Graphene nanoplatelets composite membranes for thermal comfort enhancement in performance textiles

The advent of 2D nanostructured materials as advanced fillers for polymer matrix composites has opened the doors to a plethora of new industrial applications requiring both electric and thermal management. Unique properties, in fact, can arise from accurate selection and processing of 2D fillers and their matrix. Here, we report an innovative family of nanocomposite membranes based on polyurethane (PU) and graphene nanoplatelets (GNPs), designed to improve thermal comfort in functional textiles. GNP particles were thoroughly characterized (through Raman, atomic force microscopy, high-resolution TEM, scanning electron microscope), and showed high crystallinity (I_D/I_G = 0.127), low thickness (D50 < 6–8 layers), and high lateral dimensions (D50 ≈ 3 μm). When GNPs were loaded (up to 10% wt/wt) into the PU matrix, their homogeneous dispersion resulted in an increase of the in-plane thermal conductivity of composite membranes up to 471%. The thermal dissipation of membranes, alone or coupled with cotton fabric, was further evaluated by means of an ad hoc system designed to simulate a human forearm. The results obtained provide a new strategy for the preparation of membranes suitable for technical textiles, with improved thermal comfort.     

Shielding effectiveness of carbon‐filled polycarbonate composites

In this project, varying amounts of three different carbons [carbon black (CB), carbon nanotubes (CNT), and graphene nanoplatelets (GNP)] were added to polycarbonate (PC). The resulting single filler composites were tested for shielding effectiveness (SE). The effects of single fillers and combinations of two different carbon fillers were studied via a factorial design. At the highest single filler loadings, the following SE results were obtained at 800 MHz: 18.9 dB for 10 wt % CB/PC, 18.4 dB for 8 wt % CNT/PC, and 6.3 dB for 15 wt % GNP/PC. The highest SE value of 21.4 dB was measured for the 5 wt % CB/5 wt % CNT/PC composite and could be used in SE applications (typically > 20 dB is needed). Statistically significant equations were developed that could be used to predict the SE of composites containing these fillers. In addition, it was determined that the composite SE is higher than what would be expected from the additive effect of each single filler for the CB/GNP/PC composites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42719.     

In situ fast polymerization of graphene nanosheets‐filled poly(methyl methacrylate) nanocomposites

A series of graphene nanosheets‐filled poly(methyl methacrylate) nanocomposites (GNS/PMMA) is successfully prepared by an in situ fast polymerization method with graphene weight fractions from 0.1 to 2.0 wt %. In situ polymerization is effective in well dispersing of GNS in matrixes and suitable for both low and high content of GNS. The synthesis processes of polymer composites could be simplified and fast by using industrial grade graphene. The GNS fillers are found to disperse homogeneously in the PMMA matrix. The maximum electrical conductivity of the composites achieves 0.57 S m^?1, with an extremely low percolation threshold of 0.3 wt %. The electrical conductivities are further predicted by percolation theory and found to agree well with the experimental results. The results indicate that the microstructures, thermal, electrical, and mechanical properties of PMMA polymer are significantly improved by adding a low amount of graphene nanosheets. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43423.     

Piezoresistive behavior of graphene nanoplatelets/carbon black/silicone rubber nanocomposite

Silicon rubber (SR) filled with carbon black (CB) and carbon black (CB)/graphene nanoplatelets (GNPs) hybrid fillers are synthesized via a liquid mixing method. The effects of filler type on the electrical properties and piezoresistive properties (near the region of the percolation) of the conductive SR composites are studied. It is suggested that the conductivity of the composite filled with CB/GNPs hybrid fillers in the mass ratio of 2 : 4 is much higher than that in other ratio. Percolation threshold for CB/GNPs/SR is found to be 0.18 volume fractions lower than CB/SR. Moreover, force rang and linearity of GNPs/CB/SR is higher than CB alone filling system. And the repeatability of the GNPs/CB/SR composites is better than CB/SR. Not repetitive index () of them is 0.1 and 0.18, respectively. The results suggest that the GNPs/CB/SR composites provide a new route toward fabrication of flexible piezoresistive sensors with high performance. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39778.     

Melt spinning of conductive textile fibers with hybridized graphite nanoplatelets and carbon black filler

In this study, two different carbon fillers: carbon black (CB) and graphite nanoplatelets (GNP) are studied as conductive fillers for the preparation of conductive polypropylene (PP) nanocomposites. In order to obtain a homogenous dispersion of GNP, GNP/PP composites were prepared by two different methods: solid state mixing (SSM) and traditional melt mixing (MM). The result shows that MM is more efficient in the dispersion of GNP particles compared to SSM method. PP nanocomposites containing only one conductive filler and two fillers were prepared at different filler concentrations. Based on the analysis of electrical and rheological properties of the prepared nanocomposites, it shows that a hybridized composite with equal amounts of GNP and CB has favorable processing properties. Conductive fibers with a core/sheath structure were produced on a bicomponent melt spinning line. The core materials of these fibers are the hybridized GNP/CB/PP nanocomposite and the sheath is pure polyamide. It was found that GNPs were separated during melt and cold drawing which results in the decrease of conductivity. However, the conductivity could partly be restored by the heat treatment. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2579–2587, 2013     

Investigation of the elastic properties of poly (methyl methacrylate) reinforced with graphene nanoplatelets

The technique for synthesis of poly (methyl methacrylate) (PMMA) by atom transfer radical polymerization has been strengthened by using graphene nanoplatelets (GNPs) to enhance the elastic properties of the polymer. In order to improve practical, economical and mechanical performance, the requirements for effective implementation of production control as a smart bulk polymer nanocomposite were determined for cost-effective bulk production. Three-dimensional inspection (using an ultrasound interrogation method for the whole volume under test) confirmed the synthesis of the nanocomposite to be free of agglomeration and bubbles. As a result of this elimination of defects, an enhancement in compressive strength of 42.7% was achieved and the Rockwell hardness was increased by 19.9% through the addition of GNPs at 2 wt% by mass. The deformation and mechanical failure properties have been characterized in the mechanical enhancement of the polymer nanocomposite. Elastic parameters determined using ultrasound testing identified that changes in the structural features following the addition of these GNPs were uniquely connected to the enhancements in these elastic parameters (such as Young's modulus, Poisson's ratio, shear modulus, and microhardness) of the PMMA/GNPs nanocomposite.     

Examining the contribution of factors affecting the electrical behavior of poly(methyl methacrylate)/graphene nanoplatelets composites

In this study, poly(methyl methacrylate) (PMMA)/graphene nanoplatelets (GNPs) conductive composite films with different morphologies were fabricated from the same constituent materials using four fabrication techniques, solution casting (SC), SC followed by hot pressing (SCP), melt mixing followed by SC (MSC), and melt mixing followed by hot pressing (MP). Morphologies of dispersed GNPs and electrical properties in both in-plane and perpendicular direction were investigated and compared systematically. The corresponding percolation thresholds (Φ_c) of the composites varied from 0.42 ± 0.13 vol% to 3.26 ± 0.48 vol%. The conductivities varied up to two orders of magnitude and decreased in the sequence of SC > MSC > SCP > MP. These variations were explained in terms of GNPs size, GNPs orientation, distribution and dispersion state of fillers. The contribution of the above factors in each procedure were discerned individually, the results were discussed and compared with other experimental studies and simulations as well.     

Mechanical properties of graphene nanoplatelet/epoxy composites

Because of their high‐specific stiffness, carbon‐filled epoxy composites can be used in structural components in fixed‐wing aircraft. Graphene nanoplatelets (GNPs) are short stacks of individual layers of graphite that are a newly developed, lower cost material that often increases the composite tensile modulus. In this work, researchers fabricated neat epoxy (EPON 862 with Curing Agent W) and 1–6 wt % GNP in epoxy composites. The cure cycle used for this aerospace epoxy resin was 2 h at 121°C followed by 2 h at 177°C. These materials were tested for tensile properties using typical macroscopic measurements. Nanoindentation was also used to determine modulus and creep compliance. These macroscopic results showed that the tensile modulus increased from 2.72 GPa for the neat epoxy to 3.36 GPa for 6 wt % (3.7 vol %) GNP in epoxy composite. The modulus results from nanoindentation followed this same trend. For loadings from 10 to 45 mN, the creep compliance for the neat epoxy and GNP/epoxy composites was similar. The GNP aspect ratio in the composite samples was confirmed to be similar to that of the as‐received material by using the percolation threshold measured from electrical resistivity measurements. Using this GNP aspect ratio, the two‐dimensional randomly oriented filler Halpin–Tsai model adjusted for platelet filler shape predicts the tensile modulus well for the GNP/epoxy composites. Per the authors' knowledge, mechanical properties and modeling for this GNP/epoxy system have never been reported in the open literature. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Multilayer coextrusion of graphene polymer nanocomposites with enhanced structural organization and properties

A potential advantage of platelet‐like nanofillers as nanocomposite reinforcements is the possibility of achieving two‐dimensional (2D) stiffening through planar orientation of the platelets. Forced assembly by multilayer coextrusion, which enables the in‐plane orientation of platelet‐like fillers in alternating layers, was used in this work to produce poly(lactic acid) (PLA)/graphene multilayer films. These films exhibited a multilayer structure made of alternating layers of neat PLA and PLA containing graphite nanoplatelets (GNPs). Electron microscopy revealed information on the orientation of the individual GNPs. X‐ray diffraction results indicated that the thickness of the individual GNPs was reduced during the multilayer coextrusion process. A significant reinforcement of 120% at an overall GNP loading of 1 wt % in PLA was achieved. This high effective reinforcement was attributed to the high degree of planar alignment, improved dispersion and exfoliation and increased aspect ratio of the GNPs in the composite layers after multilayer coextrusion. Improved water vapor barrier properties were also achieved as a result of the highly organized 2D nanofillers in the multilayer films. These industrial scalable multilayer nanocomposite films open up possibilities for lightweight and strong packaging materials for food and industrial applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46041.     

Ionic liquids as dispersing agents of graphene nanoplatelets in poly(methyl methacrylate) composites with microwave absorbing properties

Graphene nanoplatelets (GNP) is noncovalently functionalized with imidazolium-, pyridinium-, and vinyl-pyridinium-based ionic liquids containing bromide or bis(trifluoromethyl-sulfonyl)imide (TFSI) as the counteranions, and used to prepare poly (methyl methacrylate) (PMMA) nanocomposites by solution casting approach followed by compression molding technique. The PMMA composites loaded with 1.9 and 1.8 wt% of GNP in PMMA/GNP composite and PMMA/GNP/ionic liquids, respectively, were characterized by melting viscosity, thermogravimetric analysis and AC electrical conductivity (σ_AC). The microwave absorption properties at the X-band (8.2–12.4 GHz) frequency were measured for systems with 1 mm thickness using the metal-backed configuration. PMMA nanocomposites loaded with GNP/N-dodecyl-4-vinyl-pyridinium.TFSI (C₁₂ViPy.TFSI) displayed higher thermal stability and higher σ_AC. This system also presented the best response in terms of microwave absorbing properties, with minimum reflection loss (RL) of around −6 dB at 8.7 GHz. Triple layered composite structures with layers of different conductivities and different stacking orders were also investigated in terms of reflection loss. Broadband absorption with minimum RL ≤ −10 dB (90% of electromagnetic attenuation) in the frequency between 10.2 and 12.4 GHz and better absorbing effectiveness were observed for the PMMA/GNP-PMMA/GNP/C₁₂ViPy.TFSI-PMMA/GNP/C₁₂ViPy.Br triple-layered system with 3 mm thickness.     

Electrical conductivity and tensile properties of block‐copolymer‐wrapped single‐walled carbon nanotube/poly(methyl methacrylate) composites

Poly(methyl methacrylate) (PMMA) composites containing raw or purified single‐walled carbon nanotubes (SWCNTs) are prepared by in situ polymerization and solution processing. The SWCNTs are purified by centrifugation in a Pluronic surfactant, which consists of polyethyleneoxide and polypropyleneoxide blocks. Both the effects of SWCNT purity and non‐covalent functionalization with Pluronic are evaluated. Electrical conductivity of PMMA increases by 7 orders of magnitude upon the integration of raw or purified SWCNTs. The best electrical properties are measured for composites made of purified SWCNTs and prepared by in situ polymerization. Strains at fracture of the SWCNT/PMMA composites are nearly identical to those of the neat matrix. A certain decrease in the work to fracture is measured, particularly for composites containing purified SWCNTs (?31.6%). Fractography and Raman maps indicate that SWCNT dispersion in the PMMA matrix improves upon the direct addition of Pluronic, while dispersion becomes more difficult in the case of purified SWCNTs. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41547.     

High electrical conductivity of nylon 6 composites obtained with hybrid multiwalled carbon nanotube/carbon fiber fillers

The synergetic effect of multiwalled carbon nanotubes (MWNTs) and carbon fibers (CFs) in enhancing the electrical conductivity of nylon 6 (PA6) composites was investigated. To improve the compatibility between the fillers and the PA6 resin, we grafted γ‐aminopropyltriethoxy silane (KH‐550) onto the MWNTs and CFs after carboxyl groups were generated on their surface by chemical oxidation with nitric acid. Fourier transform infrared spectroscopy and thermogravimetric analysis proved that the KH‐550 molecules were successfully grafted onto the surface of the MWNTs and CFs. Scanning electron microscopy and optical microscopy showed that the obtained modified fillers reduced the aggregation of fillers and resulted in better dispersion and interfacial compatibility. We found that the electrical percolation threshold of the MWNT/PA6 and CF/PA6 composites occurred when the volume fraction of the fillers were 4 and 5%, respectively. The MWNT/CF hybrid‐filler system exhibited a remarkable synergetic effect on the electrically conductive networks. The MWNT/7% CF hybrid‐filler system appeared to show a second percolation when the MWNT volume fraction was above 4% and a volume resistivity reduction of two orders of magnitude compared with the MWNT/PA6 system. The mechanical properties of different types of PA6 composites with variation in the filler volume content were also studied. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40923.     

Thermal conductivity and dielectric properties of polypropylene‐based hybrid compounds containing multiwalled carbon nanotubes

In this article, we explore the possibility to develop composites with improved thermal conductivity and electrically insulating properties. The strategy adopted is to combine a thermal and electrical conductive filler (multiwalled carbon nanotubes) with secondary dielectric (but thermally conductive) fillers. To this end, particles with different compositions, sizes, and shape were used as secondary fillers and the composites, prepared by melt compounding, are characterized in terms of thermal and dielectric properties. Results show that, in ternary formulations, an increase of thermal conductivity is always verified for all kind of secondary particles. Analogously, increments in electrical conductivity are observed for ternary compounds containing larger size secondary fillers, while a significant reduction is achieved with the addition of smaller ones. This behavior is explained in terms of mutual distribution of the fillers and is consistent with direct (scanning electron microscopy) and indirect (rheological) observations. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46470.     

Effect of flake size on thermal properties of graphene oxide/poly(methyl methacrylate) composites prepared via in situ polymerization

The effect of graphene oxide (GO) flake size on thermal properties of GO/poly(methyl methacrylate) (GO/PMMA) composites prepared via in situ polymerization was investigated. Two styles of GO sheets were synthesized from different sizes of graphite powders by modified Hummers' method and GO/PMMA composites with GO of different sizes were prepared via in situ polymerization. Transmission electron microscopy verified that GO sheets produced from large graphite powders was obviously larger than that from small graphite powders. The similar number of layers and disorder degree of two types of GO sheets were proved by X‐ray diffraction and Raman, respectively. X‐ray diffraction and scanning electron microscopy results of GO/composites proved the homogenous dispersion of both two types of GO sheets in polymer matrix. Dynamic mechanical analysis and thermogravimetric analysis results showed that large GO sheets exhibit better improvement than small GO sheets in thermal properties of the composites. Compared with neat PMMA, the glass transition temperature and decomposition temperature of the composites with large GO sheets (0.20 wt %) were increased by 15.9 and 25.9 °C, respectively. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46290.     

Construction of electrostatic and π–π interaction to enhance interfacial adhesion between carbon nanoparticles and polymer matrix

In this study, an efficient method by constructing electrostatic and π–π interaction to enhance interfacial adhesion of nanocomposites was contrived. As commercial products and commonly used reinforcements, carbon nanotubes (CNTs) and graphene oxide (GO) were selected as fillers. Two kinds of interactions between carbon nanoparticles and polymer matrix were constructed by adding auxiliary comonomers (ACMs) into nanocomposites, in which one was the electrostatic interaction between quaternary ammonium cationic groups on ACMs as well as oxygen-containing groups of carbon nanoparticles, while the other was the π–π interaction between benzene rings on ACMs and conjugated structure on nanoparticles. Poly(methyl methacrylate) (PMMA) was chosen as a polymer matrix. It was found that carbon nanoparticles dramatically improved properties of nanocomposites, including thermal and mechanical performances due to the construction of electrostatic and π–π interaction on the interface. Compared with PMMA, the tensile strength of CNTs and GO reinforced nanocomposites was improved by 43.1 and 57.5%, respectively. The thermal decomposition temperature of CNTs and GO reinforced nanocomposites was improved by 21 and 23°C, respectively. Interesting and convincing results proved that the construction of multiple interactions can provide a promising method to effectively enhance interfacial adhesion of nanocomposites. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48633.     

Nanostructured thermosetting epoxy systems modified with poly(isoprene‐b‐methyl metacrylate) diblock copolymer and polyisoprene‐grafted carbon nanotubes

Nanostructured thermosetting composites based on an epoxy matrix modified with poly(isoprene‐b‐methyl methacrylate) (PI‐b‐PMMA) block copolymer were prepared through PI block segregation. Morphological structures were examined by means of atomic microscopy force microscopy. As epoxy/pristine multi‐walled carbon nanotubes (MWCNT) systems were found to present big agglomerations, with a very poor dispersion of the nanofiller, epoxy/PI‐b‐PMMA/MWCNT systems were prepared by using polyisoprene‐grafted carbon nanotubes (PI‐g‐CNT) to enhance compatibility with the matrix and improve dispersion. It was found that the functionalization of MWCNT with grafted polyisoprene was not enough to totally disperse them into the epoxy matrix but an improvement of the dispersion of carbon nanotubes was achieved by nanostructuring epoxy matrix with PI‐b‐PMMA when compared with epoxy/MWCNT composites without nanostructuring. Nevertheless, some agglomerates were still present and the complete dispersion or confinement of nanotubes into desired domains was not achieved. Thermomechanical properties slightly increase with PI‐g‐CNT content for nanostructured samples, whereas for nonnanostructured epoxy/PI‐g‐CNT composites they appeared almost constant and even decreased for the highest nanofiller amount due to the presence of agglomerates. Compression properties slightly decreased with block copolymer content, while remained almost constant with nanofiller amount. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Preparation of high‐k composites with low dielectric loss based on the double‐layer coaxial structure of inorganic/polymer

This study presents a novel and simple modification of cladding multiwalled carbon nanotubes (MWCNTs) using organic polymer and inorganic nanoparticles to synthesize a product, which has a double‐cladding coaxial structure and can be applied as filler in the dielectric field. The first layer of MWCNTs was coated with polyaniline (PANI) through the oxidation–reduction reaction mechanism using Ce(NH₄)₂(NO₃)₆ as oxidizing agent and metal precursor of cerium oxide. Cerium ions on the second cladding layer of MWCNTs were directly deposited from the solution to the surface of the PANI layer forming the double‐cladding hybrid (CeO₂/PANI@MWCNTs). The external inorganic layer provides an insulating shell, which can prevent the contact between the conductive particles and hinder the migration of electrons between the MWCNTs. The intermediate layer of PANI provides the bonding between CeO₂ and the conductive core of MWCNTs, which also shows lower conductivity than carbon nanotubes. The CeO₂/PANI@MWCNTs were compounded with epoxy (EP) resin and formed a dielectric material with the advantage of reducing dielectric loss while ensuring high dielectric constant. The dielectric constant of the coated MWCNTs/EP composites was 194.90 at 10³ Hz with the content of fillers reaching 30 wt %, which is 28 times that of the pure EP. Accordingly, the dielectric loss of 30 wt % coated MWCNTs/EP composites was only 0.09 at 10³ Hz, which is only 2.25 times that of the pure EP. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46299.     

Electrical conductivity and EMI shielding effectiveness of polyurethane foam–conductive filler composites

The morphological, electrical, and thermal properties of polyurethane foam (PUF)/single conductive filler composites and PUF/hybrid conductive filler composites were investigated. For the PUF/single conductive filler composites, the PUF/nickel‐coated carbon fiber (NCCF) composite showed higher electrical conductivity and electromagnetic interference shielding effectiveness (EMI SE) than did the PUF/multiwall carbon nanotube (MWCNT) and PUF/graphite composites; therefore, NCCF is the most effective filler among those tested in this study. For the PUF/hybrid conductive fillers PUF/NCCF (3.0 php)/MWCNT (3.0 php) composites, the values of electrical conductivity and EMI SE were determined to be 0.171 S/cm and 24.7 dB (decibel), respectively, which were the highest among the fillers investigated in this study. NCCF and MWCNT were the most effective primary and secondary fillers, and they had a synergistic effect on the electrical conductivity and EMI SE of the PUF/NCCF/MWCNT composites. From the results of thermal conductivity and cell size of the PUF/conductive filler composites, it is suggested that a reduction in cell size lowers the thermal conductivity of the PUF/conductive filler composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44373.     

Effects of facile amine‐functionalization on the physical properties of epoxy/graphene nanoplatelets nanocomposites

Graphene nanoplatelets (GNPs) have excellent thermal, electrical, and mechanical properties. The incorporation of GNPs into a polymer can remarkably enhance the thermal and mechanical properties of the polymer especially when GNPs are well dispersed in the polymer matrix with strong interfacial bonding. Therefore, in this study, GNPs were amine‐functionalized by covalently bonding 4,4′‐methylene dianiline onto their surfaces via a facile synthetic route. The amine‐functionalization was confirmed by FTIR spectroscopy and TGA. Epoxy/GNPs nanocomposites were prepared and their curing behavior, thermomechanical properties and impact strength were investigated. The amine‐functionalization increased curing rate, storage modulus, thermal dimensional stability, and impact strength of the nanocomposites. The SEM images for the fracture surface of the nanocomposite with amine‐functionalized GNPs showed a smooth and ductile failure‐like surface, resulted from the improved interfacial bonding between GNPs and the epoxy matrix. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42269.     

Enhancement of the thermal stability and mechanical properties of a PMMA/aluminum trihydroxide composite synthesized via bead milling

The use of aluminum trihydroxide (ATH) fillers as non-halogen flame retardants for polymethylmethacrylates (PMMA) creates a conflict between the mechanical properties and heat resistance of the composites. Therefore, to ensure that the PMMA mechanical properties remain satisfactory, improvements in both the filler–polymer interactions and the ability to control the size and size distribution, morphology and dispersion of the fillers are required. Thus, in the present study, bead milling was used to control both the size distribution and dispersion of ATH fillers in MMA, which had an initial average size of 0.75 μm. The dispersion was obtained by alteration of the surface characteristics of ATH fillers using a silane-based dispersing agent, (3-acryloxypropyl) trimethoxysilane (APTMS). Bead milling successfully comminuted the ATH particles and prevented the formation of ATH agglomerates. The smallest average size of the ATH particles after bead milling was 300 nm. Highly dispersed ATH filler particles were observed in the TEM images of the PMMA/ATH composites. The filler–polymer interaction, i.e. the interaction parameter (B), was calculated. The effects of volume fraction, particle size distribution, and surface modification of the fillers on the results of dynamic mechanical analysis (DMA) are discussed. The thermal stability of the PMMA/ATH composites was also investigated using thermal gravimetric analysis (TGA).