Fragmentation of polypropylene into microplastics promoted by photo-aging; release of metals, toxicity and inhibition of biodegradability.

The widespread presence of microplastics (MP) in water represents an environmental problem, not only because of the harmful effects of their size and potential to vector other pollutants, but also because of the release of additives, degradation products and residues contained in the polymer matrix. The latter includes metallic catalysts, which are often overlooked. This study focuses on the photo-aging of polypropylene (PP) and the resulting structural changes that promote its fragmentation microplastics (PP-MPs) and release of metals, as well as the resulting toxicity of leachates and their potential to inhibit biodegradation of organics in water. The pristine, photo-aged and waste PP are ground under the same regime to assess susceptibility to fragmentation. Obtained PP-MPs are submitted to leaching tests; the release of organics and metals is monitored by Total Organic Carbon (TOC) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) analysis, respectively. The leachates are assessed for their toxicity against Vibrio fischeri, Daphnia magna and Pseudokirchneriella subcapitata and their influence on the biodegradability of the glucose solution. Photo-aging induced changes in the crystallinity and morphology of the PP and manifested in the abundance of smaller MPs, as revealed by the particle size distribution. In the case of pristine PP, all particles were > 100 µm in size, while aged PP yielded significant mass fraction of MPs <100 µm. The toxicity of leachates from aged PP-MPs is higher than that of pristine and exhibits a positive correlation with portion of metals released. The biodegradability of glucose is strongly inhibited by PP-MPs leachates containing a mixture of metals in trace concentrations.

Effect of Aging on Physicochemical Properties and Size Distribution of PET Microplastic: Influence on Adsorption of Diclofenac and Toxicity Assessment.

Microplastics (MPs) are detected in the water, sediments, as well as biota, mainly as a consequence of the degradation of plastic products/waste under environmental conditions. Due to their potentially harmful effects on ecosystems and organisms, MPs are regarded as emerging pollutants. The highly problematic aspect of MPs is their interaction with organic and inorganic pollutants; MPs can act as vectors for their further transport in the environment. The objective of this study was to investigate the effects of ageing on the changes in physicochemical properties and size distribution of polyethylene terephthalate (PET), as well as to investigate the adsorption capacity of pristine and aged PET MPs, using pharmaceutical diclofenac (DCF) as a model organic pollutant. An ecotoxicity assessment of such samples was performed. Characterization of the PET samples (bottles and films) was carried out to detect the thermooxidative aging effects. The influence of the temperature and MP dosage on the extent of adsorption of DCF was elucidated by employing an empirical modeling approach using the response surface methodology (RSM). Aquatic toxicity was investigated by examining the green microalgae Pseudokirchneriella subcapitata. It was found that the thermooxidative ageing process resulted in mild surface changes in PET MPs, which were reflected in changes in hydrophobicity, the amount of amorphous phase, and the particle size distribution. The fractions of the particle size distribution in the range 100-500 µm for aged PET are higher due to the increase in amorphous phase. The proposed mechanisms of interactions between DCF and PET MPs are hydrophobic and π-π interactions as well as hydrogen bonding. RSM revealed that the adsorption favors low temperatures and low dosages of MP. The combination of MPs and DCF exhibited higher toxicity than the individual components.

Development of PE/PCL Bilayer Films Modified with Casein and Aluminum Oxide.

The studied samples were prepared from polyethylene (PE) polymer which was coated with modified polycaprolactone (PCL) film in order to obtain bilayer films. Thin PCL film was modified with casein/aluminum oxide compound to enhance vapor permeability as well as mechanical and thermal properties of PE/PCL films. Casein/aluminum oxide modifiers were used in order to achieve some functional properties of polymer film that can be used in various applications, e.g., reduction of water vapor permeability (WVTR) and good mechanical and thermal properties. Significant improvement was observed in mechanical properties, especially in tensile strength as well as in water vapor values. Samples prepared with aluminum oxide particles indicated significantly lower values up to 60%, and samples that were prepared with casein and 5% Al2O3 showed the lowest WVTR value.

Preparation of a PANI/ZnO Composite for Efficient Photocatalytic Degradation of Acid Blue.

Polyaniline/zinc oxide (PANI/ZnO) composite photocatalysts were prepared from neutral media by in situ chemical oxidation of aniline (ANI) in the presence of different amounts of diethylene glycol (DEG). The PANI/ZnO composite photocatalysts were synthesized to efficiently remove organic dye (acid blue, AB25) from model wastewater. The PANI/ZnO composite photocatalysts were studied with the intention of efficient removal of organic dye (acid blue, AB25) from wastewater to obtain low-cost heterogeneous catalysts that offer high catalytic activity and stability. The conductive PANI polymer, which absorbs Vis irradiation, was used in this work as ZnO absorbs only ultraviolet (UV) irradiation; thus, the composite photocatalysts' activity was broadened into the Vis region. Characterization of the composite photocatalysts was done by Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, scanning electron microscopy, electric conductivity, UV-Vis spectroscopy, and by specific surface area (SBET) measurements. The composites' photocatalytic activity under solar irradiation was validated by monitoring degradation of the AB25 dye. This study presented that it was possible both to prepare PANI and to prevent ZnO dissolution if in situ polymerization starts from neutral media with the addition of DEG. Additionally, efficient removal of AB25 dye, about 90% in 60 min, was achieved. The first-order rate constants of the photodegradation of AB25 by PANI/ZnO 0.02/0.024/0.04 DEG (and pure ZnO)) were computed to be 0.0272/0.0281/0.0325 (and 0.0062) min-1, indicating that the morphology and surface of the photocatalysts have significantly influenced the catalytic activity.

Stability and Synergistic Effect of Polyaniline/TiO2 Photocatalysts in Degradation of Azo Dye in Wastewater.

The polyaniline/TiO2 (PANI/TiO2) composite photocatalysts were prepared by the in situ chemical oxidation of aniline (An) in the presence of TiO2 particles. For this purpose, photocatalysts with different amounts of PANI polymer were prepared and analysed. Fourier-transform infrared (FT-IR) spectroscopy and thermogravimetric (TG) analysis indicated successful synthesis of the PANI polymer and its conductivity was also determined. The micrographs of field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) were used to explain the impact of the aniline amount on the aggregation process during the synthesis of the composites. The smallest size of aggregates was obtained for the photocatalysts with 15% of PANI (15PANI/TiO2) due to the formation of homogenous PANI. The photocatalytic activity of studied PANI/TiO2 photocatalysts was validated by monitoring the discoloration and mineralization of Reactive Red azo dye (RR45) in wastewater. The 15PANI/TiO2 sample presented the highest photocatalytic efficiency under ultraviolet A (UVA) irradiation, in comparison to pure TiO2. This was explained by the formation of uniformly dispersed PANI on the TiO2 particles, which was responsible for the synergistic PANI-TiO2 effect.