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Abundances of O, Si, Al, and Mn determined in a Luna 20 fines sample by instrumental neutron activation analysis are presented and compared with those found in Apollo lunar soil samples. The results obtained include the finding that O/Si ratios exhibit very little variability among fines samples from various lunar landing sites, whereas the Al/Si ratio is highly variable.
Review of the abundances of 24 major, minor, and trace elements measured by instrumental neutron activation analysis in Luna 20 metaigneous rocks, breccia, and soil, and in Apollo 16 soils. The similarities and differences observed are discussed. The bulk compositions of Luna 20 and Apollo 16 rocks and soils show close similarity between the two highland sites. Interelement correlations observed previously for maria are also found in highland samples. Luna 20 and Apollo 16 soils are low in alkalis. Both soils show an apparent Cd-Zn rich component similar to that observed at the mare sites and high Tl abundances relative to mare sites.
Despite the information available (Mason, 1971) on trace elements in different types of meteorites, relatively little is known about the distribution of these elements among the individual mineral phases. The mineral phases including olivine, orthopyroxene, clinipyroxene, troilite, nickel-iron, plagioclase, chromite, and the phosphates were separated from several meteorites. The purified minerals were analyzed for trace and minor elements by spark source mass spectrometry and instrumental neutron activation analysis. The elements are classified as siderophile, lithophile, and chalcophile.
Samples of ASTM type A jet fuel were analyzed for trace-element content by instrumental neutron activation techniques. Forty-nine elements were sought. Only ten, aluminum, gold, indium, lanthanum, titanium, vandium, barium, dysprosium, tellurium, and uranium, were observed at levels above the detection limits encountered; of these only aluminum, titanium, and barium were present at concentrations greater than 0.1 ppm. Estimates of exhaust gas concentrations are made, and the ambient contribution at or near airports is calculated by using the Los Angeles International Airport dispersion model. It is shown that the ambient contribution is about an order of magnitude below typical urban levels for virtually all elements sought.
Ninety sub-samples of Apollo 15 materials have been analyzed by instrumental neutron activation analysis techniques for as many as 21 elements. Soil and soil breccia compositions show considerable variation from station to station although at any given station the soils and soil breccias were compositionally very similar to one another. Mixing model calculations show that the station-to-station variations can be related to important local geologic features. These features include the Apennine Front, Hadley Rille and the ray from the craters Aristillus or Autolycus. Compositional similarities between soils and soil breccias at the Apollo 15 site indicate that the breccias and soils are related in some fundamental way, although the exact nature of this relationship is not yet fully understood.
The authors analyzed 22 Apollo 15 samples, 21 Apollo 16 samples, 4 Luna 20 samples, and 6 Apollo 17 samples for 26 to 30 major, minor, and trace elements by instrumental neutron activation analysis (INAA). Major attention is given to Apollo 16 results and recent Apollo 17 data. The roster of elements via INAA has been extended to include Nd, Ni, Ir, and Au in the Apollo 16 and 17 samples. The latter three elements are highly abundant in these samples. Sample preparation, activation conditions, and the detailed INAA analytical procedure are essentially the same as reported by Laul and Schmitt (1973).
An approach to the analysis of a very large elemental concentration data set. The particular data considered was generated by instrumental neutron activation and emission spectroscopy analyses of over 750 24-hour ambient air particulate samples collected at 16 sites in Cleveland, Ohio, during the 15 months from August 1971 thru October 1972. Examples are presented that show the use of multiple approaches to interpreting the data, including pairwise correlation statistics, selective data plotting and cluster analysis.
The techniques available for source identification are reviewed: remote sensing, injected tracers, and pollutants themselves as tracers. The use of the large number of trace elements in the ambient airborne particulate matter as a practical means of identifying sources is discussed. Trace constituents are determined by sensitive, inexpensive, nondestructive, multielement analytical methods such as instrumental neutron activation and charged particle X-ray fluorescence. The application to a large data set of pairwise correlation, the more advanced pattern recognition-cluster analysis approach with and without training sets, enrichment factors, and pollutant concentration rose displays for each element is described. It is shown that elemental constituents are related to specific source types: earth crustal, automotive, metallurgical, and more specific industries. A field-ready source identification system based on time and wind direction resolved sampling is described.
Instrumental neutron activation analyses were conducted to nine Apollo 16 samples and 23 Apollo 17 samples. Radiochemical neutron activation analyses were carried out in the case of six Apollo 16 boulder-2 rocks, five Apollo 17 soils, and one Apollo 16 soil. The elemental abundances obtained are presented in tables and the significance of the analytical results is discussed. Attention is also given to interelement correlations.
Samples of ASTM type A jet fuel were analyzed for trace element content by instrumental neutron activation techniques. Forty-nine elements were sought. Only ten, aluminum, gold, indium, lanthanum, titanium, vanadium, barium, dysprosium, tellurium, and uranium, were observed at levels above the detection limits encountered; of these only aluminum, titanium, and barium were present at concentrations greater than 0.1 ppm. Estimates of exhaust gas concentrations are made, and the ambient contribution at or near airports is calculated by using the Los Angeles International Airport dispersion model. It is shown that the ambient contribution is about an order of magnitude below typical urban levels for virtually all elements sought.
Various applications and projected applications of active microwave instruments for studying water resources. Most applications involve use of an imaging system operating primarily at wavelengths of less than 30 cm (i.e., K-, X-, and L-bands). Discussion is also included concerning longer wavelength nonimaging systems for use in sounding polar glaciers and icecaps (e.g., Greenland and the Antarctic). The section is divided into six topics: (1) stream runoff, drainage basin analysis, and floods, (2) lake detection and fluctuating levels, (3) coastal processes and wetlands, (4) seasonally and permanently frozen (permafrost) ground, (5) solid water resources (snow, ice, and glaciers), and (6) water pollution.
Concentrations of 75 chemical constituents in the airborne particulate matter were measured in Cleveland, Ohio, during 1971 and 1972. Values covering a 1-year period (45 to 50 sampling days) at each of 16 sites are presented for 60 elements. A lesser number of values is given for sulfate, nitrate, fluoride, acidity, 10 polynuclear aromatic hydrocarbon compounds, and the aliphatic hydrocarbon compounds as a group. Methods used included instrumental neutron activation, emission spectroscopy, gas chromatography, combustion techniques, and colorimetry. Uncertainties in the concentrations associated with the sampling procedures, the analysis methods, the use of several analytical facilities, and samples with concentrations below the detection limits are evaluated in detail. The data is discussed in relation to other studies and source origins. The trace constituent concentrations as a function of wind direction are used to suggest a practical method for air pollution source identification.
Compact instrument has active and reference sides consisting of tubes that elongate in response to increasing interior pressures. Relative displacement of tubes is measured by linear variable differential transformer to determine pressure on active side. Device needs no internal cooling, thus eliminating condensation problem with gases containing saturated steam.
Developments in applying aerospace medical technology to the design and production of medical equipment and instrumentation are reported. Projects described include intercranial pressure transducers, leg negative pressure devices, a synthetic speech prosthesis for victims of cerebral palsy, and a Doppler blood flow instrument. Commercialization activities for disseminating and utilizing NASA technology, and new biomedical problem areas are discussed.
Concentrations of 60 chemical elements in the airborne particulate matter were measured at 16 sites in Cleveland, OH over a 1 year period during 1971 and 1972 (45 to 50 sampling days). Analytical methods used included instrumental neutron activation, emission spectroscopy, and combustion techniques. Uncertainties in the concentrations associated with the sampling procedures, the analytical methods, the use of several analytical facilities, and samples with concentrations below the detection limits are evaluated in detail. The data are discussed in relation to other studies and source origins. The trace constituent concentrations as a function of wind direction are used to suggest a practical method for air pollution source identification.
An investigation has been conducted of the ureilites and the achondrite Chassigny to elucidate differences in their petrogenesis. The experimental studies reported include the determination of elemental abundances by instrumental neutron activation analysis. Attention is given to lithophile elements in ureilites, lithophile elements in Chassigny, the relationship between Chassigny and the nakhlites, and siderophile trace elements in the ureilites.
A total of 27 major, minor and trace element abundances in 27 fine fractions (smaller than 1 mm) of core 60009 were determined by instrumental neutron activation analysis. The core was divided into five chemically defined stratigraphic units. Unit 1, 0.5 to 11.5 cm, is characterized by low Ca and Al abundances which increase towards the base of the unit and high ferromagnesian element abundances. Unit 2, 11.5 to 19.8 cm, has higher abundances of Ca and Al and lower abundances of ferromagnesian elements than unit 1 and is much more uniform. Unit 3, 19.8 to 25.7 cm is very similar to unit 1 and may have been derived from the same source region. Unit 4, 25.7 to 29.6 cm, has the highest Ca and Al abundances of all the units defined and the lowest abundances of ferromagnesian elements. The ferromagnesian elements generally decrease in abundance towards the base of the unit. This unit exhibits a positive Eu anomaly. Unit 5, 29.6 to 31.5 cm, has the lowest Ca and Al abundances and highest ferromagnesian abundances of all the units. The unit boundaries correspond well with major unit boundaries characterized by Duke and Nagle (1974) on the basis of textural parameters, structure, composition and thickness of layers.
Results are presented for a study in which high-precision instrumental neutron activation analysis was applied to determine the abundances of seven rare-earth and nine other elements in two grain-size fractions (90 to 150 microns and less than 20 microns) of eight soils from the Taurus-Littrow Valley floor and one Apollo 11 bulk-soil fraction with grain sizes of less than 1 mm. Compositional differences between the two size fractions of two valley-floor soils are examined, and mixing of soil components is investigated. It is found that a five-component mixing model describes very adequately the chemical composition of bulk soils with grain sizes of less than 1 mm as mixtures of local Apollo 17 rock types (basalt, anorthositic gabbro, noritic breccia), orange glass, and meteorites, but does not describe well the chemical compositions of the other two size fractions. A ten-component model is used to show that the compositions of those two size fractions can be well represented as mixtures of the five components if the mineralogy and chemical composition of the basalt component are allowed to vary in the size fractions.