• Corrosion Science and Technology
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• 제13권2호
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• pp.70-80
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• 2014

Duplex stainless steels with nearly equal fraction of the ferrite(${\alpha}$) phase and austenite(${\gamma}$) phase have been increasingly used for various applications such as power plants, desalination facilities due to their high resistance to corrosion, good weldability, and excellent mechanical properties. Hyper duplex stainless steel (HDSS) is defined as the future duplex stainless steel with a pitting resistance equivalent (PRE=wt.%Cr+3.3(wt.%Mo+0.5wt.%W)+30wt.%N) of above 50. However, when HDSS is welded with gas tungsten arc (GTA), incorporation of nitrogen in the Ar shielding gas are very important because the volume fraction of ${\alpha}$-phase and ${\gamma}$-phase is changed and harmful secondary phases can be formed in the welded zone. In other words, the balance of corrosion resistance between two phases and reduction of $Cr_2N$ are the key points of this study. The primary results of this study are as follows. The addition of $N_2$ to the Ar shielding gas provides phase balance under weld-cooling conditions and increases the transformation temperature of the ${\alpha}$-phase to ${\gamma}$-phase, increasing the fraction of ${\gamma}$-phase as well as decreasing the precipitation of $Cr_2N$. In the anodic polarization test, the addition of nitrogen gas in the Ar shielding gas improved values of the electrochemical parameters, compared to the Pure Ar. Also, in the erosion-corrosion test, the HDSS welded with shielding gas containing $N_2$ decreased the weight loss, compared to HDSS welded with the Ar pure gas. This result showed the resistance of erosion-corrosion was increased due to increasing the fraction of ${\gamma}$-phase and the stability of passive film according to the addition $N_2$ gas to the Ar shielding gas. As a result, the addition of nitrogen gas to the shielding gas improved the resistance of erosion-corrosion.

• Progress in Superconductivity
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• 제7권1호
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• pp.97-101
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• 2005

Bi-22l2 tubes for fault current limiter (FCL) were fabricated by centrifugal melting process. $SrSO_4$ ($10\;wt.\;\%$) was added to Bi-2212 powder to lower the melting point of Bi-22l2 and to improve the mechanical properties. The BSCCO powder was completely melted at $1300\;^{\circ}C$ using the RF furnace and then poured into rotating steel mold. The steel mold, preheated at $450\;{\circ}C{\sim}550^{\circ}C$ for 2 hour was rotated at $1020{\sim}2520\;RPM$. The solidified BSCCO tube was cooled down to room temperature in the furnace for 48 hours and separated from the mold between Bi-2212 and the mold. $ZrO_2$ solution was used to separate it easily from the mold and Ag tape was attached in the mold inner wall of the mold to analysis electrical property. Bi-22l2 tube was often cracked when the cooling rate was high. BSCCO tubes with $70{\Phi}{\times}100\;mm,\;50{\Phi}{\times}100\;mm$ and $30{\Phi}{\times}150\;mm$ size were fabricated by centrifugal melting process. The $J_{c}s$ of tubes with $50{\Phi}{\times}100\;mm{\times}4.0\;t$ and $50{\Phi}{\times}100\;mm{\times}4.l\;t$ were 178 and $74.2\;A/cm^2$ at 77K, respectively. The processing condition for Bi-2212 tube fabrication was investigated using XRD and SEM analyses.

• 한국의류학회지
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• 제17권3호
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• pp.491-505
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• 1993

The influences of protease on the removal of various protein soils from cotton fabrics were studied. The human epidermal stratum corneum, hemoglobin and casein were used as protein soils. The soiled fabrics were denatured by steaming for 30 min. before washing and laundered using Terg-O-Tometer under washing conditions. The removal efficiency was evaluated by analysis of protein on the fabrics before and after washing by means of copper-Folin method. The relations between the removal and the characteristics of protease were discussed. Also the degradation of protein were examined by microscopy. The seperation of human epidermal stratum corneum after hydrolysis was examined by SDS-PAGE. The results obtained were as follow : 1. The protein from the soiled cotton fabric was removed effectively by adding protease. The removal of protein was increased in proportion to increasing of the enzyme concentration up to a certain point, but it began to decrease above the point. The removal effect was high in the order of casein>human epidermal stratum corneum>hemoglobin. Especially the protein was more effectively removed in ADS solution(pH 9.5) containing enzyme. 2. When protease was used with ADS. the removal of protein was efficiently showed in relatively short time(5~15min.) compared to using ADS only. It is due to the properties of this enzyme that reacts with very short time. 3. Even at low temperature the removal efficiency of enzyme was relatively higher compared with the activity of enzyme. The removal of protein soil was increased up to a maximum near $50^{\circ}C$, and then decreased. 4. The removal of protein by protease was improved with the increase of alkalinity in the pH range from 9.5 to 11.0 but it began to decrease above pH 11.0. 5. According to the increase of mechanical agitation, the removal effect was increased. But the removal efficiency of protease was more effective compared with the agitation in detergency. 6. According to the SDS-PAGE separation and micrograph it was confirmed that the human epidermal corneum was effectively hydrolysed by the enzyme added. So the fragments of protein were removed more efficiently by means of the interfacial reaction of AOS.

• 한국결정성장학회지
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• 제10권5호
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• pp.345-349
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• 2000

Micro-pulling down법을 이용하여 $Al_2O_3/ZrO_2$eutectic fiber를 제조하여 그 미세구조 및 기계적 특성과 성장속도의 관계를 조사하였다. 성장속도는 0.1~15 mm/min였으며, 직경 0.2~2 mm, 길이 500 mm의 eutectic fiber를 제조하였다. $Al_2O_3/ZrO_2$eutectic fiber의 미세구조는 성장속도에 따라 rod-shape structure에서 lameller structure를 거쳐 lamellar pattern을 갖는 cellular structure로 변화하였다. lamellar thickness는 성장속도가 1 mm/min에서 15 mm/min로 증가함에 따라 380 nm에서 110 nm로 감소하였다. 이와 같은 성장속도에 따른 lamellar thickness의 감소경향은 inverse-square-root로 나타내면, = 1 -l/2와 같이 표현할 수 있다. 여기서 는 m, 는 m/s의 단위를 갖는다. 13.1 Gpa의 hardness, 900 Mpa의 상온인장강도를 나타냈으며, 성장속도의 증가 즉, interlamellar spacing이 감소함에 따라 증가하는 경향을 나타냈다.

• 한국세라믹학회지
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• 제39권9호
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• pp.896-901
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• 2002

FHD(Flame Hydrolysis Deposition)공정은 화염 형성에 관여하는 장비의 조건들과 그에 따른 다양한 공정인자에 의하여 박막의 조성이 결정되며, 증착된 막을 치밀화하는 첨가물의 증발로 인해 열처리공정에서 조성이 변화되므로 공정인자로부터 최종적인 광도파막의 조성을 예측하는 것은 매우 어렵다. 본 연구에서는 FHD 공정에서 첨가가스의 유량을 제어하여 박막의 조성 및 광학적 특성을 예측할 수 있는 공정 분석의 기초자료를 제공하기 위하여 FTIR(Fourier Transformation Infrared Spectroscopy)측정과 ICP-AES(Inductively Coupled Plasma-Atomic Emission Spectrometry)측정을 통해 실리카 막의 조성분석에 대한 연구를 수행하였다. FTIR 흡수 스펙트럼을 통해 실리카 막에 존재하는 Si-O, B-O band를 측정하고 정성적 농도변화를 관찰 하였고, ICP-AES를 통해 Boron의 농도를 정량적으로 측정하였다. 이 두 결과로부터 FTIR을 이용한 정량적 조성분석의 기초자료인 B-O band의 흡광계수를 구하였다.

• 보존과학회지
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• 제38권3호
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• pp.217-233
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• 2022

경주 금척리 유적은 5세기 후반에서 6세기 전반에 조성된 금척리고분군(사적 제43호)과 매우 연접하며, 유적이 위치한 지역은 그 일대의 유력 지배세력의 무덤으로 알려져 있다. 신라성장에 일익을 담당했던 인근 유적과도 밀접한 관련성이 있을 것으로 추정되는 경주 금척리 유적에서 출토된 철기를 대상으로 금속학적 방법론을 도입한 연구를 진행하였다. 철기의 용도에 따른 제작기법 차이를 확인하기 위해 용도별로 분류하여 8점을 선정하고, 미세조직 및 비금속개재물을 연구하였다. 분석 결과 제작 공정은 탄소함량이 높은 소재를 사용하여 형상을 단조하는 방법과 탄소함량이 낮은 소재를 사용하여 형상 단조만을 하는 기법, 형상 단조 후 필요에 따라 강도를 높이기 위한 침탄작업을 실시하는 기법이 적용된 것으로 확인된다. 이후 부위별 기능을 고려한 제강법과 열처리기술을 선택적으로 적용하여 기계적 성질을 향상시켰으며 제련공정에는 저온환원법이 적용되었을 가능성이 크다. 또한 경주 중심부와 외곽에 위치한 유적에서 출토된 철기 유물과 비교해본 결과 제련 및 제작기술에서 상호 유사한 것이 확인된다.

• Restorative Dentistry and Endodontics
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• 제14권1호
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• pp.41-56
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• 1989

The purpose of this study was to examine the effect of temperature dependence of the behavior on the physical properties of posterior composite resins. Three light cure posterior composite resins (Heliomolar, Litefil-P, and P-50) and one chemical cure posterior composite resin (Bisfil-II) were used as experimental materials. Composite resin was placed in a cylindrical brass mold (2.5 mm high and 6.5 mm inside diameter) that was rested on a glass plate. Another flat glass was placed on top of the mold, and the plate was tightly clamped together. After the mold had been filled with the light cure composite material, the top surface was cured for 30 seconds with a light source. Chemical cure resin specimens were made in the same manner as above. Three hundreds and twenty composite resin specimens were constructed from the four composite materials. One hundred and sixty specimens of them were placed in a heater at $50^{\circ}C$, $75^{\circ}C$, $100^{\circ}C$, $125^{\circ}C$, $150^{\circ}C$, $175^{\circ}C$ and $200^{\circ}C$ for 5 minutes or 10 minutes respectively before compressive strengths were measured. Another one hundred and sixty specimens were tested for the diametral tensile strengths in the same way as above. They were randomly divided into eight groups according to the mode of heating methods as follows and stored in distilled water at $37^{\circ}C$ for 24 hours. Group $37^{\circ}C$ - specimens were stored at $37^{\circ}C$ in distilled water for 24 hours. Group $50^{\circ}C$ - specimens were heated at $50^{\circ}C$ after curing. Group $75^{\circ}C$ - specimens were heated at $75^{\circ}C$ after curing. Group $100^{\circ}C$ - specimens were heated at $100^{\circ}C$ after curing. Group $125^{\circ}C$ - specimens were heated at $125^{\circ}C$ after curing. Group $150^{\circ}C$ - specimens were heated at $150^{\circ}C$ after curing. Group $175^{\circ}C$ - specimens were heated at $175^{\circ}C$ after curing. Group $200^{\circ}C$ - specimens were heated at $200^{\circ}C$ after curing. Twenty specimens of each of four composite resins were respectively made by insertion of materials into same mold for examining the dimensional changes between before and after heating. The final eighty specimens were stored in distilled water at $37^{\circ}C$ for 24 hours before testing the dimensional changes. Compressive and diametral tensile strengths were measured crosshead speed 1mm/minute and 500Kg in full scale with a mechanical testing machine (DLC 500 Type, Shimadzu Co., Japan). Dimensional changes were determined by measuring the diametral changes of eighty specimens with micrometer (Mitutoyo Co., Japan). Results were as follows: 1. Diametral tensile strengths of specimens in all groups were increased with time heated compared with control group except for that in group $50^{\circ}C$ and the maximum diametral tensile strength was appeared in the specimen of Litefil-P heated for 10 minutes at $100^{\circ}C$. In heliomolar and P-50, it could be seen in the specimen heated for 10 minutes at $150^{\circ}C$, but in Bisfil-II, it could be found in the specimen heated for 5 minutes at $150^{\circ}C$. 2. Compressive strengths of specimens in all groups was tended to be also increased with time heated but that in group $50^{\circ}C$ and the maximum compressive strengths were showed in the same specimens conditioned as the diametral tensile strengths of four composite materials tested. 3. In Heliomolar, Litefil-P, and Bisfil-II, it was decreased in diameters of resin specimens between before heating and increased in diameters of resin specimens after storing in distilled water, but it was not in P-50. 4. There is little difference in diametral tensile strengths, compressive strengths, and dimensional changes followed by heating the resin specimens for 5 minutes and 10 minutes, but there is no statistical significances.

• 한국세라믹학회지
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• 제38권10호
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• pp.908-913
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• 2001

종이재(PA)와 대부분의 석탄회(FA)는 현재 매립에 의존하거나, 일부 시멘트의 대체재로 밖에 쓰이지 않는 폐기물로써, 이들을 자원으로 재활용한다면 환경을 보전할 뿐만 아니라 유용한 대체자원이 될 수 있는 장점이 있다. 본 연구에서는 점토를 30 wt%로 고정하고 폐기물의 양을 70 wt%로 하되, 폐기물내의 PA 대 FA의 비율은 $1:6{\sim}7:0$, 소결 온도는 $1150{\sim}1350^{\circ}C$ 범위내에서 변화시켜 제조된 소결체의 미세구조 및 물성을 분석하였다. 저온($1150{\sim}1200^{\circ}C$) 소결시에는 PA 첨가량이 증가할수록, 소결밀도가 증가한 반면, 높은 온도($1250{\sim}1350^{\circ}C$)에서 소결한 경우, PA첨가량이 증가할수록 과소결 현상이 발생하였고, 이로인해 미세구조가 불균일해지고 기공율이 증가되었다. 또한 시편의 기계적 특성은 미세구조의 균일성에 크게 좌우되었다. 예를들어 $1225^{\circ}C$에서 소결한 경우, 미세구조가 균일한 시편(10PA-60FA-30Clay)은 미세구조가 불균일한 시편(70PA-30Clay)에 비해 상대밀도값은 비슷하였으나 압축강도는 2배이상 높았다. 미세구조의 불균일성은 과소결에 인한 것으로 나타났다.

• Korean Chemical Engineering Research
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• 제56권4호
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• pp.577-584
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• 2018

본 연구는 목질계 섬유판 제조에 있어 목섬유에 대한 도계부산물인 닭털의 부분적 대체화 가능성을 검토하기 위하여 수행하였다. 닭털은 주로 케라틴계 단백질로 구성되어 있으며, 외형적으로 목섬유와 큰 차이는 없었다. 닭털의 전처리 방법에 따른 포름알데히드 흡착능을 비교한 결과, 닭털을 고온/고압에서 처리하고 분쇄한 우모분에서 가장 높았다. 한편 일반 가위로 절단한 닭털과 이를 가정용 믹서로 고해시킨 닭털의 폼알데히드 흡착량을 dinitrophenylhydrazine법으로 측정한 결과 차이는 없었다. 닭털, 고해 닭털, 우모분을 각각 목섬유의 전건무게를 기준으로 5 wt%로 혼합하여 제조한 중밀도섬유판(MDF)의 물성과 폼알데히드방출량은 닭털의 전처리 조건에 영향을 받지 않았다. 그러나 이 측정치를 목섬유만으로 제조한 MDF와 비교하였을 때, 두께팽윤율과 폼알데히드방출량은 크게 개선되었다. 따라서 현재 생산 현장에서 적용되고 있는 요소수지를 이용한 MDF 제조에 있어 목섬유와 함께 일정한 양의 닭털, 고해 닭털 또는 우모분을 첨가할 경우 치수안전성과 폼알데히드방출량이 개선된 MDF의 제조가 가능할 것으로 예상된다. 그러나 MDF제조에 있어 닭털의 사용은 현재 상황에서 목섬유와 비교하여 원료 확보의 어려움과 높은 단가로 경제성이 낮은 것으로 조사되었다. 경제성 향상을 위하여 중소형 도계장에서 발생하는 닭털을 이용하거나, 동물성 사료의 금지에 대한 대비책 및 인플루엔자 감염 조류에 대한 환경적 처리 방안으로 닭털의 섬유판 원료에 대한 부분적 대체화 기술은 향후 사용 가능성이 충분할 것으로 판단된다.

• E2M - 전기 전자와 첨단 소재
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• 제12권7호
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• pp.7-11
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• 1999

Fully sealed field emission display in size of 4.5 inch has been fabricated using single-wall carbon nanotubes-organic vehicle com-posite. The fabricated display were fully scalable at low temperature below 415$^{\circ}C$ and CNTs were vertically aligned using paste squeeze and surface rubbing techniques. The turn-on fields of 1V/${\mu}{\textrm}{m}$ and field emis-sion current of 1.5mA at 3V/${\mu}{\textrm}{m}$ (J=90${\mu}{\textrm}{m}$/$\textrm{cm}^2$)were observed. Brightness of 1800cd/$m^2$ at 3.7V/${\mu}{\textrm}{m}$ was observed on the entire area of 4.5-inch panel from the green phosphor-ITO glass. The fluctuation of the current was found to be about 7% over a 4.5-inch cath-ode area. This reliable result enables us to produce large area full-color flat panel dis-play in the near future. Carbon nanotubes (CNTs) have attracted much attention because of their unique elec-trical properties and their potential applica-tions [1, 2]. Large aspect ratio of CNTs together with high chemical stability. ther-mal conductivity, and high mechanical strength are advantageous for applications to the field emitter [3]. Several results have been reported on the field emissions from multi-walled nanotubes (MWNTs) and single-walled nanotubes (SWNTs) grown from arc discharge [4, 5]. De Heer et al. have reported the field emission from nan-otubes aligned by the suspension-filtering method. This approach is too difficult to be fully adopted in integration process. Recently, there have been efforts to make applications to field emission devices using nanotubes. Saito et al. demonstrated a car-bon nanotube-based lamp, which was oper-ated at high voltage (10KV) [8]. Aproto-type diode structure was tested by the size of 100mm $\times$ 10mm in vacuum chamber [9]. the difficulties arise from the arrangement of vertically aligned nanotubes after the growth. Recently vertically aligned carbon nanotubes have been synthesized using plasma-enhanced chemical vapor deposition(CVD) [6, 7]. Yet, control of a large area synthesis is still not easily accessible with such approaches. Here we report integra-tion processes of fully sealed 4.5-inch CNT-field emission displays (FEDs). Low turn-on voltage with high brightness, and stabili-ty clearly demonstrate the potential applica-bility of carbon nanotubes to full color dis-plays in near future. For flat panel display in a large area, car-bon nanotubes-based field emitters were fabricated by using nanotubes-organic vehi-cles. The purified SWNTs, which were syn-thesized by dc arc discharge, were dispersed in iso propyl alcohol, and then mixed with on organic binder. The paste of well-dis-persed carbon nanotubes was squeezed onto the metal-patterned sodalime glass throuhg the metal mesh of 20${\mu}{\textrm}{m}$ in size and subse-quently heat-treated in order to remove the organic binder. The insulating spacers in thickness of 200${\mu}{\textrm}{m}$ are inserted between the lower and upper glasses. The Y\ulcornerO\ulcornerS:Eu, ZnS:Cu, Al, and ZnS:Ag, Cl, phosphors are electrically deposited on the upper glass for red, green, and blue colors, respectively. The typical sizes of each phosphor are 2~3 micron. The assembled structure was sealed in an atmosphere of highly purified Ar gas by means of a glass frit. The display plate was evacuated down to the pressure level of 1$\times$10\ulcorner Torr. Three non-evaporable getters of Ti-Zr-V-Fe were activated during the final heat-exhausting procedure. Finally, the active area of 4.5-inch panel with fully sealed carbon nanotubes was pro-duced. Emission currents were character-ized by the DC-mode and pulse-modulating mode at the voltage up to 800 volts. The brightness of field emission was measured by the Luminance calorimeter (BM-7, Topcon).