Effects of spinning and drawing conditions on the crimp contraction of side‐by‐side poly(trimethylene terephthalate) bicomponent fibers

The crimp properties in the melt‐spinning and drawing processes of side‐by‐side bicomponent fibers with poly(trimethylene terephthalate)s (PTTs) of different viscosities were studied. Two PTTs of different intrinsic viscosities (1.02 and 0.92) were selected to make latent crimp yarn. The spinning and drawing conditions were changed to investigate the relation between the process conditions and crimp contraction. An orthogonal array was used to rule out the weak variables. The draw ratio, heat‐set temperature, and portion of high‐viscosity PTT were selected as variables having an effect on the crimp contraction. An analysis of the effects of the spinning and drawing conditions on the crimp contraction showed that the draw ratio was the most critical variable. Increasing the draw ratio caused a difference in the shrinkage between the two parts of PTT and caused the self‐crimping of the bicomponent fibers. Although changing the heat‐set temperature and the portion of high‐viscosity PTT did not produce a dimensional change, the crimp contraction varied with those variables. As the heat‐set temperature and the high‐viscosity portion increased, the crimp contraction increased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1322–1327, 2006     

Morphology and crystallization behavior of nylon 6‐clay/neat nylon 6 bicomponent nanocomposite fibers

Nylon 6‐clay hybrid/neat nylon 6, sheath/core bicomponent nanocomposite fibers containing 4 wt % of clay in sheath section, were melt spun at different take‐up speeds. Their molecular orientation and crystalline structure were compared to those of neat nylon 6 fibers. Moreover, the morphology of the bicomponent fibers and dispersion of clay within the fibers were analyzed using scanning electron microscopy and transmission electron microscopy (TEM), respectively. Birefringence measurements showed that the orientation development in sheath part was reasonably high while core part showed negligibly low birefringence. Results of differential scanning calorimetry showed that crystallinity of bicomponent fibers was lower than that of neat nylon 6 fibers. The peaks of γ‐crystalline form were observed in the wide‐angle X‐ray diffraction of bicomponent and neat nylon 6 fibers in the whole take‐up speed, while α‐crystalline form started to appear at high speeds in bicomponent fibers. TEM micrographs revealed that the clay platelets were individually and evenly dispersed in the nylon 6 matrix. The neat nylon 6 fibers had a smooth surface while striped pattern was observed on the surface of bicomponent fibers containing clay. This was speculated to be due to thermal shrinkage of the core part after solidification of the sheath part in the spin‐line. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 39996.     

Simulation of dry‐spinning process of polyimide fibers

As one type of high‐performance fibers, the polyimide fibers can be prepared from the precursor polyamic acid via dry‐spinning technology. Unlike the dry‐spinning process of cellulose acetate fiber or polyurethane fiber, thermal cyclization reaction of the precursor in spinline with high temperature results in the relative complex in the dry‐spinning process. However, the spinning process is considered as a steady state due to a slight degree of the imidization reaction from polyamic acid to polyimide, and therefore a one‐dimensional model based on White‐Metzer viscoelastic constitutive equation is adopted to simulate the formation of the fibers. The changes of solvent mass fraction, temperature, axial velocity, tensile stress, imidization degree, and glass transition temperature of the filament along the spinline were predicted. The effects of spinning parameters on glass transition temperature and imidization degree were thus discussed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Recent advances in core/shell bicomponent fibers and nanofibers: A review

There has been a steady progress in developing synthetic fibers in the past few years. Bicomponent fibers and nanofibers in a core/shell (C/S) configuration, including two dissimilar materials have presented unusual potential for use in many novel applications. These fibers can be produced using a variety of materials via different techniques i.e., coaxial melt spinning and electrospinning. In this review, we discuss the recent advances in C/S fibers and nanofibers’ production. The first part has been assigned to the bicomponent fibers manufacturing technology, while production and applications of C/S nanofibers have been described in the second part. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46265.     

Enhanced mechanical properties of multilayer nano‐coated electrospun nylon 6 fibers via a layer‐by‐layer self‐assembly

We reported the mechanical properties of the polyelectrolyte multilayer nano‐coated electrospun fiber mats with different number of layers. Multilayer nano‐coatings composed of layers of PSS and PAH were successfully deposited onto electrospun nylon 6 fibers via layer‐by‐layer self‐assembly. Compared with pure nylon 6 fibers, the morphology of polyelectrolyte multilayer coated nylon 6 fibers was uniform and smooth. The mechanical properties of polyelectrolyte multilayer coated random and aligned nylon 6 fibers were remarkably enhanced. Moreover, it was found that the higher degree of alignment resulted in higher tensile strength, suggesting the combined effects of the alignment, the surface nanocoating and the formation of internal networks of polyelectrolytes on nylone 6 fibers. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Melt spinning and drawing of polyethylene nanocomposite fibers with organically modified hydrotalcite

Fibers of high density polyethylene (HDPE)/organically modified hydrotalcite (LDH) were produced by melt intercalation in a two‐step process consisting of twin‐screw extrusion and hot drawing. The optimum drawing temperature was 125°C at which the draw ratios up to 20 could be achieved. XRD analysis revealed intercalation with a high degree of exfoliation for the composites with 1–2% of LDH. Higher thermal stability of nanofilled fibers was confirmed by TGA analysis. DSC data indicated that dispersed LDH particles act as a nucleating agent. Crystallization kinetics of the HDPE matrix in the composite fibers is characterized by two transition temperatures, that is, for Regimes I/II at 123°C and for Regimes II/III ranging between 114–119°C as a function of the nanocomposite composition. Fibers with 1–2% of LDH show for the drawing ratios up to 15 a higher elastic modulus, 9.0–9.3 GPa (with respect to 8.0 GPa of the neat HDPE), maintain tensile strength of 0.8 GPa and deformation at break of 20–25%. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40277.     

Preparation and radar wave absorbing characterization of bicomponent fibers with infrared camouflage

Sheath‐core bicomponent fibers were prepared by a general melt‐spinning method with polypropylene chips and various particles. The melt‐spun fibers were characterized by DSC and mass specific electrical resistance (MSER) apparatus. The electromagnetic constant was measured using a network analyzer and the absorbing wave effect was evaluated by an arch method. The results of the DSC thermogram indicated that the crystallinity of polypropylene containing particles in the core‐part slightly increased first and then kept steadily with the particles content increase. Nanoparticles in the sheath‐part did not make the crystallinity of fibers change markedly. The MSER of fibers rapidly decreased with the metal particles input. The complex permeability of fibers with Ba/Mn‐Zn ferrite was improved compared with that of fiber with single Mn‐Zn ferrite and the complex permittivity of fiber containing the 20 wt % Ba/Mn‐Zn ferrite increased with the increasing bronze content. The fibers filled with the Ba/Mn‐Zn ferrite and bronze particles had good radar absorbing effect. The input of Al particles in the sheath‐part of the fibers showed a limited effect on the radar wave absorbing properties of the fibers. The lowest infrared emissivity of the fibers including 15 wt % Al particles in sheath‐part reached 0.62. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2180–2186, 2007     

Development of high‐strength fibers from aliphatic polyketones by melt spinning and drawing

We have investigated the formation of high‐strength, high‐modulus fibers from four aliphatic polyketone resins. One resin was a perfectly alternating copolymer of ethylene and carbon monoxide, while the other three were terpolymers containing up to 6 mol % propylene. The mechanical properties were measured as a function of processing conditions, and the structures of the filaments were characterized using birefringence, WAXS, SAXS, SEM, and thermal analysis. Fibers formed from all resins develop very high molecular orientations and a microfibrillar structure. Fibers having room temperature tenacities as high as 10 gpd (～1.1 GPa) were obtained. Tensile moduli reached values as high as 120 gpd (～13 GPa). The melting point of the fibers was primarily dependent on the composition of the resin, while the maximum strength and modulus were largely determined by the maximum draw ratio achieved. The maximum draw ratio achieved in the present experiments was greater for the terpolymers than for the copolymer. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 1794–1815, 2001     

Melt spinning and drawing of 2‐methyl‐1,3‐propanediol‐substituted poly(ethylene terephthalate)

The structure and properties of fibers prepared from copolymers of poly(ethylene terephthalate) (PET) in which 2‐methyl‐1,3‐propanediol (MPDiol® Glycol is a registered trademark of Lyondell Chemical Company) at 4, 7, 10, and 25 mol% was substituted for ethylene glycol were studied and compared with those of PET homopolymer. Filaments were melt spun over a range of spinning conditions, and some filaments that were spun at relatively low spinning speeds were subjected to hot drawing. The filaments were characterized by measurements of birefringence, differential scanning calorimetry (DSC) crystallinity, melting point, glass transition temperature, wide‐angle X‐ray diffraction patterns, boiling water shrinkage, tenacity, and elongation to break. Filaments containing 25 mol% MPDiol did not crystallize in the spinline at any spinning speed investigated, whereas the other resins did crystallize in the spinline at high spinning speeds. However, compared with PET homopolymer, increasing substitution of MPDiol reduced the rate at which the crystallinity of the melt spun filaments increased with spinning speed and reduced the ultimate crystallinity that could be achieved by high‐speed spinning. The rate of development of molecular orientation, as measured by birefringence, also decreased somewhat with increasing MPDiol content. Shrinkage in boiling water decreased at high spinning speeds as the amount of crystallinity increased; however, the shrinkage decreased more slowly with increase in spinning speed as MPDiol content increased. Tenacity also decreased slightly at any given spinning speed as MPDiol content increased, but there was no significant effect on elongation to break. The addition of MPDiol in amounts up to 7 mol% increased the maximum take‐up velocity that could be achieved at a given mass throughput. This result indicates that the use of higher spinning speeds could potentially increase the productivity of melt spun yarns. Copolymer filaments spun at low speeds were readily drawn to produce highly oriented fibers with slightly less birefringence, crystallinity, and tenacity than similarly processed PET homopolymer. Preliminary dyeing experiments showed that the incorporation of MPDiol improved the dyeability of the filaments. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2598–2606, 2003     

Effect of the drawing process on the wet spinning of polyacrylonitrile fibers in a system of dimethyl sulfoxide and water

The effect of the drawing process on the structural characteristics and mechanical properties of polyacrylonitrile (PAN) fibers was comparatively studied. The protofibers extruded from the spinneret were the initial phase of stretching, which involved the deformation of the primitive fiber with the concurrent orientation of the fibrils. Wet‐spun PAN fibers observed by scanning electron microscopy exhibited different cross‐sectional shapes as the draw ratio was varied. X‐ray diffraction results revealed that the crystalline orientation of PAN fibers increased with increasing draw ratio; these differences in the orientation behaviors were attributed to the various drawing mechanisms involved. The crystalline and amorphous orientations of the PAN fibers showed different features; at the same time, the tensile properties were strongly dependent on the draw ratio. However, the stream stretch ratio had most influence on the tensile strength and the orientation of PAN fibers for the selected process parameters. Electron spin resonance proved that the local morphology and segmental dynamics of the protofibers were due to a more heterogeneous environment caused by the sequence structure. Differential scanning calorimetry indicated that the size and shape of the exotherm and exoenergic reaction were strongly dependent on the morphology and physical changes occurring during fiber formation. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1026–1037, 2007     

Formation of hollow fibers in the melt‐spinning process

This article reports an investigation of the formation of hollow fibers in a melt‐spinning process. Experimental results indicate that die swelling is largely responsible for a negative effect on hole formation. The factors that positively affect die swelling, including a decrease in temperature, a decrease in capillary length, and an increase in shear rate, are thus not recommended for the spinning of hollow fibers. For vinyl‐type polymers such as polypropylene, in which the apparent elasticity leads to serious die swelling, the formation of hollow fibers is more complex than that of a typical condensation polymer. Our results further demonstrate that when hollow fibers are being made in a variety of shapes (but of the same denier), spinning a polygonal hollow fiber is significantly more unstable than spinning a circular one. Moreover, an asymmetric bridge along the polygonal contour leads to a melt twist and interrupts the entire spinning process. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 2896–2902, 2001     

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     

Direct drawing of gel fibers enabled by twist‐gel spinning process

A new twist‐gel spinning process for ultrahigh molecular weight polyethylene fibers is demonstrated which significantly increases the extraction rate of nonvolatile spin solvent while simultaneously reducing the consumption of extraction solvent by more than 75%. Applying twist to the gel fiber enables it to be directly hot‐drawn, allowing conventional solvent extraction to proceed significantly faster. While solvent extraction effectiveness is largely enhanced, the new process does not show reduced fiber properties. The tensile strength, Young's modulus, surface morphology, and geometry are relatively unaffected when compared to fibers produced using the conventional gel‐spinning process. The new twist‐gel spinning process is expected to improve the processing efficiency of gel‐spun high‐strength fibers, promoting broad expansion of these high performance fibers into applications that were previously prohibitive due to extremely slow production. POLYM. ENG. SCI., 55:1389–1395, 2015. © 2015 Society of Plastics Engineers     

Melt spinning of poly(vinylidene fluoride) fibers and the influence of spinning parameters on β‐phase crystallinity

The effects of melt‐spinning and cold‐drawing parameters on the formation of β‐phase crystallinity in poly(vinylidene fluoride) (PVDF) fibers and ways of increasing such crystallinity were studied. Fibers were melt‐spun with four different melt draw ratios (MDRs) and were subsequently cold‐drawn at different draw ratios (λ). The maximum λ value in cold drawing was dependent on the MDR used in melt spinning. The crystalline structure of the fibers was studied mainly with differential scanning calorimetry (DSC) and X‐ray diffraction (XRD). The results showed that the degree of crystallinity in the fibers was determined by the MDR and that before cold drawing the crystalline structure of the fibers was predominantly in the α form. By cold drawing, α‐phase crystallites could be transformed into the β phase. It was established that, under certain conditions of melt spinning and cold drawing, PVDF fibers of up to 80% crystallinity, mainly in the β form, could be prepared. It was further proposed that fibers spun at a sufficiently high MDR consist to a large extent of extended‐chain crystals, and this greatly affects the melting point of PVDF. Thus, DSC melting‐point data were shown to be insufficient for determining the crystalline phase of PVDF. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Structure and property development of aromatic copolysulfonamide fibers during wet spinning process

The structure and performance changes of aromatic copolysulfonamide (co‐PSA) fibers that occurred during wet spinning process have been studied. While using different length scale characterization, including scan electron microscopy (SEM), wide‐angle X‐ray scattering (WAXS), and small‐angle X‐ray scattering (SAXS), it was found that the molecular chains of co‐PSA formed an isotropic network during coagulation which further lead to extension and orientation of these chains during the subsequent stretching. As a result, only after heat stretching and heat setting the molecular chains tended to pack into crystal lattice in the fibrils. This gave rise to a much denser structure along the spinning line and the glass transition temperature of co‐PSA fibers increased a little after heat setting. Before heat stretching, the co‐PSA fibers were in amorphous state, and only the amorphous orientation was observed within the fibers. After heat stretching at the temperature higher than T_g, the fraction of amorphous region decreased, and the crystal structure formed in the fibers, which became more perfect during heat setting. The structure development during spinning process contributed toward the improvement of thermo‐mechanical stability, tenacity and modulus of the co‐PSA fibers. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42343.     

New functional bicomponent fibers with core/sheath‐configuration using poly(phenylene sulfide) and poly(ethylene terephthalate)

Bicomponent fibers using the high‐performance polymer poly(phenylene sulfide) (PPS) together with poly(ethylene terephthalate) (PET) were melt‐spun. Both possibilities of using PPS, either as core or as sheath material, were realized to provide special functionalities like improved thermobonding capability, flame retardancy, or chemical resistance. Parameters that guarantee stable processing of PPS and PET during coaxial extrusion with different core/sheath volume ratios were explored. Microscopic studies of the cross‐sections showed holes and cavities, which were formed at the interface between PPS and PET. Possible mechanisms for cavity formation were evaluated. Results of thermal and mechanical characterization by means of TGA, DSC, and tensile testing revealed a strong influence of the processing parameters, namely draw ratio and core/sheath volume ratio, on the crystallization and the tensile strength of the drawn fibers. By changing the core/sheath volume ratio from 2 to 0.5 in the PPS/PET fiber, the crystallinity of the PET‐component was switched from 10 to 50%, whereas the crystallinity of the PPS dropped from 68 to 7%. It was determined that bicomponent fibers can exceed the strength of monocomponent fibers up to 28%. The flammability and chemical resistance of the new developed fibers were characterized. In contrary to what was expected, the encasing of PET with PPS reduced the flame retardancy, though PPS has a higher flame resistance than PET. The chemical resistance of the PET core against hydrolysis was imparted by coextruding a PPS sheath. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Melt spinning of PVDF fibers with enhanced β phase structure

Polyvinylidene fluoride (PVDF) fibers with a high amount of β phase crystal structure were prepared by melt spinning. With this technique, the cold drawing process is critical and efficient when aiming for a high amount of β phase. During the cold drawing process, more than 80% of the originally formed α phase crystal structure was converted into the β phase structure. In addition, the incorporation of 0.01 wt % of amino‐modified double wall carbon nanotube (NH₂‐DWCNT) could further enhance the β phase content in the PVDF fibers. FTIR and DSC studies showed that the addition of NH₂‐DWCNT to PVDF fibers could increase both the total crystallinity and β phase fraction in PVDF. The addition of nanoclay was found to be less efficient in this respect. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2603–2609, 2013     

Properties of PP/PET bicomponent melt blown microfiber nonwovens after heat‐treatment

Polypropylene (PP)/poly(ethylene terephthalate) (PET) bicomponent (bico) fibres are successfully melt blown in the Reicofil® meltblown (MB) pilot line commissioned at the Textiles and Nonwovens Development Center (TANDEC), the University of Tennessee, Knoxville. The bico fibers possess a cross‐sectional side‐by‐side configuration. The originally expected greater fiber crimp due to density and fine structure gradients on the different sides of the bico fibers was not commonly observed in the normal MB webs. These fabrics were exposed to dry heat for a period of time. The properties before and after the heat treatment were determined and compared to investigate the effects of heat on their properties. It was found that the bico webs are thermal dimensionally stable and many of their properties were not significantly affected. A mechanism is suggested on the thermal dimensional stability of the PP/PET bico MB webs. © 2003 Society of Chemical Industry