• 한국염색가공학회지
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• 제2권1호
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• pp.21-30
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• 1990

In order to obtain high dye uptake initially, polyethylene terephthalate (PET) filaments were dyed with C.I.Disperse Orange 3 and Red 1 in mixed solvents of tetrachloroethylene acidic solvent, ethyl alcohol and tetrachloroethylene basic solvent, DMF. The dyeing behavior in the mixed solvent of tetrachloroethylene and basic solvent, DMF, the initial uptake of disperse dyes increased rapidly. The shrinkage of PET increased when the solubility parameter values of PET fiber and mixed solvent approached graduately.

• Bulletin of the Korean Chemical Society
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• 제17권8호
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• pp.682-685
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• 1996

Photothermal properties depend on the characteristics of energy transfer processes in solution. In this study, a time-resolved single beam thermal lens experiment in various solvents is employed to investigate the energy coupling effects which govern the energy transfer processes. Interestingly, it is observed that the behaviour of the photothermal propagation in solution depends on the property of solution and the concentration of solute in a single beam thermal lens configuration. These characteristics lead us to consider the solute-solvent coupling effects as well as the solvent-solvent interactions.

• Bulletin of the Korean Chemical Society
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• 제16권4호
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• pp.326-331
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• 1995

Poly(enaryloxynitriles) containing Schiff bases were prepared from p-bis(1-chloro-2,2-dicyanovinyl)benzene (2) and various aromatic diols having Schiff base moiety by interfacial polymerization. The chemical structure of the polymers was confirmed through synthesis of their corresponding model compounds. All the polymers were soluble in polar aprotic solvents and their brittle films were cast from DMF solution. They showed a large exotherm around 340 ℃ attributable to the chemical change of dicyanovinyl group. Especially, curing of azomethine group was observed to occur at 390 ℃ by differential scanning calorimetry. According to the thermogravimetric analyses, they exhibited excellent thermal stability with 60-90% residual weight at 500 ℃ in nitrogen.

• Restorative Dentistry and Endodontics
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• 제31권4호
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• pp.290-299
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• 2006

본 연구에서는 상아질의 항복인장강도 (UTS)나 탄성계수 (E)와 같은 물리적 특성이 적용된 용매틀의 각각에 대한 Hoy의 수소결합 용해도 매개변수에 반비례한다는 가설을 설정하고 실험한 결과 가설이 입증되었으며 이를 토대로 다음과 같은 결론을 유도하여 보았다. 첫째는 탈회된 상아질의 인장 특성 및 물성이 가해진 극성 용매의 수소결합능에 밀접히 연관되어 있다는 것이며, 둘째는 낮은 수소결합능을 가진 용매는 교원섬유 층 내에서 새로운 펩타이드간 수소결합을 유도함으로써 탈회된 상아질의 인장력 및 탄성계수를 증가시킨다는 결과이다. 셋째로는 이러한 결과들을 토대로 높은 수소결합능을 가진 용매들은 새로운 펩타이드간 수소결합의 형성을 차단하여 탈회된 상아질의 구조적 특성을 유지시킬 수 있다는 결론을 도출하였다.

• Bulletin of the Korean Chemical Society
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• 제33권2호
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• pp.443-448
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• 2012

Ferrocenyl chalcones (Fc-C(O)CH=CH-Ar: Fc-Ar) with mono- and di-1-naphthalenyl moieties (Fc-1Naph and Fc-d1Naph) were prepared and spectroscopically characterized. The enone bridge was in the s-cis conformation and the $\pi$-electrons on the C=C bond were further delocalized on the bridge. The naphthalenyl moiety deviates greatly from the enone-Cp plane by $26.9(1)^{\circ}$. Cyclic voltammetry measurements for Fc-1Naph exhibit one reversible cycle for the redox of the ferrocenyl moiety at a lower potential, and one irreversible oxidation peak at the higher potential region. For Fc-d1Naph, the cyclic voltammogram is more featureless. Fluorescence properties for both compounds are active in polar solvents with $\lambda_{em}$ = 500 nm (EtOH) and $\lambda_{em}$ = 512 nm (MeOH) for Fc-1Naph and $\lambda_{em}$ = 496 nm (EtOH) and $\lambda_{em}$ = 508 nm (MeOH) for Fc-d1Naph. The intensity of Fc-d1Naph is more than twice than that of Fc-1Naph. The fluorescence properties for both compounds are inactive in the less polar solvents such as $CH_3CN$, $CH_2Cl_2$ and $CHCl_3$.

• 보존과학회지
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• 제28권3호
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• pp.229-233
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• 2012

본 연구에서는 상아 시편에 습식 세척과 약산을 통한 색상 회복 처리를 실시하고, 이에 대한 안정성 평가를 실시하였다. 사용된 상아 시편은 블랙라이트와 능형무늬 분석을 통해 진위여부를 확인하였다. 습식 세척제로는 상아 및 골각류 유물 처리에 주로 사용되는 증류수, 에틸알코올, 아세톤으로 처리하였으며, 세척 결과 표면관찰, 중량 측정, 색도 측정에서 특별한 변화가 관찰되지 않았다. 약산을 통한 색상 회복 실험에서는 UV-A, UV-B, UV-C 세 가지 파장 하에서 1주일간 인공 열화 시킨 시편을 대상으로 약산 용액인 2%와 5%로 희석된 아세트산 용액과 레몬즙을 이용해서 처리하였다. 처리 결과, 모든 시편에서 표면에 균열과 공극이 관찰되었으며, 레몬즙을 사용한 경우 시편의 색이 붉게 변색되어 유물에 적용이 불가능하다고 판단된다.

• 환경위생공학
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• 제16권1호
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• pp.72-90
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• 2001

This study was conducted to evaluate desorption efficiencies accuracy and precision by $CS_2$ and thermal desorption method for polar and non-polar organic solvents collected on activated carbon(AC), activated carbon fiber(ACF), carbosieve SIII, materials tested were Methyl alcohol, n-Hexane, Benzene, Trichloroethylene, Methyl isobutyl ketone and methyl cellosolve acetate and six different concentration levels of samples were made. The results were as follows ; 1. Accuracy on kind adsorbent and desorption method was low. In case of $CS_2$ desorption solvent, Overall B and Overall CV on AC and ACF were 43% and 6.63%, respectively. In case of thermal desorption method, accuracy of thermal desorption method appeared higher than solvent desorption method by AC 18.0%, 3.54%, ACF 2.6%, 2.57%, Carbosieve SIII 13.7% and 1.97%, respectively. 2. In the concentration level III, accuracy of thermal desorption method on adsorbent was in order as follow ; ACF > Carbosieve SIII > AC in the methyl alcohol and Carbosieve SIII > ACF > AC in the rest of them all subject material and Concentration levels showed good precision at EPA recommend standard (${\leq}{\;}30%$) 3. DEs by type of organic solvent adsorbent and desorption method are as follows ; In the case that desorption solvent is $CS_2$, DE of Methyl alcohol is AC 47.5%, DE of all materials is ACF about 50%. In the case of thermal desorption method, DE of Methyl alcohol is AC 82.0%, ACF 97.4%, Carbosieve SIII 86.3%. DE of the later case is prominently improved more than one of former. In particular, Except that DE of EGMEA is ACF 88.5%, DE of the rest of it is more than 95% which is recommend standard MDHS 72. With the result of this study, in order to measure various organic solvent occurring from the working environment, in the case of thermal desorption method, we can get the accurate exposure assessment, reduce the cost, and use ACF as thermal desorption sorbent which available with easy.

• 공업화학
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• 제1권1호
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• pp.73-82
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• 1990

로진과 말레산무수물로부터 rosin-maleic anhydride adduct (RMA)를 합성하고 이를 방향족디이소시아네이트와 반응시켜서 폴리아미드이미드를 합성하였다. 반응촉매로는 Sodium methoxide ($CH_3ONa$)를 사용하였고 반응용제로는 N-메틸-2-피롤리돈 (이하 NMP)을 사용하였다. NMP는 방향족디이소시아네이트와 부반응을 하기 때문에 중합체의 수율과 점성도가 낮았다. 부반응을 줄이기 위하여 NMP에 방향족용제인 크실렌, 아세토페논, 벤조니트릴 및 니트로벤젠을 공용제로 혼합, 사용하였다. 극성이 비교적 작은 공용제의 혼합시 공용제 혼합비율이 60%인 경우 약 70%정도, 극성이 비교적 큰 공용제의 혼합계에서는 혼합비율이 40%인 경우 90% 이상의 수율로서 높은 수율을 얻을 수 있었다. 중합체는 무정형이거나 약간의 결정성을 갖는 구조였으며 고극성용제에서만 용해하였다. 중합체의 점성도는 0.12-0.26dl/g의 범위였다. 열분석 결과 중합체의 초기분해온도는 $330^{\circ}C$ 이상으로서 양호한 열안정성을 나타내었다.

• 한국안전학회지
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• 제39권1호
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• pp.9-15
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• 2024

Hydrogen-based electricity and transportation systems are widely recognized as sustainable power sources. However, the low ignition energy of hydrogen, only 1/10th that of conventional fossil fuels, poses a safety concern involving the risk of ignition due to electrostatic discharge from facility workers. Therefore, anti-static systems are imperative for hydrogen-based electricity facilities. To address this, we propose a reliable conductive rubber mat (CRM) to ensure the safety of these facilities. Unlike conventional anti-static floors that utilize conductive paint (CP), the CRM features a uniform distribution of conductive components in chemically and mechanically stable rubber. As a result, the CRM is unyielding to polar solvents (such as ethanol and hydrosulfuric acid) and non-polar solvents (like mineral oil) without increasing its resistance. Moreover, the CRM can withstand mechanical stress. Consequently, the human-body voltage of workers on the CRM would be sufficiently low enough to protect them from hydrogen explosions, thereby enhancing overall safety.

• Bulletin of the Korean Chemical Society
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• 제23권9호
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• pp.1315-1327
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• 2002

The model compounds, 8-methoxypsoralen-CH2O(CH2)n-adenine (MOPCH2OCnAd, n=2, 3, 5, 6, 8, and 10) in which 5 position of 8-methoxypsoralen (8-MOP) is linked by various lengths of polymethylene bridge to N9 of adenine. UV absorption spectra are identical with the sum of MOPCH2OC3 and adenine absorption spectra. Solvent effects on the UV absorption and fluorescence emission spectra indicate that the lowest excited singlet state is the $(\pi${\rightarrow}$\pi*)$ state. The spectral characteristics of the fluorescence of MOPCH2OCnAd are strongly dependent upon the nature of the solvents. The fluorescence emission spectra in aprotic solvents are broad and structureless due to the excimer formation through the folded conformation accelerated by hydrophobic ${\pi}-{\pi}$ stacking interaction. Increasing polarity of the protic solvents leads to higher population of unfolded conformation stabilized through favorable solvation and H-bonding, and consequently to an increase in the fluorescence intensity, fluorescence lifetime, and a shift of fluorescence maximum to longer wavelengths. The decay characteristics of the fluorescence in polar protic solvents shows two exponential decays with the lifetimes of 0.6-0.8 and 1.6-1.9 ns in 5% ethanol/water, while MOPCH2OC3 shows 0.5 and 1.7 ns fluorescence lifetimes. The long-lived component of fluorescence can be attributed to the relaxed species (i.e., the species for which the solvent reorientation (or relaxation) has occurred), while the short-lived components can be associated with the unrelaxed, or only partially relaxed, species.