Untersuchung von Calciumisotopieeffekten bei heterogenen Austauschgleichgewichten / Investigation of Isotopic Effects of Calcium in Heterogeneous Exchange Equilibria

1972 ◽  
Vol 27 (2) ◽  
pp. 126-133 ◽  
Author(s):  
Klaus Gustav Heumann ◽  
Karl Heinrich Lieser

The following heterogeneous exchange equilibria have been examined for isotopic effects: CaCO3/Ca(aq.)2⊕. Ca-GBHA/Ca(aq.)2⊕ and Ca(Dowex 50)2⊕/Ca(aq.)2⊕ (GBHA = glyoxal-bis (2-hydroxyanil)). The isotopic ratios 44Ca/40Ca and 48Ca/40Ca were determined by means of a mass spectrometer with a thermal ion source. In the system CaCO3/Ca(aq.)2⊕, the elementary separation factor was found to be less than 1‰ or 0,5‰ per mass unit, respectively.For the exchange in the system Ca-GBHA/Ca(aq.)2⊕ in the concentration range from 0.011 to 0.84 M an elementary separation factor less than 1‰ per mass unit was found; from a three-stage experiment at a calcium concentration of 1.23 M it was concluded that the elementary isotopic effect is less than 0.4‰ per mass unit. Therefore no isotopic fractionation is to be expected for precipitation of inorganic or organic calcium salts.An enrichment of the heavier calcium isotopes in the solution was found in the case of the exchange in a Dowex 50-X12 loaded column. The isotopic effect depends on the concentration of the hydrochloric acid used as the eluent.

1972 ◽  
Vol 27 (5) ◽  
pp. 492-500 ◽  
Author(s):  
Klaus G. Heumann

The isotopic effect of calcium was determined in several heterogeneous systems with the chelating resin Dowex Al. In one column experiment the dependence of the isotopic effect on the concentration of the hydrochloric acid as the eluent was studied. In the case of a 10-2 M HCl the isotope 48Ca was enriched in the solution. In the case of a 10-4 M HCl an enrichment of the isotope 40Ca was observed in the solution. This inversion of the isotopic effect can be explained by the formation of a calcium complex in the chelating resin occurring in a 10-4 M HCl solution.In another column experiment calcium was eluated with an EDTA solution. An enrichment of the heavier calcium isotopes was found in the solution. In this case only a small separation factor was found, because calcium forms a complex in the Dowex Al resin as well as in the EDTA solution.In a static ion exchange experiment on the system Ca (DOWEX A1)2+/Ca(aq.)2+ the elementary separation factor was measured. The heavier isotopes were enriched in the solution. For the ratio 44Ca/40Ca the elementary separation factor was found to be 1.0137, in the case of 48Ca/40Ca the separation factor was 1.0214.


2020 ◽  
Author(s):  
Jianghanyang Li ◽  
Xuan Zhang ◽  
Greg Michalski ◽  
John Orlando ◽  
Geoffrey Tyndall

Abstract. The nitrogen isotopic fractionations between NO and NO2 play a significant role in determining the nitrogen isotopic compositions (δ15N) of atmospheric NO2 and nitrate. This isotopic fractionation is controlled by a combination of equilibrium isotopic effect (EIE) and Leighton Cycle induced isotopic effect (LCIE), which are poorly constrained. We quantified this isotopic fractionation process by (1) measuring the isotopic fractionation factors of EIE and LCIE in a 10 m3 atmospheric simulation chamber and (2) mathematically calculating the relative importance of EIE and LCIE. Our results showed the enrichment factors of EIE and LCIE are 1.0275 ± 0.0012, and 0.9905 ± 0.005, respectively, at room temperature. We find that EIE is the dominate factor when NOx > 20 nmol mol−1, and LCIE is more important at low NOx concentrations (


2020 ◽  
Author(s):  
Rustam Lukmanov ◽  
Marek Tulej ◽  
Valentine Riedo ◽  
Niels Ligterink ◽  
Coenraad De Koning ◽  
...  

<p>In-situ Mars exploration requires new promising instrumentation that will be capable of delivering highly accurate chemical information about soils and rocks present at the Martian surface. Specific attention is drawn to the instruments that are capable of identifying extinct or extant microbes within the bulk of various solid samples (Tulej et al., 2015; Westall et al., 2015; Wiesendanger et al., 2018). A miniature Laser Ablation/Ionization Mass Spectrometer (LIMS) developed at the University of Bern is among the valid candidates (Wurz et al., 2012). The size of the mass analyzer is only Ø 60 mm × 160 mm and thus capable of being deployed on a rover or lander platform. In this contribution, we will present data collected from a 1.88 Ga Gunflint sample using a deep UV fs laser system as ablation ion source. The gunflint chert sample contains a population of microfossils entombed in the silica matrix and was chosen as a Martian analogue. Using the high stability of the UV laser and consequent uniform ablation, we performed large-scale spectra collection (90’000) in two modes - chemical imaging and depth profiling. With the current setup, we achieved a diameter of the analytical spot of ~10 µm for the depth profiling and ~5 µm for the imaging. Our results reveal that our LIMS instrument can identify the location of the microfossil lamination area as well as single microfossils by chemical means. We show how single mass unit spectral decomposition and subsequent kernel clustering reveal masses and intensity regions unique to the microfossils and inorganic host, thus providing the opportunity for automated identification of the spectra that are collected from the microfossils. We also show how transforming spectral intensities into spectral proximities can help to navigate the rich multidimensional datasets. We also address common interpretation problems in LIMS, when multiple mineralogical inclusions contribute to the output spectra acquired within the single analytical spot using ρ-networks and Principal Component Analysis (PCA). In combination with analysis of spectral proximities, this approach is particularly useful in attempts to assess the biogenicity of the putative terrestrial microfossils as well as potential Martian microfossils. Additionally, we discuss the data analysis pipeline and chemical composition of the microfossils and surrounding inorganic host in detail. </p> <p>Tulej M., Neubeck A., Ivarsson M., Riedo A., Neuland M. B., Meyer S., and Wurz P. (2015) Chemical Composition of Micrometer-Sized Filaments in an Aragonite Host by a Miniature Laser Ablation/Ionization Mass Spectrometer. Astrobiology, 15: 669-682.</p> <p>Westall F., Foucher F., Bost N., Bertrand M., Loizeau D., Vago J. L., Kminek G., Gaboyer F., Campbell K. A., Bréhéret J.-G. and others. (2015) Biosignatures on Mars: What, Where, and How? Implications for the Search for Martian Life. Astrobiology, 15: 998-1029.</p> <p>Wiesendanger R., Wacey D., Tulej M., Neubeck A., Ivarsson M., Grimaudo V., Moreno-García P., Cedeño-López A., Riedo A., Wurz P. and others. (2018) Chemical and Optical Identification of Micrometer-Sized 1.9 Billion-Year-Old Fossils by Combining a Miniature Laser Ablation Ionization Mass Spectrometry System with an Optical Microscope. Astrobiology, 18: 1071-1080.</p> <p>Wurz P., Abplanalp D., Tulej M., Iakovleva M., Fernandes V. A., Chumikov A., and Managadze G. G. (2012) Mass spectrometric analysis in planetary science: Investigation of the surface and the atmosphere. Solar System Research, 46: 408-422.</p> <p> </p>


2020 ◽  
Vol 71 (2) ◽  
pp. 209-217
Author(s):  
Virgil Badescu

The aim of this article in continuation of Parts I [1] and II [2] is the interpretation of the TEOS mass spectrum as a precursor in the sol-gel process. In Part I [1] the primary fragmentation ions at masses 207, 193, 179 and 163 were obtained experimentally by B/E linked scan by radical induced fragmentation reactions. In Part II [2] eliminations of neutral fragments from the primary ions and the obtained ions by consecutive elimination reactions were evidenced experimentally by the B/E and B/E(1-E)1/2 linked scans. In this third and final Part of interpretation of the TEOS mass spectrum, the separation of ions by mass spectrometry at high resolutions of 5000 and 6600, relative to standard resolution 1000, and measurements of the M+1 and M+2 isotopic effects at the resolution of 5000 are presented. The separation of the ions with nominal mass 105 at high resolution is detailed.


2007 ◽  
Vol 73 (7) ◽  
pp. 2135-2143 ◽  
Author(s):  
Shaun M. Baesman ◽  
Thomas D. Bullen ◽  
James Dewald ◽  
Donghui Zhang ◽  
Seamus Curran ◽  
...  

ABSTRACT Certain toxic elements support the metabolism of diverse prokaryotes by serving as respiratory electron acceptors for growth. Here, we demonstrate that two anaerobes previously shown to be capable of respiring oxyanions of selenium also achieve growth by reduction of either tellurate [Te(VI)] or tellurite [Te(IV)] to elemental tellurium [Te(0)]. This reduction achieves a sizeable stable-Te-isotopic fractionation (isotopic enrichment factor [ε] = −0.4 to −1.0 per ml per atomic mass unit) and results in the formation of unique crystalline Te(0) nanoarchitectures as end products. The Te(0) crystals occur internally within but mainly externally from the cells, and each microorganism forms a distinctly different structure. Those formed by Bacillus selenitireducens initially are nanorods (∼10-nm diameter by 200-nm length), which cluster together, forming larger (∼1,000-nm) rosettes composed of numerous individual shards (∼100-nm width by 1,000-nm length). In contrast, Sulfurospirillum barnesii forms extremely small, irregularly shaped nanospheres (diameter < 50 nm) that coalesce into larger composite aggregates. Energy-dispersive X-ray spectroscopy and selected area electron diffraction indicate that both biominerals are composed entirely of Te and are crystalline, while Raman spectroscopy confirms that they are in the elemental state. These Te biominerals have specific spectral signatures (UV-visible light, Raman) that also provide clues to their internal structures. The use of microorganisms to generate Te nanomaterials may be an alternative for bench-scale syntheses. Additionally, they may also generate products with unique properties unattainable by conventional physical/chemical methods.


2020 ◽  
pp. 132-138
Author(s):  
О. Musich ◽  
A. Zubko ◽  
О. Demyanуuk

Isotopic effects occurring in living organisms due to metabolism are analyzed. The phenomenon of metabolism is considered in the classical sense as a combination of biochemical reactions (mainly enzyma­tic) that take place in the cells of living beings and provide the cleavage, synthesis and interconversion of complex compounds. The scope of use of natural isotopes is wide and diverse. Isotopes are carriers of information about the birth and transformation of molecules, and isotope fractionation is a chemical characteristic of a substance. Isotope metabolism consists in the intermolecular fractionation of isotopes at separate stages of biochemical reactions, namely the cleavage, synthesis and interconversion of complex compounds caused by differences in the structure and fundamental properties of isotope nuclei. It is proved that the fractionation of isotopes in chemical and biochemical reactions due to isotopic effects is based on two fundamental properties of atomic nuclei — mass and magnetic moment. The kinetic (mass-depen­ dent) isotopic effect distributes the isotopic nuclei by their masses, and the magnetic one fractionates the nuclei by their magnetic moments. The kinetic isotopic effect depends on the magnitude of the difference in the masses of isotopic molecules, temperature and the difference in the activation energies of isotopic forms. The magnetic isotope effect depends on the reaction rate in a single cell, its projection, magnetic moment and energy of electron-nuclear interaction. It is determined that the fractionation of isotopes in living organisms is that the relative content of one of the isotopes in this compound increases by reducing its content in the other. As a result, there is a fractionation of isotopes within one biological object.


Radiocarbon ◽  
1989 ◽  
Vol 31 (03) ◽  
pp. 284-291 ◽  
Author(s):  
Maurice Arnold ◽  
Edouard Bard ◽  
Pierre Maurice ◽  
Helene Valladas ◽  
J C Duplessy

The standard procedure for measuring 14C at the Gif-sur-Yvette Tandetron AMS facility is described. A new sample manipulator and automated measurements are being used and have been operational for six months. Evidence of isotopic fractionation in the sputter ion source is provided. We take this into account by measuring the 13C/12C ratio of the sample in the accelerator.


2021 ◽  
Vol 118 (52) ◽  
pp. e2114221118
Author(s):  
François Robert ◽  
Marc Chaussidon ◽  
Adriana Gonzalez-Cano ◽  
Smail Mostefaoui

Enrichment or depletion ranging from −40 to +100% in the major isotopes 16O and 24Mg were observed experimentally in solids condensed from carbonaceous plasma composed of CO2/MgCl2/Pentanol or N2O/Pentanol for O and MgCl2/Pentanol for Mg. In NanoSims imaging, isotope effects appear as micrometer-size hotspots embedded in a carbonaceous matrix showing no isotope fractionation. For Mg, these hotspots are localized in carbonaceous grains, which show positive and negative isotopic effects so that the whole grain has a standard isotope composition. For O, no specific structure was observed at hotspot locations. These results suggest that MIF (mass-independent fractionation) effects can be induced by chemical reactions taking place in plasma. The close agreement between the slopes of the linear correlations observed between δ25Mg versus δ26Mg and between δ17O versus δ18O and the slopes calculated using the empirical MIF factor η discovered in ozone [M. H. Thiemens, J. E. Heidenreich, III. Science 219, 1073–1075; C. Janssen, J. Guenther, K. Mauersberger, D. Krankowsky. Phys. Chem. Chem. Phys. 3, 4718–4721] attests to the ubiquity of this process. Although the chemical reactants used in the present experiments cannot be directly transposed to the protosolar nebula, a similar MIF mechanism is proposed for oxygen isotopes: at high temperature, at the surface of grains, a mass-independent isotope exchange could have taken place between condensing oxides and oxygen atoms originated form the dissociation of CO or H2O gas.


1984 ◽  
Vol 39 (9) ◽  
pp. 1230-1235 ◽  
Author(s):  
V. P. Tarasov ◽  
V. I. Privalov ◽  
Yu. A. Buslaev ◽  
U. Eichhoff

Changes in X-nuclei screening and scalar spin-spin X-H(D) coupling constants induced by the H-D substitutions in isotopomers [XH4-nDn] (X = N, Al, Ga) have been determined by 14,1l5N, 27 AI, 69,71Ga NMR. Isotopic chemical shifts of nuclei 51V, 53Cr, 99Tc induced by the 16O-18O substitution have been measured for tetra-oxo complexes [VO4]3-, [CrO4]2-, and [TcO4]-. The deuterium-induced secondary isotopic effect on the screening constant of the X nuclei and the scalar spin-spin X-H(D) coupling are correlated with the X-H bond length in [XHJ for the row X = N, C, B, Al, Ga, As the internuclear X-H distance increases, the isotopic shift of the X nuclei with respect to the signal from [XHJ rises linearly on H-D substitution from a negative value for [NH4]+, CH4 to a positive value (the downfield shift) for [GaH4]-. When D is substituted for H in [XH4] the X-H spin-spin coupling constant decreases for X = N, C, B, Al, Ga (the secondary isotopic effect). The magnitude and sign of the secondary isotopic effects on the screening constants of the X nuclei in [XH4] and [XO4] depend on the atomic number of the X element. With the increasing atomic number in the period the isotopic shift to high field rises in magnitude, while with the increasing atomic number in the group the isotopic upfield shift drops in the absolute value and can even change sign in the substitution of the ligand light isotope by a heavier isotope.


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