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In this work the formation of multilayers composed by carboxymethylcellulose (CMC), chitosane and bovine serum albumin (BSA) was studied by ellipsometry. First, the adsorption behavior of carboxymethylcellulose onto amino-terminated surfaces was investigated as a function of molecular weight and average degree of substitution of CMC. The influence of these parameters on the adsorbed amount of CMC onto amino-terminated substrates was absent. However, the interaction of CMC covered surfaces with chitosane and BSA was favored when the average degree of substitution of CMC was increased. The adsorption of BSA onto the polysaccharide systems was studied as a function of pH. At the isoelectric point of BSA a maximum in the adsorbed amount was found.

The adsorption of a new cellulose derivative,6-O-(2,3-bis(thiosulfato) propyl-oxy-2-hydroxy-propyl)-cellulose (TSHP), onto silver surfaces was investigated by means of ellipsometry, contact angle measurements and X-ray photoelectron spectroscopy (XPS). The results showed that the formation of a dense TSHP monolayer on silver surfaces is an irreversible and slow process. Based on XPS results a model was proposed to explain the chemisorption of TSHP on silver substrates. This model considers the homolytical cleavage of the thiosulfate groups attached to the cellulose chains with the formation of thio radicals, which bind covalently to the silver surface. The formation of silver thiolates lead to a stable TSHP monolayer on silver surfaces.

Persistent luminescent materials are present in several recent studies on new applications and novel properties. In this work, we demonstrate, for the first time, the production of translucent flexible persistent composites based on Sr2MgSi2O7:Eu2+,Dy3+ (SMSO) into cellulose ether matrix film. The composite was successfully prepared through a new optimized route of co-precipitation and microwave-assisted annealing followed by (3-aminopropyl)triethoxysilane (APTES) coating and dispersion in hydroxypropyl methylcellulose (HPMC). The SMSO@APTES/HPMC films show persistent luminescence emission at 475 nm (blue) and high transmittance in the visible range. To understand the fine distribution of the nanoparticles in the matrix, we have investigated their structure and dispersion by using Synchrotron Radiation X-ray fluorescence mapping and Scanning Transmission X-ray Microscopy. This innovative composite could bring new perspectives for the class of persistent luminescence materials, enhancing technologies in progress throwing light on new applications never perceived. [ABSTRACT FROM AUTHOR]

Composite cryogels were prepared from xanthan gum (XG) precursor gels at 20 g L-1 containing TiO2 load at 5, 10, and 20 wt% and citric acid, as crosslinker. The effect of the pH over precursor gel on the properties of the resulting cryogels was evaluated. The characterization of the XG/TiO2 cryogels comprised compression tests, swelling degree (SD) determination, Fourier transform infrared vibrational spectroscopy in the attenuated total reflectance mode (FTIR-ATR), scanning electron microscopy (SEM), and X-ray microtomography (CT) analyses. The largest compressive modulus (E) was observed for XG/TiO2 10% cryogels prepared at pH 4.0, which amounted to 100±7 kPa, whereas the E value determined for bare XG cryogels was 29±3 kPa. XG/TiO2 10% cryogels presented larger pores and thicker walls than bare XG cryogels, as evidenced by SEM and CT analyses. FTIR-ATR spectra evidenced the ester bonds stemming from the esterification among carboxylic acid groups and/or XG hydroxyl groups. XG/TiO2 10% cryogels presented SD of (61±2) gwater/gcryogel, long-term stability in water, and outstanding photocatalytic properties in the presence of Cr(VI) ions and methylene blue (MB). The photocatalytic processes for the reduction of Cr(VI) to Cr(III) and for the photobleaching of MB fitted the first-order kinetic model, yielding rate constants of 0.019 varying min-1 and 0.0096 min-1, respectively. For both processes, the XG/TiO2 10% cryogels could be recycled five times without losing shape or efficiency. [ABSTRACT FROM AUTHOR]