Polyvinyl butyral (PVB) is widely used as an interlayer material in laminated glass applications, mainly in the automotive industry, but also for construction and photovoltaic applications. Post-consumed laminated glass is a waste that is mainly landfilled; nevertheless, it can be revalorized upon efficient separation and removal of adhered glass. PVB interlayers in laminated glass are always plasticized with a significant fraction in the 20–40% w/w range of plasticizer, and they are protected from the environment by two sheets of glass. In this work, the aim is to develop a thorough characterization strategy for PVB films. Neat reference PVB grades intended for interlayer use are compared with properly processed (delaminated) post-consumed PVB grades from the automotive and construction sectors. Methods are developed to open opportunities for recycling and reuse of the latter. The plasticizer content and chemical nature are determined by applying well-known analytical techniques, namely, FT-IR, TGA, NMR. The issue of potential aging during the life cycle of the original laminated material is also addressed through NMR. Based on the findings, a sensor capable of directly sorting PVB post-consumer materials will be developed and calibrated at a later stage.
Polyvinyl butyral (PVB) is a specialty polymer primarily used as an interlayer in laminated glass applications with no current circularity plan after the end of its life. This study presents a comprehensive recycling strategy for postconsumed PVB wastes based on a remelting–restabilization approach. Thermo-oxidative degradation of PVB was analyzed under heat and shear stress conditions in an internal mixer apparatus. The degradation mechanism of plasticized PVB (p-PVB) and unplasticized PVB (u-PVB) was identified as chain scission through melt flow rate (MFR), intrinsic viscosity (IV), and yellowness index (YI) characterization. Six different antioxidant (AO) formulations were screened for their effectiveness in inhibiting degradation in both neat u-PVB and p-PVB, as well as retrieved PVB. The phenolic antioxidants 1,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene and 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-di-tert-butylphenol were found to be the most effective ones based on MFR, oxidation onset temperature (OOT), and YI evaluations, while the optimal AO concentration was determined at 0.3% w/w. Furthermore, upscaling of the process was achieved by mixing virgin PVB and high-quality retrieved PVB wastes with AOs in a twin-screw extruder. Testing of the recycled samples confirmed that the selected AOs offered resilience against degradation at reprocessing and protection during the next service life of the material.
Poly(vinyl butyral) (PVB) displays exceptional adhesion to glass surfaces and high transparency, serving as the dominant interlayer material in laminated glass composites. This study systematically investigates PVB particulate composites, focusing on the interactions between a plasticized PVB matrix and silicate or silica dispersions as reinforcements. PVB composites reinforced with glass flakes, glass fibers, and fumed silica at loadings of 2, 5, and 8 vol% were produced and characterized. Optical microscopy and thermogravimetric analysis were employed to evaluate filler incorporation and dispersion under melt mixing conditions representative of industrial extrusion. Transparency measurements assessed the optical clarity of the composites, while ATR-FTIR was used to identify chemical interactions between PVB and the fillers. Regarding mechanical performance, fumed silica increased tensile strength up to 29 MPa and reduced displacement at fracture by 120%, while high-aspect-ratio flakes and silane-treated fibers only significantly increased composite stiffness. Impact resistance was additionally evaluated, revealing a significant enhancement upon the addition of fibrous reinforcements, especially when silane-treated fibers were used. Fumed silica increased the thermal stability of PVB by 7 °C and reduced water uptake to approximately 4.5%, in contrast to glass flakes, which increased water absorption reaching up to 8–11%. Lastly, the processability of composites was monitored, showing a progressive decrease with increasing filler content for all reinforcements. Overall, this work provides a comprehensive assessment of PVB–silicate/silica interfacial interactions and highlights the design of PVB composites suitable for advanced applications or the upcycling of secondary recycled PVB grades.
Poly(vinyl butyral) (PVB) is widely used as an interlayer in laminated safety glass in automotive and construction applications. The increasing quantities of PVB arising from end-of-life laminated glass represent a waste stream with significant potential for recycling. This study investigates the durability of high-quality retrieved PVB (re-PVB) separated from laminated glass wastes and evaluates the effect of restabilization against UV aging. Neat unplasticized PVB (u-PVB) and re-PVB were subjected to artificial UV weathering (ISO 4892-3) for up to 1500 h and then characterized in terms of chemical structure, yellowness, melt flow behavior and molecular weight. The results showed that u-PVB exhibited pronounced photooxidative degradation, while re-PVB remained comparatively stable. UV–Vis spectroscopy revealed the presence of residual UV absorbers in re-PVB, indicating that the components of the initial stabilization system might remain functional after the end of its life. Unexpectedly, the restabilization of re-PVB with phenolic antioxidants (AOs) reduced its photooxidative stability, despite their established effectiveness against thermo-mechanical degradation in melt reprocessing. A possible antagonistic effect was suggested between the newly introduced AOs and the residual stabilization system. These findings highlight that re-PVB is a valuable waste, and restabilization should be carefully considered when designing its second service life.
11 August 2026 in Polymer Degradation and Stability