• 한국세라믹학회지
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• 제33권11호
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• pp.1209-1216
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• 1996

MoSi2-Al2O3 composites were prepared by thermal explosion mode of self-propagating high temperature syn-thesis (SHS) using element powders of MoO3 Mo Si and Al. The combustion products of MoSi2 which have 10, 20, 30 and 40 wt% Al2O3 showed the molten state in the range of Mo to MoO3 6:1-9.5:1, 2:1-8:1, 1:1-5:1, and 1:1-3:1 (molar ratio) respectively. The combustion products which made least seperation the molten phase from the slag phase were in Mo/MoO3=9, 5:1, 8:1, 5:1 and 3:1 (molar ratio) respectively. Particles size of MoSi2 and Al2O3 in the combustion product were decreased as the molar ratio of Mo to MoO3 increase. By XRD analysis only MoSi2 and $\alpha$-Al2O3 peaks were identified in the combusion products, In case of MoSi2 containing 20wt% Al2O3 5.1wt% Al existed into MoSi2 grains and 30.7wt% Si and 7.7wt% Mo existed into Al2O3 grains. The relative density of MoSi2 containing 10, 20, 30 and 40 wt% Al2O3 were 82.7, 85.2, and 81.9% respectively. The fracture strength of MoSi2-Al2O3 composites increased with increasing Al2O3 and that of MoSi2-20wt% Al2O3 composite was 195 MPa.

• 공업화학
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• 제9권6호
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• pp.878-883
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• 1998

Pd-ZSM-5 촉매 상에서 메탄의 연소반응을 수행하였다. 담체는 저온상압법으로 합성한 ZSM-5를 이용하였다. 담체인 ZSM-5의 $SiO_2/Al_2O_3$ 몰비 변화에 따른 메탄의 전환율 변화를 조사해 보았다. 그리고 합성한 Pd-ZSM-5 촉매의 메탄 전환율을 상업화된 Pd-ZSM-5(PQ Co.) 및 $PdO/{\gamma}-Al_2O_3$와 비교하여 보았다. $SiO_2/Al_2O_3$ 몰비 변화에 따른 메탄의 연소반응실험 결과 $SiO_2/Al_2O_3$ 몰비가 작을수록 높은 메탄의 전환율을 보였으며, Pd을 정량화시켜 메탄의 연소속도를 비교한 결과, 역시 $SiO_2/Al_2O_3$ 몰비가 작을수록 빠르게 나타났다. 합성한 Pd-ZSM-5가 상업화된 Pd-ZSM-5(PQ Co.)보다 우수한 메탄 전환율을 나타냈다. 촉매 특성 분석 결과들로부터 메탄의 연소반응에서 촉매에 흡착하는 산소의 결합세기가 반응속도에 매우 큰 영향을 미침을 알 수 있었다.

• 한국재료학회지
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• 제12권1호
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• pp.48-53
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• 2002

$Al_2O_3-SiC$ and $Al_2O_3-SiC$-TiC composite powders were prepared by SHS process using $SiO_2,\;TiO_2$, Al and C as raw materials. Aluminum powder was used as reducing agent of $SiO_2,\;TiO_2$ and activated charcoal was used as carbon source. In the preparations of $Al_2O_3-SiC$, the effect of the molar ratio in raw materials, compaction pressure, preheating temperature and atmosphere were investigated. The most important variable affecting the synthesis of $Al_2O_3-SiC$ was the molar ratio of carbon. Unreactants remained in the product among all conditions without compaction. The optimum condition in this reaction was $SiO_2$: Al: C=3: 5: 5.5, 80MPa compaction pressure under Preheating of $400^{\circ}C$ with Ar atmosphere. However there remains cabon in the optimum condition. The effect of $TiO_2$ as additive was investigated in the preparations of $Al_2O_3-SiC$. As a result of $TiO_2$ addition, $Al_2O_3-SiC$-TiC composite powder was prepared. The $Al_2O_3$ powder showed an angular type with 8 to $15{\mu}m$, and the particle size of SiC powder were 5~$10{\mu}m$ and TiC powder were 2 to $5{\mu}m$.

• Nuclear Engineering and Technology
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• 제53권12호
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• pp.3952-3965
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• 2021

In this study, volcanic ash was used as raw material to prepare waste forms with different silicon/aluminum (Si/Al) molar ratios to immobilize sodium-salt waste (SSW) containing simulated ¹³⁷Cs. Effects of Si/Al molar ratios (3:1 and 2:1) and sodium salts on sintering behavior of waste forms and immobilization mechanism of Cs⁺ were investigated. Results indicated that the main mineral phase of sintered waste-form matrixes was albite, and the formation of major phases was found to depend on Si/Al molar ratios. Si/Al molar ratio of 2 was favorable for the formation of pollucite, and the formation and crystallization of mineral phases were also decided based on physicochemical characteristics of sodium salts. Furthermore, product consistency test results indicated that the immobilization of Cs⁺ was related to Si/Al molar ratio, types of sodium salts, and glassy phase. Waste forms with Si/Al molar ratio of 2 exhibited better ability to immobilize Cs⁺, whereas the influence of sodium salts and glassy phases on the immobilization of SSW showed more complicated relationship. In waste forms with Si/Al molar ratio of 2, Cs⁺ leaching concentrations of samples containing Na₂B₄O₇·10H₂O and NaOH were low. Na₂B₄O₇·10H₂O easily transformed into liquid phase during sintering to consequently achieve low temperature liquid-phase sintering, which is beneficial to avoid the volatilization of Cs⁺ at high temperature. Results clearly reveal that waste forms with Si/Al molar ratio of 2 and containing Na₂B₄O₇·10H₂O show excellent immobilization of Cs⁺.

• 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.

• 한국세라믹학회지
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• 제30권2호
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• pp.123-130
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• 1993

Dispersed type Al2O3-SiC composite powders were synthesized from Al-isopropoxide (Al(i-OC3H7)3) and Si(OC2H5)4 precursors by hydrolysis of mixed alkoxides and carbothermal reaction method. The characteristics of the synthesized (dispersed type) Al2O3-SiC composite powders were investigated using XRD, SEM, TEM, BET and particle size analyzer. Carbothermal reaction to produce Al2O3-SiC composite was completed in 10h at 135$0^{\circ}C$ on 3~4㎤/s (0.21~0.28cm/s) of H2 flow rate and about 1/1 of carbon/oxides(=SiO2＋Al2O3) molar ratio. The synthesized powders were observed to have the mean particle size range of 0.4~1.26${\mu}{\textrm}{m}$ and showed finer particle size with increasing SiC content.

• 한국재료학회지
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• 제9권8호
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• pp.817-824
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• 1999

$Al_2$$O_3$-SiC 화합물 분말이 $SiO_2$, A1 그리고 C 분말들을 원료분말로 하여 SHS(self-propagating High-temperature Synthesis)법에 의해 제조되었다. 원료 분말에서의 몰비, 성형압력, 반응물의 초기온도의 영향이 생성물과 연소과정에 대해 연구되었다. $SiO_2$/A1/C계의 자전연소합성은 낮은 연소온도 때문에 $400^{\circ}C$ 이상으로 예열되어야 한다. 연소반응의 결과로서 최종생성물의 순도는 반응물의 순도보다 높았다. 이 계에서 $SiO_2$:Al:C의 적당한 몰비는 3.0:4.0:6.0이었고, free carbon은 30min 동안 $650^{\circ}C$에서 배소함으로써 제거되었다. 본 연구에서 상압소결은 $1700^{\circ}C$에서 powder bed를 사용한 표본의 분해를 제어하고 치밀한 소결체를 얻는데 매우 효과적이었다. hot-pressing으로 생성된 소결체는 이론비교밀도의 약 98%이었다.

• Korean Chemical Engineering Research
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• 제56권4호
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• pp.600-606
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• 2018

다양한 Si/Al 몰비를 지닌 MTT 제올라이트를 합성하여 methanol-to-olefin(MTO) 반응에서 촉매의 산성도가 미치는 영향을 조사하였다. Si/Al 몰비를 조절하기 위해 N,N,N',N'-테트라메틸-1,3-디아미노프로판을 구조유도물질(SDA)로 사용하였으며, 알루민산나트륨의 함량을 달리하여 $20SiO_2$ : 30SDA : x (=0.25~1.25)$NaAlO_2$ : 2NaOH : $624H_2O$ 조성으로 모액을 제조한 후 433 K에서 4일 동안 수열 합성하였다. 알루민산나트륨의 함량이 감소함에 따라 MTT 제올라이트의 입자 크기가 증가하였으며 또한 산점의 양도 감소하였다. 제조한 MTT 제올라이트의 촉매 활성을 평가하기 위해 673 K에서 공간속도(WHSV)가 $1.2h^{-1}$인 조건으로 MTO 반응을 수행한 결과, Si/Al 몰비가 24인 H-MTT (1.00Al) 촉매가 900분까지 90% 이상의 전환율을 유지함을 확인하였다.

• Korean Chemical Engineering Research
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• 제59권2호
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• pp.281-295
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• 2021

Si/(Si + Al) 몰비를 30 몰%까지 변화시켜 제조한 SiO2-Al2O3 복합 산화물(SA) 상에 니켈을 함침법으로 제조한 촉매 상에서 에탄올의 아민화반응에 미치는 영향을 연구하였다. 제조된 촉매의 물리·화학적 특성을 알아보기 위하여 X-선 회절분석(XRD), N2 흡착분석, 이소프로판올 승온탈착(IPA-TPD), 에탄올 승온탈착(EtOH-TPD), 수소 승온환원(H2-TPR), H2 화학흡착, 투과전자현미경(TEM) 분석을 수행하였다. SA 복합 산화물 상에서 Si/(Si + Al) = 30 몰%가 될 때까지 지속적으로 산점이 증가하였다. 담지된 Ni 금속의 분산도, 비표면적 및 산 특성 등이 촉매 반응활성에 복합적으로 영향을 미쳤다. 산점 증가와 니켈 산화물의 낮은 환원 온도는 아세토니트릴 생성에 유리하게 작용하는 것으로 사료된다. 에탄올의 전환율 측면에서는 10 wt% Ni이 담지된 Si/(Si + Al) = 10 몰% 촉매가 가장 높은 전환율을 보였으며 이를 기준으로 화산형 형태를 나타냈고, Ni 금속 분산도와 경향이 일치했다.

• 한국세라믹학회지
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• 제31권12호
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• pp.1570-1576
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• 1994

Effect of Na2O/SiO2 molar ratio, calcining temperature and addition of NaCl were investigated on the hydrothermal formation of X-type zeolite from the natural mordenite, which is a kind of rock deposited abundantly in kuryong po. Pulverized mordenite was first mixed with NaOH or NaOH-NaCl solution, and crystallized under hydrothermal condition at 90~10$0^{\circ}C$ for 10 hrs. Optimum condition for synthesis of the X-type zeolite were \circled1 the ratio Na2O/SiO2, NaCl/Al2O3 and H2O/Na2O:0.68, 11.4 and 40, respectively, \circled2 calcining temperature of starting materials: 90$0^{\circ}C$, \circled3 aging time: 48 hrs. and \circled4 crystallization temperature: 10$0^{\circ}C$. The yield of X-type zeolite under the optimum condition was about 55~60%, and the major crystallized X-type zeolite was faujasite phase. Zeolite of then type X was crystallized when NaCl was added to treating solution with in the limit 14.25 of NaCl/Al2O3 molar ratio. As the calcination temperature (from 50$0^{\circ}C$ to 95$0^{\circ}C$) of starting materials increases, yield of zeolite x increase.