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At least 325 records · Page 18Linked to original sources
USGS2002

The surface area of soil organic matter

The previously reported surface area for soil organic matter (SOM) of 560-800 m2/g as determined by the ethylene glycol (EG) retention method was reexamined by the standard BET method based on nitrogen adsorption at liquid nitrogen temperature. Test samples consisted of two high organic content soils, a freeze-dried soil humic acid, and an oven-dried soil humic acid. The measured BET areas for these samples were less than 1 m2/g, except for the freeze-dried humic acid. The results suggest that surface adsorption of nonionic organic compounds by SOM is practically insignificant in comparison to uptake by partition. The discrepancy between the surface areas of SOM obtained by BET and EG methods was explained in terms of the 'free surface area' and the 'apparent surface area' associated with these measurements.The previously reported surface area for soil organic matter (SOM) of 560-800 m2/g as determined by the ethylene glycol (EG) retention method was reexamined by the standard BET method based on nitrogen adsorption at liquid nitrogen temperature. Test samples consisted of two high organic content soils, a freeze-dried soil humic acid, and an oven-dried soil humic acid. The measured BET areas for these samples were less than 1 m2/g, except for the freeze-dried humic acid. The results suggest that surface adsorption of nonionic organic compounds by SOM is practically insignificant in comparison to uptake by partition. The discrepancy between the surface areas of SOM obtained by BET and EG methods was explained in terms of the 'free surface area' and the 'apparent surface area' associated with these measurements.

Environmental Science & Technology↗
USGS2002

Effect of ten quaternary ammonium cations on tetrachloromethane sorption to clay from water

The mineral surface of Wyoming bentonite (clay) was modified by replacing inorganic ions by each of 10 quaternary ammonium compounds, and tetrachloromethane sorption to the modified sorbents from water was studied. Tetrachloromethane sorption from solution to clay modified with tetramethyl-, tetraethyl-, benzyltrimethyl-, or benzyltriethylammonium cations generally is characterized by relatively high solute uptake, isotherm nonlinearity, and competitive sorption (with trichloroethene as the competing sorbate). For these sorbents, the ethyl functional groups yield reduced sorptive capacity relative to methyl groups, whereas the benzyl group appears to have a similar effect on sorbent capacity as the methyl group. Sorption of tetrachloromethane to clay modified with dodecyldimethyl(2-phenoxyethyl)-, dodecyltrimethyl-, tetradecyltrimethyl-, hexadecyltrimethyl-, or benzyldimethylhexadecylammonium bromide is characterized by relatively low solute uptake, isotherm linearity, and noncompetitive sorption. For these sorbents, an increase in the size of the nonpolar functional group(s) causes an increase in the organic carbon normalized sorption coefficient (Koc). No measurable uptake of tetrachloromethane sorption by the unmodified clay or clay modified by ammonium bromide was observed.

Environmental Science & Technology↗
USGS2000

Multivariate correlation between concentrations of selected herbicides and derivatives in outflows from selected U.S. midwestern reservoirs

Multivariate correlations between the concentrations of selected herbicides and herbicide derivatives in outflows from selected reservoirs in the Midwestern United States for April 1992 through September 1993 were investigated using principal component analysis (PCA) and multivariate curve resolution (MCR). Two independent sources for alachlor ethanesulfonic acid, one major source related to spring flush and seasonal runoff and another minor source related to groundwater, were identified using PCA. Results of MCR provided a semiquantitative interpretation of the environmental sources of the observed herbicide concentrations in reservoir outflows and allowed the examination of their temporal and geographical distributions. Samples with higher herbicide concentrations were collected from reservoirs in Indiana and Ohio, especially during the late spring and summer.

Environmental Science & Technology↗
USGS2002

Comparison of automated segmented-flow and discrete analyzers for the determination of nutrients in water

Water samples with specific conductances ranging from 66 to 6950 ??mho/cm at 25 ??C were analyzed for ammonia-N (NH3-N), nitrate plus nitrite-N (NO3 + NO2-N), nitrite-N (NO2-N), and phosphate-P (PO4-P) by using both a "segmented-flow" analyzer and a "discrete" analyzer. Plots of the discrete vs. the segmented-flow results showed linear correlation coefficients of 0.9980 for NH3-N, 0.9997 for NO3 + NO2-N, 0.9998 for NO2-N, and 0.9950 for PO4-P. The significances of the slope and the y intercept of each plot are discussed in terms of possible biases which may exist between the two systems. Data concerning precision and accuracy for both analyzers are presented. For the four analytes, the rate of sample analysis was 60 samples per hour on the discrete analyzer and 40 samples per hour on the segmented-flow analyzer. ?? 1981 American Chemical Society.

Environmental Science & Technology↗
USGS2002

Migration through soil of organic solutes in an oil-shale process water

The migration through soil of organic solutes in an oil-shale process water (retort water) was studied by using soil columns and analyzing leachates for various organic constituents. Retort water extracted significant quantities of organic anions leached from ammonium-saturated-soil organic matter, and a distilled-water rinse, which followed retort-water leaching, released additional organic acids from the soil. After being corrected for organic constitutents extracted from soil by retort water, dissolved-organic-carbon fractionation analyses of effluent fractions showed that the order of increasing affinity of six organic compound classes for the soil was as follows: hydrophilic neutrals nearly equal to hydrophilic acids, followed by the sequence of hydrophobic acids, hydrophilic bases, hydrophobic bases, and hydrophobic neutrals. Liquid-chromatographic analysis of the aromatic amines in the hydrophobic- and hydrophilic-base fractions showed that the relative order of the rates of migration through the soil column was the same as the order of migration on a reversed-phase, octadecylsilica liquid-chromatographic column.

Environmental Science & Technology↗
USGS2000

Beryllium-7 as a tracer of short-term sediment deposition and resuspension in the Fox River Wisconsin

Short-term (∼monthly) sediment deposition and resuspension rates of surficial bed sediments in two PCB-laden impoundments on the Fox River, WI, were determined in the summer and fall of 1998 using 7 Be, a naturally occurring radioisotope produced in the atmosphere. Decay-corrected activities and inventories of 7 Be were measured in bed sediment and in suspended particles. Beryllium-7 activities generally decreased with depth in the top 5−10 cm of sediments and ranged from undetectable to ∼0.9 pCi cm - 3 . Inventories of 7 Be, calculated from the sum of activities from all depths, ranged from 0.87 to 3.74 pCi cm - 2 , and the values covaried between sites likely reflecting a common atmospheric input signal. Activities of 7 Be did not correlate directly with rainfall. Partitioning the 7 Be flux into “new” and “residual” components indicated that net deposition was occurring most of the time during the summer. Net erosion, however, was observed at the upstream site from the final collection in the fall. This erosion event was estimated to have removed 0.10 g (cm of sediment) - 2 , corresponding to ∼0.5 cm of sediment depth, and ∼6−10 kg of polychlorinated biphenyls (PCBs) over the whole deposit. Short-term accumulation rates were up to ∼130 times higher than the long-term rates calculated from 137 Cs profiles, suggesting an extremely dynamic sediment transport environment, even within an impounded river system.

Environmental Science & Technology↗
USGS2000

Atmospheric transport, deposition, and fate of triazine herbicides and their metabolites in pristine areas at Isle Royale National Park

Trace concentrations of triazine herbicides, used in the Midwestern United States, are being transported atmospherically hundreds of kilometers and deposited by precipitation onto pristine areas, such as Isle Royale National Park (Lake Superior). Atrazine, deethylatrazine, deisopropylatrazine, and cyanazine were detected in Isle Royale rainfall from mid-May to early July (1992−1994) at concentrations of less than 0.005 to 1.8 μg/L. Analysis of predominant wind direction indicated that the herbicides originated from the upper Midwestern United States. The annual mass of herbicides deposited by rainfall varied between years, from 13.4 μg/m 2 /yr for 1992, 3.7 μg/m 2 /yr for 1993, and 54 μg/m 2 /yr for 1994. Atrazine and deethylatrazine were found also in concentrations of less than 5−22 ng/L in lakes across Isle Royale. Concentrations of atrazine in the surface layer of the lakes increased during deposition periods and decreased later in the year. The fate of triazines in shallow lakes suggests faster degradation and shorter half-lives, while deeper lakes have residence times for atrazine that may exceed 10 years.

Environmental Science & Technology↗