• 대한화학회지
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• 제12권2호
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• pp.55-60
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• 1968

芳香族誘道體 化合物의 鹽素化反應을 紫外線照射 및 ${\gamma}$-線照射下에서 行하였던 바 ethyl,${\alpha} ,{\beta} -dichloro-{\beta}$-phenyl propionate의 境遇 紫外線下에서는 主로 p-chloro 化合物이 生成되었다. 같은 反應을 ${\gamma}$-線 照射下에서 行한 結果 에스텔과 鹽素의 몰比가 1:2일 때에는 p-chloro 化合物이 主로 生成되었으나 몰比가 1:8인 境遇에는 側鎖鹽素化物이라고 判斷되는 多鹽素化合物이 生成되었다. 反應生成物을 確認하기 爲하여서 ethyl , ${\alpha} ,{\beta} -dichloro-{\beta}$-(p-chlorophenyl) propionate 및 ethyl${\alpha} ,{\beta} -dichloro-{\beta}$ -($o$-chlorophenyl) propionate 를 各各 ${\gamma}$-線 照射下에서 鹽素化시켜 보았더니 p-chloro誘道體에서는 側鎖鹽素化物을, o-chloro誘道體에서는 o,p-dichlorophenyl 化合物에 各各 該當하는 鹽素化物을 生成하였다. 化合物 確認에는 放射化 thin layer chromatography를 利用 하였으며 鹽素含量을 放射化分析法을 分析하였다. 反應結果를 鹽素化反應에 對한 芳香族의 置換基의 效果와 關聯시켜 論議하였으며 實驗方法을 記述하였다.

• Macromolecular Research
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• 제17권9호
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• pp.646-650
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• 2009

We report the fabrication of pentacene organic field-effect transistors (OFETs) using a fluorinated styrene-alt-maleic anhydride copolymer gate dielectric, which was prepared from styrene derivatives with a fluorinated side chain [$-CH_2-O-(CH_2)_2-(CF_2)_5CF_3$] and maleic anhydride through a solution polymerization technique. The fluorinated side chain was used to impart hydrophobicity to the surface of the gate dielectric and maleic anhydride was employed to improve its wetting properties. A field-effect mobility of 0.12 cm$^2$/Vs was obtained from the as-prepared top-contact pentacene FETs. Since various functional groups can be introduced into the copolymer due to the nature of maleic anhydride, its physical properties can be manipulated easily. Using this type of copolymer, the performance of organic FETs can be enhanced through optimization of the interfacial properties between the gate dielectric and organic semiconductor.

• Bulletin of the Korean Chemical Society
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• 제23권4호
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• pp.549-554
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• 2002

Thermosensitive poly(organophosphazenes) bearing methoxy-poly(ethylene glycol) (MPEG) and alkylamines as substituents have been synthesized and characterized by elemental analysis, NMR spectroscopy, GPC, and DSC. All the polymers exhibited crystallinity, which was probably induced by the MPEG side chain of the polymers. All the polymers exhibited the lower critical solution temperature (LCSTs) in the range of 28 to $94^{\circ}C$ depending on several factors such as mole ratio of the substituents, kinds of PEG and alkylamines. The higher content of MPEG and shorter chain length of alkylamines of the polymers afforded the higher LCST. The LCSTs of the polymers exhibited almost concentration-independent behavior in the range of 3-30 wt % of the polymers in aqueous solutions. The polymers showed the higher LCSTs in the acidic solutions than in the neutral and basic solutions. The ionic strength of the polymer solution affected the LCST, which decreased with increased NaCl concentration. The polymer bearing almost equimolar substitutuents with the -N-P-N- unit has shown the LCST more sensitive to NaCl and pH than that with the -N-P-O- unit. The polymers were found to degrade in acidic solution but be very stable in alkali solution as well as in the buffer solution of pH 7.4.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1997년도 춘계학술대회
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• pp.75-75
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• 1997

뛰어난 혈당강하작용을 가지고 있는 oxirane carboxilic acid의 analogue 합성과 관련하여 oxirane carboxilic acid의 기본골격을 용이하게 형성할 수 있고 동시에 다앙한 관능기를 갖는 side chain을 도입할 수 있는 방법을 개발함으로써 다양한 유도체들을 합성하는데 이용하고자 함. 방법 및 결과 $\alpha$,$\beta$-unsaturated ester로부터 dioxirane을 이용한 직접적인 epoxidation을 통해서 보통의 방법으로는 얻기 어려운 oxirane carboxilic acid의 ester를 높은 수율로 합성할 수 있는 방법이 개발되었으며 특히 분자내에 cpoxide 존재하에서도 Mitsnobu 방법을 이용한 O-alkylation에 의해 aryl ether 결합을 형성할 수 있는 방법이 개발되었으며 이들 방법을 이용하여 다양한 유도체들을 합성하였다.

• Journal of Forest and Environmental Science
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• 제6권1호
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• pp.45-60
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• 1989

리그닌 생분해의 분해경로 및 매카니즘에 관한 연구가 최근 Kirk와 Higuchi 등에 의하여 활발히 연구되고 있다. 특히, Phanerochaete chrysosporium이 생산해내는 Lignlnase를 이용하여 매우 가치있는 연구 결과를 얻고 있다. 본 총설에서는 Kirk와 Higuchi의 허가를 얻어서 그들의 논문을 중심으로 리그닌의 중요한 결합 양식 별로 즉, ${\beta}$-O-4, ${\beta}$-5, ${\beta}$-1, ${\beta}$-6, 5-5 등의 결합 모델 화합물들의 분해경로 및 매카니즘에 관하여 조사 정리하였다.

• 대한환경공학회지
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• 제22권3호
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• pp.587-595
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• 2000

국내 하수처리장에 적용되는 BNR(Biological Nutrients Removal) 공정의 효율저하 원인은 유입원수의 낮은 C/N비와 탄소 (Carbon source) 부족이 가장 큰 것으로 지적되어 왔다. 탄소원의 효율적인 공급을 위해 1차 슬러지 산 발효조(Acid fermenter)를 이용하여 SCFAs(Short-Chain Fatty Acids) 생성을 유도할 수 있다. 본 연구에서는 side-stream의 산 발효조와 조합된 $A_2/O$ 프로세스를 운전하여 영양염류 제거에 미치는 영향을 연구하였다. 그 결과 산 발효조의 최대 SCFAs생성은 중온상의 SRT 4~5일에서 약 3.000mg/L(as COD), 대략 0.10~0.16 mg SCFA(as COD)/mg 1차 슬러지(as COD)로 나타났다. 또한 생성된 SCFAs의 성상비는 Acetic, Propionic, (iso)Butyric 및 (iso)Valeric이 1, 0.7, 0.5 그리고 0.6 순으로 나타났다. BNR공정의 side-stream 산 발효조 적용에 의한 영양염류 제거효율은 크게 증가하는 것으로 나타났다. T-N은 인공하수(R1)의 경우 35% 정도의 낮은 처리효율을 나타냈으나 인공 SCFA 주입(R2) 및 발효산물 투입(R3)의 경우 제거효율 74%, 76%로 크게 향상되는 것으로 나타났다. 또한 Phosphate 는 R1의 경우 45% 의 처리효율을 나타냈으나 R2, R3의 경우 73~74% 정도로 양호한 처리효율을 나타냈다. 이는 발효산물 및 SCFA 주입에 의해 혐기조에서 인의 방출 및 호기조에서 과잉섭취가 잘 이루어졌기 때문으로 R3의 경우 인의 방출율은 $0.34g\;PO_4-P/g$ COD로 기존 연구와 비교해서 유사한 것으로 나타났다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.215-215
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• 2011

The bonding configuration and adsorption stability of alanine and leucine adsorbed on Ge(100)-2${\times}$1 surface were investigated and compared using core-level photoemission spectroscopy (CLPES) and density functional theory (DFT) calculations. The bonding configuration, stability, and adsorption energies were evaluated for two different coverage levels. In both cases, the C 1s, N 1s, and O 1s core-level spectra at a low coverage (0.30 ML) indicated that the carboxyl and amine groups participated in bonding with the Ge(100) surface in an "O-H dissociated-N dative bonded structure". At high coverage levels (0.60 ML), both this structure and an "O-H dissociation bonded structure" were present. As a result, we found that alanine adsorbs more easily (lower adsorption energy) than leucine on Ge(100) surfaces due to less steric hindrance of side chain.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2006년도 추계학술대회
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• pp.438-442
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• 2006

The degradation of Nafion membrane by hydrogen peroxide was investigated in polymer electrolyte membrane fuel cell (PEMFC). Degradation tests were carried out in a solution of $10{\sim}30%$ hydrogen peroxide containing 4ppm $Fe^{2+}$ ion which is well known as Fenton's reagent at $80^{\circ}C$ for 48hr. Characterization of degraded membranes were examined through the IR, Water-uptake, Ion exchange capacity, mechanical strength and $H_2$ permeability. After degradation, C-F, S-O and C-O chemical bonds of membrane were broken by radical formed by $H_2O_2$ decomposition. Breaking of C-F bond which is the membrane backbone reduced the mechanical strength of Nafion membrane and hence induced pinholes, resulting in increase of $H_2$ crossover through the membrane. Also the decomposition of C-O and S-O, side chain and terminal bond of membrane, decreased the ion exchange capacity of the membrane.

• 한국응용과학기술학회지
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• 제10권2호
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• pp.81-90
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• 1993

The Surfactants composed of acylated aterocollagen which is produced by the acylation of the side chain amino radicals of aterocollagen with an aliphatic acid having 12 to 18 carbon atoms will be discussed in this study. This condensation is done at moderate reaction temperature (<$25^{\circ}C$) in aqueous alkaline solution. The products of this reaction were identified by UV/VIS spectroscopy and infrared spectroscopy. For these compounds, surface active properties and physical properties including isoelectric point, Krafft point, surface tension, critical micelle concentration(cmc), foaming power, viscosity behaviour, water holding capacity, skin irritation and emulsifying power were measured respectively. The experimental results received that the products have a good emulsifying power, excellent water holding capacity while having low skin irritation. Thus, these derivatives will be expected to be used as an emulsifying agent for O/W type cosmetic emulsion.

• 한국전기전자재료학회논문지
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• 제26권11호
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• pp.810-815
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• 2013

In this study, the capacitance and dielectric loss tangent of the silicone rubber which is combined with filler (30 phr~50 phr) have been measured on the range of 100 Hz~100 kHz and $30{\sim}170^{\circ}C$. It was found that when the frequency is 0.1 kHz~100 kHz and the silicone rubber is combined with 30 phr to 50 phr of filler, the capacitance of silicone rubber has increased by about 28.6 pF to 33 pF in 30 phr of filler, about 20 pF to 46.1 pF in 40 phr of filler and about 36.4 pF to 44 pF in 50 phr of filler. It seems that the volume of dielectric loss has gradually increased due to the temperature rise and the rotating of dipole in electric field through the electric dipole generated by the Si-O group which is induced by adding of filler, or the carbonyl group which is caused by oxidation. It seems that the dielectric dispersion in 0.1 kHz is caused by molecular motion of Siloxane group in main chain, and the dielectric dispersion in 10 kHz is caused by molecular motion of Methyl group in side chain.