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G. R. Aiken

Publications and source records attributed to G. R. Aiken.

58 records · Page 4Linked to original sources

Molecular weight of aquatic fulvic acids by vapor pressure osmometry

The molecular weights of aquatic fulvic acids extracted from five rivers were determined by vapor pressure osmometry with water and tetrahydrofuran as solvents. The values obtained ranged from 500 to 950 dallons, indicating that the molecular weights of aquatic fulvic acids are not as great as has been suggested in some other molecular weight studies. The samples were shown to be relatively monodisperse from radii of gyration measurements determined by small angle x-ray scattering. THF affords greater precision and accuracy than H 2 O in VPO measurements, and was found to be a suitable solvent for the determination of molecular weight of aquatic fulvic acid because it obviates the dissociation problem. An inverse correlation was observed with these samples between the concentration of Ca ++ and Mg ++ in the river water and the radii of gyration and molecular weights of the corresponding fulvic acid samples.

Geochimica et Cosmochimica Acta↗

Chemistry and transport of soluble humic substances in forested watersheds of the Adirondack Park, New York

Studies were conducted in conjunction with the Integrated Lake-Watershed Acidification Study (ILWAS) to examine the chemistry and leaching patterns of soluble humic substances in forested watersheds of the Adirondack region. During the summer growing season, mean dissolved organic carbon (DOC) concentrations in the ILWAS watersheds ranged from 21–32 mg C l −1 in O/A horizon leachates, from 5–7 mg C l −1 in B horizon leachates, from 2–4 mg C l −1 in groundwater solutions, from 6–8 mg C l −1 in first order streams, from 3–8 mg C l −1 in lake inlets, and from 2–7 mg C l −1 in lake outlets. During the winter, mean DOC concentrations dropped significantly in the upper soil profile. Soil solutions from mixed and coniferous stands contained as much as twice the DOC concentration of lysimeter samples from hardwood stands. Results of DOC fractionation analysis showed that hydrophobia and hydrophilic acids dominate the organic solute composition of natural waters in these watersheds. Charge balance and titration results indicated that the general acid-base characteristics of the dissolved humic mixture in these natural waters can be accounted for by a model organic acid having an average p K a of 3.85, an average charge density of 4–5 μeq mg −1 C at ambient pH, and a total of 6–7 meq COOH per gram carbon.

New York↗

Preliminary data from a series of artificial recharge experiments at Stanton, Texas

A series of artificial recharge experiments was conducted by the U.S. Geological Survey at an experimental site located in Stanton, Texas. Five tests were performed from March 1977 through December 1978 to: (1) Evaluate the hydraulic properties of the aquifer; (2) test sampling and monitoring equipment; (3) compare tracers for future use in hydrologic investigations; and (4) determine the radial and vertical distribution of hydraulic properties at the site. Suites of inorganic, and both volatile and nonvolatile organic tracers were used in the tests, and comparative data were obtained from sampling points at several radial distances and depths from the injection well. Hydraulic data from aquifer tests and geologic data from core material also were obtained during the investigation.

Texas↗

Reconnaissance samplings and characterization of aquatic humic substances at the Yuma Desalting Test Facility, Arizona

Smectite clay minerals were found to be the principal compound on the surface of the cellulose-acetate, reverse-osmosis membranes at the Yuma Desalting Test Facility. These clay minerals were not present in the pumped ground water, but were blown into the conveyance canal from adjacent soils. Humic substances from the water and suspended sediments were associated with the clay films on the membrane, but no definitive results concerning their role in fouling were achieved. Microbial fouling is believed to be only a minor aspect of membrane fouling. Chemical and physical changes in humic substances were extensively studied at four points in the water-treatment process. Humic substances accounted for the largest component (over 25 percent) of organic constituents. Humic substances in the canal source water were similar to other aquatic humic substances present in natural waters. During the treatment process, these substances are brominated and decolorized. The effect of these halogenated humic substances on membrane fouling is unclear, but their presence in the reverse-osmosis product water and reverse-osmosis reject brine, along with volatile trihalomethanes, has led to environmental concerns. (USGS)

Arizona↗