• 한국진공학회:학술대회논문집
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• 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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• pp.171.1-171.1
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• 2016

재료의 표면 강화 방법 중의 하나인 질화공정을 이용하여 탄소강 S45C 소재의 질화 거동에 대하여 연구하였다. $520^{\circ}C$ 온도에서 질화 공정을 진행하여 공정시간에 따른 Kn값을 수소 센서로 측정하여 공정시간에 따른 N-potential의 변화와 그에 따른 화합물층 성장 및 화합물층의 상변화에 대해 관찰하였다. 화합물 층의 미세구조 변화는 광학현미경 및 주사전자현미경을 통해 관찰하였다. 가스 질화 처리 후 표면경도는 약 600Hv의 경도값이 측정되었고, 공정 시간이 늘어남에 따라 화합물층 및 경화깊이가 증가되고 표면 화합물이 성장하여 porous가 감소하는 것을 확인 할 수 있다. 경화깊이는 1440분 일 때 약 0.5mm 경화 깊이를 얻었고, 화합물층의 성장은 ${\varepsilon}$상(Fe2-3N)과 ${\gamma}$'상(Fe4N)으로 두 개의 상으로 형성되는 것을 관찰할 수 있었다. 시험 결과를 바탕으로 S45C 소재의 탄소 함량에 따른 lehrer diagram을 열역학 적으로 계산하고 화합물층의 형성 기구에 대해 비교 분석하였다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2008년도 춘계학술대회 논문집
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• pp.247-250
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• 2008

Biomass gasification is a promising technology for producing a fuel gas which is useful for power generation systems. In biomass gasification processes, tar formation often causes some problems such as pipeline plugging. Thus, proper tar treatment is necessary. So far, nickel (Ni)-based catalysts have been intensively studied for the catalytic tar removal. However, the deactivation of Ni-based catalysts takes place because of coke deposition and sintering of Ni metal particles. To overcome these problems, we have been using ruthenium (Ru)-based catalyst for tar removal. It is reported by Okada et al., that a Ru/$Al_2O_3$ catalyst is very effective for preventing the carbon deposition during the steam reforming of hydrocarbons. Also, this catalyst is more active than the Ni-based catalyst at a low steam to carbon ratio (S/C). Benzene was used for the tar model compound because it is the main constituent of biomass tar and also because it represents a stable aromatic structure apparent in tar formed in biomass gasification processes. The steam reforming process transforms hydrocarbons into gaseous mixtures constituted of carbon dioxide ($CO_2$), carbon monoxide (CO), methane ($CH_4$) and hydrogen ($H_2$).

• 대한용접접합학회:학술대회논문집
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• 대한용접접합학회 2004년도 춘계 학술발표대회 개요집
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• pp.316-318
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• 2004

In recent years, plastic waste has been recognized as a worldwide environmental issue. To solve the disposal problem of the plastic waste, alternative treatment such as the use of biodegradable plastic(polybutylene succinate: PBS) is indeed highly in demand due to its merit of PBS buried in soil decomposed into carbon dioxide and water. In the present study, for the production of further functional PBS with TiO$_2$ as photocatalyst, which shows the decomposition of detrimental organic compound and pollutant under ultraviolet irradiation, we attempted to prepare photocatalytic TiO$_2$ coatings on PBS substrate by HVOF and plasma spraying techniques under various conditions using three kinds of agglomerated powders (P200: 200nm, P30: 30nm, P7: 7nm). The microstructures of coatings were characterized with SEM and XRD analysis, and the photocatalytic efficiency of coatings was evaluated through the photo degradation of gaseous acetaldehyde. Therefore, such functional TiO$_2$-Plastic composite material is expected to considerably contribute to the reduction of aggravated environmental problem.

• Journal of Korean Society for Atmospheric Environment
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• 제17권E2호
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• pp.35-42
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• 2001

Recent development of photocatalytic degradation method that is mediated by TiO$_2$ is of interest in the treatment of volatile organic compounds(VOCs). In this study, trichloroethylene(TCE) and acetone were closely examined in a batch scale of photo-reactor as a function of water vapor, oxygen, and temperature. Water vapor inhibited the photocatalytic degradation of acetone, while there was an optimum concentration in TCE. A lower efficiency was found in nitrogen atmosphere than air, and the effect of oxygen on photocatalytic degradation of acetone was greater than on that of TCE. The optimum reaction temperature on photocatalytic degradation was about 45$^{\circ}C$ for both compounds. NO organic byproducts were detected for both compounds under the present experimental conditions. It was ascertained that the photocatalytic reaction in a batch scale of photo-reactor was very effective in removing VOCs such as TCE and acetone in the gaseous phase.

• 한국토양환경학회지
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• 제2권1호
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• pp.83-90
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• 1997

저농도의 난 수용성 VOC가스가 포함되어 있는 다량의 오염가스를 처리하기 위하여 흡수탑과 생물반응기의 결합체인 새로운 처리시스템을 제시하였다. 바이오스크러버의 스크러버에서는 세정액으로 기상중의 처리대상오염물질의 흡수가 일어나며 세정액은 생물반응기로 이송되어 호기성 미생물이 오염물을 분해시킨다. 본 연구에서는 폐가스중의 VOC분리를 위하여 재순환가능한 고비점용매를 사용하였다. 고비점용매를 포함한 세정액은 기/액 향류접촉이 이루어지는 흡수탑의 충전층에서 폐가스중의 오염물을 분리한다. 흡수탑은 Pall ring충전제로 채워 실제공정을 모사 하고자 하였다. 흡수처리후 생물반응기로 이송된 흡수액은 재생 후 다시 흡수탑으로 재 순환하였다. 실험에 사용된 대상가스는 농도가 400 mg/$\textrm{m}^3$ 인 톨루엔으로, 세정액이 가스흐름과 향류로 약 10~15L/min의 유량으로 충전층을 적시며 내려오는 충전탑내부로 약 100 L/min의 유량으로 도입하였다. VOC처리를 위해 제작된 본 바이오스크러버에서 고비점용매를 이용한 연속실험결과 최적운전 조건에서 약 80%의 처리율을 얻을 수 있었다.

• 한국수소및신에너지학회논문집
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• 제25권5호
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• pp.482-490
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• 2014

Gaseous sulfur compound such as $H_2S$ or COS in coal- or biomass-derived hot syngas can be purified by solid sorbents at high temperatures. In this study, we investigated the physical properties and reactivity of solid regenerable desulfurization sorbents with 37.2, 41.9, and 46.5wt% ZnO to look into the ZnO content effect. The sorbents were produced by spray-drying method to apply to a fluidized-bed process. Sulfidation and regeneration reaction were carried out using a thermogravimetric analyzer. Sorbent prepared with 46.5wt% ZnO had physical properties suitable for a fluidized-bed process applications such as spherical shape, sufficient mechanical strength and density, high porosity and surface area. It showed high sulfur sorption capacity of 10.4wt% (ZnO utilization of 57%) at reaction temperatures of 500 and $650^{\circ}C$ for sulfidation and regeneration, respectively. However, the sulfur sorption capacity and ZnO utilization were significantly reduced and dimple shape appeared when the ZnO content decreased to 37.2 and 41.9wt%. Sulfur sorption capacity and regenerability were improved as reaction temperature increased within the experimental temperatures used in this work. The reaction temperature zones of $1500{\sim}550^{\circ}C$ and $650{\sim}700^{\circ}C$ are recommended for sulfidation and regeneration, respectively, to lead best reaction performances of the ZnO-based spray-dried sorbents developed in this work.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 추계학술대회 초록집
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• pp.107-107
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• 2010

Hydrogen is an alternative fuel for the future energy which can reduce pollutants and greenhouse gases. Synthesis gas have played an important role of synthesizing the valuable chemical compound, for example methanol, DME and GTL chemicals. Renewable biomass feedstocks can be potentially used for fuels and chemical production. Current thermal processing techniques such as fast pyrolysis, slow pyrolysis, and gasification tend to generate products with a large slate of compounds. Lignocellulose feedstocks such as forest residues are promising for the production of bio-oil and synthesis gas. Pyrolysis and gasification was investigated using thermogravimetric analyzer (TGA) and bubbling fluidized bed gasification reactor to utilize forest woody biomass. Most of the materials decomposed between $320^{\circ}C$ and $380^{\circ}C$ at heating rates of $5{\sim}20^{\circ}C/min$ in thermogravimetric analysis. Bubbling fluidized bed reactor were use to study gasification characteristics, and the effects of reaction temperature, residence time and feedstocks on gas yields and selectivities were investigated. With increasing temperature from $750^{\circ}C$ to $850^{\circ}C$, the yield of char decreased, whereas the yield of gas increased. The gaseous products consisted of mostly CO, CO2, H2 and a small fraction of C1-C4 hydrocarbons.

• 한국대기환경학회지
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• 제28권3호
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• pp.306-315
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• 2012

In this study, storage stability of reduced sulfur compounds ($H_2S$, $CH_3SH$, DMS, $CS_2$, and DMDS) and $SO_2$ in sampling bags was investigated in terms of two contrasting storage approaches between forward (F) and reverse (R) direction. The samples for the F method were prepared at the same time and analyzed sequentially through time. In contrast, those of reverse (R) method were prepared sequentially in advance and analyzed all at once upon the preparation of the last sample. In addition, relative performance between two different bag materials (PVF and PEA) was also assessed by using 100 ppb standard. The response factors (RF) of gaseous RSC samples were determined by gas chromatography/pulsed flame photometric detector (GC/PFPD) combined with air server (AS)/thermal desorber (TD) system at storage intervals of 0, 1, and 3 days. There is no statistical difference in all RSCs between two storage methods. However, the results of relative recovery indicated 2.58~12.8% differences in compound type between the two storage methods. Moreover, loss rates and storage stability of $H_2S$ and $SO_2$ were considerably affected by bag materials than any other variables. Therefore, some considerations about storage methods (or bag material types) for sulfur compounds are needed if stored by sampling bag method.

• Journal of Korean Society for Atmospheric Environment
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• 제23권E1호
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• pp.16-28
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• 2007

An improved method was developed to determine gas-phase hydrogen peroxide($H_2O_2$) and organic hydro-peroxides (ROOH) in real-time, The analytical system for $H_2O_2$ is based on formation of hydroxybenzoic acid (OHBA), a strong fluorescent compound. OHBA is formed by a sequence of reactions, photoreduction of Fe(III)-EDTA to Fe(II)-EDTA, the Fenton reaction of Fe(II)-EDTA with $H_2O_2$, and hydroxylation of benzoic acid. By use of this analytical method rather than a previous similar method, Fenton reaction time was reduced from 2 min. to 30s. Air samples were collected by a surfaceless inlet to prevent inlet line losses. With a special arrangement of the sampling apparatus, sample delivery time was drastically reduced from ${\sim}5\;min\;to\;{\sim}20\;s$. The automated system was found to be sensitive, capable of continuous monitoring, and affordable to operate. A comparison of this method with a well-established one showed an excellent linear correlation, validating applicability of this technique to $H_2O_2$ determination. The system was applied to field measurements conducted during summertime of 2004 in Gwangju, South Korea. $H_2O_2$ was found to be a predominant species of peroxides. The diurnal variation of $H_2O_2$ displayed the maximum in early afternoon and the broad minimum throughout night. $H_2O_2$ was correlated positively with ozone, photochemical age, and temperature, however, negatively with $NO_x$ and relative humidity.

• 분석과학
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• 제23권5호
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• pp.446-456
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• 2010

본 연구에서는 악취성 카르보닐화합물(CC)의 채취에 많이 사용하는 DNPH cartridge의 분석 회수율을 다양한 방법으로 평가하였다. 이를 위해, 각기 다른 3종류의 DNPH cartridge (A =Waters, B = Top trading, C = Supelco) 제품을 대상으로 5가지 CC 성분들에 대하여 총 9 가지 농도단계(33~2600 nmol)의 작업용 표준시료를 제조하였다. 그리고 이들 제품들을 이용하여, 카트리지 분석 방식별, 제품별 성능을 평가하였다. 본 실험의 결과, cartridge 제품에서 acetaldehyde와 propionaldehyde 성분의 blank를 일반적으로 검출하였다. 검량 기울기 값을 비교하는 방식으로 5 가지 CC성분에 대한 제품별 회수율 비교하였다. 그 결과, 3 가지 제품 모두 CC 성분의 분자량이 증가할 경우 회수능이 감소하는 양상을 보였다. 그리고 회수율의 변화추이를 percent error(%)와 같은 변수로 살펴본 결과, 263 nmol 부터 1312 nmol 농도 범위에서 가장 안정적인 경향을 나타냈다. 이러한 점을 감안할 때, 분석 대상 CC에 대한 이상적인 농도범위와 cartridge의 선택이 정확한 분석자료를 확보하는데 중요한 요인으로 작용한다는 것을 알 수 있다.