• 한국잠사곤충학회지
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• 제41권2호
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• pp.116-121
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• 1999

This study was aimed to explain the essence of Hydroxylammonium hydrochloride(H.A.) effect on degummed silk fiber increasing the colour sites due to oxime generating reaction. H.A. in aqueous solution caues to increase the amount of [H+] and reduce pH values as the concentration of H.A. increases. The rate of [H+] absorption of silk fiker in acidic solution differs on the basic of solution pH and shows a specific uptake in each pH, the lower the pH of solution, the higher the amount [H+] absorption. The pH of solution after treating of silk fiber in H.A. and HCl, showed more remaining [H+] in H.A. solution due to [H+] releasing under the procedure of oxime production. Also it was revealed that in higher concentration of H.A. the reaction for oxime fixation in silk fiber carried out stonger and as a result the bigger gap with acid uptake curve appeared. FT-IR analysis of silk fiber treated with H.A. revealed the creating of intermolecular H-bond at the 2,981-2.930 cm-1, which was not appeared for nontraeted silk fibers and shows H-bond between N-OH group in oue chain and C=) group in another chain of silk protein. Colourimetry of dyed silk fiber after H.A. tratment showed that the silk fiber treated with the high concentration of H.A. compare to low concentration, absorbed more dyeing molecules and so Showed less percontage of Whiteness.

• Restorative Dentistry and Endodontics
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• 제31권6호
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• pp.415-426
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• 2006

자가부식 상아질 접착제의 중합 후 시간 경과에 따른 접착강도의 변화를 관찰하고, 중합률의 영향을 평가하고자 하였다. 36개의 상하악 대구치를 Single Bond (SB, 3M ESPE, USA), Clearfil SE Bond (SE, Kuraray, Japan), Xeno-III (XIII, Dentsply, Germany), 및 Adper Prompt (AP, 3M ESPE, USA)를 적용하는 4군으로 나누고, 이를 다시 미세인장접착강도 측정 시점에 따라 22$^{\circ}$C의 증류수에 보관 후 48시간에 측정한 군과 7일 후 측정한 군, 및 접착된 시편을 5000회 열순환을 시행하고 측정한 군으로 나누었다. 모래시계 형태의 접착시편을 제작하여 만능시험기 (Model 4466; Instron Co., USA)로 1 mm/min의 하중속도 하에서 미세인장접착강도를 측정하였다. 접착제의 중합률은 Fourier 변환 적외선 분광법을 이용하여 중합 직후, 48시간, 1주일에 측정하였으며, 주사전자현미경을 이용하여 파절 단면을 관찰하였다. 미세인장접착강도와 중합률 모두 시간의 경과에 따라 유의한 증가를 보였으며, 시간 경과와 재료간에 교호작용이 있었다 (미세인장접착강도, 2-way ANOVA, p = 0.018; 중합률, Repeated Measures ANOVA, p < 0.001) . XIII와 AP의 낮은 미세인장접착강도는 낮은 중합률 때문임을 확인할 수 있었다. 48시간 이후에 SE와 AP에서 접착강도가 증가 되는 것은 중합률과는 관련이 없고, 전자현미경에서 관찰되는 접착제층의 성숙에 따른 취성의 증가가 원인일 가능성이 제기된다.

• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2009년도 춘계학술대회 논문집
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• pp.411-412
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• 2009

• Bulletin of the Korean Chemical Society
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• 제10권1호
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• pp.114-116
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• 1989

• 대한치과교정학회지
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• 제27권5호
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• pp.781-789
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• 1997

본 연구는 교정치료를 위해 최근에 발거된 소구치 65개를 대상으로 발거직후 부착된 이물질을 제거하고 생리식염수에 담구어 보관한 후 법랑질을 퍼미스 및 $38\%$ 인산으로 표면 처리하고 불소가 유리되는 교정용 전색제로는 광중합형 FluoroBond, 광중합 접착제로는 Transbond, 화학중합 접착제로는 Mono-Lok 2를 선정하여 1차 부착 및 재부착시의 전단결합강도를 만능강도시험기로 측정함으로서, 치아우식 예방 및 진행 억제효과를 지닌 불소가 유리되는 교정용 전색제가 광중합형 및 화학중합형 교정용 접착제의 전단결합강도에 미치는 영향과 재부착에 의한 전단결합강도의 변화를 규명하고, 광중합형 접착제와 화학중합형 접착제 사이의 전단결합강도를 비교하여 다음의 결론을 얻었다. 1. 1차부착에 의한 전단결합강도의 크기는 Mono-Lok2군(11.84MPa), Trans bond군(10.75MPa), Light cured FluoroBond+Mono-Lok 2군(9.69MPa), Light cured FluoroBond+Transbond군(9.39MPa)순이었다. 2. 재부착에 의한 전단결합강도의 크기는 Transbond군(7.40MPa), Light cured FluoroBond+Transbond군(6.48MPa), Mono-Lok 2군(5.89MPa), Light cured FluoroBond+Mono-Lok 2군(5.15MPa)순이었다. 3. 불소가 유리되는 교정용 전색제를 적용한군과 적용하지 않은 군 모두에서 화학중합형 접착제가 광중합형 접착제보다 높은 전단결합강도를 보였으나 통계학적으로 유의한 차이는 없었다(p>0.05). 4. 불소가 유리되는 교정용 전색제를 적용한군과 적용하지 않은 군 모두에서 재부착된 광중합형 접착제가 재부착된 화학중합형 접착제보다 높은 전단결합강도를 보였으나 통계학적으로 유의한 차이는없었다(p>0.05). 5. 1차 부착된 군에 비해 재부착된 모든 군에서 전단결합강도가 현저하게 감소되었으며, 통계학적으로 유의한 차이를 보였다(p<0.05 p<0.001). 이상의 결론을 종합해볼 때 임상적으로 브라켓의 전단결합강도에 경향을 미치지 않는 불소가 유리되는 교정용 전색제를 치아 협면에 적용하여 불소의 유리에 의한 치아우식 예방 및 억제효과를 기대하는 것이 필요할 것으로 생각된다.

• 한국자기공명학회논문지
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• 제18권1호
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• pp.41-46
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• 2014

In order to obtain information on the structural geometry of $NH_4HSeO_4$ near the phase transition temperature, the spectrum and spin-lattice relaxation time in the rotating frame $T_{1{\rho}}$ for the ammonium and hydrogen-bond protons were investigated through $^1H$ MAS NMR. $T_{1{\rho}}$ for the hydrogen-bond protons abruptly decreased at high temperature and it is associated with the change in the structural geometry in $O-H{\cdots}O$ bonds. This mobility of the hydrogen-bond protons may be the main reason for the high conductivity.

• Journal of the Korean Wood Science and Technology
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• 제35권5호
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• pp.38-45
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• 2007

Flakeboards made from ring- and drum-cut flakes of Douglas-fir, hemlock, red lauan and kapur using two kinds of resin levels were evaluated for the selected properties according to flake thickness. The pH and buffering capacity of four species were determined. Those of kapur were extremely different from the other three species. These pH and buffering capacity values result in the poor internal bond strength of kapur flakeboard. The internal bond strength was affected significantly by flake thickness, resin content and species. MOR and MOE in bending strength were maximized at medium drum-cut flake thickness. Screw holding strength was not consistent for flake thickness, but it was influenced by species. Thickness swelling and water absorption of Douglas-fir and hemlock flakeboard were minimized at medium drum-cut flake thickness.

• 한국세라믹학회지
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• 제31권4호
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• pp.381-388
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• 1994

A new process which co-fires the low-firing-substrate and copper conductor was studied to achieve good bond strength and low sheet resistance of conductor. Cupric oxide is used as the precursor of conductive material in the new method and the firing atmosphere of the new process is changed sequently in air H2N2. The addition of cupric oxide and variations of firing atmosphere permited complete binder-burnout in comparison with the conventional method and contributed to the improvement of resistance and bonding behaviors. The potimum conditions of this experiment to obtain the satisfactory resistance and bond strength are as follows (binder-burnout temperature in air; 55$0^{\circ}C$, reducing temperature in H2; 40$0^{\circ}C$ for 30 min, ratio of copper and cupric oxide; 60:40~30:70 wt%). The bonding mechanism between the substrate and metal was explained by metal diffusion layer in the interface and the bond strength mainly depended on the stress caused by the difference of shrinkage and thermal expansion coefficient between the substrate and metal.

• Bulletin of the Korean Chemical Society
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• 제10권3호
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• pp.247-250
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• 1989

The molecular structure of cyclobutylmethyl ketone (c-$C_4H_7COCH_3$) has been investigated by molecular mechanics II (MM2). For the monosubstituted cyclobutane there are two possible ring conformations, the equatorial and axial form, but for the cyclobutylmethyl ketone the equatorial form is predominant conformation. For the $COCH_3$ moiety there are two stable orientations which are the equatorial-gauche and the equatorial-trans form. The equatorial-gauche form where the C = O bond is nearly eclipsing (torsional angle ${\angle}C4-C3-C2-O10=14.5^{\circ}$) one of the ${\alpha}$C-C bonds of the four-membered ring was preferred conformer with steric energy of 13.37 kcal/mol. The equatorial-trans form where the C = O bond is nearly eclipsing (${\angle}C4-C3-C2-O10=145.0^{\circ}$) the ${\alpha}$ C-H bond of the four-membered ring was less stable conformer with steric energy of 15.40 kcal/mol.

• 공업화학
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• 제33권4호
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• pp.425-430
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• 2022

L-alanine (LA, as an amino acid residue) pentamer model was used to investigate changes in the dihedral angle, intramolecular hydrogen bonding and formation energies during structural optimization. LA pentamers having four conformation types [𝛽: 𝜑/𝜓=t-/t+, 𝛼: 𝜑/𝜓=g-/g-, PP_II: 𝜑/𝜓=g-/t+ and P-like: 𝜑/𝜓= g-/g+] were carried out by quantum chemical calculations (QCC) [B3LYP/6-31G(d,p)]. In LA, 𝛽, 𝛼, and P-like types did not change by optimization, having an intra-molecular hydrogen bond: NH⋯OC (H-bond), and PP_II types in the absence of H-bond were transformed into P-like at the designated 𝜓 of 140°, and to 𝛽 at that of 160° or 175°. P-like and 𝛼 were about 0.5 kcal/mol/mu more stable than 𝛽. In order to understand the processes of the transformations, the changes of 𝜑/𝜓, distances of NH-OC (d_NH/CO) and formation energies (𝜟E, kcal/mol/mu) were examined.