• Elastomers and Composites
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• 제39권2호
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• pp.153-160
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• 2004

풀러렌($C_{70}$)을 3-picoline N-oxide, pyridine N-oxide hydrate, quinoline N-oxide, isoquinolne N-oxide의 여러가지 아민 N-옥시드를 사용하여 $25{\sim}43^{\circ}C$, 초음파 조건에서 반응시켜 풀러렌 산화물을 합성 하였다. 동일한 초음파 조건에서 여러가지 아민 N-옥시드에 대한 풀러렌 ($C_{70}$)의 반응성은 3-picoline N-oxide : pyridine N-oxide hydrate : quinoline N-oxide : isoquinoline N-oxide 처럼 동일하게 나타났다. MALDI -TOF MS, UV-vis 그리고 HPLC를 사용하여 생성된 풀러렌 산화물을 분석한 결과 [$C_{70}(O)n$] (n=1) 임을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제34권11호
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• pp.3459-3462
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• 2013

• Macromolecular Research
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• 제17권10호
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• pp.739-745
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• 2009

N,N'-(bicyclo[2,2,2]oct-7-ene-tetracarboxylic)-bis-L-amino acids 3a-g were synthesized by the condensation reaction of bicyclo[2,2,2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride 1 with two equimolars of Lalanine 2a, L-valine 2b, L-leucine 2c, L-isoleucine 2d, L-phenyl alanine 2e, L-2-aminobutyric acid 2f and L-histidine 2g in an acetic acid solution. Seven new poly(amide-imide)s PAIs 5a-g were synthesized through the direct polycondensation reaction of seven chiral N,N'-(bicyclo[2,2,2]oct-7-ene-tetracarboxylic)-bis-L-amino acids 3a-g with bis(3-amino phenyl) phenyl phosphine oxide 4 by two different methods: direct polycondensation in a medium consisting of N-methyl-2-pyrrolidone (NMP)/triphenyl phosphite (TPP)/calcium chloride ($CaCl_2$/pyridine (py), and direct polycondensation in a tosyl chloride (TsCl)/pyridine (py)/N,N-dimethylformamide (DMF) system. The polymerization reaction produced a series of flame-retardant and thermally stable poly(amide-imide)s 5a-g with high yield. The resulted polymers were fully characterized by FTIR, $^1H$ NMR spectroscopy, elemental analyses, inherent viscosity, specific rotation and solubility tests. Data obtained by thermal analysis (TGA and DTG) revealed that the good thermal stability of these polymers. These polymers can be potentially utilized in flame retardant thermoplastic materials.

• Journal of Advanced Marine Engineering and Technology
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• 제38권9호
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• pp.1045-1050
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• 2014

아산화질소($N_2O$, Nitrous Oxide)는 이산화탄소($CO_2$, Carbon Oxide), 메탄($CH_4$, Metane)이어 세 번째로 지구온난화에 기여하는 물질로 알려져 있다. $N_2O$의 지구온난화 계수는 대기 중에서 안정하고, 성층권에서 광분해 된 후 이차적인 오염의 원인이 되기 때문에 $CO_2$의 310배에 이른다. $N_2O$의 생성에 대한 조사는 보일러와 같은 연속적인 연소를 갖는 동력원에 대하여 몇몇의 연구자들에 의한 보고가 있었다. 하지만, 디젤엔진에 있어서 연료의 성분이 $N_2O$ 배출에 미치는 영향에 대한 조사는 실시되어지지 않은 상태이다. 그러므로 본 연구에서는 디젤엔진에서 연료 중에 질소와 황 농도에 의해 변화되는 $N_2O$ 배출율에 대하여 조사하였다. 실험에 사용한 엔진은 12kW/2400rpm의 4행정 직접분사식 디젤엔진이고, 실험엔진의 운전조건은 75% 부하에서 이루어졌다. 연료 중의 질소와 황 농도는 Pyridine, Indole, Quinoline, Pyrrol, Propionitrile, Di-tert-butyl-disulfide의 6 종류 첨가제를 사용하여 증가시켰다. 결과에 의하면, 질소성분 0.3% 이하를 갖는 디젤연료는 첨가제의 종류와 농도와 관계없이 $N_2O$ 배출률에 영향을 미치지 않았다. 하지만, 연료 중 황 첨가제의 증가는 배기가스 중의 $N_2O$ 농도를 증가시켰다.

• Bulletin of the Korean Chemical Society
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• 제35권7호
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• pp.2155-2158
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• 2014

• 공업화학
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• 제7권3호
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• pp.490-495
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• 1996

Organocyclosiloxane oligomer[$(R_2SiO)_n$, n=2, 3, 4, 5]와 dimethyldichlorosilane을 Pyridine N-oxide 촉매 존재하에서 개환 반응시켜 linear chlorine terminated siloxane(yields;71.2~86.5%)를 얻었다. $0^{\circ}C$에서 linear chlorine terminated siloxane과 dimethylamine을 반응시켜 amino terminated siloxane oligomer(yields;76.2~85.3%)를 얻은 후 이 화합물들과 1,4-bis(dimethylhydroxysilyl)benzene을 반응시켜 공중합체들(yields;58.0~71.0%)을 합성하였다. 이들 공중합체의 구조는 FT-IR 및 $^1H$-NMR로 확인하였으며, DSC 및 TGA thermogram을 통하여 이들 중합체들의 열적특성을 조사하였다. TGA thermogram으로부터 polymer I (n=2)의 초기분해온도는 $476^{\circ}C$로 가장 낮았고, polymer IV(n=5)가 $485^{\circ}C$로 가장 높았다. n의 수가 증가할수록 열안정성은 다소 우수한 것으로 관찰되었고, DSC thermogram에서 중합체들의 유리전이온도는 polymr IV (n=5)가 $-76^{\circ}C$로 가장 낮았으며, n의 수가 감소할수록 높게 나타났음을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제15권10호
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• pp.873-881
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• 1994

The approximate rate and stoichiometry of the reaction of excess diisobutylaluminum hydride-dimethyl sulfide complex($DIBAH-SMe_2$) with organic compounds containing representative functional group under standardized conditions (toluene, $0{\circ}C$) were examined in order to define the reducing characterstics of the reagent and to compare the reducing power with DIBAH itself. In general, the reducing action of the complex is similar to that of DIBAH. However, the reducing power of the complex is weaker than that of DIBAH. All of the active hydrogen compounds including alcohols, amines, and thiols evolve hydrogen slowly. Aldehydes and ketones are reduced readily and quantitatively to give the corresponding alcohols. However, $DIBAH-SMe_2$ reduces carboxylic acids at a faster rate than DIBAH alone to the corresponding alcohols with a partial evolution of hydrogen. Similarly, acid chlorides, esters, and epoxides are readily reduced to the corresponding alcohols, but the reduction rate is much slower than that of DIBAH alone. Both primary aliphatic and aromatic amides examined evolve 1 equiv of hydrogen rapidly and are reduced slowly to the amines. Tertiary amides readily utilize 2 equiv of hydride for reduction. Nitriles consume 1 equiv of hydride rapidly but further hydride uptake is quite slow. Nitro compounds, azobenzene, and azoxybenzene are reduced moderately. Cyclohexanone oxime liberates ca. 0.8 equiv of hydrogen rapidly and is reduced to the N-hydroxylamine stage. Phenyl isocyanate is rapidly reduced to the imine stage, but further hydride uptake is quite sluggish. Pyridine reacts at a moderate rate with an uptake of one hydride in 48 h, while pyridine N-oxide reacts rapidly with consumption of 2 equiv of hydride for reduction in 6h. Similarly, disulfides and sulfoxide are readily reduced, whereas sulfide, sulfone, and sulfonic acid are inert to this reagent under these reaction conditions.

• Bulletin of the Korean Chemical Society
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• 제8권4호
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• pp.285-291
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• 1987

The approximate rates, stoichiometries and products of the reaction of potassium triethylborohydride $(KEt_3BH)$ with selected organic compounds containing representative functional groups under the standard condition $(0^{\circ}C,$ THF) were examined in order to explore the reducing characteristics of this reagent as a selective reducing agent. Primary alcohols, phenols and thiols evolve hydrogen rapidly whereas secondary and tertiary alcohols evolve very slowly. n-Hexylamine is inert to this reagent. Aldehydes and ketones are reduced rapidly and quantitatively to the corresponding alcohols. Reduction of noncamphor gives 3% exo- and 97% endo-norboneol. Anthraquinone is cleanly reduced to 9,10-dihydro-9,10-dihydroxyanthracene stage. Carboxylic acids liberate hydrogen rapidly and quantitatively but further reduction does not occur. Anhydrides utilize 2 equiv of hydride to give an equimolar mixture of acid and alcohol. Acid chlorides, esters and lactones are rapidly and quantitatively reduced to the corresponding alcohols. Epoxides are reduced at moderate rates with Markovnikov ring opening to give the more substituted alcohols. Primary amides liberate 1 equiv of hydrogen rapidly. Further reduction of caproamide is slow whereas benzamide is not reduced. Tertiary amides are reduced slowly. Benzonitrile utilizes 2 equiv of hydride in 3 h to go to the amine stage whereas capronitrile takes only 1 equiv. The reaction of nitro compounds undergo rapidly whereas azobenzene and azoxybenzene are reduced slowly. Cyclohexanone oxime rapidly evolves hydrogen without reduction. Phenyl isocyanate utilizes 1 equiv of hydride to proceed to formanilide stage. Pyridine N-oxide and pyridine is reduced rapidly. Disulfides are rapidly reduced to the thiol stage whereas sulfoxide, sulfonic acid are practically inert to this reagent. Sulfones and cyclohexyl tosylate are slowly reduced. Octyl bromide is reduced rapidly but octyl chloride and cyclohexyl bromide are reduced slowly.

• 통합자연과학논문집
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• 제6권2호
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• pp.76-81
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• 2013

ZnO nanoparticles and vinyl pyridine were added to the mixture of MMA (methyl methacrylate), HEMA (2-hydroxy ethyl methacrylate) and NVP (N-vinylpyrrolidone) in a mould at various concentrations. Cross-linker EGDMA (ethyleneglycoldimethacrylate) and AIBN (azobisisobutyronitrile) initiator were finally added to the mixture and then heated at $80^{\circ}C$ for 60 min to prepare high-performance hydrogel ophthalmic lens. The physical properties of the hydrogel ophthalmic material were investigated by measuring the average value of refractive index, water content and optical transmittance. The refractive index of 1.429~1.450, water content of 34~41%, and visible transmittance of 78~90% were obtained. The material is possibly used to manufacture UV-block hydrogel contact lens.

• 연구논문집
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• 통권31호
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• pp.23-43
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• 2001

An experimental investigation on the reduction of nitrogen oxide emission from swirling, turbulent diffusion flames was conducted using multi air staged combustor, The combustor utilizes swirler to dampen fuel/air mixing, allowing an extended residence time for fuel pyrolysis and fuel-N conversion chemistry in an locally fuel-rich environment prior to burnout. This process also allow to reduce thermal NOx formation to lessen the temperature of reaction zone. The aerodynamic process therefore emulates the conventional staged combustion process, but without the need for the physically separate fuel-rich and -lean stages. Parametric studies on the ratios of each staged air and droplet size were carried out the feasibility of fuel/air mixing for low NOx combustion with diesel and pyridine mixed diesel fuel oil.