• Title/Summary/Keyword: PTMG

Search Result 58, Processing Time 0.02 seconds

Preparation and Properties Measurement of 2-hydroxyethyl methacrylate / Water-dispersed polyurethane composites

  • Lee, Joo-Youb
    • Journal of the Korean Applied Science and Technology
    • /
    • v.35 no.4
    • /
    • pp.1224-1229
    • /
    • 2018
  • In this study, 2-hedroxyethyl methacrylate (2-HEMA) was graft synthesized on water-dispersed polyurethane using polytetramethylene ether glycoll (PTMG), and then the film of resin was prepared and the physical properties of polyurethane resin were measured. The mechanical properties of the synthesized polyurethane resin were measured by using FT-IR, UTM, adhesion performance measuring instrument. As a result of tensile strength measurement, the tensile strength of HPUD4 with high 2-HEMA content was increased to $5.05kgf/mm^2$, the elongation was measured as 285% of the HPUD1 sample not containing 2-HEMA and adhesive strength of HPUD4 sample was measured at 9.1 sec to 635 psi.

Synthesis and Characterization of Thermoplastic Elastomer Poly(ether-b-amide) Containing Aromatic Moiety (방향족 구조가 포함된 열가소성 탄성체 Poly(ether-b-amide)의 합성 및 특성)

  • Lee, Ji Hun;Kim, Hyung Joong
    • Polymer(Korea)
    • /
    • v.38 no.5
    • /
    • pp.596-601
    • /
    • 2014
  • Polyamide (PA) oligomers, which are the hard segment of poly(ether-block-amide) (PEBA), presenting thermoplastic and high performance elastomeric properties were prepared by polycondensation between 4-aminobenzoic acid and 12-aminododecanoic acid. Subsequently PEBAs were obtained by addition polymerization of the PA oligomers and various molecular weights of poly(tetramethylene glycol) (PTMG). The structure of the final PEBA was identified by using FTIR and $^1H$ NMR and the thermal properties depending on changes in the structure of hard segment were collected by using DSC and UTM analysis. As the results, the melt temperature ($T_m$), the initial modulus, and the maximum strength of PEBAs increased with an increase in aromatic moiety up to 30% without reducing crystallinity.

Preparation of Waterborne Polyurethanes Containing Polycarbonate Component and Their Applications to the Impregnation Finishing for Artificial Leathers (폴리카보네이트 성분을 포함하는 수분산 폴리우레탄의 제조와 인공피혁 함침가공에의 응용)

  • Lee, Kyoung-Woo;Ko, Jae-Hoon;Shim, Jae-Yun;Kim, Young-Ho
    • Polymer(Korea)
    • /
    • v.33 no.2
    • /
    • pp.175-182
    • /
    • 2009
  • Waterborne polyurethanes (WPUs) based on isophorone diisocyanate and mixed polyols of poly(tetramethylene glycol) (PTMG)/polycarbonate diol (PCD) were synthesized. The variation of mechanical and dyeing properties and alkali resistance of the WPU films were analyzed according to the polycarbonate (PC) content. The tensile strength of the films increased and the elongation at break decreased with the PC content in the WPU film. The incorporation of PC component in the WPU film did not affect the alkaline hydrolysis behavior. The synthesized WPU solutions were used as impregnating resins for the production of PET artificial leathers. The prepared WPU resins showed the good color fastness to washing, rubbing, and light of the artificial leather fabrics. The improvement of the properties became greater with the PC content in the WPU resin.

A Study on Properties of the Urethane Prepolymer Synthesis with Polyether-diol and Aromatic Diisocyanate System (폴리에테르-디올과 방향족 디이소시아네이트계의 우레탄 프리폴리머 합성에 따른 특성연구)

  • Lee, Hyun-Joo;Kim, Kwang
    • Applied Chemistry for Engineering
    • /
    • v.9 no.4
    • /
    • pp.491-496
    • /
    • 1998
  • The composition of isocyanates and polyols influence prepolymeric properties of adhesive and calking sealant based on polyurethanes (PU). One component moisture curing prepolymers, which reacted with surface humidity of substrate, were synthesized in several kinds of composition. Reactivity, structural change and properties of the prepolymers were studied as a preliminary step to manufacture PU based adhesive and sealant. To study the effects of mole ratio ([NCO]/[OH]), we used toluene diisocyanate (TDI), 4, 4'-diphenylmethane diisocyanate (MDI), and ether-polyols such as PTMG and PPG which have good resistance to hydrolysis and excellent low-temperature properties. The each prepolymers could be prepared in different molecular weight without any significant structural change. The mole ratio 1.78 of [NCO] to [OH] showed the fastest reactivity. It was confirmed that effect of polyols was larger than that of isocyanates on the prepolymer in reactivity. Several kinds of compounds were manufactured with each prepolymer, and tensile and properties were tested. And the optimum quantity of curing accelerator for the PU was 0.05~0.1%. In the tensile test, TDI based PU was superior to MDI based PU, and also PTMG based PU was superior PPG based PU.

  • PDF

PBS-PTMG Segmented Block Copolymer의 Segment와 Domain 배향 거동

  • 박해동;이한섭;조창기;박영효
    • Proceedings of the Korean Fiber Society Conference
    • /
    • 1998.04a
    • /
    • pp.76-79
    • /
    • 1998
  • 일반적인 합성 섬유들은 비생분해성 고분자로 환경문제의 원인이므로 이를 대체하기 위하여 생분해성 지방족 폴리에스터가 널리 연구되고 있다.[1] 그러나, 이들의 기계적, 열적 성질이 다른 합성 섬유에 비해 떨어진다. 따라서, 생분해성 고분자의 특성을 유지하면서 기계적 성질을 향상시키기 위하여 다른 유연한 고분자와 지방족 폴리에스터를 공중합하였다.(중략)

  • PDF

Synthesis and Emulsification of Polyurethane Anionomer (음이온성 폴리우레탄의 합성 및 에멀젼화에 관한 연구)

  • Ann, Choun-Kee;Jin, Je-Yong;Lee, Gyung-Won;Choi, Sei-Young
    • Elastomers and Composites
    • /
    • v.34 no.5
    • /
    • pp.399-406
    • /
    • 1999
  • Polyurethane (PU) prepolymers were synthesized from polytetramethylene ether glycol (PTMG), 4,4'-diphenylmethane diisocyanate (MDI), toluene 2,4-diisocyanate (TDI) and isophoron diisocyanate (IPDI). After chain extention using dimethyol propionic acid (DMPA), aqueous polyurethane anionomers were prepared from triethyl amine (TEA) as a neutralizer. The effect of the content of chain extender and the degree of neutralization on the state of emulsification, adhesive strength, viscosity, glass transition temperature and physical properties of emulsion cast film were investigated using UTM, Viscometer and DSC.

  • PDF

Preparation of Waterborne Polyurethane/Silica Nanocomposites Using Tetraethylorthosilicate (Tetraethylorthosilicate를 사용한 수분산 폴리우레탄/실리카 Nanocomposite의 제조)

  • Shin, Yong Tak;Hong, Min Gi;Choi, Jin Joo;Lee, Won Ki;Lee, Gyoung Bae;Yoo, Byung Won;Lee, Myung Goo;Song, Ki Chang
    • Korean Chemical Engineering Research
    • /
    • v.48 no.4
    • /
    • pp.428-433
    • /
    • 2010
  • Waterborne polyurethane(WPU) was synthesized from isophorone diisocyanate(IPDI), poly(tetramethylene glycol)(PTMG), dimethylol propionic acid(DMPA), triethylamine(TEA), ethylenediamine(EDA) and 3-aminopropyl triethoxysilane(APS) as a coupling agent. Subsequently, WPU/silica nanocomposites with different silica contents(0 to 8 wt%) were prepared by performing sol-gel reactions with tetraethylorthosilicate in the WPU matrix. The average particle size of the nanocomposite solutions increased with increasing TEOS content. Also, the prepared nanocomposites showed better thermal stability than pure WPU.

Preparation and Properties of Aminosilane Terminated Waterborne Polyurethane (Aminosilane Terminated 수분산 폴리우레탄 코팅 용액의 제조 및 특성)

  • Shin, Yong Tak;Hong, Min Gi;Choi, Jin Joo;Lee, Won Ki;Lee, Gyoung Bae;Yoo, Byung Won;Lee, Myung Goo;Song, Ki Chang
    • Korean Chemical Engineering Research
    • /
    • v.48 no.4
    • /
    • pp.434-439
    • /
    • 2010
  • NCO terminated polyurethane prepolymers were synthesized from isophorone diisocyanate(IPDI), poly(tetramethyleneglycol)(PTMG) and dimethylol propionic acid(DMPA). Subsequently, aminosilane terminated prepolymers were prepared by capping the NCO groups of polyurethane prepolymers with different moles of aminopropyl triethoxysilane(0~0.02 mole) as a coupling agent. The average particle size of the silylated polyurethane solutions increased with increasing APS content. Also, the prepared coating films showed better thermal stability and pencil hardness than pure waterborne polyurethane.

Study on the Synthesis of Polyurethane Cationomers and Their Mechanical Properties (양이온성 폴리우레탄의 합성 및 기계적 특성에 관한 연구)

  • Ann, Choun-Kee;Jin, Je-Yong;Choi, Sei-Yong
    • Elastomers and Composites
    • /
    • v.33 no.3
    • /
    • pp.177-184
    • /
    • 1998
  • Polyurethane(PU) prepolymers were synthesized from polytetramethylene ether glycol(PTMG), with 4,4'-diphenylmethane diisocyanate(MDI), toluene 2,4-diisocyanate (TDI) and isophoron diisocyanate(IPDI). After chain extention using n-methyl-diethanol amine(n-MDEA), aqueous polyurethane cationomers were prepared by addition of glycolic acid(GA) as a quaternizer. The effect of the content of chain extender and the degree of neutralization on the stability of emulsion, adhesive strength, viscosity, glass transition temperature and physical properties of emulsion cast film were investigated using UTM, viscometer and DSC.

  • PDF

A Study on Reaction Kinetics of PTMG/TDI Prepolymer with MOCA by Non-Isothermal DSC

  • Ahn, WonSool;Eom, Seong-Ho
    • Elastomers and Composites
    • /
    • v.50 no.2
    • /
    • pp.92-97
    • /
    • 2015
  • A study on reaction kinetics for a PTMG/TDI prepolymer with 2,2'-dichloro-4,4'-methylenedianiline (MOCA), of which formulations may be generally used for fabricating high performance polyurethane elastomers, was peformed using non-isothermal differential scanning calorimetry (DSC). A number of thermograms were obtained at several constant heating rates, and analysed using Flynn-Wall-Ozawa (FWO) isoconversional method for activation energy, $E_a$ and extended-Avrami equation for reaction order, n. Urea formation reaction of the present system was observed to occur through the simple exothermic reaction process in the temperature range of $100{\sim}130^{\circ}C$ for the heating rate of $3{\sim}7^{\circ}C/min$. and could be well-fitted with generalized sigmoid function. Though activation energy was nearly constant as $53.0{\pm}0.5kJ/mol$, it tended to increase a little at initial stage, but it decreases at later stage by the transformation into diffusion-controlled reaction due to the increased viscosity. Reaction order was evaluated as about 2.8, which was somewhat higher than the generally well-known $2^{nd}$ order values for the various urea reactions. Both the reaction order and reaction rate explicitly increased with temperature, which was considered as the indication of occurring the side reactions such as allophanate or biuret formation.