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The grafting reactivities with glycidyl methacrylate (GMA) of five xylans from hardwood and cereal sources were compared. The structural property that best predicted the reactivities of xylans with GMA was the fraction of 4-O-methylglucuronic acid (MeGlcA) substitution. A comparatively high level of arabinose substitution was also positively correlated to reactivity with GMA. The impact of MeGlcA and arabinose branching groups is likely attributed to the solubilizing effect of these substituents. Consistent with this prediction, low water solubility and high lignin content were found to hinder reactivity. Even though oligomeric substrates have the advantage of water solubility, modified xylo-oligosaccharides were difficult to purify. Accordingly, delignified and high-molecular weight xylans that are soluble or dispersible in water are best suited for this type of backbone derivatization. Adsorption studies with a quartz crystal microbalance with dissipation indicated that grafting lowered the total adsorption of arabinoxylan but did not significantly affect the fraction of xylans adsorbed irreversibly on cellulose.

The aim of this work was to study the effect of solution conditions and polysaccharide structure on their Layer-by-Layer (LbL) deposition on nanofibrillated cellulose (NFC). Multilayer build-up of cellulose derivatives and chitosan on NFC model surfaces was studied using Quartz Crystal Microbalance with Dissipation (QCM-D) and Colloidal Probe Microscopy (CPM). The type of cationic polysaccharide was found to significantly affect the multilayer build-up and surface interactions. Cationic cellulose derivative quaternized hydroxyethyl cellulose ethoxylate (HECE) formed highly water-swollen layers with carboxymethyl cellulose (CMC), and the build-up was markedly influenced by both the ionic strength and pH. The ionic strength did not significantly influence the multilayer build-up of chitosan-CMC system, and adsorbed chitosan layers decreased the viscoelasticity of the system. Based on the results, it was also confirmed that electrostatic interaction is not the only driving force in case of the build-up of polysaccharide multilayers on nanofibrillated cellulose., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Films and hydrogels consisting of cellulose nanofibrils (CNF) were modified by covalent EDC/NHS coupling of luminescent, water-dispersible carbon dots (CDs). Quartz crystal microgravimetry with dissipation monitoring (QCM-D) and surface plasmon resonance (SPR) were used to investigate the attachment of CDs on carboxymethylated CNF (CM-CNF). As the first reported use of CD in nanocellulose products, we provide proof-of-concept for the synthesis of transparent and fluorescent nanopaper and for its tunable luminescence as confirmed by confocal microscopy imaging.

Cellulosic substrates were modified by using sequential adsorption of functionalized carboxymethyl cellulose (CMC) and "click" chemistry in aqueous media. First, the effect of degree of substitution (DS), and level of functionalization as well as ionic strength of the medium were systematically investigated in situ by using quartz crystal microbalance with dissipation (QCM-D) in terms of the extent of adsorption of propargyl and azido functionalized CMC. It was found that the functionalization of CMC did not prevent its adsorption on cellulose. However, it was only effective in the presence of electrolytes. Moreover, the adsorption was found to be more efficient for the functionalized CMCs with low initial DS. Next, "click" chemistry, copper (I)-catalyzed azide-alkyne cycloaddition reaction (CuAAC), was carried out for covalent attachment of different molecules on the pre-functionalized ultrathin cellulose films. The modified cellulosic surfaces were further characterized using AFM imaging and XPS. Finally, the method was successfully used in modification of nanofibrillar cellulose (NFC) in aqueous media., (Copyright © 2012 Elsevier Ltd. All rights reserved.)