• 한국전기전자재료학회논문지
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• 제19권9호
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• pp.855-861
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• 2006

Sinterability and microwave dielectric properties of $xZWO_{4}-(1-x)TiO_{2}$ ceramic systems with zinc-borosilicate glass and $TiO_{2}$ contents for LTCC(Low Temperature Co-fired Ceramics) were investigated. The addition of $3{\sim}10\;wt%$ ZBS glass ensured the sinterability below $900^{\circ}C$. In general, increasing ZBS glass content seemed to enhance the sinterability, but the quality factor($Qxf_{0}$) significantly decreased due to the formation of an excessive liquid and second phases. As for the addition of $TiO_{2}$, the dielectric constant(${\varepsilon}_{r}$) and temperature coefficient of resonant frequency(${\tau}_{f}$) showed to increase, while the quality factor($Qxf_{0}$) did not show an apparent change. The composition of $0.7xZnWO_{4}-0.3TiO_{2}$ ceramics sintered at $900^{\circ}C$ with 5 wt% ZBS glass demonstrated 21.6 in dielectric constant(${\varepsilon}_{r}$), 14,800 in quality factor($Qxf_{0}$), and $+5\;ppm/^{\circ}C$ in temperature coefficient of resonant frequency(${\tau}_{f}$).

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2004년도 International Symposium on Powder Materials and Processing
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• pp.32-32
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• 2004

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 2002년도 춘계공동학술발표회요약집
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• pp.444.1-444
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• 2002

• 공업화학
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• 제20권5호
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• pp.486-492
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• 2009

퀴놀린 습식산화는 $225^{\circ}C$와 $250^{\circ}C$에서 수행되었다. $250^{\circ}C$에서의 습식산화에서 퀴놀린은 30 min 내에 완전히 분해되었으며 총 유기탄소(TOC)는 120 min 내에 63% 감소하였다. 반면에 $225^{\circ}C$에서의 습식산화에서는 TOC는 240 min 동안 13% 감소하였다. 퀴놀린 산화 중 니코틴산과 초산이 주 중간생성물로 생성되었다. 균일촉매 $CuSO_4$ 또는 쉽게 산화되는 페놀을 첨가하여 온화한 반응조건인 $200^{\circ}C$에서의 퀴놀린 습식산화도 수행하였다. $CuSO_4$를 0.20 g/L 사용한 촉매 습식산화는 $250^{\circ}C$ 습식산화에서와 비슷한 퀴놀린 및 TOC 제거속도를 보였다. $200^{\circ}C$에서의 퀴놀린과 페놀 혼합물 습식산화에서는 퀴놀린과 페놀의 분해 개시에 필요한 자유라디칼이 생성되는 유도기간이 나타났다. 주어진 퀴놀린 초기농도에서 페놀 초기농도를 증가시킴에 따라, 퀴놀린과 페놀 분해를 위한 유도기간은 짧아졌고 습식산화 180 min 동안의 TOC 감소율은 60%에서 75%까지 증가하였다. 유도기간의 감소율은 퀴놀린에 대한 페놀 초기농도비를 증가시킴에 따라 감소하였다. 반면에 퀴놀린과 페놀 혼합물 습식산화에서의 페놀분해는 페놀 습식산화에서 보다 긴 유도기간을 필요로 하였고 서서히 진행되었다.

• 센서학회지
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• 제18권4호
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• pp.263-268
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• 2009

With the increasing number of automobiles, the problem of air pollution from the exhaust gases of automobiles has become a critical issue. The principal gases that cause air pollution are nitrogen oxide or NO$_x$(NO and NO$_2$), and CO. Because NO$_x$ gases cause acid rain and global warming and produce ozone(O$_3$) that leads to serious metropolitan smog from photochemical reaction, they must be detected and reduced. Mixtures of WO$_3$ and $In_2O_3$(WO$_3$:$In_2O_3$=10:0, 7:3, 5:5, 3:7, and 0:10 in wt.%), which are NO$_x$ gas-sensing materials, were prepared, and thick-film gas sensors that included a heater and a temperature sensor were fabricated. Their sensitivity to NO$_x$ was measured at 250$\sim$400$^{\circ}C$ for NO$_x$ concentrations of 1$\sim$5 ppm. The $In_2O_3$ thick-film sensor showed excellent sensitivity($R_{gas}/R_{air}$=10.22) at 300$^{\circ}C$ to 5-ppm NO. The response time for 70 % saturated sensitivity was about 3 seconds, and the sensors exhibited very fast reactivity to NO$_x$.

• Advances in nano research
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• 제12권3호
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• pp.291-300
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• 2022

The behavior of hydrogen species on the surface of the catalyst during the Lewis acid transformation to form Brønsted acid sites over the spherical silica-supported WO_x catalyst was investigated. To understand the structure-activity relationship of Lewis acid transformation and hydrogen bonding interactions, we explore the potential of using the in situ diffuse reflection infrared Fourier transform spectroscopy (DRIFTS) with adsorbed ammonia and hydrogen exposure. From the results of in situ DRIFTS measurements, Lewis acid sites on surface catalysts were transformed into new Brønsted acid sites upon hydrogen exposure. The adsorbed NH₃ on Lewis acid sites migrated to Brønsted acid sites forming NH⁴⁺. The results show that the dissociated H atoms present on the catalyst surface formed new Si-OH hydroxyl species - the new Brønsted acid site. Besides, the isolated Si-O-W species is the key towards H-bond and Si-OH formation. Additionally, the H atoms adsorbed surrounding the Si-O-W species of mono-oxo O=WO₄ and di-oxo (O=)₂WO₂ species, where the Si-O-W species are the main species presented on the Inc-SSP catalysts than that of the IWI-SSP catalysts.

• 공업화학
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• 제34권4호
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• pp.357-364
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• 2023

선택적 촉매 환원(SCR)은 질소산화물 배출을 줄이는 가장 효과적인 방법이지만, V₂O₅-WO₃/TiO₂ 촉매가 좁은 작동온도 (300~400℃) 범위를 가지기 때문에, V₂O₅-WO₃/TiO₂ 촉매의 작동 온도범위가 200~450℃인 새로운 촉매를 개발하였다. SCR 과정에서 생성되는 촉매 독인 황산암모늄은 350℃ 이상으로 가열함으로써 제거할 수 있다. 촉매 활성 부위의 수를 증가시키고 활성 물질의 분산을 촉진하기 위해 TiO₂ 지지체에 티타늄 이소프로폭사이드(TTIP) 처리를 여러 TTIP/TiO₂ 질량비로 진행하였다. 그 중 5 wt% TTIP 부하에서 높은 W 분산성으로 인해 열 안정성이 증가하였고 V⁵⁺가 형성되어 최적의 성능을 보였다. 5 wt% TTIP 부하로 처리된 촉매를 One-step co-precipitation으로 제조하였을 때 기존의 방법보다 더 나은 V-OH와 W-OH 분산 및 상호작용 향상이 나타나 더 낮은 온도에서 높은 촉매 활성으로 인해 향상된 성능을 보였다. 이를 향후 TTIP를 이용하여 TiO₂촉매의 표면을 개선하려는 연구자에게 이해하기 쉽게 설명하고자 하였다.

• 센서학회지
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• 제18권1호
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• pp.54-62
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• 2009

${Co_3}{O_4}$ and ${Co_3}{O_4}$-based thick films with additives such as ${Co_3}{O_4}-{Fe_2}{O_3}$(5 wt.%), ${Co_3}{O_4}-{SnO_2}$ (5 wt.%), ${Co_3}{O_4}-{WO_3}$(5 wt.%) and ${Co_3}{O_4}$-ZnO(5 wt.%) were fabricated by screen printing method on alumina substrates. Their structural properties were examined by XRD and SEM. The sensitivities to iso-${C_4}H_{10}$, $CH_4$, CO, $NH_3$ and NO gases were investigated with the thick films heat treated at $400^{\circ}C$, $500^{\circ}C$ and $600^{\circ}C$. From the gas sensing properties of the films, the films showed p-type semiconductor behaviors. ${Co_3}{O_4}-{SnO_2}$(5 wt.%) thick film heat treated at $600^{\circ}C$ showed higher sensitivity to i-${C_4}H_{10}$ and CO gases than other thick-films. ${Co_3}{O_4}-{SnO_2}$(5 wt.%) thick film heat treated at $600^{\circ}C$ showed the sensitivity of 170 % to 3000 ppm iso-${C_4}H_{10}$ gas and 100 % to 100 ppm CO gas at the working temperature of $250^{\circ}C$. The response time to i-${C_4}H_{10}$ and CO gases showed rise time of about 10 seconds and fall time of about $3{\sim}4$ minutes. The selectivity to i-${C_4}H_{10}$ and CO gases was enhanced in the ${Co_3}{O_4}-{SnO_2}$(5 wt.%) thick film.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.642-643
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• 2006

Direct reduction and carburization process was thought one of the best methods to make nano-sized WC powder. The oxide powders were mixed with graphite powder by ball milling in the compositions of WC-5,-10wt%Co. The mixture was heated at the temperatures of $600{\sim}800^{\circ}C$ for 5 hours in Ar. The reaction time of the reduction and carburization was decreased as heating temperatures and cobalt content increased. The mean size of WC/Co composite powders was about 260 nm after the reactions. And the mean size of WC grains in WC/Co composite powders was about 38 nm after the reaction at $800^{\circ}C$ for 5 hours.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.646-647
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• 2006

Nano-sized WC particles in WC/Co composite powders were synthesized by mechanochemical method. The raw powders$(WO_3,\;Co_3O_4,\;VC,\;Cr_3C_2$ and graphite) were mixed by planetary milling for 30 hours. The compositions were WC-10 and -20 wt% Co added VC and $Cr_3C_2$. The direct reduction and carburization of the mixed powders were carried at $900\;^{\circ}C$ for 1 to 3 hours under flowing Ar gas. The mean size of WC particles in WC/Co composite powders was about 16 nm. The resultant powders were compacted and sintered at $1300{\sim}1360\;^{\circ}C$ for 0.5 hour. After sintering the mean size of WC particles was about 50 nm.