• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2004.09a
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• pp.248-251
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• 2004

일반적으로 유기오염 물질의 경우 sequestration 또는 aging 현상에 의해 탈착저항성을 띠게 되는 것으로 알려져 있다. 그러나 중금속의 경우 흡/탈착반응은 탈착저항성이 없는 가역적 반응이라는 보고가 있는 반면 홉/탈착 반응은 비가역적이며 탈착저항성이 존재한다는 보고도 있다. 본 연구에서는 해양 연안 퇴적물에 대한 납의 흡/탈착 실험을 통하여 탈착 저항성을 화인하고 연속추출 실험을 수행함으로써 탈착 저항성 부분의 크기를 규명하고자 하였다. 그리고 각기 다른 pH(4, 6)에서 흡착 실험을 수행함으로써 pH에 따른 흡착친화도를 규명하였다. 그 결과 퇴적물에 대한 납의 흡착량은 높은 pH(6)에서 더 많았고, 각 pH 범위에서 납은 탈착저항성을 가지는 것으로 나타났으며, 연속추출결과 Organic Material bound부분에 66% 정도가 흡착되어 있음을 알 수 있었다.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 1996.11a
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• pp.97-101
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• 1996

산림부산물인 수피에 의한 카드뮴 이온의 선택적 흡착 현상을 이용하여 인공폐수로부터 카드뮴이온의 제거를 시도하였다. 카드뮴 이온 선택성이 우수한 소나무와 상수리 나무의 수피를 이용한 효율적인 연속식 대량 수처리 시스템의 개발을 위한 기초 실험으로 카드뮴 이온흡착 등온선을 조사하였고, batch stirred reactor, airlift reactor, packed bed column 등 여러 접촉시스템에서의 카드뮴 이온의 제거 효율을 검토하였다. 카드뮴 흡착등온선은 두 수피 모두 Langmuir 형식으로 나타났으며 소나무 수피의 최대흡착용량은 약 7 mg/g, 상수리나무 수피의 경우에는 약 8 mg/g 정도로 나타났다. Batch stirred reactor를 이용한 시스템에서 초기농도 13 ppm의 카드뮴용액 100 $m\ell$ 을 수피 10 g 과 접촉시킨 결과 30분 이내에 95% 이상 제거되는 효율성을 보여주었다. Airlift reactor를 이용한 시스템에서는 수피 30 g 을 포기농도 10 ppm 카드뮴 용액 1 liter와 접촉시킨 결과 15분 이내에 93 % 이상 제거되었으며 4 cycle 반복 운전에서도 거의 같은 성능을 유지하였고 그 이상의 cycle에서는 점점 성능이 떨어짐을 보여주었다. Packed bed column을 이용한 시스템에서는 20 g의 수피를 충전시켰을 경우 초기농도 20 ppm에서 effluent 2.5 liter 까지는 95% 정도의 제거효율을 보여주었다.

• Proceedings of the Korea Technical Association of the Pulp and Paper Industry Conference
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• 2010.04a
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• pp.193-193
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• 2010

이전의 연구에서 우리는 선응집 기술을 적용한 중질탄산칼슘의 크기에 따른 수초지의 물성을 평가하였다. 이때 선응집 기술이 적용된 충전물의 입도와 분포를 측정하기 위해 light diffraction spectroscopy (LDS) 가 사용되었다. 경질탄산칼슘과 양이온성 고분자의 흡착 현상을 알아보기 위한 이번 연구에도 LDS가 사용되었으며, 일회성으로 입자의 크기와 분포를 측정하는 것에서 더 나아가 시간의 흐름에 따라 응집체의 형성과 파괴, 재성장을 관찰할 수 있는 도구로서 역할 하였다. 본 연구에서 우리는 세 가지 경우로 나누어 경질탄산칼슘의 응집 현상을 관찰하였다. 첫째로 경질탄산칼슘에 흡착되는 양이온성 고분자의 특성, 분자량과 전하밀도, 을 달리하여 응집체의 성장과 파괴를 관찰하였다. 둘째, 양이온성 고분자로 중질탄산칼슘을 응집시켜, 경질탄산칼슘 응집체의 경우와 입도와 전단 안정성 등을 비교하였다. 마지막으로 나노 크기의 실리카 투입이, 마이크로 크기의 경질탄산칼슘 응집체가 강한 전단에 의해 파괴되었을 때, 응집체의 전단 안정성이나 재성장 측면에 도움을 주는지 관찰하였다. 내첨용 충전물로써 경질탄산칼슘의 사용이 전 세계적으로 늘고 있는 시점에서 양이온성 고분자 첨가에 의한 경질탄산칼슘의 응집 현상을 관찰하는 것은 일반적인 제지 공정에서 경질탄산칼슘의 거동을 이해하는데 도움이 될 뿐만 아니라, 내첨용 충전물 첨가에 따른 종이의 강도 저하 방지를 위한 선응집 기술의 적용에도 도움이 될 수 있을 것으로 생각한다.

• Food Science and Industry
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• v.54 no.1
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• pp.11-28
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• 2021

Air pollution caused by particulate matters (PM) has become a global issue. PM is known to threaten human health by causing respiratory and cardiovascular disease. PM can be introduced to human gastrointestinal track through food intake, causing inflammation and changes in gut microbiota. Even at low PM concentrations, prolonged exposure to PM can cause significant accumulation of PM in food products. The adsorption of PM onto food surfaces is expected to be strongly influenced by the properties of food surfaces, but few studies have been reported. This paper examines several important food surface properties that may affect the interactions between PM and food surfaces, including surface wettability, surface charge, and surface microstructure. Understanding the adsorption of PM onto food surfaces can provide useful guidance for classifying PM-sensitive foods and controlling food chains, including cultivation, processing, preservation, and cooking, to ensure food safety against PM.

• Journal of the Korean Society of Groundwater Environment
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• v.1 no.2
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• pp.100-104
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• 1994

The rock matrix diffusion provides a retarding mechanism for sorbing and especially non-sorbing radionuclides. It has to be verified not only theoretically and experimentally but also from natural phenomena, before the mechanism can be incorporated fully into transport codes. The natural analogue studies, such as the concentration variation of radionuclides in profiles perpendicular to fluid-conducting fractures and to intrusive contact zones, have been believed to provide a validation. In thermal alteration zones of Naeduckri granite intruded by a pegmatite, large alkali and alkaline earth elements such as K, Rb, Sr, and Ba were moderately migrated during thermal alteration. Li, V. and Nb were also migrated about 9cm in width from the contact between the granite and the pegmatite. The concentration variation of these elements in thermally altered zones seems to be resulted from the local migration due to the re-equilibration among the elements released from the breakdown of primary minerals in the granite. Most of these natural analogue studies simply show only the concentration variation of elements without detailed informations on the diffusion time and other important data fir interpreting the behaviour of radionuclides, because of the absence of appropriate minerals for age data. Despite this problem, natural analogue studies will be needed for transport models of radionuclides in safety assessment.

• Korean Chemical Engineering Research
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• v.58 no.3
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• pp.458-465
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• 2020

Isotherms, kinetics and thermodynamic properties for adsorption of acid fuchsin (AF) dye by activated carbon were carried out using variables such as dose of adsorbent, pH, initial concentration and contact time and temperature. The effect of pH on adsorption of AF showed a bathtub with high adsorption percentage in acidic (pH 8). Isothermal adsorption data were fitted to the Freundlich, Langmuir, and Dubinin-Radushkevich isotherm models. Freundlich isothem model showed the highest agreement and confirmed that the adsorption mechanism was multilayer adsorption. It was found that adsorption capacity increased with increasing temperature. Freundlich's separation factor showed that this adsorption process was an favorable treatment process. Estimated adsorption energy by Dubinin-Radushkevich isotherm model indicated that the adsorption of AF by activated carbon is a physical adsorption. Adsorption kinetics was found to follow the pseudo-second-order kinetic model. Surface diffusion at adsorption site was evaluated as a rate controlling step by the intraparticle diffusion model. Thermodynamic parameters such as activation energy, Gibbs free energy, enthalpy entropy and isosteric heat of adsorption were investigated. The activation energy and enthalpy change of the adsorption process were 21.19 kJ / mol and 23.05 kJ / mol, respectively. Gibbs free energy was found that the adsorption reaction became more spontaneously with increasing temperature. Positive entropy was indicated that this process was irreversible. The isosteric heat of adsorption was indicated physical adsorption in nature.

• Journal of Soil and Groundwater Environment
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• v.12 no.3
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• pp.23-28
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• 2007

A number of batch isotherm and electrokinetic experiments were conducted in order to investigate the migration of zinc and its removal efficiency during electrokinetic soil processing. Sorption and desorption characteristics of zinc spiked kaolin clay have been examined by comparison with electrically induced desorption and precipitation occurring in the anode and cathode regions, respectively. The removal efficiency of zinc under the applied voltage gradient of 300 V/m was found to be up to approximately 80 % within 4 hours of the electrokinetic treatment. The study is significant with respect to the remediation of contaminated areas.

• Korean Chemical Engineering Research
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• v.48 no.4
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• pp.534-539
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• 2010

The adsorptive removal of organic sulfur compounds including tert-butylmercaptane(TBM), tetrahydrothiophene(THT) and dimethylsulfide(DMS) in methane was investigated over NaY and copper-exchanged NaY(CuNaY) zeolites at 303 K and atmospheric pressure. In the ternary adsorption system, the preferential adsorption of THT over other sulfur compounds on NaY and the concurrent adsorption of all sulfur compounds on CuNaY were achieved, which could be explained by the breakthrough curve, the temperature-programmed desorption, and the apparent activation energy for desorption. The sulfur uptake capacity of CuNaY(2.90~3.20 mmol/g) was much higher than that of NaY(0.70~0.90 mmol/g). A comparative study indicated that the $Cu^{1+}$ sites and acidity of CuNaY were probably responsible for the strong interaction with sulfur atom and high sulfur uptake abilities.

• Korean Journal of Optics and Photonics
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• v.15 no.6
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• pp.531-538
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• 2004

Studies of adsorption isotherms with sharp step-wise layer condensation help us to better understanding of two dimensional layers. For this, an adsorption isotherm apparatus, using a phase modulated ellipsometric technique, has been constructed and an adsorption experiment has been performed. With subatomic scale resolution(∼0.3 $\AA$), the adsorption processes could be observed by ellipsometric signals. On measurement of multilayer adsorption of argon on highly oriented pyrolytic graphite(HOPG), thousands of adsorbed layers were observed at 34.04 K, which suggests that the adsorption is completely wet. On the contrary nine sharp layers of steps for adsorptions and desorptions were observed at 67.05 K. These isotherms obtained can provide a lot of information about thermodynamic states, bonding energies between adsobate and substrate, and structure transitions in the adsorbed film.

• Journal of the Korean Chemical Society
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• v.36 no.3
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• pp.351-359
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• 1992

Interaction of xenon with alkaline-earth cations in Y zeolite supercage was studied by xenon adsorption and $^{129}Xe$ NMR experiments. The CaY and the BaY samples were prepared by exchanging $Ca^{2+}$ and $Ba^{2+}$ into a high-purity NaY zeolite. Xenon adsorption isotherms of these samples were obtained by using a conventional volummetric gas adsorption apparatus in the range of 260 to 320 K and the chemical shift in the $^{129}Xe$ NMR spectrum of the adsorbed xenon was measured at 296 K. The chemical shift against pressure was quantitatively explained assuming that the xenon gas exchanged very rapidly between various adsorption sites consisting of zeolite-framework surface and alkaline-earth ion. From this analysis, it was found that the alkaline-earth ion adsorbed xenon more strongly than $Na^+$ ion and zeolite-framework surface. Baring on the difference of the adsorption strength, the number of the alkaline-earth cations present in the zeolite supercage could be estimated by analyzing the adsorption isotherm.