• Proceedings of the Korea Crystallographic Association Conference
• /
• 2002.11a
• /
• pp.49-49
• /
• 2002

A strategy for the synthesis of more stable and large periodic mesoporous organo-silica materials has been developed for the 2D hexagonal mesoporous organosilica by the core-shell approach using nonionic PEO-PLGA-PEO triblock copolymer templates. The BET surface area of the solvent-extracted hexagonal mesoporous organosilica is estimated to be 1,016 ㎡/g and the pore volume, pore diameter, and wall thickness are 1.447 ㎤/g, 65 Å, and 43 Å, respectively. More hydrophobic PLGA block than the PPO block used for templates of mesoporous silica proves to be quite effective in confining the organosilicates within the PEO phase. Reaction temperature and acid concentration of an initial solution as well as the chemical nature of the bloc k copolymer templates also demonstrate to be important experimental parameters for ordered organosilica mesophase. Moreover, the mesoporous organosilicas prepared with the PEO-PLGA-PEO block templates maintain their structural integrity for up to 25 days in boiling water at 100℃. The mesoporous materials with large pores and high hydrothermal stability prepared in this study has a potential for many applications.

• Proceedings of the Korea Concrete Institute Conference
• /
• 1998.10c
• /
• pp.197-202
• /
• 1998

The corrosion of steel reinforcements in concrete is of much concern in recent years. The mechanism of corrosion, however, is not clear yet. This study is focused on the corrosion of steel induced by internal chlorides in concrete at early ages. To examine the critical concentration of steel, half-cell potential, chemical composition of expressed pore solutions of mortars and rate of corrosion area were observed with respect to additions of chlorides, types of binders, water-binders ratio.

• Journal of Korean Society of Water and Wastewater
• /
• v.19 no.6
• /
• pp.713-719
• /
• 2005

SPME (Soild phase microextraction) has been used in the analysis of many volatile organic compounds, such as geosmin and 2-methylisoborneol (2-MIB), trihalomethanes (THMs) in drinking water. SPME fiber is characterized by high adsorption capacity (DVB/CAR/PDMS, DVB/PDMS etc.). Although the highly active adsorption capacities of the SPME fiber are often to the chemical functional group, surface properties play a significant role in determining the surface adsorption capacities. The objectives of this study were to evaluate effect of residual chlorine on analysis of geosmin and 2-MIB. Image taken by SEM before preloaded with chlorine, the surface and porous media was almost perfect spherical shape and no clogging of pores. However, after preloaded with chlorine the surface was aggregated and pore was blocked. The recovery rate of geosmin and 2-MIB coexisting with chlorine was reduced by 35 to 62%. The recovery rate with preloaded with chlorine was reduced by 25 to 43%. The lower concentration of geosmin and 2-MIB and the higher concentration of chlorine existed in water, the lower the recovery rate was.

• Journal of the Korean Crystal Growth and Crystal Technology
• /
• v.14 no.2
• /
• pp.37-46
• /
• 2004

The electrochemical adsorption of the Ag ions from aqueous solution on pelletized activated carbon monolith was investigated over wide range of operation time. The adsorption capacities of pelletized activated carbon monolith are associated with their internal porosity and are related properties such as surface area, pore size distribution. The chemical industry generates wastewater that contains toxic matters like heavy metals in small concentrations so that their economic recovery is not feasible. But, the method using activated carbon monolith can be used to withdrawal of heavy metals in waste water. After the electrochemical treatment, the quantitative properties in Ag ion solutions are also examined by pH concentration and studied elemental analysis by ICP-Atomic Emission Spectrometer and Energy Disperse X-ray (EDX) spectra. It is consider that the pH is very important factor at the reason of water pollutant with increasing acidity in industrial field. The result of quantitative analysis using Inductively Coupled Plasma-Atomic Emission Spectrometer of metal after electrochemical reaction in Ag ions solution depending on time are shown that the amount of Ag ions deposited was decreased with growth of Ag particles on the carbon surfaces as increasing electrochemically treated time. And, surface morphologies are investigated by scanning electron microscopy (SEM) to explain the changes in adsorption properties.

• Journal of Soil and Groundwater Environment
• /
• v.19 no.3
• /
• pp.15-24
• /
• 2014

Soil pollution has been recognized as a serious problem because it causes groundwater pollution through medium contacts. Although concentration of individual chemical could be more easily measured by physico-chemical analysis, it is not easy to consider the bioavailability of edaphic receptors living in soil or groundwater. To measure the toxicity of soil, the soil extracts (soil elutriates or soil suspensions in the other words) are often used due to the difficulties of extracting soil pore water. In this study, we reviewed 15 toxicity test methods found in literature to analyze the detail of each extraction method and to recommend the most frequently used extraction methods. The identified most commonly used extraction methods are as following: The 1 : 4 soil:water ratio, 24 hours shaking time, room temperature, dark, and separation of supernatant using a $0.45{\mu}m$ pore size filter.

• Journal of Korean Society of Water and Wastewater
• /
• v.23 no.6
• /
• pp.855-864
• /
• 2009

The main object of this work was to determine the influence of periodic chemical backwash on filtration resistance in membrane filtration system. In this work Hermia's models were used to investigate the fouling mechanisms involved in the microfiltration of $0.45{\mu}m$ filtered sewage feed. Batch microfiltration experiments were performed at transmembrane pressure 0.4 bar and different feed SCOD concentration (9~67 mgSCOD/L). The results showed that the best fit to experimental data corresponded to the intermediate blocking model followed by the standard and complete blocking model for all the experimental conditions tested. From the simulation results of filtration performance, it was found that in order to maintain sustainable operation of membrane filtration system, irreversible foulant component accumulated continuously on membrane surface and/or pore must be effectively removed. In addition, it was verified that periodic chemical backwash using NaOCl or NaOH effectively improved filtration performance of membrane.

• Journal of the Korean Ceramic Society
• /
• v.29 no.2
• /
• pp.107-118
• /
• 1992

Alumina supports for TiO2 ultrafiltration membrane coating were prepared by presintering disk-type preforms at 140$0^{\circ}C$. These supports showed uniform microstructures which had the apparent porosity of 40%, the pore size distribution in the range of 0.1~0.5${\mu}{\textrm}{m}$, and the water flux of 1400ι/$m^2$.h at the pressure difference of 10 atm. The optimum pH and concentration of the TiO2 sol for coating were 0.8 and 1.0 wt%, respectively, and sol particles were identified as rutile forms of 20 nm size. Crack-free alumina-supported rutile TiO2 membranes could be prepared through well controlled drying and heating the gel layer coated by the sol-gel dipping. The pore size of the TiO2 membranes heat-treated at 50$0^{\circ}C$ for 2 hrs was 30~80$\AA$, and their thickness varied from 1.1 to 3.8 ${\mu}{\textrm}{m}$ in accordence with the dipping time (4~40 min). The flux of water through this composite membrane at 10 atm was found to be in the range from 800 to 1100ι/$m^2$.hr depending on the dipping time (10~40 min). The membrane thickness increased linearly with the square root of the dipping time and the slope was 0.62 ${\mu}{\textrm}{m}$/{{{{ SQRT { min} }}.

• Journal of Korean Society of Coastal and Ocean Engineers
• /
• v.30 no.5
• /
• pp.201-206
• /
• 2018

This study investigated the changes in pore water quality of polluted sediment by mixing ratio of granulated coal ash. The mesocosm experiments were carried out with 0%, 10%, 30% and 50%, respectively, of the material mixture ratio relative to the sediments. According to the results of the experiments, pH increased depending on the mixing ratio. Phosphate and ammonia concentrations were significantly decreased in the mixing ratio of 30% and 50% compared to the control (p < 0.05). The concentration of hydrogen sulfide was reduced by 72% at the mixing ratio of 10%, and it was not detected at the mixing ratio of 30% and 50%. This study was confirmed that granulated coal ash can change the pore water quality of polluted sediments in proportion to the amount of material. However, the effect of the mixing ratio between 30% and 50% was not significantly different, thus it is concluded that mixing of 30% of the volume of the sediment is economically feasible.

• Journal of the Korean Chemical Society
• /
• v.29 no.3
• /
• pp.233-238
• /
• 1985

The non-porous and porous polystyrene divinylbenzene copolymers were prepared by the suspension polymerization method. The non-porous aminated polystyrene divinylbenzene, N-APSTDVB and the porous aminated polystyrene divinylbenzene, P-APSTDVB of 50∼100mesh size weakly basic anion exchanger were synthesized by chloromethylation followed by amination with methylamine. The functional groups of these synthesized anion exchangers were confirmed by their infrared spectra. The maximum capacity of these exchangers was 4.86meq/g. Pore volume and pore spectra were determined with a mercury porosimeter. The pore volume of P-PSTDVB increased with increasing X$_{diluent}$ at 30% of divinylbenzene. However, the pore volume of P-PSTDVB increased with increasing volume percent of divinylbenzene at constant mole fraction of diluent, X$_{diluent}$ of 0.5. The pore volume of synthesized copolymer and anion exchanger at 8% divinylbenzene and 0.5X$_{heptane}$ decreased as follows; P-PSTDVB 〉P-APSTDVB 〉N-PSTDVB. This result was attributed to the possibility that the pore volume were reduced by amination reactions. The distribution coefficients of boric acid on the N-APSTDVB anion exchanger in various concentrations of alcohol water solutions showed that as alcohol concentration increased, the distribution coefficients values decreased due to the reduced concentration of H$_2$BO$_3^-$.

• 한국해양학회지
• /
• v.28 no.3
• /
• pp.229-240
• /
• 1993

This study investigated the behaviour of sulfur species after the early diegenetic reduction of sulfate from pore solution in an anoxic intertidal flat deposit in the Banweol area of Kyeong-gi Bay, west coast of Korea. A total of seven sediment cores were collected during 1990∼1992 and were analyzed for their solid-phase sulfur species (acid-volatile sulfur, element sulfur, pyrite sulfur) as well as for chemical components in the pore solution, such as sulfate, ammonium, hydrogen sulfide, phosphate and Fe ion. The pore water sulfate oncentration was found to decrease rapidly downward from the sediment surface, while that of hydrogen sulfide, ammonium and phosphate showed and increase. The dissolved iron concentration in pore water, on the other hand, was found high in the surface layer of sediment, but fell sharply below this layer. these characteristic profiles of pore water sulfide and iron concentrations suggest that some reaction occurs between dissolved iron and sulfide ions, leading to the formation of various sulfide minerals in the sedimentary phase. The amount of inorganic sulfur species in the sediment increased downward, and showed a maximum of up to 7.9 mg/g. among the three species analyzed, acid-volatile sulfur (AVS) was dominant comprising more than 50% of the total. The amount of pyrite sulfur was greater than that of element sulfur. This implies that the formation of pyrite was restricted in this environment. the limited amount of element sulfur in this deposit may have discouraged the active formation of pyrite.