Geopolymer reinforced with E‐glass leno weaves

This study explores the viability of fiberglass‐geopolymer composites as an intermediate temperature structural ceramic composite. E‐glass fibers are cheap, readily available, resistant to heat, electricity and chemical attack. Geopolymers are refractory and can be processed at room temperature. However, pure geopolymers have low tensile strength and fracture toughness, as is typical of ceramics. In this work, tensile and flexure properties of metakaolin‐based sodium and potassium geopolymers reinforced with E‐glass leno weaves were measured and the data was analyzed by Weibull statistics. The average tensile and flexural strengths for sodium geopolymer reinforced with E‐glass leno weaves were 39.3 ± 7.2 MPa and 25.6 ± 4.8 MPa, respectively. For potassium geopolymer reinforced with E‐glass leno weaves, the average tensile and flexural strengths were 40.7 ± 9.9 MPa and 15.9 ± 4.0 MPa, respectively. The composites were heat treated for one hour at two temperatures, 300°C and 550°C and their flexure properties were studied at room temperatures. The average flexural strengths for sodium geopolymer reinforced with E‐glass leno weaves were reduced to 6.6 ± 1.0 MPa after heat treatment at 300°C, and 1.2 ± 0.3 MPa after heat treatment at 550°C, respectively. For potassium geopolymer reinforced with E‐glass leno weaves, the average flexural strengths were 6.1 ± 1.5 MPa and 1.3 ± 0.3 MPa after heat treatment at 300°C and 550°C, respectively. SEM and EDS were performed to observe the fiber‐matrix interface. XRD was done to check if the geopolymer was amorphous as expected.     

Mechanical properties of natural fiber hybrid composites based on renewable thermoset resins derived from soybean oil,for use in technical applications

Natural fiber composites are known to have lower mechanical properties than glass or carbon fiber reinforced composites. The hybrid natural fiber composites prepared in this study have relatively good mechanical properties. Different combinations of woven and non‐woven flax fibers were used. The stacking sequence of the fibers was in different orientations, such as 0°, +45°, and 90°. The composites manufactured had good mechanical properties. A tensile strength of about 119 MPa and Young's modulus of about 14 GPa was achieved, with flexural strength and modulus of about 201 MPa and 24 GPa, respectively. For the purposes of comparison, composites were made with a combination of woven fabrics and glass fibers. One ply of a glass fiber mat was sandwiched in the mid‐plane and this increased the tensile strength considerably to 168 MPa. Dynamic mechanical analysis was performed in order to determine the storage and loss modulus and the glass transition temperature of the composites. Microstructural analysis was done with scanning electron microscopy. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Curing behavior of dicyandiamide/epoxy resin system using different accelerators

Various amounts of dicyandiamide (Dicy), two grades of epoxy resins, i.e. Epiran 06 and Epikote 828, and three different accelerators including benzyl dimethyl amine (BDMA), 3-(4-chlorophenyl)-1,1-dimethyl urea (Monuron) and 2-methyl imidazole (Im) were used in curing of Dicy/epoxy resin system. Both of the used epoxy resins were based on diglycidyl ether of bisphenol A (DGEBA). The effects of type and concentration of accelerators on curing behavior were studied by differential scanning calorimetry (DSC) method in dynamic or non-isothermal mode. The optimum concentration of Dicy for curing of epoxy resins was obtained based on the glass transition temperature of the cured epoxy/Dicy formulations. The maximum glass transition temperature of 139 °C was obtained at the stoichiometric ratio of Dicy to epoxy of 0.65. The results showed that BDMA has a broader curing peak in DSC and starts the cure reaction earlier than the others. However, Monuron has a narrow curing reaction peak with good cure latency. The tensile properties of Dicy-cured Epiran 06 and Epikote 828 epoxy resins reinforced with chopped strand mat showed that these two epoxy resins have similar mechanical properties. For composites based on the Epiran 06 and Epikote 828 reinforced with 40 wt % glass chopped strand mat, tensile strength and modulus were 156 and 153.4 MPa and 11.6 and 12.4 GPa, respectively.     

Effect of interphase on mechanical properties and microstructures of 3D Cf/SiBCN composites at elevated temperatures

Interphase between the fibers and matrix plays a key role on the properties of fiber reinforced composites. In this work, the effect of interphase on mechanical properties and microstructures of 3D C_f/SiBCN composites at elevated temperatures was investigated. When PyC interphase is used, flexural strength and elastic modulus of the C_f/SiBCN composites decrease seriously at 1600°C (92 ± 15 MPa, 12 ± 2 GPa), compared with the properties at room temperature (371 ± 31 MPa, 31 ± 2 GPa). While, the flexural strength and elastic modulus of C_f/SiBCN composites with PyC/SiC multilayered interphase at 1600°C are as high as 330 ± 7 MPa and 30 ± 2 GPa, respectively, which are 97% and 73% of the values at room temperature (341 ± 20 MPa, 41 ± 2 GPa). To clarify the effect mechanism of the interphase on mechanical properties of the C_f/SiBCN composites at elevated temperature, interfacial bonding strength (IFBS) and microstructures of the composites were investigated in detail. It reveals that the PyC/SiC multilayered interphase can retard the SiBCN matrix degradation at elevated temperature, leading to the high strength retention of the composites at 1600°C.     

Amorphous self-glazed,chopped basalt fiber reinforced,geopolymer-based composites

Geopolymer composites reinforced with refractory, chopped basalt fibers, and low melting glass were fabricated and heat treated at higher temperatures. K₂O·Al₂O₃·4SiO₂·11H₂O was the stoichiometric composition of the potassium-based geopolymer which was produced from water glass (fumed silica, deionized water, potassium hydroxide), and metakaolin. Addition of low melting glass (T_m ~815°C) increased the flexure strength of the composites to ~5 MPa after heat treatment above 1000°C to 1200°C. A Weibull statistical analysis was performed exhibiting how the amorphous self-healing and self-glazing effect of the glass frit significantly improved the flexure strength of the geopolymer and ceramic composites after exposure for 1 hour to high temperatures. At 950-1000°C, the K-based geopolymer converted to primarily a crystalline leucite ceramic, but the basalt fiber remained intact, and the melted glass frit flowed out of the surface cracks and sealed them. 1150℃ was determined to be the optimum heat treatment temperature, as at ≤1200°C, the basalt fibers melt and the strength of the reinforcement in the composites is significantly reduced. The amorphous self-healing and amorphous self-glazing effects of the glass frit significantly improved the room temperature flexure strength of the heat-treated geopolymer and ceramic composites.     

In Situ Processing of Graphene/Leucite Nanocomposite Through Graphene Oxide/Geopolymer

Graphene/leucite nanocomposites (rGO/leucite) were prepared through in situ reduction of graphene oxide/geopolymer (rGO/KGP) composites. The effects of rGO on the microstructure and mechanical properties with respect to the geopolymer matrix after the high‐temperature treatment were investigated systematically. The results show that GO is first partially reduced in the geopolymeric solution and then completely under the post high‐temperature treatment. The rGO sheets undergo no interfacial reactions with the matrix even after thermal treatment. The rGO/geopolymer composites fully transform to rGO/leucite composites after being treated at 1000°C for 30 min in an argon atmosphere. Significant improvements in mechanical properties were achieved through rGO reinforcement giving flexural strength, elastic modulus, and fracture toughness of 91.1 MPa, 60.5 GPa, and 2.04 MPa·m^1/2, increased by 120%, 8%, and 1.5%, respectively, compared with the leucite matrix alone.     

Bone ash reinforced geopolymer composites

Potassium-based, geopolymer composites were made with BASF^® metakaolin and Mymensingh clay-derived metakaolin from Bangladesh. Since the natural Mymensingh clay contained 40 wt.% quartz, this same amount of quartz particulates was added to the BASF^® metakaolin to make a synthetic analog of the natural calcined clay. By analogy with bone china, bone ash or calcined hydroxyapatite (5CaO•3P₂O₅ or “HA”) particles, having a Ca: P ratio of 3.3:1, were added to make the three types of geopolymer-based composites described above. For less refractory particulate additions, dicalcium phosphate (DCP) (2CaO•P₂O₅ or “DCP”) particles, having a Ca: P ratio of 2:1, were also added to another set of geopolymers. The ambient temperature compressive and flexural strengths were measured for all of the geopolymer composites. The HA or DCP reinforced geopolymer composites were fabricated and heat-treated to 1150°C/1 h, after which they were converted to their mineralogical analogs. Their mechanical properties of compressive and 3-point flexural strengths were again measured. Flexural strengths of 22.42 ± 11.0 MPa and 31.97 ± 8.3 MPa were measured in 1 × 1 × 10 cm³ heat-treated geopolymer bars reinforced with 10 wt.% of DCP and in geopolymer reinforced with 10 wt.% DCP +40 wt.% quartz additions, respectively. Significant improvements to ambient temperature properties were observed due to the self-healing effect of the flowing amorphous DCP, whose presence was verified by SEM. The geopolymer samples exhibited reduced water absorption (WA) (on a percentage dry weight basis) of within 0.03-0.5% after being heated at 1100℃/1 h and 1125℃/1 h, as compared with those at room temperature, which varied between 2.56% and 7.89%.     

Potassium‐Based Geopolymer Composites Reinforced with Chopped Bamboo Fibers

Bamboo is a fast‐growing, readily available natural material with tensile specific strength equivalent to that of steel (250–625 MPa/g/cm³). In the pursuit of sustainable construction materials, a composite was made with potassium polysialate siloxo geopolymer as the matrix and randomly oriented chopped bamboo fibers (Guadua angustifolia) from the Amazon region as the reinforcement. Four‐point flexural strength testing of the geopolymer composite reinforced with bamboo fibers was carried out according to ASTM standard C78/C78M‐10^e1. Potassium‐based metakaolin geopolymer reinforced with 5 wt% (8 vol%) untreated bamboo fibers yielded 7.5 MPa four‐point flexural strength. Scanning electron microscopy and optical microscopy were used to investigate the microstructure. In addition, X‐ray diffraction was used to confirm the formation of geopolymer.     

Synthesis and mechanical properties of novel composites of inorganic polymers (geopolymers) with unidirectional natural flax fibres (phormium tenax)

This study reports the synthesis and mechanical properties of new inorganic polymer (geopolymer) composites unidirectionally reinforced with 4–10 vol.% natural cellulose-based fibres (NZ flax, phormium tenax). The geopolymer matrix was derived from dehydroxylated kaolinite-type clay. The mechanical properties of the fibre-reinforced composites improve with increasing fibre content, achieving ultimate flexural strengths of about 70 MPa at 10 vol.% fibre content. This represents a significant improvement on the flexural strength of the unreinforced geopolymer matrix (about 5.8 MPa), and all the composites show graceful failure, unlike the brittle failure of the matrix. Scanning electron microscopy was used to study the morphology of the fibre-matrix regions and a combination of thermogravimetric analysis (TGA) and thermal shrinkage measurements of these composites suggests that despite the formation of microcracks due to water loss from the geopolymer matrix, the fibres are thermally protected by the matrix up to 400 °C. The flax fibres do not appear to be compromised by the alkaline environment of the matrix, suggesting new possible applications for these low-cost simply prepared construction materials.     

In situ processing of MWCNTs/leucite composites through geopolymer precursor

A serial of multi-walled carbon nanotubes (MWCNTs) reinforced geopolymer composites were prepared, and then heated at elevated temperature to fabricate MWCNTs/leucite composites by in situ transformation. Effects of high-temperature treatment on the microstructure evolution and mechanical performance of the composites were investigated. The results indicated that the introduction of MWCNTs could improve the mechanical properties of geopolymer, and the optimum content was 3 wt%. The mechanical performance declined instead with the further increase in MWCNTs content up to 5 wt%, which could be attributed to the agglomeration of MWCNTs. Significant improvements in mechanical properties were achieved after the composites were treated in a temperature range from 950 °C to 1200 °C relative to their original state before heat treatment. The significant improvements could be described to the matrix densification, and leucite formation as well as the proper interface bonding state between carbon nanotube and leucite matrix.     

Amorphous self-healed,chopped basalt fiber-reinforced,geopolymer composites

Geopolymer composites containing refractory, chopped basalt fibers and low-melting glass were made and systematically heat-treated at higher temperatures. Potassium-based geopolymer of stoichiometric composition K₂O·Al₂O₃·4SiO₂·11H₂O was produced by high shear mixing from fumed silica, deionized water, potassium hydroxide, (i.e., water glass) and metakaolin. With the addition of low-melting glass (T_m ~815°C) the flexure strengths of the composites increased to ~6 MPa after heat treatment above 900°C to 1100°C. A Weibull statistical analysis was performed showing how the amorphous self-healing effect of the glass frit significantly improved the flexure strength of the geopolymer and ceramic composites after high-temperature exposure. At temperatures up to 900°C, the geopolymer-basalt composite remained amorphous and the low-melting glass frit flowed into the dehydration cracks in the geopolymer matrix. This type of composite could be described as amorphous self-healed geopolymer (ASH-G). At ~1000°C, the geopolymer converted to primarily a crystalline leucite ceramic, but the basalt fiber remained intact, and the melted glass frit flowed and sealed the cracks developed at that temperature. This type of composite could then be described as amorphous self-healed ceramic (ASH-C). A temperature of 1150°C was determined to be optimum as at 1200°C the basalt fibers melted and the strength of the reinforcement was lost in the composites. The amorphous self-healing effect of the glass frit significantly improved the room temperature flexure strength of the heat-treated geopolymer-based composites.     

Carbon‐Polymer Composite Bipolar Plate for HT‐PEMFC

Graphene reinforced carbon‐polymer composite bipolar plate is developed using resole phenol formaldehyde resin, and conductive reinforcements (natural graphite, carbon black, and carbon fiber) using compression molding technique. Graphene is reinforced into the composite to alter various properties of the composite bipolar plate. The developed composite bipolar plate is characterized and the effect of temperature on mechanical and electrical properties is investigated with an overall aim to achieve benchmark given by US‐DOE and Plug Power Inc. The flexural strength and electrical conductivity of the composites was almost stable with the increase in temperature upto 175 °C. The composite bipolar plate maintained high in‐plane and through‐plane electrical conductivities, which is about 409.23 and 98 S cm^–1, respectively, at 175 °C. The flexural strength and shore hardness of the developed composite was around 56.42 MPa and 60, respectively, at 175 °C, and on further increase in the temperature the mechanical strengths deceases sharply. The electrical and mechanical properties of the composite bipolar plates are within the US‐DoE target. However, the various properties of the composite bipolar plate could not be sustained above 175 °C.     

Biodegradable composites of poly(butylene succinate‐co‐butylene adipate) reinforced by poly(lactic acid) fibers

Biodegradable composites of poly(butylene succinate‐co‐butylene adipate) (PBSA) reinforced by poly(lactic acid) (PLA) fibers were developed by hot compression and characterized by Scanning electron microscopy (SEM), differential scanning calorimetry (DSC), dynamic mechanical analyzer, and tensile testing. The results show that PBSA and PLA are immiscible, but their interface can be improved by processing conditions. In particular, their interface and the resulting mechanical properties strongly depend on processing temperature. When the temperature is below 120 °C, the bound between PBSA and PLA fiber is weak, which results in lower tensile modulus and strength. When the processing temperature is higher (greater than 160 °C), the relaxation of polymer chain destroyed the molecular orientation microstructure of the PLA fiber, which results in weakening mechanical properties of the fiber then weakening reinforcement function. Both tensile modulus and strength of the composites increased significantly, in particular for the materials reinforced by long fiber. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43530.     

Thermoplastic composites based on poly(ethylene 2,6‐naphthalate) and basalt woven fabrics: Static and dynamic mechanical properties

Composites based on poly(ethylene 2,6‐naphthalate) and basalt woven fabrics have been investigated with the aim to develop composites with a minimum service temperature of 100°C. Laminates have been manufactured by using the film‐stacking technique. A very low void content and a good fabric impregnation has been obtained as confirmed by the morphological analysis performed with scanning electron microscopy. Static flexural modulus and strength have been measured at 20, 60, and 100°C and compared with the dynamic mechanical behavior, evaluated from −100 to 220°C. A very good agreement has been detected between static and dynamic tests, proving that the dynamic mechanical analysis can be used to estimate the flexural modulus in a wide temperature range. Poly(ethylene 2,6‐naphthalate)/basalt composites have exhibited (at 20°C) a flexural modulus and strength as high as 20 GPa and 320 MPa, respectively. The flexural modulus and the flexural strength at 100°C have been found to be equal to 18 GPa and 230 MPa, confirming that this system can retain very good mechanical properties at a service temperature of 100°C. POLYM. COMPOS., 37:2549–2556, 2016. © 2015 Society of Plastics Engineers     

Fully reacted high strength geopolymer made with diatomite as a fumed silica alternative

Geopolymers are formed by mixing of aluminosilicate sources with alkaline meta-silicate solution at room temperature. In the current study, diatomite of Turkish origin was fully utilized as a fumed silica alternative for the preparation of geopolymer, having a typical formula of K₂O•Al₂O₃•4SiO₂•11H₂O. From XRD of this sample, a broad peak centered at 28° 2θ indicated the well-known formation of amorphous geopolymer, as well as a fully reacted microstructure of geopolymer as seen by scanning electron microscopy. Additionally, geopolymer having the same formula was made by using fumed silica, in order to compare with geopolymers prepared from diatomite. The Weibull modulus was calculated from four-point bending and compressive strength testing of both geopolymer composites. The use of diatomite as a fumed silica substitute in geopolymer production resulted in a very close flexure strength 9.2 (± 4.2 MPa) when compared to geopolymer made from fumed silica 10.2 (± 3.3 MPa). There was a significantly higher compressive strength 71 (± 13.9 MPa) and Weibull modulus (5.4), than comparable properties of geopolymer made from fumed silica, which had a compressive strength 54 (± 25.8 MPa) and Weibull modulus of 2.0. The discrepancy was attributed to some self-reinforcement of the geopolymer matrix due to unreacted diatomite.     

Preparation and properties of an oxide fiber‐reinforced silica matrix composite

Oxide (Nextel? 440) fiber‐reinforced silica composites, with the density and porosity of 1.97 g/cm³ and 21.8%, were prepared through sol‐gel. Their average flexure strength, elastic modulus, shear strength, and fracture toughness at room temperature were 119.7 MPa, 25.6 GPa, 10.8 MPa, and 4.0 MPa·m^1/2, respectively. The composites showed typical toughened fracture behavior, and distinct pullout fibers were observed at the fracture surface. Their mechanical properties were performant up to 1000°C, with the maximum flexural strength of 132.2 MPa at 900°C. Moreover, the composites showed good thermal stability, even after thermal aging and thermal shock at elevated temperatures.     

An acoustic emission study on the fracture behavior of continuous glass fiber/polypropylene composites based on commingled yarn

The fracture behavior of continuous glass fiber reinforced polypropylene composites made of commingled yarn in the form of biaxial (±±45°) noncrimp warp‐knitted fabric, twill woven fabric, and swirl mat, respectively, was investigated by virtue of single edge notched tensile (SEN‐T) specimens. These composite laminates were manufactured by compression molding and cooled at two different rates (1°C/min and 10°C/min) during the last processing phase of the laminates. The failure mechanisms were studied by acoustic emission (AE) analysis. AE amplitude ranges corresponding to the individual failure modes have been identified. For biaxial noncrimp fabric reinforced materials, the failure mechanisms involved in the fracture procedure are governed by the interface related failure events. Higher cooling rate, which is accompanied by better fiber/matrix adhesion, results in not only the increase in the relative proportion of high‐amplitude failure events, but also the occurrence of a large quantity of fiber fracture events. For woven fabric and mat reinforced composites, fiber‐dominated failure mechanisms result in the higher fracture toughness when compared with biaxial noncrimp fabric composites. Under this circumstance, the change in cooling rate only results in the difference in the relative frequency of the individual failure modes. In addition, it is found out that the initiation fracture toughness of SEN‐T specimens can be easily assessed by marking the load value which corresponds to the first point of AE signals emitted stably in AE events‐displacement curves. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Mechanical and thermal properties of biphenyldiol formaldehyde resin/gallic acid epoxy composites enhanced by graphene oxide

In this study, the gallic acid‐based epoxy resin (GA‐ER) and alkali‐catalysed biphenyl‐4,4′‐diol formaldehyde resin (BPFR) are synthesized. Glass fibre‐reinforced GA‐ER/BPFR composites are prepared. Graphene oxide (GO) is used to improve the mechanical and thermal properties of GA‐ER/BPFR composites. Dynamic mechanical properties and thermal, mechanical, and electrical properties of the composites with different GO content are characterized. The results demonstrate that GO can enhance the mechanical and thermal properties of the composites. The glass transition temperature, T_g, of the BPFR/GA‐ER/GO composites is 20.7°C higher than the pure resin system, and the 5% weight loss temperature, T_d5, is enhanced approximately 56.6°C. When the BPFR: GA‐ER mass ratio is at 4 : 6 and GO content is 1.0–1.2 wt %, the tensile and impact strengths of composites are 60.97 MPa and 32.08 kJ/m² higher than the pure resin composites, respectively. BPFR/GA‐ER composites have better mechanical properties, and can replace common BPA epoxy resins in the fabrication of composites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42637.     

Erosive wear behavior and dynamic mechanical analysis of textile material reinforced polymer composites

The present analysis intends to look into the needlepunched nonwoven textile material reinforced polymer composites. The solid particle erosion wear behavior of needlepunched nonwoven fabric mat reinforced epoxy composites were assessed using silica sand particles with the size of 250, 350, and 450 μm. Taguchi analysis was also carried out on the basis of design of experiments (DoE) approach to establish the interdependence of operating parameters. Mechanical and physical properties of composites were also evaluated experimentally, and the storage modulus (E′), loss modulus (E″) and damping factor (tan δ) characteristics were analyzed with the help of dynamic mechanical analyzer (DMA) in the temperature range of 20–200°C. Surface morphology of the eroded surfaces of composites were also analyze by scanning electron microscopic (SEM) to discuss the feasible erosion mechanism on composite surfaces. The result reveals that fiber content and impact velocity has an invulnerable impact on the erosion rate of needlepunched nonwoven fabric mat‐epoxy composites. The mechanical and physical properties are meliorating with incorporation of fabric mat weight percentage in composites, and the measured damping factor (tan δ) peaks of T _g for needlepunched nonwoven fabric mat epoxy composites ranged from 100 to 110°C. POLYM. COMPOS., 38:2201–2211, 2017. © 2015 Society of Plastics Engineers     

Improved tensile strength and thermal stability of thermoplastic carbon fiber fabric composites by heat induced crystallization of in situ polymerizable cyclic butylene terephthalate oligomers

Thermoplastic carbon fiber fabric reinforced composites (CFFRCs) were prepared using a novel fast manufacturing process with a low viscosity polymerizable cyclic butylene terephthalate (CBT) resin. Structure and properties of the composites altered by thermal annealing were investigated to develop appropriate post processing of the CFFRCs for fast production and lowering the processing cost. Annealing at 200°C for 120 min resulted in improved mechanical properties and thermal stability of the polymerized CBT (pCBT) based on differential scanning calorimetry, wide‐angle X‐ray diffraction, and thermo gravimetric analysis. The tensile strength of the CFFRC compression molded at 250°C for 2 min was 440 MPa and that of the CFFRC annealed at 200°C for 120 min after compression molding was 500 MPa, which is an improvement of 550 and 625% relative to the pCBT matrix, respectively. In addition, the thermal stability of the CFFRC annealed at 250°C for 120 min improved by 10°C. Therefore, tensile strength and thermal stability of the manufactured CFFRC can be improved by using the appropriate annealing conditions. POLYM. ENG. SCI., 54:2161–2169, 2014. © 2013 Society of Plastics Engineers