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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 127 records · Page 7
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NASA NTRSDate not supplied

Stable Chlorine Isotope Measurements of Astromaterials Using the Cs-Sputter Negative Ion Source of an Accelerator Mass Spectrometer

The volatile element Cl can be lost during the formation and evolution of planetary bodies, leading to fractionation of its two stable isotopes 35Cl and 37Cl. Chlorine isotope variations (reported as δ37Cl in parts per thousand (‰) relative to Standard Mean Ocean Chloride, SMOC) [1] are documented to exceed 80‰ [2] between different lunar rock samples and have been variably interpreted as the fingerprint of degassing during accretion, magma ocean, or volcanic portions of lunar history[3,4].The large intersample and intrasample variations observed by both bulk isotope ratio mass spectrometry (IRMS) and in-situ secondary ion mass spectrometry (SIMS) methods are difficult to interpret in part because of a paucity of bulk Cl isotope measurements (Figure 1).This lack of high-precision bulk data is due to the relative rarity of IRMS laboratories capable of making these high precision measurements on small samples of precious planetary materials such as those returned by human or robotic exploration. Here we present a new method for performing high precision δ37Cl measurements using the Cs-sputter negative ion source of an existing accelerator mass spectrometer. A brief description of the methods used for this work is followed by the results of our δ37Cl measurements and a discussion of the technique’s possible applications.

Chlorine↗
NASA NTRS2022

Unexpected Repartitioning of Stratospheric Inorganic Chlorine after the 2020 Australian Wildfires

The inorganic chlorine (Cl y ) and odd nitrogen (NO y ) chemical families influence stratospheric O 3 . In January 2020 Australian wildfires injected record-breaking amounts of smoke into the southern stratosphere. Within 1-2 months ground-based and satellite observations showed Cl y and NO y were repartitioned. Compared to decadal means, lower stratospheric (LS) HCl columns declined by ~30% between March and May while ClONO 2 columns increased by 40-50%. The Cl y perturbations recovered from June to October. The LS NO 2 decreased from February to April, consistent with sulfate aerosol reactions, but returned to typical values by June - months earlier than the Cl y recovery. Transport tracers show an air mass change explains the observed O 3 decrease after April. Simulations assuming wildfire smoke behaves identically to sulfate aerosols couldn’t reproduce observed Cl y changes, suggesting that their composition and chemistry differs from sulfate aerosols. This undermines our ability to predict ozone in a changing climate.

middle atmosphere chemistry and composition↗
NASA NTRS1999

Measurements of Chlorine Partitioning in the Winter Arctic Stratosphere

Under the extremely cold conditions in the polar winter stratosphere, heterogeneous reactions involving HCl and CIONO(sub 2) on the surfaces of polar stratospheric cloud particles can release large amounts of reactive chlorine from these reservoirs leading to rapid chemical loss of ozone in the Arctic lower stratosphere during late winter and early spring.

chlorine partitioning stratosphere polar processes↗
NASA NTRS1995

Chlorine Partitioning in the Arctic Vortex During Winter 1995 Derived From Submillimeterwave Remote Sensing and in Situ Constituent Measurements

High altitude balloon flights of a combined payload of the Submillimeterwave Limb Sounder and the whole air sampler instruments were performed on 27 January 1995 and 08 March 1995. Both flights were launched from sweden as part of the Second European Stratospheric Arctic and Mid-latitude Experiment (SESAME). Results of the first flight suggest that most of the available chlorine had been converted to CLOx in the observed air parcel, while warmer air in the second flight had much more HCl than CLOx.

Arctic vortex stratosphere chlorine remote sensing↗
NASA NTRS1994

Profiles of Stratospheric Chlorine Nitrate from ATMOS/ATLAS 1 Infrared Solar Occultation Spectra

Stratospheric volume mixing ration profiles of chlorine nitrate have been retrieved from 0.01-cm(sub -1) resolution infrared solar occutation spectra recorded at latitudes between 14 degrees N and 54 degrees S by the Atmospheric Trace Molecule Spectroscopy (ATMOS) Fourier transform spectrometer during the ATLAS 1 shuttle mission (March 24 to April 2, 1992).

chlorine nitrate ATMOS/ATLAS spectroscopic paramet↗
NASA NTRS2004

Chlorine stable isotopes in sedimentary systems: does size matter?

Stable isotope abundances vary because of size differences. The chlorine stable isotope system was one of the first described theoretically, but had a slow, disappointment strewn development, relative to other elements. Method improvement gave only small, but significant, differences in compositions of geological materials. Eventually, brines and groundwater chlorides gave larger differences. Physical processes like diffusion and adsorption, probably are the main controls of groundwater compositions. Recent work on anthropogenic groundwater contaminants shows variations resulting from manufacturing processes; implying possibilities of tracing sources.

chlorine stable isotopes↗
NASA NTRS1966

Process produces chlorinated aromatic isocyanate in high yield

Tetrachloreterephthaloyl chloride reacts with sodium azide in an atmosphere of nitrogen to form a high yield of tetrachloro-p-phenylene diisocyanate. The chlorinated diisocyanate should have application as an intermediate in the preparation of polyurethane foams. The high halogen content would impart added flame resistance to these foams.

Trischler, F.↗