Isotopic fractionation in low temperature ion–molecule exchange reactions: Enrichment of22Ne in Ne+nclusters formed by association in an ionized free jet

1990 ◽  
Vol 92 (12) ◽  
pp. 7349-7355 ◽  
Author(s):  
Michael J. DeLuca ◽  
Donna M. Cyr ◽  
William A. Chupka ◽  
Mark A. Johnson
2006 ◽  
Vol 361 (1474) ◽  
pp. 1715-1720 ◽  
Author(s):  
M Anand ◽  
S.S Russell ◽  
R.L Blackhurst ◽  
M.M Grady

Recent spacecraft and lander missions to Mars have reinforced previous interpretations that Mars was a wet and warm planet in the geological past. The role of liquid water in shaping many of the surface features on Mars has long been recognized. Since the presence of liquid water is essential for survival of life, conditions on early Mars might have been more favourable for the emergence and evolution of life. Until a sample return mission to Mars, one of the ways of studying the past environmental conditions on Mars is through chemical and isotopic studies of Martian meteorites. Over 35 individual meteorite samples, believed to have originated on Mars, are now available for lab-based studies. Fe is a key element that is present in both primary and secondary minerals in the Martian meteorites. Fe-isotope ratios can be fractionated by low-temperature processes which includes biological activity. Experimental investigations of Fe reduction and oxidation by bacteria have produced large fractionation in Fe-isotope ratios. Hence, it is considered likely that if there is/were any form of life present on Mars then it might be possible to detect its signature by Fe-isotope studies of Martian meteorites. In the present study, we have analysed a number of Martian meteorites for their bulk-Fe-isotope composition. In addition, a set of terrestrial analogue material has also been analysed to compare the results and draw inferences. So far, our studies have not found any measurable Fe-isotopic fractionation in bulk Martian meteorites that can be ascribed to any low-temperature process operative on Mars.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Tong Zhu ◽  
Fabio Orlandi ◽  
Pascal Manuel ◽  
Alexandra S. Gibbs ◽  
Weiguo Zhang ◽  
...  

AbstractPreparing materials which simultaneously exhibit spontaneous magnetic and electrical polarisations is challenging as the electronic features which are typically used to stabilise each of these two polarisations in materials are contradictory. Here we show that by performing low-temperature cation-exchange reactions on a hybrid improper ferroelectric material, Li2SrTa2O7, which adopts a polar structure due to a cooperative tilting of its constituent TaO6 octahedra rather than an electronically driven atom displacement, a paramagnetic polar phase, MnSrTa2O7, can be prepared. On cooling below 43 K the Mn2+ centres in MnSrTa2O7 adopt a canted antiferromagnetic state, with a small spontaneous magnetic moment. On further cooling to 38 K there is a further transition in which the size of the ferromagnetic moment increases coincident with a decrease in magnitude of the polar distortion, consistent with a coupling between the two polarisations.


1993 ◽  
Vol 48 (12) ◽  
pp. 1737-1741 ◽  
Author(s):  
W. Preetz ◽  
E. Parzich

A technique to record Raman spectra of deeply coloured solids at low temperature (10 K) is described, using a closed cycle He-cryogenerator and moving the cell by an excentric attachment. The spectroscopic resolution is considerably enhanced as compared to room temperature or 80 K measurements. This is obvious from splittings of Raman lines observed at 10 K on the isotopomers Cs2[Pt35Cln37Cl6-n], n = 1 -5, which have been prepared by stereospecific ligand exchange reactions. As a consequence of lowered symmetry the degenerate valence vibration v2(Eg, Oh) is split into two lines for the isotopomers belonging to the point groups D4h, C4v and C2v. The isotopic effects calculated by normal coordinate analysis are in good agreement with the observed frequencies.


2013 ◽  
Vol 42 (35) ◽  
pp. 12596 ◽  
Author(s):  
Haitao Zhang ◽  
Louis V. Solomon ◽  
Don-Hyung Ha ◽  
Shreyas Honrao ◽  
Richard G. Hennig ◽  
...  

1992 ◽  
Vol 271 ◽  
Author(s):  
M. E. Villafuerte-Castrejón ◽  
A. Aragón-Piña

ABSTRACTIon-exchange reactions, particularly with molten salts, are a convenient low temperature route to prepare new materials. Six different complex oxides (KTaO3, K2Ti4O4, NaAlSiO4, Na2Si2O5,ß-NaAlO2 and K2Ge4O9) were reacted with different salts (NaCI, KC1, Na2SO4, NaNO3, LiCl and LiNO3) by the ion exchange route with molten salts. In this work, new phases and substitution reactions are reported.


Geology ◽  
2021 ◽  
Author(s):  
Jean Milot ◽  
Janne Blichert-Toft ◽  
Mariano Ayarzagüena Sanz ◽  
Chloé Malod-Dognin

Silver played a key role in the progressive monetization of early Mediterranean civilizations. We combine Pb and Ag isotopes with volatile trace elements (Bi, Sb, and As) to assess whether, during the Roman occupation of Iberia, galena constituted a significant source of silver. We find that the Pb and Ag isotopic compositions of 47 samples of galena from eight different Iberian mining provinces, many of them exploited during Roman times, are uncorrelated. This indicates that their respective isotopic variabilities depend on different petrogenetic processes. Moreover, the range of Ag isotopic abundances is approximately six times wider than that displayed worldwide by silver coins in general and Roman silver coins in particular. Although galena from the Betics provides the best fit for Pb isotopes with Roman coins, their fit with Ag isotopic compositions is at best sporadic. We suggest that, together with Sb, Bi, and As, silver is primarily derived from fluids boiled off from differentiated mantle-derived magmas. These fluids, in turn, reacted with preexisting galena and functioned as a silver trap. Lead sulfides with ε109Ag of ~0 and unusually rich in Ag, Sb, Bi, and As were the most probable sources of ancient silver, whereas samples with ε109Ag departing significantly from ~0 reflect low-temperature isotopic fractionation processes in the upper crust.


Author(s):  
I. E. Locci ◽  
M. V. Nathal

The B2 aluminide NiAl has potential as a high temperature structural material, although its lack of low temperature toughness is a major obstacle. One strategy for improving low temperature toughness is by grain refinement. Fortunately, fine grained intermetallics appear to retain their strengths to much higher fractions of their melting point than do pure metals and alloys. The purpose of this study was to investigate the effects of melt spinning and small W additions on the grain size and stability of NiAl.Two alloys of the same matrix composition, equiatomic NiAl, were examined. One also contained 0.5 W at% (NiAl+W). The alloys were cast as ribbon ∼45 pm thick by ∼2.5 mm wide using a free jet melt spinning apparatus. To simulate consolidation conditions, sections of ribbon were annealed for 1 hour at either 1273 or 1573 °K in purified argon. Optical, X-ray and electron analyses of the as-spun and annealed ribbons were performed.


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