Properties of Chitosan-Filled Polypropylene (PP) Composites: The Effect of Acetic Acid

The main objective of this research was to investigate the effect of chitosan content and chemical modification with acetic acid on mechanical and thermal properties of PP/Chitosan. It was found that the tensile strength, elongation at break and crystallinity of untreated PP/Chitosan composites decreased with increasing filler content; however, Young's modulus and thermal stability increased. The treated chitosan with acetic acid have improved the tensile strength and Young's modulus of PP/Chitosan composites. The thermal analysis results show that chemical modified chitosan had increase thermal stability and crystallinity of treated PP/Chitosan composites. The scanning electron microscopy (SEM) study of the tensile fracture surface of treated PP/Chitosan composites indicated that the presence of acetic acid increased the interfacial interaction between chitosan and polypropylene matrix.     

Alfa fiber/polypropylene composites: Influence of fiber extraction method and chemical treatments

Alfa fiber/polypropylene composites were manufactured using twin-screw extrusion. Fibers were extracted using alkaline and steam explosion methods. Three chemical treatments were also applied to the alkaline-extracted fibers: stearic acid (SA), and potassium permanganate dissolved in water (KW) and in acetone (KA). Finally, thermal annealing was applied to the composites. The results indicate that composites with steam-exploded fibers had a significantly higher melt flow index than composites with alkaline-extracted fibers. Moreover, the incorporation of fibers into the matrix increased the Young's modulus, where the optimum results were obtained utilizing the alkaline-extracted fibers. Both extraction methods also significantly decreased the water uptake, especially the steam explosion. The three chemical treatments increased the melt flow index and conversely decreased the tensile strength and Young's modulus. In addition, KW treatment decreased the water uptake. Finally, thermal annealing increased the tensile strength and Young's modulus of composites with SA-treated fibers. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47392.     

Effect of in situ surface‐modified nano‐SiO2 on the thermal and mechanical properties and crystallization behavior of nylon 1010

Nylon 1010 composites filled with two types of surface‐modified SiO₂ nanoparticles (RNS and DNS) were prepared by melt blending. The mechanical properties of the composites were evaluated. The influences of the surface‐modified nano‐SiO₂ on the thermal stability, crystallization behavior, and microstructure of nylon 1010 were investigated by thermogravimetric analysis, differential scanning calorimetry (DSC), X‐ray diffraction, and transmission electron microscopy. And the interfacial interactions between the fillers and polymer matrix were examined using a Fourier transformation infrared spectrometer. It was found that the addition of the surface‐modified nano‐SiO₂ had distinct influences on the thermal stability, mechanical properties, and crystallization behavior of nylon 1010. RNS and DNS as the fillers had different effects on the mechanical properties of nylon 1010. The composites filled with RNS at a mass fraction of 1–5% showed increased break elongation, Young's modulus, and impact strength but almost unchanged or even slightly lowered tensile strength than the unfilled matrix. The DNS‐filled nylon 1010 composites had obviously decreased tensile strength, whereas the incorporation of DNS also contributed to the increase in the Young's modulus of nylon 1010, but less effective than RNS. Moreover, the nylon 1010 composites had better thermal stability than the neat polymer matrix, and the composites filled with RNS were more thermally stable than those filled with DNS. The difference in the crystallinity of neat nylon 1010 and its composites filled with RNS and DNS was subtle, although the surface‐modified nano‐SiO₂ could induce or/and stabilize the γ‐crystalline formation of nylon 1010. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

The Effect of Waste Office White Paper Content and Size on the Mechanical and Thermal Properties of Low-Density Polyethylene (LDPE) Composites

The effect of waste office white paper (WOWP) loading and size on mechanical properties, morphology and thermal properties of LDPE/WOWP composites were investigated. The results showed that increasing of WOWP loading has increased tensile strength and Young's modulus but decreased elongation at break of composites. LDPE/WOWP composites with smaller particle size (31 μm) have higher mechanical properties. Thermal analysis results of composites with particle size (31 μm) show higher thermal stability and crystallinity than composites with particle size (77 μm). Scanning electron microscope (SEM) micrograph indicates that the smaller particle size of filler has better interaction with LDPE matrix.     

Chemical Modification of Chitosan-Filled Polypropylene (PP) Composites: The Effect of 3-Aminopropyltriethoxysilane on Mechanical and Thermal Properties

Chitosan was used as filler in polypropylene (PP) polymer. In order to improve compatibility between chitosan and PP, chitosan was chemically modified with 3-aminopropyltriethoxysilane (3-APE). The results show that the increasing of filler content decreased tensile strength and elongation at break, but increased Young's modulus of composites. The treated composites exhibit higher tensile strength and Young's modulus, but lower elongation at break compared untreated composites. The addition of 3-APE has improved thermal properties such as thermal stability and crystallinity of treated composites. SEM study of the tensile fracture surface of treated composites shows better interfacial interaction and adhesion between the chitosan-PP matrix.     

Investigation of electrical,mechanical, and thermal properties of functionalized multiwalled carbon nanotubes‐reduced graphene Oxide/PMMA hybrid nanocomposites

Electrical, mechanical, and thermal properties of the poly(methyl methacrylate) (PMMA) composites containing functionalized multiwalled carbon nanotubes (f‐MWCNTs) and reduced graphene oxide (rGO) hybrid nanofillers have been investigated. The observed electrical percolation threshold of FHC is 0.8 wt% with maximum conductivity of 1.21 × 10^?3 S/cm at 4 wt% of f‐MWCNTs. The electrical transport mechanism and magneto resistance studied of hybrid composites have also been investigated. Progressive addition of f‐MWCNTs in rGO/PMMA composite results increase in mechanical (tensile strength and Young's modulus) and thermal (thermal stability) properties of f‐MWCNTs‐rGO/PMMA hybrid nanocomposites (FHC). The increased mechanical properties are due to the efficient load transfer from PMMA matrix to f‐MWCNTs and rGO through better chemical interaction. The strong interaction between PMMA and f‐MWCNTs‐rGO in FHC is the main cause for improved thermal stability. POLYM. ENG. SCI., 59:1075–1083, 2019. © 2019 Society of Plastics Engineers     

Liquid polyoctahedral silsesquioxanes as an effective and facile reinforcement for liquid silicone rubber

Acrylo polyoctahedral silsesquioxanes (POSS), a liquid POSS derivative with reactive C=C double bond, is used to modify addition-cured liquid silicone rubber (LSR) as an effective nanofiller for the first time. Significant enhancements on mechanical properties are obtained. With addition of only 1.5 parts per hundred rubbers (phr) of acrylo POSS to fumed silica-strengthened silicones, the Young's modulus and ultimate tensile strength are increased by 432% and 66%, respectively, and the hardness of resulting LSR composites is improved as well. Proton nuclear magnetic resonance and Fourier transform infrared spectroscopies prove the efficient hydrosilylation between Acrylo POSS and hydrosiloxane directly. The thermal stability and morphology investigations also confirm that POSS is covalently incorporated into the network of silicone rubber. The increment of crosslink density is proved by extraction and swelling experiment and dynamic mechanical analysis. It can be envisioned that this simple and effective method could help produce high performance silicone rubber composites. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 46996.     

Silica‐filled polypropylene composites: The effect of ethylene diamine dilaurate and maleic anhydride grafted polypropylene on mechanical properties,water absorption,morphology, and thermal properties

The effect of two compatibilizers, i.e. ethylene diamine dilaurate (EDD) and maleic anhydride grafted polypropylene (MAPP) on the mechanical properties, water absorption, morphology, and thermal properties of silica‐filled polypropylene (PP/Sil) composites were studied. The results show that the tensile, impact and flexural strengths (up to 2 php), Young's modulus, and elongation at break (Eb) increased with increasing EDD content. However, increasing MAPP content increases the tensile strength, Young's modulus, impact and flexural strengths, and water absorption resistance. At a similar compatibilizer content, EDD exhibits higher Eb, impact and flexural strengths but lowers tensile strength, Young's modulus, and water absorption resistance compared with MAPP. Scanning electron microscopy study of tensile fractured surfaces exhibits the evidence of better silica‐PP adhesion with MAPP and EDD compared with the similar composites but without compatibilizer. Fourier transform infra red spectra provide an evidence of interaction between EDD or MAPP with PP/Sil composites. Termogravimetry analysis results indicate that the addition of EDD or MAPP slightly increases the thermal stability of PP/Sil composites. Differential scanning calorimetry also indicates that PP/Sil composites with EDD or MAPP have higher heat fusion (ΔH_f(com)) and crystallinity (X_com) than similar composites but without compatibilizer. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Phase morphology,thermomechanical, and crystallization behavior of uncompatibilized and PP‐g‐MAH compatibilized polypropylene/polystyrene blends

In this article, we discuss the phase morphology, thermal, mechanical, and crystallization properties of uncompatibilized and compatibilized polypropylene/polystyrene (PP/PS) blends. It is observed that the Young's modulus increases, but other mechanical properties such as tensile strength, flexural strength, elongation at break, and impact strength decrease by blending PS to PP. The tensile strength and Young's modulus of PP/PS blends were compared with various theoretical models. The thermal stability, melting, and crystallization temperatures and percentage crystallinity of semicrystalline PP in the blends were marginally decreased by the addition of amorphous PS. The presence of maleic anhydride‐grafted polypropylene (compatibilizer) increases the phase stability of 90/10 and 80/20 blends by preventing the coalescence. Hence, finer and more uniform droplets of PS dispersed phases are observed. The compatibilizer induced some improvement in impact strength for the blends with PP matrix phase, however fluctuations in modulus, strength and ductility were observed with respect to the uncompatibilized blend. The thermal stability was not much affected by the addition of the compatibilizer for the PP rich blends but shows some decrease in the thermal stability of the blends, where PS forms the matrix. On the other hand, the % crystallinity was increased by the addition of compatibilizer, irrespective of the blend concentration. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42100.     

Mechanical and thermal properties of chitosan‐filled polypropylene composites: The effect of acrylic acid

The mechanical properties, morphology, and thermal properties of chitosan‐filled polypropylene (PP) composites have been studied. The effect of the chemical modification of chitosan by acrylic acid treatment was also investigated. Results showed that the tensile strength and elongation at break decreased but that the Young's modulus of the composites increased with increasing filler loading. Chemical modification of chitosan with acrylic acid improved the tensile strength and Young's modulus of the composites but reduced the elongation at break. Thermogravimetric analysis showed that the addition of chitosan improved the thermal stability of the PP/chitosan composites as compared to that of neat PP. Chemical modification of chitosan had a positive effect on the thermal stability of the composites. This change was attributed to improvement of the interfacial adhesion between the chitosan and PP matrix due to formation of a covalent bond between chitosan and acrylic acid. Meanwhile, differential scanning calorimetric analysis showed that the addition of filler did not significantly change the melting temperature (T_m) of the PP/chitosan composites. The degree of crystallinity of the composites decreased with the addition of chitosan. At a similar chitosan loading, the chemically treated PP/chitosan composites exhibited higher crystallinity than the untreated composites and exhibited slightly increased T_m. A scanning electron microscopy study of the tensile fracture surface of chemically treated PP/chitosan composites indicated that the presence of acrylic acid increased the interfacial interaction between chitosan and the polypropylene matrix. J. VINYL ADDIT. TECHNOL., 2011. © 2011 Society of Plastics Engineers     

Mechanical and film formation behavior from PDMS/NaY zeolite composite membranes

In this study, polydimethylsiloxane (PDMS) and NaY zeolite doped composite membranes were prepared for the films varying from 0 to 15 NaY zeolite wt %. All the membranes were characterized by attenuated total reflectance–Fourier transform infrared (FTIR), X-ray diffraction, scanning electron microscopy, thermogravimetry/differential thermal analysis methods. The FTIR spectral results showed that there is physical interaction existing between the PDMS matrix and NaY zeolite. Additionally, film formation from the pure PDMS and PDMS/NaY composites were investigated by photon transmission technique. Activation energies corresponding to the void closure and the interdiffusion stages were calculated. The NaY zeolite added films led to the significant improvement in the mechanical properties that both the tensile strength and Young's modulus increased three times. Thermal properties of the films were also investigated and the addition of NaY zeolite into the PDMS matrix could significantly improve the thermal stability of the composite membranes. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48549.     

Interfacial strengthening of polypropylene composites via bimodal porosity in Rice husk ash: Comparison with calcium carbonate reinforcement

Polypropylene is used in the textile industry in the manufacturing of plastic yarns, tapes, etc., but its low tensile strength and Young's modulus limits its associated applications. Composites of polypropylene with reinforcement of CaCO₃ and rice husk ash were processed by compression molding. Bimodal porosity in rice husk ash particles has shown an improved interfacial anchoring effect via capillary effect resulting in enhanced mechanical properties, whereas such an effect is not observed with CaCO₃ reinforcement in polypropylene matrix. On reinforcement with 10 wt % of each of rice husk ash and CaCO₃, thermal decomposition temperature of polypropylene (333.3 °C) shifted to higher value of 415.9 °C and polypropylene Young's modulus (749.5 MPa) increased to 789.5 MPa (by 5.3%), but tensile strength decreased from 23.5 to 21.2 MPa (by 2.3 MPa only). The isolated contribution of CaCO₃ and rice husk ash has been delineated, and resulting interfacial strengths have been quantified using analytical models. Rice husk ash has shown a stronger interfacial anchoring and can effectively replace CaCO₃ as reinforcement for achieving improved mechanical and thermal properties of polypropylene composites. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 46989.     

Structural,mechanical and thermal studies of double‐molded isotactic polypropylene nanocomposites with multiwalled carbon nanotubes

Nanocomposites of isotactic polypropylene (iPP) and multiwalled carbon nanotubes (MWCNTs) with various contents of MWCNTs were fabricated by double molding techniques. X‐ray diffraction measurements reveal a development of α‐crystal with lamellar stacks having a long period of 150 Å in the neat iPP that increases to 165 Å in 2 wt % MWCNTs‐loaded composites, indicating that MWCNTs enhance crystallization of iPP as a nucleating factor. Mechanical properties, such as tensile strength, flexural strength, Young's modulus, tangent modulus, and microhardness are found to increase with increasing MWCNTs content. Thermal analyses represent an increase of crystallization and melting temperatures and a decrease of thermal stability of the composites with increasing MWCNTs. Changes in structural, mechanical, and thermal properties of the composites due to the addition of MWCNTs are elaborately discussed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Special morphology and its role in mechanical enhancement of linear low‐density polyethylene/multiwalled carbon nanotubes composites

In this work, multiwalled carbon nanotubes (MWCNTs), as reinforcing agent, were blended with linear low‐density polyethylene (LLDPE), then molded by hot compression molding to prepare LLDPE/MWCNTs composites. Tensile tests indicate that the strength, Young's modulus, and toughness are all improved for LLDPE/MWCNTs composites containing 1 and 3 wt % MWCNTs. Compared with LLDPE, the Young's modulus of LLDPE/MWCNTs composites rises from 144.8 to 270.8 MPa at 1 wt % MWCNTs content. At the same time, increases of 18.5% in tensile strength and 16.6% in yield strength are achieved. Additionally, its toughness is enhanced by 26.7% than that of LLDPE. Microstructure characterizations, including differential scanning calorimetry, X‐ray diffraction, and scanning electron microscopy were performed to investigate the variations of microstructure and further to establish the relationship between microstructure and mechanical properties. Homogeneous dispersion of MWCNTs, network formation, and development of an oriented nanohybrid shish‐kebab structure contribute to the enhanced strength and toughness. The increased crystallinity is beneficial to the reinforcement and increased modulus. Additionally, the thermal stability of the LLDPE/MWCNTs composites is enhanced as well. This work suggests a promising routine to optimize polymer/MWCNTs composites by tailoring the structural development. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45525.     

Mechanical properties and thermal stability of porous polyimide/hollow mesoporous silica nanoparticles composite films prepared by using polystyrene microspheres as the pore-forming template

The porous polyimide/hollow mesoporous silica nanoparticles (PI/HMSNs) composite films were fabricated via blending polymerization by using polystyrene (PS) microspheres as the pore-forming template. The morphologies, microstructures, thermal stability, thermal expansion coefficient (TEC), and mechanical performances of the porous PI/HMSNs films were characterized in detail. Results showed that the uniform dispersion of HMSNs benefits from the strong hydrogen-bonding interaction between the hydroxyl groups of HMSNs and poly(amic acid) chains. Both weight loss and TEC of the porous PI/HMSNs films are lower than those of the pure porous PI film. When 0.8 wt % HMSNs and 7.0 wt % PS were added into the PI matrix, the Young's modulus and tensile strength of composite film increased by about 32.4% and 68.1% compared with those of the pure porous PI film. Conclusively, the introduction of HMSNs in the porous PI matrix is an important strategy to enrich the diversity of porous structure, improve the thermal and mechanical properties of the porous PI material simultaneously. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48792.     

Mechanical and thermal properties of starch‐filled poly(D,L‐lactic acid)/poly(hydroxy ester ether) biodegradable blends

The mechanical, structural, and thermal properties of injection‐molded composites of granular cornstarch, poly(D ,L ‐lactic acid) (PDLLA), and poly(hydroxy ester ether) (PHEE) were investigated. These composites had high tensile strengths, ranging from 17 to 66 MPa, at starch loadings of 0–70 wt %. Scanning electron microscopy micrographs of fracture specimens revealed good adhesion between the starch granule and the polymer matrix, as evidenced by broken starch granules. The adhesion of the starch granules to the polymer matrix was the greatest when the matrix PDLLA/PHEE ratios ranged from zero to unity. At a PDLLA/PHEE ratio of less than unity, as the starch content increased in the composites, there was an increase in the tensile strength and modulus, with a concurrent decrease in elongation. The effects of starch on the mechanical properties of starch/PDLLA composites showed that as the starch content of the composite increased, the tensile strength and elongation to break decreased, whereas Young's modulus increased. In contrast, the tensile strength of starch/PHEE composites increased with increasing starch content. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1775–1786, 2003     

High strength poly(vinyl alcohol) films obtained by drying and then stretching freeze/thaw cycled gel

The mechanical properties of stretched poly(vinyl alcohol) (PVA), which is formed by stretching a film prepared from a freeze/thaw cycled gel, were investigated as a function of the stretching ratio. The tensile strength and Young's modulus of 800% stretched PVA annealed at 130°C were 3.4 and 119 GPa, respectively. These values were much higher than those for a PVA film prepared without freeze/thaw cycling. For a film stretched more than 600% before annealing, two melting peaks, assignable to folded and extended chain crystals, were observed around 220°C and 230°C, respectively. This indicates that a shish‐kebab structure is formed as the stretching ratio increases. After annealing at 130°C, the folded‐chain crystal transformed to an extended‐chain crystal if an extended‐chain crystal was present in the stretched film before annealing. High tensile strength and Young's modulus after annealing were due to the formation of extended‐chain crystal. Therefore, the presence of extended‐chain crystal for annealing is important to provide good mechanical properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41318.     

Structure and properties of cellulose nanocomposite films containing melamine formaldehyde

Films of high Young's modulus and low density are of interest for application as loudspeaker membranes. In the present study nanocomposite films were prepared from microfibrillated cellulose (MFC) and from MFC in combination with melamine formaldehyde (MF). The prepared materials were studied with respect to structure as well as physical and mechanical properties. Studies in SEM and calculation of porosity showed that these materials have a dense paper‐like structure. The moisture sorption isotherms were measured and showed that moisture content decreased in the presence of MF. Mechanical properties were studied by dynamical mechanical thermal measurements as well as by tensile tests. Cellulose films showed an average Young's modulus of 14 GPa while the nanocomposites showed an average Young's modulus as high as 16.6 GPa and average tensile strength as high as 142 MPa. By controlling composition and structure, the range of properties of these materials can extend the property range available for existing materials. The combination of comparatively high mechanical damping and high sound propagation velocity is of technical interest. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Agricultural residue-derived lignin as the filler of polylactic acid composites and the effect of lignin purity on the composite performance

In this study, corn stover lignin with different purities was used as filler in polylactic acid (PLA) matrix. It was found that the impurity metals present in unpurified lignin can significantly affect the performance of the composites in terms of their thermal stability, rheological behavior, mechanical properties, and hydrophobicity. Among the PLA composites, the ones fabricated with the lignin containing 4% of impurities overall had the best thermal stability and tensile strength. From melt rheology analysis, it was also found that the presence of the impurity metals decreases the complex viscosity of the composites. It is suggested that the impurity metals acted as catalysts to promote the interaction between lignin and PLA, resulting in an improved compatibility between PLA and the filler. In the present study, mechanical properties and hydrophobicity of the composites were further improved by acetylating the lignin with the optimum content of impurities. Tensile strength of the composite with the acetylated lignin was comparable to that of pure PLA, whereas the modulus increased to as high as 2.75 GPa. Overall, the study showed that unpurified lignin could be used as filler to achieve similar or better performance than the composites made with highly purified lignin fillers. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47915.     

Preparation of polyester resin/graphene oxide nanocomposite with improved mechanical strength

Graphene oxide (GO) has attracted huge scientific interest due to its unique physical and chemical properties as well as its wide‐scale applicability including facile synthesis and high yield. Here, we report preparation of nanocomposites based on GO and unsaturated polyester resin (PE). The synthesized samples were characterized by Fourier transform infrared spectroscopy, X‐ray diffraction, scanning electron microscopy, thermogravimetric analysis, and tensile strength measurements. A good dispersion of the GO sheets within the resin matrix was observed from the morphological analysis. A significant enhancement in mechanical properties of the PE/GO composites is obtained at low graphene loading. Around 76% improvement of tensile strength and 41% increase of Young's modulus of the composites are achieved at 3 wt % loading of GO. Thermal analysis of the composite showed a noticeable improvement in thermal stability in comparison to neat PE. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013