• 제목/요약/키워드: eutectic

검색결과 741건 처리시간 0.025초

LiCl-KCl 공융염 내에서 희토류염화물들의 침전 (Precipitation of Rare Earth Chlorides in a LiC-KCl Eutectic Molten Salt)

  • 조용준;양희철;은희철;김응호;김인태
    • 공업화학
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    • 제18권4호
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    • pp.361-365
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    • 2007
  • LiCl-KCl 공융염 내 존재하는 몇가지 희토류염화물($Ce/Nd/GdCl_3$)들의 산소와의 반응으로 인한 침전반응에 대한 연구를 수행하였다. 산소와의 반응으로 형성되는 희토류침전물의 형태와 산소분산 시간(최대 420 min) 및 공융염($450{\sim}750^{\circ}C$) 온도가 침전물로의 전환율에 미치는 영향을 규명하였다. 본 연구결과 산소분산 시간 및 공융염의 온도와 무관하게 $NdCl_3$$GdCl_3$는 옥시염화물(REOCl), $CeCl_3$는 산화물($REO_2$)형태로 침전되었으며 이러한 실험결과는 반응 Gibbs free energy (${\Delta}G_r$) 를 이용한 예측 결과와도 일치하였다. 희토류염화물의 침전물로의 전환특성은 전환율 개념을 도입하여 파악하였다. 전환율은 산소분산 시간이 증가함에 따라서 지수적으로 증가하였으며 $750^{\circ}C$의 공융염 온도 및 300 min 이상의 분산시간 조건에서 0.999 이상의 전환율을 나타내었다. 공융염 온도가 증가함에 따라서 전환율이 증가하였다. Ce의 경우에는 60 min 이상의 산소분산 조건에서 전 실험온도 범위에서 0.999 이상의 일정한 전환율을 나타내었다

은계(BAg) 삽입금속으로 접합된 초경합금 입자와 탄소강 브레이징부의 특성 (Characteristics of the Brazed Joint between Superhard Alloy Particles and Carbon Steel Using BAg System Insert Metals.)

  • 김광수;김상덕
    • 한국산학기술학회논문지
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    • 제9권2호
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    • pp.298-302
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    • 2008
  • 초경합금입자와 탄소강사이의 브레이징 접합부 특성을 평가하였다 선택된 두 종류의 삽입금속은 기계적 합금 공정으로 만들어졌다. 한 가지는 Cu, Zn, Ag (MIM-1) 그리고 다른 한 가지는 Cu, Zn, Ag과 Cd(MIM-2)로 구성하였다. 삽입금속들의 화학조성은 AWS BAg-20계와 BAg-2a계의 성분과 유사하였다. 그리고 상용삽입금속들(CIM-1, CIM-2) 역시 비교 평가하였다. 삽입금속들의 특성은 젖음성 시험, 전단강도 시험, 그리고 미세조직 관찰로서 나타내었다. 젖음성 시험에서 MIM-1과 CIM-1 삽입금속의 젖음각이 MIM-2와 CIM-2보다 크게 나타났고, MIM-1의 젖음각이 CIM-1보다 더 큰 값을 나타났지만 모든 경우 젖음각이 $25^{\circ}$보다 작았다. 삽입금속, MIM-1이 가장 높은 전단강도를 나타냈고, 그 값은 $2.29{\times}10^2MPa$로 측정되었다. 이 값은 상용 삽입금속의 값과 같거나 높은 것으로 나타났다. 삽입금속의 미세조직은 Cu-rich 초정영역과 Ag-rich 공정영역으로 구성되었다. MIM-1계로 만들어진 초경합금과 탄소강의 접합부는 일부 접합부 계면에 기공을 포함하지만 초정을 기지로 하는 안정적인 미세조직을 나타냈다.

Topical EMLA Cream as a Pretreatment for Facial Lacerations

  • Park, Sung Woo;Oh, Tae Suk;Choi, Jong Woo;Eom, Jin Sup;Hong, Joon Pio;Koh, Kyung S.;Lee, Taik Jong;Kim, Eun Key
    • Archives of Plastic Surgery
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    • 제42권1호
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    • pp.28-33
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    • 2015
  • Background Topical anesthetics, such as eutectic mixture of local anesthetics (EMLA) cream, can be applied to reduce pain before minor procedure. This trial evaluated EMLA as pretreatment for facial lacerations and compared pain, discomfort and overall satisfaction. Methods This trial included consecutive emergency department patients ${\geq}16years$ of age who presented with simple facial lacerations. At triage, lacerations were allotted to either the routine processing group or EMLA pretreatment group according to date of admission. Initially, the emergency department doctors inspected each laceration, which were dressed with saline-soaked gauze. In the pretreatment group, EMLA cream was applied during wound inspection. The plastic surgeon then completed primary closure following the local injection of an anesthetic. After the procedure, all patients were given a questionnaire assessing pain using the 10-point visual analog scale (VAS) ("no pain" to "worst pain"). All questionnaires were collected by the emergency department nurse before discharge. Results Fifty patients were included in the routine processing group, and fifty patients were included in the EMLA pretreatment group. Median age was 39.9 years, 66% were male, and the average laceration was 2.67 cm in length. The EMLA pretreatment group reported lower pain scores in comparison with the routine processing group (2.4 vs. 4.5 on VAS, P<0.05), and lower discomfort scores during the procedure (2.0 vs. 3.3, P=0.60). Overall satisfaction was significantly higher in the EMLA pretreatment group (7.8 vs. 6.1, P<0.05). Conclusions Pretreating facial lacerations with EMLA topical cream aids patients by reducing pain and further enhancing overall satisfaction during laceration treatment.

Sn-58Bi 솔더 페이스트와 ENIG 표면 처리된 기판 접합부의 계면 반응 및 접합강도 (Interfacial Reaction and Joint Strength of the Sn-58Bi Solder Paste with ENIG Surface Finished Substrate)

  • 신현필;안병욱;안지혁;이종근;김광석;김덕현;정승부
    • Journal of Welding and Joining
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    • 제30권5호
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    • pp.64-69
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    • 2012
  • Sn-Bi eutectic alloy has been widely used as one of the key solder materials for step soldering at low temperature. The Sn-58Bi solder paste containing chloride flux was adopted to compare with that using the chloride-free flux. The paste was applied on the electroless nickel-immersion gold (ENIG) surface finish by stencil printing, and the reflow process was then performed at $170^{\circ}C$ for 10 min. After reflow, the solder joints were aged at $125^{\circ}C$ for 100, 200, 300, 500 and 1000 h in an oven. The interfacial microstructures were obtained by using scanning electron microscopy (SEM), and the composition of intermetallic compounds (IMCs) was analyzed using energy dispersive spectrometer (EDS). Two different IMC layers, consisting of $Ni_3Sn_4$ and relatively very thin Sn-Bi-Ni-Au were formed at the solder/surface finish interface, and their thickness increased with increasing aging time. The wettability of solder joints was investigated by wetting balance test. The mechanical property of each aging solder joint was evaluated by the ball shear test in accordance with JEDEC standard (JESD22-B117A). The results show that the highest shear force was measured when the aging time was 100 h, and the fracture mode changed from ductile fracture to brittle fracture with increasing aging time. On the other hand, the chloride flux in the solder paste did not affect the shear force and fracture mode of the solder joints.

Dissolution Characteristics of Hydrophobic Drug-Soluble Carrier Coprecipitates(III) -Dissolution Behaviour of Indomethacin from Several Fast Release Solid Dispersions of Indomethacin-

  • 전인구;이민화;김신근
    • Journal of Pharmaceutical Investigation
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    • 제6권3호
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    • pp.58-69
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    • 1976
  • It is well established that dissolution is freruently the rate limiting step in the gastrointestinal absorpton of a drug from a solid dosage from. The relationship between the dissolution rate and absorption is particularly distinct when considering drugs of low solubility. Consequently, numerous attempts have been made to modify the dissolution characteristics of poorly water soluble drugs. Since dissolution rate is directly proportional to surface area, one may increase the rate by decreasing the particle size of the drug. Levy has considered a number of methods by which a drug may be presented to the GI fludids in finely divided from. The direct method is the utilization of microcrystalline or micronized particles. A second method involves the administration of solutions from which, upon dilution with gastric fluids, the dissolved drug will precipitate in the form of very fine particles. A more unique way of obtaining microcrystalline dispersions of a drug has been ercently suggested by Sekiguchi et al. They have first proposed the formation of a eutectic mixture of a poorly water soruble drug with a physiologically inert, easily soluble carrier. When such systems are exposed to water or GI fluids, the soluble carrier will dissolve rapidly and the finely dispersed drug particles will then be released. It has been suggested by Shefter and Higuchi that the formation of crystalline solvate could be a powerful tool in affecting rapid disslution of highly insoluble substances. Goldberg et al. have noted that the formation of solid solution could reduce the particle size to a minimum and increase the dissolution rate as well as the solubility of the durgs. It has also been shown that the rates of solution of drugs were appreciably increased by coprectipitating the drug with soluble polymers. The increase was found to be sensitive to the method of preparation, the molecular weight of polymer and the particular ratio of drugs to polymer. Although several investigations have demontrated that the solubility and/or dissolution rates of drugs can be increased in this manner, little information is available in the literature related to the in vivo absorption pattern of drugs orally administered as PVP coprecipitates. Recently, however, it was demonstrated that both the rate and extent of absorption of the insoluble drug could be markedly enhanced when orally administered to rats in the form of a coprecipitate with PVP. The purpose of the present investigation was to ascertain the general appility of soluble polymer coprectation technique as a method for enhancing the in vitro dissolution rate of hydrophobic indomethacin. To accomplish this aim, the dissolution characteristics of pure indomethacin, indomethcin-polymer physical mixtures and indomethacin-polymer coprecipitates were quantitatively studied by comparing their relative dissolution rates. The solubility and dissolution behavior of these systems were also examined.

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LiCl-KCl-UCl3-NdCl3 system에서 U 및 Nd 분리에 관한 기초연구 (A Basic Study on Separation of U and Nd From LiCl-KCl-UCl3-NdCl3 System)

  • 김택진;안도희;은희철;이성재
    • 방사성폐기물학회지
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    • 제16권1호
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    • pp.59-64
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    • 2018
  • 사용후핵연료을 건식처리하는 파이로프로세싱 중 전해정련 및 제련공정 후 발생되는 우라늄과 초우라늄 및 희토류 등의 염화물을 함유한 LiCl-KCl 공융염에는 특히 희토류 함량이 높기 때문에 유효자원으로 활용이 가능한 형태의 우라늄과 초우라늄의 분리/회수가 쉽지 않다. 이러한 문제점을 해결하기 위해 본 연구에서는 $LiCl-KCl-UCl_3-NdCl_3$ 시스템에서 산화제($K_2CO_3$)를 이용하여 $UCl_3$를 산화물 형태로 전환한 후 전기화학적 방법을 이용하여 $NdCl_3$를 금속형태로 분리하는 실험을 실시하였다. 실험에 앞서, 이론적 평형계산을 수행하여 우라늄 염화물을 산화물로 전환하기 위한 실험조건을 결정하였다. 상기의 실험에서 LiCl-KCl 내 $UCl_3$는 첨가제의 주입량이 이론적 반응당량에 근접하였을 때 거의 대부분이 염내에서 염화물 형태로 존재하지 않는 것으로 나타났다. 이후 액체금속음극을 이용하여 $NdCl_3$를 금속형태로 전착시켰으며, 전착실험 후 투명한 용융상의 LiCl-KCl 공융염과 갈색의 우라늄 산화침전물이 존재함이 확인되었다. 이러한 결과들을 통해 $LiCl-KCl-UCl_3-NdCl_3$ 시스템에서 우라늄 및 희토류를 각각 분리할 수 있는 방안을 수립할 수 있을 것으로 판단된다.

정전압 분극곡선법에 의한 아말감의 부식 거동에 관한 연구 (A STUDY ON THE CORROSION BEHAVIOUR OF AMALGAMS BY USING OF POTENTIOSTATIC POLARIZATION METHOD)

  • 신동훈;엄정문
    • Restorative Dentistry and Endodontics
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    • 제12권1호
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    • pp.39-49
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    • 1986
  • The purpose of this study was to observe characteristic properties through the polarization curves and SEM images from 4 different types of amalgam obtained by using the potentiostats (Princeton EG & G) & SEM (Jeol/35), and to investigate the degree of corrosion on the oxidation peak of the each phase of amalgam. After each amalgam alloy and Hg was triturated as the direction of the manufacturer by means of the mechanical amalgamator (Shofu Co.), the triturated mass was inserted into the cylindrical metal mold which was 12mm in diameter and 10.0mm in height and was condensed by using routine manner. The specimen was removed from the mold and stored at room temperature for about 24 hours. The standard surface preparation was routinely carried out. Anodic polarization measurement was employed to confirm the corrosion behaviour of the amalgams in a 0.9% saline solution (P.H: 6.8-7.0) at $37^{\circ}C$. The initial rest potential (corrosion potential) was determined after 30 minutes of immersion of specimen in electrolyte, and the potential scan was begun at the point of 100mV cathodic from the corrosion potential. The scan rate was 0.17mV/sec. in the study to observe the degree of corrosion of each phase. SEI and EPMA images on the determined oxidation peaks of each amalgam were observed. The results were as follows: 1. In the four anodic polarization curves, low copper amalgams have three oxidation peaks and high copper amalgams have two oxidation peaks, -270mV, +26mV and +179mV(SEC) in the low copper lathe cut, and -300mV, +39mV and +163mV(SEC) in the low copper spherical. -4mV and +154mV(SEC) in the Dispersalloy, and +17mV and +180mV(SEC) in the Tytin as high copper amalgams. 2. ${\gamma}_2$ phase in the low copper amalgam and ${\eta}$ phase in the high copper amalgam were the most corrodible phases and Ag-Cu eutectic in high copper amalgam was the most slowly corroded phase. 3. Low copper amalgam was more susceptible in corrosion than high copper amalgam.

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인공타액에서 아말감의 부식거동에 관한 전기화학적 연구 (ELECTROCHEMICAL STUDY ON THE CORROSION BEHAVIOUR OF DENTAL AMALGAM IN ARTIFICIAL SALIVA)

  • 김영남;엄정문
    • Restorative Dentistry and Endodontics
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    • 제13권2호
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    • pp.221-235
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    • 1988
  • The purpose of this study was to observe characteristic properties through the polarization curves and EMPA images from 4 different types of amalgam obtained by using the potentiostats (EG & G PARC) & EPMA (Jeol JSM-35), to investigate the degree of corrosion of each phase of amalgam on the oxidation peak, and to identify corrosion products from the corroded amalgam by use of X-ray diffractometer(Rigaku). After each amlgam alloy and Hg were triturated as the direction of the manufacturer by means of the mechanical amalgamator(Shofu), the triturated mass was inserted into the cylindrical metal mold which was 12mm in diameter and 10mm in height and was condensed by means of routine manner. The specimen was removed from the mold and stored at room temperature for about 7 days. The standard surface preparation was routinely carried out. Anodic polarization measurement was employed to compare the corrosion behaviours of the amalgams in 0.9% saline solution(pH6.8~7.0) and artificial saliva (pH6.8~7.0) at $37^{\circ}C$. The open circuit potential was determined after 30 minutes' immersion of specimen in electrolyte and the potential scan was begun at the potential of 100mV cathodic from the corrosion potential. The scan rate was 1mV/sec and the surface area of amalgam exposed to the solution was 0.64$cm^2$ for each specimen. All the potentials reported are with respect to a saturated calomel electrode (SCE). EPMA images on the determined oxidation peaks of each amalgam in artificial saliva were observed. X-ray diffraction patterns of each sample were recorded before and after polarization in artificial saliva (Aristaloy, Caulk Spherical, Dispersalloy and Tytin: at +770mV, +585mV, +8.10m V and +680m V respectively) by use of a recording diffractometer. Nickel filtered Cu $K_{{\alpha}_1}$ radiation was used and sample was scanned at $4^{\circ}(2{\theta})/min.$ from $25^{\circ}$ to $80^{\circ}$. The following results were obtained. 1. Oxidation peak potential in artificial saliva shifted to more anodic direction than that in saline solution. 2. The corrosion potential of high copper amalgam was more anodic than the potential of low copper amalgam. 3. The current density was lower in artificial saliva than in saline solution. 4. One of the corrosion products, AgCl was identified by X-ray diffraction analysis. 5. ${\gamma}_2$ phase was the most susceptible to corrosion and e phase was stable in low copper amalgam and ${\eta}$' phase and Ag-Cu eutectic were susceptible to corrosion in high copper amalgam.

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48 $\mu$BGA에 적용한 무연솔더의 시효처리에 대한 금속간화합물의 특성 (Characteristic of Intermetallic Compounds for Aging of Lead Free Solders Applied to 48 $\mu$BGA)

  • 신영의;이석;코조 후지모토;김종민
    • 마이크로전자및패키징학회지
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    • 제8권3호
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    • pp.37-42
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    • 2001
  • 지금 까지 전자패키지 접합에 사용되어온 Sn/37Pb 솔더는 낮은 용융온도와 우수한 물리적 특성, 그리고 저렴한 가격 등으로 널리 사용되었다. 그러나 납의 독성으로 인한 환경문제와 인체 유해성이 문제화되면서 이를 대체할 무연솔더의 요구가 시급한 실정이다. 또한 제품의 소형화에 따른 접합부의 미세화로 인한 접합부신뢰성이 요구되고 있다. 본 연구에서는 현재 Sn/37Pb 솔더를 사용하여 제품에 사용되고 있는 48 $\mu$BGA 패키지를 사용하여 Sn/Ag 계열 의 두 무연솔더인 Sn/3.5Ag/0.75Cu와 Sn/2.0Ag/0.5Cu/2.0Bi를 접합하여 장기신뢰성을 시효처리를 통하여 제시하였다. 시효처리는 $130^{\circ}C$, $150^{\circ}C$, $170^{\circ}C$ 온도에서 각각 300, 600, 900 시간동안 하였으며, 시효처리에 따른 전단강도와 각 솔더의 활성화에너지를 구하여 Sn/37Pb 솔더와 비교하였다. 두 무연솔더의 시효강도는 Sn/37Pb 솔더 보다 우수하였으며, 시효처리에 따라 형성된 솔더내부의 금속간화합물의 형상으로부터 균열의 성장과 형성에 대하여 논하였다. 이런 실험결과들로부터 두 무연솔더의 장기신뢰성 측면에서 대체가능성을 제시하였다.

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기능성화 산화 그래핀과 폴리인산암모늄을 이용한 직물 난연성 향상 (Enhanced Flame Retardancy of Cotton Fabric by Functionalized Graphene Oxide and Ammonium Polyphosphate)

  • 가동원;장성온;정현숙;진영호
    • Composites Research
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    • 제33권4호
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    • pp.177-184
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    • 2020
  • 난연 의류는 화염 및 고온 환경 속에서 착용자의 원활한 임무 수행을 돕고 추가적인 피해 확산을 방지한다. 그러나 기존 난연 의류의 높은 중량과 열 피로도는 개선이 필요하며, 친환경적인 방법으로 제작된 가볍고 편리한 난연 의류 개발이 요구되고 있다. 최근 인을 함유한 난연 물질 코팅으로 섬유에 난연성을 부여한 사례가 보고되고 있으나 이들은 국내외 방화복 및 난연 전투복 기준에 적합한 수준으로 발전될 필요성이 있다. 본 연구에서는 깊은 용융 용매로 기능성화된 산화 그래핀과 폴리인산암모늄을 동시에 섬유에 코팅하는 친환경적인 대량생산 공정을 제시한다. 코팅된 섬유는 열무게 분석(Thermogravimetric analysis), 수직불꽃저항성 시험(ASTM D6413), 콘칼로리미터법(ISO 5660-1), 한계 불꽃 확신 속도 시험(ISO 15025)으로 열 안정성 및 난연성이 시험되었다. 기능성화 산화그래핀과 폴리인산암모늄이 동시에 코팅된 직물은 단일 물질 코팅 직물보다 우수한 난연성을 보였고, 연소 이후에도 탄화된 부분의 팽창 효과로 섬유의 형상을 유지하는 것이 관찰되었다. 난연 직물의 세탁 안정성을 위해 추가적인 발수 처리 또한 시도되었다.