• 환경위생공학
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• 제10권3호
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• pp.78-84
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• 1995

Cationic surfactants can be used to modify surface of solids to promote adsorption of hydrophobic organic compounds. This behavior is due to the surfactant forming aggregate structure on the solid surface. Partition coefficients are commonly used to quantify the distribution of organic pollutants between the aqueous and particulate phases of aquatic system Partitioning of hydrophobic compounds to cetyltrimethylammonium bromide ( CTAB ) coated silicate has been investigated as a function of surfactant surface coverage at I=0 and 0.1 ionic strength. Toluene, Xylene, TCI sorption experiments demonstrated that the CTAB coated silicate was able to remove these hydrophobic organic compounds from solution The hydrophobic organic compound with the higher Kow had higher removals than lowest Kow hydrophobic organic compound.

• 한국대기환경학회지
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• 제27권3호
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• pp.337-346
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• 2011

24-hr integrated measurements of water-soluble organic carbon (WSOC) in PM2.5 were made between May 5 and September 25, 2010, on a six-day interval basis, at the Metropolitan Area Air Pollution Monitoring Supersite. A macro-porous XAD7HP resin was used to separate hydrophilic and hydrophobic WSOC. Compounds that penetrate the XAD7HP column are referred to hydrophilic WSOC, while those retained by the column are defined as hydrophobic WSOC. Laboratory calibrations using organic standards suggest that hydrophilic WSOC includes lowmolecular aliphatic dicarboxylic acids and carbonyls with less than 4 or 5 carbons, amines, and saccharides. While the hydrophobic WSOC is composed of compounds of aliphatic dicarboxylic acids with carbon numbers larger than 4~5, phenols, aromatic acids, cyclic acid, and humic-like Suwannee River fulvic acid. Over the entire study period, total WSOC accounted for on average 48% of OC, ranging from 32 to 65%, and hydrophilic WSOC accounted for on average 30.5% (9.3~66.7%) of the total WSOC. Based on the previous results, our measurement result suggests that significant amounts of hydrophobic WSOC during the study period were probably from primary combustion sources. However, on June 9 when 1-hr highest ozone concentration of 130 ppb was observed, WSOC to OC was 0.61, driven by increases in the hydrophilic WSOC. This result also suggests that processes, such as secondary organic aerosol formation, produce significant levels of hydrophilic WSOC compounds that add substantially to the fine particle fraction of the organic aerosol.

• 한국지하수토양환경학회지:지하수토양환경
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• 제17권6호
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• pp.59-68
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• 2012

This study provided sorption properties of chlorofluorocarbons (CFCs), and elucidated potential application of CFC sorption data in hydrogeochemistry. Prior sorption studies were reviewed for hydrophobic organic compounds similar to the CFCs, because there were only few CFC sorption studies. The CFCs are regarded as relatively conservative chemicals in groundwater environments based on their moderate hydrophobicity. However, thermally altered carbonaceous matter (TACM) can significantly increase sorption capacity and nonlinearity for hydrophobic organic compounds such as CFCs, compared to general soil organic matter. CFC sorption behavior are close to the sorption for reviewed organic chemicals. Therefore, the CFC sorption data can be used for determining hydrogeochemical properties and predicting transport of organic contaminants in TACM-containing aquifer environments.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2000년도 추계학술대회
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• pp.281-285
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• 2000

The effect of the presence of dissolved organic matters(DOM) on the binding of phenanthrene to cetylpyridinium chloride(CPC) coated sand was investigated. The distribution coefficient of phenanthrene increased with increase of sufactant coverage, and decreased with the presence of dissolved organic matters except for the 1.600mg/g coverage case. Both Aldrich humic acid and extracted dissolved organic matter showed the similar tendency. For the quantification of the overall distribution coefficient, this study presented mass distribution model and estimated the sorption equilibrium coefficients of hydrophobic organic compounds(HOCs) in multi system. The suggested model combined a series of sorption equilibrium relationships including the adsorption of DOMs on sorbents, the binding between HOCs and DOMs, and the sorption of HOCs on sorbents with or without DOMs.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 총회 및 춘계학술발표회
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• pp.26-29
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• 2001

Sorption/desorption Study was conducted to determine desorption-resistance hydrophobic organic compounds in natural soils with low organic carbon content. Sorption/desorption characteristics of chlorobenzene and phenanthrene for both PPI (Petro Processors, Inc. Superfund site) and BM (Bayou Manchac), soils were investigated. Desorption was biphasic including reversible and desorption-resistant compartments. The biphasic sorption parameters indicated the presence of appreciable size of desorption-resistant phase in these soils. A finite maximum capacity of desorption-resistant fraction (equation omitted) was observed after several desorption steps. The apparent organic carbon based Partition coefficient, K(equation omitted) was 10$^{4.92{\pm}0.27}$ for PPI soil and 10$^{4.92{\pm}0.27}$ for BM soil, respectively. The difference in K(equation omitted) was attributed to different characteristics in soil organic matter. The results suggest that desorption-resistance should be considered in remediation and risk assessments in natural soils and sediments.

• 대한환경공학회지
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• 제22권3호
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• pp.557-564
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• 2000

본 연구에서는 수용액 중의 유독성 유해물질로 미량으로 존재하여도 치명적 독성을 가진 난용성 유기오염물(sparingly soluble organic compounds, SSOCs)의 제거를 위한 흡착제 개발을 목표로 양이온 계면활성제(cetyltrimetylammonium bromide, CTAB)로 표면 개질된 organo-anthracite의 유기화합물 제거능을 조사하고, 흡착 특성을 분배계수 (partition coefficient, $K_d$) 로 평가함으로써 organo-anthracite의 유기물질 흡착메카니즘을 규명하고자 히였다. Organo-anthracite는 CTAB가 흡착됨에 따라 전 pH 범위에서 표면전위가 양의 값으로 상닫히 증가되었으며, 또한 표면의 소수성이 증가되어 표면전하가 pH에 비의존적으로 나타났다. pH 2~10의 용액을 탈리액으로 하여 organo-anthracite의 탈착성을 실험한 결과 0% 의 탈착율을 나타내어 전 pH 범위에서 안정함을 알 수 있었고, 이를 이용한 제거실험에서 츠기 농도 $6{\times}10^{-4}M$인 클로로포름과 벤젠이 전 pH범위에서 95% 이상 제거되었다. Organo-anthracite와 유기화합물간의 분배계수 $K_d$값은 실측치가 이론치보다 4~25배의 높은 값으로 나타났다. 이는 다른 흡착제에 비해 organo-anthracite내에서 SSOCs의 분배가 더 쉽게 이루어짐을 의미한다. 따라서, 유독성 유기오염물질을 포함하는 폐수의 처리시 흡착제로써 이용이 가능하며 또한 organo-anthracite를 매립지의 차수막으로 이용시 유독성 유기 오염물질의 이동을 보다 효과적으로 지연시킬 수 있을 것으로 사료된다.

• 한국지반공학회:학술대회논문집
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• 한국지반공학회 1999년도 봄 학술발표회 논문집
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• pp.543-550
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• 1999

Hazardous substances produced from industrial sectors have caused serious contamination of soils and groundwater. The hydrophobic organic compounds in the subsurface are hard to be decomposed, and as they soil on the soil or last as a NAPL they might contaminate the groundwater for a long time. Although we recognize the danger of contaminated subsurface, very little was known about the effective remediation technique. This paper focuses on the remediation of the p-Cresol which contaminated subsurface by applying the surfactant-enhanced description technique. Sorption characteristics of soils and organic compounds are studied, and the applications of surfactant solution are studied for effective rededication. The results from this study could be used as some data for surfactant-enhanced rededication. The flexible-wall permeameter tests are performed in which in-situ remediation is simulated. Results show that triton X-100 at 2% solution disrobes p-Cresol 1.7 times as much as water description in the flexible-wall permeameter tests.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2000년도 창립총회 및 춘계학술발표회
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• pp.129-132
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• 2000

In this research, we proposed the immobilization zone where the organic contaminant would be fixed, so that ground water could be prevented from the organic contaminants. The surfactant was adsorbed on the soil particles and the organic contaminants were partitioned into the hydrophobic tails of the surfactant in the immobilization zone. Surfactants with different molecular structures-SDDBS (sodium dodecylbenzenesulfonic acid), MADS (monoalkylated disulfonated diphenyl oxide), DADS (dialkylated disulfonated diphenyl oxide) - were used in this study. Up to the present, the research on the immolization simulated the saturated condition. But many site contaminated with organic contaminants and the zones where immobilization would be applied are unsaturated. In this research, in order to investigate the behaviors of surfactants and organic contaminants in unsaturated condition, the unsaturated columns were experimented, and their results were compared with the saturated case.

• Environmental Analysis Health and Toxicology
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• 제23권2호
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• pp.67-77
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• 2008

It has been observed that the linear relationship between the logarithm of bioconcentration factor (log BCF) of highly hydrophobic chemicals and their log $K_{ow}$ breaks when log $K_{ow}$ becomes greater than 6.0. Consequently, super hydrophobic chemicals were not thought to cause baseline toxicity as a single compound. Researchers often call this phenomenon as "hydrophobicity cutoff" meaning that bioconcentration or corresponding baseline toxicity has a certain cutoff at high log $K_{ow}$ value of hydrophobic organic pollutants. The underlying assumption is that the increased molecular size with increasing hydrophobicity prohibits highly hydrophobic compounds from crossing biological membranes. However, there are debates among scientists about mechanisms and at which log $K_{ow}$ this phenomenon occurs. This paper reviews three hypotheses to explain observed "cutoff": steric effects, kinetic or physiological limitations, and chemical activity cutoff. Although the critical molecular size that makes biological membranes not permeable to hydrophobic organic chemicals is uncertain, size effects in combination with kinetic limitation would explain observed non-linearity between log BCF and log $K_{ow}$. Chemical activity of hydrophobic chemicals generally decreases with increasing melting point at their aqueous solubility. Thus, there may be a chemical activity cutoff of baseline toxicity if there is a critical chemical activity over which baseline effects can be observed.

• Membrane and Water Treatment
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• 제5권3호
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• pp.171-182
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• 2014

Organic compounds are adsorbed on RO/NF membranes, and the adsorption may influence the rejection of organic compounds by the membranes. Because almost RO/NF membranes are composite membranes, the results obtained by adsorption experiment with using membrane pieces are unable to avoid the influence by the support membrane. In this work, the interaction between membrane polymer and organic solutes was examined by an inverse HPLC methodology. Poly (m-phenylenetrimesoylate), the constituent of skin layer of RO/NF membranes, was coated on silica gel particles and used as a stationary phase for HPLC. When water was used as a mobile phase, almost hydrophilic aliphatic compounds were not effectively adsorbed on the stationary phase, although hydrophobic compounds were slightly adsorbed. The results indicated that the hydrophilic aliphatic compounds are useful probe solutes to examine the molecular sieving effect of a membrane. When water was used as a mobile phase, the aromatic compounds were strongly retained, and therefore $CH_3CN/H_2O$ (30/70) was used as a mobile phase. It was revealed that the adsorption of aromatic compounds was controlled by stacking between solute and polymer and was hindered by non-planar structure and substituents.