Adsorption kinetics of methyl violet onto perlite

This study examines adsorption kinetics and activation parameters of methyl violet on perlite. The effect of process parameters like contact time, concentration of dye, temperature and pH on the extent of methyl violet adsorption from solution has been investigated. Results of the kinetic studies show that the adsorption reaction is first order with respect to dye solution concentration with activation energy of 13.2 kJ mol(-1). This low activation energy value indicates that the adsorption reaction is diffusion controlled. The activation parameters using Arrhenius and Eyring equations have been calculated. Adsorption increases with increase of variables such as contact time, initial dye concentration, temperature and pH.     

Degradation of the herbicide imazapyr by Fenton reactions

The degradation of the herbicide imazapyr has been carried out by three advanced oxidation processes involving iron ions as catalysts: Fentons reagent, photo-Fenton and electro-Fenton. We show that all processes are rapid and efficient. The kinetic rate constant was found to be k=5.4×10⁹ M^–1 s^–1. The mineralization of imazapyr is almost complete using the photo-Fenton and electro-Fenton processes.     

Analysis of short chain chlorinated paraffins in sediment samples from the Czech Republic by short-column GC/ECNI-MS

Top layer sediment samples from the Czech Republic were analyzed to obtain the preliminary information about contamination of the region by chlorinated paraffins. Sediment samples from three locations with different industrial discharges were taken over the period of 2 years. The analysis was performed by short-column gas chromatography-electron capture negative ion mass spectrometry (SCGC/ECNI-MS). Short chain chlorinated paraffin sediment concentrations varied between 24.00 and 45.78 ng g(-1) (dry weight, d.w.) in the Kosetice area, 16.30-180.75 ng g(-1) (dry weight) in the Zlín area and 4.58-21.57 ng g(-1) dry weight in the Beroun area. Highly chlorinated undecanes prevailed in the samples. On the basis of these results, more detailed studies should be conducted to determine the magnitude and extent of chlorinated paraffin contamination in these regions.     

Investigation of acute toxicity and the effect of 2,4-D (2,4-dichlorophenoxyacetic acid) herbicide on the behavior of the common carp (Cyprinus carpio L., 1758; Pisces,Cyprinidae)

A 96-h LC(50) values of 2,4-D [(2,4-dichlorophenoxy)acetic acid], a common contaminating agricultural herbicide, were determined on the adult common carp (Cyprinus carpio L., 1758; Pisces, Cyprinidae). The study was conducted in two stages using 130 carp. The data obtained were statistically evaluated by the use of the EPA computer program based on Finney's Probit Analysis Method and a 96-h LC(50) value for C. carpio L., 1758 was found to be 63.24 mg/l in a static bioassay test system. 95% lower and upper confidence limits for the LC(50) were 55.03 and 71.92 mg/l, respectively. Water temperature was 17+/-1 degrees C. Behavioral changes of the above mentioned species were examined for various herbicide concentrations.     

Electrochemistry: as cause and cure in water pollution—an overview

This article reviews both the pollution by the electrochemical industry and the use of electrochemistry to clean water. Main pollutants include Pd, Cd, Ni, Hg and other metals and cyanide as well as organic pollutants. The cause for water pollution by electrochemistry is due to the effluents from different electrochemical industries such as mercury from chlor-alkali industry; lead, cadmium and mercury from battery industry; heavy metals and organic contaminants from electroplating wastes; contaminants from corrosion processes; and persistent organic pollutants from the synthesis and use of pesticides, dyes and pharmaceuticals. Most pollutants can be successfully eliminated or converted to non-toxic materials by methods based on the electrochemical principles. Electrochemical depolluting methods are mainly electrodialysis, electrocoagulation, electroflotation, anodic processes, cathodic processes and electrochemical advanced oxidation processes.     

Photo-Fenton oxidation of Orange G azo dye: process optimization and mineralization mechanism

Environmental Chemistry Letters - Textile effluents containing synthetic dyes are one of the most important sources of water pollution. Several dyes are toxic to the aquatic life and...     

Bee pollens as biological indicators: An ecological assessment of pollution in Northern Turkey via ICP-MS and XPS analyses

Environmental Science and Pollution Research - In this study, pollens were collected from 25 different locations of Northern Turkey to investigate pollution monitoring. Surface chemistry of pollen...     

Integrated assessment modeling of atmospheric pollutants in the Southern Appalachian Mountains: Part II. Fine particulate matter and visibility

As part of the Southern Appalachian Mountains Initiative, a comprehensive air quality modeling system was developed to evaluate potential emission control strategies to reduce atmospheric pollutant levels at the Class I areas located in the Southern Appalachian Mountains. Six multiday episodes between 1991 and 1995 were simulated, and the skill of the modeling system was evaluated. Two papers comprise various parts of this study. Part I details the ozone model performance and the methodology that was used to scale discrete episodic pollutant levels to seasonal and annual averages. This paper (part II) addresses issues involved with modeling particulate matter (PM) and its relationship to visibility. For most of the episodes, the fractional error was approximately 50% or less for the major constituents of the fine PM (i.e., sulfate [SO4] and organics) in the region. The mean normalized errors and fractional errors are generally larger for the NO3 and soil components, but these components are relatively small. Variations in modeling bias with pollutant levels were also examined. The model showed a systematic overestimation for low levels and an underestimation for high levels for most PM species. For ammonium, the model showed better performance at lower SO4 concentrations when the measured SO4 was assumed to be completely neutralized (ammonium sulfate) and better performance at higher SO4 concentrations when the partially neutralized (ammonium bisulfate) assumption was made. The contributions of various components of PM to reductions in visibility were also calculated; SO4 was found to be the major contributor.