乙烯-丙烯酸共聚物增容导电苯胺共聚物/聚乙烯共混物的形态与性能

以乙烯-丙烯酸共聚物(EAA)为增容剂,将十二烷基苯磺酸热掺杂的苯胺/邻甲氧基苯胺共聚物〔P(An-co-oAs)-DBSA〕与线性低密度聚乙烯(LLDPE)进行熔融共混制得P(An-co-oAs)-DBSA/LLDPE/EAA导电共混物,研究了EAA用量对共混物的导电性能和力学性能的影响。结果表明,当EAA与LLDPE的质量比为30/70时,共混物的电导率最佳,随着EAA含量的增加,共混物的拉伸强度增加,扯断伸长率降低;紫外-可见光谱分析表明,EAA在共混过程中对P(An-co-oAs)有一定的二次掺杂作用;扫描电子显微镜照片显示,EAA对共混体系有良好增容作用,同时发现EAA用量过多时会对P(An-co-oAs)-DBSA产生包覆作用,这对共混物的导电性是不利的。     

Synthesis and characterization of novel poly(aniline-co-m-aminoacetophenone) copolymer nanocomposites using dodecylbenzene sulfonic acid as a soft template

A series of dodecylbenzene sulphonic acid (DBSA) doped poly(aniline-co-m-aminoacetophenone) copolymer composites of different compositions were synthesized in micellar solution of DBSA to obtain nanosphere morphology with enhanced processability. The plausible mechanism for the formation of poly(aniline-co-m-aminoacetophenone)-DBSA copolymer composite has been presented. These DBSA doped copolymer composites were characterized by UV–Visible, FTIR spectroscopy and XRD analysis techniques. UV–Vis absorption spectrum of the composites showed 325 and 637 nm which corresponds to the π–π* and n–π* transition. In FTIR spectroscopy a broad band around 2,924 cm^?1 corresponds to C–H vibration of DBSA indicating good agreement with the characteristic bands of DBSA. The sharp band at 1,292 cm^?1 is assigned to C–N stretching mode of vibration of N–Ph–N units. The X-ray diffraction of composites reveals that these composites are amorphous in nature. The number of diffraction peaks decreased with increase in the m-aminoacetophenone content. It indicates that these composites are amorphous in nature. Morphological studies (SEM) reveal that these composites have a spherical morphology with the average size of 100–200 nm. These composites exhibit electrical conductivity value of 0.744 × 10^?3 S/cm and enhanced solubility than polyaniline. Moreover, at the presented work, the DBSA doped copolymer composites were obtained in high yields by keeping an oxidant to co-monomer ratio of 1:1.     

Melt‐processed polyaniline nanofibers/LDPE/EAA conducting composites

The melt‐processable polyaniline nanofibers doped with superfluous dodecylbenzenesulfonic acid (PANI‐DBSA) were synthesized using the interfacial polymerization and thermal doping technique. Conducting composites composed of PANI‐DBSA nanofibers, low‐density polyethylene (LDPE), and ethylene‐acrylic acid copolymer (EAA) as compatibilizer were prepared by melt processing. The effects of PANI‐DBSA nanofibers on the electrical conductivity, and mechanical properties, and morphological structure of the composites were investigated. As a result, the conducting composites had lower percolation threshold (4 wt%) due to the easy formation of conducting paths for fibrillar‐like PANI‐DBSA in the LDPE matrix, which was also confirmed by the frequency dependence of the real part of the AC conductivity. The Scanning electron microscopy (SEM) images indicated that the PANI‐DBSA nanofibers were dispersed uniformly in the matrix. The mechanical properties of the composites were improved at the low PANI‐DBSA load (about 1 wt%), but they were deteriorated at high PANI‐DBSA content. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Electrochemical synthesis of poly(2‐iodoaniline) and poly(aniline‐co‐2‐iodoaniline) in acetonitrile

Poly(2‐iodoaniline) (PIANI) and poly(aniline‐co‐2‐iodoaniline) [P(An‐co‐2‐IAn)] were synthesized by electrochemical methods in acetonitrile solution containing tetrabutylammonium perchlorate (TBAP) and perchloric acid (HClO₄). The voltametry of the copolymer shows characteristics similar to those of conventional polyaniline (PANI), and it exhibits higher dry electrical conductivity than PIANI and lower than PANI. The observed decrease in the conductivity of the copolymer relative to PANI is attributed to the incorporation of the iodine moieties into the PANI chain. The structure and properties of these conducting films were characterized by FTIR and UV‐Vis spectroscopy and by an electrochemical method (cyclic voltametry). Conductivity values, FTIR and UV‐Vis spectra of the PIANI and copolymer were compared with those of PANI and the relative solubility of the PIANI and the copolymer powders was determined in various organic solvents. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1652–1658, 2003     

Electrochemical preparation of poly(2‐bromoaniline) and poly(aniline‐co‐2‐bromoaniline) in acetonitrile

Electrochemical preparation of poly(2‐bromoaniline) (PBrANI) and poly(aniline‐co‐2‐bromoaniline) [P(An‐co‐2‐BrAn)] was carried out in an acetonitrile solution containing tetrabutylammonium perchlorate (TBAP) and perchloric acid (HClO₄). The cyclic voltammograms during the copolymerization had many features similar to those for the usual polymerization of aniline. The copolymer exhibits a higher dry electrical conductivity value than that of PBrANI and a lower one than that of PANI. The observed decrease in the conductivity of the copolymer relative to PANI is attributed to the incorporation of bromine moieties into the polyaniline chain. The structure and properties of the polymer and copolymer were elucidated using cyclic voltammetry (CV), FTIR, and UV‐vis spectroscopy. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2460–2468, 2003     

Structure and oxygen‐barrier properties of (linear low‐density polyethylene/ethylene–vinyl alcohol copolymer)/linear low‐density polyethylene composite films prepared by microlayer coextrusion

Ethylene–vinyl alcohol copolymer (EVOH) and linear low‐density polyethylene (LLDPE) blends with 5% LLDPE grafted with 1% maleic anhydride (MAH; EVOH/LLDPE/LLDPE‐g‐MAH), created to increase the interfacial compatibility, were coextruded with pure LLDPE through the microlayer coextrusion technology. The phase morphology and gas‐barrier properties of the alternating‐layered (EVOH/LLDPE/LLDPE‐g‐MAH)/LLDPE composites were studied by scanning electron microscopy observation and oxygen permeation coefficient measurement. The experimental results show that the EVOH/LLDPE/LLDPE‐g‐MAH and LLDPE layers were parallel to each other, and the continuity of each layer was clearly evident. This structure greatly decreased the oxygen permeability coefficient compared to the pure LLDPE and the barrier percolation threshold because of the existence of the LLDPE/EVOH/LLDPE‐g‐MAH blend layers, and the LLDPE layers diluted the concentration of EVOH in the whole composites. In addition, the effects of the layer thickness ratio of the EVOH/LLDPE/LLDPE‐g‐MAH and LLDPE layers and the layer number on the barrier properties of the layered composites were investigated. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42211.     

Synthesis,characterization, and comparison of self‐doped,doped, and undoped forms of polyaniline,poly(o‐anisidine), and poly[aniline‐co‐(o‐anisidine)]

Polyaniline (PANI), poly(o‐anisidine), and poly[aniline‐co‐(o‐anisidine)] were synthesized by chemical oxidative polymerization with ammonium persulfate as an oxidizing reagent in an HCl medium. The viscosities, electrical conductivity, and crystallinity of the resulting polymers (self‐doped forms) were compared with those of the doped and undoped forms. The self‐doped, doped, and undoped forms of these polymers were characterized with infrared spectroscopy, ultraviolet–visible spectroscopy, and a four‐point‐probe conductivity method. X‐ray diffraction characterization revealed the crystalline nature of the polymers. The observed decrease in the conductivity of the copolymer and poly(o‐anisidine) with respect to PANI was attributed to the incorporation of the methoxy moieties into the PANI chain. The homopolymers attained conductivity in the range of 3.97 × 10^?3 to 7.8 S/cm after doping with HCl. The conductivity of the undoped forms of the poly[aniline‐co‐(o‐anisidine)] and poly(o‐anisidine) was observed to be lower than 10^?5 J/S cm^?1. The conductivity of the studied polymer forms decreased by the doping process in the following order: self‐doped → doped → undoped. The conductivity of the studied polymers decreased by the monomer species in the following order: PANI → poly[aniline‐co‐(o‐anisidine)] → poly(o‐anisidine). All the polymer samples were largely amorphous, but with the attachment of the pendant groups of anisidine to the polymer system, the crystallinity region increased. The undoped form of poly[aniline‐co‐(o‐anisidine)] had good solubility in common organic solvents, whereas doped poly[aniline‐co‐(o‐anisidine)] was moderately crystalline and exhibited higher conductivity than the anisidine homopolymer. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

Surface modification of linear low‐density polyethylene film by amphiphilic graft copolymers based on poly(higher α‐olefin)‐graft‐poly(ethylene glycol)

In this article, a series of amphiphilic graft copolymers, namely poly(higher α‐olefin‐co‐para‐methylstyrene)‐graft‐poly(ethylene glycol), and poly(higher α‐olefin‐co‐acrylic acid)‐graft‐poly(ethylene glycol) was used as modifying agent to increase the wettability of the surface of linear low‐density polyethylene (LLDPE) film. The wettability of the surface of LLDPE film could be increased effectively by spin coating of the amphiphilic graft copolymers onto the surface of LLDPE film. The higher the content of poly(ethylene glycol) (PEG) segments, the lower the water contact angle was. The water contact angle of modified LLDPE films was reduced as low as 25°. However, the adhesion between the amphiphilic graft copolymer and LLDPE film was poor. To solve this problem, the modified LLDPE films coated by the amphiphilic graft copolymers were annealed at 110° for 12 h. During the period of annealing, heating made polymer chain move and rearrange quickly. When the film was cooled down, the alkyl group of higher α‐olefin units and LLDPE began to entangle and crystallize. Driven by crystallization, the PEG segments rearranged and enriched in the interface between the amphiphilic graft copolymer and air. By this surface modification method, the amphiphilic graft copolymer was fixed on the surface of LLDPE film. And the water contact angle was further reduced as low as 14.8°. The experimental results of this article demonstrate the potential pathway to provide an effective and durable anti‐fog LLDPE film. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Synthesis and characterization of a copolymer: Poly(aniline‐co‐fluoroaniline)

In the present article, we report the chemical synthesis and characterization of poly(aniline‐co‐fluoroaniline) [poly(An‐FAn)]. The copolymerization of aniline and 2‐fluoroaniline was carried out by chemical method in acidic medium. The characterization of poly(aniline‐co‐fluoroaniline) was done using FTIR, UV‐visible spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), scanning electron micrography (SEM), and a four‐points‐probe conductivity method. X‐ray diffraction (XRD) and SEM characterization reveal crystalline nature of doped copolymer compared to undoped copolymer. The observed decrease in the conductivity of the copolymer relative to polyaniline is attributed to the incorporation of the fluoro moieties into the polyaniline chain. The chemically synthesized copolymer shows good solubility in common organic solvents, and is, therefore, technological useful. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 1460–1466, 2001     

A biodegradable diblcok copolymer poly(ethylene glycol)‐block‐poly(L‐lactide‐co‐2‐methyl‐2‐carboxyl‐propylene carbonate): Docetaxel and RGD conjugation

A diblcok copolymer monomethoxy poly (ethyleneglycol)‐block‐poly(L ‐lactide‐co‐2‐methyl‐2‐carboxyl‐propylene carbonate) (MPEG‐b‐P(LA‐co‐MCC)) was obtained by copolymerization of L ‐lactide (LA) and 2‐methyl‐2‐benzoxycarbonyl‐propylene carbonate (MBC) and subsequent catalytic hydrogenation. The pendant carboxyl groups of the copolymer MPEG‐b‐P(LA‐co‐MCC) were conjugated with antitumor drug docetaxel and tripeptide arginine‐glycine‐aspartic acid (RGD), respectively. ¹H‐NMR spectra confirmed the structure of the copolymer MPEG‐b‐P(LA‐co‐MCC/docetaxel) and MPEG‐b‐P(LA‐co‐MCC/RGD). In vitro antitumor assay indicates that the MPEG‐b‐P(LA‐co‐MCC/docetaxel) conjugate shows high cytotoxic activity against HeLa cancer cells. Cell adhesion and spreading experiment shows that copolymer MPEG‐b‐P(LA‐co‐MCC/RGD) is of benefit to cell adherence and is a promising biodegradable material for cell and tissue engineering. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Synthesis and characterization of conducting copolymer of Trans‐1‐(4‐methyl‐3′‐thienyl)‐2‐(ferrocenyl)ethene with EDOT

Ferrocene‐substituted conducting polymer namely poly(trans‐1‐(4‐methyl‐3′‐thienyl)‐2‐(ferrocenyl)ethene‐co‐3,4‐ethylenedioxythiophene) [P(MTFE‐co‐EDOT)] was synthesized and its electrochromic properties were studied. Monomer, MTFE, was obtained using 2‐(ferrocenyl)ethene and 3‐methyl‐4‐bromothiophene. The structure of monomer was determined via Fourier transform infrared spectroscopy (FTIR), ¹H‐NMR, and ¹³C‐NMR techniques. The copolymer was synthesized using this monomer and EDOT. The resulting copolymer P(MTFE‐co‐EDOT) was characterized by cyclic voltammetry, FTIR, scanning electron microscopy, atomic force microscopy, and UV–vis spectroscopy. The conductivity measurements of copolymer and PEDOT were accomplished by the four‐probe technique. Although poly(trans‐1‐(4‐methyl‐3′‐thienyl)‐2‐(ferrocenyl)ethene) [P(MTFE)] reveals no electrochromic activity, its copolymer with EDOT has two different colors (violet and gray). Band gap (E_g) and λ_max of P(MTFE‐co‐EDOT) were determined. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Noncovalent functionalization of carbon nanotube using poly(vinylcarbazole)‐based compatibilizer for reinforcement and conductivity improvement in epoxy composite

A new compatibilizer [P(GMA‐co‐VCz) copolymer] containing carbazole moiety and reactive epoxide group, which can functionalize multiwalled carbon nanotubes (MWCNTs) for making superior epoxy composites, was prepared by a simple one‐pot free radical polymerization. The designed compatibilizer could noncovalently functionalize multiwalled carbon nanotube (MWCNTs) via π‐π interaction as evidenced from fluorescence, Raman, and FTIR spectra analysis, and efficiently disperse MWCNTs in organic solvents. TEM images suggest a good wrapping of P(GMA‐co‐VCz) on MWCNTs surface. P(GMA‐co‐VCz) functionalized MWCNTs were more homogeneously dispersed in epoxy matrix than the case without compatibilizer, indicating that the compatibilizer improves the compatibility between MWCNTs and epoxy resin. In addition, the presence of epoxide groups in compatibilizer could generate covalent bonds with the epoxy matrix and improve the interface interaction between MWCNTs and epoxy matrix. As a result, mechanical and electrical properties of the epoxy composites with compatibilizer were largely improved as compared with those of composites without compatibilizer. The addition of as little as 0.15 wt % of MWCNTs to epoxy matrix affords a great increase of 40% in storage modulus and 52.5% in elongation at break. Furthermore, a sharp decrease of almost 9 orders of magnitude in volume resistivity of epoxy composite is observed. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45022.     

Thermodynamically induced self‐assembled electrically conductive networks in carbon‐black‐filled ternary polymer blends

By calculating the surface tensions of the components, composites with innovative thermodynamically induced self‐assembled electrically conductive networks were designed, prepared and investigated. Carbon black (CB) was added into a ternary blend system comprised of poly(methyl methacrylate) (PMMA), ethylene–acrylic acid copolymer (EAA) and polypropylene (PP). Scanning electron microscopy images show that the PMMA/EAA/PP ternary blend forms a tri‐continuous phase structure like a sandwich, in which PMMA and PP form a co‐continuous phase while EAA spreads at the interface of the PMMA and PP phases as a sheath. The micrographs and resistivity–temperature characteristic curve results indicate that CB fillers are selectively located at the interface of the PMMA and PP phases, namely the EAA phase. The percolation threshold of PMMA/EAA‐CB/PP composites is 0.2 vol%, which is only one‐fifth of that of PP/CB composites. Copyright © 2011 Society of Chemical Industry     

Morphology,Resistivity, and PTC behavior of EVOH/CB composites prepared by solvent‐casting saponification and precipitation saponification

Poly(ethylene‐co‐vinyl alcohol)/carbon black (EVOH/CB) composites were prepared by a solvent‐casting saponification (‐D) and precipitation saponification (‐P) methods with a poly(ethylene‐co‐vinyl acetate)/CB (EVA/CB) toluene suspension. The effects of the CB content and saponification time on the morphology, electrical resistivity, thermal, and mechanical properties of EVA/CB composites were examined. The volume resistivity (ρ _v) of the EVA/CB‐D and EVA/CB‐P samples decreased significantly with increasing CB content and the percolation threshold of such composites was determined about 10 wt%. At 10 wt% of CB content, the ρ _v of EVA/CB‐D composite decreased significantly with the saponification time, whereas ρ _v of EVA/CB‐P composites did not change. As the saponification time increased, EVA/CB25wt% composites form cavity structure which CB is usually located in oval cavities larger than the particles themselves. This oval cavity structure almost resembles extruded high‐density polyethylene (HDPE)/CB composites. The morphology and PTC behavior of prepared composites were compared with those of HDPE/CB and the mechanism of PTC and NTC effects was discussed. POLYM. COMPOS., 38:1462–1473, 2017. © 2015 Society of Plastics Engineers     

Regulation of the mechanical properties and heat resistance of the poly(l‐lactide‐co‐trimethylene carbonate) copolymer by the incorporation of a stereocomplex crystal and graphene oxide

Stereocomplex crystals of polylactide and graphene oxide (GO) were simultaneously used to regulate the mechanical properties and heat resistance of a poly(l ‐lactide‐co‐trimethylene carbonate) [P(LLA‐co‐TMC)] copolymer. The crystallization behaviors in the nonisothermal cold‐crystallization process of P(LLA‐co‐TMC)–poly(d ‐lactide) (PDLA) blends and P(LLA‐co‐TMC)–PDLA–GO composites were investigated by differential scanning calorimetry, wide‐angle X‐ray diffraction, and polarized optical microscopy. Data from the crystallization kinetics and the crystallization active energy indicated that GO both promoted nucleation and limited growth during the stereocomplex crystallization process. Three kind of samples (without crystallization, with low crystallinity, and with high crystallinity) were used to investigate the mechanical properties and heat resistance. We found a decrease in the elongation at break when the stereocomplex crystal and GO contents were increased, and this was accompanied by an improvement in the tensile strength. The change in the storage modulus value determined by dynamic mechanical analysis demonstrated that both the stereocomplex crystal and GO effectively improved the heat resistance. These results indicate that this study provided a new strategy for fabricating a P(LLA‐co‐TMC) copolymer with good comprehensive properties at was entirely different from common chemical crosslinking methods. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45248.     

Synthesis,characterization, and antitumor activity of poly(maleic anhydride‐co‐vinyl acetate‐co‐acrylic acid)

The ternary copolymerization of maleic anhydride (MA), vinyl acetate (VA), and acrylic acid (AA) [P(MA‐co‐VA‐co‐AA)], which is considered to be an acceptor–donor–acceptor system, was carried out in 1,4‐dioxane with benzoyl peroxide as an initiator at 70°C under a nitrogen atmosphere. Constants of complex formation for the monomer systems in the study were determined by UV–visible (hydrogen‐bonding complex) and ¹H‐NMR (charge transfer complex) methods, respectively. The results show that polymerization of the P(MA‐co‐VA‐co‐AA) system proceeds by an alternating terpolymerization mechanism. It is shown that the synthesized copolymers have typical polyelectrolyte behavior, ability for reversible hydrolysis–anhydrization reactions, and semicrystalline structures. In these cases, including radical polymerization, and formation of semicrystalline structures, the hydrogen‐bonding effect plays a significant role. The in vitro cytotoxicities of the synthesized terpolymer and alternating copolymer were evaluated using Raji cells (human Burkitt lymphoma cell line). The antitumor activities of prepared anion‐active copolymers were studied using methyl–thiazol–tetrazolium colorimetric assay and 50% of the cytotoxic dose of each copolymer and terpolymer were calculated. Hydrolyzed P(MA‐co‐VA‐co‐AA) and P(MA‐alt‐AA) copolymers have sufficiently high antitumor activity, which depends on the amount of hydrogen‐bonding carboxylic groups and their regular distribution in the side chain of functional macromolecules. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3425–3432, 2006     

Synthesis of poly(sodium acrylate‐co‐sodium 1‐(acryloyloxy) propan‐2‐yl phosphate) and comparative study on its swelling properties with poly(sodium acrylate) and poly(sodium acrylate‐co‐2‐hydroxypropyl acrylate)

A new superabsorbent copolymer, poly(sodium acrylate‐co‐sodium 1‐(acryloyloxy) propan‐2‐yl phosphate) [P(SA‐co‐SAPP)], was synthesized by a novel prepared monomer, 1‐(acryloyloxy) propan‐2‐yl phosphoryl dichloride. The swelling properties of the superabsorbent were investigated by comparison with poly(sodium acrylate) (PSA) and the copolymer of poly(sodium acrylate‐co‐2‐hydroxypropyl acrylate) [P(SA‐co‐HPA)]. The results showed that (1) the superabsorbent containing sodium 1‐(acryloyloxy) propan‐2‐yl phosphate had higher water absorbency at general testing conditions; (2) the swelling properties of P(SA‐co‐SAPP) and PSA were obviously influenced by pH of solutions, which were different from that of P(SA‐co‐HPA); (3) the swelling process and the saturated water absorbency of all superabsorbents were remarkably affected by cations, especially multivalent ones, while barely affected by anions. POLYM. ENG. SCI., 47:728–737, 2007. © 2007 Society of Plastics Engineers.     

Tailoring the surface architecture of poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate) scaffolds

This study was designed to determine whether the surface modifications of the various poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate) [P(3HB‐co‐4HB)] copolymer scaffolds fabricated would enhance mouse fibroblast cells (L929) attachment and proliferation. The P(3HB‐co‐4HB) copolymer with a wide range of 4HB monomer composition (16–91 mol %) was synthesized by a local isolate Cupriavidus sp. USMAA1020 by employing the modified two‐stage cultivation and by varying the concentrations of 4HB precursors, namely γ‐butyrolactone and 1,4‐butanediol. Five different processing techniques were used in fabricating the P(3HB‐co‐4HB) copolymer scaffolds such as solvent casting, salt‐leaching, enzyme degradation, combining salt‐leaching with enzyme degradation, and electrospinning. The increase in 4HB composition lowered melting temperatures (T_m) but increased elongation to break. P(3HB‐co‐91 mol % 4HB) exhibited a melting point of 46°C and elongation to break of 380%. The atomic force analysis showed an increase in the average surface roughness as the 4HB monomer composition increased. The mouse fibroblasts (L929) cell attachment was found to increase with high 4HB monomer composition in copolymer scaffolds. These results illustrate the importance of a detailed characterization of surface architecture of scaffolds to provoke specific cellular responses. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Enhanced thermoelectric performance by alcoholic solvents effects in highly conductive benzenesulfonate‐doped poly(3,4‐ethylenedioxythiophene)/graphene composites

Benzenesulfonate‐doped poly(3,4‐ethylenedioxythiophene) (PEDOT‐Bzs)/graphene thermoelectric (TE) composites with various graphene filler contents were synthesized in five different kinds of solvents. Dodecylbenzenesulfonic acid (DBSA) was used to achieve good dispersion of graphene into the PEDOT matrix. Among the synthesized PEDOT materials, the one synthesized in methanol (PEDOT‐MeOH) had the highest electrical conductivity. X‐ray photoelectron spectroscopy (XPS) analysis showed almost the same charge carrier concentration for all PEDOT materials. However, the X‐ray diffraction (XRD) analysis highlighted the enhancement of PEDOT chain stacking by shorter‐chain alcoholic solvents, as a result of which the carrier mobility and electrical conductivity were increased. The electrical conductivity and the Seebeck coefficient of the PEDOT/graphene composites were significantly improved with increasing the graphene content, which strongly depended on increased carrier mobility. The thermal conductivity of the composites exhibited relatively small changes, attributed to phonon scattering effects. The maximum TE efficiency of the PEDOT‐MeOH/graphene composite with 75 wt % graphene showed a substantially improved value of 1.9 × 10^?2, higher than that of the other PEDOT/graphene composites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42107.