ABSTRACT
Silica microparticles were synthesized from sugarcane bagasse via a green synthetic technique. The prepared silica microparticles were used to remove lead and nickel ions from their separate solutions. Microscopic analysis shows that the synthesized silica particles are spherical with good monodispersed properties. The average particle diameter of the silica microparticles is estimated to be about 432 nm. Batch adsorption experiment was employed to examine the influence of adsorbent dosage, contact time, heavy metal ion concentration and pH on the adsorption efficiency of the synthesized silica microparticles in removing the studied lead (Pb2+) and nickel (Ni2+) ions from their respective solutions. An increase in adsorbent dosage, heavy metal ion concentration, contact time and pH led to an increase in the percentage removal of Pb2+ and Ni2+ metal ions from their individual solutions. The adsorption process of Pb2+ ion onto the synthesized silica microparticles followed the Langmuir adsorption isotherm (R2 = 0.961), while, the nickel ion (Ni2+) followed the Freundlich isotherm (R2 = 0.869). The adsorption process of the studied heavy metals (Pb2+ and Ni2+) in their separate solutions favours pseudo-second-order reaction model (R2, 0.978 and 0.999) over the pseudo-first-order reaction model.
ABSTRACT
Polymer-inorganic nanocomposites are a recently developed class of materials that have altered physical or chemical properties with respect to the pure polymer, inorganic host, or their micro- and macrocomposites. Lower generation (G0.0-2.0) polyamidoamine (PAMAM) dendrimer/sodium montmorillonite (Na-MMT) nanocomposites were synthesized in a solution-phase exfoliation adsorption reaction. These are the first reports of the G0.0/ and G1.0/Na-MMT nanocomposites and of a structurally-ordered G2.0/Na-MMT. The materials were characterized using powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), and Fourier transform infrared spectroscopy (FTIR). PAMAM characteristics at acidic and basic aqueous media were studied using capillary zone electrophoresis (CZE). Pseudospherical PAMAM dendrimers in aqueous medium attain a highly flattened conformation within the confined space between MMT sheets upon nanocomposite formation. The nanocomposite structure depends on the PAMAM generation and the starting dendrimer/organic composition. G0.0 always forms monolayer structures (d = 0.42 nm), while G2.0 forms monolayer structure, mixed phase, and bilayer structures (d = 0.84 nm) at lower, intermediate, and higher organic content, respectively, showing an interesting monolayer to bilayer transition. G1.0 showed an intermediate behavior, with monolayer to mixed-phase transition at the reactant ratios studied. This monolayer arrangement of PAMAM/clay nanocomposites is reported for the first time. Maximum organic contents of G0.0 monolayer and G2.0 bilayer nanocomposites were â¼7% and â¼14%, respectively. Gallery expansions were similar to those observed with linear polymer intercalates, but the packing fractions (0.31-0.32) were 2-3 times lower. At acidic pH, the nanocomposites forming only monolayer structures are obtained, indicating a stronger electrostatic attraction between MMT and protonated PAMAM, and these nanocomposites formed more slowly and were more ordered. Na(+) ions play a significant role in nanocomposite formation. At high pH, PAMAMs show high mobility, ζ potential, and surface charge densities due to Na(+) complexation in solution. FTIR data indicates that both Na-MMT and PAMAM structural units are preserved in the nanocomposites obtained.
