• 한국광물학회지
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• 제17권2호
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• pp.147-155
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• 2004

두 양이온 유기폴리머(Hexadecyltrimethylammonium (HDTMA)과 Cetylpyridinium (CP))를 합성한 유기벤토나이트에 대해 음이온의 흡착특성을 조사하였다. 이들 유기벤토나이트는 상온에서 저면간격이 약 42.0 $\AA$으로 현저한 층간팽창을 나타냈다 유기벤토나이트 시료 0.2 g을 음이온인 질산염, 황산염, 인산염의 각 여러 농도별 용액 40 mL와 반응시킨 흡착실험을 행하였다. 그 결과, 무처리 벤토나이트는 모든 음이온에 대해서 거의 흡착능력을 보이지 않는데 비하여. 유기벤토나이트는 아주 높은 흡착성을 나타냈다. HDTMA-bentonite의 경우, 인산이온과 질산이온의 흡착률이 100 mg/L의 농도에서 약 90% 정도로 높게 나타나고, CP-bentonite의 경우, 질산이온의 흡착률이 100 mg/L의 농도에서 97%로 높게 나타났다. 음이온 및 유기벤토나이트의 종류에 따라 흡착거동이 약간차이를 나타냈다. 두 유기벤토나이트에 있어서 질산이온과 인산이온의 흡착률은 황산이온에 비해 모두 상대적으로 높게 나타났다. 이러한 유기벤토나이트의 높은 음이은 흡착성은 유해성 음이온의 제거와 같은 환경오염처리에 활용될 수 있을 것으로 생각된다.

• 한국환경과학회지
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• 제16권2호
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• pp.143-149
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• 2007

The effect of precoating of silica with polyamine surfactants on the adsorption of five model compounds containing asphalt-like functionalities was studied. Hexadecyltrimethylammonium chloride (HDTMA) and 1-hexadecylamine were used for silica precoating. The model compounds representing five asphalt functionalities were benzoic acid, phenol, benzylbenzoate, benzophenone, and quinoline. All the adsorption isotherms conformed well to the Langmuir adsorption model. All the model compounds showed decreased adsorption with the HDTMA precoating. However, two acidic compounds, benzoic acid and phenol, showed enhanced adsorption on the silica precoated with 1-hexadecylamine. In aqueous solutions, the adsorption of the acidic compounds were in the following order: silica precoated with 1-hexadecylamine > silica precoated with HDTMA > uncoated silica.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2002년도 추계학술발표회
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• pp.67-70
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• 2002

Remediation of groundwater contaminated with chlorinated organics, nitro aromatics, and heavy metals using zero valent iron (ZVI) filings has paid considerable attention in recent years. When the contaminants of high concentration leaked abundantly in subsurface environment, permeable reactive barrier technology using iron filing is taken a long time for the remediation of contaminated groundwater, The problem of contaminant shock is able to be solved using surfactant (hexadecyltrimethylammonium, HDTMA) modified bentonite (SMB) as immobilizing material. Therefore, the purpose of this research was to develop the combined remediation technology using conventional permeable reactive and immobilizing barrier for the enhanced decontamination of chlorinated compounds. Four column experiments were conducted to assess the performance of the mixed reactive materials with Ottawa sand, iron filing, and HDTMA-bentonite for trichloroethylene (TCE) removal under controlled groundwater flow conditions. TCE reduction rates with sand/iron filing/HDTMA-bentonite were highest among four column due to dechlorination of TCE by iron filing and sorption of TCE by SMB.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2004년도 총회 및 춘계학술발표회
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• pp.186-191
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• 2004

Sorption kinetics of 2-chlorophenol(2-ChP), 2,4-dichlorophenol(2,4-DChP) and 2,4,5-trichlorophenol (2,4,5-TChP), onto montmorillonite modified with hexadecyltrimethyl ammonium cations(HDTMA-mont) were investigated. One-site mass transfer model(OSMTM) and two compartment first-order kinetic model(TCFOKM) were used to analyze kinetics. As expected from the number of model parameters involved, the three-parameter TCFOKM was better than the two-parameter OSMTM in describing sorption and desorption kinetics of chlorophenols in HDTMA-mont. For all chlorophenols, the results of OSMTM analysis indicate that the predominant deprotonated speciation(at pH 9.15) exhibited higher mass transfer coefficient( $k_{s}$ ) than the protonated speciation(at pH 4.85). This is because the deprotonated speciation has stronger hydrophobic interaction than protonated speciation. Most sorption completes in three hours. The fraction of the fast sorption and the first-order sorption rate constants for the fast and slow compartments in TCFOKM were determined by fitting experimental data to the TCFOKM. The results of kinetics reveal that the fraction of the fast sorption( $f_1$) and the sorption rate constants in the fast compartments( $k_1$) were in the order 2,4,5-TChP > 2,4-DChP > 2-ChP, which agrees with the magnitude of the $K_{ow}$ . The first-order sorption rate constants in the fast compartment(10$^{0.8}$ - 10$^{1.22}$ h $r^{-1}$ ) were much larger than those in the slow compartment(10$^{-1}$.74/ - 10$^{-2}$.622/ h $r^{-1}$ ).> ).).

• 한국환경과학회지
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• 제20권2호
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• pp.185-197
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• 2011

Sorption of chlorinated pesticides such as 2,4-dichlorophenoxyacetic acid (2,4-D) and atrazine onto natural clays (montmorillonite and zeolite) modified with cationic surfactant, hexadecyltrimethyl-ammonium (HDTMA) and a natural soil was investigated using batch adsorbers. The clays were transformed from hydrophilic to hydrophobic by the cation exchange between clay surface and HDTMA up to 100% of the cation exchange capacity (CEC). Physicochemical characteristics of the sorbents such as pH, PZC (point of zero charge), organic carbon content ($f_{oc}$), fourier transform infrared spectroscopy (FT-IR), differential thermogravimetric analysis (DTGA) and X-ray diffraction (XRD) were analyzed. Sorption isotherm models such as Freundlich and Langmuir were fitted to the experimental data, resulting Langmuir model ($R^2$ > 0.986) was fitted better than Freundlich model ($R^2$ > 0.973). Sorption capacity ($Q^0$) for 2,4-D and atrazine was in the order of HDTMA-montmorillonite > HDTMA-zeolite > natural soil corresponding to the increase in organic carbon content ($f_{oc}$). The sorption of the pesticides was also affected by pH. The sorption of 2,4-D decreased with the increase in pH, whereas that of atrazine was not changed. This indicated that the sorption capacity ($Q^0$) of 2,4-D and atrazine was not affected by the solution pH because they exist as anionic (deprotonated) forms at pH above pKa. The results indicate that organoclay has a promising potential to reduce chlorinated pesticides in the effluent from golf courses.

• 한국지하수토양환경학회지:지하수토양환경
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• 제6권3호
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• pp.21-29
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• 2001

양이온성 계면활성제인 HDTMA를 이용하여 치환시킨 유기 벤토나이트의 중금속 흡착능을 알아보았다. 카드뮴과 납의 흡착량은 pH와 흡착제 대 용액 비가 증가함에 따라 증가하였다. 이 실험을 통해 적정 pH 범위와 흡착제 대 용액 비를 결정하였다. 유기 벤토나이로의 중금속 흡착은 벤토나이트에 비해 약간 감소하였으며, 두 가지 중금속이 함께 존재하는 경우 경쟁에 의해 흡착량은 더 감소하였다. 유기 벤토나이트의 경우 카드뮴에 비해 납의 흡착 감소량은 더 두드러지게 나타났다. 이러한 흡착 mechanism을 hard-soft-acid-base (HSAB) 원리를 사용하여 설명하였다.

• 자원환경지질
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• 제36권3호
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• pp.171-176
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• 2003

다환방향족 탄화수소(PAHs)와 중금속의 거동은 주로 토양 및 퇴적물내의 다양한 성분과의 상호 반응에 의해 결정된다. 토양구성 성분중 스멕타이트는 양적으로 풍부하고 큰 표면적을 가지고 있어서 오염물의 거동에 커다란 영향을 끼친다. 본 실험에서, 헥사데실트리메틸암모니움(HDTMA)으로 표면개질된 스멕타이트로 다환방향족 탄화수소에 대한 흡착 실험을 실시하였을 때, 헥사데실트리메틸암모니움의 첨가량에 따라 선형적으로 오염물의 흡착량이 증가하였다. 그러나, 트리메틸암모니움(TMA)으로 표면개질된 스멕타이트는 헥사데실트리메틸암모니움이나 도데실트리메틸암모니움(DTMA)으로 표면개질된 스멕타이트보다 다환방향족 탄화수소의 흡착능력이 떨어졌다. 한편, 동일한 스멕타이트로 물속에 존재하는 카드뮴을 제거하는 실험에서 계면활성제의 첨가량이 많지 않을 때는 카드뮴 흡착량이 높았으나, 계면활성제의 첨가량이 증가하면서 반대로 카드뮴의 흡착량은 감소하였다. 이러한 결과는 유기점토에 의한 유기 혹은 무기오염물 흡착 경향성이 점토에 첨가되는 계면활성제의 크기와 첨가량에 의해 크게 좌우됨을 보여준다. 이것은 다시 말해, 계면활성제의 첨가량에 따라 점토광물 층간에 형성되는 양이온성 계면활성제의 안정성과 배열 구조가 환경 오염물들의 효과적인 제거를 결정하는 중요한 요소임을 의미한다.

• 한국암석학회:학술대회논문집
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• 한국암석학회.한국광물학회 2000년도 공동학술발표회 논문집
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• pp.39-39
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• 2000

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2002년도 총회 및 춘계학술발표회
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• pp.114-117
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• 2002

Sorption and desorption studies were conducted to evaluate several media as a potential biobarrier for the remediation of groundwater contaminated with hydrophobic organic compounds (HOCs). Pahokee and Bion peats, Devonian Ohio shale, vermicompost, and 50% HDTMA-montmorillonite were used as model sorbents. Sorption and desorption isotherms were determined using the radiolabeled phenanthrene (Phe). Sorption capacity of Phe on several sorbents was in the order Ohio shale > 50% HDTMA-montmorillonite > vermicompost > Pahokee peat. Mineralization kinetics was investigated for Phe-sorbed sorbents using Pseudomonas putida 17484. Among the tested sorbents, active biodegradation of Phe was observed in shale and vermicompost: degradation in shale exhibited little lag time while that in shale showed a significant lag time. Results of this study indicate that sorbents used in this work can be utilized as permeable reactive biobarrier media for the remediation of HOC-contaminated groundwater.

• 한국광물학회:학술대회논문집
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• 한국광물학회.한국암석학회 2001년도 공동학술발표회 논문집
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• pp.52-52
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• 2001

Clays coated with cationic surfactants (organoclays) have been investigated due to their effectiveness in sorbing organic compounds from water The objectives of this study were to (1) study the sorption characteristics or a cationic surfactant (HDTMA) to clay minerals; (2) examine the partitioning of HOC (naphthalene) to the adsorbed surfactants within the context of the first objective, and (3) develop overall HOC distribution coefficients that consider sorbed surfactant amounts. The sorption of hydrophobic organic contaminant was due to partitioning of the organics into the organic pseudophase created by the surfactant tail groups. Sorption of naphthalene by HDTMA-clays at different surfactant surface coverages revealed that the naphthalene K$\_$d/ values were affected by the surface concentration of surfactant. In our study the kaolinite was modified with a cationic surfactant to achieve different fractional organic carbon contents and different surfactant molecule configurations on the surface. All of the sorption isotherms were nearly linear and could be described by a distribution coefficient (K$\_$d/). The sorption of naphthalene by the surfactant-modified kaolinite was found to be dependent on the bound surfactant molecule configuration as well as on the fractional organic carbon content but halloysite was not affected by the increase of surfactant amounts. Results from this investigation provide additional insight into the role that sorbed surfactant structure plays in HOC partitioning.