• 방사성폐기물학회지
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• 제20권3호
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• pp.321-338
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• 2022

The transport of radionuclides at oceanic scales can be assessed using a Lagrangian model. In this review an application of such a model to the Atlantic, Indian and Pacific oceans is described. The transport model, which is fed with water currents provided by global ocean circulation models, includes advection by three-dimensional currents, turbulent mixing, radioactive decay and adsorption/release of radionuclides between water and bed sediments. Adsorption/release processes are described by means of a dynamic model based upon kinetic transfer coefficients. A stochastic method is used to solve turbulent mixing, decay and water/sediment interactions. The main results of these oceanic radionuclide transport studies are summarized in this paper. Particularly, the potential leakage of ¹³⁷Cs from dumped nuclear wastes in the north Atlantic region was studied. Furthermore, hypothetical accidents, similar in magnitude to the Fukushima accident, were simulated for nuclear power plants located around the Indian Ocean coastlines. Finally, the transport of radionuclides resulting from the release of stored water, which was used to cool reactors after the Fukushima accident, was analyzed in the Pacific Ocean.

• 한국진공학회지
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• 제14권2호
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• pp.97-102
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• 2005

제일원리 분자동역학 방법을 이용하여 Si(001) 표면에 NO 분자 흡착을 연구하였다. NO 분자가 Si(001)의 dimer축과 나란히 흡착될 경우에 50K에서도 분해가 일어났다. 이를 에너지 장벽으로 환산해 보면 0.006eV로서 거의 무시해도 좋을 정도이다 만일 NO 분자가 표면에 수직으로 들어오면 이웃에 있는 dimer에 걸쳐서 분해가 일어났다. 이 경우는 에너지 장벽은 0.08eV 정도였으며 여전히 낮은 수준이다. 분해가 된 산소분자는 dimer와 기판 사이의 backbend로 파고들어서 (에너지 장벽 0.007eV) 안정된 구조를 만들었다. 또 dimer에 나란히 흡착된 분자 상태의 경우는 N=Si_3$를 만들기도 하는데 속전자준위분광학(core level spectroscopy) 실험 결과와 일치한다.

• 방사성폐기물학회지
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• 제3권1호
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• pp.41-47
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• 2005

Cs$^{+}$ 이온에 대해 선택성을 갖는 ferrocyanide-음이온 교환수지를 제조하여 모의 제 염폐액 내에 존재하는 Cs$^{+}$ 이온에 대한 흡착실험을 수행하였다. 제조된 이온교환 수지가 citric acid를 주제염제로 하는 제염폐액 내에 존재하는 Cs+ 이온에 대한 흡착능력은 상용 양이온교환수지에 비해 4배 이상 효과적인 것으로 나타났다. 모의 제염폐액과 선택성 이온교환수지를 접촉시킨 후 360분이 경과하면 금속이온에 대한 흡착반웅이 평형에 도달하였다. 본 연구범위에서 Co$^{2+}$ 이온농도가 필요이상 증가하게 되면 Cs$^{+}$ 이온의 흡착율은 감소하였다. 과산화수소와 히드라진을 사용한 선택성 폐 이온교환수지의 재생실험 결과 전기중성화조건을 만족시키기 위해 Cs$^{+}$ 이온이 수지로부터 용출됨을 확인하였고 열화없이 재 사용가능성을 확인하였다.

• 폴리머
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• 제31권4호
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• pp.315-321
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• 2007

본 연구에서는 방사선 중합방법으로 아민화 PONF-g-GMA 이온교환 섬유를 합성하였다. 또한 핫멜트 web spray 접착방식으로 이들과 비드 수지를 결합시켜 복합 이온교환 섬유를 제조하고 이들의 바나듐 흡착특성을 확인하였다. 복합 이온교환 섬유의 이온교환 용량은 비드보다는 낮았으며, 단일 이온교환 섬유보다는 높게 나타났으며 최대 4.18 meq/g로 나타났다. 또한, 복합 이온교환 섬유의 바나듐 흡착 파과평형은 550분으로 비드 이온교환 수지보다 빠르게 진행되었고, 섬유상 이온교환체보다는 느리게 진행되었다. 한편, 바나듐의 흡착파과 시간은 pH가 낮아짐에 따라 파과가 빠르게 진행되었으며, 바나듐 농도가 증가함에 따라 흡착 평형에 도달하는 시간은 400분 전후에서 나타났다.

• 한국세라믹학회지
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• 제39권6호
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• pp.535-539
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• 2002

이 연구는 저온균일침전법으로 제조한 루타일 상의 TiO$_2$ 나노분말을 이용하여 AgNO$_3$ 수용액 중에서 광반응 조건에 따른 Ag 이온의 광흡차 특성을 고찰하였다. 자연광을 조사하였을 경우 흡척되는 Ag의 양이 9.32ppm이며 Ag 이온의 환원 속도는 느리지만 루타일 TiO$_2$ 나노분말이 자연광에서도 광촉매 반응을 일으킨다는 것을 확인하였다. 암반응 하에서도 TiO$_2$ 나노분말 자체의 밤송이 형태 때문에 Ag흡착 반응이 진행되었으며, UV를 적용할 때에는 120분 이내에 Ag 이온이 전부 흡착되었다. 광촉매 반응이 더 중요시 됨을 알수 있었다. 흡착 반응속도상수와 흡착 평형속도상수를 계산한 결과, 각각 0.0004g/min와 1494.20(120 $m^2$/g)를 나타내었다.

• 대한화장품학회지
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• 제24권3호
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• pp.51-58
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• 1998

Generally pigment differs from dye stuff because it cannot be melted in water but also because it is stable physically and chemically. In this study you will discover the function, properties and effects of Micai-TiO$_2$-SiO$_2$pigment as abase material pigment. But until now used Mica of the base material is about 7-l5${\mu}{\textrm}{m}$ with an average diameters of 15${\mu}{\textrm}{m}$. A new characteristic superficial pigment was obtained from covering the TiO$_2$ and SiO$_2$ with the adsorption result of isoelectric point of a Mica flake, TiO$_2$ and SiO$_2$In the composition reaction study of adsorption was done as well as the physical characteristics of the superficial texture of the obtained material. L,a,b of color change as oil was absorbed, optical nature and change of reflection according to direct and diffused reflection. In the composition of Mica slurry the best result obtained was in a solution with pH 2.0 to 2.3. Following this result, we can come to the idea that electrical attraction was done during the change of electrical charge of the Mica and TiO$_2$ deposit. Also this pigment shows a big scale between the direct reflection and diffused reflection light. Using this characteristic in cosmetic, it was obtained a natural but a contrast between light and shadow making possible a sculptured make-up. Color change due to oil adsorption was insignificant which improved the last of make up.

• 산업기술연구
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• 제23권A호
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• pp.199-206
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• 2003

The charcoal-encapsulated methyl silica microcapsules were prepared by a O/W microemulsion sol-gel method, and the adsorption properties on aquatic humic acid were investigated. The capsules prepared were spherical, $100{\sim}1000{\mu}m$ in size. The size distribution was controllable by adjusting the size of charcoal powder, charcoal/methyl silica ratio, and agitating speed in O/W sol-gel process. Adsorption efficiency of charcoal for aquatic humic acid was decreased after encapsulation by methyl silica shell. The decreased adsorption efficiency can be dependent on the decrease of the BET surface area and pore volume after encapsulation. Diffusion properties of humic acid through the capsule shell also played an important role on adsorption efficiency. Therefore, the reasonable target pollutants for the capsules can be VOC or odor molecules which can overcome diffusion barrier through shell of capsules in air condition. Functionalization methods for the charcoal-encapsulated $CH_3(SiO)_n$ microcapsules by incorporation of $TiO_3$ as a phtocatalytic function and by incorporation of inorganic pigment as a color function were also investigated. $TiO_2$ coating properties were controllable by adjusting pH, temperature, and the concentration of $TiOSO_4$. In XRD measurement, the crystal form of the coated $TiO_2$ was anatase. For the colorization of the capsules, inorganic pigments were more efficient than organic dyes, and various color was introduced to the capsules using inorganic pigments.

• 대한화장품학회지
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• 제30권3호
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• pp.321-328
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• 2004

주형합성법을 이용하여 메조기공(mesoporous pore)을 지닌 나노실리카 물질들과 나노카본볼의 대량생산법이 개발되었다. 암모니아, 트리메틸아민, 아세트알데히드 그리고 메틸메르캅탄과 같은 악취 물질들이 마크로기공 코어-메조기공 쉘(macro-porous core/mesoporous shell) 구조체인 나노카본볼에 흡착되는 현상이 상업용 탈취제인 활성탄과 비교 조사되었다. 나노카본볼에서의 악취의 흡착 및 분해는 활성탄에 비해 우수하게 관측되었고 촉매가 나노카본볼 내부에 첨착되면 더욱 악취 분해 특성이 증가되었다. 나노카본볼의 우수한 흡착 및 분해 특성을 이해하기 위해 물리화학적 특성인 균일한 기공, 넓은 표면적, 큰 기공 부피에 관한 기공 특성과 악취의 분해 현상이 연구되었다. 이러한 나노카본볼은 탈취제 분야에서 많은 응용성이 있을 것으로 전망된다.

• 상하수도학회지
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• 제33권4호
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• pp.251-258
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• 2019

The physical treatment such as chemical precipitation or adsorption was usually added after biological treatment in wastewater treatment process since it was enforced to reduce the concentration of phosphate for wastewater effluent to 0.2 mg/L as P which was well known as one of main nutrient causing eutrophication in waterbody. Therefore, the new material functioned for both adsorption and disinfection was prepared with Fe and Cu, and $TiO_2$, respectively, by changing the ratio of concentration referred to tri-metal (TM). According to SEM-EDS, $TiO_2$ was 30~40% composition for any TM regardless of any synthesis condition. However, the ratio of composition for Fe and Cu was dependent on the initial Fe and Cu concentration, respectively. The removal efficiency of phosphate was obtained to 15% at low initial concentration and the maximum uptake (Q) was calculated to ~11 mg/g through Langmuir isotherm model using TM1 which was synthesized at 1000 mg/L, 1000 mg/L, and 2 g (10 g/L) for $Fe(NO_3)_3$, $Cu(NO_3)_2$, $TiO_2$, respectively. In disinfection test, the efficiency of virus removal using TM was increased with increase of dosage of TM and can be reached 98% at 0.2 g.

• Journal of Microbiology and Biotechnology
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• 제30권7호
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• pp.996-1004
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• 2020

Various genetically engineered microorganisms have been developed for the removal of heavy metal contaminants. Metal biosorption by whole-cell biosorbents can be enhanced by overproduction of metal-binding proteins/peptides in the cytoplasm or on the cell surface. However, few studies have compared the biosorption capacity of whole cells expressing intracellular or surface-displayed metal-adsorbing proteins. In this study, several constructs were prepared for expressing intracellular and surface-displayed Ochrobactrum tritici 5bvl1 ChrB in Escherichia coli BL21(DE3) cells. E. coli cells expressing surface-displayed ChrB removed more Cr(VI) from aqueous solutions than cells with cytoplasmic ChrB under the same conditions. However, intracellular ChrB was less susceptible to variation in extracellular conditions (pH and ionic strength), and more effectively removed Cr(VI) from industrial wastewater than the surface-displayed ChrB at low pH (<3). An adsorption-desorption experiment demonstrated that compared with intracellular accumulation, cell-surface adsorption is reversible, which allows easy desorption of the adsorbed metal ions and regeneration of the bioadsorbent. In addition, an intrinsic ChrB protein fluorescence assay suggested that pH and salinity may influence the Cr(VI) adsorption capacity of ChrB-expressing E. coli cells by modulating the ChrB protein conformation. Although the characteristics of ChrB may not be universal for all metal-binding proteins, our study provides new insights into different engineering strategies for whole-cell biosorbents for removing heavy metals from industrial effluents.