Interplay between physicochemical and mechanical properties of poly(ethylene terephthalate) meshes for hernia repair

Non‐medical‐grade industrial nets are often implemented in developing countries as affordable alternative to surgical meshes for hernia repair. Even if there is clear evidence about their repairing reliability, their physicochemical and mechanical properties have been not fully investigated. This works compares three industrial nets with different textile patterns, and a surgical mesh of the same polymer. Nets are autoclave‐sterilized and characterized through scanning electron microscope, Raman spectroscopy, thermogravimetric analysis , differential scanning calorimetry, and uniaxial tensile tests. Spectral and thermal analyses reveal that all samples are based on poly(ethylene terephthalate). Differences are found in phase conformations with modifications in amorphous, ordered amorphous, and crystalline domains. Changes in material characteristics do not affect mechanical properties, which are mainly ascribable to the textile pattern. Industrial nets show a stiffening behavior different from the almost linear anisotropic response of surgical mesh. However, non‐medical‐grade nets could be potentially applied for surgeries once their biocompatibility and in vivo stability have been evaluated. Non‐medical‐grade industrial nets are used as low‐cost alternative to surgical meshes for hernia repair in less developed countries. Nets sterilization modifies their phase conformation, due to the interaction with water, but do not affect mechanical properties. Even tough industrial nets show a different stiffening behavior, physicochemical characterization confirms a similarity to standard surgical meshes. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46014.     

Preparation and characterization of multi‐walled carbon nanotube/poly(ethylene terephthalate) nanoweb

Multi‐walled carbon nanotube (MWCNT)/Poly(ethylene terephthalate) (PET) nanowebs were obtained by electrospinning. For uniform dispersion of MWCNTs in PET solution, MWCNTs were functionalized by acid treatment. Introduction of carboxyl groups onto the surface of MWCNTs was examined by Fourier transform infrared (FTIR) spectroscopy and X‐ray diffraction (XRD) analysis. MWCNTs were added into 22 wt % PET solution in the ratio of 1, 2, 3 wt % to PET. The morphology of MWCNT/PET nanoweb was observed using field emission‐scanning electron microscopy (FE‐SEM) and transmission electron microscopy (TEM). The nanofiber diameter decreased with increasing MWCNT concentration. The distribution of the nanofiber diameters showed a bi‐modal shape when MWCNTs were added. Thermal and tensile properties of electrospun MWCNT/PET nanowebs were examined using a differential scanning calorimeter (DSC), thermogravimetric analyzer (TGA), dynamic mechanical analyzer (DMA) and etc. Tensile strength, tensile modulus, thermal stability, and the degree of crystallinity increased with increasing MWCNT concentration. In contrast, elongation at break and cold crystallization temperature showed a contrary tendency. Electric conductivities of the MWCNT/PET nanowebs were in the electrostatic dissipation range. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Efficient method for recycling poly(ethylene terephthalate) to poly(butylene terephthalate) using transesterification reaction

A method of recycling postconsumer poly(ethylene terephthalate (PET) using transesterification was studied. Shredded flakes of postconsumer PET waste were transesterified with higher diols, such as 1,4‐butanediol, 1,4‐cyclohexane dimethanol, and 1,6‐hexanediol, to yield copolyesters in the presence of Ti(iPrO)₄ and Sb₂O₃ as catalysts. The extent of the formation of undesirable tetrahydrofuran side products was dependent on the molar ratio of PET to1,4‐butanediol and the time of reflux during transesterification. Quantitative insertion of the butylene moiety into PET could be achieved under appropriate reaction conditions. The mechanical properties of PBT obtained by a transesterification reaction of PET with 1,4‐butanediol were comparable to those of virgin PBT (obtained by direct reaction of dimethyl terephathalate with 1,4‐butanediol). © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3720–3729, 2004     

Research on synthesis and thermal properties of poly(ethylene terephthalate) sulfonate group containing ionomer

In order to solve the poor nucleation ability and slow crystallization rate of polyethylene terephthalate (PET), we propose a new strategy to prepare PET with self-nucleation ability based on the mechanism of mutual attraction of ions. In this study, a hydroxyl-terminated sulfonate monomer, sulfonated 1,4-butanediol (SBDO) without rigid structure was synthesized as nucleating agent functionalized PET third monomer, and then PET ionomers (PETi) were prepared through melt polycondensation with different contents of SBDO. The half-crystallization time of PETi was sharply decreased in contrast with pure PET and the crystallization temperature was significantly increased from 182.6°C to 210.8°C for PETi1. Due to the high nucleation efficiency of SBDO, the crystallization temperature of PET was significantly increased, avoiding the excessive addition of traditional nucleating agents to deteriorate the mechanical properties of PET. The increased nucleation efficiency was contributed to the aggregation of SBDO induced by the ionic interactions.     

Interface adjustment between poly(ethylene terephthalate) and graphene oxide in order to enhance mechanical and thermal properties of nanocomposites

There is great interest in the use of graphene and derivatives in the production of polymer nanocomposites as it provides improvements in the properties of the materials to which they are associated. Such improvements depend heavily on filler dispersion and the interaction between the nanomaterials and the matrix. This work aimed to study the compatibility of graphene oxide (GO) with a poly(ethylene terephthalate) matrix. For this, graphite was modified using Hummers method, using reaction times of 3 and 6 h. The obtained GO was functionalized with amine, amide, and magnetite groups (FGO). The effects of the oxidation degree, functionalization and concentration of the nanofillers on the dispersion and consequently on the properties of the polymer nanocomposites were evaluated. The nanocomposites were synthesized by the solid–solid deposition method followed by the melt mixing technique. It was observed that lower concentrations of nanofiller associated with the lower degree of oxidation and functionalization improved the interaction of the nanofillers with the matrix, which resulted in better mechanical properties under tensile stresses for strain at break, maximum stress, Young's modulus and toughness. It was also observed that the glass transition and crystallization of nanocomposites increased due to a nucleating effect of the nanofillers.     

Ageing of poly(ethylene terephthalate) and poly(ethylene naphthalate) under moderately accelerated conditions

PEN is thought to have increased thermal and hydrolytic resistance in comparison to PET. However, due to a lack of research, few studies have been published on the degradation of PEN. In our research, we report on the extent of degradation in PET and PEN after ageing under contrasting environments (dry nitrogen, dry air, wet nitrogen, and wet air) at temperatures between 140°C and 190°C. A combination of analysis techniques were employed in order to characterize and track the physical and chemical changes in the aged polyester samples, enabling the effects of temperature, water, and oxygen to be mapped onto the resultant property changes of PET and PEN. The extent of degradation has been shown to differ between both polymers and the dominant degradation mechanism in PET was shown to differ with ageing temperature. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Development of active barrier systems for poly(ethylene terephthalate)

Copolymers of Poly(ethylene terephthalate) (PET) were synthesized by the melt polymerization of terephthalic acid (TPA) with ethylene glycol (EG) and with each of the active oxygen scavengers; monoolein (MO) and 3‐cyclohexene‐1,1‐dimethanol (CHEDM) in separate compositions. Proton nuclear magnetic resonance spectroscopy (¹H NMR) and 2D correlation spectroscopy (COSY) indicated that PET had reacted with both MO and CHEDM at their hydroxyl end groups. Oxygen barrier properties of the MO and CHEDM copolymers exhibited improvements of up to 40%, in comparison to an unmodified commercial PET. Effects of the oxygen scavengers on the copolymers' physical properties were investigated in terms of their crystallization, melting, and rheological behaviors. Both types of copolymers showed decreases in peak melting temperatures with increased scavenger concentrations and also crystallized more slowly as the scavenger concentrations increased. The PET/MO copolymer showed non‐Newtonian rheological behavior with higher MO concentration; while the PET/CHEDM copolymers showed Newtonian behavior within the studied range of CHEDM concentrations. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Prediction of mechanical properties of poly(ethylene terephthalate) using infrared spectroscopy and multivariate calibration

This work describes a method to determine mechanical properties (tensile strength at break and tensile modulus) of poly(ethylene terephthalate) using median infrared spectroscopy and multivariate calibration. Infrared spectroscopy is very promising for polymer process control and final product analysis because it is rapid and nondestructive. The spectra of the films were obtained using two techniques: attenuated total reflection and direct transmission. The spectra were subjected to various preprocessing procedures, such as smoothing and derivative using the algorithm Savitzy‐Golay, standard normal variate, multiplicative scatter correction and, as well, combinations of some of these preprocessing techniques. The predictive ability of the regression models were evaluated using an external validation set. The regression techniques used, partial least square and multiple linear regression, showed, in general, comparable results with root mean square error of prediction similar to the repeatability of the conventional method used to determine these mechanical properties (1.3 kgf/mm² for tensile strength at break and 29.6 kgf/mm² for tensile modulus). © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Thermomechanical and creep properties of poly(ethylene terephthalate) fibers crosslinked with disulfonyl azides

The thermomechanical and creep properties of poly(ethylene terephthalate) fibers crosslinked with 1,6‐hexanedisulfonyl azide, 1,3‐benzenedisulfonyl azide, and 2,6‐naphthalenedisulfonyl azide were investigated. Significant improvements in these properties were observed between the standard fibers and those produced by crosslinking. Cyclic loading studies highlighted minor differences not detectable by normal thermomechanical analysis. The creep at room temperature could be reduced to about one‐third of the normal values observed in the untreated fiber. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1556–1562, 2003     

Morphology and thermal and mechanical properties of phosphonium vermiculite filled poly(ethylene terephthalate) composites

A series of poly(ethylene terephthalate) (PET)/phosphonium vermiculite (P‐VMT) composites were prepared by a melt‐blending method, and we investigated the morphology and thermal and mechanical properties of the composites. We prepared P‐VMT with quaternary phosphonium salts using the common method followed by a cation‐exchange reaction. X‐ray diffraction showed that the phosphonium surfactants were partially intercalated into the vermiculite layers, The d‐spacing of the PET–clay sample was somewhat less than that of the P‐VMT because some degradation of the surfactant took place during melt processing. Compared with PET, the PET–clay composites had a lower decomposition temperature and showed a 17.4% increase in the tensile strength with a P‐VMT content of 3 wt %. Scanning electron microscopy and transmission electron microscopy demonstrated that P‐VMT had a homogeneous dispersion and good compatibility in the polymer matrix with a low content of additive and indicated that the P‐VMT content of 3 wt % was optimal. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Preparation and characterization of magnetic nanofibers with iron oxide nanoparticles and poly(ethylene terephthalate)

Iron oxide nanoparticle/Poly(ethylene terephthalate) (PET) nanowebs were obtained by electrospinning. To achieve superparamagnetic properties, iron oxide nanoparticles with diameters below 25 nm were used. Diameter distribution of iron oxide nanoparticles was measured by a particle size analyzer. Iron oxide nanoparticles were added into 16 wt % PET solution in the ratio of 5, 10, and 15 wt % to PET. The morphology of iron oxide nanoparticle/PET nanowebs was observed using field emission-scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). The nanofiber diameter increased as increasing iron oxide nanoparticle concentration. The superparamagnetic behavior of iron oxide nanoparticle/PET nanofiber was confirmed using superconducting quantum interference device (SQUID). The degree of crystallinity of iron oxide nanoparticle/PET nanowebs was calculated from a differential scanning calorimeter (DSC) results. The change of flexural rigidity and tensile properties of electrospun iron oxide nanoparticle/PET nanowebs with the external magnetic field were examined ISO 9073-7 testing method, universal testing machine and an appropriate magnet. Also, the elastic modulus of iron oxide nanoparticle/PET nanofiber was measured using nanoindentation. With applying magnetic field, the improvement in mechanical properties of field-responsive magnetic nanofibers and nanowebs was confirmed. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Preparation and properties of poly(ethylene terephthalate)/inorganic whiskers composites

To improve the crystallization and mechanical properties of poly(ethylene terephthalate) (PET), in this work, PET/SiO₂‐MgO‐CaO whiskers composites were prepared via in situ polymerization. The morphology, crystallization, and mechanical properties of the prepared composites were investigated. It was found that inorganic whiskers could be easily dispersed in PET matrix, as demonstrated by SEM and PLM. DSC and PLM observation indicated a strong nucleation capability of inorganic whiskers for PET. Mechanical analysis results showed that the glass transition temperature, tensile strength, and modulus of the composites were greatly improved. A possible chemical bonding between PET chains and the surface of whiskers was observed by FTIR, TGA, and sedimentation experiment. It could be the main reason for the good dispersion and improved properties of the prepared composites. This work is important for the application of PET due to the low cost but high reinforcing efficiency of this inorganic whisker. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Synthesis and characterization of poly(ethylene isophthalate‐co‐ethylene terephthalate) copolyesters

Poly(ethylene isophthalate‐co‐ethylene terephthalate) (PEIPET) copolymers of various compositions and molecular weights were synthesized by melt polycondensation and characterized in terms of chemical structure and thermal and rheological properties. At room temperature, all copolymers were amorphous and thermally stable up to about 400°C. The main effect of copolymerization was a monotonic increase of glass transition temperature (T_g) as the content of ethylene terephthalate units increased. The Fox equation accurately describes the T_g–composition data. The presence of ethylene terephthalate units was found to influence rheological behavior in the melt, with the Newtonian viscosity increasing as the content of ethylene terephthalate units increased. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 186–193, 2004     

Mechanical properties and microstructure of poly(ethylene terephthalate) microfiber prepared by carbon dioxide laser heating

We determined that a poly(ethylene terephthalate) microfiber was easily obtained by irradiating a carbon dioxide laser to an annealed fiber. The annealed fiber was prepared by zone drawing and zone annealing. First, an original fiber was zone drawn at a drawing temperature of 90°C under an applied tension of 4.9 MPa, and the zone‐drawn fiber was subsequently zone annealed at 150°C under 50.9 MPa. The zone‐annealed fiber had a degree of crystallinity of 48%, a birefringence of 218.9 × 10^?3, tensile modulus of 18.8 GPa, and tensile strength of 0.88 GPa. The microfiber prepared by laser heating the zone‐annealed fiber had a diameter of 1.5 μm, birefringence of 172.8 × 10^?3, tensile modulus of 17.6 GPa, and tensile strength of 1.01 GPa. The draw ratio estimated from the diameter was 9165 times; such a high draw ratio has thus far not been achievable by any conventional drawing method. Microfibers may be made more easily by laser heating than by conventional technologies such as conjugate spinning. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1955–1958, 2003     

Thermal properties of poly(ethylene terephthalate) recovered from municipal solid waste by steam autoclaving

The steam autoclaving of municipal solid waste followed by size separation was shown to be a way to recover virtually 100% of recyclable poly(ethylene terephthalate) (PET); this is a yield not attainable by a typical material recovery facility. The polymer properties of the recovered PET, which had undergone various degrees of thermal processing, were evaluated by thermogravimetric analysis, differential scanning calorimetry, gel permeation chromatography, viscometry, and solid‐state NMR to assess the commercial viability of polymer reuse. The weight‐average molecular weight (M_w) decreased as a result of autoclaving from 61,700 g/mol for postconsumer poly(ethylene terephthalate) (pcPET) to 59,700 g/mol for autoclaved postconsumer poly(ethylene terephthalate) [(apcPET)]. M_w for the reclaimed poly(ethylene terephthalate) (rPET) was slightly lower, at 57,400 g/mol. The melting temperature increased with two heat cycles from 236°C for the heat‐crystallized virgin poly(ethylene terephthalate) (vPET) pellets to 248°C for apcPET and up to 253°C for rPET. Correspondingly, the cold crystallization temperature decreased with increased processing from 134°C for vPET to 120°C for apcPET. The intrinsic viscosity varied from 0.773 dL/g for the vPET to 0.709 dL/g for rPET. Extruded samples were created to assess the potential commercial applications of the recovered rPET samples. The M_w values of the extruded apcPET and rPET samples dropped to 37,000 and 34,000 g/mol, respectively, after extrusion (three heat cycles); this indicated that exposure to heat dictated that these materials would be better suited for downcycled products, such as fibers and injected‐molded products. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2012     

Linear thermoelastic characterization of anisotropic poly(ethylene terephthalate) films

All nine independent elastic constants have been determined for a biaxially stretched poly(ethylene terephthalate) (PET) film using novel mechanical methods. The orthotropic directions and the in‐plane Poisson's ratios were first characterized using vibrational holographic interferometry of tensioned membrane samples. The out‐of‐plane Poisson's ratio was obtained by measuring the change in tension with the change in pressure for constant strain conditions. Pressure–volume–temperature (PVT) equipment was used to measure the bulk compressibility as well as the volumetric thermal expansion coefficient (TEC). The in‐plane Young's moduli were obtained by tensile tests, while the out‐of‐plane modulus was calculated from the compressibility and other elastic constants that describe the in‐plane behavior. The in‐plane TECs in the machine and transverse directions were determined using a thermal mechanical analyzer (TMA). The out‐of‐plane TEC was determined using these values and the volumetric TEC determined via PVT. The resulting compliance matrix satisfies all of the requirements of a positive‐definite energy criterion. The procedure of characterization utilized in this article can be applied to any orthotropic film. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2937–2947, 2002     

Preparation and characterization of thermally stable phosphonium organoclays and their use in poly(ethylene terephthalate) nanocomposites

Purification of montmorillonite rich bentonite followed by surface modification using organic salts was performed. The bentonite was purified by sedimentation and then surface modified by ion exchange using alkyl‐ and aryl‐based phosphonium salts. The thermal stability, morphology, melt flow, and mechanical properties of the poly(ethylene terephthalate) (PET) nanocomposites prepared with these organoclays were studied with and without using a reactive elastomeric compatibilizer. TEM results showed that the alkyl based organoclay exhibited better dispersion and thus, higher tensile strength and elongation at break in the PET/organoclay/elastomer ternary nanocomposites than the aryl‐based organoclay did. The notched Charpy impact strength of PET increased from 2.9 to 4.7 kJ m^?2 and 3.4 kJ m^?2 for alkyl and aryl phosphonium organoclay‐based ternary nanocomposites, respectively. Upon compounding PET with alkyl and aryl phosphonium organoclays, the onset decomposition temperature of PET increased from 413°C to 420°C and 424°C, respectively. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effect of trisilanolphenyl‐POSS on rheological,mechanical, and flame‐retardant properties of poly(ethylene terephthalate)/cyclotriphosphazene systems

Poly(ethylene terephthalate) (PET) chips were coated by trisilanolphenyl–polyhedral oligomeric silsesquioxane (T‐POSS) and hexakis (para‐allyloxyphenoxy) cyclotriphosphazene (PACP) using the predispersed solution method, and PET/PACP/T‐POSS hybrids were further prepared by the melt‐blending method. The influence of T‐POSS on the rheological, thermal, and mechanical properties and flame retardancy of PET/PACP composites were discussed. The results suggest that T‐POSS was homogeneously dispersed in the PET matrix, which reduced the negative effects on polymer rheology and mechanical properties. For the PET/4%PACP/1%T‐POSS sample, the tensile strength at break and T_g increased from 29.67 MPa and 81.7 °C (PET/5%PACP) to 34.8 MPa and 85.8 °C, respectively, but the sample also self‐extinguished within 2 s, and the heat release capacity was reduced by 27.9% in comparison with that of neat PET.© 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45912.     

Thermal and mechanical properties of poly(butylene terephthalate)/epoxy blends

In this study, melt blends of poly(butylene terephthalate) (PBT) with epoxy resin were characterized by dynamic mechanical analysis, differential scanning calorimetry, tensile testing, Fourier transform infrared spectroscopy, and wide‐angle X‐ray diffraction. The results indicate that the presence of epoxy resin influenced either the mechanical properties of the PBT/epoxy blends or the crystallization of PBT. The epoxy resin was completely miscible with the PBT matrix. This was beneficial to the improvement of the impact performance of the PBT/epoxy blends. The modification of the PBT/epoxy blends were achieved at epoxy resin contents from 1 to 7%. The maximum increase of the notched Izod impact strength (≈ 20%) of the PBT/epoxy blends was obtained at 1 wt % epoxy resin content. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Sequence analysis and fiber properties of a blend of poly(ethylene terephthalate) and poly(ethylene terephthalate‐co‐4,4′‐bibenzoate)

Blends of poly(ethylene terephthalate) (PET) and poly(ethylene terephthalate‐co‐4,4′‐ bibenzoate) (PETBB) are prepared by coextrusion. Analysis by ¹³C‐NMR spectroscopy shows that little transesterification occurs during the blending process. Additional heat treatment of the blend leads to more transesterification and a corresponding increase in the degree of randomness, R. Analysis by differential scanning calorimetry shows that the as‐extruded blend is semicrystalline, unlike PETBB15, a random copolymer with the same composition as the non‐ random blend. Additional heat treatment of the blend leads to a decrease in the melting point, T_m, and an increase in glass transition temperature, T_g. The T_m and T_g of the blend reach minimum and maximum values, respectively, after 15 min at 270°C, at which point the blend has not been fully randomized. The blend has a lower crystallization rate than PET and PETBB55 (a copolymer containing 55 mol % bibenzoate). The PET/PETBB55 (70/30 w/w) blend shows a secondary endothermic peak at 15°C above an isothermal crystallization temperature. The secondary peak was confirmed to be the melting of small and/or imperfect crystals resulting from secondary crystallization. The blend exhibits the crystal structure of PET. Tensile properties of the fibers prepared from the blend are comparable to those of PET fiber, whereas PETBB55 fibers display higher performance. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1793–1803, 2004