• 제목/요약/키워드: Mg particles

검색결과 736건 처리시간 0.035초

Al-Mg-Si 단조품의 시효 모델 (Aging model for Al-Mg-Si forged part)

  • 권용남;이영선;이정환
    • 한국소성가공학회:학술대회논문집
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    • 한국소성가공학회 2005년도 춘계학술대회 논문집
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    • pp.307-310
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    • 2005
  • Ageing behavior of the Al-Mg-Si alloy was modeled for the use of optimization of Al forging product. Typical precipitates of Al-Mg-Si alloy are a wide variety of metastable phases (e.g. GP zones, $\beta',\beta'$). These rod shaped particles take a role to hinder the dislocation movement. The precipitation sequence in Al-Mg-Si alloys is quite complex and the strength of precipitate particles differs with the ageing condition. In the present study, the ageing behavior of Al-Mg-Si alloy was investigated by using an industrial grade Al 6061 alloy forged product, which was a perform for an Al impeller for turbo charger. The precipitate hardening models by Esmaeili's approach were used for the analysis of ageing behavior.

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침전법과 수열처리로 제조된 수산화마그네슘 비교와 이의 저밀도 폴리에틸렌-에틸렌 비닐 아세테이트 수지 난연제 적용 (Comparison of Magnesium Hydroxide Particles by Precipitation and Hydrothermal Treatment for Flame Retardant Application to Low Density Polyethylene and Ethylene-Co-Vinyl Acetate Resin)

  • 현미경;임형미;윤준호;이동진;이승호;황진명;정상옥
    • 공업화학
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    • 제20권2호
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    • pp.234-240
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    • 2009
  • 마그네슘염과 알칼리를 출발물질로 하는 수산화마그네슘 제조에서 공정 변수가 생성되는 입자의 크기, 형상 및 응집도에 미치는 영향에 대해 완전 요인배치(full factorial) 실험계획법(Design of experiment)으로 연구하였다. 수열합성에서는 알칼리/$MgCl_2$ 몰 비가 낮을수록, $MgCl_2$ 농도와 수열처리 온도가 높을수록 평균입경은 커지고 1차 입자 크기와 2차 입자 크기가 유사하지만, 침전법으로 제조한 수산화마그네슘은 1차 입자의 응집현상으로 2차 입경은 커지며, 응집성은 알칼리원의 종류와 $MgCl_2$의 농도에 따라 달라졌다. 알칼리원의 종류에 따른 차이는 $NH_4OH$를 사용한 경우 NaOH를 사용한 것보다 입자의 크기가 커지고 분산성이 우수하였다. 크기 및 표면 상태가 다른 샘플을 선정하여 LDPE와 EVA 혼합수지에 혼합하여 난연 특성을 비교하였을 때, 50, 55% 함량에서는 일반적으로 2차 입경 크기가 감소함에 따라 LOI값은 상승하지만, UL-94에서는 1차 입자가 작은 경우에 더 우수한 등급을 받는 경우가 있었다. 60%의 높은 함량에서 입자의 제조경로와 무관하게 UL-94는 V0 등급이지만, 미립이더라도 응집성있는 경우 한계산소지수가 상대적으로 낮다는 것을 알 수 있었다.

급속혼화공정에서 응집제 주입률에 따른 미세입자의 성장특성 (Characteristics of Micro Floc in a Rapid Mixing Step at Different Coagulant Dose)

  • 전항배;박상민;박노백;정경수
    • 상하수도학회지
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    • 제21권2호
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    • pp.243-252
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    • 2007
  • Effects of alum dosage on the particle growth were investigated by monitoring particle counts in a rapid mixing process. Kaolin was used for turbid water sample and several other chemicals were added to adjust pH and ionic strength. The range of velocity gradient and mixing time applied for rapid mixing were $200{\sim}300sec^{-1}$ and 30~180 sec, respectively. Particle distribution in the synthetic water sample was close to the natural water where their turbidity was same. The number of particles in the range of $10.0{\sim}12.0{\mu}m$ increased rapidly with rapid mixing time at alum dose of 20mg/L, however, the number of $8.0{\sim}9.0{\mu}m$ particles increased at alum dose of 50mg/L. The number of $14.0{\sim}25.0{\mu}m$ particles at alum dose of 20mg/L was 10 times higher than them at alum dose of 50mg/L. Dominant particle growth was monitored at the lower alum dose than the optimum dose from a jar test at an extended rapid mixing time(about 120 sec). The number of $8.0{\sim}14.0{\mu}m$ particles was lower both at a higher alum doses and higher G values. At G value of $200sec^{-1}$ and at alum dose of 10-20mg/L, residual turbidity was lower as the mixing time increased. But at alum dose above 40mg/L and at same G value, lower residual turbidity occurred in a short rapid mixing time. Low residual turbidity at G value of $300sec^{-1}$ occurred both at lower alum doses and at shorter mixing time comparing to the results at G value of $200sec^{-1}$.

마그네슘의 금속염 환원에 의한 초미립 탄화티탄 분말 합성거동 (Synthesis and kinetic of ultrafine titanium carbide particles by Mg-thermal reduction of liquid metal chlorides)

  • 이동원;백진호;김병기
    • 한국분말재료학회지
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    • 제11권4호
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    • pp.322-327
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    • 2004
  • Ultrafine titanium carbide particles were synthesized by the reaction of liquid-magnesium and vaporized TiCl$_{4}$+C$_{x}$Cl$_{4}$(x = 1 and 2) solution. Fine titanium carbide particles with about 50 nm were successfully produced by combining Ti and C atoms released by chloride reduction of magnesium, and vacuum was then used to remove the residual phases of MgCl$_{2}$ and excess Mg. Small amounts of impurities such as O, Fe, Mg and Cl were detected in the product, but such problem can be solved by more precise process control. The lattice parameter of the product was 0.43267 nm, near the standard value. With respect to the reaction kinetics, the activation energy for the reactions of TiCl$_{4}$+C$_{2}$Cl$_{4}$and Mg was found to 69 kJ/mole, which was about half value against the use of TiCl$_{4}$+CCl$_{4}$, and such higher reactivity of the former contributed to increase the stoichiometry until the level of TiC$_{0.96}$ and decrease the free carbon content below 0.3 wt.%.

1M NaCl 용액에서 Mg-(0~6)%Zn 주조 합금의 부식 거동 (Corrosion behavior of Mg-(0~6)%Zn Casting Alloys in 1M NaCl Solution)

  • 황인제;김영직;전중환
    • 한국주조공학회지
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    • 제36권4호
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    • pp.117-125
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    • 2016
  • The effects of the Zn content on the microstructure and corrosion behavior in 1M NaCl solution were investigated in Mg-(0~6)%Zn casting alloys. The MgZn phase was scarcely observed in the Mg-1%Zn alloy, while the Mg-(2~6)%Zn alloy consisted of ${\alpha}$-(Mg) and MgZn phases. With an increase in the Zn content, the amount of the MgZn phase was gradually increased. Immersion and electrochemical corrosion tests indicated that the Mg-1%Zn alloy had the lowest corrosion rate among the alloys, and a further increase in the Zn content resulted in the deterioration of the corrosion resistance. Microstructural examinations of the corroded surfaces and EIS analyses of surface corrosion films revealed that the best corrosion resistance at 1%Zn was associated with the absence of MgZn phase particles in the microstructure and the contribution of Zn element to the formation of a protective film on the surface. A micro-galvanic effect by the MgZn particles led to the increased rate of corrosion at a higher Zn content.

Growth of magnesium oxide nanoparticles onto graphene oxide nanosheets by sol-gel process

  • Lee, Ju Ran;Koo, Hye Young
    • Carbon letters
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    • 제14권4호
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    • pp.206-209
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    • 2013
  • Nanocomposites comprised of graphene oxide (GO) nanosheets and magnesium oxide (MgO) nanoparticles were synthesized by a sol-gel process. The synthesized samples were studied by X-ray powder diffraction, atomic force microscopy, transmission electron microscopy, and energy-dispersive X-ray analysis. The results show that the MgO nanoparticles, with an average diameter of 70 nm, are decorated uniformly on the surface of the GOs. By controlling the concentration of the MgO precursors and reaction cycles, it was possible to control the loading density and the size of the resulting MgO particles. Because the MgO particles are robustly anchored on the GO structure, the MgO/GOs nanocomposites will have future applications in the fields of adsorption and chemical sensing.

Mg-Al-Si 합금에서 진동감쇠능의 변형진폭 의존성 (Strain Amplitude Dependence of Damping Capacity in Mg-AI-Si Alloy)

  • 전중환
    • 열처리공학회지
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    • 제24권3호
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    • pp.144-148
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    • 2011
  • Change in damping capacity with strain amplitude was studied in Mg-Al-Si alloy in as-cast, solution-treated and aged states, respectively. The as-cast microstructure of the alloy is characterized by eutectic ${\beta}$($Mg_{17}Al_{12}$) phase and Chinese script type $Mg_2Si$ particles. The solution treatment dissolved the ${\beta}$ phase into the matrix, while the aging treatment resulted in the distribution of continuous and discontinuous type ${\beta}$ precipitates. The solution-treated microstructure showed better damping capacity than as-cast and aged microstructures both in strain-dependent and strain-independent damping regions. The decrease in second-phase particles which weakens the strong pinning points on dislocations and distribution of solute atoms in the matrix, would be responsible for the enhanced damping capacity after solution treatment.

해수 중에서 자연상태 황토입자의 침강특성 (Settling Characteristics of Natural Loess Particles in Seawater)

  • 김성재
    • 한국수산과학회지
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    • 제32권6호
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    • pp.706-712
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    • 1999
  • 해수 중에서 자연상태의 황토입자의 침강특성에 관한 연구의 요약은 다음과 같다. 1. 2,000mg/$\ell$ 황토용액에 대한 PSD 곡선은 0 min. 침강시간에서 정규분포곡선을 나타내었고 평균입도는 31.6$\mu$m, 변동계수는 $75,6\%$로써 매우 광범위한 입도의 분포상태를 보여 주었다. 그러나 침강시간이 경과함에 따라 비정규분포곡선의 양상을 나타내었다. 한편 무게누적분포곡선에서 거의 $100\%$의 입자가 20$\mu$m 보다 큰 입자로 구성되어 있었다. 2. 해수 중에서 황토입자에 대한 $V_s/(D_{bm})^{1/2}$ 비의 값은 입자의 크기가 증가함에 따라 기하급수적으로 증가하였으며, 1 $\mu$m 입자를 중심으로 이 이상은 $V_s$$(D_{bm})^{1/2}$보다 크고 이 미만은$(D_{bm})^{1/2}$$V_s$ 보다 큰 값을 나타내었다. 20$\mu$m 크기의 입자에 대하여 $V_s/(D_{bm})^{1/2}$ 비의 값은 2,355이었다. 3. 해수 중에서 황토입자는 매우 엷은 EDL 두께 (0.4$\mu$m)를 나타냄으로써 EDL repulsive force가 거의 존재하지 않았으며, 상호 접근하는 황토입자는 모든 간격에서 LVDW attractive force가 EDL repulsive force보다 큰 값을 나타내어 항상 용이하게 floc을 형성할 수밖에 없는 조건에 있었다. 4. 해수 중의 황토입자의 $V_s/(D_{bm})^{1/2}$ 비의 값과 total interaction energy로부터 자연상태의 황토입자는 해수 중에서 외부의 강력한 전단력이 없이는 매우 확산되기 어려운 상태에 있으며, 조류의 수평운동이 적은 내만에서는 입자의 물리적 거동은 침강에 의하여 지배되는 것으로 나타났다. 5. 2,000mg/$\ell$ 황토용액에 대한 침강실험에서 대략 $22.5\%$의 황토는 격렬한 교반에도 불구하고 즉시 침강하였다. 황토농도가 400, 2,000, 10,000mg/$\ell$으로 증가함에 따라 침강특성은 개별입자침강(Type I settling or discrete settling)에서 응결침강(Type II settling or flocculation settling)의 상태로 바뀌었다. 이것은 실제 해양에서 황토입자들 끼리 floc을 형성할 정도로 많은 양의 황토를 적절한 분산장치 없이 살포하는 것은 지양해야 하며 동시에 동일한 농도의 황토용액도 살포방법에 따라 분산의 크기가 달라질 수 있음을 의미하는 것이다. 6. PVD 그래프로부터 자연상태의 황토는 급격하게 침강하는 입자와 장시간 부유하며 천천히 침강하는 입자로 구성되어 있었고 후자의 양이 전자의 양에 비하여 매우 적은 상태로 나타났다. 7. 황토를 이용하여 적조를 효과적으로 제거하기 위해서는 자연상태의 황토를 그대로 사용하기보다는 (1) 미세한 입자상태로 분쇄하고, (2) 적절한 살포장비와 분산장비를 사용하여 해수 중에서 황토입자가 넓게 부유 분산하여 적조생물과 충분한 충돌을 일으키도록 해야한다. 이것은 적어도 황토입자를 이용하여 적조를 응집 제거하려고 할 경우 피할 수 없는 기본적 원리가 되며 동시에 황토 사용량을 줄일 수 있는 하나의 방법이 된다. 8. 일반적으로 입자의 크기는 응집 및 흡착반응에 매우 중요한 인자가 된다. 황토입자는 크기가 작을수록 용이하게 분산시킬 수 있으며 더욱 효과적으로 Cochlodinium 적조를 제거할 수 있다. 실제로 어떤 황토입자의 크기가 적조 제거에 효과적인가는 현장실험을 통하여 침강속도, 수평분산범위, 적조제거효율 등을 조사하여 반드시 결정하여야 한다.

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The effects of Mg2Si(p) on microstructure and mechanical properties of AA332 composite

  • Zainon, Fizam;Ahmad, Khairel Rafezi;Daud, Ruslizam
    • Advances in materials Research
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    • 제5권1호
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    • pp.55-66
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    • 2016
  • This paper describes a study on the effects of $Mg_2Si_{(p)}$ addition on the microstructure, porosity, and mechanical properties namely hardness and tensile properties of AA332 composite. Each composite respectively contains 5, 10, 15, and 20 wt% reinforcement particles developed by a stir-casting. The molten composite was stirred at 600 rpm and melted at $900^{\circ}C{\pm}5^{\circ}C$. The $Mg_2Si$ particles were wrapped in an aluminum foil to keep them from burning when melting. The findings revealed that the microstructure of $Mg_2Si_{(p)}/AA332$ consists of ${\alpha}$-Al, binary eutectic ($Al+Mg_2Si$), $Mg_2Si$ particles, and intermetallic compound. The intermetallic compound was identified as Fe-rich and Cu-rich, formed as polygonal or blocky, Chinese script, needle-like, and polyhendrons or "skeleton like". The porosity of $Mg_2Si_{(p)}/AA332$ composite increased from 8-10% and the density decreased from 9-12% from as-cast. Mechanical properties such as hardness increased for over 42% from as-cast and the highest UTS, elongation, and maximum Q.I were achieved in the sample of 10% $Mg_2Si$. The study concludes that combined with AA332, the amount of 10 wt% of$Mg_2Si$ is a suitable reinforcement quantity with the combination ofAA332.

교반관법에 의한 Mg 기지 수소저항합금의 대량제조와 반복적 수소화 반응에 따른 수소화 특성 및 열화특성 평가 (Mass Production of Mg based Hydrogen Absorbing Alloys and Evalution of Hydrogenation and Degradation Properties by Hydriding/Dehydriding Cyclic Test)

  • 하원;이성곤;홍태환;김영직
    • 한국수소및신에너지학회논문집
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    • 제13권1호
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    • pp.13-23
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    • 2002
  • Hydrogenation properties of Mg-Ni and Mg-Ti-Ni alloys were investigated by Pressure-Composition Isotherm (PCI) test. Those alloys were fabricated by a new alloying method, Rotation-Cylinder Method (RCM). The as-cast microstructure of Mg-10 mass% Ni alloy consists of an island-like hydride forming $\alpha$-Mg phase and the eutectic structure. After 350 cyclic tests, Mg-lO mass % Ni alloy was pulverized into fine particles of 100 nm. The fine particles, which have a large specific surface area, are highly reactive with hydrogen. However, extreme pulvehzation can separate Mg from $Mg_2Ni$ in the eutectic structure, so $Mg_2Ni$ of the eutectic structure cannot behave as a dissociated hydrogen supplier.