• Environmental Engineering Research
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• 제16권3호
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• pp.149-157
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• 2011

Nanofiltration (NF) experiments were conducted to investigate fouling of Al-hydroxide precipitate and the influence of organic compound, inorganic compound, and their combination, i.e., multiple foulants. $CaCl_2$ and $MgSO_4$ were employed as surrogates of inorganic compounds while humic acid was used as surrogate of organic compound. The flux attained from NF experiments was fitted with the mathematical fouling model to evaluate the potential fouling mechanisms. Al-hydroxide fouling with a cake formation mechanism had little effect on the NF membrane fouling regardless of the Al concentration. The NF fouling by Al-hydroxide precipitate was deteriorated in presence of inorganic matter. The effect of Mg was more critical in increasing the fouling than Ca. This is because the Mg ions enhanced the resistances of the cake layer accumulated by the Al-hydroxide precipitate on the membrane surfaces. However, the fouling with Mg was dramatically mitigated by adding humic acid. It is interesting to observe that the removal of the conductivity was enhanced to 61.2% in presence of Mg and humic acid from 30.9% with Al-hydroxide alone. The influence of dissolved matter (i.e., colloids) was more negative than particulate matter on the NF fouling for Al-hydroxide precipitate in presence of inorganic and organic matter.

• Environmental Engineering Research
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• 제16권2호
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• pp.91-96
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• 2011

Limited information is available on the degradation of volatile hydrocarbons determined via the use of plate-inserted photocatalytic reactors. This has led to the evaluation of surface areas of cylindrical continuous-flow photocatalytic reactors for the degradation of three selected aromatic hydrocarbons. Three types of reactors were prepared: a double cylinder-type, a single cylindrical-type without plates and a single cylindrical-type with inserted glass tubes. According to diffuse reflectance, FTIR and X-ray diffraction (XRD) spectroscopy, the surface characteristics of a coated photocatalyst were very similar to those of raw $TiO_2$, thereby suggesting that the coated photocatalyst exhibited the same photocatalytic activity as the raw $TiO_2$. The photocatalytic degradation efficiencies were significantly or slightly higher for the single cylinder-type reactor than for the double cylinder-type reactor which had a greater catalytic surface area. However, for all target compounds, the degradation efficiencies increased gradually when the number of plates was increased. Accordingly, it was suggested that the surface area being enhanced for the plate-inserted reactor would elevate the photocatalytic degradation efficiency effectively. In addition, this study confirmed that both initial concentrations of target compounds and flow rates were important parameters for the photocatalytic removal mechanism of these plate-inserted photocatalytic reactors.

• Environmental Engineering Research
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• 제22권1호
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• pp.95-107
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• 2017

Adsorption equilibrium and kinetic behavior of two toxic heavy metals hexavalent chromium [Cr(VI)] and mercury [Hg(II)] on mustard oil cake (MOC) was studied. Isotherm of total chromium was of concave type (S1 type) suggesting cooperative adsorption. Total chromium adsorption followed BET isotherm model. Isotherm of Hg(II) was of L3 type with monolayer followed by multilayer formation due to blockage of pores of MOC at lower concentration of Hg(II). Combined BET-Langmuir and BET-Freundlich models were appropriate to predict Hg(II) adsorption data on MOC. Boyd's model confirmed that external mass transfer was rate limiting step for both total chromium and Hg(II) adsorptions with average diffusivity of $1.09{\times}10^{-16}$ and $0.97m^2/sec$, respectively. Desorption was more than 60% with Hg(II), but poor with chromium. The optimum pH for adsorptions of total chromium and Hg(II) were 2-3 and 5, respectively. At strong acidic pH, Cr(VI) was adsorbed by ion exchange mechanism and after adsorption reduced to Cr(III) and remained on MOC surface. Hg(II) removal was achieved by complexation of $HgCl_2$ with deprotonated amine ($-NH_2$) and carboxyl (COO-) groups of MOC.

• 한국수산과학회지
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• 제26권4호
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• pp.369-379
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• 1993

1992년 동계에 췌셰픽만의 꽃게자원에 대하여 예망을 사용한 연속채집법에 의한 어획 효율성을 조사하였다. 일반선형모델 분석에 따르면 26회에 걸친 야외시험 결과 어획효율성은 저질이나 수심, 사용된 조사선박에 따라 통게학적으로 유의한 차이가 나타나지 않았다. 예망효율(즉, 어획율)은 Leslies방법과 단순히 개조된 방법 등의 두 방법을 사용하여 추정하였다. 평균 어획율은 0.26 (표준오차:0.03)으로 추정되었는데 이는 한번의 예망을 사용하여 채집장소에 존재하고 있는 꽃게 가운데 단지 $26\%$($95\%$ 신뢰한계 : $20{\sim}32\%$)를 잡을 수 있다는 의미이다. 예망효율은 꽃게의 밀도가 증가함에 따라 지수적으로 감소하였다.

• 한국수자원학회:학술대회논문집
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• 한국수자원학회 2005년도 학술발표회(2)
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• pp.1179-1180
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• 2005

To immobilize the pollutants from wastewater in situ, two phosphatic clays collected from different areas in Egypt (eastern and western Sebaia, Aswan-Isna, Upper Egypt) used to remove contaminant ions from industrial wastewater. Obtained results confirmed the strong relationship between phosphatic clay and Pb elimination from wastewater. The sensitivity classification of phosphatic clay toward ions retained as described in three categories: highly sensitive to retain Pb , Al and Cr ; moderately sensitive for Mn; and weakly sensitive for Band Zn. Data suggested that large fraction of Pb removed by phosphatic clays stayed intact under a wide variation in extracting solution pH (3-11). In situ immobilization is considered a promising technique that has the potential to remove contaminant ions from wastewater. Two important factors need to be considered when applying this technique: The first, is the clay must be effective and selective under different composition of wastewater. The second, is the immobilized ions should be stable and non-leacheable under varying water conditions. Phosphatic clays with $Pb^{2+}$ were suitable to achieve these two factors. Possible mechanism for removal $Pb^{2+}$ by phosphatic clays is the formation of fluoropyromorphite through the dissolution of fluoro and hydroxyl apatite by its precipitation from solution, beside, Pb complexation at phosphatic clay surface at P-OH sites.

• Tribology and Lubricants
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• 제21권1호
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• pp.33-38
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• 2005

Fretting is the oscillatory motion with very small amplitudes, which usually occurs between two solid surfaces in contact. Fretting wear is the removal of material from contacting surfaces through fretting action. Fretting wear of steam generator tubes in nuclear power plant becomes a serious problem in recent years. The materials for the tubes usually are Inconel 690 (I-690) and Inconel 600 (I-600). In this paper, fretting wear tests for I-690 and I-600 were performed under various applied loads in water at room temperature. Results showed that the fretting wear loss of I-690 and I-600 tubes was largely influenced by stick-slip. The fretting wear mechanisms were the abrasive wear in slip regime and the delamination wear in stick regime. Also, I-690 had somewhat better wear resistance than I-600.

• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2001년도 춘계학술대회 논문집
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• pp.1117-1120
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• 2001

Chemical mechanical planarization(CMP) has emerged as the planarization technique of choice in both front-end and back-end integrated circuit manufacturing. Conventional CMP process utilize a polyurethane polishing pad and liquid chemical slurry containing abrasive particles. There have been serious problems in CMP in terms of repeatability and defects in patterned wafers. Since IBM's official announcement on Copper Dual Damascene(Cu2D) technology, the semiconductor world has been engaged in a Cu2D race. Today, even after~3years of extensive R&D work, the End-of-Line(EOL) yields are still too low to allow the transition of technology to manufacturing. One of the reasons behind this is the myriad of defects associated with Cu technology. Especially, dishing and erosion defects increase the resistance because they decrease the interconnection section area, and ultimately reduce the lifetime of the semiconductor. Methods to reduce dishing & erosion have recently been interface hardness of the pad, optimization of the pattern structure as dummy patterns. Dishing & erosion are initially generated an uneven pressure distribution in the materials. These defects are accelerated by free abrasive and chemical etching. Therefore, it is known that dishing & erosion can be reduced by minimizing the abrasive concentration. Minimizing the abrasive concentration by using Ce$O_2$ is the best solution for reducing dishing & erosion and for removal rate. This paper introduce dishing & erosion generating mechanism and a method for developing a semi-rigid abrasive pad to minimize dishing & erosion during CMP.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 추계학술발표회
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• pp.23-26
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• 2001

Batch test and column test were performed to develop the design factors for PRBs against the contaminated groundwater by ammonium and lead. Clinoptilolite, one of the natural zeolites having excellent cation exchange capacity(CEC), was chosen as the reactive material through the ion-exchange mechanism. In the batch test, the reactivity of Clinoptilolite to ammonium and lead was examined with varying the particle size of Clinoptilolite. The nit weight of Clinoptilolite showed removal efficiencies of 65 % against the ammonium and 98% against lead. The effect of particle size of Clinoptilolite was not noticeable. In the column test, the permeability was examined using flexible-wall permeameters with varying the particle size of Clinoptilolite. When the washed Clinoptilolite having the diameter of 0.42-0.85 nm was mixed with Jumunjin sands in 20:80 ratio (w/w), the highest permeability of 2$\times$10$^{-3}$ -7 x 10$^{-4}$ cm/s was achieved. The reactivity and the strength property of the mixed material were investigated using fixed wall column having 8 sampling ports on the wall and the direct shear test, respectively. Clinoptilolite was found to be a suitable material for PRBs against the contaminated groundwater with ammonium and/or heavy metals.

• 한국초전도ㆍ저온공학회논문지
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• 제22권2호
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• pp.1-6
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• 2020

Large-scale civil engineering works discharge a large amount of soil suspension contaminated with natural heavy metals. Most of the heavy metal ions due to industrial activities and minings are accumulated in the soils and the sediments of lakes and inner bays through the rivers. It is necessary to remove heavy metals from the soils and the sediments, because some of these heavy metals, such as arsenic and cadmium, have significant biological effects even in small amounts. This study proposes a new volume reduction method of the contaminated soils and sediments by superconducting magnetic separation. Our process can remove the specific minute minerals selectively, which adsorbs heavy metals depending on pH. As a fundamental study, the adsorption behaviors of arsenic and cadmium on minute minerals as a function of pH were investigated, and the adsorption mechanism was discussed based on the crystal structure and pH dependence of surface potential in each minute minerals.

• 한국지반공학회:학술대회논문집
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• 한국지반공학회 2000년도 가을 학술발표회 논문집
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• pp.435-442
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• 2000

Batch test and column test were performed to develop the design factors for permeable reactive barriers(PRBs) against ammonium and heavy metals, Clinoptilolite, a kind of natural zeolites having excellent cation exchange capacity(CEC), was choosen for the reacting materials through the ion-exchange mechanism. In the batch test, the reactivity of clinoptilolite for ammonium, lead, and copper was examined varying the initial concentration of contaminants(ammonium: 20, 40, 80 ppm, heavy metals: 10, 20, 40 ppm) and the particle size of clinoptilolites(0-0.15, 0.42-0.85, 1-1.25 mm). The reactivity is increasing as the initial concentration decrease and particle size decrease. In the column test, the permeability and the reactivity of the specimens were examined using flexible-wall permeameter. Specimens were made of clinoptilolite and Jumunjin-sand with 20 : 80 weight ratio varying particle size of clinoptilolite. The maximum permeability(1${\times}$10$\^$-4/-5${\times}$10$\^$-5/cm/s) was achieved in the specimen made of 0.42-0.85 mm clinoptilolite and sand.