• KSBB Journal
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• 제16권2호
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• pp.128-132
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• 2001

발효 배양액으로부터 균체를 제거한 후에 전분파의 흡착성 을 증가시켜주기 위하여 ammonium sulface 25% (w/v), 반응 2시간 정도면 95% 이상의 효소가 전분(힐반전분 1%, wfv)에 홉착됨올 일 수 있었다. 효소 흡착인 경우 일반전분(옥수수 전분)이 흡착율 95% 이상으로 가장 효과적이며 탈착의 경우 (탈착용액 : 증류수)에는 산화천분이 1 회 68%로 가장 효과적이었다. 또한 효소의 홉착 및 탈착에 사용되는 전분익 농도 는 효소 역가 205 U/mL 기준으로 1 % (v/v) 정도면 효소의 흡착 및 탈착에 적당하였다. 효소 흡착외 경우 $4^{circ}C$, 정도에서, 탈착의 경우 온도 $50^{circ}C$, 와 pH 8.0에서 효과적이었다 탈착 용액으로 Iris-buffer가 탈착율 98%로 가장 효과적이었다. 또한 발효배양액으토부터 균체외 제거단계의 유무에 관계없이 전분의 흡착율과 탈착율은 유사하였다.

• 공업화학
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• 제28권3호
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• pp.332-338
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• 2017

본 연구에서는 주요한 휘발성 유기화합물의 발생원인 도장공장 중에서 중소규모의 공장에 적용 가능한 저온 vacuum swing adsorption (VSA) 기술에 대하여 연구하였다. 저온 VSA 기술이란 기존의 thermal swing adsorption (TSA)의 단점을 보완하기 위하여 저온($60{\sim}90^{\circ}C$)에서 감압하여 흡착질을 탈착하는 방식이다. 국내에서 시판되고 있는 상용 활성탄을 이용하여 대표적인 VOCs인 톨루엔의 흡 탈착 특성을 랩(Lab)규모로 실험하였으며, 이를 바탕으로 $30m^3min^{-1}$ 규모의 VSA 시스템을 설계하여 실제 도장 공장에 적용하여 VSA 시스템의 현장적용 가능성에 대하여 평가하였다. 랩 규모 실험 결과, 2 mm 펠렛형 활성탄은 4 mm 펠렛형 활성탄보다 높은 톨루엔 흡착능을 나타내었으며, 이에 파일럿 규모의 VSA의 충진 활성탄으로 사용되었다. 탈착 실험에서는 $80{\sim}90^{\circ}C$의 온도와 100 torr의 압력이 최적 조건으로 결정되었다. 랩 규모 실험 결과를 바탕으로 파일럿 규모 VSA 시스템을 설계하였으며 실제 도장 공장에 현장 적용하여 95회 흡 탈착 실험을 반복 수행하였다. 수행 결과, 연속 흡 탈착 반복실험 후, 도정공장에서 배출된 VOCs를 98% 이상 효과적으로 제거 가능함을 확인하였으며 VSA 시스템의 안정적인 현장 적용이 가능함을 검증하였다.

• Environmental Engineering Research
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• 제22권2호
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• pp.169-174
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• 2017

Vacuum swing adsorption (VSA) is a promising treatment method for volatile organic compounds (VOCs). This study focuses on a VSA process for regenerating activated carbon spent with VOCs, and then investigates its adsorption capacities. Toluene was selected as the test VOC molecule, and the VSA regeneration experiments results were compared to the thermal swing adsorption process. Cyclic adsorption-desorption experiments were performed using a lab-scale apparatus with commercial activated carbon (Samchully Co.). The VSA regeneration was performed in air (0.5 L/min) at 363.15 K and 13,332 Pa. The comparative results depicted that in terms of VSA regeneration, it was found that after the fifth regeneration, about a 90% regeneration ratio was maintained. These experiments thus confirm that the VSA regeneration process has good recovery while operating at low temperatures (363.15 K) and 13,332 Pa.

• 분석과학
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• 제11권3호
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• pp.174-178
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• 1998

Formaldehyde와 resorcinol을 반응시켜 chelating 수지를 제조하였다. 이 수지는 Pb(II)나 Ni(II)와 같은 전이금속에 대해 높은 흡착능을 나타내었다. Pb(II), Ni(II), Co(II), Fe(II)와 Zn(II)의 흡착과 탈착율을 batch법으로 구하였다. 이 수지의 중요한 특성은 금속 이온과 수지의 수소 이온간의 교환과정이다. 금속이온의 흡착과 탈착의 메카니즘은 수지의 작용기인 수소 이온의 탈착과 금속 이온간의 교환반응으로 생각된다. 이 수지를 이용하여 전이금속을 농축시키고, 다른 이온들로부터 Pb(II)를 분리하는데 적용해 보았다.

• 한국산학기술학회논문지
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• 제12권5호
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• pp.2439-2444
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• 2011

기존에 주로 사용되었던 활성탄을 대체할 수 있는 활성탄소섬유를 이용하여 휘발성 유기화합물질의 흡 탈착 특성을 연구하였으며, 고정층을 이용하여 흡착 및 파과특성을 조사하였다. 활성탄소섬유중 ACFJ의 경우가 활성탄에 비하여 약1.15배 높은 흡착량을 보였으며, 흡착층의 온도가 증가함에 따라 파과시간 및 흡착량은 감소하였다. 또한 활성탄의 경우 약 99%까지 탈착하는데 20분이 소요되었으며, 활성탄소섬유의 경우 약 99% 탈착되기까지 5분이 걸려 활성탄소섬유가 약 4배 빠르게 탈착됨을 알 수 있었다.

• 한국자동차공학회논문집
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• 제14권3호
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• pp.125-132
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• 2006

Transient kinetics of $NH_3$ adsorption/desorption and of SCR(selective catalytic reduction) of NO with $NH_3$ were studied over vanadium based catalysts, such as $V_2O_5/TiO_2$ and $V_2O_5-WO_3/TiO_2$. In the present catalytic reaction process, NO adsorption is neglected while $NH_3$ is strongly chemisorbed on the catalytic surface. Accordingly, it is ruled out the possibility of a reaction between strongly adsorbed $NH_3$ and NO species in line with the hypothesis of an Eley-Rideal mechanism. The present kinetic model assumes; (1) non-activated $NH_3$ adsorption, (2) Temkin-type $NH_3$ coverage dependence of the desorption energy, (3) non-linear dependence of the SCR reaction rate on the $NH_3$ surface coverage. Thus, the surface heterogeneity for adsorption/desorption of $NH_3$ is taken into account in this model. The present study extends the pure chemical kinetic model based on a powdered-phase catalytic system to the chemico-physical one applicable to a realistic monolith reactor.

• 한국대기환경학회지
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• 제30권4호
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• pp.362-377
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• 2014

Polycyclic aromatic hydrocarbons (PAHs) have been of particular concern since they are present both in the vapor and particulate phases in ambient air. In this study, a simple method was applied to determine the vapor phase PAHs, and the performance of the new method was evaluated with a conventional method. The simple method was based on adsorption sampling and thermal desorption with GC/MS analysis, which is generally applied to the determination of volatile organic compounds (VOCs) in the air. A combination of Carbotrap (300 mg) and Carbotrap-C (100 mg) sorbents was used as the adsorbent. Target compounds included two rings PAHs such as naphthalene, acenaphthylene, and acenaphthene. Among them, naphthalene was listed as one of the main HAPs together with a number of VOCs in petroleum refining industries in the USA. For comparison purposes, a method based on adsorption sampling and solvent extraction with GC/MS analysis was adopted, which is in principle same as the NIOSH 5515 method. The performance of the adsorption sampling and thermal desorption method was evaluated with respect to repeatabilities, detection limits, linearities, and storage stabilities for target compounds. The analytical repeatabilities of standard samples are all within 20%. Lower detection limits was estimated to be less than 0.1 ppbv. In the results from comparison studies between two methods for real air samples. Although the correlation coefficients were more than 0.9, a systematic difference between the two groups was revealed by the paired t-test (${\alpha}$=0.05). Concentrations of two-rings PAHs determined by adsorption and thermal desorption method consistently higher than those by solvent extraction method. The difference was caused by not only the poor sampling efficiencies of XAD-2 for target PAHs and but also sample losses during the solvent extraction and concentration procedure. This implies that the levels of lower molecular PAHs tend to be underestimated when determined by a conventional PAH method utilizing XAD-2 (and/or PUF) sampling and solvent extraction method. The adsorption sampling and thermal desorption with GC analysis is very simple, rapid, and reliable for lower-molecular weight PAHs. In addition, the method can be used for the measurement of VOCs in the air simultaneously. Therefore, we recommend that the determination of naphthalene, the most volatile PAH, will be better when it is measured by a VOC method instead of a conventional PAH method from a viewpoint of accuracy.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2000년도 제18회 학술발표회 논문개요집
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• pp.139-139
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• 2000

We have investigated the adsorption and reaction of Cu(hfac)(vtms) on Cu(111) surface using TPD. The recombinative desorption of Cu(hfac)(vtms) reversibly occurs between 240 and 340K. The remaining Cu(hfac) after the desorption of vtms preferentially undergo the desorption between 330 and 370K as intact Cu(hfac) than the disproportionation reaction. The disprportionation reaction between adsorbed Cu(hfac) was observed to occur between 420 and 520K with an activation energy of 34~37 kcal/mol. the geometries and adsorption sites of Cu(hfac) have been also calculated by means of extended H ckel method. It is found that standing Cu(hfac) is more stable than lying-down Cu(hfac) on the Cu(111) surface and the Cu(hfac) molecule prefers to adsorb on the hollow site over the top or bridge sites. We also have investigated the surface modification effect by preadsorbed I and Na atoms on the reaction Cu(hfac)(vtms).

• Bulletin of the Korean Chemical Society
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• 제16권2호
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• pp.143-148
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• 1995

Ketene (CH2CO) adsorption on Ag(111) has been studied in ultrahigh vacuum using electron energy loss spectroscopy and temperature programmed desorption. Ketene adsorbs molecularly on Ag(111) at temperatures below 126 K. The coverage increases linearly with exposure until saturation. No multilayer formation and no shift in desorption temperature with coverage were observed, indicating a lack of attractive interaction between adsorbate molecules. The desorption activation energy is estimated to be 7.8 kcal/mol by assuming first order kinetics and a pre-exponential factor of 1013 sec-1. The adsorption geometry of ketene on the surface is determined from the relative intensities of the vibrational energy loss peaks. The CCO axis of CH2CO is found to be almost parallel to (∼4°away from) the surface and the molecular plane is almost perpendicular to the surface (∼3°tilt).

• Bulletin of the Korean Chemical Society
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• 제16권2호
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• pp.157-163
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• 1995

The adsorption and decomposition of NO on a stepped Pt(111) surface have been studied using thermal desorption spectroscopy and Auger electron spectroscopy. NO adsorbs molecularly in two different states of the terrace and the step, which are distinguishable in thermal desorption spectra. NO dissociates via a bent species at the step sites on the basis of vibrational spectrum data reported previously. The dissociation of NO is an activation process : the activation energy is estimated to be about 2 kcal/mol. Increase in the NO dissociation with adsorption temperature is explained by a process controlled by diffusion of the dissociated atomic nitrogen from the step to the terrace of the surface. In addition to NO and N2, the desorption peak of N2O is observed. We conclude that the formation of N2O is attributed to surface reaction of NO and N adsorbed on the surface.