有机累托石改性不饱和聚酯／玻璃纤维复合材料的研究

采用有机累托石改性不饱和聚酯，以改性的不饱和聚酯为基体，以两种玻璃布(EW210、CWR400-90)为增强材料，以两个不同凝胶时间的不饱和聚酯树脂体系制备三种有机累托石改性的不饱和聚酯磁璃纤维复合材料(UPB1、UPB2、UPB3)。测试了不饱和聚酯/玻璃纤维的力学性能；研究了复合材料的耐湿热性及耐介质性能；利用扫描电镜及透射电镜分析了复合材料的增强机理。结果表明，采用有机累托石改性不饱和聚酯所制备的不饱和聚酯／玻璃纤维复合材料的综合力学性能优于纯不饱和聚酯／玻璃纤维复合材料。     

Synthesis of reactive copolymers with peroxide functionality for cross-linking water-soluble polymers

A series of reactive copolymers with peroxide functionality (RCPFs) were synthesized via radical copolymerization of monomer mixtures in an organic solvent comprised of a peroxide monomer 5-(tert-butyl peroxy)-5-methylhex-1-en-3-yne, acrylamide, maleic anhydride, and butyl methacrylate. Peroxide functionality allows the RCPFs to initiate a variety of radical processes, including cross-linking of organic polymers. Hydrophilic monomer subunits (acrylamide and maleic anhydride) within the RCPF macromolecules promote cross-linking of water-soluble polymers. We aimed to investigate RCPF comonomer ratio and its effects on copolymerization kinetics and composition, as well as physico-chemical and colloidal properties. We also evaluated and characterized the kinetic parameters of the thermal decomposition of peroxide moieties in the synthesized RCPF. Findings revealed that RCPF possessed surface-active properties and reduced surface tension at its aqueous solution–air interface. The data indicated that the decomposition process complied with the first-order kinetics, and complex thermal analysis confirmed the presence of peroxide moieties. RCPFs' ability to cross-link water-soluble polymers was demonstrated on poly(acrylamide) and poly(vinyl alcohol).     

CE2908聚酯粉末涂料固化反应特性

用示差扫描量热法(DSC)在动态条件下对CE2908聚酯/异氰尿酸三缩水甘油酯(TGIC)体系的固化反应动力学进行了研究。运用温度-升温速率图外推法确定了该体系的特征参数∶凝胶温度(T0)、固化温度(Tp)和后固化温度(Tf)分别为113℃、146℃和195℃。采用Kissinger方程和Crane方程计算CE2908聚酯/TGIC酯体系的动力学参数,平均表观活化能Ea为62.32 kJ/mol、频率因子A为8.50×106min-1、反应级数n为0.95。建立了该树脂体系的固化动力学模型。利用所建立的固化动力学方程分别讨论了等温和动态条件下CE2908聚酯/TGIC的固化反应特性,为优化聚酯/TGIC体系粉末涂料固化工艺提供了理论依据,并在生产工艺中验证了其正确性。     

2011-2012年世界不饱和聚酯树脂工业进展

介绍了2011-2012年国外不饱和聚酯原料市场动态,国外企业运营情况。综述了不饱和聚酯树脂领域的研究及应用进展,涉及不饱和聚酯树脂及其复合材料的电性能、收缩性能、力学性能、生物复合材料、表面处理、阻燃性能及环保等。     

Polymer stain resistance: Prediction versus experiment

The coloration of different polymer films (from commodity and packaging films to performance films) by contact with various food coloring substances was evaluated. For this purpose, both solubility parameters as a prediction tool, and immersion experiments for time range between 24 and 1000 h were established. The two predicting tools are the Hoy and Hoftyzer‐Van Krevelen (HVK) methods. For PE and PP, HVK's method is preferred for predicting coloration. Neither of the HVK's and Hoy's methods was able to establish a coloration prediction for PET while both methods could predict the staining of PEEK. The coloration of partially and fully fluorinated polymers is well predicted by the Hoy's method. The behavior of PP/PA and PP/PA/PP multilayer films was also studied. Crystallinity degree of polymers, temperature and concentration of coloring molecules are also important parameters, which are not taken into account in solubility theories. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

The Adhesion of Irregularly-shaped 8 μm Diameter Particles to Substrates: The Contributions of Electrostatic and van der Waals Interactions

The forces needed to remove irregularly-shaped, 8 μm diameter, polyester particles from a polyester substrate were measured using an ultracentrifuge. Measurements were also made on a second set of similar particles where nanometer-size silica clusters had been placed on their surfaces. These silica clusters acted as spacers, reducing direct contact between the particle and the substrate. It was found that the separation forces for the bare particles were consistent with predictions of the JKR theory of adhesion, but were much larger than could be accounted for from simple electrostatic interactions associated with either uniformly-charged particles or particles with localized charged patches. It was found, however, that the forces needed to effect separation decreased with increasing silica concentration. For particles with 2% by weight silica clusters on their surfaces, the separation force was only about 5% of the separation forces of the bare particles. At this concentration of silica, the estimates of the separation forces obtained from JKR theory, from the uniformly-charged model, and from the localized-charged-patch model are all about equal. The numerical estimates are consistent with the experimentally-obtained values.     

Adhesion Improvement of Glass-Fibre-Reinforced Polyester Composites by Gliding Arc Discharge Treatment

A gliding arc is a plasma that can be operated at atmospheric pressure and applied for plasma surface treatment for adhesion improvement. In the present work, glass-fibre-reinforced polyester plates were treated using an atmospheric pressure gliding arc discharge with an air flow to improve adhesion with a vinylester adhesive. The treatment improved wettability and increased the polar component of the surface energy and the density of oxygen-containing polar functional groups at the surfaces. Double cantilever beam specimens were prepared for fracture mechanics characterisation (fracture resistance as a function of nominal mode mixity) of the laminate adhesive interface. It was found that gliding arc treatment significantly increases the interfacial fracture energy and fracture resistance in comparison with a standard peel ply treatment, although the mixed mode fracture energy of the gliding arc treated specimen was not as high as that of the laminate itself.     

Chemistry of the Interface Between Aluminum and Polyester Films

It has been observed that the adhesion between vacuum-evaporated aluminum and poly(ethylene isophthalate-co-ethylene sodium sulfoisophthalate) copolymer is approximately five times greater than the adhesion between vacuum-evaporated aluminum and biaxially-oriented poly(ethylene terephthalate) film. To describe the interface between the aluminum and these polymeric substrates, thermoanalytical, spectroscopic and microscopic techniques have been applied. Definite changes in surface elemental composition and chemical functionality occur upon metallization of the polymer films. Aluminized samples contained two new oxygen functionalities; one due to the aluminum oxide and the other due to an organoaluminum species. Thermal degradation, as may occur during vacuum evaporation, would be expected to yield a carboxylic acid endgroup and a vinyl endgroup for each chain scission reaction that occurred. Reaction of aluminum with these carboxylic acid endgroups is thought to be responsible for the organoaluminum oxygen peak that was observed. Based on the XPS data, however, the level of this new functionality was comparable for both types of polyester film. Thus, this new functionality may be involved in promoting aluminum/polyester adhesion, but by itself cannot explain the differences in the level of adhesion that are attained. It appears, based on the transmission electron micrographs, that the aluminum deposit penetrates the copolymer coating to a greater depth than it does the PET. The greater level of penetration could be responsible for the greater adhesion obtained between vacuum-evaporated aluminum and the copolymer film compared with the level of adhesion obtained with the PET film. Based on this work, it appears that the adhesion of the vacuum-evaporated aluminum to both polyesters has a similar chemical component (type and amount) but a different extent of the mechanical component.     

Lipase‐mediated preparation of epoxy lecithin and its evaluation as plasticizer in polyester laminates

A simple chemoenzymatic method was developed for the preparation of epoxy lecithin that contains epoxy oils and phospholipids. The parameters such as lipase concentration, hydrogen peroxide concentration, and time of the reaction were studied. The product was evaluated as a plasticizer in polyester laminates and compared with virgin polyester laminates. The laminates were prepared using various amounts of epoxy lecithin and evaluated for different properties. The epoxy lecithin modified laminates showed good impact strength, tensile, and chemical resistance properties. These laminates were also evaluated for vicat softening point and water absorption. The epoxy lecithin can be used as a plasticizer in polyester laminates. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Photoprotection of Wood Using Polyester-Type UV-Absorbers Derived from the Reaction of 2-hydroxy-4(2,3-epoxypropoxy)-benzophenone with Dicarboxylic Acid Anhydrides

Abstract

Polyester-type UV absorbers were created by reacting the epoxy-functionalized UV absorber 2-hydroxy-4(2,3-epoxypropoxy)-benzophenone (HEPBP) with maleic, phthalic, or succinic anhydride. The ability of the UV absorbers to photostabilize wood was then examined. Fourier transform infra-red (FTIR) spectroscopy confirmed that HEPBP reacted with phthalic anhydride to create a polyester that preserved the UV-absorbing benzophenone group. There was less evidence that the polyester was formed when HEPBP was reacted with maleic or succinic anhydride. HEPBP-phthalic anhydride was the most effective UV absorber at photostabilising wood. This UV absorber showed increased UV absorption around 270 nm, formed a leach-resistant film at wood surfaces and was able to restrict both weight and tensile strength losses of thin wood veneers during accelerated weathering, unlike chromium trioxide and a UV absorber-hindered amine light stabilizer. We conclude that polymeric polyester-type UV absorbers show promise as a way of photostabilizing wood and briefly discuss how more effective systems could be developed in future.