation and retention are discussed, and sample calculations are presented to illustrate the importance of properly accounting for the Soret effect in predicting tritium permeation and retention in fusion reactor structures. Neglecting the Soret effect may result in order of magnitude errors in estimating permeation and retention, while accounting for temperature sensitivity in the heat of transport will result in less significant corrections. An Appendix summarizes the development of transport equations from non-equilibrium thermodynamics to clarify the relationships between the various transport parameters involved.

Tritium saturation in plasma-facing materials surfaces

Plasma-facing components in the International Thermonuclear Experimental Reactor (ITER) will experience high heat loads and intense plasma fluxes of order 10 20 -10 23 particles/m 2 s. Experiments on Be and W, two of the materials considered for use in ITER, have revealed that a tritium saturation phenomenon can take place under these conditions in which damage to the surface results that enhances the return of implanted tritium to the plasma and inhibits uptake of tritium. This phenomenon is important because it implies that tritium inventories due to implantation in these plasma-facing materials will probably be lower than was previously estimated using classical recombination-limited release at the plasma surface. Similarly, permeation through these components to the coolant streams should be reduced. In this paper we discuss evidences for the existence of this phenomenon, describe techniques for modeling it, and present results of the application of such modeling to prior experiments.

The Safety and Tritium Applied Research (STAR) Facility: Status-2004

The Safety and Tritium Applied Research (STAR) Facility, a US DOE National User Facility at the Idaho National Engineering and Environmental Laboratory (INEEL), comprises capabilities and infrastructure to support both tritium and non-tritium research activities important to the development of safe and environmentally friendly fusion energy. Research thrusts include (1) interactions of tritium and deuterium with plasma-facing-component (PFC) materials, (2) fusion safety issues [PFC material chemical reactivity and dust/debris generation, activation product mobilization, tritium behavior in fusion systems], and (3) molten salts and fusion liquids for tritium breeder and coolant applications. This paper updates the status of STAR and the capabilities for ongoing research activities, with an emphasis on the development, testing and integration of the infrastructure to support tritium research activities. Key elements of this infrastructure include a tritium storage and assay system, a tritium cleanup system to process glovebox and experiment tritiated effluent gases, and facility tritium monitoring systems.

Verification and Validation of The Tritium Transport Code TMAP7

The TMAP code has been upgraded to version 7, which includes radioactive decay along with many features implemented in prior versions. Pursuant to acceptance and release for distribution, the code was exercised in a variety of problem types to demonstrate that it provides results in agreement with theoretical results for cases where those are available. It has also been used to model certain experimental results. In this paper, the capabilities of the TMAP7 code are demonstrated by presenting some of the results from the verification and validation process.

Deuterium transport in Cu, CuCrZr, and Cu/Be

This paper presents the results of deuterium implantation/permeation experiments and TMAP4 simulations for a CuCrZr alloy, for OFHC-Cu and for a Cu/Be bi-layered structure at temperatures from 700 to 800 K. Experiments used a mass-analyzed, 3-keV D 3 + ion beam with particle flux densities of 5 x 10 19 to 7 x 10 19 D/m 2 S. Effective diffusivities and surface molecular recombination coefficients were derived giving Arrhenius pre-exponentials and activation energies for each material: CuCrZr alloy, (2.0 x 10 -2 m 2 /s, 1.2 eV) for diffusivity and (2.9 x 10 14 m 4 /s, 1.92 eV) for surface molecular recombination coefficients; OFHC Cu, (2.1 x 10 -6 m 2 /s, 0.52 eV) for diffusivity and (9.1 x 10 -18 m 4 /s, 0.99 eV) for surface molecular recombination coefficients. TMAP4 simulation of permeation data measured for a Cu/Be bilayer sample was achieved using a four-layer structure (Cu/BeO interface/Be/BeO back surface) and recommended values for diffusivity and solubility in Be, BeO and Cu.

Storage and Assay of Tritium in STAR

The Safety and Tritium Applied Research (STAR) facility at the Idaho National Engineering and Environmental Laboratory (INEEL) is currently being commissioned to investigate tritium-related safety questions for fusion and other technologies. The tritium inventory for the STAR facility will be maintained below 1.5 g to avoid the need for STAR to be classified as a Category 3 nuclear facility. A key capability in successful operation of the STAR facility is the ability to receive, inventory, and dispense tritium to the various experiments underway there. The system central to that function is the Tritium Storage and Assay System (SAS). The SAS has four major functions: (1) receiving and holding tritium, (2) assaying, (3) dispensing, and (4) purifying hydrogen isotopes from non-hydrogen species. This paper describes the design and operation of the STAR SAS and the procedures used for tritium accountancy in the STAR facility.