• 한국세라믹학회지
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• 제32권9호
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• pp.1085-1091
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• 1995

Molybdenum disilicide (MoSi2) was synthesized from Mo, MoO3, Si and Al powders by self-propagating high temperature synthesis (SHS). The effect of processing parameters such as Mo/MoO3 molar ratio, Ar gas pressure in the reactor and pressing pressure of compacts in synthesis of MoSi2 were investigated. h-MoSi2 was transformed into t-MoSi2 with increasing the Mo/MoO3 mole ratio, and only t-MoSi2 phase was identified above 3.5 : 1 (molar ratio). The synthesized phases did not change with the variation of Ar gas pressure and pressing pressure of compacts. It was found that the combustion temperature was above 2,50$0^{\circ}C$. The products were separated into MoSi2 (s) and $\alpha$-Al2O3 by the difference of their specific grativities. Bending strength, hardness and density of sintered specimen exhibited 82 MPa, 5.368 GPa and 5.43 g/㎤, respectively.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part2
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• pp.1149-1150
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• 2006

The oxidation of (W,Mo)$Si_2$ powders has been investigated at 400, 500 and $600^{\circ}C$ for 12.0 hours in air. It was shown that the low temperature oxidation resistance of (W,Mo)$Si_2$ was worse than that of $MoSi_2$, and they showed great changes in mass, volume and colour. Especialy at $500^{\circ}C$, the amount of volume expansion of (W,Mo)$Si_2$ was as high as about $7\sim8$ times and color changed from black to yellow after 4.0h with $MoO_3$, $WO_3$, (W,Mo)$O_3$ and amorphous $SiO_2$ as main reaction products. The mass gain and oxidation rate were relatively slower at $400^{\circ}C$ and $600^{\circ}C$ than that at $500^{\circ}C$.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2001년도 하계학술대회 논문집 C
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• pp.1405-1407
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• 2001

It was studied to prepare high temperature heating elements using molybdenum disilicide($MoSi_2$). Molybdenum disilicide is widely used as material for manufacturing high temperature heating elements. $MoSi_2$ heating elements could be used at 1700-1900$^{\circ}C$. However, it is relatively expensive, and its demand depends on import. $MoSi_2$ powders was mixed with 4-5wt% of montmorillonites type bentonite as plasticizer and a small amount of $Si_3N_4$, $ThO_2$, and B as additives to prepare specimen of heating elements. Then, it was extruded, dried, sintered and machined followed by heating test. Effects of sintering conditions and amount of additives were investigated, It was sintered effectively at 1,350$^{\circ}C$ for five hours. Electrical resistivity was decreased with increasing of sintering temperature and time, and related with apparent density of the specimens. It was linealy decreased with increasing of sintered density. The heating elements thus prepared was stable at 1700$^{\circ}C$ and the physical properties such as specific electrical resistivity, hardness, apparent density, thermal expansion coefficient, and bending strength were almost identical with those of commercial heating elements.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2001년도 하계학술대회 논문집
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• pp.605-608
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• 2001

Molybdenum disilicide is widely used for manufacturing high-temperature heating elements owing to its low electrical resistivity, good thermal conductivity, and ability to withstand oxidation at high temperatures. MoSi$_2$heating elements with 4-5wt% of montmorillonite type bentonite as plasticzer and a small amount of Si$_3$N$_4$, ThO$_2$, and B as additives was manufactured. Extruded rods of 3.7mmø and 6.7mmø diameter and 400mm long were fabricated using a vacuum extruder, which were then sinrered for 4-5 hrs. at the max. temperrature of 140$0^{\circ}C$. After 10 minute's oxidation treatment, the diameter of the rod is reduced. The heating elements thus prepared was stable at 1$700^{\circ}C$ and the physical properties such as specific electrical resistivity, hardness, apparent densisty, thermal expansion coefficient, and bending strength were almost identical with thoes of commercial heating elements. In this study we have tried to gain the practical knowledge of manufacturing MoSi$_2$heating elements so that it may be utilized later in a research of pilot scale and eventually be transferred to industry.

• 한국세라믹학회지
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• 제41권1호
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• pp.62-68
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• 2004

본 연구에서는 SHS 공정에 의하여 기공의 크기를 조절함으로서 전기저항 발열 특성을 가지는 다공성 $MoSi_2$를 제조하는 공정에 관하여 연구하였다. 결함이 억제된 다공질 재료를 제조하기 위하여 Si 함량 변화 및 예열 공정을 실시하였으며, 성형체 제조에 사용되는 Mo 분말의 크기 변화에 따른 가공 형성 거동에 대하여 연구하였다. 실험 결과 합성된 $MoSi_2$ 입자의 크기는 Mo 입자의 크기와는 관계없이 연소 합성시 발열되는 발열양에 의해 좌우되었으며, 기공의 크기는 Mo 입자의 크기에 따라 결정되었다. 또한 가공 경사 $MoSi_2$ 다공질 재료를 만들기 위하여 150-300${\mu}m$ Mo 분말과 4-5${\mu}m$ Mo 분말을 단계별로 5층으로 혼합하여 합성한 결과 거시적으로 순차적인 기공 크기 분포를 나타내었으며, 이를 통하여 포집 효율등이 우수한 다공성 발열체 재료의 제조가 가능하였다.

• 대한금속재료학회지
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• 제50권9호
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• pp.653-657
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• 2012

In this study, a molybdenum disilicide ($MoSi_2$) coating process was investigated by hydrogen reduction and Si-pack cementation. At first, the metallic Mo coating was carried out by hydrogen reduction of $MoO_3$ powder at $750^{\circ}C$ for various holding times (1, 2, 3 h) in hydrogen atmosphere. A $4.3{\mu}m$ thick metallic molybdenum thin film was formed at 3 h. $MoSi_2$ was obtained by Si-pack cementation on molybdenum thin film through hydrogen reduction processing. It was carried out using $Si:Al_2O_3:NH_4Cl=5:92:3$ (wt%) packs at $900^{\circ}C$ for various holding times (30, 60, 90 min) in Ar atmosphere. When the holding time was 90 min, a $MoSi_2$ layer was coated successfully and a $15.4{\mu}m$ thickness was observed.

• 한국세라믹학회지
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• 제31권12호
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• pp.1588-1598
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• 1994

The SiC/MoSi2 composite materials were fabricated by infiltrating the mixture of molybdenum disilicide and metal silicon(MoSi2+Si=100) to a porous compact of silicon carbide and graphite under the vacuum atmosphere of 10-1 torr. The specimen were oxidized in dry air under 1 atm at 130$0^{\circ}C$~150$0^{\circ}C$ for 240 hours. The oxidation behavior was evaluated by the weight gain and loss per unit area of the oxidized samples. Also, SEM and XRD analysis of the oxidized surface of the samples were carried out. With increasing the MoSi2 content and oxidation temperature, the passive oxidation was found. The trend of weight gain of all samples was followed the parabolic rate law with the formation of a protective layer of cristobalite on the surface.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part2
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• pp.1325-1326
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• 2006

Tungsten-molydiside $W_xMo_{1-x}Si_2$ was synthesized by self-propagating high temperature synthesis (SHS). The SHS product with the initial composition of (0.5Mo+0.5W+2Si) contains 23.9% $MoSi_2$, 40.89% $WSi_2$ with remaining 9.11% Mo, 9.16% Si and 16.94%W. Lattice parameters of the $MoSi_2$ and $WSi_2$ determined by Rietvelt analysis were a=0.3206 nm, c=0.7841 nm and a=0.3212 nm, c=0.7822 nm, respectively.

• 한국재료학회지
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• 제11권3호
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• pp.164-170
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• 2001

자전고온합성반응법을 이용하여 이규화 몰리브덴-텅스텐($Mo_{1-z}$ , $W_{z}$)$Si_2$을 합성하였다. 조성 (z)을 변화시켜 성형한 원통형 시편에 합성반응 중 전달되는 온도변화를 예측하기 위하여 시편의 중앙에 열전대를 삽입하였다. 반응 선단면이 열전대를 통과할 때 가장 높은 반응온도를 보이고 이것을 단열반응 온도라 간주하였다. 따라서 본 연구에서는 이러한 온도변화를 예측하기 위하여 자전조온합성반응의 모델링을 계시하고자 하였으며, 실험을 통하여 측정한 반응온도 분포곡선의 거동을 비교하였다. 각각의 시료에 대한 실험결과 측정된 반응속도는 약 2.14~1.35mm/sec, 반응온도는 1883K~1507K의 간을 보였다. 두 항 모두 텅스텐의 함량이 증가함에 따라 감소하는 경향을 나타냈으며, 수치해석을 통하여 거의 유사한 반응온도를 얻었다. 시료의 초기온도를 증가시킬 경우 반응온도는 증가함이 예측되었고, z=0.5인 시료에 대하여 반응온도가 1900k 이상이 되기 위해서는 약 800K-900K의 예열이 필요하였다.

• 폴리머
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• 제24권2호
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• pp.237-244
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• 2000

탄화 매트릭스의 전구체로 사용된 페놀수지에 세라믹 분말인 이규화몰리브덴 (MoSi$_2$)을 0, 4, 12, 20%의 중량비로 각각 고르게 분산시켜, 여기에 PAN계 탄소섬유를 함침하여 프리프레그법을 이용하여 일방향 탄소섬유/페놀수지 복합재료를 제조하였으며, 이를 다시 탄화(110$0^{\circ}C$) 시켜서 일방향 탄소/탄소 복합재료를 제작하였다. 본 연구에서는 난소/탄소 복합재료에 산화 억제제로 사용된 MoSi$_2$의 첨가량에 따른 복합재료의 산화거동을 산화분위기 하 600-100$0^{\circ}C$의 온도범위에서 조사하였다. 그 결과, MoSi$_2$를 함유한 탄소/탄소 복합재료는 복합재료 내치 기공 감소와 산소에 대한 유동 확산 방지막의 형성으로 인하여 카본 활성종이 방해를 받아 MoSi$_2$를 함유하지 않은 것에 비해 산화속도가 감소되어 내산화성이 향상되었다. 이는 산소의 공격에 대한 보호층을 형성하는 MoSi$_2$ 고유의 특성에 따른 영향이라 사료된다.