• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2001년도 추계학술강연 및 발표대회
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• pp.7-7
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• 2001

The increasing interest in light weight materials coupled to the need for cost -effective processing have combined to create a significant opportunity for aluminum P/M. particularly in the automotive industry in order to reduce fuel emissions and improve fuel economy at affordable prices. Additional potential markets for Al PIM parts include hand tools. Where moving parts against gravity represents a challenge; and office machinery, where reciprocating forces are important. Aluminum PIM adds light weight, high compressibility. low sintering temperatures. easy machinability and good corrosion resistance to all advantages of conventional iron bm;ed P/rv1. Current commercial alloys are pre-mixed of either the AI-Si-Mg or AL-Cu-Mg-Si type and contain 1.5% ethylene bis-stearamide as an internal lubricant. The powder is compacted in closed dies at pressure of 200-500Mpa and sintered in nitrogen at temperatures between $580~630^{\circ}C$ in continuous muffle furnace. For some applications no further processing is required. although most applications require one or more secondary operations such as sizing and finishing. These sccondary operations improve the dimension. properties or appearance of the finished part. Aluminum is often considered difficult to sinter because of the presence of a stable surface oxide film. Removal of the oxide in iron and copper based is usually achieved through the use of reducing atmospheres. such as hydrogen or dissociated ammonia. In aluminum. this occurs in the solid st,lte through the partial reduction of the aluminum by magncsium to form spinel. This exposcs the underlying metal and facilitates sintering. It has recently been shown that < 0.2% Mg is all that is required. It is noteworthy that most aluminum pre-mixes contain at least 0.5% Mg. The sintering of aluminum alloys can be further enhanced by selective microalloying. Just 100ppm pf tin chnnges the liquid phase sintering kinetics of the 2xxx alloys to produce a tensile strength of 375Mpa. an increilse of nearly 20% over the unmodified alloy. The ductility is unnffected. A similar but different effect occurs by the addition of 100 ppm of Pb to 7xxx alloys. The lend changes the wetting characteristics of the sintering liquid which serves to increase the tensile strength to 440 Mpa. a 40% increase over unmodified aIloys. Current research is predominantly aimed at the development of metal matrix composites. which have a high specific modulus. good wear resistance and a tailorable coefficient of thermal expnnsion. By controlling particle clustering and by engineering the ceramic/matrix interface in order to enhance sintering. very attractive properties can be achicved in the ns-sintered state. I\t an ils-sintered density ilpproaching 99%. these new experimental alloys hnve a modulus of 130 Gpa and an ultimate tensile strength of 212 Mpa in the T4 temper. In contest. unreinforcecl aluminum has a modulus of just 70 Gpa.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2002년도 제3회 최신 분말제품 응용기술 Workshop
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• pp.25-37
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• 2002

The most important industrial application of gamma radiation in characterizing green compacts is the determination of the density. Examples are given where this method is applied in manufacturing technical components in powder metallurgy. The requirements imposed by modern quality management systems and operation by the workforce in industrial production are described. The accuracy of measurement achieved with this method is demonstrated and a comparison is given with other test methods to measure the density. The advantages and limitations of gamma ray densitometry are outlined. The gamma ray densitometer measures the attenuation of gamma radiation penetrating the test parts (Fig. 1). As the capability of compacts to absorb this type of radiation depends on their density, the attenuation of gamma radiation can serve as a measure of the density. The volume of the part being tested is defined by the size of the aperture screeniing out the radiation. It is a channel with the cross section of the aperture whose length is the height of the test part. The intensity of the radiation identified by the detector is the quantity used to determine the material density. Gamma ray densitometry can equally be performed on green compacts as well as on sintered components. Neither special preparation of test parts nor skilled personnel is required to perform the measurement; neither liquids nor other harmful substances are involved. When parts are exhibiting local density variations, which is normally the case in powder compaction, sectional densities can be determined in different parts of the sample without cutting it into pieces. The test is non-destructive, i.e. the parts can still be used after the measurement and do not have to be scrapped. The measurement is controlled by a special PC based software. All results are available for further processing by in-house quality documentation and supervision of measurements. Tool setting for multi-level components can be much improved by using this test method. When a densitometer is installed on the press shop floor, it can be operated by the tool setter himself. Then he can return to the press and immediately implement the corrections. Transfer of sample parts to the lab for density testing can be eliminated and results for the correction of tool settings are more readily available. This helps to reduce the time required for tool setting and clearly improves the productivity of powder presses. The range of materials where this method can be successfully applied covers almost the entire periodic system of the elements. It reaches from the light elements such as graphite via light metals (AI, Mg, Li, Ti) and their alloys, ceramics ($AI_20_3$, SiC, Si_3N_4, $Zr0_2$, ...), magnetic materials (hard and soft ferrites, AlNiCo, Nd-Fe-B, ...), metals including iron and alloy steels, Cu, Ni and Co based alloys to refractory and heavy metals (W, Mo, ...) as well as hardmetals. The gamma radiation required for the measurement is generated by radioactive sources which are produced by nuclear technology. These nuclear materials are safely encapsulated in stainless steel capsules so that no radioactive material can escape from the protective shielding container. The gamma ray densitometer is subject to the strict regulations for the use of radioactive materials. The radiation shield is so effective that there is no elevation of the natural radiation level outside the instrument. Personal dosimetry by the operating personnel is not required. Even in case of malfunction, loss of power and incorrect operation, the escape of gamma radiation from the instrument is positively prevented.

• 자원환경지질
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• 제30권5호
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• pp.417-431
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• 1997

Characteristics of sedimentary rocks and enrichment of toxic elements in shale and coal from the Chungnam coal field were investigated based upon geochemistry of major, trace and rare earth elements. Shale and coal of the area are interbedded along the Traissic to the Jurassic Daedong Supergroup, which can be subdivided into grey shale, black shale and coal. The coal had been mined, however all the mines are abandonded due to the economic problems. The shale and coal are characterized by relatively low contents of $SiO_2$, and $Al_2O_3$ and high levels of loss-on-ignition (LOI), CaO and $Na_2O$ in comparison with the North American Shale Composite (NASC). Light rare earth elements (La, Ce, Yb and Lu) are highly enriched with the coal. Ratios of $Al_2O_3/Na_2O$ and $K_2O/Na_2O$ in shale and coal range from 30.0 to 351.8 and from 4.2 to 106.8, which have partly negative correlations against $SiO_2/Al_2O_3$ (1.24 to 6.06), respectively. Those are suggested that controls of mineral compositions in shale and coal can be due to substitution and migration of those elements by diagenesis and metamorphism. Shale and coal of the area may be deposited in terrestrial basin deduced from high C/S (39 to 895) and variable composition of organic carbon (0.39 to 18.40 wt.%) and low contents of reduced sulfur (0.01 to 0.05 wt.%). These shale and coal were originated from the high grade metamorphic and/or igneous rocks, and the rare earth elements of those rocks are slightly influenced with diagenesis and metamorphism on the basis of $Al_2O_3$ versus La, La against Ce, Zr versus Yb, the ratios of La/Ce (0.38 to 0.85) and Th/U (3.6 to 14.6). Characteristics of trace and rare earth elements as Co/Th (0.07 to 0.86), La/Sc (0.31 to 11.05), Se/Th (0.28 to 1.06), V/Ni (1.14 to 3.97), Cr/V (1.4 to 28.3), Ni/Co (2.12 to 8.00) and Zr/Hf (22.6~45.1) in the shale and coal argue for inefficient mixing of the simple source lithologies during sedimentation. These rocks also show much variation in $La_N/Yb_N$ (1.36 to 21.68), Th/Yb (3.5 to 20.0) and La/Th (0.31 to 7.89), and their origin is explained by derivation from a mixture of mainly acidic igneous and metamorphic rocks. Average concentrations in the shale and coal are As=7.2 and 7.5, Ba=913 and 974, Cr=500 and 145, Cu=20 and 26, Ni=38 and 35, Pb=30 and 36, and Zn=77 and 92 ppm, respectively, which are similar to those in the NASC. Average enrichment indices for major elements in the shale (0.79) and coal (0.77) are lower than those in the NASC. In addition, average enrichment index for rare earth elements in coal (2.39) is enriched rather than the shale (1.55). On the basis of the NASC, concentrations of minor and/or environmental toxic elements in the shale and coal were depleted of all the elements examined, excepting Cr, Pb, Rb and Th. Average enrichment indices of trace and/or potentially toxic elements (As, Cr, Cu, Ni, Pb, U and Zn) are 1.23 to 1.24 for shale and 1.06 to 1.22 for coal, respectively.

• 한국자기학회지
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• 제25권3호
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• pp.67-73
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• 2015

본 연구는 철기(Fe based) $Fe_{73.5}Si_{13.5}B_9Nb_3Cu_1$ 나노결정 합금의 분말코어(powder core)의 연자기적 특성 향상을 위한 기초연구로서, 절연 코팅제의 첨가량 및 분말입도에 따른 투자율, 코어손실 및 DC 바이어스 특성을 주로 조사하였다. 우선 합금조성을 PFC 장치를 이용하여 비정질 합금리본을 제조한 후, 열처리, 미분쇄 및 분급하여 얻어진 합금분말에 절연 코팅제(PEI)의 첨가량을 0.5, 1.0, 2.0, 2.5 wt%로 변화시켜 $16ton/cm^2$으로 압축성형 및 결정화 열처리하여 제조한 토로이달 나노결정 분말코어($OD12.7mm{\times}ID7.62mm{\times}H4.75mm$)는 절연 코팅제 함량이 증가할수록 투자율은 감소하였지만, 코어손실 및 DC 바이어스 특성은 향상됨을 확인하였다. 이러한 이유는 합금분말 절연 코팅제 첨가량이 증가할수록 비정질 합금분말 입자가 적어져 분말코어의 성형밀도가 낮아지기 때문으로 추정되었으며, 절연 코팅제의 함량은 1 wt%가 가장 적합한 것으로 판단되었다. 또한 절연 코팅제 함량을 1 wt%로 고정하고, 합금분말의 입도에 따라 제조한 분말코어의 경우, 실효투자율 및 코어손실은 입도가 클수록 우수하였지만, DC 바이어스 특성은 인가자장이 증가함에 따라 더욱 나빠짐을 확인하였다. 그 이유는 합금분말 표면의 코팅층 두께 차이에 의한 절연효과, 잔류기공 혹은 분말코어의 성형밀도 차이 등에 기인하는 것으로 추정되었다.

• Journal of Microbiology and Biotechnology
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• 제20권6호
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• pp.1011-1017
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• 2010

A novel dioscin-glycosidase that specifically hydrolyzes multi-glycosides, such as 3-O-${\alpha}$-L-($1{\to}4$)-rhamnoside, 3-O-${\alpha}$-L-($1{\to}2$)-rhamnoside, 3-O-${\alpha}$-L-($1{\to}4$)-arabinoside, and ${\beta}$-D-glucoside, on diosgenin was isolated from the Absidia sp.d38 strain, purified, and characterized. The molecular mass of the new dioscin-glycosidase is about 55 kDa based on SDS-PAGE. The dioscin-glycosidase gradually hydrolyzes either 3-O-${\alpha}$-L-($1{\to}4$)-Rha or 3-O-${\alpha}$-L-($1{\to}2$)-Rha from dioscin into 3-O-${\alpha}$-L-Rha-${\beta}$-D-Glc-diosgenin, further rapidly hydrolyzes the other ${\alpha}$-L-Rha from 3-O-${\alpha}$-L-Rha-${\beta}$-D-Glc-diosgenin into the main intermediate products of 3-O-${\beta}$-D-Glc-diosgenin, and subsequently hydrolyzes these intermediate products into aglycone as the final product. The enzyme also gradually hydrolyzes 3-O-${\alpha}$-L-($1{\to}4$)-arabinoside, 3-O-${\alpha}$-L-($1{\to}2$)-rhamnoside, and ${\beta}$-D-glucoside from [3-O-${\alpha}$-L-($1{\to}4$)-Ara, 3-O-${\alpha}$-L-($1{\to}4$)-Rha]-${\beta}$-D-Glc-diosgenin into diosgenin as the final product, exhibiting significant differences from previously reported glycosidases. The optimal temperature and pH for the new dioscin-glycosidase is $40^{\circ}C$ and 5.0, respectively. Whereas the activity of the new dioscin-glycosidase was not affected by $Na^+$, $K^+$, and $Mg^{2+}$ ions, it was significantly inhibited by $Cu^{2+}$ and $Hg^{2+}$ ions, and slightly affected by $Ca^{2+}$ ions.

• 대한화학회지
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• 제33권4호
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• pp.366-370
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• 1989

새로운 거대고리 리간드 1,15,18-triaza-3,4 : 12,13-dibenzo-5,8,11-trioxa-cycloeicosane(NdienOdien$H_4$=$N_3O_3$)를 합성하여 $25^{\circ}C$ 95% 메탄올 용액에서 전위차계를 이용하여 양성자 첨가반응의 평형상수를 구한 결과 log $K_1$ ; log $K_2$ ; log $K_3$는 9.1; 8.1; 3.6이었다. 또한 위의 리간드와 이미 합성된 리간드 1,12,15-triaza-3,4;9,10-dibenzo-5,8-dioxa-cycloheptadecane(NdienOen$H_4$=$N_3O_2$)를 각각 Ni(II), Cu(II)의 금속이온과의 착물을 합성하여 수용액에서 산을 가해 착물의 산해리반응 속도 상수를 여러온도에서 분광광도법으로 측정하였다. 또한 활성화에너지($E_a$)와 활성화파라메타 ${\Delta}H^{\neq}$, ${\Delta}S^{\neq}$를 구하였다. 그리고 이들의 자료로부터 이 반응계의 타당한 해리메카니즘을 제안하였다.

• Journal of the Korean Wood Science and Technology
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• 제38권1호
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• pp.75-84
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• 2010

본 연구는 채취 지역 및 시기별 고로쇠나무(Acer mono) 수액의 저장기간에 따른 수액의 물성을 분석하여, 저장기간이 수액의 물성에 미치는 영향을 확인하기 위하여 수행하였다. 고로쇠나무 수액의 pH는 4.43~5.68로 함양산이 가장 낮고 남양주산이 가장 높았으나 저장기간이 길어짐에 따라 급격히 낮아졌다. 영월산 2월 22일 채취분에서 수액의 sucrose 함량이 2.06%로 가장 높았으나 4개월이 지나면서 급격히 분해되었다. Sucrose의 분해는 유기산함량의 증가에 큰 영향을 끼쳤으며 pyruvic acid가 최대 14.26 mg/$m{\ell}$까지 생성되었고, lactic acid, acetic acid, ethanol 등의 미생물의 대사산물로 여겨지는 유기산들이 발생하였다. 미량원소는 K, Ca가 93% 정도로 대부분을 차지하였으며 인제산 고로쇠나무의 전기 채취 수액의 K함량이 131.72 mg/${\ell}$로 특히 높았다. 수액 내에 특수성분으로써 비타민 C는 1.55~3.50 mg/${\ell}$ 함유되어 있음을 확인할 수 있었다. 수액의 물성은 저장기간이 늘어남에 따라 점점 변질되었지만, 지역별 전기 채취 수액의 sucrose 분해나 유기산 생성이 후기 채취 수액에 비해 상대적으로 덜 발생하였다.

• 대한금속재료학회지
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• 제48권6호
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• pp.523-532
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• 2010

Co-application of organic coating and cathodic protection has not provided enough durability to low-alloyed steels inseawater ballast tank (SBT) environments. An attempt has made to study the effect of alloy elements (Al, Cr, Cu, Mo, Ni, Si, W) on general and localized corrosion resistance of steels as basic research to develop new low-allowed steels resistive to corrosion in SBT environments. For this study, we measured the corrosion rate by the weigh loss method after periodic immersion in synthetic seawater at $60^{\circ}C$, evaluated the localized corrosion resistance by an immersion test in concentrated chloride solution with the critical pH depending on the alloy element (Fe, Cr, Al, Ni), determined the permeability of chloride ion across the rust layer by measuring the membrane potential, and finally, we analyzed the rust layer by EPMA mapping and compared the result with the E-pH diagram calculated in the study. The immersion test of up to 55 days in the synthetic seawater showed that chromium, aluminium, and nickel are beneficial but the other elements are detrimental to corrosion resistance. Among the beneficial elements, chromium and aluminium effectively decreased the corrosion rate of the steels during the initial immersion, while nickel effectively decreased the corrosion rate in a longer than 30-day immersion. The low corrosion rate of Cr- or Al-alloyed steel in the initial period was due to the formation of $Cr_2FeO_4$ or $Al_2FeO_4$, respectively -the predicted oxide in the E-pH diagram- which is known as a more protective oxide than $Fe_3O_4$. The increased corrosion rate of Cr-alloyed steels with alonger than 30-day exposure was due to low localized corrosion resistance, which is explained bythe effect of the alloying element on a critical pH. In the meantime, the low corrosion rate of Ni-alloyed steel with a longer than 30-day exposure wasdue to an Ni enriched layer containing $Fe_2NiO_4$, the predicted oxide in the E-pH diagram. Finally, the measurement of the membrane potential depending on the alloying element showed that a lower permeability of chloride ion does not always result in higher corrosion resistance in seawater.

• 전기화학회지
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• 제8권4호
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• pp.172-176
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• 2005

차세대 5V급 양극활물질로 각광받고 있는 $LiNi_{0.5}Mn_{1.5}O_4$는 기존의 $LiMn_2O_4$ spinel 물질의 $Mn^{3+}$을 $Ni^{2+}$으로 치환하여 5V 영역에서 $Ni^{2+}/Ni^{4+}$ 산화/환원 반응이 가능하게 한 물질이다. 기존의 $LiMn_2O_4$는 낮은 초기 용량과 충 방전에 따른 빠른 용량감소를 보이는 단점을 가지고 있어 이 문제를 극복하기 위해 Mn의 일부를 다른 금속으로 치환하여 $LiM_yMn_{2-y}O_4$ (M=Cr, Al, Ni, Fe, Co, Cu, Ca)을 만드는 방법이 활발히 연구되고 있다. 본 연구에서는 기계 화학적 합성법을 이용하여 합성한 $LiNi_{0.5}Mn_{1.5}O_4$의 전기화학적 특성에 대해 연구하였다. 이 물질은 기존의 $LiMn_2O_4$보다 에너지 밀도가 높으며 저가 및 친환경성 등으로 앞으로 HEV 등에서 그 활용성이 크게 기대된다. 볼밀을 이용하여 여러가지 조건(출발물질 조건, 볼밀조건, 열처리조건 등)에서 $LiNi_{0.5}Mn_{1.5}O_4$을 합성한 결과 기계화학적 방법으로는 $Ni^{2+}$가 $Mn^{3+}$를 완전히 치환하지 못하여 $4.0{\sim}4.1V$의 전압에서 $Mn^{3+}/Mn^{4+}$의 산화/환원과 관련된 peak가 발생하였다. Ni 원료 물질로써 수산화 물질을 사용하고 열처리 온도를 $800^{\circ}C$로 하였을 때 최상의 성능을 나타내었다.

• 자원환경지질
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• 제22권1호
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• pp.35-63
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• 1989

구룡산(九龍山)(또는 옥천(沃川)) 함(含)우라늄 흑연질점판암(黑鉛質粘板岩)은 옥천대(沃川帶) 서북부(西北部)에 따라 증상(層狀) 또는 부딘상(狀)으로 90km이상(以上) 연장(延長) 분포(分布)한다. 함(含)우라늄점판암(粘板岩)의 오토레디오그라프에 나타나는 퇴적(堆積), 속성(續成), 변성구조(變成構造)는 우라늄과 동시퇴적물(同時堆積物)로서 속성작용과정(續成作用過程)에서 전혀 이동(移動)하지 않고 황성변성(廣域變成) 초기(初期)에 제자리에서 미립(微粒)우라니나이트로 재결정(再結晶)하였음을 보여준다. 동시(同時)에 유기물(有機物)은 미세환장흑연(微細環狀黑鉛)으로 되었다. 라미나구조(構造)의 발달(發達)과 평균(平均) 19.64% C, 2.32% S의 함유(含有)는 함(含)우라늄흑니(黑泥) 퇴적(堆積)의 일반조건(一般條件)으로서의 극(極)히 낮은 퇴적화(堆積比), 고유기물함유(高有機物含有), 염기성황경등을 충족(充足)하였으며 Th/U가 0.07로서 해수원(海水源)임을 뜻한다. 지역별(地域別) CaO, $P_2O_5$의 평균치(平均値)가 매우좁은 범위(範圍)의 일정치(一定値)이며 높은 CaO 평균치(平均値)를 나타내어 전퇴적(全堆積)분지를 통(通)하여 동일(同一) pH(7.8-8.0)조건(條件)의 환경(環境)에서 퇴적(堆積)하였음을 나타낸다. 함(含)우라늄점판암(粘板岩)은 같은 성인(成因)의 타산장(他産狀)에 비(比)하여 미량원소(微量元素) 부화도(富化度)가 매우 높다. 고부화(高富化)의 중요(重要)한 원인(原因)으로서 미량원소(微量元素)의 소스(source)인 해수(海水)의 주기적(週期的) 교체(交替)가 요구(要求)되는데 사이크릭퇴적구조(堆積構造)는 그러한 현상(現象)을 뒷받침하여 준다. 흑니(黑泥)의 성인별(成因別) 구성광물(構成鑛物)과 원소(元素)의 수반관계(隨伴關係)에서 쇄설성광물(鑛物)에는 Si, Al, K, Na, Ti, Zr, Th, Be, B, Li, 유기물(有機物)후락숀에, U, Ni, Cu, Co, Zn, Ag, Mo, Pb, Sn, Cd, S, Fe, V, Cr, Y, 탄산염광물(炭酸鹽鑛物)에 Ca, Mg, Mn, P, Ba가 높은 상관(相關)을 나타낸다. 유기물(有機物)의 우라늄고정심전능력(固定沈澱能力)에 있어 사프로페릭(Sapropelic)형(型)보다 휴믹(Humic)형(型)에서 더 높다. 육성식물(陸性植物)의 분해물(分解物)인 휴무스(Humus)는 고대성(古生代) 중기(中期)에 출현(出現)한다. 우라늄 함유(含有) 흑니(黑泥)는 이 시대(時代)의 형성물(形成物)로서 이런 형(型)의 광상(鑛床)은 생물상(生物相)의 진화(進化)에 규제(規制)된 광화작용(鑛化作用)의 산물(産物)이다.