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Metals including Cu, Cd, Ni, Pb, Zn, Hg, Fe and Cr can be found in significant concentrations in acid mine drainage effluent from previous gold mining operations. Even at very low levels, heavy metals and their compounds are very toxic, carcinogenic, mutagenic and teratogenic. Acid mine drainage discharge must therefore be properly treated before disposal. In this study, iron removal from acid mine drainage effluent using immobilized green microalgae is explored. The impact of pH on iron metal concentrations was studied at multiple pH values between 2 and 12 using 0.1 M HCl or NaOH solutions. At pH 6, the optimal value, 82% and 90% of Fe (II) were removed from Ca-alginate beads and immobilized Desmodesmus sp., respectively. It was shown that Fe (II) ions were biosorbed by immobilized microalgae cells in a pseudo-second-order manner. This study demonstrated how immobilized green microalgae showed potential to remove iron from acid mine drainage effluent.

Wound healing is a complex dynamic biomechanical process as the body attempts to restore the integrity of traumatized or devitalized tissues. There are four stages of wound of healing that begins with hemostasis followed by inflammation, proliferation and finally weeks later wound remodeling. Full thickness wounds usually are covered with a dressing material after hemostasis, which allows for controlled hydration. We investigated the potential of a visco-liquid hemostat, polyhedral oligomeric silsesquioxane (POSS), for providing hemostasis and to maintain a microenvironment in the wound bed that would maintain moisture content and promote early re-epithelialization. We hypothesized that the hemostatic agent POSS if left in the wound bed would maintain a protective barrier and accelerate wound healing similar to using saline to irrigate the wound to keep the wound moist. We compared the early phase of wound repair (3-7 days) in a porcine full thickness wound model to evaluate the efficacy of the material. Biopsies were taken after 3 and 7 days to determine the acute response of the POSS hemostat or saline on inflammation, cell migration, concentrations of metalloproteinase (MMPs), and tissue inhibitors of metalloproteinase (TIMPs). Accelerated healing was observed in POSS treated wounds by changes in wound contraction, keratinocyte migration, and development of granulation tissue in comparison to saline treated wounds. Increased concentrations at day 3 of MMP-2, MMP-3, and in MMP-1 at day 7 in POSS treated wounds compared to saline coincide with keratinocyte migration observed in the tissue histology and changes in wound contraction. Tissue concentrations of TIMP-1 and TIMP-2 in POSS treated wounds appear to coordinate the sequence of MMP events in the healing tissue. Matrix metalloproteinase-13, a marker for tissue remodeling, was not upregulated in the early wound healing cascade in either POSS or saline treated wounds at 3 or 7 days. Overall, the data suggests POSS treatment contributed to enhanced early cell migration and wound closure compared to saline treatment.

Covalent organic frameworks (COFs) face limited processability challenges as photoelectrodes in photoelectrochemical water reduction. Herein, sub-10 nm benzothiazole-based colloidal conjugated reticular oligomers (CROs) are synthesized using an aqueous nanoreactor approach, and the end-capping molecular strategy to engineer electron-deficient units onto the periphery of a CRO nanocrystalline lattices (named CROs-Cg). This results in stable and processable "electronic inks" for flexible photoelectrodes. CRO-BtzTp-Cg and CRO-TtzTp-Cg expand the absorption spectrum into the infrared region and improve fluorescence lifetimes. Heterojunction device engineering is used to develop interlayer heterojunction and bulk heterojunction (BHJ) photoelectrodes with a hole transport layer, electron transport layer, and the main active layers, using a CROs/CROs-Cg or one-dimensional (1D) electron-donating polymer HP18 mixed solution via spinning coating. The ITO/CuI/CRO-TtzTp-Cg-HP18/SnO 2 /Pt photoelectrode shows a photocurrent of 94.9 µA cm ‒2 at 0.4 V versus reversible hydrogen electrode (RHE), which is 47.5 times higher than that of ITO/Bulk-TtzTp. Density functional theory calculations show reduced energy barriers for generating adsorbed H* intermediates and increased electron affinity in CROs-Cg. Mott-Schottky and charge density difference analyses indicate enhanced charge carrier densities and accelerated charge transfer kinetics in BHJ devices. This study lays the groundwork for large-scale production of COF nanomembranes and heterojunction structures, offering the potential for cost-effective, printable energy systems., (© 2024 The Authors. Advanced Science published by Wiley‐VCH GmbH.)

A series of crystalline, stable Metal (Metal = Zn, Cu, Ni, Co, Fe, and Mn)-Salen covalent organic framework (COF) EDA complex are prepared to continuously tune the band structure of Metal-Salen COF EDA , with the purpose of optimizing the free energy intermediate species during the hydrogen evolution reaction (HER) process. The conductive macromolecular poly(3,4-ethylenedioxythiophene) (PEDOT) is subsequently integrated into the one-dimensional (1D) channel arrays of Metal-Salen COF EDA to form heterostructure PEDOT@Metal-Salen COF EDA via the in situ solid-state polymerization method. Among the Metal-Salen COF EDA and PEDOT@Metal-Salen COF EDA complexes, the optimized PEDOT@Mn-Salen COF EDA displays prominent electrochemical activity with an overpotential of 150 mV and a Tafel slope of 43 mV dec -1 . The experimental results and density of states data show that the continuous energy band structure modulation in Metal-Salen COF EDA has the ability to make the metal d-orbital interact better with the s-orbital of H, which is conducive to electron transport in the HER process. Moreover, the calculated charge density difference indicates that the heterostructures composed of PEDOT and Metal-Salen COF EDA induce an intramolecular charge transfer and construct highly active interfacial sites., (© 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.)

High-capacity Ni-rich layered oxides are considered as promising cathodes for lithium-ion batteries. However, the practical applications of LiNi 0.83 Co 0.07 Mn 0.1 O 2  (NCM83) cathode are challenged by continuous transition metal (TM) dissolution, microcracks and mixed arrangement of nickel and lithium sites, which are usually induced by deleterious cathode-electrolyte reactions. Herein, it is reported that those side reactions are limited by a reliable cathode electrolyte interface (CEI) layer formed by implanting a nonsacrificial nitrile additive. In this modified electrolyte, 1,3,6-Hexanetricarbonitrile (HTCN) plays a nonsacrificial role in modifying the composition, thickness, and formation mechanism of the CEI layers toward improved cycling stability. It is revealed that HTCN and 1,2-Bis(2-cyanoethoxy)ethane (DENE) are inclined to coordinate with the TM. HTCN can stably anchor on the NCM83 surface as a reliable CEI framework, in contrast, the prior decomposition of DENE additives will damage the CEI layer. As a result, the NCM83/graphite full cells with the LiPF6-EC/DEC-HTCN (BE-HTCN) electrolyte deliver a high capacity retention of 81.42% at 1 C after 300 cycles at a cutoff voltage of 4.5 V, whereas BE and BE-DENE electrolytes only deliver 64.01% and 60.05%. This nonsacrificial nitrile additive manipulation provides valuable guidance for developing aggressive high-capacity Ni-rich cathodes., (© 2022 Wiley-VCH GmbH.)

Several anthropogenic activities reduce the supply of freshwater to living organisms in all ecological systems, particularly the human population. Organic matter in derived wastewater can be converted into potential energy, such as biogas (methane), through microbial transformation during anaerobic digestion (AD). To address the current lack of data and values for wastewater generation in Sub-Saharan Africa, this review analyzes and estimates (at 50% and 90% conversion rates) the potential amount of wastewater-related sludge that can be generated from domestic freshwater withdrawals using the most recent update in 2017 from the World Bank repository and database on freshwater status in Sub-Saharan Africa. The Democratic Republic of the Congo (DRC) could potentially produce the highest estimate of biogas in Sub-Saharan Africa from domestic wastewater sludge of approximately 90 billion m 3 , which could be converted to 178 million MWh of electricity annually, based on this extrapolation at 50% conversion rates. Using same conversion rates estimates, at least nine other countries, including Guinea, Liberia, Nigeria, Sierra Leone, Angola, Cameroon, Central African Republic, Gabon, and Congo Republic, could potentially produce biogas in the range of 1-20 billion m 3 . These estimates show how much energy could be extracted from wastewater treatment plants in Sub-Saharan Africa. AD process to produce biogas and energy harvesting are essential supplementary operations for Sub-Saharan African wastewater treatment plants. This approach could potentially solve the problem of data scarcity because these values for Freshwater withdrawals are readily available in the database could be used for estimation and projections towards infrastructure development and energy production planning. The review also highlights the possibilities for energy generation from wastewater treatment facilities towards wastewater management, clean energy, water, and sanitation sustainability, demonstrating the interconnections and actualization of the various related UN Sustainable Development Goals., Competing Interests: The authors declare no conflict of interest., (© 2022 University of South Africa, Florida Campus. College of Science, Engineering and Technology, 28 Pioneer Ave, Florida Park.)

The effectiveness of the adsorption process is determined by the type of adsorbent used, but some adsorbents require a significant amount of processing to achieve the desired quality, and this has become a drawback economically and environmentally. This study focused on mitigating the issue of waste management and land pollution by using amarula waste biomass, which is a low-cost adsorbent that is obtained from the industrial waste by-product. The amarula shell (AmSh) waste was found to have a higher adsorption efficiency of 30 ± 3% compared to the amarula seed (AmSe) waste and the amarula fruit (AmWa) waste, which had 19 ± 5% and 9.5 ± 0.7% efficiency, respectively. It was found that the amarula waste biomass performed better at lower adsorption temperatures. The adsorption capacity was found to decrease with an increase in the quantity of the biomass. Kinetic models were applied to the experimental data. Thermodynamic parameters were also studied to determine the spontaneity of the adsorption process. The characteristics of both the fresh and used amarula waste biomass was analyzed by using Fourier Transform Infrared Spectroscopy (FTIR), Field Emission Scanning Electron Microscopy with Energy Dispersive Spectroscopy (FESEM-EDS), Brunauer-Emmett-Teller (BET) and Thermogravimetric Analysis (TGA). It was then concluded that cellulose and hemicellulose structures in amarula waste biomass played a major role in reducing the content of dibenzothiophene in model diesel fuel., (Copyright © 2022 Elsevier Ltd. All rights reserved.)