Development and characterization of poly(trimethylene terephthalate)‐based bicomponent meltblown nonwovens

Poly(trimethylene terephthalate) (PTT)‐based mono and bico meltblown webs have been produced by using a Reicofil® Bi‐Component Meltblown Line at TANDEC, located at the University of Tennessee, Knoxville, TN. Thermal and flow properties of PTT were first examined by DSC (differential scanning calorimetry) and with a Melt Indexer for an effective experimental design through the Surface Response Methodology (SRM). The processability of meltblowing in a wide range of operating windows was extensively investigated. Melt temperature, melt throughput, air temperature, airflow rate, and DCD (distance of collector to die) were considered as primary process control variables. The produced webs were characterized for fiber diameter, bulk density, air permeability, hydrostatic head, tensile properties, and heat shrinkage. Non‐round and curly or twisted fibers were observed in the bico PP/PTT webs by SEM (scanning electrical microscope). The PTT grade studied is quite suitable for the meltblown process. The PTT/PP‐based bico webs showed enhanced barrier properties and heat resistance. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1280–1287, 2002     

Attenuating PP/PET bicomponent melt blown microfibers

This research investigated the attenuation of polypropylene (PP)/poly(ethylene terephthalate) (PET) bicomponent (bico) filaments during the melt blowing (MB) process. It was found that both mono‐ and bi‐component filaments attenuated from several hundred micrometers to a few micrometers in the first 5 centimeters from the die. However, fiber diameter distributions were found to be broad in these regions. The filaments were attenuated much slower but exhibited narrower diameter distributions as they moved further from the die. The diameters of bico MB filaments were between those of 100% PP and 100% PET filaments. The PET component in a bico filament controls the final fiber diameter. During melt blowing, filaments were aligned orderly with the airflow direction in a short distance near the die. Filament entanglements started at about 2.5 cm from the die and became more and more randomly oriented as the distance‐from‐the‐die (DFD) increased. The fiber diameter distribution of bico filaments was broader than that of 100% PP filaments. A higher airflow rate led to a narrower fiber size distribution for bico filaments.     

Preliminary study on fiber splitting of bicomponent meltblown fibers

Side‐by‐side bicomponent meltblown fiber webs were developed on REICOFIL® bicomponent (bico) meltblown line at The University of Tennessee's Textiles and Nonwovens Development Center (TANDEC), using polypropylene (PP), polyethylene (PE), polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyamide (PA), polytrimethylene terephthalate (PTT), and so forth. The posttreatment was performed by hydroentanglement to investigate the fiber‐splitting behavior in this research. Microscopy analysis and SEM were applied to examine the web structure. The change in web property after posttreatment and the adhesion mechanism of the polymer interface were also addressed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2090–2094, 2004     

Study of polypropylene/poly(ethylene terephthalate) bicomponent melt‐blowing process: The fiber temperature and elongational viscosity profiles of the spinline

Although there are significant differences between high‐speed melt spinning and melt blowing (MB), they are similar in many important components. This study, motivated by the need to better understand the bicomponent MB process, used the basic theories of high‐speed melt spinning to estimate the fiber temperature and elongation viscosity profiles of the polypropylene/poly(ethylene terephthalate) (PP/PET) bicomponent MB process. During the MB process, the filament temperature decreased dramatically within the first 2 in. from the MB die. The fiber temperature‐decay profiles of PP, PET monocomponent, and PP/PET bicomponent filaments followed similar trends. PP filaments attenuated faster than PET filaments and the bicomponent filaments attenuated at a medium rate between that of PP and PET. Accordingly, the elongational viscosity increased significantly in the first 2 in. from the die. PET filaments exhibited higher elongational viscosity than that of 100% PP filaments. The elongational viscosity profile of 75%PP/25%PET was between that of PP and PET monocomponent filaments. These data provided important information on understanding the MB process and filament attenuation. It also suggested that the filament elongational viscosity profile is the key factor in production of finer bicomponent MB fibers. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1145–1150, 2003     

Polymer distribution during bicomponent melt blowing of poly(propylene)/poly(ethylene terephthalate) and its improvement

Bicomponent melt blown (MB) microfiber nonwovens of poly(propylene) (PP) and poly(ethylene terephthalate) (PET) were produced in this study. It is interesting to analyze the polymer distribution uniformity across the web because it affects many end‐use properties. By utilizing the technique of differential scanning calorimetry (DSC), a standard working line between heat of fusion and weight percentage was constructed for mixtures of PP and PET components. The fitted equations were used for determination of a component percentage in a certain position across the MB web. Measurements were conducted from DSC re‐heating curves to achieve accurate results. The distribution of polymer varies with polymer mass ratio and processing conditions. The overall uniformity increased with the percentage of PP. When PP is the minor component in the polymer pair, it exhibits notably higher percentage in edge areas across the MB web. These results suggest the phase interface distortion of the polymer melt occurred at the entrance of the MB coat‐hanger die tip. The polymer distribution uniformity is improved by adjusting temperature profile of the MB die. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2885–2889, 2002     

Melt spinning and drawing process of PET side‐by‐side bicomponent fibers

The change of crimp contraction and shrinkage in the melt spinning and drawing process of polyethylene terephthalate (PET) side‐by‐side bicomponent fibers was studied. Regular PET and modified PET were selected to make a latent crimp yarn. The modified PET was synthesized to increase thermal shrinkage. The crimp contraction is mainly dependent on drawing conditions such as draw ratio, heat‐set temperature, and drawing temperature. Difference in shrinkage between the PET and the modified PET causes the self‐crimping of bicomponent fibers. Although changing the heat‐set temperature and the drawing temperature can not affect dimensional change, the crimp contraction varies with those variables. As the heat‐set temperature and the drawing temperature decrease, the crimp contraction increases. Difference in elongation also affects the crimp contraction in the effect of draw ratio. When the modified PET with neopentyl group was used for highly shrinkable part, the crimp contraction is greater in comparison with modified PET with dimethyl isophthalate. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1362–1367, 2006     

Interface modification of compatibilized polyethylene terephthalate/polypropylene blends: Effect of compatibilization on thermomechanical properties and thermal stability

Polyethylene terephthalate (PET) and polypropylene (PP) are incompatible thermoplastics because of differences in chemical structure and polarity, hence their blends possess inferior mechanical and thermal properties. Compatibilization with a suitable block/graft copolymer is one way to improve the mechanical and thermal properties of the PET/PP blend. In this study, the toughness, dynamic mechanical analysis (DMA), and thermogravimetric analysis (TGA) of PET/PP blends were investigated as a function of different content of styrene‐ethylene‐butylene‐styrene‐g‐maleic anhydride (SEBS‐g‐MAH) compatibilizer. PET, PP, and SEBS‐g‐MAH were melt‐blended in a single step using the counter rotating twin screw extruder with compatibilizer concentrations of 0, 5, 10, and 15 phr, respectively. The impact strength of compatibilized blend with 10 phr SEBS‐g‐MAH increased by 300% compared to the uncompatibilized blend. Scanning electron microscope (SEM) micrographs show that the addition of 10 phr SEBS‐g‐MAH compatibilizer into the PET/PP blends decreased the particle size of the dispersed PP phase to the minimum level. The improvement of the storage modulus and the decrease in the glass transition temperature of the PET phase indicated an interaction among the blend components. Thermal stability of the PET/PP blends was significantly improved because of the addition of SEBS‐g‐MAH. J. VINYL ADDIT. TECHNOL., 23:45–54, 2017. © 2015 Society of Plastics Engineers     

Molecular structures and physical properties of heat‐drawn conjugate fibers

As‐spun poly(trimethylene terephthalate) (PTT)/poly(ethylene terephthalate) (PET) side‐by‐side conjugate fibers were drawn to investigate the effects of drawing conditions on structure development and physical properties. Effects of draw ratio and heat‐set temperature were observed. In the state of an as‐spun fiber, the molecular orientation of PTT was higher than PET, whereas PET molecular orientation increased remarkably over PTT with increasing draw ratio. Crimp contraction increased sharply at a draw ratio over 2.0, where the crystalline structure of the PET developed sufficiently. A heat‐set temperature of at least 140°C was required to develop sufficient crimp contraction. The crystallinity and orientation of the PET were attributed mainly to the crimp contraction of the drawn fiber. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers     

Nanocomposite fibers of poly(ethylene terephthalate) with montmorillonite and mica: thermomechanical properties and morphology

The thermal stabilities, mechanical properties, and morphologies of nanocomposites of poly(ethylene terephthalate) (PET) with two different organoclays are compared. Dodecyltriphenylphosphonium‐montmorillonite (C₁₂PPh‐MMT) and dodecyltriphenylphosphonium‐mica (C₁₂PPh‐Mica) were used as reinforcing fillers in the fabrication of PET hybrid fibers. The variations of their properties with organoclay content in the polymer matrix and draw ratio (DR) are discussed. Transmission electron microscopy micrographs show that some of the clay layers are dispersed homogeneously within the polymer matrix on the nanoscale, although some clay particles are agglomerated. It was also found that the addition of only a small amount of organoclay is enough to improve the thermal stabilities and mechanical properties of the PET hybrid fibers. Even polymers with low organoclay contents (1–5 wt%) were found to exhibit much higher strength and modulus values than pure PET. In the case of C₁₂PPh‐MMT/PET, the values of the tensile mechanical properties of the hybrid fibers were found to decrease linearly with increases in DR from 1 to 16. However, the tensile mechanical properties of the C₁₂PPh‐Mica hybrid fibers were found to be independent of DR. Copyright © 2006 Society of Chemical Industry     

Rheological behavior of polyester blend and mechanical properties of the polypropylene–polyester blend fibers

The article deals with method of preparation, rheological properties, phase structure, and morphology of binary blend of poly(ethylene terephthalate) (PET)/poly(butylene terephthalate) (PBT) and ternary blends of polypropylene (PP)/(PET/PBT). The ternary blend of PET/PBT (PES) containing 30 wt % of PP is used as a final polymer additive (FPA) for blending with PP and subsequent spinning. In addition commercial montane (polyester) wax Licowax E (LiE) was used as a compatibilizer for spinning process enhancement. The PP/PES blend fibers containing 8 wt % of polyester as dispersed phase were prepared in a two‐step procedure: preparation of FPA using laboratory twin‐screw extruder and spinning of the PP/PES blend fibers after blending PP and FPA, using a laboratory spinning equipment. DSC analysis was used for investigation of the phase structure of the PES components and selected blends. Finally, the mechanical properties of the blend fibers were analyzed. It has been found that viscosity of the PET/PBT blends is strongly influenced by the presence of the major component. In addition, the major component suppresses crystallinity of the minor component phase up to a concentration of 30 wt %. PBT as major component in dispersed PES phase increases viscosity of the PET/PBT blend melts and increases the tensile strength of the PP/PES blend fibers. The impact of the compatibilizer on the uniformity of phase dispersion of PP/PES blend fibers was demonstrated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4222–4227, 2006     

Mechanical and thermal properties of exfoliated graphite nanoplatelets reinforced polyethylene terephthalate/polypropylene composites

Exfoliated graphite nanoplatelets (GNP) reinforced composites materials based on blend of poly(ethylene terephthalate) (PET) and polypropylene (PP) were prepared by melt extrusion followed by injection molding. 10 parts per hundred resin (phr) styrene‐ethylene‐butylene‐styrene‐g‐maleic anhydride was added to the base formulation PET/PP (70/30) as a compatibilizer. PET/PP/GNP composites 0–5 phr were prepared and characterized using field emission scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, and Fourier transform infrared (FTIR) spectroscopy analysis. The morphological studies revealed a homogenous dispersion of GNPs in PET/PP blends up to 3 phr loading after which agglomeration occurred. Flexural strength was enhanced by 80% at 3 phr GNPs loading which was the highest value obtained. Interestingly, the highest value for the impact strength was also recorded at 3 phr loading. The thermal stability of the composites were generally improved at all filler loading with the highest at 3 phr. From the overall results, it is clear that the optimum concentration of GNPs in the PET/PP/GNP system in terms of both mechanical and thermal properties was 3 phr loading. Although, the mechanical and thermal properties of the composites were improved, the FTIR analysis did not reveal any chemical interaction between GNP and the polymer matrix. POLYM. COMPOS., 35:2029–2035, 2014. © 2014 Society of Plastics Engineers     

Frictional properties of thermally bonded 3D nonwoven fabrics prepared from polypropylene/polyester bi‐component staple fiber

The frictional properties of the three‐dimensional nonwoven samples produced using the recently developed air laying and through‐air thermal bonding system are evaluated. The samples were made from commercially available polypropylene (PP)/polyester (PET) (sheath/core) bi‐component staple fiber. In particular, the effects of the process parameters on the frictional properties were investigated by employing a statistical approach involving the uniform design of experiments and regression analysis. Stick‐slip frictional traces were obtained as a result of the presence of fiber loops, overlapping of fibers at bonding points, and deformation of fibers due to melting. The effect of normal load on both the static and dynamic friction forces can be described using the power‐law relationship. Both the static and dynamic friction factors increase with increase of the thermal bonding temperature and the dwell time. POLYM. ENG. SCI., 46:853–863, 2006. © 2006 Society of Plastics Engineers     

Development and performance study of polypropylene/polyester bicomponent melt‐blowns for filtration

In this study, a new type of polypropylene (PP)/polyester (PET) bicomponent melt‐blown (bi‐MB) for filtration was developed through the melt‐blowing process with raw materials of melt‐blown (MB)‐grade PP and PET chips. The structure, porosity, and filtration performance of the bi‐MBs were tested through relevant instruments. The results show that the average fiber diameter in the bi‐MBs was 2–3.5 μm, the average pore size was 12.3–15.6 μm, and the porosity was 90–94%. The results also show that the filtration efficiency of the bi‐MBs was much higher than that of monocomponent PP MBs. It reached the highest value of 97.34% when the PP/PET ratio was 50/50 and could be used as high‐performance filter media. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Synthetic fibers and thermoplastic short‐fiber‐reinforced polymers: Properties and characterization

Among the synthetic fibers, glass fibers (GF) are most widely used in thermoplastic short‐fiber‐reinforced polymers (SFRP), as they offer good strength and stiffness, impact resistance, chemical resistance, and thermal stability at a low price. Carbon fibers (CF) are applied instead of GF, when highest stiffness is required. Other types of synthetic fibers like aramid (AF), basalt (BF), polyacrylonitrile (PAN‐F), polyethylene terephthalate (PET‐F), or polypropylene fibers (PP‐F) are rarely used in SFRP, although they offer some advantages compared with GF. The aim of this article is, to give an overview of various fiber types with regard to their mechanical properties, densities, and prices as well as the performance of their thermoplastic composites. The mechanical properties are presented as Ashby plots of tensile strength versus tensile modulus, both in absolute and specific (absolute value divided by density) values. This overview also focuses on modification of fiber/matrix interaction, as interfacial adhesion has a huge impact on composite performance. A summary of established methods for characterization of fibers, polymers, and composites completes this article. POLYM. COMPOS., 35:227–236, 2014. © 2013 Society of Plastics Engineers     

The Preparation and property of poly(lactic acid)/tourmaline blends and melt‐blown nonwoven

Poly(lactic acid) melt‐blown (MB) webs were melt‐spun by MB processing of poly(lactic acid) and poly(lactic acid)/filler blends. The effect of tourmaline particles on the structure, morphology, mechanical and filtration properties of poly(lactic acid) blends, and MB webs were reported. The blends and MB webs were characterized using differential scanning calorimetry (DSC), wide‐angle X‐ray diffraction (WXRD), scanning electron microscopy (SEM), and pore size meter (PSM). The degree of crystallinity of blends with tourmaline particles was more than that of poly(lactic acid) alone. SEM micrographs revealed a good dispersion of the additive in the blends and fiber webs. The tourmaline particles offered some benefits to the mechanical properties of the MB web. MB web samples with tourmaline had larger pore size, high surface charge density, and higher filtration efficiency. POLYM. COMPOS., 36:264–271, 2015. © 2014 Society of Plastics Engineers     

PBT/PET conjugated fibers: Melt spinning,fiber properties,and thermal bonding

This work examines the PBT/PET sheath/core conjugated fiber, with reference to melt spinning, fiber properties and thermal bonding. Regarding the rheological behaviors in the conjugated spinning, PET and PBT show the smallest difference between their melt‐viscosity at temperatures of 290°C and 260°C respectively, which has been thought to represent optimal spinning conditions. The effect of processing parameters on the crystallinity of core material‐PET was observed and listed. In order of importance, these factors are the draw ratio, the heat‐set temperature, and the drawing temperature. The crystallinity of sheath material‐PBT, however, can be considered to be constant, independent of any processing parameters. The bulk orientation, rather than the crystallinity of PET core, dominates the tenacity of PBT/PET sheath/core fiber. Moreover, heat‐set treatment after drawing is recommended to yield a highly oriented conjugated fiber. With respect to thermal bonding, PBT/PET conjugated fibers processed via high draw ratio but low‐temperature heat setting can form optimal thermal bonds at a constant bonding temperature of 10°C above the T_m of PBT.     

Bamboo fiber polypropylene composites: Effect of fiber treatment and nano clay on mechanical and thermal properties

In the current study, bamboo fibers were modified with sodium meta‐periodate in order to improve the mechanical and thermal properties of the bamboo‐clay‐polypropylene (PP) composites. Both raw and treated bamboo fibers were used in the manufacturing of the composites. The mechanical and thermal properties of the composites from modified bamboo fibers were found to increase considerably compared with those of untreated fibers. Tensile strengths of (raw bamboo fiber)/PP, (raw bamboo fiber‐clay)/PP, and (treated bamboo fiber‐clay)/PP composites showed a decreasing trend with increasing fiber loadings. However, the values for the chemically modified (bamboo fiber)‐clay‐PP composite at all mixing ratios were found to be higher than that of the original PP. The scanning electron micrographs showed that interfacial bonding between the treated fiber‐clay and matrix has significantly improved. It was determined that better dispersion of the filler into matrix occurred on 5% clay addition and fiber treatment. J. VINYL ADDIT. TECHNOL., 21:253–258, 2015. © 2014 Society of Plastics Engineers     

Crosslinked PVA nanofibers reinforced with cellulose nanocrystals: Water interactions and thermomechanical properties

Acid‐catalyzed vapor phase esterification with maleic anhydride was used to improve the integrity and thermo‐mechanical properties of fiber webs based on poly(vinyl alcohol), PVA. The fibers were produced by electrospinning PVA from aqueous dispersions containing cellulose nanocrystals (CNCs). The effect of esterification and CNC loading on the structure and solvent resistance of the electrospun fibers was investigated. Chemical characterization of the fibers (FTIR, NMR) indicated the formation of ester bonds between hydroxyl groups belonging to neighboring molecules. Thermomechanical properties after chemical modification were analyzed using thermal gravimetric analysis, differential scanning calorimetry, and dynamic mechanical analysis. An 80% improvement in the ultimate strength was achieved for CNC‐loaded, crosslinked PVA fiber webs measured at 90% air relative humidity. Besides the ultra‐high surface area, the composite PVA fiber webs were water resistant and presented excellent mechanical properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40334.     

Structural properties and superhydrophobicity of electrospun polypropylene fibers from solution and melt

Isotactic polypropylene (iPP) has successfully been electrospun from both solution and melt using an elevated temperature setup. First, PP nanofibers with two different average diameters (0.8 μm and 9.6 μm) were obtained via electrospinning of iPP in decalin, and the effect of deformation and solidification on the morphological and structural features of the resulting fibers was studied. Secondly, melt electrospun PP fibers with two different average diameters were also fabricated to compare the structures with those of solution electrospun PP fibers. DSC and XRD results show that β form crystals which can increase the impact strength and toughness of electrospun fibers are present in sub-micron scale PP fibers from solution, while fibers from melt mostly show α form crystals. The annealed fibers have changed their morphological forms into α and γ crystal forms. Finally, it is observed that electrospun PP fiber webs both from solution and melt exhibit superhydrophobicity with a water contact angle about 151° which is substantially higher than those of a commercial PP non-woven web and a compression molded PP film, 104° and 112°, respectively. Such superior hydrophobicity was observed for all PP electrospun fibers and it was not altered by the processing scheme (solution or melt) or fiber diameter (sub-micron or micron). Enhanced hydrophobicity of electrospun PP fiber webs contribute to excellent barrier performance without losing permeability when they are applied to protective clothing.     

Effect of graphene nanoplatelets presence on the morphology,structure, and thermal properties of polypropylene in fiber melt‐spinning process

Melt spinning of graphene nanoplatelets (GnPs)‐polypropylene (PP) nanocomposite fibers are reported for the first time. PP/GnPs fibers were spun with a pilot‐plant spinning machine with varying concentration of GnPs by mixing PP/GnPs masterbatch with PP. The effect of inclusion of GnPs on the morphology and crystalline structure of PP fibers was investigated. The thermal stability of the fibers was also evaluated by thermogravimetric analysis. The light microscopy images showed that the GnPs are uniformly distributed over the PP matrix. The differential scanning calorimetry (DSC) results revealed that presence of GnPs affects both the melting and crystallization behaviors. The melting peaks of PP/GnPs nanocomposite fibers were broader than that of neat PP fibers, indicating a broader crystal size distribution in PP/GnPs nanocomposite fibers as compared to the neat PP fibers. Besides, an obvious increment in the crystallization peak temperature was observed in GnPs‐PP nanocomposite fibers. The wide‐angle X‐ray diffraction spectra (WAXD) results showed that the crystal type of nanocomposite fibers did not change and was still the α‐monoclinic crystal form. Moreover, the morphology of spherulites demonstrated that GnPs increased the nucleation sites in the nanocomposite fibers which in turn restricted the crystal growth of PP chains. This finding supported the DSC and WAXD results. Activation energies were calculated by Horowitz and Metzger's method as 77.87 and 105.41 kJ/mol for neat PP and PP/0.2 wt% GnPs fibers, respectively, suggesting an increase in the thermal stability of GnPs‐PP nanocomposite fibers. POLYM. COMPOS., 36:367–375, 2015. © 2014 Society of Plastics Engineers