• Korean Journal of Metals and Materials
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• v.47 no.8
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• pp.474-481
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• 2009

The effects of final heat treatment on the mechanical and corrosion properties of a Zr alloy strip incorporating Nb were investigated. The chemical composition of the strip was Zr-1.49Nb-0.38Sn-0.20Fe-0.11Cr, and strip specimens were subjected to final heat treatment in a temperature range of $580{\sim}700^{\circ}C$. Tensile tests at room temperature and $316^{\circ}C$, along with corrosion tests in a simulated PWR loop and a 70 ppm LiOH solution environment at $360^{\circ}C$, were performed on the specimens. The mechanical properties of the strip were saturated when the specimens received final heat treatment at an elevated temperature of more than $640^{\circ}C$. However, the corrosion resistance of the strip in the simulated PWR loop and in the 70 ppm LiOH solution environment was improved with a decrease of the final annealing temperature. It is recommended that the alloy strip be finally heat-treated at a temperature of less than $620^{\circ}C$ for longer than 10 minutes in order to obtain fully recrystallized microstructures, and thereby attain enlarged tensile elongation, and to prevent the precipitation of ${\beta}-Zr$, which is known to deteriorate the corrosion resistance.

• Corrosion Science and Technology
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• v.20 no.6
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• pp.426-434
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• 2021

The effect of two different annealing temperatures on the level of the second phase precipitated in the microstructure and the corrosion behaviors of super austenitic stainless steel were examined. The sample annealed at a higher temperature had a significantly lower fraction of the sigma phase enriched with Cr and Mo elements, showing more stable passivity behavior during the potentiodynamic polarization measurement. However, after the welding process with Inconel-type welding material, severe corrosion damage along the interface between the base metal and the weld metal was observed regardless of the annealing temperature. This was closely associated with the precipitation of the fine sigma phase with a high Mo concentration in the unmixed zone (UMZ) during the welding process, leading to the local depletion of Mo concentrations around the sigma phase. On the other hand, the fraction of the newly precipitated fine sigma phase in the UMZ was greatly reduced by post-weld heat treatment (PWHT), and the corrosion resistance was greatly improved. Based on the results, it is proposed that the alloy composition of welding materials and PWHT conditions should be further optimized to ensure the superior corrosion resistance of welded super austenitic stainless steel.

• Korean Journal of Microbiology
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• v.30 no.4
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• pp.310-315
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• 1992

Absorption of $\textrm{Pb}^{2-}$ from aqueous solution was studied using Staphylococcus epidermidis. Cells of exponential phase were employed as absorbents. Uptake ratio defined as the ratio of amount of $\textrm{Pb}^{2+}$ absorbed to that of initial $\textrm{Pb}^{2+}$. Absorption of $\textrm{Pb}^{2+}$ increased with increase in cell concentration. while amount of $\textrm{Pb}^{2+}$ per unit cell mass decreased. Uptake ratio of $\textrm{Pb}^{2+}$ augmented and then diminished after exhibiting a maximum as the pH of the solution increased. Equilibrium absorption of $\textrm{Pb}^{2+}$ deviated from Freundlich isotherm especially at higher concentration of $\textrm{Pb}^{2+}$ due to the precipitation phenomena. HCI and EDTA were founded to desorb $\textrm{Pb}^{2+}$ more effectively than $\textrm{Na}_{2}\textrm{CO}_{3}$ or $\textrm{NaHCO}_{3}$. After 10 cycles of absorption and desorption. $\textrm{Pb}^{2+}$ absorption capability remained almost unchanged and the biomass had leaked out 30-40 wt/%. Uptake ratio of Pb2+ decreased in the presence of other heavy metal ions due to the competitive absorption The inhibition of $\textrm{Pb}^{2+}$ absorption appeared to have a strong correlation with ionic radius of the competing ions. Especially $\textrm{Cr}^{3-}$, $\textrm{Co}^{2+}$ or $\textrm{Fe}^{2+}$ having smaller ionic radius depressed more significantly the uptake of $\textrm{Pb}^{2+}$ than any other metal ions tested.

• Journal of the Korean institute of surface engineering
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• v.51 no.1
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• pp.54-61
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• 2018

Plasma Nitriding treatment was performed on STS 204Cu stainless steel samples at a temperature of $400^{\circ}C$ for 15 hours with varying $N_2$ content as 10%, 15% and 25%. Regardless of the content of $N_2$, S-Phase which is a hardened layer of Nitrogen (N) supersaturated phase, was formed in the surface of plasma treated samples. When $N_2$ content was 25%, the thickness of the hardened layer reached up to about $7{\mu}m$ and the surface hardness reached a value of $560Hv_{0.05}$, which is about 2.5 times higher than that of untreated sample (as received $220Hv_{0.05}$). From potentiodynamic polarization test, it was observed that compared to as received sample, the corrosion potential and the corrosion current density of the plasma treated samples were decreased regardless of the $N_2$ content, but the corrosion resistance was not increased much due to the precipitation of $Cr_2N$. On the other hand, pitting potential of the samples treated with 10% and 15% $N_2$ was higher than that of as received sample, however, the samples treated with 25% exhibited a lower pitting potential. Therefore, 10% $N_2$ content was selected as optimum plasma nitriding condition and to further increase both the thickness and surface hardness and the corrosion resistance of the hardened layer, different $CH_4$ content such as 1%, 3% and 5% was introduced into the plasma nitriding atmosphere. With 1% $CH_4$, the thickness of the hardened layer reached up to about $11{\mu}m$ and the surface hardness was measured as about $620Hv_{0.05}$, which is about 2.8 times that of as received sample. And the corrosion resistance of the plasma treated sample by using 1% $CH_4$ was improved significantly due to much higher pitting potential, and lower corrosion current density. When the $CH_4$ content was more than 1%, the thickness and surface hardness of the hardened layer decreased slightly and the corrosion resistance also decreased.

• Journal of the Korean Society of Groundwater Environment
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• v.5 no.1
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• pp.44-55
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• 1998

Imgok creek is the most severly polluted one out of the streams which have been being polluted by acid drainages from the abandoned coal mines in the Gangdong-Myeon area, the central part of the so called Gangreung coal field. Imgok creek is being mainly polluted by the drainage from Youngdong coal mine, which supplies such pollutants as Mg, Fe, Al, Si, Ca, Mn, and SO$_4$as major dissolved components and Cr, Co, Ni, Cu, Zn, Rb, Sr, Cd, Pb, and U as minor dissolved components. After the influx, the pollutants migrate mainly as dissolved solid, rather than as suspended solids along Imgok creek. The suspended solids in Imgok creek are very rich in Fe and Al, indicating that they mainly consist of the precipitates of present and past from the polluted water. Most of the dissolved components in the stream waters of Imgok creek removed from the aqueous phase by precipitation and dilution before reaching the East Sea, so that water quality of the downstreams of Imgok creek is very similar to that of unpolluted tributaries. It suggests that Imgok creek itself is now being severly polluted by the acid drainages from the abandoned coal mines, but the East Sea is relatively safe from the same pollution. The estuary and sea waters around the Goonseon estuary, which accepts Imgok creek water, certainly show no significant difference in chemical compositions from the mean oceanic water. The bottom sediments at the sampling sites of the sea waters also show no significant trend of their component variation, especially the variations of Fe, SO$_4$ and Al concentrations. These facts again supper that the acid mine drainage is not considerablly polluting the East Sea. However, the tributaries supplying the fresh water to the Imgok creek will be certainly polluted by the acid mine drainage as time passes and pollutants will have more chance to migrate in significant amount to the downstream area, which all can be a real threats to the East Sea on the pollution possibility. Therefore, it is suggested that urgently required are not only water quality and environmental improvement of the severely polluted Imgok creek but also preparation of the measures on the possible future pollution of the East Sea by the acid drainage from the abandoned coal mines in the area, while the East Sea is still not much affected by the pollution of the same kind.

• Journal of Korean Society of Environmental Engineers
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• v.29 no.8
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• pp.950-955
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• 2007

Non-point source control system which had been designed only for oil-water separation in the fields of oil refinery and garage was upgraded in this research for the removal of runoff pollutants in impervious urban area. Pollutants including oil from driveway and bridge were eliminated by two types of pathway in the system. One is the coalescence mechanism that the oil droplets in the runoff come into contact with each other in the spiral buoyant media surface and form larger coalesced droplets of oil that are carried upstream to the oil layer. The other is the precipitation that solids in runoff were settled by gravity in the system. In this research, coalescing characteristics of oil and water separation were investigated through image analyses, and efficiencies of the non-point source control system were evaluated using dust in driveway and waste engine oil. Media made of high density and high molecular weight polyethylene was indeterminate helical shape and had sleek surface by analysing SEM photographs and BET. Surface area and specific gravity of media which were measured directly were 1,428 $mm^2$ and 45.3 $kg/m^3$ respectively. From the image analyses of the oil droplets photographs which were taken by using microscope, it was proved clearly that the coalescence was the main pathway in the removal of oil from the runoff. Finally, the performances of the non-point source control system filled up with the media were suspended solid $86.6\sim95.2%$, $COD_{Cr}$, $87.3\sim95.4%$, n-Hexane extractable materials $71.8\sim94.8%$ respectively.

• Economic and Environmental Geology
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• v.54 no.2
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• pp.299-308
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• 2021

Fe(II) released from mining activities is precipitated as various Fe(III)-oxyhydroxides when exposed to an oxidizing environment including mine drainage. Ferrihydrite, one of the representative precipitated Fe(III) minerals, is easy to adsorb heavy metals and other pollutants due to the large specific surface area caused by very low crystallinity. Ferrihydrite is transformed to thermodynamically more stable goethite in the natural environment. Hence, information on the transformation of ferrihydrite to goethite and the related mobility of heavy metals in the acid mine drainage is important to predict the behaviors of those elements during ferrihydrite to goethite transition. The behaviors of heavy metals during the transformation of ferrihydrite to goethite were investigated for core samples collected from an AMD treatment system in the Heungjin-Taemaek coal mine by using X-ray diffraction (XRD), chemical analysis, and statistical analysis. XRD results showed that ferrihydrite gradually transformed to goethite from the top to the bottom of the core samples. Chemical analysis showed that the relative concentration of As was significantly high in the core samples compared with that in the drainage, indicating that As was likely to be adsorbed strongly on or coprecipitated with iron oxyhydroxide. Correlation analysis also indicated that As can be easily removed from mine drainage during iron mineral precipitation due to its high affinity to Fe. The concentration ratio of As, Cd, Co, Ni, and Zn to Fe generally decreased with depth in the core samples, suggesting that mineral transformation can increase those concentrations in the drainage. In contrast, the concentration ratio of Cr to Fe increased with depth, which can be explained by the chemical bond of iron oxide and chromate, and surface charge of ferrihydrite and goethite.