• 한국구조물진단유지관리공학회 논문집
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• 제15권1호
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• pp.215-225
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• 2011

메타카올린은 고령토나 카올린으로 알려진 카올린 광물의 풍화물로, 도자기 산업에 주로 사용되는 원료로, 일반적으로 메타카올린의 입자 크기는 시멘트보다는 작지만, 마이크로 실리카퓸보다는 크다. 본 연구에서는 콘크리트용 혼화재로 메타카올린을 사용한 콘크리트의 압축강도와 염소이온 투과저항 특성에 관한 영향에 관해 조사하였다. 메타카올린과 실리카퓸의 혼입률이 압축강도와 염소이온 투과저항에 주는 영향을 비교하기 위해 물-결합재비를 30%로 고정하고 각각 0, 5, 10, 15, 20%인 배합수준을 설정하여 비교하였다. 연구결과 메타카올린을 혼입한 콘크리트는 실리카퓸을 혼입한 콘크리트와 유사한 강도특성을 보였지만, 염소이온 투과저항성은 다소 불리한 것으로 나타났다. 따라서, 강도와 염소이온 투과저항 성능을 동시에 만족하기 위한 메타카올린의 혼입률은 10% 정도인 것으로 나타났다.

• 한국물환경학회지
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• 제20권2호
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• pp.145-150
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• 2004

This study investigated the effect of chlorine dose and chlorine reaction time for the formation of haloacetic acids (HAAs). According to the results, HAA formation was highly affected by chlorine dose and chlorine reaction time. HAA formation reached a plateau value at 30 mg/L of chlorine dose and 24 hr of chlorine reaction time. For the speciation of formed HAAs in the test water, the concentration of brominated-HAAs was significantly lower than that of chlorinated-HAAs because of low level of bromide ion concentration in the test water. It also investigated the removal efficiency of HAA precursors by several unit processes, such as ozone alone, UV alone, and combined ozone/UV system. Of them, ozone/UV system was proved as the best process to control the HAAs formation. The increase of the brominated-HAAs was observed during ozonation with and without UV irradiation showing the slight increase of total HAA concentrations.

• 한국진공학회:학술대회논문집
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• 한국진공학회 1999년도 제17회 학술발표회 논문개요집
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• pp.65-65
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• 1999

Dry etching technique provides more easy controllability on the etch profile such as anisotropic etching than wet etching process and the results of lots of researches on the characterization of various plasmas or ion beams for semiconductor etching have been reported. Chlorine-based plasmas or chlorine ion beam have been often used to etch several semiconductor materials, in particular Si-based materials. We have studied the effect of He flow rate on the Si and SiO2 dry etching using chlorine-based plasma. Experiments were performed using reactive ion etching system. RF power was 300W. Cl2 gas flow rate was fixed at 58.6 sccm, and the He flow rate was varied from 0 to 120 sccm. Fig. 1 presents the etch depth of si layer versus the etching time at various He flow rate. In case of low He flow rate, the etch rate was measured to be negligible for both Si and SiO2. As the He flow increases over 30% of the total inlet gas flow, the plasma state becomes stable and the etch rate starts to increase. In high Ge flow rate (over 60%), the relation between the etch depth and the time was observed to be nearly linear. Fig. 2 presents the variation of the etch rate depending on the He flow rate. The etch rate increases linearly with He flow rate. The results of this preliminary study show that Cl2/He mixture plasma is good candidate for the controllable si dry etching.

• 펄프종이기술
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• 제30권3호
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• pp.1-6
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• 1998

Elementally Chlorine Free (ECF) bleaching will be superior than Totally Chlorine free (TCF) bleaching, not only because they have no significant difference in effluent toxicity, but also those pulps bleached by ECF have higher brightness, strength, yield, etc., over those by TCF. With this belief, this paper focused on the chemistry of chlorine dioxide decomposition and ionization, both in water solution and in pulp slurry. Special attention was paid to chlorate ion because there have been controversies as how it is formed and what its behavior to the end pH of pulp bleaching is. As a result, during ionization of chlorine dioxide with water, both chlorate and chlorite were found to increase with increasing pH, but during ionization with pulp, chlorite was found to increase with end pH while chlorate decreased with increasing end pH. In the case of ionization with water, the disproportion equation $2CIO_2 + OH^{-} \lightarrow H_2O + CIO_3^{-} + CIO_2^{-}$ was thought to become the main reaction with the increasing pH, while in the case of ionization with pulp, the reaction $HCIO + CIO_2^{-}\lightarow H^{+} + Cl^{-} + CIO_3^{-}$ was the main reaction contributing to the formation of chlorate. Based on this above opinion, the contrary results of chlorine dioxide ionization from different researchers were discussed and explained.

• 한국수소및신에너지학회논문집
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• 제28권6호
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• pp.683-690
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• 2017

Wood pellet (WP), empty fruit bunch (EFB) and palm kernel shell (PKS) which are biomass fuels for power generation are selected to study the characteristics of torrefaction process. These biomass fuels are torrefied at $220^{\circ}C$, $250^{\circ}C$, and $280^{\circ}C$. The heating value of biomass fuels is increased depending on the torrefaction temperature. However, due to energy yield decline, it is not always desirable to torrefy biomass at higher temperature. Considering the mass yield and energy yield after torrefaction, the most proper temperature conditions for torrefaction of WP is $250-280^{\circ}C$ and for EFB, PKS are $220-250^{\circ}C$. Additionally, to investigate the phenomenons of chlorine release during torrefaction process, Ion Chromatography (IC) method was used. In the case of EFB and PKS torrefied at $300^{\circ}C$, the chlorine component has been reduced by 97.5% and 95.3% compared to the raw biomass, respectively. In conclusion, torrefied biomass can be used as alternative fuels in replacement of coals for both aspects of heating value and chlorine corrosion problems.

• 분석과학
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• 제23권1호
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• pp.45-53
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• 2010

우라늄 화합물 중에 함유된 염소를 정량하기 위하여 수증기증류 및 열가수분해를 이용한 량 염소의 분리 및 정량법을 개발하였다. 수증기 증류에 의한 시료 중의 염소를 분리하기 위하여 수증기 발생장치, 증류플라스크 및 냉각기 등으로 구성된 장치를 제작 설치하였다. LiCl 표준용액과 모의사용후핵 연료 일정량을 혼합하여 만든 우라늄 화합물 시료 중의 염소를 분리하기 위하여 혼산(0.2 M ferrous ammonium sulfate-0.5M sulfamic acid 3 mL + phosphoric acid 6 mL + sulfuric acid 15 mL)을 이용하여 $140^{\circ}C$로 증류시키고 $90{\pm}5\;mL$를 수집하였다. 열가수분해에 의한 시료 중의 염소를 분리하기 위하여 공기공급장치, 온수공급장치, 석영반응관, 연소로 및 연소보트, 그리고 휘발 염소 흡수장치로 구성된 열가수분해장치를 제작 설치하였다. 일정량의 우라늄 화합물 시료에 반응촉진제($U_3O_8$)를 가하고 1 mL/min의 공기유속과 $80^{\circ}C$의 공급수 온도를 유지하고 $950^{\circ}C$에서 1시간 반응시켜 시료 중의 염소를 분리하였다. 두 방법에 의하여 수집된 각 흡수용액은 일정부피로 희석하고 이온크로마토그래피로 정량하여 회수율을 측정하였다. 금속전환체 잔류 용융염 중의 미량 염소를 이온크로마토그래피로 정량하기 위하여 시료를 공기 및 건조 산화시키고 분쇄한 후 열가수분해하여 염소를 회수하였다.

• 한국건축시공학회지
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• 제22권6호
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• pp.577-583
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• 2022

대형 현장의 경우 다수의 레미콘사에서 콘크리트를 납품받게 되는 경우가 많으나 동일 콘크리트 배합표를 사용하더라도 재료와 제조장비의 등의 차로 인해 품질에 편차가 있을 것으로 생각된다. 하지만 그러한 검토 실적은 미비한 실정에 본 연구에서는 부산 지역의 12개 레미콘사에서 납품 받은 콘크리트를 대상으로 굳기 전 콘크리트 물성 및 압축강도, 염소이온 확산계수를 측정하였다. 굳기 전 콘크리트 물성은 기준을 만족하였고 압축강도는 설계기준 압축강도 대비 128%를 나타내었다. 염소이온 확산계수의 경우도 큰 편차없이 설계기준 압축강도별 평균값을 도출할 수 있었다. 압축강도는 강도가 높을수록 편차가 컸으며 염소이온 확산계수는 강도가 낮을수록 편차가 큰 경향을 파악할 수 있었다.

• Membrane and Water Treatment
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• 제11권3호
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• pp.201-206
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• 2020

Electrodialysis (ED) is used in wastewater treatment, during the processing and recovery of beneficial materials, to produce usable water. In this study, sulfate and chlorine ions, which are the anions majorly used for electroplating, were studied as factors affecting the recovery of copper, nickel and water from wastewater by electrodialysis. Although the removal rates of copper and nickel ions were slightly higher with the use of chlorine ions than of sulfate ions, the removal efficiencies were above 99.9% under all experimental conditions. The metal ions of the plating wastewater flowed through the ion exchange membrane of the diluate tank and the concentrate tank while all the water moved together due to electro-osmosis. The migration of water from the diluate tank to the concentrate tank was higher in the presence of a monovalent chloride ion compared to that of a divalent sulfate ion. When sulfate was the anion used, the recoveries of copper and nickel increased by about 25% and 30%, respectively, as compared to the chloride ion. Therefore, when divalent ions such as sulfate are present in the electrodialysis, it is possible to reduce the movement amount of water and highly concentrate the copper and nickel in the plating wastewater.

• 환경위생공학
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• 제21권4호
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• pp.49-60
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• 2006

The ion exchange resins have been synthesized from chlormethyl styrene - 1,4 - divinylbenzene(DVB) with 1%, 2%, 4% and 8%-crosslinking and 1-aza-18-crown-6 macrocyclic ligand by copolymerization method. Content of chlorine in styrene-DVB copolymer was decreased as crosslink increased and it is because as crosslink increased 1%, 2%, 4% and 8% DVB content increased and crosslink density increased and cavity was reduced. Functional group of resin almost disappeared as C-C1 peak around $700cm^{-1}$ was substituted with 1-aza-18-C-6 macrocyclic ligand and new peak of C-N around $1020cm^{-1}$ appeared, so it was confirmed that styrene-DVB copolymer and ligand were compounded. As crosslink increased in the analysis of element contents, it resulted in the reduction of nitrogen content and it is because as crosslink increased, it led to the reduction of chlorine content in the process of substitution reaction and it affected macrocyclic ligand substituted. Thermo analysis curve of functional synthetic resin decomposed three part of 1-aza-18-C-6, styrene, and DVB. Form of functional synthetic resin showed distortion of its particles as macrocyclic ligand was introduced to styrene-DVB copolymer and hydrogen of ligand caused substitution with chlorine element of styrene molecule.

• 한국재료학회지
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• 제20권2호
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• pp.82-89
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• 2010

Benzotriazole (B.T.A) which has been mainly used for the stabilization processing method of excavated copper and bronze artifacts is vaporized within 2~3 years after the usage because it is unstable at the acid conditions and cannot protect the surface of artifacts. In this study, NaOH method which has been used for the steel artifacts was applied as a stabilization process for the method of copper and bronze artifacts to gush chlorine ion out. For the reproduction of excavated samples, copper and bronze plates were dipped in 0.1M HCl for 26 hrs to form CuCl, rusted at $70^{\circ}C$ with RH 75% for the formation of corrosion products, and desalted in 0.1 M NaOH solution. The concentration of chlorine ion was measured by using ionchromatography. During the desalting process, a large quantity of chlorine ions was gushed out in early period and corrosion products were not additionally generated through the re-corrosion experiment. This NaOH desalting process was found to be a method of stabilization process for copper and bronze artifacts from the formation of Tenorite (CuO) during desalting as a protection layer for corrosion.