• 마이크로전자및패키징학회지
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• 제15권1호
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• pp.1-6
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• 2008

칼슘 코발트 층상 산화물계에서 $Ca_3Co_2O_6$와 $Ca_3Co_4O_9$를 기본으로 하여 열전 특성 향상을 위해 Ca 위치를 Bi, Sr, La, K로 부분 치환하고, Co위치를 Mn, Fe, Ni, Cu, Zn로 치환한 다결정 산화물을 제조하여 $300{\sim}1000K$ 까지의 열전 특성을 분석하였다. Bi가 치환된 $Ca_3Co_4O_9$계의 $Ca_{2.7}Bi_{0.3}Co_4O_9$는 전기전도도 $85.4({\Omega}cm)^{-1}, Seebeck계수 $176.2{\mu}V/K$그리고 파워팩터 $265.2{\mu}W/K^m$로 가장 높은 열전 물성치가 관찰되었다. 열전 모듈 제조를 위해서 각각의 열전반도체의 성능지수Z($10^{-4}/K$)가 0.87, 0.41의 값인 p형 열전 소재로 $Ca_{2.7}Bi_{0.3}Co_4O_9$를, n형 열전 소재로($Zn_{0.98}Al_{0.02}$)O를 선택하여 열전쌍을 제조하였다. 제조된 2쌍의 기본 열전쌍은 120K의 온도차에서 약 30mV정도의 기전력이 나타났다.

• 광물과 암석
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• 제34권1호
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• pp.1-14
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• 2021

운산 금 광상은 한반도의 3대(대유동 광상, 광양 광상) 금 광상중의 하나였다. 이 광상의 지질은 선캠브리아기의 변성퇴적암류와 중생대의 반상화강암으로 구성된다. 이 광상은 선캠브리아기의 변성퇴적암류와 중생대의 반상화강암내에 발달된 단층대를 따라 충진한 함 금 석영맥 광상으로 조산형 금 광상에 해당된다. 이 광상의 석영맥은 광물조합에 따라 1) 방연석-석영맥형, 2) 자류철석-석영맥형, 3) 황철석-석영맥형, 4) 페크마틱 석영맥형, 5) 백운모-석영맥형 및 6) 단순석영맥형으로 분류된다. 연구된 석영맥은 황철석-석영맥형이며 견운모화작용, 녹니석화작용 및 규화작용이 관찰된다. 백색운모는 유색대에서 백색석영, 황철석, 녹니석, 금홍석, 모나자이트, 저어콘, 인회석, 칼리장석 및 방해석 등과 함께 세립질 내지 중립질 입단으로 산출된다. 이 백색운모의 화학조성은 (K0.98-0.86Na0.02-0.00Ca0.01-0.00Ba0.01-0.00 Sr0.00)1.00-0.88(Al1.70-1.57Mg0.22-0.09Fe0.23-0.10Mn0.00Ti0.04-0.02Cr0.01-0.00V0.00Ni0.00)2.06-1.95 (Si3.38-3.17Al0.83-0.62)4.00O10(OH2.00-1.91F0.09-0.00)2.00로써 이론적인 이중팔면체형 운모류 값보다 Si가 높고 K, Na, Ca는 낮다. 이 광상의 엽리상 석영맥에서 산출되는 백색운모의 화학조성 변화는 팬자이틱(phengitic) 또는 Tschermark 치환[(Al3+)VI+(Al3+)IV <-> (Fe2+ 또는 Mg2+)VI+(Si4+)IV] 및 직접적인 (Fe3+)VI <-> (Al3+)VI 치환에 의해 일어났음을 알 수 있다. 엽리상 석영맥에서 산출되는 녹니석의 화학조성은 (Mg1.11-0.80Fe3.69-3.14Mn0.01-0.00Zn0.01-0.00K0.07-0.01Na0.01-0.00Ca0.04-0.01Al1.66-1.09)5.75-5.69 (Si3.49-2.96Al1.04-0.51)4.00O10 (OH)8로써 이론적인 녹니석보다 Si 함량이 높다. 이 녹니석의 화학조성 변화는 팬자이틱(phengitic) 또는 Tschermark 치환(Al3+,VI+Al3+,IV <-> (Fe2+ 또는 Mg2+)VI+(Si4+)IV) 및 팔면체적 Fe2+ <-> Mg2+ (Mn2+) 치환에 의해 일어났음을 알 수 있다. 따라서 운산 광상의 엽리상 석영맥 및 변질광물은 조산운동 시 연성전단(ductile shear) 시기에 형성되었음을 알 수 있다.

• Transactions on Electrical and Electronic Materials
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• 제13권4호
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• pp.171-176
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• 2012

As langasite $A_3BC_3D_2O_{14}$ compounds with piezoelectric properties exhibit no phase transition up to the melting point of 1,400-$1,500^{\circ}C$, many high temperature applications are expected for the SAW filter, temperature sensor, pressure sensor, and so on, based on the digital transformation of wider bandwidth and higher-bit rates. It has a larger electromechanical coupling factor compared to quartz and also nearly the same temperature stability as quartz. The $La_3Ga_5SiO_{14}$ (LGS) crystal with the $Ca_3Ga_2Ge_4O_{14}$-type crystal structure was synthesized and the crystal structure was analyzed by Mill et al. It is also an important feature that the growth of the single crystal is easy. In the case of three-element compounds such as $[R_3]_A[Ga]_B[Ga_3]_C[GaSi]_DO_{14}$ (R=La, Pr and Nd), the piezoelectric constant increases with the ionic radius of R. In this study, crystal structures of four-element compounds such as $[A_3]_A[B]_B[Ga_3]_C[Si_2]_DO_{14}$ (A = Ca or Sr, B = Ta or Nb) are analyzed by a single crystal X-ray diffraction, and the mechanism and properties of the piezoelectricity depending on the species of cation was clarified based on the crystal structure.

• 한국대기환경학회지
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• 제13권5호
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• pp.371-381
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• 1997

Precipitation sampls were collected in Chonju-city during October 1994 to September 1995 and were analysed for major ions (N $a^{+}$, $K^{+}$, $Ca^{2+}$, $Mg^{2+}$, C $l^{[-10]}$ , NO/$_3$, S $O_4$$^{2-}$) and trace metals (Al, Cd, Ni, Pb, Sr, Zn) in addition to pH, in order to understand the chemical characteristics of acid rain and to estimate the origin of the determined ions. Most rain showed a neutral or alkaline character, and only 35% had a pH lower than 5.6. S $O_4$$^{2-}$ and N $O_3$$^{[-10]}$ are identified as the primary contributors to precipitation acidity in this region. Neutralization of precipitation acidity occurs as a result of the dissolution of alkaline compounds containing $Ca^{2+}$, $Mg^{2+}$ and $K^{+}$. S $O_4$$^{2-}$ and N $O_3$$^{[-10]}$ precipitation concentrations exhibit a seasonal pattern in which higher concentrations are observed during spring months and lower concentrations during summer months. However, the seasonal behavior of $H^{+}$ concentrations differs from this pattern, in that the highest concentrations occur during autumn months, owing to the different influence of neutralization processes. In all rain, S $O_4$$^{2-}$ concentration exceeded NO/$_3$$^{[-10]}$ concentration. The contribution of maritime sources to the total S $O_4$$^{2-}$ concentration was very low or negligible. For rain strongly affacted by yellow sand, $Ca^{2+}$, $Mg^{2+}$ and $K^{+}$ ions show a sharp increase in concentration, reflecting the increased amount of dust and soil suspended in atmosphere. At the same time, S $O_4$$^{2-}$ and N $O_3$$^{[-10]}$ concentrations are at their highest levels while $H^{+}$ values are not comparably elevated, presumably beacause much of the acidity has been neutralized by alkaline substances. The seasonal variance of trace metal concentrations in rainwater is similar to that of major cations. The annual wet flux of acidic pollutants and trace metals wat calculated to be as follows: N $O_3$$^{[-10]}$ ; 2.32 g/$m^2$, S $O_4$$^{2-}$, 5.34 g/$m^2$, Al; 6.30 mg/$m^2$, Cd; 0.62 mg/$m^2$, Ni; 4.08 mg/$m^2$, Pb: 9.76 mg/$m^2$, Sr; 5.94 mg/$m^2$, Zn; 111 mg/$m^2$./$m^2$.

• 한국결정성장학회:학술대회논문집
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• 한국결정성장학회 1996년도 The 9th KACG Technical Annual Meeting and the 3rd Korea-Japan EMGS (Electronic Materials Growth Symposium)
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• pp.258-292
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• 1996

In the last year great interest appears to YBCO thin films preparation on different substrate materials. Preparation of epitaxial film is a very difficult problem. There are many requirements to substrate materials that must be fullfilled. Main problems are lattice mismatch (misfit) and similarity of structure. From paper [1] or follows that difference in interatomic distances and angles of substrate and film is mire important problem than similarity of structure. In this work we present interatomic distances and angle relations between substrate materials belonging to ABCO4 group (where A-Sr or Ca, B-rare earth element, C-Al or Ga) of different orientations and YBCO thin films. There are many materials used as substrates for HTsC thin films. ABCO4 group of compounds is characterized by small dielectric constants (it is necessary for microwave applications of HTsC films), absence of twins and small misfit [2]. There most interesting compounds CaNdAlO4, SrLaAlO4 and SrLaGaO4 were investigated. All these compounds are of pseudo-perovskite structure with space group 14/mmm. This structure is very similar to structure of YBCO. SLG substrate has the lowest misfit (0.3%) and dielectric constant. For preparation of then films of substrates of this group of compound plane of <100> orientation are mainly used. Good quality films of <001> orientations are obtained [3]. In this case not only a-a misfit play role, but c-3b misfit is very important too. Sometimes, for preparation of thin films substrates of <001> and <110> orientations were manufactured [3]. Different misfits for different YBCO faces have been analyzed. It has been found that the mismatching factor for (100) face is very similar to that for (001) face so there is possibility of preparation of thin films on both orientations. SrLaAlO4(SLA) and SrLaGaO4(SLG) crystals of general formula ABCO4 have been grown by the Czochralski method. The quality of SLA and SLG crystals strongly depends on axial gradient of temperature and growth and rotation rates. High quality crystals were obtained at axial gradient of temperature near crystal-melt interface lower than 50℃/cm, growth rate 1-3 mm/h and the rotation rate changing from 10-20pm[4]. Strong anisotropy in morphology of SLA and SLG single crystals grown by the Czochralski method is clearly visible. On the basics of our considerations for ABCO4 type of the tetragonal crystals there can appear {001}, {101}, and {110} faces for ionic type model [5]. Morphology of these crystals depend on ionic-covalent character of bonding and crystal growth parameters. Point defects are observed in crystals and they are reflected in color changes (colorless, yellow, green). Point defects are detected in directions perpendicular to oxide planes and are connected with instability of oxygen position in lattice. To investigate facets formations crystals were doped with Cr3+, Er3+, Pr3+, Ba2+. Chromium greater size ion which is substituted for Al3+ clearly induces faceting. There appear easy {110} faces and SLA crystals crack even then the amount of Cr is below 0.3at.% SLG single crystals are not so sensitive to the content of chromium ions. It was also found that if {110} face appears at the beginning of growth process the crystal changes its color on the plane {110} but it happens only on the shoulder part. The projection of {110} face has a great amount of oxygen positions which can be easy defected. Pure and doped SLA and SLG crystals measured by EPR in the<110> direction show more intensive lines than in other directions which allows to suggest that the amount of oxygen defects on the {110} plane is higher. In order to find the origin of colors and their relation with the crystal stability, a set of SLA and SLG crystals were investigated using optical spectroscopy. The colored samples exhibit an absorption band stretching from the UV absorption edge of the crystal, from about 240 nm to about 550 m. In the case of colorless sample, the absorption spectrum consists of a relatively weak band in the UV region. The spectral position and intensities of absorption bands of SLA are typical for imperfection similar to color centers which may be created in most of oxide crystals by UV and X-radiation. It is pointed out that crystal growth process of polycomponent oxide crystals by Czochralski method depends on the preparation of melt and its stoichiometry, orientation of seed, gradient of temperature at crystal-melt interface, parameters of growth (rotation and pulling rate) and control of red-ox atmosphere during seeding and growth (rotation and pulling rate) and control of red-ox atmosphere during seeding and growth. Growth parameters have an influence on the morphology of crystal-melt interface, type and concentration of defects.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2018년도 춘계학술대회 논문집
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• pp.75-75
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• 2018

Commercially pure titanium (CP-Ti) and Ti-6Al-4V alloys have been widely used in implant materials such as dental and orthopedic implants due to their corrosion resistance, biocompatibility, and good mechanical properties. However, surface modification of titanium and titanium alloys is necessary to improve osseointegration between implant surface and bone. Especially, when titanium oxide nanotubes are formed on the surface of titanium alloy, cell adhesion is greatly improved. In addition, plasma electrolytic oxide (PEO) coatings have a good safety for osseointegration and can easily and quickly form coatings of uniform thickness with various pore sizes. Recently, the effects of bone element such as magnesium, zinc, strontium, silicon, and manganese for bone regeneration are researching in dental implant field. The purpose of this study was researched on the surface morphology of PEO-treated Ti-6Al-4V alloy after anodic titanium oxide treatmentusing various instruments. Ti-6Al-4V ELI disks were used as specimens for nanotube formation and PEO-treatment. The solution for the nanotube formation experiment was 1 M $H_3PO_4$ + 0.8 wt. % NaF electrolyte was used. The applied potential was 30V for 1 hours. The PEO treatment was performed after removing the nanotubes by ultrasonics for 10 minutes. The PEO treatment after removal of the nanotubes was carried out in the $Ca(CH_3)_2{\cdot}H_2O+(CH_3COO)_2Mg{\cdot}4H_2O+Mn(CH_3COO)_2{\cdot}4H_2O+Zn(CH_3CO_2)_2Zn{\cdot}2H_2O+Sr(CH_2COO)_2{\cdot}0.5H_2O+C_3H_7CaO_6P$ and $Na_2SiO_3{\cdot}9H_2O$ electrolytes. And the PEO-treatment time and potential were 3 minutes at 280V. The morphology changes of the coatings on Ti-6Al-4V alloy surface were observed using FE-SEM, EDS, XRD, AFM, and scratch tester. The morphology of PEO-treated surface in 5 ion coating solution after nanotube removal showed formation or nano-sized mesh and micro-sized pores.

• 분석과학
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• 제9권4호
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• pp.382-391
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• 1996

세라믹스 분야, 전자요업 분야 등에서 폭넓게 사용되고 있는 티탄산바륨 소재에 대하여 신속하고 정확하게 분석할 수 있는 X-선 형광분석용 표준물질 12종을 제작하였다. 특히 매질효과 제거, 보관성, 균질성 등을 고려하면서 융제 ($Li_2B_4O_7+LiBO_2$)로 시료를 16배 희석하여 제작 하였다. 티타늄을 비롯한 몇 원소는 매트릭스의 영향을 받는 것으로 보여 실험 계수법을 사용하고 Lucas Tooth와 Price의 식을 이용해 매트릭스의 영향을 보정해 주었다. 세 곳의 분석기관에서 X-선 형광분광기로 12개의 표준물질에 포함된 15 원소에 대하여 검정곡선을 작성해 본 결과 BaO, PbO, SrO, $Fe_2O_3$, $La_2O_3$, $SnO_2$, ZnO, $ZrO_2$, CaO들은 correlation factor가 0.995를 넘는 아주 좋은 곡선을 얻었다. $SiO_2$와 $Al_2O_3$는 X-선 형광세기도 약하고 correlation factor가 낮은 검정 곡선을 보였다.

• 광물과 암석
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• 제35권2호
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• pp.83-100
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• 2022

Zhenzigou 연-아연 광상은 중국 동북지역에선 가장 규모가 큰 연-아연 광상 중의 하나로 지체구조상 Jiao Liao Ji belt내 Qingchengzi mineral field에 위치한다. 이 광상의 주변지질은 시생대의 그래뉼라이트(granulite)와 이를 관입한 고원생대의 미그마타이트질 화강암과 고-중원생대의 소딕(sodic) 화강암을 부정합으로 피복한 고원생대의 Liaohe 층군 및 이들을 관입한 중생대의 섬록암과 몬조나이틱 화강암으로 구성된다. 이 광상은 고원생대의 Liaohe 층군내 Langzishan 층 및 Dashiqiao 층내에서 층상 광체 및 맥상 광체로 산출되며 층준규제 퇴적분기형 또는 퇴적분기형 광상에 해당된다. 이 광상에서 산출되는 백색운모는 층상 광체에서만 산출되며 모암의 종류, 변질 정도, 광석광물의 유무 및 광체 형태에 따라 4 가지 형(I 형 백색운모 : 약변질(쇄설성 돌로마이트질 대리암), II 형 백색운모 : 강변질(돌로마이트질 쇄설성 암석), III 형 백색운모 : 층상광체(돌로마이트질 쇄설성 암석), IV 형 백색운모 : 층상 광체(쇄설성 돌로마이트질 대리암))으로 분류된다. I 형 백색운모는 약 변질정도를 갖는 쇄설성 돌로마이트질 대리암내 돌로마이트를 열수교대작용에 의한 돌로마이트화작용에 의해 형성된 돌로마이트와 함께 산출된다. II 형 백색운모는 강 변질정도를 갖는 돌로마이트질쇄설성 암석내 열수교대작용에 의한 칼리장석의 변질물이나 돌로마이트화작용에 의해 형성된 돌로마이트, 철백운석, 석영과 함께 산출된다. III 형 백색운모는 층상 광체를 갖는 돌로마이트질 쇄설성 암석내 열수교대작용에 의한 칼리장석의 변질물이나 돌로마이트화작용에 의해 형성된 철백운석, 방해석, 석영과 함께 산출된다. IV 형 백색운모는 층상 광체를 갖는 쇄설성 돌로마이트질 대리암내 열수교대작용에 의한 칼리장석의 변질물이나 돌로마이트, 석영과 함께 산출된다. 이들 백색운모의 화학조성은 각각 (K_0.92-0.80Na_0.01-0.00Ca_0.02-0.01Ba_0.00Sr_0.01-0.00)_0.95-0.83(Al_1.72-1.57Mg_0.33-0.20Fe_0.01-0.00Mn_0.00Ti_0.02-0.00Cr_0.01-0.00V_0.00Sb_0.02-0.00Ni_0.00Co_0.02-0.00)_1.99-1.90(Si_3.40-3.29Al_0.71-0.60)_4.00O₁₀(OH_2.00-1.83F_0.17-0.00)_2.00, (K_1.03-0.84Na_0.03-0.00Ca_0.08-0.00Ba_0.00Sr_0.01-0.00)_1.08-0.85(Al_1.85-1.65Mg_0.20-0.06Fe_0.10-0.03Mn_0.00Ti_0.05-0.00Cr_0.03-0.00V_0.01-0.00Sb_0.02-0.00Ni_0.00Co_0.03-0.00)_1.99-1.93(Si_3.28-2.99Al_1.01-0.72)_4.00O₁₀(OH_1.96-1.90F_0.10-0.04)_2.00, (K_1.06-0.90Na_0.01-0.00Ca_0.01-0.00Ba_0.00Sr_0.02-0.01)_1.10-0.93(Al_1.93-1.64Mg_0.19-0.00Fe_0.12-0.01Mn_0.00Ti_0.01-0.00Cr_0.01-0.00V_0.00Sb_0.00Ni_0.00Co_0.05-0.01)_2.01-1.94(Si_3.32-2.96Al_1.04-0.68)_4.00O₁₀(OH_2.00-1.91F_0.09-0.00)_2.00 및 (K_0.91-0.83Na_0.02-0.01Ca_0.02-0.00Ba_0.01-0.00Sr_0.00)_0.93-0.83(Al_1.84-1.67Mg_0.15-0.08Fe_0.07-0.02Mn_0.00Ti_0.04-0.00Cr_0.06-0.00V_0.02-0.00Sb_0.02-0.01Ni_0.00Co_0.00)_2.00-1.92(Si_3.27-3.16Al_0.84-0.73)_4.00O₁₀(OH_1.97-1.88F_0.12-0.03)_2.00 로써 이론적인 이중팔면체형 운모류 값보다 Si가 높고 K, Na, Ca는 낮으며 모두 백운모에 해당된다. 특히, Zhenzigou 연-아연 광상에서 산출되는 백색운모의 화학조성 변화는 팬자이틱 또는 Tschermark 치환[(Al³⁺)^VI+(Al³⁺)^IV <-> (Fe²⁺ 또는 Mg²⁺)^VI+(Si⁴⁺)^IV] 메카니즘에 의해 일어났으며 백색운모의 Fe는 Fe²⁺와 Fe³⁺ 로써 존재하지만 주로 Fe²⁺ 우세함을 의미한다. 따라서 Zhenzigou 연-아연 광상의 층상 광체에서 산출되는 백색운모들은 고원생대의 화성활동 및 녹색편암상의 변성작용에 의한 열수교대작용으로 기존에 산출되었던 광물들의 재용융 및 재침전 과정에서 형성되었으며 이들 백색운모의 화학조성 변화는 열수교대작용 동안 모암인 돌로마이트 및 쇄설성 암석의 함량 차이, 변질 정도 및 광석광물의 유무에 따른 팬자이틱 또는 Tschermark 치환[(Al³⁺)^VI+(Al³⁺)^IV <-> (Fe²⁺ 또는 Mg²⁺)^VI+(Si⁴⁺)^IV] 메카니즘에 의해 일어났음을 알 수 있다.

• 암석학회지
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• 제27권1호
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• pp.37-47
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• 2018

백두산에서 역사시대에 분화한 화산재의 시료에 대하여 다양한 방법으로 주성분과 미량성분을 분석하였다. 화산재의 주성분 원소 함량은 $SiO_2$ 58.8~71.1 wt.%, $Al_2O_3$ 9.6~16.8 wt.%, ${Fe_2O_3}^T$ 4.5~6.9 wt.%, MgO 0.1~1.7 wt.%, CaO 0.3~1.6 wt.%, $Na_2O$ 5.2~6.3 wt.%, $K_2O$ 4.3~5.9 wt.% 그리고 $TiO_2$ 1.2 wt.%이하로 분석되었다. Ba, Cu, Cr. Co, Ni, Sr, V, Zn와 Zr을 포함하는 32개 미량원소가 분석되었는데, 이들 화산재는 일부 미량원소와 경희토류 원소의 부화정도에 따라 두 그룹(그룹 A, 그룹 B)으로 구분되며, 그룹 A에는 1천년 전의 밀레니엄 분화물, 1668년과 1903년 분화물이, 그룹 B에는 1702년 분화물이 해당된다. 중금속원소인 Cu, Co, Zn, Mn 등은 소량 함유되어 나타난다. 백두산 화산재는, 섭입대 기원의 일본 사쿠라지마 화산의 화산재와 비교하여, 미량성분원소 중 Y, Nb, Pb, U, Sc, V, Ni 그리고 Cu 함량은 낮게 나타나며, Zr, Ba, Hf, Cr, Co, Zn 그리고 희토류(Eu제외) 등은 높은 함량을 나타낸다.

• 자원환경지질
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• 제25권1호
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• pp.27-39
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• 1992

Several pyrophyllite deposits occur around the Milyang area where Cretaceous andesitic rocks and spatially related granitic rocks are widely distributed. Pyrophyllite ores consist mainly of pyrophyllite, and quartz with small amount of sericite, pyrite, dumortierite, and diaspore. The andesitic rocks and spatially related granitic rocks in this area suggest that they could be formed from the same series of a calc-alkaline magma series. The contents of $SiO_2$, $Al_2O_3$, LOI(loss on ignition) are enriched, and $K_2O$, $Na_2O$, CaO, MgO, $Fe_2O_3$ are depleted in altered andesitic rocks and ores. Enrichment of As, Cr, Sr, V, Sb and depletion of Ba, Cs, Ni, Rb, U, Y, Co, Sc, Zn are characteristic during mineralization. The pyrophyllite ores can be discriminated from the altered-and unaltered wall-rocks by an increasing of $(La/Lu)_{cn}$ from 4.18~22.13 to 8.98~55.05. In R-mode cluster analysis, Yb-Lu-Y, La-Ce-Hf-Th-U-Zr, $TiO_2-V-Al_2O_3$, Sm-Eu, $CaO-Na_2O-MnO$, Cu-Zn-Ag, $K_2O-Rb$ are closely correlated. In the discriminant analysis of multi-element data, $P_2O_5$, As, Cr and $Fe_2O_3$, Sr are helpful to identify the ores from the unaltered-and altered wall-rocks. In the factor analysis, the factors of alteration of andesitic rocks and ore mineralization were extracted. In the change of ions per unit volume, $SiO_2$, $Al^{3+}$ and LOI are enriched and $Na^+$, $K^+$, $Ca^{2+}$, $Mg^{2+}$, $Mn^{2+}$ and $Fe^{3+}$ are depleted during the alteration processes. The Milyang and the Sungjin pyrophyllite deposits could be mineralized by hydrothermal alteration in a geochemical condition of low activity ratio of alkaline ions to hydrogen ion with reference to spatially related granitic rocks.