Mingtao Run

Liquid Crystalline Phase Behavior and Sol–Gel Transition in Aqueous Halloysite Nanotube Dispersions

The liquid crystalline phase behavior and sol-gel transition in halloysite nanotubes (HNTs) aqueous dispersions have been investigated by applying polarized optical microscopy (POM), macroscopic observation, rheometer, small-angle X-ray scattering, scanning electron microscopy, and transmission electron microscopy. The liquid crystalline phase starts to form at the HNT concentration of 1 wt %, and a full liquid crystalline phase forms at the HNT concentration of 25 wt % as observed by POM and macroscopic observation. Rheological measurements indicate a typical shear flow behavior for the HNT aqueous dispersions with concentrations above 20 wt % and further confirm that the sol-gel transition occurs at the HNT concentration of 37 wt %. Furthermore, the HNT aqueous dispersions exhibit pH-induced gelation with more intense birefringence when hydrochloric acid (HCl) is added. The above findings shed light on the phase behaviors of diversely topological HNTs and lay the foundation for fabrication of the long-range ordered nano-objects.

Studies on the Morphological, Rheological, Electrical, Mechanical and Thermal Properties of the PTT/SCF Composites:

Short carbon fiber reinforced poly(trimethylene terephthalate) composites (PTT/SCF) were investigated in their rheology behaviors, phase morphology, electrical, mechanical, and thermal properties by capillary rheometer, scanning electron microscope, universal tester, high insulation resistance meter, Q meter, and thermal gravimetric analyzer. PTT/SCF melt is the dilating fluid at a shear rate below 130 s-1, while it becomes pseudo-plastic fluid at a shear rate higher than 130 s- 1. Melt apparent viscosity and viscous flow activation energy increase initially, and then decrease as SCF content increases, which have maximum values with 2 wt% SCF. The interaction between SCF and PTT matrix is strong based on the observation from the fracture surface of composites. The tensile strength and rupture strength are all increased obviously with increasing SCF; while the impact strength reaches a maximum value as SCF contents is 5%. With increasing SCF content in matrix, the electrical resistivity is decreased, while the dielectric constant, and the dielectric loss tangent were increased.

Morphology, mechanical, rheological, and thermal properties study on the PTT/ABS/SCF composites

In order to improve the mechanical properties of the poly(trimethylene terephthalate) (PTT), both maleinized acrylonitrile–butadiene–styrene (ABS) and short carbon fiber (SCF) were melt-blended with PTT to prepare the composites and their morphology and properties were investigated in detail. When ABS content is fixed at 5 wt.% in composites, SCF can significantly improve the tensile and flexural strength as well as the impact strength of the matrix. The SCF has good interface adherence with the matrix. At glassy state, the storage modulus increases much with increasing SCF content. At rubbery state, the composites have larger cold-crystallization rate. At molten state, SCF first serves as lubricants and then as viscosity reinforcing agent for the matrix with increasing SCF. The composites melt exhibits increasing elastic behaviors with SCF. The composites have larger crystallization rate, but this accelerating effect decreases with excessive SCF content. The crystals formed in different composites are quite different in size or perfection.

Spherulite Morphology and Thermal Behaviors of Short Carbon Fiber/Poly(Trimethylene Terephthalate) Composites

The spherulite morphology and thermal behavior of short carbon fiber/poly (trimethylene terephthalate) (SCF/PTT) composites were investigated by polarized optical microscopy (POM), wide-angle X-ray diffraction (WAXD), and differential scanning calorimetry (DSC). The micrographs of the growing spherulites suggest the composites with more SCF content have faster nucleation rates; thus, their spherulite sizes are much smaller. Under the same cooling process, banded spherulites are detected in pure PTT as well as in SCF/PTT composites shown with decreasing band spacing with increasing radius. Melt-crystallization and melting behaviors in DSC indicate the SCF served as nucleating agents, increasing the crystallization rate of the PTT. When the samples were quenched from melt some microcrystals formed in SCF/PTT composites but not in pure PTT. When the SCF/PTT composites were heated to melt, they showed double melting peaks due to some less perfect crystals or thinner lamella formed during DSC scanning.

Mechanical Property, Crystal Morphology, and Nonisothermal Crystallization Kinetics of Poly(Trimethylene Terephthalate)/Maleinized Acrylonitrile-Butadiene-Styrene Blends

The mechanical properties, morphology, crystallization, and melting behaviors and nonisothermal crystallization kinetics of poly (trimethylene terephthalate)(PTT)/maleinized acrylonitrile-butadiene-styrene (ABS-g-MAH) blends were investigated by an impact tester, polarized optical microscopy, and differential scanning calorimetry (DSC). The results suggested that the ABS-g-MAH component served as both a nucleating agent for increasing the crystallization rate and as a toughening agent for improving the impact strength of PTT. When the ABS-g-MAH content was 5wt.%, the blend had the best toughness and a high crystallization rate. The blends showed different crystallization rates and subsequent melting behaviors due to their different ABS-g-MAH contents. The Ozawa theory and the method developed by Mo and coworkers were used to study the nonisothermal crystallization kinetics of the blends. The kinetic crystallization rate parameters suggested that the proper contents of ABS-g-MAH can highly accelerate the crystallization rate of PTT, but this effect nearly reaches saturation for ABS-g-MAH contents over 5%. The Ozawa exponents calculated from the DSC data suggested that the PTT crystals in the blends have similar growth dimensions as those in neat PTT, although they are smaller and/or imperfect. The effective activation energy calculated by the method developed by Kissinger also indicates that the blends with higher ABS-g-MAH content were easier to crystallize.

Synthesis and Characterizations of Poly(trimethylene terephthalate)-b-poly(tetramethylene glycol) Copolymers

A series of poly(trimethylene terephthalate)-b-poly(tetramethylene glycol) (PTT-PTMEG) copolymers were synthesized by two-step melt-polycondensation. The copolymers were characterized by using Fourier transform infrared spectroscopy (FTIR), 1H NMR spectroscopy, rheometer, differential scanning calorimetry (DSC), polarized optical microscopy (POM), thermal gravimetric analysis (TGA), and mechanical properties. The results suggest that by increasing the flexible PTMEG contents from 0% to 60 wt%, the copolymers show decreased glass transition temperatures, melting points, melt-crystallization temperatures, hardness, tensile strength, thermostability, and smaller spherulites dimensions; however it has much increased impact strength and elongation at breaking point. Compared with commercial poly(butylene terephthalate) (PBT)-type TPEE with 25 mol% flexible segments, PTT-type TPEE having 25 mol% flexible segments has a lower glass transition temperature, melting point, crystallization temperature, and much lower tensile strength although it has a much higher impact strength than that of PBT-type TPEE, and it is not suitably used as a commercial TPEE.

Study on Morphology, Rheology, and Mechanical Properties of Poly(trimethylene terephthalate)/CaCO3 Nanocomposites

For preparing good performance polymer materials, poly(trimethylene terephthalate)/CaCO3 nanocomposites were prepared and their morphology, rheological behavior, mechanical properties, heat distortion, and crystallization behaviors were investigated by transmission electron microscopy, capillary rheometer, universal testing machine, impact tester, heat distortion temperature tester, and differential scanning calorimetry (DSC), respectively. The results suggest that the nano-CaCO3 particles are dispersed uniformly in the polymer matrix. PTT/CaCO3 nanocomposites are pseudoplastic fluids, and the CaCO3 nanoparticles serve as a lubricant by decreasing the apparent viscosity of the nanocomposites; however, both the apparent viscosity and the pseudoplasticity of the nanocomposites increase with increasing CaCO3 contents. The nanoparticles also have nucleation effects on PTT’s crystallization by increasing the crystallization rate and temperature; however, excessive nanoparticles will depress this effect because of the agglomeration of the particles. The mechanical properties suggest that the CaCO3 nanoparticles have good effects on improving the impact strength and tensile strength with proper content of fillers. The nanofillers can greatly increase the heat distortion property of the nanocomposites.

Preparation, Morphology and Properties of Poly(Trimethylene Terephthalate)/Thermoplastic Polyester Elastomer Blends

Poly(trimethylene terephthalate)(PTT)/thermoplastic polyester elastomer (TPEE) blends were prepared and their miscibility, crystallization and melting behaviors, phase morphology, dynamic mechanical behavior, rheology behavior, spherulites morphology, and mechanical properties were investigated by differential scanning calorimetry (DSC), scanning electron microscopy (SEM), dynamic mechanical analysis (DMA), parallel-plate rotational rheometry, polarized optical microscopy (POM), wide angle X-ray diffraction (WAXD), universal tensile tester and impact tester, respectively. The results suggested that PTT and TPEE were partially miscible in the amorphous state, the TPEE rich phase was dispersed uniformly in the solid matrix with a size smaller than 2 μm, and the glass transition temperatures of the blends decreased with increasing TPEE content. The TPEE component had a good effect on toughening the PTT without depressing the tensile strength. The blends had improved melt viscosities for processing. When the blends crystallized from the melt state, the onset crystallization temperature decreased, but they had a faster crystallization rate at low temperatures. All the blends’ melts exhibited a predominantly viscous behavior rather than an elastic behavior, but the melt elasticity increased with increasing TPEE content. When the blends crystallized from the melt, the PTT component could form spherulites but their morphology was imperfect with a small size. The blends had larger storage moduli at low temperatures than that of pure PTT.

Dynamic rheological and dynamic thermomechanical properties of poly(trimethylene terephthalate)/short carbon fibre composites

The dynamic rheology and thermomechanical properties of poly(trimethylene terephthalate) (PTT)/short carbon fibre (CF) composites at different mechanical states were investigated by a rotational rheometer and a dynamic mechanical analyzer (DMA). At molten state, the composite melts were pseudo-plastic fluids, and the complex viscosity of the composite melts decreased much with increasing CF content because of the poor adhesion at the fiber/matrix interface. The viscous behavior was predominant rather than elastic behavior in the composites melt and viscous behavior was increased with increasing CF at low shearing frequency. An apparent slope change in storage modulus and loss modulus plot suggested that a structure change occurred in the melt that was dependent on shearing frequency. At glassy state, the storage modulus increased with increasing CF content, suggesting that CFs had good reinforcing effect on PTT. At glass transition region, the increasing loss modulus indicated a better toughness of the composites, and the elastic behavior was predominant rather than viscous behavior. Moreover, the glass-transition temperatures of the composites increased with 10% CF content. The composites have larger cold-crystallization rate than pure PTT.