The effect of clay type and of clay–masterbatch product in the preparation of polypropylene/clay nanocomposites

Clay containing polypropylene (PP) nanocomposites were prepared by direct melt mixing in a twin screw extruder using different types of organo‐modified montmorillonite (Cloisite 15 and Cloisite 20) and two masterbatch products, one based on pre‐exfoliated clays (Nanofil SE 3000) and another one based on clay–polyolefin resin (Nanomax‐PP). Maleic anhydride‐grafted polypropylene (PP‐g‐MA) was used as a coupling agent to improve the dispersability of organo‐modified clays. The effect of clay type and clay–masterbatch product on the clay exfoliation and nanocomposite properties was investigated. The effect of PP‐g‐MA concentration was also considered. Composite morphologies were characterized by X‐ray diffraction (XRD), field emission gun scanning electron microscopy (FEG‐SEM), and transmission electron microscopy (TEM). The degree of dispersion of organo‐modified clay increased with the PP‐g‐MA content. The thermal and mechanical properties were not affected by organo‐modified clay type, although the masterbatch products did have a significant influence on thermal and mechanical properties of nanocomposites. Intercalation/exfoliation was not achieved in the Nanofil SE 3000 composite. This masterbatch product has intercalants, whose initial decomposition temperature is lower than the processing temperature (T ～ 180°C), indicating that their stability decreased during the process. The Nanomax‐PP composite showed higher thermal and flexural properties than pure PP. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Preparation and mechanical properties of PP/PP-g-MA/Org-MMT nanocomposites with different MA content

Summary Polypropylene-clay nanocomposites were prepared by melt intercalation in a twin screw extruder using two mixing methods: two-step mixing and one-step mixing. The effect of using two different kinds of PP-g-MA (polypropylene-grafted maleic anhydride), with graft efficiencies of 0.1 and 1.0 wt% of MA and with different molecular weight, on clay dispersion and mechanical properties of nanocomposites was investigated. Three different clays, natural montmorillonite (Cloisite Na+) and chemically modified clays Cloisite 20A and Cloisite 30B were used. The relative influence of each factor was observed from structural analysis by WAXD, TEM, and mechanical properties. X-ray diffractometry (XRD) was used to investigate the intercalation effect in the nanocomposites. The results indicted that the intercalation effect and mechanical properties, specially modulus, tensile strength and impact strength, were enhanced by increasing the content of MA, using maleated PP with higher graft efficiency, and using the two step mixing conditions. Better dispersion and exfoliation were obtained when using clay 20A than 30B and natural Na+ montmorillonite. The results showed that clay dispersion and interfacial adhesion are greatly affected by the kind of maleated PP. The increase in content of polar groups gives as a result better interfacial adhesion and subsequent mechanical performance.     

Mechanical properties of polypropylene/clay nanocomposites: Effect of clay content,polymer/clay compatibility,and processing conditions

In this work, polypropylene/clay nanocomposites with 0.5, 1, 3, and 5 wt % of montmorillonite (MMT) (unmodified clay) were prepared by intensive mixing at 50 rpm and 10 min of mixing. For the highest clay content (5 wt %), the initial materials or the processing conditions were changed to study their independent effect. On one hand, 10 wt % of PP‐graft‐MA (PP‐g‐MA) was incorporated or MMT was replaced by organomodified clays (C10A and C30B). On the other side, for the initial system, the speed of rotation (100 and 150 rpm) and the mixing time (5 and 15 min) were altered. In all cases, the state of the clay inside the matrix (DRX), the degree of dispersion in the micro (SEM) and nano (TEM) scales, and the rheological and mechanical properties were analyzed. It was found that the stiffness increased with clay content, whereas tensile and impact strength did not significantly change. Although intercalated structures were observed in the composites with unmodified clay, in the composites with modified clay or PP‐g‐MA, improved dispersion of clay in PP was found. The mechanical properties increased accordingly. The degree of dispersion of the filler in the matrix appeared to be unaffected by the changes in the processing conditions introduced. Finally, the elastic modulus was modeled by using an effective filler‐parameter model based on Halpin–Tsai equations, which also allowed estimating the relative degree of dispersion. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Melt compounding of polypropylene‐based clay nanocomposites

Polypropylene (PP)‐based nanocomposites containing 4 wt% maleic anhydride grafted PP (PP‐g‐MA) and 2 wt% Cloisite 20A (C20A) were prepared using various processing devices, viz., twin‐screw extruder (TSE), single‐screw extruder (SSE), and SSE with an extensional flow mixer (EFM). Two processing methods were employed: (I) masterbatch (MB) preparation in a TSE (with 10 wt% C20A and clay/compatibilizer ratio of 1:2), followed by dilution in TSE, SSE, or SSE + EFM, to 2 wt% clay loading; (II) single pass, i.e., directly compounding of dry‐blended PP‐g‐MA/clay in TSE, SSE, or SSE + EFM. It has been indicated that the quality of clay dispersion, both at micro‐ and nanolevel, of the nanocomposites depends very much on the operating conditions during processing, such as mixing intensity and residence time, thus affecting the mechanical performance. Besides that the degradation of the organoclay and the matrix is also very sensitive to these parameters. According to results of X‐ray diffraction, field emission gun scanning electron microscopy, transmission electron microscopy, and mechanical tests, the samples prepared with MB had better overall clay dispersion, which resulted in better mechanical properties. The processing equipment used for diluting MB had a marginal influence on clay dispersion and nanocomposite performance. POLYM. ENG. SCI., 47:1447–1458, 2007. © 2007 Society of Plastics Engineers     

Preparation and mechanical properties of polypropylene/clay nanocomposites for automotive parts application

Nanocomposites of polypropylene with organically modified clays were compounded in a twin‐screw extruder by a two‐step melt compounding of three components, i.e., polypropylene, maleic anhydride grafted polypropylene (PPgMA), and organically modified clay. The effect of PPgMA compatibilizers, including PH‐200, Epolene‐43, Polybond‐3002, and Polybond‐3200, with a wide range of maleic anhydride (MA) content and molecular weight was examined. Nanocomposites' morphologies and mechanical properties such as stiffness, strength, and impact resistance were investigated. X‐ray diffraction patterns showed that the dispersion morphology of clay particles seemed to be determined in the first compounding step and the further exfoliation of clays didn't occur in the second compounding step. As the ratio of PPgMA to clay increased, the clay particles were dispersed more uniformly in the matrix resin. As the dispersibility of clays was enhanced, the reinforcement effect of the clays increased; however, impact resistance decreased. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 427–433, 2005     

Effect of Ionomeric Compatibilizer on Clay Dispersion in Polyethylene/Clay Nanocomposites

Summary: Linear low‐density polyethylene (LLDPE)/clay nanocomposites are obtained and studied by using a zinc‐neutralized carboxylate ionomer as a compatibilizer. LLDPE‐g‐MA is used as a reference compatibilizer. Two different clays, natural montmorillonite (Closite Na⁺) and a chemically modified clay Closite 20A have been used. Nanocomposites are prepared by melt blending in a twin‐screw extruder using two mixing methods: two‐step mixing and one‐step mixing. The relative influence of each compatibilizer is determined by wide‐angle X‐ray diffraction structural analysis and mechanical properties. The results are analyzed in terms of the effect of the compatibilizing agent and incorporation method in the clay dispersion, and the mechanical properties of the nanocomposites. Experimental results confirm that the film samples with ionomer show a good mechanical performance only slightly below that of the samples with maleic anhydride (MA). The two‐step mixing conditions result in better dispersion and intercalation for the nanofillers than one‐step mixing. The exfoliation of clay platelets leads to an improved thermal stability of the composite. The oxygen permeability of the clay nanocomposites, using ionomer as a compatibilizer, is decreased by the addition of the clay.

TEM image of a PE/4 wt.‐% Closite 20A nanocomposite formed using ionomer.     

Polypropylene/clay nanocomposites: An innovative one‐pot process

This work discloses a novel one‐pot preparation method of polypropylene (PP)/clay nanocomposites with high degree of clay delamination and improved thermal, mechanical and rheological properties. The in situ simultaneous synthesis of carboxylate clay from native clay and ionomer of PP‐graft maleic anhydride (PP‐g‐MA) through trihydrate sodium acetate addition, combined with water injection in the extrusion process, appears to be a valuable alternative to the use of organoclay for producing PP/PP‐g‐MA/clay nanocomposites. The influence of PP‐g‐MA graft content, and of its ionomer form, onto the clay dispersion has been especially investigated. PP‐g‐MA of low graft content is compared to a home‐made highly grafted PP‐g‐MA synthesized in the presence of N‐bromosuccinimide (NBS). The nanocomposites prepared by combining the use of NBS‐mediated PP‐g‐MA, trihydrate sodium acetate and water injection exhibit the highest clay dispersion. Thermal, rheological, and mechanical properties of the nanocomposites have been measured. POLYM. COMPOS., 36:644–650, 2015. © 2014 Society of Plastics Engineers     

Melt processing and characterization of multicomponent polymeric nanocomposites containing organoclay

Nylon 6 (Ny)/polypropylene (PP)/maleated polypropylene (PP‐g‐MA)/organoclay/wollastonite composites were prepared by melt processing. The polymers' composition was kept constant ([70PP/30Ny]/4PP‐g‐MA). Melt compounding was conducted using a twin‐screw extruder in three different methods: (1) simultaneous incorporation of the components into the compounding equipment, (2) preparation of [Ny6/clay] concentrate, and then in a second step, mixing the other components with the concentrate, and (3) mixing of PP with wollastonite and clay followed by the addition of Ny6 and PP‐g‐MA in the second step. Injection‐molded specimens were characterized in tension, scanning electron microscopy, X‐ray diffraction (XRD), and differential scanning calorimetry. The sequence of component addition greatly influences the structure and properties of the composites. Enhanced mechanical properties were achieved when the two‐step mixing procedure was used for the PP/Ny6/PP‐g‐MA/clay system (method 2) and also for the PP/Ny6/PP‐g‐MA/clay/wollastonite system (method 3). The XRD pattern of the PP/Ny6/PP‐g‐MA/clay nanocomposites produced by the two‐step mixing method does not show a characteristic basal reflection of the pristine organoclay, indicating a predominately exfoliated structure of clay. POLYM. COMPOS., 28:417–424, 2007. © 2007 Society of Plastics Engineers     

The effect of addition of poly(propylene‐g‐acrylic acid) on the morphology of poly(vinyl methylether) and isotactic polypropylene blend

The interfacial adhesion of blend of isotactic polypropylene/poly(vinyl methylether) (i‐PP/PVME) has been improved by the addition of poly(propylene‐g‐acrylic acid) (PP‐g‐AA) as a compatibilizing agent. The phase morphologies of the blends are investigated by optical microscopy (OM) and lateral force microscopy (LFM). The i‐PP/PVME (80/20) blend with no addition of PP‐g‐AA from extrusion process shows a coarse morphology with the dispersed domain size as large as several micrometers; After the addition of 2.5% PP‐g‐AA in the blends, the dispersed PVME domain size decreases greatly. The addition of 5% PP‐g‐AA results in a homogeneous morphology. The blending of PP‐g‐AA with PVME reduces the crystallization temperature of PP‐g‐AA, which is different from that of blending i‐PP with PVME. The increase of the interfacial adhesion is attributed to the specific intermolecular interaction between the acrylic acid group of PP‐g‐AA and the ether group of PVME. The specific interaction is studied by Fourier transform infrared spectroscopy. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 4098–4103, 2006     

Effect of the silane modification of clay on the tensile properties of nylon 6/clay nanocomposites

A commercially available organomodified clay, Cloisite 25A, was modified with 3‐aminopropyltriethoxysilane, 3‐(glycidoxypropyl)trimethoxysilane, and 3‐isocyanate propyltriethoxysilane to enhance its interaction with the nylon 6 matrix. Composites made of nylon 6 and clays modified with the different silane compounds were prepared by melt mixing with a twin‐screw extruder. The dispersion and degree of exfoliation of the organomodified clays were evaluated from X‐ray diffraction patterns and transmission electron microscopy images of the corresponding composites. The tensile properties of the composites were measured, and their enhancement was attributed to the work of adhesion and interfacial tension of the composites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

A spectroscopic approach for structural characterization of polypropylene/clay nanocomposite

This study focuses on the degree of dispersion and structural development of organomodified MMT clay (OMMT) during processing of polypropylene clay nanocomposites using both conventional and nonconventional characterization techniques. PP‐g‐MA and Cloisite 15A were melt blended with three different grades of PP separately in a micro‐twin screw compounder at selected screw speed and temperature. The clay was modified with fluorescent dyes and the adsorbed dye content in the clay gallery was estimated by using UV‐spectrophotometric method. The effects of residence time and molecular weight of the PP matrix on the clay dispersion were studied. The extent of dispersion and exfoliation of the clay in polymer matrix determined from the torque versus time data obtained from microcompounder. It was further supported by XRD, SEM, TEM, and DSC analysis. Offline dielectric and fluorescence spectrophotometric studies were also carried out. Changes in dielectric constant and dielectric loss with both frequency and temperature yielded quantitative information about the extent of clay exfoliation and intercalation in the polymer matrix. It was observed that with an increase in MFI (decrease in molecular weight) and mixing time, the extent of clay dispersion and exfoliation were also improved due to easy diffusion of polymer chains inside clay gallery. POLYM. COMPOS., 31:2007–2016, 2010. © 2010 Society of Plastics Engineers     

Study on dispersion and intercalation of organoclay in PP and PP‐g‐MA matrices

Understanding the complex mechanism of dispersion and intercalation of the clay tactoids can allow us to control the final morphology, homogeneity, and the macroscopic properties of clay nanocomposites. The objective of this work is a multiscale study of the dispersion state of PP/organoclay and PP‐g‐MA/organoclay composite. The microscopic investigation, WAXS diffractograms, rheological analysis, and mechanical properties were used to characterize the dispersion of organoclay in PP and PP‐g‐MA matrices during melt blending in two different shear rates. The morphological results show a system of aggregating intercalated clay particles which disperse by increasing mixing time with a strain‐controlled process and a very quick intercalation process in early mixing times for PP‐g‐MA/organoclay nanocomposite, while PP/organoclay samples only form microcomposites. The relative network modulus of these intercalated particles as a function of mixing time was obtained; and the tensile modulus of nanocomposite samples were compared with Halpin‐Tsai model prediction. POLYM. COMPOS., 2009. © 2009 Society of Plastics Engineers     

Functionalized polypropylenes in the compatibilization and dispersion of clay nanocomposites

The preparation of polypropylene (PP) nanocomposites was studied using clay and three types of modified PP (m‐PP) as compatibilizers: diethyl maleate grafted PP (PP‐g‐DEM), maleic anhydride grafted PP (PP‐g‐MA), and PP grafted with carbamyl maleamic acid (PP‐g‐UMA). The clay was made organophylic by an acid treatment with octadecylamine. PP functionalization and blending were carried out in an internal mixer. Blends of PP containing 20 and 40 wt% each of the modified PP and 5 wt% of organophilic clay (IMt), in each case, were prepared. Samples were characterized by transmission electron microscopy (TEM), differential scanning calorimetry (DSC), optical microscopy, and mechanical testing. The presence of tactoid, intercalated and exfoliated structures was observed by TEM in all the samples containing clay and modified PP, which also showed improved mechanical properties with tensile modulus as much as three times that of PP. Melting temperature did not vary significantly with the addition of clay. However, because of the clay's nucleating effect, an increase in the crystallization temperature was observed, accompanied by a slight decrease in the degree of crystallinity. The best results were obtained when PP‐g‐MA was used as the compatibilizer; intermediate results were obtained with the use of PP‐g‐UMA, followed by the results obtained when PP‐g‐DEM was used. Property enhancements were obtained when a higher percentage of modified PP was employed. POLYM. COMPOS., 27:451–460, 2006. © 2006 Society of Plastics Engineers     

Morphological structure and surface properties of maleated ethylene propylene diene monomer/organoclay nanocomposites

The phase morphology and surface properties of some maleated ethylene propylene‐diene/organoclay nanocomposites (EPDM‐g‐MA/OC) were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM) and contact angle measurements. The effect of organoclay and/or compatibilizing agent [maleic anhydride‐grafted polypropylene (PP‐g‐MA)] on the properties of the EPDM‐g‐MA nanocomposites was investigated. The quality and uniformity of nanoclay dispersion were analyzed by SEM and AFM images. The experimental results showed an intercalate structure and biphasic morphology for the binary blends based on EPDM and clay. The surface properties of the studied composites are significantly influenced by the presence of a compatibilizing agent—PP‐g‐MA. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Effect of the molecular weight of maleated polypropylenes on the melt compounding of polypropylene/organoclay nanocomposites

Maleic anhydride grafted polypropylene (PP‐g‐MA) and organically modified clay composites were prepared in a plasticorder. PP‐g‐MAs, including Polybond PB3150, Polybond PB3200, Polybond PB3000, and Epolene E43, with a wide range of maleic anhydride (MA) concentrations and molecular weights were used. The structure was investigated with X‐ray diffraction (XRD) and transmission electron microscopy (TEM). PP‐g‐MA compatibilizers gave rise to similar degrees of dispersion beyond the weight ratio of 3/1, with the exception of E43, which had the highest MA content and the lowest molecular weight. The thermal instability and high melt index were responsible for the ineffective modification by E43. Furthermore, PP‐g‐MA with a lower molecular weight and a higher melt index had to be compounded at a lower mixing temperature to achieve a reasonable level of torque for clay dispersion. Polypropylene/organoclay nanocomposites were then modified with different levels of PP‐g‐MA compatibilizers with a twin‐screw extruder. The polypropylene/E43/clay system, as shown by XRD patterns and TEM observations, yielded the poorest clay dispersion of the compatibilizers under investigation. The curves of the relative complex viscosity also revealed a systematic trend with the extent of exfoliation and showed promise for quantifying the hybrid structure of the nanocomposites. The mechanical properties and thermal stability were determined by dynamical mechanical analysis and thermogravimetric analysis, respectively. Although PP‐g‐MA with a lower molecular weight led to better clay dispersion in the polypropylene nanocomposites, it caused deterioration in both the mechanical and thermal properties of the hybrid systems. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1667–1680, 2005     

Dynamically vulcanized polypropylene/nitrile rubber blends: The effect of peroxide/bis‐maleimide curing system and different compatibilizing systems

In this study, the efficiency of dicumyl peroxide (DCP) in combination with N,N′‐m‐phenylene‐bis‐maleimide (BMI) as a crosslinking system for the polypropylene (PP)/nitrile rubber (NBR) (30 : 70 wt %) thermoplastic elastomers was investigated in the presence of compatibilizing agents. The compatibilization was carried out by maleic anhydride‐grafted‐PP (PP‐g‐MA)/amino compound and glycidyl methacrylate‐grafted‐PP (PP‐g‐GMA) with or without amino compound. They were employed in a proportion of 5 wt % together with different amounts of carboxylated NBR (XNBR). Excellent mechanical properties were achieved without the addition of compatibilizer, suggesting that BMI should act as compatibilizing agent. The other functionalized systems exerted an additional improvement on tensile properties and reprocessing ability. The mechanical and dynamic mechanical properties, oil resistance, and morphology were investigated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Evaluation of toughening mechanisms of polypropylene/ethylene–octene copolymer/maleic anhydride‐grafted poly(ethylene‐co‐octene)/clay nanocomposite

The toughness of a polypropylene (PP)/ethylene‐octene copolymer (EOC)/maleic anhydride‐grafted poly(ethylene‐co‐octene) (EOC‐g‐MA)/clay nanocomposite and blends of PP/EOC and PP/EOC/EOC‐g‐MA was investigated using Charpy impact and single‐edge‐notch tensile (SENT) tests. In order to understand the toughening mechanisms, impact fracture surfaces and damage zones of single‐edge‐notch samples were studied with scanning electron microscopy and transmission optical microscopy, respectively. It was observed that the addition of EOC‐g‐MA to PP/EOC blend led to improvements in both impact strength and fracture energy of SENT tests because of the enhanced compatibility of the blend, which resulted from reduced EOC particle size and improved interfacial adhesion, and the decreased crystallinity of PP. The incorporation of clay to PP/EOC/EOC‐g‐MA blend caused a further increase of the toughness, owing to the greater decrease in the size of elastomer particles, to the presence of clay tactoids inside the elastomer phase and presumably to debonding of clay layers during the low‐speed SENT tests. The results of microscopic observations showed that the main toughening mechanism in PP/EOC/EOC‐g‐MA blend and PP/EOC/EOC‐g‐MA/clay nanocomposite is crazing. Copyright © 2012 Society of Chemical Industry     

Solid‐state mechanical properties of polypropylene/nylon 6/clay nanocomposites

The mechanical and thermomechanical properties as well as microstructures of polypropylene/nylon 6/clay nanocomposites prepared by varying the loading of PP‐MA compatibilizer and organoclay (OMMT) were investigated. The compatibilizer PP‐MA was used to improve the adhesion between the phases of polymers and the dispersion of OMMT in polymer matrix. Improvement of interfacial adhesion between the PP and PA6 phases occurred after the addition of PP‐MA as confirmed by SEM micrographs. Moreover, as shown by the DSC thermograms and XRD results, the degree of crystallinity of PA6 decreased in the presence of PP‐MA. The presence of OMMT increased the tensile modulus as a function of OMMT loading due to the good dispersion of OMMT in the matrix. The insertion of polymer chains between clay platelets was verified by both XRD and TEM techniques. The viscosity of the nanocomposites decreased as PP‐MA loading increased due to the change in sizes of PA6 dispersed phase, and the viscosity increased as OMMT loading increased due to the interaction between the clay platelets and polymer chains. The clay platelets were located at the interface between PP and PA6 as confirmed by both SEM and TEM. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Nanocomposites of silica reinforced polypropylene: Correlation between morphology and properties

Polypropylene/fumed hydrophilic silica nanocomposites were prepared via melt mixing method using a single‐screw extruder. Comparative study with and without compatibilizing copolymer agent (maleic anhydride grafted polypropylene: PP‐g‐AM) was conducted. The obtained results were interpreted in terms of silica nanoparticle–silica nanoparticle and silica nanoparticle‐polymer interactions. These results have shown that the addition of nanofillers improves the properties of the nanocomposites. From transmission electron microscopy, it was found that agglomerations of silica particles into the PP matrix increased in average size with increasing silica contents, except in presence of the copolymer. Storage modulus values of the nanocomposites measured by dynamic mechanical thermal analysis were sensitive to the microstructure of the nanocomposites. Higher silica contents resulted in higher storage modulus, revealing that the material became stiffer. By adding the compatibilizer, a further increase of storage modulus was observed due to the finer dispersion of the filler in the matrix and the increased interfacial adhesion. Crystallization rates were found to increase with the increase of silica nanoparticles as well as PP‐g‐MA content. In addition, silica nanoparticles and the compatibilizing agent present centers of germination and nucleation of crystallites. Thus, the use of the coupling agent resulted in a further enhancement of mechanical properties of the nanocomposites due to the reduction of silica agglomeration. POLYM. ENG. SCI., 54:2187–2196, 2014. © 2013 Society of Plastics Engineers     

Relationship between branch length and the compatibilizing effect of polypropylene‐g‐polystyrene graft copolymer on polypropylene/polystyrene blends

Three polypropylene‐g‐polystyrene (PP‐g‐PS) graft copolymers with the same branch density but different branch lengths were evaluated as compatibilizing agents for PP/PS blends. The morphological and rheological results revealed that the addition of PP‐g‐PS graft copolymers significantly reduced the PS particle size and enhanced the interfacial adhesion between PP and PS phases. Furthermore, it is verified that the branch length of PP‐g‐PS graft copolymer had opposite effects on its compatibilizing effect: on one hand, increasing the branch length could improve the compatibilizing effect of graft copolymer on PP/PS blends, demonstrated by the reduction of PS particle size and the enhancement of interfacial adhesion; on the other hand, increasing the branch length would increase the melt viscosity of PP‐g‐PS graft copolymer, which prevented it from migrating effectively to the interface of blend components. Additionally, the crystallization and melting behaviors of PP and PP/PS blends were compared. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40126.