不锈钢纤维填充ABS复合材料的研究及应用

以(丙烯腈/丁二烯/苯乙烯)共聚物(ABS)树脂为主要原料,利用不锈钢纤维(SSF)进行改性,为解决SSF在树脂基体中的分散性问题,采用母料法制样。对ABS/SSF复合材料的力学性能和电学性能进行表征,并利用扫描电子显微镜、差示扫描量热仪等对其微观结构进行研究,探讨了微观结构对复合材料性能的影响。该法制备的ABS/SSF复合材料抗静电性能优异,性价比高,已用于井下探测仪器外壳。     

Effect of ultrasound on wettability between aramid fibers and epoxy resin

Good wetting of reinforced fiber by resin was a main factor in the improvement of the interface adhesion of their composites. Ultrasound with a frequency of 20 kHz was used to improve the wettability between aramid fibers and epoxy resin during the winding process of the composites. The effects of ultrasound on the viscosity and surface tension of epoxy resin and on the surface characteristics of aramid fibers were investigated. The wettability of aramid fibers and treated epoxy resin under different conditions and of aramid fibers and epoxy resin under ultrasonic online treatment were compared. The results indicated that the main action of ultrasound was to force epoxy resin to impregnate aramid fibers, in addition to the influence of ultrasound on the properties of epoxy resin and aramid fibers. The results of microdebond testing showed that the interfacial shear strength (IFSS) of aramid/epoxy composites could be 26% higher than that of untreated composites because of the improved wettability between aramid fibers and epoxy resin subjected to ultrasonic online treatment. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

Flexibility improvement of short glass fiber reinforced epoxy by using a liquid elastomer

In certain applications of fiber reinforced polymer composites flexibility is required. The aim of this study was to improve flexibility of short glass fiber reinforced epoxy composites by using a liquid elastomer. For this purpose, diglycidyl ether of bisphenol-A (DGEBA) based epoxy matrix was modified with hydroxyl terminated polybutadiene (HTPB). A silane coupling agent (SCA) was also used to improve the interfacial adhesion between glass fibers and epoxy matrix. During specimen preparation, hardener and HTPB were premixed and left at room temperature for an hour before mixing with epoxy resin to allow possible reactions to occur. In order to compare flexibility of the specimens flexural tests were conducted and the data were evaluated numerically by using a derived relation. Test data and scanning electron microscope analysis indicated that surface treatment of glass fibers with SCA, and HTPB modification of epoxy matrix improved flexural properties especially due to the strong interaction between fibers, epoxy, and rubber. It was also observed that HTPB modification resulted in formation of relatively round rubber domains in the epoxy matrix leading to increased flexibility of the specimens.     

Improvement of adhesion of Kevlar fiber to epoxy by chemical modification

Kevlar 149 fibers were surface-modified by chlorosulfonation and subsequent reaction of -SO₂O with some reagents (e.g. glycine, water, ethylenediamine, and 2-butanol) to improve the adhesion to epoxy resin. The mechanical properties and surface topography of the modified fibers were investigated at different reaction times and reagent concentrations. The surface functional groups introduced into the surface of the fibers were identified by X-ray photoelectron spectroscopy (XPS) and static secondary ion mass spectroscopy (SIMS). The interfacial shear strength (IFSS) between the fibers and epoxy resin was measured by the microbond test. The results showed that the IFSS was markedly improved (by a factor of 2.25) by the chlorosulfonation/glycine treatment and that the fiber strength was not affected. Scanning electron microscopy (SEM) was also used to study the surface topography of fibers pulled from the epoxy resin. Furthermore, energy dispersive X-ray (EDX) spectroscopy was used to qualitatively examine the amount of sulfur in the fiber surfaces and in the fracture surfaces of fibers from microbond pull-out specimens. The results of EDX examination were consistent with a change of the fracture mode from the interface between the fiber and the epoxy resin to a location within the fiber and/or epoxy resin as observed by SEM.     

Effect of fiber chemical treatment of nonwoven coconut fiber/epoxy composites adhesion obtained by RTM process

In this work untreated and alkali treated nonwoven coconut fiber mats/epoxy resin composites were manufactured using the resin transfer molding process. The alkaline solution removes some impurities present on fibers superficial layers and the effect regarding fiber/matrix adhesion were investigated by thermogravimetric analysis, dynamic mechanical analysis (DMA), scanning electron microscopy (SEM), ultrasonic C‐scan, and quasi‐static flexural test. Results show a removing of some amorphous fibers constituents, mainly waxes, extractives, and hemicellulose, revealing the fiber roughness surface but no initial degradation temperature changing. Regarding the composites, a similar interfacial adhesion was observed in both one through the results of SEM, DMA and quasi‐static flexural tests. The conclusion is that chemical treatment conditions applied on the fiber surface was been suitable to improve fiber roughness but did not the adhesion between coconut fibers mat and epoxy resin. POLYM. COMPOS., 38:2518–2527, 2017. © 2015 Society of Plastics Engineers     

Investigation of mechanical properties of unidirectional steel fiber/polyester composites: Experiments and micromechanical predictions

The article introduces steel fiber reinforced polymer composites, which is considered new for composite product developments. These composites consist of steel fibers or filaments of 0.21 mm diameter embedded in a polyester resin. The goal of this investigation is to characterize the mechanical performance of steel fiber reinforced polyester composites at room temperature. The mechanical properties of unidirectional steel fiber reinforced polyester composites (SFRP) are evaluated experimentally and compared with the predicted values by micro‐mechanical models. These predictions help to understand the role of material and process parameters on material properties. Two types of SFRP were studied: polyester resin reinforced by both steel fabric containing unidirectional fibers and steel fibers wound on a metal frame with 0° orientations. The effects of the fiber volume fraction and the role of polymer yarns (weft) on mechanical properties were analyzed through tensile, compressive, and shear tests. These tests were performed as per the standard test procedures. In particular, issues related to processing difficulties, polymer yarns effect on properties, standardized testing, and properties under various loading conditions were addressed. Microscopic observations were analyzed to assess the laminate quality and the macroscopic fracture surfaces of shear test specimens were studied by standard techniques. POLYM. COMPOS., 37:627–644, 2016. © 2014 Society of Plastics Engineers     

Unsaturated polyester‐toughened epoxy composites: Effect of sisal fiber on thermal and dynamic mechanical properties

In the present study, the mechanical and thermal properties of sisal fiber‐reinforced unsaturated polyester (UP)‐toughened epoxy composites were investigated. The sisal fibers were chemically treated with alkali (NaOH) and silane solutions in order to improve the interfacial interaction between fibers and matrix. The chemical composition of resins and fibers was identified by using Fourier‐transform infrared spectroscopy. The UP‐toughened epoxy blends were obtained by mixing UP (5, 10, and 15 wt%) into the epoxy resin. The fiber‐reinforced composites were prepared by incorporating sisal fibers (10, 20, and 30 wt%) within the optimized UP‐toughened epoxy blend. Scanning electron microscopy was used to analyze the morphological changes of the fibers and the adhesion between the fibers and the UP‐toughened epoxy system. The results showed that the tensile and flexural strength of (alkali‐silane)‐treated fiber (30 wt%) ‐reinforced composites increased by 83% and 55%, respectively, as compared with that of UP‐toughened epoxy blend. Moreover, thermogravimetric analysis revealed that the (alkali‐silane)‐treated fiber and its composite exhibited higher thermal stability than the untreated and alkali‐treated fiber systems. An increase in storage modulus and glass transition temperature was observed for the UP‐toughened epoxy matrix on reinforcement with treated fibers. The water uptake behavior of both alkali and alkali‐silane‐treated fiber‐reinforced composites is found to be less as compared with the untreated fiber‐reinforced composite. J. VINYL ADDIT. TECHNOL., 23:188–199, 2017. © 2015 Society of Plastics Engineers     

Influence of plasma treatment on properties of ramie fiber and the reinforced composites

In this research, 9 series of ramie fibers were treated under low-temperature plasma with diverse output powers and treatment times. By analysis of the surface energy and adhesion power with epoxy resin, 3 groups as well as control group were chosen as reinforced fibers of composites. The influences of these parameters on the ramie fiber and its composites such as topography and mechanical properties were tested by scanning electron microscopy (SEM), atomic force microscopy (AFM), tensile property and fragmentation test of single-fiber composites. Contact angle and surface free energy results indicated that with the increased treatment times and output powers, surface energy and adhesion work with epoxy resin improved. Compared with the untreated fibers, surface energy and adhesion work with epoxy resin grew 124.5 and 59.1% after 3 min-200 w treatment. SEM and AFM showed low temperature plasma treatment etched the surface of ramie fiber to enhance the coherence between fiber and resin, consequently fiber was not easy to pull-out. After 3 min-200 w treatment, tensile strength of ramie fiber was 253.8 MPa, it had about 30.5% more than that of untreated fiber reinforced composite. Interface shear stress was complicated which was affected by properties of fiber, resin and interface. Fragmentation test showed biggest interface shear stress achieved 17.2 MPa, which represented a 54.0% increase over untreated fiber reinforced composites.     

Mechanical properties of poly(styrene‐co‐acrylonitrile)‐modified epoxy resin/glass fiber composites

Poly(styrene‐co‐acylonitrile) was used to modify diglycedyl ether of bisphenol‐A type epoxy resin cured with diamino diphenyl sulfone and the modified epoxy resin was used as the matrix for fiber‐reinforced composites (FRPs) to get improved mechanical properties. E‐glass fiber was used as fiber reinforcement. The tensile, flexural, and impact properties of the blends and composites were investigated. The blends exhibited considerable improvement in mechanical properties. The scanning electron micrographs of the fractured surfaces of the blends and tensile fractured surfaces of the composites were also analyzed. The micrographs showed the influence of morphology on the properties of blends. Results showed that the mechanical properties of glass FRPs increased gradually upon fiber loading. Predictive models were applied using various equations to compare the mechanical data obtained theoretically and experimentally. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Effects of chemical surface pretreatment on tensile properties of a single glass fiber and the glass fiber reinforced epoxy composite

The aim of this article is to determine the effect of surface pretreatments, prior to the silanization, on the structure and tensile properties of the glass fibers and their epoxy composites. Commercial glass fibers were washed with acetone to remove the soluble portion of sizing, calcinated for the removal of organic matter, activated for surface silanol regeneration, and silanizated with glycidoxypropyltrimethoxysilane (GPS). Tensile test was carried out. The morphology of pretreated glass fibers and the fracture surfaces of the epoxy composites were observed with a scanning electron microscope (SEM). The results revealed that both apparent modulus and strength of a single glass fiber and the glass fiber/epoxy resin composites strongly depend on the fiber surface pretreatments. The acetone treatment did not change appreciably the composition and tensile properties of glass fibers, but there was a weak interface between fibers and matrix. In calcinated and acid activated fibers, the two competitive effects was observed: (1) degradation of the fibers themselves and (2) improved interfacial adhesion between the glass fibers and the epoxy matrix, once the samples was silanizated. The ATR‐FTIR results show that the surface content of Si OH increases as reflected by the increasing of the Si O band, resulting in an interaction between silane coupling agent and glass fiber. POLYM. COMPOS., 91–100, 2016. © 2014 Society of Plastics Engineers     

High-performance composite from epoxy and glass fibers: Morphology,mechanical, dynamic mechanical,and thermal analysis

Diglycidyl ether of bisphenol-A type epoxy resin cured with diamino diphenyl sulfone was used as the matrix for fiber-reinforced composites to get improved mechanical and thermal properties for the resulting composites. E-glass fiber was used for fiber reinforcement. The morphology, tensile, flexural, impact, dynamic mechanical, and thermal properties of the composites were analyzed. The tensile, flexural, and impact properties showed dramatic improvement with the addition of glass fibers. Dynamic mechanical analysis was performed to obtain the T_g of the cured matrix as well as the composites. The improved thermal stability of the composites was clear from the thermogravimetric analysis. Scanning electron micrographs were taken to understand the interfacial adhesion between the fiber and the matrix. The values of mechanical properties were compared with modified epoxy resin composite system. Predictive models were applied using various equations to compare the mechanical data obtained theoretically and experimentally. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Influence of oxygen plasma treatment parameters on the properties of carbon fiber

This study is focused on the impact of oxygen plasma treatment on properties of carbon fibers and interfacial adhesion behavior between the carbon fibers and epoxy resin. The influences of the main parameters of plasma treatment process, including duration, power, and flow rate of oxygen gas were studied in detail using interlaminar shear strength (ILSS) of carbon fiber composites. The ILSS of composites made of carbon fibers treated by oxygen plasma for 1 min, at power of 125 W, and oxygen flow rate of 100 sccm presented a maximum increase of 28% compared to composites made of untreated carbon fibers. Furthermore, carbon fibers were characterized by scanning electron microscopy (SEM), tensile strength test, attenuated total reflectance Fourier transform infrared (ATR-FTIR), and Raman spectroscopy analyses. It was found that the concentration of reactive functional groups on the fiber surface was increased after the plasma modification, as well the surface roughness, which finally improved the interfacial adhesion between carbon fibers and epoxy resin. However, high power and long exposure times could partly damage the surface of carbon fibers and decrease the tensile strength of filaments and ILSS of treated fiber composites.     

Surface modification of UHSPE fibers through allylamine plasma deposition. II. Effect on fiber and fiber/epoxy interface

The surface of ultra-high strength polyethylene (UHSPE) fibers was modified using allylamine plasma deposition to improve their adhesion to epoxy resins. Allylamine plasma polymerization was investigated at different power inputs and polymerization times. The adhesion of treated fibers to epoxy resin was studied by single-fiber, pull-out tests. A special silicon rubber mold was developed to embed the single fiber in epoxy resin. The results show that the interfacial shear strength (IFSS) increased by a factor of 2 to 3 after allylamine plasma treatments. The greatest improvement, by a factor of 3.25, was obtained at 30 W for 10 min. Scanning electron microscopy (SEM) was also used to study the surface topography of fibers pulled from the epoxy resin. In most cases, it was observed that pull-out failure occurred at the interface, as evidenced from clean fiber surfaces. In a few cases, however, fibrils were peeled from fibers. The fiber strength decreased, but initial modulus increased after the plasma treatments. The decrease in fiber strength was insignificant for treatments at a lower power input, but was significant at higher power inputs. Treatment time, however, had no significant effect on fiber strength.     

Interfacial improvement of carbon fiber/epoxy composites using a simple process for depositing commercially functionalized carbon nanotubes on the fibers

An aqueous suspension deposition method was used to coat the sized carbon fibers T700SC and T300B with commercially carboxylic acid-functionalized and hydroxyl-functionalized carbon nanotubes (CNTs). The CNTs on the fiber surfaces were expected to improve the interfacial strength between the fibers and the epoxy. The factors affecting the deposition, especially the fiber sizing, were studied. According to single fiber-composite fragmentation tests, the deposition process results in improved fiber/matrix interfacial adhesion. Using carboxylic acid-functionalized CNTs, the interfacial shear strength was increased 43% for the T700SC composite and 12% for the T300B composite. The relationship between surface functional groups of the CNTs and the interfacial improvement was discussed. The interfacial reinforcing mechanism was explored by analyzing the surface morphology of the carbon fibers, the wettability between the carbon fibers and the epoxy resin, the chemical bonding between the fiber sizing and the CNTs, and fractographic observation of cross-sections of the composites. Results indicate that interfacial friction, chemical bonding and resin toughening are responsible for the interfacial improvement of nanostructured carbon fiber/epoxy composites. The mechanical properties of the CNT-deposited composite laminate were further measured to confirm the effectiveness of this strategy.     

Characterizing high performance composite processability with dynamic fiber wettability measurements

Dynamic fiber wettability measurements are performed on T-300 carbon and Teflon fibers immersed in hexa methyl disiloxane (HMDS) silicone oil and a difunctional liquid epoxy resin, neopentyl diglycidyl ether (NPDGE). Specifically, four types of these carbon fibers, which are used to reinforce high performance composites, are studied. Decreases in the wetting force are observed for progressive immersions of all carbon fibers in the silicone oil but not observed with Teflon fibers, indicating adsorption may be occurring on the carbon surface. Perimeters determined from these wetting measurements on carbon fibers are larger than those calculated, assuming the fibers to be smooth cylinders. Scanning electron micrographs suggest this difference is attributable to surface crenulations. All carbon fibers immersed in the epoxy resin show non-zero contact angles.     

Thermal degradation of epoxy resin reinforced with polypropylene fibers

The influence of polypropylene fibers on the thermal degradation of epoxy composites was investigated with thermogravimetric analysis. Three composites with 5, 10, or 15 wt % polypropylene fibers were prepared with epoxy as a matrix material. The polypropylene fibers, used as reinforcing materials, retarded the thermal decomposition, and increasing the weight percentage of the fiber material increased the thermal stability to a certain extent. Of the three composites, the 10 wt % polypropylene fiber/epoxy resin composite showed very good thermal stability, which was indicated by the increase in the resin decomposition temperature from 280°C for the 5 wt % polypropylene fiber/epoxy resin composite to 375°C for the 10 wt % polypropylene fiber/epoxy resin composite. The Horowitz–Metzger method was used to calculate the activation energies, and the results were tabulated. A morphological analysis was carried out with scanning electron microscopy to evaluate the dispersion of the fibers in the epoxy matrix. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 500–503, 2007     

Matrix–size interactions in epoxy–glass fibers composites in relation to mechanical relaxations and effects of thermal aging

A study was carried out to examine the effect of removing the size from the surface of glass fibers in order to determine its role with respect to thermoxidative aging. Dynamic mechanical relaxation data have revealed that mechanical losses were always greater than the calculated upper bound values. The effects of removing the size from the surface glass fibers for epoxy matrix composites were found to be completely different when a fluoroligomer was used to modify the resin. Contrary to the case of the conventional epoxy resin, the characteristics of the composites containing fluoroligomer-modified resin were found to be insensitive to the removal of the size from the glass fibers surface. The presence of the size on the surface of the fibers provides an interlayer that degrades through the formation of more lightly crosslinked products than the matrix, thereby providing a large increase in dynamic mechanical losses after thermal aging. © 1995 John Wiley & Sons, Inc.     

Moisture absorption phenomenon in permeable fiber polymer composites

Studies were conducted on the moisture absorption characteristics of jute fiber composites based on polyester and epoxy resin systems, under constant humidity (ø) and ambient temperature (T) conditions. The initial slope of the moisture absorption curve (a direct measure of the composite diffusivity) increased with increased superficial fiber volume fraction (V_f), where as the time (t_m'), needed to reach the equilibrium moisture absorption value showed a reversed trend. This behavior is just a reverse to that observed¹ in case of composites with practically impermeable fibers (e.g., glass and graphite) in the same resin matrices. The theoretical expressions governing moisture diffusion phenomenon in impermeable fiber composites were modified and analyzed for the case of composites containing a permeable fiber. The experimental data obtained on the latter were then discussed in relation to the modified theory. The meaning of a correct fiber volume fraction (V_f,) as applicable to permeable fiber composites was defined.     

The effect of fiber-matrix stress transfer on the strength of fiber-reinforced composite materials

A model for the mechanism of tensile failure in oriented fiber composites based on random fragmentation of the reinforcing fibers biased by stress concentrations at fracture sites has been developed. Single-fiber composites and composite strands of 34 to 36 volume percent fiber were prepared from an epoxy resin reinforced with Hercules AS4, HMS4, and IM6G carbon fibers. Fiber strength distributions and single-fiber composite fragmentation data were used to calculate theoretical composite tensile strengths, which were then compared with experimental values. The fractures in single-fiber composites were observed in situ under cross-polarized light, and the mechanisms of interfacial failure were discussed.     

Carbon fiber cardanol-epoxy composites

Carbon fiber composites based on tetrafunctional epoxy resin N,N,N′,N′-tetraglycidyl-2,2-bis[4-(4-aminophenoxy)phenyl]propane modified with cardanol were investigated. The differential scanning calorimetric technique was used to study the curing reaction of the neat resins. The dielectric properties of the composites were compared. The use of cardanol in epoxy resins at cardanol/epoxy molar ratios less than 0.3/1 improved the chemical resistance as well as the mechanical properties of the composites, such as the flexural strength and modulus, tensile strength and modulus, and interlaminar shear strength. Higher cardanol contents decreased such properties. The highest properties of the composites were observed with the epoxy-cardanol resin having a cardanol/epoxy molar ratio of 0.3/1. © 1996 John Wiley & Sons, Inc.