• 한국대기환경학회지
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• 제13권1호
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• pp.91-98
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• 1997

Y-zeolite and ${\gamma}$-Al$_2$O$_3$ were used as supports on CO and $C_3$H$_{6}$ oxidation for diesel emission control. The catalysts composed of Pd and Pt as active components were wash coated on honeycomb type ceramic substrate. The oxidation of CO and $C_3$H$_{6}$ was carried out over prepared honeycomb in a fixed bed continuous reactor in the temperature range of 20$0^{\circ}C$~50$0^{\circ}C$ and 20,000 GHSV (h$^{-1}$ ). Surface area of Y-zeolite was larger than that of ${\gamma}$-Al$_2$O$_3$ due to channel structure of Y-zeolite. Therefore, high conversion of CO and $C_3$H$_{6}$ could be obtained because of good dispersion of active metals over Y-zeolite. The honeycomb used Y-zeolite as a support showed higher $C_3$H$_{6}$ conversion than that of ${\gamma}$-Al$_2$O$_3$ due to better cracking and isomerization activity of Y-zeolite. PdPt catalyst showed high conversion of CO and $C_3$H$_{6}$ at low temperature region, 20$0^{\circ}C$~30$0^{\circ}C$, for their synergy effects. PdPt/Y-Zeolite catalyst could achieve more than 80％ conversion of $C_3$H$_{6}$ at 30$0^{\circ}C$. The use of Y-zeolite as a support increased CO and $C_3$H$_{6}$ conversion, and decreased SO$_2$ conversion very effectively. Y-zeolite found to have a good adaptability as a support for the diesel emission after treatment system.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.212-212
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• 2011

In addition to the catalysts' activity and selectivity, the deactivation of catalysts during use is of practical importance. It is crucial to understand the phenomena of the deactivation to predict the loss of activity during catalyst usage so that the high operational costs associated with catalyst replacement can be reduced. In this study, the activity of Ru catalysts, such as nanoparticles (3~6 nm) and polycrystalline thin film (50 nm), have been investigated under CO oxidation and oxidative/reductive reaction conditions at various temperatures with the ambient pressure X-Ray photoelectron spectroscopy (APXPS). With APXPS, the surface oxides on the catalyst are measured and monitored in-situ. It was found that the Ru film exhibited faster oxidation-and-reduction compared to that of nanoparticles showing mild oxidative-and-reductive characteristics. Additionally, the larger Ru nanoparticles showed a higher degree of oxide formation at all temperatures, suggesting a higher stability of the oxide. These observations are in agreement with the catalytic activity of Ru catalysts. The loss of activity of Ru films is correlated with bulk oxide formation, which is inactive in CO oxidation. The Ru nanoparticle, however, does not exhibit deactivation under similar conditions, suggesting that its surface is covered with a highly active ultrathin surface oxide. Since the active oxide is more stable as nanoparticles than as a film, the nanoparticles showed mild oxidative/reductive behavior, as confirmed by APXPS results. We believe these simultaneous observations of both the surface oxide of Ru catalysts and the reactivity in real time enable us to pinpoint the deactivation phenomena more precisely and help in designing more efficient and stable catalytic systems.

• 유기물자원화
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• 제29권4호
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• pp.47-54
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• 2021

본 연구는 수소 경제 사회에서 누출·농축 수소에 대한 안전성 확보를 위해 Pd/TiO₂ 촉매를 허니컴 형태로 코팅하여 그 성능을 평가하였다. 열원에 노출되지 않는 액상환원법을 기반으로 촉매를 제조하였으며, 2~4 nm의 매우 작은 활성입자로 존재함을 H₂-chemisorption 분석을 통해 확인하였다. 또한 환원반응온도가 증가할수록 metal dispersion 감소 및 활성입자 크기가 증가함을 확인하였으며, 활성금속 입자 크기와 수소 산화 성능은 비례관계에 있음에 따라 수소 산화 성능 감소결과와 일치함을 확인하였다. 제조된 촉매를 실 공정에 적용할 수 있도록 허니컴 형태의 지지체에 코팅하였을 때, AS-40 바인더를 20 wt%이상 코팅하였을 때 저농도 수소 조건에서 90% 이상의 산화 성능을 관찰하였다. 이는 촉매의 부착강도를 증진시키고 촉매 탈리를 방지하여 장기적인 촉매 활성을 기대할 수 있음을 SEM 분석을 통해 확인하였다. 본 연구를 통해 가스화 등과 같은 유기물 자원화를 통해 수소 생산 및 수소 인프라 구축 사회에서 안전성을 확보할 수 있는 기초연구로, 추후 예측하지 못한 안전사고를 대응할 수 있는 시스템으로써 활용될 수 있을 것으로 판단된다.

• 대한토목학회논문집
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• 제26권4B호
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• pp.421-426
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• 2006

본 연구는 생물학적 질산화 공정에서 암모늄 이온과 활성을 가진 질산화균의 초기 농도가 질산화에 미치는 영향을 확인하고, 이에 따른 동역학식을 제시하고자 하였다. 먼저 실험에 이용된 슬러지의 질산화균 농도는 미생물 호흡률 실험으로 측정하였는데, 배양된 슬러지 중 42.8%가 활성을 가진 질산화균으로 나타났다. 암모늄 이온과 질산화균의 초기 농도를 달리하여 $N_0/X_0$비가 0.025~0.493의 조건에서 잘산화 실험을 실시하였으며, 이를 통해 암모늄 이온과 질산화균의 농도가 상이하더라도 $N_0/X_0$ 비가 동일할 경우 암모늄 산화율이 동일함을 확인하였다. 또한 $N_0/X_0$ 비와 비기질이용율의 관계는 Contois 형태의 관계식으로 표현되었으며, 최대 비암모늄산화율($q_{Nmax}$)은 4.32 gN/gVSS/day, 반 포화속도 상수($K_N{^{\prime}}$)는 0,013 gN/gVSS인 것으로 확인되었다.

• 식품과학과 산업
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• 제50권2호
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• pp.27-36
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• 2017

Today, the food packaging industry has a great interest in using active packaging to fresh food product as a solution for the future to positively provide its quality, safety and shelf life. Many researches have extensively studied functional packaging strategies in recently years. Controlled release packaging (CRP) is an innovative packaging technology in the packaging polymer matrix from which can active agents are delivered in a controlled way into the product. CRP technology is well-suited for controlling release of antimicrobial compounds and antioxidants to prevent food degradation reactions such as microbial growth and lipid oxidation. Advances in CRP technology allow food packaging manufacturers to challenge the development of better functional food packaging systems. This overview examines the most recent developments and technologies of active packaging for applying the food industry. The scope of this article has mainly been focused on controlled releasing systems.

• 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.

• 상하수도학회지
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• 제25권2호
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• pp.223-230
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• 2011

An electrolytic oxidation process was applied to remove odorous compounds from non-point odor sources including wastewater pipelines and manholes. In this study, a distance between the anode and the cathode of the electrolytic process was varied as a system operating parameters, and its effects on odor removal efficiencies and reaction characteristics were investigated. Odor precursors such as sediment organic matters and reduced sulfur/nitrogen compounds were effectively oxidized in the electrolytic process, and a change in oxidation-reduction potential (ORP) indicated that an stringent anaerobic condition shifted to a mild anoxic condition rapidly. At an electrode distance of 1 cm and an applied voltage of 30 V, a system current was maintained at 1 A, and the current density was 23.1 $mA/cm^{2}$. Under the condition, the removal efficiency of hydrogen sulfide in gas phase was found to be 100%, and 93% of ammonium ion was removed from the liquid phase during the 120 minute operating period. Moreover, the sulfate ion (${SO_4}^{2-}$) concentration increased about three times from its initial value due to the active oxidation. As the specific power consumption (i.e., the energy input normalized by the effective volume) increased, the oxidation progressed rapidly, however, the oxidation rate was varied depending on target compounds. Consequently, a threshold power consumption for each odorous compound needs to be experimentally determined for an effective application of the electrolytic oxidation.

• 한국세라믹학회지
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• 제36권5호
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• pp.555-563
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• 1999

탄소재료의 산화저항성 증진을 위해 Tri-Butyl 인산 에스테르를 함참하였다. 시편은 함침전 초산으로 전처리 한 것과 흑연재 Raw Bulk(Raw)를 함침시켜 비교하므로써 초산 세척의 효과도 아울러 조사하였다. XPS와 FTIR을 사용하여 함침처리 전후의 탄소표면의 특성을 검토한 결과 Tn-butyl phosphale로 함침된 시편(RP)의 표면에는 P-O 그룹 및 -OH Band 등의 친수성이 강한 활성기가 존재하였다. 산세척한 시편을 함침한 탄소재(AP)는 Raw보다 산화게시온도가 약 120$^{\circ}C$ 향상되었고 산화율은 1000$^{\circ}C$에서 30% 감소된 효과를 보였다. 본실험에서 구한 Raw, 초산세척 시편, 초산처리후 함침한 시편들의 Arrbenius Plot으로부터 동일한 값의 기울기를 나타내어 탄소의 산화반응 요인중에 본실험에서 처리한 내산화과정은 탄소표면의 기본적 화학반응변화에 의한 효과로 보여지지 않는다.

• 신재생에너지
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• 제4권2호
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• pp.39-44
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• 2008

Partial oxidation of methane was carried out by ceria-promoted Ni-substituted hydrotalcite-derived catalysts ($Ce_xNi_3$-HTlc ; x=$0.3{\sim}1.2$) in a fixed-bed reactor. The Ce/Ni ratio of 0.3/3 in the catalyst showed the best catalytic activity but the Ce/Ni ratio became higher above 0.3/3, the catalyst became less active in short-term tests. No ceria promoted catalyst was started to decrease $CH_4$ conversion after 20 h but the Ce/Ni ratio 0.3/3 catalyst was kept its stability in long-term tests.

• 한국연소학회:학술대회논문집
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• 한국연소학회 1997년도 제15회 KOSCO SYMPOSIUM 논문집
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• pp.1-11
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• 1997

The soot and OH radical distributions have been experimentally studied in ethylene and propane laminar diffusion flames. The integrated soot volume fraction was measured along the centerline of a flame using a laser light extinction method. Planar laser light scattering and PLIF techniques are employed for the soot and OH radical distribution measurements utilizing Nd:YAG laser and OPO, FDO system. The concentration of OH radical is rapidly decreased at the edge of sooting region, which implies the importance of OH radical species on the soot oxidation process. For ethylene flames, the addition of air in fuel moves the OH radical distribution towards the center line of a flame at the soot oxidation region, while the concentration of OH radical remains relatively high at the soot formation region. The interaction between soot particles and OH radicals becomes more active with fuel-air at the soot oxidation region. For propane flames, however, any indication of the increased interaction between soot particles and OH radicals with fuel-air was not noticed.