• Proceedings of the Membrane Society of Korea Conference
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• 1999.07a
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• pp.23-26
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• 1999

Urethane block copolymers, containing soft segments such as polydimethylsiloxane (PDMS), polytertramethylene glycol(PTMG) and PEO-PPO-PEO (Poloxamer) block copolymer, were synthesized and examined for th vapor- phase separation of toluene from nitrogen stream by using vapor permeation equipment. Generally permeabilities of PTMG and PDMS based urethane membranes were higher than those of Poloxamer based urethane membranes. Organic vapor permeability in the PDMS and PTMG soft segment urethane membranes were greater than those measured in the Poloxamer films, due to more polymer swelling. The membranes performed best with toluene, with toluene/dry N2 seletivities ranging from 120~200 and permeablilities as high as 23$\times$10-9 mol/m2sPa for saturated toluene feeds at 23$^{\circ}C$.

• Proceedings of the Korean Fiber Society Conference
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• 1996.10a
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• pp.468-472
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• 1996

A series of UV-curable polyurethane acrylate ionomer were synthesized from isophorone diisocyanate(IPDI), poly(tetramethylene ether glycol)(PTMG), 2,2-bis(hydroxymethyl)propionic acid (CMPA), triethylamine(TEA), 2-hydroxy ethyl acrylate (HEA), and dibutyl tin dilaurate (DBT) as a catalyst. 2,2-dimethoxy-2-phenyl acetophenone(DMPAP) was used as a photoinitiator. The films of UV-cured polyurethane acylate ionomer were prepared by casting the formulated materials onto a glass plate at room temperature and cured using a medium pressure mercury lamp (80 W/cm, max = 365nm). Effects of DMPA content, molecular weight of PTMG and degree of neutralization on the properties were invesigated. It is found that the storage modulus increased with increasing DMPA content. The glass transition temperature of sample A shifted to higher temperature as the content of DMPA was increased. Tensile modulus also increased with increasing DMPA content. Modulus and Tg decreased with increasing molecular weight of PTMG form 650 to 2000. With increasing the degree of nutralizaion, ionomers exhibited improved modulu.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2012.03a
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• pp.41-41
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• 2012

고급 스포츠웨어와 이너웨어 등에 많이 사용되고 있는 나일론/폴리우레탄 혼방제품은 염색에 있어서 Grin-through 현상, 인공피혁의 염료 이염 현상 등 많은 문제들이 존재한다. 본 연구의 나일론과 폴리우레탄 복합소재에서 나타나는 염색거동을 고찰하고 분석하여, 폴리우레탄 복합소재의 염색성을 개선하기 위하여 실시하였다. 폴리우레탄 복합소재는 해성분이 용출되지 않은 나일론 초극세사 소재에 폴리우레탄 수지를 함침하여 인공피혁과 같은 느낌을 주도록 직접 제조하였다. 제조된 폴리우레탄 함침 나일론 초극세사 소재의 해성분을 용출하였고, Red 색상의 밀링형 산성 염료, 함금속 염료와 반응성 염료에 따라 달라지는 염색특성 및 세탁 견뢰도 등을 고찰하였다. 본 연구를 통하여 다음과 같은 실험결과를 얻을 수 있었다. 나일론 초극세사와 폴리우레탄 수지를 준비하여 습식공정을 통해 인공피혁을 제조한 함침 소재를 알칼리 감량하였고, 감량률은 15~17% 정도로서 대부분의 해성분이 용출됨을 확인하였다. PPG와 PTMG로 구성된 폴리올을 기반으로 한 폴리우레탄 함침 피혁과 PTMG를 단독으로 사용한 함침 피혁의 염색성을 비교한 결과, PPG+PTMG 타입이 더 우수한 염색성을 나타내었다. 특히 밀링 타입과 함금속 타입 염료의 경우는 거의 2배 이상의 흡진율과 겉보기 색농도를 나타내었다. 한편, 반응성 염료의 경우는 두 종류의 폴리우레탄 필름에 거의 염착되지 않았기 때문에 앞으로의 염색실험에서 제외하였다. 견뢰도 측면에서는 각각의 피염물의 등급은 거의 유사하게 나타남을 확인하였다. 이상과 같은 결과로부터, 인공피혁 제조시 PPG+PTMG 타입의 폴리우레탄 수지를 사용하여 함침시 더 높은 색강도와 염착률을 얻을 수 있음을 알았다. 사용하는 염료의 종류를 좀 더 다양하게 하여 실험을 실시하고 폴리우레탄의 물성 및 분석 등의 추가적인 연구가 진행된다면, 인공피혁의 염색시에 발생하는 여러 가지 문제점들을 해결할 수 있을 것이다.

• Elastomers and Composites
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• v.42 no.4
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• pp.224-231
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• 2007

Polyurethane (PU) was prepared with the compositions of polytetramethylene glycol (PTMG) having two different molecular weight (250, 1000 g/mol). The optimum composition of PTMG 250/1000 was 60/40 based on the mechanical properties. PU/organoclay nanocomposites were prepared with several kinds of organoclay. The mechanical properties of nanocomposite prepared with 93A were considerable. The improvement in tensile strength and modulus for PU/organoclay nanocomposite with the application of ultrasound compared to the PU/organoclay nanocomposite without the application of ultrasound was factors of 1.2, and hardness (shore A type) increased from 90 to 95. The difference in thermal degradation was not observed. The results of transmission electron micrographs and X-ray measurements suggest that the intercalated organoclay in PU matrix was observed.

• Journal of Adhesion and Interface
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• v.23 no.4
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• pp.137-143
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• 2022

In this study, the polyurethane acrylates (PUA) resin with good adhesive and flexibility for adhesive for shoes and clothing were synthesized using that poly(tetramethylene adiphate glycol) (PTAd), poly(tetramethylene ether glycol) (PTMG) as polyester polyol and polyether polyol respectively, including 4,4'-methylene diphenyl diisocyanate (MDI), isophorone diisocyanate (IPDI), 1,4-butandiol (1,4-BD), 2-hydroxyethyl methacrylate (2-HEMA) and dibutyl amine (DBA). The effect of polyol blend in the polyurethane acrylate on thermal and mechanical properties, adhesion strength and flexural strength were studied. The glass transition temperature (T_g) of PUA was confirmed in range of -70~-40 ℃. In addition, the glass transition temperature (T_g), decomposition temperature (T_d), tensile strength adhesion strength and heat resistance were increased as increasing of PTAd amount while the elongation, water resistance and flexural properties were decreased. The synthesized polyurethane acrylate with 5:5 ratio of PTAd and PTMG indicated the highest adhesion strength and flexural properties.

• 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.

• Fibers and Polymers
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• v.3 no.4
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• pp.153-158
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• 2002

A series of waterborne polyurethanes (WBPU) were prepared from 4,4-dicyclohexylmethane diisocyanate ($H_{12}$MDI),2,2-bis(hydroxylmethyl) propionic acid (DMPA), othylenediarnine (EDA), triethylamine (TEA), and triblock glycol [TBG, ($\varepsilon$-caprolactone)$_{4.5}$-poly(tetramethylene ether) glycol (MW= 2000)-($\varepsilon$-caprolactone)$_{4.5}$: $(CL)_{4.5}$-PTMG-$(CL)_{4.5}$, MW=3000] as a soft segment. Two melting peaks of TBG at about 14$^{\circ}C$ and 38$^{\circ}C$ were observed indicating the presence of two different crystalline domains composed of CL and PTMG dominant component. The effect of soft segment content (60-75 wt%) on the colloidal properties of dispersion, and thermal and mechanical properties of WBPU films, the water vapor permeability (WVP) and water resistance (WR) of WBPU-coated Nylon fabrics, and the adhesive strength of WBPU- coated layer and Nylon fabrics was investigated. As soft segment contents increased, the water vapor permeability of WBPU- coated Nylon fabrics increased from 3615 to 4502 g/$m^2$day, however, the water resistances decreased from 1300 to 500 mm$H_2$O.O.

• Proceedings of the Korean Fiber Society Conference
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• 1999.04a
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• pp.331-334
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• 1999

• Proceedings of the Korean Fiber Society Conference
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• 1999.10a
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• pp.311-314
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• 1999

• Proceedings of the Korean Fiber Society Conference
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• 1997.10a
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• pp.126-130
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• 1997

A series of Thermoplastic polyurethane elastomers was prepared via a two-step polymerization process. The NCO/OH feed ratio of polyurethane synthesized in this study was varied from 1 to 1.3. Studies have been made on the effects of chemical and physical cross-linkina, and the properties of thermoplastic polyurethane elastomers based on isophorone diisocyanate (IPDI)/1,4-butanediol (BD)/poly(propylene glycol) (PPG, MW:2000), isophorone diisocyanate (IPDI)/BD /poly(oxytetramethylene) glycol (PTMG, MW:2000) was compared. These materials were characterized using FTIR spectrometer, dynamic mechanical thermal analyzer, and tensile retraction tester. PTMG based polyurethane elastomers showed higher elasomeric behavior than PPG based polyurethane elastomers at the same NCO/OH ratio. This feature has been connected with the specific nature of the polyols. The permanent set(%) was decreased with increasing maximum elongation from 50% to 300%.