• 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.

• Korean Chemical Engineering Research
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• v.45 no.1
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• pp.12-16
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• 2007

Temperature control of an autothermal methanol reforming reactor which uses the copper-zinc oxide catalyst was studied. Temperature at 1cm below the hot-spot point in the reactor was used for the controlled variable, and the air flow rate was used for the manipulated variable. A first order plus time delay model was identified and controller parameters were obtained by applying the IMC-PI tuning rule to the identified model. With this controller, we could control the reforming reactor temperature within ${\pm}5^{\circ}C$ over 100 hours. Change of the hot-spot point due to the catalyst degradation was investigated and it could be used to design an adaptive controller.

• Journal of the Korean Chemical Society
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• v.55 no.5
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• pp.787-793
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• 2011

An efficient three-component one-step synthesis of 2,4,5-trisubstituted imidazoles by condensation reaction of 1,2-diketones or ${\alpha}$-hydroxyketones with aromatic aldehydes and ammonium acetate using Zinc (II) [tetra (4-methylphenyl)] porphyrin as a novel and reusable catalyst under ultrasound irradiation at ambient temperature is described. In this method, ${\alpha}$-hydroxyketones as well as 1,2-diketones were converted to their corresponding 2,4,5-trisubstituted imidazoles in excellent yields.

• Bulletin of the Korean Chemical Society
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• v.18 no.4
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• pp.441-442
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• 1997

• Proceedings of the Korean Fiber Society Conference
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• 2003.10a
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• pp.1-2
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• 2003

Some new synthetic routes for the preparation of poly (isobutyl vinyl ether) (P(IBVE)) having a controllable molar mass with narrow distribution via catalytic or photoinduced living cationic polymerization and their conversion to corresponding PVA have been developed. It was found that the combination of iodomethyl methyl ether (IMME)-zinc iodide is effective in the initiation of the catalytic and the various combinations of diphenyliodonium halides, well known photocationic initiators (DPIX) with zinc halides (ZnX$_2$) are also useful in photoinduced living cationic polymerization of isobutyl vinyl ether (IBVE). Polymerization both in the catalytic and photoinduced systems precede until the full consumption of the monomer and the rate of polymerization increases as the concentration of the catalyst or photoinitiator. The number average molar mass of the resulting polymer is proportional with % conversion, which is determined by the ratio of monomer consumed and the initial values of the catalyst or initiator. The living nature was also confirmed by subsequent monomer addition technique.

• Bulletin of the Korean Chemical Society
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• v.16 no.4
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• pp.374-377
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• 1995

• Applied Chemistry for Engineering
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• v.24 no.4
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• pp.433-437
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• 2013

Electrical discharge plasma created in a multi-channel porous ceramic membrane-supported catalyst was applied to the decomposition of a volatile organic compound (VOC). For the purpose of improving the oxidation capability, the ceramic membrane used as a low-pressure drop catalyst support was loaded with zinc oxide photocatalyst by the incipient wetness impregnation method. Alternating current-driven discharge plasma was created inside the porous ceramic membrane to produce reactive species such as radicals, ozone, ions and excited molecules available for the decomposition of VOC. As the voltage supplied to the reactor increased, the plasma discharge gradually propagated in the radial direction, creating an uniform plasma in the entire ceramic membrane above a certain voltage. Ethylene was used as a model VOC. The ethylene decomposition efficiency was examined with experimental variables such as the specific energy density, inlet ethylene concentration and zinc oxide loading. When compared at the identical energy density, the decomposition efficiency obtained with the zinc oxide-loaded ceramic membrane was substantially higher than that of the bare membrane case. Both nitrogen and oxygen played an important role in initiating the decomposition of ethylene. The rate of the decomposition is governed by the quantity of reactive species generated by the plasma, and a strong dependence of the decomposition efficiency on the initial concentration was observed.

• Transactions of the Korean hydrogen and new energy society
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• v.1 no.1
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• pp.9-14
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• 1989

Mixed photocatalyst containing cadmium sulfide and zinc sulfide was prepared on silica gel powder and Nafion film. Photo-irradiation of aqueous mixture containing the photocatalysis generated hydrogen by water cleavage reaction. Use of sodium sulfide as sacrificial reagent help the photo-reaction. Evolution of the hydrogen was measured by gas chromatographic analysis. Composition of the catalyst was determined by atomic absorption spectrophotometer. 0.2 mL of of hydrogen was generated per hour. The maximun catalytic activity was obtained after 8-12 hours later. Hydrogen generation efficiency by the two different catalytic system was compared and showed that the Nafion-based catalyst is more efficient than the silicagel-based catalyst for the photoreaction.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.5 no.6
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• pp.521-525
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• 2004

Biodegradation of poly(ethylene carbonate) (PEC) and their terpolymers has been investigated in vitro. PEC has been synthesized with ethylene oxide (EO) and carbon dioxide, which is one of the greenhouse gases using Zinc glutarate has been used as catalyst Carbonate terpolymers have been prepared by the use of EO, cyclohexene oxide(CHO), and carbon dioxide. High biodegradability of PEC and terpolymers with EO. has been observed. Very low biodegradation of poly(propylene carbonate) (PPC) and poly(cyclohexene carbonate) (PCHC) has been shown. The weight loss, FT-IR and SEM have been employed to characterize biodegradability.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.12 no.2
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• pp.1027-1031
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• 2011

In order to use carbon dioxide, one of the green house gases, terpolymers have been synthesized from propylene oxide, cyclohexene oxide, and carbon dioxide with zinc glutarate as catalyst. The polymers have been investigated with FT-IR, $^1H$-NMR, DSC. The glass transition temperatures of terpolymers are dependendent upon mass ratio of the poly(alkylene carbonate by Fox equation.