New biocomposites based on thermoplastic starch and bacterial cellulose

Bacterial cellulose, produced by Acetobacter Xylinum, was used as reinforcement in composite materials with a starch thermoplastic matrix. The composites were prepared in a single step with cornstarch by adding glycerol/water as the plasticizer and bacterial cellulose (1% and 5% w/w) as the reinforcing agent. Vegetable cellulose was also tested as reinforcement for comparison purposes. These materials were characterized by different techniques, namely TGA, XRD, DMA, tensile tests, SEM and water sorption assays. All composites showed good dispersion of the fibers and a strong adhesion between the fibers and the matrix. The composites prepared with bacterial cellulose displayed better mechanical properties than those with vegetable cellulose fibers. The Young modulus increased by 30 and 17 fold (with 5% fibers), while the elongation at break was reduced from 144% to 24% and 48% with increasing fiber content, respectively for composites with bacterial and vegetable cellulose.     

Processing, compatibilization and properties of ternary composites of Mater-Bi with polyolefins and hemp fibres

Ternary composites of a biodegradable thermoplastic matrix, Mater-Bi® (MB), with various polyolefins (PP, HDPE and PS) and hemp fibres (H) were obtained by melt mixing and characterized by SEM, OM, DSC, TGA and tensile tests. The properties of composites were compared with those of MB/polyolefin and MB/H blends. Maleic anhydride functionalized polyolefins were employed as compatibilizers. Crystallization behaviour and morphology of the composites were found to be affected by the composition, phase dispersion and compatibilizer. Thermogravimetric analysis indicated that the thermal stability of the polyolefin phase and fibres was influenced by the composition and phase structure. A significant improvement of tensile modulus and strength was recorded for composites of MB with PE and PS as compared to MB/H composites. The results indicate that incorporation of polyolefins in the biodegradable matrix, compared to binary matrix/fibre system, may have significant advantages in terms of properties, processability and cost.     

Direct fluorination of Twaron fiber and the mechanical, thermal and crystallization behaviour of short Twaron fiber reinforced polypropylene composites

An experimental study of the incorporation of non-fluorinated and fluorinated Twaron fibers in polypropylene (PP) is presented. Surface modifications were made to Twaron fiber by direct fluorination technique using elemental fluorine in order to improve the interfacial adhesion between the fiber and matrix. Composites of PP/Twaron fiber (both Fluorinated and non-fluorinated) with 0.6%, 1.25%, 5% and 10% of Twaron fibers (w/w) were prepared by a solution method. Mechanical behaviour was estimated by the measurement of the tensile strength. The mechanical properties of PP improve significantly with the incorporation of Twaron fibers and fluorinated fiber composites show superior mechanical properties compared to the non-fluorinated system. The morphology was determined by scanning electron microscopy (SEM), showing good dispersion of the fibers. The thermal and crystallization behaviour of PP/Twaron fiber composites were studied by thermogravimetry (TG) and differential scanning calorimetry (DSC). The effect of fiber content and fiber surface treatments on the thermal properties was evaluated. DSC analysis exhibited an increase in the crystallization temperature and crystallinity, melting temperature upon the addition of fluorinated fibers to the PP matrix. This is attributed to the nucleating effects of the fiber surfaces. Also the thermal stability (from TG) and surface energy (determined from contact angle measurement) increased for fluorinated fiber composites. Surface modification of Twaron fibers leads to improved adhesion with the PP matrix and hence an improvement in properties of the Twaron fiber-PP composites.     

Green composites based on polypropylene matrix and hydrophobized spend coffee ground (SCG) powder

Green composites were prepared with polypropylene matrix and 20 wt.% spent coffee ground (SCG) powder for uses as a wood plastic composite (WPC). The effects of hydrophobic treatment with palmitoyl chloride on SCG powder is compared with conventional surface treatment based on silanization with (3-glycidyloxypropyl) trimethoxysilane and the use of a maleated copolymer compatibilizer (polypropylene-graft-maleic anhydride, PP-g-MA) in terms of mechanical properties, morphology, thermal properties and water uptake. Composites were previously mixed in a twin-screw co-rotating extruder and subsequently subjected to injection moulding. The comparative effect of the different surface treatments and or compatibilizers on mechanical performance was studied by flexural, impact tests and dynamic mechanical thermal analysis (DMTA-torsion); in addition, the stabilizing effect of SCG was revealed by differential scanning calorimetry (DSC) and thermogravymetric analysis (TGA). As one of the main drawbacks of wood plastic composites and natural fibre reinforced plastics is the moisture gain, water uptake tests were carried out in order to quantify the effectiveness of the hydrophobization process with palmitoyl chloride. Results show a slight increase in flexural modulus for composites with both untreated and treated/compatibilized SCG powder (20 wt.%). As expected, thermal stability is improved as indicated by an increase of more than 8% in the onset degradation temperature by DSC if compared to unfilled polypropylene. Fracture analysis by scanning electron microscopy (SEM) shows better particle dispersion for PP-SCG composites with hydrophobized SCG with palmitoyl chloride treatment; in addition a remarkable decrease in water uptake is observed for composites with hydrophobized SCG.     

New lignocellulosic fibres-reinforced composite materials: A stepforward in the valorisation of the Posidonia oceanica balls

In this work, new lignocellulosic particles obtained from Posidonia oceanica were studied to reinforce a commercial biodegradable thermoplastic matrix. First, these reinforcing fillers were characterised by Fourier-transform infrared (FT-IR) and X-ray photoelectron (XPS) spectroscopies. Then, they were used to prepare several composite films using BIOPLAST GF 106 matrix. Different P. oceanica fragment loadings, namely 0%, 10%, 20% and 30% (w/w with respect to the matrix) were investigated. The morphology of the ensuing materials was assessed by scanning electron microscopy (SEM), whereas their thermal and mechanical properties were studied by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA) and tensile tests. The obtained results showed that P. oceanica-based particles enhanced the thermo-mechanical properties of the thermoplastic matrix.     

Additive manufacturing of carbon fiber reinforced thermoplastic composites using fused deposition modeling

Additive manufacturing (AM) technologies have been successfully applied in various applications. Fused deposition modeling (FDM), one of the most popular AM techniques, is the most widely used method for fabricating thermoplastic parts those are mainly used as rapid prototypes for functional testing with advantages of low cost, minimal wastage, and ease of material change. Due to the intrinsically limited mechanical properties of pure thermoplastic materials, there is a critical need to improve mechanical properties for FDM-fabricated pure thermoplastic parts. One of the possible methods is adding reinforced materials (such as carbon fibers) into plastic materials to form thermoplastic matrix carbon fiber reinforced plastic (CFRP) composites those could be directly used in the actual application areas, such as aerospace, automotive, and wind energy. This paper is going to present FDM of thermoplastic matrix CFRP composites and test if adding carbon fiber (different content and length) can improve the mechanical properties of FDM-fabricated parts. The CFRP feedstock filaments were fabricated from plastic pellets and carbon fiber powders for FDM process. After FDM fabrication, effects on the tensile properties (including tensile strength, Young's modulus, toughness, yield strength, and ductility) and flexural properties (including flexural stress, flexural modulus, flexural toughness, and flexural yield strength) of specimens were experimentally investigated. In order to explore the parts fracture reasons during tensile and flexural tests, fracture interface of CFRP composite specimens after tensile testing and flexural testing was observed and analyzed using SEM micrograph.     

Mechanical and fracture properties of ternary PE/PA6/GF composites

This article studies the mechanical properties of short fiber reinforced polymer blends comprised of a soft thermoplastic matrix (polyethylene, PE), a rigid dispersed thermoplastic phase (polyamide-6, PA6) and glass fiber reinforcement. These ternary composites are designed as a model system to investigate the impact of the mutual interactions of the three phases on the composite mechanical properties. For this purpose two types of fibers are used, dispersed-phase and matrix-phase compatible fibers, respectively.     

Development of slate fiber reinforced high density polyethylene composites for injection molding

During the last decade the use of fiber reinforced composite materials has consolidated as an attracting alternative to traditional materials due to an excellent balance between mechanical properties and lightweight. One drawback related to the use of inorganic fibers such as those derived from siliceous materials is the relative low compatibility with conventional organic polymer matrices. Surface treatments with coupling agents and the use of copolymers allow increasing fiber–matrix interactions which has a positive effect on overall properties of composites. In this research work we report the use of slate fiber treated with different coupling agents as reinforcement for high density polyethylene from sugarcane. A silane (propyltrimethoxy silane; PTMS) and a graft copolymer (polyethylene-graft-maleic anhydride; PE-g-MA) were used to improve fiber–matrix interactions on HDPE-slate fiber. The effect of the different compatibilizing systems and slate fiber content were evaluated by scanning electron microscopy (SEM), dynamic thermomechanical analysis (DTMA) as well as mechanical properties (tensile, flexural and impact). The results show that the use of silane coupling agents leads to higher fiber–matrix interactions which has a positive effect on overall mechanical properties. Interesting results are obtained for composites containing 30 wt.% slate fiber previously treated with propyltrimethoxy silane (PTMS) with an increase in tensile and flexural strength of about 16% and 18% respectively.     

New environmentally friendly composite laminates with epoxidized linseed oil (ELO) and slate fiber fabrics

This work focuses on the development of new composite laminates based on the use of epoxidized linseed oil (ELO) as matrix and reinforcement fabrics from slate fibers with different silane treatments. The curing behavior of the ELO resin is followed by differential scanning calorimetry (DSC) and the gelation is studied by oscillatory rheometry and gel-time. Composite laminates of ELO matrix and slate fabrics are manufactured by Resin Transfer Molding (RTM) and the mechanical properties of the composite laminates are tested in tensile, flexural and impact conditions. The effects of different silane coupling agents on fiber-matrix interface phenomena are studied by scanning electron microscopy (SEM). As in other siliceous fibers, silane treatment leads to improved mechanical performance but glycidyl silane treatment produces the optimum results as the interactions between silanized slate fiber and epoxidized linseed oil are remarkably improved as observed by scanning electron microscopy (SEM).     

Wood cellulose biocomposites with fibrous structures at micro- and nanoscale

High-strength composites from wood fiber and nanofibrillated cellulose (NFC) were prepared in a semi-automatic sheet former. The composites were characterized by tensile tests, dynamic mechanical thermal analysis, field-emission scanning electron microscopy, and porosity measurements. The tensile strength increased from 98 MPa to 160 MPa and the work to fracture was more than doubled with the addition of 10% NFC to wood fibers. A hierarchical structure was obtained in the composites in the form of a micro-scale wood fiber network and an additional NFC nanofiber network linking wood fibers and also occupying some of the micro-scale porosity. Deformation mechanisms are discussed as well as possible applications of this biocomposites concept.     

Polybutene as a matrix for wood plastic composites

This study examined the feasibility of using polybutene-1 (PB-1), a ductile plastic, as a matrix for manufacturing wood plastic composites (WPCs) with improved toughness and ductility compared to currently commercialized WPCs. The processability, tensile, flexural, and impact properties of injection molded PB-1/wood-flour composite samples with varying proportions of wood flour were characterized. Analysis also included the morphology of fractured samples surface and adhesion between the polymer and wood flour using SEM. Comparisons of the mechanical properties and adhesion in the PB-1 composites to those of HDPE and PP-based WPCs found the composites made with PB-1 matrix significantly inferior in strength and stiffness (both in tensile and flexural) than their counterparts made of HDPE and PP matrices. In contrast, the processability, elongation at break, impact strength and adhesion in PB-1/wood-flour composites, superior to those of HDPE and PP, confirmed their suitability for use as a matrix in composites intended for applications subjected to high impacts.     

Grafting effects of polypropylene/polyethylene blends with maleic anhydride on the properties of the resulting wood-plastic composites

In the presented study, polypropylene (PP) and high density polyethylene (PE) were blended at the ratios of 80/20 and 20/80 to simulate recycled waste thermoplastic mixtures. The effects of in situ grafting of PP/PE blends with maleic anhydride through the extruder on the mechanical and rheological properties of resulting wood/plastic composites were investigated. Different ratios of PP and PE in the blends created distinct properties in the resulting composites. Grafting of PP and PE blends improved the tensile and flexure properties of the resulting composites. The composites exhibited a reduced water uptake and resultant dimensional swelling due to grafting with maleic anhydride. Grafting of the blends also considerably improved the interfacial bonding and enhanced the dispersion of wood in the matrix, as evidenced by rheological analysis and scanning electron microscopy.     

Influence of different carbon nanotubes on the electrical and mechanical properties of melt mixed poly(ether sulfone)-multi walled carbon nanotube composites

Commercial Udel® poly(ether sulfone) (PSU) was filled with three different commercially available multiwalled carbon nanotubes (MWCNTs) by small scale melt mixing. The MWCNTs were as grown NC 7000 and two of its derivatives prepared by ball milling treatment. One of them was unmodified (NC 3150); the other was amino modified (NC 3152). The main difference beside the reactivity was the reduced aspect ratio of NC 3150 and NC 3152 caused by ball milling process. All PSU/MWCNT composites with similar filler content were prepared under fixed processing conditions and comparative analysis of their electrical and mechanical properties were performed and were correlated with their microstructure, characterized by optical microscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). A non-uniform MWCNT dispersion was observed in all composites. The MWCNTs were present in form of agglomerates in the size of 10–60 μm whereas the deagglomerated part was homogeneously distributed in the PSU matrix. The differences in the agglomeration states correlate with the variations of properties between different PSU/MWCNT composites. The lowest electrical percolation threshold of 0.25–0.5 wt.% was observed for the shortened non-functionalized MWCNT composites and the highest for amine-modified MWCNT composites (ca. 1.5 wt.%). The tensile behavior of the three composites was only slightly altered with CNT loading as compared to the pure PSU. However, the elongation at break showed a reduction with MWCNT loading and the reduction was least for composite with best MWCNT dispersion.     

Mechanical and thermal properties of chicken feather fiber/PLA green composites

Chicken feather fiber (CFF)/reinforced poly(lactic acid) (PLA) composites were processed using a twin-screw extruder and an injection molder. The tensile moduli of CFF/PLA composites with different CFF content (2, 5, 8 and 10 wt%) were found to be higher than that of pure PLA, and a maximum value of 4.2 GPa (16%↑) was attained with 5 wt% of CFF without causing any substantial weight increment. The morphology, evaluated by scanning electron microscopy (SEM), indicated that an uniform dispersion of CFF in the PLA matrix existed. The mechanical and thermal properties of pure PLA and CFF/PLA composites were compared using dynamic mechanical analysis (DMA), thermomechanical analysis (TMA) and thermogravimetric analysis (TGA). DMA results revealed that the storage modulus of the composites increased with respect to the pure polymer, whereas the mechanical loss factor (tan δ) decreased. The results of TGA experiments indicated that the addition of CFF enhanced the thermal stability of the composites as compared to pure PLA. The outcome obtained from this study is believed to assist the development of environmentally-friendly composites from biodegradable polymers, especially for converting agricultural waste – chicken feather into useful products.     

Morphology, mechanical and thermal properties of graphene-reinforced poly(butylene succinate) nanocomposites

Graphene nanosheets (GNSs) reinforced poly(butylene succinate) (PBS) nanocomposites are facilely obtained by a solution-based processing method. Graphene nanosheets, which are derived from chemically reduced graphite oxide (GO), are characterized by AFM, TEM, XRD and Raman spectra. The state of dispersion of the GNSs in the PBS matrix is examined by SEM observations that reveals homogeneous distribution of GNSs in PBS matrix. A 21% increase in tensile strength and a 24% improvement of storage modulus are achieved by addition of 2.0 wt% of GNS. The electrical conductivity and thermal stability of the graphene-based nanocomposite are also improved. DSC measurement indicates that the presence of graphene sheets does not have a remarkable impact on the crystallinity of the nanocomposites. Therefore, the high performances of the nanocomposites are mainly attributed to the uniform dispersion of GNSs in the polymer matrix and strong interfacial interactions between both components.     

Processing and characterization of reinforced polyethylene composites made with lignocellulosic fibers from Egyptian agro-industrial residues

Lignocellulosic fibers were extracted from Egyptian industrial crops, viz. cotton stalk, rice straw, bagasse, and banana plant waste. The chemical composition of these fibers was determined. Composite materials were processed from these natural lignocellulosic fibers using low density polyethylene and acid stearic as compatibilizer, or maleated low density polyethylene. The thermal and mechanical properties were studied by differential scanning calorimetry (DSC) and tensile tests, respectively. The morphology of processed composites was studied by scanning electronic microscopy (SEM). Better compatibility and enhanced mechanical properties were obtained when using maleated LDPE as compatibilizer. The chemical composition of fibers, in terms of lignin, cellulose and hemicelluloses contents, was found to have a strong influence on the mechanical properties of the composites.     

Thermoplastic elastomers with multi-walled carbon nanotubes: Influence of dispersion methods on morphology

PBT-block-PTMO thermoplastic elastomers derived from dimethyl terephthalate (DMT), 1,4-butanediol(BD) and poly(tetramethylene glycol) (PTMG) were synthesized in the presence of oxidized multi-walled carbon nanotubes (MWCNTs) by a two-stage process involving transesterification and in situ polycondensation. Two procedures were applied to nanotubes in the polymer matrices were used. In procedure 1, nanotubes were dispersed in DMT + BD before the transesterification, while in procedure 2 nanotubes were dispersed in PTMG after transesterification. The mole ratio of the starting components was selected to produce copolymers with a constant hard to soft segment weight ratio of 45:55. Characterization of the new nanocomposites was performed by transmission electron microscopy (TEM), scanning electron microscopy (SEM), small- and wide-angle X-ray scattering (SAXS/WAXS). A better nanotube dispersion can be achieved when oxidized MWCNTs are added to the DMT + BD monomers before transesterification (procedure 1). Oxidized MWCNTs exhibit strong interfacial adhesion to the polymer matrix for both procedures.     

Influence of additives on the global mechanical behavior and the microscopic strain localization in wood reinforced polypropylene composites during tensile deformation investigated using digital image correlation

The structural integrity of polypropylene (PP) matrix composites reinforced by natural wood fibers is investigated by digital image correlation (DIC) coupled with tensile tests. The use of the material as an alternative construction material requires extensive understanding of its micromechanical properties, which primarily define its performance. Addition of several additives such as coupling agents is common practice for such materials. These ingredients improve the performance of these materials mainly by improvement of the chemical and physical interactions between the nonpolar matrix and the polar wood fibers. These interactions facilitate the transfer of the applied deformation particularly in the interphase region between the polymer matrix and the reinforcing fibers. Such localized changes can influence the performance of the material specially its micromechanical behavior. The DIC via photogrammetry was used to study the spatial distribution of the accumulated plastic surface strain, which is based on pattern recognition of the surface before and after straining. The heterogeneous strain distribution reveals a structural inhomogeneity of the material. The magnitude of local strain was much higher than the global strain, suggesting preferred regions for plastic deformation formed by the microstructure.     

Short-term creep behavior of a biodegradable polymer reinforced with wood-fibers

The short-time creep behavior at tensile and single cantilever mode of deformation for a series of biodegradable composites was thoroughly studied. The composites were based on a biodegradable polymer matrix consisted a blend of poly(butylene adipate-terephthalate) (PBAT) copolyester, produced by non-renewable resources, and Polylactic acid (PLA). The matrix was reinforced with three different wood fiber types, at 20 and 30 wt%. The experimental data were analyzed in terms of Findley's and Burger's viscoelastic models. The effect of stress and temperature and wood fiber type on the material's creep response was analytically studied, while the Burger's model parameters were related to the composites morphology. In all cases, the wood fibers improved the creep resistance of the composites.     

Sugarcane bagasse cellulose/HDPE composites obtained by extrusion

Natural fibers used in this study were both pre-treated and modified residues from sugarcane bagasse. Polymer of high density polyethylene (HDPE) was employed as matrix in to composites, which were produced by mixing high density polyethylene with cellulose (10%) and Cell/ZrO₂·nH₂O (10%), using an extruder and hydraulic press. Tensile tests showed that the Cell/ZrO₂·nH₂O (10%)/HDPE composites present better tensile strength than cellulose (10%)/HDPE composites. Cellulose agglomerations were responsible for poor adhesion between fiber and matrix in cellulose (10%)/HDPE composites. HDPE/natural fibers composites showed also lower tensile strength in comparison to the polymer. The increase in Young’s modulus is associated to fibers reinforcement. SEM analysis showed that the cellulose fibers insertion in the matrix caused an increase of defects, which were reduced when modified cellulose fibers were used.