Application of riverbed sand for the adsorptive separation of cadmium(II) from aqueous solutions has been investigated. Removal increased from 26.8 to 56.4% by decreasing the initial concentration of cadmium from 7.5 x 10-5 to 1.0 x 10-5 M at pH 6.5, 25 °C temperature, agitation speed of 100 rpm, 100 μm particle size and 1.0 x 10-2 NaClO4 ionic strength. Process of separation is governed by first order rate kinetics. The value of rate constant of adsorption, kad, was found to be 2.30 x 10-2 per min at 25 °C. Values of coefficient of mass transfer, βL, were calculated and its value at 25 °C was found to be 1.92 x 10-2 cm/s. Values of Langmuir constant were calculated. Values of thermodynamic parameters ΔG0, ΔH0 and ΔS0 were also calculated and were recorded as -0.81 kcal/mol, -9.31 kcal/mol and -28.10 cal/mol at 25 °C. pH has been found to affect the removal of cadmium significantly and maximum removal, 58.4%, has been found at pH 8.5. Process can be used for treatment of cadmium(II) rich wastewaters.

Increasing environmental concentrations of platinum group metals (PGMs), in particular platinum (Pt), rhodium (Rh) and palladium (Pd), from catalytic converters has been reported worldwide. The impact of these three metals on the uptake and use of essential mineral nutrients was examined using two plant models: the submerged aquatic plant, Elodea canadensis, and the terrestrial emergent plant, Peltandra virginica. Plants were grown for 2 weeks in nutrient solutions with either Pt⁴⁺ at concentrations between 0.05 and 5 mg/L, or a 0.1 mg/L Pt⁴⁺, Rh³⁺, Pd²⁺ mixture. Some treatments received additional Ca²⁺, Zn²⁺, or humic acid (with varying pH) to study how these conditions affected PGM uptake. Metal concentration analyses were conducted using a graphite furnace atomic absorption spectrometer (GFAAS) or an inductively coupled plasma emission spectrometer (ICP). Growth response was assessed through total chlorophyll content. There was significant Pt accumulation in plant tissues, from 55 to 326 times the concentration in nutrient solution. At pH 8, the addition of humic acid doubled Pt accumulation in comparison to the control. Additional exogenous minerals did not significantly affect PGM uptake, nor did the uptake of PGMs interfere with the uptake of Ca, Fe or Cu. Synthesis of chlorophyll in new shoots was not affected by Pt accumulation; however, visible chlorosis was observed in older shoots at 5 ppm Pt. Roadside Daucus carota samples from four heavy traffic locations in Dutchess County (New York) were also assessed for PGM content. Pt, Pd and Rh concentrations averaged 14.6, 10.2, and 0.7 μg/g, respectively.

Chemical composition of fog and rain water was studied during a 47-day experimental period. The differences between the fog and rain water were found to be significantly for most analyzed ions. H⁺, NH₄ ⁺, NO₃ -, and SO₄ ²- made up 85% of the total median ion concentration in fog and 84% in rain water. The total mean equivalent concentration was 15 times higher in the fog than in the rain water. The fog water samples were classified according to their air mass history. The analysis of the 120 h backward trajectory led to the identification of three advection regimes. Significant differences of ion concentrations between the respective classes were found. Air masses of class I travelled exclusively over the Pacific Ocean, class II were carried over the Philippines, and class III were advected from mainland China. The turbulent fog water deposition was determined by the means of the eddy covariance method. The total (turbulent plus gravitational) fog water fluxes ranged between +31.7 mg m-² s-¹ and -56.6 mg m-² s-¹. Fog water droplets with mean diameters between 15 μm and 25 μm contributed most to the liquid water flux. The sample based nutrient input was calculated on the basis of the occult and wet deposition, and the concentrations of the simultaneously collected fog and rainwater samples, respectively. The nutrient input through wet deposition was about 13 times higher than through occult deposition.

Field study at the Cervenohorske sedlo (1,013 m a.s.l.) (Hruby Jesenik Mountains, the Czech Republic, Central Europe) during 1999-2002 has been conducted in order to analyse the chemistry of rain/snow water using bulk and throughfall collector and fog/cloud water using modified passive Grunow collector. Fog water input to coniferous forest (Picea abies) was quantified using canopy balance method. For all samples pH, and the concentrations of [graphic removed] , Ca²⁺, K⁺, Mg²⁺, Na⁺, Cl-, [graphic removed] , and [graphic removed] were measured. The volume-weighted mean pH value varied from 4.92 to 5.43 in open bulk precipitation, from 4.30 to 4.71 in throughfall and from 4.66 to 5.23 in fog water. The fog droplets generally contain higher ion concentrations than rainwater. The related enrichment factors lie between 1.1 and 10.7 for the relevant species. The fog samples exhibit higher concentrations of [graphic removed] and [graphic removed] as compared to the bulk samples during 2000-2002. [graphic removed] are 5.7-10.7 times more concentrated in fog water and [graphic removed] are 3.4-7.2 times more concentrated in fog water. These differences may result from the height and characteristics of formation of the droplets. Based on canopy balance method, the annual fog water inputs were estimated to be 22 and 19% of rain and snow annual amounts in 1999 and 2000, respectively. For [graphic removed] , [graphic removed] , and [graphic removed] , the contribution of fog deposition in total (bulk + fog) deposition is estimated as 54, 47, and 42%, respectively.

Buffer capacity analysis of open atmospheric gas-liquid systems containing main acidic and basic atmospheric pollutants was carried out. Usually the buffer capacity is considered as a function of pH as an independent variable. In this work the buffer capacity is analysed including the dependence of pH on the composition of a system. Such an approach allows finding an important, from the viewpoint of atmospheric water acidification, relationship between the gas phase composition and the buffer capacity. It was found that buffer capacity of the open gas-liquid systems may be very high and it may cause the liquid phase pH to remain at low levels. The buffer capacity of the analysed systems is most strongly affected by the simultaneous presence of ammonia and strong acids in the gas phase. The higher concentrations of strong acid gases the lower NH₃ concentration is sufficient to achieve high buffer capacity. In the presence of strong acid gases, calcium ions affect both the buffer capacity and the liquid phase pH only at low NH₃ concentrations. High buffer capacity of open gas-liquid systems may be one of the reasons why the reduction in emissions of acidic gas pollutants has little effect on decrease in atmospheric water acidity.

Due to the episodic nature of rainfall and the high dissolved metal concentrations in the acid sulfate soil catchment of Clothiers Creek (NSW, Australia), active treatment was considered more appropriate than passive treatment. Alkaline reagents were added to oxidised shallow drains to remove acidities ranging from 438 to 1,837 mg/L CaCO₃. A fine limestone slurry was produced from the pounding together of limestone rock fragments within a rotating drum and, on addition to drain waters, was found to remove acidity to varying degrees of effectiveness (from 12 to 100%). The efficiency decreased as the pH of the water approached neutrality due to calcite saturation and the slow reaction rate of limestone at high pH. Hydrated lime powder was also mixed with drain water in the rotating drum though most mixing occurred once the slurry entered the drain where efficiencies ranging from 67 to 89% were observed. A powdered mixture of MgCO₃ and CaCO₃ was only 11% effective in treatment of the drainage water due to the slow rate of reaction of MgCO₃. Whilst the active treatment system was capable of treating a large acidity flux (particularly using hydrated lime) it required regular addition of reagent and the dosing of hydrated lime was particularly difficult to control. Future designs of this active treatment system should be automated to prevent adverse aquatic impacts due to overdosing.

A powerful 7.3 magnitude earthquake struck Taiwan on September 21, 1999. The stream water chemistry (pH, total alkalinity, conductivity, sodium, potassium, calcium, magnesium, ammonium, fluoride, chloride, sulfate, and nitrate) has been monitored since 1995 at the Guandaushi forestry riparian zone in central Taiwan. Collected data was used as a basis for comparing pre- and post-earthquake impacts. The pH, conductivity, and concentrations of Na, Ca, Mg, SO₄, and HCO₃ in stream water were lowest during the summer season, when stream water discharge was highest. On the other hand, the lowest concentrations of Cl, NH₄, and NO₃ in stream water occurred during the winter season, when stream water discharge was lowest. Also, K and F showed very little seasonal fluctuation in concentration. Downward trends in K and Ca were found 14 months prior to the earthquake; although, an upward trend occurred in NH₄ at the same time.

Extraction of natural gas from a confined coal aquifer requires the pumping of large amounts of groundwater, commonly referred to as produced water. Produced water from the extraction of coalbed natural gas is typically disposed into nearby constructed discharge ponds. The objective of this study was to collect produced water samples at outfalls and corresponding discharge ponds and monitor pH, electrical conductivity (EC), calcium (Ca), magnesium (Mg), sodium (Na), and alkalinity. Outfalls and corresponding discharge ponds were sampled from five different watersheds including Cheyenne River (CHR), Belle Fourche River (BFR), Little Powder River (LPR), Powder River (PR), and Tongue River (TR) within the Powder River Basin (PRB), Wyoming from 2003 to 2005. From Na, Ca, and Mg measurements, sodium adsorption ratios (SAR) were calculated, and used in a regression model. Results suggest that outfalls are chemically different from corresponding discharge ponds. Sodium, alkalinity, and pH all tend to increase, possibly due to environmental factors such as evaporation, while Ca decreased from outfalls to associated discharge ponds due to calcite precipitation. Watersheds examined in this study were chemically different form each other and most discharge ponds with in individual watersheds tended to increase in Na and SAR from 2003 to 2005. Since discharge pond water was chemically changing as a function of watershed chemistry, we predicted SAR of discharge pond water using a regression model. The predicted discharge pond water results suggested a high correlation (R ² = 0.83) to discharge well SAR. Overall, results of this study will be useful for landowners, water quality managers, and industry in properly managing produced water from the natural gas extraction.

Fluorescent dissolved organic matters (FDOM) in the groundwater-river-lake environments were investigated using three-dimensional excitation-emission matrix (EEM) and measuring the dissolved organic carbon (DOC), inorganic anions and electric conductivity (EC) in shallow groundwater, river and lake waters. DOC concentrations were high and largely varied in groundwater, 16-328 μM C (mean 109 ± 88 μM C), and in river waters, 43-271 μM C (mean 158 ± 62 μM C) and were very low in the lake Biwa waters, 89-97 μM C (mean 93 ± 2 μM C). The fluorescence properties of EEM showed that the fulvic-like components (peak C, peak A and peak M) were dominated in groundwater and river waters, but protein-like components (peak T) was in lake waters. The peak C was observed at [graphic removed] in groundwater, and 340 ± 5/432 ± 4 nm in river waters, but the lake waters detected the two peaks, 347 ± 7/441 ± 11 nm (peak C) as a minor peak and 304 ± 2/421 ± 8 nm (peak M) as a major peak. Emission wavelength of peak T was observed to shorten in wavelengths from groundwater to river and then lake waters. Peak T in lake waters showed at shorter in wavelengths (279 ± 2/338 ± 11 nm) at the middle point of Lake Biwa compared to those of lake shore site (283 ± 3/350 ± 7 nm). Photo-irradiation experiment on upstream waters suggested the changes in the fluorescence peaks of fulvic acid-like substances in lake waters, which might be caused by photo-degradation. DOC concentration was significantly correlated with inorganic anions and EC in river waters. However, such correlations were not observed in groundwater. Anion concentrations in lake waters were low with respect to DOC concentration. These results showed that the optical and chemical properties of FDOM are characteristically varied among groundwater, river and lake waters, indicating the impacts of environments to various FDOM at the same watershed level.

On the coastal plains of Finland there are approximately 3,000 km² of acid sulfate soils developed as a result of intensive agricultural drainage of waterlogged sulfide-bearing sediments. The runoff from these soils contains very high amounts of acidity and metals that have severely deteriorated the aquaculture in several downstream rivers and estuaries. Therefore, there is an urgent need to develop and test more environmental friendly ways of draining landscapes underlain with these nasty soils. In this study, over a 3-year monitoring period the effect of excess surface liming, controlled drainage and lime filter drainage of acid sulfate soils on runoff water quality (pH, sulfate, metals) was determined and assessed. The results showed that (1) the liming measures had not prevented severely acidic and metal-rich waters from forming and discharging from the soils, (2) the controlled drainage system might have reduced discharge peaks but its potential effects on the discharged water quality were nondetectable due to its small effect on the groundwater level and naturally inherited heterogeneities, and (3) the spatial and temporal variations identified for the various hydrochemical determinants were not caused by the kind of treatment applied. Therefore, on acid sulfate soil fields, like the one studied here, the short-term hydrochemical effects of the treatments tested are minor (or nonexistent) at least as long as the controlled drainage systems are not technically improved or better maintained.