• Title/Summary/Keyword: n-Butyl methacrylate(n-BMA)

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Syntheses of 70% Solids Acrylic Resin and Comparative Study in Physical Properties as Acrylic Urethane Resin Coatings (고형분 70% 아크릴수지 합성과 아크릴-우레탄 도료의 도막물성 비교 연구)

  • Kim, Seong-Kil;Park, Hyong-Jin
    • Journal of the Korean Applied Science and Technology
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    • v.38 no.2
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    • pp.476-487
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    • 2021
  • To prepare acrylic resin coatings containing 70% of solids, we used n-butyl methacrylate(BMA), methyl methacrylate(MMA), 2-hydroxyethyl methacrylate(2-HEMA), and acetoacetoxyethyl acrylate(AAEA), caprolactone acrylate(CLA) as raw materials, the glass transition temperature(Tg) of acrylic copolymer was adjusted around 50 ℃. The viscosity and molecular weight of the acrylic resins was increased with increasing OH values. Di-tert-amyl peroxide was found to be the suitable initiator to get high-solids acrylic resins. The optimum reaction conditions found in the study are 5 wt% of initiator, 4 wt% of chain transfer agent, 4 hrs of dropping time, and 140 ℃ of reaction temperature. The structure of the synthesized resins were characterized by FT-IR and 1H-NMR spectroscopy. Number average molecular weight of 1900~2600 and molecular wight distribution of 1.4~2.1 were obtained. Crosslinked acrylic urethane clear coatings were obtained by curing reaction between the synthesized acrylic resins and hexamethylene diisocyanate trimer(Desmodur N-3300), the equivalent ratio of NCO/OH was 1.2/1.0. The physical properties from the following studies were carried out: viscosity(Zahn cup #2), adhesion, drying time, pot-life, pensil hardness, and 60° specular gloss. Various properties of the acrylic urethane clear coatings were also evaluated on the coating specimens. Adhesion property to a substrate, drying time, pot-life, pencil hardness, and 60° specular gloss of prepared paint showed quite good properties. Futhermore, prepared paint containing 10% of CLA showed quite good properties for adhesion, low viscosity and high hardness.

The Kinetics of Radical Copolymerization of Styrene with Alkyl Methacrylate in a CSTR (연속반응기에서 스티렌과 메타크릴산 알킬의 라디칼 공중합 반응속도론)

  • Kim, Nam Seok;Seul, Soo Duk;Cheong, Young Eon;Park, Keun Ho;Choi, Jong jueng
    • Applied Chemistry for Engineering
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    • v.10 no.5
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    • pp.796-803
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    • 1999
  • Solution copolymerization of styrene(St.) with methyl methacrylate(MMA), ethyl methacrylate(EMA) and n-butyl methacrylate(BMA) was carried out with benzoylperoxide(BPO) as an initiator in toluene at $80^{\circ}C$ in a continuous stirred tank reactor. Reaction volume and residence time were 0.6 liters and 3hours, respectively. The monomer reactivity ratios, $r_1(St.)$ and $r_2(RMA)$ determined by both the Kelen-Tudos method and the Fineman-Ross method were $r_1(St.)=0.60(0.61),\;r_2(MMA)=0.59(0.60);\;r_1(St.)=0.65(0.62),\;r_2(EMA)=0.55(0.52);\;r_1(St.)=0.75(0.67),\;r_2(BMA)=0.63(0.56)$. The cross-termination factor $\Phi$ of the copolymer over the entire St. compositions ranged from 0.26 to 0.96. The $\Phi$ factors of St.-RMA copolymer were increased with increasing St. content. The simulated conversions and copolymerization rates were compared with the experimental results. The average time to reach dynamic steady-state was three times and half of the residence time.

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Preparation and Resistant Property of Acrylic Adhesives for Automobiles Protection (자동차 보호용 아크릴 점착제의 제조 및 내성조사)

  • Hahm, Hyun-Sik;Park, Ji-Young;Ahn, Sung-Hwan;Kim, Song-Hyoung;Hong, Suk-Young;Park, Hong-Soo
    • Journal of the Korean Applied Science and Technology
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    • v.23 no.2
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    • pp.169-176
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    • 2006
  • Acrylic adhesives for automobiles protection were prepared by emulsion polymerization. Monomers used were n-butyl acrylate(BA), acrylonitrile (AN), butyl methacrylate(BMA), glycidyl methacrylate(GMA), and acrylic acid (AA). Emulsifiers used were sodium lauryl sulfate and polyoxyethylene lauryl ether, which are an anionic emulsifier and a nonionic emulsifier respectively. Potassium persulfate was used as an initiator and polyvinyl alcohol was used as a stabilizer. Emulsion polymerization was carried out in a semi-batch reactor at $70^{\circ}C$ and agitation speed was kept at 200 rpm. Water resistance, heat resistance, acid resistance, alkali resistance and smoke resistance were examined. As a result, when each 0.03 mole of GMA and AA was introduced, the adhesion properties and various above mentioned resistances of the prepared adhesives were satisfied the standard for automobiles.

Preparation and Characteristics of Acrylic Removable Protective Coatings (박리형 아크릴 보호코팅제의 제조 및 특성)

  • Hahm, Hyun-Sik;Park, Ji-Young;Hwang, Jae-Young;Ahn, Sung-Hwan;Park, Hong-Soo
    • Journal of the Korean Applied Science and Technology
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    • v.22 no.4
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    • pp.332-338
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    • 2005
  • This study was conducted to prepare acrylic removable protective coatings by emulsion polymerization. Monomers used were n-butyl acrylate, acrylonitrile, butyl methacrylate. Emulsifiers used were sodium lauryl sulfate and polyoxyethylene lauryl ether, which are an anionic emulsifier and a nonionic emulsifier respectively. Potassium persulfate was used as an initiator and polyvinyl alcohol was used as a stabilizer. Emulsion polymerization was carried out in a semi-batch reactor at $70^{\circ}C$ and agitation speed was 200 rpm. Tensile strength, extension, peel strength, viscosity, and solid contents of the synthesized coatings were examined. The coatings prepared with BA:AN = 60:20 (in weight ratio) satisfied the standard for automobile in terms of extension and peel strength. When the concentration of BMA was in a range of $18{\sim}23$ wt%, the prepared coatings satisfied the standard for automobile in terms of peel strength and water resistance.