对苯二甲酸乙二醇酯-ε-己内酯共聚酯中硬链段结晶特性研究

利用广角X射线衍射和傅里叶变换红外光谱研究了对苯二甲酸乙二醇酯-ε-己内酯(TCL)共聚酯中对苯二甲酸乙二醇酯(ET)硬链段的晶区结构和结晶特性。结果表明,在ET硬段含量较高的TCL共聚酯中,ET链段的结晶特性与纯的聚对苯二甲酸乙二醇酯(PET)基本相同。ET硬段晶区的尺寸和结晶度均随链段序列长度的减小而减小。     

FDLC薄膜的化学结构对光学性能的影响

研究氟化类金刚石（FDLC）薄膜化学结构对光学性能的影响，用等离子体增强化学气相沉积（PECVD）法在玻璃基底上沉积氟化类金刚石（FDLC）薄膜，用俄歇能谱、傅里叶红外光谱(FTIR)、紫外 可见光分光光度计 (UV-VIS)对薄膜进行分析。分析结果表明：沉积薄膜是典型的类金刚石结构，薄膜中氟主要以C-F2键存在；随着沉积温度的提高，C-F2含量先增后减；随着F含量的增加，FDLC薄膜的sp3含量减少，sp2含量增加；光学带隙与sp2键含量密切相关，sp2含量越大，薄膜的光学带隙越小。     

聚对苯二甲酸乙二酯表面等离子体改性

纤维表面等离子体改性在学术上、工艺上都是很有意义的工作,人们对此甚感兴趣[1,2].我们利用射频电容耦合辉光放电产生等离子体,用静电双探针测量等离子体的电子温度和离子密度,用热电偶测量气体温度.研究等离子体与聚对苯二甲酸乙二酿(PET)的作用,拍摄了等离子体与PET作用时的     

对苯二甲酸乙二醇酯降解机理密度泛函的理论研究

采用密度泛函理论方法B3P86/6-31++G(d, p),对对苯二甲酸乙二醇酯一聚体降解反应机理进行了理论研究.设计了对苯二甲酸乙二醇酯一聚体纯热解、水解和醇解、水或醇作为催化剂降解过程的各种可能反应路径,对参与反应的各种中间体、过渡态及产物进行了几何结构优化和频率计算以获得热力学与动力学参数值.计算结果表明：当水或甲醇作为对苯二甲酸乙二醇酯热降解过程中的催化剂时,利用水或甲醇O-H中H提供到对苯二甲酸乙二醇酯一聚体主链酯键中O原子上形成对苯二甲酸,而乙烷基脱掉的H原子与水中羟基(-OH)或醇中甲氧基(-OCH₃)结合形成新的水或者甲醇,从而降低对苯二甲酸乙二醇酯热解过程中的反应能垒(251.4 kJ/mol→181.1 kJ/mol(甲醇)和187.5 kJ/mol(水));当水或甲醇作为对苯二甲酸乙二醇酯热降解过程中的反应物参与反应时,利用水或甲醇O-H中H提供到对苯二甲酸乙二醇酯一聚体主链乙烷基旁O原子上形成乙二醇,而水中羟基(-OH)或醇中甲氧基(-OCH₃)结合对苯二甲酸乙二醇酯一聚体主链羰基中C原子上形成对苯二甲酸或对苯二甲酸单...     

具有分子取向的拉伸高聚物(PET)中~(13)C—NMR化学位移值的估算

本文从已知的聚对苯二甲酸乙二醇酯(PET)的X-射线原子坐标和化学位移张量主值出发,计算了拉伸的PET样品,相对于外磁场不同放置方位下的~(13)C-NMR谱峰的化学位移值,很好地解释了实验结果,并得到了拉伸条件下,高聚物中分于取向的信息。     

具有分子取向的拉伸高聚物(PET)中13C-NMR化学位移值的估算

本文从已知的聚对苯二甲酸乙二醇酯(PET)的X-射线原子坐标和化学位移张量主值出发,计算了拉伸的PET样品,相对于外磁场不同放置方位下的¹³C-NMR谱峰的化学位移值,很好地解释了实验结果,并得到了拉伸条件下,高聚物中分于取向的信息。     

含氮氟化类金刚石(FN-DLC)薄膜的研究:(Ⅰ)sp结构与化学键分析

以CF4,CH4和N2为源气体,利用射频等离子体增强化学气相沉积法,在不同功率下制备了含氮氟化类金刚石膜.用俄歇电子能谱、拉曼光谱、X射线光电子能谱和傅里叶变换红外光谱对薄膜的电子结构和化学键进行了表征,并结合高斯分峰拟合方法分析了薄膜中sp2,sp3结构比率.结果表明,制备的薄膜属于类金刚石结构,不同沉积功率下,薄膜内的sp2/sp3值在2.0—9.0之间,随着沉积功率的增加薄膜内sp2的相对含量增加.膜内主要有C—Fx(x=1,2),C—C,CC和CN等化学键.沉积功率增加,C—C基团增加,膜内F的浓度降低,C—F基团减少,薄膜的关联加强,稳定性提高.     

多腔耦合微波表面波PECVD法沉积 DLC薄膜研究

报道了利用多腔耦合微波表面波等离子体增强化学气相沉积(PECVD)的方法制备类金刚石(DLC)薄膜。通过发射光谱(OES)测量,对Ar等离子体中的各种放电参数以及全部四个腔室内放电的均匀性作出评估。采用表面轮廓仪测量了薄膜的厚度;薄膜的表面形貌、组成结构通过原子力显微镜(AFM)、激光拉曼光谱和X射线衍射光谱(XPS)进行了表征。在12.5μm厚度的有机薄膜聚酯(PET)表面沉积一定厚度DLC后,通过测量水蒸气透过率(WVTR)对DLC薄膜的阻隔性能进行了研究。结果表明,这种多腔耦合微波表面波等离子体装置,不仅能够实现四个腔室同时相对均匀的放电,也能够实现单个腔室的轴向均匀放电。制备的DLC薄膜结构致密、成分均匀,可以使PET薄膜阻隔性能提高约20倍。     

多腔耦合微波表面波PECVD法沉积DLC薄膜研究

报道了利用多腔耦合微波表面波等离子体增强化学气相沉积(PECVD)的方法制备类金刚石(DLC)薄膜。通过发射光谱(OES)测量,对Ar等离子体中的各种放电参数以及全部四个腔室内放电的均匀性作出评估。采用表面轮廓仪测量了薄膜的厚度;薄膜的表面形貌、组成结构通过原子力显微镜(AFM)、激光拉曼光谱和X射线衍射光谱(XPS)进行了表征。在12.5μm厚度的有机薄膜聚酯(PET)表面沉积一定厚度DLC后,通过测量水蒸气透过率(WVTR)对DLC薄膜的阻隔性能进行了研究。结果表明,这种多腔耦合微波表面波等离子体装置,不仅能够实现四个腔室同时相对均匀的放电,也能够实现单个腔室的轴向均匀放电。制备的DLC薄膜结构致密、成分均匀,可以使PET薄膜阻隔性能提高约20倍。     

紫外光辐射法表面接枝改性PET膜

用二苯甲酮(BP)做光引发剂,聚对苯二甲酸乙二醇酯(PET)薄膜用丙烯酸进行紫外光照表面接枝改性。丙烯酸接枝率随光照时间、单体浓度增加而增加,并随引发剂浓度的变化而变化.光照时间为1h,引发剂的浓度为5×10-3mol/L,丙烯酸浓度为6%(wt%)时,接枝效果最好.通过接枝反应,羧基(—COOH)被引入到PET膜表面,提高了PET膜的亲水性和碱性染料的可染性。     

阻隔材料的气体渗透率

对气体渗透阻隔材料的渗透率与气体温度、气体压强的关系进行了理论分析,得到了在不同温度和气体压强条件下渗透率的加速因子的计算式,理论计算结果与相关文献中实验测量结果比较一致。根据加速条件下进行的水蒸气、氧气和二氧化碳对聚对苯二甲酸（PET）和环氧树脂渗透率测量的结果,计算得到在常温常压条件下这些气体对0.155 mm厚PET塑料的渗透率和对0.065 mm厚环氧树脂的渗透率。     

氢的强化刻蚀对金刚石薄膜品质的影响与sp2杂化碳原子的存在形态

用化学气相沉积方法制备了金刚石薄膜.在制备过程中，通过间歇式关闭甲烷气体，强化了氢对sp2杂化碳原子的刻蚀.用拉曼光谱和金相显微镜对薄膜进行了分析表征.结果表明，氢对sp2杂化碳原子的强化刻蚀并未影响金刚石薄膜的品质和微观结构.这一结论说明，在金刚石薄膜中，sp2杂化碳原子主要存在于金刚石晶粒表面和晶界碳原子之间,而不是以石墨或无定形碳颗粒为主要存在方式. 关键词： 化学气相沉积 金刚石薄膜 拉曼光谱 强化刻蚀     

The influence of the structures and compounds of DLC coatings on the barrier properties of PET bottles

To reduce the oxygen transmission rate through a polyethylene terephthalate (PET) bottle (an organic plastic) diamond-like carbon (DLC) coatings on the inner surface of the PET bottle were deposited by radio frequency plasma-enhanced chemical vapour deposition (RF-PECVD) technology with C₂H₂ as the source of carbon and Ar as the diluted gas. As the barrier layer to humidity and gas permeation, this paper analyses the DLC film structure, composition, morphology and barrier properties by Fourier transform infrared, atomic force microscopy, scanning electron microscopy and oxygen transmission rate in detail. From the spectrum, it is found that the DLC film mainly consists of sp³ bonds. The barrier property of the films is significantly relevant to the sp³ bond concentration in the coating, the film thickness and morphology. Additionally, it is found that DLC film deposited in an inductively coupled plasma enhanced capacitively coupled plasma source shows a compact, homogeneous and crack-free surface, which is beneficial for a good gas barrier property in PET bottles.     

Effects of the ion-beam voltage on the properties of the diamond-like carbon thin film prepared by ion-beam sputtering deposition

Diamond-like carbon(DLC) thin film is one of the most widely used optical thin films.The fraction of chemical bondings has a great influence on the properties of the DLC film.In this work,DLC thin films are prepared by ion-beam sputtering deposition in Ar and CH4 mixtures with graphite as the target.The influences of the ion-beam voltage on the surface morphology,chemical structure,mechanical and infrared optical properties of the DLC films are investigated by atomic force microscopy(AFM),Raman spectroscopy,nanoindentation,and Fourier transform infrared(FTIR) spectroscopy,respectively.The results show that the surface of the film is uniform and smooth.The film contains sp2 and sp3hybridized carbon bondings.The film prepared by lower ion beam voltage has a higher sp3 bonding content.It is found that the hardness of DLC films increases with reducing ion-beam voltage,which can be attributed to an increase in the fraction of sp3 carbon bondings in the DLC film.The optical constants can be obtained by the whole infrared optical spectrum fitting with the transmittance spectrum.The refractive index increases with the decrease of the ion-beam voltage,while the extinction coefficient decreases.     

Microstructure and tribological performance of self-lubricating diamond/tetrahedral amorphous carbon composite film

In order to smooth the rough surface and further improve the wear-resistance of coarse chemical vapor deposition diamond films, diamond/tetrahedral amorphous carbon composite films were synthesized by a two-step preparation technique including hot-filament chemical vapor deposition for polycrystalline diamond (PCD) and subsequent filtered cathodic vacuum arc growth for tetrahedral amorphous carbon (ta-C). The microstructure and tribological performance of the composite films were investigated by means of various characterization techniques. The results indicated that the composite films consisted of a thick well-grained diamond base layer with a thickness up to 150 μm and a thin covering ta-C layer with a thickness of about 0.3 μm, and sp³-C fraction up to 73.93%. Deposition of a smooth ta-C film on coarse polycrystalline diamond films was proved to be an effective tool to lower the surface roughness of the polycrystalline diamond film. The wear-resistance of the diamond film was also enhanced by the self-lubricating effect of the covering ta-C film due to graphitic phase transformation. Under dry pin-on-disk wear test against Si₃N₄ ball, the friction coefficients of the composite films were much lower than that of the single PCD film. An extremely low friction coefficient (∼0.05) was achieved for the PCD/ta-C composite film. Moreover, the addition of Ti interlayer between the ta-C and the PCD layers can further reduce the surface roughness of the composite film. The main wear mechanism of the composite films was abrasive wear.     

MOCVD growth, structure and magnetic properties of Fe films grown on GaAs (001) substrates

Thin iron films have been grown on (001) GaAs substrates by low pressure metal organic chemical vapor deposition (LP-MOCVD) at different temperatures with the pressure of 150 Torr. X-ray diffraction (XRD) analysis showed that all films have only one strong diffraction peak (110). The surface of Fe film became smooth with increasing the growth temperature. Magnetization measurements showed that the Fe films grown at different temperatures were ferromagnetic with easy axis parallel to the film surface and hard axis perpendicular to the substrates. The field dependence of magnetization along two axes showed a remarkable difference, implying that the samples have strong magnetic anisotropy. Furthermore, when the applied magnetic field is perpendicular to the Fe surface, a sharp jump in the hysteresis loop could be observed, followed by a broad shoulder, which is related to the interface effect, the existence of carbon and the formation of 180^°/90^° magnetic domains.     

Structure and gas-barrier properties of amorphous hydrogenated carbon films deposited on inner walls of cylindrical polyethylene terephthalate by plasma-enhanced chemical vapor deposition

The influence of radio-frequency (RF) power on the structure and gas permeation through amorphous hydrogenated carbon films deposited on cylindrical polyethylene terephthalate (PET) samples is investigated. The results show that a higher radio-frequency power leads to a smaller sp³/sp² value but produces fewer defects with smaller size. The permeability of PET samples decreases significantly after a-C:H deposition and the RF only exerts a small influence. However, the coating uniformity, color, and wettability of the surface are affected by the RF power. A higher RF power results in to better uniformity and it may be attributed to the combination of the high-density plasma and sample heating.     

Water vapor-induced structure modification of vertically-aligned carbon nanotube arrays and successive thin film coating for enhanced field emission properties

Vertically-aligned carbon nanotubes (VCNTs) are used as electron source in various field emission applications owing to its high aspect ratio, chemical inertness, mechanical strength and electrical conductivity. Here, we demonstrate that surface structure modification along with thin film coating enhances the field emission performance, such as turn-on voltage, emission site density, and stability. In the present study, VCNTs with different heights were grown on silicon wafers by thermal chemical vapor deposition followed by the structure modification of VCNTs using capillarity-driven water vapor condensation. We obtained various surface morphologies by varying the water vapor exposure time and heating temperature. In addition, the structure-modified VCNTs surfaces were coated with W and SiO₂ thin films using electron-beam evaporation. It was observed that W-coated VCNTs with modified surface morphology results in the best field emission performance.     

Properties of low-refractive-index films obtained by the close-spaced vapor transport technique under the sublimation of graphite in a quasi-closed volume

The properties of low-refractive-index carbon films obtained by close-spaced vapor transport at graphite sublimation are studied. The optical properties of the films are investigated by monochromatic multiple-angle ellipsometry, and their morphology is examined by AFM. It is found that the films have a columnar structure with a background surface roughness of about 1 nm. In addition, the surface of the film contains islands up to 50 nm in height with a footprint of ≈200 nm. A low-refractive-index carbon film deposited by close-spaced vapor transport on silicon tips is found to decrease the field emission threshold and drastically raise the current.     

Surface characteristics of Ni catalystic films on growth behavior of multi-walled carbon nanotubes

The effect of the surface characteristics of Ni catalyst films on the growth behavior of multi-walled carbon nanotubes (MWCNTs) were investigated using Ni catalyst films prepared by different physical vapor deposition methods, electron-beam evaporation and sputtering. The growth behavior of MWCNTs was dependent upon the surface roughness of the Ni films. After a pretreatment process with NH₃, the root mean squares of surface roughness of e-beam evaporated and sputtered Ni catalyst films increased to 16.6 and 3.2 nm, respectively. Curled-MWCNTs and carbon-encapsulated Ni nanoparticles were formed on the Ni film deposited by e-beam evaporation while vertically aligned-MWCNTs were grown on the sputter-deposited film. In addition, the surface roughness of the Ni films affected the field emission properties of the MWCNTs. This was considered to originate from the specific growth behavior of the MWCNTs which was primarily caused by the initial surface roughness of the Ni films.