• 폴리머
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• 제28권1호
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• pp.24-34
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• 2004

여러 종류의 불소고분자내로 다양한 유기용매들의 동적 흡수 평형 (혹은 팽윤) 실험을 진행하였다. 불소로 포화된 고분자는 이상적 흡수 거동을 나타내었으나 부분적으로 치환된 불소고분자는 최종 흡수단계에서 가속화되는 비이상적 흡수 거동을 나타내었다. 회귀분석에 의해 픽-확산 거동으로부터 벗어나는 정도를 최소자승법 (즉, ∑ ［측정값-예측값］$^2$)으로 구한 결과 -퍼플루오로알콕시 공중합체, 폴리(에틸렌 테트라플루오로에틸렌) 공중합체, 폴리(비닐리덴 플루오라이드), 폴리(에틸렌 클로로트리플루오로에틸렌) 공중합체에 대해 각각 3.0${\times}$$10^{-4}$, 1.75${\times}$$10^{-3}$, 8.68${\times}$$10^{-3}$, 1.75${\times}$$10^{-2}$의 수치를 나타내었다. 응력-변형 실험 결과 비-픽 확산 거동은 팽윤된 불소고분자의 기계적 성질 (탄성률과 인장 강도) 변화와 상관관계가 있음을 알 수 있었다. 비이상적 흡수 거동의 주요 원인은 치환된 수소 혹은 염소와 불소원자 간의 전기음성도 차이에 기인한 사슬 간극성 결합 구조가 침투성분의 가소화 효과에 의해 비선형적 이완이 진행되면서 비-픽 확산이 진행되기 때문이다. 따라서 부분적으로 치환된 불소고분자를 차단성 혹은 선택적 투과기능이 요구되는 분야에 적용할 때 가소화 성분에 대한 용해 및 확산 거동에 대한 신중한 고찰이 필요하다.

• 한국막학회:학술대회논문집
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• 한국막학회 2003년도 추계 총회 및 학술발표회
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• pp.164-167
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• 2003

• 한국포장학회지
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• 제8권2호
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• pp.39-43
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• 2002

Increasing use of plastics in food packaging materials has led to the issue of food-plastic packaging materials's mutual interactions. Although the plastic packaging materials are generally considered as inert, migration and sorption of fatty materials are some of the problems associated with their use. So, this work investigated the compatibility of three structurally different polymers, polypropylene (PP), polyethyleneterephthalate (PET) and ethylene vinyl alcohol copolymer (EVOH) with some structurally different food fats. The main goal was to study the sorption of food fats by the plastic films and to see what extent mechanical properties of the plastic films was affected by plasticization effect due to sorption of fatty materials. PP, PET, and EVOH films was immersed in pure triglycerides, and then extracted with hexane and analyzed for the amounts of fat migrated. The sorbed films were also investigated for change in mechanical properties. Result showed that structural factor of the films and fatty materials plays important role in th migration process. The fat with the simplest structure are migrated more easily that the fat with more complex structure. However, structural effect of migration was varied according to degree of crystallinity and density of plastic films. In addition to that, polarity of plastic film was affected migration of fatty materials significantly. Additional research is needed to justify the reason why migration of fatty materials into the films was affected by polarity and structural integrity.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2003년도 총회 및 춘계학술발표회
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• pp.434-437
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• 2003

The fate and the behavior of polycyclic aromatic hydrocarbons (PAHs) and heavy metals in the environment are mainly controlled by their interactions with various components of soils and sediments. Due to their large surface area and abundance in many soils, smectites may greatly influence the fate and transport of the contaminants in the environment. In our experiment, PAH sorption by hexadecyltrimethylammonium (HDTMA)-modified smectite linearly increased in proportion to the amount of HDTMA added on the clay. However, trimethylammonium (TMA)-modified smectite did not show superiority in its sorption of PAH compared with the HDTMA-smectite or dodecyltrimethylammonium (DTMA)-smectite. Meanwhile, the smectites modified with the same cationic surfactants adsorbed Cd$^{2+}$ (heavy metal) significantly from water at low surfactant loading level, but the Cd$^{2+}$ adsorption linearly decreased as the loading of surfactant increased. The result shows that the sorption tendency of organoclays for organic or inorganic contaminants was significantly influenced by the amount and size of the surfactants added on the clay. It means that the stabilization and configuration of cationic surfactant formed on the clay interlayer according to the loading amount of each surfactant of different sizes may be an important factor in effectively sorbing environmental pollutants.nts.

• 상하수도학회지
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• 제21권1호
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• pp.27-36
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• 2007

Milled Korean pine (Pinus densiflora) wood was used to evaluate its adsorption capacity of Cu(II) ions from aqueous solution by running a series of batch experiments. Prior to the tests, the milled woods were pretreated with 1N NaOH, 1N $NHO_3$, and distilled water, respectively, to examine the effect of pretreatment. Within the tested pH range in this study between 3 and 6, copper adsorption efficiency of NaOH-treated wood(96~99%) was superior than $NHO_3$-treated wood(19~31%) and distilled water-treated wood(18~35%). Adsorption behavior of copper onto both raw and $NHO_3$-treated woods was mainly attributed to interaction with carboxylic acid group. For NaOH-treated wood, carboxylate ion produced by hydrolysis was a major functional group responsible for Cu sorption. NaOH treatment of wood changed the ester and carboxylic acid groups into carboxylate group, whereas $NHO_3$ treatment did not affect the production of functional groups which could bind copper. A pseudo second-order kinetic model fitted well for the sorption of copper ion onto NaOH-treated wood. A batch isotherm test using NaOH-treated wood showed that equilibrium sorption data were better represented by the Langmuir model than the Freundlich model.

• 한국재료학회지
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• 제27권3호
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• pp.166-171
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• 2017

Removal of phosphate from environmental water has become more important to prevent eutrophication. In the present study, sorption behavior of phosphate onto magnesite was investigated under different conditions. The optimum pH of phosphate adsorption was determined to be 6.0. The adsorption capacity was found to decrease with increasing temperature, which indicates that a low temperature was beneficial for phosphate adsorption. The sorption capacity for phosphate was found to be 10.2 mg/g at an initial concentration of 100 mg/L and a dose of 2 g/L. The first order kinetic equation and Freundlich isotherm model fit the data well. Phosphate adsorption on magnesite was explained by electrostatic attraction and weak physical interactions.

• 한국암석학회:학술대회논문집
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• 한국암석학회.한국광물학회 2000년도 공동학술발표회 논문집
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• pp.35-38
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• 2000

• Nuclear Engineering and Technology
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• 제18권3호
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• pp.194-199
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• 1986

수용액중에 극미량의 Am의 거동이 pH변화에 따라 변화하는 것을 원심분리법으로 조사하였다. 이 연구에서 평형시간을 2~3주 연장, 방사성 코로이드 형성에 있어서의 시간효과를 조사하였다. 또한 실리카겔 및 Fe$^{3+}$ 등 외부 물질을 첨가하여 그 효과를 조사하였으며, 또한 진한 전해질물질의 효과도 아울러 조사하였다. 그 결과, pH 6에서 Am은 불순입자, 또는 용기벽과 이온 흡착과정으로 급속히 흡착이 일어났다. 외부물질의 첨가는 Am의 흡착을 촉진하였으며, 진한 전해질물질의 첨가로 흡착이 방해되었다. pH 7에서 Am은 pH 6조건과는 전혀 다른 거동을 나타내었다. 일부 Am은 용기 기벽에서 빠른 흡착이 일어났으며, 1~2일 후에 일부는 탈착되었다.

• Journal of Radiation Protection and Research
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• 제10권1호
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• pp.3-13
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• 1985

주요 핵분열 생성물인 세슘-137, 장수명 핵종과 세륨-144, 희토류원소 그리고 부식 생성물인 코발트-60등의 제올라이트 A, 제올라이트 F-9(Faujasite) 그리고 비정형 제올라이트에 대한 흡착거동을 염농도 0.01 M부터 2.0 M 질산과 질산암모늄 그리고 교반시간 15분부터 90분까지 15분 간격으로 검토하였다. Kd 값은 Batch 실험방법으로 구했다. 결론으로 주요핵종의 분리 제거의 최적조건은 비정질 제올라이트, 0.01 M-질산과 0.1 M-질산암모늄, pH 4, 교반시간 한시간 그리고 가장 효율높은 핵종은 세슘 -137이다.

• 한국대기환경학회지
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• 제26권1호
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• pp.77-84
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• 2010

The diffusion and partition coefficients of polyurethane foam (PUF) are estimated using a microbalance experiment and small chamber test. The microbalance is used to measure sorption/desorption kinetics and equilibrium data. When the diffusion condition is controlled in the chamber of the sample, interactions between volatile organic compounds (VOCs) and PUF can lead to the estimation of a relatively homogenous rate of mass transfer in the interiors and surfaces of PUF. The estimates of the material/air partition coefficient (K) and the material-phase diffusion coefficient (D) are shown to be independent of the concentrations of VOCs. This approach, if applied to a diffusion-controlled or physically-based model, can facilitate more precise prediction of their source/sink behavior. Although further research and more rigorous validation is needed, an emission model applied with the diffusion and partition coefficients from this research holds promise for the improvement of reliability in predicting the behavior of VOCs emitted from porous building materials by D and K.