Alkylphenol ethoxylates and brominated flame retardants in water, fish (carp) and sediment samples from the Vaal River, South Africa.

Alkylphenol ethoxylates (APEs) and brominated flame retardants (BFRs) are known to be bio-accumulative, persistent, and endocrine disruptors and can cause adverse health effects in animals and humans. In this study, environmental samples were collected from sites along the Vaal River, South Africa in order to determine the concentrations of APEs and BFRs in water, sediment, and fish samples. The highest concentrations of these pollutants were observed from discharge of the Rietspruit WWTW. Measurable levels of both APEs and BFRs were observed with APEs exhibiting higher concentrations than BFRs in all the matrices. The concentrations observed for APEs and BFRs were as follows: 1.00-3.85 µg/L APEs, 0.09-0.26 µg/L PBDEs, ND- 0.14 PBBs and 0.51-1.77 µg/L HBCD for water samples; 47-63 ng/g lipid APEs, 3.24-12.4 ng/g lipid PBB, 4.63-33 ng/g lipid PBDEs and 10-13 ng/g lipid HBCD for fish; and 40-184 ng/g (wet weight (ww)) APEs, 2.93-5.9 ng/g (ww) PBB, 10-24 ng/g (ww) PBDEs, and 15-52 ng/g (ww) HBCD for sediment samples. The concentrations of APEs and BFRs in water samples were found to be in the range with the results reported in the literature while the concentration in fish and sediment were lower than the concentrations reported in other studies.

Preparation and use of maize tassels' activated carbon for the adsorption of phenolic compounds in environmental waste water samples.

The determination and remediation of three phenolic compounds bisphenol A (BPA), ortho-nitrophenol (o-NTP), parachlorophenol (PCP) in wastewater is reported. The analysis of these molecules in wastewater was done using gas chromatography (GC) × GC time-of-flight mass spectrometry while activated carbon derived from maize tassel was used as an adsorbent. During the experimental procedures, the effect of various parameters such as initial concentration, pH of sample solution, eluent volume, and sample volume on the removal efficiency with respect to the three phenolic compounds was studied. The results showed that maize tassel produced activated carbon (MTAC) cartridge packed solid-phase extraction (SPE) system was able to remove the phenolic compounds effectively (90.84-98.49%, 80.75-97.11%, and 78.27-97.08% for BPA, o-NTP, and PCP, respectively). The MTAC cartridge packed SPE sorbent performance was compared to commercially produced C18 SPE cartridges and found to be comparable. All the parameters investigated were found to have a notable influence on the adsorption efficiency of the phenolic compounds from wastewaters at different magnitudes.

Improved derivatization protocol for simultaneous determination of alkylphenol ethoxylates and brominated flame retardants followed by gas chromatography-mass spectrometry analyses.

An improved derivatization protocol for the simultaneous determination of alkylphenol ethoxylates and brominated flame retardants with heptafluorobutyric anhydride under triethylamine amine base was investigated. The derivatization reaction was completed in 30 min at 50 °C using hexane as solvent. Under these conditions, it was observed that alkylphenol ethoxylates and tetrabromobisphenol A were derivatized successfully in the presence of hexabromocyclododecane, lower congeners of polybrominated biphenyls and polybrominated diphenyl ethers. The improved protocol was applied to the recover of the analytes of interest from a simulated water sample after solid phase extraction. The recoveries achieved were above 60%. The limit of detection and limit of quantification ranged from 0.01-0.20 and 0.05-0.66 µg L(-1), respectively. The improved derivatization procedure was also successfully applied to determine trace amounts of these compounds in environmental water samples. The concentrations of the targeted analytes from the environmental samples were determined from limit of quantification. The levels of the targeted compounds in the environmental samples ranged from nd-7.63 ±2.83 µg L(-1).

Susceptibility of riparian wetland plants to perfluorooctanoic acid (PFOA) accumulation.

As plants have been shown to accumulate organic compounds from contaminated sediments, there is a potential for long-lasting ecological impact as a result of contaminant accumulation in riparian areas of wetlands, particularly the accumulation of non-biodegradable contaminants such as perfluorooctanoic acid (PFOA). In this study, commonly found riparian wetland plants including reeds, i.e., Xanthium strumarium, Phragmites australis, Schoenoplectus corymbosus, Ruppia maritime; Populus canescens, Polygonum salicifolium, Cyperus congestus; Persicaria amphibian, Ficus carica, Artemisia schmidtiana, Eichhornia crassipes, were studied to determine their susceptibility to PFOA accumulation from PFOA contaminated riparian sediment with a known PFOA concentration, using liquid chromatography/tandem mass spectrometry (LC/MS/MS). The bioconcentration factor (BCF) indicated that the plants affinity to PFOA accumulation was; E. crassipes, > P. sali-cifolium, > C. congestus, > P. x canescens, > P. amphibian, > F. carica, > A. schmidtiana, > X. strumarium,> P. australis, > R. maritime, > S. corymbosus. The concentration of PFOA in the plants and/or reeds was in the range 11.7 to 38 ng/g, with a BCF range of 0.05 to 0.37. The highest BCF was observed in sediment for which its core water had a high salinity, total organic carbon and a pH which was near neutral. As the studied plants had a higher affinity for PFOA, the resultant effect is that riparian plants such as E. crassipes, X. strumarium, and P. salicifolium, typified by a fibrous rooting system, which grow closer to the water edge, exacerbate the accumulation of PFOA in riparian wetlands.

Perfluorooctanoate and perfluorooctane sulfonate in South African river water.

This study examined the prevalence of perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS) in river water samples (n = 56) and suspended solids (n = 5) from three major Western Cape rivers, in South Africa. Solid phase extraction (SPE) followed by liquid chromatography combined with electrospray tandem mass spectrometry (LC-MS/MS) using an analytical method developed in ISO 25101 (2009), PFOS and PFOA concentration in river water and in suspended solids from the rivers was investigated and quantified. From the results, PFOA and PFOS were detected in all the river water samples and were found in concentrations up to 314 and 182 ng/L for Diep River; 390 and 47 ng/L for Salt River; and 146 and 23 ng/L for Eerste River, respectively. In suspended solids, concentrations for PFOS and PFOA were 28 and 26 ng/g for Diep River; 16 and less than limit of detection for Eerste River; and 14 and 5 ng/g for Salt River, respectively. Some of these concentrations are higher than those previously reported in similar studies in various countries, and this suggests there is a cause for concern, in the Western Cape, South Africa, particularly in catchments where river and ground water is drawn for agricultural purposes in the province.

Total petroleum hydrocarbons and trace metals in street dusts from Tshwane Metropolitan area, South Africa.

This study reports the level of total petroleum hydrocarbons (TPHs) and trace metals in dusts from some petroleum handling facilities (gasoline stations), selected high traffic density roads and residential areas within the Tshwane Metropolitan area in South Africa. Total petroleum hydrocarbons in dust samples were extracted using soxhlet extraction and isolated gravimetrically after column cleanup, while total trace metals in dust samples were digested using mineral acid digestion and analyzed using atomic absorption spectrometry (AAS). The mean TPH level from the residential sites ranged from 206 +/- 20.3-300 +/- 36.4 microg g(-1) while those from gasoline stations and high traffic density roads varied between 562 +/- 43.9-340 +/- 62.6 microg g(-1) and 404 +/- 32.7-852 +/- 55.4 microg g(-1) respectively. Mean concentrations of analyzed trace metals at residential areas ranged from 0.04 +/- 0.02-0.07 +/- 0.03 microg g(-1); ND; 0.21 +/- 0.01-0.34 +/- 0.02 microg g(-1); 0.66 +/- 0.06-2.11 +/- 0.82 microg g(-1); 18.7 +/- 0.86-33.4 +/- 0.83 microg g(-1) and 0.07 +/- 0.04-0.23 +/- 0.01 microg g(-1) for Cd, Pb, Cu, Zn, Mn and Cr respectively. Mean levels from gasoline stations ranged between 0.05 +/- 0.02-0.17 +/- 0.07; 0.08 +/- 0.02-0.12 +/- 0.04; 0.21 +/- 0.04-4.34 +/- 0.60; 7.44 +/- 0.40-13.0 +/- 0.56; 23.36 +/- 4.37-131 +/- 10.5 and 0.05 +/- 0.02-0.17 +/- 0.05 microg g(-1) while those from high traffic density roads ranged from 0.07 +/- 0.04-0.10 +/- 0.04; ND-0.30 +/- 0.05; 0.67 +/- 0.05-3.80 +/- 0.82; 2.40 +/- 0.25-10.6 +/- 0.96; 19.8 +/- 1.03-108 +/- 4.44 and 0.06 +/- 0.02-0.12 +/- 0.04 microg g(-1) also in the above metal order. Contamination by TPH and trace metals both at gasoline stations and high traffic density roads is revealed by their significantly higher values compared to those of residential areas.

Potential for local and systemic bacterial infection in some occupational groups in Benin City, Nigeria.

BACKGROUND: Many Third World countries may not have adequate facilities for rapid sensitivity testing of antibiotics as an aid to diagnosis and chemotherapy. It may therefore be valuable to relate bacterial carriage on the skin to type of work a person does. METHODS: Given areas of skin in workers from 10 occupational groups were sampled. The bacteria obtained were analyzed after growth on appropriate media. The sensitivity profiles of potential pathogens isolated from these groups, as well as of those (Staphylococcus aureus only) isolated from patients with certified infections, were carried out and the results were analyzed. RESULTS: Staphylococcus aureus constituted the most widely and frequently isolated potential pathogen. Proteus mirabilis, Escherichia coli, and Klebsiella species were also frequent colonizers of skin. There was a statistical relationship between work type and overall prevalence of bacteria on skin (p less than 0.01). Most isolates of the work groups were highly sensitive to gentamicin and cefuroxine but not to penicillin G, ampicillin, and trimethoprim plus sulfamethoxazole; isolates from infected persons were generally more resistant than were the community-acquired ones. CONCLUSIONS: A relationship may exist between the types of bacteria carried on the skin and the type of work in which a person is engaged.