Exploring the Effects of Stereo-Defect Distribution on Nonisothermal Crystallization and Melting Behavior of β-Nucleated Isotactic Polypropylene/Graphene Oxide Composites.

In this work, using two isotactic polypropylene (iPP) resins with similar average isotacticity and molecular weight but different uniformities of stereo-defect distribution, the β-nucleated iPP/graphene oxide (β-iPP/GO) composites (NPP-A and NPP-B) were prepared to investigate the effect of stereo-defect distribution on the nonisothermal crystallization kinetics and polymorphic melting behavior of the composites by means of scanning electron microscopy, wide-angle X-ray diffraction, and differential scanning calorimetry. The results showed that more uniform stereo-defect distribution led to a slight increase of the crystallization rate and decrease of the crystallization activation energy . NPP-B with more uniform stereo-defect was more favorable for the formation of a large amount of β-phase.

Effect of structure regulation of hyper-branched polyester modified carbon nanotubes on toughening performance of epoxy/carbon nanotube nanocomposites.

In this paper, carboxylic multi-walled carbon nanotubes (MWCNTs-COOH) were modified by a series of hyperbranched polyesters (HBP) with different molecular structures (different branching degree) through surface grafting, and then the epoxy resin (EP)/carbon nanotube composites were prepared to explore the influences of structure regulation of HBP modified carbon nanotubes on the toughening performance of the composites. The results of Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA) of various HBP grafted carbon nanotubes confirmed that the HBP were successfully grafted onto MWCNTs-COOH an esterification reaction between the carboxyl groups of MWCNTs-COOH and the hydroxyl groups of HBP, meanwhile, the higher the branching degree of the HBP, the higher its grafting ratio onto carbon nanotubes. Furthermore, the outcome of dynamic thermal mechanical analysis (DMA) indicated that the addition of MWCNTs-COOH increased the storage modulus and glass transition temperature ( ) of the pure EP, and surface grafting of various HBP onto MWCNTs-COOH decreased the and peak height of mechanical loss of composites.

Influences of Hyperbranched Polyester Modification on the Crystallization Kinetics of Isotactic Polypropylene/Graphene Oxide Composites.

In this study, the hyperbranched polyester grafted graphene oxide (GO-H202) was synthesized, and the isotactic polypropylene/graphene oxide (iPP/GO) composites were prepared. Results of X-ray photoelectron spectra (XPS), Fourier transform infrared (FT-IR), and transmission electron microscopy (TEM) revealed the successful synthesis of GO-H202, while thermogravimetric analysis (TGA) indicated that the weight ratio of grafting was about 35 wt %. Differential scanning calorimetry (DSC) and polarized optical microscopy (POM) were carried out to investigate the role of GO and GO-H202 on the crystallization kinetics of the composites.

Investigation on cure kinetics of epoxy resin containing carbon nanotubes modified with hyper-branched polyester.

The cure kinetics of epoxy resin cured by diethyltoluene diamine (D-EP), D-EP/multi-walled carbon nanotube (D-EP/CNT) composites and D-EP/hyper branched polyester functionalized CNTs (D-EP/CNTs-H20) were investigated by non-isothermal differential scanning calorimetry (DSC). Results revealed that the presence of CNTs shifted the cure temperature to a lower temperature and accelerated the curing of D-EP, and the addition of CNTs-H20 exhibited a stronger effect in accelerating the cure of D-EP. Activation energies were calculated based on the Kissinger approach and Ozawa approach respectively.