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Chemical fractionations in meteorites
Chemical fractionations in meteorites - acceptance of chondrites as average samples of nonvolatile planetary matter
Lack of chemical fractionation in major and minor elements during agglutinate formation
Rhodes et al. (1975, 1976) and Adams et al. (1975) have reported that the agglutinate fraction of the soils on the lunar surface displays a marked enrichment in Fe, Mg, Ti, K, and La, and a depletion in Ca, Na, Al, and Eu, relative to the bulk soils. The reported investigation is concerned with a testing of the theory of chemical fractionation involving magnetic separation which was developed in connection with these findings. Soils 64421 and 71501 were sieved and the magnetic fractions separated according to the method developed by Adams and McCord (1973). Analyses of agglutinitic glass did not indicate any appreciable chemical fractionation for the major and minor elements accompanying the agglutination process. It was found that most, if not all fractionations reported can be accounted for completely by the magnetic nonagglutinate impurities in the agglutinate fraction. It is, therefore, concluded that there appears to be no reason to make use of any chemical fractionation theory, whose validity remains to be demonstrated.
Chemical Fractionation is not a Constant: Revisiting Bomb Vapor Chemistry
The debris produced by a nuclear explosion forms a hazard to response, can serve as a record used to interpret the event, and may persist in the environment necessitating long term management. Hence, understanding the radiochemical inventory of nuclear debris remains an important area of study, particularly the behavior and resulting distribution of actinides and fission products. Despite formation in a high energy environment, it has been recognized for decades that the chemical and isotopic composition of debris rarely, if ever, captures a homogenized blend of the bomb products. Instead, during cooling and debris formation, a variety of chemical processes cause separation of the different constituents. This process of chemical fractionation creates debris with a variety of different radionuclide inventories. Here we provide an overdue re-examination of our historic basis for understanding chemical fractionation in nuclear explosions through the context of new characterization of a large set of historical nuclear test data. Finally, we then discuss the implications of our findings for advancing models of radionuclide distribution and postdetonation chemical fractionation.
Chemical fractionation in systems condensing from the gas phase
The development of chemical fractionation in particles condensing from a gas is described in terms of the intrinsic properties of the components and their mutual interaction through the nucleation, growth, and agglomeration processes. Possible ranges in the degree of fractionation are discussed in terms of a simple three-species configuration, and an example is given of the numerical description of this phenomenon.
Chemical fractionations in meteorites. IV - Abundances of fourteen trace elements in L- chondrites- Implications for cosmothermometry
Chemical fractionations in meteorites, considering trace elements abundance in L chondrites and implications for cosmothermometry
Chemical fractionation of the lunar regolith by impact melting
Impact-produced agglutinitic glass in both lunar highland and mare soils is enriched in mafic elements, in potassium, phosphorus, and sulfur, and in most lithophile elements, whereas it is depleted in plagioclase components including europium. It is proposed that the chemical fractionation is the result of a multistage partial-melting mechanism that accompanies micrometeoroid impacts into soils. The process would be expected to occur on solar system bodies that have an impact-produced regolith.
Chemical fractionation of siderophile elements in impactites from Australian meteorite craters
The abundance pattern of siderophile elements in terrestrial and lunar impact melt rocks was used extensively to infer the nature of the impacting projectiles. An implicit assumption made is that the siderophile abundance ratios of the projectiles are approximately preserved during mixing of the projectile constituents with the impact melts. As this mixture occurs during flow of strongly shocked materials at high temperatures, however there are grounds for suspecting that the underlying assumption is not always valid. In particular, fractionation of the melted and partly vaporized material of the projectile might be expected because of differences in volatility, solubility in silicate melts, and other characteristics of the constituent elements. Impactites from craters with associated meteorites offer special opportunities to test the assumptions on which projectile identifications are based and to study chemical fractionation that occurred during the impact process.
Isotope ratios and chemical fractionation of CO in Lynds 134
A radio observation of (C-12)(O-17) in the dust cloud Lynds 134 is reported, and the question of the (C-13)(O-16)/(C-12)(O-18) ratio across this cloud is considered. A value of approximately 0.28 is obtained for the (C-12)(O-17) column-density ratio, and it is shown that the (C-13)(O-16)/(C-12)(O-18) ratio is very different at two positions in the cloud separated by about 3.75 arcmin. (C-13)(O-16)/(C-12)(O-18) column-density ratios are calculated on the assumption of LTE and found to have a mean value of 4.8 at six positions in the most obscured part of the cloud; the same ratio is determined to be much larger and variable outside the cloud core. It is suggested that chemical fractionation of CO is occurring in this cloud, that (C-13)(O-16) is considerably enriched in its outer regions, and that the cloud's C-12/C-13 ratio is approximately 104.
Experimental Set-up for the Study of Chemical Fractionation and Aerosol Dynamics
Experimental investigations of chemical fractionation/phase partition and aerosol dynamics in high-temperature environment were reviewed and discussed. Particle composition and size distribution are the key data for aerosol dynamics predictive model and simulation. However, there were no particle size distribution available from the previous works. Nucleation, condensation, and coagulation are three key physical processes driving the fractionation or phase partition thereby the aerosol dynamics. A new approach was proposed to experimentally observe fractionation/phase partition and provide data for validating the predictive model for aerosol dynamics in the simulation of bomb debris formation.
Chemical fractionations in meteorites. VIII - Iron meteorites and the cosmochemical history of the metal phase
The chemical composition of the metal phase of iron meteorites is traced through an idealized traditional history from condensation, oxidation, and accretion in the nebula to melting, segregation, and freezing in a parent body, considering the following fifteen elements: Au, Co, Cu, Fe, Ga, Ge, Ir, Mo, Ni, Os, Pd, Pt, Re, Rh, and Ru. Twelve iron meteorite groups resolved by Scott and Wasson (1975) are considered in the framework of cosmochemical historical analysis. The parent bodies of five of these groups seem to have had a traditional history. The others seem to have had more unusual histories. For example, the composition of the metal in group IVB matches that predicted for the metal condensate at 1270 K, implying accretion at high temperatures; and the metal in group IVA has a composition indicative of aggregates undergoing progressive stages of partial melting.
Chemical fractionations in group IIIAB iron meteorites - Origin by dendritic crystallization of an asteroidal core
Results of an investigation of the crystallization history of the asteroidal core that produced nearly 200 iron meteorites of group IIIAB are presented. The accuracy of the published distribution of coefficients between solid and liquid metal for seven elements and their dependence on the concentrations of S and P are critically assessed to develop a nonideal fractional crystallization model that reproduces all of the major features of the overall chemical trends in group IIIAB. It is suggested that the apparent distribution coefficient of S was was much higher than its equilibrium value (not greater than 0.01) and that it increased during crystallization. In the present preferred model the apparent distribution coefficient for S increases from 0.6 to 0.8, while the S concentration of the liquid increases from 6 to 13 wt pct. It is inferred that light S-rich liquid accumulates preferentially at the top of the core and in structural traps formed by the advancing solid.
Chemical fractionation in iron meteorites and its interpretation.
Published analyses of trace and minor elements in iron meteorites have been compiled and the distributions interpreted with the chemical groups defined by Wasson. When each element is plotted against Ni on log scales, groups are often clearly resolved with all the members of a group falling within the limits of sampling and analytical error on a straight line. Two fractionations have occurred, a primary event which established the bulk composition of each group and a secondary event which fractionated the elements within each group. Group I appears to have escaped the secondary fractionation. An examination of possible fractionation mechanisms suggests that the secondary process took place during solidification of iron cores in the parent bodies. The elements Ir, Os, Pt, Ru and Rh would be enriched in the early Ni-poor solid whilst As, Au, Co, Mo, P, Pd and Sb would concentrate in later solid and produce the observed positive correlations with Ni.-
Chemical fractionation in the solar nebula
The sequence of condensation of minerals from a cooling gas of solar composition has been calculated from thermodynamic data assuming complete chemical equilibrium is maintained. The results suggest that the Ca-Al-rich inclusions in Allende and other carbonaceous chondrites are aggregates of the highest temperature condensates. Complete condensation of these elements is followed 100 deg later, by the onset of the crystallization of nickel-iron, forsterite and enstatite. Transport of Ca-Al-rich refractory condensates from one part of the nebula to another before the condensation of these lower-temperature phases may have been responsible for the refractory element fractionations between the different classes of chondrites and possibly for the inferred refractory element enrichment of the moon.
Chemical fractionation in the solar nebula
The sequence of condensation of minerals from a cooling gas of solar composition has been calculated from thermodynamic data over the pressure range 0.001-0.00001 atm, assuming that complete chemical equilibrium is maintained. The results suggest that the Ca-Al-rich inclusions Allende and other carbonaceous chondrites are aggregates of the highest temperature condensates. Complete condensation of these elements is followed, 100 deg later, by the onset of the crystallization of nickel-iron, forsterite and enstatite. Transport of Ca-Al-rich refractory condensates from one part of the nebula to another before the condensation of these lower-temperature phases may have been responsible for the refractory element fractionations between the different classes of chondrites and possibly for the inferred refractory element enrichment of the Moon. The temperature gap between the condensation temperatures of nickel-iron and forsterite increases with increasing total pressure. Because pressure and temperature probably increased with decreasing heliocentric distance in the solar nebula, Mercury may have accreted from a condensate assemblage having a higher metal/silicate ratio than Venus or Earth which may, in turn, have formed from less oxidized material than Mars.
Are C1 chondrites chemically fractionated - A trace element study
Six C1 chondrite samples and a C2 xenolith from the Plainview H5 chondrite were analyzed by radiochemical neutron activation for a large variety of elements, including rare earths. The sample processing is described, including the irradiation, chemical procedure, rare earths separation, counting techniques, radiochemical purity check, and chemical yields. The results of consistency checks on a number of elements are discussed. Abundances for siderophiles, volatiles, and rare earths are presented and discussed. Tests are presented for fractionation of rare earths and other refractories, compositional uniformity of C1's, and interelement correlations. There is no conclusive evidence for nebular fractionation affecting C1's. Three fractionation-prone rare earths have essentially the same relative abundances in C1's and all other chondrite classes, and hence are apparently not fractionated in C1's.
Chemical fractionations in meteorites. I.
Condensation history of cooling gas of cosmic composition, stressing chondrite fractionation patterns
Chemical fractionations in meteorites. II.
Abundance of volatile elements in meteorites, comparing chondrite decrease for evidence of fractionations in solar nebula