Influence of ethylene glycol pretreatment on effectiveness of atmospheric pressure plasma treatment of polyethylene fibers

For atmospheric pressure plasma treatments, the results of plasma treatments may be influenced by liquids adsorbed into the substrate. This paper studies the influence of ethylene glycol (EG) pretreatment on the effectiveness of atmospheric plasma jet (APPJ) treatment of ultrahigh molecular weight polyethylene (UHMWPE) fibers with 0.31% and 0.42% weight gain after soaked in EG/water solution with concentration of 0.15 and 0.3 mol/l for 24 h, respectively. Scanning electron microscopy (SEM) shows that the surface of fibers pretreated with EG/water solution does not have observable difference from that of the control group. The X-ray photoelectron spectroscopy (XPS) results show that the oxygen concentration on the surface of EG-pretreated fibers is increased less than the plasma directly treated fibers. The interfacial shear strength (IFSS) of plasma directly treated fibers to epoxy is increased almost 3 times compared with the control group while that of EG-pretreated fibers to epoxy does not change except for the fibers pretreated with lower EG concentration and longer plasma treatment time. EG pretreatment reduces the water contact angle of UHMWPE fibers. In conclusion, EG pretreatment can hamper the effect of plasma treatment of UHMWPE fibers and therefore longer plasma treatment duration is required for fibers pretreated with EG.     

Three different low-temperature plasma-based methods for hydrophilicity improvement of polyethylene films at atmospheric pressure

Three different low-temperature plasma-based methods were used to improve the surface hydrophilicity of polyethy- lene （PE） films, and all the modification processes were carried out by employing an atmospheric pressure plasma jet （APPJ） system. （a） PE films were directly modified by APPJ using a gas mixture of He and 02. （b） Acrylic acid （AA） was introduced into the system and a polymer acrylic acid （PAA） coating was deposited onto the PE films. （c） AA was grafted onto the PE surface activated by plasma pre-treatment. It was found that the hydrophilicity of the PE films was significantly improved for all the three methods. However, the samples modified by Process （a） showed hydrophobicity recovery after a storage time of 20 days while no significant change was found in samples modified by Process （b） and Process （c）. The Fourier transform infrared spectroscopy （FTIR） results indicated that the most intensive C=O peak was detected on the PE surface modified by Process （c）. According to the X-ray photoelectron spectroscopy （XPS） analysis, the ratios of oxygen-containing polar groups for samples modified by Process （b） and Process （c） were higher than that modified by Process （a）.     

Surface wettability of atmospheric dielectric barrier discharge processed Armos fibers

Wettability of Armos fibers has been investigated after exposed to dielectric barrier discharge (DBD) plasma, which was performed at atmospheric pressure in air while varying the sample treatment time between 9 and 27 s. Contact angles and surface free energy of the original and plasma-treated fibers were measured with dynamic contact angle analysis (DCAA) to reveal the correlation between the fiber wettability and the surface treatment, including surface composition and topography modifications, which were evaluated by X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM), respectively. It was found by XPS analysis that the O/C atomic ratio on Armos fiber surface can be increased from 0.134 to 0.248 after the 18 s exposure to the plasma and many polar functional groups were proved to be incorporated into the surface, which aided good wetting. In addition, AFM observations revealed the changes of fiber surface microstructure, showing significant enhancement of the surface roughness after the treatment, which could also bring the fiber better wettability. What's more, the impacts of fiber surface treatment on its tensile properties were characterized by single fiber tensile strength (SFTS) testing. Results showed that Armos fibers exhibited only slight reductions in their tensile strengths with the great enhancement in fiber surface free energy.     

等离子体处理的聚丙烯和聚乙烯的粘合体

采用射频辉光放电等离子体和介质阻挡放电等离子体对聚丙烯（PP）和聚乙烯（PE）进行处理后,使用聚氨酯进行粘接,并测试了混合粘合体的剪切强度。介质阻挡放电功率是100 W时,等离子体处理对混合粘合体的剪切强度无影响。介质阻挡放电的功率为200 W、处理时间20 s时,等离子体处理效果最佳,剪切强度为1.58 MPa,是未处理的混合粘合体的14.36倍。介质阻挡放电的功率是300 W时,样品在10 s内就被击穿。射频辉光放电等离子体中,使用空气处理后最大剪切强度为1.60 MPa（100 W,3 min）,使用氮气处理后的最大剪切强度为1.57 MPa（200 W,3 min）。通过扫描电镜（SEM）对等离子体处理前后的PP表面形貌观察,发现未处理样品的表面比较平滑,而经等离子体放电处理后的样品表面变得疏松,出现了大量泡状物质,表面粗糙程度提高。     

等离子体处理的聚丙烯和聚乙烯的粘合体

采用射频辉光放电等离子体和介质阻挡放电等离子体对聚丙烯（PP）和聚乙烯（PE）进行处理后,使用聚氨酯进行粘接,并测试了混合粘合体的剪切强度。介质阻挡放电功率是100 W时,等离子体处理对混合粘合体的剪切强度无影响。介质阻挡放电的功率为200 W、处理时间20 s时,等离子体处理效果最佳,剪切强度为1.58 MPa,是未处理的混合粘合体的14.36倍。介质阻挡放电的功率是300 W时,样品在10 s内就被击穿。射频辉光放电等离子体中,使用空气处理后最大剪切强度为1.60 MPa（100 W,3 min）,使用氮气处理后的最大剪切强度为1.57 MPa（200 W,3 min）。通过扫描电镜（SEM）对等离子体处理前后的PP表面形貌观察,发现未处理样品的表面比较平滑,而经等离子体放电处理后的样品表面变得疏松,出现了大量泡状物质,表面粗糙程度提高。     

单模光纤的磁光效应

本文利用琼斯(Janes)矩阵叙述了单模光纤磁光效应的理论,导出了既具有双折射又具有法拉第效应的琼斯矩阵形式,并利用Mueller矩阵导出电流传感器系统输出光强与法拉第旋转角之间的关系.     

The Influence of Air Counter‐Flow Through Powder Materials as a Means of Reducing Cohesive Flow Problems

The cohesive behavior of aerated solids controls fluidization behavior of bulk materials. Very cohesive materials cannot be easily fluidized. However, aeration is often used in contact bed situations to help maintain some cohesive materials in flowable conditions. The cohesive properties of aerated materials are not well understood. This paper presents a new test method to measure the effect of aeration on cohesive flow properties. These measurements could be used along with new design equations to predict arching and stable rathole formation of cohesive materials in aerated process equipment. Experimental results on fine silica powder and fluid catalytic cracking (FCC) catalyst show the evolution of the yield locus shape and the effective yield locus shape as a function of the degree of aeration. It was found that both the cohesion intercept and the yield locus slope are functions of the degree of aeration.     

The interaction of an atmospheric pressure plasma jet using argon or argon plus hydrogen peroxide vapour addition with bacillus subtilis

This paper reports that an atmospheric pressure dielectric barrier discharge plasma jet, which uses argon or argon + hydrogen peroxide vapour as the working gas, is designed to sterilize the bacillus subtilis. Compared with the pure argon plasma, the bacterial inactivation efficacy has a significant improvement when hydrogen peroxide vapour is added into the plasma jet. In order to determine which factors play the main role in inactivation, several methods are used, such as determination of optical emission spectra, high temperature dry air treatment, protein leakage quantification, and scanning electron microscope. These results indicate that the possible inactivation mechanisms are the synergistic actions of chemically active species and charged species.     

A modified fractional model to describe the viscoelastic behavior of solid amorphous polymers: The effect of physical aging

Amorphous polymers are viscoelastic materials. When they are subjected to dynamical loads, their behavior can be modeled by transform functions of stress and strain in the complex plane. In our work, a model based on the fractional calculus concept is proposed in order to predict the viscoelastic behavior of polymethylmethylacrylate (PMMA) over a wide temperature range between (T_g -190°C) and (T_g +15°C). The extended fractional solid model is shown to be capable of describing experimentally observed dynamic viscoelastic behavior over a wide temperature range, including multiple relaxations, using a limited number of free parameters. Structural recovery of PMMA was studied by dynamic mechanical spectrometry, and its effect on the different parameters is also discussed. Furthermore, from the fractional differential and fractional integral formulations. most of the relevant viscoelastic functions that quantify the degree of molecular mobility of amorphous polymers, like E(t), E?(τ). and H(t), can be derived analytically.