• The Journal of Engineering Research
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• v.6 no.2
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• pp.119-124
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• 2004

In this research montmorillonite intercalations complexes as organophilic clay compounds which have very different properties as the starting clay mineral were synthesized by the substitution of metal ions which exist in the montmorillonite layers with the organic cations which have long alkyl chain by the cation exchange reaction. Thereafter the obtained products dried in high vacuum were treated with the various swelling liquids such as dist. water, methanol, acetone, ether and acetonitrile in order to know the swelling behaviour of the synthesized complexes. Especially for this research Korean and Turkish clays were selected to compare the intercalations complexes of both clays and their swelling behaviour.

• The Journal of Natural Sciences
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• v.5 no.1
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• pp.77-86
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• 1992

By cation-exchange-reaction long-chain organic cationic tensides can be intercalated in the montmorillonite layer space, and thus intercalations-complexes of montmorillonite with different properties of materials can be obtained. Such intercalations-complexes are finding strong technical appliances in many areas and are also used very often as model-systems for studying behaviors of materials. Therefore in this research intercalations-complexes of montmorillonite with organic cationic tensides ad model-systems were synthesized and their behabiors under various different conditions were studied.

• Journal of the Korean Ceramic Society
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• v.38 no.5
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• pp.431-437
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• 2001

본 연구에서는 양이온 교환반응에 의해 Na-Mont와 R$_{11}$SO$_4$로부터 R$_{11}$SO$_4$-Mont 층간화합물을 합성한 후, 이 R$_{11}$SO$_4$-Mont 층간화합물을 다시 제 4차 유기 양이온인 (Et)$_4$N$^{+}$ 이온 및 (Bu)$_4$N$^{+}$ 이온과 반응시켜 그 거동을 살펴보았다. R$_{11}$SO$_4$-Mont를 (Et)$_4$N$^{+}$이온과 반응시켰을 대보다 (Bu)$_4$N$^{+}$ 이온과 반응시킨 경우에 좀 더 큰 층간거리가 얻어졌다. R$_{11}$SO$_4$-Mont를 (Et)$_4$N$^{+}$이온 및 (Bu)$_4$N$^{+}$과 반응시켜 얻은 층간화합물을 다시 아세토니트릴, 에탄올 및 디옥산과 팽윤반응을 수행한 결과 층간거리가 확장되었으나, 이는 Na-Mont를 R$_{11}$SO$_4$와 48시간 교환 반응시킨 후에 교환용액 하에서 얻은 R$_{11}$SO$_4$-Mont의 층간거리에 불과했다. 원소분석결과, R$_{11}$SO$_4$-Mont와 (Bu)$_4$N$^{+}$를 반응시킬 경우 반응이 반응식 b에 의거 진행되고, (Bu)$_4$N-Mont를 R$_{11}$SO$_4$와 반응시킬 경우에는 반응식 c에 의거 진행됨을 예측할 수 있었다.의거 진행됨을 예측할 수 있었다.

• The Journal of Engineering Research
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• v.7 no.1
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• pp.79-87
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• 2005

[TEACOOH]-Montmorillonite intercalations complex obtained from Na-Montmorillonite and 10-Carboxy-n-decyldimethylethylammonium bromide(organic cation) was reacted with the monomer($\varepsilon$-caprolactone) to achieve the [TEACOOH]-$\varepsilon$-caprolactone-Montmorillonite intercalations complex. From intercalations complex Montmorillonite/Polycaprolactone Nanocomposite in which montmorillonite(inorganic material) is chemically linked with the polycaprolactone(organic polymer) was formed at $220^{\circ}C$ for 48 h. The basal spacing for the sample obtained after polymerization, extraction with methanol and dried at $65^{\circ}C$ in high vacuum for 24 h was 50.7 $\AA$.

• Journal of the Korean Applied Science and Technology
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• v.34 no.4
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• pp.799-806
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• 2017

The potential use of modified clays in the adsorption of vapor phase benzene and toluene was investigated. The modified clays OC-CPC, IOC, and Al-PILC were prepared for comparative purposes and were characterized using infrared spectroscopy, thermogravimetric analysis, and X-ray diffraction. It was confirmed the intercalation of the aluminium pillar in IOC and Al-PILC, as well as the introduction of cetylpyridinium. The adsorption studies showed a great affinity of benzene and toluene for OC-CPC due to the hydrophobic character that resulted and also to the increase in the interlaminar distance. IOC showed a lower affinity for the benzene and toluene, followed by Al-PILC. Natual clay had no affinity for benzene and toluene due to its hydrophilic nature. Clay materials having a laminar structure can be chemically modified, changing their physiochemical characteristics, such as interlaminar distance, surface area, pore size, and chemical affinity. In this study, it was focused on obtaining modified clays to be used for the adsorption of volatile organic chemicals.

• Analytical Science and Technology
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• v.13 no.3
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• pp.338-345
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• 2000

The intercalated compounds of alkylsulfonate into hydrated and dehydrated zinc were synthesized. From the XRD, FT-IR, TGA, elemental analysis data, and the molecular size, the orientation of the intercalated alkylsulfonates was determined. For the hydrated compounds, alkylsulfonates were intercalated into hexaqua zinc layer with the bilayer structure of $32.9^{\circ}$ angle of inclination. For the dehydrated compounds, alkylsulfonates were directly bonded to zinc ion with the bilayer structure of $51.4^{\circ}$ angle of inclination.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.9 no.6
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• pp.580-584
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• 1999

The synthesis and characterization of intercalated compound of decansulfonate into hydrated nickel is presented. The compound shows a layered structure as determined by high temperature powder X-ray diffraction (HTXRD). The layer distance of the product is increased from 24.7 $\AA$ to 30.5 $\AA$ by increasing the temperature which is in turn accomplished by changing the structure of the intercalated nickel compound. From the X-ray diffraction data and the decanesulfonate size, the orientation of the decanesulfonate onto the nickel layer is determined. The molecular axis of the decanesulfonate with bilayer structure is tilted to the perpendicular of the nickel layer.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.8 no.1
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• pp.36-41
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• 1998

Intercalation compounds of alkyl sulfonates into layered double hydroxides (LDH) have been directly synthesized. From the X-ray diffraction data and the alkyl sulfonates size, the orientation of the intercalated alkyl sulfonate into the layered double hydroxide was determined. The intercalated alkyl sulfonate is arranged with molecular chain perpendicular to the hydroxide layer with an antiparallel pattern.

• Journal of the Mineralogical Society of Korea
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• v.19 no.2 s.48
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• pp.123-128
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• 2006

Beidellite, a member of the dioctahedral smectite group, was synthesized hydrothermally from dickite. Organophilic [DEACOOH]-beidellite intercalation complex was formed by the cation exchange reaction between synthetic Na-beidellite and [DEACOOH]Br. The products dried in high vacuum were treated with various organic solvent such as methanol, ethanol, acetone, ether, acetonitrile and caprolactam in order to determine the swelling behaviour of the prepared complexes. After drying under high vacuum, basal spacing of [DEACOOH]-beidellite shows 15.1 ${\AA}$, and it changed to 19.4, 29.9, 15.9, 16.8, 14.8, 26.5 and 14.8 ${\AA}$ under distilled water, methanol, ethanol, acetone, ether, acetonitrile and caporlactam, respectively. Especially, the characteristics of the intercalation complexes and their swelling behavior of the synthetic beidellite and natural montmorillonite were compared.

• Analytical Science and Technology
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• v.13 no.1
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• pp.66-71
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• 2000

The intercalated compound of dodecanesulfonate into hydrated cobalt was synthesized. The compound shows a layered structure as determined by high temperature X-ray diffraction. The layer distance of the product is increased from $19.1{\AA}$ to $34.7{\AA}$ by increasing the temperature from $30^{\circ}C$ to $200^{\circ}C$. We can control the layer distance by varying the temperature which is accomplished by changing from the monolayer to the bilayer structure of the intercalated dodecanesulfonate.