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A target for production of radioxenons

A liquid cesium target has been developed which permits the production and identification of the neutron deficient isotopes of xenon. The thick target yields of Xe-127 and Xe-129 m were measured for proton energies between 28 and 40 MeV. Production of Xe-129 m, as indicated by the presence of a 196 keV line in the gamma ray spectra, occurred at all proton energies; Xe-127 was produced at proton energies above 33 MeV. Both accumulated on the target with the same time constant, and the cross sections were comparable in magnitude. The radioxenons were removed from the target by a stream of carrier gas so that chemical separation was unnecessary.

Blue, J. W.

A target design for irradiation of NaI at high beam current

A solution to the targetry problems encountered when the iodine nucleus is a target for cyclotron irradiation is given as a target design. A target based on this design was used in 30 microampere irradiations of 46 MeV alpha particles for one-half hour without significant damage. Such an irradiation produces 6 to 7 mCi of Cs-129. This target should also be considered for cyclotron production of the radioisotopes Cs-127, I-123, and Xe-127.

Blue, J. W.

A target design for irradiation of NaI at high beam current.

A solution to the targetry problems encountered when the iodine nucleus is a target for cyclotron irradiation is given as a new target design. A target based on this design has been used in 30 microampere irradiations of 46 MeV alpha particles for one-half hour without significant damage. Such an irradiation produces 6 to 7 mCi of Cs-129, an isotope useful in nuclear medicine. This target should also be considered for cyclotron production of the radioisotopes Cs-127, I-123, and Xe-127.

Blue, J. W.

Gamma ray spectrometer experiment, NaI(Tl) detector crystal activation

Preliminary results are presented of data on the extent of the cosmic ray-induced activity obtained by a sodium iodide thallium-activated crystal flown onboard the Apollo 17 command module. Qualitative identification is reported for the following: Na-24, I-123, I-124, I-125, I-126, and Xe-127.

Trombka, J. I.

A target for production of radioxenons

A liquid cesium target has been developed which allows the production and separate identification of the neutron deficient isotopes of xenon. The present report describes irradiations utilizing 34 to 41 MeV protons to produce millicurie quantities of Xe-127 and Xe-129m. At higher energies, however, the target could be used without modification to produce xenon isotopes as light as 119.

Blue, J. W.

Trapping of xenon in ice - Implications for the origin of the earth's noble gases

Although the earth's atmosphere contains Ne, Ar, and Kr in about C1,2-chondrite proportions, Xe is depleted about 20-fold. To test the suggestion that the 'missing' Xe is trapped in Antarctic ice, distribution coefficients for Xe in artifically formed frost at -20 to -60 C were measured, using Xe-127 tracer. The values are 0.098 + or - 0.004 cc STP/g atm for trapping and less than 5 cc STP/g atm for trapping plus adsorption. If these results are representative of natural ice, then the Antarctic ice cap contains less than 1 percent of the atmospheric Xe inventory, or not greater than about 0.001 the amount needed for a C1,2-chondrite pattern. Two possibilities remain for the 'missing' Xe, both on the premise that the earth's noble gases, along with other volatiles, came from chondritic material: (1) xenon is preferentially retained in the mantle and lower crust, due to the strong affinity of Xe for clean silicate surfaces and amorphous carbon; and (2) the source material of the earth's volatiles had high, relatively unfractionated, Ar/Xe and Kr/Xe ratios, like the non-carbonaceous noble gas carriers in C3O and E-chondrites.

Wacker, J. F.

Laboratory simulation of meteoritic noble gases. I - Sorption of xenon on carbon: Trapping experiments

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.

Wacker, J. F.

Laboratory simulation of meteoritic noble gases. II - Sorption of xenon on carbon: Etching and heating experiments

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.

Zadnik, M. G.