The screening of emerging micropollutants in wastewater in Sol Plaatje Municipality, Northern Cape, South Africa.

Although pollutants pose environmental and human health risks, the majority are not routinely monitored and regulated. Organic pollutants emanate from a variety of sources, and can be classified depending on their chemistry and environmental fate. Classification of pollutants is important because it informs fate processes and apposite removal technologies. The occurrence of emerging contaminants (ECs) in water bodies is a source of environmental and human health concern globally. Despite being widely reported, data on the occurrence of ECs in South Africa are scarce. Specifically, ECS in wastewater in the Northern Cape in South Africa are understudied. In this study, various ECs were screened in water samples collected from three wastewater treatment plants (WWTPs) in the province. The ECs were detected using liquid chromatography coupled to high resolution Orbitrap mass spectrometry following Oasis HLB solid-phase extraction. The main findings were: (1) there is a wide variety of ECs in the WWTPs, (2) physico-chemical properties such as pH, total dissolved solids, conductivity, and dissolved organic content showed reduced values in the outlet compared to the inlet which confirms the presence of less contaminants in the treated wastewater, (3) specific ultraviolet absorbance of less than 2 was observed in the WWTPs samples, suggesting the presence of natural organic matter (NOM) that is predominantly non-humic in nature, (4) most of the ECs were recalcitrant to the treatment processes, (5) pesticides, recreational drugs, and analgesics constitute a significant proportion of pollutants in wastewater, and (6) NOM removal ranged between 35 and 90%. Consequently, a comprehensive database of ECs in wastewater in Sol Plaatje Municipality was created. Since the detected ECs pose ecotoxicological risks, there is a need to monitor and quantify ECs in WWTPs. These data are useful in selecting suitable monitoring and control strategies at WWTPs.

Photocatalytic Degradation of Single and Binary Mixture of Brilliant Green and Rhodamine B Dyes by Zinc Sulfide Quantum Dots.

We present the preparation of octadecylamine-capped ZnS quantum dots from bis(morpholinyldithiocarbamato)Zn(II) complex. The complex was thermolyzed at 130 °C in octadecylamine at different times, to study the effect of reaction time on the morphological and photocatalytic properties of the ZnS quantum dots. Powder X-ray diffraction patterns confirmed a hexagonal wurtzite crystalline phase of ZnS, while HRTEM images showed particle sizes of about 1-3 nm, and energy band gaps of 3.68 eV (ZnS-1), 3.87 eV (ZnS-2), and 4.16 eV (ZnS-3) were obtained from the Tauc plot for the ZnS nanoparticles. The as-prepared ZnS were used as photocatalysts for the degradation of brilliant green, rhodamine B, and binary dye consisting of a mixture of brilliant green-rhodamine B. The highest photocatalytic degradation efficiency of 94% was obtained from ZnS-3 with low photoluminescence intensity. The effect of catalytic dosage and pH of the dyes solution on the photocatalytic process shows that pH 8 is optimal for the degradation of brilliant green, while pH 6.5 is the best for photocatalytic degradation of rhodamine B. The degradation of the binary dyes followed the same trends. The effect of catalytic dosage shows that 1 mg mL-1 of the ZnS nano-photocatalyst is the optimum dosage for the degradation of organic dyes. Reusability studies show that the ZnS quantum dots can be reused five times without a significant reduction in degradation efficiency.

Enhanced Photocatalytic Degradation of Ternary Dyes by Copper Sulfide Nanoparticles.

We report the effect of thermolysis time on the morphological and optical properties of CuS nanoparticles prepared from Cu(II) dithiocarbamate single-source precursor. The as-prepared copper sulfide nanoparticles were used as photocatalysts for the degradation of crystal violet (CV), methylene blue (MB), rhodamine B (RhB), and a ternary mixture of the three dyes (CV/MB/RhB). Powder XRD patterns confirmed the hexagonal covellite phase for the CuS nanoparticles. At the same time, HRTEM images revealed mixed shapes with a particle size of 31.47 nm for CuS1 prepared at 30 min while CuS2 prepared at 1 h consists of mixtures of hexagonal and nanorods shaped particles with an average size of 21.59 nm. Mixed hexagonal and spherically shaped particles with a size of 17.77 nm were obtained for CuS3 prepared at 2 h. The optical bandgaps of the nanoparticles are 3.00 eV for CuS1, 3.26 eV for CuS2 and 3.13 eV for CuS3. The photocatalytic degradation efficiency showed that CuS3 with the smallest particle size is the most efficient photocatalyst and degraded 85% of CV, 100% of MB, and 81% of RhB. The as-prepared CuS showed good stability and recyclability and also degraded ternary dyes mixture (CV/MB/RhB) effectively. The byproducts of the dye degradation were evaluated using ESI-mass spectrometry.

Morphological Studies, Photocatalytic Activity, and Electrochemistry of Platinum Disulfide Nanoparticles from Bis(morpholinyl-4-carbodithioato)-platinum(II).

Bis(morpholinyl-4-carbodithioato)-platinum(II) was synthesized and characterized using spectroscopic techniques and single-crystal X-ray crystallography. The Pt(II) complex crystallized in a monoclinic space group P21/n with a Pt(II) ion located on an inversion center coordinated two morpholinyl dithiocarbamate ligands that are coplanar to form a slightly distorted square planar geometry around the Pt(II) ion. The complex was thermolyzed at 120, 180, and 240 °C to prepare PtS2 nanoparticles. Powder X-ray diffraction patterns confirmed the hexagonal crystalline phase for the as-prepared PtS2 nanoparticles irrespective of thermolysis temperature. Bead-like shaped PtS2-120 nanoparticles with a particle size in the range of 12.46-64.97 nm were formed at 120 °C, while PtS2-180 prepared at 180 °C is quasi-spherical in shape with particles in the range of 24.30-46.87 nm. The PtS2-240 obtained at 240 °C is spherical with particles in the range of 11.45-46.85 nm. The broad emission maxima of the as-prepared PtS2 nanoparticles are ascribed to the particles' broad size distributions. The photocatalytic degradation of methylene blue by the PtS2 nanoparticles shows a maximum efficiency of 87% for PtS2-240 after 360 min. The effects of photocatalytic dosage, irradiation time, pH medium, and scavengers were also evaluated. Cyclic voltammetry of the PtS2 nanoparticles showed a reversible redox reaction, while the electrochemistry of the as-prepared PtS2 indicates that the electron transfer process is diffusion-controlled.