• Journal of Institute of Convergence Technology
• /
• v.1 no.2
• /
• pp.33-36
• /
• 2011

Ionic liquids based on formate and hydrogen carbonate anions were synthesized for use as solvents for the effective dissolution of cellulose and the regenerated cellulose was in the native lattice.

• Proceedings of the Korean Society of Dyers and Finishers Conference
• /
• 2012.03a
• /
• pp.51-51
• /
• 2012

Cellulose is extremely difficult to dissolve cellulose in water and most common organic solvents due to their stiff molecular structure, close chain packing and intermolecular hydrogen bonds. Recently, cellulose solutions using ionic liquids (ILs) as a green solvent have been known to form cholesteric liquid crystalline phase at high cellulose concentration. In this study, the phase transition and rheological behaviors of concentrated cellulose/[AMIM]Cl solution were investigated using polarized optical microscopy and rheometry. Studies were conducted to characterize the influence of cellulose concentration on the phase transition of the cellulose solution and the mechanical properties of the regenerated fibers spun from the anisotropic cellulose/[AMIM]Cl solutions.

• Journal of the Korean Wood Science and Technology
• /
• v.31 no.6
• /
• pp.1-7
• /
• 2003

The phase transformation from cellulose I into cellulose II in woods by way of Na-cellulose I was examined by x-ray diffraction analysis.The formation of Na-cellulose I in woods increased with the increase of treating time in alkali solution. When compression wood was treated with 20% NaOH solution at room temperature for 1 day, the x-ray diagram showed only Na-cellulose I. On the other hand, the x-ray diagram of tension wood showed a mixture of cellulose I and Na-cellulose I. Cellulose I of tension wood could not be transformed completely into Na-cellulose I even after 10-day treatment, but was transformed into Na-cellulose I after 30-day treatment. Na-cellulose I of compression and tension woods was converted to the cellulose I pattern and the mixture of cellulose I and cellulose II, respectively, after washing with water and drying at 20℃. Cellulose I regenerated from Na-cellulose I in wood could not be converted to cellulose II by delignification. Thus, it revealed that the delignification of the alkali-treated wood did not affect their cellulose structures. From the results, therefore, it can be concluded that lignin in woods prevents the formation of the stable Na-cellulose I and the conversion from cellulose I to cellulose II. This means that the conversion of chain polarity of wood cellulose hardly occurs during mercerization because cellulose microfibrils are fixed by lignin which not to be intermingled.

• Journal of the Korean Wood Science and Technology
• /
• v.20 no.1
• /
• pp.38-45
• /
• 1992

Fine and alkali-swollen structures of native cellulose fibers were investigated by x-ray diffraction methods. The results of fine structures are shown in Table 1. In meridional x-ray diffractograms, the relative intensity ratio R of (002) to (004) for cellulose I was ca. 0.05 and for regenerated cellulose it was ca. 0.45. It was considered that the transformation from cellulose I to cellulose II resulted from the packing or conformational change of cellulose chain. Finally. although cellulose I was not detected in the alkali-swollen celluloses treated for 1 hr to 24 hrs, washing and drying them resulted in the generation of considerable amounts of cellulose I and the amount decreased with increasing alkali duration.

• Archives of Craniofacial Surgery
• /
• v.20 no.5
• /
• pp.289-296
• /
• 2019

Background: Topical hemostatic agents are used when ligation, electrocauterization, or other conventional hemostatic methods are impractical. Because a hemostatic agent is a foreign body, it can cause foreign body reactions, inflammation, and infections that can interfere with the wound healing process. Therefore, we should select hemostatic agents after considering their effects on wound healing. Here, we compared the effects of hemostatic agents on wound healing in a rectus abdominis muscle defect in rats. Methods: Twelve Sprague Dawley rats were subjected to creation of a $6{\times}6mm$ defect in the rectus abdominis muscle and divided into four groups: control group; group A, Tachosil fibrin sealant patch; group B, Surgicel Fibrillar oxidized regenerated cellulose; and group C, Surgicel Snow oxidized regenerated cellulose. For the histologic analysis, biopsies were performed on the 3rd, 7th, and 27th days. Results: The foreign body reaction was the weakest in group A and most significant in group C. The inflammatory cell infiltration was the weakest in group A and similar in groups B and C. Muscle regeneration differed among periods. The rats in group A were the most active initially, while those in group C showed prolonged activity. Conclusion: Tachosil and Surgicel administration increased inflammation via foreign body reactions, but the overall wound healing process was not significantly affected. The increased inflammation in the Surgicel groups was due to a low pH. We recommend using Tachosil, because it results in less intense foreign body reactions than Surgicel and faster wound healing due to the fibrin action.

• Proceedings of the Korean Fiber Society Conference
• /
• 2001.10a
• /
• pp.215-218
• /
• 2001

이산화탄소($CO_2$)를 사용한 셀룰로오스 카보네이트 유도체의 제조 및 재생 셀룰로오스 섬유 제조와 관련한 기초 연구성과를 이미 발표한 바 있다[1~3]. 이번 연구에서는 일정한 조건에서 제조된 셀룰로오스 카보네이트 유도체의 용해온도, 셀룰로오스 카보네이트 함량, 10% 수산화나트륨 수용액내의 산화아연의 함량 변화에 따른 용해성을 평가하여 상그림표를 작성하였다. (중략)

• Journal of Korea Technical Association of The Pulp and Paper Industry
• /
• v.45 no.3
• /
• pp.27-35
• /
• 2013

Cotton linter pre-treatment methods using electron beam and sulfuric acid were investigated to prepare high quality regenerated fibers for fabrics. So far, NaOH was used to reduce the degree of polymerization (DP) of the cotton linter for ease of dissolving by cellulose solvent. Two pre-treatment methods were developed to reduce the consumption of the chemicals (NaOH) and to control the DP of cellulose more precisely. Changes in ${\alpha}$-cellulose contents and brightness by the pre-treatments were also important concerns. Both electron beam irradiation and sulfuric acid were shown to be effective on controlling the DP of cellulose and to reduce the chemical consumption, but reduced ${\alpha}$-cellulose contents as well in this study. Sulfuric acid pre-treatment, which needed additional washing process after the pre-treatment when comparing to the electron beam irradiation method, gave the highest brightness and the highest reduction of ${\alpha}$-cellulose content.

• Polymer(Korea)
• /
• v.37 no.1
• /
• pp.52-60
• /
• 2013

Partially hydrolyzed cellulose acetate (CA) fibers were prepared by treating CA fibers in aqueous $Na_2CO_3$ solutions of various concentrations. The deacetylation of CA fibers was confirmed through FTIR spectra and WAXD patterns. The hydrolysis was confined to the surface part of the CA fiber by controlling the treatment conditions. The resultant fibers had a sheath-core structure with a sheath component of regenerated cellulose and a core of non-hydrolyzed cellulose acetate. The SEM images of the surface-hydrolyzed CA fibers, the core of which was dissolved out using acetone as the solvent, showed that the sheath thickness increased with increasing alkaline concentration, indicating an increase in the hydrolyzed fiber, i.e., regenerated cellulose. Polarized FTIR analysis of the polyimide film rubbed with velvet fabrics of surface-hydrolyzed CA fibers showed that polyimide molecules were preferentially oriented to the rubbing direction.

• Fibers and Polymers
• /
• v.3 no.1
• /
• pp.1-7
• /
• 2002

Cellulose carbonate was prepared by the reaction of cellulose pulp and $CO_2$ with treatment reagents, such as aqueous $Zncl_2$ (20-40 wt%) solution, acetone or ethyl acetate, at -5-$0^{\circ}C$ and 30-40 bar ($CO_2$) for 2 hr. Among the treatment reagents, ethyl acetate was the most effective. Cellulose carbonate was dissolved in 10% sodium hydroxide solution containing zinc oxide up to 3 wt% at -5-$0^{\circ}C$. Intrinsic viscosities of raw cellulose and cellulose carbonate were measured with an Ubbelohde viscometer using 0.5 M cupriethylenediamine hydroxide (cuen) as a solvent at $20^{\circ}C$ according to ASTM D1795 method. The molecular weight of cellulose was rarely changed by carbonation. Solubility of cellulose carbonate was tested by optical microscopic observation, UV absorbance and viscosity measurement. Phase diagram of cellulose carbonate was obtained by combining the results of solubility evaluation. Maximum concentration of cellulose carbonate for soluble zone was increased with increasing zinc oxide content. Cellulose carbonate solution in good soluble zone was transparent and showed the lowest absorbance and the highest viscosity. The cellulose carbonate and its solution were stable in refrigerator (-$5^{\circ}C$ and atmospheric pressure).

• Proceedings of the Korean Society for Noise and Vibration Engineering Conference
• /
• 2009.10a
• /
• pp.198-201
• /
• 2009

Due to piezoelectric property of regenerated cellulose paper, a green energy harvester using an electro-active paper (EAPap) was studied. In order to design the green energy harvester, we simulated cymbal type energy harvesting structures for single and multi-stacked layers of EAPap films. From the simulation, the optimized material orientation, thickness of harvesting structure was selected. By measuring of the induced output voltage by applying stress on energy harvester will be explained in detail. Therefore we propose the feasibility of the nature-friendly piezoelectric EAPap as a new green energy harvesting material.