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首页> 外文期刊>The Korean journal of chemical engineering >Chemical structure and surface morphology of plasma polymerized-allylamine film
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Chemical structure and surface morphology of plasma polymerized-allylamine film

机译:等离子体聚合烯丙胺薄膜的化学结构和表面形态

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In this study, we conducted the plasma polymerization of allylamine using radio frequency (RF) glow discharge with continuous wave (CW) in order to make an organic thin film with an amine functional group retained. Allylamine as a monomer was deposited on a glass in a bell-jar type plasma reactor and polymerized to plasma-polymerized allylamine (PPAa). The parameter to control the property of plasma polymer was input power at other conditions remaining constant. The chemical structure and the surface morphology of plasma-polymerized allylamine (PPAa) film were characterized by contact angle measurement, Attenuated Total Reflection Fourier Transform Infrared (ATR-FTIR), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscopy (SEM). The property of PPAa film was highly dependent upon the plasma input power. The input power, which determines the plasma density, results in a property of PPAa thin film such as hydrophilicity, high retention of functionality of PPAa's surface. Surface energy calculated by contact angle measurement indicated that increasing input power (from 30 W to 90 W) decreased the hydrophilic property of PPAa due to loss of amine functional group and high cross-linking. The increase of the energy causes the films to be harder. ATR-FTIR and XPS results showed that high input energy fragmented the amine group from monomer with increasing nitrogen atomic content and nitrile group. The high retention of amine groups seems mainly favored by low input power ( < 30 W). From thickness measurement using α-stepper, the deposition rates were 0.43, 0.83, 1.11, 1.37 nm/s at 30, 50, 70, 90 W, respectively. The change of surface morphology of plasma-polymerized thin films was investigated after soaking the PPAa film into ethanol. Due to weak adhesion with substrate and internal stress in plasma polymer film, the surface morphology of PPAa film revealed some irregular network pattern.
机译:在这项研究中,我们使用具有连续波(CW)的射频(RF)辉光放电进行烯丙基胺的等离子体聚合,以制得保留有胺官能团的有机薄膜。在钟罩式等离子体反应器中将烯丙胺作为单体沉积在玻璃上,并聚合成等离子体聚合的烯丙胺(PPAa)。控制等离子体聚合物性能的参数是在其他条件下保持恒定的输入功率。通过接触角测量,衰减全反射傅立叶变换红外(ATR-FTIR),X射线光电子能谱(XPS),扫描电子显微镜(SEM)表征了等离子聚合烯丙胺(PPAa)膜的化学结构和表面形态。 。 PPAa膜的性能高度依赖于等离子体输入功率。确定等离子体密度的输入功率会导致PPAa薄膜的特性,例如亲水性,PPAa表面功能的高度保留。通过接触角测量计算的表面能表明,由于胺官能团的丧失和高交联性,输入功率的增加(从30 W到90 W)降低了PPAa的亲水性。能量的增加导致膜变硬。 ATR-FTIR和XPS结果表明,随着氮原子含量和腈基含量的增加,高输入能量将胺基团与单体分开。胺基团的高保留似乎主要是由于低输入功率(<30 W)所致。从使用α-步进器的厚度测量,在30、50、70、90 W下的沉积速率分别为0.43、0.83、1.11、1.37 nm / s。将PPAa膜浸泡在乙醇中后,研究了等离子体聚合薄膜的表面形态变化。由于与基质的粘附力弱和等离子体聚合物薄膜的内应力,PPAa薄膜的表面形态显示出一些不规则的网状图案。

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