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Reactions of aqueous aluminum species at mineral surfaces

Aqueous aluminum solutions containing 4.5 ? 10 4 molar aluminum in 0.01 molar NaC104 were partly neutralized with NaOH to give OH:A1 mole ratios from 1.40 to 2.76. Measured amounts of montmorillonite, kaolinite, volcanic ash, or feldspathic sand were added to provide an area of inert surface. Reactions that occurred during 100 days of aging were compared with those in similar solutions without added surfaces, studied in earlier work. Adsorption of monomeric species Al(H20)6+3, AlOH(H2O)5+2, and Al(OH)2(H2O 4? on the added surfaces follows a cation exchange mass law equilibrium model, and adsorption is essentially complete in 1 hour. Only minor changes in monomeric aluminum species occurred after that. Rapid adsorption of polynuclear aluminum hydroxide species also occurs and follows the pattern of the Langmuir adsorption isotherm. In the absence of surfaces, the polynuclear ions slowly increase in size and become microcrystalline gibbsite during aging. Electron micrographs showed microcrystalline gibbsite was present or surfaces after aging only 2 days. However, the analytical data suggest this material must have been adsorbed after it had already attained a near-crystalline state. Adsorbed polynuclear aluminum hydroxide species were not extensively converted to microcrystalline gibbsite during 100 days of aging.

Water Supply Paper

The role of water in the formation of reversed micelles: An antimicellization agent

Micellization of sodium bis(2-ethylhexyl) phosphate in n-heptane has been studied under controlled environmental conditions by dynamic and static light scattering. The results clearly show that a trace amount of water has a very dramatic effect on reversed micellization. In contrast with results in the literature, water can function as an antimicellization agent. The generality of and the evidence for supporting the current view that water is a prerequisite for the formation of reversed micelles are discussed and criticized.

Langmuir

The solubilities of some major and minor element minerals in ground waters associated with a sandstone-hosted uranium deposit

Ground-water samples from 41 wells penetrating basal Oakville sandstone (Miocene) in S Texas were chemically analysed to identify chemical changes related to nearby U orebodies. The coverage included a 240 km 2 area which contains several fault-related U deposits. Factors affecting the hydrochemistry include: 1) relatively high permeabilities of buried fluvial-channel sediments; 2) upwards leakage of brines along growth faults into the aquifer; 3) development of a redox interface (Eh = 0 volts) within the aquifer; and 4) the semi-arid climate. Variations in the saturation index (SI) for chemically reduced minerals of U, As, Mo, Se and for associated minerals such as pyrite outlined the position of known deposits. The SI increases towards zero as the deposits are approached from updip distances of 3-4.5 km, then decreases again downdip. The radiogenic pathfinders Ra and Rn showed very strong anomalies with ore, but diminished to background levels at short distances from ore. A strong He anomaly is deflected in the direction of ground-water flow away from the ore.-R.A.H.

Bulletin de Mineralogie