• 한국식품과학회지
• /
• 제26권4호
• /
• pp.428-435
• /
• 1994

쌀전분의 다각적 이용을 위하여 고순도의 멥쌀전분과 찹쌀전분을 Alkali 침지법에 의해 제조하여 각각 드럼 건조기와 압출성형기로 변성전분을 제조한 후 특성을 검토하였다. 청값은 찹쌀전분이 가장 낮았으며 변성 후 L값이 감소하였다. 수분용해지수는 압출성형기로 제조한 변성전분들이 높은 값을 나타내었으며 수분흡수지수는 드럼건조기로 제조한 변성전분들이 높았다. Cold-Water-Solubility는 측정에서는 드럼건조기를 이용한 멥쌀변성전분이 가장 높았다. 각 시료들의 광투과도는 온도 증가에 따라 일정한 양상을 보이지 않았다. 드럼건조기로 제조한 멥쌀변성전분은 전단속도의 증가에 따라 점조성지수가 급격히 증가하였으며 항복응력도 가장 높은 값을 나타내었다. Gel Permeation Chromatography에 의하면 전분을 변성시킴에 따라 분자길이의 절단과 아밀로오스 분해가 일어남을 알 수 있었으며 X-선 간섭도형측정(XRI)에 의한 간섭도형은 피크를 상실한 V도형의 X-선 회절양상을 보임으로서 결정구조가 무정형으로 변화 된 것을 알 수 있었다.

• 한국식품영양학회지
• /
• 제20권4호
• /
• pp.349-355
• /
• 2007

Periodate-oxidized soluble starch was reacted with papain at pH 4.0, pH 7.0, and pH 9.7, and an oxidized soluble starch-papain conjugate was produced. When compared with native papain, the specific activity decreased to 60%, in both the modified papain reacted with 0.4% $NaBH_4$ and in the modified papain not reacted with $NaBH_4$. The specific activity decreased to 70% in the modified papains reacted with 1.5% $NaBH_4$ and 4.0% $NaBH_4$, respectively. The reduction by $NaBH_4$ did not have an effect in the thermal stability of either the modified or nonmodified papain. An activity of 54.7% remained in the papain modified at pH 4.0, which was incubated at $80^{\circ}C$ for 40 min. The papains modified at pH 7.0 and pH 9.7 and incubated for 40 min at two different temperatures, respectively, were stable to $60^{\circ}C$, and at $80^{\circ}C$ their activities at 56.3% and 44.1 %, respectively. The modified papain's thermal stability pattern was similar to that of native papain, with no increase in its statbility. In the range of pH $2.0{\sim}13.0$, the stability of the papain modified at pH 4.0 decreased greatly between pH $3.0{\sim}5.0$, but it was similar to the native papain at other pH values. The stability of the papain modified at pH 7.0 showed a similar pattern to the native papain at pH $2.0{\sim}6.0$, while its stability increased when moving into the alkali pH range. The papain modified at pH 9.7 also had increased stability, when moving into the alkali range. The results of Hammerstein milk casein, which was reacted with the papains modified at pH 4.0, pH 7.0, and pH 9.7, respectively, and analyzed by FPLC, showed different peaks according to the different modification pHs, and the greatest peak differences were observed with the modification at pH 9.7.

• Applied Biological Chemistry
• /
• 제12권
• /
• pp.75-81
• /
• 1969

세균성(細菌性) Sericinase를 생사(生絲)의 정련(精練)과 고치 해서(解舒)에 이용(利用)하고자 유용균(有用菌)을 분리(分離) 선별(選別)하였으며 이 균(菌)이 생성(生成)하는 Sericinase 의 여러 효소학적(酵素學的) 성질(性質)을 조사(調査)하여 생사정련(生絲精練)에 적용(適用)한 결과(結果)를 타정련법(他精練法)과 비교검토(比較檢討)하였다. 1. 생사정련작용(生絲精練作用)과 견제교작용(繭除膠作用)이 강(强)하며 견(絹) Fibroin에 대(對)해서는 전연(全然) 작용(作用)하지 아니하는 Sericinase를 생성(生成)하는 세균(細菌) 일주(一走)를 분리(分離) 선별(選別)하였다. 2. 본(本)균주(菌株)에 의(依)해 생성(生成)된 Sericinasedml 최적작용(最適作用) pH는 7.5에 위치(位置)하였으며 최적작용(最適作用) 온도는 $50^{\circ}C$였다. 이 온도(溫度)에서는 견섬유(絹纖維)의 modification 등(等)은 일어나지 않을 것으로 믿어지며 3. 본(本) 효소(酵素)는 free incubation에 있어서는 $Ca^{++}$이 효소실활(酵素失活)을 촉진(促進)하며 기질(基質)에 사용(使用)할 때는 Ca-oxalate 일 경우(境遇) 효소작용(酵素作用)을 촉진(促進)하므로 작잠등(?蠶等)으 해서(解舒)에 유용(有用)할 것으로 믿어지며 4. 본(本) 효소(酵素)는 견사(絹絲) 중(中)의 Sericin을 거의 완전(完全)하게 분해(分解)하는 것으로 믿어지며 5. 본(本) 효소(酵素)를 사용(使用)하여 졍련(精練)한 견(絹)을 조사(調査)한 바그 생사표면(生絲表面)의 상태(狀態), Fibroin의 손상(損傷), 촉감(觸感), 정련효과(精練效果) 등(等)이 타(他) 정련법(精練法) 즉(卽) 석감법, Alkali법(法), Alkali 석(石) 감법보다 우수(優秀)하였으며, 고급정련볍(高級精練法)에만 이용(利用)하는 papain이나 pancreatin과 같은 효과(效果)를 얻을 수 있으리라 기대(期待)된다.

• Bulletin of the Korean Chemical Society
• /
• 제35권5호
• /
• pp.1506-1510
• /
• 2014

A kinetic study on nucleophilic substitution reaction of 5-nitro-8-quinolyl picolinate (6) with alkali-metal ethoxides (EtOM; M = K, Na, and Li) in anhydrous ethanol is reported. The plot of $k_{obsd}$ vs. [EtOM] curves upward in the absence of crown ethers but is linear with significantly decreased reactivity in the presence of crown ethers. Dissection of $k_{obsd}$ into $k_{EtO}$- and $k_{EtOM}$ (i.e., the second-order rate constants for the reactions with the dissociated $EtO^-$ and ion-paired EtOM, respectively) has revealed that the ion-paired EtOM is significantly more reactive than the dissociated $EtO^-$ (e.g., $k_{EtOM}/k_{EtO^-}$ = 33.4-141). This indicates that the reaction of 6 is catalyzed by $M^+$ ions in the order $Na^+$ > $Li^+$ > $K^+$ and the catalytic effect disappears in the presence of a proper crown ether. Picolinate ester 6 is much more reactive and is more strongly catalyzed by $M^+$ ions than 5-nitro-8-quinolyl benzoate (5). It has been concluded that $M^+$ ions catalyze the reaction of 6 by increasing electrophilicity of the reaction center through a cyclic transition state, which is structurally not possible for the reaction of 5.

• 한국염색가공학회지
• /
• 제19권2호
• /
• pp.14-23
• /
• 2007

This research article explores the use of phthalocyanine reactive dye on nylon substrate. The effect of factors such as pH, temperature, liquor ratio and alkali addition on level of dye exhaustion, fixation and total fixation efficiency. Low pH, high temperature and low liquor ratio were found to be suitable conditions for maximum % exhaustion values. The effect of sulphatoethylsulphone(SES) and vinylsulphone(VS) form of the dyes on level of dye fixation was also discussed. The optimized exhaustion (%E), fixation(%F) and total fixation efficiency were determined. Modification of the dyeing process with alkali addition displayed that dye fixation(%) increased by alkali addition. Vinylsulphone(VS) moiety of the dye was found to be superior to. maximum fixation (%F). Appropriate predictable empirical models, relatively a new approach in dyeing processes, were developed incorporating interactions effects of temperature, pH and liquor ratio for predicting % exhaustion, fixation and total fixation efficiency. The significance of the mathematical model developed was ascertained using microsoft excel regression(solver) analysis module. High correlation coefficient was obtained (R2=0.9895 for % exhaustion, R2=0.9932 for fixation, R2=0.9965 for total fixation efficiency) for the model which shows prominent prediction capacity of the model for my conditions. The predictable polynomial equations developed from tile experimental results were thoroughly analyzed by ANOVA (Analysis of Variance) statistical concepts.

• 한국식품영양학회지
• /
• 제3권2호
• /
• pp.123-132
• /
• 1990

Sweet potato $\beta$-amylase is a tetrameric enzyme consisting of four identical polypeptide chains with a molecular weight of 5.6$\times$104, though most of the other $\beta$-amylases are monomeric enzymes. But, the relationship between subunit structure and catalytic function of the enzyme is not known. This study was done to know what the function of the subunit structure of the enzyme is. We obtained the monomer from the enzyme by the treatment of SDS, alkali pH buffer and urea. But the monomer had not activity. We tried to prepare the active monomer from the enzyme by the modification with periodate-oxidized soluble starch , In the result, we succeeded in isolating an active monomer as an oxidized soluble starch-conjugated form The active monomer had 57% of the original activity, 13.2% of the sugar and the molecular weight was estimated to be 5.4$\times$104. This results suggest that the tetrameric form of the enzyme is a most stable one and exists in nature, and the subunit structure of the enzyme Plays an important role in stabilization but not catalytic function.

• Advanced Composite Materials
• /
• 제17권1호
• /
• pp.89-99
• /
• 2008

Using a Dynamic Mechanical Analyzer (DMA), mechanical properties like modulus and phase transition temperature of polyester composites of banana fibers (treated and untreated) are measured simultaneously. The shifting of phase transition temperature is observed in some treatments. The performance of the composite depends to a large extent on the adhesion between polymer matrix and the reinforcement. This is often achieved by surface modification of the matrix or the filler. Banana fiber was modified chemically to achieve improved interfacial interaction between the fiber and the polyester matrix. Various silanes and alkalies were used to modify the fiber surface. Chemical modification was found to have a profound effect on the fiber/matrix interaction, which is evident from the values of phase transition temperatures. Of the various chemical treatments, simple alkali treatment with 1% NaOH was found to be the most effective.

• International Journal of Concrete Structures and Materials
• /
• 제3권2호
• /
• pp.97-101
• /
• 2009

It has been known that acid-resistant concretes on the liquid glass basis have high porosity (up to 18${\sim}$20%), low strength and insufficient water resistance. Therefore they can not be used as materials for load-bearing structural elements. Significant increasing of silicate matrix strength and density was carried out by incorporation of special liquid organic alkali-soluble silicate additives, which block of superficial pores and reduces concrete shrinkage deformation. It was demonstrated that introduction of tetrafurfuryloxisilane additive sharply increases strength, durability and shock resistance of silicate polymer concrete in aggressive media. This effect is attributable to hardening of contacts between silicate binder gel globes and modification of alkaline component owing to "inoculation" of the furan radical. The optimal concrete composition with the increased strength, chemical resistance in the aggressive environments, density and crack resistance was obtained.

• Macromolecular Research
• /
• 제13권3호
• /
• pp.229-235
• /
• 2005

Various alkoxyamine initiators for nitroxide mediated radical polymerization (NMRP) were prepared in high yields by a simple substitution reaction of nitroxide anions with benzyl bromide. The required nitroxide anions were easily generated by treating either nitroxide free radicals or hydroxy amine with an alkali metal such as sodium or potassium in THF. This method is both practical and efficient, since the ionic conditions prevent other side reactions from occurring, such as the self-coupling or oligomerization reactions that are observed in the case of radical trapping conditions. To demonstrate the utility of the resulting alkoxyamine initiators, end- and telechelic-alkoxyamine PEG macroinitiators derived from the alkoxyamines were synthesized by a simple chemical modification, and used for the preparation of PEG-b-PS and PS-b-PEG-b-PS block copolymers by NMRP.

• Bulletin of the Korean Chemical Society
• /
• 제33권2호
• /
• pp.519-523
• /
• 2012

A kinetic study is reported on nucleophilic displacement reactions of benzyl 2-pyridyl carbonate 6 with alkalimetal ethoxides, EtOM (M = Li, Na, and K), in anhydrous ethanol at $25.0{\pm}0.1^{\circ}C$. The plots of pseudo-firstorder rate constant $k_{obsd}$ vs. [EtOM] curve upward, a typical phenomenon reported previously for alkaline ethanolysis of esters in which alkali-metal ions behave as a Lewis-acid catalyst. The kobsd value for the reaction of 6 with a fixed EtOK concentration decreases rapidly upon addition of 18-crown-6-ether (18C6), a complexing agent for $K^+$ ion up to [18C6]/[EtOK] = 1.0 and then remains constant thereafter, indicating that the catalytic effect exerted by K+ ion disappears in the presence of excess 18C6. The reactivity of EtOM towards 6 increases in the order $EtO^-$ < EtOLi < EtONa < EtOK, which is contrasting to the reactivity order reported for the corresponding reactions of 2-pyridyl benzoate 4, i.e., $EtO^-$ < EtOK < EtONa < EtOLi. Besides, 6 is 1.7 and 3.5 times more reactive than 4 towards dissociated $EtO^-$ and ion-paired EtOK, respectively. The reactivity difference and the contrasting metal-ion selectivity are discussed in terms of electronic effects and transition-state structures.