• Bulletin of the Korean Chemical Society
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• 제31권7호
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• pp.1869-1874
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• 2010

By reducing PVP with $H_2NOH$.HCl and NaOH 2:2:1 mass ratios in aqueous ethanol, poly-N-vinyl pyrrolidone oxime [PVPO] was prepared with 92% yield. Applying the sol-gel concept, orthosilicic acid [OSA] was made by hydrolyzing TEOS with ethanol in 1:0.5 molar ratios using 1 N KOH aqueous solution as a catalyst. The OSA + PVPO + $_L$-Valine ($\alpha$-amino acid) were mixed with pure ethanolic medium in 1:2:2 mass ratios and refluxed at $78^{\circ}C$ and 6 pH for 6.5 h. A white residue of poly-N-vinyl pyrrolidone oximo-L-valyl-siliconate [POVS] appeared after 5 h. The heating of reaction mixture was stopped and the contents were brought to NTP. The residue formation of POVS was intensified with lowering a temperature and completely solidified within 5 h, was filtered using a vacuum pump with Whatmann filter paper no. 42. The residue of POVS was washed several times with 20% aqueous cold ethanolic solution and dried in vacuum chamber at $25^{\circ}C$ for 24 h. The MP was noted above $350^{\circ}C$. Structural and internal morphology were analyzed with IR and $^1H$-NMR, and SEM respectively. A drug loading and transporting ability of the POVS in water and at pH = 5 and 8 was determined chromatographically.

• 대한전기학회논문지:전기물성ㆍ응용부문C
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• 제48권2호
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• pp.69-75
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• 1999

The characteristics of $H_2$ gas detection have been investigated using the Pt-MIS capacitor composed of the LPCVD nitride on the oxide. The flat band voltage shift is measured as 0.1 V in 1,000 ppm $H_2$ gas ambient and to be independent of Pt catalyst thickness. It is found that the flatband voltage shift is proportional to the hydrogen concentrations. The response and recovery time of Pt-MIS capacitor are 5 mins and 25 mins respectively. The samples of 30nm thick Pt revealed much higher sensitivity than that of 150nm samples. The samples of 150nm Pt showed that the flatband voltage shift of the device is due to the formation of the dipole layer of the adsorbed hydrogen atoms at the Pt-insulator interface.

• 한국전기전자재료학회논문지
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• 제19권3호
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• pp.292-300
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• 2006

In order to improve energy efficiency in the dilute trichloroethylene removal using the nonthermal plasma process, the barrier discharge treatment combined with manganese dioxide was experimentally studied. Reaction kinetics in this process was studied on the basis of final byproducts distribution. Decomposition efficiency was improved to about $99\;\%$ at the specific energy of 40 J/L with passing through manganese dioxide. C=C ${\pi}$ bond cleavage of TCE substances gave DCAC, which has the single bond of C-C through oxidation reaction during the barrier discharge plasma treatment. Those DCAC were broken easily in the subsequent catalytic reaction due to the weak bonding energy about $3{\sim}4\;eV$ compared with the double bonding energy in TCE molecules. Oxidation byproducts of DCAC and TCAA from TCE decomposition are generated from the barrier discharge plasma treatment and catalytic surface chemical reaction, respectively. Complete oxidation of TCE into COx is required to about 400 J/L, but $CO_2$ selectivity remains about $60\;\%$.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2011년도 추계학술대회 초록집
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• pp.109.2-109.2
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• 2011

바이오디젤의 생산은 원료유의 순도와 촉매 종류, 알코올의 양, 반응시간, 반응 온도와 같은 다양한 조건을 이용하여 최적의 조건을 찾아내는 것이 중요하며 이는 곧 생산단가와 직결된다. 바이오디젤 전환 시 고체촉매를 이용하면 후처리 공정의 단순화가 가능하며 글리세린의 순도가 약 98%로 매우 높아져 고부가 물질 생산 원료로 활용이 가능하다는 장점이 있으며 생산 단가를 4~20% 가량 낮출 수 있다. 본 연구에서는 바이오디젤의 경제적인 생산을 위하여 정제공정을 단순화 시킬 수 있는 방안으로 3종의 고체촉매를 이용하여 동 식물성 유지의 바이오디젤로 전환 실험을 수행 하였다. 촉매 활성화를 위하여 고체촉매를 $700^{\circ}C$에서 3~5시간 소성하고 동 식물성 유지를 이용 전이에스테르화 반응실험을 수행하여 30분 간격으로 시료를 수집 하였다. 실험 결과, 동물성 폐유지로부터 반응 120분 후에 최대 90% 이상의 지방산 메틸에스테르로의 전환율을 얻을 수 있었으며 식물성 유지인 팜유에서는 86%, 유채유에서는 64%의 전환율을 나타냈다. 동 식물성 유지의 초기 산가는 0.45~2mg KOH/g 사이로 나타났다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2011년도 추계학술대회 초록집
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• pp.73.2-73.2
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• 2011

합성천연가스(SNG: Synthetic Natural Gas)를 얻기 위해, 석탄 가스화로부터 얻은 합성가스는 일반적으로 수소와 일산화탄소의 비가 3.0($H_2$/CO)이 되도록 수성가스전환(WGS)반응을 거친 후 메탄화반응기로 유입되며, 가능하면 낮은 온도에서 메탄 전환율이 높은 메탄화 반응의 특성상 강한 발열반응이 수반되므로 이를 낮추는 것이 중요하다. 또한, 최종생성물내의 메탄 농도를 높이기 위해 WGS 이후 탈황과 동시에 이산화탄소를 제거하기 위한 공정이 요구된다. 본 연구에서는 정제된 합성가스의 WGS와 이산화탄소 제거가 생략된 공정을 개발하기 위해, 상업용 촉매에 대하여 수소의 농도가 낮은 합성가스를 이용하여 스팀과 이산화탄소에 대한 메탄화반응 특성을 평가하였다. 또한, 이산화탄소의 존재여부에 따라 스팀으로 메탄화반응과 WGS가 동시에 일어날 수 있는 최적의 운전조건을 얻고자 하였다.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2000년도 제1회 학술대회 논문집
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• pp.55-56
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• 2000

We report the fabrication of carbon nanostureture films with excellent electron-emission characteristics on chrome electrodes using a pre-deposited transition metal catalyst layer. The emission current densities of 1 ${\mu}A/cm^2$ and 1 $mA/cm^2$ were measured at the electric field of 2.5 and 4.8 $V/{\mu}m$, respectively, and the current fluctuation of less than 2.5% was observed at the average current density 211 ${\mu}A/cm^2$ for the measurement duration of 20 minutes. We counted more than ${\sim}10^4$ emission sites per $cm^2$ from the emission images, and also noticed good mechanical stability. Moreover, we were able to fabricate good electron-emitting carbon films on chrome electrodes on Corning glass substrates at the nominal temperature below $650^{\circ}C$.

• 한국표면공학회지
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• 제49권6호
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• pp.521-529
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• 2016

In this study, titanium nanotubes, prepared by anodization method, showing high surface and strong chemical stability in acidic and basic media, have been employed for the application to the electrodes for water splitting in KOH solution. Due to its high polarization resistance of $TiO_2$ itself, proper catalysts are essentially required to reduce overpotentials for water oxidation and reduction. Most of academic literature showed noble metal catalysts for foreign dopants in $TiO_2$ electrodes. From commercialization point of view, screening of low-cost catalyst is important. Herein, we propose molybdenum oxide as low-cost catalysts among various catalysts tested in the experiments, which exhibits the highest performance for hydrogen evolution reaction in highly alkaline solution. We showed that molybdenum oxide doped electrode can be operated in extreme acidic and basic conditions as well.

• KSBB Journal
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• 제27권1호
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• pp.51-56
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• 2012

This research was to investigate the polyester preparation using waste ethylene glycol (EG) generated from the wastepaper pretreatment process. Waste EG was obtained from using EG five times repeatedly in the pretreatment of wastepaper. The hydroxyl value of the waste EG was 441 mg KOH/g and its composition was 0.68% cellulose, 6.5% hemicellulose, 6.1% lignin, and 86.7% EG. Maleic acid was used as carboxylic acid. The effect of reaction temperature and time except carboxyl group/hydroxyl group ratio on the crosslinkage of the prepared polyester was marginal. Citric acid, lithium hydroxide and dicumyl peroxide were used as additive or catalyst to enhance the crosslinkage of polyester. Among them, 10% of citric acid was found to be most effective. The crosslinkage was 86% when the polyester was prepared at an optimum condition such as $130^{\circ}C$ and 15 minutes, 1.5 of C/H ratio, and 10% of citric acid, and its insoluble percentage in boiling water for 6 hours was 47%. The weight loss of the prepared polyester was approximately 40% when it was buried in damp soil for 5 months, indicating that it is readily biodegradable. This results can provide some information for future development of wastepaper pretreatment by organic solvent.

• 한국축산식품학회지
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• 제41권4호
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• pp.731-738
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• 2021

Herein, a novel analytical method using a high-performance liquid chromatography-fluorescence detector (HPLC/FLD) is developed for rapidly measuring an L-carnitine ester derivative in infant powdered milk. In this study, solid-phase extraction cartridges filled with derivatized methanol and distilled water were used to effectively separate L-carnitine. Protein precipitation pretreatment was carried out to remove the protein and recover the analyte extract with a high recovery (97.16%-106.56%), following which carnitine in the formula was derivatized to its ester form. Precolumn derivation with 1-aminoanthracene (1AA) was carried out in a phosphate buffer using 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) as the catalyst. Method validation was performed following the AOAC guidelines. The calibration curves were linear in the L-carnitine concentration range of 0.1-2.5 mg/L. The lower limit of quantitation and limit of detection of L-carnitine were 0.076 and 0.024 mg/L, respectively. The intra- and interday precision and recovery results were within the allowable limits. The results showed that our method helped reduce the sample preparation time. It also afforded higher resolution and better reproducibility than those obtained by traditional methods. Our method is suitable for detecting the quantity of L-carnitine in infant powdered milk containing a large amount of protein or starch.

• Korean Chemical Engineering Research
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• 제48권3호
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• pp.322-326
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• 2010

수소발생용으로 사용되는 $NaBH_4$ 수용액의 저장과정 중에 $NaBH_4$ 안정성에 대해 연구하였다. $NaBH_4$의 안정성을 증가시키기 위해 NaOH와 KOH를 사용하였으며, $NaBH_4$의 저장 중 가수분해반응에 미치는 알칼리와 $NaBH_4$ 농도, 온도 그리고 저장 용기 재질의 영향을 실험하였다. 알칼리농도가 증가할수록 $NaBH_4$가 수용액 중에서 안정화되기 때문에 수소발생 속도가 감소하였다. $NaBH_4$ 농도를 10에서 15 wt%로 증가시켰을 때 안정성이 감소하다 15 wt% 이상으로 농도를 증가시켰을 때는 pH의 증가에 의해 안정성이 증가하였다. $NaBH_4$ 농도를 25 wt%, NaOH 3.0 wt%일 때 수소발생 활성화 에너지 값은 115.1 kJ/mol 로 촉매를 사용했을 때보다 활성화 에너지 값이 1.5~4.0배 높았다. 유리나 스텐리스-스틸에 저장된 $NaBH_4$ 용액의 안정성이 플라스틱에 저장된 $NaBH_4$ 용액의 안정성보다 더 높았다.