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Controlled change of structure and properties of nanometer polymer layers deposited by electron beam polymerization from vapour phase

机译:通过电子束聚合从气相沉积的纳米聚合物层的结构和性能的控制变化

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Electron beam polymerization of monomers from vapour phase is advanced method of thin polymer layers (TPL) deposition on solid substrates. The structure features and properties of TPL formed from tetrafluoroethylene and methylmethacrylate vapour at different E-beam current densities were found to be different strongly. In 1-10 μA/cm2 field the low molecular mass PTFE films with tape and disk supramolecular structures formed. These films are low thermostable (to 250-300) because of sublimation under heating. Macromolecules in these films are regulated (mesomorphic state). The polymer chain axes are oriented perpendicularly toward substrate surface. In 102-103 μA/cm2 field the films with high thermostability (400-450) form. These films are probably crosslinked. In 104-106 μA/cm2 field the amorphous, strongly crosslinked, high thermostable, high uniform films form. Polymethylmethacrylate (PMIMA) films formed at 1-10 μA/cm2 rapidly dissolve in organic solvents. The PMMA films deposited at 102-103 μA/cm2 only swell in organic solvents. The observed differences of structure and properties of films deposited by E-VDP method are caused probably by different balance of chain polymerization and polyrecombination mechanisms in the film deposition processes. In highest current density range the polyrecombination mechanism predominates. In low current density the main mechanism of deposition is the radical-chain polymerization. The results obtained show great possibilities of controlled change of properties of E-VDP films deposited from the same precursor.
机译:来自气相的单体的电子束聚合是固体衬底上的薄聚合物层(TPL)沉积的先进方法。发现由四氟乙烯和甲基甲基丙烯酸甲酯蒸汽形成不同电子束电流密度的TPL的结构特征和性质被发现强烈。在1-10μA/ cm2场中,用胶带和盘上分光结构的低分子量PTFE膜。由于加热下的升华,这些薄膜是低温恒温(至250-300)。这些薄膜中的大分子是调节(中间形态)。聚合物链轴垂直朝向基底表面定向。在102-103μA/ cm2中,具有高热稳定性(400-450)形式的薄膜。这些薄膜可能交联。在104-106μA/ cm2场中,无定形,强烈交联,高温,高均匀的薄膜形式。在1-10μA/ cm 2下形成的聚甲基丙烯酸酯(PMIMA)膜在有机溶剂中迅速溶解。在102-103μA/ cm 2下沉积的PMMA膜仅在有机溶剂中膨胀。观察到通过E-VDP方法沉积的薄膜的结构和性质的差异可能是通过膜沉积方法中的链聚合和聚重组机制的不同平衡。在最高电流密度范围内,聚合物机构主要占主导地位。在低电流密度中,沉积的主要机理是自由基链聚合。得到的结果表明,由相同前体沉积的E-VDP膜的性能变化的极大可能性。

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