To effectively combat global warming, an enormous reduction in CO₂ emissions is required. Cameroon, which is currently the largest emitter of CO₂ in the CEMAC subregion, has committed to reducing its greenhouse gas emissions by 32% by 2035. However, previous studies in Cameroon have only addressed the relationship between economic growth, energy consumption, and CO₂ emissions without estimating all causal relationships at the same time. Moreover, no study has yet decomposed this country’s CO₂ emissions to date. To fill these research gaps and further assess the determinants of these CO₂ emissions, an extended Kaya identity and the Logarithm Mean Divisia Index (LMDI I) have been applied in this paper to identify, quantify, and explain the main drivers of Cameroon’s CO₂ emissions from 2007 to 2014. Seven effects were measured and the main findings show that carbon intensity and the emission factor increased by 0.57% and 107.50% respectively. Regarding contributions to the increase of CO₂ emissions, the population effect was the most positive followed by the activity effect, whereas the energy intensity, the substitution of fossil fuels and the penetration of renewable energies have contributed to reduce the CO₂ emission. To enable Cameroon to not only achieve the goals of its vision but also develop a low-carbon economy, this paper provides some proposed avenues that should be considered by policymakers.

Traditional medicine (TM) including Ayurvedic medicines, traditional Chinese medicines and nutraceuticals are popular across the globe as dietary supplements and traditional and alternative medicines. Health risks from these remedies continue to present serious concerns, with occurrences of poisoning by metals and metalloids present at concentrations above acceptable regulatory standards. This review overviews the prevalence of TM use, cases of metal and metalloid poisoning following TM consumption, and forms of TM contamination and adulteration. The review summarises regulations by the World Health Organization (WHO) and other relevant bodies. Finally, the review recommends how to protect consumers.

In this study, the removal of ciprofloxacin hydrochloride (a fluoroquinolone antibiotic) by using various effective adsorbents such as activated carbon, montmorillonite, modified montmorillonite (commercial name Cloisite 20A), and alumina was investigated. Adsorption experiments were performed to determine and compare the adsorption capacities of these adsorbents. The adsorption capacities of adsorbents were examined at different initial concentrations of ciprofloxacin hydrochloride. Activated carbon was found to be having the best adsorption capacity for the removal of ciprofloxacin hydrochloride. For the solution having an initial ciprofloxacin hydrochloride concentration of 4 ppm, the adsorption capacities of adsorbents were obtained as 1.86 mg g⁻¹ for activated carbon, 1.67 mg g⁻¹ for modified montmorillonite, 1.15 mg g⁻¹ for alumina, and 0.60 mg g⁻¹ for montmorillonite. And also, about 92% of the ciprofloxacin hydrochloride was removed from the water using the activated carbon. In addition, Langmuir, Freundlich, and Temkin isotherm models were employed to express the adsorption process. For all adsorbents, Freundlich isotherm model provided best fitting to the experimental data because of very high values of R² (> 0.99). Kinetic models of pseudo-first order, pseudo-second order, Elovich, and Weber-Morris intraparticle diffusion model were utilized to evaluate the experimental adsorption data. Adsorption kinetics data were well represented by pseudo-second order kinetic model with values of R² (> 0.999).

China is a massive mercury emitter, responsible for a quarter of the world’s mercury emissions, which transit the atmosphere and accumulate throughout its watercourses. The Changjiang (Yangtze) River is the third largest river in the world, integrating mercury emissions over its 1.8 × 10⁶ km² catchment and channelling them to the East China Sea where they can be buried. Despite its potential global significance, the importance of the East China Sea as a terminal mercury sink remains poorly known. To address this knowledge gap, total mercury and methylmercury concentrations were determined from 51 surface sediment samples revealing their spatial distribution, whilst demonstrating the overall pollution status of the East China Sea. Sedimentary mercury distributions beneath the East China Sea are spatially heterogeneous, with high mercury concentrations (> 25 ng g⁻¹) corresponding to areas of fine-grained sediment accumulation. In contrast, some sites of fine-grained sediment deposition have significantly lower values of methylmercury (< 15 ng g⁻¹), such as the Changjiang estuary and some isolated offshore areas. Fine-grained particles and organic matter availability appear to exert the dominant control over sedimentary mercury distribution in the East China Sea, whereas in situ methylation serves as an additional control governing methylmercury accumulation. Estimated annual sedimentary fluxes of mercury in the East China Sea are 51 × 10⁶ g, which accounts for 9% of China’s annual mercury emissions.

Solutions with 0.65 mM of the antituberculosis drug isoniazid (INH) in 0.050 M Na₂SO₄ at pH 3.0 were treated by electro-Fenton (EF) and UVA photoelectro-Fenton (PEF) processes using a cell with a BDD anode and a carbon-PTFE air-diffusion cathode. The influence of current density on degradation, mineralization rate, and current efficiency has been thoroughly evaluated in EF. The effect of the metallic catalyst (Fe²⁺ or Fe³⁺) and the formation of products like short-chain linear aliphatic carboxylic acids were assessed in PEF. Two consecutive pseudo-first-order kinetic regions were found using Fe²⁺ as catalyst. In the first region, at short time, the drug was rapidly oxidized by ●OH, whereas in the second region, at longer time, a resulting Fe(III)-INH complex was much more slowly removed by oxidants. INH disappeared completely at 300 min by EF, attaining 88 and 94% mineralization at 66.6 and 100 mA cm⁻², respectively. Isonicotinamide and its hydroxylated derivative were identified as aromatic products of INH by GC-MS and oxalic, oxamic, and formic acids were quantified by ion-exclusion HPLC. The PEF treatment of a real wastewater polluted with the drug led to slower INH and TOC abatements because of the parallel destruction of its natural organic matter content.

Since nitrosamine disinfection by products is highly carcinogenic, they have attracted considerable attention due to their increased presence in ambient waterways and potable water supplies. For the present study, the potential formation of nitrosamines from corresponding precursor secondary amines during ozonation was investigated. The results revealed that five nitrosamines were observed during the ozonation of their corresponding secondary amines. The molar yields initially increased and then decreased with longer contact times and higher ozone doses. These phenomena indicated that ozone not only promoted nitrosamine formation but also degraded the formed nitrosamines. High pH had a positive influence on nitrosamine formation at room temperature. Further, coexisting substances including nitrate, nitrite, humic acid, and tert-butanol inhibited the generation of nitrosamines due to hydroxyl radical (·OH) competition and scavengers, whereas in the presence of hydroxylamine, nitrosamine formation increased considerably without ozone due to its capacity for independent formation between secondary amines and hydroxylamine. Further, the generation of nitrosamines from secondary amines was primarily attributed to O₃ and ·OH oxidation, which was produced through the decomposition of ozone. The transformation pathways were mainly comprised of the indirect routes between the O₃/·OH intermediates. The findings of this study were helpful toward expanding the knowledge of nitrosamine formation during the corresponding precursor secondary amine ozonation process.

Magnetic activated carbon (MAC) was fabricated to improve biohydrogen (bio-H₂) production. The MAC exhibited higher biocatalytic capability and better microbial immobilization than activated carbon (AC) during the bio-H₂ process. Glucose supplemented with 200 mg/L MAC obtained the highest H₂ yield of 214 mL/g glucose, much higher than that (130 mL/g glucose) of the control group without MAC. Suitable dosage such as 300 mg/L AC or 200 mg/L MAC promoted volatile fatty acid (VFA) formation and H₂ generation. Besides, the metabolites showed that AC or MAC did not change the bio-H₂ evolution pathway. Some possible biochemical mechanisms were as follows: MAC served as a microbial carrier to promote cell colonization and electron transfer rate, and it released Fe³⁺ to enhance glucose acidogenesis and Fe²⁺ to increase microbial concentration and activity in the bio-H₂ evolution. Graphical Abstract Magnetic activated carbon (MAC) was fabricated and subsequently used in bio-H₂ process through glucose-fed anaerobic mixed bacteria at 37 °C. The MAC acted as a carrier of anaerobes to promote cell growth and electron transfer rate, and released Fe³⁺ to increase glucose acidogenesis and Fe²⁺ to improve microbial concentration and activity in the bio-H₂ evolution process.

Successive applications of pig manure increase Cu and Zn contents in soils and may cause toxicity to plants. However, plants may have defense strategies that reduce Cu and Zn availability in rhizosphere soil. The study aimed to evaluate growth of white oats (Avena sativa) and Cu and Zn availability in rhizosphere soil subjected to long-term applications of pig slurry (PS) and pig deep litter (PL). The study was carried out with samples of a Typic Hapludalf soil from an 11-year experiment with annual fertilization of 180 kg N ha⁻¹ as pig slurry (PS180) and pig deep litter (PL180) and a control (C) treatment. White oats were grown in pots with soil collected at 0.0–0.10 m depth. Thirty-five and 70 days after emergence (DAE), rhizosphere (RS) and bulk soil (BS) were analyzed to determine Cu and Zn availability. Plant growth, tissue Cu and Zn concentration, and content (concentration X dry weight) were measured. The application of pig manure for 11 years increased available soil Cu and Zn, as well as tissue concentration and content. Dry matter yield and plant height in PL180 were similar to those found in plants grown in the control treatment, while plants grown in PS180 had higher dry matter than in C. We found few differences in soil chemical characteristics and Cu and Zn contents between RS and BS. The high Cu concentrations in roots, especially in soil treated with PL180, show that Cu retention in the roots prevents excess Cu transport to white oat shoots.

Sodium diclofenac (DCF) is a common analgesic and anti-inflammatory drug, which has become an environmental problem due to its growth and accumulation into water bodies. In this work, commercial (with excipients) and analytical (pure) DCF mineralization was studied by means of heterogeneous catalytic ozonation. The process was carried out with magnetite (Fe₃O₄) as a catalyst, which preserves its physical and chemical properties during the process. The best results of mineralization were obtained after a 40-min treatment of 35 mg/L analytical DCF solution, with a 0.5 g/L catalyst concentration. These results showed the highest organic load decrease, measured as dissolved organic carbon (DOC) and chemical oxygen demand (COD), with 94 and 89%, respectively. In addition, the percentage of organic load decrease was compared between the conventional and the catalyzed process. Besides, reaction products were identified by gas chromatography–mass spectrometry (GC-MS) and the catalytic properties were identified by Mössbauer spectroscopy, which showed the catalyst maintained its nature after the process. Finally, the results obtained show that the heterogeneous catalytic process could be an efficient degradation treatment for emerging contaminants such as DCF.

Climate change may result in increased variability in rainfall intensity in the future, leading to more frequent flooding and a substantial loss of lives and properties. To mitigate the impact from flooding events, flood control facilities need to be designed and operated more efficiently, which requires a better understanding of the relationship between climate change and flood events. This study proposed a framework combining the Hydrologic Engineering Center’s Hydrologic Modeling System (HEC-HMS) and the Coupled Model Intercomparison Project Phase 5 (CMIP5) general circulation models to assess the impact of climate change on flood events. HEC-HMS is one of the most commonly used hydrologic models in the USA, and CMIP5 provides the latest climate data for potential future climate scenarios. The proposed approach is applied to the Nippersink Creek watershed, which shows that 10-, 25-, 50-, and 100-year precipitations for the low, medium, and high emission scenarios are all greater than the historic observations. The corresponding 10-, 25-, 50-, and 100-year floods are remarkably higher than in the historic observations for the three climate scenarios. The high emission scenario results in dramatically increased flood risks in the future. The case study demonstrates that the framework combining HEC-HMS and CMIP5 is easy to use and efficient for assessing climate change impacts on flood events. It is a valuable tool when complicated and distributed hydrologic modeling is not an option because of time or monetary constraints.