Commercialization in the meat-processing industry has emerged as one of the major agrobusiness challenges due to the large volume of wastewater produced during slaughtering and cleaning of slaughtering facilities. Slaughterhouse wastewater (SWW) contains proteins, fats, high organic contents, microbes, and other emerging pollutants (pharmaceutical and veterinary residues). It is important to first characterize the wastewater so that adequate treatment techniques can be employed so that discharge of this wastewater does not negatively impact the environment. Conventional characterization bulk parameters of slaughterhouse wastewater include pH, color, turbidity, biochemical oxygen demand (BOD), chemical oxygen demand (COD), total organic carbon (TOC), total suspended solids (TSS), total nitrogen (TN), total phosphorus (TP), and coliform counts. Characterization studies conducted have revealed the effects of the pollutants on microbial activity of SWW through identification of toxicity of antibiotic-resistant strains of bacteria. Due to the high-strength characteristics and complex recalcitrant pollutants, treatment techniques through combined processes such as anaerobic digestion coupled with advanced oxidation process were found to be more effective than stand-alone methods. Hence, there is need to explore and evaluate innovative treatments and techniques to provide a comprehensive summary of processes that can reduce the toxicity of slaughterhouse wastewater to the environment. This work presents a review of recent studies on the characterization of SWW, innovative treatments and technologies, and critical assessment for future research.

Natural materials are widely used in the field of environmental remediation and are appreciated for their surface physical and chemical properties. Clay constitutes a typical example. In this work, we report the evaluation of sorbent and photocatalytic potentials of local clay of two irrigated rice field waters in the degradation of crystal violet. The structural, textural and compositional properties of the local clay were investigated by Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD) and X-ray Fluorescence (XRF) analysis. The analysis results showed that these materials were composed mainly of quartz and kaolinite. The efficiency of these adsorbents (Y. Clay and L. Clay) to eliminate crystal violet dye from aqueous medium was examined at different initial concentrations, pH, contact time, adsorbent dose and the possible interference of inorganic salts from fertilizers. Kinetic studies showed that the adsorption process was well described by the pseudo-second order model and the equilibrium modelling results fitted adequately to the Freundlich model. The maximum amount of uptake capacity achieved at pH 2.0 was 18.40 (mg·g⁻¹) and 20.40 (mg·g⁻¹), respectively, for Y. Clay and L. Clay. The evaluation of the photocatalytic potential showed that the raw clay samples do not show photocatalytic activities during the 30 min of exposure to UV light. On the other hand, their photocatalytic potential is manifested when loaded with titanium dioxide (TiO₂). Clays coupled with TiO₂ under UV light showed an improvement in the degradation of the crystal violet dye by 15%. The synergistic effects between the high photocatalytic activity of TiO₂ and the strong adsorption capacity of clays can be one promising technique for in situ remediation of contaminated soaked rice field.

In this study, TiO₂ nanospheres (TiO₂-NS) were synthesized by the solvothermal method. Firstly, the synthesized nanomaterial was characterized by X-ray diffraction (XRD), Fourier Transformed Infrared (FTIR), scanning electron microscopy (SEM) and UV-Vis Diffuse Reflectance Spectroscopy (DRS). To study the photocatalytic degradation of Tartrazine (TTZ) and Naphthol Blue Black (NBB) in a binary mixture, the influence of some key parameters such as pH, pollutant concentration and catalyst dose was taken into account under visible and UV light. The results show a 100% degradation efficiency for TTZ after 150 min of UV irradiation and 57% under visible irradiation at 180 min. The kinetic study showed a good pseudo-first-order fit to the Langmuir–Hinshelwood model. Furthermore, in order to get closer to the real conditions of textile wastewater, the influence of the presence of salt on TiO₂-NS’s photocatalytic performance was explored by employing NaCl as an inorganic ion. The optimum conditions provided by the Response Surface Methodology (RSM) were low concentrations of TTZ (2 ppm) and NBB (2.33 ppm) and negligible salt (NaCl) interference. The percentage of photodegradation was high at low pollutant and NaCl concentrations. However, this yield became very low as NaCl concentrations increased. The photocatalytic treatment leads to 31% and 53% of mineralization yield after 1 and 3 h of visible light irradiation. The synthesis of TiO₂-NS provides new insights that will help to develop an efficient photocatalysts for the remediation of contaminated water.

This study focused on fluoride (F⁻) contamination of water sources in Bahimi village, Cameroon. After the first investigation, results revealed that all water samples collected had elevated concentrations of fluoride ions (2.3 ± 0.1) mg/L to (4.5 ± 0.2) mg/L above the WHO guidelines (less than 1.5 mg/L). To mitigate the F⁻ levels, the use of bone char (BC) as an adsorbent material was proposed and its performance was tested. BC was prepared from bovine bones at different calcination temperatures (350 °C, 450 °C, 550 °C and 650 °C) and residence times (1 h and 2 h). The prepared materials were characterized in detail by SEM/EDS, BET, FTIR, and XRD. The BET findings indicated that the surface area of BC samples decreased with increasing calcination temperature and residence time. At a lower heating temperature and holding time (350 °C, 1 h), the prepared BC exhibited a higher specific surface area (112.3 ± 0.3) m²/g and adsorption capacity for F⁻ in the sampled water. Also, the batch adsorption experiments showed that the optimized adsorbent dose of 8 g/L facilitates the reduction in the F⁻ level of the sampled water below the acceptable limit level (1.5 mg/L) within 5 min of treatment. The presence of Ca²⁺ and Mg²⁺ in natural water has a positive effect on the removal of F⁻ in BC resulting in a high adsorption performance range of (72.5 ± 1.4)% to (80.3 ± 0.6)%. It was found that the adsorption of Ca²⁺ on the BC surface occurs via cation exchange with Na⁺. However, an increase in dissolved organic carbon (DOC) in the treated water limited the application of BC. Overall, the study presented a cost-effective adsorbent for the removal of this recalcitrant ion in the water source.