Due to the 2011 labelling of styrene monomer as "reasonably anticipated to be a human carcinogen" by the National Institutes of Health's National Toxicology Program (NTP) and the controversy over whether styrene oligomers mimic the physiological effects of estrogen, an updated review of styrene monomer and oligomers in food and food contact materials (FCMs) was performed. The concentrations of styrene monomer and oligomers were determined in 24 polystyrene (PS) products and ranged from 9.3 to 3100 mg kg(-1) for the styrene monomer, 130-2900 mg kg(-1) for the sum of three styrene dimers, and 220-16,000 mg kg(-1) for the sum of six styrene trimers. Foods in contact with PS packaging had styrene monomer concentrations ranging from 2.6 to 163 ng g(-1); dimer concentrations from the limit of quantitation (LOQ) to 4.8 ng g(-1) and trimer concentrations were all below the LOQ (2 ng g(-1)). Diffusion coefficients (Dp) and partition coefficients (K) were also calculated for styrene dimers and trimers. The results presented here indicate that styrene monomer concentrations in foods have not significantly changed since the 1980s and monomer concentrations in food packaging quantified in this study were all below USFDA limits. Although styrene dimers and trimers are present in higher concentrations in PS FCMs than the monomer, their migration to food is limited because of their high K values (4 × 10(2) to 2 × 10(6)) and their low diffusion coefficients in PS products. Additionally, diffusion coefficients calculated using USFDA-recommended food simulants and Arrhenius plots describing the temperature dependence of styrene dimers and trimers can be used in future calculations of dietary intake of the styrene oligomers.
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http://dx.doi.org/10.1080/19440049.2013.878040 | DOI Listing |
Polymers (Basel)
December 2024
Centro de Física de Materiales (CSIC-UPV/EHU)-Materials Physics Center (MPC), P. M. de Lardizábal 5, 20018 San Sebastián, Spain.
This work connects the calorimetric responses of different rubber-resin blends with varying resin contents with their alpha relaxation dynamics. We used differential scanning calorimetry and broadband dielectric spectroscopy to characterize the calorimetric and dielectric responses of styrene-butadiene, polybutadiene, and polyisoprene with different resin contents. To model the results, we used the Gordon-Taylor equation combined with an extension of the Adam-Gibbs approach.
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December 2024
College of Electromechanical Engineering, Qingdao University of Science and Technology, Qingdao 266061, China.
Pyrolysis is recognized as a promising technology for waste plastics management. Although there have been many studies on pyrolysis of waste plastics, there is still a lack of in-depth research on the mechanism of synergistic effect between mixed plastics and the mechanism of product formation. In this paper, based on the pyrolysis characteristics of Polystyrene, Polyethylene, and mixed plastics (Polystyrene/Polyethylene), it is demonstrated that a synergistic effect exists in the co-pyrolysis of Polystyrene/Polyethylene and affects the pyrolysis behavior and pyrolysis products.
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December 2024
Institute of Polymer and Dye Technology, Faculty of Chemistry, Lodz University of Technology, Stefanowskiego Street 16, 90-537 Lodz, Poland.
This study aimed to investigate the properties of tin(II) oxide (SnO) as an unconventional cross-linking agent for chloroprene (CR) and styrene-butadiene (SBR) rubbers compositions. The use of tin(II) oxide results from the need to reduce the use of zinc oxide as a cross-linking agent due to environmental regulations and its toxic impact on aquatic environments. The studied elastomeric blends can be cross-linked with tin(II) oxide, and the results demonstrate the significant potential of this oxide in such applications.
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December 2024
Institute of Integrated Natural Sciences, University Koblenz, Universitätsstr. 1, 56070 Koblenz, Germany.
Tire wear particles (TWPs) are among the most relevant sources of microplastic pollution of the environment. Nevertheless, common analytical methods like IR and Raman spectroscopy are highly impaired by additives and filler materials, leaving only thermogravimetric methods for chemical analysis of TWPs in most cases. We herein present quantitative NMR spectroscopy (qNMR) as an alternative tool for the quantification of the polymeric material used for the production of tires, including natural rubber (NR), styrene-butadiene-copolymer (SBR), polyethylene-co-propylene (EPR) and polybutadiene (BR).
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December 2024
Polymer Extrusion Lab, The University of Texas at El Paso, El Paso, TX 79968, USA.
In the work presented here, we explore the upcycling of polyethylene terephthalate (PET) that was derived from water bottles. The material was granulated and extruded into a filament compatible with fused filament fabrication (FFF) additive manufacturing platforms. Three iterations of PET combined with a thermoplastic elastomer, styrene ethylene butylene styrene with a maleic anhydride graft (SEBS-g-MA), were made with 5, 10, and 20% by mass elastomer content.
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