Mechanical properties and nonisothermal crystallization kinetics of polyamide 6/functionalized TiO2 nanocomposites

Titanium dioxide (TiO₂) nanoparticles were pretreated with excessive toluene‐2,4‐diisocyanate (TDI) to synthesize TDI‐functionalized TiO₂ (TiO₂‐NCO), and then polymeric nanocomposites consisting of polyamide 6 (PA6) and functionalized‐TiO₂ nanoparticles were prepared via a melt compounding method. The interfacial interaction between TiO₂ nanoparticles and polymeric matrix has been greatly improved due to the isocyanate ( NCO) groups at the surface of the functionalized‐TiO₂ nanoparticles reacted with amino groups ( NH₂) or carboxyl ( COOH) groups of PA6 during the melt compounding and resulted in higher tensile and impact strength than that of pure PA6. The nonisothermal crystallization kinetics of PA6/functionalized TiO₂ nanocomposites was investigated by differential scanning calorimetry (DSC). The nonisothermal crystallization DSC data were analyzed by the modified‐Avrami (Jeziorny) methods. The results showed that the functionalized‐TiO₂ nanoparticles in the PA6 matrix acted as effective nucleation agents. The crystallization rate of the nanocomposites obtained was faster than that of the pure PA6. Thus, the presence of functionalized‐TiO₂ nanoparticles influenced the mechanism of nucleation and accelerated the growth of PA6 crystallites. POLYM. COMPOS., 35:294–300, 2014. © 2013 Society of Plastics Engineers     

Nanocomposites of PVC/TiO2 nanorods: Surface tension and mechanical properties before and after UV exposure

In this study, nanocomposites of poly(vinyl chloride) (PVC), using the synthesized titanium dioxide (TiO₂) nanorods and commercial nanopowder of titanium dioxide (Degussa P25) were produced by melt blending. The presence of TiO₂ nanorods in PVC matrix led to an improvement in mechanical properties of PVC nanocomposites in comparison with unfilled PVC. The photocatalytic degradation behavior of PVC nanocomposites were investigated by measuring their structural change evaluations, surface tension, and mechanical properties before and after UV exposure for 500 h. It was found that mechanical and physical properties of PVC nanocomposites are not reduced significantly after UV exposure in the presence of TiO₂ nanorods in comparison with the presence of TiO₂ nanoparticles, which can be due to the amorphous structure of the synthesized nanorods. Therefore, it can be concluded that TiO₂ nanorods led to an improvement in photostability and mechanical properties of PVC nanocomposites. The interfacial adhesion between TiO₂ nanorods and PVC matrix was also investigated. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Characterization of in situ prepared nanocomposites of PS and TIO2 nanoparticles surface modified with alkyl gallates: Effect of alkyl chain length

Incorporation of surface modified TiO₂ nanoparticles into polystyrene (PS) matrix was achieved by in situ bulk radical polymerization of styrene. The surface of TiO₂ nanoparticles was modified with four amphiphilic esters of the gallic acid (octyl, decyl, lauryl and cetyl gallate), which have different lengths of hydrophobic alkyl chain (C8–C16). FTIR and UV‐Vis spectroscopy measurements confirmed the formation of a charge transfer complex between surface Ti atoms and gallic esters. Microstructural characterization of the synthesized nanocomposites revealed that the best dispersion of TiO₂ nanoparticles in PS was achieved when the TiO₂ surface was modified with octyl gallate. The presence of surface modified TiO₂ nanoparticles by different alkyl gallates does not have an influence on the molecular weight and glass transition temperature of PS matrix. On the other hand, thermal and thermo‐oxidative stability of PS were significantly improved by incorporation of surface modified TiO₂ nanoparticles. The most pronounced improvement of thermal and thermo‐oxidative stability was observed for TiO₂ nanoparticles surface modified with octyl gallate. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Interfacial interactions and performance of polyamide 6/modified attapulgite clay nanocomposites

Attapulgite (AT) clay was firstly treated with sodium polyacrylate (PAS), then polyamide 6 (PA6)/AT nanocomposites were prepared by simple melt compounding. Transmission electron microscope (TEM) and Fourier transform infrared spectrometry (FT‐IR) of treated AT confirm the success of purifying and surface modification of the original AT by PAS. X‐ray diffraction spectra for the nanocomposites show that the microstructure of AT in PA6 matrix is almost unchanged. It indicates that a strong interfacial adhesion exists between AT and PA6 matrix through analyzing fracture surfaces of the nanocomposites, the variation of glass transition temperature (T_g) obtained by dynamic mechanical analysis, and interfacial interaction factors; field emission scanning electron microscopy on the fracture surfaces of the nanocomposites shows that a uniform dispersion of AT is obtained. The above two aspects conform to the improvement of mechanical and thermal properties of the nanocomposites. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Effects of carbon‐coated titanium dioxide nanoparticles as a photostabilizer on the photodegradation of rigid poly(vinyl chloride)

In this study, nanocomposites of rigid poly(vinyl chloride) (UPVC) using the synthesized carbon‐coated titanium dioxide (TiO₂) nanoparticles and commercial powder of titanium dioxide (with rutile structure) were prepared by melt blending. The presence of carbon‐coated TiO₂ nanoparticles with rutile structure in UPVC matrix led to an improvement in photo stability of UPVC nanocomposites in comparison with commercial UPVC. The photocatalytic degradation behavior of nanocomposites was investigated by measuring their structural changes, surface tension, and mechanical and morphological properties before and after UV exposure for 700 h. It was found that mechanical and physical properties of UPVC nanocomposites are not considerably reduced after UV exposure in the presence of carbon‐coated TiO₂ nanoparticles even in small percentage of nanoparticles in comparison with the presence of commercial TiO₂ particles. Therefore, it can be concluded that UPVC/TiO₂ nanocomposite with low content of carbon‐coated TiO₂ nanoparticles(0.25 wt %) illustrated high stability under light exposure. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40228.     

Mechanical and Antibacterial Properties of Polypropylene/Polyamide 6 Blends-TiO2 Nanocomposites

Polypropylene/Polyamide 6 (PP/PA6) blends-TiO₂ nanocomposites have been prepared via melt blending PP/PA6 with TiO₂ nanoparticles, which were pretreated with toluene-2,4-di-isocyanate. The functionalized-TiO₂ can react with the terminal amino and carboxyl groups at PA6, interfacial interaction and compatibility between TiO₂ and matrix have been greatly improved resulted in higher tensile and impact strength than that of those filled with pristine TiO₂ or pure PP/PA6 blends, and they have strong antimicrobial abilities against Bacillus subtilis, Staphylococcus aureus and Escherichia coli. The average efficiency of antibacterial is over 90% within 2.0 h. Mechanical and antibacterial properties can achieve their maximum with 3.0 wt%TiO₂.     

Enhancement of mechanical and tribological properties in ring‐opening metathesis polymerization functionalized molybdenum disulfide/polydicyclopentadiene nanocomposites

This study focuses on the possibility of improving performance properties of polydicyclopentadiene (PDCPD) nanocomposites for engineering applications using nanoparticles. In this article, molybdenum disulfide/polydicyclopentadiene (MoS₂/PDCPD) nanocomposites have been prepared by in situ ring‐opening metathesis polymerization using reaction injecting molding (RIM) process. To enhance the interfacial adhesion between the fillers and PDCPD matrix, the surface modified MoS₂ nanoparticles hybridized with dialkyldithiophosphate (PyDDP) were successfully prepared by in situ surface grafting method. The effect of low MoS₂ loadings (<3 wt %) on the mechanical and tribological behaviors of PDCPD was evaluated. The results indicated that the friction coefficient of the MoS₂/PDCPD nanocomposites was obviously decreased and the wear resistance of nanocomposites was greatly improved by the addition of PyDDP‐hybridized MoS₂ nanoparticles; meanwhile, the mechanical properties were also enhanced. The MoS₂/PDCPD nanocomposites filled with 1 wt % PyDDP‐hybridized MoS₂ exhibited the best mechanical and anti‐wear properties. The friction coefficient was shown to decrease by more than 40% compared to pure PDCPD by incorporating just 1 wt % hybridized MoS₂ nanoparticles, and modest increase in modulus and strength was also observed. The reinforcing and wear‐resistant mechanisms of MoS₂/PDCPD nanocomposites were investigated and discussed by scanning electron microscopy. The well interfacial compatibility between the particle/matrix interfaces played an important role for the improved mechanical and tribological properties of MoS₂/PDCPD nanocomposites in very low MoS₂ loadings. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Nanocrystalline Fe‐Ni alloy/polyamide 6 composites of high mechanical performance made by ultrasound‐assisted master batch technique

The focus of this study is to improve the dispersion state of nanocrystalline (nc) Fe‐Ni particles in polyamide 6 (PA6) matrix and the filler‐matrix interfacial interactions to provide Fe‐Ni alloy/PA6 nanocomposites of remarkable mechanical performance for engineering applications. nc Fe₄₀Ni₆₀ particles were chemically synthesized. Then Fe₄₀Ni₆₀/PA6 nanocomposites of various nanofiller loading were prepared by compounding via a newly modified master batch technique called ultrasound assisted master batch (UMB), followed by injection molding (IM). Their mechanical properties, morphology and structural parameters were characterized and compared with the corresponding properties of Fe₄₀Ni₆₀/PA6 nanocomposites made by solution mixing (SM) and IM. The study reveals that the UMB process is more cost effective and time efficient, simpler and easier to scale up compared with the SM process. In addition, UMB nanocomposites exhibit superior mechanical properties and distinctive morphology compared with the corresponding SM ones. Moreover, structural analyses indicate that physical structural changes occurred in PA6 due to presence of alloy particles are affected differently by the different compounding methods, profound understanding of such phenomenon is focused throughout the article. These distinctive advantages recommend that UMB technique can be of great potential in commercial production of polymer nanocomposites (PNCs). It is concluded that the sonication of nc Fe₄₀Ni₆₀ particles in dilute polymer solution during UMB compounding, a new step that is incorporated for the first time in the master batch process, is mainly responsible for the good wetting between nanoparticles and polymer chains, strong filler‐matrix interactions and consequently the remarkable mechanical performance of UMB PNCs. POLYM. COMPOS., 35:2343–2352, 2014. © 2014 Society of Plastics Engineers     

Improvement of interfacial interaction,dispersion, and properties of chlorosulfonated polyethylene/sio2 nanocomposites using CSPE‐g‐Sio2 nanoparticles synthesized under ultrasonics

Chlorosulfonated polyethylene (CSPE) is a widely used elastomer because of the resistance to gases and aggressive chemicals, fire‐retarding, and electric insulating properties. Silica nanoparticles were usually introduced into the elastomer to improve its critical properties. However, there were some problems of strong aggregation and poor dispersion of nanoparticles in the nanocomposites. In this work, an efficient approach of grafting matrix CSPE onto silica surface was proposed to solve the problems. CPSE‐g‐SiO₂ nanoparticles were prepared via an in situ radical reaction between  Cl in CSPE and Si OH on silica surface under ultrasonics. The successful chemical graft reaction was confirmed using Fourier transform infrared, ultraviolet–visible spectroscopy, ¹H‐NMR, and X‐ray photoelectron spectroscopy. Thermogravimetric analysis indicated that the grafting amount of CSPE was 4.68 wt%. Grafting CSPE onto silica surface significantly improved the dispersion of CSPE‐g‐SiO₂ nanoparticles in CSPE matrix and the interfacial interaction. Therefore, the mechanical, thermal stability, damping capacity, and rheology properties of CSPE/CSPE‐g‐SiO₂ nanocomposites were improved. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Effect of dendrimer‐like PAMAM grafted attapulgite on the microstructure and morphology of Nylon‐6

The effect of dendrimer‐like polyamidoamine grafted attapulgite (ATP‐PAMAM) on the microstructure and morphology of Nylon‐6 (PA6) was investigated. The ATP‐PAMAM nanoparticles were prepared by treating attapulgite (ATP) with heat and acid followed by grafting with polyamidoamine (PAMAM) molecules, which was confirmed by Fourier transform infrared spectroscopy (FT‐IR), thermogravimetric analysis (TGA), and dispersion state in formic acid. The X‐ray diffraction (XRD) analysis result indicated that the grafting modification was occurred on the surface of fibrous crystals and did not shift the crystal structure of ATP. PA6/ATP‐PAMAM (G_2.0) nanocomposites with different modified ATP content were prepared by melt compounding in a twin screw extruder. XRD measurements suggested that the intensity of diffraction peak of α crystalline form of PA6 decreased gradually as the inclusion of ATP‐PAMAM(G_2.0) into the PA6 matrix, while that of γ crystalline form increased gradually. The results of molau experiment and scanning electron microscopy (SEM) observation showed not only a uniform dispersion of ATP‐PAMAM(G_2.0) in the PA6 matrix but also a strong interfacial adhesion between them. Mechanical investigation (by tensile test) showed an obvious improvement in the presence of surface modified ATP. POLYM. COMPOS., 35:627–635, 2014. © 2013 Society of Plastics Engineers     

Surface modification of titanium dioxide nanoparticles by polyaniline via an in situ method

BACKGROUND: Nanoparticulate titanium dioxide (TiO₂) has the advantages of high chemical stability, high photocatalytic activity to oxidise pollutants in air and water, relatively low price and non‐toxicity. However, its high surface energy leads to the aggregation of nanoparticles. In addition, the wide band gap of TiO₂ (3.2 eV) only allows it to absorb ultraviolet (UV) light (<387 nm), which represents just a small fraction (3–5%) of the solar photons. These factors have limited its use in many fields. In this study, nanoparticulate TiO₂ was modified by polyaniline (PANI) in order to enhance its photoactivity under UV light and sunlight illumination. RESULTS: TiO₂ nanoparticles were modified by PANI via a chemical oxidative method. The introduction of small amounts of PANI enhanced the dispersion of TiO₂ nanoparticles and improved the photocatalytic activity under UV light. In addition, the band gap energies of all PANI/TiO₂ nanocomposites were lower than that of neat TiO₂ nanoparticles, so the PANI/TiO₂ nanocomposites can be excited to produce more electron–hole pairs under sunlight, which could result in higher photocatalytic activities. CONCLUSION: The modification of nanoparticulate TiO₂ by PANI can increase its photoactivity in the process of phenol degradation under UV light and sunlight illumination. Copyright © 2008 Society of Chemical Industry     

Location of functionalized-TiO<Subscript>2</Subscript> nanoparticle in an immiscible PP/PA6 blends and its effect on the compatibility of the components

Nanocomposites based on 70/30 (w/w) polypropylene (PP)/polyamide 6 (PA6) immiscible blends and functionalized-TiO₂ nanoparticles were prepared via melt compounding. The influences of TiO₂ on the morphology of nanocomposites were investigated. Scanning electron microscopy results revealed the domain size of the dispersed PA6 phase decreased in presence of functionalized-TiO₂ and the TiO₂ nanoparticles were preferentially located at the PA6 phase and at the interfacial region between PP and PA6, which were ascertained by differential scanning calorimetry. The functionalized-TiO₂ nanoparticles played the compatibilizer for the immiscible PP/PA6 blends, increasing the interaction of the two phases in certain extent. Therefore, a clear compatibiliting effect was induced by the TiO₂ in the immiscible PP/PA6 blends.     

Synthesis and characterization of bionanocomposites of poly(lactic acid) and TiO2 nanowires by in situ polymerization

Bionanocomposites from biopolymers and inorganic nanoparticles are of great interest for packaging materials due to their enhanced physical, thermal, mechanical, and processing characteristics. In this study, poly(lactic acid) (PLA) nanocomposites with covalent bonding between TiO₂ nanowire surface and PLA chains were synthesized through in situ melt polycondensation. Molecular weight, structure, morphology, and thermal properties were characterized. Fourier transform infrared spectroscopy confirmed that PLA chains were covalently grafted onto TiO₂ nanowire surface. Transmission electron microscopy images also revealed clearly a third phase presence on the nanowires after the grafting process. Those grafted PLA chains exhibited significantly increased glass transition temperature and thermal stability, compared with pure PLA. The weight-average molecular weight of PLA/2% TiO₂ nanowire bulk nanocomposites increased by 66% compared with that of pure PLA. The electron microscopy results showed that strong interfacial interaction and homogeneous distribution were achieved between inorganic nanowires and organic PLA matrix in the bulk nanocomposites. The PLA matrix in bulk nanocomposites exhibited elevated glass transition temperature and decreased crystallization ability as the TiO₂ nanowire concentrations were increased from 0 to 2%.     

Preparation and properties of polylactide–silica nanocomposites

Poly(lactic acid) (PLA)/SiO₂ nanocomposites were prepared via melt mixing with a Haake mixing method. To improve the dispersion of nanoparticles and endow compatibility between the polymer matrix and nanosilica, SiO₂ was surface‐modified with oleic acid (OA). The interfacial adhesion of the PLA nanocomposites was characterized by field‐emission scanning electron microscopy. The storage modulus and glass‐transition temperature values of the prepared nanocomposites were measured by dynamic mechanical thermal analysis. The linear and nonlinear dynamic rheological properties of the PLA nanocomposites were measured with a parallel‐plate rheometer. The effects of the filling content on the dispersability of the OA–SiO₂ nanoparticles in the PLA matrix, the interface adhesion, the thermomechanical properties, the rheological properties, and the mechanical properties were investigated. Moreover, the proper representation of the oscillatory viscometry results provided an alternative sensitive method to detect whether aggregation formed in the polymeric nanocomposites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Friction and wear behavior of the hybrid PTFE/cotton fabric composites filled with TiO2 nanoparticles and modified TiO2 nanoparticles

A chemical grafting method was applied to modify TiO₂ nanoparticles through covalently introducing glycidoxypropyltrimethoxy silicane (KH560) followed by polyoxymethylene onto the particles to overcome the disadvantages generated by the agglomeration of nanoparticles. TiO₂ nanoparticles unmodified and modified were introduced into hybrid polytetrafluoroethylene (PTFE)/cotton fabric composites. Friction and wear test demonstrated that TiO₂ nanoparticles unmodified and modified can significantly increase the wear resistance of hybrid PTFE/cotton fabric composites but cannot reduce the friction coefficient. Fabric composites filled with grafted TiO₂ nanoparticles exhibited a lower wear rate due to the disintegration of agglomeration and the improvement of interfacial adhesion between filler/matrix. POLYM. ENG. SCI., 2009. © 2008 Society of Plastics Engineers     

Nanocomposites of polypropylene/titanate nanotubes: morphology,nucleation effects of nanoparticles and properties

High-quality titanate nanotubes (TiNT) were mixed with modified polypropylene (PP*) by a batch melt-mixing procedure. To improve compatibility between the nanofiller and the matrix, polypropylene (PP) was modified by electron beam irradiation. Effects of TiNT nanoparticles on crystallization, mechanical, thermal and rheological properties of the modified polypropylene were studied and compared with the analogous systems filled with commercial micro- (mTiO₂) and nano- (nTiO₂) titanium dioxide particles. Nucleation effects of the TiO₂-based fillers on PP* crystallization were investigated in detail. The microstructure of the PP*/TiNT nanocomposites shows well-dispersed TiNT sparse aggregates (clouds), penetrated by the polymer. A large-scale structure in the nanocomposite melts confirmed also rheology. In comparison to the matrix characteristics, the stiffness and microhardness of the TiNT nanocomposites increase by 27 and 33 %, respectively. The enhancement in mechanical properties demonstrates that the quality titanate nanotubes can be used as an efficient filler in non-polar polymers using the polymers modified by irradiation. In the case of the nanocomposites containing nTiO₂-anatase particles, the increase in these mechanical characteristics is lower. The investigated changes in the rate of crystallization indicate a marked nucleation effect of the nanotubes. The crystallization kinetics data, processed by the Avrami equation, suggest 3-dimensional crystal growth in the polypropylene matrix. The observed improvement in mechanical properties of the TiNT nanocomposites is induced not only by the nanofiller reinforcement but also by the changes of supermolecular structure of the polymer matrix due to nucleated crystallization.     

Isothermal crystallization and melting behaviors of nano TiO2‐modified polypropylene/polyamide 6 blends

Titanium dioxide (TiO₂) nanoparticles were functionalized with toluene‐2,4‐diisocyanate and then polypropylene/polyamide 6/(PP/PA6) blends containing functionalized‐TiO₂ were prepared using a twin screw extruder. Isothermal crystallization and melting behavior of the as‐prepared composites were investigated using differential scanning calorimetry and wide‐angle X‐ray diffraction. Isothermal crystallization analysis shows that the TiO₂ nanoparticles have two effects on PP/PA6 blends, i.e., it can favor the improvement of crystallization ability and decrease the crystallization rate of PP/PA6 blends. The improvement of crystallization ability is superior over decreasement of crystallization rate of PA6 chains caused by TiO₂, therefore PA6 in PP/PA6/TiO₂ nanocomposites have higher crystallization rate than that of PA6 in pure PP/PA6 blends, which indicated TiO₂ nanoparticles favored the crystallization of PA6. The TiO₂ nanoparticles show no effects on the equilibrium melting temperature (T) values of PP phase but decreases the T values of PA6 phase. In addition, the TiO₂ nanoparticles did not change the crystalline polymorph of PP/PA6 blends basically; however, favored the formation of β‐PP. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Interfacial agent effect on rheological response and crystallite characteristics in germicidal polypropylene/titanium dioxide nanocomposites

Germicidal nanocomposites based on metallocene isotactic polypropylene (iPP) and titanium dioxide (TiO₂) nanoparticles have been prepared at a constant TiO₂ content of 2 wt%. Different quantities of a polypropylene wax partially grafted with maleic anhydride (PP‐g‐MAH) are employed to improve the polymer‐nanoparticle compatibility. Remarkable biocidal capabilities of these TiO₂ nanocomposites have been found and their crystalline structure and thermal and rheological responses explored. Several very interesting features have been found in these germicidal nanocomposites. On the one hand, rheological parameters do not change significantly with respect to those exhibited by pure iPP. This is extremely advantageous for the processing of these compounds since they can be transformed under similar conditions to those employed for iPP. On the other hand, the existence of two polymorphs is observed independent of the amount of compatibilizer used. The enhancement in polymer‐nanoparticle interactions by effect of the interfacial (PP‐g‐MAH) component is appraised looking at dynamical mechanical relaxations as a function of temperature and at crystallization processes of the various nanocomposites. Copyright © 2012 Society of Chemical Industry     

The effect of the interface structure of different surface‐modified nano‐SiO2 on the mechanical properties of nylon 66 composites

The nylon 66‐based nanocomposites containing two different surface‐modified and unmodified SiO₂ nanoparticles were prepared by melt compounding. The interface structure formed in different composite system and their influences on material mechanical properties were investigated. The results indicated that the interfacial interactions differed between composite systems. The strong interfacial adhesion helped to increase tensile strength and elastic modulus of composites; whereas, the presence of modification layer in silica surface could enhance the toughness of composites, but the improvement of final material toughness was also correlated with the density of the adhered nylon 66 chains around silica nanoparticles. In addition, the results also indicated that the addition of surface‐modified silica nanoparticles has a distinct influence on the nonisothermal crystallization behavior of the nylon 66 matrix when compared with the unmodified silica nanoparticle. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Effects of nanoparticle treatment on the crystallization behavior and mechanical properties of polypropylene/calcium carbonate nanocomposites

Effects of nanoparticle surface treatment on the crystallization behavior and mechanical properties of polypropylene (PP)/CaCO₃ nanocomposites were investigated by using differential scanning calorimetry (DSC), polarized optical microscope (POM), X‐ray diffraction (XRD), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). The results demonstrated that the interfacial interaction formed between PP and nanoparticles significantly influenced the thermal and mechanical properties of nanocomposites. It was found that CaCO₃ nanoparticles modified by a single aluminate coupling agent (CA‐1) could improve the onset crystallization temperature more effectively than that modified by a compound surface‐treating agent (CA‐2) could. However, there is no significant difference in total rate of crystallization for the two PP/CaCO₃ nanocomposites (PPC‐1 and PPC‐2), which contained CA‐1 and CA‐2, respectively. In contrast, CA‐2 modified nanoparticles could cause smaller spherulites and induce much more β‐phase crystal in nanocomposites than that of CA‐1 modified nanoparticles. This may be explained by a synergistic effect of aluminate coupling agent and stearic acid in CA‐2, which also resulted in an improved toughness for PPC‐2. © 2006 Wiley Periodicals, Inc. J Appl PolymSci 102: 3480–3488, 2006