• Journal of the Korean Crystal Growth and Crystal Technology
• /
• v.25 no.6
• /
• pp.272-279
• /
• 2015

$Y_2O_3:Eu^{3+}$ is an excellent red-emitting phosphor, which has been widely used for display devices due to highly luminescent property and chemical stability. In this study, $Y_2O_3:Eu^{3+}$ red phosphors were prepared using the solid state reaction and RF thermal plasma synthesis. The particle size of $Y_2O_3:Eu^{3+}$ phosphors obtained by the solid state reaction varied from 10 to $20{\mu}m$, and 30~100 nanometer sized $Y_2O_3:Eu^{3+}$ particles were obtained from a liquid form of raw material through RF thermal plasma synthesis without an additional heat treatment. Photoluminescence measurements of the obtained $Y_2O_3:Eu^{3+}$ particles showed a red emission peak at 611 nm ($^5D_0{\rightarrow}^7F_2$). PL intensity of red nano phosphors prepared by RF thermal plasma synthesis was comparable to that of red phosphors prepared by the solid state reaction, indicating that nano-sized $Y_2O_3:Eu^{3+}$ red phosphors could be successfully synthesized using one-step process of RF thermal plasma.

• Journal of the Korean Mathematical Society
• /
• v.44 no.3
• /
• pp.499-509
• /
• 2007

Let m, n be positive integers or monic polynomials in $\mathbb{F}_q[T]$ with n|m. Let $K_m\;and\;K^+_m$ be the m-th cyclotomic field and its maximal real subfield, respectively. In this paper we define two matrices $D^+_{m,n}\;and\;D^-_{m,n}$ whose determinants give us the ratios $\frac{h(\mathcal{O}_{K^+_m})}{h(\mathcal{O}_{K^+_n})}$ and $\frac{h-(\mathcal{O}_K_m)}{h-(\mathcal{O}_K_n)}$ with some factors, respectively.

• Korean Journal of Materials Research
• /
• v.27 no.6
• /
• pp.339-344
• /
• 2017

A series of $CaNb_2O_6:Dy^{3+}$, $CaNb_2O_6$:$Eu^{3+}$ and $CaNb_2O_6:Dy^{3+}$, $Eu^{3+}$ phosphors were prepared by solid-state reaction process. The effects of activator ions on the structural, morphological and optical properties of the phosphor particles were investigated. XRD patterns showed that all the phosphors had an orthorhombic system with a main (131) diffraction peak. For the $Dy^{3+}$-doped $CaNb_2O_6$ phosphor powders, the excitation spectra consisted of one broad band centered at 267 nm in the range of 210-310 nm and three weak peaks; the main emission band showed an intense yellow band at 575 nm that corresponded to the $^4F_{9/2}{\rightarrow}^6H_{13/2}$ transition of $Dy^{3+}$ ions. For the $Eu^{3+}$-doped $CaNb_2O_6$ phosphor, the emission spectra under ultraviolet excitation at 263 nm exhibited one strong reddish-orange band centered at 612 nm and four weak bands at 536, 593, 650, and 705 nm. For the $Dy^{3+}$ and $Eu^{3+}$-codoped $CaNb_2O_6$ phosphor powders, blue and yellow emission bands due to the $^4F_{9/2}{\rightarrow}^6H_{15/2}$ and $^4F_{9/2}{\rightarrow}^6H_{13/2}$ transitions of $Dy^{3+}$ ions and a main reddish-orange emission line at 612 nm resulting from the $^5D_0{\rightarrow}^7F_2$ transition of $Eu^{3+}$ ions were observed. As the concentration of $Eu^{3+}$ ions increased from 1 mol% to 10 mol%, the intensities of the emissions due to $Dy^{3+}$ ions rapidly decreased, while those of the emission bands originating from the $Eu^{3+}$ ions gradually increased, reached maxima at 10 mol%, and then slightly decreased at 15 mol% of $Eu^{3+}$. These results indicate that white light emission can be achieved by modulating the concentrations of the $Eu^{3+}$ ions incorporated into the $Dy^{3+}$-doped $CaNb_2O_6$ host lattice.

• Korean Journal of Crystallography
• /
• v.6 no.1
• /
• pp.36-42
• /
• 1995

Two types of single crystals of the title compound [6-(2-pyridyl)-3, 5-hexadiyn-ol, PyHxD] were obtained by solution of n-hexane/CH2C12 and n-hexane/Et2O, and their molecular conformations are proved identical in spite of different of space groups; C22H18N2O2 (I), Mr=343.70, Monoclinic, Pa, a=14.595(2), b=5.413(2), c=12.218(2)Å, β=96.86(1)°, V=958.3Å3, Z=2, Dx=1.19 Mgm-3, λ(MoKα)=0.71069Å, μ=0.072mm-1, F(000)=360.0, T=292K, R=0.104 for 756 unique observed reflections. An asymmetric unit contains a dimer connected by two N-H…O intermolecular hydrogen bonds. C11H9NO (II), Mr=171.85, Monoclinic, P21/a, a=14.611(2), b=5.423(6), c=12.191(2)Å, β=96.89(1)°, V=959.0Å3, Z=4, Dx=1.19 Mgm-3, λ(MoKα)=0.71069Å, μ=0.072mm-1, F(000)=360.0, T=293K, R=0.066 for 824 unique observed reflection. The structural asymmetric unit contains a molecule, but two N-H…O hydrogen bonds related by controsymmetry make the molecules form a dimer. In both structure, the dihedral angle between the planar pyridyl ring and the plane defined by C(10)-C(11)-O connected by linear diyne chain is approximately normal, and the molecules are stacked along b-axis with the unit repeat of b-axis.

• Journal of Magnetics
• /
• v.1 no.1
• /
• pp.1-3
• /
• 1996

The $YBa_2Cu_3O_{7-x}$ structure has been fluorinated by a gas phase exchange technique. The ${^19}F$NMR (nuclear magnetic resonance) spin-lattice relaxation rate (1/T1) measurements on a fluorinated sample gave superconducting energy gap of $2\Delta=4.6kT_c$.

• Journal of Korean Society of Steel Construction
• /
• v.14 no.1
• /
• pp.95-104
• /
• 2002

In this paper, research for dynamic wheel loads of 3-D vehicle model considering tire enveloping model is carried out. Heavy trucks with 2-axles and 3-axles are modeled by 7-d.o.f. and 8-d.o.f., in which contact length of tire and pitching of tandem spring axles is considered. Dynamic equations of vehicle are derived by using the Lagrange's equation and solution of the equation is calculated by 5th Runge-Kutter method. The validity of the developed 3-D vehicle model is demonstrated by comparing the results obtained by the present method and experimental data by Whittemore. The maximum impact factors of tire force are calculated when vehicle models of 8ton and 15ton dump truck are running on the different class roads with 1.0km and on the various step bump.

• Proceedings of the Korean Society of Medical Physics Conference
• /
• 2003.09a
• /
• pp.42-42
• /
• 2003

목적 : 조사면 크기에 따른 금속쐐기와 가상쐐기에 의한 6 MV 와 15 MV 엑스선의 출력 및 상부와 하부 에 설치하는 금속쐐기의 출력을 비교하고자 한다. 대상 및 방법 : Varian Clinac21EX(미국)는 두부의 상부와 하부에 설치하는 각각의 금속쐐기와 제한기에 의한 가상쐐기 기능을 가지고 있다. 금속쐐기의 쐐기각은 네 가지 (15$^{\circ}$, 30$^{\circ}$, 45$^{\circ}$, 60$^{\circ}$)이며 투과력에 무관하게 한 쐐기각에 대한 쐐기는 사하부는 각 1 개이고, 가상쐐기는 일곱 가지 ($10^{\circ}$, 15$^{\circ}$, 20$^{\circ}$, 25$^{\circ}$, 30$^{\circ}$, 45$^{\circ}$, 60$^{\circ}$) 이다. 각 쐐기에 대하여 3$\times$3～20$\times$20 $\textrm{cm}^2$ 의 조사면 크기에서 6 및 15 MV 엑스선의 쐐기출력인수 (wedge field output factor)를 $d_{max}$와 10 $\textrm{cm}^2$ 깊이에서 측정하였다. 조사면크기와 측정깊이에 따른 쐐기출력인수의 변화추이를 관찰하였다. 쐐기출력인수 O $F_{Wdg}$는 다음과 같다. O $F_{Wdg}$(r)= $D_{Wdg}$(r)/ $D_{op}$ ( $r_{0}$) 여기서 $r_{0}$와 r은 각각 민조사면의 기준조사면크기, 쐐기조사면크기이다. 하부쐐기에 대한 상부쐐기의 출력인수의 상대적인 백분율 차이, %ROD=l00$\times$(O $F_{upWdg}$/O $F_{lowWdg}$ lowWdg/ - 1)를 구하였다. 조사면크기와 깊이에 따른 %ROD의 변화추이를 평가하였으며 쐐기 각각에 대하여 출력인수를 측정해야하는지 평가하였다. 결과 : 금속쐐기에 대한 쐐기출력인수는 방사선의 투과력과 깊이에 관계없이 조사면 크기가 커짐에 따라 증가하였으나 가상쐐기의 쐐기출력인수는 쐐기각이 작은 경우에는 조사면크기가 커짐에 따라 증가하다가 감소하였으며 최대값을 보이는 조사면크기는 쐐기각이 커짐에 반하여 감소하였으며 투과력에 관계없이 60。 쐐기에 대해서는 조사면 크기가 4 cm(A/P=1) 이상에서 조사면크기가 커짐에 따라 감소하였다. 6 MV 엑스선 에 대한 10 cm 깊이에서 15。 쐐기와 15 MV 엑스선에 대한 10 cm 깊이에서 45。 쐐기의 A/P 가 1.5보다 작은 조사면을 제외하고는 조사면의 크기가 커짐에 따라 %ROD는 감소하였다. $d_{max}$에서는 15。 쐐기와 30。 쐐기에 대해서는 %ROD가 음수였으며 절대값이 증가하였다. 이는 곧 조사면의 크기가 커짐에 따라 상부쐐기의 쐐기출력계수가 하부쐐기와 접근하고 드디어는 상부쐐기의 출력인수가 하부쐐기의 출력인수보다 작아질 수도 있다는 것을 의미하고 있다. 또한 %ROD 는 쐐기각이 클수록 변화가 컸으며, 조사면 크기가 커짐에 따라 10 cm 깊이에서보다 $d_{max}$에서 더 급하게 감소하였다. %ROD 는 6 MV 엑스선에 대해서는 -0.52～4.18 % 였고, 15 MV 엑스선에 대해서는 -0.44-4.18 % 였다. 결론 : 두 가지 투과력의 엑스선이 방출되는 선형가속기의 상하부 쐐기와 가상쐐기의 출력인수를 측정하여 비교하였다. 결과에서 얻어진 결론은 아래와 같다. 1. 조사면의 크기가 커짐에 따라 금속쐐기의 출력계수 는 증가하였으나 가상쐐기의 경우는 증가하다가 감소하거나 큰 쐐기각에 대해서는 감소만 하였다. 2. 상부쐐 기와 하부쐐기는 쐐기출력인수가 4% 이상 차이가 날 수 있으므로 독립적으로 측정하여 이용하여야 할 것이다.것이다.다.

• Journal of the Korean Electrochemical Society
• /
• v.16 no.3
• /
• pp.184-189
• /
• 2013

$Ba_2SiO_4:Eu^{2+}$ ($B_2S:Eu^{2+}$) powders were prepared by firing the dry gel obtained by the sol-gel and the hybrid process (sol-gel and combustion), respectively, and their structure and luminescence were investigated. Tetraethyl orthosilicate (TEOS) was used as a Si source. The phase transition was observed with the TEOS content. With 1.2M TEOS, the powders prepared by the sol-gel process without prior calcination were composed of the $B_2S:Eu^{2+}$ single phase, whereas those by the sol-gel and the hybrid process with prior calcination consisted of the dominant $B_2S:Eu^{2+}$ and minor $BaSiO_3:Eu^{2+}$ ($BS:Eu^{2+}$) phases and their emission intensities were approximately two times higher than those without prior calcination. The hybrid process could reduce the process time innovatively compared to the sol-gel process, even though the former was a little inferior to the latter in the emission intensity of $B_2S:Eu^{2+}$. With 1.1M TEOS, the $B_2S:Eu^{2+}$ single phase was obtained by the hybrid process, and its green emission was observed at 505 nm originated from the $4f^65d^1{\rightarrow}4f^7$ transition of $Eu^{2+}$ ions.

• Journal of the Korean Crystal Growth and Crystal Technology
• /
• v.17 no.4
• /
• pp.156-159
• /
• 2007

The red emission properties of $Mn^{4+}$ doped $SrAl_{12}O_{19}$ prepared by the solid-state reaction was investigated, in order to verify its potential to act as the red emitting phosphor of white LEDs. The emission spectrum exhibits a narrow band between $600{\sim}700 nm $ with four sharp peaks occurring at about 643, 656, 666, 671 nm due to the $^2E\to^4A_2$ transition of $Mn^{4+}$. The excitation spectrum exhibits a broad band between $200{\sim}500 nm$ with three peaks occurring at about 338, 398 and 468 nm, respectively. Moreover, the relative emission intensity of $SrAl_{12}O_{19}:Mn^{4+}$ with or without $CaF_2$ and MgO fluxes measured at excitation source 390 nm. The relative emission intensity of $SrAl_{12}O_{19}:Mn^{4+}$ containing 0.67mol% MgO was approximately 30% higher than that of the base composition sample. Strontium hexa-aluminate measured at room temperature as a function of the substituted Mg concentration. MgO was added to replace part of the $Al_2O_3$. Also, the relative emission intensity of $SrAl_{12}O_{19}:Mn^{4+}$ containing 0.67 mol% MgO and 0.67 mol% $CaF_2$ was approximately about 48% higher than that of the base composition $SrAl_{12}O_{19}:Mn^{4+}$.

• Mycobiology
• /
• v.51 no.3
• /
• pp.148-156
• /
• 2023

Penicillium oxalicum strain can be isolated from the Bletilla striata (Thunb.) Reichb. f. tubers. Its solid-state fermentation products are concentrated by percolation extraction. Separation and purification have been conducted to the ethyl acetate extracts by preparative HPLC. Based on the use of spectrometry, we have determined 17 known compounds, 12,13-dihydroxy-fumitremorgin C (1), pseurotin A (2), tyrosol (3), cyclo-(L-Pro-L-Val) (4), cis-4-hydroxy-8-O-methylmellein (5), uracil (6), cyclo-(L-Pro-L-Ala) (7), 1,2,3,4-tetrahydro-4-hydroxy-4-quinolin carboxylic acid (8), cyclo-(Gly-L-Pro) (9), 2'-deoxyuridine (10), 1-(b-D-ribofuranosyl)thymine (11), cyclo-(L-Val-Gly) (12), 2'-deoxythymidine (13), cyclo-(Gly-D-Phe) (14), cyclo-L-(4-hydroxyprolinyl)-D-leucine (15), cyclo-(L)-4-hydroxy-Pro-(L)-Phe (16), uridine (17). Here, we report compounds 1-3, 5, 7-8, 11-12, 14-17 are first found and isolated from this endophyte.