• Proceedings of KOSOMES biannual meeting
• /
• 2009.06a
• /
• pp.145-147
• /
• 2009

Nutrients in wastewater should be removed prior to release in the receiving waters to prevent the occurrence of eutrophication. In this study, seawater is used to remove ammonia and phosphate by the formation of struvite ($MgNH_{4}PO_{4}{\cdot}6H_{2}O$). It aims to know the optimum conditions for the removal of nutrients using seawater as source of magnesium ions. Experiments were performed using jar tester and pH of ammonium-phosphate solutions were adjusted Samples were drawn at different mixing times. It was shown that simultaneous removal of ammonia and phosphate is rapid, with no significant reduction beyond 10 min of mixing Another important parameter is pH, where range 10-11 showed the optimum nutrient removal. Increase in the volume of seawater, which meant an increase in magnesium ions also lead to better removal.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
• /
• 2003.09a
• /
• pp.417-421
• /
• 2003

Three kinds of surfactant systems - cationic surfactant (system 1), combinition of two cationic surfactants (system 2), and combination of two cationic surfactant and non-ionic surfactant (system 3) - for the simultaneous removal of nitrate and phosphate by micellar-enhanced ultrafiltration (MEUF) were investigated. The highest removal efficiencies of nitrate and phosphate were observed in system 2, which were 90 % of nitrate and 72 % of phosphate. The COD of permeate in system 3 was the lowest, because the added non-ionic surfactant made critical micelle concentration (CMC) lower than that of other surfactant systems. In all systems, the flux decline was similar.

• Journal of Korean Society on Water Environment
• /
• v.27 no.4
• /
• pp.516-522
• /
• 2011

This study was performed to investigate the removal characteristics of phosphate by adsorption on olivine, which is generated as industrial by-products from quarry. The adsorption of phosphate on olivine was significantly achieved within 1 hour and equilibrated after 3 hours. The adsorption capacity of phosphate was enhanced with decreasing pH. The maximum adsorption capacity was observed to be 0.463 mg/g in the condition of pH 3. The $Ca^{2+}$ and $Mg^{2+}$ ion amount per adsorbent eluted from olivine was increased with decreasing pH. The precipitation test showed that phosphate in aqueous phase under the condition of pH 3 ~ 9 could be eliminated largely by adsorption on olivine, not precipitation. Freundlich adsorption model were successfully applied to describe the adsorption behavior of phosphate on olivine. The $q_m$ of Langmuir adsorption model were 1.3369 mg/g, 1.0544 mg/g, 1.0288 mg/g at pH 3, 6 and 9, respectively. The $K_F$ of Freundlich adsorption model were 0.4247 mg/g, 0.3399 mg/g, 0.2942 mg/g at pH 3, 6 and 9, respectively. The olivine showed high feasibility as a adsorbent for the removal of $PO_4$-P.

• Journal of Korean Society of Water and Wastewater
• /
• v.23 no.1
• /
• pp.113-119
• /
• 2009

The feasibility of using cork oak bark for phosphorus removal from wastewater was evaluated in this study. Recently, development of more cost-effective media while maintaining high efficiency in pollutants removal has received concern. Barks have a negative surface charge and, hence, tend to show a high affinity to bind cations, and they need to undergo chemical modification to increase their adsorption capacity of anions. Bark was hydrolyzed by HCl solution and it received modification using an aqueous solution of high molecular weight polyethylenimine(PEI). Surface modification with HCl and PEI resulted in a decrease of specific surface area of the bark from $1.932 m^2/g$ to $1.094 m^2/g$. The adsorption experiments were carried out in batch tests and the data were fitted to the Langmuir isotherm and Freundlich isotherm equations. Phosphate removal rate was higher at the lower solution pH possibly due to the form of phosphate ion in solution. For the initial phosphate concentration of 10 mg/L, maximum adsorption was 20.88 mg P/g at pH 3 and 12.02 mg P/g at pH 5. Mechanism of phosphorus sorption onto the HCl-PEI bark was examined through FT-IR spectrometer. Ion exchange between $NH^+$ and $H_2PO_4{^-}$ appeared to be a key mechanism of phosphate adsorption onto the HCl-PEI bark surface.

• Journal of Korean Society on Water Environment
• /
• v.20 no.3
• /
• pp.231-235
• /
• 2004

To investigate removal effects of nutrients in stormwater runoff by soil of riparian protection zone, soil column experiment was conducted for 20 months. Artificial stormwater runoff containing phosphate and nitrate was applied on the surface of soil column twice a week, and phosphate and nitrate concentrations were measured from the leached water. Soil of riparian protection zone reduced the released amount of infiltrated water to the surrounding water. After infiltration of 1m depth of soil column, average removal rates of phosphate and nitrate were 97.7 % and 74.7 %, respectively. As main mechanisms of phosphate are adsorption to soil particle and utilization by plants, periodical replacement of soil and harvesting of plant at the end of growing season are required. For the removal of nutrients in stormwater runoff by the soil layer, soil of riparian protection zone has higher hydraulic conductivity to infiltrate stormwater. Sandy soil having hydraulic conductivity of about $1{\times}10^{-2}cm/s$ range might be appropriate for this purpose.

• Clean Technology
• /
• v.16 no.4
• /
• pp.258-264
• /
• 2010

This study estimated the possibility of phosphate removal characteristics to utilize EAF(electric arc furnace) slag as submarine cover material. The major phosphate removal mechanism was a certain formation of HAP precipitation occurred by the ionization reaction between $Ca^{2+}$ and $OH^-$, which were leached from the EAF Slag. Another phosphate removal mechanism was the adsortion of EAF slag surface. As a result of $PO_4{^-}-P$ removal characteristics using continuous column reactor, $PO_4{^-}-P$ concentration decreased rapidly after 3 days and 10 days later, it show under 0.5 ppm. The result as applied in real sea water, shows that the phosphate removal effects were 93~98% by the subaqueous sediment removal using the EAF slag. In conclusion, EAF slag is useful in $PO_4{^-}-P$ removal and control and it is possible to use without additional process like crush and selection.

• Nuclear Engineering and Technology
• /
• v.8 no.2
• /
• pp.69-76
• /
• 1976

This experiment has been carried out for the removal of long-lived radioactive-nuclides (Sr-90, Ru-106, Cs-137 and Ce-144) contained in the low-level radioactive effluents from the spent fuel reprocessing plant and nuclear power plant, in order to determine the decontaminability of various chemical coagulants and domestic clay mineral (montmorillonite). Phosphate process showed prominent efficiency for the removal of Ce-144, and lime-soda process did good removal efficiency for Sr-90. About Cs-137 copper-ferrocyanide process is much desirable. In phosphate or lime-soda process, most favorable removal efficiency was obtained at more than pH 11. The montmorillonite treated with sodium chloride showed a considerable improvement in the removal of the radioactive-nuclides. By a combined chemicals-montmorillionite process, the radioactive-nuclides could be more effectively removed than by the only chemicals process.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
• /
• 2004.09a
• /
• pp.350-353
• /
• 2004

in order to develop a new technique for the removal of arsenic compoundsfrom acidified water, the removal of arsenic compounds by an acidophilic moss, Jungermannia vulcanicola Steph. was investigated in this study. The result of vial tests for arsenic removal is dependent on the biological activity of moss. The presence of phosphate inhibited the arsenic removal. And the acclimatization of moss by the media containing arsenic increased the its capability of arsenic remova.

• Environmental Engineering Research
• /
• v.18 no.4
• /
• pp.267-276
• /
• 2013

This study presents a comparison of different protocols for the synthesis of iron-loaded zeolites, and the results of their application, as well as that of zeolite-A (Z-A), to the removal of ammonium and phosphate from aqueous media. Zeolites prepared by three methods were evaluated: iron-incorporated zeolites (IIZ), iron-exchanged zeolites (IEZ), and iron-calcined zeolites (ICZ). The optimal iron content for preparing of IIZ, as determined via scanning electron microscopy and X-ray photoelectron spectroscopy analyses, expressed as molar ratio of $SiO_2:Al_2O_3:Fe$, was below 0.05. Ammonia removal revealed that the iron-loaded zeolites have a higher removal capacity than that of Z-A due, not only to ion-exchange phenomena, but also via adsorption. Greater phosphate removal was achieved with IEZ than with ICZ; additionally, no sludge production was observed in this heterogeneous reaction, even though the coagulation process is generally accompanied by the production of a large amount of undesired chemical sludge. This study demonstrates that the developed synthetic iron-loaded zeolites can be applied as a heterogeneous nutrient-removal materials with no sludge production.

• Journal of Korean Society of Environmental Engineers
• /
• v.33 no.2
• /
• pp.143-148
• /
• 2011

In this work, a composite formed by adding loess with lanthanium ("La-Loess") was proposed for effective removal of phosphate found in confined water bodies such as lake and reservoir. It was found that the theoretical maximum amount of lanthanum that can be attached to Loess was 2.68 mg La/g Loess. The phosphate removal was enhanced as an added amount of La-Loess composite increased. Furthermore, there was a noticeable difference in phosphate removal between Loess and La-Loess as the latter required 1.5 to 10 times less Loess than the former. Both Isotherm equations of Freundlich and Langmuir can be used to explain the phosphate adsorption characteristics in using La-Loess composites. The phosphate removal was very effective in the pH range of 5~8, which means that the proposed adsorbent can be directly applied to natural water without adjusting pH. Also, the La-Loess composites were well settled within 30 min without causing turbidity in water. Consequently, the proposed La-Loess can be strongly recommended for phosphate removal in confined water bodies.