• Elastomers and Composites
• /
• v.35 no.4
• /
• pp.281-287
• /
• 2000

Waterborne polyurethane(PU) microgel dispersions were synthesized with different mole ratio of polytetramethylene glycol(PTMG) to dimethylol propionic acid(DMPA). Particle size distribution, thermal and mechanical properties of the PU microgels were investigated. Particle size of the microgels was distributed in the range of $98{\sim}$680{\mu}m$ and decreased with increasing the mole ratio of DMPA and 1,2,6-hexanetriol. Glass transition temperature and melting temperature of the microgels were in the range of $-79.7 {\sim}-78.1^{\circ}C$, $22{\sim}24^{\circ}C$ respectively. Tensile strength and elongation of the PU microgel films were maximum in the case of 60/40 mole ratio of PTMG/DMPA.

• Elastomers and Composites
• /
• v.33 no.3
• /
• pp.149-158
• /
• 1998

SBR latex, polyurethane latex and epoxy latex were separately mixed with polyvinyl acetate emulsion. The various physical properties were examined for the mixtures. Epoxy mixtures gave a transparent film. Both polyurethane and SBR mixtures showed opaque film with high viscosity. In SBR and polyurethane increase in hardness was dependent on the evaporation rate of water, but in epoxy it was dependent on the degrees of crosslink. Epoxy's showed excellent water-resistance. SBR showed a good flexural strength and impact strength. When vinyl acetate emulsion was mixed with less than 10% latex paper tube showed the ductile fracture, but over latex content 20%, it showed the brittle fracture.

• Elastomers and Composites
• /
• v.48 no.4
• /
• pp.256-262
• /
• 2013

We synthesized thermoplastic polyurethane elastomer (TPU) with different contents of sulfuric acid group, and characterized their physical properties such as mechanical, thermal and grip properties. And the results were compared with carboxylic acid-introduced TPU. Wet slip, tensile strength and abrasion properties were increased by the introduction of acid group. Mechanical properties increased with increasing the acid content up to 0.3 wt%. However, wet slip was continually increased as the acid content increased due to increase of hydrophilicity of TPU.

• Elastomers and Composites
• /
• v.44 no.3
• /
• pp.329-335
• /
• 2009

Four series of novel liquid crystalline polyurethanes were synthesized by the polyaddition reaction of diisocyanates such as 2,6-tolylene diisocyanate (2,6-TDI), 2,5-tolylene diisocyanate (2,5-TDI), 2,4-tolylene diisocyanate (2,4-TDI), and 1,4-phenylene diisocyanate (1,4-PDI) with 4,4'-bis(5-hydroxypentoxy)biphenyl (BP5). 4,4'-bis(5-hydroxypentoxy)biphenyl exhibited a smectic type mesophase. Mesophase was found for all synthesized liquid crystalline polyurethanes except 1,4-PDI/BP5. The structures and the thermal properties of polyurethanes were studied by using FT-IR and ^1H$ NMR spectroscopy, DSC measurements and a polarizing microscope equipped with a heating stage.

• Proceedings of the Korean Fiber Society Conference
• /
• 1998.04a
• /
• pp.85-90
• /
• 1998

고무와 같은 유연성과 탄성을 가지면서 가유 필요없이 열가소성 성형기로 성형이 가능한 열가소성 탄성체는 1958년 E.I DuPont에 의해 폴리우레탄계 탄성섬유가 최초로 개발된 이래 낮은 생산원가와 대량생산이 쉬운 이점 때문에 많은 종류의 화합물이 개발되어 사용되고 있다.(중략)

• Elastomers and Composites
• /
• v.48 no.2
• /
• pp.141-147
• /
• 2013

Polyurethanes containing no mesogenic unit were prepared by polyaddition reaction of homo- and copolyurethanes based on para-type 1,4-phenylene diisocyanate (1,4-PDI), 2,6-bis($\omega$-hydroxypentoxy)naphthalene (BHN5) with 1,4-bis($\omega$-hydroxypentoxy)benzene (BHB5). All copolyurethanes showed monotropic liquid crystallinity, when measurements were performed under shearing. For example, a polyurethane Poly(50/50, mol%) with $[\eta]$=0.32 dL/g exhibited liquid crystallinity in the temperature range from $223^{\circ}C$ to $211^{\circ}C$ in the cooling stage. In contrast, two homopolyurethanes exhibited no explicit mesomorphic behavior, which was observed by DSC (Differental Scanning calorimeter) and measurement and polarized microscopic observation. The mesomorphic behavior of synthesized polyurethane was identified and characterized by differential scanning calorimetry, polarized optical microscope and X-ray.

• Elastomers and Composites
• /
• v.39 no.4
• /
• pp.286-293
• /
• 2004

Ester- and ether-based thermoplastic polyurethanes of different hardness were injection molded at different mold temperatures and effects of mold temperature on the physical properties of TPUs were investigated. Glass transition temperatures of soft segments of TPUs were hardly changed by mold temperatures. The phase separation of soft and hard segments of injection molded TPUs were affected little by mold temperatures. However, crystallinity of hard segments, temperature range of rubbery plateau, and tensile strength of injection molded TPUs decreased with increasing mold temperatures for TPUs of high hardness. However, injection molded TPUs of low hardness showed increases of crystallinity of hard segments, temperature range of rubbery plateau, and tensile strength with increasing mold temperatures. Different physical properties of injection molded TPUs depending on mold temperatures were attributed to different crystallization and physical crosslinking effects of hard segments.

• Elastomers and Composites
• /
• v.37 no.1
• /
• pp.39-48
• /
• 2002

Linear and crosslinked polyurethane dispersions were synthesized with 2,4-toluene diisocyanate, dimethylol propionic acid, polyoxypropylene glycol and polyoxypropylene glycerin. The structures of these polyurethanes were characterized by $^1H-NMR$ and FT-IR and the properties were measured with DSC, TGA, Instron and AFM etc. In case of linear polyurethane dispersion, the particle size, viscosity and glass transition temperature of polyurethanes increased with higher molecular weight of polyol and the degree of crosslinking. The crosslinked polyurethanes which contains more than 15% of polyoxypropyleneglycerin didn't from dispersion, when mixtures by polyoxypropyleneglycol and polyoxypropyleneglycerin were used as polyols. Thus, we synthesized crosslinked polyurethanes with 5%, 8%, 13% and 15% weight percents of polyoxypropylene glycerin as polyol mixtures.

• Journal of Adhesion and Interface
• /
• v.19 no.1
• /
• pp.5-12
• /
• 2018

The purpose of this study is to evaluate the adhesive properties of polyurethane mixed aqueous dispersions by omitting the primer, dealing with the preparation of skins for synthetic leather with excellent adhesion by omitting the pre-treatment process. The two-component mixed polyurethane water dispersion was prepared by synthesizing an ester-based polyurethane resin (PU-T) and a carbonate-based polyurethane resin (PU-C) to obtain the final resin. As a result of measuring the peel strength of the adhesive specimens omitting the pre-treatment agent, it was confirmed that the state adhesive strength (ethylene vinyl acetate (middle): $4.2kg_f/cm$ and rubber (outsole): $4.4kg_f/cm$) there was. This makes it possible to omit the pre-treatment process which has been indispensably used in the shoe manufacturing process, thereby reducing the process time and reducing the amount of volatile organic compounds (VOCs) generated in the pre-treatment product, resulting in environmentally advantageous.

• Elastomers and Composites
• /
• v.37 no.4
• /
• pp.258-264
• /
• 2002

In this work, the influence of thermal treatment on surface properties of silicas and mechanical interfacial properties of silicas/polyurethane composites was investigated. The surface properties of thermally treated silicas were studied in the context of Fourier Transform-IR (FT-IR), solid-state 29Si NMR spectroscopy, and contact angle. And the mechanical interfacial properties of the silica/polyurethane composites were evaluated by composite tearing energy (GIIIC). As a result, it was found that the thermally treated silica surfaces became hydrophobic in nature, due to the condensation of surface hydroxyls and the formation of siloxane bonds, resulting in increasing the London dispersive component of surface free energy. From which, the increase of the London dispersive component of the silicas led to an improvement of the dispersion of silicas in a polyurethane matrix, finally resulting in improving the tearing energy (GIIIC) of the silicas/polyurethane composites.