Mechanical properties,stress‐relaxation,and orientation of double bubble biaxially oriented polyethylene films

Biaxially oriented linear low density polyethylene (LLDPE) films were produced using the double bubble process with different machine direction (MD) orientation levels and the same transverse direction (TD) blow‐up ratio. Their mechanical behavior was characterized in terms of the tensile strength and tear resistance. The viscoelastic behavior of oriented films was studied using dynamic‐mechanical thermal analysis (DMTA). The microstructure and orientation were characterized using microscopy, X‐ray diffraction pole figures, and birefringence. The results indicate that MD ultimate tensile strength increases and the TD one decreases with MD stretching ratio. Tear propagation resistance, in general, remained mainly constant in TD and decreased in MD, as the draw ratio was increased. The morphology analyses exhibit a typical biaxial lamellar structure for all samples with different lamellar dimensions. Orientation of c‐axis in crystalline phase, molecular chain in amorphous phase along MD increased with draw ratio. In most crystals, a‐axis was located in the normal direction (ND) and the b‐axis in the ND–TD plane. A good correlation was observed between c‐axis orientation factor and MD mechanical properties. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3545–3553, 2006     

Improved dielectric performance of polypropylene/multiwalled carbon nanotube nanocomposites by solid‐phase orientation

By means of a die‐drawing technique in the rubbery state, the effect of the orientation of the microstructure on the dielectric properties of polypropylene (PP)/multiwalled carbon nanotube (MWCNT) nanocomposites was examined in this study. The viscoelastic behavior of the PP/MWCNT nanocomposites with MWCNT weight loadings ranging from 0.25 to 5 wt % and the dielectric performance of the stretched PP/MWCNT nanocomposites at different drawing speeds and drawing ratios were studied to obtain insight into the influences of the dispersion and orientation state of the MWCNTs and matrix molecular chains. A viscosity decrease (ca. 30%) of the PP/MWCNT‐0.25 wt % (weight loading) melt was obviously due to the free volume effect. Differential scanning calorimetry (DSC) and wide‐angle X‐ray diffraction were adopted to detect the orientation structure and the variation of crystal morphology of the PP/MWCNTs. Melting plateau regions, which indicated the mixed crystallization morphology for the stretched samples, were found in the DSC patterns instead of a single‐peak for the unstretched samples. We found that the uniaxial stretching process broke the conductive MWCNT networks and consequently increased the orientation of MWCNTs and molecular chains along the tensile force direction; this led to an improvement in the dielectric performance. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42893.     

X‐ray diffraction study of iPP/cand iPP/TiO2 composites relating to micromechanical properties

Composites of isotactic polypropylene with various contents of white clay or titanium dioxide TiO₂ were prepared by extrusion molding. The extruded composites were melt‐pressed at two different temperatures, and, thereafter, either slowly cooled, or quenched to room temperatures. It is shown that the structure of all the samples, as revealed by wide‐angle X‐ray scattering and small‐angle X‐ray scattering (SAXS), depends on the processing conditions. The lack of SAXS maxima in the composites suggests that the presence of the microadditives hinders the stacking of iPP lamellae. Furthermore, the microindentation hardness H in the slowly cooled composites is influenced by the type and amount of the filler used. However, in the quenched samples H depends only on the amount of the filler used, and not on its type. In case of the quenched iPP/clay composites, the relationship between H and the Young's modulus E is found to be H/E ≈ 0.12, in good agreement with Struik's theoretical predictions of σ_e ≈ E/30, in consonance with results previously obtained for a series of polyethylene samples with different morphology. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

The effect of talc on the crystallization of isotactic polypropylene

Isotactic polypropylene (iPP) has been crystallized in the presence of talc under the quiescent state and shear flow of injection molding. The resulting morphology has been investigated by means of polarizing microscopy, transmission electron microscopy, and wide angle X‐ray diffraction. In the quiescent state, the iPP lamellae grew from the surface of talc and the transcrystalline region was formed at the interface between iPP melt and the talc. The nucleation of iPP was very frequent on the cleavage plane of talc. The X‐ray diffraction pattern of the transcrystal showed a*‐axis orientation to the crystal growing direction. In injection‐molded samples of the talc‐filled iPP, the morphology of lamella growing from talc appeared as same as that of the transcrystal. However, the crystalline orientation of injection‐molded talc‐filled iPP, in which the b axis was oriented to the thickness direction and the a* and the c axis was oriented to the flow direction, was quite different from that of the transcrystal. This b‐axis orientation results from the orientation of the plate plane of talc, which induces the nucleation and the crystallization under shear flow. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1693–1703, 2001     

Properties of aligned poly(L‐lactic acid) electrospun fibers

Poly(L‐lactic acid) (PLLA)‐aligned fibers with diameters in the nano‐ to micrometer size scale are successfully prepared using the electrospinning technique from two types of solutions, different material parameters and working conditions. The fiber quality is evaluated using scanning electron microscopy (SEM) to judge fiber diameter, diameter uniformity, orientation, and appearance of defects or beads. The smoothest fibers, most uniform in diameter and defect free, were found to be produced from 10% w/v chloroform/dimethylformamide solution using an accelerating voltage from 10–20 kV. Addition of 1.0% multiwalled carbon nanotubes (MWCNT) into the electrospinning solution decreases fiber diameter, improves diameter uniformity, and slightly increases molecular chain alignment. The fibers were cold crystallized at 120°C and compared with their as‐spun counterparts. The influences of the crystalline phase and/or MWCNT addition were examined using fiber shrinkage, temperature‐modulated calorimetry, X‐ray diffraction, and dynamic mechanical analysis. Crystallization increases the glass transition temperature, T_g, slightly, but decreases the overall fiber alignment through shrinkage‐induced buckling of the fibers when heated above T_g. MWCNT addition has little impact on T_g, but significantly increases the orientation of crystallites. MWCNT addition slightly reduces the dynamic modulus, whereas crystallization increases the modulus in both neat‐ and MWCNT‐containing fibers. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41779.     

Dielectric properties of irradiated polymer/multiwalled carbon nanotube and its amino functionalized form

The polymer/multiwalled carbon nanotube [poly(vinyl alcohol) (PVA)/carboxyethyl acrylate (CEA)]‐multiwalled carbon nanotube (MWCNT) and its amino functionalized (PVA/CEA)‐MWCNT‐NH₂ nanocomposite samples were successfully synthesized by the chemical method in the form of films. The samples were irradiated with gamma‐ray doses of 50 and 100 kGy and with ion beam fluence of 2.5 × 10¹⁸ and 3.75 × 10¹⁸ ions cm^?2. The prepared nanocomposite samples were characterized using X‐ray diffraction and thermogravimetric analysis. The X‐ray diffraction and thermogravimetric analysis confirm the existence of the chemical crosslinking occurred in the polymer compositions. The AC electrical conductivity, electrical modulus, dielectric constant, and dielectric loss in the frequency range 10²–10⁶ Hz are measured at room temperature. The electrical conductivity is increased with MWCNT doping, gamma‐irradiation, and by ion beam irradiation. A comprehensive analysis of the results revealed that dielectric properties are improved due to the induced physicochemical changes and conductive networks induced by ion beam irradiation. The behavioral effect of these embedded nanoparticles in a PVA matrix on the microstructural, dielectric, and electric properties is analyzed for possible device applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46647.     

Resistive Switching Behaviors of Sol‐Gel‐Derived MgNb2O6 Thin Films on ITO/glass Substrate

In this study, transparent amorphous MgNb₂O₆ (MNO) films were fabricated via the sol‐gel method to form an Al/MNO/indium tin oxide/glass structure. The resistive switching (RS) behavior of the devices was investigated. From the DC voltage sweep test, the air‐annealed MNO samples exhibited stable and reproducible bipolar resistive switching (BRS) behavior; however, the samples annealed in an O₂‐rich environment showed no RS property. These results suggest that the RS behavior of the MNO memory devices is highly related to the oxygen vacancy concentration and distribution within the MNO films. In addition, forming‐free unipolar resistive switching (URS) behavior was observed when the MNO films were annealed under an N₂H₂ atmosphere. In order to determine the origin of the BRS and URS behaviors, cross‐sectional high‐resolution transmission electron microscopy images of the MNO samples were acquired. The RS behavior of the MNO films can be ascribed to the release and recombination of electrons and oxygen vacancies.     

Crystallization and orientation development in fiber and film processing of polypropylenes of varying stereoregular form and tacticity

We investigated the crystallization and orientation development in melt spinning and tubular blown film extrusion of several different types of polypropylenes, including conventional high tacticity isotactic polypropylenes (iPP) and metallocene catalyst low tacticity iPPs and syndiotactic polypropylenes (sPP). The fiber and film samples were characterized by wide‐angle X‐ray diffraction (WAXD), birefringence and differential scanning calorimetry (DSC). In melt spinning iPP, we found that the mesomorphic structure of iPP is more readily formed in lower tacticity fibers, and significant amounts of hexagonal β‐form crystals are found in low tacticity iPP fibers spun at high draw‐down ratios. Low tacticity iPP fibers exhibited a significant decrease in the crystalline chain‐axis orientation at high draw‐down ratios, resulting from increased epitaxially branched lamellae. Melt‐spun sPP fibers exhibit Form I helical structure at low spinning speeds and Form III zigzag all trans structure at high spinning speeds. We found that the level of spinline stress is the governing factor for this structural change. Melt‐spun sPP fibers exhibit much higher chain‐axis (c‐axis) orientation factors (f_c) and lower birefringence than iPP fibers spun at the same spinline stresses. In tubular blown sPP films, the a‐axis of Form I unit cell tends to orient perpendicular to the film surface, while the b‐axis of monoclinic α unit cell does so in iPP blown films.     

Orientation and property correlations for LLDPE blown films

The orientation and property correlations of biaxially oriented polyethylene (PE) blown films have been studied. A linear low density polyethylene (LLDPE) (DOWLEX ? 2045A) was used to fabricate films at different conditions with blow up ratio, die gap, and frost line height as the variables. The White‐Spruiell orientation factors of crystal unit cells, amorphous chains, and Herman's orientation factors of lamellae were determined from wide‐angle X‐ray diffraction pole figure, birefringence, and small angle X‐ray scattering (SAXS). A general orientation pattern with the crystal unit cell a‐axis preferentially oriented to MD, b‐axis to TD, lamellae stacking along the MD, and amorphous chains preferentially to the MD has been found for all films in this study. A correlation between the orientation of each element of the morphology hierarchy has been revealed. Key mechanical properties including dart impact and Elmendorf tear strength in both MD and TD have been determined. Good correlation has been found among these properties. Most importantly, these properties have excellent correlation to the orientation. These correlations have been linked to underlying morphology and microdeformation mechanisms. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 898–907, 2006     

Shear flow‐induced orientation and structural recovery of multiwalled carbon nanotube in poly(ethylene oxide) matrix

In the present work we studied the flow induced multiwalled carbon nanotube (MWCNT) orientation and the mechanisms governing the kinetics of nanotube reorientation and three‐dimensional network restructuring in poly(ethylene oxide) (PEO)/MWCNT nanocomposites. For this purpose, the linear and nonlinear viscoelastic experiments including frequency sweep, time sweep and transient tests were performed on PEO/MWCNT samples varying in MWCNT content. The extent as well as kinetics of network restructuring was found to be strongly dependent upon the amount of preshearing (shear rate and shearing time) and MWCNT concentration. The results also showed two mechanisms for structural recovery; a fast restructuring at the beginning due to rejoining of clusters and unoriented adjacent nanotube and much slower recovery in the longer annealing times due to Brownian motion. The latter mechanism was found to be uncompleted over 3600 s annealing. This was supported by a_ij (orientation tensors) calculated based on transmission electron micrograph. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41753.     

Detecting structural orientation in isoprene rubber/multiwall carbon nanotube nanocomposites at different scales during uniaxial deformation

Enhanced strain‐induced crystallization (SIC) behavior in isoprene rubber/multiwall carbon nanotube (IR/MWCNT) nanocomposites was analyzed in terms of structural orientation during uniaxial deformation. In situ synchrotron wide‐angle X‐ray diffraction and small‐angle X‐ray scattering (SAXS) reveal the molecular orientation in IR/MWCNT composites at different scales. The inclusion of MWCNTs leads to a decrease in the molecular orientation at small strain due to the promotion of SIC. Meanwhile, the presence of MWCNTs induces a large‐scale orientation within the vulcanized rubber network based on SAXS results. Considering the heterogeneous nature of the vulcanized network, the nucleation process during SIC is discussed from the viewpoint of thermodynamics. The oriented large‐scale structure in IR/MWCNT composites is composed of local rubber chains stretched up MWCNTs, from which the additional nuclei are induced. By forming a bound rubber layer around MWCNTs through attractive interactions, MWCNTs can amplify the local strain of rubber segments and form a highly oriented large‐scale structure, but without altering the overall molecular orientation level. The evolution of detailed structural orientation in MWCNT‐filled rubber composites during deformation is revealed for the first time. © 2017 Society of Chemical Industry     

Ionic occupation,structures, and microwave dielectric properties of Y3MgAl3SiO12 garnet‐type ceramics

The Y₃MgAl₃SiO₁₂ ceramics with pure phase were successfully synthesized by solid‐state sintering reaction method for the first time. Their microwave dielectric properties were investigated as a function of sintering temperature. Their microstructure characteristics and ionic occupation sites of tetrahedral and octahedral units were characterized and analyzed by SEM& energy dispersive spectrometer (EDS) and Rietveld refinement of X‐ray powder diffraction data. Crystal structure of Y₃MgAl₃SiO₁₂ is isostructural to Y₃Al₅O₁₂ with a cubic garnet structure and space group of Ia‐3d, which contains YO₈ dodecahedra, (Mg/Al_oct)O₆ octahedral, and (Si/Al_tet)O₄ tetrahedral units. The Qf and ε_r values of different samples are strongly dependent on the distribution of grain sizes, grain sizes, and porosity. The samples sintered at 1550°C exhibit optimized microwave dielectric properties with relative permittivity (?_r) of 10.1, Qf values of 57 340GHz (at 9.5 GHz), and τ_f values of ?32 ppm/°C. Such properties indicate potential application of Y₃MgAl₃SiO₁₂ as microwave substrates.     

Crystal structures and orientation development in tubular film extrusion of syndiotactic polypropylene and isotactic polypropylene

The differences in behavior of isotactic polypropylene (iPP) and syndiotactic polypropylene (sPP) in tubular film extrusion are qualitatively described. The crystalline form and orientation in the films were characterized using wide‐angle X‐ray diffraction (WAXD) patterns, pole‐figure analysis and birefringence. The sPP films had the crystalline form of the disordered Form I and the a‐crystallographic axis was found to be preferentially oriented in the film normal direction (ND) under the conditions of biaxial stresses. High transverse orientations were developed in the sPP films. In the iPP films, the monoclinic crystalline form was found and the b‐crystallographic axis was preferentially oriented in the ND. The birefringence of the films showed trends very similar to the crystalline orientations characterized by WAXD in both iPP and sPP films.     

Morphological effect of fillers on graphite reinforced polydicyclopentadiene based composites

Graphite reinforced polydicyclopentadiene (polyDCPD) composites were synthesized via the in situ ring‐opening metathesis polymerization (ROMP) of DCPD with vapor‐grown carbon fiber (VGCF), acidified multiwall carbon nanotube (a‐MWCNT), and mildly oxidized graphene oxide (MOGO) as distinctive reinforcing fillers, respectively. We studied the morphological effect of the fillers on the mechanical and thermal properties of graphite/polyDCPD composites. Mechanical property tests showed that the addition of VGCF greatly strengthened the tensile strength, the introduction of a‐MWCNT dramatically extended the elongation at break, whereas the incorporation of MOGO enhanced both performances of the resulting composites. Impact tests showed that the maximum mechanical performances of a‐MWCNT/polyDCPD and MOGO/polyDCPD composites both were got with 0.4 wt% of fillers (a‐MWCNT and MOGO) loading. Meanwhile, all of the reinforced composites exhibited increased thermal stabilities compared with the unfilled polyDCPD, confirmed by increased T_gs and thermal decomposition temperatures at 5 wt% weight loss. POLYM. COMPOS., 35:1918–1925, 2014. © 2014 Society of Plastics Engineers     

Structure and properties of melt‐spun PET/MWCNT nanocomposite fibers

Polyethylene terephthalate (PET) melt‐spun fibers were modified with multiwall carbon nanotubes (MWCNT) to obtain conductive microfibers smaller than 90 μm in diameter. Physical properties such as crystallinity and orientation of as‐spun fibers were studied by X‐ray diffraction, Raman spectroscopy, and microscopy techniques at different draw ratios (DR) and MWCNT concentrations. Morphological and orientation analysis of MWCNT after melt‐spinning process showed agglomerates formation and highly oriented CNTs. The study of the orientation of PET crystalline phase in drawn fibers proved that the addition of nanoparticles decreases the orientation of crystalline units inside the fibers. The orientation of MWCNT as well as that of PET chains was studied using Raman spectroscopy at different DR and a high degree of CNT orientation was observed under high DR conditions. Mechanical and electrical properties of as‐spun fibers were also investigated. Our results showed that it was possible to achieve conductive fibers at a MWCNT concentration of 2% w/w, and more conductive fibers using higher DR were also obtained without increasing the MWCNT concentration. Mechanical properties results showed interestingly high value of maximum tensile strain at break (ε_max) of nanocomposite fibers, up to three times more than pure PET fibers. POLYM. ENG. SCI., 50:1956–1968, 2010. © 2010 Society of Plastics Engineers     

Polyethylenimine‐functionalized multiwalled carbon nanotube for the adsorption of hydrogen sulfide

Functionalized multiwalled carbon nanotubes (MWCNTs) were synthesized with ethane diamine and polyethylenimine (PEI) with molecular weights of 1800 [MWCNT‐PEI weight‐average molecular weight (M_w) = 1800] and 70,000 (MWCNT‐PEI M_w = 70,000), respectively. The structures and properties of the ethane diamine functionalized MWCNTs and PEI‐functionalized MWCNTs were characterized by Raman spectroscopy, thermogravimetric analysis, X‐ray powder diffraction, and scanning electron microscopy. An increase with the D/G (D, Disorder band; G, Graphite) ratio of the functionalized MWCNTs in the Raman spectra proved that the ethane diamine and PEI were successfully bonded to the surface of the pristine MWCNTs. The results of TGA also confirmed this. In addition, the structure of the functionalized MWCNTs showed no significant changes compared with the pristine MWCNTs; this was confirmed by X‐ray powder diffraction. Hydrogen sulfide (H₂S) sorption on the functionalized MWCNTs was studied by UV spectroscopy. As expected, the results of UV spectroscopy shows that the MWCNTs bonded with higher molecular weight PEI had a more excellent H₂S adsorption efficiency than those bonded with low‐molecular‐weight PEI and ethane diamine, a micromolecular amine. The effects of the pH and temperature on the adsorption of H₂S were also studied. Under the conditions investigated, the maximum first‐time H₂S adsorption efficiency of 1.94 mmol/g was observed for MWCNT‐PEI (M_w = 70,000) in the 60 mg/L sodium hydrosulfide (NaHS) aqueous solution. In addition, the H₂S reversible adsorption of the functionalized MWCNTs was conducted, and the second‐time H₂S adsorption efficiency of MWCNT‐PEI (M_w = 70,000) reached 1.83 mmol/g in the 60 mg/L NaHS aqueous solution. The results demonstrate that the MWCNTs decorated with high‐molecular‐weight PEI were potentially excellent and reversible H₂S adsorbents. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44742.     

In situ polymerization and photophysical properties of poly(p‐phenylene benzobisoxazole)/multiwalled carbon nanotubes composites

Poly(p‐phenylene benzobisoxazole)/multiwalled carbon nanotubes (PBO‐MWCNT) composites with different MWCNT compositions were prepared through in situ polymerization of PBO in the presence of carboxylated MWCNTs. The nanocomposite's structure, thermal and photophysical properties were investigated and compared with their blend counterparts (PBO/MWCNT) using Fourier transform infrared spectra, Raman spectra, Wide‐angle X‐ray diffraction, thermogravimetric analysis, UV‐vis absorption, and photoluminescence. The results showed that MWCNTs had a strong interaction with PBO through covalent bonding. The incorporation of MWCNTs increased the distance between two neighboring PBO chains and also improved the thermal resistance of PBO. The investigation of UV‐vis absorption and fluorescence emission spectra exhibited that in situ PBO‐MWCNT composites had a stronger absorbance and obvious trend of red‐shift compared with blend PBO/MWCNT composites for all compositions. This behavior can be attributed to the efficient energy transfer through forming conjugated bonding interactions in the PBO‐MWCNT composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of luminance of samples on color discrimination ellipses: Analysis and prediction of data

Four data sets are analyzed to quantify three effects of luminance of samples on chromaticity discrimination: on ellipse area, axis dimensions (a and b), and a/b ratio. Ellipses for aperture, surface, and simulated surface colors in CIE 1931 and 1964 x, y, Y color spaces are shown to reduce axis dimensions with higher luminance by different functions for the major and minor axes. Reduction is greater for major than minor axes, thus improving ellipse circularity. The functions plot straight lines in log‐log scale as power law equations, except luminances below 3 cd/m². We give formulae to predict a and b axes, a/b ratio, and ellipse area for almost any luminance in x, y, Y spaces. Effect of luminance is remarkable on ellipse area, which on average halves with every 3.5 times higher luminance. To illustrate the substantial effects of luminance, RIT‐DuPont ellipses are predicted for three levels of equal luminance at 42, 212, and 2120 cd/m². In the latter, ellipses are much smaller and are nearer circular than in the former. Higher luminance is known to improve color discrimination, so reduced ellipse area is to be expected but does not occur in CIELAB and DIN99 spaces because of lack of luminance‐level dependency. We discuss our results' implications on uniform color space. Weber fraction ΔY/Y indicates brightness discrimination decreases with increasing luminance and is thus independent of chromaticity discrimination. © 2005 Wiley Periodicals, Inc. Col Res Appl, 30, 186–197, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/col.20107     

Hybridizing MWCNT with nano metal oxides and TiO2 in epoxy composites: Influence on mechanical and thermal performances

In this study, the effects of multi‐walled carbon nanotubes (MWCNT), and its hybrids with iron oxide (Fe₂O₃) and copper oxide (CuO) nanoparticles on mechanical characteristics and thermal properties of epoxy binder was evaluated. Furthermore, simultaneous effects of using MWCNT with TiO₂ as pigment and CaCO₃ as filler for epoxy composites were determined. To investigate effects of nano‐ and micro‐particles on epoxy matrix, the samples were evaluated by TGA and DTA. It was found that the hybrid of MWCNT with nano metal oxides caused considerable increment in the tensile and flexural properties of epoxy samples in comparison to the single MWCNT containing samples at the same filler contents. Significant improvement in the thermal conductivity of epoxy samples was obtained by using TiO₂ pigment along with MWCNT. The TiO₂ pigment also caused considerable improvement in mechanical properties of the epoxy matrix and the MWCNT containing nanocomposite. The best mechanical and thermal properties of epoxy nanocomposites were obtained at 1.5 wt % of MWCNT and 7 wt % of TiO₂ that it should be attributed to particle network forming of the particles which cause better nano/micro dispersion and properties. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43834.     

Interaction of melt spinning and drawing variables on the crystalline morphology and mechanical properties of high-density and low-density polyethylene fiber

An experimental study of the spinnability and the variation in crystallinity and orientation in high-density and low-density polyethylene fibers with melt spinning and drawing conditions has been carried out. Three polymers (two high-density and one low-density) and eicosane (C₂₀H₄₂) were studied. The maximum spinnability was in the lower molecular weight high-density polyethylene. Hermans-Stein a, b, and c crystallographic axis orientation factors were computed from wide-angle x-ray scattering patterns. In the spun fiber, small take-up velocities cause the b axis to become perpendicular to the fiber axis in each fiber. The c axis increasingly orients itself parallel to the fiber axis as take-up velocity increases. The a axis orientation is different for each polymer. The results are interpreted in terms of modern theories of crystalline morphology, specifically the development of row structures. In the drawing experiments, the two high-density polyethylenes necked. A phenomenological theory of necking is discussed. The a, b, and c axis orientation factors were determined for different stages of drawing. In the necked regions and in completely drawn fibers, the c axis was parallel to the fiber axis and the a and b axes are perpendicular to the fiber axis. The tangent Young's modulus and tensile strength of the spun fibers increased with take-up velocity and in the drawn fibers were an order of magnitude higher than in the spun fiber. The mechanical properties of spun fiber may be correlated with the c axis (Hermans) orientation factor. The drawn fiber shows significant variations in Young's modulus and tensile strength at constant unit cell orientation.