• 박물관보존과학
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• 제30권
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• pp.23-46
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• 2023

동아대학교 석당박물관 소장 지자총통은 조선 중기에 사용하던 전장유통식 중화기무기로 천자총통 다음으로 큰 화기류이다. 지자총통의 표면에는 표면 이물질들로 인해 고유의 색상이 가려져 있는 상태로, 보존처리가 필요한 상황으로 판단되었다. 안정적인 보존처리를 위해 감마선(γ선), X선 비파괴 투과조사, 내시경카메라 관찰을 실시하여 내부 구조와 보존상태를 파악하였고, p-XRF 성분분석, SEM-EDS 성분분석, XRD 분석 등을 활용하여 지자총통의 재질 성분과 표면 오염물 등에 관한 성분분석을 진행하였다. 휴대용현미경 관찰과 정밀 3D스캔으로 지자총통 표면 명문의 상태, 새김형태 등을 확인하였다. 감마선, X선 비파괴 투과조사 결과, 지자총통 내부에 다량의 기포가 관찰되었으며, 육안관찰로 확인되는 표면의 채플릿은 비파괴투과조사 결과로는 확인되지 않았다. p-XRF 성분분석 결과 지자총통은 구리(Cu), 주석(Sn), 납(Pb) 합금으로 만들어진 청동으로 확인되었으며, SEM-EDS를 활용한 표면 이물질 성분분석 결과, 백색이물질은 칼슘(Ca), 황(S), 티타늄(Ti)이 주성분으로 확인되었다. 티타늄은 백색수정액의 주성분인 이산화티타늄(TiO₂)으로 추정되었으며, 적색이물질은 바륨(Ba)이 주성분으로 확인되어 페인트의 체질안료인 황산바륨(BaSO₄)으로 추정되었다. 티타늄과 바륨을 주성분으로 하는 백색과 적색 오염물은 근래에 이르러 표면에 묻은 것으로 추정된다. 황색이물질은 알루미늄(Al), 규소(Si)로 확인되어 토양성분에서 유래한 것으로 추정했다. 백색이물질의 XRD 성분분석결과 황화칼슘(CaS)으로 확인되었고, SEM-EDS와 XRD 성분분석결과로 백색이물질은 석고(CaS)로 확인하였다. 성분분석의 결과를 토대로 표면 이물질 제거, 안정화처리, 강화처리를 진행하였다. 보존처리를 진행하던 중에 휴대용 현미경과 정밀 3D스캔을 통해 알려지지 않았던 명문 우(右), 병(兵), 상(上), 이(二)를 발견하였다. 또한, 명문의 새김방법과 깊이, 너비 등을 측정하였다. 우병상(右兵上)은 창원 합포성 내 위쪽이며, 이(二)는 두 번째 돈대로 파악할 수 있다.

• 대한기계학회논문집B
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• 제29권11호
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• pp.1229-1238
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• 2005

The objective of the present study was to investigate the efficacy of physical water treatment (PWT) technologies using different catalytic materials and an electronic anti-fouling device in the mitigation of mineral fouling in a once-through flow system with mini-channel heat exchanger. Effects of flow velocity and water hardness on the effectiveness of PWT technologies were experimentally studied. The artificial water hardness varied from 5.0 to 10 mo1/m$^{3}$ as CaCO$_{3}$. For 10 mo1/m$^{3}$ solution, fouling resistance reduced by 13-40$\%$ depending on flow velocity and types of PWT devices. On the other hand, fouling resistance reduced by 21-29$\%$ depending on the PWT devices for 5 mo11m3 solutions. The PWT device using alloy of Cu and Zn as catalyst (CM2) was slightly more effective than the others. SEM photographs of scale produced from the 10 mol/m$^{3}$ solution at 1.0 m/s indicated that calcium carbonate scales without PWT devices were needle-shaped aragonite, which is sticky, dense and difficult to remove. Scales with the PWT devices showed a cluster of spherical or elliptic shape crystals. Both the heat transfer test results and SEM photographs strongly support the efficacy of PWT technologies using catalytic materials and an electronic anti-fouling device in the mitigation of mineral fouling.

• Transactions on Electrical and Electronic Materials
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• 제1권2호
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• pp.32-37
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• 2000

Effect of alloying element additions to Ag on thermal conductivity and electrical conductivity of sheath materials for Bi-Pb-Sr-Ca-Cu-O(BSCCO) tapes has been characterized. The thermal conductivity at low temperature range (10~300K) of Ag and Ag alloys were evaluated by both direct and indirect measurement techniqueas and compared with each other, It was observed that the thermal conductivity decreases with increasing the content of alloying element such as Au, Pd and Mg. Thermal conductivity of pure Ag at 3 0K was measured to be 994.0 W(m.K) on the other hand, the corresponding values of $Ag_{0.9995}Mg_{0.0005}$, $Ag_{0.974}$, $Au_{0.025}$, $Mg_{0.001}$, $Ab_{0.973}$, $Au_{0.025}$, $Mg_{0.002}$ and $Ag_{0.92}$, $Pb_{0.06}$, $Mg_{0.02}$ were 342.6, 62.1, 59.2 and 28.9 W(m.K), respectively, indicating 3 to 30 times lower than that of pure Ag. In addition, the thermal conductivity of pure Ag measured by direct and indirect measurement techniques was 303.2 and 363.8 W(m.K) The difference in this study is considered to be within an acceptable error range compared to the reference data.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2009년도 제38회 동계학술대회 초록집
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• pp.277-277
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• 2010

The capacity of the carbonaceous materials reached ca. $350\;mAhg^{-1}$ which is close to theorestical value of the carbon intercalation composition $LiC_6$, resulting in a relatively low volumetric Li capacity. Notwithstanding the capacities of carbon, it will not adjust well to the need so future devices. Silicon shows the highest gravimetric capacities (up to $4000\;mAhg^{-1}$ for $Li_{21}Si_5$). Although Si is the most promising of the next generation anodes, it undergoes a large volume change during lithium insertion and extraction. It results in pulverization of the Si and loss of electrical contact between the Si and the current collector during the lithiation and delithiation. Thus, its capacity fades rapidly during cycling. We focused on electrode materials in the multiphase form which were composed of two metal compounds to reduce the volume change in material design. A combination of electrochemically amorphous active material in an inert matrix (Si-M) has been investigated for use as negative electrode materials in lithium ion batteries. The matrix composited of Si-M alloys system that; active material (Si)-inactive material (M) with Li; M is a transition metal that does not alloy with Li with Li such as Ti, V or Mo. We fabricated and tested a broad range of Si-M compositions. The electrodes were sputter-deposited on rough Cu foil. Electrochemical, structural, and compositional characterization was performed using various techniques. The structure of Si-M alloys was investigated using X-ray Diffractometer (XRD) and transmission electron microscopy (TEM). Surface morphologies of the electrodes are observed using a field emission scanning electron microscopy (FESEM). The electrochemical properties of the electrodes are studied using the cycling test and electrochemical impedance spectroscopy (EIS). It is found that the capacity is strongly dependent on Si content and cycle retention is also changed according to M contents. It may be beneficial to find materials with high capacity, low irreversible capacity and that do not pulverize, and that combine Si-M to improve capacity retention.

• Restorative Dentistry and Endodontics
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• 제22권1호
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• pp.1-33
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• 1997

The objective of this study was to analyze the in vitro and in vivo corrosion products of low and high copper amalgams. The four different types of amalgam alloy used in this study were Fine cut, Caulk spherical, Dispersalloy, and Tytin. After each amalgam alloy and Hg were triturated according to the directions of the manufacturer by means of the mechanical amalgamator(Amalgam mixer. Shinhung Co. Korea), the triturated mass was inserted into a cylindrical metal mold which was 12mm in diameter and 10mm in height. The mass was condensed by 150Kg/cm compressive force. The specimen was removed from the mold and aged at room temperature for about seven days. The standard surface preparation was routinely carried out by emery paper polishing under running water. In vitro amalgam specimens were potentiostatically polarized ten times in a normal saline solution at $37^{\circ}C$(potentiostat : HA-301. Hukuto Denko Corp. Japan). Each specimen was subjected to anodic polarization scan within the potential range -1700mV to+400mV(SCE). After corrosion tests, anodic polarization curves and corrosion potentials were obtained. The amount of component elements dissolved from amalgams into solution was measured three times by ICP AES(Inductive Coupled Plasma Atomic Emission Spectrometry: Plasma 40. Perkim Elmer Co. U.S.A.). The four different types of amalgam were filled in occlusal and buccal class I cavities of four human 3rd molars. After about five years the restorations were carefully removed after tooth extraction to preserve the structural details including the deteriorated margins. The occlusal surface, amalgam-tooth interface and the fractured surface of in vivo amalgam corrosion products were analyzed. In vivo and in vitro amalgam specimens were examined and analyzed metallographically by SEM(Scanning Electron Microscope: JSM 840. Jeol Co. Japan) and EDAX(Energy Dispersive Micro X-ray Analyser: JSM 840. Jeol Co. Japan). 1. The following results are obtained from in vitro corrosion tests. 1) Corrosion potentials of all amalgams became more noble after ten times passing through the in vitro corrosion test compared to first time. 2) After times through the test, released Cu concentration in saline solution was almost equal but highest in Fine cut. Ag and Hg ion concentration was highest in Caulk spherical and Sn was highest in Dispersalloy. 3) Analyses of surface corrosion products in vitro reveal the following results. a)The corroded surface of Caulk spherical has Na-Sn-Cl containing clusters of $5{\mu}m$ needle-like crystals and oval shapes of Sn-Cl phase, polyhedral Sn oxide phase. b)In Fine cut, there appeared to be a large Sn containing phase, surrounded by many Cu-Sn phases of $1{\mu}m$ granular shapes. c)Dispersalloy was covered by a thick reticular layer which contained Zn-Cl phase. d)In Tytin, a very thin, corroded layer had formed with irregularly growing Sn-Cl phases that looked like a stack of plates. 2. The following results are obtained by an analysis of in vivo amalgam corrosion products. 1) Occlusal surfaces of all amalgams were covered by thick amorphous layers containing Ca-P elements which were abraded by occlusal force. 2) In tooth-amalgam interface, Ca-P containing products were examined in all amalgams but were most clearly seen in low copper amalgams. 3) Sn oxide appeared as a polyhedral shape in internal space in Caulk spherical and Fine cut. 4) Apical pyramidal shaped Sn oxide and curved plate-like Sn-Cl phases resulted in Dispersalloy. 5) In Tytin, Sn oxide and Sn hydroxide were not seen but polyhedral Ag-Hg phase crystal appeared in internal space which assumed a ${\beta}_l$ phase.

• 보존과학회지
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• 제26권2호
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• pp.157-169
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• 2010

이 연구는 부여 쌍북리유적에서 출토된 도가니 내부 유리 및 청동용융물질과 금동보살입상의 재료학적 특성 및 고고과학적 상관관계를 규명한 것이다. 도가니 내부의 유리질 용융물질은 주로 황록색과 적갈색을 띠는 PbO-$SiO_2$계의 납유리로서 바륨과 안정제의 함량이 낮은 특징이 있다. 금속용융물질은 Cu, Sn, Pb의 합금으로 이루어진 청동으로 밝혀졌으며, 낮은 불순물 함량으로 미루어 고순도로 정련된 구리를 이용하여 제작되었음을 알 수 있다. 주석의 원광석으로는 석석이 이용된 것으로 판단된다. 금동보살입상의 청동소지도 구리의 함량이 높고 불순물의 함량이 낮아 고도로 정련된 원료를 사용하였으며, 쌍북리 유적의 공방에서 숙련된 기술을 바탕으로 제작되었을 가능성이 충분하다. 또한 표면에는 고순도의 금을 아말감기법으로 도금한 것으로 밝혀졌다. 한편 도가니 내 납유리와 청동물질 및 금동보살입상의 납동위원소비는 일관된 결과를 보여주지 않는 것으로 보아 납광석의 원산지 해석에는 무리가 있는 것으로 판단된다.