• Proceedings of the KIEE Conference
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• 1995.07c
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• pp.1048-1050
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• 1995

Lead-acid battery is used widely as a power source at a automobile, industrial machines, folk lifts, U.P.S. etc. Lead-acid battery is cheaper than arty other secondary battery, but this battery has many disadvantages such as heavy, low energy density, environment problem etc. In this article, we introduce cyclic voltammetry methods to investigate corrosion behaviour of positive grids of Pb-Ca alleys.

• Progress in Superconductivity
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• v.2 no.2
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• pp.65-70
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• 2001

$Pb/Bi_2Sr_2CaCu_2O_{8+\delta}$-single-crystal junctions with the tunneling direction along the c axis of the crystal were fabricated to obtain an s-wave-superconductor/d-wave-superconductor Josephson junctions. The tunneling R (T) curves and current-voltage characteristics show distinct features which can be explained only under the assumption that the order parameter of high-$T_c/Bi_2Sr_2CaCu_2O_{8+{\delta}}$ superconductors has a pure d-wave symmetry, which is in contrast to the case of $YBa_2Cu_3O_{7+{\delta$}}$erconductors where a minor s-wave component is also present..

• Proceedings of the KIEE Conference
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• 1992.07b
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• pp.744-746
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• 1992

In this study, we investigated structural, electrical characteristics and studied the conditions which improved hydrostatic constants in hydrophones as we changed x = 0.1, 0.25, 0.35, 0.4 and y = 0.04, 0.08, 0.12, 0.16 in $(Pb_{1-x}Ca_x)[(Mg_{1/3}Nb_{2/3})_yTi_{1-0.01}Mn_{0.01}]O_3$ ceramics in which Ca was substituted with Pb and $Pb(Mg_{1/3}Nb_{2/3})O_3$ was added to decrease sintering temperature in $PbTiO_3$. When Ca was substituted 0.25[mol], the largest electro-mechanical anisotropy ($k_t/k_p$) was found ($k_t{\fallingdotseq}50,k_p{\fallingdotseq}4$), and the less $Pb(Mg_{1/3}Nb_{2/3})O_3$ and the stronger poling field, the larger this anisotropy was. When Ca=0.25[mol], $Pb(Mg_{1/3}Nb_{2/3})O_3=0.08[mol]$ were substituted, ($k_t/k_p$)(=12, 3) was large, permittivity was low and hydrostatic constants were high. Therefore, this composition is promising as wide band ultrasonic devices in water.

• The Transactions of the Korean Institute of Electrical Engineers
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• v.41 no.7
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• pp.766-772
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• 1992

Bi-Sr-Ca-Cu-O superconducting system has both the low and high Tc phases. We added Pb and sintered for 200hrs. in OS12T atmosphere in order to get the superconductor above critical temperature 100K. Superconducting properties of the Bi(Pb)SrCaCuO system doped Sb were also investigated. When Sb of 0.1mol is added, the sintering time becomes shorter than that doped Pb only. We could get the critical temperature 102K at the samples sintered for 24hrs. and 109K for 210hrs.

• Korean Journal of Materials Research
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• v.17 no.3
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• pp.147-151
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• 2007

Cu-free multi-component sol, of which final oxide composition becomes $Bi_{1.9}Pb{0.35}SrCaO,\;Bi_{1.8}Pb_{0.2}SrCaO\;and\;Bi_{1.5}SrCaO$, respectively, was prepared through sol-gel route and coated on a bare Cu substrate. Starting materials were metal-alkoxides as follows.; [$Bi(OC_{2}H_{5})_{3}\;Pb(O^{1}C_{3}H_{7})_{2},\;Sr(O^{i}C_{3}H_{7})_{2},\;Ca(OC_{2}H_{5})_{2}$] as a reagent grade. Transparent light yellowish sol was obtained in the case of $Bi_{1.9}Pb_{0.35}SrCaO\;and\;Bi_{1.8}Pb_{0.2}SrCaO$ composition and $Bi_{1.5}SrCaO$ composition's sol was light greenish. Each sol was repeatedly dip-coated on Cu substrate four times and pre-heated at $400^{\circ}C$ and finally heat-treated in the range of $740{\sim}900^{\circ}C$. In the results, crystalline phases confirmed by XRD were (2201) orthorhombic and monoclinic phases. However, only $Bi_{1.9}Pb_{0.35}SrCaO_{x}$ composition showed pseudo-superconductive behavior after heat-treatment at $900^{\circ}C$ for 12 seconds and then onset temperature was 77 K, even though it did not exhibit zero resistance below Tc.

• The Transactions of The Korean Institute of Electrical Engineers
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• v.59 no.1
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• pp.120-122
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• 2010

In this paper the effect of constituent content on superconductivity and phase in BiPbSrCaCuO system was reported. The zero resistance temperature reaches as high as 100k when dophant Sb was decreased dramatically with increasing Sb content in BiPbSrCaCuO system while the corresponding phase was changed fundamentally.

• Economic and Environmental Geology
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• v.50 no.6
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• pp.497-508
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• 2017

This study was carried out to document and diagnose the conditions of the seated stone statue of Buddhist Master Seungga in Seunggasa temple immediately after its conservation treatment, which was found to be long covered in surface of white materials. The stone Halo was researched along with the Statue, and basic data was secured through precisely examination and nondestructive diagnosis. The result from the surface deterioration evaluation shows that both the Statue and Halo had a little bit of physical deterioration, although their level of chemical deterioration was proportionally higher due to discoloration. The physical property diagnosis using ultrasonic measurements on the Statue and Halo showed that the average ultrasonic velocity was found to be 3,570 m/s and 3,373 m/s, respectively, which corresponds to grade III, an indication of a favorable physical property. The surface covered materials were detected to be Ca, Ti, Pb, Fe, Al and Si, emanating from Hobun (Oster shell powder; $CaCO_3$) or lime ($CaO{\cdot}Ca(OH)_2$) and silicate minerals. Furthermore, Ti and Pb seems to be the component of the white coloring pigments, titanium white ($TiO_2$) and white lead ($2PbCO_2{\cdot}Pb(OH)_2$). Therefore, the seated stone statue of Buddhist Master Seungga is presumed to be painted with Hobun or lime and thereafter painted over with titanium white and white lead.

• Environmental Engineering Research
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• v.11 no.1
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• pp.54-61
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• 2006

An electron probe microanalysis (EPMA) investigation can provide quantitative and qualitative insight into the nature of the surface and bulk chemistry on solidified waste forms(SWF). The proportion of Pb in grain areas is below 0.3 wt. %, and the proportion near the border of the grain slightly increases to 0.98 wt. % but in the inter-particle areas farther from the grain, the concentration of Pb markedly increases. It is apparent that very little Pb diffuses into the tricalcium silicate($C_3S$) particles and most of the Pb exists as precipitates of sulfate, hydroxide, and carbonate in the cavity areas between $C_3S$ grains. Calcite additions on Pb-doped SWF are also observed to induce deeper incorporation of lead into the cement grains with EPMA line-analysis of cross-sections of cement grains. The line-analysis reveals the presence of $0.2{\sim}5$ weight % Pb over $5\;{\mu}m$ from cement grain boundaries. In the inter-particle areas, the ratio of Ca, Si, Al and S to Pb is relatively similar even at some distance from the grain border and the Pb (wt. %) ratio is reasonably constant throughout the whole inter-particles area. It is apparent that the enhanced development of C-S-H on addition of calcite can increasingly absorbs lead species within the silica matrix.

• Korean Journal of Pharmacognosy
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• v.13 no.3
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• pp.102-105
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• 1982

Nine trace elements in Bear Galls(Fel Ursi) studied in this paper are Na, Mg, K, Ca, Cu, Zn, Fe, Pb and Ge. The contents of Na, Mg, K, Ca, Cu, Zn, Fe, Pb are determined by atomic absorption spectrometry and Ge is determined by graphite atomic absorption spectrometry. In both methods, the sample is digested with nitric-perchloric acid and then ashed. The results of analysis are shown in table and the result obtained from this study are as follows. a. The highest content of trace element of Bear Gall is Na and other elements are getting lower in order of K, Mg, Ca, Ge, Zn, Fe, Cu, and Pb. b. Particularly the content of Ge in Bear Gall was determined.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2001.05a
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• pp.211-216
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• 2001

수용액상에서 게 껍질에 의한 납 이온 제거시 납 이온 메카니즘을 규명하기 위하여 납이온 제거에 미치는 pH의 영향에 대해 조사하였다. 게 껍질에 의한 납 이온의 제거는 게껍질 내에 함유되어 있는 CaC $O_{3(S)}$의 용해에 따른 미세침전에 의한 제거가 대부분인 것으로 나타났다. pH가 증가하면 납 이온 제거량도 증가하였고 이온교환에 의해 발생되는 칼슘 이온의 유출은 납 이온 제거를 더욱 증가시키고 게 껍질 내의 $CO_{3}^{2-}$는 납 이온의 침투로 게 껍질 내부에 $PbCO_{3(S)}$ 형태의 복합체를 형성하는 것으로 판단되었다. 납 이온의 제거는 대부분 게 껍질 내 $PbCO_{3(S)}$의 용해로 인해 발생되는 $Pb_{3}(CO_{3}){2}(OH)_{2(S)}$와 $PbCO_{3(S)}$의 침전으로 이루어졌다. 수용액 중의 납 이온은 게 껍질 내 CaC $O_{3(S)}$의 용해를 가속화시키며 게 껍질 내부에서도 납 이온의 침전물이 발생하는 것으로 관찰되었다.