By using a transmission electron microscope equipped with an energy dispersive spectrometer, it was possible to detect the morphological, structural, and chemical characteristics of individual asbestos fibers and clay minerals without any realignment of the equipment. A rapid and convenient procedure for semiquantitative analysis is proposed. Analyses are given for 21 hydrous silicates, asbestos and clay minerals, by both ordinary chemical and energy dispersive methods. The energy dispersive results were comparable to those obtained by chemical analysis. Application of this procedure to asbestos fibers proved this method to be practical and valid for characterization of asbestos in environmental and tissue samples.

A series of mixed iron and titanium oxide coprecipitates ranging in composition between 0 < Ti/Ti + Fe < 1 was synthesized and aged under varying conditions of pH, temperature and time in order to establish a working model for pedogenic titanium and titano-ferric oxides. X-ray powder diffraction (XRD), selective chemical dissolution, magnetic susceptibility, charge distribution and electron optical data indicate that the freshly prepared Fe-Ti oxides consist of an Fe-rich (Ti-ferrihydrite) phase (Ti/Ti + Fe ⩽ 0.70) having pH-dependent positive charge and a Ti-rich phase (Ti/Ti + Fe ⩾ 0.7) with permanent and pH dependent negative charge.

Synthetic Ti-ferrihydrite and amorphous TiO2 were completely soluble in acid ammonium oxalate (2 hr extraction in the dark) whereas poorly crystalline anatase (width at half height, WHH > 2.0°2θ) was partly oxalate soluble. NH4-oxalate soluble Ti was particularly high in soils developed under a cool montane climate (afro-alpine) and lower in soils of warmer subtropical climate, which contain anatase and rutile.

Several mixed Fe-Ti crystalline phases were identified after aging NH3 coprecipitates of Fe and Ti nitrate at 70°C and pH 5.5 for 70 days:

1. (1) goethite and hematite in the composition range 0 < Ti/Ti + Fe ⩽ 0.20; at low Ti concentrations (<5 mole %) goethite was favored and/or hematite inhibited

2. (2) microcrystalline pseudorutile in the composition range 0.20 ⩽ Ti/Ti + Fe ⩽ 0.70

3. (3) anatase and ferriferous anatase in the range 0.70 ⩽ Ti/Ti + Fe < 1.0; with decreasing proportion of Ti the crystal-Unity of anatase decreased.

The results suggest that secondary or pedogenic Ti-Fe oxides can form by coprecipitation and crystallization in the weathering solution, and emphasize the essential role of water (as opposed to dry oxidation) in the alteration of primary titaniferous minerals.

An infrared method has been developed for estimating kaolinite in sediments. Hydroxyl stretching bands of kaolinite in sediments can be recorded by using a differential technique which eliminates the overlapping owing to other mineralic constituents present. By adding known amounts of an appropriate standard to the sample and by measuring intensities of the OH bands before and after the addition it is possible to calculate the proportion of kaolinite in the test sample. The choice of the added standard is made from characteristic features of the hydroxyl stretching bands.

Dehydroxylated sericites were stirred in the various salt solutions, or washed several times with various salt solutions using a centrifuge. By these treatments a seriate of the 2M type was easily transformed into an interstratified mineral of the rectorite type when a sericite was treated with sodium salts, and random mixed-layer mineral was formed from 1M sericite. The formation of a rectorite-type mixed-layer mineral from 2M sericite can be explained by the (OH) bond direction after the extraction of the potassium ions.

Analytical data from aqueous dissolution studies of minerals, mineral systems, and naturally equilibrated solutions such as surface waters and groundwaters provide the basic ingredients necessary to calculate comparative solubility (or activity) products (CKs) and comparative free energies of formation (CΔGf0) of possible minerals or hypothetical minerals. Using a thermodynamic approach, quasi-thermodynamic values are obtained which can help in understanding the relative stabilities of different but similar materials and changes in reacting systems. Illite equilibrated solutions demonstrated that: 1) there is a 5 kcal spread in comparative free energies of formation of the five illites used, 2) the comparative stabilities remain about the same when highly simplified but similar hypothetical mineral formulas are considered, and 3) some of these illites are probably not the most stable phase in a closed chemical system at standard temperature and pressure.

A “mineral index system” composed of common rock-forming minerals, products of chemical weathering and perhaps hypothetical minerals is proposed, which offers a means of studying naturally equilibrated solutions. Such a system can show changes with respect to CΔGf0 of these minerals at a particular site through time or in relationship to spatial distribution and geologic changes through synchronous sampling at different sites.

Clay minerals were used as indicators for determining the source of sediment in recently dredged harbors along the north shore of Long Island Sound. Amount and characteristics of clay minerals in sediments from the dredged channels were compared to their amount and characteristics in the surrounding soils and in sediments from Long Island Sound. Clay minerals in sediments from the channels were similar in amount and characteristics to clay minerals in sediments from Long Island Sound but differed from those in the surrounding soils in the watershed. Thus, the main source of deposits in the channels is the bottom sediment of Long Island Sound which is transported to the channels by tidal action. These conclusions are supported by recent studies of the bottom currents in the Sound.

Low albite and maximum microcline were the two feldspars identified in Coal Measures mudrocks. Standard feldspars were then used to spike a mudrock base to construct standard working curves based on X-ray powder diffraction peak areas. Boehmite was added as an internal standard and also to correct for orientation effects. The samples were ignited at 950°C before the addition of the internal standard. This is advantageous for several reasons, but a disadvantage is that albite was found to undergo partial conversion to K-feldspar. The conversion was not total and the original albite content could be determined. This method is an extension of an existing method for quartz and therefore feldspars and quartz can be determined simultaneously.

The flint-clay facies, originally proposed from widespread stratigraphie evidence, is represented by four of its six members within a single commercial deposit of Cheltenham refractory clay in Missouri. Scan electron micrographs show progressive changes in texture from plastic refractory clay (as in ball-clay “swirl” texture) through semi-plastic, semi-flint, to typical flint clay (recrystallized, well-ordered kaolinite). Micrographic evidence supports the interpretation of the origin of the Cheltenham clay earlier made from field and macroscopic evidence. Source material from nearby residual, weathered clay was transported into paludal basins, “digested,” partly recrystallized to kaolinite, brecciated and reconsolidated, essentially completed before being covered by younger Pennsylvanian-age sediments.