SiO2-kaolinite affecting the surface properties of ternary poly(vinyl chloride)/silica/kaolinite nanocomposites

The products from the dispersion of nanoscale particulates such as the layered clays or the spherical inorganic minerals within the polymeric matrices are called polymeric nanocomposites. In this paper, we prepared poly(vinyl chloride) (PVC) based nanocomposites containing SiO₂-kaolinite by melt compounding. The influence of SiO₂-kaolinite on the surface properties of PVC was investigated by the use of various surface analysis techniques including a ttenuated total reflectance spectroscopy (ATR), wide angle X-ray diffractometry (WAXD), atomic force microscopy (AFM), scanning electron microscopy (SEM), electron dispersive X-ray spectrometer (EDX), contact angle measurement (CAM), and reflectance spectroscopy (RS). ATR spectroscopy showed possible interaction between layered kaolinite and PVC at surface. Microscopic methods illustrated an increased surface roughness compared to the pure PVC. Contact angle measurements of the resultant PVC nanocomposites demonstrated that the wettability of substrates depends on the surface interactions between kaolinite layers and PVC matrix. Optical properties of nanocomposite films were finally measured by the aid of reflectance spectrophotometer. It can be seen from optical studies that reflectance values were increased after incorporation of SiO₂-kaolinite in nanocomposite.     

Enhanced mechanical and thermal properties of hybrid graphene nanoplatelets/multiwall carbon nanotubes reinforced polyethylene terephthalate nanocomposites

The effects of graphene nanoplatelets (GNP) and multiwall carbon nanotube (MWCNT) hybrid nanofillers on the mechanical and thermal properties of reinforced polyethylene terephthalate (PET) have been investigated. The nanocomposites were melt blended using the counter rotating twin screw extruder followed by injection molding. Their morphology, mechanical and thermal properties were characterized. Combination of the two nanofillers in composites formulation supplemented each other which resulted in the overall improvement in adhesion between fillers and matrix. The mechanical properties and thermal stability of the hybrid nanocomposites (PET/GNP1.5/MWCNT1.5) were significantly improved compared to PET/GNP3 and PET/MWCNT3 single filer nanocomposites. However, it was observed that GNP was better in improving the mechanical properties but MWCNT resulted in higher thermal stability of Nanocomposite. The transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM) revealed uniform dispersion of the hybrid fillers in PET/GNP1.5/MWCNT1.5 nanocomposites while agglomeration was observed at higher filler content. The MWCNT prevented the phenomenal stacking of the GNPs by forming a bridge between adjacent GNP planes resulting in higher dispersion of fillers. This complimentary geometrical structure is responsible for the significant improvement in the thermal stability and mechanical properties of the hybrid nanocomposites.     

Morphological, optical and electromagnetic characterization of polybutylene terephthalate/silica nanocomposites

Polybutylene terephthalate (PBT) composites containing 1 %, 3 % and 5 % silica nanoparticles were prepared by melt compounding method. The characteristics of the nanocomposites were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA), tensile strength test (TST), reflectance spectroscopy (RS), electromagnetic transition test (ETT) and atomic force microscopy (AFM). XRD method showed successful incorporation of silica into the polymer matrix. SEM and AFM results showed the presence of silica aggregates on the surface of PBT sheets. Thermal analysis results demonstrated some changes in crystallinity of PBT after addition of silica. The PBT/silica nanocomposites were found to have higher electromagnetic reflection compared with the pure PBT. Silica nanoparticle is thus suggested as a good candidate for electromagnetic shielding purposes.     

Assessing the relationship among fabric constructional parameters, fractional reflectances and cover factors of polyester fabrics by experimental and mathematical methods

This paper focuses on the assessment of the relation among constructional properties, fractional reflectances and cover factors of fabrics woven from polyester yarns. A novel equation for the calculation of the relation between fractional reflectance and fabric cover factor was proposed and the usage of the equation was assessed by reflectance measurements. 48 polyester fabrics having different constructional parameters were used and the fabrics differed from each other by their cover factors. The warp yarn type and count, warp density and warp yarn twist were the same but weft yarn count, weft yarn fiber count and weft density were different for the fabrics in the experimental sub-groups. The reflectance measurements were conducted on the pretreated but undyed fabric samples as well as on the individual yarn systems of the same fabrics. Fabrics with the same cover factors exhibited different fractional reflectances. Reflectances were found to be dependent on the cover factor as well as on yarn fiber fineness, yarn count, yarn density and fabric weave. The changes in crimp of the yarns according to different construction parameters also governed the changes in fractional reflectances of fabric surfaces. The proposed equation was tested according to different fabric construction parameters and it was concluded that fiber fineness and weave pattern were among the most important parameters which govern the total light reflectances from the fabric surfaces, although they are not incorporated in the calculation of the fabric cover factors. The proposed equation was used to explain the effects of these components on the reflectance behavior of the fabric surfaces and on fabric cover.     

Thermal and mechanical properties of modified CaCO3 filled poly (ethylene terephthalate) nanocomposites

Poly(ethylene terephthalate) (PET)/CaCO₃ and PET/modified-CaCO₃ (m-CaCO₃) nanocomposites were prepared by melt blending. The morphology indicated that m-CaCO₃ produced by reacting sodium oxalate and calcium chloride, was well dispersed in PET matrix and showed good interfacial interaction with PET compared to CaCO₃. No significant differences in the thermal properties such as, glass transition, melting and degradation temperatures, of the nanocomposites were observed. The thermal shrinkage of PET at 120 °C was 10.8 %, while those of PET/CaCO₃ and PET/m-CaCO₃ nanocomposites were 2.9–5.2 % and 1.2–2.8 %, respectively depending on filler content. The tensile strength of PET/CaCO₃ nanocomposite decreased with CaCO₃ loading, whereas that of PET/m-CaCO₃ nanocomposites at 0.5 wt% loading showed a 17 % improvement as compared to neat PET. The storage modulus at 120 °C increased from 1660 MPa for PET to 2350 MPa for PET/CaCO₃ nanocomposite at 3 wt% loading, and 3230 MPa for PET/m-CaCO₃ nanocomposite at 1 wt% loading.     

Preparation of new polymer nanocomposites based on poly(lactic acid)/fatty nitrogen compounds modified clay by a solution casting process

In this study, different organoclays (OMMTs) were prepared using various fatty nitrogen compounds (FNCs) and natural clay, sodium montmorillonite (MMT). The clay modification was carried out by stirring the clay particles in an aqueous solution of fatty amides (FA), fatty hydroxamic acids (FHA), and carbonyl difatty amides (CDFA). These OMMTs were then used for nanocomposites production to improve the property balance of poly(lactic acid) (PLA) by solution casting process. All sets of OMMTs and nanocomposites were characterized using various apparatuses. In the nanocomposites, where the clay surface is pretreated with FA, FHA and CDFA, the basal spacing of the clay increased to 2.94, 3.26 and 3.80 nm, respectively The X-ray diffraction (XRD) and transmission electron microscopy (TEM) results confirmed the production of nanocomposites. PLA modified clay nanocomposites show higher thermal stability and significant improvement of mechanical properties in comparison with pure PLA.     

Surface modification of polyester fibers by thermal reduction with silver carbamate complexes

In this study, the surface of polyester fiber was modified by means of thermal treatment with a silver carbamate complex. We used scanning electron microscopy (SEM), an X-ray diffraction technique (XRD), and X-ray photoelectron spectroscopy (XPS) to allow a detailed characterization of the silver-coated polyethylene terephthalate (PET) fibers. The results revealed remarkable changes in the surface morphology and microstructure of the silver film after thermal reduction. On SEM, the silver nanoparticles (AgNPs) were seen to be uniformly and densely deposited on the fiber surface. The XRD pattern of the silver-coated fiber indicated that the film has a crystalline structure. A continuous layer of AgNPs, between 30 and 100 nm in size, was assembled on the PET fibers. The PET/Ag composite was found to impart high conductivity to the fibers, with an electrical resistivity as low as 0.12 kΩ·cm.     

New biopolymer nanocomposites based on epoxidized soybean oil plasticized poly(lactic acid)/fatty nitrogen compounds modified clay: Preparation and characterization

Biodegradable polymers, such as poly(lactic acid) (PLA) have attracted a lot of attention in the scientific community recently due to a rapid growth of intensive interest in the global environment for alternatives to petroleum-based polymeric materials. Fatty nitrogen compounds (FNCs), fatty amides (FA), fatty hydroxamic acids (FHA), and carbonyl difatty amides (CDFA), which were synthesized from vegetable oils, were used as one of organic compounds to modify natural clay (sodium montmorillonite). The clay modification was carried out by stirring the clay particles in an aqueous solution of FA, FHA, and CDFA, by which the clay layer thickness increased from 1.23 to 2.61, 2.84 and 3.19 nm, respectively. The modified clay was then used in the preparation of the PLA/epoxidized soybean oil (ESO) blend nanocomposites. They were prepared by incorporating 2% of CDFA-MMT and 3% of both FA-MMT and FHA-MMT. The interaction of the modifier in the clay layer was characterized by X-ray diffraction (XRD), and Fourier transform infrared (FTIR). Elemental analysis was used to estimate the presence of FNCs in the clay. The nanocomposites were synthesized by solution casting of the modified clay and a PLA/ESO blend at the weight ratio of 80/20, which has the highest elongation at break. The XRD and transmission electron microscopy (TEM) results confirmed the production of nanocomposites. PLA/ESO modified clay nanocomposites show higher thermal stability and significant improvement of mechanical properties in comparison with those of the PLA/ESO blend. The novelty of this study is use of FNCs which reduces the dependence on petroleum-based surfactants.     

Thermal properties of Poly(trimethylene terephthalate)/Poly(ethylene terephthalate) melt blends

The thermal behavior, morphology, ester-interchange reaction of Poly(trimethylene terephthalate) (PTT)/Poly(ethylene terephthalate) (PET) melt blends were investigated over the whole composition range(xPTT/(1-x)PET) using a twinscrew Brabender. The melt blends were analyzed by differential scanning calorimetry (DSC), nuclear magnetic resonance spectroscopy (¹³C-NMR), and scanning electron microscopy (SEM). Single glass transition temperature (T _g ) and cold crystallization temperature (T _cc ) were observed in all melt blends. Melt blends were found to be due to the ester-interchange reaction in PTT/PET blend. Also the randomness of copolymer increases because transesterification between PTT and PET increases with increasing blending time. This reaction increases homogeneity of the blends and decreases the degree of crystallinity of the melt blends. In PTT-rich blends, mechanical properties decrease with increase of PET content compared with that of pure PTT. And, in PET-rich blends, tensile modulus decreases with increase of PTT content, but tensile strength and elongation is similar to that of pure PET.     

Preparation of electrospun LA-PA/PET/Ag form-stable phase change composite fibers with improved thermal energy storage and retrieval rates via electrospinning and followed by UV irradiation photoreduction method

In this paper, novel electrospun LA-PA/PET/Ag phase change composite fibers with different amount of Ag nanoparticles were prepared via the technique of electrospinning followed by UV irradiation method. The morphological structure, thermal energy storage properties, thermal energy storage and release rates of prepared LA-PA/PET/AgNO₃ and LA-PA/PET/Ag composite fibers were investigated by scanning electron microscope (SEM), high-resolution transmission electron microscope (HR-TEM), differential scanning calorimeter (DSC), and the measurement of melting and freezing times, respectively. The SEM images revealed that electrospun LA-PA/PET/AgNO₃ and LA-PA/PET/Ag composite fibers possessed the smooth morphologies with cylindrical shape. The corresponding average fiber diameters gradually decreased with increasing content of the AgNO₃ in the solutions, and slightly smaller than those of the LA-PA/PET composite fibers with oblate morphology and wrinkled surfaces. Yellow-brown coloration of electrospun LA-PA/PET/Ag phase change composite fibers were observed after UV irradiation treatment, which demonstrated that Ag ions were successfully reduced to Ag nanoparticles. The TEM images revealed that these reduced Ag nanoparticles were homogenously dispersed within the composite fibers. The results from DSC measurements indicated that the phase change temperatures and enthalpies of electrospun LA-PA/PET/Ag phase change composite fibers with different Ag content have not be influenced by the UVirradiation treatment. The thermal energy storage and release rates of electrospun LA-PA/PET/Ag phase change composite fibers were also improved due to the combination of reduced Ag nanoparticles. These UV-irradiated electrospun phase change composite fibers with excellent thermal energy storage properties can be acted as a novel form-stable PCMs for the applications related to storage and retrieval of thermal energy.     

Immobilization of TiO2 nanoparticles on PET fabric modified with silane coupling agent by low temperature hydrothermal method

PET fabric was first modified with silane coupling agent KH-560, and then was loaded with a layer of nano-scaled TiO₂ particles using tetrabutyl titanate as precursor by low temperature hydrothermal method, followed by dyeing with Disperse Blue 56. The morphology, crystalline phase, chemical modification, thermal stability and optical property of PET fiber before and after treatments were studied by scanning electron microscope, X-ray diffraction, X-ray photoelectron spectroscopy, thermal gravimetric and diffuse reflectance spectrum techniques. The properties of tensile, air permeability, luster, ultraviolet (UV) protection, photocatalytic activity, K/S value and color fastness were also measured. It was found that compared with the TiO₂-coated fabric without modification with KH-560, the loading of TiO₂ nanoparticles on the surface of the TiO₂-coated fabric modified with KH-560 was obviously improved. The pure anatase TiO₂ nanoparticle was grafted onto the fiber surface. The onset decomposition temperature increased. The absorbing capability to ultraviolet radiation was enhanced. The properties of tensile, air permeability, luster, K/S value and color fastness changed slightly. The UV protection ability and photodegradation of methyl orange under UV illumination were enhanced to some extent.     

Mercerization mediated modification of cellulosic fibers with NIPAAm and some compounds with antioxidant activity

A two step process was used for the modification of a cellulose/chitin mixed fibers: the first step was an alkali treatment with a NaOH solution (20 %), which was followed by the reaction with one of the reagents such as Nisopropylacrylamide, p-hydroxybenzoic acid, gallic acid, or eugenol. Both the samples activated with the alkali treatment and modified with chemicals were characterized by attenuated total reflectance Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy and thermal analysis. Results revealed the morphological and structural changes of the fiber surface after the surface grafting, which significantly altered the cellulose/chitin mixed fiber properties. Thermal analysis results showed an increase in the thermal stability of the treated samples. Antioxidant activity of cellulose/chitin mixed fibers modified with phenolic compounds showed that the efficiency depends on the chemical nature of phenolic compound.     

End-capped polyethylene terephthalate having superior carbonaceous char yield

End-capping of PET with triphenyl phosphate (TPP), bisphenol A bis(diphenyl phosphate) (BDP), or resorcinol bis(diphenyl phosphate) (RDP) as phosphorous containing flame retardants was performed by using benzoyl peroxide as initiator. ³¹P NMR and FT-IR spectroscopy were used to evaluate end-capping of PET and structural changes of specimens. From thermal characteristics evaluated by differential scanning calorimetry and thermogravimetric analysis, BDP and RDP end-capped PETs show flame retarding mechanisms similar to those of blended counterparts. However, TPP end-capped PET presented superior carbonaceous char yields of up to 46.7 %, which was attributed to the condensed-phase action of TPP anchored at the ends of PET.     

Surface-Modified Cellulose Nanocrystal-incorporated Poly(butylene succinate) Nanocomposites

In this work, surface acetylation of cellulose nanocrystals was performed to improve their interfacial adhesion with hydrophobic polymer matrix and to restore their thermal stability by removing the sulfate groups. The morphological, chemical, and thermal characteristics of the surface-modified cellulose nanocrystals (ACNs) were confirmed by field emission-transmission electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. Furthermore, poly(butylene succinate) (PBS)/ACNs nanocomposites were also prepared via melt-mixing process, and the reinforcing effects of ACNs on the thermal, mechanical, and biodegradable properties of the nanocomposites were investigated. The Young’s modulus and tensile strength of the PBS/ACN nanocomposites increased from 115.36 and 33.67 MPa for the neat PBS to 130.55 MPa and 39.97 MPa, respectively. The thermal stability and biodegradability of the nanocomposites also increased with increasing ACN content.     

Polyvinylpyrrolidone/Carbon Nanotube/Cotton Functional Nanocomposite: Preparation and Characterization of Properties

In the last decade, preparation of multifunctional composites have attracted researchers around the World for multi-purpose application. In this regard, we produced polyvinylpyrrolidone/carbon nanotubes/cotton (PVP/CNTs/cotton) nanocomposite by coating cotton fabric via pad-dry-cure under UV irradiation. Several characterization methods were used to investigate the functionality and durability including scanning electron microscopy, thermo-gravimetric analysis, flammability test, reflectance spectroscopy, tensile strength test, water absorption and antibacterial analysis. The interactions among PVP molecular chains, CNT particles and cellulose were confirmed by Raman spectroscopy. We observed a uniform coating of PVP/CNTs on the fiber surface. An advantage of our developed method was the strong interfacial interaction among compositions, high durability along with multifunctional properties. PVP/CNT nanocomposite was able not only to improve the thermal stability of cotton, but also provided a reduced flammability and good antibacterial properties. Here, we confirm a simple and versatile method for fabrication of PVP/CNTs/cellulose nanocomposite for multi-purpose applications.     

Functinalization of poly(ethylene terephthalate) fibers by grafting of maleic acid/methacrylamide monomer mixture

Functionalized poly(ethylene terephthalate) (PET) fibers were synthesized by grafting of maleic acidmethacrylamide (MAA-MAAm) monomer mixtures by using benzoylperoxide as initiator onto PET fibers in an aqueous medium. The functionalized fibers were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimeter, and scanning electron microscopy. The effects of reaction conditions, such as monomer mixture ratio, monomer mixture and initiator concentration, polymerization time, and temperature on grafting were investigated. In alone grafting of MAA, grafting was not observed. However, the use of MAAm as a comonomer increased the amount of MAA inserted to the PET fiber up to 40.7 %. An increase in the temperature between 75 and 95 °C and also, increase in monomer mixture concentration between 0.50 and 1.00 M increased the grafting rate and saturation graft yield. The graft yield has shown an increase up to an initiator concentration of 1.0×10⁻² M and decreased afterwards. The grafting increased the dyeability with disperse, acidic and basic dyes, and water absorption capacity but decreased the thermal stability of the fibers.     

Effect of phase transformation on physical and biological properties of PVA/CaFe<Subscript>2</Subscript>O<Subscript>4</Subscript> nanocomposite

The thermal treatment method was employed to achieve higher homogeneity of calcium ferrite (CaFe2O4) and Poly (vinyl alcohol) (PVA) nanocomposites. The influences of phase transformation on physical and biological properties of calcined specimens were investigated by various experimental techniques including X-ray diffraction (XRD), Transmission Electron Microscopy (TEM), high resolution Field emission scanning electron microscope (FESEM) and Fourier transform infrared spectroscopy (FT-IR). Heat treatment was conducted at temperatures between 723 and 923 K, so that a phase transformation occurred from cubic to orthorhombic spinel structure at 923 K. The chemical analysis of the PVA/CaFe₂O₄ nanocomposite was performed by energy dispersion X-ray analysis (EDXA), demonstrated the PVA/CaFe₂O₄ nanocomposites contained the elements of C, Ca, Fe, and O. The formed nanocomposites exhibited ferromagnetic behaviors which were confirmed by using a vibrating sample magnetometer (VSM). The calcined specimens were carried out to an antimicrobial or antifungal test.     

Functionalization of graphene nanosheets and its dispersion in PMMA/PEO blend: Thermal,electrical, morphological and rheological analyses

Graphene nanoplatelet (GnP) was chemically functionalized by amine groups for improvement of compatibility in poly(methyl methacrylate) (PMMA)/poly(ethylene oxide) (PEO) blend. PMMA/PEO (90/10) nanocomposites with non-functionalized GnP and functionalized GnP (FGnP) were prepared by solution casting method. Successful grafting of amine groups on the GnP surface was confirmed by Fourier transform infrared (FT-IR) and X-ray diffraction (XRD) analysis. The Transmission electron microscopy (TEM) images showed that the dispersion state of FGnP was better than that of GnP in PMMA/PEO nanocomposites. The effects of FGnP and GnP on rheological, thermal and electrical properties of PMMA/PEO nanocomposites were investigated by various methods. The results indicated that the FGnP-based nanocomposites had higher storage modulus, glass transition temperature and thermal stability as compared to the GnP-based nanocomposites. The electrical conductivity of the nanocomposites with FGnP was better than that of GnP-based nanocomposites. The higher conductivity was attributed to homogeneous and well dispersion state of FGnP in PMMA/PEO nanocomposites.     

Thermal properties of copolyetherester/silica nanocomposites

Thermal properties of copolyetherester/silica nanocomposites were examined by using DSC and TGA. The segmented block copolyetheresters with various hard segment structures and hard segment contents (HSC) were synthesized and their silica nanocomposite films were prepared by solution casting method. The nano-sized fumed silica particles were found to act as a nucleating agent of the copolyetheresters. The nanocomposites always showed reduced degree of supercooling or faster crystallization than the corresponding copolyetheresters. The nanocomposites also showed increased hard segment crystallinity except HSC 35 sample which had short hard segment length. In case of 2GT [poly(ethylene terephthalate)] copolyetheresters, which were not developed commercially because of their low crystallization rate, the hard segment crystallinity increased considerably. The copolyetherester/silica nanocomposites showed better thermal stability than copolyetheresters.     

Graphene Oxide/Polyester Fabric Composite by Electrostatic Self-Assembly as a New Recyclable Adsorbent for the Removal of Methylene Blue

A novel graphene oxide/polyester (GO/PET) composite fabric as a recyclable adsorbent was prepared via electrostatic self-assembly. The structure, morphology, and properties of the GO/PET composite fabrics were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), Fourier transformed infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), and contact angle (CA), respectively. The absorption property was evaluated by the absorption amount and removal efficiency of methylene blue (MB) solution on the GO/PET composite fabric. The results indicated that the absorption amount was found to be 21.80 mg/g and the removal efficiency reached 99.93 % under the experimental conditions of GO concentration of 2 mg/ml, initial concentration of 50 mg/l, and area of 64 cm². The experimental parameters were investigated including the concentration of GO, the initial concentration of MB solutions, and adsorbent area. Simultaneously, according to a series of dynamic analysis, the absorption process revealed that the kinetics was well-described by pseudo-second-order model. This study showed that the GO/PET composite fabric could be a recyclable, efficient adsorbent material for the environmental cleanup.