Background: Pharmaceuticals is one of the groups of contaminants of emerging concern that are resistant to decomposition or removal by most of the existing water and wastewater treatment procedures, hence the need to develop techniques to facilitate the removals of this group of organic contaminants from water systems. In this study, needle-like SnO₂ nanoparticles was synthesised and loaded on exfoliated g-C₃N₄ nanosheet through a hydrothermal method, for use as sensitive visible light induce-photocatalyst for the decomposition of tetracycline in aqueous systems. The synthesised composites was characterized and analysed for the nature of the heterojunction between the SnO₂ nanoparticle and g-C₃N₄ nanosheet using microscopic and spectroscopic techniques. Results: The composites were of improved surface properties and enhanced visible-light absorption. The synthesised SnO₂/g-C₃N₄ nanocomposites with various amounts of SnO₂ (10–50 mg), employed in the degradation of tetracycline under visible light irradiation, were of good degradation efficiency. The degradation efficiencies of tetracycline by 1 wt.%, 2 wt.%, 3 wt.% and 5 wt.% SnO₂/g-C₃N₄ photocatalyst were 81.54%, 90.57%, 95.90% and 92.15% as compared to g-C₃N₄ and SnO₂ with 40.92% and 51.32% degradation efficiencies. The synergistic interaction between the needle-like SnO₂ and exfoliated g-C₃N₄ nanosheet promoted the separation of photogenerated electron holes pairs, which enhanced their migration rate between SnO2 and g-C3N4 heterojunction, thereby facilitating the degradation of tetracycline. The ·O₂⁻ was noted to be the major reactive species in the photocatalytic of the 3 wt.% SnO₂/g-C₃N₄ nanocomposite. Conclusion: The fabricated SnO₂ nanoparticles anchored on exfoliated g-C₃N₄ showed good performance for the decomposition of tetracycline in water, with possible application on other pharmaceuticals having same moiety (similar chemical structures).

The best management options for cover cropping are largely unknown, including the growth patterns of cover crop (CC) species, optimum termination stages and termination methods. A greenhouse experiment was conducted to explore the following: (i) Effect of two termination stages (vegetative and flowering) on the chemical composition (N and C:N) of four CCs; (ii) Short-term impacts of living CCs and residues on soil pH, total N, urease and phosphatase activities at the two termination stages, and under two termination methods (slash and spray). Species tested as CCs were, vetch (Vicia dasycarpa L.), field pea (Pisum sativum L.), oats (Avena sativa L.), rye (Secale cereal L.) and a control (no CC). The experiment was set up in a randomized block design with three replications. Soil was sampled at kill and one year after CC kill. Delaying termination from vegetative till flowering stage decreased N in the tissue of P. sativum, A. sativa, V. dasycarpa and S. cereal by 59%, 65%, 44% and 56%, respectively, while their C:N ratios increased. Cover crop presence had no effect on soil pH. Living CCs had no significant effect on soil N concentration. The activities of urease and phosphatase were stimulated by all the living CC species. Unlike urease, all CC residues had a positive impact on phosphatase activity at one year. Only P. sativum and V. dasycarpa residues increased soil N concentration in the short-term. Compared to flowering, termination at vegetative stage improved soil N concentrations and phosphatase activity at both sampling times. Termination method had no effect on soil N, urease and phosphatase activity at one year. The significant interaction (P < 0.05) of sampling time, CC and termination stage effects on soil N concentration and phosphatase activity observed in this study indicates that these management approaches can optimize CC benefits and improve soil chemical and biological properties.

The detection and quantitation of pharmaceutical compounds (PCs) in different environmental matrices is still a challenge, due to their extremely low (ng-μg) concentrations and the lack of rapid and sensitive analytical techniques. A number of techniques, such as enzyme-linked immunosorbent assay (ELISA), chromatography, electrophoresis, and electrochemical methods have been explored. These methods are limited by their poor sensitivity. In this study, a hyphenated liquid chromatography-mass spectrometric (LC-MS) method was developed, validated, and tested for the detection and quantification of seven active pharmaceutical compounds, with solid-phase extraction for analytes recovery and separation of interference from the aqueous matrix. The sensitivity achieved for the method allowed for LODs (μg/L) of 0.0439, 0.0684, 0.1219, 0.0710, 0.1129, 0.0447, 0.0837 and LOQs (μg/L) of 0.1462, 0.2281, 0.4065, 0.2367, 0.3763, 0.1492, 0.2792, for lamivudine, acetaminophen, vancomycin, ciprofloxacin, sulfamethoxazole, diclofenac, and ivermectin, respectively, within a linear range of 0.01–0.1 μg/mL. Other ICH validation parameters are also discussed. The different PCs were positive in 61 % of the tested surface waters, with diclofenac present only in two of the sampling points. The concentrations at which they occurred were variable and ranged between ND and 398.98 μg/L.

A multi-residue method for the determination of the occurrence and prevalence levels of selected veterinary pharmaceutical residues in surface water was developed on a high performance liquid chromatography coupled to ultraviolet-visible (HPLC-UV) detector, and tested with the intent of profiling their distribution. The limit of detection (LOD) and limit of quantitation (LOQ) achieved for the selected pharmaceuticals; acetaminophen, diclofenac, salicylic acid, tetracycline, chloramphenicol, ciprofloxacin, bisphenol-A, 17β-estradiol, estriol, and ivermectin ranged between 0.06-3.45 μg L-1 and 0.17-10.35 μg L-1 respectively. Other International Conference on Harmonization (ICH) parameters for validation of analytical procedures were also evaluated and discussed. Pharmaceutical residues were recovered from surface water samples collected from around livestock farms in Cape Town, South Africa by solid phase extraction (SPE), and thereafter separated and quantified using a validated method on a HPLC-UV-detector. Most frequently detected residues were: acetaminophen (56%), diclofenac (53), tetracycline (72%), 17β-estradiol (73%); chloramphenicol (68%), and salicylic acid (67%), with significantly high (p > 0.05) spatial variability in the concentration distributions of the pharmaceuticals in the surface waters.