• Proceedings of the Korean Institute of Building Construction Conference
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• 2018.05a
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• pp.27-28
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• 2018

Deterioration of reinforced concrete structures due to salt corrosion is a phenomenon that can be easily seen, and the main reason for deterioration is chloride ion. Therefore, researches are actively conducted to control chlorine ion penetration worldwide. The purpose of this study is to evaluate the chloride ion fixation capacity of Portland cement paste containing Hydrotalcite. For this purpose, cement paste containing 0%, 2.5%, and 5% of Hydrotalcite was sealed and cured for 28 days, and the cured cement paste was crushed. Chloride ion solution was prepared at a concentration of 0.5M using NaCl, and the powdered cement paste was reacted for a specific time in aqueous chloride ion solution. After the reaction, the concentration of the chloride ion aqueous solution was measured using a silver nitrate potentiometric titrator, and the reacted cement paste was analyzed using XRD and FT-IR.

• Journal of Korean Society for Atmospheric Environment
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• v.5 no.2
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• pp.42-54
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• 1989

This study was carried out to investigate the phenomena of acid precipitation. The pH value, electro conductivity and major anions (sulfate, nitrate and chloride) were measured by automatic acid rain monitor and ion chromatography at 5 points in Seoul area from Jan. to Dec. 1988. 1. The acidity of rainfall was in order winter (4.31) spring (4.77) fall (4.94) summer (5.31). Rainfall with a pH of less than 5.6 was appeared 83.2 percent. 2. The range of the highest appearence frequency rate both at Hannam-dong and Songsu-dong was from pH 4.6 to 5.0 and appeared 30.7 percent and 38.3 percent respectively, Bang-i-dong was 36.3 percent in the ranged from pH 4.1 to 4.5 and Guro and Ssangmun-dong were 26 percent and 30.3 percent in the ranged from pH 5.1 to 5.5 respectively. 3. The sulfate and nitrate ion concentration in earlier rainwater ranged from 0.1 ppm to 50.2 ppm and from 0.01 ppm to 15.8 respectively. The earlier rainwaters were generally more acidic than the after rainwaters. 4. The order of the major anion concentration in rainwater was $SO_4^{2-} > Cl^- > NO_3^-$ and the acidity of it was more effective by sulfate ion than others. The correlation between pH value and anions concentration was shown positive correlationship at Guro-dong and Bang-i-dong and negative correlation at Hannam-dong but not at the other sites.

• Korean Journal of Environmental Agriculture
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• v.5 no.2
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• pp.135-140
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• 1986

K-bentonite was made by ion exchange reaction in $K^{\ast}$ ion saturated aqueous solution. K-bentonite had a slow releasing effect in different soils such as sand, sandy loam and clayey loam, but the effect was the best in sand. The growth of radish and lettuce was better in the plot fertilized with K-bentonite than with KCl in sand culture in field condition. There was no effects on the growth of radish grown in pot in glass house. Vitamin C, nitrate content, thiocyanate ion content and dry weight of radish were not affected by K-bentonite and KCl in both pot and field culture. The commercial production of K-bentonite was discussed.

• Polymer(Korea)
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• v.39 no.1
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• pp.157-164
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• 2015

In this study, we synthesized poly(vinylimidazole-co-trifluoroethylmethacrylate-co-divinylbenzene) (PVTD) copolymer and introduced functional group through quaternization reaction for removing nitrate from drinking water. Also, optimizing conditions (reaction time, reaction temperature and functionalized agents concentration) for introducing the functional group were confirmed. The basic properties such as water uptake, swelling ratio, electrical resistance, ion exchange capacity and anion permselectivity for removing nitrate from drinking water were measured. The optimal values of water uptake, electrical resistance and ion exchange capacity of synthesized anion exchange membrane were 51.2%, $5.4{\Omega}{\cdot}cm^2$, and 1.04 meq/g, respectively.

• Polymer(Korea)
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• v.25 no.3
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• pp.311-317
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• 2001

In this study, we synthesized bead-type GMA-DVB copolymer using glycidylmethacrylate (GMA) with high reactivity and hydrophilicity. Macrorecticular anion exchanger containing the trimethylammonium group were then prepared by amination with trimethylammonium chloride. We observed that the size of $NO_3^-$ is smaller than that of $SO_4^{2-}$ which disturb $NO_3^-$ removal in most of coexistent anions in ground water. Thus we investigated selective affinity for $NO_3^-$ and properties of individual ion exchangers with various DVB content. For each resins, we confirmed formation of copolymer by FT-IR spectrometer and investigated ion exchange capacity, swelling ratio, the amination yield and the effect with degree of crosslinking on adsorbability for nitrate. When amount of DVB is 4 wt%, amination yield, ion exchange capacity and swelling ratio was 384.3%, 3.25 meq/g and 77.1%, respectively. In these result, it can found that synthetic optimal condition is 4 wt% DVB content for monomer.

• Bulletin of the Korean Chemical Society
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• v.31 no.1
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• pp.47-51
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• 2010

A powder, containing 80 percent of blue cobalt aluminate $(CoAl_2O_4)$ crystallites, was synthesized at $210 ^{\circ}C$ using a (metal nitrate-malonic acid-ammonium hydroxide-ammonium nitrate) system. The optimal amount of concentrated ammonia water and initial decomposition temperature were determined for the blue $CoAl_2O_4$ crystallites preparation. Three $CoAl_2O_4$ precursor pastes, corresponding to the various amounts of concentrated ammonia water, were prepared by evaporating the initial solutions in an electric furnace fixed at $80 ^{\circ}C$ under a vacuum of 25 torr. The initial solution was used to dissolve the starting materials. The powder with the maximum content (80%) of blue $CoAl_2O_4$ crystallites was prepared when the prepared precursor was decomposed at $210 ^{\circ}C$. The blue $CoAl_2O_4$ crystallite content in the prepared sample decreased with increasing initial decomposition temperature. For 0.2 mole of the $Al^{3+}$ ion, the chemical compositions of the precursor corresponded to molar ratios of 0.4, 1.40, 2.56 and 2.00 for the $Co^{2+}$ ion, malonic acid, ammonia and ammonium nitrate per mole of the $Al^{3+}$ ion, respectively. The blue $CoAl_2O_4$ crystallite content in the sample decreased with the amount of ammonia deviated from the optimal value. The characteristics of the powders were examined using X-ray diffraction, optical microscopy, Fourier transformation infrared spectroscopy and the Brunauer-Emmett-Teller technique.

• Journal of Korean Society of Occupational and Environmental Hygiene
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• v.31 no.1
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• pp.22-30
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• 2021

Objectives: The objectives of this study were to develop a quality control protocol of inorganic acids using ion chromatograph and to evaluate analytical proficiency of the legally designated agencies. Methods: This study prepared inorganic acid samples by injecting three anion certified solutions (chloride, nitrate, and sulfate) on the quartz filters. To investigate the storage stability and concentration consistency of the samples, 240 samples for each anion were tested at weeks 0, 2, 4, 8, 12, and 16 while storing at 4℃ and 25℃. To evaluate analytical proficiency, two separate testings were administrated for six skilled analysts and 46 analysts affiliated with legally designated agencies. Results: Average recoveries of the three ions after 16 weeks of storage were fairly high (over 95%). In addition, average recoveries (chloride = 97%, nitrate = 96%, and sulfate = 103%) after 16 weeks of storage at low temperate were relatively higher than those (94%, 93%, and 98%) at room temperature. The coefficients of variation (CV) for the three ions were less than 5% except for the sulfate sample at 5.56 ㎍ (CV = 12.4%). The average ratios of the concentration values analyzed by the legally designated agencies to the injected concentrations were close to 1. However, their CVs were relatively greater (chloride ≤ 49%, nitrate ≤ 14%, and sulfate ≤ 28%), which implies a need for quality control. Conclusions: The quality control protocol used in this study for the three inorganic acids can be utilized in the quality control for ion chromatography.

• Journal of Environmental Health Sciences
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• v.22 no.3
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• pp.64-71
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• 1996

Measurement of concentration and size distribution of TSP, ammonium, nitrate and sulfate were made from Mar., 1991. to June., 1992 in Seoul. The seasonal variation of concentration and size distribution of aerosols has been investiated. Aerosol were collected and size frationated by Andersen air sampler. Size classified samples were extrated with deionized water and analyzed for ammonium, nitrate and sulfate by ion chromatography. As the results of measurement, the average of concentration and MMAD(mass median aerodynamic diameter) were $118.58 \mu g/m^3$, and $2.77 \mu m$ for TSP, $1.92 \mu g/m^3$ and $1.35 \mu m$ for ammonium, $1.34 \mu g/m^3$ and $1.58 \mu m$ for nitrate, $8.52 \mu g/m^3$ and $2.15 \mu m$ for sulfate. The Seasonal variation of concentration and size distribution was observed for ammonium, nitrate and sulfate. The concentration peak of TSP was observed in coarse particles in spring and observed in fine particles in winter. The concentration's distribution of TSP, ammonium, nitrate and sulfate was observed bimodal type during all season.

• Journal of Biosystems Engineering
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• v.28 no.4
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• pp.335-342
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• 2003

A simple disposable thick-film potentiometric strip has been developed and evaluated for hydroponics application. The strip consisted of low ion-selective electrodes (ISE) fabricated by screen-printing technology. The electrochemical responses of ion sensors for nitrate, ammonium, potassium, and magnesium were measured with specially designed 16-channel low voltage signal transducers. The analytical characteristics of the sensors were comparable with those of conventional ISE sensors. The thick-film sensors exhibit linear relationships over five concentration decades. The concentration of N $O_3$ - ion in standard solution can be determined by direct potentiometric measurements without any conditioning before measurements. However, measurement of $K^{+}$, N $H_4$$^{+}$, and $Mg^{2+}$ ionic concentrations in nutrient solutions seems not feasible.

• Microbiology and Biotechnology Letters
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• v.40 no.4
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• pp.414-418
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• 2012

The quantity of research on microbial fuel cells has been rapidly increasing. Microbial fuel cells are unique in their ability to utilize microorganisms and to generate electricity from sewage, pig excrement, and other wastewaters which include organic matter. This system can directly produce electrical energy without an inefficient energy conversion step. However, with MFCs maximum power production is limited by several factors such as activation losses, ohmic losses, and mass transfer losses in cathodes. Therefore, electron acceptors such as nitrate and ferric ion in the cathodes were utilized to improve the cathode reaction rate because the cathode reaction is very important for electricity production. When 100 mM nitrate as an electron acceptor was fed into cathodes, the current in single-cathode and dual-cathode MFCs was noted as $3.24{\pm}0.06$ mA and $4.41{\pm}0.08$ mA, respectively. These values were similar to when air-saturated water was fed into the cathodes. One hundred mM nitrate as an electron acceptor in the cathode compartments did not affect an increase in current generation. However, when ferric ion was used as an electron acceptor the current increased by $6.90{\pm}0.36$ mA and $6.67{\pm}0.33$ mA, in the single-cathode and dual-cathode microbial fuel cells, respectively. These values, in single-cathode and dual-cathode microbial fuel cells, represent an increase of 67.1% and 17.6%, respectively. Furthermore, when supplied with ferric ion without air, the current was higher than that of only air-saturated water. In this study, we attempted to reveal an inexpensive and readily available electron acceptor which can replace platinum in cathodes to improve current generation by increasing the cathode reaction rate.