Justice M. Thwala

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.

Viscoelastic and shear viscosity studies of colloidal silica particles dispersed in monoethylene glycol (MEG), diethylene glycol (DEG), and dodecane stabilized by dodecyl hexaethylene glycol monoether (C12E6).

Silica dispersions stabilized by a nonionic surfactant, dodecyl hexaethylene glycol monoether (C 12E 6), were studied using rheological measurements. The viscosity-shear rate flow behavior of silica in monoethylene glycol (MEG) is shear thinning at low shear rates, leading to a Newtonian plateau at high shear rates for all dispersions studied. All rheological properties showed an increase above a critical surfactant concentration. The dispersions were stable at low levels of C 12E 6 concentrations because of electrostatic repulsions as deduced from the zeta potentials of silica that were on the order of about -30 to -65 mV in monoethylene glycol (MEG). Instability on further addition of C 12E 6 to the silica particles, a phenomenon normally obtained with high-molecular-weight polymers, was observed in MEG. Viscoelatic measurements of silica in monoethylene glycol at various surfactant concentrations showed a predominantly viscous response at low frequency and a predominantly elastic response at high frequencies, indicative of weak flocculation. Instability is explained in terms of hydrophobic and bridging interactions. Restabilization observed at high surfactant concentration was due to the steric repulsion of ethoxy groups of micellar aggregates adsorbed on silica particles. The study also revealed that the presence of trace water introduced charge repulsion that moderated rheological measurements in glycol media and introduced the charge reversal of silica particles in dodecane.

Rheological studies of stability of colloidal silica particles dispersed in monoethylene glycol (MEG) stabilized by dodecyl hexa ethylene glycol monoether (C12E6).

The steady shear viscosity, dynamic viscoelasticity, and high shear wave rigidity modulus were measured for silica dispersions stabilized by a nonionic surfactant, dodecyl hexa ethylene glycol monoether (C(12)E(6)). Electrokinetic measurements were also obtained to help understand the role of charge on the stability of the silica particles in nonaqueous media. The dispersions were found to be stable at low levels of C(12)E(6) concentrations due to electrostatic repulsions as deduced from zeta potential data. Zeta potentials of silica particles in mono ethylene glycol (MEG) were of the order of (-)20-(-)70 mV, signifying the importance of electrostatic stabilization normally reported in aqueous media. Instability on further addition of C(12)E(6) to silica particles in MEG, a phenomenon normally obtained with high molecular weight polymers, is explained in terms of micellar bridging and hydrophobic interactions. The extended Derjaguin-Landau-Verwey-Overbeek (DLVO) theory is used to model the effect of C(12)E(6) on particle stability. Viscoelasticity of silica in MEG in the presence of C(12)E(6) is also reported. Viscoelasticity was found to be due to weak flocculation resulting in a free energy increase and a decrease in configurational entropy as the dispersion was weakly strained. Viscoelastic measurements are modeled using a mode-coupling model.