• Polymer(Korea)
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• v.38 no.5
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• pp.650-655
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• 2014

The degradation characteristics of perfluoropolyether (PFPE) derivatives currently being used as computer hard disk lubricants have been investigated. Especially, we considered the effects of end group on degradation behavior of PFPE derivatives. It was found that the degradation of PFPE derivatives in the presence of $Al_2O_3$ involves two degradation mechanisms such as thermal degradation and Lewis acid disproportionation by $AlF_3$ which was mainly formed by oxide-to-halide reaction between $Al_2O_3$ and the degraded PFPE. The end groups were strongly related to Lewis acid disproportionation of PFPE derivatives, and it is due to the difference of electron donating ability in the each end groups. Even if PFPE derivatives have same repeating unit in the main chain, Lewis acid disproportionation was prohibited by higher electron donating ability by the end group which caused the high electron density at the acetal group in the repeating unit.

• Clean Technology
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• v.19 no.3
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• pp.333-341
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• 2013

This paper presents results on $CO_2$ gasification of 17 raw coals containing a wide range of volatile matter (21-57 wt%). The gasification is performed using a TGA under $CO_2$ and also under $N_2$ atmosphere. An amount of weight loss with increasing temperature is proportional to that of volatile matter in a coal under $N_2$ atmosphere. Reactivity of $CO_2$ gasification also increases with a content of volatile matter. However, the correlation is a little scattered. Oxygenated functional groups in a coal are generally reactive and therefore, an increase in O/C ratio leads to enhanced reactivity. However, $CO_2$ reactivity is affected by neither H/C ratio nor a content of ashes that possibly activate the gasification reaction. These findings are also applicable to steam coal gasification and the reactivity series are confirmed in the test at a fixed bed reactor.

• Composites Research
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• v.15 no.2
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• pp.40-47
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• 2002

The di-functional epoxy resins, i.e., diglycidylether of bisphenol A(DGEBA) and diglycidylethere of bisphenol F(DGEBF) were initiated by cationic catalyst, i.e., benzylquinoxalinium hexafluoroantimonate(BQH) using electron-beam(EB) technique. And the effect of structure of DGEBA and DGEBF on thermal stabilities and cure behaviors was investigated. According to the experimental results, the decomposed activation energy based on Horowitz-Metzger method was higher in the case of DGEBA, but intergral procedural decomposition temperature(IPDT) of DGEBA was lower than DGEBF. This could be interpreted in terms of high crosslink density resulted from hydroxyl bond of DGEBF backbone. It was confirmed in increasing the hydroxyl band at $7000\;cm^{-1}$ and $5235\;cm^{-1}$ using near-infrared spectroscopy(NIRS).

• Journal of the Korean Chemical Society
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• v.22 no.6
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• pp.370-379
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• 1978

The specific rate constants for the oxidation reactions of carbon monoxide on a unit catalytic surface area were measured. The catalysts used were NiO made from $Ni(NO_3)_2,\;and\;Ni(OH)_2$, and Mn$O_2$ made from Mn$(NO_3)_2$. At low pressure the reaction rate was found to be of second order and the activation energies were 12 kcal/mole (on NiO made from Ni$(NO_3)_2$, 17 kcal/mole (on NiO made from Ni$(OH)_2)$) and 18 kcal/mole (on Mn$O_2$). Plausible reaction mechanisms were proposed from the experimentally determined reaction orders.

• Clean Technology
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• v.18 no.4
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• pp.426-431
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• 2012

Carbon-rich coal can be utilized as a fuel for direct carbon fuel cell (DCFC). However, left-behind ash after the electrochemical oxidation may hinder the electrochemical reactions. In this study, we produced ash-free coal (AFC) by thermal extraction and then tested it as a fuel for DCFC. DCFC was built based on solid oxide electrolyte and the electrochemical performance of AFC mixed with $K_2CO_3$ was compared with AFC only. Significantly enhanced power density was found by catalytic steam gasification of AFC. However, an increase of the power density by catalytic pyrolysis was negligible. This result indicated that a catalyst activated the steam gasification reactions, producing much more $H_2$ and thus increasing the power density, compared to AFC only. Results of a quantitative analysis showed much improved kinetics in AFC with $K_2CO_3$ in agreement with DCFC results. A secondary phase of potassium on yttria-stabilized zirconia (YSZ) surface was observed after the cell operation. This probably caused poor long-term behavior of AFC with $K_2CO_3$. A thin YSZ (30 ${\mu}m$ thick) was found to be higher in the power density than 0.9 mm of YSZ.

• Journal of Life Science
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• v.13 no.1
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• pp.105-109
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• 2003

Epoxide hydrolase (EH) gene from Aspergillus niger #33 was cloned from cDNA library generated by reverse transcriptase-polymerase chain reaction (RT-PCR). The nucleotide sequence analysis revealed that the deduced amino acid sequence was almost similiar to that of A. niger LCP521 previously reported. The cloned EH gene was transformed into Saccharomyces cerevisiae and expressed by addition of galactose. The recombinant S. cerevisiae showed hydrolytic activity toward racemic phenyl oxirane substrate based on chiral GC analysis, and can be used as a potential biocatalyst for the preparation of chiral phenyl oxirane.

• Proceedings of the Korean Society of Propulsion Engineers Conference
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• 1998.04a
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• pp.31-31
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• 1998

위성체의 보조추진시스템은 임구궤도까지의 궤도진입 및 임무궤도상에서의 속도 또는 자세제어에 필요한 임펄스를 제공한다. 단일하이드라진 추력기는 하이드라진(H$_2$H$_4$)과 자발적 촉매(Shell 405)의 발열 및 흡열 열분해 반응에 의해 발생하는 질소($N_2$), 수소(H$_2$), 암모니아(NH$_3$), 혼합가스를 노즐을 통해 방출하므로써 요구되는 impulse를 얻는다. 단일하이드라진 추력기 설계는 주입기, 촉매대, 노즐과 기타 설계 형태에 따른 다지관, 링, 스크린, 지지판 등의 부수적인 부품으로 구성된다. 추력기 제작 과정은 크게 piece-parts 기계가공, HEA(Head End Assembly)와 TCA(Thrust Chamber Assembly)로 구성되고 각 세부공정마다 전수시험 및 검사를 가진다. 연소시험설비는 최소 모사진 공 수준이 고도 100,000 ft(8.4 torr)를 만족시킬 수 있는 진공설비, 시험제어부, 성능변수 측정 및 처리부, 추진제 가압 공급부, 기타 환경 안전 및 부대 설비로 구성된다. 추력기 연소성능시험 절차는 추진제 충전 및 오염 여부 표본 검사, 가압 및 공급 라인 이상여부 확인, 추력기 장착, 추진제 가압 및 공급, 시험장치 보정, 진공 모사 및 연소성능시험, data 처리 등으로 구성된다.

• Journal of Korean Society of Forest Science
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• v.65 no.1
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• pp.12-23
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• 1984

This study was carried out to investigate on the catalytic pyrolysis products of hardwood (Alnus hirsuta (Spach) Rupr. Quercus acutissima Carruters, Robinia pseudoacacia L., and Populus tomentaglandulosa T. Lee) and comparing the rate of catalytic pyrolysis from untreated wood (ordinary wood) with that of treated wood with catalizer (Ammonium phosphate, Ammonium sulfate, Ammonium chloride and Urea). The results were summerized as follows; 1) It is the Populus tomentiglandulosa T. Lee that the species has the most content of holocellulose and pentosan. And Populus tomentiglandulosa exhibited high yield of the distillate in pyrolysis products by Ammonium phosphate with catalizer. 2) The distillate of pyrolysis products is decreased in accordance with increasing catalytic concentration. And untreated wood (ordinary wood) with catalizer has the most distillate of pyrolysis products. 3) The yield of charcoal in pyrolysis products is increased in accordance with increasing catalytic concentration and lignin content of species. 4) The caloric values of charcoal in pyrolysis products is decreased with increasing catalytic concentration. And untreated wood (ordinary wood) with catalizer had the most caloric values, but the caloric values of charcoal did not show statistically significent difference at 5% levels in catalizer.

• Resources Recycling
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• v.21 no.2
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• pp.34-40
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• 2012

$Pt_{10}$/C, $Pt_9Mn_1$/C, $Pt_7Mn_3$/C electrocatalysts for Polymer Electrolyte Membrane Fuel Cells(PEMFCs) were synthesized by reduction with HCHO and their activity as a oxygen reduction reaction(ORR) was examined at half cell. The electrochemical oxygen reduction reaction(ORR) was studied by using a glaasy carbon electrode through cyclic voltammetric curves(CV) in a 1 M $H_2SO_4$ solution. The ORR activities of $Pt_9Mn_1$/C were higher than $Pt_{10}$/C, $Pt_7Mn_3$/C. Also potential-current curves of $Pt_9Mn_1$/C at 0.9, 0.8, 0.7, 0.6V for 5minutes respectively were higher than $Pt_{10}$/C, $Pt_7Mn_3$/C. Physical characterization was made by using x-ray diffraction(XRD) and transmission electron microscope(TEM). The TEM images of $Pt_9Mn_1$/C, $Pt_{10}$/C catalysts showed homogenous particle distribution with particle size of about 2.7 nm, 3 nm respectively and then the XRD results showed that the crystalline structure of the synthesized catalysts are seen FCC structure.

• Applied Chemistry for Engineering
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• v.19 no.1
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• pp.17-26
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• 2008

With the effectuation of Kyoto Protocol on the United Nations Framework Convention on the Climate Change, the emission reduction of greenhouse gases became an urgent issue and has been competitively secured among countries as the form of certificates through clean development mechanism (CDM) or joint implementation (JI). Nitrous oxide ($N_2O$) is one of the major greenhouse gases along with carbon dioxide ($CO_2$) and methane ($CH_4$) having warming potential 310 times that of carbon dioxide and chemically very stable in the atmosphere to give a life time of more than 120 years so that it reaches to the stratosphere to act as an ozone depleting substance. $N_2O$ hardly decomposes and thus, besides to the adoption of thermal decomposition at high temperature, selective catalytic reduction methods are usually used at temperatures over $400^{\circ}C$ in which the presence of NOx acts as a major impeding material in the decomposition process. In this article, the sources of various $N_2O$ generation, catalytic reduction processes and the status and trends of emission trade with CDM projects for greenhouse gas reduction are summarized and discussed on a condensed basis.