Graded glass mat–reinforced polypropylene

In the impregnation process, when pressure is applied, the dry fiber preform is first compressed and then unloads as the matrix flows within the pores. It has been shown earlier that for glass mat–reinforced thermoplastic (GMT) materials, the time to provide complete infiltration of the matrix is significantly shorter than the unloading time of the reinforcement. This effect is exploited here to control the processing time in order to provide full infiltration but limited relaxation of the fiber bed, thereby producing a graded fiber content structure. Symmetric glass fiber/polypropylene (PP) composites were impregnated for different processing times to produce parts with a higher fiber content on the surface, decreasing towards the center. The elastic modulus in bending of the GMT parts was measured by a three‐point flexure test while the distribution of fibers in the matrix was quantified using optical microscopy combined with image analysis. The flexural modulus of GMT was found to decrease with the impregnation time, in good agreement with the prediction from infiltration and mechanics theory. Controlled processing could therefore be used to maximize the bending stiffness of GMT. POLYM. COMPOS., 26:361–369, 2005. © 2005 Society of Plastics Engineers.     

Fatigue of three advanced SiC/SiC ceramic matrix composites at 1200°C in air and in steam

High‐temperature mechanical properties and tension‐tension fatigue behavior of three advanced SiC/SiC composites are discussed. The effects of steam on high‐temperature fatigue performance of the ceramic‐matrix composites are evaluated. The three composites consist of a SiC matrix reinforced with laminated, woven SiC (Hi‐Nicalon?) fibers. Composite 1 was processed by chemical vapor infiltration (CVI) of SiC into the Hi‐Nicalon? fiber preforms coated with boron nitride (BN) fiber coating. Composite 2 had an oxidation inhibited matrix consisting of alternating layers of silicon carbide and boron carbide and was also processed by CVI. Fiber preforms had pyrolytic carbon fiber coating with boron carbon overlay applied. Composite 3 had a melt‐infiltrated (MI) matrix consolidated by combining CVI‐SiC with SiC particulate slurry and molten silicon infiltration. Fiber preforms had a CVI BN fiber coating applied. Tensile stress‐strain behavior of the three composites was investigated and the tensile properties measured at 1200°C. Tension‐tension fatigue behavior was studied for fatigue stresses ranging from 80 to 160 MPa in air and from 60 to 140 MPa in steam. Fatigue run‐out was defined as 2 × 10⁵ cycles. Presence of steam significantly degraded the fatigue performance of the CVI SiC/SiC composite 1 and of the MI SiC/SiC composite 3, but had little influence on the fatigue performance of the SiC/SiC composite 2 with the oxidation inhibited matrix. The retained tensile properties of all specimens that achieved fatigue run‐out were characterized. Composite microstructure, as well as damage and failure mechanisms were investigated.     

Unidirectional hemp and flax EP‐ and PP‐composites: Influence of defined fiber treatments

In some technical areas, mainly in the automotive industry, glass fiber reinforced polymers are intended to be replaced by natural fiber reinforced polymer systems. Therefore, higher requirements will be imposed to the physical fiber properties, fiber‐matrix adhesion, and the quality assurance. To improve the properties of epoxy resins (EP) and polypropylene (PP) composites, flax and hemp fibers were modified by mercerization and MAH‐PP coupling agent was used for preparing the PP composites. The effects of different mercerization parameters such as concentration of alkali (NaOH), temperature, and duration time along with tensile stress applied to the fibers on the structure and properties of hemp fibers were studied and judged via the cellulose I–II lattice conversion. It was observed that the mechanical properties of the fibers can be controlled in a broad range by using appropriate mercerization parameters. Unidirectional EP composites were manufactured by the filament winding technique; at the PP matrix material, a combination with a film‐stacking technique was used. The influence of mercerization parameters on the properties of EP composites was studied with hemp yarn as an example. Different macromechanical effects are shown at hemp‐ and flax‐PP model composites with mercerized, MAH‐PP‐treated, or MAH‐PP‐treated mercerized yarns. The composites' properties were verified by tensile and flexural tests. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2150–2156, 2004     

Long jute fiber‐reinforced polypropylene composite: Effects of jute fiber bundle and glass fiber hybridization

Two types of long jute fiber pellet consisting of twisted‐jute yarn (LFT‐JF/PP) and untwisted‐jute yarn (UT‐JF/PP) pellets are used to prepare jute fiber–reinforced polypropylene (JF/PP) composites. The mechanical properties of both long fiber composites are compared with that of re‐pelletized pellet (RP‐JF/PP) of LFT‐JF/PP pellet, which is re‐compounded by extrusion compounding. High stiffness and high impact strength of JF/PP composites are as a result of using long fiber. However, the longer fiber bundle consequently affects the distribution of jute fiber. The incorporation of 10 wt % glass fibers is found to improve mechanical properties of JF/PP composites. Increasing mechanical properties of hybrid composites is dependent on the type of JF/PP pellets, which directly affect the fiber length and fiber orientation of glass fiber within hybrid composites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41819.     

Preparation and performance characteristics of short‐glass‐fiber/maleated styrene–ethylene–butylene–styrene/polypropylene hybrid composites

Eighty/twenty polypropylene (PP)/styrene–ethylene–butylene–styrene (SEBS) and 80/20 PP/maleated styrene–ethylene–butylene–styrene (SEBS‐g‐MA) blends reinforced with 30 wt % short glass fibers (SGFs) were prepared by extrusion and subsequent injection molding. The influence of the maleic anhydride (MA) functional group grafted to SEBS on the properties of SGF/SEBS/PP hybrid composites was studied. Tensile and impact tests showed that the SEBS‐g‐MA copolymer improved the yield strength and impact toughness of the hybrid composites. Extensive plastic deformation occurred at the matrix interface layer next to the fibers of the SGF/SEBS‐g‐MA/PP composites during impact testing. This was attributed to the MA functional group, which enhanced the adhesion between SEBS and SGF. Differential scanning calorimetry measurements indicated that SEBS promoted the crystallization of PP spherulites by acting as active nucleation sites. However, the MA functional group grafted to SEBS retarded the crystallization of PP. Finally, polarized optical microscopy observations confirmed the absence of transcrystallinity at the glass‐fiber surfaces of both SGF/SEBS/PP and SGF/SEBS‐g‐MA/PP hybrid composites. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1303–1311, 2002     

Process–structure–property relationship in ternary short‐glass‐fiber/elastomer/polypropylene composites

Short‐glass‐fiber (SGF)‐reinforced polypropylene (PP) composites toughened with a styrene/ethylene butylene/styrene (SEBS) triblock copolymer were injection molded after extrusion. Furthermore, a maleic anhydride (MA)‐grafted SEBS copolymer (SEBS‐g‐MA) was used as an impact modifier and compatibilizer. The effects of the processing conditions and compatibilizer on the microstructure and tensile and impact performance of the hybrid composites were investigated. In the route 1 fabrication process, SGF, PP, and SEBS were blended in an extruder twice, and this was followed by injection molding. In route 2, or the sequential blending process, the elastomer and PP were mixed thoroughly before the addition of SGF. In other words, either PP and SEBS or PP and SEBS‐g‐MA pellets were premixed in an extruder. The produced pellets were then blended with SGF in the extruder, and this was followed by injection molding. The SGF/SEBS‐g‐MA/PP hybrid fabricated by the route 2 process exhibited the highest modulus, yield stress, tensile stress at break, Izod impact energy, and Charpy drop weight impact strength among the composites investigated. This was due to the formation of a homogeneous SEBS elastomeric interlayer at the SGF and matrix interface of the SGF/SEBS‐g‐MA/PP hybrid. This SEBS rubbery layer enhanced the interfacial bonding between SGF and the matrix of the SGF/SEBS‐g‐MA/PP hybrid. The correlations between the processing, microstructure, and properties of the hybrids were investigated. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1384–1392, 2003     

玻纤毡增强聚丙烯复合材料的增容及力学性能

通过玻璃纤维(GF)毡与双螺杆挤出相容剂改性聚丙烯(PP)膜的多层叠合,以熔融浸渍法制得PP基GF毡增强热塑性塑料(GMT)复合材料,研究了相容剂PP接枝马来酸酐(PP-g-MAH)和PP接枝丙烯酸(PP-g-AA)的用量(为PP基体质量的百分数)及其复配改性,以及相容剂改性PP基体分布和毡体种类对GMT力学性能的影响。结果表明,PPg-MAH可明显提高GMT的拉伸与弯曲性能,但降低了冲击性能;PP-g-AA可明显提高GMT的冲击性能,但不利于拉伸与弯曲性能的提高,只有当PP-g-AA用量超过5%后,拉伸性能才有所提升。在PP-g-MAH用量为3%的条件下,将其与不同用量的PP-g-AA进行复配改性没有对GMT力学性能产生协同作用。在各相容剂用量相近(3%~3.5%)的情况下,与相容剂复配改性GMT相比,以两层PP-g-AA改性PP为芯层、PP-g-MAH改性PP为上下表面层作为改性基体分布时,GMT拉伸与弯曲强度分别提高17%和27%、缺口冲击强度提高48%;而以两层PP-g-MAH改性PP为芯层、PP-g-AA改性PP为上下表面层作为改性基体分布时,在不损失强度与刚性的同时,缺口冲击强度提高了88%。采用连续GF毡的GMT力学性能比采用短切GF毡的GMT高,尤其是缺口冲击强度提高了89.6%。     

Preparation and mechanical properties of high‐performance short ramie fiber‐reinforced polypropylene composites

Short ramie fiber (RF) was used to reinforce the polypropylene (PP). The composites were prepared in a twin‐screw extruder followed by injection molding. The experimental results showed that both the strength and the modulus of the composites increase considerably with increasing RF content. The tensile strength and flexural strength are as high as 67 and 80 MPa by the incorporation of ramie up to 30 wt %. To the best of our knowledge, this is one of the best results for short natural fiber‐reinforced PP composites. However, the preparation method in this study is more simple and economic. This short RF‐reinforced PP composites extend the application field for short‐nature fiber‐reinforced PP composites. Morphological analysis revealed that it is the high aspect ratio of the fiber and good interfacial compatibility that result in the high performance of the composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Injection molding of long sisal fiber–reinforced polypropylene: Effects of compatibilizer concentration and viscosity on fiber adhesion and thermal degradation

A two‐step process was used to obtain long sisal fiber‐polypropylene (SF/PP)–reinforced thermoplastic composites, using maleic anhydride grafted polypropylene (MA‐g‐PP) as a compatibilizer. At a first stage, modified polypropylenes (mPP) were used for an extrusion impregnation process, for the preparation of composite pellets containing about 70 wt% of SF. SF/mPP pellets with a large aspect ratio were prepared by continuous extrusion impregnation of a continuous SF yarn, using a single screw extruder and an adequate impregnation die. The mPP used were MA‐g‐PP and regular polypropylene (PP), modified by reaction with different amounts of an organic peroxide. The composite pellets were thus dry blended with regular PP pellets in an injection machine hopper, and injection molded to obtain composite tensile specimens with a minimum quantity of modified polypropylene, minimum fiber breakage and thermal degradation, and excellent mechanical properties. It is shown that the fiber breakage is reduced to a minimum, even for recycled composites, due to the presence of the low‐viscosity polymer layer wetting the SF fibers. The bulk composite effective viscosity and the fiber breakage extent and thermal degradation during the injection‐molding step are found to be closely related. Blending with much less expensive mPP at the impregnation stage optimizes the amount of expensive MA‐g‐PP. POLYM. ENG. SCI., 45:613–621, 2005. © 2005 Society of Plastics Engineers     

Impact toughness,viscoelastic behavior,and morphology of polypropylene–jute–viscose hybrid composites

In this investigation, we studied the impact toughness and viscoelastic behavior of polypropylene (PP)–jute composites. In this study, we used viscose fiber as an impact modifier and maleated PP as a compatibilizer. The toughness of the composites was studied with conventional Charpy and instrumental falling‐weight impact tests. The composites’ viscoelastic properties were studied with dynamic mechanical analysis. The results show that the incorporation of viscose fibers improved the impact strength and toughness to 134 and 65% compared to those of the PP–jute composites. The tan δ peak amplitude also increased with the addition of the impact modifier and indicated a greater degree of molecular mobility. The thermal stability of the composites was evaluated with thermogravimetric analysis. The addition of 2 wt % maleated polypropylene (MAPP) to the impact‐modified composite improved the impact strength and toughness to 144 and 93%, respectively. The fiber–matrix morphology of the fracture surface and the Fourier transform infrared spectra were also studied to ascertain the existence of the type of interfacial bonds. Microstructural analysis showed the retention of viscose fibers in the composites compared to the more separated jute fibers. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42981.     

Development and physico‐mechanical behavior of LDPE–sisal prepreg‐based composites

Low‐density polyethylene (LDPE)‐coated sisal fiber prepreg was prepared by using solution coating process. These coated fiber prepregs were consolidated to make composites having different weight fraction of sisal fibers in a hot compression‐molding machine. This experimental study reveals that higher loading of sisal fiber up to 57wt% in LDPE–sisal composites is possible by this technique. Mechanical and abrasive wear characteristics of these composites were determined. The tensile strength of composites increased with the increase in sisal fiber concentration. Coating thickness of LDPE was varied by changing the viscosity of LDPE–xylene solution that manifested to different weight fraction of fiber in sisal–LDPE composites. Mechanical, dynamic mechanical, and abrasive wear characteristics of these composites were determined. The tensile strength and modulus of sisal composites reached to 17.4 and 265 MPa, respectively, as compared to 7.1 and 33MPa of LDPE. Storage modulus of sisal composites LD57 reached to 2.7 × 10⁹ MPa at 40°C as compared to 8.1 × 10⁸ MPa of LDPE. Abrasive wear properties of LDPE and its composites were determined under multi‐pass mode; pure LDPE showed minimum specific wear rate. The specific wear rate of composites decreased with the sliding distance. Increase of coated sisal fiber content increased the specific wear rate at all the sliding distances, which has been explained on the basis of worn surface microstructures observed by using SEM. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Processing–formulation–performance relationships of polypropylene/short flax fiber composites

This work is a comprehensive study of the effect of extrusion process parameters and formulation on the properties of polypropylene (PP)/short flax fiber composites. The parameters that were varied during the twin‐screw extrusion process were screw configuration, revolutions per minute (rpm), extrusion temperature, and flow rate. The effect of the feeding zone location of cellulosic fiber was also considered. This study investigates the effect of the formulation, cellulosic fiber content, the presence of a coupling agent, and of a reactive additive on composite performance. The composites were characterized in terms of morphology and microstructure, fiber length, rheological, thermal, and mechanical properties. Sensibility to humidity and recyclability were also considered. When compared with as‐received PP, the tensile strength of injection‐molded parts increased with cellulosic content by up to 40 vol %, and the tensile modulus increased 3.5 times when a combination of coupling and reactive agents was used. Exposed to controlled humidity of 50% during 1 year, these composites exhibited a very low level of humidity uptake around 0.85 wt %. The processability of these materials using a cast film line and the mechanical properties of extruded sheets are also presented. Furthermore, these materials demonstrate a good recyclability using injection molding by keeping the integrality of their mechanical properties after five reprocessing cycles. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41528.     

Effect of coupling agents on the thermal and mechanical properties of polypropylene–jute fabric composites

Composites with different jute fabric contents and polypropylene (PP) were prepared by compression molding. The composite tensile modulus increased as the fiber content increased, although the strain at break decreased due to the restriction imposed on the deformation of the matrix by the rigid fibers. Moreover, and despite the chemical incompatibility between the polar fiber and the PP matrix, the tensile strength increased with jute content because of the use of long woven fibers. The interfacial adhesion between jute and PP was improved by the addition of different commercial maleated polypropylenes to the neat PP matrix. The effect of these coupling agents on the interface properties was inferred from the resulting composite mechanical properties. Out‐of‐plane instrumented falling weight impact tests showed that compatibilized composites had lower propagation energy than uncompatibilized ones, which was a clear indication that the adhesion between matrix and fibers was better in the former case since fewer mechanisms of energy propagation were activated. These results are in agreement with those found in tensile tests, inasmuch as the compatibilized composites exhibit the highest tensile strength. Scanning electron microscopy also revealed that the compatibilized composites exhibited less fiber pullout and smoother fiber surface than uncompatibilized ones. The thermal behavior of PP–compatibilizer blends was also analyzed using differential scanning calorimetry, to confirm that the improvements in the mechanical properties were the result of the improved adhesion between both faces and not due to changes in the crystallinity of the matrix. Copyright © 2006 Society of Chemical Industry     

Mechanical,thermal, and morphological properties of maleic anhydride‐g‐polypropylene compatibilized and chemically modified banana‐fiber‐reinforced polypropylene composites

Composites were prepared with chemically modified banana fibers in polypropylene (PP). The effects of 40‐mm fiber loading and resin modification on the physical, mechanical, thermal, and morphological properties of the composites were evaluated with scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Infrared (IR) spectroscopy, and so on. Maleic anhydride grafted polypropylene (MA‐g‐PP) compatibilizer was used to improve the fiber‐matrix adhesion. SEM studies carried out on fractured specimens indicated poor dispersion in the unmodified fiber composites and improved adhesion and uniform dispersion in the treated composites. A fiber loading of 15 vol % in the treated composites was optimum, with maximum mechanical properties and thermal stability evident. The composite with 5% MA‐g‐PP concentration at a 15% fiber volume showed an 80% increase in impact strength, a 48% increase in flexural strength, a 125% increase in flexural modulus, a 33% increase in tensile strength, and an 82% increase in tensile modulus, whereas the heat deflection temperature increased by 18°C. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Quiescent crystallization of natural fibers–polypropylene composites

The effect of natural fibers (vetiver grass and rossells) on quiescent crystallization of polypropylene (PP) composites was analyzed in this study. Also, equilibrium melting temperature (T) of the composites was elucidated. Natural fiber‐PP composites showed lower T when compared to neat PP. Thermal analysis was performed via differential scanning calorimeter to study the crystallization kinetics. Natural fiber‐PP composites exhibited higher rate of crystallization than that of neat PP. Furthermore, spherulitic growth rate and transcrystallinity of the composites were investigated under a polarized light optical microscope. It was found that the growth rates of the composites were lower than that of neat PP. The spherulitic growth rates combined with the crystallization rates were used to calculate number of effective nuclei. It was shown that the number of effective nuclei of the composites was higher than that of neat PP. This suggested that natural fibers could act as a nucleating agent in the composite. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Experimental investigation of the influence of the compounding process and the composite composition on the mechanical properties of a short flax fiber–reinforced polypropylene composite

Polypropylene (PP) composites containing 20 wt% short flax fibers are prepared, and the process parameters such as throughput, rotational speed, and screw configuration are varied during melt compounding with a corotating intermeshing twin‐screw extruder. The investigations reveal that low rotational speeds, high throughputs, and moderate shear energy inputs by the screw configuration led to an optimum set of mechanical properties. To investigate the influence of different composite compositions on the mechanical properties, composites with fiber contents between 0 and 40 wt% and maleic anhydride‐grafted PP (PP‐g‐MA) contents between 0 and 7 wt% are prepared. Increasing fiber contents enhance the Young's modulus and decrease the elongation at break and the notched impact strength. The tensile strength is barely affected. The addition of PP‐g‐MA increases the tensile strength as well as the elongation at break, whereas the Young's modulus is not influenced. Thus, PP‐g‐MA enhances the adhesion between PP and flax fibers significantly. POLYM. COMPOS., 36:2282–2290, 2015. © 2014 Society of Plastics Engineers     

Effects of the chemical foaming agents,injection parameters,and melt‐flow index on the microstructure and mechanical properties of microcellular injection‐molded wood‐fiber/polypropylene composites

Wood‐fiber‐reinforced plastic profiles are growing rapidly in nonstructural wood‐replacement applications. Most manufacturers are evaluating new alternative foamed composites, which are lighter and more like wood. Foamed wood composites accept screws and nails better than their nonfoamed counterparts, and they have other advantages as well. For example, internal pressures created by foaming give better surface definition and sharper contours and corners than nonfoamed profiles have. In this study, the microfoaming of polypropylene (PP) containing hardwood fiber was performed with an injection‐molding process. The effects of different chemical foaming agents (endothermic, exothermic, and endothermic/exothermic), injection parameters (the mold temperature, front flow speed, and filling quantity), and different types of PP (different melt‐flow indices) on the density, microvoid content, physicomechanical properties, surface roughness, and microcell classification of microfoamed PP/wood‐fiber composites were studied. A maleic anhydride/polypropylene copolymer (MAH‐PP) compatibilizer was used with the intention of improving the mechanical properties of microfoamed composites. The microcell classification (from light microscopy) and scanning electron micrographs showed that an exothermic chemical foaming agent produced the best performance with respect to the cell size, diameter, and distance. The polymer melt‐flow index and the variation of the injection parameters affected the properties and microstructure of the microfoamed composites. The density of the microfoamed hardwood‐fiber/PP (with a high melt‐flow index) composites was reduced by approximately 30% and decreased to 0.718 g/cm³ with an exothermic chemical foaming agent. Tensile and flexural tests were performed on the foamed composites to determine the dependence of the mechanical properties on the density and microvoid content of the foamed specimens, and these properties were compared with those of nonfoamed composites. MAH‐PP improved the physicomechanical properties up to 80%. With an increase in the mold temperature (80–110°C), the surface roughness was reduced by nearly 70% for the foamed composites. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1090–1096, 2005     

Poly(propylene)–poly(propylene)‐grafted maleic anhydride–organic montmorillonite (PP–PP‐g‐MAH–Org‐MMT) nanocomposites. II. Nonisothermal crystallization kinetics

The nonisothermal crystallization kinetics of poly(propylene) (PP), PP–organic‐montmorillonite (Org‐MMT) composite, and PP–PP‐grafted maleic anhydride (PP‐g‐MAH)–Org‐MMT nanocomposites were investigated by differential scanning calorimetry (DSC) at various cooling rates. Avrami analysis modified by Jeziorny and a method developed by Mo well‐described the nonisothermal crystallization process of these samples. The difference in the exponent n between PP and composite (either PP–Org‐MMT or PP–PP‐g‐MAH–Org‐MMT) indicated that nonisothermal kinetic crystallization corresponded to tridimensional growth with heterogeneous nucleation. The values of half‐time, Z_c; and F(T) showed that the crystallization rate increased with the increasing of cooling rates for PP and composites, but the crystallization rate of composites was faster than that of PP at a given cooling rate. The method developed by Ozawa can also be applied to describe the nonisothermal crystallization process of PP, but did not describe that of composites. Moreover, the method proposed by Kissinger was used to evaluate the activation energy of the mentioned samples. The results showed that the activation energy of PP–Org‐MMT was much greater than that of PP, but the activation energy of PP–PP‐g‐MAH–Org‐MMT was close to that of pure PP. Overall, the results indicate that the addition of Org‐MMT and PP‐g‐MAH may accelerate the overall nonisothermal crystallization process of PP. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 3093–3099, 2003     

PP-g-MAH预浸渍玻璃纤维毡对GMT界面改性的作用

采用含有马来酸酐接枝聚丙烯(PP–g–MAH,简称MPP)的聚丙烯(PP)树脂对玻璃纤维(GF)毡预浸渍,进行增强体改性,通过直接浸渍工艺、增强体预浸渍工艺、累加浸渍工艺等不同工艺制备GF毡增强PP热塑性复合材料(GMT)。对不同工艺制备的GMT界面形态进行了扫描电子显微镜分析,并测定了预浸渍处理后GF的疏水性,研究了预浸渍工艺中MPP的用量对GMT拉伸、弯曲、冲击等力学性能的影响。结果表明:采用含MPP的PP树脂进行增强体预浸渍改性的方法,改性树脂对GF的包覆效果良好,经预浸渍改性法处理的GF,其疏水性增强;并可以获得与PP/MPP改性树脂直接浸渍GF毡时相似的界面改性效果和相近的GMT力学性能;样品界面改性效果相近的情况下,增强体预浸渍改性方法所需的MPP用量明显少于改性树脂直接浸渍时的用量。     

Elektrophoretische Abscheidung zur Herstellung von faserverstärkten Keramik‐ und Glasmatrix‐Verbundwerkstoffen — Eine Übersicht

In this paper, we review the application of the electrophoretic deposition (EPD) technique in the fabrication of fibre reinforced composites, with particular emphasis on composites with glass and ceramic matrices containing metallic or ceramic fibre fabric reinforcement. The review covers research published in the last 10 years. EPD has been used to infiltrate preforms with tight fibre weave architectures using different nano‐sized ceramic particles, including silica and boehmite sols, as well as dual‐component sols of mullite composition. The principles of the EPD technique are briefly explained and various factors affecting the EPD behaviour of ceramic sols and their optimisation to obtain high infiltration of the fibre preforms are considered. Overall, the analysis of the published data and our own results demonstrate that EPD, being simple and inexpensive, provides an attractive alternative for ceramic infiltration and coating of fiber fabrics, even if they exhibit tight fibre weave architectures.