甲氧基代多个氧化乙烯结构交联型酚醛聚合物的合成

采用对甲氧基苯酚、多缩乙二醇二氯化物为原料, 合成了五个4,4'-二甲氧基多缩乙二醇二苯醚新单体; 分别经甲醛、2,6-二羟甲基对甲氧基苯酚聚合, 得到二个系列甲氧基代多个氧化乙烯结构交联型酚醛聚合物。这些聚合物含有假冠醚结构单元, 配合容量在0.9-3.0mmol/g之间, 可作为配合树脂使用, 富集分离多种金属离子。     

Influence of interfacial reaction on interfacial performance of carbon fiber and polyarylacetylene resin composites

The influence of interfacial reaction on interfacial performance of carbon fiber/polyarylacetylene resin composites was studied. For this purpose, vinyltrimethoxysilane containing a double bond was grafted onto the carbon fiber surface to react with the triple bond of polyarylacetylene resin. The reaction between polyarylacetylene resin and vinyltrimethoxysilane was proved by reference to the model reaction between phenylacetylene and vinyltrimethoxysilane. Surface chemical analysis by XPS, surface energy determination from the dynamic contact angle, and the interfacial adhesion in composites was evaluated by interfacial shear strength test as well. It was found that vinyltrimethoxysilane, which can react with polyarylacetylene resin, had been grafted onto the carbon fiber surface. Furthermore, because the reaction between polyarylacetylene resin and vinyltrimethoxysilane took place at the interface, the interfacial adhesion in composites was significantly increased, and the improvement of interfacial adhesion was all attributed to the interfacial reaction.     

Dielectric breakdown phenomena in Al2O3 filled DGEBA/MDA/SN composite system

Dielectric breakdown phenomena by electrical treeing deterioration was investigated in the new epoxy resin system DGEBA/MDA/SN filled with Al₂O₃. As the filler content increased, the maximum electric field at breakdown increased and then decreased with increase of defects such as voids, impurities and delamination or peeling between filler and matrix. As the electrode separation increased, the breakdown voltage increased, but the breakdown strength decreased and then saturated to 17 kV/mm. Also, the maximum electric field at the tip when the system was failed increased. The electrical tree initiated from the side of the needle electrode was not from the tip where the reinforced field is the highest. The electrical tree was blocked by the filler. The interface condition of filler and polymer matrix played an important role in the electrical treeing resistance. The final breakdown phenomena showed fan-type crack as observed in the non-filled system.     

Inorganic-organic interpenetrating frameworks: oxi-hydroxide iron (III) inside poly-4-vinylpyridine-methacrylic acid-N,N'-methylenebisacrylamide. Part I: Synthesis and macrostructure

A carboxylic gel-type resin, poly-4-vinylpyridine-methacrylic acid-N, N'-methylenebisacrylamide is designed and synthesized in order to be able to incorporate both Fe^III and, potentially, also Au^III in its polymer framework. Along with the gradual substitution of H⁺ with Na⁺, of Na⁺ with Fe³⁺/3 and after a very controlled and gradual precipitation of Fe^III as oxihydroxides induced by the hydrolysis of urea directly inside the nanoporous domains of the metalated resin particles, an organic-inorganic composite is obtained. The material is characterized with TGA, ESEM, XRMA and Mössbauer spectroscopy.     

Thermal behavior of chemically treated and untreated sisal fiber reinforced composites fabricated by resin transfer molding

Using thermogravimetric analysis (TGA), the thermal behavior of sisal fibers and sisal/polyester composites, fabricated by resin transfer molding (RTM), has been followed. Chemical treatments have been found to increase the thermal stability, which has been attributed to the resultant physical and chemical changes. Scanning electron microscopy (SEM) and infrared (FT-IR) studies were also performed to study the structural changes and morphology in the sisal fiber during the treatment. The kinetic studies of thermal degradation of untreated and treated sisal fibers have been performed using Broido method. In the composites, as the fiber content increases, the thermal stability of the matrix decreases. The treated fiber reinforced composites have been found to be thermally more stable than the untreated derivatives. The increased thermal stability and reduced moisture behavior of treated composites have been correlated with fiber/matrix adhesion.     

Sorption characteristics of water,oil and diesel in cellulose nanofiber reinforced corn starch resin/ramie fabric composites

Nowadays, utilisation of biodegradable materials has become necessary in order to maintain global environmental and ecological balance. Fully biodegradable nano 'Green' textile composites have been prepared from cellulose nanofibers reinforced corn starch resin and ramie fabric. Nanofibers having dimensions of approximately 1 μm long and 20–30 nm in diameter are used in the study. The nanofibers were incorporated in corn starch resin via ball mill mixing using ceramic balls. Textile composites were fabricated by pasting the reinforced resin onto the ramie fabric and by hot compression molding technique. Interactions at the fiber–matrix interface and the compatibility between cellulose and corn starch resin molecules will affect the properties of the system. The well dispersed cellulose nanofibers contribute higher interfacial area and good fiber networking within the matrix resin. This will lead to better barrier properties. Sorption characteristics of water, oil and diesel in the textile composites were analysed and the influence of nano fibers and macro fibers on the transport phenomena was investigated. The kinetics of sorption-diffusion process was investigated. Kinetic parameters such as n, k, diffusion coefficient, permeability, solubility parameter, % swelling index, etc., were analysed. The presence of cellulose nanofibers influences the sorption mechanism. The water sorption mechanism in the nanocomposites was found to exhibit slight deviation from Fickian mode. Structure–property relationships of the nanocomposites were evaluated.     

Studies on interface in polyester/fly-ash particulate composites

Fly ash (FA)-general purpose unsaturated polyester resin (GPR) particulate composites have been made. The effect of surface treatment of FA with two different silane coupling agents (CAs) on the mechanical properties like tensile, flexural, impact strength and hardness, thermal properties like thermal stability and morphological properties (SEM) of FA-GPR composites are studied. The properties of FA-CA-GPR are also compared with that of GPR and CaCO₃ -GPR. An enhancement in the tensile, flexural, and impact strength and moduli are observed when FA is surface treated with CA. Hardness is also found to increase with CA-treated FA-filled GPR. A suitable mechanism for the chemical reaction taking place at the interface in the presence of CAs is proposed.     

Improvement of resin impregnation into glass cloth by silane treatment in resin transfer molding

An evaluation method was proposed for resin impregnation using resin transfer molding of unsaturated polyester matrix composites with silane-treated glass cloth. The determination of whitening of the composite was carried out as a parameter of incompleteness of resin impregnation. The change of whitening with silane concentration was compared with the bending modulus as a parameter of chemical reinforcement. The materials used were unsaturated polyester resin as a matrix and methacryloxypropyltrimethoxysilane as a silane coupling agent for glass cloth. Resin transfer molding was used to produce four plies of glass cloth laminates by impregnating the resin. The silane-treated glass cloth repressed whitening above 0.026 w/w% of silane in aqueous solution, while the chemical reinforcement due to silane gave no appearance below 0.2 w/w% based on the bending test of the laminates. The large difference between the concentrations suggested that silane has a couple of functions, that is, chemical reinforcement and physico-chemical resin wettability.     

Anisotropic orientation of the carbon fiber/liquid crystalline epoxy resin composites

Anisotropic orientation of carbon fiber (CF)/liquid crystalline epoxy (LCE) resin composite was readily induced during curing on a CF surface along a long molecular axis of CF. Orientation of LCE was confirmed with polarized optical microscope (POM) and wide angle X-ray diffractometer (WAXD). In addition, anisotropic ordering of LCE was correlated with curing rate, dynamic mechanical properties and thermal expansion behaviors of CF/LCE composite. Curing of LCE was accelerated in the presence of CF and the rubbery modulus of the CF/LCE composites cured at low temperature was enhanced by long-range, long axis orientational ordering of the LCE resin along a CF surface. Fully cured CF/LCE composite showed a negative coefficient of thermal expansion in the fiber direction. These results obtained in this study are interpreted in terms of structural changes occurring during curing.     

ADSORPTION OF 1,2,4-ACID BY WEAKLY BASIC RESIN： ISOTHERMS, THERMODYNAMICS AND KINETICS

The adsorption properties, including the adsorption isotherms, thermodynamics and kinetics, of l-amino-2-naphthol-4-sulfonic acid (1,2,4-acid) onto weakly basic resin ND900 are investigated. Both the Langmuir and Freundlich equations can give a good fit to the adsorption isotherms, which indicates an endothermic and a favorable adsorption in our study range. A high yield in elimination of about 45.21%-97.28% is obtained for the tested adsorption systems. The capacity and affinity of the adsorption increase with temperature, due to the phenomena of “solvent-motivated” effects. The value of ΔH is 51.59 kJ/mol, which indicates a chemical adsorption and then expects the poor desorption property of ND900. The negative value of ΔG indicates the spontaneous nature of the adsorption process, and the positive value of ΔS shows the increased randomness at the solid/solution interface during the adsorption process. The value of the adsorption rate constant lower than 0.013 min^-1 is indicative of a slow adsorption rate. The intra-particle diffusion must be one of the rate limiting steps.