• 한국세라믹학회지
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• 제33권9호
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• pp.1045-1049
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• 1996

Pressureless-sintered polycrystalline alumina and carbon steel were joined with Ag-33.5Cu-1.5Ti (wt%) brazing alloy. SEM observation revealed that two reaction layers with different thicknesses were continuously formed between the alumina and the brazing alloy. A thick layer formed on the brazing alloy side was identified as Ti3(Cu0.93Al0.07)3O phase with diamond cubic structure. Another thin layer adjacent to the alumina was revealed as $\delta$-TiO phase of which the crystal structure was HCP with a lattice parameter of a0=0.419 nm and c0=0.284 nm. It was confirmed using XPS analysis that $\delta$-TiO was formed directly by a redox reaction of alumina with titanium ir, molten brazing alloy.

• Journal of Photoscience
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• 제6권2호
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• pp.57-60
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• 1999

The reaction of [1.1.1]propellane with singlet methylene afforded 1,3-dimethylenecyclobutane and [l.1.1.1]paddlane (3). Various minor products were also produced. The reaction of [1.1.1]propellane with triplet methylene afforded 1,3-dimethylenecyclobutane (2) and various minor products. But even trace of [1.1.1.1]paddlane was not detected. The mechanism for the addition of singlet methylene involved [1.1.1.1]paddlane intermediate The addition of triplet methylene led to diradical intermediate. In order to reveal the reaction pathway for generation of various ruiner products, various studies were carried out under the same condition.

• Archives of Pharmacal Research
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• 제12권4호
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• pp.259-262
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• 1989

The reaction of the sodium salts of 4-methoxy and 4, 7-dimethoxy 6-hydroxy benzofuran-5-carboxylic acid with ethyl chloroformate yields the corresponding dicarbethoxy derivatives. The N-substituted amides were obtained by treating the latter compounds with amines. The corresponding hydrazides were synthesized by the reaction of hydrazine hydrate on the dicarbethoxy derivatives which spontaneously cyclized to 5-substituted-2, 3- dihydro-1, 3, 4, -oxadiazol-2-one. Also the reaction with phenyl hydrazine has been studied. The dicarbethoxy derivatives and N-substituted amides were tested against Gram positive and Gram negative bacteria in vitro. Most of the compounds posses moderate or slight activity against Gram positive bacteria.

• 한국미생물·생명공학회지
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• 제18권5호
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• pp.466-470
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• 1990

아스콜빈산 (Ascorbic acid, AA)과 Aflatoxin ($B_1\; AFB_1$) 의 반응생성물 ($37^{\circ}C$ pH5에서 5일간 반응) 그리고 산화제(cupric ion, $Cu^{2+}$)와 환원제(cysteine) 존재하에서 얻어진 동 반응생성물의 돌연변이 유발성에 대한 특성을 Salmonella assay system에 의하여 살펴보았다. AA와 $AFB_1$의 반응생성물의 돌연변이 유발성은 대조군인 $AFB_1$의 경우보다 73 감소하였고, $Cu^{2+}$이 첨가된 AA와$AFB_1$반응생성물의 돌연변이 유발성은 더욱 감소되어 거의 돌연변이성을 나타내지 않았다. 그리고 cysteine의 존재하의 AA와 $AFB_1$ 반응생성의 돌연변이 유발성은 $AFB_1$ 단독보다는 약간 낮고, $Cu^{2+}$나 AA+$AFB_1$ 반응생성물보다는 약간 높은 경향을 보였다. 그러므로 AA와 $AFB_1$의 반응 체계에 있어서 AA는 $AFB_1$의 분해 또는 전환에 영향을 주고 있으며 동 반응생성물은 $AFB_1$ 단독이 갖는 돌연변이 유발성보다는 현저히 낮았고 이 때 산화환원제의 존재 역시 돌연변이성에 영향을 주었다.

• 대한환경공학회지
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• 제29권7호
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• pp.810-819
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• 2007

물유리와 수산화나트륨 용액을 이용하여 플라이 애쉬와 고로슬래그의 알칼리 활성에 관한 연구를 수행하였다. 플라이 애쉬/슬래그 시멘트 페이스트(FSC)의 반응생성물과 미세구조를 관찰하기 위하여 XRD, FTIR, $^{29}Si$ and $^{27}Al$ NMR, TGA and SEM 분석을 수행하였다. 무정형 상태 또는 저급 결정구조를 가진 calcium silicate hydrate와 aluminosilicate 겔이 각각 고로슬래그와 플라이 애쉬의 알칼리 활성반응에 의해 생성되었다. 실험결과, 물유리 모듈 1.0과 1.2가 플라이 애쉬와 고로슬래그의 알칼리 활성반응을 위해 적정한 것으로 나타났다. 물유리 모듈 1.0과 1.2로 알칼리 활성화된 FSC 페이스트는 플라이 애쉬와 고로슬래그의 알칼리 활성반응에 의해 생성된 겔 형태의 반응생성물과 물유리에 의한 또 다른 수화물(즉 실리카겔)에 의해 좀 더 단단하고 연속적이 모체가 형성되었음을 보여주었다.

• Preventive Nutrition and Food Science
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• 제2권3호
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• pp.232-235
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• 1997

This study was investigated to determine antimutagenic effects of enzymatic browning reaction products (PEBRPs) obtained by reaction of polyphenol compouns with oxidase extracted from potato. Catechol (Ca) PEBRPs showed the strongeest inhibitor effects with 90% inhibition on benzo-($\alpha$)-pyrene(B($\alpha$)P) induced mutagenesis in Salmonella typhimurium TA98, but he least with40% inhibition on the 2-aminofluorene (2-AF) induced mutagenesis in TA98. The strong antimutagenic activities with 80% inhibition were observed in the presence of 100$\mu\textrm{g}$/plate of hydroquinone(HQ)-PEBRP on the B($\alpha$)P or 3-amino-1,4-dimethyl-5H-pyrido[4,3-b]indole(Trp-P-1) induced mutagenesis in TA98, whereas HQ-PEBRP showed the least antimutagenic effect on 2-AF-induced mutagenesis. The addition of 100$\mu\textrm{g}$ hydroxyhydroquinone(HHQ)-PEBRP to the plate led to approximately 82% inhibitory effects on 2-AF or Trp-P-1 induced mutagenesis in TA98, whereas the least antimutagenicity was obsrved in the4-nitroquinoline-1-oxide(4-NQO) induced mutagenesis in the presence of 100$\mu\textrm{g}$/plate of HHQ-PEBRP. More than 80% inhibiton were observed in the presence of 200$\mu\textrm{g}$/plate of Pyrogalol(Py)-PEBRP on the B($\alpha$)P or Trp-P-1 induced mutagenesis in TA98, but the least with 38% inhibition on 4-NQO induced mutagenesis in TA98. The results indicate that enzymatic browing reaction products of potato have a strong modulatory effect on mutagen induced mutagenesis in TA98.

• 콘크리트학회지
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• 제6권2호
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• pp.108-117
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• 1994

국내에서는 아직 알칼리-골재 반응으로 인한 피해가 보고되지는 않았지만, 해사와 쇄석의 사용이 증가하고 있어 이에 대한 연구가 시급히 진행되어야 할 것으로 사료되어, 화학법(KS F 2545, ASTMC 289)과 모르터바법(KS F 2546, ASTM C 227)을 중심으로 실험을 행하여 국내산 쇄석1종과 국외산 쇄석 1종이 유해로 판정되었으며, 첨가알칼리성량 및 종류를 달리하여 실시한 모르터바법 시험결과 첨가 알카리로 NaCl사용시 가장 높은 팽창을 하였다. 또한, 모르터바의 표면 및 내부의 반응생성물을 SEM에 의한 관찰과 EDXA에 의한 성분분석을 실시하여 알칼리와 실리카성분으로 이루어진 알칼리 실리케이트 겔임이 판명되어 국내에서 알칼리 반응성을 나타내는 골재의 존재가 처음으로 확인되었다.

• Bulletin of the Korean Chemical Society
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• 제20권4호
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• pp.422-426
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• 1999

The Grignard reactions of bis(chloromethyl)dimethylsilane (1) with trimethylchlorosilane (2) in THF give both the intermolecular C-Si coupling and intramolecular C-C coupling products. At beginning stage, 1 reacts with Mg to give the mono-Grignard reagent ClCH2Me2SiCH2MgCl (1) which undergoes the C-Si coupling reaction to give MC2Si(CH2SiMe3)2 3, or C-C coupling to a mixture of formula Me3SiCH2(SiMe2CH2CH2)nR1 (n = 1, 2, 3, ..; 4a, R1I = H: 4b, R1 = SiMe3). In the reaction, two reaction pathways are involved: a) Ⅰ reacts with 2 to give Me3SiCH2SiMe2CH2Cl 6 which further reacts with Mg to afford a Me2SiCH2Mel-SiCH2MgCl (Ⅱ) or b) I cyclizes intramolecularly to a silacyclopropane intermediate A, which undergoes a ring-opening polymerization by the nucleophilic attack of the intermediates I or Ⅱ, followed by the termination reaction with H2O and 2, to give 4a and 4b, respectively. As the mole ratio of 2/1 increased from 2 to 16 folds, the formation of product 3 increased from 16% to 47% while the formation of polymeric products 4 was reduced from 60% to 40%. The intermolecular C-Si coupling reaction of the pathway a becomes more favorable than the intramolecular C-C coupling reaction of the pathways b at the higher mole ratio of 2/1.

• 한국미생물·생명공학회지
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• 제26권3호
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• pp.264-268
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• 1998

덱스트란수크라제는 Sucrose를 이용하여 덱스트란의 합성을 촉진하는데 sucrose이외에 다른 탄수화물이 효소 반응기 중에 존재하는 경우에는 Sucrose의 glucose를 이 탄수화물에 전달하는 반응을 촉진하여 새로운 구조의 산물을 생산한다. Leuconostoc mesenteroides B-742CB로 부터 얻은 덱스트란수크라제를 이용하여 플루란을 변형하고 그 조건을 최적화 하고자 했다. 수용성 변형 플루란은 이론적 수율의 57%(<$\pm$5)를 얻었다. 플루란 변형의 최적 조건으로는 pH 5.2, 28$^{\circ}C$ 에서 기질 0.37%(w/v)와 반응한 효소의 농도와 Sucrose농도가 각각 0.1 U/$m\ell$과 48mM일 때였다. 변형 플루란을 pullulanase, endodextranase로 처리하여 변형 전의 플루란과가수분해 상태를 비교 분석한 결과 변형전의 산물에 비해 이들 가수 분해 효소에 대해 더 저항성을 보였다. 변형 플루란을 methylation과 산가수분해 후 TLC한 결과 sucrose의 glucose가 플루란 glucose의 C3, C4, C6 위치의 free-OH group에 수식된 새로운 구조의 변형 플루란임을 확인하였다.

• 한국수소및신에너지학회논문집
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• 제19권1호
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• pp.56-63
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• 2008

In this study, thermochemical degradation of hemicellulose by Acetone-Solvolysis, the effects of reaction temperature, conversion yield, degradation properties and degradation products were investigated. Experiments were performed in a tube reactor by varying reaction temperature from $200{\circ}C$ to $400{\circ}C$ at 40 min of reaction time. The liquid products from pyrolysis-liquefaction of hemicellulose contained various kinds of ketones. ketones, as 4-methyl-3-penten-2-one, 3-methylene-2-pentanone, 22,6-dimethyl-2, 5-heptadien-4-one, 4-methyl-2-pentanone, 5-methyl-2-hexanone, 3,5,5-trimethyl-2-cyclohexen-1-one, and bezenes. as 1,4-dimethylbenzene, 1-methyl-2-(1-methylethyl)-benzene, 1,4-dimethyl-2-(2-methylpropyl)benzene, 4-secbutyl-ethyl benzene, could be used as high-octane-value fuels and fuel additives. Combustion heating value of liquid products from thermochemical conversion processes of hemicellulose was in the range of $6,680{\sim}7,170cal/g$. After 40min of reaction at $400{\circ}C$ in Acetone-Solvolysis of hemicellulose, the energy yield and mass yield was as high as 72.2% and 41.2g oil/100g raw material, respectively.