首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Macroporous poly(dicyclopentadiene) YFe2O3/Fe3O4 nanocomposite foams by high internal phase ennulsion templating
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Macroporous poly(dicyclopentadiene) YFe2O3/Fe3O4 nanocomposite foams by high internal phase ennulsion templating

机译:高内相模板法制备大孔聚二环戊二烯YFe2O3 / Fe3O4纳米复合泡沫

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The high internal phase emulsion (HIPE) templating approach to macroporous poly(dicyclopentadiene) γFe2O3/Fe3O4 nanocomposite foams via ring opening metathesis polymerisation was elaborated and the influence of the formulation of the HIPE on structural and mechanical properties of the magnetic composite foams of 80% nominal porosity was studied. HIPEs solely stabilized with the nanopartlcles resulted in considerably shrunken monolithic specimens characterized by an open cellular morphology with cavities bigger than 265 urn. Nanopartlcles were situated in the bulk and on the surface of the polymeric foam skeleton. Precise control over the feature sizes could not be obtained in this case. In contrast, HIPE formulations co-stabilized with a surfactant yielded samples of good casting quality characterized by a fully open cellular morphology in all cases. The cavity and the window size could be controlled by the amount of surfactant in the emulsion. A low surfactant loading of 1.5 v% with respect to the monomer yielded diameters of the cavities of the order of 20 nm interconnected with windows with diameters in the order of 4 urn, while 10 v% surfactant resulted in smaller cavities (10 μm) and windows (2 nm). All these feature sizes are hardly affected by the nanoparticle loading which was varied from 1 to 30 wt%. Surfactant stabilized and cured HIPEs featured the nanopartlcles predominantly on the surface of the cavities. Mechanical properties of the composite foams were assessed by stress-strain tests and revealed a strengthening of the foams prepared with 10 v% surfactant upon addition of the nanopartlcles. Indicative of the strengthening is an increase of the Young's modulus from 13 ± 2 MPa in the case of a sample without nanopartlcles to 104 ± 4 MPa in the case of the composite foam with 15 wt% nanopartlcles. This trend was accompanied by a decrease of the elongation at break from 21 ± 4 to less than 1%. Specimens prepared with 1.5 v% surfactant are ductile and gave the same high Young's modulus (104 ± 9 MPa) irrespective of the nanoparticle loading and became stronger upon raising the nanoparticle amount reaching an ultimate strength of 3.4 ± 0.4 MPa at an elongation at break of 13 ± 4%.
机译:阐述了通过开环复分解聚合制备大孔聚(二环戊二烯)γFe2O3/ Fe3O4纳米复合泡沫的高内相乳液(HIPE)模板方法,HIPE的配方对80%磁性复合泡沫的结构和力学性能的影响研究了名义孔隙率。仅用纳米颗粒稳定的HIPEs导致整体样品明显收缩,其特征是具有开放的细胞形态,空腔大于265微米。纳米颗粒位于本体中并且在聚合物泡沫骨架的表面上。在这种情况下,无法获得对特征尺寸的精确控制。相反,与表面活性剂共稳定的HIPE制剂可产生具有良好浇铸质量的样品,其特征是在所有情况下均具有完全开放的细胞形态。空腔和窗口尺寸可以通过乳液中表面活性剂的量来控制。相对于单体而言,表面活性剂的负载量低至1.5 v%,与直径为4 urn的窗口相互连接的腔体直径约为20 nm,而表面活性剂10 v%则导致腔体更小(10μm)和窗口(2纳米)。所有这些特征尺寸几乎不受纳米粒子负载的影响,纳米负载在1至30 wt%之间变化。表面活性剂稳定和固化的HIPEs主要在腔体表面形成纳米颗粒。通过应力-应变测试评估了复合泡沫的机械性能,结果表明,加入纳米颗粒后,用10 v%表面活性剂制备的泡沫增强了。增强的指示是杨氏模量从无纳米颗粒的样品的13±2 MPa增加到含15 wt%纳米颗粒的复合泡沫的104±4 MPa。这种趋势伴随着断裂伸长率从21±4降低到小于1%。用1.5 v%表面活性剂制备的样品具有延展性,并且与纳米颗粒负载无关,具有相同的高杨氏模量(104±9 MPa),并且随着纳米颗粒量的增加,在断裂伸长率达到3.4±0.4 MPa时,其强度会提高。 13±4%。

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