• Title/Summary/Keyword: molar ratios

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Synthesis, Characterization and Catalytic Evaluation of Zinc Fluorides for Biodiesel Production

  • Indrayanah, Sus;Marsih, I Nyoman;Murwani, Irmina Kris
    • Journal of the Korean Chemical Society
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    • v.62 no.1
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    • pp.7-13
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    • 2018
  • The potential of zinc fluorides with different molar ratios of Zn/F was applied as a solid catalyst in the simultaneous reaction of transesterification and esterification of crude palm oil (CPO) for biodiesel production. These materials were prepared by the fluorolytic sol-gel technique with different fluorine contents. The resulting samples were investigated using elemental analysis, XRD, FT-IR, TG/DTG, $N_2$ physisorption measurements and SEM. The results exhibited that the presence of fluorine strongly affected the catalytic activity in the biodiesel production. The catalysts with smaller fluorine contents (${\leq}1$) showed the best performance in all of the observed samples, yields from 92.94 to 89.95, 87.38 and 85.21% with increasing fluorine contents, respectively. The yield toward the formation of biodiesel depended on the phase and particle sizes of catalysts, but it was not influenced by surface area, pore size, and volume of the samples. The recovered catalyst showed a gradual decrease in activity over three cycles of same reactions.

Effect of Silica-Alumina Adsorbent on the Efficiency of Paclitaxel Purification (파클리탁셀 정제 효율에 미치는 실리카-알루미나 흡착제의 영향)

  • Oh, Hyeon-Jeong;Jung, Kyeong Youl;Kim, Jin-Hyun
    • Clean Technology
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    • v.19 no.3
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    • pp.342-346
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    • 2013
  • Several types of mesoporous silica-alumina adsorbents with varied $SiO_2/Al_2O_3$ ratios were prepared by spray pyrolysis and were used for the purification of the anticancer agent paclitaxel. When $S_{0.5}A_{0.5}$ (Silica/Alumina molar ratio = 0.5/0.5) was used, the highest purity (~27%) and yield (~63%) of paclitaxel were obtained from adsorbent treatment and hexane precipitation. Removal of impurities was confirmed by TGA analysis of the organic substances that were adsorbed to the adsorbent.

Fabrication and Machinability of Mullite-ZrO2-Al2TiO5 Ceramics

  • Shin, Young Been;Lee, Won Jae;Kim, Il Soo
    • Journal of the Korean Ceramic Society
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    • v.52 no.6
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    • pp.423-428
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    • 2015
  • The machinability of materials is an important factor in engineering applications. Many ceramic components that have complex shapes require machining, typically using diamond tools, which leads to high production cost. Machinable ceramics containing h-BN have recently been developed, but these materials are very expensive because of high cost of raw materials and machining. Therefore the development of low-cost machinable ceramics is desirable. In this study, mullite-$ZrO_2$ ceramics were prepared additions of $Al_2TiO_5$. $ZrSiO_4$, $Al_2O_3$, and $Al_2TiO_5$ powders mixed at various molar ratios with sintering at 1400, 1500, and $1600^{\circ}C$ for 1 hr. Phase formation and microstructure of the sintered ceramics were observed by XRD and SEM, respectively. The machinability of each specimen was tested using the micro-hole machining method. The machinability results show that the ceramics sintered at temperatures over $1500^{\circ}C$ can be used as good low-cost machinable mullite-$ZrO_2-Al_2TiO_5$ ceramics.

Characterization and Manufacturing for Solar Cells $CuInS_2$ Nanopowder by polyol process (Polyol process를 이용한 태양전지용 $CuInS_2$ 나노분말 제조 및 특성평가)

  • Lee, Dae-Girl;Lee, Nam-Hee;Oh, Hyo-Jin;Yun, Yeong-Ung;Hwang, Jong-Sun;Kim, Sun-Jae
    • Proceedings of the KIEE Conference
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    • 2009.04a
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    • pp.30-32
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    • 2009
  • In this study, $CuInS_2$ powders have been synthesized using polyol process of a mixture of copper nitrate, indium nitrate, and thiourea with various stoichiometric molar ratios in ethylene glycol at 196$^{\circ}C$. As boiling time goes by, the color of metal ion mixed solutions were changed transparent green to dark green and finally fumed to black by reduction of $OH^-$ radicals. The prepared powders were fully characterized by SEM, XRD and UV-Vis. The particle shape of black colored powders showed sphere with about 30 nm in particle size compared to those with dark green colored powders showed irregular shape with about 1 ${\mu}m$ in particle size. The XRD results showed highly crystallized $CuInS_2$. The UV-Vis spectra showed broad shoulder at 430 and 780 nm corresponding to 2.78 and 1.58 eV for the dark green colored one and black colored one, respectively.

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Variation in Fucoidan Contents and Monosaccharide Compositions of Korean Undaria pinnatifida (Harvey) Suringar (Phaeophyta)

  • Lee, Yoo-Kyung;Lim, Dong-Jung;Lee, Yoon-Hee;Park, Yong-Il
    • ALGAE
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    • v.21 no.1
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    • pp.157-160
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    • 2006
  • Three different forms of Undaria pinnatifida, the southern form (U. pinnatifida f. typica), the northern form (U. pinnatifida f. distans), and Samcheok form (recently cultivated strain), were examined for the contents and compositions of fucoidans. Fucoidans were extracted from the dried edible portions of three forms of U. pinnatifida in low pH condition, mainly by ethanol precipitation and CaCl2 treatment. It was shown that Samcheok form contains 1.8 and 3.5 times more fucoidans than the northern and the southern forms, respectively. The monosaccharide compositions of individual fucoidans were also varied. The fucoidans from the southern and the northern forms were shown to be composed of mainly fucose and galactose with the molar percentage ratios of 83.5%:16.5% and 87.4%:12.6%, respectively, indicating that these are F-type fucoidans. The fucoidan from Samcheok form, however, consisted of fucose (62.7%), galactose (32.9%), and small amount of glucose (4.4%). The results of this study showed that both amount and monosaccharide compositions of fucoidans are variable depending on U. pinnatifida forms.

Nano-particles of Mechanochemical Synthesis

  • Urakaev, Farit Kh.
    • Journal of the Speleological Society of Korea
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    • no.71
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    • pp.5-11
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    • 2006
  • A theoretical investigation of the solid phase mechanochemical synthesis of nano sized target product on the basis of dilution of the initial powdered reagent mixture by another product of an exchange reaction is presented. On the basis of the proposed 3 mode particle size distribution in mechanically activated mixture, optimal molar ratios of the components in mixture are calculated, providing the occurrence of impact friction contacts of reagent particles and excluding aggregation of the nanosized particles of the target reaction product. Derivation of kinetic equations for mechanochemical synthesis of nanoscale particles by the final product dilution method in the systems of exchange reactions is submitted. On the basis of obtained equations the necessary times of mechanical activation for complete course of mechanochemical reactions are designed. Kinetics of solid phase mechanosynthesis of nano TlCl by dilution of initial (2NaCl+$Tl_2SO_4$) mixture with the exchange reaction product (diluent,$zNa_2SO_4$, z=z*=11.25) was studied experimentally. Some peculiar features of the reaction mechanism were found. Parameters of the kinetic curve of nano TlCl obtained experimentally were compared with those for the model reaction KBr+TlCl+zKCl=(z+1) KCl+TlBr (z=z1*=13.5), and for the first time the value of mass transfer coefficient in a mechanochemical reactor with mobile milling balls was evaluated. Dynamics of the size change was followed for nanoparticle reaction product as a function of mechanical activation time.

Microstructure of Cured Urea-Formaldehyde Resins Modified by Rubber Latex Emulsion after Hydrolytic Degradation

  • Nuryawan, Arif;Park, Byung-Dae
    • Journal of the Korean Wood Science and Technology
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    • v.42 no.5
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    • pp.605-614
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    • 2014
  • This study investigated microstructural changes of cured urea-formaldehyde (UF) resins mixed with aqueous rubber latex emulsion after intentional acid etching. Transmission electron microscopy (TEM) was used in order to better understand a hydrolytic degradation process of cured UF resins responsible for the formaldehyde emission from wood-based composite panels. A liquid UF resin with a formaldehyde to urea (F/U) molar ratio 1.0 was mixed with a rubber latex emulsion at three different mixing mass ratios (UF resin to latex = 30:70, 50:50, and 70:30). The rate of curing of the liquid modified UF resins decreased with an increase of the rubber latex proportion as determined by differential scanning calorimetry (DSC) measurement. Ultrathin sections of modified and cured UF resin films were exposed to hydrochloric acid etching in order to mimic a certain hydrolytic degradation. TEM observation showed spherical particles and various cavities in the cured UF resins after the acid etching, indicating that the acid etching had hydrolytically degraded some part of the cured UF resin by acid hydrolysis, also showing spherical particles of cured UF resin dispersed in the latex matrix. These results suggested that spherical structures of cured UF resin might play an important role in hindering the hydrolysis degradation of cured UF resin.

Synthesis Processing of the Fine (Ni, Zn)-ferrite Powder for $CO_2$ Decomposition of the Flue Gas in the Iron Foundry (제철소의 연소배가스 $CO_2$ 분해용 (Ni, Zn)-ferrite 미세분말 합성공정 연구)

  • 김정식;안정률
    • Journal of the Korean Ceramic Society
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    • v.37 no.2
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    • pp.164-167
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    • 2000
  • Flue gases in the iron foundry consist of 15~20% CO2 as an air pollution gas whose emission should be mitigated in order to protect the environment. In the present study, ultrafine powders of NixZn1-xFe2O4 as a potential catalyst for the CO2 decomposition were prepared by the coprecipitation methods. Oxygen deficient ferrites (MeFe2O4-$\delta$) can decompose CO2 as C and O2 at a low temperature of about 30$0^{\circ}C$. The XRD result of synthesized ferrites showed the spinel structure of ferrites and ICP-AES and EDS quantitative analyses showed the composition similar with initial molar ratios of the mixed solution prior to reaction. The BET surface area of the (Ni, Zn)-ferrites was about 77~89.5$m^2$/g and their particle size was observed about 10~20 nm. The CO2 decomposition efficiency of the oxygen deficient (Nix, Zn1-x)-ferrites was the highest at x=0.3, and the ternary (Ni, Zn)-ferrites was better than that of binary Ni-ferrites.

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Synthesis of Bioceramics Based on Glass-Ceramics of $CaO-P_2O_5$ System ($CaO-P_2O_5$계 결정화유리로 된 생체세라믹스의 합성에 관한 연구)

  • 김병호;박인용
    • Journal of the Korean Ceramic Society
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    • v.23 no.3
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    • pp.67-77
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    • 1986
  • various properties and manufacturing conditions were investigated in order to synthesize the glass-ceramics of $CaO-P_2O_5$ system for bioceramics. Compositions of easy unidirectional crystallization were between 47.5 and 50, 0mol% CaO For the glass rods prepared by pulling them to about 3 times the original rod length unidirectional crystallization was easier than original glass rods. These samples were crystallized in the axial direction at 15${\mu}{\textrm}{m}$/min in an electric furnace with a temperature gradient of about 3$0^{\circ}C$/cm at 57$0^{\circ}C$. Bending strengths of surface and unidirectionally crystallized samples were investigated with various CaO/$P_2O_5$ molar ratios. The bending strengths of unidirectionally crystallized samples were larger than those of surface -crystallized samples and the value of 47.5CaO.52.5 $P_2O_5$ was 1650kg/$cm^2$. XRD patterns showed that major phase is $\beta$-Ca(PO3) with minor phase 2CaO.$P_2O_5$ Relative crystal-linity of surface-crystallized sample was inversely propertional to the bending strenth. SEM of fracture surface of unidirectionally crystallized samples revealed an unidirectionally aligned structures.

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Detection of Escherichia coli O157:H7 Using Immunosensor Based on Surface Plasmon Resonance

  • Oh, Byung-Keun;Kim, Young-Kee;Bae, Young-Min;Lee, Won-Hong;Choi, Jeong-Woo
    • Journal of Microbiology and Biotechnology
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    • v.12 no.5
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    • pp.780-786
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    • 2002
  • An immunosensor based on surface plasmon resonance (SPR) with a self-assembled protein G layer was developed for the detection of Escherichia coli O157:H7. A self-assembled protein C layer on a gold (Au) surface was fabricated by adsorbing the mixture of 11-mercaptoundecanoic acid (MUA) and hexanethiol at various molar ratios and by activating chemical binding between free amine (-$NH_2$) of protein G and 11-(MUA) using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDAC) in series. The formation of a self-assembled protein G layer on an Au substrate and the binding of the antibody and antigen in series were confirmed by SPR spectroscopy. The surface morphology analyses of the self-assembled protein G layer on the Au substrate, monoclonal antibody (Mab) against E. coli O157:H7 which was immobilized on protein G, and bound E. coli O157:H7 extracts on Immobilized Mab against E. coii O157:H7 were performed by atomic force microscopy (AFM). The detection limit of the SPR-based immunosensor for E. coli O157:H7 was found to be about $10^4$ cells/ml.