聚丙烯共混表面改性剂的研究

由不同链长的甲基丙烯酸长链醇酯。少量改性剂与聚丙烯共混，能大幅增加聚丙烯表面润湿性与粘接性，而拉伸强度与熔点却变化不大。通过ＥＳＣＡ与接触角分析，发现极性基团大表面富集，添加不同改性剂使材料表面富集的极性基浓度与粘接强度产生差异。     

Adhesive properties of polypropylene (PP) and polyethylene terephthalate (PET) film surfaces treated by DC glow discharge plasma

In this study, the adhesive properties of the plasma modified polypropylene (PP) and polyethylene terephthalate (PET) film surfaces have been investigated. Hydrophilicity of these polymer film surfaces was studied by contact angle measurements. The surface energy of the polymer films was calculated from contact angle data using Fowkes method. The chemical composition of the polymer films was analyzed by X-ray photoelectron spectroscopy (XPS). Atomic force microscopy (AFM) was used to study the changes in surface feature of the polymer surfaces due to plasma treatment. The adhesion strength of the plasma modified film was studied by T-peel strength test. The results showed a considerable improvement in surface wettability even for short exposure times. The AFM and XPS analyses showed changes in surface topography and formation of polar groups on the plasma modified PP and PET surfaces. These changes enhanced the adhesive properties of polymer film surfaces.     

Photoinduced hydrophobic surface of graphene oxide thin films

Graphene oxide (GO) thin films were deposited on transparent conducting oxide substrates and glass slides by spin coating method at room temperature. The wettability of GO thin films before and after ultraviolet (UV) irradiation was characterized with water contact angles, which increased from 27.3° to 57.6° after 3 h of irradiation, indicating a photo-induced hydrophobic surface. The UV-vis absorption spectra, Raman spectroscopy, X-ray photoelectron spectroscopy, and conductivity measurements of GO films before and after UV irradiation were taken to study the mechanism of photoinduced hydrophobic surface of GO thin films. It is demonstrated that the photoinduced hydrophobic surface is ascribed to the elimination of oxygen-containing functional groups on GO molecules. This work provides a simple strategy to control the wettability properties of GO thin films by UV irradiation.     

Polymer films with surfaces unmodified and modified by non-thermal plasma as new substrates for cell adhesion

The surface properties of biomaterials, such as wettability, polar group distribution, and topography, play important roles in the behavior of cell adhesion and proliferation. Gaseous plasma discharges are among the most common means to modify the surface of a polymer without affecting its properties. Herein, we describe the surface modification of poly(styrene) (PS) and poly(methyl methacrylate) (PMMA) films using atmospheric pressure plasma processing through exposure to a dielectric barrier discharge (DBD). After treatment the film surface showed significant changes from hydrophobic to hydrophilic as the water contact angle decreasing from 95° to 37°. All plasma-treated films developed more hydrophilic surfaces compared to untreated films, although the reasons for the change in the surface properties of PS and PMMA differed, that is, the PS showed chemical changes and in the case of PMMA they were topographical. Excellent adhesion and cell proliferation were observed in all films. In vitro studies employing flow cytometry showed that the proliferation of L929 cells was higher in the film formed by a 1:1 mixture of PS/PMMA, which is consistent with the results of a previous study. These findings suggest better adhesion of L929 onto the 1:1 PS/PMMA modified film, indicating that this system is a new candidate biomaterial for tissue engineering.     

Electric properties and surface characterization of transparent Al-doped ZnO thin films prepared by pulsed laser deposition

We grew 2 wt.% Al-doped ZnO (AZO) films on 5.08 cm-diameter polymer substrates at room temperature by the pulsed laser deposition (PLD) technique added the beam-rastering function. The structural properties, surface morphology, resistivity, mobility and chemical bonding states of AZO/polymer films were measured. The structuring of polymer surface by atmospheric plasma can occur at nm scales and can influence adhesion, optical and wettability properties of the materials. With increasing plasma treatment power, surface hydrophilicity and roughness for PET and PES polymer increased, respectively.     

Surface modification of polymers by ion-assisted reaction

This paper deals with a new surface modification technique of polymers, the so-called ion-assisted reaction (IAR) to improve the surface properties of polymers and provides outstanding experimental results regarding wettability and adhesion of various polymers. In the IAR, polymer surfaces were subjected to low energy ion irradiation at different dosage in reactive gas environment. Dramatic improvements in wettability and surface energy are observed for the IAR-treated polymer surfaces and can be explained by the addition of functional groups, responsible for the increase of polar component in surface energy. The formation of functional groups results from the interaction among ion, reactive gas and polymer chain involved in IAR treatment, depending on the reactive ion species, the flow rate of the reactive gas and the irradiating ion fluence. The improvement in adhesion between the IAR-treated polymers and coating materials was explained in terms of the increased surface energy as well as surface roughness in the polymers modified by the IAR and possible adhesion enhancement mechanism is to be discussed.     

Improvement of ternary recycled polymer blend reinforced with date palm fibre

This paper investigates the study and preparation of date palm fibre reinforced recycled polymer blend composites. This is the first paper which describes the recycled polymer ternary blends of (1) recycled low density polyethylene (RLDPE), (2) recycled high density polyethylene (RHDPE) and (3) recycled polypropylene (RPP). The date palm fibre reinforced composites (C_D00) were prepared by maintaining constant weight% of fibre of 20 wt% without any fibre treatment. Maleic anhydride (MA) was used as the compatabilizer (1 and 2 wt%) and the effect of compatabilizer on the blend matrix composites was studied. The mechanical, thermal, morphological properties, water absorption and chemical resistance properties were evaluated for these composites and also studied for pure blend matrix (C₀₀). Date palm fibre improved the tensile strength and hardness of recycled polymer blend matrix. Further improvement was achieved with 1% MA (C_D1), which showed that 1% MA treated composites (C_D1) had higher tensile strength, modulus and hardness properties. Thermal stability and water absorption were improved by 1% MA. These improvements were demonstrated at the nanoscale level by the decrease in roughness appearing in Atomic Force Spectroscopic Microscopy analysis indicating that flow is better under this concentration. The SEM analysis also showed that the fibre matrix adhesion improved by adding 1 wt% (C_D1) of MA. The melting and crystallisation temperatures of the blends did not change with the addition of date palm fibre and MA, indicating that the additives did not influence the melting and crystallisation properties of the composites. The chemical resistance test results showed that these composites are resistance to all chemicals but more weight gain observed in solvents. 2 wt% of MA (C_D2) caused poor adhesion between the polymer chains and fibres as well as polymer chain scission.     

Flow behavior in surface-modified microchannels with polymer nanosheets

The paper describes water flow behavior in surface-modified microchannels. We prepared straight-type microchannels which had rectangular cross sections with four different combinations of microchannel surface wettability; cleaned glass substrates served as hydrophilic microchannel walls and the microchannel walls coated with polymer Langmuir–Blodgett (LB) films were used as hydrophobic surfaces. The polymer LB films were successfully transferred onto glass substrates by vertical dipping method. The flow rates and the water meniscus shape strongly depended on the microchannel surface wettability. The decrease in flow rate with the increasing number of hydrophobic (polymer LB film) surface was attributed to the higher adhesion energy of hydrophobic surface. The Reynolds number was also characterized to be in the order of 10^− 1, implying a specific feature of microchannel; laminar flow.     

An effective surface modification of carbon fiber for improving the interfacial adhesion of polypropylene composites

A simple and effective modification for carbon fiber (CF) was presented in our work. CF was coated with ethylene–methyl acrylate–glycidyl methacrylate (E–MA–GMA) terpolymer through solution dipping. A uniform layer of 2.0 wt.% E–MA–GMA was confirmed on CF by IR, TGA and SEM. XPS showed that surface oxygen-containing functional groups were obviously increased after modification, which were advantageous to promote the reactivity of CFs. The treatment turned out to be helpful in enhancing the interfacial adhesion by micro-droplet experiment and the interfacial shear strength was 157% higher. The physical properties of PP/mCF composites were improved by static and dynamic mechanical analysis and the improvement was more noteworthy when maleic anhydride grafted PP (MAPP) was added to the matrix, which was consistent with the fracture morphology. The ultimate flexural strength, impact energy and tensile strength were increased by 139.3%, 233.9% and 126.1%. Besides, the mechanical performance of PP composites with 0–30 wt.% CFs were all significantly enhanced by CF surface treatment in combination with MAPP modification. We believed that the excellent performance was not caused by fiber length or crystallinity, it was mainly due to the superior interfacial interaction by intermolecular chain entanglement, as well as chemical reaction between E–MA–GMA and MAPP.     

The influence of the additives composition and concentration on the properties of SnOx thin films used in photocatalysis

The aim of this study is to investigate the influence of different organic additives on the surface properties of SnO_x thin films used for photocatalytic degradation of methylene blue. The films were obtained by anodic oxidation of tin substrate in electrolyte solutions containing green additives based on hydrophobic and hydrophilic maleic anhydride copolymers. The hydrophobic copolymer leads to the formation of thin films with increased specific area which generates a larger interfacial area between the layers and the dye solution. The consequence is an improvement in the photocatalytic efficiency: up to 16% compared to less than 5% for samples electrodeposited without polymer. The hydrophilic copolymer presence in the electrolyte solution leads to higher grain size and lower surface energy which significantly reduce the photocatalytic properties of the layers. The use of copolymers can be a tool for enhancing the surface roughness and film's wettability and thus the photodegradation efficiency.     

Effects of CO2 laser irradiation on the wettability and human skin fibroblast cell response of magnesia partially stabilised zirconia

Human skin fibroblast cells in vitro responses on the surface of a bioinert zirconia ceramic partially stabilised with magnesia partially stabilised zirconia (MgO-PSZ) bioinert ceramic before and after CO₂ laser treatment were investigated to find the interrelationship between the cell adhesion, wettability and laser parameters. Contact angle, θ, measurements of a set of test liquids were a clear indication that surface treatment of the MgO-PSZ with a CO₂ laser brought about a reduction in θ, indicating that the wettability of the MgO-PSZ had been enhanced. A relationship was found between the wettability and the microstructure of the MgO-PSZ surface and laser processing parameters. It was subsequently deduced that the factors active in causing the observed modification in the wettability of the MgO-PSZ were the increases in the surface O₂ content and the polar component of the surface energy, γ_sv^p, the latter resulting from surface melting and resolidification. Moreover, the investigation into the human skin fibroblast cell response revealed that the CO₂ laser treatment of the MgO-PSZ had resulted in a surface favourable for cell adhesion, as the extent of cell attachment and adhesion on the MgO-PSZ surface was enhanced depending on laser parameters. Such an improvement in cell adhesion, which could be greatly beneficial to developing enhanced bonding at the tissue and implant interface, was influenced by the surface properties of the modified MgO-PSZ, particular wettability.     

类金刚石薄膜的表面性能研究

利用微波-ECR等离子体源全方位离子注入设备,采用PSII与PSII+PECVD工艺在医用316L不锈钢上制备碳改性薄膜.Raman光谱分析表明,薄膜为典型的类金刚石(DLC) 薄膜.静态接触角测量技术研究表明:在酸碱溶液中,DLC薄膜表面价键遭到破坏,稳定性降低.不同工艺制备的DLC薄膜表面能在40mN/m左右,极性分量大于色散分量,呈现出疏水性质.DLC薄膜表面能高低取决于表面碳碳键与粗糙度的变化.     

Surface properties of aromatic polymer film during thermal treatment

Aromatic polyimide films are processed from polyamic acid solutions. This process involved the simultaneous loss of solvent and chemical conversion of polyamic acid to polyimide, and implied structural reorganization which led to changed physical properties. Polymer films generated from benzophenonetetracarboxylic dianhydride and 4,4′-diamino-3,3′-dimethyl diphenylmethane have been investigated at different stages of thermal treatment. The surface polarity, which was determined by the presence of polar COOH and CONH groups, changed during polyamic acid thermal treatment. These polar groups were removed step by step by imidization process leading to the modification of the physical properties of the polymer film.     

Polycarbonate surface cell's adhesion examination after Nd:YAG laser irradiation

Nd:YAG laser treatment was used in order to increase surface cell adhesion aspects of polycarbonate (PC) films prepared via melt process. The treatment was carried out under different wavelengths and beam diameters. ATR-FTIR and UV spectra obtained from different samples before and after laser treatment in air showed that laser irradiation has induced some chemical and physical changes in surface properties. The irradiated films were also characterized using scanning electron microscopy (SEM) and contact angle measurements. Effect of pulse numbers on the surface properties was also investigated. Cell culture test was used to evaluate cell adhesion property on the PC films before and after treatment. The results obtained from this test showed that after laser treatment, the cells were attached and proliferated extensively on the Nd:YAG laser treated films in comparison with the unmodified PC. Moreover, it was revealed that a decrease in the laser beam diameter and an increase in the irradiated pulse numbers increased surface wettability and caused a better cell attachment on the polymer surface.The obtained results also showed that a decrease in the laser beam diameter and an increase in the irradiated pulse numbers increased surface wettability and caused a better cell attachment on the polymer surface.     

Anti-fouling properties of polylactic acid film modified by pegylated phosphorylcholine derivatives

Anti-fouling properties are important for both pharmaceutical and biomedical applications of polylactic acid (PLA). In this study, highly hydrated hydrophilic bilayers containing phosphatidylcholine (PC) and polyethylene glycol (PEG) were applied to PLA films to prevent the protein adsorption and blood platelet adhesion. The PLA films were coated with three PLA copolymers of PC and PEG, namely, a PLA-b-PEG block copolymer with a PC group on the end of a PEG chain (PC-PEG-PLA), a poly[2-methacryloyloxyethyl phosphatidylcholine (MPC)]-PLA graft copolymer (PMPC-g-PLA), and a PMPC-PLA graft copolymer with PEG serving as a spacer (PMPC-g-(PEG-b-PLA)). The influence of the copolymer structure on the anti-fouling properties of PLA film was then investigated. The results showed that the introduction of PC and PEG polar copolymers decreased the water-contact angle (WCA) and increased the equilibrated degree of hydration (H_eq) of the PLA surface significantly. The PMPC-g-(PEG-b-PLA) copolymer achieved the lowest WCA value and the highest H_eq value as it provided a higher density of PC on the outer surface. In addition, the strong hydration of the PEG and PC groups efficiently suppressed the bovine serum albumin (BSA) and fibrinogen (Fg) adsorption and subsequently inhibited platelet adhesion. The above results demonstrated that a good “anti-fouling” surface layer on the PLA substrate could be achieved by a combination of PEG and PC in copolymers.     

Preparation,surface properties,and MC3T3-E1 cell response of mesoporous hydroxyapatite thin films

Mesoporous hydroxyapatite (meso-HA) thin films were fabricated by a sol–gel method using cetyltrimethyl ammonium bromide as the template. The phase, surface morphology, and mesoporous structure of the meso-HA films were characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The uniform thin films consisted of meso-HA spherical particles with different pore size (2.0 or 3.1 nm) were prepared on the glass substrate at different pH value (pH 3.0 or 7.0). The introduction of mesopores would enhance the surface area of HA. Water contact angle was also measured on the non-mesoporous and meso-HA thin films, revealing the promotion of surface wettability in the mesoporous ones. In vitro cytocompatibility of HA films were evaluated by cell adhesion and proliferation tests using MC3T3-E1 cells. After 3 days of culture on the samples, the cells spread in an elongated shape and were well adhered to the surface of the meso-HA films. Moreover, the cells proliferation on the meso-HA films was higher than that on the non-mesoporous films. There are significant differences in the cell density between the control group and the meso-HA films with the pores sized in 2.0 nm after being cultured for 2 and 3 days (P < 0.05). The results suggested that the presence of mesopores could influence the surface and biological properties of HA films, and the mesoporous structure would enhance the cell response of HA.     

含氟嵌段共聚物蜂窝状多孔膜制备与表征

采用原子转移自由基聚合(ATRP)方法,合成聚苯乙烯(PS)大分子引发剂,再引发甲基丙烯酸十二氟庚酯制备嵌段共聚物(PS-b-PDFHMA)。将嵌段共聚物与纳米二氧化钛(TiO_2)复合,利用静态呼吸图法制备抑菌性多孔膜。通过傅里叶变换红外光谱、核磁共振氢谱、凝胶渗透色谱等对嵌段共聚物结构、组成及相对分子质量进行分析和表征;利用扫描电子显微镜对多孔膜表面形貌和膜层结构进行观察;利用接触角测试仪和微生物粘附实验研究多孔膜表面润湿性及对微生物粘附的影响。结果表明,以水滴为模板的多孔膜相较于不含孔薄膜疏水性有一定改善,但细菌粘附量提高,与TiO_2复合后,多孔膜表面粗糙度上升,水接触角可达136°,其表面细菌粘附量明显下降。     

低温等离子体碳纤维表面处理技术研究

采用低温等离子体法对碳纤维表面进行处理,并通过滴水试验、SEM、XPS测试处理效果。与阳极氧化法相比,低温等离子体法能更有效地改变碳纤维的表面性质。滴水试验表明经等离子体处理的碳纤维表面呈极性,与水的润湿性好;SEM测试结果表明,低温等离子体法处理的碳纤维表面沟槽比阳极氧化法的更多,前者表现出更强的表面修饰性;XPS测试结果表明,经等离子体和阳极氧化法处理后的碳纤维表面均含有羧基、羟基、羰基,低温等离子体处理后的碳纤维表面的极性官能团总含量为17%。     

The mechanism of adhesion and printability of plasma processed PET films

Of the several techniques available for the surface modification, plasma processing has proved to be very appropriate. The low temperature plasma is a soft radiation source and it affects the material only over a few hundred Å deep, the bulk properties remaining unaffected. Plasma surface treatment also offers the advantage of greater chemical flexibility. PET films are widely used for packaging and electrical insulation. The studies of adhesion and printability properties are important. In the present study PET films are treated in air plasma for different time of treatment. The improvement in adhesion is studied by measuring T-peel and Lap shear strength. In addition, printability of plasma treated PET films is studied by cross test method. It has been found that printability increases considerably for plasma treatment of short duration. Therefore it is interesting to study the surface composition and morphology by contact angle measurement, ESCA and AFM. Surface energy and surface roughness can be directly correlated to the improvement in above-mentioned surface related properties. It has been found that the surface oxidation occurs containing polar functional groups such as C-O, COO. A correlation of all such observations from different techniques gives a comprehensive picture of the structure and surface composition of plasma treated PET films.     

Preparation of the HIPS/MA graft copolymer and its compatibilization in PA6/HIPS blends

The graft copolymer of high impact polystyrene (HIPS) grafted with malice anhydride (MA) (HIPS-g-MA) was prepared with melt mixing in the presence of a free-radical initiator. The grafting reaction was confirmed by IR analyses and the amount of MA grafted on HIPS was evaluated by a titration method. 1–5 wt% of MA can be grafted on HIPS. HIPS-g-MA is miscible with HIPS. Its anhydride group can react with the PA6 during melt mixing the two components. The compatibility of HIPS-g-MA in the HIPS/PA6 blends was evident. Evidence of reactions in the blends was confirmed in the morphology and mechanical properties of the blends. A significant reduction in domain size was observed because of the compatibilization of HIPS-g-MA in the blends of HIPS and PA6. The tensile mechanical properties of the prepared blends were investigated and the fracture surfaces of the blends were examined by means of the scanning electron microscope (SEM). The improved adhesion in a 16%HIPS/75%PA6 blend with 9%HIPS-g-MA copolymer was detected. The morphology of fibrillar ligaments formed by PA6 connecting HIPS particles was observed.