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首页> 外文期刊>Journal of Applied Polymer Science >Foam Stability and Polymer Phase Morphology of Flexible Polyurethane Foams Synthesized from Castor Oil
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Foam Stability and Polymer Phase Morphology of Flexible Polyurethane Foams Synthesized from Castor Oil

机译:蓖麻油合成的柔性聚氨酯泡沫的泡沫稳定性和聚合物相形态

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摘要

Foam stability and segmented polymeric phase morphology of polyurethane foams synthesized partially and completely from castor oil are investigated. Preliminary analysis of the impact of alterations in the polymeric phase on macroscopic stress dissipation in foams is also carried out. The stability and morphology show unique trends depending on the concentration of castor oil used in foam synthesis. While low and intermediate concentrations of castor oil does not significantly affect the foaming process; at high concentrations, the volumetrically expanding liquid matrix remains in a nonequilibrium state during the entire foaming period, resulting in significant foam decay from top. This increases the final foam cell density and decreases the plateau border thickness at bottom. In the polymeric phase of castor oil based foams, the fraction of monodentate urea increases at the cost of non-hydrogen bonded urea. These monodentate urea domains undergo flocculation in foams synthesized completely from castor oil, thus prominently modifying the segmented morphology. The glass transition temperature of soft segments of partially substituted foams shows moderate increase, with indications of phase mixing between the polyether and castor oil generated urethane domains. Foams synthesized entirely from castor oil have significant sol fraction due to unreacted oligomers. The microscopic alterations in polymeric phase reduce the elastic recovery of partially substituted castor oil foams compared to its viscous dissipation under an applied stress.
机译:研究了由蓖麻油部分和全部合成的聚氨酯泡沫的泡沫稳定性和分段的聚合物相形态。还进行了聚合物相变化对泡沫宏观应力消散的影响的初步分析。取决于泡沫合成中所用蓖麻油的浓度,稳定性和形态显示出独特的趋势。蓖麻油的中低浓度不会显着影响发泡过程;在高浓度下,体积膨胀的液体基质在整个发泡期间保持非平衡状态,从而导致泡沫从顶部显着衰减。这增加了最终的泡沫孔密度,并减小了底部的平台边界厚度。在蓖麻油基泡沫的聚合物相中,单齿脲的比例以非氢键结合的脲为代价而增加。这些单齿脲结构域在完全由蓖麻油合成的泡沫中经历絮凝,从而显着改变了分段的形态。部分取代的泡沫的软链段的玻璃化转变温度显示出适度的升高,表明在聚醚和蓖麻油生成的氨基甲酸酯域之间发生了相混合。完全由蓖麻油合成的泡沫由于未反应的低聚物而具有显着的溶胶分数。与在施加应力下的粘性耗散相比,聚合物相的微观变化降低了部分取代的蓖麻油泡沫的弹性回复率。

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