Bhekie B. Mamba

Chitosan-based nanomaterials: A state-of-the-art review

This manuscript briefly reviews the extensive research as well as new developments on chitosan based nanomaterials for various applications. Chitosan is a biocompatible and biodegradable polymer having immense structural possibilities for chemical and mechanical modification to generate novel properties and functions in different fields especially in the biomedical field. Over the last era, research in functional biomaterials such as chitosan has led to the development of new drug delivery system and superior regenerative medicine, currently one of the most quickly growing fields in the area of health science. Chitosan is known as a biomaterial due to its biocompatibility, biodegradability, and non-toxic properties. These properties clearly point out that chitosan has greater potential for future development in different fields of science namely drug delivery, gene delivery, cell imaging, sensors and also in the treatment as well as diagnosis of some diseases like cancer. Chitosan based nanomaterials have superior physical and chemical properties such as high surface area, porosity, tensile strength, conductivity, photo-luminescent as well as increased mechanical properties as comparison to pure chitosan. This review highlights the recent research on different aspect of chitosan based nanomaterials, including their preparation and application.

Dendrimers, mesoporous silicas and chitosan-based nanosorbents for the removal of heavy-metal ions: A review

The application of nanomaterials as nanosorbents in solving environmental problems such as the removal of heavy metals from wastewater has received a lot of attention due to their unique physical and chemical properties. These properties make them more superior and useful in various fields than traditional adsorbents. The present mini-review focuses on the use of nanomaterials such as dendrimers, mesoporous silicas and chitosan nanosorbents in the treatment of wastewater contaminated with toxic heavy-metal ions. Recent advances in the fabrication of these nanoscale materials and processes for the removal of heavy-metal ions from drinking water and wastewater are highlighted, and in some cases their advantages and limitations are given. These next-generation adsorbents have been found to perform very well in environmental remediation and control of heavy-metal ions in wastewater. The main objective of this review is to provide up-to-date information on the research and development in this particular field and to give an account of the applications, advantages and limitations of these particular nanosorbents in the treatment of aqueous solutions contaminated with heavy-metal ions.

Synthesis and DNA binding studies of Ni(II), Co(II), Cu(II) and Zn(II) metal complexes of N1,N5-bis[pyridine-2-methylene]-thiocarbohydrazone Schiff-base ligand.

The thiocarbohydrazone Schiff-base ligand with a nitrogen and sulphur donor was synthesized through condensation of pyridine-2-carbaldehyde and thiocarbohydrazide. Schiff-base ligands have the ability to conjugate with metal salts. A series of metal complexes with a general formula [MCl2(H2L)]·nH2O (MNi, Co, Cu and Zn) were synthesized by forming complexes of the N1,N5-bis[pyridine-2-methylene]-thiocarbohydrazone (H2L) Schiff-base ligand. These metal complexes and ligand were characterized by using ultraviolet-visible (UV-Vis), Fourier Transform Infrared (FT-IR), 1H and 13C NMR spectroscopy and mass spectroscopy, physicochemical characterization, CHNS and conductivity. The biological activity of the synthesized ligand was investigated by using Escherichia coli DNA as target. The DNA interaction of the synthesized ligand and complexes on E. coli plasmid DNA was investigated in the aqueous medium by UV-Vis spectroscopy and the binding constant (Kb) was calculated. The DNA binding studies showed that the metal complexes had an improved interaction due to trans-geometrical isomers of the complexes than ligand isomers in cis-positions.

Spectral, thermal and in vitro antimicrobial studies of cyclohexylamine-N-dithiocarbamate transition metal complexes

Transition metal complexes of the type [M(L)(2)] and those containing monodentate phosphines of the type [M(L)(2)(PPh(3))] {M=Ni, Co, Cu and Zn; L=cyclohexylamine-N-dithiocarbamate; PPh(3)=triphenylphosphine} have been synthesized. The complexes were characterized using IR, UV-vis, NMR spectroscopy, and thermal analysis (TGA). The (1)H NMR, (13)C NMR and (31)P NMR showed the expected signals for the dithiocarbamate and triphenylphosphine moieties. The spectral studies in all compounds revealed that the coordination of metals occurs via the sulphur atom of the dithiocarbamate ligand in a bidentate fashion. Thermal behavior of the complexes showed that the complexes were more stable than their parent ligands. The ligand moiety is lost in the first step and the rest of the organic moiety decomposes in the subsequent steps. Furthermore, the ligand and their metal complexes were screened in vitro for their antibacterial activity against Escherichia coli, Staphylococcus aureus, Salmonella typhi, Enterococcus faecalis, Pseudomonas aeruginosa and Bacillus cereus and antifungal activities against Aspergillus flavus, Aspergillus carbonarius, Aspergillus niger and Aspergillus fumigatus. The metal complexes exhibited higher antimicrobial activity than the parent ligands. Generally, the zinc complexes were effective against the growth of bacteria with Zn(L)(2) displaying broad spectrum bacteriocidal activity at concentrations of 50microg/mL; and Ni(L)(2) was more effective against the growth of fungi at concentrations of 100-400microg/mL under laboratory conditions.

Ion-imprinted polymers for environmental monitoring of inorganic pollutants: synthesis, characterization, and applications.

Ion imprinting has become one of the fast-growing technologies that have gained a lot of attention recently especially in the area of materials science. One of them is called the ion-imprinted polymers (IIPs). The IIPs are synthesized on the principles of enzyme phenomenon whereby a polymer is altered by a polymerization that takes place in the presence of a template that will be later removed to create cavities that will recognize only the analyte of interest. This specific and selective affinity for the target species decreases the chances of competition with other different types of ions. The imprinting technique started with the discovery of the bulk polymerization method where by the monomer, initiator, crosslinker, and template are mixed together and allowed to polymerize, and then the resulting polymer is ground and sieved to get particles with sizes suitable for the polymers application. The IIPs have got some attractive qualities for use in environmental applications which include their stability and inexpensiveness and have a wide range of synthesis options with each suiting a certain unique application. Apart from environmental work, IIPs have applications in many other areas such as in membranes, in drug delivery, and in biosensors as alternatives to antibodies just to mention a few. This review focuses on the synthesis, types of imprinting, characterization, and applications of IIPs.

Removal of Escherichia coli and Faecal Coliforms from Surface Water and Groundwater by Household Water Treatment Devices/Systems: A Sustainable Solution for Improving Water Quality in Rural Communities of the Southern African Development Community Region

There is significant evidence that household water treatment devices/systems (HWTS) are capable of dramatically improving microbially contaminated water quality. The purpose of this study was to examine five filters [(biosand filter-standard (BSF-S); biosand filter-zeolite (BSF-Z); bucket filter (BF); ceramic candle filter (CCF); and silver-impregnated porous pot (SIPP)] and evaluate their ability to improve the quality of drinking water at the household level. These HWTS were manufactured in the workshop of the Tshwane University of Technology and evaluated for efficiency to remove turbidity, faecal coliforms and Escherichia coli from multiple water source samples, using standard methods. The flow rates ranged from 0.05 L/h to 2.49 L/h for SIPP, 1 L/h to 4 L/h for CCF, 0.81 L/h to 6.84 L/h for BSF-S, 1.74 L/h to 19.2 L/h and 106.5 L/h to 160.5 L/h for BF The turbidity of the raw water samples ranged between 2.17 and 40.4 NTU. The average turbidity obtained after filtration ranged from 0.6 to 8 NTU (BSF-S), 1 to 4 NTU (BSF-Z), 2 to 11 NTU (BF), and from 0.6 to 7 NTU (CCF) and 0.7 to 1 NTU for SIPP. The BSF-S, BSF-Z and CCF removed 2 to 4 log10 (99% to 100%) of coliform bacteria, while the BF removed 1 to 3 log (90% to 99.9%) of these bacteria. The performance of the SIPP in removing turbidity and indicator bacteria (>5 log10, 100%) was significantly higher compared to that of the other HWTS (p < 0.05). The findings of this study indicate that the SIPP can be an effective and sustainable HWTS for the Southern African Development Community (SADC) rural communities, as it removed the total concentration of bacteria from test water, can be manufactured using locally available materials, and is easy to operate and to maintain.

Stabilisation of silver and copper nanoparticles in a chemically modified chitosan matrix

This work describes the stabilisation of silver and copper nanoparticles in chemically modified chitosan colloidal solution. Chitosan-N-2-methylidene-hydroxy-pyridine-6-methylidene hydroxy thiocarbohydrazide (CSPTH) was used as a stabilising and reducing agent for silver and copper nanoparticles. The modified chitosan derivatives and the synthesised nanoparticles were characterised by Fourier transform infrared (FT-IR) spectroscopy, Ultraviolet-visible (UV-Vis) spectroscopy and X-ray diffraction (XRD). Particle size, morphology and segregation of the nanoparticles were determined by transmission electron microscopy (TEM). The size of the nanoparticles was found to be less than 20 nm and 50 nm for silver and copper nanoparticles, respectively. These nanoparticles were stabilised in a chemically modified chitosan solution and their properties were studied using fluorescence spectroscopy, photoluminescence spectroscopy and surface-enhanced Raman scattering (SERS). The optical properties of silver nanoparticles in surface plasmon band (SPB) were enhanced at 407 nm compared to those of copper nanoparticles. Fluorescence (400 nm and 756 nm), photoluminescence (450 and 504 nm) and Raman scattering (1382 and 1581 cm(-1)) properties for the copper nanoparticles were superior to those of the silver nanoparticles.

Preparation, characterization, and application of polypropylene-clinoptilolite composites for the selective adsorption of lead from aqueous media

A polymer composite of polypropylene (PP) and clinoptilolite (CLI) for the adsorption of lead has been prepared using the melt-mixing compounding technique in a rheomixer. Characterization of the composite was performed using scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), Brunuer-Emmett-Teller (BET), and Fourier transform infrared spectroscopy (FTIR). The influence of contact time, pH, initial metal-ion concentration, temperature, and pretreatment on the adsorption of lead (Pb) by the PP-CLI composite was investigated. Optimum pH was found to be between pH 6 and pH 8 while the maximum sorption of lead at optimal pH was 95%. No difference was observed between the adsorption behavior of composites functionalized with 20% and 30% clinoptilolite, respectively, while the pretreatment with HCl and NaCl made a slight difference to the adsorption capacity of composites. The findings from this study on the lead adsorption behavior of CLI-PP composite may have potential applications in wastewater and water purification works.

Bacteria–Polymeric Membrane Interactions: Atomic Force Microscopy and XDLVO Predictions

Atomic force microscopy (AFM) in conjunction with a bioprobe developed using a polydopamine wet adhesive was used to directly measure the adhesive force between bacteria and different polymeric membrane surfaces. Bacterial cells of Pseudomonas putida and Bacillus subtilis were immobilized onto the tip of a standard AFM cantilever, and force measurements made using the modified cantilever on various membranes. Interaction forces measured with the bacterial probe were compared, qualitatively, to predictions by the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory with steric interactions included. The XDLVO theory predicted attractive interactions between low energy hydrophobic membranes with high energy hydrophilic bacterium (P. putida). It also predicted a shallow primary maximum with the most hydrophilic bacterium, B. subtilis . Discrepancies between predictions using the XDLVO theory and theory require involvement of factors such as bridging effects. Differences in interaction between P. putida and B. subtilis are attributed to acid-base interactions and steric interactions. P. putida is Gram negative with lipopolysaccharides present in the outer cell membrane. A variation in forces of adhesion for bacteria on polymeric membranes studied was interpreted in terms of hydrophilicity and interfacial surface potential calculated from physicochemical properties.

Enhanced visible-light photocatalytic activity of multi-elements-doped ZrO2 for degradation of indigo carmine

Abstract In this study, C,N,S-doped ZrO 2 and a series of Eu doped C,N,S-ZrO 2 photocatalysts were synthesized by a coprecipitation method using thiourea as the source of C, N and S and Eu(NO 3 )·6H 2 O as source of Eu. The materials were characterized by X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), UV-visible diffuse reflectance spectroscopy, scanning electron microscopy (SEM)/energy dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). Indigo carmine (IC) was chosen as a model for organic pollutants and used to evaluate the photocatalytic performance of the photocatalysts under simulated solar light. Commercial ZrO 2 was used as a reference material. XRD and Raman results indicated the formation of both tetragonal and monoclinic phase ZrO 2 with particle size ranging from 8-30 nm. Multi-element doping had a great influence on the optical responses manifested as red shift in the absorption edge. The highest photocatalytic activity towards IC was observed for the Eu,C,N,S-doped ZrO 2 (0.6 mol.% Eu) sample ( k =1.09×10 −2 min −1 ). The commercial ZrO 2 showed the lowest photodegradation activity ( k =5.83×10 −4 min −1 ). The results showed that the control of Eu doping in the C,N,S-ZrO 2 was very important in reducing electron-hole recombination. The synergistic effect of Eu, C, N, and S in the ZrO 2 matrix led to enhanced utilization of simulated solar energy for the degradation of IC through narrowing of bandgaps.