• 대한치과보철학회지
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• 제34권4호
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• pp.791-799
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• 1996

교정치료을 위해 발거된 소구치를 사용하며 레진에 고정한 후 직경 4mm이상의 법랑질 평면을 얻었다. 직경 4mm의 아크릴릭 봉을 길이 5mm로 해서 Ni-Cr 비귀금속 합금으로 주조한 후, 사용될 표면을 전기화학적 식각처리 하였다. 각 실험군당 시편 42개를 I군은 Panavia 21, II군은 Superbond, III군은 All-Bond로 세멘트 한 후 1일, 15일, 그리고 30일에 각 군당 14개의 시편을 임의로 취득하여 인스트론 만능시험기에 특별히 만든 Jig를 사용하여 거상하고 cross-head speed 1mm/min으로 전달결합강도를 측정하였다. 세멘팅한 후 1일에 측정한 전달결합강도는 Panavia-21의 I군에서 $32.7{\pm}9.9kg$중, Super-bond의 II군에서 $25.9{\pm}5.9kg$중, 그리고 All-Bond의 III군에서 $23.5{\pm}7.2kg$중의 순으로 나타났으며, I군이 II군과 III군에 대하여 통계학적인 유의성이 있었다(P<0.01). 세멘팅후 15일에 측정한 전단결합강도는 II군이 $34.6{\pm}10.4kg$중, I군에서 $23.1{\pm}8.7kg$중, 그리고 III군에서 $10.9{\pm}7.2kg$중으로 II군이 I과 III군에 대해, I군은 III군에 대해 통계학적 유의성이 있었다(P<0.01) 세민팅후 30일에 측정한 전달결합강도는 II군에서 $33.0{\pm}12.9kg$중, I군에서 $31.0{\pm}8.6kg$중, 그리고 III군에서 $13.6{\pm}6.6kg$중으로 II군과 I군이 III군에 대해 통계학적인 유의성이 있었다(p<0.01). 저장기간에 따른 전달결합강도 비교에서 III군에서 1일에서의 전단결합강도가 15일과 30일에서의 전단결합강도보다 통계학적으로 유의성 있게 높았다(P<0.01).

• Bulletin of the Korean Chemical Society
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• 제32권7호
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• pp.2423-2427
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• 2011

Pseudo-first-order rate constants ($k_{obsd}$) have been measured spectrophotometrically for nucleophilic substitution reactions of 3,4-dinitrophenyl diphenylphosphinothioate 9 with alkali metal ethoxides (EtOM, M = Li, Na, K) in anhydrous ethanol at $25.0{\pm}0.1^{\circ}C$. The plot of $k_{obsd}$ vs. [EtOM] is linear for the reaction of 9 with EtOK. However, the plot curves downwardly for those with EtOLi and EtONa while it curves upwardly for the one with EtOK in the presence of 18-crown-6-ether (18C6). Dissection of $k_{obsd}$ into $k_{EtO^-}$ and $k_{EtOM}$ (i.e., the second-order rate constant for the reaction with dissociated $EtO^-$ and ion-paired EtOM, respectively) has revealed that the reactivity increases in the order $k_{EtOLi}$ < $k_{EtONa}$ < $k_{EtO^-}$ ${\approx}$ $k_{EtOK}$ < $k_{EtOK/18C6}$, indicating that the reaction is inhibited by $Li^+$ and $Na^+$ ions but is catalyzed by 18C6-crowned $K^+$ ion. The reactivity order found for the reactions of 9 contrasts to that reported previously for the corresponding reactions of 1, i.e., $k_{EtOLi}$ > $k_{EtONa}$ > $E_{EtOK}$ > $k_{EtO^-}$ ${\approx}$ $k_{EtOK/18C6}$, indicating that the effect of changing the electrophilic center from P=O to P=S on the role of $M^+$ ions is significant. A four-membered cyclic transition-state has been proposed to account for the $M^+$ ion effects found in this study, e.g., the polarizable sulfur atom of the P=S bond in 9 interacts strongly with the soft 18C6-crowned $K^+$ ion while it interacts weakly with the hard $Li^+$ and $Na^+$ ions.

• 대한화학회지
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• 제36권2호
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• pp.205-211
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• 1992

아세트아미드(AA)의 CO기와 희토류 금속이온(Ln(II))을 포함하는 몇 가지 lanthanide shift reagent(LSR) 사이의 상호작용을 이해하기 위하여 AA의 $2{\nu}_{C=0}$ + amide III 조합띠를 $15^{\circ}$ ${\sim} 45^{\circ}C$에서 조사하였다. 묽은 $CCl_4$ 용액속에서 하나의 AA가 사용된 LSR에 배위되어 1 : 1 AA-LSR 복합체를 이루며, Ln(Ⅲ)이온에 대한 AA의 배위 위치는 카르보닐의 산소임을 알았다. 온도 및 농도에 따른 이 조합띠의 변화로부터 Ln(III)${\cdot}$O=C 결합에 대한 여러가지 열역학적 함수들을 구했다. Eu$(dpm)_3$, Yb$(dpm)_3$ 및 Pr$(dpm)_3$에 대한 AA의 결합의 세기를 나타내는 ${\Delta}H^{\circ}$는 각각 -39.1, -28.4 및 -25.5kJ/mol이다. 이들 값을 비교해보면 AA 분자가 배위될 때 중심금속이온의 ionic potential 효과보다는 이미 배위되어 있는 커다란 dpm 분자에 의한 입체장애효과가 더 큼을 알 수 있다.

• Journal of Welding and Joining
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• 제28권3호
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• pp.92-98
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• 2010

Ferritic stainless steels, which have relatively small thermal expansion coefficient and excellent corrosion resistance, are increasingly being used in vehicle manufacturing, in order to increase the lifetime of exhaust manifold parts. But, there are limits on use because of the problem related to cosmetic resistance, corrosions of condensation and high temperature salt etc. So, Aluminum-coated stainless steel instead of ferritic stainless steel are utilized in these parts due to the improved properties. In this investigation, Al-8wt% Si alloy coated 409L ferritic stainless steel was used as the base metal during Gas Tungsten Arc(GTA) welding. The effects of coated layer on the microstructure and hardness were investigated. Full penetration was obtained, when the welding current was higher than 90A and the welding speed was lower than 0.52m/min. Grain size was the largest in fusion zone and decreased from near HAZ to base metal. As welding speed increased, grain size of fusion zone decreased, and there was no big change in HAZ. Hardness had a peak value in the fusion zone and decreased from the bond line to the base metal. The highest hardness in the fusion zone resulted from the fine re-precipitation of the coarse TiN and Ti(C, N) existed in the base metal during melting and solidification process and the presence of fine $Al_2O_3$ and $SiO_2$ formed by the migration of the elements, Al and Si, from the melted coating layer into the fusion zone.

• Bulletin of the Korean Chemical Society
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• 제29권6호
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• pp.1157-1161
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• 2008

2,6-Dinitrophenol (2,6-DNP) complexes with lanthanide series including yttrium (except Pm, Tm, and Lu) have been synthesized and their crystal structures have been analyzed by X-ray diffraction methods. Singlecrystal X-ray structure determinations have been performed at 296 K on the Ce$\rightarrow$Yb species and shown them to be isomorphous, triclinic, P1, a = 8.6558(2)$\rightarrow$8.5605(3) $\AA$, b = 11.8813(3)$\rightarrow$11.6611(4) $\AA$, c = 13.9650(3) $\rightarrow$13.8341(5) $\AA$, $\alpha$ = 73.785(1)$\rightarrow$73.531(2)o, $\beta$ = 74.730(1)→74.903(2)${^{\circ}}$, $\gamma$ = 69.124(1)→ 69.670 $(2){^{\circ}}$, V = 1266.86(5)→1221.53(7) $$\AA^{3}$$, Z = 2. In Ln(III) complexes, three 2,6-DNP ligands coordinate directly to the metal ion in the bidentate fashion. The nine coordinated Ln(III) ion forms slightly distorted tri-capped trigonal prism. There are no water molecules in the crystal lattice. The dependences of metal to ligand bond lengths are discussed on the atomic number of lanthanide elements. The thermal properties of lanthanide complexes of 2,6- DNP have also studied by TG-DTG and DSC thermal analysis methods.

• 한국재료학회지
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• 제20권6호
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• pp.319-325
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• 2010

3-D IC integration enables the smallest form factor and highest performance due to the shortest and most plentiful interconnects between chips. Direct metal bonding has several advantages over the solder-based bonding, including lower electrical resistivity, better electromigration resistance and more reduced interconnect RC delay, while high process temperature is one of the major bottlenecks of metal direct bonding because it can negatively influence device reliability and manufacturing yield. We performed quantitative analyses of the interfacial properties of Al-Al bonds with varying process parameters, bonding temperature, bonding time, and bonding environment. A 4-point bending method was used to measure the interfacial adhesion energy. The quantitative interfacial adhesion energy measured by a 4-point bending test shows 1.33, 2.25, and $6.44\;J/m^2$ for 400, 450, and $500^{\circ}C$, respectively, in a $N_2$ atmosphere. Increasing the bonding time from 1 to 4 hrs enhanced the interfacial fracture toughness while the effects of forming gas were negligible, which were correlated to the bonding interface analysis results. XPS depth analysis results on the delaminated interfaces showed that the relative area fraction of aluminum oxide to the pure aluminum phase near the bonding surfaces match well the variations of interfacial adhesion energies with bonding process conditions.

• 대한치과보철학회지
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• 제41권5호
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• pp.656-673
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• 2003

Statement of problem : Long-term exposure of dental porcelain to saliva during temporary cementation of a porcelain-fused to metal (PFM) restoration could affect mechanical strength of dental porcelain if the restoration is refired. Purpose : This work was performed to verify the effect of water on the mechanical strength in aged dental porcelain. Material and method : 63 specimens(Vintage Metalbond opaque and opal powder) were distributed to three experimental groups ; non-water immersed control, immersed and pedried, and immersed and non-predired groups. The changes in flexural strength and fracture toughness after specimen refiring related to Fourier Transform Infrared (FT-IR) spectroscopy. Results : 1. The FT-IR reflectances assigned to molecular bonds of $H_2O$ were noted as significantly different between the first-fired group and three refired groups and between two water-immersed groups and control group after refiring(p<0.05). They were also significantly different between predried group and non-predried group after refiring(p<0.05) 2. For opal specimens, FT-IR absorbances for hydrogen bond of $H_2O$ and silanols were significantly higher in non-predried group than in predreid group(p<0.05). 3 Predried opal group showed the highest mean flexural strength(p<0.05). Non-predried group indicated higher mean flexural strength than control group(p<0.05). 4. The mean fracture toughness for predired group was higher than non-predried group(p<0.05). 5. The difference of leucite crystal size is noted between control group and water-immersed, predried group in scanning electron microscopic study(${\times}10000$).

• Journal of Microbiology and Biotechnology
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• 제26권9호
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• pp.1650-1656
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• 2016

The SCO0284 gene of Streptomyces coelicolor A3(2) is predicted to encode an α-galactosidase (680 amino acids) belonging to glycoside hydrolase family 27. In this study, the SCO0284 coding region was cloned and overexpressed in Streptomyces lividans TK24. The mature form of SCO0284 (641 amino acids, 68 kDa) was purified from culture broth by gel filtration chromatography, with 83.3-fold purification and a yield of 11.2%. Purified SCO0284 showed strong activity against p-nitrophenyl-α-D-galactopyranoside, melibiose, raffinose, and stachyose, and no activity toward lactose, agar (galactan), and neoagarooligosaccharides, indicating that it is an α-galactosidase. Optimal enzyme activity was observed at 40℃ and pH 7.0. The addition of metal ions or EDTA did not affect the enzyme activity, indicating that no metal cofactor is required. The kinetic parameters V_max and K_m for p-nitrophenyl-α-D-galactopyranoside were 1.6 mg/ml (0.0053 M) and 71.4 U/mg, respectively. Thin-layer chromatography and mass spectrometry analysis of the hydrolyzed products of melibiose, raffinose, and stachyose showed perfect matches with the masses of the sodium adducts of the hydrolyzed products, galactose (M+Na, 203), melibiose (M+Na, 365), and raffinose (M+Na, 527), respectively, indicating that it specifically cleaves the α-1,6-glycosidic bond of the substrate, releasing the terminal D-galactose.

• 대한화학회지
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• 제39권5호
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• pp.356-363
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• 1995

유기 리간드(디크로로 비스[η-싸이크로 펜타디엔닐])을 가지고 전이금속 4가$(Nb^{4+}와\;Mo^{4+}$와의 착물들에 대한 거동을 UV-vis 분광학적, 자기적, 그리고 전기화학적 방법에 의해 조사하였다. 2 또는 3개의 에너지 흡수띠가 이들 착물들의 스펙트라에 의해 관찰되었다. 결정장 갈라짐 에너지 크기와 스핀 짝지움 에너지 그리고 결합 세기는 착물들의 스펙트라로부터 얻어졌다. 이들은 비편재화이고, 낮은 스핀 상태이며 그리고 강한 결합 세기임을 알았다. 자기쌍극자 모멘트는 상자기성과 반자기성 착물이었다. 착물들의 산화환원 과정은 비수용매속에서 순환 전압전류법에 의해서 조사되었다. Nb-C 착물의 산화환원 반응과정은 일전자의 확산과 반응 전류에 의한 짝-단일 반응이었고 또한 Mo-C 착물에서는 일전자의 반응전류에 의한 짝-단일 반응이었다.

• 한국진공학회지
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• 제6권2호
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• pp.159-164
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• 1997

X-선 광전자 분광법 (x-ray photoelectron spectroscopy: SPS)과 반사 고에너지 전 자 회절법(reflection high energy electron diffraction: RHEED)을 이용하여 상온과 고온(약 300~$500^{\circ}C$)에서 알칼리금속(AM)/Si(111)7$\times$7표면에 1 monolayer(ML)의 AM을 흡착시키면 Si(111)7$\times$7표면에 비해 산소의 초기 부착 계수(initial sticking coefficient)와 산소의 포화량 은 증가하지 않았다. Si(111)7$\times$7-AM표면에 산소의 주입량을 증가시키면서 측정한 O ls 스 펙트럼으로부터 AM이 흡착된 Si(111)7$\times$7표면에 흡착되는 산소원자는 Si-O, AM-O 두 종 류의 결합형태를 가지는 것으로 생각되며 이중에서 AM-O 결합의 산화과정상에서의 역할 에 대하여 논의하였다. 상온과는 달리 고온에서는, Si(111)3$\times$1-AM표면으로 구조가 변화하 면서 산소의 흡착이 급격히 떨어지는 것을 관측할 수 있었다. 이때 3$\times$1-AM표면을 형성시 키는 AM종류의 산화에 대한 의존성을 살펴보았다.