• Title/Summary/Keyword: solid-phase synthesis

Search Result 313, Processing Time 0.025 seconds

Characteristics of Spodumene Powders Synthesized by Polyvinyl Alcohol Solution Technique (Polyvinyl Alcohol 폴리머 용액법으로 합성한 스포듀민 분말의 특성연구)

  • Lee, Sang-Jin;Park, Ji-Eun
    • Journal of Powder Materials
    • /
    • v.18 no.1
    • /
    • pp.35-40
    • /
    • 2011
  • LAS-system ceramic powder, spodumene ($Li_2O{\cdot}Al_2O_3{\cdot}4SiO_2$), was successfully synthesized by a chemical solution technique employing PVA(polyvinyl alcohol) as an organic carrier. The PVA content affected the microstructure of porous precursor gels and the crystalline development. The optimum PVA content contributed to homogeneous distribution of metal ions in the precursor gel and it resulted in the synthesis of glass free $\beta$-spodumene powder having a specific surface area of $7.57\;m^2/g$. The agglomerated $\beta$-spodumene powders were also enough soft to grind to fine powders by a simple ball milling process. The microstructures of the densified powder compacts were strongly dependant on the minor phases of spodumene solid solution and amount of liquid phase, which were formed from the inhomogeneous precursors.

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

  • 안영수;한문희;김종오
    • Journal of the Korean Ceramic Society
    • /
    • v.33 no.6
    • /
    • pp.693-699
    • /
    • 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$0^{\circ}C$.

  • PDF

Eutectic Ceramic Composites by Melt-Solidification

  • Goto, Takashi;Tu, Rong
    • Journal of the Korean Ceramic Society
    • /
    • v.56 no.4
    • /
    • pp.331-339
    • /
    • 2019
  • While high-temperature ceramic composites consisting of carbides, borides, and nitrides, the so-called ultra-high-temperature ceramics (UHTCs), have been commonly produced through solid-state sintering, melt-solidification is an alternative method for their manufacture. As many UHTCs are binary or ternary eutectic systems, they can be melted and solidified at a relatively low temperature via a eutectic reaction. The microstructure of the eutectic composites is typically rod-like or lamellar, as determined by the volume fraction of the second phase. Directional solidification can help fabricate more sophisticated UHTCs with highly aligned textures. This review describes the fabrication of UHTCs through the eutectic reaction and explains their mechanical properties. The use of melt-solidification has been limited to small specimens; however, the recently developed laser technology can melt large-sized UHTCs, suggesting their potential for practical applications. An example of laser melt-solidification of a eutectic ceramic composite is demonstrated.

Synthesis of Liquid Crystalline Copolyurethanes Containing Imide Unit

  • Lee, Dong-Jin;Lee, Tae-Jung;Kim, Han-Do
    • Proceedings of the Korean Fiber Society Conference
    • /
    • 1998.10a
    • /
    • pp.94-97
    • /
    • 1998
  • We have been studying :he synthesis of thermotropic polyurethanes, based on structural modifications by means of (i) the introduction of bulky substituent group in the aromatic ring to decrease the degree of lateral packing, (ii) the copolymerization of two kinds of monomers having different alkylene lengths to lower the regularity of the polymer structure, and (iii) the use of nonlinear monomers to lower the persistence length of the polymer chain in the liquid crystalline phase and to decrease the lateral interactions in the solid state. (omitted)

  • PDF

Synthesis of Titanium Diboride and Composites by Carbothermic Reduction of Titanium Oxide and Boric Oxide

  • Yoon, Su-Jong;Jha, Animesh
    • The Korean Journal of Ceramics
    • /
    • v.4 no.4
    • /
    • pp.387-393
    • /
    • 1998
  • The formation of titanium diboride ($TiB_2$ ) via the reduction of $TiO_2$ with boric oxide and carbon was studied in a partially reducing atmosphere of argon mixed with 4 vol.%H2. The effect of reaction time, temperature, partial pressure of nitrogen and $TiO_2/B_2_O3$ stoichiometric ratio on the reducibility of oxides has been studied. The phases formed were analysed by using X-ray rowder diffraction and scanning sosctron microscopic techniques. In this paper, we also investigated the presence of $CaC_2$ as a reducing agent on the reducibility of oxide mixtures and on the Ti-B-C-Ca-O phase equilibria. The morphology of $TiB_2$ formed in the presence of $CaC_2$ is compared with the microstructure of $TiB_2$ formed as a consequence of carbothermic reduction. The observed variation in $TiB_2$ crystals formed is also explained.

  • PDF

Synthesis of Functional Microspheres and Biomedical Applications (기능성 Microspheres의 합성 및 생의학적 응용)

  • Kim, J.H.;Kim, W.S.
    • Proceedings of the KOSOMBE Conference
    • /
    • v.1993 no.05
    • /
    • pp.7-14
    • /
    • 1993
  • Nowadays, microspheres are expected to be applied to biomedical areas and many studies are being performed. For biomedical applications, many kinds of microspheres were synthesized by emulsion polymerization, emulsifier-free emu]sion polymerization, and emulsifier-free emulsion polymerization with ionic surface-active comonomers. Further synthesis techniques about microencapsulation and magnetic microspheres are introduced. Among the practical applications of microspheres, some interesting subjects are introduced. These include solid-phase immunoassays, labeling and identification of lymphocyte populations, extracorporeal and hemoperfusion systems, drug delivery systems, and immunomagnetic cell separation. In addition, basic theories, problems and research trends are also introduced.

  • PDF

Synthesis of NiTi Alloy Powder by the Reaction of NiO-TiH2 Mixing Powders (NiO-TiH2 혼합분말의 반응을 이용한 NiTi 합금분말 제조)

  • Jeon, Ki Cheol;Lee, Han-Eol;Yim, Da-Mi;Oh, Sung-Tag
    • Journal of Powder Materials
    • /
    • v.22 no.4
    • /
    • pp.266-270
    • /
    • 2015
  • The synthesis of NiTi alloy powders by hydrogen reduction and dehydrogenation process of NiO and $TiH_2$ powder mixtures is investigated. Mixtures of NiO and $TiH_2$ powders are prepared by simple mixing for 1 h or ball milling for 24 h. Simple-mixed mixture shows that fine NiO particles are homogeneously coated on the surface of $TiH_2$ powders, whereas ball milled one exhibits the morphology with mixing of fine NiO and $TiH_2$ particles. Thermogravimetric analysis in hydrogen atmosphere reveals that the NiO and $TiH_2$ phase are changed to metallic Ni and Ti in the temperature range of 260 to $290^{\circ}C$ and 553 to $639^{\circ}C$, respectively. In the simple-mixed powders by heat-up to $700^{\circ}C$, agglomerates with solid particles and solidified liquid phase are observed, and the size of agglomerates is increased at $1000^{\circ}C$. From the XRD analysis, the presence of liquid phase is explained by the formation and melting of $NiTi_2$ inter-metallic compound due to an exothermic reaction between Ni and Ti. The simple-mixed powders, heated to $1000^{\circ}C$, lead to the formation of NiTi phase but additional Ni-, Ti-rich and Ti-oxide phases. In contrast, the microstructure of ball-milled powders is characterized by the neck-grown particles, forming $Ni_3Ti$, Ti-oxide and unreacted Ni phase.

Process variables of gamma-type aluminum trihydride in wet chemical synthesis (감마형 삼수소 알루미늄 습식합성반응의 공정변수 연구)

  • Yang, Yo-Han;Kim, Woo-Ram;Gwon, Yoon-Ja;Park, Mi-Jeong;Kim, Jun-Hyung;Cho, Young-Min
    • Journal of the Korean Applied Science and Technology
    • /
    • v.35 no.1
    • /
    • pp.214-222
    • /
    • 2018
  • Alane(aluminum trihydride, $AlH_3$) is a candidate material involving high energetic capacity for solid propellant or explosives. In this study aluminum trihydride-etherate ($AlH_3{\cdot}(C_2H_5)_2O$) was synthesized through a wet process, and solid alane was extracted by controlled crystallization. Alane crystals were grown during the crystallization step with phase conversion of aluminum trihydride-etherate to alane using an anti-solvent. Stable crystal forms were found by a 2 hour crystallization process at $85^{\circ}C$. Finally the extracted solid aluminium trihydride consisted mainly of ${\gamma}-type$ with $50-100{\mu}m$ in size.

Synthesis and Characterization of Y-doped SrTiO3 Powder by Pechini Method (Pechini법에 의한 Y-doped SrTiO3 분말의 합성)

  • Yoon, Mi-Young;Song, R.H.;Shin, D.R.;Hwang, Hae-Jin
    • Journal of Powder Materials
    • /
    • v.17 no.1
    • /
    • pp.59-64
    • /
    • 2010
  • 8 mol% Y-doped $SrTiO_3$ powder was synthesized by Pechini method from titanium isopropoxide, strontium nitrate, yttrium nitrate, citric acid and ethylene glycol. A $Y_2Ti_2O_7$ pyrochlore phase-free perovskite powder was obtained by calcining a polymeric resin, which was prepared from a precursor solution, at $500^{\circ}C$ in an air atmosphere. Low temperature calcination could lead to a fine-grained microstructure. In the case of a solid-state reaction, an extended heat-treatment at high temperature in a reduced atmosphere needed to obtain a single phase perovskite $SrTiO_3$.