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The solubilities of many substances are significantly affected by specific ions, as demonstrated by the Hofmeister series of proteins. Cellulose has a resistant fibrillar structure that hinders its swelling and dissolution. Certain inorganic salt solutions are effective swelling agents and solvents for cellulose. However, the precise effects of these ions on cellulose are not fully understood. In this study, we studied the intermediate structures of cellulose fibers during their swelling process in ZnCl 2 and LiBr solutions via in situ X-ray diffraction. Two swollen phases with characteristic morphologies were observed for both salt treatments. Only the surfaces of the fibers were swollen in ZnCl 2 , whereas the ions penetrated the fibers and formed complexes with cellulose while the morphology of the fibers was maintained in LiBr. Our findings clarify the reasons that ZnCl 2 has been used as an excellent swelling agent, whereas LiBr has been used as a good solvent for cellulose.

A hydrogel was prepared from a polysaccharide, enzymatically synthesized through a one-pot reaction in aqueous solution, and its properties as a functional material were evaluated. Enzymatic synthesis using glucosyltransferase K obtained from Streptococcus salivarius ATCC 25975 was performed with sucrose as a substrate. The synthetic product was unbranched linear (1 → 6)-α-d-glucan with a high molecular weight, M w : 1.0-3.0 × 10 5 . The synthesized (1 → 6)-α-d-glucan was insoluble in water and crystallized in a monoclinic unit cell, which is consistent with the hydrated form of dextran. Transparent and highly swellable (1 → 6)-α-d-glucan hydrogels were obtained by crosslinking with diglycidyl ethers. The hydrogels showed no syneresis and no volume change during compression, resulting in the retention of shape under repeated compression. The elastic moduli of these hydrogels (<60 kPa) are smaller than those of other polysaccharide-based hydrogels having the same solid contents. The oven-dried gels could be restored to the hydrogel state with the original transparency and a recovery ratio greater than 98%. The mechanism of water diffusion into the hydrogel was investigated using the kinetic equation of Peppas. The properties of the hydrogel are impressive relative to those of other polysaccharide-based hydrogels, suggesting its potential as a functional biomaterial., Competing Interests: The authors declare no competing financial interest., (© 2020 The Authors. Published by American Chemical Society.)

Enzymatic hydrolysis was conducted with Pseudomonas lipase for film samples of graft copolymers of cellulose acetate (CA) and butyrate (CB) with poly(epsilon-caprolactone) (PCL), CA-g-PCL, and CB-g-PCL, respectively. The two trunk polymers CA and CB, both having the degree of acyl substitution (DS) of >2, are respectively immiscible and miscible with PCL. A hindrance effect of the cellulose ester trunks on the enzymatic attack to the PCL component was observed for the two copolymer series; the situation was more conspicuous in the use of CB trunks. After the selective hydrolytic degradation of the PCL component, a topographical study by AFM revealed that the CA and CB constituents as residues formed a protuberant structure on the surface of the respective film specimens. The altitude and regularity of the protuberances were variant depending on the initial copolymer composition. In a phase-imaging mode of AFM, a hydrolyzed film of CA-g-PCL with an extremely low graft-density (acetyl DS > 2.95) showed particularly larger CA domains of >25 nm in diameter. The domain sizes were in accordance with a heterogeneity scale in the original intercomponent mixing state estimated by (1)H spin-lattice relaxation time (T(1)(H)) measurements in solid-state (13)C NMR spectroscopy. The present results demonstrate a high potential in application of the PCL-grafted cellulosic copolymers as spatiotemporally biodegradation-controllable materials.