• 한국산학기술학회논문지
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• 제14권5호
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• pp.2544-2549
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• 2013

고성능 고분자/클레이 나노 복합재료의 제조 과정에는 친수성을 보이는 클레이 원료 물질인 $Na^+$-MMT (sodium monmorilonite)를 친유성을 갖도록 유기화된 계면활성제로처리하여 개질하는 과정이 필수적이다. 이를 위하여 이 연구에서는 VDAC (vinylbenzyldimethyl-dodecylammonium chloride)를 간단한 화합물로부터 합성하였고 이를 이용하여 양이온 교환반응에 의하여 $Na^+$-MMT를 개질한 후 $VDA^+$-MMT를 제조하였다. 이를 스티렌과 혼합하여 in-situ 중합에 의하여 나노복합재료를 제조하였고 클레이의 분산성 및 차단특성을 연구하였다. 연구 결과 PS/$VDA^+$-MMT 나노 복합재료의 경우 클레이의 분산이 $Na^+$-MMT와 비교할 때 현저히 증가함을 확인하였고 이로 인해 유기 용매에 대한 차단 특성이 매우 우수함을 확인하였다.

• 자원환경지질
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• 제27권6호
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• pp.507-521
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• 1994

Bentonite occurs in the Janggi Conglomerate of Tertiary age and consists mainly of montmorillonite with Mg as predominant interlayer cations. The bentonite was reacted with various concentrations of sulfuric acid (0.8~1.5M) for various reaction time (1-10h) at $103^{\circ}C$. Cation exchange capacity, exchangeable cations, surface area and solid acidity of the original bulk and acid activated bentonites were measured. Chemical analysis, X-ray diffraction, differential thermal analysis and infrared spectroscopy were used to characterize the changes in structure and properties of the acid activated bentonite. The dissolution of octahedral cations occurs not only from the edge of the clay platelets but also throughout the whole clay structure creating vacant octahedral sites. These lattice defects are created by $H^+$ diffused into the smectite layers. The cations leached possibly from the octahedral sheets are adsorbed on the interlayer exchange sites. They are exchanged with hydronium ions again by stronger acid attack. These reactions create wedge-shaped pores resulting in the increase of the surface area and the changes the morphology in the lattice structure.

• Journal of Photoscience
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• 제6권3호
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• pp.91-96
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• 1999

Zeolites and microporouos materials continue to attract attention as novel hosts for photochemical reactions. Zeolities are attractive because of their ability to selectivity exchange and incorporate species within the void spaces and interconnecting channels, providing a spatial arrangement of molecules. Our research has primarily focused on intrazeolitic electron transfer from excited Ru(bpy)32+ in supercages of zeolite Y to a series of bipyridinium ions. In the Ru(bpy)32+ viologen-zeolite Y samples, the slowing of the back electron transfer from the bipyridinium radical cation to Ru(bpy)32+ allows for charge propagation via self exchange between diquat molecules. This provides an opportunity for permanent charge separation. When the migrating charge on the diquat radical within the zeolite reaches the surface, it can be transferred to a neutral viologen (PVS) in solution, resulting in permanent charge separation. The advantage of long-lived charge separation can be exploited for useful chemistry if suitable catablysts can be assembled on the zeolities. We have studied Ru(bpy)2 as water oxdiation catalysts. We have demonstrated that synthesis of RuO2 fibers on a zeolite via thermal decomposition of Ru3(CO)12 leads to the most active water decomposition catalyst reported to date. Because of the extensive interest of photochemical water reduction to H2, much is known about catalytic systems usin gone electron catalyst, and even more importantly, that no reaction of viologen occurred with H2 over this catalyst. The present challenge is to incorporate all these elements of the system into an architecture and we are examining zeolite membranes for this purpose.

• 대한화학회지
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• 제24권5호
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• pp.356-360
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• 1980

팔면체 구조를 갖는 Co(Ⅲ) glycine methyl ester 착물을 합성하고 원소분석과 적외선 스펙트럼 및 핵자기공명스펙트럼을 이용하여, 이들 착물의 구조에 관하여 고찰하였다. 이들 중 $[Co(gly)_2(glycinemethylester)Cl]Cl_2$ 착물은 양이온 교환수지인 Dowex 50W-X8을 이용하여 분히하였으며, 가능한 기하학적 이성질체는 $C_1-cis(0-0), C_2-cis(0-0), trans(0-0)$ 형태의 구조를 가지고 있음을 확인하였다.

• 한국세라믹학회지
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• 제14권2호
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• pp.95-103
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• 1977

Characteristics of Ham Pyong clay and clay-organic complexes were investigated by means of geological exploration, chemical analysis, X-ray diffraction, differential thermal analysis, electron microscopy, thermal mechanical analysis, cation exchange capacity and viscosity measurement. The results are as follows; 1) This caly is a transported clay which has black and white colors, and the amounts of deposit are estimated about 1, 600, 000M/T. 2) The major mineral phases identified by X-ray diffraction are kaolinite, sericite and halloysite and the minor phases are quartz and feldspar, these mineral phases can be seperated very easily by the elutriation method. 3) It was supposed that the black colored clay involved a certain clay-organic complexs by the mechanism of intercalation as well as surface absorption. 4) The clay-organic complexes in clay seemed to improve dispersity, to increase the fluidity of clay-water slips, to decrease the firing shrinkage and to promote the thermo-chemical reaction at temperature range up to 50$0^{\circ}C$, but not to effect on the resulted firing color.

• 대한방사선기술학회지:방사선기술과학
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• 제13권2호
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• pp.43-49
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• 1990

[ $^{111}$ ]In has wide applications in nuclear medicine for labelling and in-vivo distribution studies. A method is developed for the production of carrier free $^{111}$In using the reaction $^{nat.}Cd(p,\;xn)$ $^{111}$In with MC-50 cyclotron. Carrier free $^{111}$In was separated from the irradiated metallic cadmium by liquid-liquid extraction and cation exchange chromatography. The yield of $^{111}$In at EOB is $0.8mCi/{mu}\;Ahr$ and the nuclidic purity is over 99%. $^{111}In-DTPA\;and\;^{111}In-bleomycin$ were prepared for medical study.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2003년도 추계학술발표회
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• pp.132-135
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• 2003

Solution chemistry, sorbate chemistry, and sorbent chemistry were widely investigated to find important factors that affect PAH sorption on mineral surfaces and to elucidate its microscopic mechanism. The solution chemistry, pH and ionic strength caused measurable change of HOC sorption reaction to minerals. The detectable change of Ka occurred at a pH region crossing the PZC (Point of Zero Charge) of each mineral. The PAH hydrophobicity, one of sorbate chemistry, was observed to have a strong correlation with PAM sorption to mineral. Mineral surface area was not found to be a predominant factor controlling PAH sorption. The mineral type might be more likely to play a crucial role in controlling the PAH sorption behavior. The CEC (Cation Exchange Capacity) of mineral, representing surface charge density, has meaningful correlation with regression slope of sorption coefficients (log $K_{d}$) versus aqueous activity coefficients (log Υ$_{w}$).).).

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2002년도 생물공학의 동향 (X)
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• pp.500-503
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• 2002

In order to improve the physical properties of food such as texture and food self-life. Transglutaminase(mTG) from Streptoverticillum morbarense was prepared. In the preliminary experiments, presence of proteases in the crude enzyme did not improve the texture of dough, which mean the inteference of mTG reaction by the proteases. Among the cation exchange resins tested for the removal of proteases, Monoplus S 100(Bayer, Germany) was the most efficient resin with 20 fold increase in the mTG/protease activity ratio. By further purification steps with a quaternary ammonia salt resin and a gel permeation chromatography, proteases were effectively removed from the preparation. Therefore, the improvement of flour texture was shown by adding the protease-free mTG.

• 한국세라믹학회지
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• 제31권3호
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• pp.282-290
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• 1994

In this research, the organic salt [RCOOH] Br with long alkyl-chain was synthesized, and the organophilic [RCOOH]-Montmorillonite was formed by cation-exchange-reaction between Na-Montmorillonite and synthesized organic salt [RCOOH] Br. After drying of the organophilic [RCOOH]-Montmorillonite at $65^{\circ}C$ in high vaccum, the experiments for the probability of forming its complexes with various swelling-solutions as dist, water, methanol, ethanol, acetonitrile, propionitrile, butyronitrile, toluene and n-decanol were performed, and the corresponding basal spacings obtained were 17.44$\AA$, 31.86$\AA$, 34.38$\AA$, 30.37$\AA$, 32.39$\AA$, 35.04$\AA$, 14.16$\AA$ and 14.63$\AA$ respectively.

• 공학논문집
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• 제6권2호
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• pp.119-124
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• 2004

본 연구에서는 양이온교환방응에 의해 몬모릴로나이트 층 내의 금속 양이온을 긴 알킬 사슬을 갖는 유기 양이온으로 치환시켜 물성이 전혀 다른 유기 점토화합물인 몬모릴로나이트 층간 화합물을 합성한 후, 이 층간화합물을 증류수, 메탄올, 아세톤, 에테를 및 아세토니트릴 등과 같은 상이한 팽윤액체와 반응시켜 팽윤거동에 대하여 연구하였다. 특히 연구에 사용된 점토로는 한국산과 터키산의 두 가지 상이한 몬모릴로나이트를 선정하여 두 점토의 층간화합물 및 팽윤거동에 대하여 비교.분석하였다.