Geology topics
Publications and source records attributed to F.O. Simon.
Platinum, palladium and rhodium have been determined in 18 U.S. Geological Survey reference materials by graphite furnace atomic absorption spectrometry after preconcentration by the classical leadfree assay technique. A comparison with literature values shows clearly the need for additional data on these samples before “best” values can be assigned.
Rhenium is determined by spectrophotometry of the tellurium sol formed by the reduction of tellurate by stannous chloride under the catalytic influence of rhenium. A detailed investigation of the conditions for high sensitivity and stability at lowest concentration levels of rhenium is presented as well as the behavior of 26 ions. The method is applied to the determination of some tenths of 1 p.p.m. or more of rhenium in a 1-mg. aliquot of mineralized rocks, mixtures of molybdenite and rocks, and molybdenite concentrates. The practical quantity limit of detection is 2x -10 gram of rhenium. Samples are decomposed with a mixture of CaO, CaCl 2 , and MgO. On leaching, most constituents of the sample are precipitated either as calcium salts or hydroxides, except for rhenium and a small amount of molybdenum which pass into the filtrate. Residual molybdenum is removed by extraction with 8-quinolinol in chloroform. Better than 95% recoveries are obtained with two fusions with flux.
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Approximately 20 kg of the Herrin (No. 6) coal was collected from a strip mine in St. Clair County, Ill. A 10-kg portion was ground to -60 mesh, homogenized, and riffled into 128 splits of 70-80 g each. Homogeneity of these splits was confirmed by moisture, ash, and sulfur analyses of six randomly selected splits. Results of these analyses were within the ASTM (American Society for Testing and Materials) guidelines for interlaboratory precision. Splits of the Herrin (No. 6) coal were then transmitted to more than 30 laboratories for analysis. Low-temperature plasma oxidation was used to isolate inorganic matter for quantitative chemical and mineralogical analysis. Despite a wide variation in ashing conditions, only minor variations in ash yields were obtained; these variations were attributed to differences in operating temperature and moisture content. Mineralogical analyses of low-temperature ash (LTA) concentrates prepared by five different laboratories indicated variations within the limits of analytical error. The mean values, in weight percent, for the major minerals are as follows: calcite, 9; quartz, 20; pyrite, 23; kaolinite, 14; and illite+mixed-layer clays, 31. Normative mineralogical calculations and Fourier transform infrared analysis (FTIR) yielded results similar to those obtained from X-ray diffraction (XRD). Choosing appropriate mineral standards was found to be critical for the proper use of analytical techniques such as XRD and FTIR. Good interlaboratory agreement was obtained for most major, minor, and trace elements despite differences in analytical procedures and in the type of sample analyzed (coal, high-temperature ash, or LTA). Discrepancies between analyses for zinc, strontium, manganese, and iron may be attributed to sampling inhomogeneity problems. Mossbauer spectroscopy showed that approximately 44 percent of the pyritic sulfur was lost through weathering in the first year after preparation of the interlaboratory sample. Szomolnokite and possibly coquimbite and jarosite were also identified. Scanning electron microscopy studies indicated ubiquitous pyrite framboids and, less commonly, euhedral crystals, skeletal grains, irregularly shaped particles, and vein fillings. Minor accessory minerals such as rare-earth phosphates and possibly silicates, zircon, barium sulfate, titanium oxide, and sphalerite were also found. The textural evidence indicates that the minerals in the banded material are detrital whereas the minerals occurring as vein and pore fillings are authigenic. Magnetic measurements indicate that coal crushed in a steel pulverizer is contaminated by small quantities of abrasion fragments from the crusher, which seriously affect the measured magnetic properties of the coal.
The pattern of sulfur transformation in peat across the Everglades basin indicates that pyrite formation in organic-rich swamps depends on the use of organic oxysulfur compounds in dissimilatory respiration by sulfur-reducing bacteria. This paragenesis explains the primary distribution of sulfur compounds in low-sulfur coals and possibly in most coals and many organic-rich soils and sediments. It also accounts for the occurrence of framboidal pyrite bound in fossil tissue in coal and sediments.
This report includes all the analytical data on 617 coal samples from 8 states east of the Mississippi River. The samples from each state are, Pennsylvania 71, Ohio 40, West Virginia 252, Virginia 72, Kentucky 27, Tennessee 27, Alabama 20, and Indiana 108. The U.S. Geological Survey has quantitatively determined the amounts of 35 major, minor and trace elements in each sample. It has also searched for 35 other trace elements using semi-quantitative spectrographic methods. In addition, the Coal Analysis Section of the Department of Energy has provided proximate and ultimate analyses, Btu, forms of sulfur, free swelling index, and ash fusion temperatures on 491 samples. Comparison of the geometric means of these samples with 331 bituminous coal samples of the Appalachian region reported by Swanson and others (1976) are as follows. As shown by the means for ultimate and proximate analyses small differences exist between the two sets of data, only the moisture content and oxygen are significantly different. The forms of sulfur and heat of combustion are also similar. The means for the major and minor oxides in ash are similar for SiO 2 , Al 2 O 3 , CaO, MgO, K 2 O 3 and TiO 2 . Na 2 O is significantly lower and Fe 2 O 3 and MnO higher in the analyses of the 617 samples of this report. Most means for the trace elements in the coals studied for this report are lower. Only Be is significantly higher in these coals.
A method is described for the atomic-absorption determination of beryllium in geological materials, that utilizes electrothermal atomization after a separation by solvent extraction. Samples are decomposed with hydrofluoric acid and nitric acid in Teflon-lined pressure decomposition vessels. Beryllium is isolated by its extraction as beryllium acetylacetonate at pH 8 into xylene and back-extraction in 3 M hydrochloric acid. The method has been successfully applied to the determination of beryllium in 14 U.S. Geological Survey standard rocks. Four subsamples from four bottles of each standard sample were analysed in random order. The mean beryllium contents (ppm) are: AGV-1, 1.98; PCC-1, 0.024; MAG-1, 2.84; BHVO-1, 0.90; DTS-1, 0.026; SCo-1, 1.74; SDC-1, 2.52; BCR-1, 1.44; GSP-1, 1.22; SGR-1, 0.86; QLO-1, 1.83; RGM-1, 2.21; STM-1, 8.75; G-2, 2.29. An analysis of variance shows that all the samples may be considered homogeneous at F 0.95 except AGV-1 and DTS-1 which may be considered homogeneous at F 0.99 .
Chemical leaching and analysis of the sulflde portion of rocks from a section of the Basal zone of the Stillwater Complex demonstrate that mole fractions of nickel, copper, cobalt, and sulfur in the sulfldes show trends and repeating patterns when plotted against stratigraphic position. These patterns are attributed to differentiation of immiscible sulflde liquids probably in response to differentiation of basaltic magma. Changes in composition of the immiscible sulflde liquids could most readily take place during the collection of the sulflde from the basaltic magma or during the crystallization of the sulflde liquid to the present assemblages of minerals.
Thallium was determined in 16 USGS standard rocks by atomic absorption spectroscopy in which a heated graphite atomizer was used after extraction as thallium iodide into amyl acetate. Four subsamples from four bottles of each standard sample, except G-1 and W-1, were analyzed in random order, and the average thallium contents in parts per million (as Tl) were AGV-1, 0.41; GSP-1, 1.63; G-2, 1.08; BCR-1, 0.35; SDC-1, 0.80; MAG-1, 0.79; BHVO-1, 0.049; SCO-1, 0.79; SGR-1, 0.34; QLO-1, 0.23; RGM-1, 1.07 ; STM-1, 0.30; DTS-1, <0.005; and PCC-1, <0.005. The analysis of variance showed that all samples may be considered homogeneous at F 0.975 and only GSP-1 may be considered heterogeneous at F 0.95 . The Tl contents of G-1 and W-1 are 1.0 and 0.12 ppm, respectively.
Chromium, determined by neutron-activation analysis in a suite of rocks and minerals from the southern California batholith, shows Cr concentrated in the mafic differentiates, decreasing as the more felsic rocks are approached. This trend is evident for samples of the Woodson Mountain Granodiorite from a single differentiated stock. The distribution of Cr in the minerals from the rocks of the southern California batholith shows that Cr was depleted in the magma during the course of crystallization. The data indicate that the minerals were in equilibrium with the magma during crystallization, and the distribution coefficient (Cr in biotite/Cr in hornblende) is correlated with differentiation indices, indicating either temperature or compositional dependence. The average distribution coefficient (Cr in biotite/Cr in hornblende) is 1.18, which compares favorably with the average values found by other investigators for other suites. ?? 1976.
Arsenic in soil and rock samples may be determined in part-per-million concentrations using a radiochemical-isotope dilution method. Arsenic in the sample plus added As 76 tracer is separated as arsine and determined spectrophotometrically as a molybdenum blue complex. The As 76 activity in the absorbing solution allows corrections for chemical losses. A lower limit of 1 ppm is determinate in a 0.5-g sample.
A gravity‐feed, pneumatic‐ejection sample changer has been developed. The changer is suitable for both flat and well‐type detectors and permits the continuous use of gamma‐ray spectroscopy equipment 24 h a day, 7 days a week. The electronic circuitry has a fail‐safe feature which stops the operation of the changer if a malfunction occurs.
Fire-asay preconcentration followed by neutron-activation analysis permits the determination of as little as 0.5 ppM of platinum and 0.5 ppM of palladium on a 20-g sample. Platinum and palladium are separated with carriers and beta-counted. Results for the platinum and palladium content of seven U.S.G.S. standard rocks are presented.