Peter Papoh Ndibewu

Hazardous chemicals are transported on rail and road networks. In the case of accidental spillage or terror attack, civilian and military first responders must approach the scene equipped with appropriate personal protective equipment. The plausible manufacturing of chemical protective polymer material, from photocatalyst anatase titanium dioxide (TiO₂) doped low-density polyethylene (LDPE), for cost-effective durable lightweight protective garments against toxic chemicals such as 2-chloroethyl ethyl sulphide (CEES) was investigated. The photocatalytic effects on the physico-chemical properties, before and after ultraviolet (UV) light exposure were evaluated. TiO₂ (0, 5, 10, 15% wt) doped LDPE films were extruded and characterized by SEM-EDX, TEM, tensile tester, DSC-TGA and permeation studies before and after exposure to UV light, respectively. Results revealed that tensile strength and thermal analysis showed an increasing shift, whilst CEES permeation times responded oppositely with a significant decrease from 127 min to 84 min due to the degradation of the polymer matrix for neat LDPE, before and after UV exposure. The TiO₂-doped films showed an increasing shift in results obtained for physical properties as the doping concentration increased, before and after UV exposure. Relating to chemical properties, the trend was the inverse of the physical properties. The 15% TiO₂-doped film showed improved permeation times only when the photocatalytic TiO₂ was activated. However, 5% TiO₂-doped film exceptionally maintained better permeation times before and after UV exposure demonstrating better resistance against CEES permeation.

We report on the detection of an organic pollutant mostly found in local streams and wastewater treatment plants, specifically on triclosan detected in the Umbogintwini Industrial Complex (UIC), located on the south coast of Durban, KwaZulu-Natal in South Africa. Triclosan was successfully extracted from effluent samples using molecularly imprinted membrane adsorbents (MIMs) before quantification and removal using high-performance liquid chromatography (HPLC). This was done through fabrication of a polyvinylidene fluoride polymer using selective microparticles and molecularly imprinted polymers by means of phase inversion and an immersion precipitation method which results in enhanced hydrophilicity and membrane performance. The optimisation of experimental parameters – i.e. contact time and sample size – was performed through different stages of analysis. The synthesised MIMs exhibited an outstanding adsorption efficiency of 97% for triclosan in relation to those of non-imprinted membranes (NIMs) and pristine membranes at 92% and 88%, respectively. The analytical method employed had limits of detection and quantification of 0.21 and 0.69 parts per billion (ppb or μg/L) in wastewater effluent, respectively. The obtained efficiency results show great potential for future use of membrane and molecular imprinting technology, and that MIMs can be adopted as adsorbents for water treatment. The fast and highly selective methodology presented in this work could also be employed for the examination of persistent organic pollutants in the future to combat water scarcity in South Africa. Significance: The key finding of this work is the incorporation of molecularly imprinted polymers with a membrane adsorbent to improve the performance of the membrane. An unexpected finding was the existence of pollutants like triclosan in water within the boundaries of the KwaMakhutha community, near the human settlement. Among the MIMs, NIMs and bare membranes, higher removal efficiencies were displayed by the synthesised MIMs against the discovered pollutants. This work could open doors for advanced research in the community.

Open access peer-reviewed chapter

A brief review has been herein done of technologies involved in the exploitation of lignin, in order to provide an introduction to the subject from the perspective of a fast technologically advancing economy. Lignocellulosic materials and biomass have historically been utilised from since time memorial, but a new conversation is emerging on the role of these materials in modern bioeconomies. This new discourse needs to help us understand how technologies for managing and processing lignocellulosic materials both as biosynthetic moieties, biogenic wastes or simply renewable biopolymer—both established and novel—should be deployed and integrated (or not) to meet developmental requirements of the sustainability paradigm. The world is caught in the middle of green technology advocating for more and more focus on renewable sources of manufacturing raw materials and that of the molecularly imprinted/synthesised or genetically engineered ones. The utilisation of lignins (from renewable sources) in both the industry as the base for the formulation of ionic liquids (with yet a wider industrial applications), and also is a potential scaffold material for functionally modified imprinted polymers (LCIPS) for the selective recovery of base metals and gold, respectively, evidently incorporates the bioeconomy aspirations.

This study reports the synthesis of gold nanoparticles from a gold precursor salt (HAuCl₄·3H₂O) using Moringa oleifera bark broth, a cheap renewable material, without adding external surfactant, capping agent or template. Biomolecules responsible for reducing Au³⁺ to Au⁰ and stabilization of the resulting nanoparticles were extracted from the bark, and the synthesis was monitored for precursor concentration, percentage broth, pH of reaction media and reaction time. The biosynthesized nanoparticles were characterized using spectroscopic (FTIR and UV-Vis) techniques, advanced microscopic imaging (HRTEM, SEM/EDS), and Zeta potential measurements. Distinct color change from yellow to wine red was observed, indicative of the formation of gold particles at nanoscale. The SPR band was found at around 550 nm, in agreement with conventional synthetic protocols. The particles were stable with a net negative surface charge (–20 mV), a contribution associated with the protein nature of the broth. Addition of Pb²⁺ to the polydisperse nanoparticle suspension resulted in a color shift, to a faint blue color, coupled with a corresponding SPR shift to higher wavelengths, depending on the concentration of Pb²⁺ added. This color change is attributed to the aggregation of the colloidal particles due to complexation effects of the metal ions with the biomolecules on the surface of the nanoparticles.

The objective of this study was to (1) measure the concentration of four anions (Cl^-, F^-, , and ) and nine other elements (Al, Ba, Ca, K, Mg, Mn, Fe, Ni, and Si) in two nontraditional biopolymeric chemical stabilizers (EBCS1 and EBCS2), (2) investigate consequent environmental toxicity risk implications, and (3) create awareness regarding environmental health issues associated with metal concentration levels in enzyme-based chemical stabilizers that are now gaining widespread application in road construction and other concrete materials. Potential ecotoxicity impacts were studied on aqueous extracts of EBCS1 and EBCS2 using two thermodynamic properties models: the Pitzer–Mayorga model (calculation of the electrolyte activity coefficients) and the Millero–Pitzer model (calculation of the ionic activity coefficients). Results showed not only high concentrations of a variety of metal ions and inorganic anions, but also a significant variation between two chemical stabilizing mixtures. The mixture (EBCS2) with the lower pH value was richer in all the cationic and anionic species than (EBCS1). Sulfate ( ) concentrations were found to be higher in EBCS2 than in EBCS1. There was no correlation between electrolyte activity and presence of the ionic species, which may be linked to a possible high ionic environmental activity. The concentrations of trace metals found (Mn, Fe, and Ni) were low compared to those of earth metals (Ba, Ca, K, and Mg). The metal concentrations were higher in EBCS1 than in EBCS2. Data suggest that specific studies are needed to establish “zero” permissible metal ecotoxicity values for elements and anions in any such strong polyelectrolytic enzyme-based chemical stabilizers.