Morphology,electrical resistance,electromagnetic interference shielding and mechanical properties of functionalized MWNT and poly(urea urethane) nanocomposites

The functionalized multi‐walled carbon nanotubes (MWNT) had been prepared by free radical reaction with vinyltriethoxysilane. Polydimethylsiloxane (PDMS)‐based poly(urea urethane) (PUU) was also synthesized. PUU was further end‐capped with aminopropyltriethoxysilane (A‐silane), or with phenyltrimethoxysilane (P‐silane). Fourier transform infrared (FTIR), Raman spectra and thermogravimetric analysis (TGA) confirmed the functionalization of MWNT. The M_n and M_w of PUU were 85,123 and 235,876 g/mol, respectively. Both A‐silane end‐capped PUU and P‐silane end‐capped PUU showed improved dispersion of MWNT compared with that of PUU and MWNT. Moreover, the reduced discrepancy of surface electrical resistance of the two sides of the MWNT/PUU nanocomposite film was found due to the homogeneous dispersion of MWNT. The microwave absorption and tensile strength of MWNT/PUU were also improved by the well dispersion of MWNT in PUU matrix. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1096–1105, 2006     

Isothermal crystallization kinetics of polypropylene with silane functionalized multi‐walled carbon nanotubes

Multi‐walled carbon nanotubes (MWNTs) were functionalized with a silane coupling agent. The MWNTs were first coated with inorganic silica by a sol‐gel process and then grafted with 3‐methacryloxypropyltrimethoxysilane (3‐MPTS). The effect of raw MWNTs and silane‐functionalized MWNTs on the crystallization behavior of poly(propylene) (PP) was investigated by means of polarized optical microscopy, differential scanning calorimetry, and wide‐angle X‐ray diffraction. Results obtained from isothermal crystallization experiments indicate that 3‐MPTS functionalization affects the crystallization and melting behavior of PP/MWNTs composites remarkably, which can be attributed to the fact that 3‐MPTS functionalization of MWNTs leads to a uniform dispersion of MWNTs in PP matrix resulting in the good nucleating effect of MWNTs. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 1616–1624, 2007     

“Click” coupling between alkyne‐decorated multiwalled carbon nanotubes and reactive PDMA‐PNIPAM micelles

Covalent functionalization of alkyne‐decorated multiwalled carbon nanotubes (MWNTs) with a well‐defined, azide‐derivatized, thermoresponsive diblock copolymer, poly(N,N‐dimethylacrylamide)‐poly(N‐isopropylacrylamide) (PDMA‐PNIPAM) was accomplished by the Cu(I)‐catalyzed [3 + 2] Huisgen cycloaddition. It was found that this reaction could simultaneously increase the molecular size and bonding density of grafted polymers when PDMA‐PNIPAM micelles were employed in the coupling system. On the other hand, attachment of molecularly dissolved unimers of high‐molecular weight onto the nanotube resulted in low‐graft density. The block copolymer bearing azide groups at the PDMA end was prepared by reversible addition–fragmentation transfer polymerization, which formed micelles with a diameter of ～40 nm at temperatures above its critical micelle temperature. Scanning electron microscopy was utilized to demonstrate that the coupling reaction was successfully carried out between copolymer micelles and alkyne‐bearing MWNTs. FTIR spectroscopy was utilized to follow the introduction and consumption of alkyne groups on the MWNTs. Thermogravimetric analysis indicated that the functionalized MWNTs consisted of about 45% polymer. Transmission electron microscopy was utilized to image polymer‐functionalized MWNTs, showing relatively uniform polymer coatings present on the surface of nanotubes. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7187–7199, 2008     

Synthesis of polystyrene brush on multiwalled carbon nanotubes treated with KMnO4 in the presence of a phase‐transfer catalyst

Multiwalled carbon nanotubes (MWNTs) were effectively functionalized with KMnO₄ in the presence of a phase‐transfer catalyst at room temperature. The hydroxyl functionalized MWNTs were reacted with a vinyl‐group carrying silane‐coupling agent and the terminal vinyl groups were used to fabricate polystyrene (PS) brushes by solution polymerization. Finally, PS‐encapsulated MWNTs were obtained. The synthesis results were verified from FT‐Raman, thermal gravimetric analysis, energy dispersive X‐ray analysis, and transmission electron microscope. PS‐encapsulated MWNTs had much improved dispersion stability in hydrophobic medium, toluene since grafted hydrophobic PS interacts with media and has improved compatibility. This functionalization technique would provide a facile route to prepare various polymer brushes on the surface of MWNTs to improve the dispersion of MWNTs for potential applications. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4413–4420, 2007     

Preparation and electromagnetic interference shielding characteristics of novel carbon‐nanotube/siloxane/poly‐(urea urethane) nanocomposites

Poly(urea urethane) (PUU) with a poly(dimethylsiloxane) soft segment was synthesized. Different types of conductive fillers—carbon nanotube (CNT), silver‐coated carbon nanotube (CNT–Ag), and nickel‐coated carbon nanotube (CNT–Ni)—were blended with PUU to form partially conductive polymer composites. The results showed that highly conductive metals could improve the conductivity of CNTs significantly. When the filler contents were 3, 4, and 5 parts per hundred parts of resin (phr), the PUU/CNT composites possessed electromagnetic interference shielding effectiveness (SE) at 8.5, 28.4, and 26.0 dB as the electromagnetic wave frequencies were 12.3, 16.2, and 15.9 GHz, respectively. SE of the composites that contained CNT–Ni and CNT–Ag increased with the filler loading. At the same modified‐CNT loading, the CNT–Ni‐filled composites had a higher SE than those filled with CNT–Ag. Tensile stresses ranged from 5.7 to 15.6 MPa (a 177.3% increase) when the CNT concentration reached 8 phr. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 345–358, 2005     

Novel diblock copolymer‐grafted multiwalled carbon nanotubes via a combination of living and controlled/living surface polymerizations

Diels–Alder cycloaddition reactions were used to functionalize multiwalled carbon nanotubes (MWNTs) with 1‐benzocylcobutene‐1′‐phenylethylene (BCB‐PE) or 4‐hydroxyethylbenzocyclobutene (BCB‐EO). The covalent functionalization of the nanotubes with these initiator precursors was verified by FTIR and thermogravimetric analysis (TGA). After appropriate transformations/additions, the functionalized MWNTs were used for surface initiated anionic and ring opening polymerizations of ethylene oxide and ε‐caprolactone (ε‐CL), respectively. The OH‐end groups were transformed to isopropylbromide groups by reaction with 2‐bromoisobutyryl bromide, for subsequent atom transfer radical polymerization of styrene or 2‐dimethylaminoethyl methacrylate to afford the final diblock copolymers. ¹H NMR, differential scanning calorimetry (DSC), TGA, and transmission electron microscopy (TEM) were used for the characterization of the nanocomposite materials. TEM images showed the presence of a polymer layer around the MWNTs as well as the dissociation of MWNT bundles. Consequently, this general methodology, employing combinations of different polymerization techniques, increases the diversity of diblocks that can be grafted from MWNTs. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1104–1112, 2010     

Poly(butylene terephthalate)‐functionalized MWNTs by in situ ring‐opening polymerization of cyclic butylene terephthalate oligomers

Poly(butylene terephthalate) (PBT) had been covalently attached onto the surface of multiwalled carbon nanotubes (MWNTs) by a “grafting from” method based on in situ ring‐opening polymerization (ROP) of cyclic butylene terephthalate oligomers (CBT) using MWNT‐supported initiator (MWNT‐g‐Sn). The Sn? O bond grafted on the surface of MWNTs, which was confirmed by X‐ray photoelectron spectroscopy, provided the initiating sites for ROP of CBT. Fourier transformed infrared spectroscopy and nuclear magnetic resonance were used to confirm the chemical structure of MWNT‐graft‐PBT copolymer and emission transmission electron microscope was utilized to observe the nanostructure of the PBT functionalized MWNTs. A distinct core–shell structure with PBT layer as the shell could be observed after functionalization of PBT despite it was not uniform. The results of thermogravimetric analysis indicated that the grafting ratio of PBT was about 59.3%. Furthermore, the solubility of the PBT functionalized MWNTs in phenol/tetrachloroethane had also been investigated. Copyright © 2010 John Wiley & Sons, Ltd.     

Multiwalled Carbon Nanotubes Functionalized by Hyperbranched Poly(urea‐urethane)s by a One‐Pot Polycondensation

Summary: Hyperbranched poly(urea‐urethane)‐functionalized multiwalled carbon nanotubes (MWNT‐HPUs) have been synthesized by a one‐pot polycondensation of tolylene 2,4‐diisocyanate and diethanolamine in the presence of MWNTs terminated with multiple hydroxy groups. FT‐IR, Raman, ¹H NMR, and ¹³C NMR spectra reveal that the HPU trees are covalently grafted onto the MWNT surfaces. After a high density of HPU trees (83.5 wt.‐%) is attached to the MWNTs, core‐shell nanostructures with MWNTs as the core and the HPU trees as the shell are formed. A loose and uniform nanotube network can be observed by TEM, SEM, and AFM. The resulting MWNT‐HPUs are soluble in polar solvents such as dimethylformamide, dimethylacetamine, 1‐methyl‐2‐pyrrolidinone, and dimethyl sulfoxide.

Hyperbranched poly(urea‐urethane)s functionalized multiwalled carbon nanotubes.     

Effect of interaction between poly(ethylene terephthalate) and carbon nanotubes on the morphology and properties of their nanocomposites

Poly(ethylene terephthalate) (PET) nanocomposites were prepared by melt‐extruding mixtures of PET and functionalized multiwalled carbon nanotubes (MWNTs) with some interaction with PET molecules. For the functionalization of MWNTs, benzyl isocyanate and phenyl isocyanate with different molecular flexibility were employed on the surface of the MWNTs via chemical modification, respectively. The reaction for functionalization of MWNTs was confirmed by FTIR and transmission electron microscopy (TEM) measurements. TEM observations indicated that both benzyl and phenyl isocyanate groups covered the surface of the MWNTs after functionalization. The PET nanocomposites containing isocyanate groups showed improved mechanical properties, including the tensile strength and tensile modulus, compared with those with pristine and acid‐treated nanotubes. These improvements were ascribed to π–π interactions between the aromatic rings of PET molecules and the isocyanate group in MWNTs. The functionalized MWNTs showed a better dispersion of carbon nanotubes in the matrix polymer and a different fractured cross‐section morphology in scanning electron microscope measurements relative to the pristine MWNTs. The crystallinity of the functionalized MWNT‐PET nanocomposites was significantly higher than that of the pristine and acid‐treated MWNTs. FTIR results indicated that the presence of carbon nanotubes induced trans‐conformation of PET chains, and trans conformation was particularly dominant in PET composites incorporating MWNT‐phenyl. © 2008 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 900–910, 2008     

Modification of carboxyl‐functionalized single‐walled carbon nanotubes with biocompatible,water‐soluble phosphorylcholine and sugar‐based polymers: Bioinspired nanorods

We report here the successful functionalization of single‐walled carbon nanotubes with bioinspired sugar and phosphocholine polymeric structures via surface‐initiated atom transfer radical polymerization. The surface‐polymer‐coated carbon nanotubes have been systematically analyzed by Raman, infrared, ultraviolet–visible, and nuclear magnetic resonance spectroscopy and high‐resolution transmission electron microscopy, which give strong evidence of successful functionalization. The successful aqueous dispersion of the functionalized carbon nanotubes also indicates that functionalization has been achieved. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6558–6568, 2006     

Polymorphism of nylon‐6 in multiwalled carbon nanotubes/nylon‐6 composites

The effects of pristine and amino‐functionalized multiwalled carbon nanotubes (MWNTs) on the crystallization behaviors of nylon‐6 were investigated by differential scanning calorimetry and X‐ray diffraction. The results indicate the presence of polymorphism in nylon‐6 and its composites, which is dependent on the MWNTs concentration and the cooling rate. More MWNTs and slow cooling from the melt favors the formation of α crystalline form. With the increase in cooling rates, the crystallinity of neat nylon‐6 decreases, and that of the composites decreases initially but increases afterward. Moreover, the degree of crystallinity of the composites is higher than neat nylon‐6 under high cooling rates, counter to what is observed under low cooling rates. The heterogeneous nucleation induced by MWNTs and the restricted mobility of polymer chains are considered as the main factors. Furthermore, addition of MWNTs increases the crystallization rate of α crystalline form but amino‐functionalization of MWNTs weakens this effect. The influence of thermal treatment on the crystalline structure of MWNTs/nylon‐6 composites is also discussed. A γ–α phase transition takes place at lower temperature for MWNTs/nylon‐6 composites than for nylon‐6. The annealing peaks of the composites annealed at 160 °C are higher than that of neat nylon‐6, and the highest annealing peak is obtained for amino‐functionalized MWNTs/nylon‐6 composites. This phenomenon is closely related to the different nucleation and recrystallization behaviors produced by various MWNTs in confined space. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1499–1512, 2006     

Preparing a polystyrene‐functionalized multiple‐walled carbon nanotubes via covalently linking acyl chloride functionalities with living polystyryllithium

A new method was developed for preparing polystyrene‐functionalized multiple‐walled carbon nanotubes (MWNTs) through the termination of anionically synthesized living polystyryllithium with the acyl chloride functionalities on the MWNTs. The acyl chloride functionalities on the MWNTs were in turn obtained by the formation of carboxyls via chemical oxidation and their conversion into acyl chlorides. The polystyrene‐functionalized MWNTs had good dispersion in common organic solvents, and this indicated good compatibility for the preparation of styrenic nanocomposite materials. The synthesis results and characterization data for the functionalized MWNTs, collected via Fourier transform infrared, thermogravimetric analysis, solid‐state NMR, and electron microscopy, are presented and discussed. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5802–5810, 2004     

Effect of nanotube functionalization on the properties of single‐walled carbon nanotube/polyurethane composites

A commercially available aliphatic thermoplastic polyurethane formulated with a methylene bis(cyclohexyl) diisocyanate hard segment and a poly(tetramethylene oxide) soft segment and chain‐extended with 1,4‐butanediol was dissolved in dimethylformamide and mixed with dispersed single‐walled carbon nanotubes. The properties of composites made with unfunctionalized nanotubes were compared with the properties of composites made with nanotubes functionalized to contain hydroxyl groups. Functionalization almost eliminated the conductivity of the tubes according to the conductivity of the composites above the percolation threshold. In most cases, functionalized and unfunctionalized tubes yielded composites with statistically identical mechanical properties. However, composites made with functionalized tubes did have a slightly higher modulus in the rubbery plateau region at higher nanotube fractions. Small‐angle X‐ray scattering patterns indicated that the dispersion reached a plateau in the unfunctionalized composites that was consistent with the plateau in the rubbery plateau region. The room‐temperature modulus and tensile strength increase was proportionally higher than almost all increases seen previously in thermoplastic polyurethanes; however, the increase was still an order of magnitude below what has been reported for the best nanotube–polymer systems. Nanotube addition increased the hard‐segment glass transition temperature slightly, whereas the soft‐segment glass transition was so diffuse that no conclusions could be drawn. Unfunctionalized tubes suppressed the crystallization of the hard segment; whereas functionalized tubes had no effect. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 490–501, 2007     

Multiwalled carbon nanotubes covalently functionalized with poly(N‐vinylcarbazole) via RAFT polymerization: Synthesis and nonliner optical properties

The poly(N‐vinylcarbazole)‐grafted MWNTs (MWNT‐PVK) hybrid materials were synthesized in the presence of S‐1‐Dodecyl‐S′‐(α, α′‐dimethyl‐α″‐acetic acid) trithiocarbonate (DDAT)‐covalently functionalized multiwalled carbon nanotubes (MWNT‐DDAT) as reversible addition–fragmentation chain transfer (RAFT) agent. Incorporation of the PVK moieties onto the MWNTs surface can considerably improve the solubility and processability of MWNTs. For all MWNT‐PVK hybrid materials, they are soluble in some common organic solvents such as toluene, THF, chloroform, DMF and others. In contrast to the UV/Vis spectrum of DDAT‐PVK, which was synthesized by use of DDAT as RAFT agent under the same synthetic condition, in the visible region, the absorption spectrum of MWNT‐PVK exhibited a typical electronic absorption characteristics of solubilized carbon nanotubes, in which the absorbance decreases gradually in the range of 350–600 nm. At the same level of linear transmission the MWNT‐PVK with 79.2% PVK moieties in the material structure possesses best optical limiting performance in comparison with the other MWNT‐PVK composites, MWNTs and C₆₀. The significant NLO responses manifest the MWNT‐PVK materials suitable candidate for viable optical limiting devices. Light scattering, originating from the thermal‐induced microplasmas and/or microbubbles, is responsible for the optical limiting. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3161–3168, 2010     

Poly(lactic acid) composites with poly(lactic acid)‐modified carbon nanotubes

This work reports the study of the effect of chemical functionalization of carbon nanotubes on their dispersion in poly(lactic acid). The nanotubes were functionalized by the 1,3‐dipolar cycloaddition reaction, generating pyrrolidine groups at the nanotube surface. Further reaction of the pyrrolidine groups with poly(lactic acid) was studied in solution and in the polymer melt. The former involved refluxing the nanotubes in a dimethylformamide/polymer solution; the latter was carried out by direct melt mixing in a microcompounder. The carbon nanotubes collected after each process were characterized by thermogravimetry and by X‐ray photoelectron spectroscopy, showing evidence of polymer bonded to the nanotube surface only when the reaction was carried out in the polymer melt. The composites with polymer modified nanotubes present smaller average agglomerate area and a narrower agglomerate area distribution. In addition, they show improved tensile properties at low CNT concentration and present lower electrical resistivity. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3740–3750     

Synthesis and self‐assembly of polystyrene‐grafted multiwalled carbon nanotubes with a hairy‐rod nanostructure

Polystyrene‐grafted multiwalled carbon nanotubes (PS‐g‐MWNTs) with a hairy‐rod nanostructure were synthesized by the in situ free‐radical polymerization of styrene in the presence of multiwalled carbon nanotubes (MWNTs) terminated with vinyl groups. To quantitatively study the molecular weight and composition of polystyrene (PS) chains in PS‐g‐MWNTs, PS‐g‐MWNTs were fully defunctionalized by hydrolysis. The results showed that 1 of every 100 carbon atoms in MWNTs was functionalized at the tips and outer walls of the carbon nanotubes and grafted by PS with a weight‐average molecular weight of 9800 g/mol; therefore, a uniform thin layer (ca. 8–10 nm) of a PS shell was formed on the outer wall of MWNTs. PS‐g‐MWNTs were soluble in dimethylformamide and tetrahydrofuran. The thermal stability and glass‐transition temperature of PS in PS‐g‐MWNTs were obviously increased. Nanopins were formed on the glass substrates by the self‐assembly of PS‐g‐MWNTs, and the dewetting effect between the glass substrate and PS chains covered MWNTs during the evaporation of the solution. Both the length and diameter of the nanopins increased with the solution concentration. When PS‐g‐MWNTs were compression‐molded, MWNTs were dispersed uniformly in the PS matrix and formed good networks, such as circlelike and starlike structures, because of the entanglements of hairy PS chains on MWNTs. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3869–3881, 2006     

Preparation and characterization of waterborne poly(urethane urea) with well‐defined hard segments

A series of polyester‐based poly(urethane urea) (PUU) aqueous dispersions with well‐defined hard segments were prepared from polyester polyol, 4,4′‐diphenylmethane diisocyanate, dimethylolpropionic acid, 1,4‐butanediol, isophorone diisocyanate, and ethylenediamine. These anionic‐type aqueous dispersions had good dispersity in water and were stable at the ambient temperature for more than 1 year. For these aqueous dispersions, the particle size decreased as the hard‐segment content increased, and the polydispersity index was very narrow (<1.10). Films prepared with the PUU aqueous dispersions exhibited excellent waterproof performance: the amount of water absorption was as low as 5.0 wt %, and the contact angle of water on the surface of this kind of film was as high as 103° (this led to a hydrophobic surface). The water‐resistant property of these waterborne PUU films could be well correlated with some crystallites and ordered structures of the well‐defined hard segments formed by hydrogen bonding between the urethane/urethane groups and urethane/ester groups, as well as the degree of microphase separation between the hard and soft segments in the PUU systems. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2606–2614, 2005     

Poly(γ‐benzyl‐L‐glutamate)‐functionalized single‐walled carbon nanotubes from surface‐initiated ring‐opening polymerizations of N‐carboxylanhydride

Single‐walled carbon nanotubes (SWCNTs) have been functionalized with poly(γ‐benzyl‐L ‐glutamate) (PBLG) by ring‐opening polymerizations of γ‐benzyl‐L ‐glutamic acid‐based N‐carboxylanhydrides (NCA‐BLG) using amino‐functionalized SWCNTs (SWCNT‐NH₂) as initiators. The SWCNT functionalization has been verified by FTIR spectroscopy and transmission electron microscopy. The FTIR study reveals that surface‐attached PBLGs adopt random‐coil conformations in contrast to the physically absorbed or bulk PBLGs, which exhibit α‐helical conformations. Raman spectroscopic analysis reveals a significant alteration of the electronic structure of SWCNTs as a result of PBLG functionalization. The PBLG‐functionalized SWCNTs (SWCNT‐PBLG) exhibit enhanced solubility in DMF. Stable DMF solutions of SWCNT‐PBLG/PBLG with a maximum SWCNTs concentration of 259 mg L^?1 can be readily obtained. SWCNT‐PBLG/PBLG solid composites have been characterized by differential scanning calorimetry, thermogravimetric analysis, wide/small‐angle X‐ray scattering (W/SAXS), scanning electron microscopy, and polarized optical microscopy for their thermal or morphological properties. Microfibers containing SWCNT‐PBLG and PBLG can also be prepared via electrospinning. WAXS characterization reveals that SWCNTs are evenly distributed among PBLG rods in solution and in the solid state where PBLGs form a short‐range nematic phase interspersed with amorphous domains. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2340–2350, 2010     

Functionalized multi‐walled carbon nanotubes with poly(N‐(2‐hydroxypropyl)methacrylamide) by RAFT polymerization

In this study, we grafted water‐soluble biocompatible polymer, poly(N‐(2‐hydroxypropyl)methacrylamide) (PHPMA), onto the surface of multi‐walled carbon nanotubes (MWNTs). The reversible addition‐fragmentation chain transfer (RAFT) agents, dithioesters, were successfully immobilized onto the surface of MWNTs first, PHPMA chains were then subsequently grafted onto MWNTs via RAFT polymerization by using dithioesters immobilized on MWNTs as RAFT agent. FTIR, XPS, ¹H NMR, Raman and TGA were used to characterize the resulting products and to determine the content of water‐soluble PHPMA chains in the product. The MWNTs grafted with PHPMA chains have good solubility in distilled water, PBS buffer, and methanol. TEM images of the samples provide direct evidence for the formation of a nanostructure that MWNTs coated with polymer layer. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2419–2427, 2006     

Nylon 610/functionalized multiwalled carbon nanotube composite prepared from in‐situ interfacial polymerization

Pristine multiwalled carbon nanotubes (P‐MWNTs) were functionalized with 4‐chlorobenzoic acid via “direct” Friedel‐Crafts acylation in polyphosphoric acid (PPA)/phosphorous pentoxide (P₂O₅) medium. The resultant 4‐chlorobenzoyl‐functionalized MWNTs (F‐MWNTs) were soluble in chlorinated solvents such as dichloromethane, chloroform, and carbon tetrachloride. A large scale of nylon 610/F‐MWNT composite could be conveniently prepared by in situ interfacial polymerization of 1, 6‐hexamethylenediamine (HMDA) in an aqueous phase, and sebacoyl chloride with F‐MWNTs in an organic phase. Similarly, nylon 610/P‐MWNT composite was also prepared for comparison. The state of F‐MWNTs dispersion in nylon 610 matrix was distinctively better than that of P‐MWNTs, which could be clearly discerned by both naked eye and scanning electron microcopy (SEM). As a result, the tensile strength of nylon 610/F‐MWNT composite was 4.9‐fold higher than that of nylon 610/P‐MWNT composite. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6041–6050, 2008