• Macromolecular Research
• /
• 제17권7호
• /
• pp.483-490
• /
• 2009

Stable poly(styrene-co-divinylbenzene) [P(St-co-DVB)] micro spheres with narrow size distribution were synthesized in the presence of 2,2'-azobis(2,4-dimethyl valeronitrile) (V-65) and co-initiator in an acetone/water mixture in the precipitation polymerization at $53^{\circ}C$ for 24 h. Potassium peroxodisulfate (KPS), ammonium peroxodisulfate (APS) and sodium peroxodisulfate (NaPS) were used as co-initiators. The optimum ratio of acetone to water for the formation of a narrow distribution of P(St-co-DVB) particles was 49:11 (g/g). The optimum co-initiator compositions for narrow distribution were 9:1 (g/g) for V-65 to KPS, 11:1 for V-65 to APS and 6:1 for V-65 to NaPS. The yield for these compositions was $54{\sim}57%$ and the largest particle size was obtained with the lowest zeta-potential and CV values. From the XPS measurements, the charge density was increased but the zeta potential decreased with increasing sulfur content, implying that the sulfate group provides the electrostatic stabilization on the particle surface. This suggested that the self-crosslinking between styrene and DVB, the electrostatic stabilization of initiators, and the balanced hydrophobic and hydrophilic properties of the solvents are responsible for the formation of stable P(St-co-DVB) spherical particles with narrow size distribution.

• Macromolecular Research
• /
• 제12권5호
• /
• pp.519-527
• /
• 2004

Stable poly(methyl methacrylate-co-divinylbenzene) (poly(MMA-co-DVB)) microspheres were prepared by precipitation polymerization using acetonitrile as the main medium under various polymerization conditions, including modifications of the agitation speed, monomer and initiator concentrations, DVB content in the monomer mixture, and the use of various cosolvents. Gentle agitation was required to obtain smooth spherical particles. The individually stable microspheres were obtained at monomer concentrations of up to 15 vol% in an acetonitrile medium. The number-average diameter increased linearly with respect to increases in the monomer and initiator concentrations. We found, however, that the uniformity of the microspheres was independent of the variation of the polymerization ingredients because nuclei formation was solely influenced by the crosslinking reaction of the monomers. We obtained higher yields for the polymerization at higher concentrations of monomer and initiator. The concentration of DVB in the monomer mixture composition played an important role in determining not only the size of the microspheres but also the yield of the polymerization. In addition, although we employed various cosolvents as the polymerization medium, we found that acetonitrile/2-methoxyethanol was the only system that provided spherical particles without coagulation. This finding indicates that the precipitation polymerization is strongly dependent on the solvent used as the medium.

• 한국정보디스플레이학회:학술대회논문집
• /
• 한국정보디스플레이학회 2004년도 Asia Display / IMID 04
• /
• pp.1208-1211
• /
• 2004

When irradiated with visible light in HPDLC, photoinitiator and coinitiator produce a radical for photopolymerization. According to the kinds of photoinitiator and coinitiator, quantity and rate of produced a radical is different. It is influence on photopolymerization rate relate on diffraction efficiency. Thus, this paper is about the effect of photoinitiator/coinitiator combinations in terms of diffraction efficiency and real-time first order diffraction efficiency.

• Journal of Photoscience
• /
• 제5권2호
• /
• pp.63-67
• /
• 1998

New photoinitiator systems of dimethylphenacylsulfonium butyltnphenylborate (DMPSB) as a donor-acceptor initiator and styryl dyes have been investigated for free radical polymerization of an acrylate with visible lasers (488, 514 and 647 nm). DMPSB was able to be sensitized by many styryl dyes. When polymerized with pentaerythrithol triacrylate, the sensitivity value of the photosensitive layer containing DMPSB was higher than that of an tetrabutylammonium butyltnphenylborate (TBAB) as an electron donating initiator or a dimethylphenacylsulfonium tetrafiuoroborate (DMPS) as an electron accepting initiator. The sensitivity values of the photosensitive layer containing the photoinitiator systems had a close relation to the free energy changes between the excited singlet styryl dyes and DMPSB.

• 한국자동차공학회논문집
• /
• 제18권3호
• /
• pp.69-73
• /
• 2010

The melt grafting of unsaturated silanes onto polypropylene (PP) in a twin-screw extruder and crosslinking in hot water were studied to enhance impact strength of polypropylene. The influence of grafting formulations on the melt flow rates of grafted PP and the gel percentages of crosslinked PP was investigated. 3-methacryloylpropyltrimethoxysilane (VMMS) unsaturated silane monomer was used. Benzoyl peroxide, (BPO) and Dicumyl peroxide (DCP) were used as an initiator. When benzoyl peroxide (BPO) was used as an initiator, higher gel percentage and impact strength than those of DCP has been observed. The maximum impact strength was obtained with 0.7 phr of BPO and 2phr of VMMS. The value is 8.7 kgf-cm/cm and it is on a parity with the value of with 20 phr of EOR mixed to PP.

• Elastomers and Composites
• /
• 제28권3호
• /
• pp.191-197
• /
• 1993

The graft copolymerization of methyl methacrylate(MMA) onto natural rubber latex(NRL) initiated by t-butyl hydroperoxide(t-BHPO) was investigated in aquous medium. The grafting percentage, grafting efficiency and total conversion were observed in various reaction conditions such as monomer, initiator and emulsifier concentration, reaction temperature, reaction time and agitation speed. The optimum conditions for the graft copolymerization onto natural rubber latex were as follows ; At given monomer concentration of $3{\times}10^{-2}mole/l$, the maximum grafting percentage was appeared in the case of grading in initiator concentration of $4{\times}10^{-2}mo1e/l$ and emulsifier concentration of 0.2wt.% at $40^{\circ}C$ for 5hrs.

• 폴리머
• /
• 제38권1호
• /
• pp.16-23
• /
• 2014

A novel poly(AM-DMDAAC)/MMT superabsorbent nanocomposites are prepared by radical polymerization using ammonium persulfate (APS) and anhydrous sodium sulfite as a free radical initiator and N,N-methylene bisacrylamide (MBA) as a crosslinker. In this paper, an optimization study on the synthesis of superabsorbent nanocomposites is carried out. Orthogonal array experiment indicates that the optimized conditions is acrylamide (AM) content 23 wt%, diallyl dimethyl ammonium chloride (DMDAAAC) content 6 wt%, montmorillonite (MMT) content 4 wt%, initiator content 0.2 wt% and crosslinker content 0.02 wt%. Under the optimization syntheses conditions concluded, the maximum water absorbency in distilled water is $659.53g{\cdot}g^{-1}$ and in 2 wt% sodium chloride solution is $116.25g{\cdot}g^{-1}$. Compared with the range values of different factors ($R_j$), the order of significance factors in distilled water is C (MMT) > B (DMDAAC) > A (AM) > D (crosslinker) > E (initiator). MMT is intercalated during polymerization reaction and a nanocomposite structure is formed as shown by TEM analysis and XRD analysis.

• Macromolecular Research
• /
• 제16권2호
• /
• pp.120-127
• /
• 2008

Glycidyl methacrylate linked poly(dimethylsiloxane) (GMA-PDMS) was synthesized and used as a stabilizer for the dispersion polymerization of methyl methacrylate (MMA) in supercritical $CO_2$. This study examined the effect of the concentrations of the stabilizer, 2,2'-azobisisobutyronitrile (AIBN) initiator, and MMA on the yield, molecular weight, and morphology of the poly(methyl methacrylate) (PMMA) product. PMMA was obtained in 94,6% yield using only 0,87 wt% GMA-PDMS, When the AIBN concentration was increased from 025 to 1.06 wt%, the molecular weight and particle size of the PMMA decreased from 56,600 to 21,600 and from 4.1 to $2.7{\mu}m$, whereas the particle size distribution increased from 1.3 to 1.9. The $M_n$ of the PMMA product ranged from 41,600 and 55,800 under typical polymerization conditions. The PMMA particle diameter ranged from 1.8 to $11.0{\mu}m$ and the particle size distribution ranged from 1.4 to 1.8.

• 폴리머
• /
• 제32권2호
• /
• pp.116-124
• /
• 2008

본 연구는 식물유래 생분해성 고분자인 poly(lactic acid)(PLA)의 가공성을 향상시키기 위하여 기능성 단량체인 glycidyl methacrylate(GMA)와 반응 개시제를 첨가하여 반응압출법으로 PLA를 개질한 후 겔화도, 열적성질, 유변학적 특성 및 생분해도를 조사하였다. 개질 PLA및 순수 PLA의 열적특성은 시차열량분석기(DSC)를 이용하여 측정하였고 유변학적 특성은 복합점도(${\eta}^*$), 저장 탄성률(G'), log G' vs. log G" 선도를 이용하여 분석 비교하였다. GMA가 포함되지 않고 개시제로만 개질된 PLA의 복합점도 및 저장탄성률도 순수 PLA보다 증가하였지만, 여기에 GMA를 첨가하여 개질하면 더욱 향상된 복합점도와 저장탄성률을 갖는 개질 PLA를 얻을 수 있었다. 개시제의 함량에 따라 최고 높은 복합점도 및 저장탄성률 증가 효과를 보이는 최적의 GMA함량이 존재하였다. 그리고 GMA가 함유된 개질 PLA의 생분해도는 약간 낮아지는 경향을 보였다.

• 대한화학회지
• /
• 제23권6호
• /
• pp.402-411
• /
• 1979

Pyrrolidone의 음이온중합의 새로운 개시제로서 Pyrrolidone-N-sulfonyl chloride를 합성하고, 이 개시제에 의한 중합반응기구를 제안하였으며, 중합결과를 분석 고찰하여 다른 개시제의 경우와 비교하였다. Pyrrolidone-N-sulfonyl chloride의 농도를 작게할 수록 합성되는 고분자의 점도가 증가함을 관찰하였으며, 개시제의 KOH에 대한 비율이 0.25일때 중합속도 및 중합수율이 가장 큰 결과를 얻었다. PNSC/KOH 촉매작용에 의한 pyrrolidone의 음이온 중합은, $CO_2$/KOH 촉매작용의 경우에 비하여 일반적으로 중합속도가 빠르고, 중합수율도 높았다.