• Title/Summary/Keyword: poly(caprolactone diol)

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Preparation of Exfoliated PCL/Clay Nanocomposite and Its Characterization (박리형 PCL/Clay 나노복합재료 제조와 특성)

  • 유성구;박대연;배광수;서길수
    • Polymer(Korea)
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    • v.25 no.3
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    • pp.421-426
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    • 2001
  • 11-Aminododecanoic acid, to insert the functional group of -COOH reacted with the end group of poly($\varepsilon$-caprolactone) diol, and cetyltrimethylammonium bromide (CTMA), to increase the d-spacing of Montmorillonite (MMT), were intercalated into $Na^+;_-$MMT. The modified MMT was reacted with poly(${varepsilon}-caprolactone$) diol ($M_n{=2000$) in THF solution at $80^{\circ}C$ for 4 hrs. After reaction, poly(${varepsilon}-caprolactone$) ($M_n{=80000$) was mixed into the solution for 12 hrs. To prepare the PCL/clay nanocomposite film this solution was cast into the silicon mold at $60^{\circ}C$ in vacuum oven for 6 hrs. From the results of XRD and TEM, it was found that the exfoliated PCL/clay nanocomposite were prepared. The effects of the amount of MMT on the mechanical properties and thermal properties of PCL/clay nanocomposites have been investigated by tensile tester and DSC. Because the MMT was dispersed homogeneously in PCL matrix, the Young's modulus of the nanocomposite were found to be excellent. However, MMT dispersed in PCL matrix had almost no effect on the tensile strength of the composites. The crystallization temperature of PCL increased in proportion to 3 wt% MMT in the PCL matrix.

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Full-atomistic simulations of poly(ϵ-caprolactone) diol models with CVFF and CGenFF

  • Chang, Yin;Chang, Shu-Wei
    • Multiscale and Multiphysics Mechanics
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    • v.1 no.4
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    • pp.327-340
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    • 2016
  • Poly(${\epsilon}$-caprolactone) (PCL) diol, with good biodegradation and biocompatibility, is one of the widely used soft segments (SSs) in composing bio-polyester-urethanes (Bio-PUs), which show great potential in both biomedical and tissue engineering applications. Properties of Bio-PUs are tunable by combining SS monomers with different molecular weights, structures, modifications, and ratio of components. Although numbers of research have reported many Bio-PUs properties, few studies have been done at the molecular scale. In this study, we use molecular dynamic (MD) simulation to construct atomistic models for two commonly used PCL diol SSs with different molecular weights 1247.58 Da and 1932.42 Da. We compare the simulation results by using two widely used classical force fields for organic molecules: Consistent Valence Force Field (CVFF) and CHARMM General Force Field (CGenFF), and discuss the validity and accuracy. Melt density, volume, polymer conformations, transition temperature, and mechanical properties of PCL diols are calculated and compared with experiments. Our results show that both force fields provide accurate predictions on the properties of PCL diol system at the molecular scale and could help the design of future Bio-PUs.

Preparation and Physical Properties of the Polyurethane Microgels Based on Poly(caprolactone) diol/Poly(ethylene glycol) (Poly(caprolactone) diol/Poly(ethylene glycol)을 기초로 한 폴리우레탄 마이크로겔의 합성 및 특성)

  • Lim, Jeong-Soo;Kim, Kong-Soo;Lee, Moo-Jae;Lee, Young-Geun
    • Polymer(Korea)
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    • v.25 no.1
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    • pp.41-48
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    • 2001
  • Polyurethane(PU) microgels were synthesized from poly(caprolactone) diol(PCD) and/or poly(ethylene glycol)(PEG), diisocyanate and 1,2,6-hexane triol by solution polymerization method. A critical gelation concentration of the PU microgels with, mole ratios of PCD/PEG were the important factors influencing the formation and property microgel or macrogels. The physical and thermal properties of the PU microgels prepared with depending upon the structure of diisocyanate, mole ratio of PCD/PEG, and molecular weight of PEG were investigated. It was found that PU microgels were distributed by polydisperse, spherical small particles below 300nm and showed the properties of low viscosity.

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Kinetics on the Synthesis of Poly(caprolactone diol) and Aliphatic Lsocyanate by FTIR Spectroscopy (FTIR을 이용한 폴리(카프로락톤 다이올)과 지방족 이소시아네이트의 반응속도 연구)

  • Kang, Suk-Hwan;Yang, Yun-Kyu;Kwak, Noh-Seok;Kang, Yun-Uk;Hwang, Taek-Sung
    • Polymer(Korea)
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    • v.29 no.1
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    • pp.59-63
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    • 2005
  • Kinetic study of a reaction between poly(caprolactone diol) and aliphatic isocyanate was investigated by FTIR spectroscopy. The reaction rate was obtained from analyzing the absorbance change of NCO peak (2265 $cm^{-1}$) in series IR spectra. In the results, the overall reaction between PCL and isocyanate conformed to the simple second-order law, and the rate constant increases with increasing reaction temperature. The activation energies obtained from the evaluation of kinetic data were 25.4∼30.9 kJ/mol for hexamethylene diisocyanate and 16.8∼22.1 kJ/mol for cyclohexylmethane diisocyanate, respectively.

Preparation and Biodegradability of Microsphere Prepared from Biodegradable Microgel (생분해성 Microgel로부터 약물을 담지한 Microsphere의 제조 및 그의 생분해성)

  • Kim, Kong Soo;Kang, Seok Ho;Kim, Jeong Muk
    • Applied Chemistry for Engineering
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    • v.9 no.4
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    • pp.591-594
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    • 1998
  • Biodegradable microsphere containing bovine serum albumine (BSA) as a model drug were prepared with the microgel based on poly(caprolactone diol) by a modified solvent evaporation method. The influence of the stirring speed, the concentration of microgel and the mixing rate but increased with increasing the concentration of microgel in methylene chloride. The biodegradability of microsphere in 100 unit/mL of lipase solution was investigated. A lot of small pores appeared on the surface of microsphere after 3 hours of incubation time and the pores and cracks were developed with increasing the incubation time and microsphere lost their own shape after 36 hours of incubation time.

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Application of Polycarbonate Diol Prepared with Carbon Dioxide in the Field of Waterborne Polyurethane (이산화탄소를 이용하여 제조된 폴리카보네이트 디올의 수분산 폴리우레탄에 응용)

  • Lim, Jae-Woo;Oh, Hyoung-Jin;Kim, Young-Jo;Jeong, Kwang-Eun;Yim, Jin-Heong;Ko, Young-Soo
    • Polymer(Korea)
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    • v.34 no.6
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    • pp.507-510
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    • 2010
  • Poly(cyclohexane carbonate) diol was synthesized by the alternating copolymerization of cyclohexene oxide and $CO_2$ over Cr based transition metal catalysts. The prepared PCCD was applied as a precursor for the preparation of waterborne polyurethane (PUD) in order to investigate an application field of carbon dioxide-based polycarbonate. The scratch resistance and thermal properties of PUDs, which was prepared with two kinds of polymeric diols (PCD and PCCD) were investigated. The scratch resistance and thermal decomposition temperature of PUD film prepared with PCCD is worse than those prepared with PCD, poly(hexamethylene carbonate) glycol. While, glass transition temperature of PUD film prepared with PCCD was higher than that prepared with PCD. It might be due to the rigid cyclohexane structure in the PCCD.

Preparation and Physical Properties of Polycaprolactone Diol-based Water-based Polyurethanes for Split Leather Coatings (스플릿 레더 코팅을 위한 폴리 카프로 락톤 디올 기반 수성 폴리 우레탄의 제조 및 물리적 특성)

  • Lee, Joo-Youb
    • Journal of the Korean Applied Science and Technology
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    • v.37 no.1
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    • pp.49-55
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    • 2020
  • In this study, isophorone diisocyanate (IPDI) and dimethylolbutanoic acid (DMBA) were used on the basis of poly caprolactone diol (3M, 3.5M, 4M, 4.5M) for the synthesis of water-based polyurethanes for coating on skin layers of leather. Tensile strength, elongation, and adhesive strength of the prepared samples were measured. As a result of measuring the tensile strength, the tensile strength was found to be 4.09 kgf / ㎟ when 3 moles were applied, and 1.071 kgf / ㎟ when 4.5 moles were applied. Elongation was 366 % when 3 moles of PCL were applied, and 709 % at 4.5 moles. Adhesive strength was 2.887 kgf / cm when 3 moles of PCL was applied and 0.998 kgf / cm when 4.5 moles were applied.

Miscibility of TPU(PCL diol)/PCL Blend and its Effect on PCL Crystallinity

  • Ajili Shadi Hassan;Ebrahimi Nadereh Golshan
    • Proceedings of the Polymer Society of Korea Conference
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    • 2006.10a
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    • pp.371-372
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    • 2006
  • Poly(${\varepsilon}-caprolactone$) (PCL) is a highly crystalline polymer that is miscible with several amorphous polymers including chlorinated polyether, poly(vinylchloride), poly(hydroxyether) and Bisphenol A polycarbonate. The crystallization behavior of miscible blend of amorphous/crystalline polymers has widely been studied. Generally a depression of the crystallization ability has been found with addition of amorphous component because of the reduction of chain mobility, the change of free energy of nucleation as a result of a specific interaction, and so on [1]. In this work, for the first time, the blend of PCL and copolymer of polyurethane containing polycaprolactone as a soft segment is considered. The structural similarity of TPU soft segment with PCL affects on formation of the miscible component and crystallization behavior of PCL in the blend. This has been studied using differential scanning calorimetry (DSC) and Wide-angle X-ray Scattering (WAXS).

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Effect of polyol on urethane to increase the cavitation resistance (우레탄수지에서 캐비테이션 저항을 높이기 위한 Polyol의 영향)

  • Lee, Iksoo;Kim, Nackjoo;Pak, Daewon
    • Journal of the Korean Applied Science and Technology
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    • v.31 no.4
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    • pp.628-634
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    • 2014
  • In this study, a new paint which is able to resist the cavitation erosion is tried to be developed by using urethane added with polyol such as poly propylene glycol(PPG), poly carbonate diol(PCD), polycaprolactone polyol (PCL-1), and poly caprolactone-tetramethylene gylcolether polyol(PCL-2). The new paint synthesized by adding polyol was characterized with physical properties and resistivity to cavitation erosion. Among polyol, the prepolymer added with PCD showed high hardness and wear resistance. However, due to too high in viscosity, the prepolymer added with PCL-1 was selected as a paint. The paint added with PCL-1 showed high resistivity to cavitation erosion and its surface was monitored by using Scanning Electron Microscope.

Synthesis and Characteristics of 2 Step-curable Shape Memory Polyurethane (2단계 경화형 형상기억 폴리우레탄의 합성 및 분석)

  • Noh, Geon Ho;Lee, Seungjae;Bae, Seong-Guk;Jang, Seong-Ho;Lee, Won-Ki
    • Journal of Environmental Science International
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    • v.27 no.11
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    • pp.1023-1028
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    • 2018
  • Shape memory materials are widely used in high-tech industries. Although shape memory polymers have been developed, they have a disadvantage, only unidirectional resilience. Shape memory polymers with bi-directional recovery resilience have been actively studied. In this study, a bidirectional shape memory polyurethane was synthesized using poly(${\varepsilon}$-caprolactone) diol, methylene dicyclohexyl diisocyanate, and hydroxyethyl acrylate. The first physical curing occurred between hard segments and hydrogen bondings when the solution was dried. The second curing in acrylate groups was performed by UV exposure. A degree of curing was analyzed by infrared spectroscopy. The shape memory properties of 2 step-cured polyurethanes were investigated as a function of UV curing time.