• 제목/요약/키워드: acrylic viscosity agent

검색결과 22건 처리시간 0.017초

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

  • 정충호;김성래;박형진;김명수;박홍수;박신자
    • 한국응용과학기술학회지
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    • 제19권4호
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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.

음이온성 아크릴아미드와 아크릴산의 역유화 중합에 관한 연구 (A Study on the Inverse Emulsion Polymerization of Anionic Arcrylamide and Acrylic Acid)

  • 이기창;최희천;최봉종;이광일
    • 한국응용과학기술학회지
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    • 제6권1호
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    • pp.1-7
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    • 1989
  • To developed new process for obtaining maximum molecular weight of anionic acrylamide and acrylic acid copolymer by inverse emulsion polymerization. Concentration of initiator, reducing agent, surfactant and mole ratio of acrylamide-acrylic acid were studied for the process. Semi-batch processes with method of redox, control of reaction temperature, feeding method of monomer and reaction time, was suitable for maximum molecular weight of P(AMAC) from this process obtained $3.09\;{\time}\;10^6({\bar{M}}n.)$ and $4.41\;{\time}\;10^6({\bar{M}}w.)$ in molecular weight measured by the intrinsic viscosity method. inverse emulsion polymerization mechanism of P(AMAC) does not followed the Smith-Ewart and Medvedev theory, but selected for concentration of initiator, reducing agent, surfactant, water solubility of monomer.

Structural Adjustment of In-Situ Surface-Modified Silica Matting Agent and Its Effect on Coating Performance

  • Xu, Qingna;Ji, Tongchao;Tian, Qingfeng;Su, Yuhang;Niu, Liyong;Li, Xiaohong;Zhang, Zhijun
    • Nano
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    • 제13권12호
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    • pp.1850137.1-1850137.9
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    • 2018
  • A series of silica surface-capped with hexamethyldisilazane (denoted as $H-SiO_2$) were prepared by liquid-phase in-situ surface-modification method. The as-obtained $H-SiO_2$ was incorporated into acrylic amino (AA) baking paint to obtain AA/$H-SiO_2$ composite extinction paints and/or coatings. $N_2$ adsorption-desorption tests were conducted to determine the specific surface area as well as pore size and pore volume of $H-SiO_2$. Moreover, the effects of $H-SiO_2$ matting agents on the physical properties of AA paint as well as the gloss and transmittance of AA-based composite extinction coatings were investigated. Results show that $H-SiO_2$ matting agents possess a large specific surface area and pore volume than previously reported silica obtained by liquid-phase method. Besides, they have better dispersibility in AA baking paint than the unmodified silica. Particularly, $H-SiO_2$ with a silica particle size of $6.7{\mu}m$ and the dosage of 4% (mass fraction) provides an extinction rate of 95.2% and a transmittance of 79.3% for the AA-based composite extinction coating, showing advantages over OK520, a conventional silica matting agent. Along with the increase in the silica particle size, $H-SiO_2$ matting agents cause a certain degree of increase in the viscosity of AA paint as well as a noticeable decrease in the gloss of the AA-based composite extinction coating, but they have insignificant effects on the hardness and adhesion to substrate of the AA-based composite coatings. This means that $H-SiO_2$ matting agents could be well applicable to preparing low-viscosity and low-gloss AA-based matte coatings.

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

  • 정동진;박형진;김성래;함현식;박홍수;김성길
    • 한국응용과학기술학회지
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    • 제20권1호
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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.

아세토아세톡시기 함유 90% 고형분인 아크릴수지의 하이솔리드 도료에의 적용 (Application of Acrylic Resins Containing Acetoacetoxy Group and 90% Solid Contents to High-Solid Coatings)

  • 박홍수;김보배;김지현;박은수;윤현돈;이영준;연제원;가은지;이지수
    • 한국응용과학기술학회지
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    • 제25권3호
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    • pp.322-331
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    • 2008
  • In order to synthesize high-solid coatings, acrylic resins (HSAs) containing 90% solid content were first synthesized, then the synthesized HSAs were cured with a curing agent, isocyanate, at room temperature to obtain high-solid coatings. In the HSAs synthesis, conversion was in a range of $82{\sim}87%$, and viscosities and number-averaged molecular weight ($M_n$) of the HSAs were in a range of $4380{\sim}8010$ cP and $1540{\sim}1660$, respectively. From the correlation between $T_g$ value, viscosity and $M_n$, it was found that, with increasing $T_g$ value, viscosity increases rapidly and molecular weight increases slowly. From the visco-elasity measured by the pendulum method, it was found that the curing time decreased with increasing $T_g$ values. From the tests of physical properties of the coatings' film, $60^{\circ}$ specular gloss, impact resistance and heat resistance were proved to be good and pencil hardness, drying time and pot-life were proved to be poor.

잠재적 화재.폭발 위험 지역 작업용 녹전환형 중방식 코팅제의 특성에 관한 연구 (A Study on the Properties of the Heavy Duty Rust-Converting Agent used in the Potential Hazard Areas of Fire & Explosion)

  • 강영구
    • 한국안전학회지
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    • 제13권3호
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    • pp.102-111
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    • 1998
  • This study was concerned with the development of a heavy duty rust-converting agent, the function of which is to form metal complex coatings, containing vinyl halide-acrylic terpolymer emulsion, defoamer, emulsifying agent, glass flakes, chelating agent such as gallotannic acid, gallic acid, and pyrogallic acid, and other additives. The resulted emulsion products(Sample No.1~No.5) were characterized through test either in the forms of emulsions, which include Viscosity, Penetration rate, Acidity and Film drying rate test, or in the forms of coated layer on rusty steel substrates by FT-IR, which include hardness, gloss, salt spray, adhesion and flame retardant test. The test results are as follows ; Penetration rate(0.1~0.4 mm/min), Solid content(70%), Acidity (pH 1.8~2.0), Specific gravity(1.30~1.35), Film drying rate(108min, RH 40% ; 150min, RH 80%), Gloss(83~92, incident angle $60^{\circ}$; 88~97, incident angle $85^{\circ}$), Pencil hardness(4H~5H), Adhesion (100/100), Salt spray test(>720Hr), LOI(%) value(38%), Vertical burning test(UL 94-v-l). According to the various performance of specimens show above, the evaluation of the availability of this heavy duty rust-converting agent can be concluded that all the samples(No.1~No.5) are capable of being used in the field of chemical plant and in the hazard areas of fire and explosion potential. It was observed that the properties of sample No.2, especially gloss and hardness, were much better than that of the other samples.

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선택된 단량체와 가교제에 의한 아크릴고무의 물성 변화에 관한 연구 (A Study on Property Change of Acrylic Rubber by Selected Monomers and Crosslinking Agent)

  • 김준호;조을룡
    • Elastomers and Composites
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    • 제47권1호
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    • pp.75-81
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    • 2012
  • 주단량체로 에틸 아크릴레이트, 부틸 아크릴레이트, 메톡시에틸 아크릴레이트, 가교 단량체로 글리시딜 메타아크릴레이트를 유화중합하여 아크릴고무를 제조한 후, 가교제로써 2,2-bis[4-(4-aminophenoxy)phenyl]propane를 첨가하여 고무컴파운드를 제조하였다. 주단량체의 조성에서 에틸 아크릴레이트의 함량이 증가하면 내열성이 증가하는 경향을 보였는데 이는 아크릴고무의 유리전이온도가 감소되었기 때문이다. 또한 에틸 아크릴레이트의 에스테르 그룹 농도가 3개의 주단량체 중 가장 높기 때문에 에틸 아크릴레이트 함량이 증가할수록 내유성이 향상되었다. 2,2-Bis[4-(4-aminophenoxy)phenyl]propane의 함유량에 따른 영향은 2 phr 첨가까지 인장강도와 신장율은 증가하지만, 그 이상의 첨가에서는 가교밀도의 증가에 따른 점성과 탄성이 감소하여 그 값들이 감소하였다.

카르복실화 스티렌-부타디엔 라텍스의 중합시간 단축과 안정성 개선을 위한 연구 (Study for Reducement of Polymerization Time and Improvement of Stability in Manufacturing Carboxylated Styrene-butadiene Latex)

  • 조을룡
    • Elastomers and Composites
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    • 제37권1호
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    • pp.31-38
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    • 2002
  • 카르복실화 스티렌-부타디엔 라텍스의 중합시간은 사용되는 부타디엔 모노머가 공액 이중결합을 가진 화학적 구조로 인하여 라디칼 중합시 홀 전파의 비편재화로 인해 아크릴 에멀젼의 제조시 보다 중합시간이 매우 길다. 또한 라텍스 자체가 고분자와 분산매의 분리 없이 사용되기 때문에 라텍스의 안정성은 대단히 중요하다. 물성의 저하없이 반응시간을 단축하기 위하여 기존에 사용하던 연쇄이동제인 사염화탄소 대신 tert-dodecylmercaptane 과 ${\alpha}$-methylstyrene dimer를 혼합 사용하여 반응시간을 14시간에서 12시간으로 줄일 수 있었다. 반응 성장단계에서 아크릴산의 투입량을 0.3 part로 제한하여 라텍스의 점도 상승을 막고 초기중합단계 직후에 아크릴아미드를 0.1 part 첨가하여 라텍스 입자의 내부영역과 외부영역의 고분자 사슬의 상호간확산을 막아 단단하면서도 접착력을 유지할 수 있는 라텍스의 합성 결과를 얻었다.

유변학적 특성과 표면장력측정을 통한 음이온성 폴리머와 비이온성 계면활성제의 상호작용에 대한 연구 (Investigation of the Interactions between Anionic Polymer and Nonionic Surfactant with Rheological and Surface Tension Measurements)

  • 이정노;김동주;고하영
    • 한국응용과학기술학회지
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    • 제24권2호
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    • pp.160-166
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    • 2007
  • The rheological properties and surface tensions of polymer solutions and polymer-surfactant mixed solutions were investigated. The polymers used in this study were a homopolymer of acrylic acid crosslinked with an allyl ether of pentaerythritol, an allyl ether of sucrose, or an allyl ether of propylene (CARBOMER), acylate/C10-30 alkyl acylate crosspolymer (AAAC), and ammonium acryloydimethyltaurate/VP copolymer (ADTV). A solubilizing agent PEG-40 hydrogenated castor oil (HCO-40) and an emulsifying agent polyoxyethylene (20) sorbitan monostearate (POLYSORBATE 60) made the micelles intervening between AAAC polymers, resulting in the increase of viscosity. However, HCO-40 made this behavior over the wider range of surfactant concentration than POLYSORBATE 60. From the view point of surface tensions in the same range of surfactant concentration, AAAC/HCO-40 solution showed the area of increasing surface tension with surfactant concentration in contrast to the AAAC/POLYSORBATE 60 solution showing no increasing area.

수용성 아크릴 변성 알키드 수지의 합성과 물성 2. MA 및 TMPTA 공중합체에 의한 변성 (Synthesis and Characterization of Acrylic-Modified Water-Reducible Alkyd Resin 2. Modification by MA and TMPTA Graft Copolymerization)

  • 조영호;강기준;노시태
    • 공업화학
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    • 제5권4호
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    • pp.698-705
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    • 1994
  • Linseed oil fatty acid(LOFA), phthalic anhydride(PAA) 및 maleic anhydride(MA), trimethylol propane(TMP)을 사용하여 기본적인 유장(oil length) 50%의 중유성 기본 알키드를 합성하고 trimethylol propane triacrylate(TMPTA)를 그라프트 공중합시켜 MA/TMPTA 변성 알키드 수지를 제조하였다. 수지의 산가는 MA 첨가량으로 제어하였으며, 수용화에는 N,N-dimethylethanol amine(DMEA)를 사용하였다. TMPTA의 첨가량 변화에 의한 분자량, 유리 전이온도, 수용화 후의 점성도 및 그라프트율을 측정하였으며, 가교도막의 경화온도별 겔분율 변화를 조사하였다. 또한 멜라민 수지 경화 도막의 내열성, 내자외선성, 내수성 및 저장 안정성을 측정하고, TMA/TMPTA 변성 알키드 수지의 물성과 비교하였다. TMPTA의 첨가량이 증가할수록 수용화 후의 점성도, 겔분율, 그라프트율 및 분자량이 증가하였으며, 유리 전이온도(Tg)는 감소하였다. 고형분 함량에 따른 점성도 변화는 고형분 30%일 때보다 40%일 때가 더 낮게 나타났으며, 중화도에 따른 점성도 변화는 중화도가 높을수록 낮은 점성도를 나타내썼다. 내열성, 내자외선성, 내수성은 MA/TMPTA 변성 알키드 수지가 TMA/TMPTA 변성 알키드 수지보다 우수하였으나, 저장 안정성은 TMA/TMPTA 변성 알키드 수지가 우수함을 알 수 있었다.

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