• 공업화학
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• 제9권2호
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• pp.294-299
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• 1998

입자당 한 개 이상의 성장라디칼이 있는 일반계에서 근사적인 psedo-homopolymerization (PHP)방법의 신뢰성을 간접적으로 증명하기 위하여, 벌크중합의 Mayo-Lewis식이 Interval II 동안 유화중합의 순간공중합조성식으로부터 확률적으로 유도됨을 보였다. Ballard등에 의하여 제안된 유화공중합의 확장된 Smith-Ewart식으로부터 0-1계(입자당 1개 이하의 성장라디칼이 있는 계)에 대하여 완전해를 얻었다. 이 해를 사용하여 입자당 평균라디칼수와 순간공중합조성이 몇 분 이내에 정상상태에 도달함을 예측할 수 있었다. 따라서 0-1계에 국한하여 PHP근사방법의 신뢰성을 직접 증명할 수 있었다. 모델계산의 목적으로 Styrene-butadiene(St-Bu)과 Styrene-methyl methacrylate(St-MMA)계를 예로 들었다.

• 공업화학
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• 제9권2호
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• pp.300-305
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• 1998

세 종류의 모노머로 구성된 삼모노머중합의 동력학을 입자성장이 끝난 interval II 동안 pseudo-homopolymerization (PHP) 방법에 의하여 연구하였다. 삼모노머중합의 Smith-Ewart 확장식과 순간중합조성식을 단일유화중합의 해당식과 유사하게 나타낼 수 있었다. 입자당 평균라디칼수와 순간중합조성을 라텍스입자내의 모노머조성을 변화시킴으로써 입자당 자유라디칼수가 한 개 이하인 계에서 예측하였다. 모델계산의 예로서 Styrene-Methyl methacrylate-Acrylonitrile(SMA)계의 속도상수들을 사용하였다.

• Nuclear Engineering and Technology
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• 제9권2호
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• pp.65-74
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• 1977

High dose rates꼭 전자선을 이용하여 Polyester 직포에 acrylic acid를 중합 반응시켰다. Homopolymerization inhibitor로서 cation 을 첨가시키면 hoinopolymerization 뿐만 아니라 graft효율도 감소되었다. Graft 중합 반응 속도는 선량율이 1.6$\times$$10^{6}$rad/sec에서부터 10$\times$$10^{6}$ rad/sec 사이에서 선량율의 0.82승에 비례하였다. Acrylic acid가 graft 중합 반응된 Polyester 직포는 흡습성, 제전성 효과 등이 크게 증진되었다.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1992년도 제1차 학술발표초록집
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• pp.7-7
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• 1992

• Bulletin of the Korean Chemical Society
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• 제22권6호
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• pp.629-632
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• 2001

• Bulletin of the Korean Chemical Society
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• 제34권9호
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• pp.2720-2724
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• 2013

Polynorbornenes prepared by vinyl addition pathway are known to have some desirable characteristics for wider application but they have some critical drawbacks such as brittleness, poor solubility and adhesion. In order to improve these drawbacks, extensive research for the successful homo- and copolymerization of polar functionalized norbornene with olefin has been carried out. Even though considerable advance has been achieved in the polymerization of polar functionalized monomers, successful catalytic systems for the homopolymerization of polar functionalized norbornene are rare. In this study, a novel successful catalytic system for the polymerization of polar functionalized norborene is proposed. This system employs Pd ${\beta}$-diketiminate/borate cocatalyst in water/organic mixed solvents and it is unique due to introduction of water as a component of solvents. Polymers obtained in this study show high Mw with narrow PDI. Effects of several reaction parameters to the polymer activity and properties are investigated and optimal catalytic system are proposed.

• 한국재료학회지
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• 제11권9호
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• pp.786-791
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• 2001

$\alpha$,$\omega$-Bis(4-glycidyloxybenzylidene-4-aminophenyl)methane (BGBAM) was synthesized from the initial materials, 4-hydroxylbenzaldehyde (HBA), 4,4'-methylenedianiline (MDA) and epichlorohydrin. The DSC trace for BGBAM shows two endotherms associated with the liquid crystalline phase transition around $104.2^{\circ}C$ and the isotropic transition around $171.2^{\circ}C$, and it also has a broad exotherm in the range of $178~300^{\circ}C$ due to the anionic homopolymerization of BGBAM. DSC curve for the curing of BGBAM with hexamethylene diamine (HMD) shows an endothermic peak around $93^{\circ}C$ attributed to the melting of BGBAM. It also has three exothermic peaks around $128.4^{\circ}C$ and $180.2^{\circ}C$ associated with the epoxide-amine reaction and weak peak in the range of $200~263^{\circ}C$ related to the anionic homopolymerization between the unreacted epoxide groups. The activation energy values of cure reaction by Kissinger method are 66.5, 67.3 and 90.6 kJ/mol for $T_{pl},\; T_{p2}\; and \;T_{p3},\; respectively$. The kinetic parameters by isoconverional method are similar value to those from Kissinger method.

• 대한화학회지
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• 제62권3호
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• pp.191-202
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• 2018

The aim of this work is to study Monte Carlo simulation of ethylene (co)polymerization over Ziegler-Natta catalyst as investigated by Chen et al. The results revealed that the Monte Carlo simulation was similar to sum square error (SSE) model to prediction of stage II and III of polymerization. In the case of activation stage (stage I) both model had slightly deviation from experimental results. The modeling results demonstrated that in homopolymerization, SSE was superior to predict polymerization rate in current stage while for copolymerization, Monte Carlo had preferable prediction. The Monte Carlo simulation approved the SSE results to determine role of each site in total polymerization rate and revealed that homopolymerization rate changed from site to site and order of center was different compared to copolymerization. The polymer yield was reduced by addition of hydrogen amount however there was no specific effect on uptake curve which was predicted by Monte Carlo simulation with good accuracy. In the case of copolymerization it was evolved that monomer chain length and monomer concentration influenced the rate of polymerization as rate of polymerization reduced from 1-hexene to 1-octene and increased when monomer concentration proliferate.

• 폴리머
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• 제32권4호
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• pp.366-371
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• 2008

The controlled/living cationic polymerization of $\alpha$-methylstyrene (${\alpha}MeSt$) and sequential block copolymerization of isobutylene (IB) with ${\alpha}MeSt$ were achieved using 2-chloro-2,4,4-trimethylpentane (TMPCl)/titanium tetrachloride ($TiCl_4$)/titanium isopropoxide ($Ti(OiPr)_4$)/2,6-ditert-butylpyridine (DtBP) initiating system in $CH_3Cl$/hexane(50/50 v/v) solvent mixture at $-80^{\circ}C$. The polymerization rate decreased with increasing $[Ti(OiPr)_4]/[TiCl_4]$ ratio in the homopolymerization of ${\alpha}MeSt$. The effects of $[Ti(OiPr)_4]/[TiCl_4]$ ratios and $PIB^+$ molecular weight on the polymerization rate and blocking efficiency were also investigated. Well-defined poly(isobutylene-b-$\alpha$-methylstyrene)s were demonstrated by $^1H$-NMR and triple detection SEC; refractive index (RI), multiangle laser light scattering (MALLS) and ultraviolet (UV) detectors. Blocking efficiencies for the poly(isobutylene-b-$\alpha$-methylstyrene)s of almost 100% were obtained when ${\alpha}MeSt$ was induced by PIB's of $M_n\;{\geq}\;41000$ at $[Ti(OiPr)_4]/[TiCl_4]=1$. Differential scanning calorimetry (DSC) of the block copolymers showed two glass transition temperatures, thereby demonstrating microphase separation.

• 멤브레인
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• 제23권3호
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• pp.220-225
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• 2013

친수성 단량체를 polyvinylidene fluoride (PVDF) 분리막 표면에 열중합으로 lamination하여 분리막을 친수화하였다. 친수화 처리 후 접촉각은 $95^{\circ}$에서 $55^{\circ}$까지 감소하였고 수투과량은 10배 이상 증가하였으며 bovine serum albumin (BSA) 흡착량은 1/4 수준으로 감소하였다. 열중합 공정에서 각 공정변수별 영향을 조사하였고 이를 최적화하였다. 단량체 중 dimethyl oxobuthyl acrylamide (DOAA)가 친수성이 높아 다른 단량체에 비하여 친수화 효과가 우수하였다. 단량체의 농도가 증가함에 따라 성능이 향상되었으나 30 wt% 이상의 경우 homopolymerization을 유발하여 성능을 저하시켰다. 개시제로 사용되었던 azobis (isobutyronitrile)(AIBN)의 활성 온도 범위가 benzoyl peroxide (BPO)의 활성온도 범위보다 넓기 때문에 높은 친수화 효율을 나타내었다. 개시제를 먼저 도포시켜주고 단량체를 나중에 첨가하는 2단계 lamination 방식이 일괄 공급하는 1단계 방식보다 친수화도는 크게 향상됐지만 pore blocking현상이 나타나면서 순수투과도는 매우 감소하였다.