• Journal of the korean society of oceanography
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• v.35 no.1
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• pp.16-33
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• 2000

In order to measure the vertical fluxes of particles and reactive radionuclides such as thorium and polonium isotopes, Dunbar-type sediment traps were freely deployed at the Ulleung Basin and in warm and cold water masses around the polar front of the East Sea. We estimated the ratios of the catched (F) to the predicted $^234$Th fluxes (P) using natural tracers pair $^234$Th-$^238$U. The F/P ratios are decreased with increasing water depth. Whereas the concentrations of suspended particles are homogeneous in water column, the mass fluxes are also decreased with increasing water depth like the F/P ratios. These facts indicate that organic matters of settling particles are destructed within the euphotic layer due to decomposition. Whereas regenerations of sinking particles are negligible in the cold water mass, about 80% of them are regenerated in the warm water mass during falling of large particles. These downward mass fluxes are closely correlated with their primary productions in euphotic zone. The activities of $^234$Th, $^228$Th and $^210$Po in the sinking material were increased with water depth. Because $^234$Th steadily produced in the water column are cumulatively adsorbed on the surface of sinking particles, vertical $^234$Th fluxes were observed to increase with water depth. Therefore, these sinking particles play important roles in transporting the particle reactive elements like thorium from surface to the deep sea. The scavenging processes including adsorption and settling reactions generate radio-disequilibrium between daughter and parent nuclides in water column. The activity ratios of $^234$Th/$^238$U and $^228$Th/$^228$Ra were observed to be < 1.0 in the surface water and approached to be equilibrium below the thermocline. The extent of the deficiency of daughter nuclides compared to the parents nuclide was highly correlated with the vertical particle flux. Because most of the $^210$Po in the surface water are scavenged on a labile phase and are recycled at sub-surface depths (< 200 m), the $^210$Po are always observed to be excess activities compared to $^226$Ra in surface water.

• Resources Recycling
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• v.14 no.6 s.68
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• pp.60-63
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• 2005

It was possible to understand the adsorption characteristics of ions in aqueous environment based on the variations of PZC and IEP of particles when adsorption of ions on particle surface occurred. The specific adsorption of $Cu^{2+}$ ion upon chalcopyrite surface provoked a lowered PZC, which was considered to be due to increased adsorption of OH- ion via the electrostatic attraction between the two ions. On the contrary, IEP of chalcopyrite was observed to rise when Cu2+ was specifically adsorbed on its surface. The reason for this could be explained by the necessity of the increase of pH to offset the positively increased surface potential of chalcopyrite for the reestablishment of IEP. Neither PZC or IEP of chalcopyrite was observed to change when non-specific adsorption occurred since no change in the surface potential of chalcopyrite was invoked under this condition.

• Proceedings of the Korea Institute of Fire Science and Engineering Conference
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• 1997.11a
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• pp.130-137
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• 1997

Intumescent inorganic and organic coatings which dintr one from the other by the type of gas formers and the mechanisms of foam formation have been obtained and investigated. Inorganic intumescent coatings are the compositions based on water glass and mineral additives with different dispersity. Mineral additives contain adsorbed and absorbed water and carbonates which are destructed with the carbon dioxide and water evolution during the flame action on coating. The decreasing of mineral additives particle sizes under the mechanical milling with the fraction precipitation promotes the foam coke formation with less defects. Here the main structure of comparing compositions does not change. In organic coatings based on epoxy-polymers the polyammonium phosphate additive is used. It is the cabonization catalyst and the foam agent. The polyammonium phosphate of various dispersity employed is uniformly distributed on the polymeric matrix. The decreasing of the particle sizes leads to the increasing of the fire resistant properties of the intumescent coa-ting. The fire resistant analysis of the coating during more than an hour: the coating back side the temperature on plastic or wooden materials does not exceed 423K, and on metal-573K.

• Bulletin of the Korean Chemical Society
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• v.19 no.9
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• pp.934-942
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• 1998

$^13CO$ chemisorbed on platinum particles in L-zeolite has been investigated by static and magic angle spinning NMR spectroscopy. The representative spectra are composed of a broad asymmetric peak with a center of gravity at 230±30 ppm and a sharp symmetric peak at 124±2 ppm which is tentatively assigned to physisorbed $CO_2$, on inner walls of L-zeolite. Overall, the broad resonance component is similar to our previous results of highly dispersed (80-96%) CO/Pt/silica or CO/Pt/alumina samples, still showing metallic characters. The principal difference is in the first moment value. The broad peak in the spectra is assigned to CO linearly bound to Pt particles in the L-zeolites, and indicates a distribution of isotropic shifts from bonding site to bonding site. The NMR results reported here manifest that the Pt particles inside of the L-zeolites channels are not collectively the same with the ones supported on silica or alumina with similar dispersion in terms of Pt particle shape and/or ordering of Pt atoms in a particle. As a result, Pt particles of CO/Pt/L-zeolite were agglomerated accompanying CO desorption upon annealing. There were no definite changes in the NMR spectra due to differences of exchanged cations. Comparison of our observation on CO/Pt/L-zeolite with Sharma et al.'s reveals that even when the first moment, the linewidtb, and the relaxation times of the static spectra and the dispersion measured by chemisorption are similar, the properties of Pt particles can be dramatically different. Therefore, it is essential to take advantage of the strengths of several techniques together in order to interpret data reliably, especially for the highly dispersed samples.

• Journal of the Korean Society for Marine Environment & Energy
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• v.9 no.3
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• pp.176-186
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• 2006

Distribution characteristics of organophosphorous pesticides(OPs) in water and suspended particles were studied in Asan Bay, Korea, from June 2004 to October 2005. 28 organophosphorous pesticides could be detected in Asan Bay during this study. The most commonly and abundantly measured OPs in the surface waters were IBP (max=$6,343.7ng\;l^{-1}$). DDVP, diazionon, ethoprophos and methidathion were also observed at relatively high concentrations. Their maximum concentrations exceeded $100ng\;l^{-1}$ in almost every month. Malathion, mevinphos, ph orate and chlorfenvinphos were also detected at relatively high concentrations. Many OPs more frequently appeared in summer than in winter due to the intensive application of pesticides in summer months. The concentration of OPs generally decreased with increasing distance from the mouth of Asan Bay. This result implies progressive dilution of these pesticides in the marine environment. Measured concentrations of diazinon were well below $20,000ng\;l^{-1}$ which is a limit set by the seawater quality standard of Korea. The concentrations of malathion and parathion in the surface waters of Asan Bay did not exceed the seawater quality standard of Korea($250,000\;and\;60,000ng\;l^{-1}$ respectively). OPs adsorbed on suspended particles were also studied. DDVP, phorate, stirofos, EPN, azinphos-methyl and IBP had higher adsorption capacity onto suspended particles than other pesticides. Calculated pesticide-particle adsorption coefficient($K_d-particle$) for samples collected in Asan Bay were closely related to the reported pesticides-soil adsorption coefficient ($K_d-soil$).

• Analytical Science and Technology
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• v.13 no.3
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• pp.332-337
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• 2000

The study on the nitrogen adsorption, surface properties and water adsorption capacity of the carbonaceous desiccants derived from phenolic resin was carried out. In the nitrogen adsorption study on the carbonaceous desiccants, Type II isotherm for each sample was obtained. Furthermore, the adsorbed volume decrease with water washing of the desiccant. The $S_{BET}$ of the carbonaceous desiccants was $648.7m^2/g$ before washing and $189.3m^2/g$ after washing, respectively. The morphology of needlelike formation before washing and spherical particle after washing with water were observed from SEM micrographs. Finally, from the water adsorption effects, the percentage of the water loading capacity was 25-63%, and the capacity was good at relatively low humidity.

• Journal of Environmental Health Sciences
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• v.20 no.4
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• pp.36-44
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• 1994

A study was carried out in order to investigate the removal efficiencies and removal characteristics of heaw metals such as Pb, Cd, Cr, Cu in raw water by one of conventional water treatment processes. The coagulants used in this study were Alum and PAC. Three kinds of water samples were provided: kaolin water, kaolin water mixed with humic acid and raw water from Han River mixed with suspended matter deposited on raw water inlet pipe. Heaw metals were added to the water samples with their respective turbidity, and jar tests were performed. In the results from heaw metal removal studies, lead might be adsorbed or exchanged on the particle surface (SS) rather than react with organic matter added. Cadmium was affected on the dissolved organic matter. Chromium was affected by the both dissolved organic matter and SS concentration, and the restabilization and the enmeshment appeared at moderate (50~80 NTU) and high (100 NTU) turbidity as defined in this experimenL The removal efficiency of copper was relatively little affected by the dissolved organic matter but by SS concentration in comparison with other heavy metals. In these studies as to the raw water turbidities and concentration of heaw metals, it is proved out that the removal efficiency on heaw metals in both cases of PAC and Alum as coagulants was not significantly different.

• Journal of the Korean Ceramic Society
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• v.23 no.2
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• pp.21-30
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• 1986

Pure submicron $SrTiO_3$ powders had been synthesized with chemical wet process that $5N-NH_4OH$ solution was sprayed into the mixed solution of $SrTiO_3$, $TiCl_4$ and $H_2O_2$ with $N_2$ carrier gas. The characteristic properties of powders obtained from this experiment were as follows. The optimum synthesis condition in reaction bath was above PH 8.5 and under $25^{\circ}C$ The particle size of precipitated SrTiO(OH) powders dried at 6$0^{\circ}C$ was under 0.01${\mu}{\textrm}{m}$ and uniform. Amorphous precipitated complex powders emitted adsorbed water at 15$0^{\circ}C$ less that and crystalline $SrTiO_3$powders was produced from calcining the complex at 30$0^{\circ}C$. Sintered body of SrTiO3 fired at 133$0^{\circ}C$ showed that relative dielectric constant was 228 at 1MHZ and bulk density was 4.73g/$cm^3$.

• Journal of the Korean Applied Science and Technology
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• v.27 no.2
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• pp.183-187
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• 2010

Core-Shell polymers of silicone dioxide-styrene system were prepared by sequential emulsion polymerization. In inorganic/organic Core-Shell composite particle polymerization, silicone dioxide adsorbed by surfactant sodium dioctyl sulfosuccinate (EU-DO133L) was prepared initially and then core silicone dioxide was encapsulated emulsion by sequential emulsion polymerization using styrene at the addition of potassium persulfate (KPS) as an initiator. We found that $SiO_2$ core shell of $SiO_2$/styrene structure was formed when polymerization of styrene was conducted on the surface of $SiO_2$ particles, and the concentration sodium dioctyl sulfosuccinate (EU-DO133L) was 0.5~2.0g. The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer and morphology of latex by scanning electron microscope(SEM).

• Journal of Korean Society of Water and Wastewater
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• v.31 no.4
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• pp.281-287
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• 2017

Mill scale, an iron waste, was used to separate magnetite particles for the adsorption of phosphate from aqueous solution. Mill scale has a layered structure composed of wustite (FeO), magnetite ($Fe_3O_4$), and hematite ($Fe_2O_3$). Because magnetite shows the highest magnetic property among these iron oxides, it can be easily separated from the crushed mill scale particles. Several techniques were employed to characterize the separated particles. Mill scale-derived magnetite particles exhibited a strong uptake affinity to phosphate in a wide pH range of 3-7, with the maximum adsorptive removal of 100%, at the dosage of 1 g/L, pH 3-5. Langmuir isotherm model well described the equilibrium data, exhibiting maximum adsorption capacities for phosphate up to 4.95 and 8.79 mg/g at 298 and 308 K, respectively. From continuous operation of the packed-bed column reactor operated with different EBCT (empty bed contact time) and adsorbent particle size, the breakthrough of phosphate started after 8-22 days of operation. After regeneration of the column reactor with 0.1N NaOH solution, 95-98% of adsorbed phosphate could be detached from the column reactor.