• 한국대기환경학회지
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• 제6권2호
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• pp.161-167
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• 1990

The reaction of sulfur dioxide with cupric oxide supported on zeolite was investigated over a temperature range of $250{\sim}450^{{\circ}C$. After the completion of the $SO_2$ removal reaction, the cupric sulfate produced was regenerated to copper by hydrogen or LPG. The experimental results showed that the removal efficiency of $SO_2$ was improved with temperature increase and with $SO_2$ inlet concentration decrease. The reaction of $SO_2$ with CuO/Zeolite was well explained by the shrinking unreacted core model using first order chemical reaction control and diffusion control. THe reaction rate constant and the effective diffusivity were respectively as follows: 1k (cm/s) = 2.519 exp[-10991 (cal/mol)/RT] $De(cm^2/s) = 2.06 \times 10^{-5} exp[-8380 (cal/mol)/RT]$

• The Korean Journal of Ceramics
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• 제5권3호
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• pp.284-287
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• 1999

CuO catalyst-coated alumino-silicate fiber filters were prepared for the simultaneous removal of particulate matter and gaseous contaminants such as NOx and SOx. Hot gas cleaning experiments similar to Shell UOP process other than the catalyst supporting materials were carried out between 300 and $500^{\circ}C$ for the evaluation of the gas removal efficiency of the catalytic filter. Experimental results showed that removel efficiency for $SO_2$ was greater than 99% in the temperature range 450~$500^{\circ}C$ and more than 90% of NO was collected between 350 and $370^{\circ}C$. It was found that the higher the CuO content, the higher the removal efficiency for $SO_2$. Removal efficiency for NO was more affected by the gas cleaning temperature than by the CuO content in the catalyst-filter.

• 한국지하수토양환경학회지:지하수토양환경
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• 제26권1호
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• pp.45-53
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• 2021

The removal of 2,4-dichlorophenoxyacetic acid (2,4-D) in aqueous solution by coupled electro-oxidation and Fe(II) activated persulfate oxidation process was investigated. The electrochemical oxidation was performed using carbon sheet electrode and persulfate using Fe(II) ion as an activator. The oxidation efficiency was investigated by varying current density (2 - 10 mA/㎠), electrolyte (Na2SO4) concentration (10 - 100 mM), persulfate concentration (5 - 20 mM), and Fe(II) concentration (10 - 20 mM). The 2,4-D removal efficiency was in the order of Fe(II) activated persulfate-assisted electrochemical oxidation (Fe(II)/PS/ECO, 91%) > persulfate-electrochemical oxidation (PS/ECO, 51%) > electro-oxidation (EO, 36%). The persulfate can be activated by electron transfer in PS/ECO system, however, the addition of Fe(II) as an activator enhanced 2,4-D degradation in the Fe(II)/PS/ECO system. The 2,4-D removal efficiency was not affected by the initial pHs (3 - 9). The presence of anions (Cl- and HCO3-) inhibited the 2,4-D removal in Fe(II)/PS/ECO system due to scavenging of sulfate radical. Scavenger experiment using tert-butyl alcohol (TBA) and methanol (MeOH) confirmed that although both sulfate (SO4•-) and hydroxyl (•OH) radicals existed in Fe(II)/PS/ECO system, hydroxyl radical (SO4•-) was the predominant radical.

• 한국환경보건학회지
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• 제23권3호
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• pp.102-108
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• 1997

It has been studied that SO$_2$ removal efficiency of anthracite-bituminous coal blend combustion in a fludized bed coal combustor. The objectives of this study were to investigate SO$_2$ removal characteristics of coal blend combustion with Ca/S, anthracite fraction, bed temperature, and limestone size. The experimental results were presented as follows First, the effect of the desulfurization by the dia size of limestone was great and SO$_2$ removal efficiency was highest in limestone dia 631 $\mu$m. Second, as air velocity increased, the desulfurization rate decreased a little. But the difference of the desulfurization rate according to air velocity was not too large. As the height of fluidized bed combustor increased regardless of air velocity, SO$_2$ concentration tends to increase largely. Third, as Ca/S mole ratio incresed, SO$_2$ desulfurization rate incresed rapidly up to Ca/S mole ratio 3 while the desulfurization rates did not increse too largely in the range of more than the level. Forth, the bed temperature had a great effect on the desulfurization rate and the desulfurization rate tended to increase slightly as anthracite fraction increased.

• Korean Chemical Engineering Research
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• 제47권4호
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• pp.512-517
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• 2009

순산소 연소에서 $SO_2$ 농도는 배가스의 재순환으로 인해 기존의 공기연소에 비해 3배 이상 높게 나타나고, $CO_2$ 농도와 $SO_2$ 농도가 높기 때문에 탈황현상이 기존의 공기 연소와는 다르게 나타난다. 본 연구에서는 순산소 연소조건에서 로내탈황 특성을 알아보기 위해 Drop Tube Furnace(DTF)를 이용하여, 반응온도, 유입 $SO_2$ 농도 그리고 Ca/S 비 등의 운전변수에 따른 $SO_2$ 제거효율을 측정하였으며 수분의 영향에 대해서도 알아보았다. 반응온도, 유입 $SO_2$ 농도 그리고 Ca/S 비가 증가함에 따라 $SO_2$ 제거효율은 증가하였고 유입가스 내 수분이 존재할 경우 $SO_2$ 제거효율은 약 4~6% 증가하는 것으로 나타났다.

• 한국물환경학회지
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• 제24권6호
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• pp.659-669
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• 2008

Two sets of four parallel activated sludge reactors (ASRs) maintaining an MLSS of 3000 mg/L were operated to investigate the effect of DO, HRTs and bio-contact media (BCM) packing ratios on the removal efficiency of organic matters and nitrogen. Packing ratios of BCM to BCM-ASR systems 1, 2, 3, and 4 were 0% (suspended growth only), 10%, 15% and 20%, respectively. All systems were operated at an HRT of 4 hr, 6 hr, and 8 hr, respectively; DO concentration was maintained 0.5~1.0 mg/L and 1.5~2.0 mg/L for each HRT condition. In terms of TSS, TCODcr and SCODcr removal efficiency, all systems had a similar level of the removal efficiency under varied HRTs, and DO. But organic removal efficiency of systems with BCM was approximately 3~5% higher than systems without BCM at the same HRT and the DO. About the nitrification efficiency, with high DO (1.5~2.0 mg/L), as HRT (4 hr, 6 hr, 8 hr) or BCM packing ratio increased, the slight increment of nitrification efficiency was observed. However, under the low DO (0.5~1.0 mg/L), increase of BCM packing ratio and HRT resulted in large increase of the nitrification efficiency. At the same HRT and BCM packing ratio, the nitrification efficiency increased greatly with up to 15% as DO increased. When the HRT increased from 4hr to 8hr, the denitrification efficiency slightly increased by 5~10% only, under all DO conditions. Systems with BCM had higher denitrification efficiency, ranged 62.7~91.1% than systems without BCM showed 32.1~65.6%. And the increase in BCM packing ratio from 10% to 20% resulted in about 14~16% denitrification efficiency increment. BCM packing ratio showed great effect on the denitrification. The increase of the DO (from 0.5~1.0 mg/L to 1.5~2.0 mg/L) at the same HRT and BCM packing ratio resulted in slight decrease of denitrification efficiency with up to 7% for systems with BCM. But for systems without BCM, the denitrification efficiency decreased with up to 28%. In all system, the denitrification efficiency had more influence on the TN removal efficiency than nitrification efficiency. So, BCM packing ratio (0%, 10%, 15%, 20%) has greater effect on the TN removal than HRT and DO. The TN removal efficiency increased as packing ratio of BCM increased with up to 45%. As a result, the highest TN removal efficiency was observed 73.7% at the condition showed the highest denitrification efficiency that DO of 0.5~1.0 mg/L, an HRT of 8 hr, and 20% of BCM packing ratio was maintained.

• 공업화학
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• 제5권5호
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• pp.836-842
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• 1994

가스분사반응기(Jet bubbling reactor)에서의 가스분사관의 최적 설계조건과 $SO_2$ 제거효율에 미치는 운전변수들의 영향을 검토하였다. 효과적인 기-액 접촉을 위한 가스분사관의 설계에 있어서 가장 중요한 인자는 Reynolds number로서 Reynolds number를 12,000 이상으로 하고 가스분사관과 가스분사구멍에서의 Reynolds number가 동일하게 되도록 가스분사관을 설계하는 것이 가스분사관 설계의 최적조건인 것으로 판단된다. ${\Delta}P$, pH, 유입 $SO_2$농도, 석회석 입자크기 등 공정의 운전변수 중에서 $SO_2$ 제거효율에 가장 큰 영향을 미치는 변수는 ${\Delta}P$였으며 pH 4.0하에서 90% 이상의 $SO_2$ 제거효율을 얻기 위해서는 ${\Delta}P$를 230mmAq 이상으로 유지시켜야 하였다. 실험결과 3.0 정도의 낮은 pH 하에서도 높은 $SO_2$ 제거효율이 얻어졌으며 이러한 이유는 강제산화에 의해 흡수액내의 $HSO{_3}{^-}$이온이 $SO{_4}{^{2-}}$ 이온으로 거의 완전한 산화가 일어나 흡수액 내의 $SO_2$ 평형분압이 매우 낮은 상태로 유지되었기 때문으로 생각된다. 또한 흡수액의 pH 5.0 이하의 조건에서는 $SO_2$ 흡수에 사용된 석회석의 입자크기에 관계없이 모두 99.5% 이상의 높은 석회석 이용률을 나타내었다.

• 한국안전학회지
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• 제6권4호
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• pp.26-33
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• 1991

To remove SO$_2$ from flus gas, cupric oxide, manganese oxide and iron oxide were studied with varying loading value. The experiment was carried out in a flow reactor and the reactants were prepared by impregnation method using alumina. The reaction temperature was varied from 30$0^{\circ}C$ to 45$0^{\circ}C$. Experimental results showed that all of these metal oxides were effective on SO$_2$ removal reaction and cupric oxide was the best reactant. The sample with 10wt％ loading value was better reactant than with 20wt％ because in case of 20wt％ loading, metal dispersion on the alumina surface was not uniform. And the SO$_2$ removal efficiency was increased with the reaction temperature.

• 한국재료학회지
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• 제16권2호
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• pp.75-79
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• 2006

The effect of ozone and/or ultrasound treatments on the efficiency of slurry removal in post sliced cleaning (PSC) of silicon ingot was studied. Efficiency of slurry removal was evaluated as functions of time, temperature and surfactant with DOE (Design of Experiment) method. Residual slurries were observed on the wafer surface in case of cleaning by ozone or ultrasound separately. However, a clean wafer surface was appeared when cleaned with ozone and ultrasound simultaneously. It has found that cleaning time was the main effect among temperature, time and surfactant. Elevated temperature, addition of surfactant and high ozone concentration helped to accelerate efficient removal of slurry. The improvement of removal efficiency seems to be related to the formation of more active OH radicals. The highly cleaned surface was achieved at 10 wt% ozone, 1 min and 10 vol% surfactant with ultrasound. Application of ozone and ultrasound might be a useful method for PSC process in wafer cleaning.

• 상하수도학회지
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• 제22권3호
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• pp.307-314
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• 2008

In this study, the effects of applied voltage, solution pH and coexistence of other ions such as sulfate ion (${SO_4}^{2-}$) and chloride ion ($Cl^-$) were investigated on the removal of nitrate-nitrogen ($NO_3{^-}-N$) from ground water by electrodialysis. The examined operating conditions were evaluated for optimizing the removal efficiency of $NO_3{^-}-N$. Real ground water samples taken from a rural area of Yongin city and artificial ones with components similar to the real ground water were tested for the study, which contained $NO_3{^-}-N$ concentration of 17mg/L that exceeds current drinking water quality standard of 10 mg/L. The increase in the removal rate of $NO_3{^-}-N$ was observed as the applied voltage increased from 5V to 30V, while no significant increase in the removal rate appeared at the applied voltage beyond 20V during a given operating time. The removal rate appeared to get lower at both acidic and basic condition, compared to neutral pH. Coexistence of of ${SO_4}^{2-}$and $Cl^-$ demanded much longer operating time to achieve a given removal rate or to meet a certain level of treated water concentration. When nitrate ion was combined with ${SO_4}^{2-}$and $Cl^-$, the removal rate was reduced by 4.29% and 10.83%, respectively.