• 제목/요약/키워드: b-y Ions

검색결과 590건 처리시간 0.027초

$BaORe_2O_3TiO_2$ (Re=La, Nd, Y)계 고주파 유전체의 결정구조 분석 및 온도계수 au_\varepsilon$와의 관련성 (Analysis of the Crystal Structure and the Relation with the Temperature Coefficient au_\varepsilon$ in $BaORe_2O_3TiO_2$ (Re=La, Nd, Y) Microwave Dielectric Ceramics)

  • 김정석;강현주;심해섭;이창희;천채일
    • 한국세라믹학회지
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    • 제36권2호
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    • pp.136-144
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    • 1999
  • 텅스템브론즈형 고주파 유전체의 $BaORe_2O_3TiO_2$(BLT)와 $BaO(Nd({0.77}Y_{0.23})_2O_34TiO_2(B(NY)T)$의 결정구조를 Rietveld 정밀화법으로 분석하였다. 양이온은 X-선 데이터로부터, 산소이온은 중성자 데이터로부터 정밀화한 'combined법'에 의해 가장 신뢰성이 높은 결정구조분석 결과를 얻었다. Mateeva 등이 처음 제시한 결정구조의 결정학적 모순점을 해결하였다. BaORe2O34TiO2(Re=La, Nd, Y) 유전체는 $3\times2$개의 페롭스카이트 블록과 이 블록사이에 형성된 4개의 pentagon-channel로 이뤄진다. Ti-O6팔면체는 tilted 및 변형된 구조를 갖고 있고, 이에 의해 같은 z-층에 있는 Ba 및 Re 이온의 변위되어 초격자(c$\approx$ 7.6$\AA$)를 형성된다. Re 이온반경이 작은 B(NY)T의 Ti-O6 팔면체가 tilting 및 변형이 큰 것으로 나타났다. 유전상수 $\varepsilon_{\gamma}$과 온도계수 $au_\varepsilon$은 BLT의 경우 각각 $109.5, -180 ppm/^{\circ}C$였고, B(NY)T 경우 $76, +40ppm/^{\circ}C$이었다. Re 이온 크기가 작은 시료의 $\tau$$\varepsilon$이 +값을 나타내었다. 복합 페롭스카이트에서 관찰되는 $\tau_\varepsilon$과 팔면체 tilting과의 관계를 본 텅스텐 브론즈 구조재료에서 고찰하였다.

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ICRF Wave Propagation and Absorption on KSTAR Plasma

  • Ju, M.H.;Hong, B.G.;Han, J.M.;Mau, T.K.
    • 한국원자력학회:학술대회논문집
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    • 한국원자력학회 1997년도 춘계학술발표회논문집(2)
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    • pp.583-588
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    • 1997
  • For the efficient current drive, the structure of ICRF wave propagation and absorption in a tokamak plasma should be first investigated. In this paper, two dimensional study on FWCD as well as ICRF minority ion heating for the KSTAR [Korea Superconducting Tok Amak Research] [1] plasma was performed using the full wave code of TORIC [2]. The ICRF wave propagation and absorption structures, the competitive power absorption between electrons and ions and the coupling of antenna/plasma are investigated.

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$PbO-B_2O_3$ 계 유리의 상분리에 미치는 $P_2O_5$의 영향 (Effect of $P_2O_5$ on the Phase Separation of $PbO-B_2O_3$ Glasses)

  • 최춘식;김철영
    • 한국세라믹학회지
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    • 제22권4호
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    • pp.47-53
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    • 1985
  • Various amount of $P_2O_5$ were added to $PbO-B_2O_3$ binary glass system to investigate its effect on the phase separation and physical properties of the glass. Experiments such as infrared spectroscopy scanning electron microscopy thermal expansion softening point and microhardnesses were done. Phase separation with $B_2O_3$ rich phase matrix and PbO rich phase droplet was observed for the glasses con-taining less than 10m/o of PbO while the opposite morphology of phase separation for the glasses containing more than 11m/o of PbO. By adding increasing amount of $P_2O_5$ their phase separation region was extended to the glass containing more than 20m/o of PbO. These effects can be interpreted in terms of the inoic field strength difference of each ions in the glasses. The abrupt changes of physical properties such as softening point thermal expansion and microhardness were observed for the glass with around 10m/o of PbO in this system. These changes are by the matrix composition change from TEX>$B_2O_3$ rich phase to PbO rich phase depending on PbO concentration.

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Structural Insight into Dihydrodipicolinate Reductase from Corybebacterium glutamicum for Lysine Biosynthesis

  • Sagong, Hye-Young;Kim, Kyung-Jin
    • Journal of Microbiology and Biotechnology
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    • 제26권2호
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    • pp.226-232
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    • 2016
  • Dihydrodipicolinate reductase is an enzyme that converts dihydrodipicolinate to tetrahydrodipicolinate using an NAD(P)H cofactor in L-lysine biosynthesis. To increase the understanding of the molecular mechanisms of lysine biosynthesis, we determined the crystal structure of dihydrodipicolinate reductase from Corynebacterium glutamicum (CgDapB). CgDapB functions as a tetramer, and each protomer is composed of two domains, an Nterminal domain and a C-terminal domain. The N-terminal domain mainly contributes to nucleotide binding, whereas the C-terminal domain is involved in substrate binding. We elucidated the mode of cofactor binding to CgDapB by determining the crystal structure of the enzyme in complex with NADP+ and found that CgDapB utilizes both NADH and NADPH as cofactors. Moreover, we determined the substrate binding mode of the enzyme based on the coordination mode of two sulfate ions in our structure. Compared with Mycobacterium tuberculosis DapB in complex with its cofactor and inhibitor, we propose that the domain movement for active site constitution occurs when both cofactor and substrate bind to the enzyme.

비자성 이온 Ga, In이 치환된 유화물 스피넬의 뫼스바우어 분광학 연구 (The Effect of Non Magnetic ion Substitution for the FeCr2-xMxS4(M=Ga, In) by Mossbauer Spectroscopy)

  • 손배순;김삼진;김철성
    • 한국자기학회지
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    • 제16권1호
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    • pp.6-10
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    • 2006
  • 단일상 $FeCr_{2-x}M_xS_4$ (M=Ga, In; x=0.1, 0.3)에 대하여 x-선 회절기(XRD), 진동 시료 자화율 측정기(VSM), 뫼스바우어 분광기를 이용하여 비자성 이온의 치환효과를 연구하였다. 결정구조는 Rietveld프로그램을 이용하여 공간그룹이 Fd3m[Fe, Ga, In(8a); Cr, Ga, In(160); S(32e) (u, u, u)]인 입방 스피넬 구조임을 확인하였다. 비자성 이온 Ga이 치환된 시료의 경우, Ga이 치환 될수록 격자상수가 10.007에서 $9.996\;{\AA}$,으로 감소하는 반면, In이 치환된 시료의 경우, In이 치환 될수록 격자상수가 10.029에서 $10.092\;{\AA}$로 증가함을 확인하였다 VSM측정 결과 Ga과 In이 치환 될수록 Neel온도는 각각 180에서 188K, 173에서 160K로 변화하였는데, 이것은 격자상수의 변화에 따른 사면체 자리(A자리)와 팔면체 자리(B 자리)의 초교환 상호작용 세기의 변화로 해석 할 수 있었다 $4.2K\~300K$의 온도범위에 걸쳐서 뫼스바우어 스펙트럼을 분석한 결과 Fe이온이 각각 A자리와 B자리에 점유함을 확인 할 수 있었다. 이것은 비자성 이온 Ga과 In 이 A자리의 Fe이온의 비대칭적인 전하 분포를 야기시키는 것으로 해석할 수 있었다. 또한 Cr-S의 결합거리를 비교해 본 결과, $FeCr_{2-x}Ga_xS_4$(x=0.3)와 RFeCr_{2-x}In_xS_4$ (x=0.3)가 각각 2.41, $2.43\;{\AA}$$FeCr_{2-x}Ga_xS_4$(x=0.3)의 결합거리가 작아 공유 결합력이 커짐에 따라 비대칭적인 전하 분포를 유도함으로 해석할 수 있다. 이는 큰 전기 사중극자를 유도하는 결과와 일치함을 알 수 있었다.

Ion Beam Modified ppolyimide: A Study of the Irradiation Effect

  • Lee, Y.S.;Lim, K.Y.;Chung, Y.D.;Lee, K.M.;Choi, B.S.;Whang, C.N.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 1998년도 제14회 학술발표회 논문개요집
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    • pp.132-132
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    • 1998
  • Ion bombardment in the keV range is known to induce drastic chemical modifications in organic and inoranic molecular comppounds. A degrading effects in orgainc materials such as the release of ppolymer compponents and the chemistry of the iradiation pprocess have been observed. The work to be described was carried out in order to understand the irradiation effect better. The sampple(ppolyimide : Kappton ) Were irradiated by Ar+, Ne+, H+ ions and electrons (3 keV) to fluence ranging from ~1$\times$1015 to ~1$\times$1017 ions/$cm^2$ at room tempperature. The impplant was usually rastered over an area of a few $cm^2$ . These ion impplantation were carried out in an electron sppectrometer ESCA 5700 (ppHI Ltd) at a residual gas ppressure of ~5$\times$10-10 Torr. X-ray pphotoelectron sppectroscoppy(XppS) measurements were made using a monochromatized Al Ka(1486.6 eV) excitation source. The pphotoemitted electrons were detected by hemisppherical analyser with a ppass energy of 23.5 eV. Core-level binding energies were referenced to the Fermi level. To avoid the charging effect it was used the neutralizer. We studied the irradiation effects on ppolyimide with Ar+, Ne+, He+ ions and electrons by XppS which 추 pprovide detailed information concerning the bonding-induced changes.

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크랜베리 수용액 색상의 특성 및 안정성 (Characteristics and Stability of the Color of the Cranberry Solution)

  • 김진현;이재하;백창규
    • 한국식품영양과학회지
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    • 제32권6호
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    • pp.806-811
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    • 2003
  • 크랜베리 수용액의 색상 안정성 에 대한 pH, 열, 광, 당, 유기산, 금속이온, 비타민 C, $B_1$, $B_3$$B_{6}$의 영향을 조사하였다. 크랜베리 수용액의 색상은pH가 낮을수록 농색화 효과가 높았고 pH가 높아질수록 최대흡수파장이 장파장 쪽으로 이동하는 bathochromic shift현상이 관찰되었다. 열의 영향에 대한 실험 결과, 색상의 반감기가 37$^{\circ}C$에서 34일, 9$0^{\circ}C$에서 91분, 12$0^{\circ}C$에서 29분으로 온도가 높을수록 색상의 반감기가 급격하게 짧아졌다. 광에 의해 색상의 안정성이 크게 저하되었는데, 형광보다 일광에 대한 영향이 더 컸으며 저장 시 광을 차단함으로써 안정성을 증진시킬 수 있었다. 당류 첨가는 오히려 무첨가구에 비해서 저장 안정성을 저하시켰고 fructose가 색상 저하를 가장 촉진하는 것으로 나타났다. 유기산 중 fumaric acid, citric acid, malic acid, acetic acid 순으로 색상 안정성에 효과가 있었으며 특히 fumaric acid는 색상안정화에 크게 기여하였다. 금속이온 중 $Na^{+}$$Mg^{2+}$은 색상안정화에 기여하였으나 $Mn^{2+}$은 색상의 안정성을 가장 크게 저하시켰고 다음으로 F $e^{2+}$, $K^{+}$, $Ca^{2+}$순으로 저하시켰다. 비타민 C와 $B_1$은 크랜베리 수용액 색상의 안정성을 저하시켰으며 특히 비타민 C는 색상의 안정성을 크게 저하시켰다. 반면 $B_3$, $B_{6}$는 색상의 안정성에 미약하게 기여하였다.

Improved Magnetic Anisotropy of YMn1-$xCrxO_3 $ Compounds

  • Yoo, Y.J.;Park, J.S.;Kang, J.H.;Kim, J.;Lee, B.W.;Kim, K.W.;Lee, Y.P.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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    • pp.218-218
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    • 2012
  • Recently, hexagonal manganites have attracted much attention because of the coexistence of ferroelectricity and antiferromagnetic (AFM) order. The crystal structure of hexagonal manganites consists of $MnO_5$ polyhedra in which $Mn^{3+}$ ion is surrounded by three oxygen atoms in plane and two apical oxygen ions. The Mn ions within Mn-O plane form a triangular lattice and couple the spins through the AFM superexchange interaction. Due to incomplete AFM coupling between neighboring Mn ions in the triangular lattice, the system forms a geometrically-frustrated magnetic state. Among hexagonal manganites, $YMnO_3$, in particular, is the best known experimentally since the f states are empty. In addition, for applications, $YMnO_3$ thin films have been known as promising candidates for non-volatile ferroelectric random access memories. However, $YMnO_3$ has low magnetic order temperature (~70 K) and A-type AFM structure, which hinders its applications. We have synthesized $YMn1_{-x}Cr_xO_3$ (x = 0, 0.05 and 0.1) samples by the conventional solid-state reaction. The powders of stoichiometric proportions were mixed, and calcined at $900^{\circ}C$ for $YMn1_{-x}Cr_xO_3$ for 24 h. The obtained powders were ground, and pressed into 5-mm-thick disks of 1/2-inch diameter. The disks were directly put into the oven, and heated up to $1,300^{\circ}C$ and sintered in air for 24 h. The phase of samples was checked at room temperature by powder x-ray diffraction using a Rigaku Miniflex diffractometer with Cu $K{\alpha}$ radiation. All the magnetization measurements were carried out with a superconducting quantum-interference-device magnetometer. Our experiments point out that the Cr-doped samples show the characteristics of a spin-glass state at low temperatures.

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Preparation of Metal-p-aminobenzyl-DOTA Complex Using Magnetic Particles for Bio-tagging in Laser Ablation ICP-MS

  • Yoon, S.Y.;Lim, H.B.
    • Bulletin of the Korean Chemical Society
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    • 제33권11호
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    • pp.3665-3670
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    • 2012
  • Metal-p-$NH_2$-Bn-DOTA (paraammionobenzyl-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid: ABDOTA) complex was synthesized and purified for bio-tagging to quantify biological target materials using laser ablation (LA)-ICP-MS. Since the preparation of a pure and stable tagging complex is the key procedure for quantification, magnetic particles were used to purify the synthesized metal-ABDOTA complex. The magnetic particles immobilized with the complex attracted to a permanent magnet, resulting in fast separation from free un-reacted metal ions in solution. Gd ions formed the metal-complex with a higher yield of 64.3% (${\pm}3.9%$ relative standard deviation (RSD)) than Y ions, 52.3% (${\pm}2.5%$ RSD), in the pH range 4-7. The complex bound to the magnetic particles was released by treatment with a strong base, of which the recovery was 81.7%. As a reference, a solid phase extraction (SPE) column packed with Chelex-100 resin was employed for separation under similar conditions and produced comparable results. The tagging technique complemented polydimethylsiloxane (PDMS) microarray chip sampling in LA-ICP-MS, allowing determination of small sample volumes at high throughputs. For application, immunoglobulin G (IgG) was immobilized on the pillars of PDMS microarray chips and then tagged with the prepared Gd complex. IgG could then be determined through measurement of Gd by LA-ICP-MS. A detection limit of 1.61 ng/mL (${\pm}0.75%$ RSD) for Gd was obtained.

Bi$_2$Sr$_2$Ca$_{1-x}$Na$_x$Cu$_2$O$_{8+y}$ 산화물 고온초전도체의 Ca 위치에 Na 치환 효과 (Effect of Na Substitution for the Ca Site in the Bi$_2$Sr$_2$Ca$_{1-x}$Na$_x$Cu$_2$O$_{8+y}$ Superconductors)

  • 이민수;송승용;이종용;송기영;최봉수
    • 한국세라믹학회지
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    • 제35권10호
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    • pp.1007-1013
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    • 1998
  • The samples of Bi2Sr2Ca1-xNaxCu2O8+y with various carrier concentration were synthesized by substituting Na for Ca ion. The superconducting properties hall coefficients and X-ray powder diffraction were measur-ed the sampled. Single phase samples were obtained for 0$\leq$x<0.3 of Bi2Sr2Ca1-xNaxCu2O8+y In the single phase the critical temperature. {{{{ { T}_{c } }} and carrier concentration increase with the increase of Na concentration pass through a maximum and then decreases. In the range of x$\geq$0.7 to the Na doped samples however we observed the metal-semiconductor transition. The c-axis seemed to decrease and a and b-axes increase with increasing Na concentration in the single phase. Decreasing of c-axis while increasing x is due to the smaller size of {{{{ {Na}^{+1 } }} ions to the {{{{ { Ca}^{+2 } }} ions. In the range of x>0.3 however the trend becomes ambiguous due to the inclusion of the 10K phase and impurity phase.

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