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Polyurethanes were prepared from toluene diisocyanate (TDI), 1-4-butane diol (BDO) and polycaprolactone-based triols with varying molecular weights. Among each molecular weight triol-based urethane, hard segment content was varied from 20% to 70%. Differential scanning calorimetry, tensile testing, and Iosipescu shear testing were done on all the various urethanes prepared. Thermal characterization data revealed the dependence of phase separation on hard segment content as well as on the triol molecular weight. Tensile data and Iosipescu shear data further confirmed the observations made from the DSC data. The data further indicated that phase separation can greatly improve the modulus of cross-linked segmented urethanes. Adhesion of these urethanes to glass surface was evaluated using soda-lime float glass plate. Urethane samples were cast on the air side of the glass plates and adhesion was measured in shear mode. Adhesion data indicated that in addition to hard segment content, modulus, cross-link density, and molecular weight of the triols, phase separation seems to be a major factor in controlling adhesion. Surfaces of the failed adhesion samples were also analyzed and the failure mode was found to be cohesive, in varying degree, with the different urethane systems. 相似文献
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Maltose long-chain fatty acid esters (MFAE), esterified at the 6 and 6′ position, were synthesized with stearic, palmitic,
myristic, and oleic groups. Synthesis yields were 15–20% based on initial maltose present, and structural confirmation was
obtained using plasma desorption mass spectrometry and nuclear magnetic resonance spectroscopy. These surfactants have surface
tensions in the range of 34–36 dyn/cm at their critical micelle concentrations (CMC) of approximately 10−5–10−6 mol/L. The increased chain lengths have a marked effect, reducing CMC values for MFAE by approximately three orders of magnitude
over similar carbohydrate-based dodecyl chain sources. Within chain lengths between 14 and 18 carbons, the rate of change
in CMC is significant and decreases with increasing chain length for MFAE. The melting points of MFAE are approximately 40°C,
and the heat capacities range from 1.6 to 1.9 J/g·K. These numbers are comparable to those of sucrose esters, indicating their
applicability in similar uses. However, because MFAE, unlike sucrose, possess an anomeric carbohydrate carbon position, these
surfactants maintain their reducing nature and are susceptible to further derivatization. They are also synthesized from renewable,
economical carbohydrates and lipids and may provide an excellent alternative to pertrochemical-derived products. 相似文献
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Jia Bing Dai Xing Yuan Zhang Jing Chao Chen Yan Bai 《Journal of Coatings Technology and Research》2007,4(3):283-288
A novel core–shell type fluorinated acrylic and siliconated polyurethane (FSiPUA) hybrid emulsion was prepared by seeded emulsion
polymerization using siliconated polyurethane (SiPU) as a seed and forming the structure with SiPU as a shell and the copolymer
of butyl acrylate (BA) with 2,2,2-trifluoroethylmethacrylate (TFEMA) as a core. SiPU was synthesized using isophorone diisocyanate
(IPDI), polytetramethylene ether glycol (PTMG), polypropylene glycol (PPG), dihydroxybutyl-terminated polydimethylsiloxane
(PDMS), dimethylol propionic acid (DMPA), 1,6-hexanediol (HDO) and triethylamine (TEA). The contents of siloxane and fluorine
were determined according to the feed ratio. Fourier transform infrared spectroscopy (FTIR) was used to identify the chain
structure of SiPU and FSiPUA. Investigation of transmission electron microscopy (TEM) confirmed the core–shell structure of
FSiPUA emulsion and gave the particle size at about 50 nm. The measurement results of water contact angles and the solvent
absorptions in water and n-octane for cured films showed that the water and the oil repellency for FSiPUA had been improved significantly with a suitable
content of fluorine and siloxane. 相似文献
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介绍了1,4-环己烷二甲酸的物化性质、性能特点及应用,并综述了其专利制备技术的研究进展。 相似文献
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