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EN
Polymer-polymer interactions and miscibility for chitosan (Ch) and partially hydrolysed polyacrylamide (HPAM) have been investigated using dilute solution viscosity. The intrinsic viscosity, [η], and the viscosity interaction parameters, bm, have been determined for the binary (solvent/polymer) and ternary (solvent/polymer A/polymer B) systems. Degree of miscibility of these polymer mixtures was estimated on the basis of two criteria. The final result depends on (i) the applied extrapolation method used for determination of the interaction parameters, (ii) the assumed miscibility criteria, and (iii) the blend composition.
EN
Polyacrylamide-zeolite composite was prepared by direct polymerization of polyacrylamide in suspensions of β-zeolite. Phytic acid was then immobilized on the composite surface. Fourier transform infrared spectrometry (FT-IR), X-Ray Diffraction (XRD) and Thermal gravimetry (TG) techniques were employed to characterize the synthesized adsorbent. The adsorptive features of the composite and the modified composite were investigated for the removal of Pb2+ from aqueous solution in view of dependency on pH, time, ion concentration, temperature, selectivity, kinetics and reusability. The adsorption isotherms were evaluated with reference to the Langmuir and Freundlich models. Thermodynamic of the system was calculated. ΔG<0 indicated that the adsorption process was spontaneous. Good compatibility of the adsorption kinetics to the pseudo-second-order model predicted that the rate-controlling step was a chemical sorption. The selectivity experiments showed that the adsorbents were selective toward Pb2+ in the presence of Zn2+ and Cd2+. The reusability of the adsorbent was tested for four regeneration cycles.
EN
In the present paper, the results of rheological measurements in solutions of chitosan (Ch) with partially hydrolyzed polyacrylamide (HPAM) are presented. Aqueous acetic acid, lactic acid and aqueous acetic acid/NaCl were used as solvents for chitosan, HPAM and Ch/HPAM solution blends. The criterion of miscibility of solution blends, based on the additivity rule of apparent shear viscosity (ηa) has been discussed. The rheological parameters from power law (Ostwald de Waele model) and activation energy of viscous flow (Ea) have been calculated from the flow curves and Arrhenius plots, respectively. It was found that studied polymer solutions exhibited the non-Newtonian behaviour with shear-thinning and/or shear-thickening areas. The final result depends on the thermodynamic goodness of the solvent and on the blend composition.
EN
The surface properties of chitosan acetate (ChA), polyacrylamide (PAM) and ChA/PAM mixtures have been investigated by the tapping-mode atomic force microscopy (AFM) and monitored by contact angle measurements. Chitosan is blended with polyacrylamide in acetic acid solution and this solution is cast to prepare the mixture film. Measurements of the contact angle for two different liquids (diiodomethane and glycerol) on the surface of chitosan acetate. The surface free energy (γs) as well as dispersive (gsd) and polar (gsp) components were calculated from contact angle values by Owens-Wendt methods using an appropriate computer program. The values of polar and dispersive components of surface free energy show that PAM films are more polar than chitosan acetate films. In the case of ChA/PAM mixtures, the values of surface free energy and polar component are reduced significantly compared with pure polymers. This behavior indicates rather hydrophobic character of this surface. The changes of topography images were considered by determining the root mean square (RMS) deviation in the image data. The study of blends by AFM showed a completely different morphology when compared with pure components. The roughness of blends increases with the increase of ChA content. This may indicates a strong interaction between the polymeric components.
EN
In the present work, the results of Fourier transform infrared (FTIR) and atomic force microscopy (AFM) studies of films of chitosan acetate (ChA), polyacrylamide (PAM), and their mixtures are presented. The morphology of the ChA and PAM films and their mixtures was studied by tappingmode atomic force microscopy (AFM). The topography images were considered by determining the root mean square (RMS) deviation in the image data. The study of mixtures by AFM showed a completely different morphology when compared with pure components. The roughness of mixtures increases with the increase of ChA content but is significantly reduced after UV exposure. This may indicate a strong interaction between the polymeric components. The FTIR spectroscopy also supports the obtained results. The miscibility of polymer mixtures is related to interactions between the functional groups of the polymeric components.
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