No abstract

No abstract

No abstract

The functionalization of poly(ethylene terephthalate) (PET) surface films by reactions with multifunctional amines such as triethylenetetramine (TETA), and tetraethylenepentamine (TEPA) was investigated. For the functionalization of PET films surface we used a new way of treatment, a \u27sandwich model\u27. Physical-chemical properties of functionalized PET films were analysed. Qualitative and quantitative determination of the introduced amine groups were examined by means of Fourier Transform Infrared Attenuated Total Reflexion(FTIR - ATR), X-ray photoelectron spectroscopy (XPS), and potentiometric titration. Gained wetting properties were determined by using contact angle measurements and thoroughly analysed by acid-base approach. In addition, surface topography was investigated by atomic force microscopy (AFM). The amount of the introduced amino groups after TETA incorporation has been found to be two times higher as compared to TEPA. Wetting properties were significantly improved after aminolysis. Surface free energy was higher for PET - TETA treated film than that observed for PET - TEPA treated which is in accordance with titration results. The collagen immobilization onto PET treated films was evidenced by using AFM and subsequently by using XPS

Surface of biaxially oriented poly(ethylene terephthalate) films was chemically modified by exposure to ethylenediamine (EDA), triethylenetetramine (TETA), and tetraethylenepentamine (TEPA) for different treatment times. Variable angle attenuated total reflection Fourier transform infrared (ATR‐FTIR) spectroscopy was used in conjunction with weight loss measurements, scanning electron microscopy (SEM), and atomic force microscopy to establish the surface modification and to draw the depth profile of the newly created species, with emphasis on amide group. A clear differentiation was found between the effects of the three amines studied: EDA produces the highest amidation degree but, because of its deep penetration into the film, leads to delamination of rather thick layers, TETA reacts at and near surface and develops surface cracks without delamination, and TEPA is the mildest reactant, generating amide groups on the surface without visible deterioration of the sample. It was proved that the amide II absorption band became weaker with increasing analyzed depth, with a pronounced heterogeneity near the surface. SEM micrographs showed the development of cracks onto the surface at longer aminolysis time, which allowed a better understanding of ATR‐FTIR observations. Assuming an exponential decay for the depth profile spectrally obtained, the surface concentration of amide groups and the decay constant were determined for the amines and reaction times used. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010

No abstract

No abstract

Hemp fibres used as a reinforcing agent and three polymeric matrices (polypropylene, bicomponent, recycled polyester) were used to obtain composite materials by needle punching and heat pressing. The influence of the hemp/matrix ratio and the nature of the matrix on the properties of the composites were analysed. The obtained composites were characterised by physical–mechanical indices, thermal analysis (thermogravimetry (TG), differential thermogravimetry (DTG) and Differential Scanning Calorimetry (DSC)), Fourier Transform Infrared Spectroscopy (FTIR-ATR) analysis, Scanning Electron Microscopy (SEM) and Chromatic measurements. The mechanical properties of composites are influenced by both the hemp/matrix ratio and the nature of the matrix. The thermal stability of composites decreased as the amount of hemp increased (for the same mass losses, the decomposition temperature decreased significantly for composites containing a quantity of hemp greater than 50%). Regarding the nature of the matrix, for the same mass loss, the highest decomposition temperature was presented by the composites containing recycled polyester as matrix, and the lowest one was presented by composites containing polypropylene fibres as matrix. The FTIR and SEM analyses highlight the changes that occurred in the structure of the composite, changes determined both by the amount of hemp in the composite and by the nature of the matrix.