• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2006년도 춘계학술대회 논문집
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• pp.103-104
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• 2006

Wear of valve seating face and seat insert seating face influence the performance of engine, so they are important. To manufacture good quality valve and seat insert which have wear resistance the relations between wear factors and wear of the two seating faces have to be inspected. Cycle number is one of the important wear factors wearing the two seating faces and it can translate into mileage in rear car. But little is blown. Test variable is only cycle number and the cycle numbers are $2.0{\times}10^6,\;4.0{\times}10^6\;6.0{\times}10^6,\;8.0{\times}10^6$. And the other test conditions were fixed. Rmax of valve seating face and seat insert seating face increase linearly as cycle number is increased. Rmax of valve seating face were smaller than seat insert seating face in each cycle number. Reaction production by tribological reaction and sliding wear was found on the two faces.

• 환경위생공학
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• 제16권4호
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• pp.62-68
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• 2001

The advantages of hydrogen peroxide dissolution method were no discharge of noxious matter when dissolution of iron wire which used as the center supporter, reactions occur in room temperature and easy to recover dissolved iron. This study was aimed at gathering the basic data of iron wire dissolution- recovery process and proposes the reaction condition of iron wire dissolution- recovery process rind the factors influencing those reactions. The results were as follows : 1 . Hydrogen peroxide dissolution method used hydrochloric acid as the catalyst. 1. In the dissolution of iron wire(1.668 g), the condition of reaction was E1702(30 ml), HCI(20 ml) and $H_2O$(200 ml) ; time of the reaction was 18 min. P.W.(Piece weight) was 7.75 mg, and C.R. was $2.34{\;}{\Omega}$ 2. In the dissolution of iron wire(1.529 g), the condition of reaction was H7O2(30 ml), HCI(20 ml) and $H_2O$(200 ml), time of the reaction was 21 min., P.W.(Piece weight) was 7.73 mg, and C.R. was $2.35{\;}{\Omega}$. Hydrogen peroxide dissolution method used sulfuric acid as the catalyst. 1. In the dissolution of iron wire(0.834 g), the condition of reaction was $H_2O$(65 ml), $H_2SO_4$(5 ml) and 1702(5 ml) ; time of the reaction was 5 min.30 sec, P.W.(Piece weight) was 7.74 mg, and C.R. was $2.33{\;}{\Omega}$ 2. In the dissolution of iron wire(1.112 g), the condition of reaction was $H_2O$(65 ml), $H_2SO_4$(5 ml) and $H_2O_2$(5 ml) ; time of the reaction was 4 min.30 sec, P.W.(Piece weight) was 7.75 mg, and C.R. was $2.33{\;}{\Omega}$. Hydrogen peroxide dissolution method used hydrochloric acid and sulfuric acid as the catalyst confirmed a clean technology, because there were not occurred a pollutant discharged in the existing method.

• 한국미생물생명공학회:학술대회논문집
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• 한국미생물생명공학회 1978년도 추계학술대회
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• pp.209.4-209
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• 1978

Previously, we reported the inhibitory substane which reacts on venoms proteinases and haemorrha-ghagic factors. The active substsnce was originated from soil fungi. This report describes the results of molecular weight determination, the activity by the derivatives, and also the reaction in vivo by the administration of sample L175-68-B.

• Archives of Pharmacal Research
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• 제8권4호
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• pp.261-266
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• 1985

Many monoterpen-erivatives are contained in edible plants. Some monoterpen-derivatives have been assessed as negative factors in the food safety. Among them thuone and 4-caranone are important toxic constituents of many plant essential oils. In this study, convenient detection methods of thujone and 4-caranone in oil were developed. The colour reactions of toxic thujone and 4-caranone were performed in oder to detect those in foods and oils. Sodium pentacyanonitrosylferrate (II) react with thujone to produce thujzoximinocarboxylic acid which becomes the six ligand in the ferrate complex (red colour reaction for thujone). Sodium pentacyanonitrosylferrate (II) cleaves 4-caranone to the red ferrate complex of caranketonic acid.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.171-172
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• 2006

The effect of the preparation factors, such as the feeding mode and rate of raw materials, the reaction temperature and the surfactant on the size distribution of molybdenum trioxide particle were investigated by orthogonal test. The optimum conditions for the preparation of $MoO_3$ precursors are as following; opposite feeding fast, reaction temperature of $60^{\circ}C$ and adding dispersant.

• 한국표면공학회지
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• 제33권5호
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• pp.381-386
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• 2000

It was found that colloidal silica sprayed to the galvanized steel sheet apparently made the molten zinc layer solidified to be the randomly oriented fine grains. Its spraying effect was also little affected by steel temperature that had been considered as one of the major operating factors in this process. From the results of surface analysis, it is considered that aluminum dissolved in coating layer reduces silica to silicon by the oxidation-reduction reaction, and that the reduced silicon acts as a more effective nucleus in solidification reaction than phosphate salt, siica and alumina.

• 한국전기화학회:학술대회논문집
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• 한국전기화학회 2001년도 추계총회 및 학술발표회
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• pp.29-29
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• 2001

• Bulletin of the Korean Chemical Society
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• 제18권5호
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• pp.471-473
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• 1997

• 자원리싸이클링
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• 제24권6호
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• pp.3-8
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• 2015

일정 온도에서 중량 변화를 통하여 가스화 반응 특성을 살펴볼 수 있는 열중량 분석기(thermobalance)를 이용하여 하수슬러지의 수증기 가스화 특성 및 발생 가스의 농도 분석을 실시하였다. 반응 온도 및 수증기의 분압이 증가할수록 가스화 반응이 촉진되어 반응 속도가 증가하는 것으로 나타났다. 반응 kinetics 해석은 기체-고체 화학반응의 세 가지 모델이 이용되었다. 이 중 하수슬러지 촤의 수증기 가스화는 modified volumetric reaction model이 반응 kinetics를 가장 잘 나타내었으며, 이 때 activation energy와 빈도 인자는 각각 155.5 kJ/mol, $14,087s^{-1}atm^{-1}$로 분석되었다. 또한, 수증기의 분압에 따른 반응 차수는 0.68이었다. 합성가스의 발생 특성을 살펴보고자 $900^{\circ}C$에서 생성 합성가스를 분석한 결과 수소의 농도가 가장 높았으며 수증기 분압이 증가할수록 생성기체의 농도 특히 수소 농도가 급격히 증가하였다. 가스화와 동시에 수성가스화 변환반응이 진행되어 생성기체의 수소 생성 농도가 일산화탄소에 비하여 2-4배 높은 값을 나타내었다.

• 한국작물학회지
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• 제51권1호
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• pp.89-94
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• 2006

Traditionally fatty acid composition used to be analysed by a GC and the sample preparation process includes lipid extraction from sample and subsequent methyl esters preparation, which are time-consuming and cumbersome. As an alternative, simultaneous extraction/methylation methods are being developed for rapid and simplified sample preparation. To optimize one-step extraction/methylation method for analysis of fatty acid composition in brown rice, various reaction factors such as sample to reaction solution ratio, reaction time and temperature, shaking intensity were changed and resultant fatty acid composition data were evaluated in comparison with previous reports. The ratio of sample weight to reaction solution volume was the most critical factor in that higher sample to reaction solution ratio caused overestimation of palmitic acid and linoleic acid composition, resulting in underestimation of oleic acid. Lower reaction temperature also induced overestimation of linoleic acid and underestimation of oleic acid. Reaction duration and the intensity of shaking prior to and during the reaction, however, caused no significant changes in analysis results. In conclusion, the optimum condition was mixing 5 grains (about 0.2 g) of brown rice with $680{\mu}L$ of extraction/methylation mixture and $400{\mu}L$ of heptane, followed by reaction at $80^{\circ}C$ for 2 hours.