• Korean Chemical Engineering Research
• /
• 제61권3호
• /
• pp.472-478
• /
• 2023

본 연구에서는 공기청정기 필터용 활성탄의 아세트알데하이드 제거 특성이 금속 촉매 첨착 및 관능기 도입 방법을 사용하여 조사되었다. 야자각 차의 KOH 활성화를 통해 고 비표면적(1700 m²/g)과 미세기공이 발달한 활성탄을 제조하였으며, 금속촉매 첨착과 관능기 개질을 위해 침지 후 기공 내 건조조건에 따른 첨착 효율을 조사하였다. 제조된 활성탄의 물성은 비표면적 및 기공 분석(BET), 유도결합 플라즈마 분광 분석(ICP), 유기 원소 분석(EA) 및 푸리에변환 적외선 분광 분석(FT-IR) 등을 통해 분석하였으며, 활성탄 성능 확인을 위해 침지 농도에 따른 아세트알데하이드 흡착성능을 가스크로마토그래피(GC)로 분석하였다. 첨착용액의 농도가 증가함에 따라 금속촉매 첨착량은 증가하였으며, 비표면적은 감소하는 경향을 보였다. 각 금속촉매 첨착 및 표면개질 활성탄의 파과시험 결과 MgO10@AC, CaO10@AC, EU10@AC, H-U3N1@AC 조성에서 우수한 아세트알데하이드 흡착성능을 보여주었다. 흡착성능이 가장 뛰어난 MgO10@AC에 대해 파과 시간은 533.8 분, 흡착량은 57.4 mg/g으로 측정되었으며, 이는 활성탄에 나노 크기의 MgO 촉매를 첨착할 경우 아세트알데하이드의 카보닐기와 상호작용하여 흡착성능이 개선됨을 알 수 있었다.

• 분석과학
• /
• 제20권6호
• /
• pp.516-523
• /
• 2007

2N급(99 %)의 실리카를 3N급(99.9 %)으로 향상시키기 위해서 널리 이용되고 있는 산 침출법(acid leaching)들의 정제효과와 실리카광물에 존재하는 불순물의 분석법에 대한 연구를 수행하였다. 산 침출법에 이용한 용액은 0.2M-oxalic acid (pH1.5, 2.5), conc-Aqua regia, 2.5 %-HCl/HF, 1 %-$HNO_3/HF$의 다섯 종류이었으며, 각 방법의 불순물 정제특성과 침출시간에 따른 침출효율을 조사하였다. 실리카광물과 침출용액중의 불순물 분석은 중성자방사화분석법(neutron activation analysis; NAA), 유도결합 플라즈마 원자방출 분석법(inductively coupled plasma atomic emission spectrometry; ICP-AES), 원자흡광 분광분석법(atomic absorption spectrometry; AAS), x-선 형광분석법(x-ray fluorescence; XRF), 그리고 습식분석법(wet analysis; WA)의 여섯 가지 방법을 이용하였으며, 불순물의 농도와 종류에 따른 분석법들의 장단점을 조사하였다. 실험에 사용한 실리카광물은 습식 비중선별 및 자력선별과 같은 물리적 정제를 거친 순도 99 %급의 실리카로서 $100-150{\mu}m$ 범위의 입도분포를 가지는 분말들이었다. 실리카중 주요 불순물은 Al, Fe, Na, Ca 및 Ti 이었으며 수백에서 수천 mg/kg의 농도로 존재하고 있었다. 산 침출방법과 불순물의 종류에 따른 정제효과를 비교한 결과 2.5 %-HCl/HF 침출방법이 가장 효과적이었으며 이 방법으로 99.1 % 실리카 분말을 99.8 %까지 순도를 향상시킬 수 있었다. 또한 실리카광물과 침출용액의 불순물의 종류와 함량에 따른 최적의 분석기술을 결정할 수 있었다.

• 청정기술
• /
• 제7권3호
• /
• pp.215-223
• /
• 2001

A present semiconductor cleaning technology is based upon RCA cleaning technology which consumes vast amounts of chemicals and ultra pure water(UPW) and is the high temperature process. Therefore, this technology gives rise to the many environmental issues, and some alternatives such as electrolyzed water(EW) are being studied. In this work, intentionally contaminated Si wafers were cleaned using the electrolyzed water. The electrolyzed water was generated by an electrolysis system which consists of three anode, cathode, and middle chambers. Oxidative water and reductive water were obtained in anode and cathode chambers, respectively. In case of NH4Cl electrolyte, the oxidation-reduction potential and pH for anode water(AW) and cathode water(CW) were measured to be +1050mV and 4.8, and -750mV and 10.0, respectively. AW and CW were deteriorated after electrolyzed, but maintained their characteristics for more than 40 minutes sufficiently enough for cleaning. Their deterioration was correlated with CO2 concentration changes dissolved from air. Contact angles of UPW, AW, and CW on DHF treated Si wafer surfaces were measured to be $65.9^{\circ}$, $66.5^{\circ}$ and $56.8^{\circ}$, respectively, which characterizes clearly the eletrolyzed water. To analyze the amount of metallic impurities on Si wafer surface, ICP-MS was introduced. It was known that AW was effective for Cu removal, while CW was more effective for Fe removal. To analyze the number of particles on Si wafer surfaces, Tencor 6220 were introduced. The particle distributions after various particle removal processes maintained the same pattern. In this work, RCA consumed about $9{\ell}$ chemicals, while EW did only $400m{\ell}$ HCl electrolyte or $600m{\ell}$ NH4Cl electrolyte. It was hence concluded that EW cleaning technology would be very effective for promoting environment, safety, and health(ESH) issues in the next generation semiconductor manufacturing.

• 분석과학
• /
• 제33권4호
• /
• pp.186-196
• /
• 2020

A simple and rapid preconcentration method of actinide from seawater using Actinide resin was developed and tested with the seawater spiked with a known U and Th. The developed method of Actinide resin based on column chromatography is less time-consuming and requires less labor compared with a typical co-precipitation technique for preconcentration of actinides. U and Th, which are relatively weak-bonded with Actinide resin among actinides, were used to determine the optimum flow rate of seawater sample and evaluate the capacity of Actinide resin to concentrate actinides from seawater. A flow rate of 50 mL min^-1 was available with Actinide resin 2 mL (BV, bed volume). When 5 or 10 L of seawater containing U were loaded on Actinide resin (2 mL, BV) at 50 mL min^-1, the recovery of U was 93 % and 86 %, respectively. For extraction of actinides bound with Actinide resin, we compared three methods: solvent extraction, ashing-acid digestion, and ashing-microwave digestion. Ashing-microwave digestion method shows the best performance of which is the recovery of 100 % for U and 81 % for Th. For the preconcentration of actinides in 200 L of seawater, a typical coprecipitation method requires 2-3 days, but the developed method in this study is achieved the high recovery of actinides within 12 h.

• 한국자기학회지
• /
• 제14권5호
• /
• pp.163-168
• /
• 2004

나노 두께의 NiFe의 자기적 특성을 살펴보기 위해 Si(100)/ $SiO_2$(200 nm)/Ta(5 nm)/N $i_{80}$F $e_{20}$(1～15 nm)의 구조를 ICP형 헬리콘 스퍼터로 제작하였다. 제작된 시편의 자기적 물성은 SQUID를 이용하여 $\pm$50 Oe에서의 4.2K와 300K에서 각각의 M-H loop를 측정하여 자기탄성에너지 변화와 보자력을 확인하였다. 또한 SQUID로 4.2K-300K에서의 M-T curve를 통해 온도에 따른 포화자화를 두께에 따라 살펴보았다. TEM을 사용하여 제작된 시편의 각 계면간의 미세구조를 살펴보았다 나노두께의 NiFe는 3 nm 이하에서는 $B_{bulk}$=0, $B_{surf}$=-3${\times}$$10^{-7}$(J/$m^2$)의 자기 탄성계수를 보였으며, 보자력은 급격히 증가하는 것을 확인하였다. 나노 두께의 퍼말로이는 계면효과에 의해서 벌크특성과 다른 자기탄성계수, 보자력, Ms의 변화가 발생하였다. 따라서 나노급 소자를 제작할 때 이러한 변화를 고려하여 설계하여야 하였다.

• 한국세라믹학회지
• /
• 제42권3호
• /
• pp.178-181
• /
• 2005

Silicon oxynitride (SiON) 막은 플라즈마 화학기상증착법(PECVD)으로 $SiH_4,\;N_2O$와 $N_2$ 가스를 사용하여 $SiO_2/Si$ 위해 증착되었다. 증착 변수에 따라서 SiON 막의 굴절률은 prism coupler를 사용하여 1552nm 파장에서 $1.4480\~1.4958$까지 변화하였다. 평판 광도파로 코어로 사용되는 SiON 막의 두께는 $6{\mu}m$이고, buffer 막과의 굴절률 차이(An)는 $0.36\%$이다. 또한 식각 공정으로 $SiO_2$ 막 위에 증착된 SiON 막은 건식식각을 통해서 수행되었다. 광화이버에 $1.55{\mu}m$ 파장의 레이저론 입력단에 조사하였다. 결과적으로 저굴절률 차이 SiON 광도파로를 제작하였으며, 출력단에서 single-mode 형상을 확인하였다.

• Bulletin of the Korean Chemical Society
• /
• 제28권8호
• /
• pp.1375-1382
• /
• 2007

A column preconcentration method with pulverized Amberlite XAD-4 loaded with bismuthiol I (BI) has been developed for the determination of trace Cd(II) and Cu(II) in various real samples by flame atomic absorption spectrophotometry. Various experimental conditions, such as the size of XAD-4, adsorption flow rate, amount of bismuthiol I, stirring time for adsorbing bismuthiol I on XAD-4, pH of sample solution, amount of XAD-4- BI, desorption solvent, and desorption flow rate, were optimized. Also, the adsorption capacity and the adsorption rate of Cd(II) and Cu(II) on XAD-4-BI were investigated. The interfering effects of various concomitant ions were investigated, Bi(III), Sn(II) and Fe(III) were found to affect the determination. But the interference by these ions was completely eliminated by adjusting the amount of XAD-4-BI resin to 0.70 g, although the adsorption flow rate was slower. For Cd(II) our proposed technique obtained a dynamic range of 0.5-40 ng mL-1, a correlation coefficient (R2) of 0.9913, and a detection limit of 0.3 ng mL-1. For Cu(II), the corresponding values were 2.0-120 ng mL-1, 0.9921 and 1.02 ng mL-1. To validate this proposed technique, the aqueous samples (stream water, reservoir water, tap water and wastewater), the diluted brass sample and the plastic sample, as real samples, were used. Recovery yields of 91-103% were obtained. These measured data were not different from ICP-MS data at 95% confidence level. Our proposed method was also validated using rice flour CRM (normal, fortified) samples. From the results of our experiment, we found that the technique we present here can be applied to the determination of Cd(II) and Cu(II) in various real samples.

• 한국환경과학회지
• /
• 제13권12호
• /
• pp.1079-1088
• /
• 2004

In order to understand chemical characteristics and dewfall formation in western Busan area, we analysed monthly distribution of dewfall, and investigated the correlation between dewfall formation amount and meteoro­logical factors. This study used the modified teflon plate $(1m{\times}1m)$ at Silla university in Busan from August 2002 to April 2003. In order to estimate qualitatively water soluble components, IC, ICP and UV methods for water soluble ions are also used respectively. Dewfall amount of sampling periods (47 day) collected 3.8 mm. Meteorological conditions for the formation of dewfall above $50\;g/m^{2}$ showed that temperature diurnal $range(^{\circ}C)\;was\;5.6^{\circ}C$ above, cloud amounts (1/10) at dawn of the sampling day was 7/10 below, mean wind speed at dawn (0~6hr) of the sampling day was 4.4 m/sec below, and mixing ratio at 6hr of the sampling day was 3.2 g/kg above. Distribution of water soluble ions in dewfall founded the highest concentration (206.1\;{\mu}eq/{\ell}\;for\;SO_{4}^{2-},\;42.4\;{\mu}eq/{\ell}\;for\;NH_{4}^{+},\;249.2\;{\mu}eq/{\ell}\;for\;Ca^{2+},\;and\;42.0\;{\mu}eq/{\ell}\;for\;Mg^{2+})$ during the March, the lowest concentration $(73.0\;{\mu}eq/{\ell}\;for\;SO_{4}^{2-},\;4.6\;{\mu}eq/{\ell}\;for\;NH_{4}^+\;and\;72.7\;{\mu}eq/{\ell}\;for\;Ca^{2+})$ during the August. Monthly equivalent ratio of $[SO_{4}^{2-}]/[NO_{3}^-]$ showed the highest value (4.99) during the October, the lowest value (1.84) during the August, and the mean value was 3.45.

• 한국수소및신에너지학회논문집
• /
• 제26권5호
• /
• pp.416-422
• /
• 2015

Lithium Ion capacitor (LIC) is a new storage device which combines high power density and high energy density compared to conventional supercapacitors. LIC is capable of storing approximately 5.10 times more energy than conventional EDLCs and also have the benefits of high power and long cycle-life. In this study, LICs are assembled with activated carbon (AC) cathode and pre-doped graphite anode. Cathode material of natural graphite and artificial graphite kinds of MAGE-E3 was selected as the experiment proceeds. Super-P as a conductive agent and PTFE was used as binder, with the graphite: conductive agent: binder of 85: 10: 5 ratio of the negative electrode was prepared. Lithium doping condition of current density of $2mA/cm^2$ to $1mA/cm^2$, and was conducted by varying the doping. Results Analysis of Inductively Coupled Plasma Spectrometer (ICP) was used and a $1mA/cm^2$ current density, $2mA/cm^2$, when more than 1.5% of lithium ions was confirmed that contained. In addition, lithium ion doping to 0.005 V at 10, 20 and $30^{\circ}C$ temperature varying the voltage variation was confirmed, $20^{\circ}C$ cell from the low internal resistance of $4.9{\Omega}$ was confirmed.

• 한국환경농학회지
• /
• 제40권1호
• /
• pp.67-72
• /
• 2021

BACKGROUND: Biological iron redox transformation alters iron minerals, which may act as effective adsorbents for arsenate [As(V)] in the environments. In the viewpoint of alleviating arsenate, microbial Fe(III) reduction was sought under high concentration of As(V). In this study, Fe(III)-reducing bacteria were isolated from the wild plant rhizosphere soils collected at abandoned mine areas, which showed tolerance to high concentration of As(V), in pursuit of potential agents for As(V) bioremediation. METHODS AND RESULTS: Bacterial isolation was performed by a series of enrichment, transfer, and dilutions. Among the isolated strains, two strains (JSAR-1 and JSAR-3) with abilities of tolerance to 10 mM As(V) and Fe(III) reduction were selected. Phylogenetic analysis using 16S rRNA genesequences indicated the closest members of Pseudomonas stutzeri DSM 5190 and Paenibacillus selenii W126, respectively for JSAR-1 and JSAR-3. Ferric and ferrous iron concentrations were measured by ferrozine assay, and arsenic concentration was analyzed by ICP-AES, suggesting inability of As(V) reduction whereas ability of Fe(III) reduction. CONCLUSION: Fe(III)-reducing bacteria isolated from the enrichments with arsenate and ferric iron were found to be resistant to a high concentration of As(III) at 10 mM. We suppose that those kinds of microorganisms may suggest good application potentials for As(V) bioremediation, since the bacteria can transform Fe while surviving under As-contaminated environments. The isolated Fe(III)-reducing bacterial strains could contribute to transformations of iron minerals which may act as effective adsorbents for arsenate, and therefore contribute to As(V) immobilization