Adsorption of Phenol and Chlorophenols by HDTMA Modified Halloysite Nanotubes.

The adsorption of phenol, 2-, 3-, 4-chlorophenol, 2-, 4-dichlorophenol and 2-, 4-, 6-trichloro-phenol on halloysite nanotubes modified with hexadecyltrimethylammonium bromide (HDTMA/halloysite nanocomposite) was investigated in this work by inverse liquid chromatography methods. Morphological and structural changes of the HDTMA/halloysite nanocomposite were characterized by scanning and transmission electron microscopy (SEM, TEM), Fourier-transform infrared spectrometry (FT-IR) and the low-temperature nitrogen adsorption method. Specific surface energy heterogeneity profiles and acid base properties of halloysite and HDTMA/halloysite nanocomposite have been determined with the inverse gas chromatography method. Inverse liquid chromatography methods: the Peak Division and the Breakthrough Curves Methods were used in adsorption experiments to determine adsorption parameters. The obtained experimental adsorption data were well represented by the Langmuir multi-center adsorption model.

Methods for the determination of levoglucosan and other sugar anhydrides as biomass burning tracers in environmental samples - A review.

Nowadays, there is a great pressure on finding an alternative source of energy. One such source is biomass combustion. Biomass is any organic matter such as wood, crops, seaweed, and animal wastes that during combustion emits energy but also smoke and solid residue. Biomass burning tracers, such as levoglucosan, mannosan and galactosan, are sugar anhydrides produced during burning of biomass that contain cellulose and hemicellulose. Analysis of environmental samples for tracers is the source of information about the type of biofuel burned. In this article, a literature review of the preparation and determination of biomass burning tracers for environmental samples was presented. The review discusses the preparation of different samples (particulate matter, soils, sediments, biological samples), extraction, derivatization, and determination. Amongst determination methods the most popular was gas chromatography with mass spectrometry but other techniques were also used, such as high-performance liquid chromatography with aerosol charge detection, capillary electrophoresis with pulsed amperometric detection, and ion chromatography with pulsed amperometric detection.

Conception of the Mercury Deposition Coefficient Based on Long-term Stream Intensity Measurements of Mercury Species TGM and TPM.

For many years, atmospheric mercury has been perceived as a global pollutant. Transport of mercury compounds in the atmosphere and its deposition on the earth's surface is an important issue that requires knowledge regarding the circulation of the various forms of this metal between environmental components. There are many numerical models that can be used to study and image this phenomenon. These models are based on data concerning mercury emission sources, concentrations of this contaminant on modelling areas and meteorological data to assess air mass inflow on a regional and global scale. A method to assess mercury deposition fluxes on a local scale based only on stream intensity analysis of mercury is proposed in this study. Mercury deposition fluxes (bulk) that were assessed by the MDC method at the Zloty Potok station (regional background station for the Silesian Agglomeration) varied from 22.8 µg · m-2 · year-1 (an 8-month period in 2013) to 54.2 µg · m-2 · year-1 in 2012. Developing procedures to estimate the mercury deposition coefficient (MDC) is useful in areas where only meteorological parameters and mercury concentrations in the atmospheric air are measured. The obtained deposition coefficient values enable quantification of a selected pollutant concentration and its potential impact resulting from deposition.

Study of photodegradation and photooxidation of p-arsanilic acid in water solutions at pH = 7: kinetics and by-products.

The paper presents the kinetics and proposed pathways photodegradation and photooxidation of p-arsanilic acid, in a neutral environment by ozone and hydrogen peroxide. The results showed that in a neutral environment, photoozonation process was characterized by the highest decomposition rate constant (k) (k = 31.8 × 10(-3) min(-1)). The rate constants decreased in the order UV/O3 > O3 > UV/H2O2 > H2O2 > UV. It was also found that under pH = 7, decomposition of p-arsanilic acid leads mainly to the formation of aniline, which undergoes secondary reactions. Intermediate products of oxidation and photooxidation by hydrogen peroxide like nitrobenzene, nitrophenol, azobenzenes, and phenylazophenol were identified depending on processes. However, in the photodegradation process, formation of nitrasone as a reaction product of p-arsanilic acid with oxygen in the singlet state was observed. In the case of ozonation and photoozonation, in addition, aniline formation of carboxylic acids was observed.

Application of advanced oxidation processes for cleaning of industrial water generated in wet dedusting of shaft furnace gases.

The paper presents results of studies into advanced oxidation processes in 03 and 03/UV systems. An advanced oxidation process (AOP) was conducted to reduce the load of impurities in circulating waters from wet de-dusting of shaft furnace gases. Besides inorganic impurities, i.e. mainly arsenic compounds (16 g As L(-1) on average), lead, zinc, chlorides and sulphates, the waters also contain some organic material. The organic material is composed of a complex mixture that contains, amongst others, aliphatic compounds, phenol and its derivatives, pyridine bases, including pyridine, and its derivatives. The test results show degradation of organic and inorganic compounds during ozonation and photo-oxidation processes. Analysis of the solutions from the processes demonstrated that the complex organic material in the industrial water was oxidized in ozonation and in photo-oxidation, which resulted in formation of aldehydes and carboxylic acids. Kinetic degradation of selected pollutants is presented. Obtained results indicated that the O3/UV process is more effective in degradation of organic matter than ozonation. Depending on the process type, precipitation of the solid phase was observed. The efficiency of solid-phase formation was higher in photo-oxidation with ozone. It was found that the precipitated solid phase is composed mainly of arsenic, iron and oxygen.

Methods for determination of polybrominated diphenyl ethers in environmental samples--review.

Polybrominated diphenyl ethers (PBDEs) are a group of persistent organic pollutants. They are used as flame retardants in plastics, paints, varnishes and textile materials. PBDEs pose great risk to the environment because of their high persistence and ability to get into the environment easily due to the lack of chemical bonds with the matrix of materials, to which they are added. Global research studies confirmed the occurrence of those compounds in the majority of elements of water and land environment. Analysis of PBDEs in environmental samples is one of the specific analytical methods of criteria that comprise low detection limits and high selectivity. The analysis of PBDEs in environmental samples is one of the specific analytical methods, in which the main criteria are low detection limits and high selectivity. In this article, a literature review of methods for environmental sample preparation and analysis of the PBDE content was presented. The article discusses the potential of modern extraction techniques such as: solid-phase microextraction, single-drop microextraction, dispersive liquid-liquid microextraction, microwave-assisted extraction, cloud point extraction, hollow fibre-liquid phase microextraction and others for the separation of PBDEs from environmental samples with a complex matrix. Among the methods for qualitative and quantitative determination of PBDEs, a particular focus was put on gas chromatography/mass spectrometry with various injection techniques and different types of sample ionisation.

Lead Speciation in the Dusts Emitted from Non-Ferrous Metallurgy Processes.

The paper presents results for the speciation analysis of lead in dusts derived from dedusting of technological gasses from metallurgical processes of non-ferrous metals with different elementary content, made in accordance with two equal sequential extractions. Analytical procedure A provided possibilities for determination of fraction of Pb(2+), metallic lead and fraction containing mainly lead sulfides. The second procedure (procedure B) was sequential extraction in accordance with Tessier. The results obtained in accordance with procedure A indicate that, regardless of the dust origin, the dominant group of Pb compounds is composed of lead salts which are soluble under alkaline conditions or lead compounds that form plumbites in the reaction with NaOH.

Synthesis of 2-deoxy-hexopyranosyl derivatives of uridine as donor substrate analogues for glycosyltransferases.

A series of 2-deoxy-hexopyranosyl derivatives of uridine have been synthesized as analogues of UDP-sugar. These compounds were tested as inhibitors against bovine beta-1,4-galactosyltransferase I in fluorescent assays and showed no significant inhibition.

Application of biosurfactants and non-ionic surfactants for removal of organic matter from metallurgical lead-bearing slime.

The paper presents evaluation of different extracting solutions used for removal of organic matter, especially polycyclic aromatic hydrocarbons (PAHs), from slime produced in copper smelting. A series of extraction experiments was conducted using biosurfactants and non-ionic surfactant solutions of various concentrations. The results showed that the efficiencies of organic matter removal by biosurfactants were at the level of 20-30% and depended on the type of the used biosurfactant. Biolen Biogrease L, and mixture of alkylobenzenesulfonic acid and oxyethylene fatty alcohol were effective for removal of polycyclic aromatic hydrocarbons (above 50%), whereas Zymbiose-enz. was ineffective. Non-ionic surfactants were found to be more effective in removing organic matter than biosurfactants. In the case of non-ionic surfactants the removal efficiencies depended on the concentration. Increase of Tween 80 concentration caused decrease in the efficiency of organic matter removal. The similar results were obtained for Nonoxynol 14. By contrast, the increase of Nonoxynol 10 concentration resulted in increase of organic matter removal efficiency.

Photo-degradation of chlorophenols in the aqueous solution.

The review presents the chlorophenols photo-degradation kinetics and mechanism in the aquatic environment under UV-vis in the presence of hydroxyl radicals and singlet oxygen. The influence of experimental parameters e.g. pH, dissociation degree, presence of oxidants in solution, number and position of Cl atoms on the quantum yield and reaction rate constant of chlorophenols are discussed. Mechanisms of photolysis, reaction with hydroxyl radicals, singlet oxygen and secondary reactions for mono-, di-, tri-, tetra- and pentachlorophenol are proposed. The pathways for intermediate reactions e.g. dechlorination, oxidation, dimerization for chlorophenols are also presented.

Fate of PCDD/PCDF during mechanical-biological sludge treatment.

In this preliminary study the seventeen 2,3,7,8-substituted congeners of PCDD/PCDF were analyzed at the inlet and outlet water and for three sewage sludge samples taken from different treatment stages to check behaviours of PCDD/PCDF at a municipal wastewater treatment plant (MWTP) in Poland. At the inlet (untreated sewage) water dominated PCDD congeners, whereas in the outlet (treated water) dominated the PCDF congeners. The octaCDD, 1,2,3,4,6,7,8-heptaCDD/CDF and octaCDF congeners dominated in all of the sludge samples. The total toxicity load gradually increased in the series excess, digested and dewatered sludge and amounted to 12.2, 14.4 and 16.9ngI-TEQkg(-1).

Sources and transformations of chlorophenols in the natural environment.

The present review updates our knowledge about chlorophenols, their chemical reactions and transformations in the natural environment, as well as factors affecting kinetics and mechanisms of these processes. Effects of pH of the environment and structure of molecules (also the number of chlorine atoms and their position in the molecule) on the behaviour of these compounds in the natural environment are also discussed. In addition, ways of propagation of chlorophenols in the natural environment are presented and discussed on the background of their physical and chemical properties, which influence the propagation rate in the ecosystems.