• Journal of Korea Foundry Society
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• v.22 no.3
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• pp.109-113
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• 2002

A good fluidity of high strength Al-alloys is required to cast thin wall castings needed to reduce the weight of cast parts. The fluidity, measured as the length to which the metal flows in a standard channel, is affected by many factors, such as the pouring temperature, solidification type of the alloy, the channel thickness, melt head, mold materials and temperature, coating etc. Therefore the experimentally measured fluidity scatters very much and makes it difficult to estimate the fluidity of a melt with a few measurements. The effect of Ti content and grain refinement on the fluidity of high strength aluminum alloy was investigated with a test casting with 8 thin flow channels to reduce the scattering of the fluidity results. The fluidity of Al-4.8%Cu-0.6%Mn Al-6.2%Zn-1.6%Mg-1.0%Cu and well-known commercial aluminum alloy, A356 was tested. Initial content of Ti was varied from 0 to 0.2wt% and Al-5Ti-B master alloy was added for grain refinement. The flow length varied linearly with superheat. By adding Ti and Al-5Ti-B, the fluidity increased. The grain size decreased by adding grain refiner at the same time. The fluidity depended on the degree of grain refinement. The fluidity of the alloy solidifying in mushy type is improved by grain refinement, because grain refinement increases the solid fraction at the time of flow stoppage.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2018.06a
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• pp.74-74
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• 2018

Ti-6Al-4V alloys have been widely used as orthopedic materials because of their excellent corrosion resistance and mechanical properties. However, it does not bind directly to the bone, so it requires a surface modification. This problem can be solved by nanotube and micropore formation. Plasma electrolytic oxidation (PEO) treatment for micropore, which combines high-voltage spark and electrochemical oxidation, is a new way of forming a ceramic coating on light metals such as titanium and its alloys. This method has excellent reproducibility and can easily control the shape and size of the Ti alloy. In this study, formation of bioactive surface by PEO-treatment after $2^{nd}$ ATO technique of Ti-6Al-4V alloy was invesgated by various instrument. Nanotube oxide surface structure was formed on the surface by anodic oxidation treatment in 0.8 wt.% NaF and 1M $H_3PO_4$ electrolytes. After nanotube formation, nanotube layer was removed by ultrasonic cleaning. PEO-treatment was carried out at 280V for 3 minutes in the electrolytic solution containing the bioactive substance (Mg, Zn, Mn, Sr, and Si). The surface of Ti-6Al-4V alloy was observed by field emission scanning electron microscopy (FE-SEM, S-4800 Hitachi, Japan). An energy dispersive X-ray spectrometer (EDS, Inca program, Oxford, UK) was used to analyze the spectra of physiologically active Si, Mn, Mg, Zn, and Sr ions. The PEO film formed on the Ti-6Al-4V alloy surface was characterized using an X-ray diffractometer (TF-XRD, X'pert Philips, Netherlands). It is confirmed that bioactive ions play an essential role in the normal bone growth and metabolism of the human skeletal tissues.

• Journal of the Korean GEO-environmental Society
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• v.2 no.3
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• pp.37-45
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• 2001

The characteristics of drinking groundwater quality was analyzed by investigating observed data during 1995-1997 in Daejeon city. As the analysis of observed data, the 30.1% of them were over the drinking water quality standards in Daejeon city and the unfit ratios of each region were 36.4% at Dong-Gu, 32.3% Daedeog-Gu, 31.2% Jung-Gu, 30.0% Seo-Gu and 25.2% at Yusoung-Gu. It was found that the items over the drinking water quality standards were 24 items and all of the mean concentration of water quality items were under the drinking water quality standard except Fe and Mn in 1997. The mean concentration of Fe was $1.31mg/{\ell}$ over the water quality at Daedeog-Gu and that of Mn was $0.53mg/{\ell}$ at Jung-Gu. The concentrations of $NH_3$-N, Mn, Fe, Al and F were increased rapidly in 1997, so that the cause of increasing also must be examined closely. It was found that the rainfall and unfit ratio(unfit frequency/test frequency) of E-coli and bacteria had the hydrologic persistance. The coefficient of correlation between them was 0.525. On the rainfall over 100mm, it was 0.673 and on the rainfall over 150mm, it was 0.641. The correlation between E-coli and rainfall was higher than that between bacteria and rainfall.

• Journal of Korean Society of Environmental Engineers
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• v.28 no.7
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• pp.704-712
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• 2006

This research was designed to investigate the removal of heavy metals, such as $Al^{3+}$, $Cu^{2+}$, $Mn^{2+}$, $Pb^{2+}$ and $Zn^{2+}$, by adsorption on clay minerals. Bentonite(Raw-Bentonite), $Ca^{2+}$ and $Na^+$ ion exchanged bentonite(Ca- and Na-Bentonite) and montmorillonite, such as KSF and K10 from Sigma Aldrich, were used as adsorbents. The component of five inorganic adsorbents was analyzed by XRF, and the concentration of metal ions was measured by ICP. The cation exchange capacity(CEC) and the particle charge of adsorbents were measured. The initial concentration range of metal ions was $10{\sim}100$ mg/L. From the experimental results, it was shown that the adsorption equilibrium was attained after $1{\sim}2$ hours. The maximum percentage removal of $Al^{3+}$, $Cu^{2+}$, $Pb^{2+}$ and $Zn^{2+}$ on Na-Bentonite were more than 98% and that of $Mn^{2+}$ was 66%. $Al^{3+}$ was leached out from KSF with the higher concentration of hydrogen ion. Percentage removals of $Pb^{2+}$ and $Zn^{2+}$ on KSF were 88% and 59%, respectively. In general, the percentage removal of metal ions was decreased with the higher initial concentration of metal ions. The adsorption capacity of metal ions on Na-Bentonite was $1.3{\sim}19$ mg/g. Freundlich equation was used to fit the acquired experimental data. As the results, the adsorption capacity of metal ions was in the order of Na-Bentonite$\gg$Raw-Bentonite$\cong$K10>Ca-Bentonite>KSF. Freundlich constant, K of Na-Bentonite was the largest for metal ions. The order K of Na-Bentonite was Al>Cu>Pb>Zn>Mn, and the adsorption intensity(1/n) was determined to be $0.2{\sim}0.39$.

• Korean Journal of Soil Science and Fertilizer
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• v.37 no.3
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• pp.184-191
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• 2004

Forest soils were collected from various sites adjacent to the heavy industrial complexes and soil solutions were extracted to characterize the chemical properties and to find factors affecting forest decline by acid deposition. Concentrations of $NO_3{^-}$, $SO{_4}^{2-}$, $F^-$ and Al in the soil solutions collected from industrial complexes were 2-33 times higher than those from the non-industrial areas. pH and Al concentrations were significantly correlated with $NO_3{^-}$ and $SO{_4}^{2-}$ concentrations. Forest soils from Onsan and Ulsan regions had very low Ca and Mg concentrations in the soil solutions. In these sites, the molar ratios of Ca/Al and Mg/Al were also lower than 2 and 1, respectively. Aluminum concentrations in the A and B horizons were 547 and $683mg\;kg^{-1}$, respectively, which were considered to be high enough to inhibit tree growth. Magnesium deficiency in A horizon and high concentrations of Al and Mn in B horizon were considered as the major limiting factors for tree growth by inhibiting the uptake of Ca and Mg and causing the imbalance of nutrients in both soil solution and trees.

• Journal of Ocean Engineering and Technology
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• v.33 no.6
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• pp.615-619
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• 2019

Various fluorides, i.e., CaF₂, Na₃AlF₆, K₂SiF₆, MnF₃, MgF₂, were added to the flux cored wire, and their effects on the oxygen content of the weld metal were investigated. The investigation showed that the oxygen content of weld metal was not influenced by the type of metallic elements in the fluoride; rather, it was influenced by the stability of the arc during welding. While the wire containing MgF₂ showed the most stable arc and the least amount of oxygen in the weld metal, the wire containing MnF₃ showed the least stable arc and the greatest amount of oxygen. Since the deoxidation of the weld metal was not affected by the deoxidation elements, such as Ca and Mg, it was possible to predict the oxygen content of the weld metal by the equilibrium Si-Mn deoxidation thermodynamic model.

• Journal of Pharmaceutical Investigation
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• v.6 no.3
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• pp.10-13
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• 1976

Trace Element in Deer Horn have been determined Ca, Mg, Fe, Zn, Mn, Al, As, Co and as were detected by partition paper chromatography and spectroscopic method.

• Proceedings of the Korean Magnestics Society Conference
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• 2000.09a
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• pp.429-430
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• 2000

• Journal of Environmental Health Sciences
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• v.30 no.5 s.81
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• pp.455-468
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• 2004

The purpose of this paper is to understand the time series and origin of a chemical component and to compare the difference during yellow sand episodes for analysis $PM_{10}$ chemical components in the region of west in Korean Peninsula, 1999-2001. An annual mean concentration of $PM_{10}$ is $29.1\;{\mu}g/m^3$. A monthly mean and standard deviation of $PM_{10}$ concentration are very high in spring but there is no remarkably seasonal variation. Also, water soluble ionic component of $PM_{10}$ be influenced by double more total anion than total cation, be included $NO_{3}^-\;and\;SO_{4}^{2-}$ for the source of acidity and $NH_{4}^+$ to neutralize. Tracer metals of $PM_{10}$ slowly increases caused by emitted for soil and ocean (Fe, Al, Ca, Mg, Na) and Zn, Pb, Cu, Mn for anthropogenic source. According to method of enrichment factor (E.F) and statistics, assuming that the origin of metal component in $PM_{10}$ most of element in the Earth's crust e.g. Mg, Ca, Fe originates soil and Cu, Zn, Cd, Pb derives from anthropogenic sources. The ionic component for $Na^{+}\;Cl^-,\;Mg^{2+}\;and\;Ca^{2+}$ and Mg, Al, Ca, Fe originated by soil component largely increase during yellow sand period and then tracer metal component as Pb, Cd, Zn decrease. According to factor analysis, the first group is ionic component ($Na^+,\;Mg^{2+},\;Ca^{2+}$) and metal component (Na, Fe, Mn and Ni) be influenced by soil. The second group, Mg, Cr also be influenced by soil particle.

• Journal of the Korean Ceramic Society
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• v.33 no.8
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• pp.928-934
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• 1996

Quantitative analysis each portland cement components was conducted by standard calibration method using X-ray fluorescence spectrometer. Standard sample and the unknown sample were prepared by fused cast bead method. In checking the errors of standard cement 227A372 the relative errors of constituents such as CaO, SiO2, Al2O3, Fe2O3, MgO and SrO were less than 1% and the relative errors of constituents such as So3, K2O, TiO2, Na2O P2O5, and Mn2O3 were less than 5% Sample preparation was mainly contributed to the errors. Compared with general wet chemical method the results of X-ray fluorescence analyses were more precise and accurate. Moreover it is possible to analyze precisely a little amount of the constituents such as SrO, Mn2O3 and P2O5 the analyses of which were very difficult using the wet chemical method.