• 제목/요약/키워드: Precipitate

검색결과 710건 처리시간 0.029초

THE EVALUATION OF MICROSTRUCTURE AND MECHANICAL PROPERTIES OF FRICTION STIR WELDEDAL-MG-SI ALLOY

  • Lee, Won-Bae;Yeon, Yun-Mo;Jung, Seung-Boo
    • 대한용접접합학회:학술대회논문집
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    • 대한용접접합학회 2002년도 Proceedings of the International Welding/Joining Conference-Korea
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    • pp.499-504
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    • 2002
  • The microstructural change associated with the hardness profile in friction stir welded, age-hardenable 6005 Al alloy had been evaluated. Frictional heat and plastic flow during friction stir welding created the fine recrystallized grain (Stir Zone, SZ), the elongated and recovered grain (Thermo-Mechanical Affected Zone, TMAZ) in the weld zone. Heat affected zone (HAZ), which could be only identified by hardness test because there is no difference in the grain structure compared with that of the base metal, was formed beside the weld zone. A softened region had been formed near the weld zone during friction stir welding process. The softened region was characterized by the dissolution and coarsening of the strengthening precipitate during the friction stir welding. The sound joints of 6005 Al alloys were successfully formed under a wide range of the friction stir welding conditions.

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균일침전법에 의한 Yttrium Iron Garnet 분말의 합성 및 결정화 (Synthesis of Yttrium Iron Garnet Powder by Homogeneous Precipitation and its Crystallization)

  • 안영수;한문희;김종오
    • 한국세라믹학회지
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    • 제33권6호
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    • pp.693-699
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    • 1996
  • YIG precursor powder was obtained by homogeneous precipitation in chloride salt solution by thermal decom-position of urea. It was found that ferric ions precipitated prior to yttrium ions. The precipitate was minute and spherical in shape. The precipitate formed consisted of the mixture of amorphous and ferric oxyhydroxide. Crystallization of YIG was proceeded by solid state reaction of intermediate YFeO3 and Fe2O3 in the temperature range of 85$0^{\circ}C$ to 140$0^{\circ}C$. Single phase of YIG was obtained by heat-treatment of the powder at 140$0^{\circ}C$ for 6 hrs in air. The powder calcined was molded into pellets and sintered in air. The maximum density of 4,92 g/cm3(95.1% of theoretical density) was obtainable for the pellet sintered at 145$0^{\circ}C$ using the powder calcined at 90$0^{\circ}C$.

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물이 해동한 다음 발생하는 휜 침전물의 정성분석 및 이온의 변화 (Study on White Precipitate in Most of Waters after Thawing)

  • 윤수철;박해룡;윤형식;김창수
    • 한국식품위생안전성학회지
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    • 제17권1호
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    • pp.15-19
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    • 2002
  • The objectives of this study were to investigate the change of silicon, cations and anions dissolved in water before and after thawing, and analyzed what the white-colored precipitate (WP) farmed after thawing was composed of. The silicon concentration that has been changed might have been compared with the weight of WP under water-free state. The major component of WP has been approved to be a silicon, while calsium was only a little contained. As the weight of WP has been nearly equal to the reduced silicon concentration, the weight of its could be changeable calculated by silica (SiO$_2$) molecular weight. Therefore, WP could have been presumed to be a silica. The more silicon concentration was increased, the more weight of silicon was increased. Except for the sample "C", the amounts of cations and anions could be found to be unchangeable nearly. As a result of that, WP has been apparent to be silica itself while most of ions (excluded with Si) of any others were not changed.

습식합성에 의한 Mn-Zn Ferrite의 생성반응에 관한 연구 (Formation Reaction of Mn-Zn Ferrite by Wet Process)

  • 이경희;이병하;허원도;황우연
    • 한국세라믹학회지
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    • 제30권1호
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    • pp.25-33
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    • 1993
  • Formation reaction of Mn-Zn ferrite depending on various synthetic conditions of wet process was investigated using FeCl2.nH2O(n≒4), MnCl2.4H2O, ZnCl2 as starting materials. A stable intermediate precipitate was formed by the addition of H2O2. And the precipitate was hard to transform to spinel phase of Mn-Zn Fe2O4. Single phase of Mn-Zn Fe2O4 spinel was obtained above 8$0^{\circ}C$ reaction temperature. The powder had spherical particle shape and 0.02~0.05${\mu}{\textrm}{m}$ particle size. Fe(OH)2 solid solution, -FeO(OH) solid solution, -FeOOH, Mn-Zn Fe2O4 spinel were formed with air flow rate 180$\ell$/hr. However, single phase of Mn-Zn Fe2O4 spinel with cubic particle shape and 0.1~0.2${\mu}{\textrm}{m}$ particle size was formed with synthetic conditions of 8$0^{\circ}C$ and 90 munutes. The particle shape of the -FeOOH was needle-like.

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알콜 탈수법에 의한 Mn-Zn Ferrite 분체 제조시 pH의 영향 (Effect of pH on the Preparation of Manganese Zinc Ferrite Powder by Alcoholic Dehydration of Citrate/formate Solution)

  • 김창범;신효순;이대희;김창현;이병교
    • 한국세라믹학회지
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    • 제32권10호
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    • pp.1123-1130
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    • 1995
  • In the preparation of manganese zinc ferrite powders by alcoholic dehydration of citrate/formate solution. The effect of pH change on precipitation was investigated. The pH range for obtaining stable precipitates was studied. The glassy phase was obtained when the pH value of solution is higher than 5, and the formation mechanism of glassy phase was suggested. Below pH 5, the stable precipitates were formed, and the optimal pH was 2. Formation of glassy phase was accounted for the change of surface charge by pH change. The change of surface charge is caused by the interparticular agglomeration. The precipitate was redissolved into the water on the surface of precipitate itself and through the polymerization, it agglomerated. This mechanism is tought to be similar to that of viscous flow.

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수산화물과 옥살산염의 열분해에 의한 $SnO_2$미분말의 합성 ($SnO_2$ Powder Preparation from Hydroxide and Oxalate and its Characterization)

  • 이종흔;박순자
    • 한국세라믹학회지
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    • 제27권2호
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    • pp.274-282
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    • 1990
  • SnO2 powder was prepared by hydroxide method and oxalate method. In hydroxide method, the pH dependence of powder characteristics was investigated by using buffer solution. As increasing the pH of solution, SnO2 powder size was decreased because nucleation rate was inctreased by more supersaturation of solution. Also, we found that the powder by our method has larger specific surface area in comaprison with other method. And the degree of agglomeration of precipitate with the change of precipitation temperature was investigated in oxalate method. The SnC2O4 was angular shape precipitate, and the size of the SnC2O4 was increased with the increase of precipitation temperature in methanol solvent.

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내마모 철계 소결합금(Fe-5Cr-lMo-2Cu-0.5P-3C)에서 정합변형이 액상석출물의 모양에 미치는 영향 (The Effect of Elastic Anisotropy on the Shape of a Liquid Precipitate in a Wear-Resistant Fe-Base Alloy(Fe-5Cr- lMo-2Cu-0.5P-3C))

  • 신형상
    • 한국분말재료학회지
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    • 제1권1호
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    • pp.60-65
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    • 1994
  • When a commercial prealloyed Fe-powder(Fe-5Cr-lMo-2Cu-0.5P-3C) is liquid phase sintered at 116$0^{\circ}C$, liquid precipitates with various shapes form within solid grains during the initial stage of sintering. The shape of a liquid precipitate changes pith the increment of their size from sphere(with radius<0.3$\mu\textrm{m}$), a transient polyhedron with more than 7 faces(1~2 $\mu\textrm{m}$), cuboid(3~5 $\mu\textrm{m}$), and finally to sphere(>5 $\mu\textrm{m}$). The shapes of liquid precipitates closely resemble the growth shapes predicted on the basis of solid-liquid interfacial energy and the coherency strain energy with anisotropic elastic constants in the diffusion zone around the precipitates.

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석출물과 전위에 기인한 초음파 비선형성 파라미터 (Ultrasonic Nonlinearity Parameter Due to Precipitate and Dislocation)

  • 김정석;박익근
    • 한국정밀공학회지
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    • 제25권7호
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    • pp.131-138
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    • 2008
  • The microstructural effects on the ultrasonic nonlinearity were investigated in isothermally degraded ferritic 2.25Cr-1Mo steel and low cycle fatigued copper. The variation in ultrasonic nonlinearity (${\beta}/{\beta}_0$) was interpreted as resulting from microstructural changes supported by the electron microscopy and X-ray diffraction, in addition to the mechanical test (Victor's hardness and ductile-brittle transition temperature). The ultrasonic nonlinearity of 2.25Cr-1Mo steel increased abruptly in the initial 1,000 h of degradation, and then changed little due to the coarsening of carbide and precipitation of stable $M_6C$ carbide during isothermal degradation. The ultrasonic nonlinearity of copper increased with the fatigue cycles due to the evolution of dislocation cell substructure.

Uranium(VI) Phosphate Precipitate Formation in a Carbonate Solution

  • Im, Hee-Jung;Park, Kyoung-Kyun;Park, Yeong-Jae;Kim, Won-Ho
    • 한국원자력학회:학술대회논문집
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    • 한국원자력학회 2005년도 춘계학술발표회
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    • pp.311-312
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    • 2005
  • The precipitation of U(VI) in the presence of phosphate and carbonate was investigated in the pH range of 4 to 13 and the following was obtained as a result of this experimental condition. U(VI) precipitates as a $NaUO_{2}PO_{4}$ at pH<9 but as mixtures of phosphate, hydroxides and/or carbonate at pH>9. The portion of the phosphate in the precipitate decreases almost linearly to near zero with an increasing pH in the range of 9 to 13. The U(VI) phosphate is dissolved by the carbonate complex formation at pH<10.5. The ternary complex of a carbonate and phosphate is not found.

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지렁이(지룡)의 해열성분에 관한 연구 (Studies of Antipyretic Component of the Earthworm)

  • 김영은;이왕규;윤희정
    • 약학회지
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    • 제25권4호
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    • pp.137-143
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    • 1981
  • In order to confirm the exact antipyretic component in the earthworm, etherial extract of American earthworm(Red Worm) was fractionated into five fractions by using silica gel column chromatography and thin layer chromatography. The fraction including free fatty acids was found to possess artipyretic response and standard arachidonic acid showed marked antipyretic response on typhoid vaccinated rabbits. Arachidonic acid was identified from the free fatty acid fraction of the earthworm by using gas liquid chromatography. Thus it was considered that the antipyretic activity of the free fatty acid may be due to the presence of arachidonic acid. Lipid-free earthworm powder was extracted with phosphate buffer (pH, 8.0, 0.1M) and all the proteins was salted out by ammonium sulfate. The crude precipitate was dialyzed and the impure proteins were eliminated at pH 5.4 and 4.6. The remaining protein solution was fractionated with various concentrations of acetone. The acetone fractions were identified by using S.D.S. polyacrylamide gel electrophoresis and disc gel electrophoresis. The precipitate at 85% acetone concentration and the remaining proteins in the supernatant did not exhibit the antipyretic activity.

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