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Cellulose–chitosan gels were prepared using a LiOH/urea aqueous solution for a co-dissolution. After cellulose and chitosan were dissolved by a freeze–thaw process, the hydrogels were prepared via regeneration in methanol and washing with water. Finally, freeze-dried cellulose–chitosan gels were obtained via solvent exchange (water → ethanol → t-butyl alcohol) followed by freeze-drying. The chitosan...
Herein, we present a new process for the preparation of cellulose-chitosan foams using an aqueous lithium bromide (LiBr) solution. After obtaining hydrogels via dissolution-regeneration from an aqueous LiBr solution and methanol, cellulose-chitosan foams were prepared via solvent exchange (water → ethanol → t-butyl alcohol) followed by freeze-drying. The amino group content and elemental analysis...
s Herein, we present a new process for the formation of cell spheroids in three-dimensional culture systems using cellulose hydrogel film. Transparent cellulose hydrogel film were prepared via dissolution-regeneration with a LiOH/urea aqueous solution and methanol. The cell viability of the cellulose hydrogel film was equivalent to that of cell tissue culture plate, revealing no cytotoxicity. Spheroids...
Crosslinked cellulose-chitosan beads were obtained via dissolution-regeneration of cellulose and chitosan by a LiOH/urea aqueous solution, followed by the crosslinking of chitosan via dialdehyde cellulose (DAC). This crosslinking reaction involved the Schiff base formation between the aldehyde groups of DAC and the amino groups of chitosan and subsequent reduction. DAC was prepared through periodate...
Here, we present a new process for the preparation of cellulose–silk fibroin hydrogels using a concentrated lithium bromide (LiBr) aqueous solution. After mixing, the solutions of cellulose and silk fibroin that had each been dissolved separately in aqueous LiBr, the cellulose forms a gel as the solution cools to approximately 70°C, and silk fibroin is regenerated via treatment in methanol. Three...
Three β-chitin structures [anhydrous, di-hydrate, mono-ethylenediamine (EDA)] recently determined by synchrotron X-ray and neutron fiber diffraction were reviewed from the viewpoint of molecular interactions. Both water and EDA molecules interact with the chitin chains through multiple hydrogen bonds. When water complexes with chitin, the hydrogen bonding pattern rearranges with the replacement of...
We investigated the crystal structure of alkali-celluloses, Na-cellulose IIA and II(Cu), formerly known as Na-cellulose IIB, by synchrotron X-ray diffraction. Na-cellulose IIA, formed from cellulose I by high-concentration NaOH treatment, has a fiber repeat of 15 Å and a threefold-like helical conformation. Na-cellulose II(Cu), prepared by treating cellulose I with copper-saturated alkali solution,...
A protocol was developed to freeze-trap (at 150 K) cellulose as it is undergoing liquid ammonia pretreatment, and then to collect X-ray diffraction data from the freeze-trapped reactants as the reaction is allowed to proceed and ammonia is allowed to melt and then evaporate, leaving ammonia-cellulose I. Cellulose adopts a new two-chain crystal form, which we call low temperature phase ammonia-cellulose...
A new all-aqueous process of the dissolution/regeneration of cellulose was developed. Cellulose was completely dissolved in the 54–60 wt% lithium bromide aqueous solutions in the temperature range of 110–130 °C within a dissolution time of 1 h. Then, the cellulose was directly regenerated from the solution by cooling down to approximately 70 °C and removing the salts with water, yielding a translucent...
Surface and structural properties of cellulose hydrogel prepared from LiOH/urea solvent with alcoholic coagulation were examined. As coagulants, alcohols from methanol to butanol were employed. Alcohol with high water miscibility (MeOH, EtOH, 1-PrOH, 2-PrOH, and t-BuOH) gave a nano-porous structure consisting of a fibrous network of cellulose, while alcohol with low water miscibility (1-BuOH, 2-BuOH,...
To elucidate the role of urea in dissolution of cellulose in aqueous alkali-urea solvent, the dissolution process was monitored by differential scanning calorimetry and X-ray diffractometry. Urea had no direct interaction with cellulose in dissolution process, but promoted the decrease of crystallinity. Moreover, the addition of urea increased the dissolved fraction of cellulose in the solvent by...
The neutron structure of a complex of EDA with cellulose has been determined to reveal the location of hydrogen atoms involved in hydrogen-bonding. EDA disrupts the hydrogen-bonding pattern of naturally occurring cellulose by accepting a strong hydrogen-bond from the O6 hydroxymethyl group as the conformation of this group is rotated from tg to gt. The O3-H·O5 intrachain hydrogen-bond commonly found...
The highly crystalline β-chitin from diatom Thalassiosira weissflogii was esterified via intercalation with succinic anhydride followed by simple heating, maintaining the original crystalline order. Due to the introduced free carboxyl groups, the chitin ester crystal showed ion exchange ability for metal cations in aq. solution. Heavy metal cations such as Pb2+ bound to the β-chitin succinate gave...
Adsorption–complexation of cellulose by hydrazine solutions in water and toluene was studied for native cellulose of varied crystallinity. Penetration of hydrazine into cellulose takes place more readily in hydrazine solution of higher concentration and with cellulose of lower crystallinity, but the equilibrium uptake was nearly independent of crystallinity. Complexation from toluene solution takes...
We prepared two cellulose hydrates, Na-cellulose IV and cellulose II hydrate, along with their respective anhydrous forms, cellulose II and II′, from microcrystalline cellulose. X-ray diffractometry analysis showed that the structure of the hydrophobic stacking sheet was conserved in the samples, but the distance between the sheets was in the order: cellulose II hydrate > Na-cellulose IV > cellulose...
Cellulose-synthetic polymer nanocomposite films were prepared by immersion of cellulose gel in polymer solutions followed by dry casting. The cellulose hydrogel was prepared from aqueous alkali-urea solution. As the synthetic polymer, polystyrene (PS) and poly(methyl methacrylate) (PMMA) were used. The polymer content could be changed between 10 and 80% by changing polymer concentration of immersing...
A technique of immobilizing an enzyme/antibody was developed using cellulose hydrogel prepared from an aqueous alkali-urea solvent. Partial oxidation by sodium periodate activated the cellulose gel for introducing aldehyde groups. Proteins were covalently introduced to cellulose gel by a Schiff base formation between the aldehyde and the amino groups of proteins, and stabilized by a reduction of imines...
Highly crystalline cellulose samples from green algae (cellulose I) and mercerized ramie (cellulose II) were treated with anhydrous hydrazine and the resulting complexes were analyzed by synchrotron X-ray diffraction and thermogravimetry. Cellulose I-hydrazine complex could be fully described by a two-chain monoclinic unit cell, a = 0.879 nm, b = 1.076 nm, c = 1.038 nm, and γ = 122.0°, with space...
The hydrogen bond arrangement in a complex of cellulose with ammonia has been studied using neutron crystallography in combination with molecular dynamics simulations. The O6 atom of the hydroxymethyl group is donor in a highly occupied hydrogen bond to an ammonia molecule. This rotating ammonia molecule is donor in partially occupied and transient hydrogen bonds to the O2, O3 and O6 atoms of the...
Structural changes during the treatment of films of highly crystalline microfibers of Cladophora cellulose with ethylenediamine (EDA) have been studied by time-resolved X-ray microprobe diffraction methods. As EDA penetrates the sample and converts cellulose I to EDA-cellulose I, the measured profile widths of reflections reveal changes in the shapes and average dimensions of cellulose I and EDA-cellulose...
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