• 제목/요약/키워드: polymerization reaction

검색결과 612건 처리시간 0.025초

Syndiotactic Polymerization of Amino-functionalized Styrenes Using (Pentamethylcyclopentadienyl)titanatrane/MMAO Catalyst System

  • Kim, Young-Jo;Park, Sung-Jin;Han, Yong-Gyu;Do, Young-Kyu
    • Bulletin of the Korean Chemical Society
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    • 제25권11호
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    • pp.1648-1652
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    • 2004
  • A set of unprecedented syndiospecific dimethyl- and diethylamino-functionalized polystyrenes was prepared by catalytically polymerizing the corresponding monomers using (pentamethylcyclopentadienyl)titanatrane/MMAO catalytic system. Dialkylamino-functionalized styrene monomers were synthesized by Wittig reaction from the corresponding aldehyde in high yield. The resulting polymers are soluble in polar organic solvents such as THF and show good thermal stability. The chemical transformation of the syndiospecific poly(4-diethylaminostyrene) also gave new polar polymers, namely syndiotactic poly(4-diethylaminostyrene hydrochloride), which is unattainable by traditional synthetic methods.

The polymerization rate and the degree of conversion of composite resins by different light sources

  • Ryoo, Joo-Hee;Kwon, Hyuk-Choon
    • 대한치과보존학회:학술대회논문집
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    • 대한치과보존학회 2003년도 제120회 추계학술대회 제 5차 한ㆍ일 치과보존학회 공동학술대회
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    • pp.565-566
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    • 2003
  • The clinical performance of light polymerized composite resins is greatly influenced by the quality of the light curing unit used. Commonly used halogen light curing units(LCUs) have some specific drawbacks such as decreasing light output with time. To overcome this, the blue LED LCUs are newly developed and introduced. The purpose of this study was to observe the reaction kinetics and the degree of polymerization of composite resins when cured by different light sources and to evaluate the effectiveness of the blue LED LCUs compared with conventional halogen LCUs.(omitted)

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Polymerization of Tetrahydrofuran with New Transition Metal Catalyst and Its Mechanism: (p- Methylbenzyl)- o -cyanopyridinium Hexafluoroantimonate

  • 강준원;한양규
    • Bulletin of the Korean Chemical Society
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    • 제18권4호
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    • pp.433-438
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    • 1997
  • (p-Methylbenzyl)-o-cyanopyridinium hexafluoroantimonate, a new catalyst, was synthesized by the reaction of o-cyanopyridine with α-bromo-p-xylene followed by exchange of counteranion with SbF6θ. We examined the effect of the catalyst on the bulk polymerization of tetrahydrofuran under various conditions. The catalytic activity was best in the presence of 1 : 1 of epichlorohydrin used as cocatalyst versus catalyst concentration. The resulting polymers had relatively low conversions in 1.0-40%. Their number average molecular weights were in the range of 800 to 5300. Propagation rate increased with increase in temperature according to an Arrhenius expression giving an activation energy of 62 KJ/mol. We also found catalyst proceeds via a cationic mechanism.

Theoretical Study on Polymerization of Oxepane High Explosives

  • Kim, Joon-Tae
    • 통합자연과학논문집
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    • 제5권3호
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    • pp.175-181
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    • 2012
  • Oxepane high explosives substituted to explosive group such as azido, nitrato and hydrazino are investigated theoretically the acid catalyzed reaction using the semiempirical MINDO/3, MNDO and AM1 methods to use as the guidelines of high explosives. The nucleophilicity and basicity of oxepane high explosives can be explained by the value of negative charge on oxygen atom of oxepane and the reactivity in propagation step can be represented by the value of positive charge on carbon atom and low electrophile LUMO energy. It was known that carbenium ion was favorable due to the stable energy (19.507~32.101 Kcal/mol) between oxonium ion and carbenium ion in the process of cyclic oxonium ion of oxepane high explosives being converted to open carbenium ion in oxepane high explosives. The value of concentration of cyclic oxonium ion and open carbenium ion in equilibrium status was found to be a major determinant of mechanism, it was expected to react faster in the prepolymer propagation step in SN1 mechanism than in that of $S_N2$.

Chromatic Detection of Cholesterol Using Polydiacetylene Vesicles

  • Min Jae Shin
    • 공업화학
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    • 제34권6호
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    • pp.660-664
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    • 2023
  • In this study, a new system to determine the concentration of cholesterol using a color change was developed. The system comprised diacetylene vesicles and cholesterol oxidase (ChOx). 10,12-Pentacosadiynoic acid (PCDA) was used as the diacetylene compound, and PCDA vesicles were formed using sonication. The H2O2 produced during the reaction between cholesterol and ChOx was used to initiate the polymerization of the PCDA in the vesicles. During polymerization, the vesicles changed from colorless to blue. Therefore, the cholesterol concentration was proportional to the intensity of the blue color. The absorption at 665 nm indicated that the blue color was directly proportional to the cholesterol concentration. This indicates that the system can be used for cholesterol detection. The minimum cholesterol concentration detected using this system was 1.0 mM.

소수성 실리카를 안정제로 하는 현탁중합 II. 카본블랙을 함유하는 폴리스티렌 복합체 입자의 합성 (Suspension Polymerization with Hydrophobic Silica as a Stabilizer II. Preparation of Polystyrene Composite Particles Containing Carbon Black)

  • 박문수
    • 폴리머
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    • 제30권6호
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    • pp.505-511
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    • 2006
  • 물을 반응매체로 하고 카본블랙을 함유하는 폴리스티렌 복합체를 현탁중합법을 이용하여 입자형태로의 합성을 시도하였다. 안정제로는 소수성 실리카를, 개시제로는 지용성 안정제인 azobisisobutyronitrile (AIBN)을 선택하였다. 반응은 $75^{\circ}C$로 고정하였다. 안정제의 농도를 물에 대하여 $0.17{\sim}3.33wt%$까지 변화시킨 결과 1.67 wt%에서 최소 평균입경인 $7.96{\mu}m$의 입자가 형성되었다. 가교제인 divinylbenzene(DVB)은 단량체에 대하여 $0.1{\sim}1.0wt%$까지 변화시킨 결과 가교제의 농도가 증가함에 따라 입자간의 응집이 발생하며 평균입경이 크게 증가하였다. 카본블랙의 농도가 단량체에 대하여 1.0 wt%에서는 단량체만으로 구하여진 입자의 입경에 비하여 평균입경이 큰 폭으로 증가하였다. 이는 혼합물이 분산에 필요한 최소점도에 미치지 못하며 균일한 분산이 이루어지지 못한 결과 발생한 것으로 사료된다. 단량체 대비 3.0 wt% 카본블랙 혼합물의 경우에는 혼합물의 점도 증가로 인한 분산의 향상으로 평균입경이 감소하였다. 이 두 농도의 경우 중합반응 이전의 혼합물의 예비입자 및 중합반응 후의 고분자복합체 입자의 입경은 유사한 경향을 나타내었다. 카본블랙의 농도가 단량체 대비 5.0 및 7.5 wt%에서는 혼합물의 점도가 큰 폭으로 상승하고 그 결과 균일한 분산이 이루어지며 예비입자의 평균입경은 감소하였으나, 중합반응 과정에서 입자응집 현상이 발생하며 고분자 복합체의 평균입경은 다시 증가하였다.

유기티타늄을 촉매로 한 폴리트리메틸렌테레프탈레이트 합성에 관한 연구 (Synthesis of Poly(trimethylene terephthalate) Using an Organic Titanium Compound as a Catalyst)

  • Pio Sifuentes;Kim, Kap-Jin
    • 한국섬유공학회:학술대회논문집
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    • 한국섬유공학회 2003년도 봄 학술발표회 논문집
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    • pp.335-336
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    • 2003
  • The synthesis of poly(trimethylene terephthalate) (PTT), whose application is being expanded very rapidly to new apparel and carpet materials, was investigated by melt condensation polymerization using 1,3-propanediol (PDO) and terephthalic acid (TPA). No catalyst was used in the 1st step reaction (esterification), but tetrabutyl titanate(TBT) was used as a polyesterification catalyst ranging from 25 to 75 ppm based on the weight of TPA used in the 2nd step reaction (polyesterification). The molar ratio of PDO to TPA was set as 2.2:1. The effect of reaction conditions on the color and intrinsic viscosity of the final product was investigated. (omitted)

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솔젤법으로 제작한 $TiO_2-V_2O_5$ 세라믹스의 물성 (Properties of $TiO_2-V_2O_5$ Ceramics Prepared by Sol-Gel Method)

  • 유도현
    • 전기학회논문지
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    • 제56권7호
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    • pp.1255-1260
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    • 2007
  • [ $TiO_2-V_2O_5$ ] sol was prepared using sol-gel method. Sol changed to gel with hydrolysis and polymerization. DTA properties of gel powder had endothermic reaction due to evaporation of propanol about $80^{\circ}C$, had exothermic reaction due to combustion of propanol about $230^{\circ}C$ and had exothermic reaction due to combustion of alkyl group about $350^{\circ}C$. Crystalline properties of gel powder retained amorphous phase at $50^{\circ}C$, retained anatase phase from $400^{\circ}C\;to\;600^{\circ}C$ and had all rutile phase over $700^{\circ}C$ at 0.01mole $V_2O_5$ additive. The capacitance of thin films increased with increasing heat treatment temperature and thin films had best properties at $700^{\circ}C$. The capacitance of thin films increased a lot with decreasing measurement frequency.

Development of Click Chemistry in Polymerization and Applications of Click Polymer

  • Karim, Md. Anwarul
    • 고무기술
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    • 제13권1호
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    • pp.1-9
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    • 2012
  • Click chemistry had enjoyed a wealthy decade after it was introduced by K.B.Sharpless and his co-worker on 2001. Since there is no optimized method for synthesis of click polymer, therefore, this paper introduced three click reaction methods such as catalyst, non-catalyst and azide-end capping for fluorene-based functional click polymers. The obtained polymers have reasonable molecular weight with narrow PDI. The polymers are thermally stable and almost emitted blue light emission. The synthesized fluorene-based functional click polymers were characterized to compare the effect of click reaction methods on polymer electro-optical properties as well as device performance on quasi-solid-state dye sensitized solar cells (DSSCs) applications. The DSSCs with configuration of $SnO_2:F/TiO_2/N719$ dye/quasi-solid-state electrolyte/Pt devices were fabricated using these click polymers as a solid-state electrolyte components. Among the devices, the catalyzed click polymer composed device exhibited a high power conversion efficiency of 4.62% under AM 1.5G illumination ($100mW/cm^2$).These click polymers are promising materials in device application and $Cu^I$-catalyst 1, 3-dipolar cycloaddition click reaction is an efficient synthetic methodology.

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석유계 잔사유 및 coal-tar의 핏치 개질 특성 (Characterization of Pitch Derived from Petroleum Residue and Coal-tar)

  • 김지홍;김형기
    • 한국수소및신에너지학회논문집
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    • 제27권5호
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    • pp.612-619
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    • 2016
  • Pitch synthesis reaction was studied based on the effect for chemical composition of feedstock. Feedstock was selected as pyrolyzed fuel oil (PFO) and coal-tar (CT), which are by-products in petroleum and steel industry. Pitch was prepared at $420^{\circ}C$ for 180 minutes on atmospheric pressure by thermal treatment. Thermal stability and softening point (SP) of the prepared pitches were investigated and their molecular weight distribution was analyzed by MALDI-TOF. PFO has various aliphatic compounds and coal-tar has high aromaticity with 3 wt% of primary quinoline insolubles. The thermal property of PFO was enhanced with polymerization reaction during the thermal treatment with increased molecular weight range. But CT was inferior to PFO because of side reaction by hetero elements. CTP was appeared molecular weight by 0~200 m/z.