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The adsorption abilites of cotton cellulose fibers are very often modified by alkaline treatments in form of alkaline purification or mercerization using high concentration of NaOH. We tried to determine the correlation between morphological modifications and the adsorption abilities of cotton fibers using several methods: the analysis of microscope images of fibers by image processing and the analysis of the electrokinetic surface properties which express the adsorption behavior of fibers. The longitudinal images and cross‐sections of native and modified cotton fibers were analyzed and the parameters: form factor, wall thickness, cross‐section area, fiber diameter, lumen area were calculated using image processing. The adsorption behavior of native and NaOH modified polymers was investigated by the determination of electrokinetic properties. The zeta potential (ζ) was calculated from streaming potential measurements as a function of pH and surfactant concentration in the liquid phase. The results indicate that only a correct combination between the morphological modifications and electrokinetic behavior of fibers leads to a desirable adsorption mechanism which causes a specific adsorption of components of the liquid phase.

Water soluble cellulose derivatives are highly required products for many practical purposes, expanding the limited applications of pure cellulose, caused by highly ordered hydrogen bond network and high crystallinity. In this connection, this paper, presents a new approach to obtain water soluble carboxyl-functionalized cellulosic materials, combining two of the most common selective oxidation protocols for cellulose, i.e. the nitroxyl mediated and periodate, in one-shot reaction. It was found that, under specific reaction conditions, fully oxidized, 2,3,6-tricarboxy cellulose can be obtained in high amounts. The other valuable oxidized fractions were found to possess large amounts of carboxylic groups, as determined by potentiometric titration. 13 C-NMR evidenced the presence of three distinctive carboxylic groups in the fully oxidized product, whereas for the partially oxidized samples, 13 C CP-MAS solid-state NMR did not detect any carbonyl signals. The oxidized products were characterized by means of FTIR and X-ray 2 photoelectron spectroscopy (XPS). Moreover, the changes on the degree of polymerization occurred after oxidative treatments were viscometrically determined.

In this study, sulphated polysaccharides were investigated in respect to their blood compatibility properties (hemocompatibility). Pure chitosan was treated with sulphating agents such as SO(3)/pyridine complex and chlorosulfonic acid (HClSO(3)) to obtain 3,6-O-sulfochitosan with low and high concentration of sulfur. These synthetically derived materials and the commercially available sulphated polysaccharides heparin and dextran sulfate, both with high concentrations of sulfur, were coated onto PET foils to act as surfaces with strong antithrombotic activity. This treatment should lead to better blood compatibility properties of PET materials for medical applications. To examine this, the optimized free hemoglobin method was applied to determine the antithrombotic activity of these surfaces. Glass as the standard thrombotic surface and a heparin-coated PET surface as a surface well-known for its strong antithrombotic activity were used as internal references. The experiments showed that dextran sulfate and sulphated chitosan with high concentrations of sulfur demonstrated the same antithrombotic activity as heparin over the whole period of measurement time. In addition, a relationship between the sulfur concentration in these sulphated polysaccharides and their blood compatibility properties can be demonstrated in this article.

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The adsorption behavior of chitosan on poly(ethylene terephthalate) (PET) model film surface was studied using the quartz crystal microbalance (QCM) technique. QCM with a dissipation unit (QCM-D) represents a very sensitive technique for adsorption studies at the solid/liquid interface in situ, with capability of detecting a submonolayer of adsorbate on the quartz crystal surface. Chitosan as well as PET were chosen for this study due to their promising biocompatible properties and numerous possibilities to be used in biomedical applications. As a first step, PET foils were activated by alkaline hydrolysis in order to increase their hydrophilicity. Model thin films were prepared from PET foils by the spin coating technique. The chemical composition of the obtained model PET films was analyzed using X-ray photoelectron spectroscopy (XPS) and their morphology was characterized by atomic force microscopy (AFM). Furthermore, the adsorption behavior of chitosan on these activated PET films and the influence of adsorption parameters (pH, ionic strength and chitosan solution concentration) were investigated in detail. Additionally, the surface chemistry and morphology of the PET films and the chitosan coated PET films were analyzed with XPS and AFM.