Investigation of combined stress state failure criterion for glass fiber/epoxy interface by the cruciform specimen method

The interfacial failure criterion under combined stress state in a glass fiber/epoxy composite is investigated by the cruciform specimen method. Experiments were conducted by using specimens with a fiber whose angle from the loading direction is varied in order to make various stress state of normal and shear at the interface. Finite element analysis is performed to calculate the interfacial stress distribution. By combining the experimental measurement of the specimen stress at the interfacial debonding initiation and the finite element stress analysis, it is possible to obtain the interfacial stress state at interfacial failure. A method to determine the interfacial failure criterion and the interfacial failure initiation location simultaneously is proposed in the present study. We conclude the value of the interfacial shear strength is higher than that of the interfacial normal strength for the material system used in the present study.     

Interconnected multi-walled carbon nanotubes reinforced polymer-matrix composites

A modified method for interconnecting multi-walled carbon nanotubes (MWCNTs) was put forward. And interconnected MWCNTs by reaction of acyl chloride and amino groups were obtained. Scanning electron microscopy shows that hetero-junctions of MWCNTs with different morphologies were formed. Then specimens of pristine MWCNTs, chemically functionalized MWCNTs and interconnected MWCNTs reinforced epoxy resin composites were fabricated by cast moulding. Tensile properties and fracture surfaces of the specimens were investigated. The results show that, compared with pristine MWCNTs and chemically functionalized MWCNTs, the chemically interconnected MWCNTs improved the fracture strain and therefore the toughness of the composites significantly.     

Effect of oxygen plasma treatment of PPTA and PBO fibers on the interfacial properties of single fiber/epoxy composites studied by Raman spectroscopy

The interfacial micromechanics of single poly(p-phenylene terephthalamide (PPTA) and poly(p-phenylene benzobisoxazole (PBO) fibers embedded in an epoxy resin has been investigated by determining the interfacial shear stress distributions along the fiber length. The effects of an oxygen plasma treatment on the interfacial shear stress of the fiber-epoxy systems are analyzed. Raman spectroscopy was used to map the stress distributions along the fiber when the composite is subjected to a small axial tensile strain (3.5% for PPTA and 2.5% for PBO). The quality of the interface or adhesion was improved after the surface treatment, supporting the ability of plasma oxidation to enhance the adhesion of high-performance fibers to epoxy resins. The tensile behavior of fiber-reinforced systems was different in each case. PPTA reinforcements underwent fragmentation, likely by fiber microfailure, whereas debonding or bridging is the most probable fragmentation mechanism in the case of PBO.     

Influence of the interphase zone on the nanoparticle debonding stress

One of the most appealing features concerned with nanomodification of polymeric resins for structural applications is the perspective of obtaining high toughness even at low nanofiller volume fractions. Such performances are related to the energy dissipated through the damage mechanisms taking place at the nanoscale. Among these, nanoparticle debonding could take an important role either as a mechanism itself or as a trigger for phenomena like plastic void growth or matrix shear yielding. In the present work, a model for the hydrostatic tension related to debonding is presented. The model accounts for some important issues inherently related to the nanoscale with particular reference to the emergence of an interphase surrounding the nanoparticle. Results can be useful in view of a multi-scale modelling of the problem.     

Study on interfacial adhesion strength of single glass fibre/polypropylene model composites by altering the nature of the surface of sized glass fibres

Polypropylene (PP) compatibly sized glass fibres (GFs) were treated with boiling water and toluene, respectively, to reveal the interactions of water and toluene with different components in the sizing of sized GF and their influences on the interfacial adhesion strength of GF/PP model composites. Compared to control GF/PP model composites, about 30% increase of interfacial adhesion strength was achieved for composites with water-treated GF, whereas a small decrease of interfacial adhesion strength was revealed for composites with toluene-treated GF. X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Zeta-potential measurement, and water contact angle measurement demonstrated that the boiling water-treated GFs posses a more polar and hydrophilic surface with homogeneously distributed derivatives of 3-aminopropyltriethoxysilane, which is related to a higher interfacial adhesion strength for water-treated GF/PP model composites. In contrast, hot toluene-treated GFs led to a more hydrophobic surface with low molar mass PP and surfactants enriching on the outermost surface.     

Interfacial shear strength of a glass fiber/epoxy bonding in composites modified with carbon nanotubes

In recent years, carbon nanotubes (CNTs) grown on fibers have attracted a lot of interest as an additional reinforcing component in conventional fiber-reinforced composites to improve the properties of the fiber/matrix interface. Due to harsh growth conditions, the CNT-grafted fibers often exhibit degraded tensile properties. In the current study we explore an alternative approach to deliver CNTs to the fiber surface by dispersing CNTs in the fiber sizing formulation. This route takes advantage of the developed techniques for CNT dispersion in resins and introduces no damage to the fibers. We focus on unidirectional glass fiber/epoxy macro-composites where CNTs are introduced in three ways: (1) in the fiber sizing, (2) in the matrix and (3) in the fiber sizing and matrix simultaneously. Interfacial shear strength (IFSS) is investigated using single-fiber push-out microindentation. The results of the test reveal an increase of IFSS in all three cases. The maximum gain (over 90%) is achieved in the composite where CNTs are introduced solely in the fiber sizing.     

Effect of interface debonding on the thermal conductivity of microencapsulated-paraffin filled epoxy matrix composites

Microcapsules containing phase change materials (microPCMs) can be filled in polymeric matrix forming smart temperature-controlling composites. The aim of this study was to investigate the effect of interface debonding on the thermal conductivity of microPCMs containing paraffin/epoxy composites. The shell thickness and average size of microPCMs were controlled by regulating the core/shell ratios and emulsion stirring rates. Test results indicated that the thermal conductivity (K_e) of all composites decreased after a thermal shock treatment. SEM and thermography measurements were applied to observe the interface behaviors of composites after a violent thermal treatment process. It was proved that the interface debonding was generated because of the mismatch of expansion coefficient between shell and epoxy. A modeling analysis of the relative thermal conductivity (K_r) indicated that the effective approach to decrease the debonding is to enhance the molecule tangling degree between shell and matrix.     

Modification of surface functionality of multi-walled carbon nanotubes on fracture toughness of basalt fiber-reinforced composites

In this work, we studied the influence of surface functionality of multi-walled carbon nanotubes (MWCNTs) on the mechanical properties of basalt fiber-reinforced composites. Acid and base values of the MWCNTs were determined by Boehm's titration technique. The surface properties of the MWCNTs were determined FT-IR, and XPS. The mechanical properties of the composites were assessed by measuring the interlaminar shear stress, fracture toughness, fracture energy, and impact strength. The chemical treatments led to a change of the surface characteristics of the MWCNTs and of the mechanical interfacial properties of MWCNTs/basalt fibers/epoxy composites. Especially the acid-treated MWCNTs/basalt fibers/epoxy composites had improved mechanical properties compared to the base-treated and non-treated MWCNTs/basalt fibers/epoxy composites. These results can probably be attributed to the improved interfacial bonding strength resulting from the improved dispersion and interfacial adhesion between the epoxy resin and the MWCNTs.     

Influence of hard segment content and nature on polyurethane/multiwalled carbon nanotube composites

Knowledge of how polyurethanes, PU, complexity affects their derived multiwalled carbon nanotube, MWCNT, composites could shed important clues for preparing future tailored PU/MWCNT elastic, strong and electrically conductive composites. In this regard, hard segment content and nature, along with MWCNT functionalisation, are believed to have great influence on both nanoscale PU/MWCNT self assembling mechanisms and on final composites properties. In this work the effect of PU hard segment content into composites was analysed. According to the results, a preferential interaction of nanotubes with polyurethanes hard segments can be assumed although nanotubes introduction hindered both soft and hard segments crystallisation. In all cases carbon nanotubes percolative network formation seemed to be crucial for obtaining significant reinforcement, being observed at this stage, a reduction of ductility, phenomena which is related to an increase on hard domains interconnections by MWCNT. The hard to soft segment ratio into PU plays a crucial role on determining the stress transfer to MWCNT. In addition, PU hard domains nature has important effect on nanotubes reinforcing character, this fact being related to the different PU intrinsic morphologies as well as different PU-MWCNT interactions.     

Characterization of fibre/matrix interfaces in carbon/carbon composites

The present paper proposes an approach to characterizing fibre/matrix (F/M) interface in carbon/carbon (C/C) composites with respect to both modes of loading that may be expected: opening or shearing. Push-out and tensile tests were used. The former tests involve the shearing mode whereas the latter ones involve the opening one. Push-out tests use a diamond indenter to load the fibres. The interface sliding shear stress was obtained from the load-fibre displacement curve. The tensile tests were conducted on specimens having fibres oriented at 90° with respect to loading direction in order to preferentially open the interfaces. Interface opening strength was extracted from the composite tensile stress–strain behaviour. The specimens were examined under load and after ultimate failure by optical microscopy (OM). The mechanical properties of the F/M interfaces were then discussed.     

Effect of pectin and hemicellulose removal from hemp fibres on the mechanical properties of unidirectional hemp/epoxy composites

The objective of this study was to investigate the effect of pectin and hemicellulose removal from hemp fibres on the mechanical properties of hemp fibre/epoxy composites. Pectin removal by EDTA and endo-polygalacturonase (EPG) removed epidermal and parenchyma cells from hemp fibres and improved fibre separation. Hemicellulose removal by NaOH further improved fibre surface cleanliness. Removal of epidermal and parenchyma cells combined with improved fibre separation decreased composite porosity factor. As a result, pectin removal increased composite stiffness and ultimate tensile strength (UTS). Hemicellulose removal increased composite stiffness, but decreased composite UTS due to removal of xyloglucans. In comparison of all fibre treatments, composites with 0.5% EDTA + 0.2% EPG treated fibres had the highest tensile strength of 327 MPa at fibre volume content of 50%. Composites with 0.5% EDTA + 0.2% EPG → 10% NaOH treated fibres had the highest stiffness of 43 GPa and the lowest porosity factor of 0.04.     

Fracture toughness and creep performance of PMMA composites containing micro and nanosized carbon filaments

Chopped carbon fiber (CCF), multiwall carbon nanotubes (MWCNTs) and carbon nanofibers (CNFs) were introduced to polymethylmethacrylate (PMMA) via melt compounding. Fracture toughness and creep performance of these composites are presented. A constant volume concentration of 1 vol.% was used. Dispersion was evaluated on both micro- and nano-scales. Flexural modulus was also measured.     

Experimental characterization of thermo-oxidation-induced shrinkage and damage in polymer-matrix composites

This paper focuses on the experimental characterization of thermo-oxidation in carbon-fiber-reinforced polymers (CFRPs) exposed to “high” temperatures (up to 150 °C) and “high” oxygen pressures (up to 5 bars), at the microscopic scale. Unidirectional IM7/977-2 composite specimens were aged at 150 °C under atmospheric air and under oxygen pressure (1.7 bars and 5 bars): periodic tests were carried out to characterize degradation phenomena after different aging times. The thermo-oxidation-induced resin shrinkage and fiber/matrix debonding were measured on the CFRP sample surface by confocal interferometric microscopy (CIM) and scanning electron microscopy (SEM). The results show that thermo-oxidation-induced degradation strongly depends on aging time, distance between fibers and partial oxygen pressure.     

Interface damage study of hydrothermally aged glass-fibre-reinforced polyester composites

Two types of glass-fibre-reinforced polyester composites have been immersed in water at different temperatures (from 30 to 100°C) and subjected to gravimetric analysis, mechanical tests, and microscopic observations. Three types of damage have been identified: osmotic cracking in the matrix, at the interphase and interfacial debonding. It is suggested that matrix osmotic cracking is responsible for weight loss. The decrease of interlaminar shear strength (ILSS) is explained mainly by interfacial debonding, induced by differential swelling, and by osmotic cracking at the interphase but the matrix also contributes to the decrease. In summary, composite lifetime is greatly dependent on the ability of the matrix to microcrack under the service conditions.     

NaBF4 as a hygrothermal durability enhancer for glass fibre reinforced polypropylene composites

The long term performance of composite materials is highly desired for their expanding application range. Tuning the interphase properties has been proven to be a practical way to enhance the performance of composites. In this study, short glass fibre (GF) reinforced polypropylenes (PPs) with improved hygrothermal durability were obtained by incorporating NaBF₄ into the sizing and thus the interphases of GF/PP composites. Detailed investigations were performed on the surface properties of sized GFs and the mechanical properties of virgin and aged composites. It was found that the retention in both ultimate tensile strength and Charpy impact toughness of aged composites monotonically increased with increasing NaBF₄ content. The improvement in hygrothermal durability was related to the enhanced fibre/matrix adhesion strength induced by the presence of NaBF₄ as indentified by fracture surface analysis using field-emission scanning electron microscopy and single fibre pull-out test.     

Thermal and mechanical properties of phenolic-based composites reinforced by carbon fibres and multiwall carbon nanotubes

The thermal, mechanical and ablation properties of carbon fibre/phenolic composites filled with multiwall carbon nanotubes (MWCNTs) were investigated. Carbon fibre/phenolic/MWCNTs were prepared using different weight percentage of MWCNTs by compression moulding. The samples were characterized by scanning electron microscopy (SEM), flexural tests, thermal gravimetric analysis and oxyacetylene torch tests. The thermal stability and flexural properties of the nanocomposites increased by increasing MWCNTs content (wt% ⩽1), but they decreased when the content of MWCNTs was 2 wt%. The linear and mass ablation rates of the nanocomposites after modified with 1 wt% MWCNTs decreased by about 80% and 52%, respectively. To investigate the material post-test microstructure, a morphological characterization was carried out using SEM. It was shown that the presence of MWCNTs in the composite led to the formation of a strong network char layer without any cracks or opening.     

Interfacial load transfer in carbon nanotube/ceramic microfiber hybrid polymer composites

Growing carbon nanotubes (CNTs) on the surface of fibers has the potential to modify fiber–matrix interfacial adhesion, enhance the composite delamination resistance, and possibly improve its toughness and any matrix-dominated elastic property as well. In the present work aligned CNTs were grown upon ceramic fibers (silica and alumina) by chemical vapor deposition (CVD) at temperatures of 650 °C and 750 °C. Continuously-monitored single fiber composite (SFC) fragmentation tests were performed on pristine as well as on CNT-grown fibers embedded in epoxy. The critical fragment length, fiber tensile strength at critical length, and interfacial shear strength were evaluated. Significant increases (up to 50%) are observed in the fiber tensile strength and in the interfacial adhesion (which was sometimes doubled) with all fiber types upon which CNTs are CVD-grown at 750 °C. We discuss the likely sources of these improvements as well as their implications.     

The poly(urethane-ionic liquid)/multi-walled carbon nanotubes composites

In the paper, a novel kind of imidazolium based poly(urethane-ionic liquid)/multi-walled carbon nanotubes (PUIL/MWCNT) composites was facilely prepared by uncovalent ways. The imidazolium based ionic liquid (IL) greatly improved the dispersion of pristine MWCNTs in PUIL by the π-cation interaction formed between the imidazolium cation and the π-electron of MWCNTs. The PUIL/MWCNT composites showed obviously increased modulus, glass transition temperature and tensile strength in comparison with PU/MWCNT composites. The thermal and mechanical properties of the PUIL/MWCNT composites presented significant increase with low load of the MWCNTs. It indicated the interactions between PUIL and MWCNTs played an important role to enhance the performances of the composites.     

Mixed resin and carbon fibres surface treatment for preparation of carbon fibres composites with good interfacial bonding strength

The objective of this work is to improve the interlaminar shear strength of composites by mixing epoxy resin and modifying carbon fibres. The effect of mixed resin matrix’s structure on carbon fibres composites was studied. Anodic oxidation treatment was used to modify the surface of carbon fibres. The tensile strength of multifilament and interlaminar shear strength of composites were investigated respectively. The morphologies of untreated and treated carbon fibres were characterized by scanning electron microscope and X-ray photoelectron spectroscopy. Surface analysis indicates that the amount of carbon fibres chemisorbed oxygen-containing groups, active carbon atom, the surface roughness, and wetting ability increases after treatment. The tensile strength of carbon fibres decreased little after treatment by anodic oxidation. The results show that the treated carbon fibres composites could possess excellent interfacial properties with mixed resins, and interlaminar shear strength of the composites is up to 85.41 MPa. The mechanism of mixed resins and treated carbon fibres to improve the interfacial property of composites is obtained.     

Increasing the through-thickness thermal conductivity of carbon fiber polymer-matrix composite by curing pressure increase and filler incorporation

The low through-thickness thermal conductivity limits heat dissipation from continuous carbon fiber polymer-matrix composites. This conductivity is increased by up to 60% by raising the curing pressure from 0.1 to 2.0 MPa and up to 33% by incorporation of a filler (?1.5 vol.%) at the interlaminar interface. The 7-μm-diameter 7-W/m K-thermal-conductivity continuous fiber volume fraction is increased by the curing pressure increase, but is essentially unaffected by filler incorporation. The thermal resistivity is dominated by the lamina resistivity (which is contributed substantially by the intralaminar fiber-fiber interfacial resistivity), with the interlaminar interface thermal resistivity being unexpectedly negligible. The lamina resistivity and intralaminar fiber-fiber interfacial resistivity are decreased by up to 56% by raising the curing pressure and up to 36% by filler incorporation. The curing pressure increase does not affect the effectiveness of 1-mm-long 10-μm-diameter 900-1000-W/m K-thermal-conductivity K-1100 carbon fiber or single-walled carbon nanotube (SWCNT) as fillers for enhancing the conductivity, but hinders the effectiveness of carbon black (CB, low-cost), which is less effective than K-1100 or SWCNT at the higher curing pressure, but is almost as effective as K-1100 and SWCNT at the lower curing pressure. The effectiveness for enhancing the flexural modulus/strength/ductility decreases in the order: SWCNT, CB, K-1100.