• 한국응용과학기술학회지
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• 제25권2호
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• pp.115-122
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• 2008

The hydrosilylation is an addition reaction of Si-H bond to unsaturated double bonds, which provides a convenient mechanism to synthesize poly(dimethylsiloxane-co-methylsiloxane)copolymer having siloxy units in polymer backbone. In this study, Poly(dimethylsiloxane-co-methylsiloxane) copolymer was synthesized through the polymerization reaction of cyclopentasiloxane with poly(methyl-hydrogen) siloxane. Silicone-hydrogen functional group of the poly(dimethylsiloxane-co-methylsiloxane) copolymer was substituted to the alkyl groups by hydrosilylation. And their structure was analyzed with FT-IR, H-NMR and GPC instruments, respectively. Surface tension of the synthetic compounds is increased from 22dyne/cm to 25dyne/cm according to increase additional EO moles. The cmc which was evaluated by surface tension was ranged $10^{-5}$ to $10^{-4}mol/L$ and it was decreased according to increase of dimethyl siloxyl content. HLB number of these surfactants was evaluated 9.5 to 11.5 range. These silicone surfactants is applied to self-emulsifier defoamer and personal care products as surface tension depressant, emulsifier, foam control agent.

• Bulletin of the Korean Chemical Society
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• 제18권8호
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• pp.874-880
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• 1997

Various classes of phospholipids were investigated for the structural determination of fatty acyl groups by fast atom bombardment tandem mass spectrometry (FAB-MS/MS). Phospholipids were desorbed by FAB as molecules chelated with sodium ion (or ions). Collision-induced dissociation (CID) of intact sodium adduct molecular ions ([M+Na]+, [M-H+2Na]+ or [M+Na-2H]-) produced a series of homologous fragment ions via the charge-remote fragmentation along the fatty acid chains. These ions were found useful to locate the double bond positions even for the polyunsaturated fatty acid chains. The regiospecificity of the acyl chain linkages in phosphatidylcholine (PC) could also be determined based on the ratio of relative abundance of the product ions (i.e., [M+Na-85-R2COOH]+ vs [M+Na-85-R1COOH]+) in CID-MS/MS of [M+Na]+. These are generated by the loss of fatty acyl groups at sn-1 and sn-2, respectively, together with the choline group. In all the phospholipid compounds investigated, loss of the fatty acid at the sn-2 position was dominant. The present method was applied to the structural determination of molecular species of phosphatidylglycerols (PG) isolated from cyanobacterium Synechocystis sp. PCC 6803.

• Bulletin of the Korean Chemical Society
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• 제11권5호
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• pp.427-430
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• 1990

Cholesteryl aniline ($C_{33}H_{51}N$) is monoclinic, space group $P2_1$, with a = 9.020(3), b = 6.000(1), c = 27.130(9)${\AA},\;{\beta} = 98.22(2)^{\circ}$, Z = 2, Dc = 1.06 g/cm$^3$ and Dm = 1.04 g/cm$^3$. A diffraction data set was collected with Mo-$K_{\alpha}$ radiation (${\lambda} = 0.7107 {\AA}$) on a diffractometer with a graphite monochromator to a maximum 2${\theta}$ value of 50$^{\circ}$, by the ${\omega}-2{\theta}$ scan technique. The coordinates of the non-hydrogen atoms and their anisotropic temperature factors were refined by full-matrix least-squares methods to final R of 0.058. In cholesteryl group, bond distances were normal except in tail part, where high thermal vibration resulted in apparent shortening of the C-C distances. The crystal structure consists of bilayers of thickness $d_{001} = 27.13 {\AA}$, in each of which there is the tail to tail arrangement of molecules aligned in the unit cell with their long axes approximately parallel to the [104] axis. The two halves of the double layer are related to each other by the screw axis.

• 공업화학
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• 제32권2호
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• pp.219-223
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• 2021

Considering the current COVID 19 pandemic, herein, we developed a material that can be used to fabricate a device for checking the body temperature of a person who has been exposed to influenza or corona virus. This material was formed by mixing pluronic F127 (F127) with a polydiacetylene (PDA) vesicle, which was formed with 10,12-pentacosadiynoic acid. The color of the system started to change from blue to light purple at 37 ℃, finally turning reddish at 40 ℃. Thus, the developed material can be used to detect changes in body temperature, and thus, detect signs of fever. The mixing ratio of the PDA vesicle and F127 was an important factor for controlling the temperature at which the color change started. The results showed that the color change accompanied by the separation of the PDA vesicle with F127. We believe that this phenomenon plays an important role in reducing the conjugation length in the double and triple bond of PDA.

• Elastomers and Composites
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• 제53권4호
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• pp.202-206
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• 2018

Five solution styrene butadiene rubber/neodymium butadiene rubber (SSBR/NdBR) composites were manufactured using different ratios of SSBR and NdBR. In this study, the composites were reinforced with NdBR and silica to confirm the physical properties of SSBR used for treads of automobile tires and the dispersibility with silica. The morphologies of the rubber composites were observed using field-emission scanning electron microscopy (FE-SEM). The crosslinking behaviors of the composites were tested using a rubber process analyzer (RPA), and the abrasion resistances were tested using a National Bureau of Standards (NBS) abrasion tester. The hardness values, tensile strengths, and cold resistances of the composites were also tested according to ASTM standards. Increased NdBR content yielded composites with excellent crosslinking properties, abrasion resistances, hardnesses, tensile strengths, and cold resistances. The crosslinking point increased due to the double bond in NdBR, thereby increasing the degree of crosslinking in the composites. The NdBR-reinforced composites exhibited excellent abrasion resistances, which is explained as follows. In SSBR, a breakage is permanent because a resonance structure between styrene and SSBR forms when the molecular backbone is broken during the abrasion process. However, NdBR forms an additional crosslink due to the breakdown of the molecular backbone and high reactivity of the radicals produced. In addition, the low glass transition temperature (Tg) of NdBR provided the rubber composites with excellent cold resistances.

• Bulletin of the Korean Chemical Society
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• 제17권3호
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• pp.257-262
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• 1996

p-(2-Vinyloxyethoxy)benzylidenemalononitrile 2 and methyl p-(2-vinyloxyethoxy)benzylidenecyanoacetate 3 was prepared by the condensation of p-(2-vinyloxyethoxy)benzaldehyde 1 with malononitrile or methyl cyanoacetate, respectively. Vinyl ether monomers 2 and 3 polymerized quantitatively with radical initiators in γ-butyrolactone solution at 65 ℃. The trisubstituted terminal double bond participated in the vinyl polymerization and radical polymerization of 2 and 3 led to swelling polymers 4 and 5 that were not soluble in common solvents due to cross-linking. Under the same polymerization conditions ethylvinyl ether polymerized well with model compounds of p-methoxybenzylidenemalononitrile 6 and methyl p-methoxybenzylidenecyanoacetate 7, respectively, to give 1:1 alternating copolymers 8 and 9 in high yields. Polymers 4 and 5 showed a thermal stability up to 300 ℃ without any characteristic Tg peaks in DSC thermograms. Alternating copolymers 8 and 9 were soluble in common solvents such as acetone and DMSO, and the inherent viscosities of the polymers were in the range of 0.36-0.74 dL/g. Films cast from acetone solution were cloudy and tough and Tg values obtained from DSC thermograms were in the range of 59-60 ℃.

• Bulletin of the Korean Chemical Society
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• 제18권3호
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• pp.274-280
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• 1997

The rates and stoichiometry of the reaction of gallane-trimethylamine with selected organic compounds containing representative functional groups were examined in tetrahydrofuran solution under standardized conditions (THF, 0 ℃). And its reducing characteristics were compared with those of aluminum hydride-triethylamine(AHTEA). The rate of hydrogen evolution from active hydrogen compounds varied considerably with the nature of the functional group and the structure of the hydrocarbon moiety. Alcohols, phenol, amines, thiols evolved hydrogen rapidly and quantitatively. Aldehydes and ketones were reduced moderately to the corresponding alcohols. Cinnamaldehyde was reduced to cinnamyl alcohol, which means that the conjugated double bond was not attacked by gallane-trimethylamine. Carboxylic acids, esters, and lactones were stable to the reagent under standard conditions. Acid chlorides also were rapidly reduced to the corresponding alcohols. Epoxides and halides were inert to the reagent. Caproamide and nitrile were stable to the reagent, whereas benzamide was rapidly reduced to benzylamine. Nitropropane, nitrobenzene and azoxybenzene were stable to the reagent, whereas azobenzene was reduced to 1,2-diphenylhydrazine. Oximes and pyridine N-oxide were reduced rapidly. Di-n-butyl disulfide and dimethyl sulfoxide were reduced only slowly, but diphenyl disulfide was reduced rapidly. Finally, sulfones and sulfonic acids were inert to the reagent under the reaction.

• 대한설비공학회지:설비저널
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• 제9권2호
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• pp.93-103
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• 1980

A small domestic solar water heating system in thermosyphonic flow was tested in Seoul. The system consisted of four flat plate aluminium roll bond type collectors of total effective area $3.28m^2$ and a $280{\iota}$ storage tank. It was tilted $52^{\circ}$ relative to the horizon. And the collector plate, collector tube and storage tank were equiped with 14 thermocouples. As the results, the following facts were found; 1) To provide water at $55^{\circ}C$ for a family of four in Seoul, a collector area of $3-4m^2$ and a storage capacity of $180{\iota}- 200{\iota}$ are suggested. And this system can supply hot water at above $45^{\circ}C$ day about. 2) In the late afternoon hours, it might be advantageous to stop the flow in the system as heat losses to the environment increase unduly. 3) Without any hot water consumption throughout the day, water temperature distributions inside the storage tank was found almost linear. This indicates essentially no mixing inside the storage tank. 4) In case of a small domestic solar water heating system, it is better to employ a single transparent cover rather than double one.

• Journal of the Korean Wood Science and Technology
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• 제38권4호
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• pp.316-322
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• 2010

본 연구의 목적은 폐식용유를 오존산화 처리에 의한 구조적 변성을 시도하고 이를 pMDI와 반응시켜 목재접착제로 개발하고자 하는 것이다. 폐식용유를 사용하여 1, 2, 3시간 오존산화 처리 한 후 화학적 변화를 알아보기 위하여 FT-IR을 측정하였다. 또한 접착강도를 조사하기 위하여 상태, 내수, 내온수, 반복끓임 실험을 하였다. FT-IR 측정 결과, 폐식용유의 오존산화가 진행될수록 불포화 이중결합에 기인한 3,010 $cm^{-1}$ 부근의 흡수가 사라지고 1,700 $cm^{-1}$ 부근의 카르복실기의 흡수가 크게 나타났다. 특히 3시간대에 3,010 $cm^{-1}$ 부근에 이중결합이 거의 사라짐을 알 수 있었다. 3시간 처리한 폐식용유의 상태 접착력 시험 결과, 폐식용유: pMDI 비율이 1 : 0.5일 때 8.08 kgf/$cm^2$, 1 : 0.75일 때 9.53 kgf/$cm^2$, 1 : 1일 때 44.16 kgf/$cm^2$ 1 : 2일 때 58.08 kgf/$cm^2$, 1 : 3일 때 61.41 kgf/$cm^2$, 1 : 4일 때는 46.95 kgf/$cm^2$를 나타내어 MDI와의 적정당량이 1 : 2, 1 : 3 부근에서 결정됨을 알 수 있었다. 중량비 1 : 2, 1 : 3만을 선택하여 각각 내수, 내온수, 반복끓임 상태로 접착강도 시험을 실시하였다. 내수 접착강도에서는 1 : 3의 경우가 더 높은 값을 보였으나 실험조건이 강화된 내온수, 반복 끓임에서는 혼합비율 1 : 2와 1 : 3이 비슷한 값을 나타내었다.

• 한국식품과학회지
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• 제36권3호
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• pp.398-402
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• 2004

신소재로 각광 받고 있는 chitosan의 낮은 수용성을 극복하기 위하여 chitosan 유도체인 safrolechitosan(SaCs) 및 eugenolchitosan(EuCs)을 제조하고, Ubbelohde 점도계를 사용하여 이들의 점도평균분자량을 측정한 결과, chitosan 및 chitosan유도체인 EuCs와 SaCs의 경우 각각 $1.2{\times}10^{5}\;Da,\;7.8{\times}10^{5}\;Da$ 및 $7.5{\times}10^{5}\;Da$인 것으로 확인되었다. Chitosan과 chitosan유도체의 구조분석을 위한 IR spectrum에서 SaCs의 경우, safrole의 공유결합에 의한 chitosan내 amine기와의 반응으로 인하여 순수 chitosau보다 amide II 흡수띠가 $1,553cm^{-1}$으로 이동함을 알 수 있었는데, 이것은 chitosan내의 1차 amine기와 safrole의 이중결합이 반응하여 공유결합을 형성함으로써 흡수띠의 이동현상이 나타난 결과이다. 또한, safrole이 반응하면서 safrole내의 vinyl기를 의미하는 특징적인 peak인 C=C 및 $H_{2}C=$의 $1,611cm^{-1}$와 $1,442cm^{-1}$에서의 흡수띠가 사라졌으며, EuCs의 경우에도 반응물질로 사용된 eugenol내의 vinyl기를 나타내는 $1,612cm^{-1}$ 및 $1,434cm^{-1}$에서의 흡수띠가 사라짐을 확인하였다. 또한 $^{1}H-NMR\;spectrum$을 확인한 결과, 합성유도체의 경우 safrole과 eugenol 간량체의 5.7-6.0ppm에서 나타난 이중결합($H_{2}C=CH-$) peak가 사라지고, SaCs는 2.1-2.2ppm에서, 그리고 EuCs는 1.9와 2.2ppm에서 단일결합($-CH_{2}-CH_{2}-$)의 peak가 생성됨을 알 수 있었으며, safrole과 eugenol이 chitosan에 그라프트된 후 safrole과 eugenol의 영향으로 chitosan내의 $H_{3}-H_{6}$의 수소 숫자가 상대적으로 감소하여 3.1-3.9ppm에서 나타나는 peak의 크기가 작아짐도 확인하였다. 이상의 결과들을 종합해 볼때, SaCs 및 EuCs를 합성하기 위한 그라프트 반응이 정상적으로 일어났음을 알 수 있었다.