Effect of fly ash and coupling agent on the structural, morphological, thermal, and mechanical properties of polyamide 6/acrylonitrile‐butadiene‐styrene blend

In the present study, coal fly ash (FA) was used as a reinforcement in a thermoplastic matrix blend of polyamide 6/acrylonitrile‐butadiene‐styrene (PA/ABS). In the first part of this work, the as‐received FA (raw FA) was sieved with a 25 μm sieve to obtain FA with particle size less than 25 μm (FA)....

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Veröffentlicht in:Polymer composites 2021-07, Vol.42 (7), p.3518-3538
Hauptverfasser: Ez‐Zahraoui, Siham, Kassab, Zineb, Ablouh, El‐houssaine, Sehaqui, Houssine, Bouhfid, Rachid, Alami, Jones, El Achaby, Mounir, Qaiss, Abou El Kacem
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container_end_page 3538
container_issue 7
container_start_page 3518
container_title Polymer composites
container_volume 42
creator Ez‐Zahraoui, Siham
Kassab, Zineb
Ablouh, El‐houssaine
Sehaqui, Houssine
Bouhfid, Rachid
Alami, Jones
El Achaby, Mounir
Qaiss, Abou El Kacem
description In the present study, coal fly ash (FA) was used as a reinforcement in a thermoplastic matrix blend of polyamide 6/acrylonitrile‐butadiene‐styrene (PA/ABS). In the first part of this work, the as‐received FA (raw FA) was sieved with a 25 μm sieve to obtain FA with particle size less than 25 μm (FA). Then, the physicochemical properties of the raw FA and the FA were determined. Afterwards, FA was used to prepare a masterbatch of 20 wt% FA and 80 wt% PA by twin‐screw extrusion. Using this masterbatch, composites with different FA contents (4.5, 9, 14, and 18.5 wt%), with and without styrene‐(ethylene‐butylene)‐styrene grafted with maleic anhydride (SEBS‐g‐MA) (S‐g‐M), were produced by extrusion, which was followed by injection molding. Subsequently, several characterization techniques were performed to investigate the effect of FA loading and the S‐g‐M coupling agent on the structural, morphological, thermal, and mechanical properties of the developed composites. The results showed that incorporating FA particles in the matrix blend improved the thermal stability and crystallinity, the Young's modulus, the tensile strength, and torsional properties of the composites. In contrast, the addition of S‐g‐M coupling agent to the polymer composites improved the interfacial adhesion between FA particles and the matrix blend. This further enhanced the structural, morphological, thermal, and mechanical properties of the polymer composites. Overall, the use of FA as an inorganic filler improves the thermal and mechanical properties of polymer composites and shows a potential for promising applications.
doi_str_mv 10.1002/pc.26076
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In the first part of this work, the as‐received FA (raw FA) was sieved with a 25 μm sieve to obtain FA with particle size less than 25 μm (FA). Then, the physicochemical properties of the raw FA and the FA were determined. Afterwards, FA was used to prepare a masterbatch of 20 wt% FA and 80 wt% PA by twin‐screw extrusion. Using this masterbatch, composites with different FA contents (4.5, 9, 14, and 18.5 wt%), with and without styrene‐(ethylene‐butylene)‐styrene grafted with maleic anhydride (SEBS‐g‐MA) (S‐g‐M), were produced by extrusion, which was followed by injection molding. Subsequently, several characterization techniques were performed to investigate the effect of FA loading and the S‐g‐M coupling agent on the structural, morphological, thermal, and mechanical properties of the developed composites. The results showed that incorporating FA particles in the matrix blend improved the thermal stability and crystallinity, the Young's modulus, the tensile strength, and torsional properties of the composites. In contrast, the addition of S‐g‐M coupling agent to the polymer composites improved the interfacial adhesion between FA particles and the matrix blend. This further enhanced the structural, morphological, thermal, and mechanical properties of the polymer composites. 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In the first part of this work, the as‐received FA (raw FA) was sieved with a 25 μm sieve to obtain FA with particle size less than 25 μm (FA). Then, the physicochemical properties of the raw FA and the FA were determined. Afterwards, FA was used to prepare a masterbatch of 20 wt% FA and 80 wt% PA by twin‐screw extrusion. Using this masterbatch, composites with different FA contents (4.5, 9, 14, and 18.5 wt%), with and without styrene‐(ethylene‐butylene)‐styrene grafted with maleic anhydride (SEBS‐g‐MA) (S‐g‐M), were produced by extrusion, which was followed by injection molding. Subsequently, several characterization techniques were performed to investigate the effect of FA loading and the S‐g‐M coupling agent on the structural, morphological, thermal, and mechanical properties of the developed composites. The results showed that incorporating FA particles in the matrix blend improved the thermal stability and crystallinity, the Young's modulus, the tensile strength, and torsional properties of the composites. In contrast, the addition of S‐g‐M coupling agent to the polymer composites improved the interfacial adhesion between FA particles and the matrix blend. This further enhanced the structural, morphological, thermal, and mechanical properties of the polymer composites. 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In the first part of this work, the as‐received FA (raw FA) was sieved with a 25 μm sieve to obtain FA with particle size less than 25 μm (FA). Then, the physicochemical properties of the raw FA and the FA were determined. Afterwards, FA was used to prepare a masterbatch of 20 wt% FA and 80 wt% PA by twin‐screw extrusion. Using this masterbatch, composites with different FA contents (4.5, 9, 14, and 18.5 wt%), with and without styrene‐(ethylene‐butylene)‐styrene grafted with maleic anhydride (SEBS‐g‐MA) (S‐g‐M), were produced by extrusion, which was followed by injection molding. Subsequently, several characterization techniques were performed to investigate the effect of FA loading and the S‐g‐M coupling agent on the structural, morphological, thermal, and mechanical properties of the developed composites. The results showed that incorporating FA particles in the matrix blend improved the thermal stability and crystallinity, the Young's modulus, the tensile strength, and torsional properties of the composites. In contrast, the addition of S‐g‐M coupling agent to the polymer composites improved the interfacial adhesion between FA particles and the matrix blend. This further enhanced the structural, morphological, thermal, and mechanical properties of the polymer composites. Overall, the use of FA as an inorganic filler improves the thermal and mechanical properties of polymer composites and shows a potential for promising applications.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1002/pc.26076</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0002-3660-6835</orcidid><orcidid>https://orcid.org/0000-0002-7799-3392</orcidid><orcidid>https://orcid.org/0000-0001-6694-3739</orcidid></addata></record>
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subjects ABS resins
acrylonitrile‐butadiene‐styrene
blend
Butadiene
Coupling agents
Extrusion molding
Fly ash
Injection molding
Maleic anhydride
Mechanical properties
Modulus of elasticity
Morphology
polyamide 6
Polyamide resins
polymer composites
Polymer matrix composites
Polymers
Reagents
Styrenes
Tensile strength
thermal and mechanical properties
Thermal stability
Thermodynamic properties
title Effect of fly ash and coupling agent on the structural, morphological, thermal, and mechanical properties of polyamide 6/acrylonitrile‐butadiene‐styrene blend
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