• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.4 no.1
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• pp.40-49
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• 1999

A laboratory flume experiment, using turbulence-generating acryl tank and natural sediments, was conducted to investigate the effects of salinity, concentration of suspended sediment, turbulence and clay minerals on the flocculation and settling of fine-grained suspended sediments. While experiments were run, a sequence of water samples were taken near the bottom of the tank to analyze the variations of size distribution and relative contents of clay minerals. The results of the salinity experiment indicate that median settling velocity ($W_{50}$) increases linearly with salinity. Different settling processes of suspended sediments under variable concentrations appear to be predictable, depending upon the range of the suspension concentration. At concentrations less than 200 mg/l, $W_{50}$ is rarely varied with concentration probably because of the individual--grain settling mode. In the range of 200 to 13,000 mg/l show $W_{50}$ and concentration a good relationship following an empirical formula: $W_{50}=0.45C^{0.44}$. This relationship, however, no longer holds in concentrations exceeding 13,000 mg/l; instead, a more or less reverse one is shown. This result suggests an effect of hindered settling. The turbulence effect is somewhat different from that of concentration. Turbulence accelerates the flocculation and settling susepended sediments at low concentration (200 mg/l), whereas at high concentration turbulence breaks floes down and impedes the settling. Size distribution of suspended sediments sampled near the bottom of the tank tend to be more negatively skewed and leptokurtic in turbulent conditions compared to those in static conditions. The clay mineral analysis from the sequential water samples shows that over time the content of smectite decreases most rapidly with illite remaining concentrated in suspension. This means that smectite, among other clay minerals, plays the most effective role in the flocculation of fine-grained sediment in saline water.

• Applied Chemistry for Engineering
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• v.9 no.2
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• pp.243-248
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• 1998

This study investigated the separation and the property of palladium precipitate formed by ascorbic acid in a simulated radioactive liquid waste, which was composed of 10 elements((Pd, Ru, Rh, Nd, Cs, Sr, Fe, Ni, Zr, Mo). Pd was separated selectively by using reduction characteristics of metal ions contained in the simulated waste with ascorbic acid. When the nitric acid concentration was 0.5 M, the Pd over 99.5% was precipitated by adding 0.04 M ascorbic acid. Nitric acid concentration is important at the reduction reaction of Pd ion. The precipitation yield of Pd was decreased as the concentration of nitric acid was increased. The Pd precipitate was re-dissolved in reaching at an equilibrium when the concentration of nitric acid was high and ascorbic acid was added with a small amount. The Pd precipitate formed by ascorbic acid was Pd metal and was aggregated by particles less than $1.0{\mu}m$.

• Applied Chemistry for Engineering
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• v.18 no.6
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• pp.545-551
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• 2007

HCl concentration, reaction temperature, and $Ti^{4+}$ concentration are the decisive factors in determining the structure of precipitates in the process of synthesis of $TiO_2$ particles from aqueous $TiCl_4$ solution by precipitation and the volumetric proportion of brookite phase in $TiO_2$ particles can be controlled by these factors. Pure brookite-type $TiO_2$ nanoparticles were synthesized by heating the aqueous $TiCl_4$ solution with no more than 1.0 M of $Ti^{4+}$, in which the concentration of HCl was kept in the range of about 2.53~6.41 M during reaction, at the temperature below $70^{\circ}C$ for 20 h. Also, Pure brookite was finally transformed to a rutile phase via an anatase phase through heat-treatment.

• Applied Chemistry for Engineering
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• v.10 no.7
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• pp.996-1002
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• 1999

The oxalate precipitation of lanthanide and actinide by oxalic acid was investigated in the simulated radioactive liquid waste, which was composed of 17 elements of alkali, alkaline earth(Cs, Rb, Ba, Sr), transition metal(Zr, Fe, Mo, Ni, Pd, Rh), lanthanide(La, Y, Nd, Ce, Eu) and actinide(Np, Am) in nitric acid solution. The effect of concentrations of nitric acid and ascorbic acid on the precipitation yield of each element in the simulated solution was examined at 0.5 M oxalic acid concentration. The precipitation yields of the elements were usually decreased with nitric acid concentration, nevertheless, the precipitation yields of lanthanide and actinide were more than 99%. Palladium was precipitated due to the reduction of Pd(II) into Pd metal by the addition of ascorbic acid in the oxalate precipitation and then, the precipitation yields of Mo, Fe, Ni, Ba decreased by 10~20% with concentration of ascorbic acid. The reductive precipitation of Pd(II) into Pd metal by the addition of ascorbic acid into the simulated radwaste occurred at below 1 M nitric acid concentration and its yield showed maximum at the ascorbic acid concentration of 0.01~0.02 M. The hydrazine suppressed the reductive precipitation of Pd by the ascorbic acid.

• Journal of Korea Water Resources Association
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• v.38 no.2
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• pp.133-142
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• 2005

The settling concentration of fine suspended solid particles(alumina(Al$_2$O$_3$) and quartz(SiO$_2$)) is investigated with the physico-chemical effects(initial concentration, pH and NaCl). Laboratory tests have confirmed the significant influence of increasing initial concentration and salinity which can lead to flocculation due to the intermolecular attraction. Furthermore, the influence of the pH value on the concentration-time corves of alumina has been on firmed. Besides a numerical model to predict the behaviour of cohesive deposit under still water is analyzed by solving the unsteady one-dimensional diffusion-advection equation with a explicit, implicit, Crank-Nicolson and finite difference scheme. The model predicts the existence of an equilibrium concentration. Application of the model with implicit centered difference to data from settling experiments shows a similar distribution.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1993.04a
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• pp.58-58
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• 1993

면역 조절능이 우수하고 독성이 적은 신물질의 개발을 목표로 하여 초유에 들어있는 면역물질을 검색한 결과 초유로부터 자연 살해 세포의 기능을 활성화시키는 물질을 순수분리 하였다. 이 물질은 초유의 유청으로부터 ammonium sulfate에 의한 침전, DEAE-cellulose ion exchange, Sephadex G-200 gel filtration 등의 방법에 의하여 분리되었으며, 초유의 유청 100ml로부터 최종 수득량은 1.2 mg이었다. 이 물질은 SDS-polyacrylamide gel electrophoresis에서도 분자량의 변화가 없는 것으로부터 interchain disulfide bond가 없음을 확인할 수 있었다. 이 물질은 실온에 방치하거나 또는 37$^{\circ}C$로 가온하면 침전을 형성하고, 생성된 침전물을 4$^{\circ}C$로 냉각시키면 다시 용해되는 특이한 특성을 갖고 있으며, 침전이 형성되는 정도는 농도, 온도 및 이온 강도에 비례하여 증가하는 것으로 나타났다. 침전에 최적 pH는 중성인 것으로 나타났다. 이 물질을 사람의 말초혈액으로부터 분리한 림파구의 배양액에 가하고 18 시간동안 배양한 결과 림파구의 적 백혈병 암세포인 K-562 세포에 대한 자연 살해능이 증가됨을 확인할 수 있었다. 자연살해 세포의 활성화는 1.0 - 0.01$\mu\textrm{g}$/ml의 농도 범위에서 확인되었다.

• Journal of the Korean Society of Hazard Mitigation
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• v.9 no.4
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• pp.107-113
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• 2009

This paper considers the influence of floc on the sedimentation rate for the cohesive material. The effects of floc density and size changes were also taking into consideration during the experiment. The settling velocity of a discrete floc was measured in a quiescent water column. Floc diameter and density were investigated using a modified Stokes equation with some constants such as water density, viscosity, material density and the floc fractal dimension $n_f$ obtained from the relationship between the floc diameter and the floc settling. The floc diameter of quartz and alumina increased at increasing initial concentrations. The floc size of quartz with increasing NaCl concentration varied between approximately 0.8 um to $10{\mu}m$. Floc density decreased as floc size increased. The floc settling velocity and the floc diameter have a straight line relationship on a logarithm. The floc fractal dimension nf was 2.65 with increasing of initial concentration and 2.93 with increasing of NaCl. The exponent n to predict the settling velocity was proposed and varied from 1 to 1.93.

• Economic and Environmental Geology
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• v.55 no.5
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• pp.531-540
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• 2022

Various iron minerals that precipitate in acid mine drainage have a great influence on the concentration change and mobility of trace elements in the drainage during phase transition to other minerals as well as the precipitation process. This study investigated the change of mineral properties and the behaviors of trace elements influenced by pH and time for the precipitates collected from the acid mine drainage treatment system of the Dalsung mine, where schwertmannite is mainly precipitated. However, the main mineral precipitated in the drainage was goethite, suggesting schwetmannite has already undergone a phase transition to goethite to some extent, and it was observed that at higher pH, the peak width at half maximum of XRD peak was narrower. This can be interpreted as the transformation of small amount of amorphous schwetmannite to goethite or an increase in the crystallinity of goethite, and it showed that the higher the pH, the greater this change was. The concentration of Fe was also greatly affected by the pH values, and as the pH increased, the concentration of Fe in the drainage decreased. With increasing time, the Fe concentration increased and then decreased, which can be interpreted to indicate the dissolution of schwertmannite and precipitation of goethite. This mineral change probably resulted in the rapid increase of the concentration of S at initial stage, but its concentration was stabilized later. The concentration of S is also related to the stability of schwetmannite, showing a high concentration at a low pH at which schwertmannite is stable and a low concentration at a high pH at which goethite is stable. The trace elements present as cations in the drainage also showed a close relationship with the pH, generally the lower the pH, the higher the concentration, due to the solubility changes by the pH, and the precipitation and the changes in mineral surface charge at high pH. On the other hand, in the case of As, existing as an anion, although it showed a high concentration at low pH, its concentration increased with time at all pH values, which is probably related to the concentration of Fe which can be coprecipitated in the drainage, and the increase of As concentration with time is also considered to be related to the decrease in schwertmannite rather than the mineral surface charge.

• Korean Journal of Food Science and Technology
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• v.27 no.1
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• pp.86-91
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• 1995

In order to expand the utility of alginic acid in the food industry, we have investigated to prepare low viscous alginic acid using a method for degradation of alginic acid with the enzyme system of Vibrio sp. AL-145. The enzyme showed maximum activity at pH 8.0 and $37^{\circ}C$, and was stable in the pH range 7.5 to 8.5 and at temperature up to $30^{\circ}C$, and 0.5M NaCl needed for the enzyme activity. The viscosity of alginic acid decreased with the reaction time courses regardless of alginic acid and enzyme concentration, and 90% of viscosity decreased with 60 min of reaction time, but the changes of reducing sugar not exhibited. The soluble concentration of partially degradated alginic acid(PDA) in water was about 10%(w/v), and adsorption capacity of $Ca^{2+}$ ion increased with increasing the concentration of PDA. The alcohol concentration on precipitation of PDA was higher than Na-alginic acid.

• Journal of Korea Soil Environment Society
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• v.3 no.3
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• pp.21-31
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• 1998

A study on the acid leaching and precipitation has been conducted to remove arsenic from the closed-mine tailings. HCI and H$_2$SO$_4$were used as the leach liquor of arsenic and the tailing obtained from the Da-Duck Mine, which was already closed several decades ago, was also used as the source of arsenic. The effect of the concentration of acid, leaching time and the slurry density on the leaching efficiency of arsenic has been examined. In addition, pH controls and the addition of sodium sulfide were also attempted to remove the arsenic compound as the precipitation from the leachate. After 1 hr leaching by HCI, 40 to 86% of arsenic was leached out depending on the concentration of acid or the slurry density while 47 to 77% of it was leached out by $H_2$$SO_4$. The leaching of arsenic by both acids was almost accomplished within 10 min. and after that only a slight increase in leaching efficiency was observed with leaching time. When the leach liquor was used repeatedly for the leaching of arsenic, the concentration of arsenic in the leach liquor was found to increase continuously although the leaching efficiency was diminished. As far as the precipitation of arsenic in the leachate was concerned, more than 99% of arsenic could be precipitated through the addition of sodium sulfide as the precipitator while the pH controls resulted in the precipitation of up to 84%.