• 공업화학
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• 제23권3호
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• pp.253-258
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• 2012

본 연구는 $Pd/TiO_2$ 촉매를 이용한 $CH_4$, CO 동시 산화반응에서 활성점 및 Pd의 산화 상태에 대한 영향을 조사하였다. Pd 함량이 증가할수록 Pd 종(PdO)의 결정성장을 야기시켜 $CH_4$ 산화반응 활성을 증진시켰다. 열처리를 통해 제조된 촉매표면의 Pd 산화상태에 따라 $CH_4$과 CO의 산화반응 활성이 상이한 결과를 나타내었다. XRD와 $H_2-TPR$ 분석으로 소성촉매는 $Pd^{2+}$종, 환원촉매는 $Pd^0$종이 우점하고 있음을 확인하였다. 또한, BET분석을 통해 촉매 활성인자인 비표면적 및 기공부피보다는 Pd의 산화상태가 촉매 활성에 미치는 중요한 인자임을 알 수 있었다. FT-IR 분석을 이용하여 Pd의 산화상태에 따른 $CH_4$과 CO의 반응 메커니즘을 확인할 수 있었다.

• 공업화학
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• 제32권3호
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• pp.237-242
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• 2021

미세먼지와 함께 질소산화물, 황산화물, 휘발성 유기화합물, 암모니아 비롯한 유발물질에 대한 동시 저감기술은 엄격해지는 환경규제와 실질적인 저감효과 제고를 위해 꾸준히 주목받아 왔다. 오존산화에 의한 비수용성 질소산화물 고속산화 공정은 전통적으로 적용되고 있는 선택적 촉매환원 공정에 비해 공간절약형 시스템 적용을 가능하게 할 뿐만 아니라 운영비용 절감 측면에서 매우 효과적인 방법으로 평가되고 있으며 황산화물을 비롯한 산성가스와 동시 저감이 가능한 공정 구현이 가능하다는 장점까지 있다. 본 논문에서는 오존 고속산화 공정에 대한 기술 이슈 및 개발 동향을 소개하며 향후 산업적 이용 확대를 위한 개발 방향에 대해서 고찰하고자 한다.

• Applied Microscopy
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• 제43권4호
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• pp.173-176
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• 2013

The oxidation behavior of the crystallized $Al_{87}Ni_3Y_{10}$ alloy has been investigated with an aim to compare with that of the amorphous $Al_{87}Ni_3Y_{10}$ alloy. The oxidation at 873 K occurs as follows: (1) growth of an amorphous aluminum-yttrium oxide layer (~10 nm) after heating up to 873 K; and (2) formation of $YAlO_3$ crystalline oxide (~220 nm) after annealing for 30 hours at 873 K. Such an overall oxidation step indicates that the oxidation behavior in the crystallized $Al_{87}Ni_3Y_{10}$ alloy occurs in the same way as in the amorphous $Al_{87}Ni_3Y_{10}$ alloy. The simultaneous presence of aluminum and yttrium in the oxide layer significantly enhances the thermal stability of the amorphous structure in the oxide phase. Since the structure of aluminum-yttrium oxide is dense due to the large difference in ionic radius between aluminum and yttrium ions, the diffusion of oxygen ion through the amorphous oxide layer is limited thus stabilizing the amorphous structure of the oxide phase.

• 전기화학회지
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• 제5권4호
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• pp.209-211
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• 2002

The simultaneous sensing of nitric oxide (NO) and its metabolite, nitrite $(NO_2^-)$ has been studied by Osteryoung square-wave voltarnmetery (OSWV) in physiological pH solution (0.1 M phosphate buffer solution, pH 7.2). Using an electrochemically pretreated glassy carbon (GC) electrode, OSWV was successfully applied to observe the well-separated oxidation peaks at ca. 0.58 and 0.80V vs. Ag/AgCI for NO and $(NO_2^-)$, respectively. This clear separation between the NO and $(NO_2^-)$ oxidation peaks may be due to the formation of surface oxides (e.g., quinone (C=O) or carboxylic $(COO^-)$ group) and surface defects introduced by the electrochemical pretreatment of GC electrodes.

• 한국지하수토양환경학회지:지하수토양환경
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• 제24권4호
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• pp.1-10
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• 2019

Recently, groundwater contamination by mixed occurrence of arsenic (As) and nitrate ($NO_3{^-}$) has been a serious environmental issue all around world. In this study, we investigated the microbial As(III) oxidation characteristic under denitrification process to examine the feasibility of the microbial consortia in wetland sediment to simultaneously treat these two contaminants. The detail objectives of this study were to investigate the effects of $NO_3{^-}$ on the oxidation of As(III) in anaerobic environments and observe the microbial community change during the As oxidation under denitrification process. Results showed that the As(III) was completely and simultaneously oxidized to As(V) under denitrification process, however, it occurred to a much less extent in the absence of sediment or $NO_3{^-}$. In addition, the significant increase of As(III) oxidation rate in the presence of $NO_3{^-}$ suggested the potential of As oxidation under denitrification by indigenous microorganisms in wetland sediment. Genera Pseudogulbenkiania, and Flavisolibacter were identified as predominant microbial species driving the redox process. Conclusively, this study can provide useful information on As(III) oxidation under denitrifying environment and contribute to develop an effective technology for simultaneous removal of As(III) and $NO_3{^-}$ in groundwater.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.208-209
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• 2011

In this work, we developed self-assembled monolayers (SAMs) of alkanethiols on gold that can release amine groups, when an electrical potential was applied to the gold. The strategy was based on the introduction of the electroactive carbamate group, which underwent the two-electron oxidation with simultaneous release of the amine molecules, to alkanethiols. The synthesis of the designed thiol compounds was achieved by coupling isocyanate-containing compound with hydroquinone. The electroactive thiols were mixed with hydroxyl-containing alkanethiol [$HS(CH_2)_{11}OH$] to form mixed monolayers, and cyclic votammetry was used for the characterization of the release. The mixed SAMs showed a first oxidation peak at +540 mV (versus Ag/AgCl reference electrode), demonstrating irreversible conversion from carbamate to hydroqinone with simultaneous release of the amine groups. The second and third cycles showed typical reversible redox reaction of hydroquinone and quione: the oxidation and reduction occurred at +290 mV and -110 mV, respectively. The measurement of ToF-SIMS further indicates that electrochemical-assisted chemical reaction successfully released amine groups. This new SAM-based electrochemistry would be applicable for direct release of biologically active molecules that contain amine groups.

• 공업화학
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• 제32권6호
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• pp.659-663
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• 2021

반도체 제조공정에서 발생하는 미세먼지와 질소산화물 동시처리를 위하여 오존산화, 습식중화 및 습식전기집진 기술들을 직접화한 10 CMM급 복합오염물질 제거시스템을 개발하였으며, NOx 제거효율 증대를 위한 공정변수 제어 및 최적화를 진행하였다. 특히, 전원공급장치를 포함한 습식전기집진장치 핵심부품 안정성 평가를 위해 30일 동안의 장기운전도 병행하였다. 오존산화 기반 DeNOx 공정에서 가장 중요한 운전변수인 O₃/NO 비율은 1.5 부근에서 최적화하였으며, 습식중화 공정의 운전변수를 최적화하여 중화반응에 의한 제거효율 기여도를 확인하였다.

• 공업화학
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• 제21권2호
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• pp.178-182
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• 2010

다양한 $TiO_2$를 담체로 한 Pt계 촉매에서 NOx, soot의 동시 제거 반응에 대한 연구를 수행하였다. 실험은 각 촉매를 NOx와 soot의 반응을 독립 또는 동시에 반응시킨 조건으로 수행하였으며 그 결과 $TiO_2$의 종류에 따라 서로 상이한 NOx 제거능력과 soot 산화력을 나타내었다. 또 NOx 독립 실험 시 생성된 $NO_2$ 양과 soot 산화시작온도가 저온으로 이동하는 정도가 관계가 있었다. 담체의 물성 중 Pt의 뭉침현상에 결정적 역할을 미치는 비표면적과 촉매의 환원력에 영향을 미치는 crystallite size가 NO의 $NO_2$ 전환반응에 밀접한 관계를 가지는 것으로 조사되었다. 따라서 반응의 중요한 인자는 촉매에 사용되는 담체의 물리화학적 특성임을 알 수 있었다.

• 한국대기환경학회지
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• 제18권2호
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• pp.139-148
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• 2002

Both UV Photolysis and Phtocatalytic Oxidation Processing are an emerging technology for the abatemant of Volatile Organic Compounds (VOCs) in atmospheric -pressure air streams. However, each process has some drawbacks of their own. The former is little known as an application for air pollution treatment, so it has been a rare choice in the field. Therefore we have to do more experiment and study for its application for treatment of VOCs. Although the latter has been used in the industrial fields, it still has a difficulty in decomposing high concentrations of VOCs. To solute these problems, we have been studying simultaneous application of those two technologies. We have studied the effects of background gas composition and gas temperature on the decomposition chemistry. It has shown that concentration of TCE and B.T.X., diameter of reactor, and wavelength of lamp have effects on decomposition efficiency. When using Photolysis Process only, the rates of fractional conversion of each material are found at TCE 79%, Benzene 65%, Toluene 68%, Xylene 76%. In case of Photocatalytic Oxidation Process only, the rates of fractional conversion decreased drastically above 30 ppm. When there two methods were combined, the rates of fractional conversion of each material are enhanced such as TCE 93%, Benzene 75%, Toluene 81%, Xylene 90%. Therefore, we conclude that the combination of Photolysis-Photocatalytic Oxidation process is more efficient than each individual process.

• Journal of Electrochemical Science and Technology
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• 제8권4호
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• pp.274-281
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• 2017

This paper describes the simple fabrication of an electrode modified with electrochemically reduced graphene oxide (ERGO) for the simultaneous electrocatalytic detection of dopamine (DA), ascorbic acid (AA), and uric acid (UA). ERGO was formed on a glassy carbon (GC) electrode by the reduction of graphene oxide (GO) using linear sweep voltammetry. The ERGO/GC electrode was formed by subjecting a GO solution ($1mg\;mL^{-1}$ in 0.25 M NaCl) to a linear scan from 0 V to -1.4 V at a scan rate of $20mVs^{-1}$. The ERGO/GC electrode was characterized by Raman spectroscopy, Fourier transform infrared spectroscopy, contact angle measurements, electrochemical impedance spectroscopy, and cyclic voltammetry. The electrochemical performance of the ERGO/GC electrode with respect to the detection of DA, AA, and UA in 0.1 M PBS (pH 7.4) was investigated by differential pulse voltammetry (DPV) and amperometry. The ERGO/GC electrode exhibited three well-separated voltammetric peaks and increased oxidation currents during the DPV measurements, thus allowing for the simultaneous and individual detection of DA, AA, and UA. The detection limits for DA, AA, and UA were found to be 0.46, 77, and $0.31{\mu}M$ respectively, using the amperometric i-t curve technique, with the S/N ratio being 3.