• Proceedings of the SAREK Conference
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• 2006.06a
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• pp.1119-1124
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• 2006

The objectives of this paper are to investigate the performance of silica gel-water adsorption refrigeration system with heat recovery process from the system experiment. This system can be driven by waste heat at near ambient temperature from $60^{\circ}C$ to $90^{\circ}C$. The cooling capacity and coefficient of performance(COP) were measured from various experimental conditions. An experimental results revealed the influence of operating temperatures(hot, cooling and chilled water), water flow rates, and adsorption-desorption cycle times on cooling capacity and COP. Under the standard conditions of $80^{\circ}C$ hot water, $25^{\circ}C$ cooling water, $14^{\circ}C$ chilled water inlet temperatures and 420sec cycle time, a cooling capacity of 1.14kW and a COP for cooling of 0.55 can be achieved.

• Journal of Soil and Groundwater Environment
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• v.18 no.3
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• pp.65-72
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• 2013

Adsorption of melamine was examined using columns packed with granular activated carbon (GAC). Raw GAC was sieved with 20, 40, 60 and 80 mesh to determine the influence of adsorbent particle size on reaction and diffusion. The mass ratio of the adsorption capacity of GAC for melamine ranged from 9.19 to 11.06%, and adsorption rates increased with decreasing particle size within this range. Rate constants between 3.295 ~ 4.799 $min^{-1}$ were obtained using a pseudofirst-order equation that was used to determine adsorption kinetics. A surface diffusion model was adapted to take into account the unsteady-state equation of a spherical adsorbent by converting the surface concentration from a constant to a variable governed by a dispersion equation. The calculated values were fit with the experimental results by using the diffusion coefficients as regression parameters. The modified equation exhibited a more precise agreement with respect to the sum of the absolute error (SAE).

• Journal of the Korean Electrochemical Society
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• v.15 no.1
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• pp.54-66
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• 2012

The phase-shift method and correlation constants, which are unique electrochemical impedance spectroscopy techniques for studying the linear relationship between the phase shift ($90^{\circ}{\geq}-{\varphi}{\geq}0^{\circ}$) vs. potential (E) behavior for the optimum intermediate frequency ($f_o$) and the fractional surface coverage ($0{\leq}{\theta}{\leq}1$) vs. E behavior, are proposed and verified to determine the Frumkin, Langmuir, and Temkin adsorption isotherms and the related electrode kinetic and thermodynamic parameters. At Ni/0.5 M $H_2SO_4$ and 0.1M LiOH aqueous solution interfaces, the Frumkin and Temkin adsorption isotherms (${\theta}$ vs. E) of H for the cathodic hydrogen ($H_2$) evolution, interaction parameters (g), equilibrium constants (K), standard Gibbs energies (${\Delta}G^0_{\theta}$) of H adsorption, and rates of change (r) of ${\Delta}G^0_{\theta}$ with ${\theta}$ have been determined using the phase-shift method and correlation constants. A lateral repulsive interaction (g>0) between the adsorbed H species appears. The value of K in the alkaline aqueous solution is much greater than that in the acidic aqueous solution.

• Clean Technology
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• v.14 no.1
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• pp.47-52
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• 2008

Among various mass transfer models to express adsorption rates for any adsorption processes, the linear driving force (LDF) model is used most. The present investigation aims at finding whether this model may be applied to real adsorption process for separation and removal of benzene. Comparison of numerical simulation results calculated by the LDF model with experimental data allowed us to find the mass transfer coefficients that are most appropriate for a specific adsorption process. Various breakthrough curves were obtained from experiments performed at many different temperatures and pressures, which in turn produced suitable mass transfer coefficients. These dependencies of mass transfer coefficient on temperature and pressure were represented by an Arrhenius type- and a power law type empirical equation, respectively.

• Journal of Environmental Health Sciences
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• v.33 no.5
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• pp.456-461
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• 2007

This study was carried out two point view that reuse of sludge and adsorption of benzene, toluene and o-xylene of VOCs in cast, carbonized cast and activated carbon. The cation exchange capacity of cast and carbonized cast were 59.2, 112 meq/100g, respectively. The specific surface were 560, $800m^2/g$, respectively. The average removal rates of benzene by 50g cast of 50% hydrous cast, anhydrous cast, carbonized cast, activated carbon were 15.0, 41.2, 88.2, 99.4% in 60min of retention time. The average removal efficiency of toluene by 50 g cast of 50% hydrous cast, anhydrous cast, carbonized cast, activated carbon were 12.5, 34.2, 88.2, 99.5% in 60 min of retention time. The average removal rates of o-xylene 50 g cast of 50% hydrous cast, anhydrous cast, carbonized cast, activated carbon were 8.8, 28.5, 84.8, 98.1% in 60min of retention time. The adsorption efficiency of test absorbent was in order of Activated Carbon > Carbonized Cast > Cast.

• Applied Chemistry for Engineering
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• v.9 no.5
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• pp.689-697
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• 1998

In this work, we studied the equilibrium, rate and rate determining step of uranium adsorption on RGP resins of MR type prepared by varying the degree of crosslinking and the amount of diluent. The equilibrium of uranium adsorption on RGP resins were well explained by Frendrich isotherm as well as Langmuir isotherm model. The amount of adsorption and adsorption rate increase with the adsorption temperature. The heat of the adsorption was 11 kcal/mol. The adsorption rates of uranium on RGP resins were decreased in the order of RGP-10(50)>RGP-1(50)>RGP-2(50)>RGP-5(50)>RGP-0(50) and RGP-2(75)>RGP-2(100)>RGP-2(50)>RGP-2(30)>RGP-2(0). The diffusion resistance of uranium into RGP resin increased as follows; molecular diffusion < pore diffusion < surface diffusion. On the other hand, the surface diffusion was more dominative than the pore diffusion in intraparticle region. Thus, this result indicates that the adsorption mechanism of uranium on RGP resins is intraparticle diffusion controlled.

• Journal of the Korean Chemical Society
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• v.28 no.3
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• pp.194-202
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• 1984

The adsorption properties of organo sulfur compounds on cation exchanged natural zeolites from n-heptane were investigated. The equilibrium adsorbed amounts were dependent upon the exchanged cation and the nature of organo sulfur compounds such as length, volume, electronical structure. The increasing orders of equilibrium adsorbed amounts were thiophene derivatives, disulfide, sulfide mercaptane and thiophene, benzothiaphene, dibenzothiophene. And $Co^{+2}$-zeolite was the most prominent adsorbant. Rate determining step of the adsorption at initial stage was intraparticle diffusion into the transitional pores of zeolite. These adsorption rates were dependent upon the bulkiness of adsorbate. Finally, preadsorbed water didn't affect these adsorption until the cation exchanged natural zeolite contained 2.26${\times}10^{-3}$ mol/g of water. It indicated that water preferentially occupied the micro pores of the cation exchanged natural zeolites.

• Nuclear Engineering and Technology
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• v.54 no.8
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• pp.3017-3026
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• 2022

The ¹³¹Cs radioisotope with a short half-life time and high average radiation energy can treat the cancer effectively in prostate brachytherapy. The typical ¹³¹Cs production processes have a separation step of the cesium from ¹³¹Ba to obtain a high specific radioactivity. Herein, we suggested a novel ¹³¹Cs separation method based on the Ba²⁺ adsorption of alginate beads. It is necessary to reduce the affinity of alginate beads to cesium ions for a high production yield. The carboxyl group of the alginate beads was replaced by a sulfonate group to reduce the cesium affinity while reinforcing their affinity to barium ions. The modified beads exhibited superior Ba²⁺ adsorption performances to native beads. In the fixed-bed column tests, the saturation time and adsorption capacity could be estimated with the Yoon-Nelson model in various injection flow rates and initial concentrations. In terms of the Cs elution, the modified alginate showed better performance (i.e., an elution over 88%) than the native alginate (i.e., an elution below 10%), indicating that the functional group modification was effective in reducing the affinity to cesium ions. Therefore, the separation of cesium from the barium using the modified alginate is expected to be an additional option to produce ¹³¹Cs.

• Particle and aerosol research
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• v.18 no.3
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• pp.79-86
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• 2022

Many commercial air purifiers currently have deployed granular activated carbon (GAC) filters for removing volatile organic compounds in the indoor air. GACs are generally used to remove gaseous contaminants in the air through adsorption by the inner surfaces of pores. In addition, airborne particles can be also filtered by the surface adsorption of the GACs, which can improve the life-time of the particulate filters. In this study, the filtration efficiency of GACs to ultrafine particles through surface adsorption was investigated at different volume flow rates by deploying a continuous particle filtration system. The polydisperse sodium chloride (NaCl) particles were generated by a set of an atomizer and a diffusion dryer, and then mixed with particle-free air at different volume flow rates. The penetration of ultrafine particles and pressure drop for each experimental condition were measured to figure out the effect of the volume flow rate on the surface adsoprtion of the GACs to particles, ~ 2 mm. The particle filtration efficiency of the GACs decreased as the volume flow rate increased from 4 to 14 lpm. However, the 5 times thicker GAC filter layer decreased the penetration of ultraparticles than a preious study. The filtration efficiency of the single granule was also higher than the previous result in the literature with smaller granule filter materials.

• Membrane and Water Treatment
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• v.15 no.2
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• pp.51-57
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• 2024

The removal of phosphorus, especially phosphate-form phosphorus, is necessary in wastewater treatment. Biofouling induced by the quorum sensing mechanism is also a major problem in membrane bioreactor (MBR), which reduces membrane flux. This study introduces lanthanum-doped quorum quenching (QQ) beads into MBR, confirming their inhibitory effect on biofouling due to Rhodococcus sp. BH4 and their capacity for phosphorus removal through lanthanum adsorption. A batch test was conducted to access the phosphate adsorption of lanthanum-QQ (La-QQ) beads and lab-scale MBR to verify the effect of inhibition. The study aimed to identify distinctions among the MBR, QQ MBR, and La-QQ MBR. In the batch test, the phosphate removal rate increased as the volume of beads increased, while the unit volume removal rate of phosphate decreased. In the lab-scale MBR, the phosphate removal rates were below 20% in the control MBR and QQ MBR, whereas the La-QQ MBR achieved a phosphate removal rate of 74%. There was not much difference between the ammonia and total organic carbon (TOC) removal rates. Regarding the change in transmembrane pressure(TMP), 3.7 days were taken for the control MBR to reach critical pressure. In contrast, the QQ-MBR took 9.8 days, and the La-QQ MBR took 6.1 days, which confirms the delay in biofouling. It is expected that La-QQ can be used within MBR to design a more stable MBR process that regulates biofouling and enhances phosphate removal.