Employment of passive sampling in monitoring indoor air quality in selected residences in a Tri-city area in Poland

Time-weighted average concentrations of selected volatile compounds were measured in chosen residences in a Tri-City area of Poland by means of passive sampling. The results were compared to those obtained by dynamic technique – sorption tubes filled with Tenax TA sorbent. Results obtained by employing the two techniques were similar. Total volatile organic compound (TVOC) parameters were also determined. An attempt was also made to evaluate the influence of outdoor air pollutants on indoor air quality.     

Study of sorptive properties of trap systems for selective enrichment of volatile organic compounds from tobacco smoke samples

There is a dearth of data on the consumer product concentrations of iron, lead, and nickel for accurate comparison to be made. The levels of these elements were determined in 85 samples of six different classes of personal care products commonly used in Nigeria using atomic absorption spectrophotometry. The results of the analysis showed that the range of the mean concentrations of Fe was 0.485–1.108 ppm, Pb ND–0.163 ppm, and Ni ND-0.160 ppm. The analytical data have demonstrated that the selected consumer products are possible sources of iron, lead, and nickel exposure. Users can be exposed to these metals directly through dermal contact or inhalation. The regulations relating to cosmetic products give no limit values for heavy metals in cosmetic products, hence, it was difficult to establish if the values obtained in this study are safe or not. Prolonged use of soaps, creams, and detergent containing these elements may pose threat to human health and the environment. This could be responsible for various skin diseases such as allergic skin, follicular and pigmentary disorders, which are common among the users (exposed groups) of these products in Nigeria. A body of evidence has presented a rare example of systemic allergic dermatitis caused by topical application of a mercury-containing cosmetic to the upper lip of a 32-year-old Turkish patient.     

Male reproductive toxicity of organophosphorous compounds: a review

Fertility is declining in many countries and there has been substantial interest in the potential adverse effects of exposure to environmental hazardous chemicals, including pesticides on male reproduction. Organophosphorous compounds (organophosphates, OP) constitute a heterogeneous category of chemicals specifically designed for the control of pests or plant diseases. OP are known to produce reproductive toxicity, resulting in a decrease in the fertility levels of humans and animals. This review article mainly focused on toxicity of some OP such as acephate, chlorpyrifos, diazinon, dimethoate, fenitrothion, malathion, and monocrotophos especially dealing with reproductive toxicity in males. Furthermore, this review deals with mode of action and clinical syndromes of OP. Considerable lab studies on animals concluded that OP produce adverse effects on male reproductive system.     

Detection and quantitation of trace levels of low molecular weight halocarbons (LMHs) associated with commercial sodium humate

Examination of vapor above commercial sodium humate and above 10wt% aqueous humate solution by gas chromatography (GC) revealed the presence of chloroform and trichloroethylene. Further examination of the aqueous humate by the purge and trap procedure confirmed the association of chloroform and trichloroethylene with the humate. GC/mass spectrometry analyses of methylene chloride extract of the humate established the association of LMHs with the humate. Improved headspace capillary GC technique showed that the humate contained not only chloroform, trichloroethylene but several other LMHs in the range 190 to 4000ng·kg^‐1.     

Effect on benthic communities of a major input of organic matter and other pollutants (coast off Barcelona,Western Mediterranean)

Benthic communities on soft bottoms off Barcelona, at and around two main pollution sources, the mouth of the Besòs River and the outlet of the submarine pipeline draining wastewater and organic sludges from the wastewater treatment plant of Sant Adrià del Besòs, have been studied. Samples were obtained with a Van Veen grab from 36 stations covering a 100 km² grid, between 10 and 70 m in depth. The effect of both pollution sources is clearly seen both at the species (the following macrofauna groups have been studied: Polychaeta, Mollusca, Echinodermata and Crustacea Decapoda) and community levels. The distribution of species and individuals numbers, species diversity and a pollution index, and of some selected (indicator) polychaeta species, all clearly define the degree of environmental degradation and the extent of the areas under the influence of the organic pollution.     

Effect Of pH on the complexation of U(II) with organic matter dissolved in resh waters

In the present work we study the effect of pH on the complexation of copper with organic matter dissolved in fresh surface waters. Samples collected in rivers of Galicia (NW of Spain) were titrated with copper solution at pH values in the range 5.5–7.5. Copper concentration was measured by DPASV technique. The complexation parameters were obtained from the simple model of 1 : 1 complex formation. The obtained values show a linear increase of the logarithm of the conditional stability constant as the pH increases.     

Aqueous high‐temperature chemistry of arsenic‐containing compounds in water at 300°C

Arsenic compounds, and especially organo‐arsenic derivatives, are highly toxic and many have been manufactured as chemical warfare agents. This study was designed to provide background information relevant to the potential application of aquathermolysis techniques for the detoxification of such potent military warfare agents. Six arsenic‐containing compounds with structural features which mimic known agents were studied in neutral superheated water: 4‐aminophenylarsine oxide, 4‐arsanilic acid, 4‐nitrophenylarsonic acid, 5, 10‐dihydro‐10‐ethylphenarsazine, tetraphenylarsonium chloride hydrate, and (3‐cyanopropyl)dimethyl(2‐phenethyl)arsonium bromide. Most of these compounds were moderately susceptible to hydrolysis for 1h at 300°C. o‐ and p‐Aminosubsituted arsenic compounds were more reactive than compounds with an electron‐withdrawing group substituent. Aromatic C—As bonds were more resistant to cleavage than aliphatic C—As bonds.     

Diazinon leaching through a sandy soil amended with different humic materials

The water leaching of diazinon (O,O‐diethyl‐O‐2‐isopropyl‐6‐methylpyrirnidin‐4‐yl phosphoroth‐ioate) through soil columns, was studied after column amendments with two well characterized humic acids (HA), in both liquid and solid state, and with the original raw organic materials, an oxidized coal and a leonardite, from which the HA were extracted. The percolation curves and the pesticide distribution over the soil columns showed that the addition of the raw organic materials and the solid HAs reduced significantly the mobility of the pesticide along the soil column. The oxidized coal was more effective than the leonardite original material; the different origin of the two carbon‐rich materials had an influence on the diazinon movement along the soil columns and such difference was enhanced with increasing addition rates. Moreover, incubation at field capacity for two months of the soil columns treated with raw oxidized coal and leonardite, largely enhanced the described effects on pesticide behaviour. A complete adsorption of diazinon on columns and a practical absence of leaching was observed when the HA from both materials were added in dissolved form. These results were explained with the swelling of the humic micelles in water and the enhanced availability of inner hydrophobic surfaces for the strong adsorption of diazinon. The water diffusion into the solid humic materials after two months incubation, also explains their high pesticide retention capacity. This work indicates the usefulness of either solid o dissolved humic substances, with the proper hydrophobic character, in preventing the vertical leaching of non‐polar organic pesticides in soils.     

Determination and QSPR analysis of log Kow and log Koc for fluorine containing benzene derivatives

Octanol‐water partition coefficients (Kow) and soil organic carbon sorption coefficients (Koc) were determined for 14 fluorinated benzene derivatives. Quantitative structure‐property relationships were developed using molecular connectivity indices and quantum chemical parameters to analyze the most significant factors influencing these physico‐chemical properties of the compounds. The substitution by F in benzene derivatives has greater influence on Koc than on Kow.     

Source and material balance of total organic halogen pollution in the Ayase River system,Japan

The total organic halogen (TOX) pollution in the highly polluted Ayase River system was investigated. Using the concentration of coexisting linear undecylbenzenesulfonate and the difference in the flowing water volume between summer and winter, the fractions of domestic and agricultural wastewaters in the whole water column were calculated and the variety of the TOX sources in the river was estimated. The river carried about 100 kgCl of TOX materials in one day; about 50 kgCl of the materials was from residential area in the basin. The contribution of agricultural drainage from paddy field was not negligible in summer. Highly contribution of industrial wastewater was observed in a tributary Furuayase River basin while the amount of TOX loaded in the area was widely varied; 0–105 kgCl of the materials was discharged as industrial wastewater.