• Journal of Korean Society of Occupational and Environmental Hygiene
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• v.9 no.2
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• pp.19-31
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• 1999

Most breakthrough tests are conducted at higher concentration levels compared to those in the field of air-purifying respirator applications. For example, typical challenge concentrations for breakthrough tests agains tcarbon tetrachloride are ranged between 250-1000 ppm although applicable concentrations range for air-purifying cartridge is 5-50 ppm for carbon tetrachloride. However, no guarantee has been made that isotherms derived from the experiment at high challenge concentrations could estimate adsorption capacity at the lower concentration range where workers wear usually air-purifying respirators. Three models of adsorption isotherms (Freundlich, Langmuir and Dubinin/Radushkevich(D/R) isotherms) that have been commonly applied for respirator cartridge testing were evaluated. Adsorption capacity at each challenge concentration was calculated from the Reaction Kinetic equation fitted for the breakthrough data. These data were used for derivation of three isotherms. In general, the D/R isotherm has given the best agreement between estimated adsorption capacities and experimentally measured. If the challenge concentration of 100 ppm is included for derivation of models, Freundlich and D/R models could succes sfully produced good estimations for adsorption capacities at 50 ppm level. Estimated adsorption capacities by both models ranged in 94 - 109 % of the experimentally measured. However, Langmuir model gives underes timation in all cases.

• Journal of the Korean Society of Tobacco Science
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• v.18 no.2
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• pp.150-159
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• 1996

In this study, to obtain the basic data for the optimum moisture control system, moisture adsorption characteristics, adsorption isotherms models for water and surface physical characteristics of burley and flue-cured tobacco were investigated. By the hypothesis' the phenomenon of moisture adsorption of tobacco is the same as the first order reaction, the wetting constant (k) and equilibrium moisture content were obtained. And activation energy, frequency factors were also calculated by applying its data to Arrhenius equation. The Kamei's empirical formula of moisture adsorption isotherms showed the best agreement with the experimental data and its correlation coefficient (r) was 0.997. It can be seen that specific surface area of burley is 157 m2/g, that of flue-cured is 152 m2/g, -△H1 of adsorbed monolayer is 45,972 J/mol, 45,486 J/mol, respectively, and the condensation heat (40,595 J/mol) being caught in adsorbed multilayer is less than that of monolayer.

• Journal of Soil and Groundwater Environment
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• v.27 no.6
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• pp.11-21
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• 2022

Sorption of phenanthrene (PHE) and pyrene (PYR) in several sorbents, i.e., natural soil, BionSoil^®, Pahokee peat, vermicompost and Devonian Ohio Shale and a surfactant (hexadecyltrimethyl ammonium chloride)-modified montmorillonite (HDTMA-M) were investigated. Pyrene exhibited higher sorption tendency than phenanthrene, as predicted by its higher octanol to water partition coefficient (K_ow). Several sorption models: linear, Freundlich, solubility-normalized Freundlich model, and Polanyi-Manes model (PMM) were used to analyze sorption isotherms. Linear isotherms were observed for natural soil, BionSoil^®, Pahokee peat, vermicompost, while nonlinear Freundlich isotherms fitted for Ohio shale and HDTMA-M. The relationship between sorption model parameters, organic carbon content (f_oc), and elemental C/N ratio was studied. In the binary competitive sorption of phenanthrene and pyrene in natural soil, competition between the solutes caused reduction in the sorption of each solute compared with that in the single-solute system. The ideal adsorbed solution theory (IAST) coupled with the single-solute Freundlich model was not successful in describing the binary competitive sorption equilibria. This was due to the inherent nature of linear sorption of phenanthrene and pyrene in natural soil. The result indicates that the applicability of IAST for the prediction of binary competitive sorption is limited when the sorption isotherms are inherently linear.

• Computers and Concrete
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• v.13 no.6
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• pp.695-707
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• 2014

This study investigated the chloride binding isotherms of various cement types, especially the contributions of C-S-H and AFm hydrates to the chloride binding isotherms were determined. Ordinary Portland cement (OPC), Modified cement (MC), Rapid-hardening Portland cement (RHC) and Low-heat Portland cement (LHC) were used. The total chloride contents and free chloride contents were analyzed by ASTM. The contents of C-S-H, AFm hydrates and Friedel's salt were determined by X-ray diffraction Rietveld (XRD Rietveld) analysis. The results showed that OPC had the highest chloride binding capacity, and, LHC had the lowest binding capacity of chloride ions. MC and RHC had very similar capacities to bind chloride ions. Experimental equations which distinguish the chemically bound chloride and physically bound chloride were formulated to determine amounts of the bound chloride basing on chloride binding capacity of hydrates.

• KIEE International Transactions on Electrophysics and Applications
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• v.11C no.3
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• pp.81-84
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• 2001

The trans and cis forms of N-alkyl-4-styrylpyridinium derivatives (CnSP: n= 4, 8, 12, 16) were successfully synthesized and purified. The derivatives of styrylpyridinium cause photoisomerization when they are illuminated with UV light. The pressure-area isotherms of CnSP and their derivatives were studied to reveal the effect of alkyl chain length. The photoisomerization of CnSP monolayers at the air/water interfaces was indirectly studied by measuring surface tension changes with photoirradiation on the water surface. The characteristics of CnSP were furthermore studied with UV-vis, surface pressure-area isotherms, surface potential-area isotherms, Brewster Angle Microscopy (BAM) at the air/water interface, and optical diffraction efficiency on the ultrathin films.

• Carbon letters
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• v.9 no.1
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• pp.1-7
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• 2008

The ability of cow dung ash without any pretreatment to remove color from textile dyes N Blue RGB, Green B and EOSIN YWS from aqueous solution has been investigated in this work. Cow dung ash, an ecofriendly and low cost adsorbent was prepared by burning cow dung cakes in the muffle furnace at $500^{\circ}C$. The adsorption was achieved under different pH and adsorbate concentration. The data was fitted to simple polynomial and the isotherms similar to Langmuir and Freundlich isotherms.

• Textile Coloration and Finishing
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• v.24 no.4
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• pp.239-246
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• 2012

The binding isotherms of ionic dyes with Poly(vinylpyrrolidone) in aqueous solution were determined by the dynamic dialysis technique. The shape of the isotherms of cationic dye, C. I. Basic Red 18 with poly(vinlypyrrolidone) showed a partition type. It suggests that the binding involves a non-cooperative mode. Isotherms of an anion dye, a synthesized dye by coupling of diazotized m-trifluoromethylaniline with 2-naphthol-6-sulfonic acid, were sigmoid type and showed multimode interaction. The results were interpreted by the McGhee von Hippel theory. The thermodynamic parameters for the complex formation of the dyes-polymer were calculated from their temperature dependences of the intrinsic binding constant.

• Korean Chemical Engineering Research
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• v.47 no.6
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• pp.747-754
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• 2009

In this study, adsorption isotherms of o-DCB(ortho-dichlorobenzene) on an activated carbon heated at $1000^{\circ}C$ for 24 hours were obtained by experiment and were predicted by using molecular simulation. The initial molecular structure of the activated carbon was designed on the basis of its molecular formula and functional groups ratio measured experimentally. Then, the molecular structure was optimized using the COMPASS(condensed-phase optimized molecular potentials for atomistic simulation studies) force field. The particle porosity, specific surface area, and particle density obtained from the optimized molecular structure of activated carbon were compared with those experimental data. The errors between experimental data and simulation results of the particle porosity, specific surface area, and particle density were shown as 7.6, 3.8, and 2.8%, respectively. Adsorption isotherms constants of o-DCB are calculated by the GCMC(grand canonical Monte Carlo) method in the optimized molecular structure of activated carbon. The simulation result of the adsorption isotherms showed an error of under 3%, compared to that of experimental data. Adsorption isotherms, adsorption heat and pore diffusivity of 2,3,7,8-TCDD(tetrachlorodibenzo-p-dioxin) was finally obtained in the same molecular structure of the activated carbon as used for o-DCB. Thus, adsorption characteristics of persistent organic pollutants on activated carbon, which are not easy to experimentally evaluate, are predicted by the molecular simulation.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.04a
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• pp.330-333
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• 2002

Immobilization isotherms for methyl tort-buty1 ether (MTBE) in sodium dodecy1 sulfate(SDS) and cetylpyridinium chloride (CPC) were investigated for application to micellar enhanced remediation. Headspace solid-phase microextraction was used to analyze immobilization isotherms. Maximum partitioning coefficients of MTBE were 48 L/mol and 9 L/mol for SDS and CPC, respectively, The values decreased gradually as the MTBE mole fraction in the micelles increased.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.09a
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• pp.103-106
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• 2002

Solubilization isotherms for methyl tort-butyl ether (MTBE) in sodium dodecyl sulfate(SDS), dowfax 8390, sodium dodecylbenzenesulfonate and cetylpyridinium chloride (CPC) were investigated for application to micellar enhanced remediation. Dowfax 8390 showed maximum extent of solubilization among surfactants tested in this study. It seems that sulfate group in anionic surfactants playes a important role in solublization of MTBE. Chemical shiftes in NMR of surfactant and MTBE supports this point.