Modification of pine pulp during oxygen delignification by xylan self-assembly.

Self-assembly is a technique of preparing functional materials based on targeted intermolecular interactions involving different macromolecules. In this work, hardwood xylan was disassembled from wood and birch bleached kraft pulp using pressurized hot water extraction (HWX) and cold alkali extraction (CAX), respectively. The extracted biopolymers were characterized using gas chromatography (GC), size exclusion chromatography (SEC) and Fourier transform infrared spectroscopy (FTIR), and subsequently added into an oxygen delignification reactor containing pine kraft pulp. The assembly of xylan-pulp fiber was characterized using advanced time-of-flight secondary ion mass spectrometry (ToF-SIMS) and imaging. The xylan-pine pulp assembly was not significantly removed during the whole elemental chlorine free bleaching sequence or during low consistency refining. Modified fibers had superior mechanical properties compared to the reference pulp. Our concept can be easily applied in the pulp and paper industry, and it opens new possibilities for the utilization of fully bio-based fibers in new materials.

Photoresponsive cellulose fibers by surface modification with multifunctional cellulose derivatives.

Eucalyptus bleached kraft pulp fibers were modified by adsorption of novel bio-based multifunctional cellulose derivatives in order to generate light responsive surfaces. The cellulose derivatives used were decorated with both cationic groups (degree of substitution, DS of 0.34) and photoactive groups (DS of 0.11 and 0.37). The adsorption was studied by UV-vis spectroscopy, surface plasmon resonance (SPR) and time-of-flight secondary ion mass spectroscopy (ToF-SIMS). The adsorption isotherms followed the Freundlich model and it turned out that the main driving force for the adsorption was electrostatic interaction. Moreover, strong indications for hydrophobic interactions between the fibers and the derivatives and the derivatives themselves were found. ToF-SIMS imaging revealed an even distribution of the derivatives on the fiber surfaces. The modified fibers underwent fast photocrosslinking under UV-irradiation as demonstrated by light absorbance and fluorescence measurements. Thus, our results proved that the modified fibers exhibited light-responsive properties and can potentially be used for the manufacture of smart bio-based materials.