• 제목/요약/키워드: IPNs

검색결과 23건 처리시간 0.018초

Synthesis and Physical Properties of pH-sensitive Semi-IPN Hydrogels Based on Poly( dimethylaminoethyl methacrylate-co-PEG dimethacrylate) and Poly(acrylic acid)

  • Kim Goo-Myun;Jo Won-Ho
    • Fibers and Polymers
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    • 제7권3호
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    • pp.223-228
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    • 2006
  • Hydrogels of semi-interpenetrating polymer networks (semi-IPNs) were prepared by two step reactions. Dimethylaminoethyl methacrylate (DMAM) and poly(ethylene glycol)-dimethacrylate (PEGDM) were copolymerized to yield hydrogels, and then acrylic acid (AA) monomer were adsorbed in the hydrogels followed by polymerization of AA to produce semi-IPNs. The swelling behavior of semi-IPNs depends largely on pH of medium, showing that the degree of swelling of the semi-IPNs exhibits a minimum at pH 6.0. It is observed that the elastic modulus of semi-IPNs is closely related to its swelling behavior.

Polyetherimide/Dicyanate Semi-interpenetrating Polymer Networks Having a Morphology Spectrum

  • Kim, Yu-Seung;Min, Hyun-Sung;Kim, Sung-Chun
    • Macromolecular Research
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    • 제10권2호
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    • pp.60-66
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    • 2002
  • The morphology, dynamic mechanical behavior and fracture behavior of polyetherimide (PEI)/dicyanate semi-interpenetrating polymer networks (semi-IPNs) with a morphology spectrum were analyzed. To obtain the morphology spectrum, we disported PEI particles in the procured dicyanate resin containing 300 ppm of zinc stearate catalyst. The semi-IPNs exhibited a morphology spectrum, which consisted of nodular spinodal structure, dual-phase morphology, and sea-island type morphology, in the radial direction of each dispersed PEI particle due to the concentration gradient developed by restricted dissolution and diffusion of the PEI particles during the curing process of the dicyanate resin. Analysis of the dynamic mechanical data obtained by the semi-IPNs demonstrated that the transition of the PEI-rich phase was shifted toward higher temperature as well as becoming broader because of the gradient structure. The semi-IPNs with the morphology spectrum showed improved fracture energy of 0.3 kJ/$m^2$, which was 1.4 times that of the IPNS having sea-island type morphology. It was found that the partially introduced nodular structure played a crucial role in the enhancement of the fracture resistance of the semi-IPNs.

우레탄을 기초로 한 IPN 탄성체의 성질 (Properties of Urethane-Based IPN Elastomers)

  • 민성기;박찬영
    • 한국인쇄학회지
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    • 제22권2호
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    • pp.37-54
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    • 2004
  • IPNs have interpenetrating motion and phase separation behavior of independent polymers, respectively, and also these are affected by the physical interaction of polymer components. First of all, 2- and 3-component IPNs based on PU are prepared by combination with two or three components of PU, PMMA, PS and epoxy resin. And then the entire physical properties concerning morphological and mechanical behaviors of these IPNs are measured by employing FT-IR, SEM, Rheovibron, and DSC, etc. Compared with pure component, Tg's of IPN are shifted to higher temperature in all IPN kinds, and these are considered in attribution to internal movement of glass transition temperature or partial phenomenon of interpenetration. Rheovibron measurement results in a broader distribution with peaks of tan${\delta}$ or E", and this morphologically represents a medium degree of partially mixed IPNs in confirmation of SEM photographs.

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Drug Release from Bioerodible Hydrogels Composed of $Poly-{\varepsilon}-Caprolactone/poly(Ethylene{\;}glycol)$ Macromer Semiinterpenhetrating Polymer Networks

  • Kim, Sung-Ho;Ha, Jeong-Hun;Jung, Yong-Jae;Cho, Chong-Su
    • Archives of Pharmacal Research
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    • 제18권1호
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    • pp.18-21
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    • 1995
  • Poly(ethylene glycol)(PEG) macrocers teminated with acrylate groups and semi-interpenetrating polymer networks (IPNs) composed of poly-.epsilon.-capolactone(PCL) and PEG macromer were syntheswized with the aim of obtaining a bioerodible hydrogel that could be used to release drugs for implantable delivery system. Polymerization of PEG macromer resulted in the formation of cross-linked gels due to the multifunctionality of macromer. Non-crosslinked PCL chains were interpenetrated into the cross-linked three-dimensions networks of PEG. The IPNs, largw drug loading lower concentration of PEG macromer in the IPNs concentration and the higher molecular weight of PEG macromer. Also, 5-FU was more fast released than hydrocortisone to the increased water solubility.

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Drug Release from Ph-sensitive Interpenetrating Polymer Net-works Hydrogel Based on Poly(ethylene glycol) Macromer and Poly (acrylic acid)Prepared by UV Cured Method

  • Kim, In-Sook;Kim, Sung-Ho;Cho, Chong-Su
    • Archives of Pharmacal Research
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    • 제19권1호
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    • pp.18-22
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    • 1996
  • Acrylate-terminated poly (ethylene glycol) (PEG) macromer was prepared by the reaction of PEG with acryloyl chloride. Photopolymerization of PEG macromer resulted in the formation of cross-linked PEG network. Interpenetrating polymer networks (IPNs) based on PEG and poly(acrylic acid) (PAA) was obtained via template polymerization of AA to the PEG network by UV curing. The swelling degree of the IPNs hydrogel increased with an increase of pH value due to the association-dissociation between carboxylic acid of PAA and either of PEG through hydrogen bounding. The swelling-deswelling behavior proceeded reversibly for the IPNs upon changing pH. Release of indomethacin from the IPNs demonstrated "on-off" regulation with pH fluctuation.

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UV 경화형 키토산/지방족 폴리에스터 Hydrogel IPN 제조 및 약물투과 (Synthesis, Properties and Permeation of Solutes through Hydrogels based on Poly(ethylene glycol)-co-Poly(lactones) diacrylate Macromers and Chitosan)

  • 조성민;김소연;이영무;성용길;조종수
    • 대한의용생체공학회:학술대회논문집
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    • 대한의용생체공학회 1998년도 추계학술대회
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    • pp.229-230
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    • 1998
  • Triblock copolymers from poly(ethylene glycol) (PEG) and D,L-lactide or $\varepsilon$-carprolactone were synthesized to prepare semi-interpenetrating polymer network (semi-IPN) with chitosan by U.V. irradiation method. Then, solute permeation through these semi-IPNs hydrogels were investigated. The structures of semi-IPNs were confirmed by FT-IR spectroscopy and wide angle X-ray diffractometer (WAXD). Equilibrium water content (EWC) of these hydrogels was in the range of 67-75%. The crystallinity, thermal properties and mechanical properties of semi-IPNs hydrogels were studied. All the hydrogels revealed a remarkable decrease in crystallinity as compared with PEG macromer itself. The tensile strengths of semi-IPNs hydrogels in dry state were rather high, but those of hydrogels in wet state decreased drastically. The permeabilities of solutes of hydrogels followed the swelling behaviors and were regulated by solute size.

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진동·충격음 흡수성 목질계 복합재료의 개발 -폭 넓은 감쇠곡선을 나타내는 고분자의 합성- (Development of Vibration and Impact Noise Damping Wood-Based Composites -Synthesis of the Polymer Showing a Broad Damping Peak)

  • 이현종
    • Journal of the Korean Wood Science and Technology
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    • 제27권2호
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    • pp.15-22
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    • 1999
  • 진동 충격음 흡수성능을 지니는 샌드위치구조 목질 복합재료 제조용 폴리머는 넓은 온도범위(또는 주파수 범위)에서 높은 손실계수를 지니면서, 동시에 $5{\times}10^7\sim-10^9\;dyne/cm^2$의 탄성율을 지녀야 한다. 본실험에서는 이러한 점탄성 거동율 나타내는 고분자재료의 제조를 목적으로 에폭시 수지/아크릴 수지 상호침투망목고분자(IPNs)를 동시망목형성법으로 합성하였다. 고분자의 동적 점탄성은 Rheovibron을 사용하여 110Hz에서 측정하였으며, 복합체의 손실계수 및 동탄성 계수는 Rheovibron을 개조한 양단지지 강제 휨 진동법으로 주파수 110Hz에서 측정하였다. 동력학적 측정 결과, 손실탄성율의 최대값 온도 및 손실계수의 최대값 온도가 이동하고, 유리전이 영역이 확대되어, 이 IPNs계는 부분 상용계임을 알 수 있었다. 특히, 70/30 및 50/50 조성의 Epikote871/P(n-BMA) IPNs는 넓은 온도 범위에서 비교적 높은 손실계수 및 적당한 탄성율을 나타냈다. 또한 이를 적층한 목질 복합체는 넓은 온도 범위에서 비교적 높은 진동흡수 계수를 나타냈다.

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폴리우레탄-에폭시 IPNs의 강인성 (The Toughness of Polyurethane and Epoxy Resins IPNs)

  • 김종석;홍석표
    • 공업화학
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    • 제9권3호
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    • pp.445-450
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    • 1998
  • 에폭시수지와 caster oil(CO)형 폴리우레탄(PU)은 상호침투고분자(IPNs)를 형성하였다. 사슬연장제인 polypropylene ether glycol(PPG)와 가교제인 CO를 사용하여 두 종류의 폴리우레탄을 제조했다. CO를 이용한 COPU/epoxy의 동시중합 상호침투고분자(SINs)는 PPG를 이용한 PPGPU/epoxy SINs보다 상용성이 좋았다. PPGPU/epoxy SINs의 전조성에서 가교구조의 얽힘정도가 감소함에 따라 굴곡강도가 감소하였다. COPU/epoxy SINs은 PPGPU/epoxy SINs에 비해 기계적 물성과 파괴인성이 우수하였다. 실험 결과, 모든 SINs의 파괴단면에서 폴리우레탄의 공동화에 의한 응력백화 현상보다는 전단변형과 크랙의 편향이 관찰되었다.

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폴록사머-폴리아크릴산 IPNs의 약물 조절 방출 (Drug Release Control of Poloxamer-Poly(acrylic acid) Interpenetrating Polymer Networks)

  • 변은정;박주애;이승진;김길수
    • 약학회지
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    • 제41권1호
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    • pp.22-29
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    • 1997
  • Poloxamer-poly (acrylic acid) (PAA) interpenetrating polymer networks (IPNs) were prepared via matrix polymerization of acrylic acid with poloxamer prepolymer. The equilibrium s welling of poloxamer/PAA IPNs was determined in various pH medium. The swelling of poloxamer/PAA IPNs was more affected by pH difference compared with the swelling of homo PAA gel due to protonation and deprotonation of the PAA network, followed by reversible formation and dissociation of the interpolymer complex due to hydrogen bonding between acidic hydrogens and ether oxygens. Nonionic/anionic/cationic drugs were incorporated into IPN matriceds as a model drug and their release behavior was studied. Nonionic, drug revealed release patterns depending solely on pH dependent swelling kinetics. In contrast, the release of ionic drugs was significantly affected by ionic drug-polymer interaction as well as the swelling kinetics.

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