• 한국환경과학회지
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• 제10권6호
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• pp.451-459
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• 2001

Adsorption characteristics of triadimefon and diniconazole(pesticide) by natural zeolite($CLI_N$) and several synthetic zeolites were Investigated. The synthetic zeolites used En this study were as follows: Faujasite synthesized from coal fly ash($FAU_F$); Zeolite synthesized from the mixture of FAU and Na-Pl synthesized from the ratio of Cheju scoria 6 to coal fly ash 4 by weight($(FAU + Na-Pl)_{SF}$); waste fluid catalytic cracking catalyst($FCC_W$). The distribution coefficient, $K_D$ and Freundlich constant, $K_F$ decreased in the fellowing sequence : $FCC_W ＞ FAU_F ＞ (FAU + Na-Pl)_{SF} ＞CLI_N$ among the zeolites. The distribution coefficient and the adsorption capacity of $(FAU + Na-Pl)_{SF}$ for pesticides were 4.4 and 2.6 times higher for triamefon, and 2.0 and 2.4 times higher for diniconazole than those of $CLI_N$, respectively.

• 한국환경과학회지
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• 제12권10호
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• pp.1061-1069
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• 2003

The adsorption behaviors of strontium and cesium ions on fly ash, natural zeolites, and zeolites synthesized from fly ash were investigated. The zeolites synthesized from fly ash had greater adsorption capabilities for strontium and cesium ions than the original fly ash and natural zeolites. The maximum adsorption capacity of synthetic zeolite for strontium and cesium ions was 100 and 154 mg/g, respectively, It was found that the Freundlich isotherm model could fit the adsorption isotherm. The distribution coefficients (K$\_$d/) for strontium and cesium ions were also calculated from the adsorption isotherm data, The distribution coefficients decreased with increasing equilibrium concentration of strontium and cesium ions in solution. By studying the removal of cesium and strontium ions in the presence of calcium, magnesium, sodium, potassium, sulfate, nitrate, nitrite, and EDTA (in the range of 0.01 - 5 mM) it was found that these coexistence ions competed for the same adsorption sites with strontium and cesium ions.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 총회 및 춘계학술발표회
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• pp.7-10
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• 2001

Adsorption of the pesticides (phosphamidon, fenitrothion, triadimefon and diniconazole) in natural zeolite (CL $I_{N}$) and several synthetic zeolites was incestigated. The pesticides were not adsorbed on zeolites (Na-Pl, SOD, ANA, JBW and CAN) synthesized from Jeju scoria. The distribution coefficient ( $K_{D}$) and the Freundlich constant ( $K_{F}$) decreased in the following sequences. FC $C_{W}$ (waste catalytic cracking catalyst)>FA $U_{F}$ (FAU Synthesized from coal fly ash)>(FAU+Na-Pl)$_{SF}$ (the mixture of FAU and Na-Pl synthesized from the ratio of Jeju scoria 6 to coal fly ash 4 by weight)>CL $I_{N}$ among the zeolites; diniconazole>fenitrothion> triadimefon>phosphamidon. As the temperature was increased, the amount of pesticide adsorbed per unit mass of zeolite increased for FC $C_{W}$, FA $U_{F}$ and (FAU+Na-Pl)$_{SF}$ but it decreased for CL $I_{N}$, for all the pesticides used in this study. It was independent of pH for phosphamidon, fenitrothion and triadimefon, but decresed as pH was increased for all the zeolites used in this study.y.udy.y.y.y.y.y.y.

• Journal of Photoscience
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• 제8권1호
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• pp.27-32
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• 2001

Photoreduction of Methyl Orange Catalyzed by Nile Red-Adsorbed TiO$_2$/Y zeolites. Nile Red was successfully adsorbed on TiO$_2$/Y zeolites and the absorption profile is very broad with maxima, ca. 630 nm. The peak is largely red-shifted compared to that observed in hydrocarbon solvents. Furthermore, a broad and largely Stokes shifted emission band as observed around 660 nm. The largely Stokes shifted emission band should be originated from the excited state structural changes. In order to understand the photocatalytic activities of Nile Red-adsorbed TiO$_2$/Y zeolite, the photoreduction of Methyl Orange(5.0$\times$10$^{-5}$ M) was studied using visible light beyond 320 nm. Methyl Orange was effectively reduced by Nile Red-adsorbed TiO$_2$/Y zeolite, indicating the photocatalytic activity of Nile Red-adsorbed TiO$_2$ zeolites was enhanced by about eight times higher than that of TiO$_2$/Y zeolite.

• Korean Chemical Engineering Research
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• 제56권6호
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• pp.909-913
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• 2018

A hydrocarbon trap (HT) plays an important role of controlling vehicle emissions in the so-called cold emission period by holding hydrocarbons until three way catalysts (TWCs) are thermally activated. In this study, we have investigated the adsorption characteristics of cation (H, La, K, and Ag)-exchanged ZSM-5 zeolites for hydrocarbons (propylene, n-butane, and toluene) by DFT (density functional theory)-based computational chemistry. Cation exchange is to improve the hydrothermal stability of zeolites and their adsorption capacity, thereby rendering cation-exchanged zeolites promising materials for HT. The idea of cluster approximation makes the calculation of adsorption energies superbly efficient in computation. The results showed that Ag-exchanged ZSM-5 would be the best for the adsorption of all three adsorbates, without often encountered Ag oxidation in experiments. Besides, the hydrothermal stability of La-exchanged ZSM-5 was confirmed from the change of geometrical parameters by cation exchange, and it showed good adsorption capacity for propylene and toluene. Hydrogen-exchanged ZSM-5 was also good for hydrogen adsorption, but had poor hydrothermal stability.

• 공업화학
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• 제18권4호
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• pp.344-349
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• 2007

마이크로파 가열(microwave heating)에 의하여 제올라이트 NaY를 합성하였으며, 그 결과를 기존의 가열 방법(conventional heating)에 의하여 합성한 결과와 비교하였다. 같은 승온 속도를 사용하였을 때는 마이크로파에 의하여 가열하였을 때가 기존의 가열 방법에 비하여 NaY 결정 생성의 유도 기간(induction period)이 감소하였으며 결정의 생성 속도가 증가하였다. 또한 마이크로파의 사용 여부와 관계없이 승온 속도가 빠를 때도 유도 기간이 감소하고 결정 생성 속도가 증가하였다. 빠른 승온 속도에서 합성하였을 때 최종 결정의 크기가 크며, 이는 마이크로파의 사용에 의하여 더욱 증가하였다. 빠른 승온 속도에서는 반응 시간이 짧아져서 NaY의 합성에 소모되는 에너지 소모량은 감소하였다. 본 연구의 조건에서는 에틸렌글리 콜조(ethylene glycol bath)를 사용한 기존 가열 방법에서의 에너지 소모량이 마이크로파 가열보다 적게 나타났는데, 이는 마이크로파 에너지를 사용하는 것이 항상 효율적인 것만은 아니라는 것을 말해준다. 그러나 승온 속도를 적절히 조절하면 마이크로파 가열에 의해서 에너지 면에서 보다 효율적으로 NaY를 합성할 수 있다는 것을 알 수 있었다

• 대한화학회지
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• 제31권1호
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• pp.14-24
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• 1987

실리카 및 제올라이트의 OH기 또는 교환된 양이온과 CO분자간의 상호작용과 전자구조를 살펴보기 위하여 CNDO/2계산을 행하였다. 실리카의 OH기와 CO분자간의 상호작용에너지는 약 12kcal/mol이었고, 그 결합거리, R(O-H${\cdots}$C)는 2.6${\AA}$이었다. 여러가지의 양이온과 CO분자와의 결합강도는 $H^+ < Na^+ < Li^+$의 순이었는데, 그것은 양이온의 정전기적 장의 세기와 일치하였다. 또한 OH기나 양이온과 결합하고 있는 CO분자의 결합차수는 OH-CO type의 경우를 제외하고는 모두 증가하였다. 제올라이트에 있는 양이온을 떼어내는데 필요한 에너지는 $H^+ > Li^+ > Na^+$의 순이었으며, 이것은 제올라이트의 골격으로부터 양이온으로 이동되는 전하의 양과 관계가 있다.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2003년도 가을 학술논문집
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• pp.215-219
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• 2003

현재 국내에서 개발 중인 사용후 핵연료의 금속전환공정에서 발생이 예상되는 LiCl 염폐기물을 제올라이트로 고정화한 후 최종 고화체를 만드는 기술을 개발 중에 있다. 여러 혼합조건에 대해 고정화 생성물의 결정을 분석한 결과 모든 혼합조건에서 제올라이트 A형이 제올라이트 Li-A으로 전이되었으며, 일부 혼합조건에서는 Minor phase로 소달라이트 형도 발견되었다. 자유염 발생이 최소가 되는 혼합조건은 Cs, Sr 핵종이 포함된 LiCl 제올라이트 비가 1.0인 조건이었다.

• 대한화학회지
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• 제32권2호
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• pp.149-155
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• 1988

ZSM-5, ZSM-8, ZSM-11 및 실리카라이트를 포함하는 펜타실 제올라이트들을 여러가지 유기양이온과 실리카졸을 사용하여 합성하고 반응온도, 교반, 숙성시간 등 합성조건을 변화시키므로서 균일한 크기와 모양을 갖는 결정을 얻었다. TEA-OH(수산화 사에틸암모늄), TPA-OH, TBA-OH 및 Choline이 유기양이온으로 사용되었으며 콜로이달 실리카(Snowtex)를 실리카원으로 사용했다. 합성 실험은 $2{\ell}$ 압력 반응기 (parr제품)와 자체 제작된 자석식 반응기를 사용하였으며, 반응물 조성(실리카/알루미나 비), 반응온도 등이 펜타실 제올라이트 합성의 중요한 인자임을 알았다.

• 대한화학회지
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• 제58권1호
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• pp.72-75
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• 2014

In the presence of zeolites, 4,4'-dibromobiphenyl could be region-selectively nitrated by the action of nitrogen dioxide and molecular oxygen. The ratio of 4,4'-dibromo-2-nitrobiphenyl to 4,4'-dibromo-3-nitrobiphenyl could reach 14 in a high yield of 90%. Zeolites could be easily regenerated by heating and reused four times to give the results similar to those obtained with fresh catalyst. Compared with the classic nitration method, no nitric acid and sulfuric acid were used, which suggested that the method was an environmentally economic process.