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Study on thermal, water barrier and mechanical properties of polyurethane clay nanocomposite prepared by solution intercalation method

机译:溶液插层法制备聚氨酯粘土纳米复合材料的热,阻水及力学性能研究

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摘要

In this thesis, a series of polyurethane (PU) nanocomposite was fabricated by using the solution intercalation polymerization by employing chloroform with the incorporation of nanoclay Cloisite B30. The interaction between the nanoclay Cloisite B30 and PU matrices is the major factor in determining the structure in the PU nanocomposite, which was aimed at achieving a good dispersion with slighter agglomerates. The thermal characterization was conducted through thermal conduction, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Thermal conductivity of the PU nanocomposite increased with increase in the nanoclay loading. The results show that there was significant effect of the nanoclay on lowering the melting temperature of the PU nanocomposite. Hence, the thermal degradation behaviour of PU increased by the incorporation of the nanoclay up to 16 oC for 96 % PU/4 % B30. The addition of the nanoclay results in the enhancement of the thermal stability. The morphology of PU nanocomposite was investigated using the field emission scanning emission microscopy (FESEM), scanning emission microscopy (SEM) and X-ray diffraction (XRD), while chemical structure analysis was analysed using Fourier transform infrared spectrometer (FTIR). FESEM micrographs demonstrated fewer agglomerates formed in the PU nanocomposite while an even distribution of nanoclay in SEM was obtained. The degree of crystallinity of PU nanocomposite was directly increased according to Cloisite B30 content, which shows that good intercalated structure has been attained. FTIR indicated that there was no chemical structure alteration in PU nanocomposite. The barrier properties of the PU nanocomposite films were studied through the water absorption and water permeability analysis. Water absorption analysis presented that the highest percentage of water absorption was in the 98% PU/2% B30 with 14.9 %. Meanwhile, the water permeability revealed an improvement through the increase in nanoclay loading due to the formation of the tortuosity of the transport path in the PU nanocomposite. The highest decrement in the water permeation rate amounting to 56 % for 3 bar and 68 % for 4 bars were obtained in 98% PU/2% B30 however for 2 bar, there was no volume of water penetrate through the sample. The tensile strength and elongation of the PU nanocomposite at break were improved by the incorporation of the nanoclay. The tensile stress for the pristine PU was valued at 0.40 MPa while the highest tensile stress at 0.93 MPa was observed for the sample with 96 % PU/4 % B30 film. Meanwhile, the percentage of the elongation at break of the sample is the maximum with 106 % for the sample with 96 % of PU/4 % of B30. The results exhibited that the tensile strength and elongation at break of the nanocomposites dramatically increased with the incorporation of the nanoclay. This improvement was dependent on the content of the nanoclay as well as the formation structure of the nanoclay in the PU matrices.
机译:本文采用氯仿与纳米粘土Cloisite B30的溶液插层聚合,制备了一系列聚氨酯(PU)纳米复合材料。纳米粘土Cloisite B30与PU基质之间的相互作用是决定PU纳米复合材料中结构的主要因素,其目的是使较小的附聚物达到良好的分散性。通过热传导,热重分析(TGA)和差示扫描量热法(DSC)进行热表征。 PU纳米复合材料的热导率随纳米粘土负载的增加而增加。结果表明,纳米粘土对降低PU纳米复合材料的熔融温度具有显著作用。因此,对于96%PU / 4%B30,通过掺入高达16 oC的纳米粘土,可以提高PU的热降解性能。纳米粘土的添加导致热稳定性的增强。使用场发射扫描发射显微镜(FESEM),扫描发射显微镜(SEM)和X射线衍射(XRD)研究了PU纳米复合材料的形态,同时使用傅立叶变换红外光谱仪(FTIR)分析了化学结构。 FESEM显微照片表明,在PU纳米复合材料中形成的团聚物较少,而在SEM中获得的纳米粘土分布均匀。 PU纳米复合材料的结晶度随Cloisite B30含量的增加而直接增加,表明已获得良好的插层结构。 FTIR表明PU纳米复合材料中没有化学结构改变。通过吸水率和透水性分析研究了PU纳米复合膜的阻隔性能。吸水率分析表明,吸水率最高的是98%PU / 2%B30和14.9%。同时,由于PU纳米复合材料中传输路径的曲折性的形成,水渗透性通过增加纳米粘土负载而显示出改善。在98%PU / 2%B30中,水渗透率的最高减量分别为3 bar的56%和4bar的68%,但是对于2 bar,则没有水透过样品。通过掺入纳米粘土可以改善PU纳米复合材料断裂时的拉伸强度和伸长率。原始PU的拉伸应力值为0.40 MPa,而带有96%PU / 4%B30膜的样品的最高拉伸应力为0.93 MPa。同时,对于具有96%的PU / 4%的B30的样品,样品的断裂伸长率百分比最大,为106%。结果表明,随着纳米粘土的掺入,纳米复合材料的拉伸强度和断裂伸长率显着增加。这种改善取决于PU基体中纳米粘土的含量以及纳米粘土的形成结构。

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    Norayuni Azizi;

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  • 年度 2016
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