Exploring the Surface Potential of Recycled Polyethylene Terephthalate Composite Supports on the Collagen Contamination Level.

With a significant number of features (namely being multipurpose, inexpensive and durable), thermoplastic polymers, most often named plastics, are part of our daily routine, with an increasing production over the last decade. Among them, polyethylene terephthalate (PET), high-density polyethylene (HDPE) and polypropylene (PP) are distinguished as the five most commonly used plastics in various fields, mainly in the packaging industry. Even if it is difficult to imagine the world without plastics, the boosted plastic assembly comes with huge plastic waste, creating a number of challenges, as the most important threat for our environment, but also opportunities for recycling. Currently, a special attention is dedicated on how to improve the current recycling methods or to find new ones, since the quality of recycled plastics and potential chemical or biological contaminations are two problematic aspects. Understanding the properties of each thermoplastic polymer and the interaction with possible contaminants may be the key for an efficient recycling process. The aim of this paper was to evaluate the surface behaviour of different composite supports based on recycled PET before and after interaction with collagen (used as a biological contaminant). The surface contamination bias of PET supports was studied through different techniques: scanning electron microscopy (SEM), water uptake through swelling studies, contact angle measurements and attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR).

The Impact of the Azo-Chromophore Sort on the Features of the Supramolecular Azopolyimide Films Desired to Be Used as Substrates for Flexible Electronics.

High-performance supramolecular polyimide systems were synthesized via a simple and innovative approach using two types of azo-chromophores, leading to concomitant special properties: high thermostability, the ability to be processed in the form of films with high flexibility, adequate morphological features, and good structuring capacity via phase mask ultraviolet (UV) laser irradiation, induced by the presence of the azo groups (-N=N-). The dimension and the anisotropy degree of the micro/nano patterns obtained on the surface of the flexible films (determined by atomic force microscopy) depend on the azo-dye type used in the supramolecular azopolyimide synthesis, which were higher when the azo-chromophore containing a -cyano group (-C≡N) was used. The molecular dynamics method, an excellent tool for an in-depth examination of the intermolecular interactions, was used to explain the morphological aspects. Energetic, dynamic and structural parameters were calculated for the two systems containing azo-chromophores, as well as for the pristine polymer system. It was highlighted that the van der Waals forces make a major contribution to the intermolecular interactions. The results from the combination of the dynamic analysis and the concentration profile explain the better mobility of the polyimide chains with a maximum content of azo groups in the cis configuration compared to the other systems. Taking all these data into account, the surfaces of the films can be tuned as required for the proposed applications, namely as substrates for flexible electronis.

Artificial Neural Network Modeling of Glass Transition Temperatures for Some Homopolymers with Saturated Carbon Chain Backbone.

The glass transition temperature (Tg) is an important decision parameter when synthesizing polymeric compounds or when selecting their applicability domain. In this work, the glass transition temperature of more than 100 homopolymers with saturated backbones was predicted using a neuro-evolutive technique combining Artificial Neural Networks with a modified Bacterial Foraging Optimization Algorithm. In most cases, the selected polymers have a vinyl-type backbone substituted with various groups. A few samples with an oxygen atom in a linear non-vinyl hydrocarbon main chain were also considered. Eight structural, thermophysical, and entanglement properties estimated by the quantitative structure-property relationship (QSPR) method, along with other molecular descriptors reflecting polymer composition, were considered as input data for Artificial Neural Networks. The Tg's neural model has a 7.30% average absolute error for the training data and 12.89% for the testing one. From the sensitivity analysis, it was found that cohesive energy, from all independent parameters, has the highest influence on the modeled output.

New Strategy for Inducing Surface Anisotropy in Polyimide Films for Nematics Orientation in Display Applications.

The operability of liquid crystal displays is strongly impacted by the orientation aspects of nematics, which in turn are affected by the alignment layer surface features. In this work, two polyimide (PI) structures are obtained based on a cycloaliphatic dianhydride and aromatic or aliphatic diamines with distinct flexibility. The attained PI films have high transmittance (T) for visible radiations, i.e., at 550 nm T > 80%. Here, a novel strategy for creating surface anisotropy in the samples that combines rubbing with a cloth and stretching via pressing is reported. Birefringence and atomic force microscopy (AFM) scans reveal that the generated orientation of the chains is affected by the chemical structure of the polymer and order of the steps involved in the surface treatment. Molecular modeling computations and wettability tests show that the PI structure and produced surface topography are competitive factors, which are impacting the intensity of the interactions with the nematic liquid crystals. The achieved results are of great relevance for designing of reliable display devices with improved uniform orientation of liquid crystals.

Evaluation of Local Mechanical and Chemical Properties via AFM as a Tool for Understanding the Formation Mechanism of Pulsed UV Laser-Nanoinduced Patterns on Azo-Naphthalene-Based Polyimide Films.

Aromatic polyimides containing side azo-naphthalene groups have been investigated regarding their capacity of generating surface relief gratings (SRGs) under pulsed UV laser irradiation through phase masks, using different fluencies and pulse numbers. The process of the material photo-fluidization and the supramolecular re-organization of the surface were investigated using atomic force microscopy (AFM). At first, an AFM nanoscale topographical analysis of the induced SRGs was performed in terms of morphology and tridimensional amplitude, spatial, hybrid, and functional parameters. Afterward, a nanomechanical characterization of SRGs using an advanced method, namely, AFM PinPoint mode, was performed, where the quantitative nanomechanical properties (i.e., modulus, adhesion, deformation) of the nanostructured azo-polyimide surfaces were acquired with a highly correlated topographic registration. This method proved to be very effective in understanding the formation mechanism of the surface modulations during pulsed UV laser irradiation. Additionally to AFM investigations, confocal Raman measurements and molecular simulations were performed to provide information about structured azo-polyimide chemical composition and macromolecular conformation induced by laser irradiation.