• 제목/요약/키워드: $LN_2O$

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$xMgTiO_3$(1-x) ($Na_{1/2}Ln_{1/2}$) $TiO_3$(Ln = La, Pr, Nd, Sm)의 초고주파 유전특성에 관한 연구 (Microwave Dielectric Characteristics of the $xMgTiO_3$(1-x) ($Na_{1/2}Ln_{1/2}$) $TiO_3$(Ln = La, Pr, Nd, Sm)Systems)

  • 김덕환;임상규;안철
    • 전자공학회논문지D
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    • 제35D권10호
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    • pp.51-59
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    • 1998
  • (Na½Ln½) TiO₃(Ln = La, Pr, Nd, Sm)은 양의 온도계수(190 ∼ 480ppm/℃), 고유전율(99∼127)의 특성을 갖고 있다. 반면에 MgTiO₃는 음의 온도계수(-45ppm/℃), 저유전손실(110,000㎓)을 갖고 있다. 그래서 xMgTiO₃(1-x) (Na½Ln½) TiO₃의 유전특성에 관심을 갖게 되었고, 초고주파 대역에서의 유전특성을 측정하고 미세구조를 관찰하여, 몰비변화와 소결온도변화에 따른 경향성을 파악하였으며, 그 원인을 연구하였다. 그 결과 MgTiO₃와 (Na½Ln½) TiO₃는 구조적으로 새로운 고용체나 이차상을 형성하지 않는 혼합상을 이루고 있었다. 그리고 이들의 유전특성은 (Na½Ln½) TiO₃와 MgTiO₃의 중간 값을 나타냈고, logarithmic mixing rule로써 유전특성을 예측할 수 있다. 이중에서 온도에 안정한 조성은 Ln = La, Pr, Nd으로 치환되었을 경우 각각 x = 0.9, 0.87, 0.84이었다. 이때의 유전율은 22 ∼25, Qf값은 55000 ∼ 28000㎓를 나타내었다. 이로써 온도에 안정한 유전특성을 갖는 새로운 유전체 재료를 개발하였으며, 특히 Ln = La으로 치환되었을 경우 다른 조성에 비하여 유전특성이 좋을 뿐아니라, 소결온도 범위가 넓어 공정상의 잇점을 가지고 있다.

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Lanthanide-Oxalate Coordination Polymers Formed by Reductive Coupling of Carbon Dioxide to Oxalate: [Ln2(3,5-pdc)2(C2O4)(H2O)4]·2H2O (Ln = Eu, Sm, Ho, Dy; pdc = Pyridinedicarbox

  • Huh, Hyun-Sue;Lee, Soon W.
    • Bulletin of the Korean Chemical Society
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    • 제27권11호
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    • pp.1839-1843
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    • 2006
  • Hydrothermal reactions of $Ln(NO_3)_3{\cdot}5H_2O $ (Ln = Eu (1), Sm (2), Ho (3), Dy (4)) with 3,5-pyridinedicarboxylic acid (3,5-pdcH2) in the presence of 4,4'-bipyridine led to the formation of the 3-D Ln(III)-coordination polymers with a formula unit of $[Ln_2(3,5-pdc)_2(C_2O_4)(H_2O)_4]{\cdot}2H_2O$. These polymers contain a bridging oxalate ligand ($C_2O_4\;^2$). On the basis of GCMS study of the mother liquor remaining after the reaction, we proposed that the $C_2O_4\;^2$ formation proceeds in three steps: (1) Ln(III)-mediated decarboxylation of $3,5-pdcH_2$ to give $CO_2$, (2) the reduction of $CO_2$ to $CO_2\;^{\cdot}$ by the Ln(II) species, and (3) the reductive coupling of the two $CO_2\;^{\cdot}$ radicals to the oxalate ($C_2O_4\;^2$) ion. All polymers were structurally characterized by X-ray diffraction.

Correlation between Structures and Ionic Conductivities of $Na_2Ln_2Ti_3O_{10}$ (Ln=La, Nd, Sm, and Gd)

  • 박길응;변송호
    • Bulletin of the Korean Chemical Society
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    • 제17권2호
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    • pp.168-172
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    • 1996
  • The variations of the structural detail of layered perovskite-type oxides, Na2Ln2Ti3O10 (Ln=La, Nd, Sm, Gd), have been refined by Rietveld analyses of their powder X-ray diffraction data. Although the c-axis strongly decreases from Ln=La to Nd, Sm, or Gd, the length of Na-O bond along the c-axis that is regarded as the sodium layer spacing is not dependent on the unit cell parameter. Such a behavior is explained by the fact that Na-O bond is in competition with Ti-O one of the perovskite slab. Increased covalency of this Ti-O bond by the lattice contraction leads to weakening of the attaching strength of Na ion. This picture is consistent with the experimental observation that Na ion conductivity of Na2Ln2Ti3O10 increases from Ln=La to Nd, Sm, or Gd despite strong contraction of the unit cell volume.

Preparati on and Characterization of $LnTaO_4$ (Ln = La, Nd, Sm, Dy, Er and Tm)

  • Fujita, Atsushi;Matsushita, Hiroaki;Katsui, Akinori
    • 한국분말야금학회:학술대회논문집
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    • 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part2
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    • pp.1116-1117
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    • 2006
  • Lanthanide tantalite $LnTaO_4$ (Ln= La, Nd, Sm, Dy, Er and Tm) was synthesized by a solid state reaction between mixed powders of $Ln_2O_3$ and $Ta_2O_5$. The single-phase $LnTaO_4$ was prepared by sintering at temperatures of 1423-1673 K in air. The SEM observation showed that the particles were provided with the growth steps and the depeloped facets. The photocatalytic activity for water splitting of $LnTaO_4$ prepared was measured under UV light irradiation. The activity obtained was higher than that previously reported. These results suggested the crystallinity of $LnTaO_4$ photocatalysts correlates closely with the efficiency of water splitting.

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$CH_3OH$ 용매에서 란탄족 원소{Ln(Ⅲ)=Pr, Sm, Gd, Dy}-거대고리 착물과 보조 리간드 간의 화학평형 (제2보): 주게원자가 산소인 염기를 중심으로 고찰. (Chemical Equilibria of Lanthanides{Ln(Ⅲ)=Pr, Sm, Gd, Dy}-Macrocyclic Complexes with Auxiliary Ligands in $CH_3OH$(PartⅡ):Study of the Coordination of Oxygen-Containing Bases.)

  • 변종철;박유철;한충훈
    • 대한화학회지
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    • 제43권6호
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    • pp.628-635
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    • 1999
  • 활성화된 $Mn(IV)O_2$를 이용하여 2,6-bis(hydroxymethyl)-4-methylphenol로부터 2,6-diformyl-p-cresol과 2-hydroxy-3-hydroxymethyl-5-methylbenzaldehyde를 제조하였다. 2-hydroxy-3-hydroxymethyl-5-methylbenzaldehyde와 ethylenediamine 및 1,3-diaminopropane의 축합반응에 의해 6-배위 칸막이 리간드, $H_4L[A]와\; H_4L[B]$를 각각 얻었다. methanol에서 2,6-diformyl-p-cresol과 1,2-diaminobenzene으로부터 부분적으로 환원된 거대고리, $H_4[20]DOTA$를 얻을 수 있었다. 이 $H_4[20]DOTA$와 lanthanide(IlI) nitrate 간의 반응 또는 methanol에서 주형과정(template procedure)에 의해 일핵 착물, $[Ln(IIl)(H_2[20]DOTA)(ClO_4)(H_2O)]\;{\cdot}\;3H_2O과\; [Ln([20]DOTA)(NO_3)(H_2O)](NO_3)_2\;{\cdot}\;xH_2O$를 각각 합성하였다. $[Ln([20]DOTA)(NO_3)(H_2O)](NO_3)_2\;{\cdot}\;xH_2O$를 2일 정도 methanol에 정치함으로써 얻은 $[Ln([20]DOTA)(NO_3)(CH_3OH)]^{2+}$에서 배위된 $CH_3OH$이 주게원자가 O인 보조리간드, $L_a$(=salicylic acid, p-chlorobenzoic acid, benzoic acid, acetic acid, 4-bromophenol)에 의해 치환될 때 평형상수 (K)를 25$^{\circ}C$, ${\mu}$=0.1M $NaClO_4$에서 분광학적 방법으로 결정하였다. 이 때 평형상수(K) 값들은 보조리간드 pKa 크기의 반대 경향인 salicylic acid>p-chlorobenzoic acid>benzoic acid>acetic acid>4-bromophenol 순서로 나타났다.

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Hydrothermal Synthesis of LaCO3OH and Ln3+-doped LaCO3OH Powders under Ambient Pressure and Their Transformation to La2O2CO3 and La2O3

  • Lee, Min-Ho;Jung, Woo-Sik
    • Bulletin of the Korean Chemical Society
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    • 제34권12호
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    • pp.3609-3614
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    • 2013
  • Orthorhombic and hexagonal lanthanum(III) hydroxycarbonate ($LaCO_3OH$) and $Ln^{3+}$-doped $LaCO_3OH$ ($LaCO_3OH:Ln^{3+}$, where Ln = Ce, Eu, Tb, and Ho) powders were prepared by a hydrothermal reaction under ambient pressure and characterized by thermogravimetry, powder X-ray diffraction, infrared and luminescence spectroscopy, and field-emission scanning electron microscopy. The polymorph of $LaCO_3OH$ depended on the reaction temperature, inorganic salt additive, species of $Ln^{3+}$ dopant, and solvent. The calcination of orthorhombic $LaCO_3OH:Ln^{3+}$ (2 mol %) powers at $600^{\circ}C$ yielded a mixture of hexagonal and monoclinic $La_2O_2CO_3:Ln^{3+}$ powders. The relative quantity of the latter increased with decreasing ionic radius of the $Ln^{3+}$ dopant ion and increasing doping concentrations. On the other hand, the calcination of hexagonal $LaCO_3OH:Ln^{3+}$ (2 mol %) powders at $600^{\circ}C$ resulted in a pure hexagonal $La_2O_2CO_3:Ln^{3+}$ powder, regardless of the species of $Ln^{3+}$ ions (Ln = Ce, Eu, and Tb). The luminescence spectra of $LaCO_3OH:Ln^{3+}$ and $La_2O_2CO_3:Ln^{3+}$ were measured to examine the effect of their polymorph on the spectra.

PE/$LN_2O$ 하이브리드 로켓 모터의 연소특성에 관한 연구 (A Study on the Combustion Characteristic in Hybrid Rocket Motor using PE/$LN_2O$)

  • 김기훈;이정표;김수종;조정태;김학철;우경진;성홍계;문희장;김진곤
    • 한국추진공학회:학술대회논문집
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    • 한국추진공학회 2009년도 춘계학술대회 논문집
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    • pp.233-236
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    • 2009
  • 산화제는 $LN_2O$, 고체연료는 HDPE(High Density PolyEthlene)를 사용하여 산화제의 상 및 연료포트 직경에 따른 하이브리드 로켓 모터의 연소특성을 비교 분석하였다. 불완전한 액적의 기화와 연료와 산화제의 혼합으로 인해 산화제로 $GN_2O$ 보다 $LN_2O$를 적용했을 때, 연소효율이 낮게 나타났다. O/F비에 따른 화염온도변화 및 끝 단면적에서의 연소반응으로 인해 $LN_2O$$GN_2O$를 사용하였을 경우 고체연료의 초기 포트 직경에 따른 후퇴율의 경향이 달리 나타났다.

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Synthesis and Structures of Two Lanthanide Complexes Containing a Mixed Ligand System: [Ln(Phen)2(L)3(HL)]·H2O [Ln = La, Ce: Phen = Phenanthroline: HL = Salicylic Acid]

  • Iravani, Effat;Nami, Navabeh;Nabizadeh, Fatemeh;Bayani, Elham;Neumuller, Bernhard
    • Bulletin of the Korean Chemical Society
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    • 제34권11호
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    • pp.3420-3424
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    • 2013
  • The reaction of $LnCl_3{\cdot}7H_2O$ [Ln = La (1), Ce (2)] with salicylic acid (HL) and 1,10-phenanthroline (Phen) at $20^{\circ}C$ in $H_2O$/ethanol gave after work-up and recrystallization two novel lanthanide complexes with general formula $[Ln(Phen)_2(L)_3(HL)]{\cdot}H_2O$. Compounds 1 and 2 were characterized by IR and UV-Vis spectroscopy, TGA, CHN as well as by X-ray analysis. According to these results, compounds 1 and 2 are isostructural and contain $Ln^{3+}$ ions with coordination number nine. Complexes 1 and 2 consist of two Phen, one neutral HL and three L anions (two L anions act as monodentate ligands and the third one is chelating to $Ln^{3+}$). Thermal decomposition led to primary loss of the Phen molecules. Then HL molecules and finally L moieties left the material to give $Ln_2O_3$.

R-P Phase $Ln_{1-x}Sr_{2-x}Mn_2O_7$(Ln=La, Pr, Gd, Eu, Er, Nd, Sm)의 합성 및 특성연구 (Syntheses and Characteristics of R-P Phase $Ln_{1-x}Sr_{2-x}Mn_2O_7$(Ln=La, Pr, Gd, Eu, Er, Nd, Sm))

  • 송민석;서상일;이재열
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 1999년도 춘계학술대회 논문집
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    • pp.337-340
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    • 1999
  • Since the first reports of CMR(colossal magnetoresistance) effects in some single crystal R-P Phase Ln$_{1-x}$ Sr$_{2-x}$Mn$_{2}$O$_{7}$ 1996. many researches have been carried out to find optimum compositions and processing conditions in this system. In this study, layered perovskite R-P Phase Ln$_{1-x}$ Sr$_{2-x}$Mn$_{2}$O$_{7}$ (x=0.4, Ln=-La, Eu, Gd, Nd, Pr, Sm) phases were synthesized by solid state reaction and their structures were refined by Rietveld method. Electrical and magnetic properties were measured drown to 20K and compare with those of R-P Phase Ln$_{1-x}$ Sr$_{2-x}$Mn$_{2}$O$_{7}$ Phases.es.es.es.es.es.

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$Ca_{2-X}-Ln_{x}MnO_{4}$상의 합성과 결정구조 정밀화 {Ln=Gd, Nd, Pr, Sm} (Syntheses and structure refinement of $Ln_{x}MnO_{4}$ {Ln=Gd, Nd, Pr, Sm})

  • 서상일;이재열
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2000년도 하계학술대회 논문집
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    • pp.726-729
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    • 2000
  • Though L $a_{1+x}$S $r_{2-x}$M $n_2$ $O_{7}$ n=2 R-P phases have been well known to have CMR effect, it was generally believed that n=1 phase was insulating. But recently monolayered perovskite $Ca_{2-x}$L $n_{x}$Mn $O_4$phase has been reported to show magnetoresistance. In this study, layered perovskite $Ca_{2-x}$L $n_{x}$Mn $O_4$ (x=0, 0.5, Ln=Pr, Nd, Sm, Gd) phases were synthesized by solid state reaction and their structures were refined by Rietveld method. The space groups of $Ca_2$Mn $O_4$, N $d_{0.5}$C $a_{1.5}$Mn $O_4$phases were refined as C2cb and Fmmm, respectively.y.ely.y.y.y.y.y.y.

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