• Journal of the Mineralogical Society of Korea
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• v.17 no.2
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• pp.147-155
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• 2004

Anion adsorption properties of organobentonites modified by two cationic polymers, hexadecyltrimmethylammonium (HDTMA) and cetylpyridinum (CP), were investigated. The organobentonites showed the significant expansion of basal spacing to 42.0 $\AA$ at room temperature. The adsorption experiments were conducted for the 0.2 g of organobentonites with 40 mL solutions of various concentrations of anions such as nitrate, sulfate and phosphate. As a result, the organobentonites showed excellent adsorption capacities for those anions whereas untreated bentonite showed very low adsorption capacity. Adsorption rate of HDTMA-bentonite was about 90% for 100 mg/L solutions of nitrate and phosphate, and that of CP-bentonite was 97% for 100 mg/L solution of nitrate. Adsorption behaviors were slightly different for the different organobentonites and anions. Both organobentonites showed relatively higher adsorption rate for nitrate and phosphate than sulfate. Therefore, these organobentonites showing high anion adsorption capacities can be used far the removal of deleterious anions in the treatment of environmental pollution.

• Journal of the Mineralogical Society of Korea
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• v.22 no.1
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• pp.23-34
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• 2009

The adsorption of iodide on untreated bentonite and bentonites modified with organic cation (i.e., hexadecylpyridinium chloride monohydrate ($HDP^+$)) was investigated, and the organobentonites were characterized using uptake measurements, ${\mu}$-XRD, and electrophoretic mobilities measurement. Uptake measurements indicate that bentonite has a high affinity for $HDP^+$. Our ${\mu}$-XRD study indicates that organobentonites significantly expanded in basal spacing and organic cations were substantially intercalated into the interlayer spaces of bentonite. The electrophoretic mobility indicates that organobentonite tht is modified with organic cations in excess of the CEC of bentonite is completely different from untreated bentonite in the surface charge distribution. We found significant differences in adsorption capacities of iodide depending on the bentonite properties as follows: iodide adsorption capacities were 439 mmol/kg for the bentonite modified with $HDP^+$ at an equivalent amount corresponding to 200% of the CEC of bentonite whereas no adsorption of iodide was observed for the untreated bentonite. The molecular environments of iodine adsorbed on organobentonites were further studied using I K-edge and $L_{III}$-edge x-ray absorption spectroscopy (XAS). The X-ray absorption near-edge structure (XANES) of iodine spectra from organobentonites was similar to that of KI reference solution. Linear combination fitting of EXAFS data suggests the fraction of iodine reacted with the organic compound increased with increasing loading of the organic compound on organobentonites. In this study, we observed significant differences in the adsorption environments of iodide depending on the modified property of bentonite and suggest that an organobentonite has potential as reactive barrier material around a nuclear waste repository containing anionic radioactive iodide.

• KSCE Journal of Civil and Environmental Engineering Research
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• v.26 no.6B
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• pp.677-682
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• 2006

Dodecyldimethylethylammonium (DDDEA), a cationic surfactant, and aluminum metal ions were used with bentonite to synthesize to synthesize an improved organo bentonite. Among three different synthesis procedure for organo bentonites, aluminium-pillared bentonite showed the highest DDDEA sorption, which indicated that aluminium-pillared organo bentonite would exhibit the highest sorption capacity for organic contaminants. Aluminium pillared organo bentonite also showed a high sorption capability for phosphorus, while it did not exhibit strong sorption for nitrate. In the meantime, more desorption was observed with aluminium-pillared organo bentonite than ordinary organo bentonites.

• Journal of Soil and Groundwater Environment
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• v.6 no.3
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• pp.21-29
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• 2001

Organobentonite modified with hexadecyltrimethylammonium (HDTMA) was used to quantify adsorption of heavy metals. Adsorption of cadmium and lead increased with increasing pH and soil/solution ratio. Based on these experiments, an optimal soil/solution ratio and an optimal pH was selected. Adsorption experiments with cadmium and lead were conducted to quantify adsorption selectivity on bentonite and organobentonite. Adsorption of heavy metals on organobentonite was slightly reduced relative to bentonite. Because of competition between cadmium and lead, adsorption of each metal was reduced due to the presence of the other. Adsorption selectivity of cadmium was higher than lead. This study used the principle of hard soft-acid-base (HSAB) to interpret adsorption.

• Journal of the Mineralogical Society of Korea
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• v.15 no.4
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• pp.243-257
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• 2002

Ca-type and Na-type bentonites show the great difference of some physicochemical properties. Na exchanged bentonite is mainly used for the foundry and construction materials in domestic utilization. This study tries to identify in detail the differences of some physicochemical properties and thermal properties between Ca-type and Na-type bentonites. Also the adsorption behavior and interlayer expansion for the HDTMA (Hexadecyltrimethylammonium) exchanged and CP (Cetylprydinium) exchanged Ca-type and Na-type bentonites were compared. Na-type bentonite shows the strong alkaline property, high viscosity and swelling compared to Ca-type bentonite. However, two types are very similar for the cation exchange capacity and MB (Methylene Blue) adsorption. The decomposition of adsorbed and interlayer water of Na-type bentonite is caused in the lower temperature than Ca-type bentonite. And Ca-type bentonite shows the decomposition of structural water in the lower temperature than Na-type bentonite. The interlayer expansion of montmorillonite resulted to the intercalation of HDTMA and CP into bentonite is so strongly caused from 12～15 $\AA$ to $40\AA$ (basal spacing). HDTMA-bentonite is almost expanded to $37～38\AA$ when 200% CEC equivalent amount of HDTMA is added, and CP-bentonite is fullly expanded to 40 $\AA$ in the 140% CEC equivalent amount of CP It means that CP causes the stronger interlayer expansion of montmorillonite and easier adsorption than HDTMA. Adsorption behaviors of CP into bentonite is so stable and continuously sorbed in the proportion to the treatment of amount until 200% of the CEC equivalents. CP-bentonite shows the same adsorption behavior regardless of Ca-type or Na-type montmorillonite.

• Polymer(Korea)
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• v.38 no.1
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• pp.62-68
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• 2014

To improve the compatibility of bentonite with rubber matrix, organo-modified bentonite was synthesized with a silane coupling agent, [3-(2-aminoethylamino)propyl]trimethoxysilane (AEAPTMS) in the suspension of bentonite. The structure and characteristics of organo-modified bentonite were investigated using FTIR-spectroscopy, thermogravimetric analysis (TGA) and X-ray diffraction (XRD). Ethylene-propylene-diene monomer (EPDM) rubber/organo-bentonite composites were compounded by a two-roll mill. The vulcanization and mechanical properties were studied. Results showed that the concentration of hydrochloric acid and $H_2O$ in the synthesis had significant influence on the modification of bentonite, which further contributed to the properties of the composites. Filled with 20 phr modified bentonite, the tensile strength and elongation at break of the rubber increased from 1.95 to 4.8 MPa and 300% to 500%, respectively.

• Proceedings of the Mineralogical Society of Korea Conference
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• 2000.10a
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• pp.31-42
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• 2000

1. 선진국의 경우 한 사업체에서 광산-가공산업체-연구소를 운영하는 시스템으로서 제품규제부터 시작하여 계속적인 용도개발이 가능하다. 2. 한국의 벤토나이트 광업 및 가공산업체의 현황이 일본의 5분의 1규모이며 년간 생산량 및 수요량이 100,000톤 규모로서 세계 15위권에 해당된다. 3. 벤토나이트 광업의 영세화로 효율적이고 장기적인 개발이 되지 못한다. 4. 광량의 고갈 및 개발 침체로 수입량이 증대되고 있다. 5. 새로운 용도개발이 요구된다. 특히 최근 증대되는 cat litter용, 흡착제용등 우선 개발이 용이한 용도개발을 추진해야 하며 다음으로 방사성 폐기물 처분장 liner 및 brick용, 폐수처리용 유기-벤토나이트, 쓰레기매립장 liner용과 화장품용등의 부가가치를 향상시킬 수 있는 용도개발이 시급하다고 본다.

• The Journal of Engineering Geology
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• v.9 no.2
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• pp.89-100
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• 1999

This study was carried out to assess the physicochemical properties of domestic bentonites and zeolites from Tertiary Formation as the candidate material for a engineered barrier of a radioactive waste repository. Natural bentonite and zeolite samples were collected from nine bentonite mines and six zeolite mines in Yeonil-Gampo area. The commercial products of bentonite and zeolite were obtained from local companies. The collected samples were investigated to study the following physicochemical properties: X-ray diffraction patterns, swelling, cation exchange capacity(CEC), specific surface area, montmorillonite content, pH, organic carbon content, thermal property, microstruciure and chemical composition. Based on the physicochemical properties of bentonite and zeolite, the bentonites from U-41 and G-46 mines and the zeolites from Daedo and Y-1 mines are regarded as the most desirable candidate materials.

• Proceedings of the Mineralogical Society of Korea Conference
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• 2005.05a
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• pp.58-59
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• 2005

• Journal of the Korea Organic Resources Recycling Association
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• v.22 no.2
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• pp.17-26
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• 2014

In this study, the adsorption efficiency of mixed heavy metals from an aqueous solution was examined using bentonite. The physical and chemical properties of bentonite was analyzed via scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR), Further, heavy metal adsorption was characterized using Freundlich and Langmuir equations. Equilibrium adsorption data were fitted well to the Langmuir model for bentonite. The adsorption uptake of heavy metals was high and followed the order $Pb^{2+}$ > $Cu^{2+}$ > $Cd^{2+}$ > $$Zn^{2+}{\sim_=}Ni^{2+}$$. The results also showed that adsorption uptake slightly increased as increasing pH from 6 to 10. The bentonite surface was observed viay SEM and FT-IR; Si-O and Si-O-Al were found to be the main functional groups by FT-IR analysis. From these results, the adsorption mechanisms of heavy metal were not only surface adsorption and ion exchange, but also surface precipitation. Thus, bentonite could be a useful adsorbent for treating heavy metal in aqueous solution.