• Journal of Soil and Groundwater Environment
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• v.6 no.4
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• pp.41-50
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• 2001

The use of clay has been the favored method of reducing or eliminating hazardous contaminants in the leachate from landfills. But, neither natural clays nor organoclays modified with surfactants are able to effectively sorb both heavy metals and organic contaminants. Therefore, the objective of this study is to determine the optimal amount of surfactant added on the clay mineral to effectively remove both of them. For this purpose, Na-Bentonite as the natural clay, and hexadecyltrimethylammonium (HDTMA) as the cationic surfactant were used, Chlorobenzene and lead ($Pb^{2-}$) were selected as representative contaminants. Experimental result showed that chlorobenzene sorption increased with increasing HDTMA to bentonite, ratios. On the contrary, the removal rate of lead decreased as the amount of HDTMA increased. The removal of chlorobenzene was influenced by the amount of HDTMA added to the bentonites rather than initial concentration of chlorobenzene, but the removal of lead was much more influenced by the initial concentration of lead. The adsorption of lead was not affected by chlorobenzene, and vice versa. The competitive sorption between the heavy metal and the organic contaminant was not present.

• Polymer(Korea)
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• v.26 no.3
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• pp.381-388
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• 2002

The properties of polyurethane (PU) nanocomposites with organoclay have been compared in terms of their thermo-mechanical properties, morphology, and gas permeability. Hexadecylamine-montmorillonite ($C_{16}$-MMT) was used as an organoclay to make PU hybrid films. The properties were investigated as a function of organoclay content (1-4 wt%) in the PU matrix. Transmission electron microscopy (TEM) photographs showed that most clay layers were dispersed homogeneously into the matrix polymer in nano-scale, although some particles of clay were agglomerated. We also found that the addition of only a small amount of organoclay was enough to improve the thermal stabilities and mechanical properties of PU hybrid films while gas permeability was reduced. Even at low organoclay content (<5 wt%), the PU nanocomposite showed much better thermo-mechanical properties, and lower gas permeability than pure PU.

• Polymer(Korea)
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• v.34 no.4
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• pp.326-332
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• 2010

Nanocomposite films were prepared by blending poly(amic acid)(PAA), poly(o-hydroxyamide)( PHA) and organically modified montmorillonite (OMMT) that has a layered structure. XRD, SEM and TEM were used to study the morphology of PAA/PHA nanocomposites, and DMA, TGA, UTM, LOI and PCFC techniques were used to characterize the mechanical and thermal properties, and flame retardancy of the nanocomposites. TEM images revealed that OMMT layers were well dispersed in the PAA/PHA matrix and showed exfoliation and intercalation behavior. The addition of 3 wt% OMMT to the PAA/PHA blend increased the initial modulus of PAA/ PHA blend to 3.68 GPa that was ca. 48% higher than that of the control PAA/PHA blend. Above 4 wt%, however, both the initial modulus and the tensile strength were found to decrease, which might be due to the aggregation of OMMT in PAA/PHA matrix. When the OMMT content was below 3 wt%, the thermal stability and flame retardancy of the PAA/PHA nanocomposites increased with increasing OMMT content.

• Proceedings of the Materials Research Society of Korea Conference
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• 2003.03a
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• pp.226-226
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• 2003

일반적으로, 고분자 매트릭스에 층상 점토광물이 분산되어 얻어지는 복합재료는 세가지 형태를 이룬다. 첫째 통상의 복합재료는 고분자 매트릭스 내에 점토입자가 고루게 분산된 상태를 말하며, 둘째 점토 층 사이에 고분자 모노머나 올리고머가 일부분 삽입된 삽입형 복합재료(intercalated composite)이며, 셋째 점토 층 사이에 삽입된 모노머나 올리고머의 경화 또는 중합반응을 통해 점토내의 한층 한층 균일하게 매트릭스 내에 분산된 박리형 나노복합소재(exfoliated nanocomposite) 이다. 이들 복합재료들 중 박리형 나노복합소재는 적은 양의 점토가 단위 층으로 고분자 매트릭스에 완전히 분산되어 다양한 물성의 향상이 기대되는 재료이다. 따라서 최근 고분자의 기계적 강도, 팽윤 저항성 그리고 차폐특성 둥 전반적인 물성을 향상시키는 방법으로 층상 점토광물의 층 사이에 다양한 유기물을 삽입하여 층간거리를 확장시킨 유기 점토광물을 제조하고 이를 고분자 소재에 첨가하여 박리형 나노복합소재를 제조하는 방법이 많은 연구가 수행되고 있다.

• Polymer(Korea)
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• v.27 no.4
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• pp.377-384
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• 2003

High impact polystyrene/organically modified layered silicate (HIPS/OLS) nanocomposites by in situ polymerization were synthesized to investigate the effect of clay on the particle size and properties of rubber. In the OLS, the montmorillonite having benzyl group showed best dispersion in polystyrene phase. With the addition of clay, the intercalated peak from XRB was confirmed, but the peak gradually shifted to lower angle as rubber concentration increased. Thus, it is speculated that the organoclay disperses better in rubber phase than in polystyrene phase. The average rubber particle size increased and the particle size distribution widened as the amount of clay increased, which may be caused by the increase of the viscosity ratio of rubber to polystyrene phases and the unstable dispersion. The materials having clay showed improved thermal properties from thermogravimetric analysis. Rheological properties such as complex viscosity and storage modulus increased as the amount of clay increased.

• Polymer(Korea)
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• v.31 no.5
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• pp.428-435
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• 2007

The thermomechanical property, morphology, and gas permeability of nanocomposites of ultra high molecular weight polyethylene (UHMWPE) with two different organoclays are compared. Hexamethylene benzimidazole-mica ($C_{16}BIMD-Mica$) and Cloisite 25A were used as reinforcing fillers in the formation of UHMWPE hybrid films. Dispersions of organoclays with UHMWPE were carried out by using the solution intercalation method at different organoclay contents to produce nano-scale composites. Transmission electron microscopy (TEM) micrographs show that some of the clay layers are dispersed homogeneously within the polymer matrix on the nano-scale, although some clay particles are agglomerated. We also found that the addition of only a small amount of organoclay is enough to improve the thermomechanical property and gas barrier of the UHMWPE hybrid films. In general, Cloisite 25A is more effective than $C_{16}BIMD-Mica$ in increasing both the thermomechanical property and the gas barrier in a UHMWPE matrix.

• Polymer(Korea)
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• v.24 no.6
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• pp.794-801
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• 2000

The effect of chain length and packing density of intercalated surfactants, annealing temperature, and annealing time on static melt intercalation of thermoplastic polymers was examined using x-ray and FTIR spectroscopy. Although melt intercalation of polymers was not successful when alkyl chains in organosilicates form a lateral monolayer structure, the type and structure of surfactants could not much affect final interlayer distances of most polymer/silicate hybrids. As annealing time increases, interlayer distance in organosilicates increases while the dispersity of the spacing between silicate layers decreases. However, the dispersity of interlayer spacing as well as interlayer distance in organosilicates increase with annealing temperature.

• Polymer(Korea)
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• v.32 no.4
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• pp.347-352
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• 2008

High impact polystyrene (HIPS) nanocomposites with organically modified montmorillonite (organoclay) via in situ polymerization were synthesized, and the effects of organoclay incorporation on material properties were investigated. Organoclays having a reactive group, vinylbenzyltrimethyl clay (VBC) and octadecylvinylbenzyldimethyl clay (ODVC), were prepared by the ion-exchange reactions of sodium montmorillonite with vinylbenzyltrimethyl ammonium chloride (VBTMAC) and octadecylvinylbenzyldimethyl ammonium bromide (ODVBDAB), respectively, and a commercial organoclay, $Cloisite^{(R)}$ 10A(C10A), was used for comparison. It was confirmed that the X-ray diffraction (XRD) peak of the nanocomposites prepared by ODVC disappeared, which indicates the exfoliation of silicate layers. On the contrary, the XRD peak of the nanocomposites prepared by C10A shifted to lower angle, indicative of the intercalation of polymer chains into silicate layers. Rheological properties such as storage modulus and complex viscosity increased with increasing organoclay.

• Journal of the Mineralogical Society of Korea
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• v.15 no.4
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• pp.305-314
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• 2002

The dehydration of hexadecyltrimethylammonium (HDTMA)-exchanged montmorillonite has been studied using X-ray diffractometry (XRD) and differential scanning calorimetry (DSC). The dehydration in HDTMA-montmorillonite seems to influence the swelling behavior of the organo-clay during heating. The basal d(001) spacing vs temperature curve of the HDTMA-montmorillonite has one broad swelling edge with a shoulder on the low-temperature side. We believe that the shoulder at $100^{\circ}C$ for the HDTMA-montmorillonite is due to interlayer swelling induced by the initial rearrangement of surfactants, and the second edge at $200^{\circ}C$ is caused by interlayer swelling resulting from the secondary vertical reorientation of alkyl chains. It seems that the dehydration of organo-clay induces a reorientation of the alkyl chains by transition to more vertical position relative to the silicate sheets, allowing instantly greater d-spacing.

• Mineral and Industry
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• v.14 no.1
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• pp.48-61
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• 2001