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Results for “Clay Minerals”

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At least 289 records · Page 16Linked to original sources
USGS2000

Stanford-USGS shrimp-RG ion microprobe: A new approach to determining the distribution of trace elements in coal

The distribution of Cr and other trace metals of environmental interest in a range of widely used U.S. coals was investigated using the Stanford-USGS SHRIMP-RG ion microprobe . Using the oxygen ion source, concentrations of Cr (11 to 176 ppm), V (23 to 248 ppm), Mn (2 to 149 ppm), Ni (2 to 30 ppm), and 13 other elements were determined in illite/smectite, a group of clay minerals commonly present in coal. The results confirm previous indirect or semi-quantitative determinations indicating illite/smectite to be an important host of these metals. Calibration was achieved using doped aluminosilicate-glass synthetic standards and glasses prepared from USGS rock standards. Grains for analysis were identified optically, and confirmed by 1) precursory electron microprobe analysis and wavelength-dispersive compositional mapping, and 2) SHRIMP-RG major element data obtained concurrently with trace element results. Follow-up investigations will focus on the distribution of As and other elements that are more effectively ionized with the cesium primary beam currently being tested.

ACS Division of Fuel Chemistry, Preprints↗
USGS2010

Potential of kaolin-based particle film barriers for Formosan subterranean termite (Isoptera: Rhinotermitidae) control

Effects of three particle film products on Formosan subterranean termites, Coptotermes formosanus Shiraki, were evaluated in feeding, tunneling, and contact assays. The particle films, hydrophobic M96-018 and hydrophilic Surround and Surround WP are based on the inert clay mineral kaolin. In 2-week long no-choice feeding tests, significant mortality occurred only with M96-018-coated wood. When a choice was provided, M96-018 and Surround were consumed at higher rates than untreated wood. Surround WP did not differ from controls in either test. In the tunneling assay termites were given the option of crossing a kaolin-sand mixture to reach an alternate food source. After 3-weeks, rates of 1% and 5% M96-018 provided an effective barrier to Formosan termite tunneling, while termites were not stopped by rates as high as 20% Surround and Surround WP. Dust treatments of all three formulations caused significant increases in mortality within 24 h, with mortality rates ranging from 72.0 - 97.3% within 72 h of treatment. The particle films were most effective when moisture levels were low, suggesting that desiccation was the mechanism for mortality. All particle films showed potential for use in above ground applications while hydrophobic M06-018 has the most potential as a soil barrier to subterranean termites.

Sociobiology↗
USGS1989

Diagenesis of hydrocarbon-bearing rocks in the Middle Ordovician Simpson Group, southeastern Anadarko Basin, Oklahoma

Quartzarenites and subarkoses in the Middle Ordovician Simpson Group in the Gulf Costello No. 1 and Sunray-DX Parker No. 1 Mazur wells, southeastern Anadarko basin, have undergone a complex diagenetic and petroleum-migration history. During early burial, petroleum migrated locally through sandstones; patches of bitumen in calcite and bitumen-lined quartz overgrowths containing oil-bearing inclusions reflect the introduction of petroleum-bearing fluids at shallow depths. Stable-isotope data reveal that early calcite precipitated at near-surface temperatures from fluids dominated by marine carbon. At moderate to deep burial, calcite dissolution, followed by ferroan-dolomite and clay-mineral precipitation, occurred at about the same time as the rocks reached levels of thermal maturity sufficient for the generation of hydrocarbons. Maximum paleotemperatures during deep burial are estimated from maturation models to have reached 250°F in the Costello well and 300°F in the Mazur well. Maturation-derived temperatures in the Costello well are consistent with preliminary homogenization temperatures (210-250°F) for oil inclusions along microscopic healed fractures that formed during deep burial, thus supporting an Early to Middle Pennsylvanian timing for the generation and migration of late-stage hydrocarbons. The early petroleum phase, emplaced while the rocks were at shallow burial depths, migrated from mature source rocks deeper in the basin.

Oklahoma↗
USGS1976

Method and importance of obtaining humic and fulvic acids of high purity

A detailed procedure incorporating centrifugation, pressure filtration, dialysis, resin exchange, and freeze drying is given for the extraction and purification of fulvic and humic acids from soils and sediments. By use of the procedure humic acids have been prepared which have less than 0.22 percent ash. The isolation of relatively ash-free natural organic matter preparations is an essential prerequisite to the characterization of organic reactivity in natural systems. Inorganic impurities of amorphous and crystalline clay minerals and various inorganic metal ions often lead to numerous complications and errors during experimentation with organic matter because the inorganic substances associated with the organic phase cause variable reactivity of the organic substances.

Journal of Research of the U.S. Geological Survey↗
USGS1977

Chemical structure of humic acids - Part 1, a generalized structural model

A new model is proposed for the structure of humic acids. In this model humic acid is pictured as being made up of a hierarchy of structural elements. At the lowest level in this hierarchy are simple phenolic, quinoid, and benzene carboxylic acid groups. These groups are bonded covalently into small particles. Particles of similar chemical structure are linked together by weak bonds to form "homogeneous" aggregates. Two or more different types of aggregates may be linked together to form mixed aggregates. Complexes of humic acid and clay minerals are also formed.

Journal of Research of the U.S. Geological Survey↗
USGS2009

Systematic approaches to comprehensive analyses of natural organic matter

The more that is learned of the chemistry of aquatic natural organic matter (NOM) the greater is the scientific appreciation of the vast complexity of this subject. This complexity is due not only to a multiplicity of precursor molecules in any environment but to their associations with each other and with other components of local environments such as clays, mineral acids and dissolved metals. In addition, this complex system is subject to constant change owing to environmental variables and microbial action. Thus, there is a good argument that no two NOM samples are exactly the same even from the same source at nearly the same time. When ubiquity of occurrence, reaction with water treatment chemicals, and subsequent human exposure are added to the list of NOM issues, one can understand the appeal that this subject holds for a wide variety of environmental scientists.

Annals of Environmental Science↗
USGS1987

CLAYFORM: a FORTRAN 77 computer program apportioning the constituents in the chemical analysis of a clay or other silicate mineral into a structural formula

The FORTRAN 77 computer program CLAYFORM apportions the constituents of a conventional chemical analysis of a silicate mineral into a user-selected structure formula. If requested, such as for a clay mineral or other phyllosilicate, the program distributes the structural formula components into appropriate default or user-specified structural sites (tetrahedral, octahedral, interlayer, hydroxyl, and molecular water sites), and for phyllosilicates calculates the layer (tetrahedral, octahedral, and interlayer) charge distribution. The program also creates data files of entered analyses for subsequent reuse. ?? 1987.

Computers & Geosciences↗
USGS2002

Characterization of soils and rock at an active oil production site: Effects of brine and hydrocarbon contamination

An active oil production site (Osage-Skiatook petroleum environmental research Site B) in Osage County, Oklahoma is under study to determine the impacts on soils and rock of brine and hydrocarbon spills. The goals of the soil and rock characterization are to 1) document and identify the type, degree, and areal extent of brine and hydrocarbon releases, 2) understand controls on the movement and retention of brine and hydrocarbons, and 3) determine the role of solid phases, such as clay and iron-bearing minerals, in natural mitigation. The types and amounts of clay minerals and oxidizers (particularly iron) are important because of the capacity of clay minerals to exchange cations that are dissolved in brines and the capacity of reactive ferric iron species to oxidize hydrocarbons. Characterization of soils and rock includes visual and microscopic description, X-ray diffraction of bulk and clay fraction samples, separation of size fractions, determination of cation exchange capacity, bulk chemical composition, and selective extraction of iron species. Results suggest that much of the brine and hydrocarbon contamination occurs in the shallow subsurface (< 240 cm) where the soil profile varies from dark brown topsoil to reddish orange sand to greenish-gray clay. A layer of iron-stained colluvium that is present in the shallow subsurface consists of pebbles and coarse sand and forms an important conduit for fluid movement. Unusually high percentages (as much as 97 % of total iron) of reduced iron may record the passage of hydrocarbon-rich ground water. Clay minerals are abundant in some samples and are dominated by kaolinite, mixed layer illite-smectite, and smectite. The correlation of grain size and clay mineral content with soil leachate results will be discussed and high percentages of sodium on exchange sites in clay are expected in areas of past spills of produced water.

Oklahoma↗
USGS2018

Dual-phase mass balance modeling of small mineral particle losses from sedimentary rock-derived soils

Losses of small mineral particles can be a significant physical process that affects the elemental composition of soils derived from sedimentary rocks. Shales, in particular, contain abundant clay-sized minerals that can be mobilized by simple disaggregation, and solutional weathering is limited because the parent rock is composed primarily of recalcitrant minerals previously subjected to continental weathering. Here, the dual-phase mass balance model is employed to quantify losses of small mineral particles as water dispersible colloids (WDCs) from three previously studied soil profiles along a hill slope at the Susquehanna Shale Hills Critical Zone Observatory (SSHO). WDCs were isolated from soil in the laboratory to determine their mineralogical and elemental compositions. Clay minerals dominated WDCs, including illite, vermiculite, and chlorite inherited from the parent shale, along with neoformed kaolinite. Quartz present in bulk soil was generally excluded from WDCs. Elements of low solubility and/or bound in recalcitrant forms, like Rb in illite, were employed in tracer ratios in the dual-phase model. Aluminum, Ga, and Rb were enriched in WDCs, and Zr and Hf were partially excluded. Six different combinations of elements into tracer ratios (Al/Zr, Ga/Zr, Rb/Zr, Al/Hf, Ga/Hf, Rb/Hf) each yielded similar model results. Mass losses of WDCs were large, ranging from − 68 ± 7% to − 15 ± 5% relative to soil parent material in different parts of the profiles. Mass losses via solution were smaller, ranging from − 7 ± 2% to a gain of 6 ± 1% in part of one profile. Losses of WDCs account for > 90% of total mass loss, surpassing chemical dissolution, and therefore dominate the weathering portion of denudation at SSHO. Zirconium concentrations were 97–158 ppm in the generally ≤ 1 μm WDCs, suggesting colloidal, Zr-bearing phases. Model-quantified losses of Zr via WDCs were large, with a median loss of 41% relative to parent material. Such losses indicate systematic underestimates of weathering by traditional mass balance that uses Zr as an index element. Losses of Ca, Mg, and K via WDCs exceeded losses via solution, countering assumptions of base cation losses primarily via mineral dissolution. The results illustrate a geochemical fingerprint of physical weathering and the ability of the dual-phase model to quantify that weathering process.

Chemical Geology↗
USGS2023

Stream sediment geochemistry in mineral exploration: A review of fine-fraction, clay-fraction, bulk leach gold, heavy mineral concentrate and indicator mineral chemistry

Stream sediment surveys support early-stage reconnaissance mineral exploration and regional assessment programmes, enhanced by recent improvements in analytical method detection limits, continuously improving mineral chemistry, and new approaches to the interpretation of geochemical data. Sediment surveys may be used to predict catchment basin lithology, mineralization type based on pathfinder geochemistry, and geological features based on indicator mineral chemistry. Sediment surveys that target a finer-fraction sediment sample led to the discovery of the La Colosa gold deposit, Colombia. The Batu Hijau porphyry Cu–Au deposit in Indonesia was discovered based on an anomalous clay-sized fraction sample 12 km downstream. In an arid region with poorly developed drainages and minor topographic relief, the Ag-base-metal Navidad District in Argentina was discovered with clay-fraction sediment geochemistry. Heavy mineral concentrate (HMC) sediment surveys that include mineral chemistry determinations have led to global diamond discoveries. HMC surveys contributed to discovery of the Ring of Fire Ni–Cu–PGE and chromite district, Ontario, Canada. Discoveries and geochemical mapping can assist advancement of the application of stream sediment geochemistry in those global areas for which lithologies and deposits are exposed. Stream sediment surveys continue to be one of the most cost-effective geochemical methods for covering large areas for mineral exploration.

Geochemistry: Exploration, Environment, Analysis↗
USGS2006

Sediments from bay St. George, Newfoundland

Sediments cored to a depth of about 1 m in Bay St . George , Newfoundland , were examined for grain‐size distribution and minerals. The sediments are light brown silty clays, the principal minerals of which are chlorite and muscovite mica. The scarce sand consists of fresh detrital grains of blue‐green amphibole, biotite, epidote, zoisite, magnetite, garnet, hypersthene, apatite, chlorite, and scarce zircon. Quartz, plagioclase feldspar, and muscovite are abundant. These minerals are all present in the rocks of the adjacent land areas and have been deposited in the sediments with little alteration or change due to weathering. The clay minerals of the sediments are predominantly muscovite and chlorite with a slight admixture of vermiculite and montmorillonite. There is very little mixed‐layering of these minerals. Montmorillonite may be due to diagenetic changes after deposition of these clays in the marine environment of the bay .

Newfoundland↗
USGS2024

Hyperspectral (VNIR-SWIR) analysis of roll front uranium host rocks and industrial minerals from Karnes and Live Oak Counties, Texas Coastal Plain

VNIR-SWIR (400–2500 nm) reflectance measurements were made on the surfaces of various cores, cuttings and sample splits of sedimentary rocks from the Tertiary Jackson Group, and Catahoula, Oakville and Goliad Formations. These rocks vary in composition and texture from mudstone and claystone to sandstone and are known host rocks for roll front uranium occurrences in Karnes and Live Oak Counties, Texas. Spectral reflectance profiles, 569 in total, were reduced to 125 representative spectral signatures, which were analyzed using the U.S. Geological Survey's (USGS) Material Identification and Characterization Algorithm (MICA). MICA uses an automated continuum-removal procedure together with a least-squares linear regression to determine the fit of observed sample spectral absorption features to those of reference mineral standards in a spectral library. The reference minerals include various clay, mica, carbonate, ferric and ferrous iron minerals and their mixtures. In addition, absorption feature band-depth analysis was done to identify rock surfaces exhibiting absorption features related to uranium and zeolite minerals, which were not included in the command files used to execute MICA. Rocks from each of the four geologic units produced broadly similar spectral signatures as a result of comparable mineral compositions, but there were some notable differences. For example, Ca- and Na-montmorillonite was matched most frequently to the spectral absorption features in 2-μm (∼2000–2500 nm) wavelengths, while goethite occurred often at 1-μm (∼400–1000 nm) wavelengths. The latter is related to limonitic iron-staining in and around oxidized zones of the uranium roll front as described in previous papers. Rocks of the Jackson Group differed from those of the Catahoula, Oakville and Goliad units in that the former exhibited spectral features we interpret as being due to the presence of lignite-bearing mudstone layers. Goliad rocks exhibit spectral features related to dolomite, gypsum, anhydrite, and an unidentified green clay mineral that is possibly glauconite . Jackson Group rocks also exhibit weak but well-resolved absorption features at 964 and 1157 nm related to either or both zeolite minerals clinoptilolite and heulandite. These zeolite minerals and a few spectra exhibiting hydrous silica absorption features are indicative of alteration of volcanic glass in tuffaceous mudstone and claystone layers. A few sample spectra exhibited strong absorption features at around 1135 nm related to the uranium mineral coffinite. Both the 1135 nm coffinite and 1157 nm zeolite absorption features overlap somewhat, potentially making them difficult to distinguish without additional hyperspectral field, laboratory or remote sensing data. The results of this study were compared to mixtures of minerals described for ore, gangue and alteration minerals in deposit models for sandstone-hosted uranium, sedimentary bentonite and sedimentary zeolite. Use of these spectra can help facilitate mapping of both waste materials from the legacy mining of the above commodities, as well as future exploration and resource assessment activities.

Texas↗
USGS2010

Mineral resource of the Month: Clay

Clays were one of the first mineral commodities used by people. Clay pottery has been found in archeological sites that are 12,000 years old, and clay figurines have been found in sites that are even older.

Earth↗
USGS2004

Mineral resource of the month: clays

Clays represent one of the largest mineral commodities in the world in terms of mineral and rock production and use. Many people, however, do not recognize that clays are used in an amazingly wide variety of applications. Use continues to increase worldwide as populations and their associated needs increase. Robert Virta, clay and shale commodity specialist for the U.S. Geological Survey, has prepared the following information about clays.

Geotimes↗
USGS1996

Trace elements and organic contaminants in stream sediments from the Red River of the North Basin

To assess the presence and distribution of a variety of hydro-phobic chemicals in streams in the Red River of the North Basin, bottom sediments were analyzed for trace elements, organochlorines, and polycyclic aromatic hydrocarbons (PAHs). Glaciolacustrine clays and carbonate minerals are common in fine sediments of the region, and can help explain the distribution of many elements. Aluminum (Al), an indicator of glaciolacustrine clay minerals, correlates strongly (r>0.75, p<0.05) with Cr, Co, Fe, La, Li, K, Sc, and Ti; and moderately (0.55<r<0.75) with Ce, Cu, Ga, Nd, Ni, Th, V, and Y. Excluding the tributary Pembina River Basin, Eu, Nb, Ce, La, Nd, and Ni also have strong correlations with Al. Al correlates negatively with major elements associated with carbonate minerals (Ca, Mg, and inorganic carbon). No significant correlations with Al, Ca, or Mg were observed for As, Pb, Mn, Hg, Se, or Ag, which implies that these elements have different environmental sources or behaviors than glaciolacustrine clays or carbonate minerals. Reduction-oxidation processes may influence Mn distribution. Lead (Pb) and mercury (Hg) are known to be anthropogenically enriched in the environment--their distribution may indicate environmental enrichment in Red River of the North Basin streams. Organochlorines detected are limited to traces of DDT and its metabolites (mostlyp,p'-DDE). Fourteen PAHs, which are constituents of fossil fuels and of combustion byproducts, were detected in at least halfthe sediment samples; pyrene and fluoranthene were detected in about 90 percent of samples. The contaminants detected in this study were present at low levels, likely indicative of diffuse or remote sources; they occur widely in the environment.

Minnesota, North Dakota, South Dakota↗