• 한국염색가공학회지
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• 제6권2호
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• pp.47-54
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• 1994

Cotton fiber, NaOH-mercerized cotton fiber, cotton fabric, and NaOH-mercerized cotton fabric have been treated by liquid ammonia at -33.4$^{\circ}C$. The fine structures, bending properties, tensile strengthes, shrinkages for laundering, and wrinkle recoveries were studied. The treatment of cottons with liquid ammonia brought about the transition of crystal lattice ; transforming cellulose I crystal of original cotton to cellulose I and III crystal, and cellulose II crystal of mercerized cotton to cellulose II and III crystals. The degree of crystallinities were decreased in the order of liquid ammonia>NaOH/liquid ammonia>NaOH-treated cotton. However moisture regain and water absorbency for liquid ammonia-treated cotton were lower than that of NaOH-treated cotton because of a difference in swelling actions of the agents. It seems caused by intermicrofibrillar pores produced in swelling processes. The bending rigidity and bending hysteresis were decreased remarkly by liquid ammonia treatment. Therefore softness and dimensional stability were improved. The liquid amminia and NaOH/liquid ammonia-treated cottons moreover show excellent properties in tensile strength, anti-shrinkage for laundering, and wrinkle recovery.

• 한국염색가공학회지
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• 제7권1호
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• pp.10-22
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• 1995

Cellulosic fabrics, i.e. rayon, polynosic, and linen were treated with liquid ammonia at -33.4$^{\circ}C$. The fine structures, bending properties, tensile strength, wrinkle recoveries, and dyeing properties of the treated fabrics were studied. Dyeing was carried out with two direct dyes, C. I. Direct Red 2 and Blue 1. The liquid ammonia treatment for three fabrics brought about the transition of crystal lattices and the decrease of crystallinity; transforming cellulose I structure of original linen to cellulose I and III structure, and cellulose II structure of original rayon and polynosic to cellulose II and III structure. Moisture regain of liquid ammonia- treated polynosic and linen was higher than that for untreated, and water absorbency of liquid ammonia-traeated fabrics was all lower than that of untreated. Also, bending properties of treated fabrics were not improved compared with those of untreated ones. The rayon treated with liquid ammonia was increased not only the apparent diffusion coefficient and the rate of dyeing but also equilibrium dye adsortion, whereas polynosic and linen were increased only equilibrium dye adsortion. It is suggested that the pore sizes of liquid ammonia-treated rayon, polynosic, and linen are much smaller than that of liquid ammonia-treated cotton.

• 임산에너지
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• 제18권2호
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• pp.62-69
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• 1999

목재 세포벽중의 셀룰로오스의 알칼리 팽윤구조는 리그닌에 의해 크게 영향을 받는다. 본 연구에서는 알칼리 팽윤특성에 관한 리그닌의 영향을 명확히 하기 위하여 신갈나무의 정상재 및 부후재를 이용하여 X선 회절법과 자외선 현미경법에 의해 검토하였다. 그 결과, 목재 셀룰로오스는 고농도의 알칼리 수용액 중에서 머서화 처리를 하여도 결정변태가 일어나지 않으며 탈리그닌 후에도 결정의 변화는 없었다. 즉, 목재세포벽중의 셀롤로오스 결정은 리그닌의 존재에 의해 알칼리 팽윤이 억제되어 결정의 변태는 발생하지 않으며 탈리그닌 후에도 결정의 구조는 변화되지 않는 것으로 생각되었다.

• 공업화학
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• 제9권3호
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• pp.348-354
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• 1998

아크릴산의 셀룰로오스에 대한 방사선 그라프트 반응에서 가교제로서 다관능성 단량체를 첨가할 경우 그라프트 반응에 미치는 영향을 알아보기 위하여 작용기가 2개인 1,2-propandiol dimethacrylate(PDDMA)와 작용기가 3개인 1,1,1-trimethylolethane triacrylate(TMETA)를 아크릴산에 대한 부피분율로 첨가하여 그라프트 반응을 수행하였다. 그라프트 반응시 다관능성 단량체의 함량, 조사선량, 반응온도, 반응시간 등이 그라프트율에 미치는 효과에 대하여 조사하였다. 아크릴산에 가교제로서 다관능성 단량체를 첨가하여 그라프트 반응을 시킬 때 2관능성 단량체인 PDDMA 는 0.75부피%, 3관능성 단량체인 TMETA는 1.0부피%에서 최대의 그라프트율을 나타내었다. 아크릴산에 PDDMA가 소량 함유된 그라프트 반응에서 그라프트용액에 산을 첨가하면 그라프트율은 감소하였으며 강산일수록 감소현상은 증가하였고, TYMETA는 산을 첨가하여 그라프트 반을을 시키면 그라프트율은 증가하였다. 3관능성 단량체인 TMETA가 포함된 그라프트 반응에서 $FeSO_4{\cdot}7H_2O$와 산을 동시에 첨가하면 산을 첨가하지 않은 경우보다 높은 그라프트율을 나타냈고, 산만을 첨가하면 과다한 단일중합체의 형성으로 그라프트 반응을 수행할 수가 없었다.

• 미생물학회지
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• 제14권2호
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• pp.65-74
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• 1976

Atternaria sp. was isolated from soil and crude cellulases were prepared from wheat bran culture of the fungus. The activities of the crude enzyme were studied on five different subvstrates and some phsical properties were also examined, crude enzymes were purified by column chromatography on DEAE Sephadex and Sephadex, Isozymes were separated some of which were active specifically on DEAE cellulose and some were primarily active on cellulose and CM-cellulose. The optimal points of pH and temperature for the crude enzyme were varied depending on the substrates ; On cellulose they were at pH 6.0 and 40.deg.C, on CM-cellulose at pH's 4.0 and 6.0 and 60.deg.C, and on DEAW-cellulose at pH 5.0 and 50.deg.C. Two active fractions, F-1 and F-II on Na-CMC was used as substrate the Km values of crude enzyme, F-I and F-II were calculated to be $4{\times}10^{-5}$ , 1.1 * 10$^{-4}$ , and $1.25{\times}10^{-4}mN$ resepctively. The Ki value of $Cu^{++}$ for crude enzyme was$4{\times}^{-4}mN$ , while that of $Nm^{++}$ while in the same concentration of $Mn^{++}$ it reached to 91%. Some 57% activity of F-1 was inhibited in s mN $Cu^{++}$, whereas it was inhibited as much as 81% in the same concentration above the concentration of 0.3 mM with tis activity reaching up to 137% in 2 mM. On the other hand the F-11 was inhibited by the presence of M $n^{++}$ and some 67% activity was inhibited at 2mM.

• 한국수소및신에너지학회논문집
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• 제16권2호
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• pp.159-169
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• 2005

Cellulose, consisted of 45 wt% in wood, is usable as fuels and heavy oil additives if depolymerized to monomer unit, because the chemical structures are similar to high octane materials found in gasoline. In this study, thermochemical degradation by solvolysis reaction of cellulose such as the effect of reaction temperature, reaction time and type of solvent on conversion yield and degradation products were investigated. It was found that the effectiveness of the solvent on the sovolysis reaction was as follows; acetone>n-butanol>tetralin. When acetone was used as a solvent, the highest cellulose conversion was observed to be 91.8% at 500$^{\circ}C$, 40min. Combustion heating value of liquid products from thermochemical conversion processes was in the range of 7,330${\sim}$7,410cal/g. The energy yield and mass yield in acetone-solvolysis of cellulose was as high as 66.8% and 37.0 g oil/100g raw material after 40min of reaction at 400$^{\circ}C$. Various aliphatic and aromatic compounds were detected in the cellulose solvolysis products. The major components of the solvolysis products, that could be used as fuel, were mesityl oxide, mesitylene, isophorone.

• Journal of the Korean Wood Science and Technology
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• 제29권1호
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• pp.60-67
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• 2001

소나무(Pinus densiflora)재의 1차조직과 2차조직의 조직구조, 미세구조 및 머서화(mercerization)에 의한 셀룰로오스의 결정구조 변화를 검토하였다. 그 결과, 1차조직의 세포는 원형에 가깝고 내강이 크며 배열이 무질서한 데 비하여, 2차조직의 세포는 장방형이고 비교적 규칙적인 배열을 갖고 있다. 섬유장은 1차조직 $200{\sim}250{\mu}m$, 2차조직 $1,500{\sim}1,600{\mu}m$였으며, 내강경은 1차조직 $40{\sim}50{\mu}m$, 2차조직 $10{\sim}20{\mu}m$였다. 그리고 1차조직과 1차방사조직은 2차조직의 세포에 비해 미목화된 세포가 많았다. 1차조직과 2차조직에서 셀룰로오스 결정의 면간격과 미결정 폭의 차이는 없었으나 상대결정화도는 각각 23%와 35%로 다소 차이가 있었다. 배향성에 있어서 1차조직의 미결정은 무배향을 나타냈으나 2차조직의 미결정은 섬유축에 $20{\sim}30^{\circ}$의 배향성을 나타냈다. 머서화 과정 동안에 1차조직 셀룰로오스 결정은 셀룰로오스 II로 변화되었지만 2차조직의 셀룰로오스 결정은 거의 변화되지 않았다. 따라서 양 조직간의 결정변태의 차이는 목화 정도의 차이에 의한 리그닌의 영향으로 생각되었다.

• 한국동물학회지
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• 제36권3호
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• pp.367-372
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• 1993

재생쥐간에서 분리한 topoisomerase II에서 protein kinase 활성이 발견되었다. ,topo II 활성 및 kinase 활성은 hydroxyapatite, phosphocellulose, double strand DNA cellulose chromatography 등의 순수 분리 과정 중에도 서로 분리되지 않았으며 glycerol gradient sedimentation 분석에서도 같은 분획에서 활성이 존재하였다. Kinase는 topo II 저해제인 N-ethylmaleimide와 novobiocin 등에 의해 그 활성이 저해되었다. 그러나 이러한 증거들 만으로 kinase 활성이 topo II가 아닌 다른 polypeptide에 의한 것일 가능성을 완전히 배제 할 수는 없다. Topo II와 결합된 kinase 활성에는 Mg++가 절대적으로 필요하였으며 다른 일가 또는 이가 이온으로는 그 효과가 대체되지 않았다. Histone H1은 kinase 활성을 증가 시키며 또 kinase에 의해 강하게 인산화된다. 이러한 효과는 다른 histone 류 및 casein 등에 의해 대체되지 않았다.

• 한국식품과학회지
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• 제16권3호
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• pp.322-328
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• 1984

Pizopus oryzae가 생산(生産)하는 glucoamylase를 유안(硫安)및 acetone 분획(分劃)과 이온교환수지의 column chromatography에 의하여 정제(精製)하였다. 즉(卽) 조효소액(粗酵素液)을 유안분획(硫安分劃) acetone 분획(分劃), DEAE-cellulose column chromatography, CM-cellulose column chromatography에 의(依)하여 두가지형(型)의 glucoamylase를 분리정제(分離精製)하였으며 이들을 각각(各各) glucoamylase I과 II라고 하였다. Glucoamylase I과 II의 Specific activity는 각각(各各) 157.6U/mg protein (조효소액(粗酵素液)의 37.5배(倍)) 164.7U/mg protein (조효소액(粗酵素液)의 39.2배(倍)) 이었고 수율(收率)은 각각(各各) 4.3%, 3.8%이었다. Glucoamylase I과 II는 polyacrylamide disc gel electrophoresis와 SDS-polyacrylamide gel electrophoresis에 의(依)하여 각각(各各) 단일(單一)한 band를 나타내었고 이 단백질(蛋白質) band는 옥도염색(沃度染色)에 의(依)해 glucoamylase 활성(活性)을, PAS염색(染色)에 의(依)해 glycoprotein임을 확인(確認)하였다.

• Journal of Microbiology and Biotechnology
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• 제8권6호
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• pp.568-574
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• 1998

Two types of chitosanases produced from Aspergillus fumigatus KH-94 were purified by ion exchange and gel permeation chromatography. Molecular weights of the enzymes are 22.5 kDa (chitosanase I) and 108 kDa (chitosanase II). pI, optimum pH, and temperature of chitosanase I are 7.3, 5.5, and 70-$80^{\circ}C$, respectively, and those of chitosanase II are 4.8, 4.5~5.5, and 50~$60^{\circ}C$, respectively. Activities of both chitosanases were increased by $Mn^{2+}$ but inhibited by $Cu^{2+}$ and $Hg^{2+}$ . Chitosanase I has endo-splitting activity that hydrolyzes chitopentaose, chitohexaose, and chitosan to chitobiose, chitotriose, and chitotetraose, whereas chitosanase II has exo-splitting activity that hydrolyzes chitobiose and chitosan to glucosamine. Chitosanase II was found to have transglycosylation activity also in the reaction of 2% more chitooligosaccharides as a substrate and at the initial reaction. The higher degree of deacetylation, the stronger activities of chitosanase Iand II toward chitosans. Both chitosanases could hydrolyze chitosan and glycol chitosan but not chitin, cellulose, and carboxymethyl cellulose. To produce higher degree of polymerization of chitooligosaccharides, chitosanase I was used and yielded 80% of recovery.