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Achieving high photoelectrochemical conversion efficiency requires the logical layout of a composite photocatalyst with optimal charge separation and transfer with ideal light harvesting capabilities to enhance the photocatalytic performance and the degradation rate towards organic pollutants. Herein, a novel In2O3/WO3@Ti4N3Tx S-scheme heterojunction was successfully synthesized and confirmed through valence band VB-XPS and Mott Schottky combined analysis. The formed MXene-doped In2O3/WO3@Ti4N3Tx S-scheme significantly enhances the charge flow and spatial separation with an improved oxidation and reduction ability. An in-built interfacial electric field at the WO3-In2O3 boundary enhanced the light-harvesting capacity, whereas Ti4N3Tx MXene offers a unique electron trapping effect which effectively lowers high charge carrier recombination rate-related photocatalytic deficit. It preserves the exceptional redox potency of the photocatalyst by providing a directed acceleration and effective separation of the photogenerated charges. A high carrier density (ND = 7.83 × 1021 cm-3) with a lower negative flat band (VFB = -0.064 V vs. Ag/AgCl) was obtained by Mott-Schottky analysis for 3 wt% In2O3/WO3@Ti4N3Tx, an indicator that a low overpotential is needed to activate photocatalytic reactions. This study, therefore, provides a novel thought for the design and fabrication of an S-scheme heterojunction for photocatalytic reactions for mineralization of organic pollutants in water and clean energy production.

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Ocean acidification (OA) is becoming a potential threat to marine organisms, especially in calcifying marine invertebrates. So far, along the Kenya Coast, there has been little research on the impact of OA on cockle (Anadara antiquata), particularly on their physiological impacts induced by exposure to acidified seawater. Hence, this study aimed to investigate the physiological and biochemical responses of Anadara antiquata under present and future predicted seawater pH. In this study, the Anadara antiquata was exposed to three pH treatments (pH 7.90, 7.60, and 7.30) for 8 weeks to mimic future OA and to understand the physiological and biochemical effects on the organisms. Condition index, energy reserves (glycogen and protein), and cellular damage (e.g., lipid peroxidation level) were measured. Condition index (CI) showed no significant difference at different pH treatments (pH 7.90, 7.60, and 7.30), whereas the survival Anadara antiquata was slightly reduced after 8 weeks of exposure to pH 7.30. Glycogen and protein content were not affected at reduced pH (7.60 and 7.30). However, after 8 weeks of exposure to pH 7.60 and 7.30, Anadara antiquata showed a slight decrease in lipid peroxidation, an indication of cellular damage. The physiological and biochemical parameters analyzed (glycogen and protein content; lipid peroxidation levels) showed useful biomarkers to assess ocean acidification impacts in cockle.

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The information on pharmaceutical compounds' distribution and their possible risks in marine ecosystems along the Kenya coast is limited especially in the peri-urban creeks. Hence, this study aimed to determine pharmaceutical residue levels and distribution in selected peri-urban creeks in Mombasa and Gazi bay. The target compounds were analgesic (acetaminophen), antibiotics (trimethoprim and sulfamethoxazole), antiepileptic (carbamazepine), and antiretroviral (nevirapine). Pharmaceutical residues in grab surface seawater in wet and dry seasons ranged from below detection limit (BDL)-1065.6 µg L-1 and BDL-71.3 µg L-1, respectively. The concentration of the pharmaceutical residues was high in Tudor creek in the dry and wet seasons with a mean concentration of 63.3 µg L-1 and 233.1 µg L-1 respectively compared to Makupa creek (dry season, 54.2 µg L-1; wet season 16.2 µg L), and Mtwapa creek (dry season, 43.1 µg L-1; wet season, 15.0 µg L-1). Gazi Bay being used as a control site had a mean concentration of 21.3 µg L-1 and 3.1 µg L-1 during the dry season and wet season respectively. Acetaminophen and nevirapine were the most ubiquitous compounds in seawater since they were found in all seawater samples collected. Risk quotients (RQ) for invertebrates and algae based on the mean concentrations of the analytes were estimated to provide a preliminary environmental risk assessment. The results suggest that the studied acetaminophen, trimethoprim, sulfamethoxazole, and carbamazepine in seawater pose low (0.01 ≤ RQ < 0.1) to medium (0.1 ≤ RQ < 1) ecological risk whereas nevirapine poses medium to high (RQ ≥ 1) ecological risk to the ecosystems of Mombasa periurban creeks and Gazi bay. Further research, however, is encouraged on the distribution of pharmaceuticals in the marine environment and the long-term synergistic effects of mixtures of these compounds on marine biota.

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Rift Valley fever (RVF) is a mosquito-borne zoonotic disease that is caused by the Rift Valley fever virus (RVFV); Bunyaviridae: Phlebovirus. RVF disease can affect several different species, including ruminants, camels and humans and thus present a dual threat to public health and livestock food production in endemic regions. In livestock, the RVFV infection is characterised by an acute hepatitis, abortion and high mortality rates in new-born animals. The current RVF diagnostic techniques have shown good sensitivity. However, they require extensive sample processing and complex instrumentation. Owing to speed, low cost, ease of use, and most importantly, the ability to diagnose diseases at sites where they are managed, lateral flow immunoassays (LFIA) are the most widely used point-of-care (POC) tools for disease diagnosis. In this study, a lateral flow assay (LFA) device that is able to detect antibodies against RVFV, with a minimum detectable concentration of 0.125 mg/mL, was successfully developed. The LFA also successfully detected RVFV antibodies in reference RVFV sera. Protein A (ProA), which has the ability to bind immunoglobulins from different species, was used in the detection probe, giving the developed RVFV LFA potential for multi-species diagnosis.

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The impact of worldwide water scarcity, further exacerbated by environmental pollution, necessitates the development of effective water treatment membranes. Herein, we report the synthesis and characterization of nanocomposite membranes containing hyperbranched polyethyleneimine (HPEI) stabilized bi-and trimetallic nanoparticles. These membranes were prepared by blending a pre-grafted Polyethersulfone (PES) powder with the Pd@Fe@HPEI and Pd@FeAg@HPEI nanoparticles followed by phase inversion. The membranes, together with stabilized nanoparticles, were characterized by several analytical techniques, such as attenuated total reflectance-Fourier transform infra-red spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffractometry (XRD), optical contact angle (OCA), scanning electron microscopy (SEM), atomic force microscopy (AFM), and high-resolution transmission electron microscopy (HRTEM). These techniques revealed the elemental composition, zerovalent nature of the nanoparticles, and their small and even size distribution. Surface analysis showed chemical bonding between the polymeric functional groups and the supported nanoparticles. Furthermore, the nanocomposite membranes were found to be hydrophilic. Additionally, the membranes were investigated for swelling (water uptake), porosity, pore size, pure water permeation fluxes, and they indicated a decreased protein adhesion property. As such, the membranes fabricated in this work indicate the required properties for application in water treatment.

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The development of a strategy to stabilise the cubic phase of HfO2 at lower temperatures is necessary for the emergence of unique properties that are not realised in the thermodynamically stable monoclinic phase. A very high temperature (>2600 °C) is required to produce the cubic phase of HfO2, whereas the monoclinic phase is stable at low temperature. Here, a novel rapid synthesis strategy was designed to develop highly crystalline, pure cubic-phase HfO2 nanoparticles (size <10 nm) using microwave irradiation. Furthermore, the as-prepared nanoparticles were converted to different morphologies (spherical nanoparticles and nanoplates) without compromising the cubic phase by employing a post-hydrothermal treatment in the presence of surface modifiers. The cytotoxicities and proliferative profiles of the synthesised cubic HfO2 nanostructures were investigated over the MCF-7 breast cancer cell line, along with caspase-3/7 activities. The low-temperature phase stabilisation was significantly attributed to surface imperfections (defects and deformations) induced in the crystal lattice by the desirable presence of Na2S·xH2O and NaOH. Our work provides unprecedented insight into the stabilisation of nanoscale cubic-phase HfO2 in ambient environments; the method could be extended to other challenging phases of nanomaterials.

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Currently in South Africa, online flue gas desulphurisation (FGD) is being utilized as one of the most effective methods for total sulphur reduction in coal samples during the combustion process. However, the main disadvantage associated with FGD is the formation of its by-products (FGD gypsum). The latter is mostly formed in low grade quality, thereby bringing secondary pollution problems and extra disposal costs. Therefore, the current study describes the development of total sulphur extraction in coal under microwave heating using different dilute alkaline solutions such as NaOH, NaOH-H2O2, NH4OH, and NH4OH-H2O2. The experimental conditions were as follows: 150 °C, 5 min and 10% (m/v or v/v) for temperature, extraction time and reagent concentration, respectively. The most effective alkaline reagent for coal desulphurisation was observed to be NaOH-H2O2 with total sulphur reduction of 55% (from the inductively coupled plasma-optical emission spectrometry (ICP-OES) results). The NaOH-H2O2 reagent also showed significant morphological changes in coal as observed from the SEM images and effective demineralisation as revealed by the powder X-ray diffractometer (P-XRD) results. Additionally, desulphurisation results obtained from the developed microwave-assisted dilute alkaline extraction (MW-ADAE) method were quite comparable with the published work. The proposed total sulphur reduction method is advantageous as compared to some of the literature reported coal desulphurisation methods as it requires a short period (5 min) of time to reach its completion. Additionally, the proposed method shows excellent reproducibility (% RSD from 0.5 to 1); therefore, it can be utilized for routine analysis. Graphical abstract ᅟ.

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In this research paper a comparative study has been carried out for the removal of methyl violet dye using unfunctionalized and functionalized cellulose. The functionalization was achieved through esterification of cellulose with furan-2,5-dione. The functionalization of the cellulose was evidenced using BET, FT-IR, SEM and TGA. The adsorption isotherm data was fitted using different isotherm models like Langmuir, Freundlich, Temkin, Flory-Huggins and Dubinin-Kaganer-Radushkevich models and found to follow Langmuir and Temkin isotherm models with high value of correlation coefficients. Functionalized cellulose (106.38 mg g(-1)) showed higher dye removal capability than unfunctionalized cellulose (43.668 mg g(-1)). The kinetics of adsorption was investigated using pseudo first order, second order, Elovich, liquid film diffusion and intra-particle diffusion models. The mechanism of adsorption was found to follow pseudo second order rate equation. Thermodynamic studies showed that the adsorption process was endothermic and spontaneous.

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Aflatoxins are a group of mycotoxins that have deleterious effects on humans and are produced during fungal infection of plants or plant products. An electrochemical immunosensor for the determination of aflatoxin B(1) (AFB(1)) was developed with AFB(1)antibody (AFB(1)-Ab) immobilized on Pt electrodes modified with polyaniline (PANi) and polystyrene sulphonic acid (PSSA). Impedimetric analysis shows that the electron transfer resistances of the Pt/PANi-PSSA electrode, the Pt/PANi-PSSA/AFB(1)-Ab immunosensor and Pt/PANi-PSSA/AFB(1)-Ab incubated in bovine serum albumin (BSA) were 0.458, 720 and 1,066 kOmega, respectively. These results indicate that electrochemical impedance spectroscopy (EIS) is a suitable method for monitoring the change in electron transfer resistance associated with the immobilization of the antibody. Modelling of EIS data gave equivalent circuits which showed that the electron transfer resistance increased from 0.458 kOmega for the Pt/PANi-PSSA electrode to 1,066 kOmega for the Pt/PANi-PSSA/AFB(1)-Ab immunosensor, indicating that immobilization of the antibody and incubation in BSA introduced an electron transfer barrier. The AFB(1) immunosensor had a detection limit of 0.1 mg/L and a sensitivity of 869.6 kOmega L/mg.

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