Utilization of nSiO2, fly ash, and nSiO2/fly ash composite for the remediation of triphenyltin (TPT) from contaminated seawater

The removal of triphenyltin chloride from contaminated simulated seawater with adsorption method was discussed. The adsorbents used are fly ash, nSiO₂, and nSiO₂/fly ash composite. The results showed that the adsorption of the adsorbents increases with increase in the adsorbent dose, contact time, pH, stirring speed, initial TPT concentration, and decreased with increase in temperature. The adsorption fitted well with the Freundlich isotherm, showing that the adsorbent and TPT combined with function groups and the adsorption kinetics followed the pseudo-second-order kinetic model. The thermodynamic parameters were also evaluated. Optimal conditions for the adsorption of TPT from simulated seawater were applied to TPT removal from natural seawater. A higher removal efficiency of TPT (>99 %) was obtained for the nSiO₂/fly ash composite but not for fly ash and nSiO₂.     

Trace zinc and copper concentration in roadside surface soils and vegetation—measurement of local atmospheric pollution in Alice, South Africa

Surface soil and grass samples were collected from ten locations perpendicular to a major road in Alice and were analyzed for zinc and copper. The results revealed an association between zinc concentration and distance from road traffic. An association was also revealed between soil zinc and grass zinc which suggests same source for the metal in samples. The results for copper did not show any correlation between sample concentration and distance from road traffic. Neither did it show any correlation between soil zinc and soil copper or between grass zinc and grass copper which suggests different sources for the elements.     

Levels of organochlorine pesticide residues in marine-, surface-, ground- and drinking waters from the Eastern Cape Province of South Africa

Persistent organochlorine pesticides (OCPs) such as DDT and its metabolites (DDDs and DDEs). chlordane, hexachlorobenzene (HCB), heptachlor and endosulfan were determined in drinking-, ground-, surface- and marine waters from the Eastern Cape Province of South Africa. Percentage recoveries of the OCPs from spiked river water ranged from 71.03 +/- 8.15% (dieldrin) to 101.25 +/- 2.17% (alpha-BHC). The levels of OCPs ranged from 5.5 ng/L (2,4-DDD) to 160 ng/L (HCB) in the water samples. Some endocrine disrupting OCPs such as DDT, DDE, heptachlor, endosulfan and chlordane were detected.     

Catalytic activities of ultra-small β-FeOOH nanorods in ozonation of 4-chlorophenol

We report the catalytic properties of ultra-small β-FeOOH nanorods in ozonation of 4-chlorophenol (4-CP). XRD, TEM, EDS, SAED, FTIR and BET were used to characterize the prepared material. Interaction between O₃ and β-FeOOH was evident from the FTIR spectra. The removal efficiency of 4-CP was significantly enhanced in the presence of β-FeOOH compared to ozone alone. Removal efficiency of 99% and 67% was achieved after 40 min in the presence of combined ozone and catalyst and ozone only, respectively. Increasing catalyst load increased COD removal efficiency. Maximum COD removal of 97% was achieved using a catalyst load of 0.1 g/100 mL of 4-CP solution. Initial 4-CP concentration was not found to be rate limiting below 2 × 10^− 3 mol/L. The catalytic properties of the material during ozonation process were found to be pronounced at lower initial pH of 3.5. Two stage first order kinetics was applied to describe the kinetic behavior of the nanorods at low pH. The first stage of catalytic ozonation was attributed to the heterogeneous surface breakdown of O₃ by β-FeOOH, while the second stage was attributed to homogeneous catalysis initiated by reductive dissolution of β-FeOOH at low pH.     

Bioaccumulation of metals in black mussels (Mytilus galloprovincialis) in Cape Town Harbour, South Africa

Heavy metal concentrations in black mussels (Mytilus galloprovincialis) collected from Cape Town Harbour were determined using energy dispersive X-ray fluorescence (EDXRF) and inductively coupled plasma-mass spectrometry (ICP-MS). EDXRF showed that tissue portions of the mussels contained K, Ca, Fe, Cu, Zn, Si, Sr, Al and Au, while the shell portion contained K, Ca, Fe, Cr, Zn, Si and Sr. In addition to these metals, EDXRF also revealed the presence of Al in the shells of the largest mussels. Highest concentrations of Cu and Zn were recorded in the tissues of the smallest mussels. Due to poorer detection limits of EDXRF, ultra-trace elements (Mn, Pb, As, Hg, V, Cr, Sn, Cd, Ni and Co) were determined in mussels using ICP-MS. The average metal concentrations found in the mussels are as follows; Pb (7.30 ± 0.67), Cd (1.98 ± 0.13), Hg (4.92 ± 0.60), As (6.94 ± 0.04), Sn (2.63 ± 0.13), Ni (1.88 ± 0.05), Cr (3.54 ± 0.05), V (4.17 ± 0.23), Co (0.74 ± 0.01) and Mn (35.20 ± 1.46). ANOVAs, Pearson correlation and principal component analysis (PCA) were employed in data analysis. The order of the abundance of metals in the mussels is Mn > Pb > As > Hg > V > Cr > Sn > Cd > Ni > Co. The average metal concentrations found in the mussels were higher than the permissible Food and Agriculture Organization (FAO) limits and other international guidelines.     

Determination of selected steroid hormones in some surface water around animal farms in Cape Town using HPLC-DAD

In this study, a method for the simultaneous determination of two steroid hormones, 17β-estradiol (E2) and estriol (E3), and a hormone mimicking polycarbonate, bisphenol-A (BPA), was developed and validated. This was thereafter used for the determination of the levels of the hormones in surface water collected around some livestock farms. The sensitivity of the method allowed the LODs and LOQs of the hormones and mimic hormone in the range 1.14–2.510 and 3.42–7.53 μg/L, respectively. The results revealed wide variability in the concentrations of E2 and E3, while BPA was not detected at any of the sampling stations. The concentration of E3 ranged between <1.14 and 45.5 μg/L (N = 120) in station 2 water. The highest concentration of E2 (15.7 μg/L, N = 80) was observed in water from station 1. The varied concentrations may be connected with the nature and sources of release, inconsistencies in analyte distribution due to dynamics of water flow pattern and the physical/chemical properties of the receiving water bodies.     

Assessment of polybrominated diphenyl ethers in sediment of Asunle stream of the Obafemi Awolowo University,Ile-Ife,Nigeria

Assessment of levels of polybrominated diphenyl ethers (PBDEs) from the sediment of Asunle stream, an adjourning stream of the Obafemi Awolowo University dumpsite, has been carried out. Sediment samples were collected from the stream at six locations for a period of 8 months, composed of 4 months each of wet (May–Aug) and dry (Nov–Feb) seasons. Soxhlet extraction was employed for the isolation of all the target compounds from the sediment samples. Extracts were further subjected to multi-layer column chromatography employing different forms of silica gel. The prepared samples were analyzed using GC-MS. The overall mean concentrations of the total PBDEs ranged from 1.80 to 9.46 ng/g. The results showed that the concentrations of the PBDEs were slightly higher during the wet season than those during the dry season. In all the studied locations, BDE28, BDE47, BDE99, BDE100, BDE153, and BDE154 were detected in all the sediment samples at concentrations that ranged from 0.73 to 10.43 ng/g. Results of this study indicated that BDE153 was the major pollutant of the Asunle stream sediments.     

Polybrominated diphenyl ethers (PBDEs) and 2,2′,4,4′,5,5′-hexabromobiphenyl (BB-153) in landfill leachate in Cape Town, South Africa

An assessment of the concentrations of selected polybrominated diphenyl ether (PBDE) congeners as well as BB 153 in leachate samples collected from three landfill sites within the city of Cape Town was conducted. A liquid–liquid extraction technique was employed for the isolation of all the target compounds from the leachate samples. Extracts obtained were further subjected to multi-layer column chromatography employing different forms of silica gel. The prepared samples were analysed using a high capillary gas chromatograph equipped with a micro-electron capture detector (GC-μECD). The overall mean concentrations of the total PBDEs, including BDE 209 ranged between 5.65 and 2,240, 0.28–20.5 and 1.66–1,170 ng/l for Bellville, Coastal Park, and Vissershok landfill sites, respectively. The mean concentrations of BB 153, which were generally low in most of the samples analysed, were 70.4, 7.14 and 8.16 ng/l for Bellville, Coastal Park and Vissershok sites, respectively. The influence of precipitation on the characteristics and quantity of leachate produced from the landfill sites investigated was most pronounced during the August/September sampling regime. Generally, the trend observed in this study clearly indicated a wide variation in the levels of these contaminants in all the landfill sites studied from one sampling period to the other. However, the principal component analysis revealed that the release of these contaminants might be associated with two or three possible sources. This study further confirmed the relevance of landfill leachate as an important source of PBDE contamination of the environment, especially the groundwater and surface water sources.     

Determination of phthalate ester plasticizers in the aquatic environment of Southwestern Nigeria

Water from the Lagos, Oyo, Osun, Ondo, and Delta states of Nigeria and the cities' water treatment plants had been analized for the presence of ubiquitous phthalate esters using liquid chromatography. Extraction with CH₂Cl₂ and liquid chromatography was used for compound separation. Several phthalate esters, dimethyl- (DMP), diethyl- (DEP), and di-n-butyl- (DBP) were found present at levels of 10 mg L⁻¹ to 1472 mg L⁻¹ in river water and 91 mg L⁻¹ to 1219 mg L⁻¹ in tap water from the cities' water treatment plants. A study of uncontaminated water was done to establish blank levels.     

Occurrence of polybrominated diphenyl ethers (PBDEs) and 2,2’,4,4’,5,5’-hexabromobiphenyl (BB-153) in water samples from the Diep River, Cape Town, South Africa

Until recently, studies reporting the concentrations of polybrominated diphenyl ethers (PBDEs) as well as polybrominated biphenyls (PBBs) are generally scarce in the literature. Consequently, this study was aimed to investigate the occurrence and concentrations of certain PBDE congeners (BDE 28, 47, 100, 99, 154, 153, 183 and 209) and BB 153 in river water samples collected bi-monthly from the Diep River. The routine analyses of the target compounds were performed using a high-capillary GC–microelectron capture detection, while their structural elucidation was assessed using GC-TOF-MS technique. The overall mean concentrations of the sum of the eight PBDE congeners were 2.60, 4.83 and 4.29 ng/L for the upstream, point of discharge and downstream sampling points, respectively. Similarly, the overall mean concentrations of BB 153 were 0.25, 4.85 and 1.56 ng/L for the upstream, point of discharge and downstream sampling points, respectively. BDE 47 was the dominant congener found in these samples contributing between 19 and 26 % to the total PBDEs across the sampling points. The statistical analyses performed on the results obtained showed that all the congeners, except BDE 209 in certain instances, had strong positive correlations with one another, thus suggesting that these contaminants could be emanating from the same source. In this study, potential sources of these pollutants other than WWTP discharges into the investigated river were also identified. However, the relatively high concentrations of the target compounds found at the point of discharge sampling point coupled with the large volume of treated effluent being discharged suggested that the contributions from this source could be very significant over time.