Beckry Abdel-Magid

The effects of ultraviolet (UV) light and moisture environments on the properties of continuous fiber-reinforced thermoplastic composites were investigated in this study. Materials included carbon fiber-reinforced polyphenylene sulfide (CF/PPS), glass fiber-reinforced polyphenylene sulfide (GF/PPS), glass fiber-reinforced polypropylene (GF/PP), and glass fiber-reinforced polyethylene terephthalate (GF/PET). Fiber orientation was noted to affect the response of the materials to UV and moisture environments. For CF/PPS, UV exposure led to enhanced unidirectional tensile and flexure properties, and quasi-isotropic compression strength, but reduced in-plane shear properties of cross-ply laminates and the short-beam shear strength of unidirectional laminates. Exposure to moisture had minimal effect on CF/PPS laminates. UV light caused a slight decrease in tensile strength and strain of unidirectional samples of GF/PPS and a slight increase in these properties with various degrees in quasi-isotropic samples. Exposure to moisture was noted to cause a reduction in most of the mechanical properties with various degrees in unidirectional and quasi-isotropic GF/PPS laminates. For GF/PP, exposure to UV and moisture decreased the tensile and compressive strengths of unidirectional and quasi-isotropic laminates. However, a notable increase in flexure strength was observed in both laminates after UV exposure. The GF/PET quasi-isotropic laminates showed reduced tension, compression, and flexure strengths but increased impact resistance and short-beam strength under UV exposure, while moisture decreased in-plane shear properties of cross-ply laminates and increased the glass transition temperature of unidirectional laminates. Vertical burn and surface flammability and smoke generation tests showed high flame resistance of CF/PPS and GF/PPS composites, and less so for GF/PP and GF/PET composites. The findings highlight the various responses of the materials to extreme environments.

Continuously reinforced thermoplastic composites are widely used in structural applications due to their toughness, light weight, and shorter process cycle. Moreover, they provide flexibility in design and material selection. Unlike thermoset composites, continuous fiber content to maximize mechanical properties in thermoplastic composites has not been well investigated. In this paper, three thermoplastic systems are investigated to study the optimum content of continuous fiber reinforcement. These systems include carbon fiber/polyphenylene sulfide (PPS), glass fiber/PPS, and glass fiber/high-density polyethylene (HDPE). Tapes were made at several fiber contents, and samples were compression molded and tested using thermo-gravimetric analysis (TGA), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), tensile, 3-point flexure, and short-beam shear tests. Results revealed that higher fiber content led to an increase in the glass transition and melt transition temperatures of the polymer. Some mechanical properties increased with fiber content and then began to decrease upon further addition of fibers, while other properties, such as ductility and interfacial bond strength, decreased with more reinforcement. Furthermore, the optimum fiber contents to maximize mechanical properties are different for different properties and different materials.

In this paper, a polyacrylic elastomer latex with butyl acrylate (BA) as the core and methyl methacrylate (MMA) copolymerized with glycidyl methacrylate (GMA) as the shell, named poly(BA-MMA-GMA) (PBMG), was synthesized by seeded emulsion polymerization. Cellulose nanocrystal (CNC) was dispersed in the polyacrylic latex to prepare PBMG/CNC dispersions with different CNC contents. The dried product was mixed with polylactic acid (PLA) to fabricate PLA/PBMG/CNC blends. The addition of PBMG and PBMG/CNC improved the mechanical properties of the PLA matrix. Differential scanning calorimetry (DSC) was used to investigate the non-isothermal crystallization kinetics. The Avrami equation modified by the Jeziorny, Ozawa and Mo equations was used to analyze the non-isothermal crystallization kinetics of PLA and its blends. Analysis of the crystallization halftime of non-isothermal conditions indicated that the overall rate of crystallization increased significantly at 1 wt% content of CNC. This seemed to result from the increase of nucleation density and the acceleration of segment movement in the presence of the CNC component. This phenomenon was verified by polarizing microscope observation.

In this paper, a polyacrylic elastomer latex with butyl acrylate (BA) as the core and methyl methacrylate (MMA) copolymerized with glycidyl methacrylate (GMA) as the shell, named poly(BA-MMA-GMA) (PBMG), was synthesized by seeded emulsion polymerization. Cellulose nanocrystal (CNC) was dispersed in the polyacrylic latex to prepare PBMG/CNC dispersions with different CNC contents. The dried product was mixed with polylactic acid (PLA) to fabricate PLA/PBMG/CNC blends. The addition of PBMG and PBMG/CNC improved the mechanical properties of the PLA matrix. Differential scanning calorimetry (DSC) was used to investigate the non-isothermal crystallization kinetics. The Avrami equation modified by Jeziorny, and the Ozawa, and Mo’s equations were used to analyze the nonisothermal crystallization kinetics of PLA and its blends. Analysis of crystallization halftime of nonisothermal conditions indicated that the overall rate of crystallization increased significantly at 1 wt% content of CNC. This seemed to result from the increase of nucleation density and the acceleration of segment movement in the presence of CNC component. This phenomenon was verified by polarizing microscope observation.

In this manuscript, the durability of the E-glass/epoxy composite was determined under a seawater environment. The effect of harsh environment was investigated in terms of seawater absorption, microstructure and degradation in mechanical properties. E-glass epoxy composite specimens were conditioned in gulf seawater at 23 °C, 65 °C and 90 °C for the period of 12 months. It was observed that the mass of the samples increased after the immersion of 12 months at 23 °C and 65 °C whereas it reduced at 90 °C. The salt deposition was observed at the surface of specimens without any crack for the seawater conditioning at 23 °C and 65 °C. The swelling and crack formation were significantly visible on the surface of the specimen immersed for 12 months at 90 °C. It indicates that the degradation mechanism accelerated at elevated temperature results fiber/matrix debonding. The tensile test indicates slight variation in the elastic modulus and reduction in strength of E-glass epoxy composite by 1% and 9% for specimens immersed at 23 °C and 65 °C respectively. However, at 90 °C, the tensile strength sharply decreased to 7% and elastic modulus significantly increased in the exposure of 12 months. A prediction approach based on a time-shift factor (TSF) was used. This model predicted that the strength retention of E-glass/Epoxy composite will be reduced to 7% in 450 years after immersion in seawater at 23 °C. Lastly, the activation energy for the degradation of the composite was calculated.

A series of poly(n-butyl acrylate-co-methacrylic acid) with different contents of acrylic crosslinking agent (1,4-butanediol dimethacrylate, BDDA) latexes, named as poly(BA-co-MAA-co-BDDA), PBMABD, were synthesized via a two-stage sequential emulsion polymerization. During the polymerization, the particle sizes of the PBMABD latexes and conversions including instantaneous conversion and overall conversion of monomers were monitored online by dynamic light scattering (DLS) technology and gravimetric analysis in half-hour intervals, respectively. The overall conversions at the end of emulsion polymerization with different crosslinking agent contents were high, and the latex particles grew in a spherical shape without secondary particles during the growth process. The adhesive properties, including loop tack force, peel force and shear resistance, were evaluated systematically according to Fédération Internationale des Fabricants et Transformateurs d'Adhésifs et Thermocollants sur Papiers et Autres Supports (FINAT) test methods. When the content of the crosslinking agent was 0.5 wt%, a best equilibrium among the adhesive properties could be achieved. The adhesive properties of the PBMABD polymer were closely related to its viscoelastic behaviour and molecular structure, such as gel content and various molecular weight parameters.

A new epoxy-based composite with higher toughness and thermal conductivity was developed. First, a poly(n-butyl acrylate)/poly(methyl methacrylate-co-glycidyl methacrylate) (PBMG) core–shell structured latex was prepared by seeded emulsion polymerization to toughen the epoxy resin (EP). Second, boron nitride particles were modified into nano-scale sheets and added to the epoxy/PBMG blend to improve the thermal conductivity of the resulting composite material. The properties of the constituent materials were determined prior to fabrication and testing of the composite product. The monomer conversion in the emulsion polymerization process of the PBMG was checked by determining the solid particle content. The PBMG particle size was characterized by dynamic laser scattering, and the morphology of the particles was characterized by scanning and transmission electron microscopy. The exfoliation of the modified boron nitride (MBN) flakes was verified by TEM and Raman microscopy. The mechanical properties and the thermal conductivity of the EP/PBMG/MBN composite were determined at various constituent contents. Results showed that the unnotched impact strength of the composite increased by 147%, the flexural strength increased by 49.1%, and the thermal conductivity increased by 98% compared with pristine EP at a PBMG content of 5 wt% and MBN content of 7 wt%. With the enhanced properties and ease of fabrication, the developed composite has good potential for application in high-end industries such as microelectronics packaging.

A new cyanate ester resin-based composite with higher toughness and thermal conductivity was developed. First, a poly(n-butyl acrylate)/poly(methyl methacrylate-co-acrylamide) (PBMAM) core–shell structured latex was prepared by seeded emulsion polymerization. Second, hexagonal boron nitride (h-BN) particles were modified by a surface coupling agent, 3-(2-amino ethyl amino)propyl trioxysilane, to improve the dispersion in cyanate ester resin (BADCy). Third, PBMAM and the modified boron nitride were mixed with BADCy resin to increase mechanical properties and thermal conductivity. The monomer conversion in the emulsion polymerization process of the PBMAM was monitored by determining the solid content. Its particle size was characterized by dynamic laser scattering, and the morphology of the particles was characterized using scanning and transmission electron microscopes. The modified boron nitride (ABN) was verified by FTIR and TGA measurements. The mechanical properties and thermal conductivity of the BADCy/PBMAM/ABN composites were determined at various BN contents. Results showed that the unnotched impact strength of the composite increased by 151% and the thermal conductivity increased by 85% at a PBMAM content of 5 wt% and ABN content of 6 wt%. With the enhanced properties and ease of fabrication, the developed composites have good potential for application in high-end industries such as microelectronic packaging.