Preparation of Poly(o-toluidine)/Nano ZrO2/Epoxy Composite Coating and Its Application for Corrosion Protection of Steel

The main objective was to study the anticorrosion performance of poly（o-toluidine）/nano ZrO2/epoxy composite coating.Poly（o-toluidine）/nano ZrO2 composite was prepared by in situ polymerization of o-toluidine monomer in the presence of nano ZrO2 particles.Fourier transformation infrared spectroscopy（FT-IR）,UV-visible spectroscopy（UV-vis）,X-ray diffraction（XRD）,Scanning electron microscopy（SEM）,and Thermogravimetric analysis（TGA） were used to characterize the composition and structure of the composite.Poly（o-toluidine）/nano ZrO2 composite was mixed with epoxy resin through a solution blending method and the three components poly（o-toluidine）/nano ZrO2/epoxy composite coating was coated onto the surface of steel sample by the brush coating method.The anticorrosion performance of poly（o-toluidine）/nano ZrO2/epoxy composite coating on steel sample was studied by polarization curve and electrochemical impendence spectroscopy in 3.5% Na Cl solution as corrosion environment and also compared with that of poly（o-toluidine）/epoxy composite coating and pure epoxy coating.It was observed that the composite coating containing poly（otoluidine）/nano ZrO2 composite has got higher corrosion protection ability than that of poly（o-toluidine）.The electrochemical measurement results demonstrated that poly（o-toluidine） fillers improve the electrochemical anticorrosion performance of epoxy coating and the addition of nano ZrO2 particles increases the tortuosity of the diffusion pathway of corrosive substances.

Comparison of Chain Structures between High-speed Extrusion Coating Polyethylene Resins by Preparative Temperature Rising Elution Fractionation and Cross-fractionation

Two polyethylene（PE） resins（samples A and B） are synthesized as high-speed extrusion coatings with similar minimum coating thickness and neck-in performance but different maximum coating speeds. Both samples are separated into seven fractions using preparative temperature rising elution fractionation. The microstructures of the original samples and their fractions are studied by high-temperature gel permeation chromatography, Fourier transform infrared spectroscopy, 13 C nuclear magnetic resonance spectroscopy, differential scanning calorimetry, and successive self-nucleation/annealing thermal fractionation. Compared with sample B, sample A has a broader MWD, more LCB contents, and less SCB contents. Moreover, sample A contains slightly more 30 ℃ and 50 ℃ fractions with lower molecular weights, and more fractions at 75 ℃ and 85 ℃ with higher molecular weight. The chain structure and its distribution in the two PE resins are studied in detail, and the relationship between the chain structure and resin properties is also discussed.