• 제목/요약/키워드: Bonding ability

검색결과 125건 처리시간 0.032초

의사이성분계, Li2Cr2O4-MgCr2O4와 Li2Cr2O4-MgAl2O4에서의 LiCrO2 고용체 형성과 결합구조 (Solid Solution and Defect Structure of LiCrO2 in the Pseudo-binary Systems : Li2Cr2O4-MgAl2O4)

  • 정영서;오근호;김호기
    • 한국세라믹학회지
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    • 제25권1호
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    • pp.35-41
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    • 1988
  • In the system of Li2O-MgO-Al2O3-Cr2O3, the crystalline solid solution of LiCrO2 along the pseudo-binary join between rocksalt structure(LiCrO2) and spinel structure(MgCr2O4 or MgAl2O4) have been investigated by x-ray diffraction techniques. In this study, order-disorder phase transition of LiCrO2 was observed and the unit cell of the disordered LiCrO2 structure has been established. It has been found that LiCrO2 makes a solid solution over a wide range with MgAl2O4, while not with MgCr2O4. This difference was explained as being due to the ability of oxygen lattice distortion which depended on the relative sizes and chemical bonding characteristics of the substituted ions.

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다이아몬드성 탄소 박막의 전계 전자 방출 특성에 관한 연구 (A Study on Field Electron Emission Characteristics of Diamond-Like Carbon)

  • 여선영;표재학;김중균;황기웅
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 1996년도 추계학술대회 논문집 학회본부
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    • pp.203-205
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    • 1996
  • DLC(Diamond-Like Carbon) films were prepared by Inductively Coupled Plasma(ICP) CVD system. It was confirmed that the field emission characteristics are closely related to the richness of C-H bonding incorporated in the DLC. According to Fowler-Nordheim equation, it is thought that the ability of DLC to emit electron at relatively low voltage is due to the field enhancement caused by the nodules of ${\sim}100nm$ size on the surface of DLC. The electric field to start field emission was about $1.4{\times}10^9V/m$ in case of DLC film deposited at input power of 400W and substrate bias of -100V.

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Quantification of Crystallinity Change in Celluloses during Refining

  • Kim, Chul-Hwan;Yang, Jae-Kyung;Park, Jong-Yawl
    • 펄프종이기술
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    • 제32권5호
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    • pp.8-13
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    • 2000
  • X-ray diffraction technique was used to quantify change of cellulose crystallinity during refining. XRD data confirmed that fiber wall delamination was caused by the structural conversion of celluloses which occurred in a liquid medium during refining. The quantified crystallinity of celluloses in pulp fibers was closely associated with the change of fiber wall delamination, which was defined by measurement of fiber wall thickness. In particular, it was well recognized that low intensity beating showed a better response in the change of crystallinity than high intensity one. The decrease o cellulose crystallinity during refining considerably enhanced the improvement of interfiber bonding ability of a dried sheet.

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Micellar Effects on Intramolecular Charge Transfer Emission from Biphenylcarboxylic Acids

  • Yoon, Min-Joong;Cho, Dae-Won;Kang, Seong-Gwan;Lee, Min-Yung
    • Bulletin of the Korean Chemical Society
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    • 제14권6호
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    • pp.704-708
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    • 1993
  • The intramolecular charge transfer (ICT) phenomena of the photoexcited 2-biphenylcarboxylic acid (2BPCA) and 4-biphenylcarboxylic acid (4BPCA) have been investigated in some surfactant micellar solutions. The ICT emission of 4BPCA and 2BPCA in aqueous solution at sufficiently low pH (1-3) has been observed to be markedly quenched and blue-shifted upon addition of a cationic surfactant, cetyltrimethylammonium chloride (CTAC) in contrast to little change in anionic sodium dodecyl sulfate (SDS) and neutral Brij 35. An anionic emission band has been observed to be enhanced at expense of the ICT emission as a function of the concentration of CTAC. These results with the micellar effects on the fluorescence decay kinetics of 4BPCA suggest that formation of the ICT state of the excited acids is inhibited by CTAC-induced proton transfer as well as the decrease in the polarity and/or hydrogen-bonding ability of the micellar microenvironment entrapping the acids.

Photophysical Properties of Khellin-Dimethylfumarate C$_4$-Cyclomonoadduct

  • Shim, Sang-Chul;Kang, Ho-Kwon
    • Bulletin of the Korean Chemical Society
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    • 제7권6호
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    • pp.458-461
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    • 1986
  • The fluorescence intensity of khellin-dimethylfumarate C$_4$-cycloadduct (KDF) is very sensitive to temperature and to the nature of solvents, especially hydrogen-bonding ability. The fluorescence quantum yields of KDF in ethanol and isopentane at 77K are 0.73 and 0.54, respectively, both of which are much larger than the room temperature values. The phosphorescence lifetime is very long and decreases with decreasing the solvent polarity. The phosphorescence and fluorescence quantum yield ratio is very small and decreases with decreasing solvent polarity. The solvent relaxation plays an important role in the excited states of KDF. The internal conversion is a major decay process of the excited singlet state of KDF in all the solvents used at room temperature.

5-Bromo-Ph4-BTPhen Ligand for Selective Removal of Strontium and Cobalt From Water

  • Jang, Jiseon;Harwood, Laurence M.;Cowell, Joe;Afsar, Ashfaq;Lee, Dae Sung
    • 한국방사성폐기물학회:학술대회논문집
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    • 한국방사성폐기물학회 2018년도 춘계학술논문요약집
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    • pp.183-183
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    • 2018
  • In this study, 5-bromo-2,9-bis(5,6-diphenyl-1,2,4-triazin-3-yl)-1,10-phenanthroline (5-bromo-Ph4-BTPhen) was synthesized and evaluated for its ability to remove major radionuclides ($Cs^+$, $Sr^{2+}$, and $Co^{2+}$). The synthesized ligand removed both $Sr^{2+}$ and $Co^{2+}$ from $1mg\;L^{-1}$ aqueous solutions with extraction efficiencies of up to 99% at neutral and alkaline pH. The $Sr^{2+}$ and $Co^{2+}$ removal efficiencies decreased as a consequence of the higher bonding strengths of competing metal ions to the N-donor atoms in the cavity of the ligand; competing divalent ions affected the $Sr^{2+}$ and $Co^{2+}$ removal efficiencies more than monovalent ions.

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Characterion of Calcium Phosphate Films Grown on Surgicl Ti-6AI-4V By Ion Beam Assisted Deposition

  • Lee, I-S.;Song, J-S.;Choi, J-M;Kim, H-E.
    • 한국진공학회지
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    • 제7권s1호
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    • pp.30-36
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    • 1998
  • The plasma-spray technique is currently the most frequently used method to produce calcium phosphate coatings. Hydroxyapatite(HAp), one form of calcium phosphate, is preferred by its ability to form a direct bond with living bone, resulting in improvements of implant fixation and faster bone healing. Recently, concerns have been raised regarding the viable use and long-term stability of plasma-spray HAp coatings due to its nature of comparatively thick, porous, and poor bonding strength to metal implants. Thin layers (maximum of few microns) of calcium phosphate were formed by an e-beam evaporation with and without ion bombardments. The Ca/P ration of film was controlled by either using the evaporants having the different ration of Ca/P with addition of CaO, or adjusting the ion beam assist current. The Ca/P ration had great effects on the structure formation after heat treatment and the dissolution bahavior. The calcium phosphate films produced by IBAD exhibited high adhesion strength.

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MeOH-1,1,2,2-Tetrachloroethane 혼합용매에서 tert-Butyl Halides의 이온화에 미치는 분광용매화변수들의 협동효과 (Cooperative Effects of Solvatochromic Parameters on the Ionizations of tert-Butyl Halides in MeOH-1,1,2,2-Tetrachloroethane Mixtures)

  • 사공열;김시준;주재범
    • 대한화학회지
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    • 제30권3호
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    • pp.265-272
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    • 1986
  • MeOH-1,1,2,2-tetrachloroethane 혼합용매에서 할로겐화삼차부틸(t-BuCl, t-BuBr, t-BuI)의 가메탄올 분해반응을 속도론적으로 연구하였으며, 이온화에 미치는 용매효과를 고찰하기 위하여 6가지 indicater를 이용한 분광용매화비교법을 적용하였다. 이결과 할로겐화삼차부틸의 가메탄올 분해반응에 미치는 용매화의 작용은 용매의 극상-편극성에 기인되는 상호작용이 주된 것이긴 하지만 halide leaving group의 living ability에 미치는 electrophilic assistance와 t-Butyl 양이온쪽에 대한 nucleophilic assistance도 상당히 작용함을 알 수 있다. 특히 hydrogen bonding에 의한 electrophilic assistance는 basicity가 큰 leaving group일수록 커지며 ($I^-), 탄소 중심일수록 커짐을 밝힐 수 있었다. (t-BuCl

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치과용 지르코니아 이장재 처리에 따른 지르코니아와 도재의 전단결합강도 비교 (Shear bond strength of a layered zirconia and porcelain according to treatment of zirconia liner)

  • 서정일;박원욱;김양근
    • 대한치과기공학회지
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    • 제39권1호
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    • pp.43-52
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    • 2017
  • Purpose: Physical and chemical properties of gold is most suitable to be restored of teeth to its original state. Recently zirconia was used instead of gold because of esthetical and intimacy of human body. Because of high strength and high abrasion resistance of zirconia, all zirconia artificial tooth lead to wear the original tooth of opposite site. To preserve this original tooth, zirconia artificial tooth covered with dental ceramic glass was used. When joining the zirconia core and dental ceramic glass, difference of their thermal expansion coefficient and wetting ability is generated the residual stress at interface lead to crack. In order to solve this problem, intermediate layer what is called zir-liner was imported to decrease the residual stress and increase the bonding strength. Methods: In this study, to identify the optimum conditions for manufacturing process, various methods to rough the surface of zirconia core were adopted, and vary the thickness of interlayer, and analyzed bond strength. Results: Bond strength of sanding specimens group showed higher than that of non-sanding specimens group, and once applied intermediate layer with sanding specimens showed highest bond strength with 28 MPa. SEM photomicrographs of zirconia cores fired at $1500^{\circ}C$ showed parallel straight lines in sanding and pockmarked surface in blasting surfaces as abrasion traces. Observation of the destruction section after shear test by SEM were carried out. Liner applied non-sanding group and non-liner applied sanding group all showed interfacial crack. Sandblasting group with non-liner showed remained dental ceramic glass on the surface of zirconia. Sandblasting group with once applied liner showed partially remained liner and dental ceramic glass on the surface of zirconia. XRD analysis revealed that sandblasting group showed higher monoclinic peaks than other specimens group and this result was due to the high collision energy for stress induced phase transformation. Conclusions: A study on the improvement of bonding strength between zirconia and dental ceramic glass steadily carried out for the future to practical use.

티오프로피온 아미드의 수소 결합 능력에 대한 근 적외선 분광학 연구 (The Near Infrared Spectroscopic Studies on the Hydrogen Bonding Ability of Thiopropionamide)

  • 주설아;박정희;윤창주;최영상
    • 대한화학회지
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    • 제39권11호
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    • pp.837-841
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    • 1995
  • 사염화탄소 속에서 티오프로피온아미드(TPA)와 triethylphosphine oxide(TEPO), triethylphosphine oxide(TPPO), trimethylphosphate(TMP), 그리고 tributyl phosphate(TBP)간의 수소 결합에 대한 열역학적 상수들을 근적외선 분광법을 이용하여 구하였다. TPA의 .nu./.alpha./+amide 2 조합띠는 TPA 단위체 및 수소 결합을 이룬 TPA의 띠로 이루어져 있음이 확인되어 이 띠를 두 개의 Lorentzian-Gaussian 곱함수의 띠로 분해하였다. 온도 및 농도의 변화에 따른 이 조합띠의 변화기로부터 TPA와 TEPO, TPPO, TMP, TBP의 수소 결합 엔탈피는 각각 -21.4, -16.8, -12.8, -12.9kJ/mol이었다. 이 결과는 치환기의 inductive effect 및 steric effect로 설명할 수 있다.

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