Preparation, crystallization, electrical conductivity and thermal stability of syndiotactic polystyrene/carbon nanotube composites

A homogeneous dispersion of multi-walled carbon nanotubes (MWCNTs) in syndiotactic polystyrene (sPS) is obtained by a simple solution dispersion procedure. MWCNTs were dispersed in N-methyl-2-pyrrolidinone (NMP), and sPS/MWCNT composites are prepared by mixing sPS/NMP solution with MWCNT/NMP dispersion. The composite structure is characterized by scanning electron microscopy and transmission electron microscopy. The effect of MWCNTs on sPS crystallization and the composite properties are studied. The presence of MWCNTs increases the sPS crystallization temperature, broadens the crystallite size distribution and favors the formation of the thermodynamically stable β phase, whereas it has little effect on the sPS γ to α phase transition during heating. By adding only 1.0 wt.% pristine MWCNTs, the increase in the onset degradation temperature of the composite can reach 20 °C. The electrical conductivity is increased from 10^{−10∼−16} (neat sPS) to 0.135 S m⁻¹ (sPS/MWCNT composite with 3.0 wt.% MWCNT content). Our findings provide a simple and effective method for carbon nanotube dispersion in polymer matrix with dramatically increased electrical conductivity and thermal stability.     

A facile route to develop electrical conductivity with minimum possible multi‐wall carbon nanotube (MWCNT) loading in poly(methyl methacrylate)/MWCNT nanocomposites

Today, we stand at the threshold of exploring carbon nanotube (CNT) based conducting polymer nanocomposites as a new paradigm for the next generation multifunctional materials. However, irrespective of the reported methods of composite preparation, the use of CNTs in most polymer matrices to date has been limited by challenges in processing and insufficient dispersability of CNTs without chemical functionalization. Thus, development of an industrially feasible process for preparation of polymer/CNT conducting nanocomposites at very low CNT loading is essential prior to the commercialization of polymer/CNT nanocomposites. Here, we demonstrate a process technology that involves in situ bulk polymerization of methyl methacrylate monomer in the presence of multi‐wall carbon nanotubes (MWCNTs) and commercial poly(methyl methacrylate) (PMMA) beads, for the preparation of PMMA/MWCNT conducting nanocomposites with significantly lower (0.12 wt% MWCNT) percolation threshold than ever reported with unmodified commercial CNTs of similar qualities. Thus, a conductivity of 4.71 × 10^?5 and 2.04 × 10^?3 S cm^?1 was achieved in the PMMA/MWCNT nanocomposites through a homogeneous dispersion of 0.2 and 0.4 wt% CNT, respectively, selectively in the in situ polymerized PMMA region by using 70 wt% PMMA beads during the polymerization. At a constant CNT loading, the conductivity of the composites was increased with increasing weight percentage of PMMA beads, indicating the formation of a more continuous network structure of the CNTs in the PMMA matrix. Scanning and transmission electron microscopy studies revealed the dispersion of MWCNTs selectively in the in situ polymerized PMMA phase of the nanocomposites. Copyright © 2012 Society of Chemical Industry     

Characterization of conductive multiwall carbon nanotube/polystyrene composites prepared by latex technology

Conductive multiwall carbon nanotube/polystyrene (MWCNT/PS) composites are prepared based on latex technology. MWCNTs are first dispersed in aqueous solution of sodium dodecyl sulfate (SDS) driven by sonication and then mixed with different amounts of PS latex. From these mixtures MWCNT/PS composites were prepared by freeze-drying and compression molding. The dispersion of MWCNTs in aqueous SDS solution and in the PS matrix is monitored by UV–vis, transmission electron microscopy, electron tomography and scanning electron microscopy. When applying adequate preparation conditions, MWCNTs are well dispersed and homogeneously incorporated in the PS matrix. The percolation threshold for conduction is about 1.5 wt% of MWCNTs in the composites, and a maximum conductivity of about 1 S m⁻¹ can be achieved. The approach presented can be adapted to other MWCNT/polymer latex systems.     

Modified carbon nanotube composites with high dielectric constant, low dielectric loss and large energy density

Flexible dielectric polystyrene based composites containing multi-walled carbon nanotubes (MWCNTs) were reported. The MWCNTs were coated with polypyrrole (PPy) by an inverse microemulsion polymerization. Transmission electron microscopy, X-ray photoelectron spectroscopy and Raman spectroscopy indicated that the MWCNTs were coated with PPy. Our composites presented a stable high dielectric constant (∼44), rather low loss (<0.07), and large energy density (up to 4.95 J cm⁻³). The largely-enhanced dielectric performance originates from the organic shell PPy, which not only ensure good dispersion of MWCNTs in the polymer matrix but also screen charge movement to shut off leakage current. Such MWCNT composites can be used to store charge and electrical energy and play a key role in modern electronics and electric power systems.     

Coupling activity of ionic liquids between diene elastomers and multi-walled carbon nanotubes

In order to ensure better rubber/multi-walled carbon nanotube (MWCNT) compatibility and to enhance the dispersibility, a series of ionic liquids has been tested in regard to an improved interaction between rubber and carbon nanotubes. We found that in the presence of especially one ionic liquid, namely, 1-allyl-3-methyl imidazolium chloride, for the blend of solution-styrene-butadiene and polybutadiene rubber, used as basic elastomer, a three fold increase of tensile strength was achieved with only ∼3 wt.% MWCNT loading. At this low concentration of MWCNTs the sample can be stretched up to 456% without mechanical failure. The use of this ionic liquid additionally results in higher electrical conductivity (10⁻² S cm⁻¹) at low concentration (<3 wt.%) of MWCNTs. Dynamic mechanical analysis confirmed the specific interaction of CNTs and diene rubber chains by showing an extra relaxation process at relatively higher temperature (∼T_g + 130 K) in the temperature sweep measurements. Raman spectroscopic analysis also supported the specific interaction between MWCNTs and rubber molecules with the help of 1-allyl-3-methyl imidazolium chloride. Transmission electron microscopic images confirm the good dispersion of the MWCNTs along with a ‘cellular’-like structure of the CNTs in the rubber matrix.     

Electrical and mechanical properties of acrylonitrile‐butadiene‐styrene/multiwall carbon nanotube nanocomposites prepared by melt‐blending

The electrical properties in polymer/carbon nanotube (CNT) nanocomposites are governed not only by the degree of dispersion but also to a greater extent on the aspect ratio of the CNTs in the final composites. Melt‐mixing of polymer and CNTs at high shear rate usually breaks the CNTS that lowers the aspect ratio of the nanotubes. Thus, homogeneous dispersion of CNTs while retaining the aspect ratio is a major challenge in melt‐mixing. Here, we demonstrate a novel method that involves melt‐blending of acrylonitrile‐butadiene‐styrene (ABS) and in situ polymerized polystyrene (PS)/multiwalled CNT (MWCNT) nanocomposites, to prepare electrically conducting ABS/MWCNT nanocomposites with very low CNT loading than reported. The rationale behind choosing PS/MWCNT as blending component was that ABS is reported to form miscible blend with the PS. Thus, (80/20 w/w) ABS/(PS/MWCNT) nanocomposites obtained by melt‐blending showed electrical conductivity value ≈1.27 × 10^?6 S cm^?1 at MWCNT loading close to 0.64 wt %, which is quite lower than previously reported value for ABS/MWCNT system prepared via solution blending. Scanning electron microscopy and differential scanning calorimetry analysis indicated the formation of homogenous and miscible blend of ABS and PS. The high temperature (100°C) storage modulus of ABS (1298 MPa) in the nanocomposites was increased to 1696 MPa in presence of 0.64 wt % of the MWCNT. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Synergistic effect of dual nanofillers (MWCNT and Ni–Al LDH) on the electrical and thermal characteristics of polystyrene nanocomposites

The advantage of using 3D hybrid filler containing carboxylic acid functionalized multiwalled carbon nanotubes (c‐MWCNTs) and sodium dodecyl sulfate modified Ni–Al layered double hydroxide (sN‐LDH) over c‐MWCNTs and sN‐LDHs acting alone was investigated. PS/c‐MWCNT composites proved to be good for improvement of properties, but not to an appreciable level, especially in case of electrical conductivity, flame retardancy, rheology, and water vapor permeability. Hence, a combination of 0.3 wt % of c‐MWCNT and 3 wt % of sN‐LDH was optimized as additives to assist in the full expression of the filler traits in the nanocomposite and to obtain a versatile nanocomposite with properties specific to both the fillers. This approach slightly decreases the dispersion challenge faced with handling high loadings of CNT and also the intrinsic limitations specific to the individual fillers (i.e., inertness of CNTs and low conductivity of LDHs). Moreover, the anion/anionic repulsion of organically modified CNT/LDH facilitates effective dispersion of the additive opposing adhesion. FTIR and Raman spectroscopy provided evidence for incorporation and proper dispersion of the additives in the polymer matrix, with XRD and TEM confirming a well‐dispersed morphology of the nanocomposites. In this work, focus is made on the improvement of thermal stability, flame retardancy, melt rheology, hardness, electrical conductivity, and water vapor permeability of PS/0.3 wt % c‐MWCNT/3 wt % sN‐LDH nanocomposites over PS/0.3 wt % c‐MWCNT, making use of the synergistic effect of c‐MWCNT coupled with sN‐LDH on polystyrene. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46513.     

Synergistic effect of multiwalled carbon nanotubes and an intumescent flame retardant: Toward an ideal electromagnetic interference shielding material with excellent flame retardancy

To shield undesirable electromagnetic waves caused by electronic devices and simultaneously resolve the flame safety of the electronic components, an electromagnetic interference (EMI) shielding material with excellent flame‐retardant properties is urgently needed. The synergistic effect of the intumescent flame retardant (IFR) and multiwalled carbon nanotubes (MWCNTs) for polystyrene (PS) nanocomposites prepared by melt blending was investigated. The results show that addition of certain amounts of IFRs facilitated the dispersion of MWCNTs in the PS matrix, and the percolation threshold of the MWCNTs in the PS matrix also decreased from 1.67 ± 0.05 to 1.29 ± 0.04 wt %. Moreover, the EMI shielding efficiencies (SEs) of the PS–MWCNT–IFR composites were consistently higher than those of the PS–MWCNT composites without the addition of the IFRs at the same MWCNT content; this indicated that the synergistic effect of the MWCNTs and IFRs effectively improved the EMI SE of the PS–MWCNT–IFR composites. Furthermore, the limiting oxygen index (LOI) testing results show that the LOI values of the PS–MWCNT composites were consistently higher than 27%; this indicated that the PS–MWCNT composites effectively met the needs of flame safety; this indicated that the PS–MWCNT–IFR composite is a novel and promising candidate for an ideal EMI shielding material with excellent flame‐retardant properties for today's electronic devices. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45088.     

Enhanced electrical conductivity of nylon 6 composite using polyaniline-coated multi-walled carbon nanotubes as additives

Aggregation in polymer composites is one of the major obstacles in the carbon nanotubes (CNTs) applications. Authentic CNTs are known to have very good electrical conductivity and mechanical strengths. Surface functionalization can avoid aggregation and help dispersion of CNTs, but reduces CNT’s electrical conductivities and mechanical strengths dramatically. It needs a good way to resolve the above dilemma situation; i.e., poor dispersion-good conductivity vs. good dispersion-poor conductivity. Herein, we demonstrate that in-situ polymerized polyaniline (PANI)-coated CNTs have good polymer matrix compatibility, and are superior electrically conductive fillers to nylon 6 composites. In this report, multi-walled CNTs (MWCNTs) were surface-modified with poly(acrylic acids) (PAA), followed by further coating with PANI. The electrical conductivity of (PANI-MWCNTs)-nylon 6 composite thin film was increased from 10⁻¹² to 7.3 × 10⁻⁵ S/cm in the presence of 1 wt% PANI-coated MWCNTs prepared by physical mixing of PANI and PAA-grafted MWCNTs. When in-situ polymerized PANI-coated MWCNTs were added, the electrical conductivity of MWCNTs-nylon 6 composite was further enhanced by 3 orders to be 3.4 × 10⁻² S/cm at the same 1 wt% loading of MWCNTs. Both Fourier-transformed infrared and uv-visible absorption spectra indicate that there exist very strong site-specific charge transfer interactions between the quinoid rings of PANI and MWCNTs, which results in the superior electrical conductivity of MWCNT-nylon 6 composite.     

Polystyrene composites containing crosslinked polystyrene‐multiwalled carbon nanotube balls

Crosslinked polystyrene‐multiwalled carbon nanotube (PS‐MWCNT) balls, which act as conductive microfillers, were prepared by the in situ suspension polymerization of styrene with MWCNTs and divinyl benzene (DVB) as a crosslinking agent. The diameters of the synthesized crosslinked PS‐MWCNT balls ranged from 10 to 100 μm and their electrical conductivity was about 7.7 × 10^?3 S/cm. The morphology of the crosslinked PS‐MWCNT balls was observed by scanning electron microscopy and transmission electron microscopy. The change in the chemical structure of the MWCNTs was confirmed by Raman spectroscopy and Fourier transform infrared spectroscopy. The mechanical and electrical properties of the PS/crosslinked PS‐MWCNT ball composites were investigated. It was found that the tensile strength, ultimate strain, Young's modulus, and impact strength of the PS matrix were enhanced by the incorporation of the crosslinked PS‐MWCNT balls. In addition, the mechanical properties of the PS/crosslinked PS‐MWCNT ball composites were better than those of the PS/pristine MWCNT composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Highly dispersed carbon nanotube reinforced cement based materials

The remarkable mechanical properties of carbon nanotubes (CNT) suggest that they are ideal candidates for high performance cementitious composites. The major challenge however, associated with the incorporation of CNTs in cement based materials is poor dispersion. In this study, effective dispersion of different length multiwall carbon nanotubes (MWCNTs) in water was achieved by applying ultrasonic energy and in combination with the use of a surfactant. The effects of ultrasonic energy and surfactant concentration on the dispersion of MWCNTs at an amount of 0.08 wt.% of cement were investigated. It is shown that for proper dispersion the application of ultrasonic energy is absolutely required and for complete dispersion there exists an optimum weight ratio of surfactant to CNTs. For a constant ratio of surfactant to MWCNTs, the effects of MWCNT type (short and long) and concentration on the fracture properties, nanoscale properties and microstructure of nanocomposite materials were also studied. Results suggest that MWCNTs improve the nano- and macromechanical properties of cement paste.     

The production of functionalized multiwall carbon nanotube/amino acid-based poly(amide–imide) composites containing a pendant dopamine moiety

The high compatibility of amino-acid based poly(amide–imide) (PAI) as a polymer matrix for acid-modified multi-walled carbon nanotubes (MWCNTs) is discussed. PAI was synthesized from the direct polycondensation reaction of N,N′-(pyromellitoyl)-bis-l-isoleucine with a dopamine-based diamine, 3,5-diamino-N-(3,4-dihydroxy-phenethyl)benzamide, in a medium consisting of a molten salt, tetrabutylammonium bromide, and triphenyl phosphite as the activator under microwave radiation. To obtain a homogeneous dispersion of MWCNTs in the PAI matrix, acid-functionalized MWCNTs were used. Composites containing 5, 10, and 15 wt.% MWCNT–COOH exhibited a relatively good dispersion on the macroscopic scale. MWCNT/PAI composite films have been prepared by casting a solution of precursor polymer containing MWCNTs into a thin film and its tensile properties examined. Incorporation of MWCNTs improved the mechanical properties significantly. Composites were also characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning and transmission electron microscopy, and thermal gravimetric analysis. The thermal stability of the composites containing the CNTs was improved due to the increased interfacial interaction between the PAI matrix and the modified CNTs and their good dispersion.     

High dispersion ability of fluorene‐based polyester as a polymer matrix for carbon nanotubes

The high compatibility of fluorene‐based polyester (FBP‐HX) as a polymer matrix for multiwalled carbon nanotubes (MWCNTs) is discussed. A low surface resistivity due to the fine dispersion of MWCNTs in FBP‐HX and polycarbonate (PC) is reported. With a solution‐casting method, a percolation threshold with the addition of between 0.5 and 1.0 wt % MWCNTs was observed in the MWCNT/PC and MWCNT/FBP‐HX composites. Because of the coverage of FBP‐HX on the MWCNTs, a higher surface resistivity and a higher percolation ratio of the MWCNT/FBP‐HX composites were achieved compared with the values for the MWCNT/PC composites. In the MWCNT/FBP‐HX composites, MWCNTs covered with FBP‐HX were observed by scanning electronic microscopy. Because of the coverage of FBP‐HX on the MWCNTs, FBP‐HX interfered with the electrical pathway between the MWCNTs. The MWCNTs in FBP‐HX were covered with a 5‐nm layer of FBP‐HX, but the MWCNTs in the MWCNT/PC composites were in their naked state. MWCNT/PC sheets demonstrated the specific Raman absorption of the MWCNTs only with the addition of MWCNTs of 1 wt % or above because of the coverage of the surface of the composite sheet by naked MWCNTs. In contrast, MWCNT/FBP‐HX retained the behavior of the matrix resin until a 3 wt % addition of MWCNTs was reached because of the coverage of MWCNTs by the FBP‐HX resin, induced by its high wettability. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

A flexible graphene/multiwalled carbon nanotube film as a high performance electrode material for supercapacitors

A flexible graphene/multiwalled carbon nanotube (GN/MWCNT) film has been fabricated by flow-directed assembly from a complex dispersion of graphite oxide (GO) and pristine MWCNTs followed by the use of gas-based hydrazine to reduce the GO into GN sheets. The GN/MWCNT (16 wt.% MWCNTs) film characterized by Fourier transformation infrared spectra, X-ray diffraction and scanning electron microscope has a layered structure with MWCNTs uniformly sandwiched between the GN sheets. The MWCNTs in the obtained composite film not only efficiently increase the basal spacing but also bridge the defects for electron transfer between GN sheets, increasing electrolyte/electrode contact area and facilitating transportation of electrolyte ion and electron into the inner region of electrode. Electrochemical data demonstrate that the GN/MWCNT film possesses a specific capacitance of 265 F g⁻¹ at 0.1 A g⁻¹ and a good rate capability (49% capacity retention at 50 A g⁻¹), and displays an excellent specific capacitance retention of 97% after 2000 continuous charge/discharge cycles. The results of electrochemical measurements indicate that the freestanding GN/MWCNT film has a potential application in flexible energy storage devices.     

The cutting of multi-walled carbon nanotubes and their strong interfacial interaction with polyamide 6 in the solid state

The cutting of multi-walled carbon nanotubes (MWCNTs) using solid state shear milling (S³M) method and their strong interfacial interaction with polyamide 6 (PA6) in the solid state were studied. Transmission electron microscopy showed that after milling, the CNTs were greatly reduced in length, and disentangled, being straighter with open ends. Fourier transform infrared spectra and differential scanning calorimeter analysis indicated the existence of strong interfacial interactions between MWCNTs and PA6 of the pan-milled PA6/CNTs powder. It was further quantified by thermogravimetric analysis that about 30 wt.% of PA6 formed a strong combining force with CNTs after pan-milling. The mechanism of cutting CNTs and the reason for their strong interfacial interactions with PA6 in the solid state were discussed. A fine and homogeneous dispersion of CNTs throughout PA6 matrix was observed by scanning electron microscopy. The tensile properties of the composites prepared by the S³M method were significantly improved compared to those of pure PA6 and composites prepared by conventional melt mixing. Upon incorporation of only 1.5 wt.% MWCNTs, the tensile modulus of PA6 was enhanced from 2448 MPa to 4439 MPa, by about 80%, and the tensile strength was increased by about 23%.     

Influence of rigid segment content on the piezoresistive behavior of multiwall carbon nanotube/segmented polyurethane composites

Tensile piezoresistive properties of multiwall carbon nanotube (MWCNT)/segmented polyurethane (SPU) composites comprising 15, 30, and 50 wt % rigid segment (RS) contents and 2, 4, and 6 wt % MWCNT contents are investigated. The physicochemical properties of such composites are used to better understand their mechanical and piezoresistive behavior. Infrared spectra shows that for 15 and 30 wt % RS composites the addition of MWCNTs promotes a more structured RS domain which increases the phase separation, while for 50 wt % RS composites the MWCNTs disrupt the RS domains of the polymer with a high phase separation. Overall, MWCNT content has less effect on the phase separation than RS content. The composites with 6 wt % MWCNT content reached electrical conductivities of the order of ～10^?1 S/m using 15 and 50 wt % RS polymers. Upon deformation, composites with 15 wt % RS and 4 wt % MWCNT achieved changes in electrical resistance of the order of 5000 times their unstrained value, which are outstanding values that can be exploited for applications such as human motion detection. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44448.     

Mechanical and electrical properties of multi walled carbon nanotube/ABC block terpolymer composites

Composites of multi-walled carbon nanotubes (MWCNTs) in ABC block terpolymer matrices of different compositions are studied. The composites were obtained by dispersion of MWCNTs in poly(styrene-block-butadiene-block-methyl methacrylate) (SBM) in a selective solvent for the M block, followed by solvent evaporation and compression molding. The structures of the MWCNT/SBM composites are investigated by transmission electron microscopy. The processing conditions, i.e. solvent cast or compression molding, induce different non-equilibrium microstructures and the MWCNTs modify the SBM organization only locally. We show that by fixing the processing procedure we are able to obtain samples with reproducible microstructure and properties. The electrical conductivity thresholds of these composites are lower than 1 wt.%. The reinforcing effect of the MWCNTs measured by dynamical mechanical analysis is mainly related to the SBM microstructures of the matrix and to the MWCNT dispersion quality.     

Properties of surface‐modified multiwalled carbon nanotube filled poly(ethylene terephthalate) composite films

Poly(ethylene terephthalate) (PET)/multiwalled carbon nanotube (MWCNT) composites were prepared by in situ polymerization. To improve the dispersion of MWCNTs in the PET matrix, functionalized MWCNTs having acid groups (acid‐MWCNTs) and acetic groups (acetic‐MWCNTs) on their surfaces were used. The functional groups were confirmed by infrared spectrometry. Scanning electron microscopy showed that acetic‐MWCNTs had a better dispersion in the PET matrix than pristine MWCNTs and acid‐MWCNTs. A reaction between PET and acetic‐MWCNTs was confirmed by a shift of the Raman G band to a higher frequency and an increase of the complex viscosity in the rheological properties. The composites containing functionalized MWCNTs showed a large increase in their tensile strengths and moduli. The values of the strengths and moduli of the PET/acetic‐MWCNT composites were higher than those of the PET/acid‐MWCNT composites. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Carbon nanohorn and graphene nanoplate based polystyrene nanocomposites for superior electromagnetic interference shielding applications

In this article is reported the preparation of carbon nanohorn (CNH)/graphene nanoplates (GNP)/polystyrene (PS) nanocomposites through in‐situ bulk polymerization of styrene monomer in the presence of CNH, followed by the addition of suspension polymerized GNP/PS bead during polymerization of styrene, as next‐generation multifunctional material for high electrical conductivity and electromagnetic interference shielding effectiveness (EMI SE) applications. Morphological analysis revealed selective dispersion of CNH in bulk polymerized PS matrix, where GNP/PS beads were randomly distributed. The formation of continuous CNH–CNH conductive path and GNP–CNH–GNP or CNH–GNP–CNH conductive network throughout the PS matrix at exceptionally low loading of CNH (1.0 wt %) and GNP (0.15 wt %) leads to high electrical conductivity (6.24 × 10^?2 S cm^?1) and EMI SE ～(?24.83 dB) when the nanocomposites was prepared in the presence of 75 wt % GNP/PS bead. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42803.     

Influence of chemical functionalization of carbon nanotubes on their dispersibility in alkyl methacrylate polymer matrix

Nanocomposites based on poly(methyl methacrylate) (PMMA) and poly(methyl methacrylate‐co‐octadecyl methacrylate) (M/O) matrices and four different types of multiwall carbon nanotubes: pristine, oxidized (MWCNT–COOH), methyl ester (MWCNT–COOCH₃), and dodecyl ester (MWCNT–COOC₁₂H₂₅) functionalized, were prepared in situ by radical (co)polymerization. The effectiveness of preparation of nanocomposites regarding dispersion and distribution of various MWCNT in polymer matrices was sized by Scanning electron microscopy. In case of PMMA matrix, the best dispersion and distribution were accomplished for MWCNT–COOCH₃ due to their chemical resemblance with polymer matrix. After the introduction of 10 mol % of octadecyl methacrylate in polymer matrix a fairly good dispersion and distribution of MWCNT–COOCH₃ were retained. The addition of 1 wt % of MWCNTs caused a significant reduction in the degree of polymerization of the PMMA matrix. But at the same time, the present MWCNTs increased storage modulus of PMMA nanocomposites except for dodecyl ester functionalized MWCNT. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46113.