• 제목/요약/키워드: Functional monomer

검색결과 154건 처리시간 0.023초

기능성 복합 라텍스의 합성과 열분해 특성에 관한 연구 (A Study on Synthesis of Functional Composite Latex and Characteristics of Thermal Decomposition)

  • 권재범;김남석;이내우;설수덕
    • 한국안전학회지
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    • 제19권2호
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    • pp.47-53
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    • 2004
  • Emulsion polymerization ws carried out using Alkyl methacrylate(RMA) like MMA, EMA, BMA and Styrene Monomer(SM) for core-shell latex preparation. It was synthesized at $80^{\circ}C$ in the presence of anionic surfactant SLS(Sodium Lauryl Sulfate). FT-IR and DSC analysis are used to confirm the synthesized core-shell emulsion latexes. Moreover DSC and TGA were used to investigate the thermal characterisitcs of them. The differences of the decomposition rate and the activation energy from TGA and DSC analysis are not so big. It considers that the pendent group is not affect of the thermal characteristics and stability on core-shell latexes, which is synthesized with RMA and Styrene. For investigating combustion products, LC50 values were calculated by FED(Fractional Effective Dose)from the Pyrolyzer-Mass sepctrometer.

Acetoacetoxy기 함유 하이솔리드 도료용 아크릴 수지의 합성 (Synthesis of Acrylic Resins for High-Solid Coatings Containing Acetoacetoxy Group)

  • 유혁재;정동진;정충호;함현식;박홍수;김태옥
    • 한국응용과학기술학회지
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    • 제20권3호
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    • pp.221-229
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    • 2003
  • A copolymer ${\sim}$550cps ; $M_n$, 2590${\sim}$2850 ; and conversion, 82${\sim}$89%, respectively. It was found from the plotting of $T_g$ versus viscosity and $T_g$ versus molecular weight that viscosity increased with $T_g$ while number averaged molecular weight decreased with increasing $T_g$.

하이솔리드 도료용 카프로락톤기 함유 80% 고형분인 아크릴수지의 합성 (Synthesis of Acrylic Resins Containing Caprolactone Group and 80% Solid Contents for High-Solid Coatings)

  • 박홍수;조혜진;심일우;정충호;김영근
    • 한국응용과학기술학회지
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    • 제23권1호
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    • pp.85-91
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    • 2006
  • Acrylic resins (HSCs : EA/EMA/2-HEMA/CLA) which contain 80% solid content were synthesized by the copolymerization of monomers (ethyl acrylate, ethyl methacrylate, 2-hydroxyethyl methacrylate) and functional monomer (caprolactone acrylate : CLA) which improves the crosslinking density and physical properties of films. The physical properties of the prepared acrylic resins (HSCs) containing CLA, are as follows: viscosity 1440$^{\sim}$2630 cps ; $M_n$ 1590$^{\sim}$1660 ; and conversions, 81$^{\sim}$86%, respectively. From the correlation of $T_g$ values, viscosities, and $M_n$ of the HSCs, it was found thst viscosity and $M_n$ increased with $T_g$ value.

Caprolactone기 함유 하이솔리드 도료용 아크릴수지의 최적 합성조건 (Optimum Synthesis Condition of Acrylic Resins for High-Solid Coatings Containing Caprolactone Group)

  • 정동진;유혁재;김성길;김명수;박홍수;김태옥
    • 한국응용과학기술학회지
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    • 제21권3호
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    • pp.197-203
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    • 2004
  • Acrylic resins ($HSC_s$ : EA/EMA/2-HEMA/CLA) which contain 70% solid content were synthesized by the copolymerization of monomers (2-hydroxyethyl methacrylate, ethyl acrylate, and ethyl methacrylate) and functional monomer (caprolactone acrylate : CLA) which improves the crosslinking density and physical properties of films. The physical properties of the prepared acrylic resins (HSCs) containing CLA, are as follows : viscosity 245${\sim}$515 cps ; $M_n$ 2670${\sim}$2840 ; and conversions, 83${\sim}$91%, respectively. From the correlation of $T_g$ values, viscosities, and $M_n$ of the HSCs, it was found that viscosity and $M_n$ increased with $T_g$ value.

플라즈마 중합에 의한 프탈릭 안하이드라이드 고분자 박막 필름 제조 연구 (Polymer Thin Film of Phthalic Anhydride via Plasma Polymerization)

  • 강현민;;백관열;윤태호
    • 접착 및 계면
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    • 제10권1호
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    • pp.17-22
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    • 2009
  • Polymer thin films were prepared by radio frequency (RF) plasma polymerization of phthalic anhydride (PA). First, monomer vaporization temperature ($100{\sim}160^{\circ}C$) was optimized by evaluating the thermal properties of thin films using differential scanning calorimeter (DSC) and measuring the root-mean-square (RMS) roughness with atomic force microscope (AFM) at the fixed plasma power of 10 W and time of 5 min in a continuous-wave (CW) mode. Plasma power (5~20 W) was then optimized by measuring the film solubility in solvents such as toluene, acetone, dimethylsulfoxide (DMSO) and 1 methylpyrrolidine (NMP). Next, pulsed mode plasma polymerization was also studied by varying the duty cycle of on-time (5, 20%) under optimized conditions of continuous-wave (CW) mode ($120^{\circ}C$, 10 W) in order to increase the anhydride functional groups. Finally, polymer thin films were characterized by Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analyzer (TGA) and ${\alpha}$-step.

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방사선 중합법에 의한 Kapok 이온교환 섬유의 합성 (Preparation of Son Exchange Kapok Fiber by Radiation Polymerization)

  • 조인희;강필현;임윤묵;최재학;황택성;노영창
    • 폴리머
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    • 제31권6호
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    • pp.512-517
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    • 2007
  • [ $Co_{60}\;{\gamma}-ray$ ] 방사선 조사법을 이용하여 kapok 섬유에 styrene, glycidylmethacrylate(GMA) 또는 acrylic acid(AAc)를 그래프트 공중합 반응하여 합성한 공중합체의 그래프트율은 단량체의 농도와 방사선 조사량에 따라 증가하는 것으로 나타났으며, 또한 합성된 이온교환 섬유의 도입된 관능기를 확인하고 이온교환 능을 측정하였으며, SEM과 FT-IR을 통하여 이온교환 섬유의 표면과 구조를 분석하였다.

Structure and Luminescence Properties of Poly(1-hexyl-3,4-dimethyl-2,5-pyrrolylene)

  • Kang, Jun-Gill;Kim, Tack-Jin;Park, Chang-Moon;Woo, Lee-Sang;Kim, In-Tae
    • Bulletin of the Korean Chemical Society
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    • 제25권5호
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    • pp.704-710
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    • 2004
  • A poly(1-hexyl-3,4-dimethyl-2,5-pyrrolylene) (PHDP) was prepared and its luminescence in tetrahydrofuran (THF) was studied. When PHDP is excited by UV light, it produces very strong blue luminescence. The quantum yield of PHDP (Q = 36.9%) is much greater than that of the monomer, 1-hexyl-3,4-dimethylpyrrole (HDP) with Q = 0.61%. The principal luminescence of PHDP has a single decay component with ca. 1 ns, whereas the decay of HDP is complicated. The molecular structure and conformational behavior of HDP and the oligomers up to trimer have been also determined by ab initio Hartree-Fock (HF/6-31$G^{**}$), density functional theory (DFT-B3LYP/6-31$G^{**}$), and semiempirical (ZINDO) methods. According to the results of calculations, it is proposed that the enhanced quantum yield of the polymer PHDP results mostly from the ${\pi}$-conjugation between neighboring pyrrole rings.

Effect of plasma polymerized film on fouling of heat exchangers

  • Kim, Ki-Hwan;Park, Sung-Chang;doo-Jin choi;Jung, Hyung-Jin;Ha, Sam-Chul;Kim, Chul-Hwan;Koh, Seok-Keun
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 1999년도 제17회 학술발표회 논문개요집
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    • pp.160-160
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    • 1999
  • To reduce the fouling of heat exchangers, the plasma polymerized films was coated on the heat exchangers, and an effect of plasma polymerized film on fouling of heat exchangers was investigated. Monomer and reactive gases were used as the precursors of plasma polymerization. Plasma polymerized films were deposited with process parameters of pressure, power, and ratio of gases. Plasma polymerized films could be served as functional layers of good wettability and high resistance to corrosion. Wettability of plasma polymerized film could be controlled by the ratio change gas mixture. Hydrophilicity of plasma polymerized films on heat exchanger in air conditioner can provide improvement in performance of heat exchanger which results from good water drainage, decrease of pressure drop. DC-plasma polymerized films improve resistance to corrosion whcih is related to deposit formation in heat exchangers. The difference in the build up of fouling deposits between bare substrate and plasma polymerized substrate was investigated by scanning electron microscopy (SEM). An effect of plasma polymerized film on fouling of heat exchangers was discussed in terms of surface properties such as wettability, surface chemical state.

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Effect of Solvent on Swelling, Porosity and Morphology of Transparent Poly (HEMA)

  • Pathak Tara Sankar;Kim Lae-Hyun;Chung Kun-Yong
    • Korean Membrane Journal
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    • 제8권1호
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    • pp.67-73
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    • 2006
  • Transparent materials are well known but preparation of transparent poly 2-hydroxyethyl methacrylate {poly (HEMA)} material by varying solvent is a new one and economically reliable. This material is prepared from hydroxyl based monomer HEMA by radical polymerization using benzoyl peroxide (BPO) as initiator and isobutanol, 2-butanol, 1-butanol, hexane and toluene as a solvent. The reaction temperature, time and stirring speed were set at $70^{\circ}C$, 4 hrs and 150 rpm, respectively. The polymer was characterized for functional group by IR spectroscopy. It was observed that the intensity of band at $1637 cm^{-1}$ a characteristic band of C=C stretching disappeared indicating that it was completely consumed after polymerization. It was observed that swelling percentage increases with increase as time passes but after a certain time a constant swelling percentage is achieved. SEM pictures reveals that poly (HEMA) prepared by different solvent shows pore with a distinguishable void up to several micrometers. The BET surface area, cumulative pore volume and average pore diameter is greater in poly (HEMA) prepared by hexane as a solvent compared to other solvents. Poly (HEMA) prepared by 1-butanol as a solvent shows higher glass transition temperature compared to other solvents. Poly (HEMA) prepared by different solvents shows $90{\sim}94%$ light transmission property from light transmission measurement and looks transparent.

하이솔리드 아크릴/이소시아네이트 도료의 경화반응과 도막물성 (Curing Reaction and Physical Properties of High-Solid Acrylic/Isocyanate Coatings)

  • 박홍수;심일우;조혜진;김성길;김명수
    • 한국응용과학기술학회지
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    • 제22권4호
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    • pp.371-378
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    • 2005
  • In the previous study, three kinds of monomers and the functional monomer, acetoacetoxyethyl methacrylate (AAEM), which could improve the film property and cross-linkage, were polymerzied into acrylic resin copolymers (HSA-98-20, HSA-98-0, HSA-98+20) containing 80% solid content. In this study, the high-solid coatings(HSA-98-20C, HSA-98-0C, HSA-98+20C) were prepared by the curing reaction between acrylic resins containing 80% solid content and isocyanate at room temperature. Various properties were examined for the film coated with the prepared high-solid coatings. The introduction of AAEM in the coatings enhanced the abrasion resistance and solvent resistance of coatings, which indicated the possible use of high-solid coatings for top-coating materials of automobile. The curing times measured by viscoelastic measurement were 350, 264, and 212 min for HSA-98-20C, HSA-98-0C, and HSA-98+20C, respectively. This shows that the curing times become shorter with increasing $T_g$ values.