• 제목/요약/키워드: solution polymerization

검색결과 484건 처리시간 0.028초

Toluene 용액 캐스팅에 의한 차출용 전도성 Polyaniline-HIPS 블렌드 제조 (Preparation of the Conducting Polyaniline-HIPS Blends for Injection Molding by Toluene Solution Casting)

  • 이종혁;김은옥
    • 폴리머
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    • 제33권3호
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    • pp.203-206
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    • 2009
  • 화학적 산화중합에 의한 Polyaniline Emeraldine salt(PANI-salt)는 도펀트로 존재하는 HCl과 같은 양성 자산으로 인한 금속성 사출금형 부식이 발생한다. 본 연구에서는 비극성 유기용매인 톨루엔, 포펀트와 계면활성제 역할을 하는 dodecylbenzenesulfonic acid(DBSA)를 사용하여 유화 중합법으로 PANI-salt를 합성한 후, 공용매 toluene에서 PANI-salt와 high impact polystyrene(HIPS)를 다양한 비율로 solution-cast 혼합하여 PANI-HIPS 블렌드를 얻었다. PT-IR과 UV-Vis.로 PANI-salt 구조를 확인하였고, PANI-HIPS 블렌드의 모폴로지, 열적 및 전기적 특성을 확인하였다. PANI(50 mL)와 HIPS(1 g)을 혼합하여 사출온도 $103^{\circ}C$, 사출압력 120 psi 하에서 사출한 PANI-HIPS 사출품에서 가장 높은 전기전도도($6.02{\times}10^{-5}\;S/cm$)가 나타났다.

Synthesis and Performance Evaluation of Linear Polycarboxylate Dispersant of Glacial Acrylic Acid - Maleic Acid- Sodium Methallyl Disulfonate for Ceramics

  • Kommanapalli, Kiran Kumar;Lyot, Pierre;Sunkara, Jhansi Rani;Checule, Pierrick
    • 한국세라믹학회지
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    • 제55권2호
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    • pp.126-134
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    • 2018
  • Using aqueous solution free radical polymerization with glacial acrylic acid (GAA), maleic anhydride (MA) and sodium methallyl disulfonate (SMADS), a novel linear polycarboxylate dispersant was synthesized for ceramics. Dispersant linear structural characterization was done by FTIR, $^1H$ NMR, HPLC and GPC, and the ratio of monomers was determined using an orthogonal experiment. This research is focused on the effects of polymerization temperature, monomer mole ratios and dosage of initiator on ceramic slurry viscosity with linear polycarboxylate dispersant for ceramic dosage rate of 0.30% (based on dry slurry), all of which were investigated by single factor test. The best polymerization conditions for linear GAA-MA-SMADS are when n(AA) : n(MA) : n(SMADS) equals 3.0 : 1.0 : 0.5, the molecular weight of the polymer is 4600 daltons, the initiator sodium persulfate accounts for 7% of the total mass of polymerized monomers, the polymerization temperature is $90^{\circ}C$ and the reaction time is 2 h. The ceramic body slurry viscosity drops from $820mPa{\cdot}s$ to $46mPa{\cdot}s$ when the concentration of the polycarboxylate dispersant is 0.30%.

Tricaprylmethylammonium Chloride에 의한 Methyl Methacrylate의 라디칼 중합 (Radical Polymerization of Methyl Methacrylate with Tricaprylmethylammonium Chloride)

  • 박상욱;문진복;하유수;김종현
    • 공업화학
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    • 제4권2호
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    • pp.300-307
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    • 1993
  • $Na_2S_2O_4$ 수용액과 $CCl_4$-toluene 용액의 2상에서 유기상에 용해하는 tricaprylmethylammonium chloride 상이동 촉매를 사용하여 methyl methacrylate의 라디칼 중합속도를 측정하여, 액-액 불균일계 접촉계면을 통한 라디칼 중합반응기구를 해석하였다. MMA의 중합속도는 수용액상에 존재하는 $Q^+$ 이온의 농도와 ${S_2O_4}^{-2}$ 이온의 농도의 제곱근에 정비례하고 $CCl_4$와 MMA의 농도에 각각 정비례하였다.

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Preparation of Honeycomb-patterned Polyaniline-MWCNT/Polystyrene Composite Film and Studies on DC Conductivity

  • Kim, Won-Jung;Huh, Do-Sung
    • Bulletin of the Korean Chemical Society
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    • 제33권7호
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    • pp.2345-2351
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    • 2012
  • Conductive honeycomb-patterned polystyrene (PS) thin films were prepared by the formation of a polyaniline (PANI) thin layer on the surface of the patterned PS thin films using simple one-step chemical oxidative polymerization of aniline. The in situ chemical oxidation polymerization of aniline hydrochloride solution on the patterned structure of the PS films was conducted in the presence of multiwalled carbon nanotubes (MWCNT) to prepare the PANI-MWCNT/PS composite film. The concentration (wt %) of MWCNT was varied in the range of 1%-3% by weight. The dependence of surface morphology of the PANI/PS and PANI-MWCNT/PS composite film to the polymerization time was observed by scanning electron microscopy. The room temperature DC conductivity was obtained by the four-probe technique. The conductivity of the PANI-MWCNT/PS composite film was affected both by the MWCNT concentration and polymerization time. In addition, DC electrical field was loaded during the oxidative polymerization to affect the distribution of the MWCNT included in the composite film, varying the loading voltage in the range of 0.1-3.0 V. The conductivity of the PANI-MWCNT/PS composite film was increased as loading voltage rose. However, this increase stops at a voltage higher than the critical value.

Fabrication and Processing Method of Ophthalmic Hydrogel Tinted Lens Containing Indium Tin Oxide-Composited Materials

  • Lee, Min-Jae;Lee, Kyung-Mun;Sung, A-Young
    • 한국재료학회지
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    • 제28권12호
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    • pp.685-690
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    • 2018
  • In this study, a multifunctional ophthalmic lens material with an electromagnetic shielding effect, high oxygen permeability, and high water content is tested, and its applicability is evaluated. Metal oxide nanoparticles are applied to the ophthalmic lens material for vision correction to shield harmful electromagnetic waves; the pyridine group is used to improve the antibacterial effect; and silicone substituted with urethane and acrylate is employed to increase the oxygen permeability and water content. In addition, multifunctional tinted ophthalmic lens materials are studied using lens materials with an excellent antibacterial effect (2,6-difluoropyridine, 2-fluoro-4-pyridinecarboxylic acid) and functional (UV protection, high wettability) lens materials (2,4-dihydroxy benzophenone, 2-hydroxy-4-(methacryloyloxy)benzophenone). To solve problems such as air bubbles generated during the polymerization process for the manufacturing and turbidity of the lens surface, polymerization conditions in which the defect rate is minimized are determined. The results show that the polymerization temperature and time are most appropriate when they are $110^{\circ}C$ and 40 minutes, respectively. The optimum injection amount of the polymerization solution is 350 ms. The turbid phenomenon that appears in lens processing is improved by 10 to 95 % according to the test time and conditions.

醋酸纖維素의 醋化溫度가 分子量分配曲線에 미치는 影響 (Study on the Molecular Weight Distribution Curve of Cellulose Triacetate Acetylated Under Various Temperatures)

  • 김동일;노익삼;차경모
    • 대한화학회지
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    • 제4권1호
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    • pp.44-50
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    • 1957
  • Fibrous cellulose triacetate prepared from purified cotton under various temperatures was dissolved in the solution of 70%, monochloroacetic acid and it was fractionated using water as a precipitant. Eight fractions were obtained through the stepwise precipitation. Degree of polymerization and molecular weight of each fraction were measured viscometrically. Integral and differential molecular weight distribution curve were drawn for each sample prepared under various temperatures and were carefully observed. On this experimental study, following conclusions were obtained: Fractional precipitation can be carried out for fibrous cellulose triacetate in the solution of 70% monochloroacetic acid using water as a precipitant. The differences on the shapes of molecular weight distribution curve were occured on account of the various acetylation temperatures. At the relatively higher acetylation temperatures, the cellulose was randomly degraded and the portion of low degree of polymerization was increased. Commercial acetate, therefore, may not be prepared at above 40$^{\circ}C$ according to the molecular weight distribution curve regardless of higher viscosity and average degree of polymerization. It was concluded that the optimum acetylation temperature for commercial acetate was approximately 30$^{\circ}C$.

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Synthesis of Polypropylene-Polystyrene Copolymer via Ultrasonic Irradiation-Initiated Polymerization of Styrene in Polypropylene Solution

  • Kim, Hyungsu;Kim, Jihye;Kim, Miwha;Seyoung Oh;Lee, Jaewook
    • Macromolecular Research
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    • 제9권3호
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    • pp.150-156
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    • 2001
  • Polystyrenes(PS) were grafted onto polypropylene(PP) in the PP solution by ultrasonic irradiation-initiated polymerization of styrene. The resulting products consisted of mixtures of homopolymers and PP-PS copolymer because of the homopolymerization of styrene itself and copolymerization with PP. The dependency of the designated polymerization on sonication times was investigated to monitor the evolution lion of the copolymerization. Formation of the PP-PS copolymer was confirmed by FTIR analysis of the reaction products after a proper separation procedure of free PS and PP-PS copolymer. It was found that the tendency for the formation of PP-PS copolymer was closely related with the phase behavior of the PP/styrene mixture which was also influenced by sonication time. In order to verify the effectiveness of the PP-PS copolymer as a compatibilizer for PP/PS blend, melt mixing of PP/PS/PP-PS was performed in a batch mixer. During the mixing, the average torque was higher for the blend containing PP-PS copolymer influencing compatibilization. In accordance with the results from FRIR analysis and torque measurement, the PS domain size remarkably decreased in the PP/PS/PP-PS blend.

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The Synthesis of Cellulose-graft-poly (L-lactide) by Ring-opening Polymerization and the Study of Its Degradability

  • Dai, Lin;Xiao, Shu;Shen, Yue;Qinshu, Baichuan;He, Jing
    • Bulletin of the Korean Chemical Society
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    • 제33권12호
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    • pp.4122-4126
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    • 2012
  • Cellulose-graft-poly (L-lactide) (cellulose-g-PLLA) was successfully prepared via ring-opening polymerization (ROP) by using 4-dimethylaminopyridine (DMAP) as an organic catalyst in an ionic liquid 1-allyl-3-methylimidazolium chloride (AmimCl). The structure and morphology of the polymer was characterized by nuclear magnetic resonance (NMR) and transmission electron microscope (TEM). From wide-angle X-ray powder diffraction (WAXD) and degradation test (by acid, alkaline, PBS and enzyme solution), changes in the crystalline structure as a result of degradation was also investigated. The results indicated that materials which have low degree of crystallinity showing higher degradability, however, in acid liquor, enzyme solution, alkaline liquor and PBS system, the degradation rate of the polymer decreased by the above sequence. Moreover, with the further increase of graft degree of this material, its degradation degree decreased.

Natural Rubber-polyacrylamide Graft 공중합체의 합성 (Synthesis of Natural Rubber-g-polyacrylamide Polymer)

  • Son, Cha Hoo;Kim, Kyung Hwan;Park, Tchun Wook
    • 한국염색가공학회지
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    • 제7권4호
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    • pp.45-53
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    • 1995
  • Natural rubber(NR)-polyacrylamide(PAAm) graft copolymers(GP)(toluene soluble GP : TSGP, water dispersible GP : WDGP) have been synthesized as coupling agents by pre-emulsification methods based on "inverse emulsion graft polymerization" technique. The polymerization was carried out at $65^{\circ}C$ using Azobisisobytyro nitrile(AIBN) as an initiator in the inverse emulsion system formed by inxing NR toluene solution with inverse emulsion of awueous AAm solution emulsified with $Tween^{\#}$ 80 in toluene. The mechanism of inverse emulsion graft copolymerization was studied on AAm conversion, % grafting, grafting efficiency, NR conversion, production ratio of TSGP and amount of GP(sum of TSGP and WDGP). The reaction has been confirmed through use of optical microscope to proceed via adsorption of emulsifier colloid particles onto the stretched NR molecule. From the analysis of the effects of various polymerization conditions on the grafting, it has also been found that the present rection system can easily yield high(over 90%) grafting efficiency and AAm conversion and relatively high(over 80%) NR conversion.onversion.

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