• Journal of Korean Society of Water and Wastewater
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• v.20 no.3
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• pp.367-375
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• 2006

Sequencing Batch Reactor (SBR) is well adopted for community wastewater treatment for its simplicity, performance and various advantageous treatment options. SBR is now drawing attention for its process modification such as coupled with membrane bioreactor, reverse osmosis or applying different media to achieve high removal efficiency. This study focused on the improved efficiency of carbon, nitrogen and phosphorous removal by applying zeolite materials called bioceramics to the SBR. Two laboratory-scale SBR units were operated in the same operating conditions - one with bioceramics called Bioceramic SBR (BCSBR) and the other without bioceramics used as control. Routine monitoring of COD, TP, $NH_3-N$, $NO_3-N$ was performed throughout this study. COD removal was about 80% to 100% and phosphorous removal was about 60% in the process whereas $NH_3-N$ removal efficiency was found to be 99.9% in the BCSBR unit. Addition of bioceramics also improved sludge characteristics such as sludge dewaterability, specific gravity and particle size. BCSBR can withstand high ammonia shock loading leading to the better treatment capacity of high ammonia containing wastewater. The cause of improved removal efficiencies within the biological reactor could be attributed to the biochemosorption mechanisms of bioceramics. Absorption/adsorption or desorption capacity of bioceramics was tested through laboratory experiments.

• Nuclear Engineering and Technology
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• v.55 no.2
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• pp.516-522
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• 2023

The co-precipitation process plays a key role in the decontamination of radionuclides from low and intermediate levels of liquid waste. For that reason, the removal of Cs ions from waste solution by the co-precipitation method was carried out. A simulated liquid waste (¹³³Cs) was prepared from a 0.1 M CsCl solution, while wastewater generated by washing steel ash served as a representative of radioactive cesium solution (¹³⁷Cs). By co-precipitation, potassium ferrocyanide was applied for the adsorption of Cs ions, while nickel nitrate and iron sulfate were selected for supporting the precipitation. The amount of residual Cs ions in the CsCl solution after precipitation and filtration was determined by ICP-OES, while the radioactivity of ¹³⁷Cs was measured using a gamma-ray spectrometer. After cesium removal, the amount of cesium appearing in both XRD and SEM-EDS was analyzed. The removal efficiency of ¹³³Cs was 60.21% and 51.86% for nickel nitrate and iron sulfate, respectively. For the ash-washing solution, the removal efficiency of ¹³⁷Cs was revealed to be more than 99.91% by both chemical agents. This implied that the co-precipitation process is an excellent strategy for the effective removal of radioactive cesium in waste solution treatment.

• Journal of Wetlands Research
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• v.14 no.4
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• pp.629-635
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• 2012

This study was conducted to evaluate the removal behaviors of DOM(dissolved organic matter) and phosphorus in eutrophic lake water by coagulation process with PAC(powdered activated carbon). It was observed that the removal characteristic of soluble matter was different from that of dissolved one, and the removal of DOM was effected by both pH and coagulant dosage. It was founded that PAC could increase the removal efficiency by an adsorption of DOM in coagulation process. A formation of soluble and colloidal matters resulted in the degradation of phosphorus removal efficiency in a chemical precipitation process. The phosphorus removal efficiency could be enhanced by an absorption of colloidal matter and dissolved complex with PAC addition. In addition, the PAC addition caused the increase of floc density in coagulation process, that led to the rise of sedimentation rate, and resulted in a significant improvement of solid-liquid separation efficiency.

• Proceedings of the SAREK Conference
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• 2008.06a
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• pp.714-719
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• 2008

In a domestic construction field, after floor is constructed, protector for construction surface is set up to prevent the surface of the floor being scratched and polluted. However, the problem is that contaminants discharged with the removal of the protector for construction surface exert a bad influence for the indoor air quality. In the research, it tested to the contaminant reduction performance of the adsorption protector for construction surface using powder of charcoal by the alternative proposal of such protectors for construction surface

• Journal of the Korean Society of Tobacco Science
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• v.2 no.1
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• pp.8-16
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• 1980

The cavity of triple filter was filled with the mixture of clinoptilolite and charcoal(1:1, V/V). The particle size of clinoptilolite was 30$\pm$5 A.S.T.M mesh. The reduction effects of the important gaseous components by this mixture were obtained as follows: 1) In comparison with the normal cellulose acetate niter, the contents of nicotine and T.P.M. were reduced about 35% and 22% respectively. 2) Many aliphatic and cyclic compounds were also substantially reduced in an average of 60%. 3) In contrast with the charcoal, the removal efficiency of clinoptilolite was revealed as higher (15-20%) in case of aliphatic compounds than the one (10-15%) of cyclic compounds. The above results showed us that the removal function of gaseous components was quite complementary each other (charcoal and clinoptilolite).

• Journal of Korean Society of Environmental Engineers
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• v.29 no.2
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• pp.205-213
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• 2007

We have studied NOM(natural organic matters) adsorption and biodegradation on 3 kinds of activated carbon and a anthracite. Coal based activated carbon showed the highest DOC(dissolved organic carbon) adsorption capability and roconut(samchully), wood (pica) in the order among the 3 kinds of activated carbon(F400). The biomass amount and activity also showed on coal, wood and coconut based activated carbon in the order. Over 15 minutes EBCT(empty bed contact time) needed to achieve 10 to 17% average removal efficiency and $18\sim24%$ maximum removal efficiency of NOM biodegradation in biofilter using anthracite. Hydrophobic and below 10,000 dalton NOM was much easier to adsorb into the activated carbon than hydrophilic NOM, THMFP(trihalomethane formation potential) and BDOC (biodegradable dissolved organic carbon)$_{slow}$ were much easier than HAA5FP(haloacetic acid 5 formation potential) and $BDOC_{rapid}$ to adsorb into the activated carbon. Hydrophilic and below 1,000 dalton NOM was much easily biodegraded and HAA5FP and $BDOC_{rapid}$ was easier than THMFT and $BDOC_{slow}$ to biodegrade in the biofilter.

• Journal of the Mineralogical Society of Korea
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• v.18 no.4 s.46
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• pp.267-276
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• 2005

The study is to determine the feasibility of activated red mud as an anti-red tide material. The red mud, a byproduct of Bayer process for the production of alumina from bauxite, contained hematite, boehmite, calcite, sodalite, quartz, zircon, anatase and an unknown phase. In the adsorption study of the red mud, its adsorption efficiencies for heavy elements were close to $100\%$ except $92\%$ In As. These results seem to be attributed by the high adsorption ability of iron oxides for heavy elements. As a result of leaching tests with the red mud at various pHs (pH $1\∼13$), the high leaching efficiencies for As, Cu and Zn at low pHs (at acidic condition) were obtained. It indicated that removal efficiency of heavy elements could be excellent in acidic treatment of red mud. The activated red mud, red mud reacted with acid, contained hematite, boehmite and so on, and desorption of heavy metals from the activated red mud increased with increasing temperature. The grain of the activated red mud was tens nm in size. The removal efficiency for 5 types of plankton was generally in inverse proportion to pH, especially to final pH. Of five plankton types, Prorocentrum minimum and Alexandrium tamarense promptly were removed more than $90\%$ as soon as the activated red mud was sprayed and $100\%$ after 30 minutes. These results indicated that the activated red mud seems to be a promising anti-red tide material.

• Journal of Korean Society of Environmental Engineers
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• v.37 no.3
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• pp.145-151
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• 2015

In order to remove Sr ions and Cs ions from aqueous solution, PS-zeolite beads were prepared by immobilizing zeolite with polysulfone (PS). The prepared PS-zeolite beads were characterized by SEM, XRD, FT-IR, and TGA. The optimum condition to prepare PS-zeolite beads was 1.25 g of PS content and 2 g of zeolite A. The removal efficiencies of Sr and Cs ions by the PS-zeolite beads increased as the solution pH increases and nearly reached a plateau at pH 4. The PS-zeolite beads prepared in this study showed a remarkably high selectivity for Sr ion and Cs ion under the coexistence of ions such as $Na^+$, $K^+$, $Mg^{2+}$, and $Ca^{2+}$. Zeolite particles detached from the PS-zeolite beads were not observed on this experiments, and also the PS-zeolite beads maintained the morphological structure on a SEM image. The removal efficiencies of Sr ions and Cs ions by PS-zeolite beads were maintained over 90% even after five adsorption-desorption cycles. These results implied that the prepared PS-zeolite beads could be an available adsorbent for the adsorption of Sr and Cs ions. These results suggest that the PS-zeolite can potentially be used as an adsorbent in radioactive ions removal for the treatment of industrial wastewater.

• Journal of the Mineralogical Society of Korea
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• v.16 no.4
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• pp.321-331
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• 2003

We researched the variation of mineral composition with depth and the Cu adsorption behavior of Hwangto in the Okjong area, Hadong. The 4 Hwangto samples were collected from depth 10 cm, 25 cm, 2∼3 m and under 3 m from surface, and analyzed using the X­ray Diffractometer. The Hwangto samples were mostly composed of clay minerals such as kaolinite and halloysite. Two samples from 10 cm and 25 cm contained Fe or Al hydroxide minerals, for example goethite or gibbsite. As depth increases, the content of quartz decreases but that of kaolinite increases. The amount of Cu removal was rapidly rised from pH 4, and reached about 90％ at pH 6 and above 90％ at pH 7. It is regarded that the trend of Cu removal was affected by the difference in mineral composition. It was relatively well matched between experimental value and calculated value by MINTEQA2 program in the case of high Cu concentration. From this study the precipitation has important role for the removal of Cu ions, particularly in the case of high Cu concentration. However, it was discord between experimental value and calculated one in the dilute concentration circumstances. The reason may be the mistake in parameters, insufficient reaction time, and inadequate consideration of reaction site in mineral surface.

• Journal of Korean Society of Environmental Engineers
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• v.22 no.5
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• pp.837-847
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• 2000

For the treatment of wastewaters generated from beer industry and petrochemical company with high organic and nitrogen contents, laboratory scale of A/O Pure-Oxygen Biofilm (POB) process was developed and studied by means of the comparative economic analysis with extended aeration process. When the wastewater of beer company was initially treated by the A/O POB process in the ranges of 70 to 150 mg TOC/L diluted with tap water, higher than 92% of TOC removal was accomplished in the all ranges. In case of petrochemical wastewater, the initial TOC removal was as low as 52%, though, it increased to 86% after 32 days of operation and also the TKN removal marked 71% after 27 days. Continuous high removal rates were monitored in both the TOC and TKN parameters during the experimental period. Due to the cost for PSA (Pressure Swing Adsorption) setting and biomass supporting media installation, the initial construction cost of A/O POB process was 2.9 times higher than that of extended aeration process. However, the advantages such as low sludge production, no need for sludge recycling and low energy consumption allow the A/O POB process to have 2.5 times lower operation and maintenance costs. Consequently, in the long term of operation, it is likely that A/O POB process would show higher performance as well as cost effectiveness compared to extended aeration process.