Polyethylene Samples Research Articles

Study on the effects of aging on the pyrolysis of plastic and the synergistic mechanisms of co-pyrolysis with lignite

Co-pyrolysis of waste plastic with low-rank coal explored how photoaging impacts the pyrolysis of plastics and delves into the synergistic mechanisms involved in co-pyrolysis. The results of elemental analysis, X-ray powder diffraction and Fourier transform infrared spectroscopy showed that photoaging primarily involves oxidizing and breaking the aliphatic chains in polyethylene (PE), as well as generating oxygen-containing functional groups like hydroxyl (-OH), carbonyl (-C=O), and ether (-C-O), thereby reducing the crystallinity of PE. The results of individual plastic pyrolysis showed that photoaging is beneficial to the generation of gas and tar. Pyrolysis tar of PE samples contains significant amounts of alcohols, and olefins and alkynes (O&As). The results of co-pyrolysis indicated that photoaging can enhance the yields of gas and oil from the co-pyrolysis between PE and Naomaohu (NMH) coal. Co-pyrolysis effectively reduced the relative content of O&As in the tar from the pyrolysis of PE samples alone by 8.0%-29.0%. The synergistic mechanism of co-pyrolysis between aged PE and NMH involved supplying a significant quantity of hydrogen and hydroxyl radicals by NMH, which react with alkyl radicals generated from PE pyrolysis, leading to the production of additional alkanes and alcohols. These findings offered new insights for a deeper understanding of the co-pyrolysis behaviors between waste plastic and lignite.

Tearing properties, crystallization behavior, microstructure, and morphology of LLDPE with different short branched chain distributions

Abstract The length and distribution of comonomers with short-chain branching (SCB) have a significant influence on the crystallization behavior and crystal structure of polymers, as well as the mechanical properties of the material. This study investigates the crystallization behavior and properties of linear low-density polyethylene (LLDPE) samples with similar density, molecular weight, and branching degree but varying SCB distributions. The results show that LLDPE with butene as the comonomer has a stronger ability to suppress crystallization compared to LLDPE with hexene as the comonomer due to its more uniform SCB distribution. Additionally, among LLDPEs with comonomers of octene, hexene, and butene, the LLDPE with the most uniform SCB distribution exhibits the weakest crystallization ability. Small-angle X-ray scattering (SAXS) and scanning electron microscopy (SEM) results indicate that LLDPE with more uniform distribution of SCB has smaller long-period and more regular lamellar structure. Therefore, LLDPE with more uniform SCB distribution exhibits weaker inhibition ability towards crystallization, leading to less agglomerated phases and weaker phase separation, resulting in higher tear strength.

Influence of interface voltage on charge build-up under high voltage

Abstract The interface voltage appearing when two materials are brought into contact was measured with a high sensitive pressure-wave-propagation measurement setup in various low density and high density polyethylene samples coated either with aluminum or gold electrodes. The samples were then tested under high voltage (40 kV/mm) for 24 h to assess the correlation between interface voltage and charge injection at 22 °C. Aluminum electrodes induce a positive interface voltage toward the insulator favoring electron injection at the cathode while gold electrodes induce a negative interface voltage toward the insulator favoring hole injection at the anode. After the injections due to interface voltage, charges diffuse more easily in low density polyethylene that triggers a subsequent injection due to heterocharges buildup.

Quantitative Raman analysis of microplastics in water using peak area ratios for concentration determination

This study presents a novel analytical method for the quantitative and qualitative analysis of microplastics (MPs) in deionized (DI) water using Raman spectroscopy. Raman peak area ratios of 1295 cm−1 for polyethylene (PE) and 637 cm−1 for polyvinylchloride (PVC) to the broad H2O peak were utilized to establish a calibration model for the concentration of MPs dispersed in DI water at 0.1 wt% to 1.0 wt%. The calibration model demonstrated R2 values of 0.98537 for PE and 0.99511 for PVC, indicating high linearity between the peak area ratio and concentration. The calibration model was validated using mixed PE and PVC samples to confirm its applicability to real-world water bodies, where multiple types of MPs are present. The calculated standard error of calibration (SEC) and relative standard error of calibration (%RSEC) values further confirmed the accuracy of the predictions, providing a robust approach for detecting and quantifying MPs in aquatic environments.

Multimodal Non-Destructive In Situ Observation of Crystallinity Changes in High-Density Polyethylene Samples with Relation to Optical Parameters during Tensile Deformation

Abstract: Many non-destructive optical testing methods are currently used for material research, providing various information about material parameters. At RECENDT, a multimodal experimental setup has been designed that combines terahertz (THz) spectroscopy, optical coherence tomography (OCT), infrared (IR), and Raman spectroscopy with a tensile test stage. This setup aims to gather material information such as crystallinity and optical parameters of high-density polyethylene (HDPE) during a tensile test. The setup compares common IR and Raman spectroscopy and the less common optical methods THz and OCT. Complementarity is achieved through different frequency ranges and measurement approaches, resulting in different measured optical material parameters and depths. During tensile testing, HDPE samples with varying crystallinity were analysed, and the determined optical parameters such as refractive index, birefringence, scattering coefficient of decay, and penetration depth can be correlated with the change in crystallinity. These findings demonstrate that the optical methods and their outcomes can be interconnected. With further optimization of the experimental setup, it would be possible to observe the alignment of fibres in fibre composite panels and the stress distribution of polymers effectively. This opens interesting possibilities for polymer characterization in the future, including quality control during moulding processes and material testing.

Measuring Oxygen Solubility in Amorphous and Semicrystalline Polyolefins Using Test Particle Insertion: A Comparative Study of Polyethylene and Isotactic Polypropylene.

The test particle insertion method is used to study the solubility of oxygen in two commonly used polymers: polyethylene (PE) and isotactic polypropylene (iPP). Amorphous samples for both polymers were prepared by means of Monte Carlo and molecular dynamics simulations, and the oxygen solubility was measured across different temperatures. The solubility-temperature dependence for iPP proved to be nonmonotonic due to the interplay between binding and reorganizational enthalpy, while for PE, it appeared to be monotonic based on the available data in the studied temperature range. A broad comparison to experiments and simulations is included. Further oxygen insertions were also performed in semicrystalline PE and iPP samples at ambient temperature, and the obtained values were compared to a linear relationship which correlates the solubility in the purely amorphous phase with the solubility in the crystalline phase. The solubility of PE closely follows the linear relationship, while iPP exhibits some divergence. All the semicrystalline samples were previously annealed at elevated temperatures for long periods (a few μs), and a strong effect of annealing was observed on the structure and the solubility of iPP. A well-developed iPP lamellar structure emerged at longer annealing times, while PE develops that structure already in the early crystallization stages. The solubility of semicrystalline iPP samples with lamellar morphology exhibited better agreement with extrapolated solubility values of the amorphous state─the extrapolation was made using a linear relationship connecting solubility in the purely amorphous phase and solubility in mixed phases (amorphous and crystalline). Results on the correlation of the solubility with the local structural ordering are also present.

Synthesis of Ultralow-Density Polyethylene Elastomers Using Triarylnaphthyl Iminopyridyl Ni(II) Catalysts.

Recently, the chain-walking ethylene polymerization strategy has garnered widespread attention as an efficient and straightforward method for preparing polyolefin elastomers. In this study, a series of 2,4,8-triarylnaphthyl iminopyridyl nickel catalysts were synthesized and used in ethylene polymerization. These catalysts demonstrated moderate catalytic activity (105 g mol-1 h-1), producing high-molecular-weight (up to 145.5 kg/mol) polyethylene materials with high branching degrees (75-95/1000C) and correspondingly low melting points. Detailed analysis using 13C NMR spectroscopy revealed that the polyethylenes primarily featured methyl and long-chain branches. Mechanical testing of the polyethylene samples obtained from catalysts Ni1-Ni3 exhibited moderate stress at break (4.64-6.97 MPa) coupled with a very high strain at break (1650-3752%), indicating their very good ductility. Furthermore, these polyethylenes showcased great elastic recovery abilities, with strain recovery values ranging from 72% to 85%. In contrast, the polyethylene produced by Ni4 displayed notably inferior tensile strength (0.16 MPa) and tensile recovery (43%). To the best of our knowledge, this study represents the inaugural utilization of a nickel iminopyridyl catalyst in the preparation of a polyethylene thermoplastic elastomer.

Application of interlayer perforation and installation of transparent elements in the technology of duplicated decorative polymer films

Objectives. To develop technologies for producing multilayer films of transparent thermoplastic polymers; to study methods of modifying their supramolecular structure; and to determine their optical properties by means of optical-polarization methods for the use of modified films as decorative and design materials in modern architecture.Methods. Industrial samples of polystyrene, low-density polyethylene, polypropylene, and polyvinyl chloride films from various manufacturers (Don Polimer, Vektor, and Sibur) were the objects of the study. The optical properties of the films were studied by means polarized-light spectrophotometry. In order to modify the supramolecular structure of the polymers, the surfaces of the films were treated under isometric conditions with volatile solvents or their aqueous solutions. Parts of the layers of multilayer films were removed by cutting with a punching knife using a press or with a manual device for perforating printing materials.Results. The spectral characteristics of multilayer films of several transparent thermoplastic polymers in polarized light were determined. The study showed that a wide palette of colors and contrasting images can be obtained by mechanically removing part of the layers of multilayer films. The phenomenon of pseudo-disappearance of the outermost layer was discovered after treatment of a stack of films under isometric conditions with volatile solvents or their aqueous solutions.Conclusions. Based on the example of large-scale production thermoplastics, it was shown that a combination of technological methods of stacking, perforation, and local plasticization of films of transparent thermoplastic polymers can produce pleochroic multicolor materials for a range of human activities. The possibility of hidden coding of information on multilayer packaging materials, and its visualization and instrumental reading in polarized light was confirmed by color differential and contrast of 150 and 60 units, respectively. It was also shown that several monochrome tones of different lightness and brightness can be obtained by varying the number of layers or perforating the films in multilayer materials.

Accurate pulse time distribution determination using MLEM algorithm in integral experiments

Integral experiments play a crucial role in advancing nuclear science and technology by providing critical data that validate theoretical models and enhance reactor designs. This study presents a novel approach to accurately determine pulse time distribution in integral experiments conducted with pulsed accelerators. By strategically placed monitors and shields at angles of 0° and 90° relative to the beam direction, neutron flight times from the target are measured, and a response matrix for neutron emission at different times is constructed through simulation. The Maximum Likelihood Expectation Maximization (MLEM) algorithm is employed for pulse time reconstruction, with the gamma ray flight time spectrum from monitors used as the initial spectrum to streamline the computational process. Experimental validation using a standard polyethylene sample and n-p scattering cross-sections confirms the accuracy of the method. Results are compared across multiple nuclear databases such as CENDL-3.2, ENDF/B-VIII.0, JENDL-5.0, and JEFF-3.3 libraries. The developed method significantly enhances the precision of pulse time distribution determination, thereby improving the quality and reliability of experimental data obtained from integral experiments conducted with pulsed accelerators.

Improving flame resistance and shielding properties for cross-linked polyethylene (XLPE) using nanoclay filler

Polymers play an essential role in both industry and medical fields due to their diverse and adaptable properties. In this work, prepared crosslinking polyethylene (XLPE) samples with hydrophilic bentonite nanoclay fillers (H2Al2O6Si) at concentrations of 0, 1, 2.5, 4, and 5 wt% enhance their flame-retardant and radiation shielding efficiency. The research investigated flame retardancy and thermal stability parameters. The XLPE/H2Al2O6Si nanocomposite polymer sheets were exposed to a collimated beam of fast neutrons using an Am/Be neutron source (5 Ci) and to gamma radiation using a 137Cs point source (5 μCi) to assess their radiation shielding properties. The study found that uniform dispersion of nanoclay particles enhanced the thermal properties of the composite, forming a char layer that acted as a barrier, slowing thermal decomposition and reducing the heat release rate. Limiting oxygen index (LOI) increased from 28% to 34%, and burning rate improved with higher nanoclay concentrations. Additionally, absorption and optical band gap calculations decreased with increasing filler concentrations. Radiation attenuation capabilities increased by approximately 40% for neutrons and 30% for gamma radiation compared to pure XLPE. The study concluded that incorporating nanoclay fillers into XLPE enhances its shielding capabilities and improves flame resistance properties, making the prepared samples suitable for various industrial applications.

An automatic method for accurate signal-to-noise ratio estimation and baseline correction of Raman spectra of environmental microplastics

In this study, we introduced a k-iterative double sliding-window (DSW^k) method for the estimation of spectral noise, signal-to-noise ratio (SNR), and baseline correction. The performance was evaluated using simulated spectra and compared against other commonly employed methods. Convergent evaluation determined that a k value of 20 strikes an optimal balance between convergence and computational intensity. The DSW^k method demonstrated outstanding performance across different spectral types (flat baseline, baseline with elevation, baseline with fluctuation, baseline with elevation and fluctuation) coupled with SNR values from 10 to 1000, achieving results that ranged from 1.01 to 1.08 times of the reference value in estimating spectral noise. It also showed that the estimated SNR values are 0.89 to 0.93 times of the reference value, demonstrating a 74.5 % − 131.7 % improvement over the conventional method in spectra with elevated and/or fluctuating baselines. Additionally, the DSW^k method proved effective in correcting baselines and identifying polymers in environmental samples of polyethylene (PE), polypropylene (PP), and polystyrene (PS), despite the limitation of reducing the peak height in spectra with low SNR. This method offers the potential to enhance the automatic and accurate evaluation of spectral quality and could assist in the development of guidelines for more rapid parameter adjustments in Raman measurements.

Segmentation of beach plastic fragments’ contours based on self-organizing map and multi-shape descriptors: A rapid indication of fragmentation and wearing types

Environmental plastic fragments have been verified as byproducts of large plastic and its secondary pollutants including micro and nanoplastics. There are few quantitative studies available, but their contours have values for the weathering mechanisms. We used geometric descriptors, fractal dimensions, and Fourier descriptors to characterize field and artificial polyethylene and polypropylene samples as a means of investigating the contour characteristics. It provides a methodological framework for contour classification. Unsupervised classification was performed using self-organizing neural networks with size-invariance parameters. We revealed the isometric phenomenon of plastic fragments during fragmentation, i.e., that the degree of contour rounding and complexity increase and decrease, respectively, with decreasing fragment size. With an average error rate of 8.9 %, we can distinguish artificial samples from field samples. It was also validated by the difference in Carbonyl Index between groups. We propose a two-stage process for plastic fragmentation and give three types of contour features which were key in the description of fragmented contours, i.e., size, complexity, and rounding. Our work will improve the accuracy of characterizations regarding the weathering and fragmentation processes of certain kinds of plastic fragments. The contour parameters also have the potential to be applied in more realistic scenarios and varied polymers.

Microplastic identification in marine environments: A low-cost and effective approach based on transmitted light measurements

Microplastics have become a significant concern for the well-being of marine ecosystems. Small fragments of plastic debris are released into the environment from both the direct disposal of plastic products and the deterioration of larger items. Ingestion of microplastics by marine life can result in detrimental effects, including physical harm and the accumulation of toxic chemicals in their tissues. The aim of this research is to design a compact and cost-effective measurement system for effectively detecting and quantifying microplastics in marine environments. The proposed system uses a 2.4-inch liquid-crystal display (LCD) panel and a digital USB microscope, both of which are connected to a single-board computer, with a dedicated python-based graphical user interface (GUI). Specifically, the light transmitted through plastic and organic samples was measured in order to identify and classify them. Various types of materials, such as polypropylene, polyvinyl chloride, polycarbonate, polyethylene, and organic algae samples, were tested and the metrological performance of the system has been estimated. The transmittance of the samples analyzed was primarily influenced by their opacity and thickness. In general, thicker materials exhibited significantly lower transmittance values. This trend was particularly evident in organic components and opaque plastic samples, where transmittance was significantly low. In addition, the experimental results suggest that the colour of the material also affects transmittance, although as a secondary factor. The employed technique could be used to identify and distinguish samples based on material properties, thereby allowing the proposed system to be a valuable tool for further research on microplastics in marine environments.

The influence of low-temperature shear on crystallization of shish-kebab of unimodal/ bimodal C4 short-chain branching polyethylene

The shish crystal, a crucial structure in the formation of shish-kebab crystals, has drawn widespread attention due to its highly oriented chain arrangement, significantly enhancing the mechanical properties of products. This study utilizes polyethylene samples with longer C4 short branches, employing in-situ synchrotron SAXS/WAXD to investigate the influence of short branch length and content on the formation of shish-kebab crystals in unimodal and bimodal polyethylene under low-temperature shear conditions (with supercooling degrees of 13.5 °C and 10.5 °C). The results reveal that the presence of C4 short-chain branching affects system crystallization, but low-temperature shear induces stronger mechanical action on the melt, resulting in better-oriented lamellar crystals compared to high-temperature shear (superheat degrees of 22.5 °C and 19.5 °C), achieving higher orientation. This achieves the control of shish-kebab crystal generation through the stretched network mechanism. Both types of samples with different C4 short-chain branching contents generate shish-kebab crystals during the shear stage, with relatively higher short-chain branching content inducing more shish crystal formation but with less regular structure. The bimodal polyethylene exhibit higher proportions and absolute amounts of final shish crystals compared to the unimodal polyethylene, indicating that high molecular weight portions are conducive to shish crystal generation under shear. The result demonstrates the feasibility of generating shish-kebab crystals during the low-temperature shear process of PE in the presence of C4 branches using the stretched network mechanism under shear flow conditions. Moreover, controlling the degree of entanglement of molecular chains by adjusting shear temperature, branch content, and branch length can modulate two formation mechanisms of shish crystals—coil-stretch transition mechanism at high temperature and stretched network mechanism at low-temperature.

Safety assessment of the substance amines, di-C14-C20-alkyl, oxidised, from hydrogenated vegetable oil, for use in food contact materials.

The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP) assessed the safety of amines, di-C14-C18-alkyl, oxidised, renamed by the Panel as amines, di-C14-C20-alkyl, oxidised, from hydrogenated vegetable oil. The substance amines, bis(hydrogenated tallow alkyl) oxidised, consisting of the same components, but originating from tallow, is currently authorised as FCM substance No 768. The vegetable-sourced substance is intended to be used at up to 0.1% w/w as antioxidant and/or stabiliser in the manufacture of polyolefin food contact materials (FCM) and articles intended for contact with dry, aqueous and acidic foods. The substance is a mixture consisting of linear N,N-dialkyl hydroxylamines and their corresponding amine, nitrone and oxime derivatives, as well as further components: tert-N-oxides, secondary amides and carboxylic acids. Specific migration was tested from polyethylene samples in 10% ethanol and 3% acetic acid for 2 h at 100°C followed by 10 days at 60°C. None of the non-authorised components were detected to migrate at detection limits (LoD) in the range 0.003-0.029 mg/kg. The LoD of authorised carboxylic acids was 0.35 mg/kg. The Panel reassessed the genotoxicity studies carried out on FCM No 768 and evaluated two new bacterial reverse mutation tests on the nitrone and oxime derivatives as well as new (qualitative/quantitative) structure-activity relationship (Q)SAR analyses on other components. The Panel concluded that the substance did not raise a concern for genotoxicity. The Panel concluded that the substance is not of safety concern for the consumers if it is used as an additive at 0.1% w/w in the manufacture of polyolefin FCM intended to be in contact with foods simulated by food simulants A, B, C and E, except for infant formula and human milk, for storage above 6 months at room temperature and below, including hot-fill conditions and heating up to 100°C for 2 h.

Polyethylene, whose surface has been modified by UV irradiation, induces cytotoxicity: A comparison with microplastics found in beaches

Microplastics, plastic particles 5 mm or less in size, are abundant in the environment; hence, the exposure of humans to microplastics is a great concern. Usually, the surface of microplastics found in the environment has undergone degradation by external factors such as ultraviolet rays and water waves. One of the characteristics of changes caused by surface degradation of microplastics is the introduction of oxygen-containing functional groups. Surface degradation alters the physicochemical properties of plastics, suggesting that the biological effects of environmentally degraded plastics may differ from those of pure plastics. However, the biological effects of plastics introduced with oxygen-containing functional groups through degradation are poorly elucidated owing to the lack of a plastic sample that imitates the degradation state of plastics found in the environment. In this study, we investigated the degradation state of microplastics collected from a beach. Next, we degraded a commercially available polyethylene (PE) particles via vacuum ultraviolet (VUV) irradiation and showed that chemical surface state of PE imitates that of microplastics in the environment. We evaluated the cytotoxic effects of degraded PE samples on immune and epithelial cell lines. We found that VUV irradiation was effective in degrading PE within a short period, and concentration-dependent cytotoxicity was induced by degraded PE in all cell lines. Our results indicate that the cytotoxic effect of PE on different cell types depends on the degree of microplastic degradation, which contributes to our understanding of the effects of PE microplastics on humans.

SINGLE-STAGE AND SIMPLE FABRICATION OF PE FILMS DECORATED WITH HALLOYSITE NANOTUBES

Background. Environmental pollution with plastic waste is a global problem that requires the search for effective and safe ways of disposal or processing of secondary raw materials. The use of catalysts for this purpose is a promising direction for research. Objective. In this work, a method of introduction of nanomaterials on the surface of a polyethylene film by partially dissolving the upper layer of the polymer in a heated nanomaterial suspension, namely aluminosilicate halloysite nanotubes in cyclohexane, was developed. Methods. Thermogravimetric, optical, and dynamic mechanical analyses of synthesised samples were carried out, and their properties were compared with reference samples of pure polyethylene and treated without the addition of nanomaterial. Results. It was achieved by the introduction of halloysite nanotubes in the amount of a maximum of 2.83 % by mass after immersion of the film in the suspension at a temperature of 50 °C for 120 seconds. The resulting film showed a wetting angle value of 77.11o, while for the reference sample without HNT it was 99.24o, which indicates the presence of hydrophilic nanotubes in the PE surface layer. Conclusions. At the same time, the synthesised samples showed a significant decrease in mechanical properties, such as elasticity and tensile strength, due to the destructive effect of the solvent on the polymer.

Safety assessment of the substance 'phosphorous acid, triphenyl ester, polymer with 1,4-cyclohexanedimethanol and polypropylene glycol, C10-16 alkyl esters', for use in food contact materials.

The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP) assessed the safety of the substance 'phosphorous acid, triphenyl ester, polymer with 1,4-cyclohexanedimethanol and polypropylene glycol, C10-16 alkyl esters', when used as an additive in all types of polyolefins. The substance is a polymer containing ≤ 13% w/w of a low molecular weight fraction (LMWF, < 1000 Da). A polyethylene sample with 0.15% w/w of the substance was used in a comprehensive set of migration tests with food simulants. The specific migration was up to 0.014 and 0.023 mg/kg in 4% acetic acid and 10% ethanol, respectively. Migration into olive oil was estimated by the Panel to be up to 5.3 mg/kg under worst-case conditions of use. The migrating LMWF species were comprehensively identified. Those without phosphorous were either without alerts for genotoxicity or listed in Regulation (EU) 10/2011 with worst-case migrations well below their respective specific migration limits. Toxicological studies were performed using phosphite and phosphate versions of the substance enriched in its LMWF. The substance does not raise a concern for genotoxicity. From a repeated dose 90-day oral toxicity study in rats with a 50:50 phosphite:phosphate blend, the Panel identified a NOAEL of 250 mg/kg bw per day for each component of the blend. No delayed neurotoxicity in hens was observed. The CEP Panel concluded that the substance does not raise a safety concern for the consumer if its LMWF is not higher than 13% w/w, if it is used at up to 0.15% w/w in polyolefin materials and articles intended for contact with all food types, except for infant formula and human milk, for long-term storage at room temperature and below, after hot-fill and/or heating up to 100°C for up to 2 h, and if its migration does not exceed 5 mg/kg food.

Safety assessment of the substance calcium tert-butylphosphonate for use in food contact materials.

The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids assessed the safety of calcium tert-butylphosphonate, which is intended to be used as a nucleating agent up to 0.15% w/w for the manufacture of polyolefin food contact materials (FCM) and articles for single and repeated use, in contact with all types of food, including infant formula and human milk. Specific migration was tested using polyethylene samples in 10% ethanol, 3% acetic acid and 95% ethanol for 2 h at 100°C, followed by 238 h at 40°C. Results for all three simulants were near or below the limit of detection of 10 μg/kg. As the solubility of the substance is far above the reported migration and above 60 mg/kg food, no assessment of the particle fraction was needed, and the conventional risk assessment was followed. The substance did not induce gene mutations in bacterial cells and structural chromosomal aberrations in mammalian cells, thus, did not raise concern for genotoxicity. The Panel considered that the use of the substance did not give rise to safety concern related to neurotoxicity for the general population, but this conclusion could not be applied to infants below 16 weeks of age, due to their specific sensitivity and the absence of dedicated data. The Panel concluded that calcium tert-butylphosphonate does not raise a safety concern for the consumer if it is used as a nucleating agent up to 0.15% w/w in the manufacture of polyolefin FCM that are intended to be in contact with all types of food for storage above 6 months at room temperature and below, including temperatures up to 100°C for maximum 2 h and up to 130°C for short durations. The Panel could not evaluate the safety of use to manufacture FCM for contact with infant formula and human milk.

Thermal Analysis of Combustible Components of Municipal Solid Waste

The use of municipal solid waste as a raw material for alternative fuel is a promising direction for waste recycling and substitution of solid fossil fuels. Therefore, selecting of fuel composition and studying of its properties is an urgent task. The aim of this work is thermal characteristics analysis of the combustible components of municipal solid waste, which are the most common in Ukraine, for further selection of a fuel composition that will satisfy the consumer's requirements. The goal is achieved by studying the thermal destruction of samples by thermogravimetry and differential thermal analysis when materials are heated to 1000 ºС in the presence of air oxygen. Paper, cardboard, plastic, biodegradable film, textiles, leather, wood were investigated in this work. The most important results are the received data on the characteristic temperatures of destruction stages, content of water, organic and mineral substances, ash, as well as the calculated values of rate and conditional thermal effect of decomposition of organic substances. Strong formation of gaseous substances was registered for samples of polyethylene and biodegradable film, polyethylene terephthalate and cotton fabric. These features should be considered in the technologies of production and combustion of fuel. The significance of the results also lies in the fact that it is recommended to use data on the thermal stability of materials in order to prevent their ignition during drying when developing fuel production technology. In addition, the calculated values of the conditional thermal effect made it possible to evaluate the thermal characteristics of the studied materials as components of solid alternative fuels.