• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2011년도 제45차 학술발표회
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• pp.63-63
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• 2011

통상적으로 코팅가공시 수지의 흐름성을 개선하기 위해서 코팅수지(점도 : 50,000~60,000 Cps)의 점도를 10,000 Cps 이하로 낮추어서 작업을 진행한다. 이때 MEK(Methyl Ethyl Ketone), TOL(Toluene), DMF(Dimethyl Formamide) 등과 같은 유기용제를 사용하여 점도를 조절한다. 본 연구는 기존에 표면처리 코팅용 수지 배합시 유기용제를 사용하는 대신 물을 사용하여 점도 조절이 가능한 표면처리 코팅용 hydrophilic PU 수지를 연구하였다. Prepolymer 법으로 합성한 수지가 One-shot법으로 합성한 수지보다 water dilution 안정성이 우수하며, 친수성 polyol과 소수성 polyol의 비율이 6/4정도가 될 때 water dilution된 수지의 안전성, 투습도 등의 물성이 가장 이상적으로 발현 되는 것을 확인 할수 있었고, 50part의 물과 희석 후 5일 이후에도 상분리가 되지 않음을 확인 할 수 있었다. 개발된 수지의 적용성을 평가한 결과, J-knife를 이용하여 knife over roll 방식으로 $200{\mu}m$의 gap으로 80/120/$140^{\circ}C{\times}10m/min.$의 다단건조 공정으로 진행했을 때 최적의 물성을 얻을 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제21권7호
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• pp.685-689
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• 2000

The complexation reaction between Pb2+,TI and Cd2+ions and macrocyclic ligands, 18-crown-6 ( 18C6) and dibenzo- 18-crown-6 (DB 18C6), was studied in dimethylsulfoxide (DMSO)-nitromethane (NM) and dimethyl-formamide (DMF)-nitromethane binary system s by square wave polarography (SWP) technique. The stoichiometry and stability of the complexes were determined by monitoring the shifts in half-waves or peak potentials of the polarographic waves of metal ions against the Iigand concentration. In most cases, the stability constants of complexes increase with increasing amounts of the nitromethane in mixed binary solvents used in this study. The complexes formed between 18C6 and DB18C6 and these metal cations in all cases had a stoichiometry of 1 : 1. The results obtained show that there is an inverse relationship between the formation constant of complexes and the donor number of solvents based on a Gatmann donocity scale and the stability constants show a high sensitivity to the composition of the mixed solvent systems. A linear behavior was observed for variation of log Kf of I8C6 complexes vs the composition of the mixed solvent systems in NM/DMSO and NM/DMF,but a non-linear behavior was observed in the case of DB 18C6 complexes in these binary systems. In most of the systems investigated, the Pb2+ cation forms a more stable complex with the 18C6 than other two cations and the order of selectivity of this Iigand for cations is: Pb2+ > TI+,Cd2+.

• 대한안전경영과학회지
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• 제2권2호
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• pp.95-108
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• 2000

Electrochemical charateristics of activated carbon fiber cloth(ACFC) electrode were studied with propylene carbonate(PC), ${\gamma}$-butyrolactone(GBL) and N,N-dimethyl-formamide(DMF) as a solvent and tetraethylammoniumtetrafluoroborate(TEABF$_4$), tetraethylammoniumhexafluorophosphate(TEABF$_{6}$), tetrabutylammoniumtetrafluoroborate(TBABF$_4$) and tetrabutylammonium hexafluorophosphate(TBAPF$_6$) as an electrolytes(active material). The concentrations of electrolytes were in the range of 0.2~1.2 N, the volume ratios of PC and DMF as a mixed solvent system, were 90：10, 80：20, 70：30, 60：40, 50：50, and 40：60 vol%. Electrochemical characteristics such as electric conductivity, internal resistance, and electric capacitance of fabricated unit cells were measured after the moisture of activated material was removed with molecular sieve. Electrochemical characteristics were better in mixed solvents system than in mono solvent system. The mono solvent system of 1.0 N electrolyte of GBL/TEABF$_4$ with activated carbon cloth electrodes showed better result but the mixed solvent system with PC and DMF/TEABF$_4$(50：50 vol%) and the concentration of 1.0 N electrolyte showed the best characteristics. Internal resistance was 3.47 $\Omega$ and specific capacitance was 19.1 F/g respectively.y.

• Bulletin of the Korean Chemical Society
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• 제24권6호
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• pp.817-823
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• 2003

We have performed ab initio calculation on the active site of HIV-1 protease. The FEP method was used to determine the binding free energy of four different of protonated states of HIV-1 protease with inhibitor. The structure of the active site and hole structure was taken from the X-ray crystallographic coordinates of the C₂ symmetric inhibitor A74704 protease bound. The active site was modeled with the fragment molecules of binding pocket, acetic acid/ acetate anion (Asp25, Asp125), formamide (amide bond of Thr26/Gly27, Thr126/ Gly127), and methanol as inhibitor fragment. All possibly protonated states of the active site were considered, which were diprotonated state (0, 0), monoprotonated (-1, 0),(0, -1) and diunprotonated state (-1, -1). Once the binding energy Debind, of each model was calculated, more probabilistic protonated states can be proposed from binding energy. From ab-initio results, the FEP simulations were performed for the three following mutations: Ⅰ) Asp25 … Asp125 → AspH25 … Asp125, ⅱ) Asp25 … Asp125 → Asp25 … AspH125, ⅲ) AspH25 … Asp125 → AspH25 … AspH125. The free energy difference between the four states gives the information of the more realistic protonated state of active site aspartic acid. These results provide a theoretical prediction of the protonation state of the catalytic aspartic residues for A74707 complex, and may be useful for the evaluation of potential therapeutic targets.

• 멤브레인
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• 제20권1호
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• pp.76-86
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• 2010

본 연구에서는 비용매 첨가제 BE와 습도 및 노출 시간이 정밀여과막의 구조, 투과특성에 미치는 영향을 살펴보았다. 멤브레인은 PES/DMF/TSA/PVP/BE 혼합 용액을 물에 침지하여 제조하였다. 다양한 농도의 BE가 첨가된 캐스팅 용액들을 공기 중의 수분이 흡착될 수 있도록 상대습도 60%와 80%로 달리하여 40초와 90초 동안 노출시켰으며, 그 결과로 만들어진 멤브레인 투과 성능과 표변 및 단면 구조와의 연관성을 조사하였다. 멤브레인의 특성은 capillary flow porometer, FE-SEM 및 순수 투과 장치를 이용하여 이루어졌다. PES 멤브레인의 표면 구조는 상대 및 노출 시간에 의해 크게 영향을 받는다. 또한 BE의 첨가는 특정한 습도와 노출 시간에서 표면 및 내부의 구조의 조절이 용이함을 확인할 수 있었다.

• 한국전기전자재료학회논문지
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• 제30권12호
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• pp.822-827
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• 2017

Mg/Al layered double hydroxide with two-dimensional (2D) nanostructures was synthesized by a hydrothermal technique. The morphology and aspect ratio of $Mg_4Al_2(OH)_{14}3H_2O$ were controlled by the concentration and kinds of the hydrolysis agent, and temperature. The aspect ratio of $Mg_4Al_2(OH)_{14}3H_2O$ layered double hydroxides with the 2D hexagonal crystal structure was tailored from about 12.6 to about 45.7. The intercalated $CO{_3}^{2-}$ anions of the synthesized 2D $Mg_4Al_2(OH)_{14}3H_2O$ layered double hydroxides were exchanged to $NO_3{^-}$ anions. The bulk 2D $Mg_4Al_2(OH)_{14}3H_2O$ layered double hydroxides with the increased space between two layers due to the anion exchange were exfoliated in a formamide solution. The aspect ratio of the exfoliated 2D $Mg_4Al_2(OH)_{14}3H_2O$ layered double hydroxides increased to 570.3.

• 전기화학회지
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• 제11권4호
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• pp.304-308
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• 2008

Noble Poly (lithium 2-acrylamido-2-methyl propane sulfonate) and its copolymer with N-vinyl formamide based on trihexyl (tetradecyl) phosphonium acetate [$(C_6H_{13})_3$ P ($C_{14}H_{29}$) $CH_3COO$; $P_{66614}$ $CH_3COO$] and trihexyl (tetradecyl)phosphonium bis(trifluoromethane sulfonyl) amide ([$(C_6H_{13})_3P(C_{14}H_{29})$] [TFSA];$P_{66614}TFSA$) were prepared and analyzed to determine their characteristics and properties. The ionic conductivity of a copolymer based $P_{66614}TFSA$ ionic liquid system exhibits a higher conductivity ($8.9{\times}10^{-5}Scm^{-1}$) than that of a copolymer based $P_{66614}CH_3COO$ system ($1.57{\times}10^{-5}Scm^{-1})$. The charge on the TFSA anion is spread very diffusely through the S-N-S core and particularly in the trifluoromethane groups, and this diffusion results in a decreased interaction between the cation and the anion. The viscosity of $P_{66614}TFSA$ (39 cP at 343 K) and $P_{66614}CH_3COO$ (124 cP at 343 K), which is very hydrophobic, was fairly high. High viscosity leads to a slow rate of diffusion of redox species. The ionic conductivity of copolymer of a phosphonium ionic liquid system also exhibits higher conductivity than that of a homopolymer system. Phosphonium ionic liquids were thermally stable at temperatures up to $400^{\circ}C$.

• Applied Biological Chemistry
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• 제25권3호
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• pp.177-181
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• 1982

Dicofol의 각종(各種) 유기용매(有機溶媒)에 대(對)한 안정성(安定性)을 조사(調査)하기 위하여 $-5^{\circ}C$에서 7일간(日間) 방치(放置)하여 그 침전생성유무(沈澱搬成有無)를 조사(調査)하고, $50^{\circ}C$에서 56일간(日間) 처리(處理)한 다음 각종용매(各種溶媒)에 대(對)해서 Dicofol의 분해형태(分解形態)를 T.L.C.로 확인(確認)하였으며, 그 주성분(主成分) 분해율(分解率)을 2주(週)간격으로 gas chromatography로 측정(測定)하였다. 그 결과(結果) Dicofol 수화제(水和劑)와 N.N-dimethylformamide 및 cyclohexanone용액(溶液)에서는 Dicofol의 주성분(主成分) 분해율(分解率)이 각각(各各) 1.2%, 6.7%, 13.3%이었으나 xylene, toluene, M.I.B.K. 및 isophorone용액(溶液)에서는 거의 주성분(主成分) 분해(分解)가 일어나지 않았다. 그러나 $-5^{\circ}C$에서 7일간(日間) 방치(放置)하였을 때 isophorone 을 제외(除外)한 xylene, toluene 및 M.I.B.K. 용액(溶液)에서는 침전(沈澱)이 생성(生成)되어 Dicofol의 용제(溶劑)로서는 적합하지 못하였다. 이러한 사실(事實)로 미루어 볼 때 공시(供試)된 각종(各種) 유기용매중(有機溶媒中)에서 Dicofol의 제제상(製劑上) 가장 적합한 용매(溶媒)는 isophorone임을 알았다.

• 한국산학기술학회논문지
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• 제10권6호
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• pp.1287-1291
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• 2009

시안화물을 포름아미드로 변환시키는 nitrilase의 일종인 시안 수화효소 (cyanide hydratase, CHT) 를 진균류인 Neurospora crassa 와 Aspergillus nidulans로부터 유전자 조작을 통하여 His에 태그 또는 언태그된 형태로 대장균에 형질변환시켜 발현하였다. 발현된 효소를 고정 metal affinity chromatography로 정제하였다. 정제된 효소들의 pH 안정성, 동력학적 매개변수의 값을 검토하였다. 실험 결과 N. crassa 의 CHT가 50% 정도 더 넓은 pH 안정 범위를 가졌고 3배 가량 turnover rate도 높았다. 반면 A. nidulans CHT의 Km 값 (효소포화 용량)이 N. crassa CHT보다 더 크게 나타났다. 두 진균류에서 CHT의 유도발현은 질소성분과 상관없이 KCN에 의해 가능하였으며, 생분해 실험결과 N. crassa CHT에 의해 최대 82%/h의 시안분해가 가능하였다.

• 대한치과보철학회지
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• 제45권6호
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• pp.795-804
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• 2007

Statement of problem. Nano-scale calcium-phosphate coating on the anodizing titanium surface using ion beam-assisted deposition (IBAD) has been recently introduced to improve the early osseointegration. However, not much is known about their surface characteristics that have influence on tissue-implant interaction. Purpose. This study was aimed to investigate microtopography, surface roughness, surface composition, and wettability of the titanium surface modified by the anodic oxidation and calcium phosphate coating using IBAD. Material and methods. Commercially pure titanium disks were used as substrates. The experiment was composed of four groups. Group MA surfaces represented machined surface. Group AN was anodized surface. Group CaP/AN was anodic oxidized and calcium phosphate coated surfaces. Group SLA surfaces were sandblasted and acid etched surfaces. The prepared titanium discs were examined as follows. The surface morphology of the discs was examined using SEM. The surface roughness was measured by a confocal laser scanning microscope. Phase components were analyzed using thin-film x-ray diffraction. Wettability analyses were performed by contact angle measurement with distilled water, formamide, bromonaphtalene and surface free energy calculation. Results. (1) The four groups showed specific microtopography respectively. Anodized and calcium phosphate coated specimens showed multiple micropores and tiny homogeneously distributed crystalline particles. (2) The order of surface roughness values were, from the lowest to the highest, machined group, anodized group, anodized and calcium phosphate deposited group, and sandblasted and acid etched group. (3) Anodized and calcium phosphate deposited group was found to have titanium and titanium anatase oxides and exhibited calcium phosphorous crystalline structures. (4) Surface wettability was increased in the order of calcium phosphate deposited group, machined group, anodized group, sandblasted and acid etched group. Conclusion. After ion beam-assisted deposition on anodized titanium, the microporous structure remained on the surface and many small calcium phosphorous crystals were formed on the porous surface. Nanoscale calcium phosphorous deposition induced roughness on the microporous surface but hydrophobicity was increased.