Current Topics in Plastic Recycling

This chapter presents an overview of current trends in plastic recycling and focuses on specific topics of interest. Firstly, there are presented all methods used for plastic recycling, along with the advantages and disadvantages of each method. Extra attention is paid to chemical recycling and especially, pyrolysis (thermal and catalytic), which is an environmentally friendly method that results in the formation of value-added products. Emphasis is given on three case studies where there are difficulties as regards the recycling of the plastic part: polymeric blends, since the existence of mixed plastic wastes may be challenging for their recycling; plastics originating in multilayer packaging, since the multilayer packaging consists of various materials, including plastics, paper, and metals that may be an obstacle for the recycling of the plastic part; and brominated flame-retarded plastics from waste electric and electronic equipment (WEEE), since in this case safe handling is required in order to avoid environmental contamination and a pretreatment step before recycling may be of paramount importance. These three case studies along with the mentioned difficulties and suggestions in order to overcome them are presented here, with the aim of offering insights for future studies on the management of plastic materials.

FTIR INVESTIGATION ON CRYSTALLINITY OF HYDROXYPROPYL METHYL CELLULOSE-BASED POLYMERIC BLENDS

Two series of polymeric blends have been prepared based on hydroxypropyl methyl cellulose (HPMC)/polyacrylic acid (PAA) (1:1, 1:2, 1:3, 1:4) and HPMC/sodium alginate (SA) (1:30, 2:30, 3:30, 4:40) and investigated by Attenuated Total Reflectance–Fourier Transform Infrared Spectroscopy (ATR-FTIR). IR analysis confirmed the interaction between the polymeric components in the blend and the degree of structural organization. Crystallinity changes in the blends were observed as a function of a number of experimental parameters, such as temperature, composition and HPMC concentration, by determining the quantitative crystallinity indexes: Total Crystallinity Index (TCI), Lateral Order Index (LOI) and Hydrogen Bond Index (HBI).

The Study of Recycled Ethylene Propylene Diene Monomer (EPDM-r)/Polypropylene (PP) Polymeric Blends

In this study, recycled ethylene propylene diene monomer (EPDM-r) were blended with polypropylene (PP) by compounding via heated two roll mills with the various ratio of EPDM-r. Certain blends were included with PP-g-MA as a compatibilizer. In tensile tests, the increasing of EPDM-r content in blends resulted in the reduction of tensile strength and Young’s Modulus but increased elongation at break. Furthermore, the presence of compatibilizer in blends enhanced the tensile properties. It was found all the samples with compatibilizer performs better results in tensile strength, Young’s Modulus, and elongation at break than samples without compatibilizer. On the other hand, the aging affected were studied on compatibilized and uncompatibilized blends. It was found that aging affects the samples by decreasing the tensile strength, Young’s Modulus, and elongation at break. The crosslink density had been found higher in the blends with high EPDM-r content as the EPDM-r had the ability to swell. The morphological study related to the structure with the tensile properties. It was confirmed that the presence of a compatibilizer increased the compatibility between EPDM-r and PP matrix.

Optical Heating Controlled With a Thermoplasmonic Metasurface

We develop a photothermal technology to control optical heating of polymer and liquid crystal films through a refractory titanium nitride (TiN) metasurface. The metasurface represents an array of identical square-shaped TiN nanoantennas on a Si substrate. Upon CW laser illumination, a TiN nanoantenna experiences anomalous Joule heating at a plasmon resonance. A temperature rise provides a unique opportunity for locally probing phase transitions. In the case of heterogeneous PMMA thin films or polymeric blends, a controlled optical heating is needed to probe the glass transition temperature (Tg) of their constituents. Here, we model a controlled thermal response originating from the TiN nanoantenna under CW laser illumination by using FDTD/FEM methods.

Effect of Direct Fluorination on the Transport Properties and Swelling of Polymeric Materials: A Review

Fluorine-containing polymers occupy a peculiar niche among conventional polymers due to the unique combination of physicochemical properties. Direct surface fluorination of the polymeric materials is one of the approaches for the introduction of fluorine into the chemical structure that allows one to implement advantages of fluorinated polymers in a thin layer. Current review considers the influence of the surface interaction of the polymeric materials and membranes with elemental fluorine on gas, vapor and liquid transport as well as swelling and related phenomena. The increase in direct fluorination duration and concentration of fluorine in the fluorination mixture is shown to result mostly in a reduction of all penetrants permeability to a different extent, whereas selectivity of the selected gas pairs (He-H2, H2-CH4, He-CH4, CO2-CH4, O2-N2, etc.) increases. Separation parameters for the treated polymeric films approach Robeson’s upper bounds or overcome them. The most promising results were obtained for highly permeable polymer, polytrimethylsilylpropyne (PTMSP). The surface fluorination of rubbers in printing equipment leads to an improved chemical resistance of the materials towards organic solvents, moisturizing solutions and reduce diffusion of plasticizers, photosensitizers and other components of the polymeric blends. The direct fluorination technique can be also considered one of the approaches of fabrication of fuel cell membranes from non-fluorinated polymeric precursors that improves their methanol permeability, proton conductivity and oxidative stability.

Multiphoton Laser Fabrication of Hybrid Photo-Activable Biomaterials

The possibility to shape stimulus-responsive optical polymers, especially hydrogels, by means of laser 3D printing and ablation is fostering a new concept of “smart” micro-devices that can be used for imaging, thermal stimulation, energy transducing and sensing. The composition of these polymeric blends is an essential parameter to tune their properties as actuators and/or sensing platforms and to determine the elasto-mechanical characteristics of the printed hydrogel. In light of the increasing demand for micro-devices for nanomedicine and personalized medicine, interest is growing in the combination of composite and hybrid photo-responsive materials and digital micro-/nano-manufacturing. Existing works have exploited multiphoton laser photo-polymerization to obtain fine 3D microstructures in hydrogels in an additive manufacturing approach or exploited laser ablation of preformed hydrogels to carve 3D cavities. Less often, the two approaches have been combined and active nanomaterials have been embedded in the microstructures. The aim of this review is to give a short overview of the most recent and prominent results in the field of multiphoton laser direct writing of biocompatible hydrogels that embed active nanomaterials not interfering with the writing process and endowing the biocompatible microstructures with physically or chemically activable features such as photothermal activity, chemical swelling and chemical sensing.

Special Issue: “Environmentally Friendly Polymeric Blends from Renewable Sources”

The aim of this Special Issue is to highlight the progress in the manufacturing,characterization, and applications of environmentally friendly polymeric blends from renewable resources [...]

Effects of Repulsion Parameter and Chain Length of Homopolymers on Interfacial Properties of An/Ax/2BxAx/2/Bm Blends: A DPD Simulation Study

We explored the effects of the repulsion parameter (aAB) and chain length (NHA or NHB) of homopolymers on the interfacial properties of An/Ax/2BxAx/2/Bm ternary polymeric blends using dissipative particle dynamics (DPD) simulations. Our simulations show that: (i) The ternary blends exhibit the significant segregation at the repulsion parameter (aAB = 40). (ii) Both the interfacial tension and the density of triblock copolymer at the center of the interface increase to a plateau with increasing the homopolymer chain length, which indicates that the triblock copolymers with shorter chain length exhibit better performance as the compatibilizers for stabilizing the blends. (iii) For the case of NHA = 4 (chain length of homopolymers An) and NHB (chain length of homopolymers Bm) ranging from 16 to 64, the blends exhibit larger interfacial widths with a weakened correlation between bead An and Bm of homopolymers, which indicates that the triblock copolymer compatibilizers (Ax/2BxAx/2) show better performance in reducing the interfacial tension. The effectiveness of triblock copolymer compatibilizers is, thus, controlled by the regulation of repulsion parameters and the homopolymer chain length. This work raises important considerations concerning the use of the triblock copolymer as compatibilizers in the immiscible homopolymer blend systems.

Blends Containing Amphiphilic Biopolymers. Compatibility Behavior

: This mini-review deals with the miscibility behavior of two biopolymers, chitosan, and alginate. It is well known that the miscibility in multifunctional polymers blends is favored due to specific interactions, which origin a negative heat of mixing. Particular interest is focused on functionalized polymers because they are the most suitable way to obtain interacting polymers, producing a single-phase material. Due to the polyfunctionality of chitosan (CS) and other biopolymers, they can be taken into account as a basis of a strongly interacting polymer. They would allow obtaining compatible polymeric materials. For this reason, blends containing CS with different vinyl polymers have been studied. The most significant polymeric blends with these natural polymers will be analyzed in this review. Chitosan is obtained from the biopolymer chitin through sequential processes of demineralization, deproteinization, and deacetylation. The native chitin is obtained by direct separation from the marine crustaceans shell, abundant on the sea coasts. Some classic results that relate to the polymeric blends containing amphiphilic polymers will be discussed. Another biopolymer of the coast is Sodium Alginate (SA). Alginate also allows the formation of compatible polymer blends. Results in this regard will also be analyzed in this review.

Graphene-Based Materials Immobilized within Chitosan: Applications as Adsorbents for the Removal of Aquatic Pollutants

Graphene and its derivatives, especially graphene oxide (GO), are attracting considerable interest in the fabrication of new adsorbents that have the potential to remove various pollutants that have escaped into the aquatic environment. Herein, the development of GO/chitosan (GO/CS) composites as adsorbent materials is described and reviewed. This combination is interesting as the addition of graphene to chitosan enhances its mechanical properties, while the chitosan hydrogel serves as an immobilization matrix for graphene. Following a brief description of both graphene and chitosan as independent adsorbent materials, the emerging GO/CS composites are introduced. The additional materials that have been added to the GO/CS composites, including magnetic iron oxides, chelating agents, cyclodextrins, additional adsorbents and polymeric blends, are then described and discussed. The performance of these materials in the removal of heavy metal ions, dyes and other organic molecules are discussed followed by the introduction of strategies employed in the regeneration of the GO/CS adsorbents. It is clear that, while some challenges exist, including cost, regeneration and selectivity in the adsorption process, the GO/CS composites are emerging as promising adsorbent materials.