• Title/Summary/Keyword: acrylic/urea coating

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Preparation and Physical Properties of High-Solids Acrylic/Urea Coatings (하이솔리드 아크릴/우레아 도료의 제조와 도막물성 연구)

  • Jung, Choong-Ho;Kim, Sung-Rae;Park, Hyong-Jin;Kim, Myung-Soo;Park, Hong-Soo;Park, Shin-Ja
    • Journal of the Korean Applied Science and Technology
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    • v.19 no.4
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    • pp.311-319
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    • 2002
  • Environmental friendly acrylic/urea high-solid paint(MUHC) were prepared through the curing reaction of acrylics resin(EBHC) containing 70wt% of solids content and butylated urea curing agent. The synthesis of EBHC Was done at $150^{\circ}C$ for 6 hours, and the results were obtained as follows : $M_{n}=1830{\sim}2190$, $M_{w}$ $3290{\sim}4000$, $M_{w}/M_{n}$=1.80{\sim}1.83$ viscosity=$110{\sim}352$ cps, and conversion=$82{\sim}92$%. After the film was coated with MUHC, the various physical properties were measured. They showed that enhancement of the coating properties such as adhesion, flexibility, abrasion resistance, impact resistance, and water resistance could be expected through introdl1cing caprolactone acrylate component in acrylics resin for the high-solids content acrylics/urea coatings.

Preparation and Properties of Polydimethylsiloxane Modified Urea with Multi Acrylate Group Coating Materials (Multi Acrylate기를 갖는 Polydimethylsiloxane 변성 Urea 코팅 액의 제조와 그 특성)

  • Bak, Seung Woo;Kang, Ho-Jong;Kang, Doo Whan
    • Polymer(Korea)
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    • v.38 no.6
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    • pp.720-725
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    • 2014
  • Aminopropyl terminated polydimethylsiloxane was synthesized by hydrosilylation reaction with hydride terminated polydimethlysiloxane and allyl amine. Polydimethylsiloxane modified urea with isocyanate group was prepared from cyclic trimer of hexamethyldiisocyanate with aminopropyl terminated polydimethylsiloxane. Polydimethylsiloxane modified urea/acrylate resin (PUA) was prepared from the urethane reaction of PU with isocyanate group and 2-hydroxyethylmethacrylate. PUA structure was analyzed by FTIR and NMR. Coating materials were prepared by mixing PUA, acrylic monomer, photo-initiator, and solvent and coated on PET film to obtain flexible hard coating film by UV irradiation.

Acrylic/Urea Crosslinked Polymers for High-Solid Coatings Applications (아크릴/우레아 가교 폴리머의 하이솔리드 도료에의 적용)

  • Chung, Dong-Jin;Park, Hyong-Jin;Kim, Sung-Rae;Hahm, Hyun-Sik;Park, Hong-Soo;Kim, Seong-Kil
    • Journal of the Korean Applied Science and Technology
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    • v.20 no.1
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    • pp.8-19
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    • 2003
  • Environmental friendly acrylics/urea high-solid paints (BEHCU) were prepared through the curing reaction of acrylics resin(BEHC) containing 70wt% of solids content and butylated urea curing agent. BEHC was synthesized by addition copolymerization of caprolactone acrylate(CLA), 2-hydroxypropyl methacrylate(2-HPMA), ethyl methacrylate, and n-butyl acrylate. The addition polymerization of these monomers, especially including flexible CLA monomer and 2-HPMA monomer with OH funtional group, under appropriate reaction conditions resulted in polymers with controlled glass transition temperature($T_g$) and crosslinking density. The molecular weight($M_w$) of these polymers(BEHCs) was 2940${\sim}$3240 and polydispersity ($M_w/M_n$) was in the range of 1.61${\sim}$1.72. The viscosity and the molecular weight of these acrylic resins increased with increasing $T_g$. The coated films were prepared using curing reaction between BEHC resin and butylated urea curing agent at 100$^{\circ}C$ for 30 minutes. Our experimental resulted showed that enhancement of the coating properties such as adhesion, flexibility, impact resistance, water resistance, and abrasion resistance could be expected through introducing CLA component in acrylic resin for the high-solid content acrylics/urea coatings.

Development of Mixed Pesticides Containing Herbicide and Topdressing Fertilizer for Paddy Rice (벼 제초제(除草劑)와 분약비(分蘖肥) 혼합약제(混合藥劑)의 개발(開發))

  • Park, Yang-Ho;Lee, Byung-Moo;Park, Seung-Soon;Lee, In-Yong;Kim, Young-Koo;Park, Young-Sun
    • Korean Journal of Environmental Agriculture
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    • v.13 no.3
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    • pp.279-287
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    • 1994
  • To develop mixed pesticides of herbicide and topdressing fertilizer for paddy rice, twelve mixtures were formulated with combination of urea coated with different level of acrylic acid wax(AAW) and four herbicides, which were thiobencarb, pretilachlor, mefenacet + bensulfuron-methyl and mefenacet + bensulfuron-methyl + dymron, and effects of the mixtures for weed control, phytotoxicity and rice tillering were investigated in the laboratory and the field experiments. Release rates of active ingredient of herbicides in the distilled water were over 90% during 24 hours same as that of the reference herbicides. The release rates of nitrogen showed different patterns according to coated level of granular urea with acrylic acid wax. Optimum release rate of nitrogen as $NH_4-N$ was obtained by 5.5% AAW coating on urea for thiobencarb or pretilachlor mixture, and by 4.0% AAW coating on urea for mefenacet + bensulfuron-methyl or mefenacet + bensulfuron-methyl + dymron mixture. The pesticide active ingredients of the mixtures were stable, which showed $3.7{\sim}8.0%$ of degradation rate after 90 days of storage under $50^{\circ}C$. Effects on weed control of mixtures were acceptable for both annual and perennial weeds, while ACRI-M9213 mixture showed considerable phytotoxicity at double dose of standard. When treated the mixed pesticides to paddy rice, rice growth status including culm length, ear length, panicle number and polished rice yield exhibited no significant differences compared with the conventional treatment.

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Nitrogen Release and Polymer Degradation Properties of Polymer-Coated Urea Fertilizer in Soil (고분자 피복요소비료의 질소용출 및 토양중 분해특성)

  • Kang, Byung-Hwa;Ha, Byoung-Yeun;Park, Ki-Do;Park, Moon-Su;Sohn, Bo-Kyoon;Jeong, Yeun-Kyu;Heo, Jong-Soo;Cho, Ju-Sik
    • Korean Journal of Soil Science and Fertilizer
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    • v.35 no.5
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    • pp.264-271
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    • 2002
  • Nitrogen releasing characteristics of polymer-coated urea(PCU) that made acrylic synthetic resins were studied in incubated soil, water and paddy soil. Also, their correlations and degradation patterns of coating material were tested. Releasing rate of nitrogen from PCU decreased with increasing coating rate. N001(coating rate 8.5%) and N003(coasting rater 6.3%) were low releasing amount at the early stage, whereas N005(coating rate 4.8%) was released over 80% within 20 days. Relationship of the releasing rate between incubated soil($25^{\circ}C$) and paddy soil could be described as follows : $Y=-0.0011X^2+2.2931X-50.264(R^2=0.9884)$ for N001, $Y=-0.0016X^2+1.1587X+5.5064(R^2=0.9805)$ for N003 and $Y=-0.03X^2+6.499X-243.22(R^2=0.9422)$ for N005, respectively (Y: release rate at field condition, X: experiment period). Relationship of the releasing rate between incubated water($30^{\circ}C$) and paddy soil can be described as follows : $Y=0.0011X^2+2.2601X-25.329(R^2=0.9884)$ for N001, $Y=-0.0306X^2+4.4994X-76.307(R^2=0.955)$ for N003 and $Y=-0.0164X^2+3.7764X-108.22(R^2=0.9422)$ for N005. After 150 days, coating materials of N001, N003, and N005 in incubated soil were degraded approximately 23%, 22% and 15%, respectively. Also The scanning electron microscope examination of coating material revealed that particle surface became gradually shattered with the time after the soil treatment.