• Macromolecular Research
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• v.10 no.6
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• pp.365-368
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• 2002

Thermoplastic polyurethanes (TPUs) with different hard segment length has been prepared from a fixed molar ratio of poly(tetramethylene ether glycol), 4,4'-diphenylmethane diisocyanate, and 1,4-butanediol by different polymerization procedures. Results reveal that the on-set temperature of endotherms ( $T_{cc}$ ) due to the crystallization of hard segments by cooling the TPUs from melt and the peak temperature of endotherms due to the melting of hard segments ( $T_{mh}$ ) by heating the TPUs increased and levelled off with increasing the hard segment length of TPUs. It has also been observed that soft segment glass transition temperature ( $T_{gs}$ ) of TPU decreased slightly with increasing the hard segment length, which explains less mixing of soft segments and hard segments. In tensile measurement of TPUs, strain hardening is observed with increasing the hard segment length, which is attributed to the strain induced crystallization of soft segments.

• Polymer(Korea)
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• v.31 no.6
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• pp.543-549
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• 2007

We synthesized various polyurethanes(PU) haying different hard segments with different molecular weights of the soft segment to explore the effect of structure on the dispersion of silver particle in the phase of synthesized polyurethanes matrix. The thermal stability was increased by increasing the number of aromatic compound, while the degree of dispersion for silver particle was decreased. Silver particles showed better dispersion in the PU matrix having aromatic compounds when the soft segments were held constant. On the contrary, when the hard segment was held constant, silver particles on the PU matrix haying low $M_w$ of soft segment showed better dispersion than high $M_w$ of soft segment because poor chain mobility of low $M_w$ of soft segment restricted re-aggregation of silver particle. A sheet resistance of composite materials showed different aspects. In this case, the inter connection between silver particles was more important than its dispersion. In this study, the NDI-PEG 900/silver particle composite film showed the best thermal stability and electro conductivity.

• Textile Coloration and Finishing
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• v.5 no.4
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• pp.60-66
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• 1993

Aqueous polyurethane(PU) anionomer dispersions were prepared from isophorone diisocyanate (IPDI), polytetramethylene adipate glycol(PTAd) and dimethylol propionic acid(DMPA) as potential anionic centers. The effects of polyol molecular weight(Mn) on the state of dispersion, thermal, mechanical, and viscoelastic properties and swelling of emulsion cast film were determined. With increasing Mn of PTAd, particle size of emulsion and soft segment T$_{g}$ decreased, and solvent swell, emulsion viscosity, and hard segment $T_{g}$ increased. Tensile strength showed minimum with PTAd 1000, and elongation at break generally increased with the Mn of PTAd. These results were possibly nterpreted in terms of soft segment-hard segment phase separation and crystallization of high molecular weight PTAd.

• Proceedings of the Korean Fiber Society Conference
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• 1998.10a
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• pp.66-69
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• 1998

Most segmented polyurethanes are prepared from a two-step method where the polyol is end-capped with an excess of diisocyanate, followed by chain extension with stoichiometric amount of chain extender, In the final polymer the hard and soft segments tend to segregate, due to thermodynamic immiscibility and the differences in chemical structure between hard and soft segments, and produce a phase separated morphology of hard segment-rich and soft segment-rich phase. (omitted)

• Proceedings of the Korean Fiber Society Conference
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• 1998.04a
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• pp.5-8
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• 1998

Polyurethane elastomers are segmented cocoplymer with an [HS]n-type structure. Typically, these materials are two-phase systems, prepared from relatively polar and stiff component called the hard segment(H) and relatively flexible component known as the soft segment(S). Diisocyanate and chain extender together form the hard segment, which is dispersed within a matrix of the soft segment, composed of the macrodiolos.(omitted)

• Proceedings of the Korean Fiber Society Conference
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• 2003.04a
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• pp.350-351
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• 2003

Polyurethane은 물리적, 화학적 성질이 매우 다른 두 segment(hard/soft)로 이루어진 block copolymer로서 hard segment의 화학적 구조가 hard segment의 packing정도에 영향을 미쳐, PU의 미세상분리 현상을 결정하며 결과적으로 PU의 물리적 성질에 큰 영향을 미치게 된다$^1$. 본 연구에서는 hard segment의 packing을 향상시켜 PU은 열적 기계적 특성을 향상시키기 위하여 방향족환으로 구성되어 있어 aromatic diol의 일종인 hydroxyquinone-di-(beta-hydroxyl)ether(HQEE)를 chain extender로 사용하여 PU를 합성하였다. (중략)

• Proceedings of the Korean Fiber Society Conference
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• 1998.10a
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• pp.33-36
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• 1998

Segmented block copolyetheresters defined as copolymers having sequences of alternating polyester hard blocks and polyether soft blocks create labile physical cross-links upon crystallization of hard polyester blocks Since the nature of the physical interlocking is a crystallite formed exclusively from the crystallizable hard segment, the hard segment content (HSC) and hard segment length (HSL) will play an important role in determining the properties such as mechanical property and dynamic mechanical property. (omitted)

• Fibers and Polymers
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• v.4 no.3
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• pp.114-118
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• 2003

The prepolymer and the final polyurethane (PU) block copolymer were synthesized by reacting 4,4-methylene bis(phenylisocyanate) with poly(tetramethylene glycol) and the prepolymer with 1,4-butanediol as a chain extender, respectively, to investigate the relation between phase separation and it's resulting properties. According to FT-IR data, the phase separation of hard and soft segments in the prepolymer and the PU block copolymer grew bigger by increasing the hard segment content, and the PU showed more dominant phase separation than the prepolymer. The heat of fusion due to soft segments decreased in both the prepolymer and the PU by increasing the hard segment content, whereas the heat of fusion due to hard segments increased in the PU did not appear in the prepolymers. The breaking stress and modulus of the prepolymer increased by increasing the hard segment content, and the elongation at break decreased gradually, and the PU showed the highest breaking stress and modulus at 58% hard segment content. However, the best shape recovery of the PU was obtained at 47% hard segment content due to the existence of proper interaction among the hard segments for shape memory effect. Consequently, the mechanical properties and shape memory effect of the PU were influenced by the degree of phase separation, depending on the incorporation of chain extender as well as the hard segment content.

• Journal of Korean Ophthalmic Optics Society
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• v.6 no.1
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• pp.119-124
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• 2001

Dimethyl terephthalate (DMT). 1.4-butanediol (1.4-BD) and poly (tetramethylene ether) glycol (PTMG) in the molecular weight of 2000 (g/mol) were used to synthesize poly(ether-b-ester) thermoplastic elastomers (TPEEs). The final copolymers were annealed to improve thermal stability at elevated temperatures and mechanical properties. This study showed that as the proportion of soft segment increases melting temperature and degree of crystallinity of TPEEs decrease constantly. In case of mechanical properties like flexural strength and flexural elastic modulus. $35-PTMG^{2000}$ indicates the highest values due to more efficient physical interlock.

• Proceedings of the Korean Fiber Society Conference
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• 2003.10b
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• pp.195-196
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• 2003

Polyurethane(PU)은 물리적 화학적 성질이 매우 다른 두 segment(hard/soft)로 이루어진 block copolymer로서 상온에서 미세상분리된 구조를 가진다. 이런 미세 상분리 구조는 PU의 물리적 성질을 결정하는 가장 중요한 요소이며, hard segment(H/S)의 화학적 구조에 따른 PU사슬의 강직성은 H/S의 packing및 상분리도에 큰 영향을 미친다. 본 연구에서는 H/S의 화학적 구조를 변화시켜 사슬의 강직성이 서로 다른 다양한 PU을 합성하였으며 Synchrotron SAXS와 FTIR-dichioism을 이용하여 PU 사슬의 강직성에 따른 거시적인 domain의 변형거동과 미시적인 사슬의 변형거동을 관찰 하였다. (중략)