• 공업화학
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• 제7권5호
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• pp.861-868
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• 1996

n-butene의 i-butene으로의 골격 이성질화 반응은 발열반응으로서 열역학적으로 저온($100^{\circ}C{\sim}150^{\circ}C$)에서 최고수율을 나타내며 반응 mechanism은 carbonium ion의 형성과 methyl기의 골격치환에 따른 2step으로 규정된다. 산처리되어 강산점을 가지는 zeolite, alumina와 비교하여, $Pt/MoO_3/SiO_2$ 촉매 사용시 $110^{\circ}C$ 등온 환원반응 실험으로 설명되는 Proton의 증가된 표면 이동 속도는 골격 이성질화 반응시 carbonium ion의 형성을 빠르게 촉진시킬 수 있으며, 이에 따라 $110^{\circ}C$에서 1-butene의 수율은 최대치로 나타나며 부산물은 생성되지 않는다. $110^{\circ}C$에서의 등온 환원반응에서 $Pt/MoO_3/SiO_2$가 $Pt/MoO_3/Al_2O_3$보다 높은 proton spillover 속도를 보이지만 약 90분 경과한 $MoO_3$ 표면의 proton 포화상태에서는 i-butene의 반응수율이 같고, $MoO_3$가 없는 zeolite, $Pt/SiO_2$보다 높은 전환율을 보이므로 proton spillover에 의한 carbonium ion의 생성이 반응속도를 조절하는 것으로 나타난다. $Pt/MoO_3/SiO_2$에서 산점의 증가, Pt 및 $MoO_3$ 함량의 증감은 i-butene 수율에 영향을 미치지 않으며, 이는 proton spillover에 의한 Pt 표면위의 carbonium ion의 형성이 속도 결정 단계이기 때문인 것으로 사료된다.

• Bulletin of the Korean Chemical Society
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• 제26권4호
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• pp.614-618
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• 2005

The complex of the composition LaL(N$O_3)_3\;(H_2O)_2$ is prepared by the reaction of La($NO_3)_3{\cdot}6H_2O$ with Nethylmorpholine in aqueous medium. The ligand is involved in the complex as a neutral species where the chelation occurs via the oxygen of the ligand moiety and the nitrate groups as bidentate ligand. The chemical structure of the studied complex is confirmed through IR, XRD, and thermal analysis data. The complexation equilibria of La(III) with N-ethylmopholine is studied in aqueous medium at ionic strength I = 0.1 mol${\cdot}dm^{-3}\;KNO_3$ and at 25, 35 and 45 ${^{\circ}C}$, respectively. The thermodynamic parameters $\Delta$G, $\Delta$H and $\Delta$S values were calculated to prove the association with the complex formation. It is clearly observed that the process is accompanied by absorption of heat, i.e. endothermic process, while the entropy does not change greatly attributed to the release of constant number of water molecules during chelate formation.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2012년도 춘계학술발표회 논문집
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• pp.167-168
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• 2012

Films of CrN, $Cr_{40}Zr_9N$, and $Cr_{31}Zr_{16}N$ were deposited on a steel substrate by closed field unbalanced magnetron sputtering, and their oxidation behaviors at $700^{\circ}C$ and $800^{\circ}C$ for up to 60h in air were investigated. All the deposited films were composed of the CrN phase. Zirconium atoms in $Cr_{40}Zr_9N$ and $Cr_{31}Zr_{16}N$ films partially dissolved in the CrN phase. They advantageously refined the columnar structure, reduced the surface roughness, and increased the microhardness. The CrN film displayed relatively good oxidation resistance, owing to the formation of the highly protective $Cr_2O_3$ on its surface. The $Cr_{40}Zr_9N$ and $Cr_{31}Zr_{16}N$ films oxidized to $Cr_2O_3$ as the major phase and ${\alpha}-ZrO_2$ as the minor one. They oxidized primarily by the inward transport of oxygen. The addition of Zr could not increase the oxidation resistance of the CrN film, because the formed $ZrO_2$ that was intermixed in the $Cr_2O_3$-rich oxide layer was oxygen permeable, and developed the compressive stress in the oxide scale owing to the volume expansion during its formation.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2013년도 춘계학술대회 논문집
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• pp.53-54
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• 2013

Nano-multilayered CrAlSiN films consisting of crystalline CrN nanolayers and amorphous AlSiN nanolayers were deposited by cathodic arc plasma deposition. Their oxidation characteristics were studied between 600 and $1000^{\circ}C$ for up to 70 h in air. During their oxidation, the amorphous AlSiN nanolayers crystallized. The formed oxides consisted primarily of $Cr_2O_3$, ${\alpha}-Al_2O_3$, $SiO_2$. The outer $Al_2O_3$ layer formed by outward diffusion of Al ions. Simultaneously, an inner ($Al_2O_3$, $Cr_2O_3$)-mixed layer formed by the inward diffusion of oxygen ions. $SiO_2$ was present mainly in the lower part of the oxide layer due to its immobility. The CrAlSiN films displayed good oxidation resistance, owing to the formation of oxide crystallites of $Cr_2O_3$, ${\alpha}-Al_2O_3$, and amorphous $SiO_2$.

• 한국재료학회지
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• 제14권11호
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• pp.780-785
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• 2004

The degradation mechanism of soft magnetic properties of $Fe-Hf-N/Cr/SiO_2$ thin films reacted with a bonding glass was investigated. When $Fe-Hf-N/Cr/SiO_2$ films were annealed under $600^{\circ}C$ without the bonding glass, the compositions and the soft magnetic properties of Fe-Hf-N layers were not changed. However, after reaction with the bonding glass at $550^{\circ}C$, the soft magnetic properties of the film were degraded. At $600^{\circ}C$, the saturation magnetization of the reacted film decreased to 13.5 kG, and its coercivity increased to 4 Oe, and its effective permeability decreased to 700. It was founded that O diffused from the glass into the Fe-Hf-N layers during the reaction and generated $HfO_2$ phases. It was considered that the soft magnetic properties of the $Fe-Hf-N/Cr/SiO_2$ films reacted with the bonding glass were primarily degraded by the formation of the Fe-Hf-O-N layer of which the Fe content was below 60 $at\%$, and secondarily degraded by the Fe-Hf-O-N layer above 70 $at\%$.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2011년도 춘계학술대회 및 Fine pattern PCB 표면 처리 기술 워크샵
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• pp.33-35
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• 2011

Films of CrAlN and CrZrN were deposited on a steel substrate by closed field unbalanced magnetron sputtering, and their oxidation behaviors were investigated. CrAlN films consisted of dense, polycrystalline CrN and AlN fine columns. The formed oxides consisted primarily of crystalline $Cr_2O_3$ incorporated with $Al_2O_3$. The oxide layers were thin and compact so as to make CrAlN films more protective than CrN films. In case of CrZrN films, Zr atoms were dissolved in the CrN phase. Zr atoms advantageously refined the columnar structure, reduced the surface roughness, and increased the micro-hardness. However, the addition of Zr did not increased oxidation resistance, mainly because Zr was not a protective element. All the deposited films displayed relatively good oxidation resistance, owing to the formation of the highly protective $Cr_2O_3$ on their surface. The $Cr_{40}Zr_9N$ and $Cr_{31}Zr_{16}N$ films oxidized to $Cr_2O_3$ as the major phase and ${\alpha}-ZrO_2$ as the minor one, whereas the CrN film oxidized to $Cr_2O_3$.

• 한국세라믹학회지
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• 제29권6호
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• pp.471-479
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• 1992

AlN powder was synthesized by carbothermal reduction and nitridation using Al2(SO4)3.18H2O as the starting material. The synthesized AlN powder was fine but contained oxygen. Therefore carbonaceous material (carbon black or phenol novolac) was added teogether with the sintering aids (CaO, CaF2, CaCl2, Y2O3 and YF3). It was found that pressureless sintering at 1700~180$0^{\circ}C$ after deoxidation at 150$0^{\circ}C$ suppressed the formation of second phase (27R) and reduced the contents of lattice oxygen within AlN ceramics.

• 한국진공학회지
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• 제1권1호
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• pp.183-189
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• 1992

텅스텐 실리사이드를 축적전극으로 하는 얇은 N/O(SiO2/Si3N4) 구조막의 특성을 다 결성 실리콘의 경우와 비교 평가하였다. 누설전류 및 항복전압이 향상되었고 축적용량은 감 소하였다. 용량 감소의 원인중의 하나는 텅스텐 실리사이드 상의 산화막 성장률이 다결성 실리콘 위에서 보다 빠른 것이고 둘째는 열처리에 따라 다결정 실리콘 내 도판트 불순물이 텅스텐 실리사이드를 통하여 외향확산하여 다결정 실리콘 내에 공핍층을 형성하게 되고 공 핍층 용량으로 인하여 축적용량이 감소하게 된다.

• 자원환경지질
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• 제14권2호
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• pp.55-76
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• 1981

Southwestern contact zone of the Boeun granodiorite occurs near the thrust fault between the Ogcheon Group and Majeonri Limestone Formation. Ogcheon Group, metasediments composed of the Munjuri Formation, Changri Formation, and unconformably overlying Hwanggangri Formation, belongs to greenschist facies of regional metamorphism accompanied with deformation of two fold axes, $N10^{\circ}E$ and $N45-65^{\circ}E$ directions. Basic metamorphic rocks occurring in the Changri and Limestone Formations are the meta-basalts and meta-diabases of tholeiitic basalt series. The meta-basalts intruded in the Changri Formation as sills, whereas the meta-diabases in the Changri and Limestone Formations as stocks in appearance. They are considered to have emplaced before the formation of two fold axes and related with the thrust fault, based on the geologic setting of the area. The metamorphic facies are identified to be greenschist facies to epidote-amphibolite facies for the meta-basalt, and epidote-amphibolite facies for the meta-diabases. It is interpreted that such a variety of facies was related from the combination of earlier deuteric alteration and later regional metamorphism. The metasediments in southwestern contact zont of the Boeun granodiorite which is a product of later syntectonic intrusion of middle Jurassic in age, show pyroxene-hornfels facies near the contact and amphibole-horenfels facies away from the contact to the mineral zoning in the contact metamorphic aureole of the Limestone Formation, based on the paragenetic analysis of mineral assemblages. The Limestone in the area appears to be considerably $SiO_2-CaO-MgO-CO_2-H_2O$ can be adopted to evaluate equilibrium conditions of the mineral assemblages in each mineral zone. It is revealed that a temperature gradient was existed accross the contact aureole ranging from the higher igneous side to lower sedimentary side, whereas no clear trend of $XCO_2$ variation appears but high mole fraction. The tremolite diopside-quartz-calcite assemblages occurs in common through the most mineral zones of contact aureole that is in good agreement with the equivalent reaction curve which extends over a wide range of $T-XCO_2$ conditions.

• 해양환경안전학회지
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• 제21권2호
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• pp.188-193
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• 2015

일반적으로 선박용 디젤엔진의 아산화질소($N_2O$)배출률은 이산화황($SO_2$)배출률과 밀접한 상관성을 갖고 있고, 선박에서 사용되는 연료의 다양성은 $N_2O$배출특성에 영향을 미친다고 받아들여져 왔다. 최근의 연구보고에 의하면 연료 연소에서 발생한 충분한 일산화질소(NO)가 존재할 경우, 배기의 $SO_2$배출률이 $N_2O$생성에 미치는 영향은 NO의 영향보다 막대하게 크다. 그러므로 $SO_2$성분으로부터 기인하는 $N_2O$생성은 NOx저감을 위한 배기가스 재순환(EGR) 시스템에서 중요한 인자로 작용한다. 본 실험적인 연구의 목적은 $SO_2$유량 증가를 갖는 디젤엔진의 흡기가 배기의 $N_2O$배출률에 미치는 영향에 대하여 조사하는 것이다. 실험에 사용된 테스트 엔진은 2600rpm에서 12kW의 출력을 갖는 4행정 직접분사식 디젤엔진이고, 운전조건은 75% 부하에서 실시되었다. 0.499%($m^3/m^3$)의 $SO_2$표준가스는 흡기의 $SO_2$농도를 변화시키기 위해 사용되었다. 결과적으로 황 성분을 포함하지 않는 연료는 $SO_2$를 배출시키지 않았고, 흡기 중에 $SO_2$표준가스의 증가에 따른 배기의 $SO_2$배출률은 $SO_2$흡입률과 비교하여 거의 같은 비율이었다. 또한, 흡기의 $SO_2$유량 상승은 $N_2O$배출률을 상승시켜 배기 중의 $N_2O$는 흡기의 $SO_2$혼합기에 의해 생성되었다. 결국 황 성분을 함유한 연료는 연소 중에 $SO_2$를 형성하고 배기 중의 $N_2O$는 연소실에 존재하는 NO와 $SO_2$의 반응에 의해 발생된다고 할 수 있다.