• 폴리머
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• 제27권3호
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• pp.195-200
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• 2003

알지네이트는 곁사슬에 강한 음이온을 가지고 있어 전기장 하에서 구동 특성을 발현할 수 있다. 본 연구에서는 가교제로 CaCl$_2$를 사용하여 가교 알지네이트 필름을 제조하였고, 제조된 필름의 열적 특성, 기계적 특성 및 전기적 구동 특성을 열중량 분석, 인장 강도 실험 및 전기응답 실험을 통하여 조사하였다. 가교제의 농도가 증가함에 따라 필름의 초기 분해 온도와 인장 강도가 증가하였다. 또한 팽윤비는 사슬 내 자유부피와 정전기적 반발력에 기인하여 가교제 농도의 감소와 pH가 증가함에 따라 증가하였다. 저기 자극에 의하여 알지네이트 필름은 유연한 물리적 거동을 발현하였다. 전기장에서 전압, 이온 강도 및 저해질 용액의 종류에 따라서 필름의 응답 속도 띤 거동에 영향을 주었다. 가교제의 농도가 5 wt%일 때 가장 좋은 굽힘 거동과 반복 회복성을 보였으며, NaCl과 KCl 전해질 용액의 이온 강도가 0.1 M일 때 가장 높은 전기 반응성을 나타냈다. 또한 전압이 증가됨에 따라 전하의 이동이 활발해지고 따라서 굽힘 거동이 증가하였다.

• 폴리머
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• 제31권4호
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• pp.315-321
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• 2007

본 연구에서는 방사선 중합방법으로 아민화 PONF-g-GMA 이온교환 섬유를 합성하였다. 또한 핫멜트 web spray 접착방식으로 이들과 비드 수지를 결합시켜 복합 이온교환 섬유를 제조하고 이들의 바나듐 흡착특성을 확인하였다. 복합 이온교환 섬유의 이온교환 용량은 비드보다는 낮았으며, 단일 이온교환 섬유보다는 높게 나타났으며 최대 4.18 meq/g로 나타났다. 또한, 복합 이온교환 섬유의 바나듐 흡착 파과평형은 550분으로 비드 이온교환 수지보다 빠르게 진행되었고, 섬유상 이온교환체보다는 느리게 진행되었다. 한편, 바나듐의 흡착파과 시간은 pH가 낮아짐에 따라 파과가 빠르게 진행되었으며, 바나듐 농도가 증가함에 따라 흡착 평형에 도달하는 시간은 400분 전후에서 나타났다.

• 폴리머
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• 제31권4호
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• pp.322-328
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• 2007

촉매인 potassium(K)을 2회 분할 투입하는 음이온 개환중합반응으로 ${\varepsilon}-caprolactam$을 분산매인 liquid paraffin 내에서 분간 중합하여 $4{\sim}7\;{\mu}m$의 직경을 가지는 단분산된 구형의 polyamide 6 (Nylon 6) micro-particle를 제조하였다. 융착 방지제의 농도, 촉매의 양, 개시제의 양에 따라 생성된 입자 크기, 형태, 그리고 분포의 변화를 비교 분석하였다. 그 결과 개시제인 $PCl_3$의 양이 단량체의 $0.97{\sim}1.17\;wt%$일 때 약 90.6%의 수율을 얻었으며, 또한 촉매를 $1.3{\sim}1.4\;wt%$ 정도로 투입하였을 경우 가장 안정된 구형의 미세입자가 제조되고 높은 수율이 얻어짐을 알 수 있었다.

• 한국염색가공학회지
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• 제6권2호
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• pp.10-16
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• 1994

Neutral salts have negative or positive effects on the rates of many chemical reactions and also on the rates of acidic and alkaline hydrolysis of carboxylic esters. The direction of neutral salt effects on the hydrolysis of ester depends on the charge of esters. Neutral salts accelerate alkaline hydrolysis of esters with negative charge, but decelerate alkaline hydrolysis of esters with positive charge, and have little effect on the alkaline hydrolysis of neutral esters. It is expected that the rate of the alkaline hydrolysis of Poly(ethylene terephthalte) (PET), polymeric solid carboxylic polyester with carboxyl end group at the polymer end, is also influenced positively by neutral salts. In the present work, to clarify the mechanism of the neutral salt effect on the alkaline hydrolysis of PET, many salts with different anions like NaF, NACl, NaBr, NaI were added to the aqueous alkaline solutions. Then PET was hydrolyzed with aqueous solutions of many salts in alkali metal hydroxides under various conditions. Some conclusions obtained from the experimental results were summarized as follows. The reaction rate of the alkaline hydrolysis of PET was increased by the addition of neutral salts and In k was increased nearly linearly with the square root of ionic strength of reaction medium. This fact suggested that the ionic strength effect by Debye-Huckel and Bronsted theory was exerted on the reaction. The specific salt effect was also observed. The reaction rate was increased with the decrease in the nucleophilicity of anions of neutral salts, i.e., in the order of $F^-$ <$Cl^-$<$Br^-$<$I^-$. It was thought that the reaction rate was increased in the order of $F^-$ <$Cl^-$<$Br^-$<$I^-$. because the completion of anions with $OH^-$ for carbonyl carbon became weaker with the decrease in the nucleophilicity and with the increase in the size of anions.

• 한국광물학회지
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• 제16권1호
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• pp.107-123
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• 2003

본 연구는 0가 철 (ZVI)의 설치위치와 전극의 배열에 따른 다양한 조합의 전기적 투수성 반응벽을 대상으로 트리클로로에틸렌의 탈염소화 반응에 의한 정화시 ZVI의 부식에 기인하는 광물상침전물에 대해 알아보고, 이에 대한 조절 요소를 알아보고자 한다. 광물학적 연구 결과, 지하수 유입부의 ZVI 시료는 상대적으로 많은 레피도크로사이트, 훼리하이드라이트 혹은 철 수산화물과 (phospho)siderite가 산출되는 반면, 용출부의 ZVI 시료는 아카가나이트, 자철석/마그헤마이트, 그리고 중간 산물인 green rust (CR) I 과 CR II가 산출되었다. 이러한 광물 조합의 변화는 용존 산소 및 pH의 상승에 주로 기인한 것으로 나타났다. 또한 전기적 투수성 반응벽 내에 산출되는 광물상 침전물들의 조절 요소들은 (1) pH, (2) 용존산소, (3) 철의 부식시 중간 산물, (4) 음이온 종류 등으로 밝혀졌다.

• BMB Reports
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• 제41권3호
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• pp.259-265
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• 2008

Three peroxidase (POD) cDNAs were isolated from dehydration-treated fibrous roots of sweetpotato (Ipomoea batatas) plant via the screening of a cDNA library, and their expressions were assessed to characterize functions of each POD in relation to environmental stress. Three PODs were divided into two groups, designated the basic PODs (swpb4, swpb5) and the anionic PODs (swpa7), on the basis of the pI values of mature proteins. Fluorescence microscope analysis indicated that three PODs are secreted into the extracellular space. RT-PCR analysis revealed that POD genes have diverse expression patterns in a variety of plant tissues. Swpb4 was abundantly expressed in stem tissues, whereas the expression levels of swpb5 and swpa7 transcripts were high in fibrous and thick pigmented roots. Swpb4 and swpa7 showed abundant expression levels in suspension cultured cells. Three POD genes responded differently in the leaf and fibrous roots in response to a variety of stresses including dehydration, temperature stress, stress-associated chemicals, and pathogenic bacteria.

• Journal of Pharmaceutical Investigation
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• 제22권4호
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• pp.289-300
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• 1992

The counter-transport phenomena in the hepatic transport of 1-anilino-8-naphthalene sulfonate (ANS) were kinetically investigated by analyzing the plasma disappearance-time profiles and the transport into the isolated hepatocytes. In vivo "counter transport phenomena" were simulated based on the perfusion model which incorporated the carrier-mediated transport and the saturable intracellular binding. The condition that the mobility of carrier-ligand complex is greater than that of free carrier is not essential for the occurrence of counter-transport phenomenon. To examine the inhibitory effects on the initial uptake of a ligand by the liver, it is necessary to judge whether the true counter-transport mechanism (trans-stimulation) is working or not. The initial plasma disappearance curves of ANS were then kinetically analyzed based on a two-compartment model, in which the ligand is eliminated only from the peripheral compartment (liver compartment). No effects on the initial plasma disappearance rates of ANS were observed after preloading of bromophenol blue (BPB) or rose bengal (RB) in the liver. Inhibitory effect of BPB or RB on the initial uptake (or efflux) rates of ANS by the isolated hepatocytes were not observed, suggesting that the true counter transport mechanism is not working. In conclusion, checking the preloading effects of transstimulation on the initial uptake of a ligand by the liver could be a useful criterion for carrier cycling and common use of the same carrier between two ligands. However, one cannot exclude those possibilities even if the preloading effects cannot be observed.

• 폴리머
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• 제34권2호
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• pp.89-96
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• 2010

Methyl methacrylate(MMA), ethyl acrylate(EA), n-butyl acrylate(BA), styrene(St) 단량체를 수용성 개시제인 ammonium persulfate(APS)와 음이온 유화제인 sodium dodecyl benzene sulfonate(SDBS)를 사용하여 organic/organic core-shell 구조의 접착바인더를 중합 후 부직포와 피혁에 함침시키고 플라즈마 표면 처리 후 속도론적인 해석과 기계적인 물성을 평가하였다. Core-shell 바인더 중합시 전환율은 단량체의 조성이 등몰에서 MMA/EA, MMA/BA core-shell 복합입자 모두 90% 이상이 되었다. 등몰에서 부직포/부직포에 core-shell 복합입자를 함침시키고 플라즈마 처리 후의 상태접착 박리강도는 MMA/St, EA/BA, BA/MMA, EA/St, EA/MMA의 순으로 되었고, 또한 부직포/피혁에 core-shell 복합입자를 함침시키고 플라즈마 처리 후의 상태접착 박리강도는 MMA/BA, BA/EA, MMA/EA, St/MMA, EA/St의 순으로 되었다.

• 한국식품영양학회:학술대회논문집
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• 한국식품영양학회 2001년도 동계 학술심포지움
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• pp.126-126
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• 2001

The Rhus verniciflua contains alkly(en)-catechol type allergens with a saiurated or unsaturated alkly chain of 15 or 17 carbon atoms. It has been recognized as an extremely active allergen causing skin reactions similar In poison ivy. The allergic contact dermatitis induced by the urushiol is known to be mediated be T lymphocytes whicht specifically recognize the hepten urushiol. Therefore. direct use of this plant as a medicinal purpose might imply a considerable hazard in Korea. In this study, using the established method for the detoxification from the stem bark of Rhus verniciflua, an strong antioxidant substance was isolated and characterized DPPH (diphenypricryl hydrazyl) assay measures hydrogen atom-donating activity and hence provides a measure of free radical scavenging antioxidant activity. DPPH, a purple-colored stable free radical, is reduced to yellow-colored diphenylpicryl hydrazine by antioxidants to deducing agents. Antioxidative effects of the water extract from RV were measured by DPPH assay. Twenty microliters of the extract was added to 1ml of 100mM DPPH solution in ethanol The mixture was shaken and left to stand for 10min at room temperature. The crude water extracts was purified by using HPLC method with a DEAE (anionic type), CN, ODS column. The purified compound remained stable at pH 3.0-6,0, but unstable above pH 6.5. It was stable heat at 10$0^{\circ}C$ for 4 hours, but still had about 80% of residual activity after treatment at 10$0^{\circ}C$ for 5 hours. The elemental composition of the HR-EI mass spectrum at m/z 170.02 was estimated the empirical formula as $C_{7}$ $H_{6}$ $O_{5}$. $C_{10}$ $H_4$ $O_2$N$_1$, $C_{5}$ $H_4$ $O_4$N$_3$, $C_{8}$$H_2O$$_1$N$_4$. In antimicrobial test, no inhibition was observed against Gram-positive and negative bacteria. This compound was stronger than that of commercial antioxidant by DPPH test, such as BHT, BHC at the same concentration (20$\mu$g/ml).ml).

• Korea-Australia Rheology Journal
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• 제14권4호
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• pp.189-201
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• 2002

The interaction between hydrophobically modified hydroxyethyl cellulose (hmHEC), containing approximately 1 wt% side-alkyl chains of $C_{16}$, and an anionic sodium dodecyl sulphate (SDS) surfactant was investigated. For a semi-dilute solution of 0.5 wt% hmHEC, the previously observed behaviour of a maximum in solution viscosity at intermediate SDS concentrations, followed by a drop at higher SDS concentrations, until above the cmc of surfactant when the solution resembles that of the unsubstituted polymer, was confirmed. Additionally, a two-phase region containing a hydrogel phase and a water-like supernatant was found at low SDS concentrations up to 0.2 wt%, a concentration which is akin to the critical association concentration, cac, of SDS in the presence of hmHEC. Above this concentration, SDS molecules bind strongly to form mixed micellar aggregates with the polymer alkyl side-chains, thus strengthening the network junctions, resulting in the observed increase in viscosity and elastic modulus of the solution. The shear behaviour of this polymer-surfactant complex during steady and step stress experiments was examined In great detail. Between SDS concentrations of 0.2 and 0.25 wt%, the shear viscosity of the hmHEC-polymer complex network undergoes shear-induced thickening, followed by a two-stage shear-induced fracture or break-up of the network. The thickening is thought to be due to structural rearrangement, causing the network of flexible polymers to expand, enabling some polymer hydrophobic groups to be converted from intra- to inter-chain associations. At higher applied stress, a partial local break-up of the network occurs, while at even higher stress, above the critical or network yield stress, a complete fracture of the network into small microgel-like units, Is believed to occur. This second network rupture is progressive with time of shear and no steady state in viscosity was observed even after 300 s. The structure which was reformed after the cessation of shear is found to be significantly different from the original state.