Microcellular poly(hydroxybutyrate‐co‐hydroxyvalerate)‐hyperbranched polymer–nanoclay nanocomposites

The effects of incorporating hyperbranched polymers (HBPs) and different nanoclays [Cloisite® 30B and halloysite nanotubes (HNT)] on the mechanical, morphological, and thermal properties of solid and microcellular poly(hydroxybutyrate‐co‐hydroxyvalerate) (PHBV) were investigated. According to the X‐ray diffraction (XRD) and transmission electron microscopy (TEM) analyses, Cloisite 30B exhibited a combination of exfoliation and heterogeneous intercalation structure for both solid and microcellular PHBV–12% HBP–2% Cloisite 30B nanocomposites. TEM images indicated that HNTs were uniformly dispersed throughout the PHBV matrix. The addition of 2% nanoclays improved the thermal stability of the resulting nanocomposites. The addition of HBP+poly(maleic anhydride‐alt‐1‐octadecene) (PA), Cloisite 30B, and HNT reduced the average cell size and increased the cell density of the microcellular components. The addition of (HBP+PA), Cloisite 30B, and HNT also increased the degree of crystallinity for both solid and microcellular components in comparison with neat PHBV. Also, with the addition of 12% (HBP+PA), the area under the tan‐δ curve, specific toughness, and strain‐at‐break of the PHBV–HBP nanocomposite increased significantly for both solid and microcellular specimens, whereas the storage modulus, specific Young's modulus, and specific tensile strength decreased. The addition of 2% nanoclays into the PHBV–HBP nanocomposites improved the storage modulus, specific Young's modulus, and specific tensile strength of the PHBV–HBP–nanoclay‐based nanocomposites, but they were still lower than those of the neat PHBV. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers     

Effect of lactic acid chain length on thermomechanical properties of star‐LA‐xylitol resins and jute reinforced biocomposites

Star‐shaped bio‐based resins were synthesized by direct condensation of lactic acid (LA) with xylitol followed by end‐functionalizing of branches by methacrylic anhydride with three different LA chain lengths (3, 5 and 7). The thermomechanical and structural properties of the resins were characterized by ¹³C NMR, Fourier transform IR spectroscopy, rheometry, DSC, dynamic mechanical analysis (DMA), TGA and flexural and tensile tests. An evaluation of the effect of chain length on the synthesized resins showed that the resin with five LAs exhibited the most favorable thermomechanical properties. Also, the resin's glass transition temperature (103 °C) was substantially higher than that of the thermoplast PLA (ca 55 °C). The resin had low viscosity at its processing temperature (80 °C). The compatibility of the resin with natural fibers was investigated for biocomposite manufacturing. Finally, composites were produced from the n5‐resin (80 wt% fiber content) using jute fiber. The thermomechanical and morphological properties of the biocomposites were compared with jute‐PLA composites and a hybrid composite made of the impregnated jute fibers with n5 resin and PLA. SEM and DMA showed that the n5‐jute composites had better mechanical properties than the other composites produced. Inexpensive monomers, good thermomechanical properties and good processability of the n5 resin make the resin comparable with commercial unsaturated polyester resins. © 2017 Society of Chemical Industry     

Effect of an alkalized‐modified halloysite on PLA crystallization,morphology, mechanical,and thermal properties of PLA/halloysite nanocomposites

Poly(lactic acid) (PLA)/alkalized halloysite nanotube (HNTa) nanocomposites were prepared by melt mixing. The morphology, crystallization behavior, mechanical properties, and thermal stability of the nanocomposites were investigated in comparison with those of the pristine PLA. HNTa can nucleate PLA, leading to a lower recrystallization temperature and higher crystallinity. Infrared spectra revealed that the hydroxyl groups of the PLA interacted with the external hydroxyl groups of HNTa nanofillers via hydrogen bonding. The thermal stability of the nanocomposites was improved with the addition of HNTa. The PLA/HNTa nanocomposites exhibited higher modulus and tensile strength than those of the PLA composites containing unmodified halloysite nanotubes (HNTs). The improvement in properties was probably due to a better dispersion of the HNTa in the PLA matrix compared to that of the unmodified HNTs. Therefore, the facile alkali treatment of HNTs offers a low cost nanofiller for the preparation of PLA based nanocomposites with high tensile modulus and tensile strength. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44272.     

Electromagnetic interference shielding properties of PEDOT/PSS–halloysite nanotube (HNTs) hybrid films

Poly(3,4‐ethylenedioxythiophene)/poly(4‐styrene sulfonate) (PEDOT/PSS) films hybridized with halloysite nanotubes (HNTs) were for the first time investigated for electromagnetic interference (EMI) shielding. The hybridization of the HNTs induced EMI properties for the pristine PEDOT/PSS films, and the content of the HNTs in the hybrid films significantly influenced the EMI properties of the hybrid films. The highest EMI shielding effectiveness of the hybrid film is ?16.3 dB in the measured frequency range from 2 to 13 GHz for the PEDOT/PSS film hybridized with 75% HNTs, using a sample with 4.5 mm thick. The contribution of EMI shielding effectiveness in the hybrid films is mainly due to dielectric loss rather than magnetic loss. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44242.     

Compatibilizing effect of halloysite nanotubes in polar–nonpolar hybrid system

This article explores the effect of halloysite nanotubes (HNTs) and modified HNTs (M‐HNTs) on the properties of immiscible blend system based on polar polyoxymethylene (POM) and nonpolar polypropylene (PP) polymers. HNTs have been modified by N‐(β‐aminoethyl)‐γ‐aminopropyltrimethoxysilane (APTMS). Modification is confirmed by Fourier transform infrared spectroscopy (FTIR), also FTIR confirms the interaction between polymer blend and HNTs/M‐HNTs. Morphology of the nanocomposites are demonstrated by scanning electron microscope (SEM) and dispersion of HNTs/M‐HNTs are observed by transmission electron microscope (TEM). In nanocomposites, average dispersed domain sizes reduce in the presence of HNTs/M‐HNTs but significant reduction has been observed in the case of M‐HNT‐filled nanocomposites rather than unmodified HNT‐filled nanocomposites. The M‐HNT acts as a reinforcing agent as well as bridging tool in polar–nonpolar hybrid system. Modification of HNTs brings compatibility in between the blend partners and reveals improved dynamic mechanical, thermal, and tensile properties than that of the pure blend system. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39587.     

Simultaneous improvement in strength,toughness, and thermal stability of epoxy/halloysite nanotubes composites by interfacial modification

This work investigated the effect of silane modification of halloysite nanotubes (HNTs) on the mechanical properties of epoxy/HNTs nanocomposites. Three kinds of silane coupling agents, including 3‐(2‐aminoethyl)‐aminopropyltrimethoxysilane (AEAPS), (3‐glycidyloxypropyl)‐trimethoxysilane (GPTMS), and octyltriethoxysilane (OTES), were employed. It was shown that the modified HNTs exhibited a better dispersion in the epoxy matrix compared with pristine one. Because of strong interfacial interaction between AEAPS modified HNTs and the epoxy matrix, the nanocomposites exhibited the highest glass transition temperature and modulus among all the samples. On the other hand, AEAPS and GPTMS modified HNTs/epoxy nanocomposites showed enhanced tensile strength and toughness. The toughing mechanisms were identified by the SEM micrographs of the fracture surfaces of the different kinds of samples. In this study, simultaneous enhancement of strength, toughness, and thermal stability of epoxy by the modified HNTs provides a novel approach to produce high‐performance thermosets. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43249.     

Effect of halloysite nanotubes on mechanical properties and flammability of soy protein based green composites

To address the growing emphasis on the use and development of sustainable materials, bio‐based polymers and fibers are processed to prepare entirely bio‐based fiber‐reinforced ‘green’ composites. To enable these new materials to perform in lightweight vehicle and infrastructural applications, they must be characterized both structurally and in terms of their various performance characteristics. The results of preparation and characterization of bio‐based composites comprising jute fabric and soy protein concentrate (SPC) modified with glycerol and/or halloysite nanotubes (HNT) are reported herein as a first look at the flammability of these bio‐based nanocomposites. The results reveal that SPC has lower flammability (heat release capacity) than petrochemical‐based resins, such as epoxies and vinyl esters. In addition, incorporating 5% mass fraction of HNT is found to reduce the composite flammability, while having no negative impact on the mechanical properties. Copyright © 2012 John Wiley & Sons, Ltd.     

Mechanical and thermal properties of SEBS‐g‐MA compatibilized halloysite nanotubes reinforced polyethylene terephthalate/polycarbonate/nanocomposites

In this study, the effect of maleic anhydride grafted styrene‐ethylene‐butylene‐styrene (SEBS‐g‐MA) content on mechanical, thermal, and morphological properties of polyethylene terephthalate/polycarbonate/halloysite nanotubes (PET/PC/HNTs) nanocomposites has been investigated. Nanocomposites of PET/PC (70 : 30) with 2 phr of HNTs were compounded using the counter rotating twin screw extruder. A series of formulations were prepared by adding 5–20 phr SEBS‐g‐MA to the composites. Incorporation of 5 phr SEBS‐g‐MA into the nanocomposites resulted in the highest tensile and flexural strength. Maximum improvement in the impact strength which is 245% was achieved at 10 phr SEBS‐g‐MA content. The elongation at break increased proportionately with the SEBS‐g‐MA content. However, the tensile and flexural moduli decreased with increasing SEBS‐g‐MA content. Scanning electron microscopy revealed a transition from a brittle fracture to ductile fracture morphology with increasing amount of SEBS‐g‐MA. Transmission electron microscopy showed that the addition of SEBS‐g‐MA into the nanocomposites promoted a better dispersion of HNTs in the matrix. A single glass transition temperature was observed from the differential scanning calorimetry test for compatibilized nanocomposites. Thermogravimetric analysis of PET/PC/HNTs nanocomposites showed high thermal stability at 15 phr SEBS‐g‐MA content. However, on further addition of SEBS‐g‐MA up to 20 phr, thermal stability of the nanocomposites decreased due to the excess amount of SEBS‐g‐MA. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42608.     

Highly dispersed polyamide‐11/halloysite nanocomposites: Thermal,rheological, optical,dielectric, and mechanical properties

Bio‐based polyamide 11 and natural halloysite nanotubes (HNTs) were used for the preparation of PA‐11/HNT nanocomposites with varying nanotubes concentrations by melt extrusion using a masterbatch dilution process. The prepared nanocomposites were analyzed for microstructural changes, transparency, thermal stability, rheological behavior, dielectric, and mechanical properties. The HNT nanotubes are well dispersed in PA‐11 matrix in the studied composition range as shown by microscopy and spectrophotometry. Interestingly, good halloysite dispersion in PA‐11 matrix increases the tensile strength and Young modulus of PA‐11 without sacrificing the ductility. Highly dispersed nanotubes also bring favorable changes in the thermal stability, dielectric, and rheological characteristics of PA‐11. Additionally, glass transition temperature, crystallization temperature, and degree of crystallinity of the nanocomposites tend to increase with increase in nanotubes loading. Thus, PA‐11 can become a tailor‐made material with multifunctional characteristics, thanks to the addition of HNTs. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Surface modification of halloysite nanotubes with l‐lactic acid: An effective route to high‐performance poly(l‐lactide) composites

To improve the interfacial bonding between halloysite nanotubes (HNTs) and poly(l ‐lactide) (PLLA), a simple surface modification of HNTs with l ‐lactic acid via direct condensation polymerization has been developed. Two modified HNTs were obtained: HNTs grafting with l ‐lactic acid (l‐HNTs) and HNTs grafting with poly(l ‐lactide) (p‐HNTs). The structures and properties of l‐HNTs and p‐HNTs were investigated. Then, a series of HNTs/PLLA, l‐HNTs/PLLA and p‐HNTs/PLLA composites were prepared using a solution casting method and were characterized by polarized optical microscopy (POM), field scanning electron microscopy, and tensile testing. Results showed that l ‐lactic acid and PLLA could be easily grafted onto the surface of HNTs by forming an Al carboxylate bond and following with condensation polymerization, and the amounts of the l ‐lactic acid and PLLA grafted on the surface of the HNTs were 5.08 and 14.47%, respectively. The surface‐grafted l ‐lactic acid and PLLA played the important role in improving the interfacial bonding between the nanotubes and matrix. The l‐HNTs and p‐HNTs can disperse more uniformly in and show better compatibility with the PLLA matrix than untreated HNTs. As a result, the l‐HNTs/PLLA and p‐HNTs/PLLA composites had better tensile properties than that of the HNTs/PLLA composites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41451.     

Mechanical and electrical multifunctional poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate)—multiwall carbon nanotube nanocomposites

In this work, nanocomposites of poly(hydroxybutyrate‐co‐hydroxyvalerate) PHBV and multiwalled carbon nanotubes (MWNT) were prepared by melt blending. Mechanical, thermal, morphological, and electrical properties of the prepared PHBV/MWNT nanocomposites were investigated. Differential scanning calorimetry (DSC) and X‐ray diffraction (XRD) results showed MWNT effectively enhanced the crystallization and nucleation of PHBV. Dynamic thermo‐mechanical and static uniaxial mechanical tensile and compressive properties were increased by the addition of MWNT. MWNT observed in the nanocomposites using transmission electron microscopy (TEM) showed dimensions similar to separated nanotubes inferring a good dispersion. The presence of nanotubes in close vicinity with each other formed an interconnecting network that led to the formation of electrically conductive nanocomposites. The electrical resistance of the nanocomposites was reduced with the addition of MWNT. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Surface‐modified halloysite nanotubes reinforced poly(lactic acid) for use in biodegradable coronary stents

Poly(lactic acid) (PLA) was reinforced halloysite nanotubes (HNTs) in this study. To improve dispersion and interfacial adhesion of HNTs within the PLA matrix, HNTs were surface modified with 3‐aminopropyltriethoxysilane (ASP) prior to compounding with PLA. PLA/ASP‐HNTs nanocomposites were characterized by differential scanning calorimetry (DSC), Fourier transfer infrared spectroscopy (FTIR), surface wettability, thermogravimetric analysis, transmission electron microscopy (TEM), and tensile testing. The hemocompatibility and cytocompatibility of PLA and PLA composites were investigated and the in vitro degradation process of PLA/ASP‐HNTs composites was investigated for a period of 6 months by gel permeation chromatography, FTIR, weight loss measurement, DSC, and tensile testing. PLA and all PLA composites were blood compatibile and non‐cytotoxic. TEM analysis revealed that HNTs agglomeration in PLA matrix was reduced by surface treatment with ASP. ASP‐HNTs had better reinforcing effect than unmodified HNTs evidenced by tensile testing. ASP‐HNTs appeared to increase the hydrolytic degradation process as measured by weight measurement. PLA/ASP‐HNTs composites displayed 12.1% weight loss and 30.6% average molecular weight reduction while retaining 74% of Young's modulus by the 24th week of degradation. Based on this data, the reinforcement of PLA using ASP‐HNTs may prove beneficial for applications such as biodegradable stents. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46521.     

Influence of the processing methods on the properties of poly(lactic acid)/halloysite nanocomposites

The influence of processing methods on the thermo‐mechanical properties of poly (lactic acid) (PLA) nanocomposites were investigated by preparing nanocomposites reinforced by halloysite nanotubes (HNTs) (from 0 to 10 [w/w%]) using solution casting (SC) and melt compounding (MC) methods. Statistical analysis revealed that the processing methods have a significant influence on the tensile properties, where nanocomposites prepared by MC have higher tensile properties compared to those by SC. Experimental results illustrated higher tensile strength and a drop in ductility under the higher strain rate as compared to the low strain rate for PLA/HNTs nanocomposites. At lower concentrations micrographs revealed that, HNTs dispersion was better for SC films as compared to MC, but more prominent HNTs aggregation at higher loadings. MC nanocomposites exhibited a high crystallinity as compared to SC, due to the recrystallization and nucleation effects. The thermal stability and activation energy increased with addition of HNTs, regardless of the processing methods. POLYM. COMPOS., 37:861–869, 2016. © 2014 Society of Plastics Engineers     

Poly[(3‐hydroxybutyrate)‐co‐(3‐hydroxyvalerate)]/layered double hydroxide nanocomposites

BACKGROUND: The thermomechanical performance of poly[(3‐hydroxybutyrate)‐co‐(3‐hydroxyvalerate)] (PHBV) is associated with its crystallization. Enhanced nucleation using a stearate‐functionalized synthetic layered double hydroxide (LDH) presents a potential solution. RESULTS: PHBV crystallization varied with concentration of LDH. At lower LDH concentration, thermal history‐induced cold crystallization was present. The extent of this order–disorder transition decreased with increasing LDH concentration and was completely eliminated at 7 wt% LDH. PHBV did not have a melt recrystallization peak but the introduction of LDH resulted in an increasingly pronounced melt recrystallization with increasing LDH concentration. Polarized optical microscopy coupled with differential scanning calorimetry and wide angle X‐ray diffraction (WAXD) analysis indicated increased lamella thickness in the nanocomposites compared to pure PHBV. WAXD and transmission electron microscopy showed that the nanocomposites had an intercalated but aggregated dispersion. CONCLUSION: The concentration of nanofiller provides unique effects in PHBV. Mechanical performance was found to scale with composition as determined using dynamic mechanical analysis and tensile testing. Copyright © 2008 Society of Chemical Industry     

Thermal,mechanical, and rheological properties of poly(ε‐caprolactone)/halloysite nanotube nanocomposites

Naturally available halloysite nanotubes (HNTs) with hollow nanotubular structures were used as reinforcement in poly(ε‐caprolactone) (PCL). The PCL/HNT nanocomposites were prepared by melt mixing the polymer with as‐received HNTs up to 10 wt % in an internal batch mixer. Transmission electron microscopy analysis indicated that the HNTs were dispersed uniformly on the nanoscale throughout the PCL matrix. Differential scanning calorimeter studies revealed that the PCL crystallinity was decreased in the nanocomposites, and the HNTs dispersed in the PCL matrix led to an increase in the non‐isothermal crystallization temperature of the PCL. Tensile and dynamic mechanical tests showed great enhancement in strength and stiffness at low HNT content, while still maintaining the ductility of the PCL. The glass transition temperature (T_g) of the pristine PCL was substantially increased with increase in filler loading, which indicates good reinforcing effect imparted by the addition of HNT. Melt rheological studies revealed that the nanocomposites exhibited strong shear thinning behavior, and a percolated network of HNT particles was formed. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Viscoelastic behavior and constitutive modeling of PP/HNT composites prepared by water‐assisted extrusion

Poly(propylene) (PP) nanocomposites containing 5, 10, and 15 wt% unmodified halloysite nanotubes (HNTs) were prepared using extrusion with and without water injection. Scanning electron microscopy micrographs show that HNT aggregates prepared by water injection are smaller than those prepared by conventional melt extrusion (without water injection). The nanocomposites prepared by water injection exhibit higher storage modulus (G′) and complex viscosity (η*) values than those by conventional melt extrusion. Stress relaxation results indicate that the interaction between HNTs and PP matrix at low concentration (5 wt%) is stronger than its non‐water injection counterpart. Subsequently, for 5 wt% HNT sample, the transient viscosity is simulated numerically using the Kaye–Bernstein–Kearsley–Zapas (K‐BKZ) integral constitutive equation along with experimentally determined damping functions. It is found that the samples prepared by water injection exhibit a more obvious overshoot behavior than conventional samples and the Papanastasiou‐Scriven‐Macosko (PSM) model can predict the transient viscosity of the samples more accurately than Wagner model. Further, the relationship between the dispersion of HNTs and the damping factors in the constitutive models is discussed. The results of this investigation would improve the theoretical understanding of possible polymer–filler interaction during shear flow. POLYM. ENG. SCI., 59:1585–1592 2019. © 2019 Society of Plastics Engineers     

Synthesis of poly(AA‐co‐AM) superabsorbent composites by reinforcement of halloysite nanotubes

A novel poly(acrylic acid‐co‐acrylamide)/halloysite nanotubes [PAA‐AM/HNTs] superabsorbent composite was synthesized by free radical polymerization with using HNTs as an inorganic additive. The composite was characterized by Fourier transform infrared spectroscopy, scanning electron microscope, and thermogravimetric analysis. The results revealed that HNTs and PAA‐AM were combined well together to form a porous structure with a pore size of about 10 μm, and HNTs were uniformly distributed in the composite. The thermal stability was improved by adding HNTs in the composite. The influences of contents of initiator and halloysite, neutralization degree of AA, and molar ratio of AM to AA on water absorbency were investigated. The water absorbency and the water retention capacity were improved after adding HNTs into PAA‐AM. The composite containing 10% HNTs had the highest water absorbency of 1276 g/g in distilled water. Moreover, PAA‐AM/HNTs composite also had a high swelling rate within 60 min and could maintain 78% initial swelling capability after five reswelled test. The substantial enhancement of swelling properties enables PAA‐AM/HNTs suitable for numerous practical applications. POLYM. COMPOS., 36:229–236, 2015. © 2014 Society of Plastics Engineers     

The morphology and degradation behavior of electrospun poly(3‐hydroxybutyrate)/Magnetite and poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate)/Magnetite composites

Electrospinning of biodegradable poly(3‐hydroxybutyrate) (PHB)/magnetite and poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV)/magnetite composites in 2,2,2‐trifluoroethanol (TFE) and chloroform are investigated to develop nonwoven nanofibrous structure. Ultrafine PHB/magnetite fibers are obtained and the resulting fiber diameters are in the range of 690–710 nm and 8.0–8.4 µm for the polymer dissolved in TFE and chloroform. The surface of PHB composites fiber fabricated in chloroform contains porous structures, which are not observed for the sample of PHB composites fiber dissolved in TFE. The fiber diameters for PHBV5/magnetite composites are in the range of 500–540 nm and 2.3–2.5 µm, depending on the use of TFE and chloroform. The average diameters of PHBV5/magnetite composite fibers are smaller than those of PHB/magnetite composites fiber. All electrospun PHB/magnetite and composite fibers are superparamagnetic. The degradation behaviors of PHB/magnetite and PHBV5/magnetite composite fibers were investigated using Caldimonas manganoxidans. For the fabricated composite fibers, it is found that the degradation rate increased with the increasing loading of magnetite nanoparticles. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41070.     

Crystallization and mechanical behavior of covalent functionalized carbon nanotube/poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) nanocomposites

To improve the dispersity of multi‐walled carbon nanotubes (MWCNTs) in poly(3‐hydroxybutyrate‐co?3‐hydroxyvalerate) (PHBV) matrix, MWCNTs functionalized with carboxyl groups, hydroxyl groups, and atactic poly (3‐hydroxybutyrate) (ataPHB) through acid oxidation, esterification reaction, and “grafting from” method, respectively, were used to fabricate nanofiller/PHBV nanocomposites. The crystallization behavior, dispersion of MWCNTs before and after functionalization in PHBV matrices, and mechanical properties of a series of nanocomposites were investigated. The differential scanning calorimetry, wide‐angle X‐ray diffraction, and polarized optical microscope results suggested that the four types of MWCNTs acted as effective heterogeneous nucleation agents, inducing an increase in the crystallization rate, crystallinity, and crystallite size. Scanning electron microscope observations demonstrated that functionalized MWCNTs showed improved dispersion comparing with MWCNTs, suggesting an enhanced interfacial interaction between PHBV and functionalized MWCNTs. Consequently, the mechanical properties of the functionalized MWCNTs/PHBV nanocomposites have been improved as evident from dynamic mechanical and static tensile tests. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42136.     

Hemocompatibility of electrospun halloysite nanotube‐ and carbon nanotube‐doped composite poly(lactic‐co‐glycolic acid) nanofibers

One of the major problems of nanofiber scaffold or other devices like cardiovascular or blood‐contacting medical devices is their weak mechanical properties and the lack of hemocompatibility of their surfaces. In this study, halloysite nanotubes (HNTs) and carbon nanotubes (CNTs) were incorporated within poly(lactic‐co‐glycolic acid) (PLGA) nanofibers and the mechanical property and hemocompatibility of both types of composite nanofibers with different doping levels were thoroughly investigated. The morphology and internal distribution of the doped nanotubes within the nanofibers were characterized using scanning electron microscopy and transmission electron microscopy. Mechanical properties of the electrospun nanofibers were tested using a material testing machine. The hemocompatibility of the composite nanofibers was examined through hemolytic and anticoagulant assay, respectively. We show that the doped HNTs or CNTs are distributed in the nanofibers with a coaxial manner and the incorporation of HNTs or CNTs does not significantly change the morphology of the PLGA nanofibers. Importantly, the incorporation of HNTs or CNTs within PLGA nanofibers significantly improves the mechanical property of PLGA nanofibers, and PLGA nanofibers with or without doping of the HNTs and CNTs display good anticoagulant property and negligible hemolytic effect to human red blood cells. With the enhanced mechanical property, great hemocompatibility, and previously demonstrated biocompatibility of both HNTs‐ and CNTs‐doped composite PLGA nanofibers, these composite nanofibers may be used as therapeutic artificial tissue/organ substitutes for tissue engineering applications. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013