• 헤리티지:역사와 과학
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• 제36권
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• pp.267-297
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• 2003

The plain coarse pottery from the Unjeonri Bronze Age relic sites in the Cheonan, Korea were studied on the basis of clay mineralogy, geochemistry and archaegeological interpretations. For the research, the potteries are utilized at the analysis for 6 pieces of plain coarse potteries. Color of the these potteries are mainly light brown, partly shows the yellowish brown to reddish brown. The interior, surface and inside of the pottery appear as different colors in any cases. Original source materials making the Unjeonri potteries are used of mainly sandy clay soil with extreme coarse grained irregularly quartz and feldspar. The magnetic susceptibility of the Unjeonri pottery range from 0.20 to 1.20. And the Unjeonri soil's magnetic susceptibility agree almost with 0.20 to 1.30. In the same magnetization of soil and pottery, the results revealed that the Unjeonri soil and low material of pottery are same produced by identical source materials. The Unjeonri potteries and soil are very similar patterns with all characteristics of soil mineralogy, geochemical evolution trend. The result seems to be same relationships between the behavior and enrichment patterns on the basis of a compatible and a incompatible elements. Consequently, the Unjeonri potteries suggest that made the soil to be distributed in the circumstance of the relic sites as the raw material are high in a greater part. In the Unjeonri soil, the kaolinite is common occurred minerals. However, in the Unjeonri pottery, the kaolinite was not detected in all broken pieces. The kaolinite was presumed to destroy crystal structure during the firing processes of over $550^{\circ}C$. The quartz is phase transition from ${\alpha}$-quartz to ${\beta}$-quartz at $573^{\circ}C$, but the Unjeonri pottery did not investigated any phase transition evidences of quartz. The chorite was detected within the mostly potteries and soils. As the results, the Unjeonri potteries can be interpreted by not experiencing a firing temperature over $800^{\circ}C$. The colloidal and cementing materials between the quartz and low materials during the heating did not exist in the internal part of the potteries. An any secondary compounds by heating does not appear within the crack to happen during the dry of the pottery. The hyphae group are kept as it is with the root tissue of an organic matters to live in the swampy land. In the syntheses of all results, the general firing condition to bake and make the Unjeonri pottery is presumed from $550^{\circ}C$ to $800^{\circ}C$. However, the firing condition making the Unjeonri pottery can be different firing temperature partially in one pottery. Even, the some part of the pottery does not take a direct influence on the fire.

• 청정기술
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• 제28권2호
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• pp.110-116
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• 2022

본 연구에서는 NdFeB 영구자석 스크랩으로부터 회수한 철(Fe) 부산물을 이용하여 산화철(FeO_x) 나노입자를 합성하였고, 열처리 온도가 FeO_x 나노입자의 물성에 미치는 영향을 관찰하였다. 이를 위해 D.I. water에 약 10 wt%로 희석한 철 부산물 용액에 2.0 M 암모니아(NH₄OH) 용액을 투여하여 산화철 전구체를 석출하였고, 이를 300 ℃, 400 ℃, 500 ℃ 및 600 ℃로 각각 열처리하여 FeO_x 나노 입자를 합성, 열처리 온도에 따른 FeO_x 나노 입자의 물성을 관찰하였다. X-ray diffraction (XRD) 분석 결과 열처리 온도가 증가할수록 <104> 회절 피크가 성장하여 500 ℃ 이상에서 α-Fe₂O₃ 결정구조와 일치하는 회절 피크가 검출되었다. BET (Brunauer-Emmett-Teller) 비표면적 분석 결과 400 ℃ 이상에서 열처리 온도가 증가할수록 비표면적이 감소하는 경향을 나타내었다. HRTEM (high resolution transmission electron microscope) 관찰 결과 rod 형 나노입자가 관찰되었고, 열처리 온도 증가에 따라 나노입자의 크기가 증가하는 경향을 나타내었다.

• 분석과학
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• 제21권2호
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• pp.123-128
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• 2008

졸-겔법에 의한 코디어라이트계 전구체(precursor) 제조 시 마그네슘 에톡사이드를 사용하면 황금색을 띠는 불투명한 전구체 용액이 되고, 조핵제인 5%-$Zr(OC_3H_7)_4$ 첨가 시에는 투명한 코디어라이트를 얻을 수 있다. 적외선 흡수 분광 분석에서 $SiO_2$ 성분은 $1045cm^{-1}$에서 흡수 피크를 확인 할 수 있었으며, 동시에 $1140cm^{-1}$과 $940cm^{-1}$의 두 개 피크 분리는 열처리 한 겔체인 $SiO_4$ 신축 진동이고, $Al_2O_3$ 성분은 $580cm^{-1}$과 $680cm^{-1}$의 흡수 피크로 보아 $Al_2O_6$ 망목 구조이고, MgO 성분은 $575cm^{-1}$에서 MgO 신축 진동 임을 알 수 있었다. X-선 회절 분석에서 코디어라이트계 전구체 : 물 몰비 1:5의 경우 반응 소결 온도 $1000^{\circ}C$ 이상에서는 ${\mu}$-cordierite 결정상이 나타남을 알 수 있었고, 코디어라이트계 전구체 : 암모니아 몰비 1:5 건조 겔체의 경우 $1050^{\circ}C$에서는 ${\mu}$-cordierite와 ${\alpha}$-cordierite가 공존 하다가 $1100^{\circ}C$에서는 ${\alpha}$-cordierite만이 존재함을 알 수 있었다.

• 자원환경지질
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• 제56권6호
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• pp.817-830
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• 2023

This study investigates the age of the surficial rocks in the Arunta region using Uranium-Lead (U-Pb) geochronological dating. Rock samples were collected at four locations, Cattle-Water Pass (CP 1610), Gough Dam (GD 1622 and GD 1610), and London-Eye (LE 1601), within the Strangways Metamorphic Complex and crushed by selFragging. Subsequently, the zircon grains were imaged using Cathodoluminescence (CL) analysis and the U-Pb (uranium and lead) isotope ratios and the chrono-stratigraphy were measured. The imaged zircon revealed an anomalous heterogeneous crystal structure. Ellipses of the samples at locations GD1601, CP1610, and GD1622 fall below the intercept indicating the ages produced discordant patterns, whereas LE1601 intersects the Concordia curve at two points, implying the occurrence of an event of significant impact. For the rock sample at CP1610, the estimated mean age is 1742.2 ± 9.2 Ma with mean squared weighted deviation (MSWD) = 0.49 and probability of equivalence of 0.90; 1748 ± 15 Ma - MSWD = 1.02 and probability of equivalence of 0.40 for GD1622; and 1784.4 ± 9.1 Ma with MSWD of 1.09 and probability of equivalence of 0.37 for LE1601. But for samples at GD1601, two different age groups with different means occurred: 1) below the global mean (1792.2 ± 32 Ma) estimated at 1738.2 ± 14 Ma with MSWD of 0.109 and probability of equivalence of 0.95 and 2) above it with mean of 1838.22 ± 14 Ma, MSWD of 1.6 and probability of equivalence of 0.95. Analysis of the zircon grains has shown a discrepancy in the age range between 1700 Ma and 1800 Ma compared to the ASO dated to have occurred between 440 and 300 Ma. Moreover, apparent similarity in age of the core and rim means that the mineral crystallized relatively quickly without significant interruptions and effect on the isotopic system. This may have constraint the timing and extent of geological events that might have affected the mineral, such as metamorphism or hydrothermal alteration.

• 대한화학회지
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• 제63권6호
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• pp.453-458
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• 2019

Synthesis of ZnCo₂O₃ oxide is performed by sol-gel method via nitrate-citrate route. Powder X-ray diffraction (XRD) study shows monoclinic unit cell having lattice parameters: a = 5.721(1) Å, b = 8.073(2) Å, c = 5.670(1) Å, β = 93.221(8)°, space group P_2/m and Z = 4. Average crystallite sizes determined by Scherrer equation are the range ~14-32 nm, whereas SEM micrographs show nano-micro meter size particles formed in ZnCo₂O₃. Endothermic peak at ~798 K in the Differential scanning calorimetric (DSC) trace without weight loss could be due to structural transformation and the endothermic peak ~1143 K with weight loss is due to reversible loss of O₂ in air atmosphere. Energy Dispersive X-ray (EDX) analysis profile shows the presence of elements Zn, Co and O which indicates the purity of the sample. Magnetic measurements in the range of +12 kOe to -12 kOe at 10 K, 77 K, 120 K and at 300 K by PPMS-II Physical Property Measurement System (PPMS) shows hysteresis loops having very low values of the coercivity and retentivity which indicates the weakly ferromagnetic nature of the oxide. Observed X-band EPR isotropic lineshapes at 300 K and 77 K show positive g-shift at g_iso ~2.230 and g_iso ~2.217, respectively which is in agreement with the presence of paramagnetic site Co²⁺(3d⁷) in the oxide. DC conductivity value of 2.875 ×10^-8 S/cm indicates very weakly semiconducting nature of ZnCo₂O₃ at 300 K. DRS absorption bands ~357 nm, ~572 nm, ~619 nm and ~654 nm are due to the d-d transitions ⁴T_1g(⁴F)→²E_g(²G), ⁴T_1g(⁴F)→⁴T_1g(⁴P), ⁴T_1g(⁴F)→⁴A_2g(⁴F), ⁴T_1g(⁴F)→⁴T_2g(⁴F), respectively in octahedral ligand field around Co²⁺ ions. Direct band gap energy, E_g~ 1.5 eV in the oxide is obtained by extrapolating the linear part of the Tauc plot to the energy axis indicates fairly strong semiconducting nature of ZnCo₂O₃.

• 대한치과보철학회지
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• 제43권3호
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• pp.363-378
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• 2005

Statement of problem. Hydroxyapatite(HA) coated titanium surfaces have not yet showed the reliable osseointegration in various conditions. Purpose. This study was aimed to investigate microstructures, chemical composition, and surface roughness of the surface coated by the hydrothermal method and to evaluate the effect of hydrothermal coating on the cell attachment, as well as cell proliferation. Material and Methods. Commercially pure(c.p.) titanium discs were used as substrates. The HA coating on c.p. titanium discs by hydrothermal method was performed in 0.12M HCl solution mixed with HA(group I) and 0.1M NaOH solution mixed with HA(group II). GroupⅠ was heated at 180 $^{\circ}C$ for 24, 48, and 72 hours. GroupⅡ was heated at 180 $^{\circ}C$ for 12, 24, and 36 hours. And the treated surfaces were evaluated by Scanning electron microscopy(SEM), Energy dispersive X-ray spectroscopy(EDS), X-ray photoelectron spectroscopy(XPS), X-ray diffraction method(XRD), Confocal laser scanning microscopy(CLSM). And SEM of fibroblast and 3-(4,5- dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide(MTT) assay were used for cellular responses of the treated surfaces. Results. The color of surface changed in both groups after the hydrothermal process. SEM images showed that coating pattern was homogeneous in group II, while inhomogeneous in group I. H72 had rosette-like precipitates. The crystalline structure grew gradually in group II, according to extending treatment period. The long needle-like crystals were prominent in N36. Calcium(Ca) and phosphorus(P) were not detected in H24 and H48 in EDS. In all specimens of group II and H72, Ca was found. Ca and P were identified in all treated groups through the analysis of XPS, but they were amorphous. Surface roughness did not increase in both groups after hydrothermal treatment. The values of surface roughness were not significantly different between groups I and II. According to the SEM images of fibroblasts, cell attachments were oriented and spread well in both treated groups, while they were not in the control group. However, no substantial amount of difference was found between groups I and II. Conclusions. In this study during the hydrothermal process procedure, coating characteristics, including the HA precipitates, crystal growth, and crystalline phases, were more satisfactory in NaOH treated group than in HCl treated group. Still, the biological responses of the modified surface by this method were not fully understood for the two tested groups did not differ significantly. Therefore, more continuous research on the relationship between the surface features and cellular responses seems to be in need.

• 한국재료학회지
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• 제19권2호
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• pp.61-67
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• 2009

Electrolessly deposited Co (Re,P) was investigated as a possible capping layer for Cu wires. 50 nm Co (Re,P) films were deposited on Cu/Ti-coated silicon wafers which acted as a catalytic seed and an adhesion layer, respectively. To obtain the optimized bath composition, electroless deposition was studied through an electrochemical approach via a linear sweep voltammetry analysis. The results of using this method showed that the best deposition conditions were a $CoSO_4$ concentration of 0.082 mol/l, a solution pH of 9, a $KReO_4$ concentration of 0.0003 mol/l and sodium hypophosphite concentration of 0.1 mol/L at $80^{\circ}C$. The thermal stability of the Co (Re,P) layer as a barrier preventing Cu was evaluated using Auger electron spectroscopy and a Scanning calorimeter. The measurement results showed that Re impurities stabilized the h.c.p. phase up to $550^{\circ}C$ and that the Co (Re,P) film efficiently blocked Cu diffusion under an annealing temperature of $400^{\circ}C$ for 1hr. The good barrier properties that were observed can be explained by the nano-sized grains along with the blocking effect of the impurities at the fast diffusion path of the grain boundaries. The transformation temperature from the amorphous to crystal structure is increased by doping the Re.

• 한국진공학회지
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• 제22권5호
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• pp.250-256
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• 2013

양전자 소멸 분광법으로 발광 박막 시료에 3.0 MeV 에너지를 가진 양성자 빔을 $0.0{\sim}20.0{\times}10^{13}$ protons/$cm^2$의 조사에 의해 생성된 결함을 측정하여 박막구조 특성에 대하여 실험하였다. 동시 계수 도플러 넓어짐 양전자 소멸법 스펙트럼의 수리적 해석 방법인 S-변수를 사용하고, 양전자 수명 측정 방법에 의한 양전자 수명 ${\tau}_1$과 ${\tau}_2$, 이에 따른 세기 $I_1$과 $I_2$를 사용하여, 박막구조에 대한 결함 특성 변화를 측정하였다. 측정된 S-변수는 박막에 조사된 양성자의 빔 조사량에 따라 양성자가 빈자리에 포획되어 감소하는 값을 보였다. 양전자 수명 ${\tau}_1$은 증가하고, ${\tau}_2$은 일정한 값을 나타내었으나, 반면에 세기 $I_1$과 $I_2$는 큰 변화가 없었다. 그 이유는 양성자 조사 빔의 변화에 따라서 단일 빈자리의 크기는 증가하고, 다 결정체 알갱이 빈자리 때문에 양성자에 의한 다수의 빈자리 결함의 양은 큰 차이가 없기 때문이다. 그리고 Bragg 피크로 인하여 박막 시료의 특정 깊이에 결함을 형성하여 박막 전체의 결함으로 잘 나타나지 않기 때문으로 판단된다.

• 한국재료학회지
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• 제9권1호
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• pp.46-50
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• 1999

액상반응법에 의해 $\textrm{Zn}_{2-x}\textrm{Mn}_{x}\textrm{SiO}_{4}$ 녹색 형광체를 합성한 후 소성온도($900^{\circ}C$-$1200^{\circ}C$) 및 Mn 활성제 농도(x=0.01~0.20)에 따른 발광특성과 결정특성을 조사하였다. 147nm와 254nm 여기원을 사용한 경우 형광체의 소성온도가 $900^{\circ}C$에서 $1200^{\circ}C$로 증가함에 따라 상대발광피크강도는 약 4배 이상 크게 증가하였다. XRD 분석결과 $1100^{\circ}C$이상의 소성온도에서 $\textrm{Zn}_{2}\textrm{SiO}_{4}$:Mn 녹색 형광체에서 나타나는 전형적인 willemite 결정구조를 보여주었다. $1200^{\circ}C$의 온도로 소성된 $\textrm{Zn}_{2-x}\textrm{Mn}_{x}\textrm{SiO}_{4}$형광체 시료의 경우 147nm 여기원에서 Mn 활성제 농도가 x=0.02에서 최대 발광강도를 나타내었으며 x=0.10 이상에서 발광강도가 급격히 저하하는 농도 칭 현상이 나타났다. SEM 분석결과 형광체 입자는 구형에 가까운 형상을 보여주었으며 $1200^{\circ}C$에서 소성된 형광체 입자크기는 약 2~3$\mu\textrm{m}$이었다.EX>이었다.

• 대한환경공학회지
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• 제30권5호
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• pp.560-566
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• 2008

본 연구에서는 산업폐기물 소각장 비산재의 고형화시 시멘트와 폐석분을 일정 비율로 첨가하여 하나의 공시체로 만든 후, 압축강도와 중금속의 용출특성을 비교 분석하여 비산재의 고형화시 고화제로 사용되는 시멘트의 일부를 대체할 수 있는지를 평가하였다. 각 시료의 입도와 SEM 분석 결과, 폐석분의 입도가 작게 나타났으며, 비산재가 시멘트나 폐석분의 혼합시 조밀성이 향상되고 뚜렷한 결정구조를 나타내는 것을 관찰할 수 있었다. 각 시료의 XRD 분석 결과, 비산재의 경우 CaO성분이 다량 함유되어 있었으며, 폐석분에 경우 SiO$_2$성분이 다량 포함되어 있어 고화제로 사용되는 시멘트와 혼합시 수화반응 및 Pozzolan반응에 기여할 것으로 판단된다. 공시체의 압축강도의 경우, 비산재에 시멘트와 폐석분 혼합 첨가시에 각 첨가비율에 따른 모든 압축강도가 10 kgf/cm$^2$을 초과하고 있었으며, 시멘트 단독으로 첨가할 때 보다 시멘트와 폐석분을 혼합하여 첨가할 때 더욱 높은 압축강도를 나타냈다. 중금속 용출시험 결과, 폐석분을 혼합 14일 양생 시, 시멘트 150 kg/m$^3$에 폐석분 80$\sim$100 kg/m$^3$을 주입하는 것으로 국내의 폐기물 관리기준 Pb 3 mg/L를 만족하는 것으로 나타났다.