• Journal of the Mineralogical Society of Korea
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• v.21 no.3
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• pp.307-312
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• 2008

Rietveld analysis using synchrotron X-ray powder diffraction data collected at 15 K reveals that CFC-13 ($CF_{3}Cl;$ chlorotrifluoromethane) sorbed on Na,K-LSX binds through fluorine to sodium ions around the single 6-ring aperture in the supcrgage.

• 한국신재생에너지학회:학술대회논문집
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• 2011.05a
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• pp.145.2-145.2
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• 2011

메탄 하이드레이트는 낮은 온도와 높은 압력 조건에서 물분자들의 격자구조에 메탄가스분자가 포획되어 수소결합으로 형성되는 외관상 얼음과 비슷한 결정성 화합물이다. $1m^3$의 메탄 하이드레이트는 표준상태에서 $172m^3$의 메탄가스와 $0.8m^3$의 물로 분해되며, $-10^{\circ}C{\sim}-20^{\circ}C$의 온도에서는 하이드레이트 입자표면에서 생성되는 얼음막으로 인하여 상압에서도 안정하게 존재하는 자기보존 효과를 가지고 있다. 따라서 이와 같은 특징을 천연가스 수송 및 저장의 방법으로 이용할 경우 $-162^{\circ}C$의 초저온을 만들고 유지시키기 위하여 고가의 설비를 필요로 하는 기존의 LNG 수송방법을 대체할 수 있다. 특히 연간 천연가스 소비량을 0.4 ~ 1.0 million ton으로 가정했을 때, 하이드레이트 수송방법은 LNG 수송에 비해 18 ~ 25% 정도의 비용을 절약할 수 있는 경제적인 방법으로 알려져 있다. 그러나 하이드레이트를 인공적으로 제조할 경우 물분자와 가스분자의 반응율이 낮기 때문에 하이드레이트가 생성되기까지 많은 시간이 소요되며, 하이드레이트에 포획되는 가스분자의 양도 적다. 따라서 본 연구에서는 이와 같은 문제점을 해결하기 위하여 다공성 물질인 천연 제올라이트와 제올라이트 13X를 이용하여 제올라이트 혼합유체를 제조하였으며, 메탄가스와 반응시켜 하이드레이트를 생성시키는 실험을 수행하였다. 그 결과, 하이드레이트 생성 시 천연 제올라이트와 제올라이트 13X 모두 0.01 wt%의 혼합비율에서 가장 좋은 효과를 나타내었으며, 하이드레이트에 포획된 가스의 양은 같은 과냉도 조건에서 천연제올라이트와 제올라이트 13X 혼합유체를 이용하여 하이드레이트를 생성 시켰을 때, 증류수보다 각각 4배, 5배 높음을 보였다. 또한 낮은 과냉도에서 하이드레이트 생성 시 제올라이트, 제올라이트13X 혼합유체에서 하이드레이트 생성시간이 증류수에서 하이드레이트를 생성시킬 때보다 빨라짐을 확인하였다.

• Korean Chemical Engineering Research
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• v.44 no.3
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• pp.243-247
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• 2006

MFI zeolite membranes were prepared on anodic alumina (Anodisc) as support. First, silicalite-1(${\approx}1.2{\mu}m$) seed crystals were attached to the surface of the support via chemical bonding, and the a- and b-axis oriented zeolite membranes could be synthesized on the support coated with the monolayer of the seed crystals by secondary growth hydrothermal synthesis. The zeolite membranes prepared were characterized using scanning electron microscope and analyzed by X-ray diffraction.

• Korean Chemical Engineering Research
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• v.43 no.6
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• pp.691-695
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• 2005

Zeolite membranes on various supports such as filter paper, cotton fiber, and glass fiber filter were prepared by secondary growth hydrothermal synthesis. First, zeolite NaA (${\approx}0.5{\mu}m$) and silicalite-1 (${\approx}0.2{\mu}m$) crystals were synthesized as zeolite seed crystals, and they were attached to the surfaces of the supports via chemical bonding. Zeolite NaA or silicalite-1 membranes could be synthesized on the supports coated with the seed crystals. The prepared zeolite membranes were observed by scanning electron microscope and analyzed by X-ray diffraction.

• Membrane Journal
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• v.9 no.2
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• pp.97-106
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• 1999

A and 2SM-5 type zeoli tic crystal films were synthesized on porous supports from the reaction mixture of 1.9 ${SiO}_2$1.5 $Na_20-Al_2O_3-40$ $H_20$ and $Si0_2$-0.l3 $Na_2O$-52 $H_20$-O.l2 TPAOH composition, respectively. The zeolite films were characterized by XRD and SEM. The 2SM -5 crystals grown on the porous matrix were very closely bound together. It was so difficult to obtain the perfectly intergrown crystals in the case of A-type zeolite and this crystal was transformed into P-type zeolite membrane with a prolonged reaction time. The densely intergrown A type zeolite crystal membrane could be also synthesized by the hydrothermal treatment at 100$^{\cirt}C$ after pressing the reaction mixture without addition of water. The pervaporation performance of the synthesized porous inorganic membranes was investigated for alcohol and water mixtures. A-type zeolite membrane crystallized as a thin film showed the selective \'Jermeability of water from the mixtures through the molecular sieving activity of micropores.

• Applied Chemistry for Engineering
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• v.4 no.4
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• pp.731-738
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• 1993

This study showed the adsorption behavior of Cs and Sr into the inorganic ion-exchanger zeolites such as 4A, 13X, AW300, AW500 and natural. It was found that the best type of zeolite is AW500 for Cs and 13X for Sr in terms of ion-exchange capacity. The temperature effect was also examined for the following systems : AW500-Cs, AW300-Cs, natural zeolite-Cs, 4A-Sr and 13X-Sr. Experiments showed that the effect of temperature on the ion-exchange capacity is negligible in all cases except for the systems of 4A-Sr and natural zeolite-Cs. The enhancement in the ion-exchange capacity for 4A-Sr would be caused by the Sr ion movement and the multilayer adsorption due to the heterogeneous characteristics of ion-exchange site. The distribution coefficient was increased with pH of the solution which is in equilibrium with zeolite particles. The values of $K_d$ in the systems of AW500-Cs and 4A-Sr were found to be about $10^3cm^3/g$ and $10^3{\sim}10^4cm^3/g$ respectively.

• Journal of the Mineralogical Society of Korea
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• v.19 no.4 s.50
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• pp.301-310
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• 2006

Smectites were synthesized from Na-P type and Na-A type zeolites by the hydrothermal synthetic method, and their physicochemical properties were studied. The optimal synthetic conditions for producing smectite were $290^{\circ}C$, 72 hr and $75{\sim}100kgf/cm^2$ in autogenous pressure. pHs of initial reaction solutions for the synthesis of smectites from Na-P type and Na-A type zeolite s were pH 6 and pH 10, respectively. The synthetic smectite was confirmed as $12{\AA}$-beidellite by a series of analysis such as X-ray diffraction analysis with random and oriented mounts, ethylene glycol treatment, and Greene-Kelly test, and their several physicochemical properties were studied.

• Proceedings of the Korean Ceranic Society Conference
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• 2003.10a
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• pp.129.2-129
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• 2003

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.8 no.1
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• pp.55-63
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• 1998

A and Y type zeolitic crystal films were synthesized on porous supports from the reaction mixture of 1.9 $SiO_2-1.5\;Na_2O-Al_2O_3-40\;H_2O$ and 10 $SiO_2-7\;Na_2O-Al_2O_3-280\;H_2O$ composition, respectively. The zeolite film was characterized by XRD and SEM. The crystals grown on the porous matrix were very closely bound together and the thickness of membrane was about 8-15$\mu \textrm{m}$. The densely intergrown crystals could be also synthesized by the hydrothermal treatment at $100^{\circ}C$ after pressing the reaction mixture without addition of water. A zeolite membrane crystallized as a thin film showed the selective permeability of water from water and methanol mixture through the molecular sieving activity of micropores.

• Journal of the Mineralogical Society of Korea
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• v.6 no.2
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• pp.116-121
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• 1993

A single crystla of zeolite $Na_{78}Rb_{28}-X$ (approximate composition) was prepared by exposing $Na_{92}-X$ at $350^{\circ}C$ to 0.1 Torr of rubidium vapor, and its structure was determined by single-crystal x-ray diffraction methods in the cubic space group, Fd3, ${\alpha}=25.045(4){\AA}$. The structure was refined to the final error indices $R_1=0.082$ and $R_2=0.084$ with 353 for which I>$3{\sigma}(I)$. Only about 28 of the 92 $Na^+$ ions per unit cell were reduced and only about 14 of the 28 $Na^0$ atoms produced were retained within the zeolite. A $Na_5{^{4+}}$ cluster is present within each sodalite cavity. It is a centered tetrahedron (like $CH_4$) with bond $length=2.80(2){\AA}$ and angle tetrahedral by symmetry, and shows the full symmetry of its site. $T_d$, at the center of the sodalite cavity. Each of the four terminal atoms of the $Na_5{^{4+}}$ cluster bond to three framework oxygens at $2.36(2){\AA}$. At the centers of some double 6-rings are sodium atoms which bridge linearly between $Na_5{^{4+}}$ clusters to form agglomerations such as short zig-zag chains $Na_5{^{4+}}$ clusters. Delocalized electrons, located primarily on the sodiums at centers of the sodalite and (likely) double-six-ring cavities, contribute to the stability of the clusters.