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PBT Matrix (pbt + matrix)
Selected AbstractsSynthesis and properties of poly(butylene terephthalate)/multiwalled carbon nanotube nanocomposites prepared by in situ polymerization and in situ compatibilizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Fangjuan Wu Abstract A novel cyclic initiator was synthesized from dibutyl tin(IV) oxide and hydroxyl-functionalized multiwalled carbon nanotubes (MWNTs) and was used to initiate the ring-opening polymerization of cyclic butylene terephthalate oligomers to prepare poly(butylene terephthalate) (PBT)/MWNT nanocomposites. The results of Fourier transform infrared and NMR spectroscopy confirmed that a graft structure of PBT on the MWNTs was formed during the in situ polymerization; this structure acted as an in situ compatibilizer in the nanocomposites. The PBT covalently attached to the MWNT surface enhanced the interface adhesion between the MWNTs and PBT matrix and, thus, improved the compatibility. The morphologies of the nanocomposites were observed by field emission scanning electron microscopy and transmission electron microscopy, which showed that the nanotubes were homogeneously dispersed in the PBT matrix when the MWNT content was lower than 0.75 wt %. Differential scanning calorimetry and thermogravimetric analysis were used to investigate the thermal properties of the nanocomposites. The results indicate that the MWNTs acted as nucleation sites in the matrix, and the efficiency of nucleation was closely related to the dispersion of the MWNTs in the matrix. Additionally, the thermal stability of PBT was improved by the addition of the MWNTs. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Synthesis and characterization of poly(butylene terephthalate)/mica nanocomposite fibers via in situ interlayer polymerizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007Jin-Hae Chang Abstract Intercalated nanocomposites consisting of poly(butylene terephthalate) (PBT) incorporated between mica layers were synthesized from dimethyl terephthalate (DMT) and 1,4-butanediol (BD) by in situ interlayer polymerization. PBT nanocomposites of varying organoclay content were melt-spun to produce monofilaments. The samples were characterized using wide angle X-ray diffraction, electron microscopy, thermal analysis, and tensile testing. Some of the clay particles were found to be well dispersed in the PBT matrix, but other clay particles were agglomerated at a size level greater than approximately 20 nm. The glass transition temperatures (Tg) and the thermal degradation properties (TDi) of undrawn PBT hybrid fibers were found to improve with increases in the clay content. At draw ratio (DR) = 1, the ultimate tensile strengths of the hybrid fibers increased with the addition of clay up to a critical content and then decreased. However, the initial moduli monotonically increased with increases in the amount of organoclay in the PBT matrix. The ultimate strengths were found to decrease linearly with increases in DR from 1 to 18. In contrast to the trend for the tensile strengths, the initial moduli of the hybrid fibers increased only slightly with increases in DR up to 18. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] On Toughness and Stiffness of Poly(butylene terephthalate) with Epoxide-Containing Elastomer by Reactive ExtrusionMACROMOLECULAR MATERIALS & ENGINEERING, Issue 8 2004Zhong-Zhen Yu Abstract Summary: To obtain a balance between toughness (as measured by notched impact strength) and elastic stiffness of poly(butylene terephthalate) (PBT), a small amount of tetra-functional epoxy monomer was incorporated into PBT/[ethylene/methyl acrylate/glycidyl methacrylate terpolymer (E-MA-GMA)] blends during the reactive extrusion process. The effectiveness of toughening by E-MA-GMA and the effect of the epoxy monomer were investigated. It was found that E-MA-GMA was finely dispersed in PBT matrix, whose toughness was significantly enhanced, but the stiffness decreased linearly, with increasing E-MA-GMA content. Addition of 0.2 phr epoxy monomer was noted to further improve the dispersion of E-MA-GMA particles by increasing the viscosity of the PBT matrix. While use of epoxy monomer had little influence on the notched impact strength of the blends, there was a distinct increase in the elastic stiffness. SEM micrographs of impact-fracture surfaces indicated that extensive matrix shear yielding was the main impact energy dissipation mechanism in both types of blends, with or without epoxy monomer, and containing 20 wt.-% or more elastomer. SEM micrographs of freeze-fractured surfaces of PBT/E-MA-GMA blend illustrating the finer dispersion of E-MA-GMA in the presence of epoxy monomer. [source] Crystallization and thermal behavior of multiwalled carbon nanotube/poly(butylenes terephthalate) compositesPOLYMER ENGINEERING & SCIENCE, Issue 6 2008Defeng Wu Multiwalled carbon nanotube/poly(butylene terephthalate) composites (PCTs) were prepared by melt mixing. The nonisothermal crystallization and thermal behavior of PCTs were respectively investigated by X-ray diffractometer, polarized optical microscope, differential scanning calorimeter, dynamic mechanical thermal analyzer, and thermogravimetric analyzer. The presence of nanotubes has two disparate effects on the crystallization of PBT: the nucleation effect promotes kinetics, while the impeding effect reduces the chain mobility and retards crystallization. The kinetics was then analyzed using Ozawa, Mo, Kissinger, Lauritzen-Hoffman, and Ziabicki model, and the results reveal that the nucleation effect is always the dominant role on the crystallization of PBT matrix. Thus the crystallizability increases with increase of nanotube loadings. In addition, the presence of nanotubes nearly has no remarkable contribution to thermal stability because nanotubes also play two disparate roles on the degradation of PBT matrix: the Lewis acid sites to facilitate decomposition and the physical hindrance to retard decomposition. Hence the nanotubes act merely as inert-like filler to thermal stability. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Influence of the degree of grafting on the morphology and mechanical properties of blends of poly(butylene terephthalate) and glycidyl methacrylate grafted poly(ethylene- co -propylene) (EPR)POLYMER INTERNATIONAL, Issue 8 2006SL Sun Abstract Poly(ethylene- co -propylene) (EPR) was functionalized to varying degrees with glycidyl methacrylate (GMA) by melt grafting processes. The EPR- graft -GMA elastomers were used to toughen poly(butylene terephthalate) (PBT). Results showed that the grafting degree strongly influenced the morphology and mechanical properties of PBT/EPR- graft -GMA blends. Compatibilization reactions between the carboxyl and/or hydroxyl of PBT and epoxy groups of EPR- graft -GMA induced smaller dispersed phase sizes and uniform dispersed phase distributions. However, higher degrees of grafting (>1.3) and dispersed phase contents (>10 wt%) led to higher viscosities and severe crosslinking reactions in PBT/EPR- graft -GMA blends, resulting in larger dispersed domains of PBT blends. Consistent with the change in morphology, the impact strength of the PBT blends increased with the increase in EPR- graft -GMA degrees of grafting for the same dispersion phase content when the degree of grafting was below 1.8. However, PBT/EPR- graft -GMA1.8 displayed much lower impact strength in the ductile region than a comparable PBT/EPR- graft -GMA1.3 blend (1.3 indicates degree of grafting). Morphology and mechanical results showed that EPR- graft -GMA 1.3 was more suitable in improving the toughness of PBT. SEM results showed that the shear yielding properties of the PBT matrix and cavitation of rubber particles were major toughening mechanisms. Copyright © 2006 Society of Chemical Industry [source] | ||||||||||