Comments on 'Xe129 and the origin of CCF xenon in meteorites' by R. S. Lewis and E. Anders
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The diffusion of Xe in olivine, a major mineral in both meteorites and lunar samples, was studied. Xe ions were implanted at 200 keV into single-crystal synthetic-forsterite targets and the depth profiles were measured by alpha particle backscattering before and after annealing for 1 hour at temperatures up to 1500 C. The fraction of implanted Xe retained following annealing was strongly dependent on the implantation dose. Maximum retention of 100% occurred for an implantion dose of 3 x 10 to the 15th power Xe ions/sq cm. Retention was less at lower doses, with (approximately more than or = 50% loss at one hundred trillion Xe ions/sq cm. Taking the diffusion coefficient at this dose as a lower limit, the minimum activation energy necessary for Xe retention in a 10 micrometer layer for ten million years was calculated as a function of metamorphic temperature.
The production of electrostatic ion cyclotron waves by a perpendicular ion beam in the F-region ionosphere is described. The ion beam experiment was part of the Porcupine program and produced electrostatic hydrogen cyclotron waves just above harmonics of the hydrogen cyclotron frequency. The plasma process may be thought of as a magnetized background ionosphere through which an unmagnetized beam is flowing. The dispersion equation for this hypothesis is constructed and solved. Preliminary solutions agree well with the observed plasma waves.
The diffusion of Xe in olivine, a major mineral in both meteorites and linear samples, was studied. Xe ions were implanted at 200 keV into single-crystal synthetic-forsterite targets and the depth profiles were measured by alpha particle backscattering before and after annealing for 1 hour at temperatures up to 1500 C. The fraction of implanted XE retained following annealing was strongly dependent on the implantation dose. Maximum retention of 100 percent occurred for an implanting dose of 3 x 10 to the 15th power Xe ions/sq cm. Retention was less at lower doses, with approximately more than or = 50 percent loss at one hundred trillion Xe ions/sq cm. Taking the diffusion coefficient at this dose as a lower limit, the minimum activation energy necessary for Xe retention in a 10 micrometer layer for ten million years was calculated as a function of metamorphic temperature. Previously announced in STAR as N83-18528
A novel trapped gas analysis protocol is applied to five shales in which the samples are sealed in air to eliminate the possibility of gas loss in the preanalysis laboratory vacuum exposure of a conventional protocol. The test is aimed at a determination concerning the hypothesis that atmospheric noble gases occur in the same proportion as planetary gases in meteorites, and that the factor-of-23 deficiency of air Xe relative to planetary Xe is made up by Xe stored in shales or other sedimentary rocks. The results obtained do not support the shale hypothesis.
Highly volatile elements (e.g., T1, Pb, B, C1, Br, etc.) in the Earth's crust occur in C-chondrite proportions, and so do the atmospheric noble gases Ne, Ar, and Kr. This has led to the suggestion that the Earth acquired its volatiles from a late veneer of C-chondrite-like material. A glaring exception is Xe, which is depleted approx. 20x relative to Ne, Ar, Kr. Three explanations are discussed for the depletion: (1) Xe is preferentially trapped in the crust, either in sediments (3) or in Antarctic ice (4); (2) the Earth's noble gas inventory is non-chondritic (5); or (3) Xe is incompletely outgassed from the mantle.
The sorption of Xe-127 at 5 x 10 to the -7th atm onto carbon black, pyrolyzed polyvinylidene chloride, and pyrolyzed acridine at 100-1000 C for 5 min-240 h is measured experimentally by gamma spectrometry. The results are presented in tables and graphs and characterized in detail. The tightly bound Xe remaining in the samples after 4000 min pumping at temperatures above 100 C is found to comprise two components: a low-temperature component attributed to physisorption within an atomic-scale labyrinth of micropores, and a high-temperature component due to volume diffusion. The implications for the trapping of noble gases near grain surfaces of amorphous carbon in meteorites are considered.
The release of trapped Xe from amorphous-C phases of meteorites is simulated experimentally by HNO3 etching of carbon-black and pyrolyzed polyvinylidene chloride samples exposed to Xe-127 for 0.5-240 h at 100-1000 C and then degassed for 9 h or more at the same temperatures, as reported by Wacker et al. (1985). The results are presented in tables and graphs and characterized in detail. Samples exposed at 100-200 C are found to lose most of their Xe after etching to a depth of only about 20 pm, while those exposed at 800-1000 C exhibit a second more tightly bound component extending to a depth of 3 nm, indicative of diffusion of Xe during exposure and resembling planetary Xe. The higher noble-gas concentrations measured in meteorites are attributed to rate-controlled Xe uptake over a long period in the solar nebula.
As a first step in an experimental program to study the behavior of noble gases produced in situ in minerals, a suite of minerals and pure chemicals were irradiated with 14.5 MeV neutrons at LLNL's Rotating Target Neutron Source (RTNS-II) and production rates for noble gases were determined. While neutron effects in meteorites and lunar samples are dominated by low-energy neutron capture, more energetic cosmic-ray secondary neutrons can provide significant depth-dependent contributions to production of cosmogenic nuclides through endothermic reactions such as (n,2n), (n,np), (n,d) and (n,alpha). Production rates for nuclides produced by cosmic-ray secondary neutrons are therefore useful in interpreting shielding histories from the relative abundances of cosmogenic nuclides. Absolute production cross sections were calculated from isotope dilution analyses of NaCl, Mg, CsCl, and Ba(NO3)2 samples, assuming purity, stoichiometry, and quantitative noble gas retention and extraction. Relative production cross sections determined from neon isotopic ratios in the mineral samples were also considered in evaluating the neon production cross sections. Results are presented.
Results from a series of experiments to determine the effect of accelerator grid mount geometry on the performance of the J-series ion optics assembly are described. Three mounting schemes, two flexible and one rigid, are compared for their relative ion extraction capability over a range of total accelerating voltages. The largest ion beam current, for the maximum total voltage investigated, is shown to occur using one of the flexible grid mounting geometries. However, at lower total voltages and reduced engine input power levels, the original rigid J-series ion optics accelerator grid mounts result in marginally better grid system performance at the same cold interelectrode gap.
The I-Xe systems of six Allende inclusions (five Eggs and the Pink Angel) appear to have been altered by nonnebular secondary processes. Evidence for this includes temperature-ordered variations in the initial I isotopic composition within several objects (with older apparent I-Xe ages associated with higher extraction temperatures) and the absence of primitive I-Xe ages. The span of apparent ages seen in Allende objects (10 Myr or more) is probably too long to reflect any nebular process, so at least some alteration probably occurred ont the parent body. The range in initial (Pu-244)/(U-238) ratios for the Eggs (0.003-0.014) includes the current best estimates of the bulk solar system value (0.004-0.007). For Egg 3, the Pu/U ratio varies by a factor of two between extractions, probably the result of fractionation of Pu from U among different phases.
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The most readily and widely studied of the extinct radionuclides in meteorites is I-129, and there is an extensive data base for meteorite chronology based on this isotope, but also significant uncertainty about how to interpret many of the data. If the data are interpreted as a straightforward chronology, a time span is inferred for most meteorite classes that appears too long for the events being dated to have taken place in the nebula.
Xe has been compressed in a diamond-anvil cell to approximately 200 GPa. The metallization of Xe by band-gap closure was investigated by obtaining optical data in both the metallic and insulating states. In the metallic state, the pressure dependence of the plasma frequency was determined from absorption data fitted with a free-electron model. In the insulating state, the pressure dependence of the band gap was determined from absorption data fitted with an indirect-band-gap model. The optical data indicate that the insulator-to-metal transition in Xe occurs at 132(5) GPa.
The neutrino burst from the collapsed core in Type II supernovae liberates free neutrons by nu, nu-prime(n) reactions which drive isotopic abundances several mass steps heavier. The neutron fluence in the He shell, abetted by another burst 10 s later from alpha, n reactions, is about right for rendering Xe-136, the most abundant Xe isotope. The Xe isotopic composition is a good match to Xe-H, the unshielded neutron-rich Xe component abundant in carbonaceous meteorites. The He shell is implicated because it is the only C-rich shell in massive stars that can be expected to condense solid carbon thermally, a requirement for locating the Xe-H in meteoritic diamonds, which are so common as to require an abundant Galactic source of unoxidized carbon.
The sorption of Ne, Ar, Kr, and Xe was studied in carbon black, acridine carbon, and diamond in an attempt to understand the origin of trapped noble gases in meteorites. The results support a model in which gases are physically adsorbed on interior surfaces formed by a pore labyrinth within amorphous carbons. The data show that: (1) the adsorption/desorption times are controlled by choke points that restrict the movement of noble gas atoms within the pore labyrinth, and (2) the physical adsorption controls the temperature behavior and elemental fractionation patterns.
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The time dependence and the intensity of the primary scintillation light in liquid Xe excited by Am-241 alpha particles and Bi-207 internal-conversion electrons were measured at different electric-field strengths. High-purity liquid Xe was used to fill a parallel-plate ionization chamber equipped with a CaF2 window coupled to a UV-sensitive photomultiplier tube. The effect of the specific ionization density on the scintillation light and the time correlation between the light signal and the charge signal is reported. It is demonstrated that the fast scintillation signal produced in liquid Xe by an ionizing particle provides an ideal trigger in a detector aiming at a complete three-dimensional event reconstruction with an excellent background rejection capability.