• 대한의용생체공학회:의공학회지
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• 제25권5호
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• pp.383-389
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• 2004

본 연구에서는 치과용 티타늄(CP-Ti)과 Ti-25wt%Pd를 인산염계 실리카$.$알루미나 주형재로 주조 후 SEM/EDS, XRD, XPS를 이용하여 주조시 생성되는 표면반응생성물을 조사하였다. Ti-25wt%Pd는 CP-Ti에 비하여 융점이 현저이 감소하여 주조체의 표면반응이 상대적으로 적게 발생하였다. 또한 인산염계 실리카$.$알루미나 주형재를 소성한 결과 주형재는 $SiO_2$, $Al_2$ $O_3$, P$_2$ $O_{5}$, $Mg_3$(P $O_4$)$_2$, AlP $O_4$, $Mg_2$ $SiO_4$, MgAl$_2$ $O_4$의 성분들로 구성되어 있었으며, 표면반응생성물은 CP-Ti 주조체의 경우 $Ti_{5}$Si$_3$ 와 Ti $O_2$로, Ti-25wt%Pd 주조체의 경우 Ti $O_2$ 와 $SiO_{x}$ 로 구성되어 있었다.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2005년도 International Meeting on Information Displayvol.II
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• pp.1338-1342
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• 2005

We have synthesized an $Eu^{2+}$-activated $Sr_3MgSi_2O_8$ blue phosphor and $Ba_2SiO_4$ green phosphor and $Ba^{2+}$ co-doped $Sr_3SiO_5$ red phosphor investigated an attempt to develop white LEDs by combining it with a GaN blue LED $chip(\lambda_{em}=405 nm)$. Three distinct emission bands from the GaN-based LED and the $(Sr_3MgSi_2O_8:Eu\; +\; Ba_2SiO_4:Eu\; +\; Ba^{2+}\; co-doped\; Sr_3SiO_5:Eu)$ phosphor are clearly observed at 460nm, 520 nm and at around 600 nm, respectively. These three emission bands combine to give a spectrum that appears white to the naked eye. Our results show that GaN (405 nm chip)-based $(Sr_3MgSi_2O_8:Eu\; +\; Ba_2SiO_4:Eu\; +\; Ba^{2+}\; co-doped\; Sr_3SiO_5:Eu) exhibits a better luminous efficiency than that of the industrially available product InGaN (460 nm chip)-based YAG:Ce.

• 대한화학회지
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• 제43권2호
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• pp.206-212
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• 1999

본 연구의 목적은 기존의 $Zn_2SiO_4:Mn$형광체에 새로운 co-dopant를 첨가하여 발광특성을 향상시키는 것이다. co-dopant로서 선정한 Mg와 Cr이온들은 Zn자리를 치환하는 것으로 알려져 있으며 실제로 co-doping 시 각각 발광휘도와 decay time을 개선시키는 효과를 거두었다. $Zn_2SiO_4:Mn$에 Mg와 Cr이온들이 co-doping될 시에는 lattice 및 $Mn^{2+}$의 에너지 준위를 변화시키는 것으로 추정되어 발광휘도 및 decay time의 변화를 일으키는 것으로 해석된다. 특히 이 원소들은 발광과정에 긍정정인 영향을 끼쳐 Mg는 발광휘도를 중가시키고 Cr은 decay time을 감소시키는 결과를 얻었다. $Zn_2SiO_4:Mn,\;Mg$ 형광체의 발광휘도 개선은 DV-X${\alpha}$ embedded cluster 계산방법으로 설명할 수 있었고 반면에 $Zn_2SiO_4:Mn,\;Cr$ 형광체가 decay time을 줄이는 원인은 Mn이온과 Cr이온사이에 energy transfer가 일어나 발생되는 것으로 추정된다.

• 대한방사선기술학회지:방사선기술과학
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• 제20권1호
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• pp.65-69
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• 1997

[ $Mg_2SiO_4(La.Ho)$ ] thermoluminescent phosphor was made by putting the $MgCl_2.6H_2O$ and $SiO_2$ and by doping the rare earth element of $LaCl_3.7H_2O$ and $HoCl_3$. The heating rate is $10^{\circ}C/sec$ for the thermoluminescent phosphor. Two peaks are found in the measured $Mg_2SiO_4(La.Ho)$ Tl glow curve at $152^{\circ}C$ and $205^{\circ}C$ when the heating rate is $5^{\circ}C/sec$. The peak value at $205^{\circ}C$ is the most sensitive to X-ray among the glow peaks. The activation energy of the main peak has been estimated by the peak shape method. The estimated activation energies for Ho and La are $0.52{\sim}1.77\;eV$ respectively.

• 한국광물학회지
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• 제28권4호
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• pp.333-341
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• 2015

동아광산에서 채취한 암석 시료의 X-선 회절분석 결과 주 구성광물은 백운석(Dolomite : $CaMg(Co_3)_2$, 투각섬석(Tremolite : $Ca_2Mg_5Si_{18}O_{22}(OH)_2$), 활석(Talc : $Mg_3Si_4O_{10}(OH)_2$), 방해석(Calcite : $CaCO_3$)이며, 소량의 석영(Quartz : $SiO_2$)을 포함하고 있다. 편광현미경 관찰 결과 종횡비는 일반적으로 정의하는 3 : 1의 수치보다 높은 값을 나타내며 신장방향에 대한 소광각은 $8.0-19.5^{\circ}$의 범위로 사소광을 나타낸다. 주사전자현미경 관찰 결과 석면의 장경은 $5{\mu}m$ 이상이고 최대 $250{\mu}m$ 정도이며 종횡비는 3 : 1 정도이다. 암석시료에서 나타나는 석면결정은 벽개면을 따라 성장하고 있으며 결정의 끝부분이 침상형태를 나타낸다. 에너지분산분광분석결과 투각섬석이 주 구성광물인 시료는 대체로 Fe의 함량이 높게 나타난다.

• 공업화학
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• 제8권4호
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• pp.582-588
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• 1997

고체산 촉매인 헤테로폴리산 촉매를 이용하여 대기오염 방지를 위한 옥탄가 향상제인 TAME, ETBE 및 MTBE 합성반응에 대한 실험을 고정층 상압유통식 반응장치에서 수행하였다. 일반적으로 TAME, ETBE 및 MTBE 합성반응에서 헤테로폴리산에 hetero원자와 poly원자를 치환시켜 비교한 결과, 배위된 poly원자가 W, hetero원자가 Si인 $H_4SiW_{12}O_{40}$ 촉매의 활성이 가장 우수하였고, 또한 치환된 금속에 따라 촉매의 활성이 달랐으며 이는 촉매의 산성질과 관련이 있음을 알 수 있었다. 헤테로폴리산 촉매를 이용한 합성반응에서 TAME 경우는 $FeHPW_{12}O_{40}$과 $K_3PM_{o12}O_{40}$이 비교적 활성이 좋았으나, ETBE나 MTBE 경우에 비해서는 다소 활성이 낮았다. 그리하여 본 연구에서는 활성이 좋은 헤테로폴리산 촉매들을 선정하여 각각에 대하여 1:1로 다음과 같이 혼합하여 $H_4SiW_{12}O_{40}$ : $Sr_2SiW_{12}O_{40}$, $H_4SiW_{12}O_{40}$ : $NaH_2PW_{12}O_{40}$, $Fe_{1.5}PW_{12}O_{40}$ : $Mg_2SiW_{12}O_{40}$ 및 $Mg_2SiW_{12}O_{40}$ : $Ba_2SiW_{12}O_{40}$ 실험한 결과, 혼합촉매들이 각각의 단일성분 촉매때보다 TBA의 전화율과 ETBE나 MTBE의 선택율이 더욱 향상되었음을 알 수 있었다.

• 한국세라믹학회지
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• 제23권5호
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• pp.25-34
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• 1986

This study was to refined the crystal structure of solid solution to determine the position and amount of Al in diopside and to relate crystal structure changes and properties of solid solution. Single crystals of the solid solution in the system CaO.MgO.$2 SiO_2-Al_2O_3$ were made from the melt with slow cooling and used to refine the structure. The following were obtained. 1. Tetrahedra rotated around axis parallel to the direction which the angle 03-03-03 became small. 2. Tetrahedron became large and regular. Average T-O bond distance increased 0.53 percent. 3. M1 octahedron became small and average M1-O bond distance decreased 1.1 percent. 4, M2 polyhedron became small and average M2-O bond distance decreased 0.37 percent Polythedron was affected not so much compared with any cation site. 5. Distance between metal ions distances between T and oxygens which were coordinated with M2 and meighboring tetrahedron distances between M2 and oxygens which coordinated with M1 and M2 were not changed almost. 6. $Al^{3+}$ substituted 4Mg^{2+}$ and $Si^{4+}$

• 한국재료학회지
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• 제24권12호
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• pp.658-662
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• 2014

$Eu^{2+}/Dy^{3+}$-doped $Sr_2MgSi_2O_7$ powders were synthesized using a solid-state reaction method with flux ($NH_4Cl$). The broad photoluminescence (PL) excitation spectra of $Sr_2MgSi_2O_7:Eu^{2+}$ were assigned to the $4f^7-4f^65d$ transition of the $Eu^{2+}$ ions, showing strong intensities in the range of 375 to 425 nm. A single emission band was observed at 470 nm, which was the result of two overlapping subbands at 468 and 507 nm owing to Eu(I) and Eu(II) sites. The strongest emission intensity of $Sr_2MgSi_2O_7:Eu^{2+}$ was obtained at the Eu concentration of 3 mol%. This concentration quenching mechanism was attributable to dipole-dipole interaction. The $Ba^{2+}$ substitution for $Sr^{2+}$ caused a blue-shift of the emission band; this behavior was discussed by considering the differences in ionic size and covalence between $Ba^{2+}$ and $Sr^{2+}$. The effects of the Eu/Dy ratios on the phosphorescence of $Sr_2MgSi_2O_7:Eu^{2+}/Dy^{3+}$ were investigated by measuring the decay time; the longest afterglow was obtained for $0.01Eu^{2+}/0.03Dy^{3+}$.

• 한국세라믹학회지
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• 제23권1호
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• pp.51-59
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• 1986

It was the first time the MgO-C brick was developed for the lining materials in the hot spots in electric are furnace in 1972. MgO-C brick is high registant to thermal and structural spalling. Futhermore for the reason that carbon is hard to react with slag and MgO is high fireproof MgO-C brick shows a high corrosion registance to slag attack compared with conventional basic refractories. Owing to their excellent properties the use of MgO-C refractories are being developed widely in the field of shaped refractories and even in that of monolithic refractories. In this paper the oxidation of carbon the infiltration of slag into the brick texture and effects of additions were investigated. The results obtained were as follows : 1) The use of fused MgO-clinker and high purity carbon as raw materials increased the corosion registance and hot modulus of rupture of MgO-C brick. 2) As the oxidation reaction of the carbon proceeded the slag infiltrated into the brick texture. And then the slag components reacted with the MgO grains and formed low melting point compounds particulary CaO.MgO.$SiO_2$ and 3CaO.MgO.$2SiO_2$ that resulted in the wear of the brick. 3) It is recongnized the Al, Si, $B_3C$ effects on the oxidation registant properties of MgO-C brick by contribu-ting to the decrease of permeability according to the formation of $Al_4C_3$, SiC, $B_2O_3$ and the decrease of open pores relating to the formation of MgO.Al2O3, $SiO_2$, 3MgO.$B_2O_3$ at the decarbonized layer.

• 한국세라믹학회지
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• 제33권3호
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• pp.307-312
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• 1996

In following addition of 0.3, -0.6, 0.8, 1.0 and 5 weight percent MgSiF66H2O studies have been made of the setting and hardening characteristics of ordinary portland cement. MgSiF66H2O retarded the setting time of ordinary portland cement and extended the induction pariod of the hydration. In ordinary portland cement the setting characteristics were drastically altered especially at high MgSiF66H2O contents. Evidence was also obtained by the formation of a KSiF6 which was very fine particle. The results wee as follows. 1. Slump was slightly decreased when MgSiF66H2O added. 2. Setting time was retarded depending on the amount of retarding agent 2 to 8 hours 3. Compressive strength was almost same or some increased in comparision with opc. 4. When MgSiF66H2O was added to cement paste K2SiF6 were formed It was fine-sized distributed uniformly in cement grain and caused retardation of cement setting.