Influence of Different Stabilization Systems and Multiple Ultraviolet A (UVA) Aging/Recycling Steps on Physicochemical, Mechanical, Colorimetric, and Thermal-Oxidative Properties of ABS

Commercially mass-polymerized acrylonitrile–butadiene–styrene (ABS) polymers, pristine or modified by stabilization systems, have been injection molded and repeatedly exposed to ultraviolet A (UVA) radiation, mechanical recycling, and extra injection molding steps to study the impact of such treatments on the physicochemical, mechanical, colorimetric, and thermal-oxidative characteristics. The work focus on mimicking the effect of solar radiation behind a window glass as relevant during the lifetime of ABS polymers incorporated in electrical and electronic equipment, and interior automotive parts by using UVA technique. The accelerated aging promotes degradation and embrittlement of the surface exposed to radiation and causes physical aging, deteriorating mechanical properties, with an expressive reduction of impact strength (unnotched: up to 900%; notched: up to 250%) and strain at break (>1000%), as well as an increase in the yellowing index (e.g., 600%). UV-exposition promotes a slight increase in the tensile modulus (e.g., 10%). The addition of antioxidants (AOs) leads to a limited stabilization during the first UVA aging, although the proper AO formulation increases the thermal-oxidative resistance during all the cycles. Mechanical recycling promotes an increase in strain at break and unnotched impact strength alongside a slight decrease in tensile modulus, due to disruption of the brittle surface and elimination of the physical aging.This research was funded by the European Union’s Horizon 2020 Research and Innovation Program, grant number 730308

Pushing forward the predictive power of kinetic Monte Carlo simulations for detailed (de)polymerization chemistries

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Performance analysis of kinetic Monte Carlo algorithms for synthesis of linear polymers

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How increasingly powerful PRE modeling tools allow to unlock the full potential of FRP and RDRP in aqueous emulsion

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A novel interpretation of measured and simulated PLP data

Figure 1 - Simulated ν dependency of the observed kp in vinyl acetate PLP at 323 K. Case 1 (♦): chain length independent head-to-tail prop., Case 2 (■): chain length dependent head-to-tail prop., Case 3 (●): chain length dependent head-to-tail, head-to-head, tail-to-tail, and tail-to-head prop., and Case 4 (▲): Case 3 with backbiting by head and tail radicals, and mid-chain prop. Pulsed laser polymerization (PLP) is an interesting technique to study individual reactions.1-4 In PLP, photoinitiator radical fragments are generated at laser pulses with a frequency ν (or dark time Δt = ν-1). Depending on the PLP conditions and the monomer type, the molar mass distribution (MMD) can possess specific characteristics, allowing the determination of intrinsic rate coefficients. Most known is that under well-chosen conditions a multimodal MMD with inflection points Lj (j = 1, 2, …) is obtained, allowing the determination of the propagation rate coefficient kp ([M]0: initial monomer concentration): (1) In this contribution, kinetic Monte Carlo (kMC) modeling is applied to allow a further understanding and exploitation of PLP. For PLP of acrylates, regression analysis to low frequency inflection point data at various solvent volume fractions is proposed as an additional new method to estimate the backbiting rate coefficient kbb.5 Moreover, it is demonstrated that photodissociation, chain initiation and termination reactivities can be extracted from the complete PLP MMD.6 For the first time, the ratio of MMD peak heights has been used for the fast and reliable estimation of the photodissociation quantum yield,Φ.7 For PLP of vinyl acetate a unique combination of ab initio calculated rate coefficients and kMC simulations is considered to explain the experimental8 ν dependency of the observed kp (cf. Case 4 in Figure 1; Eq. (1) with kpobs). Via a stepwise extension of the kMC model (cf. 4 cases in Figure 1), the ν dependency is attributed to backbiting of tail radicals formed via head-to-head propagation.9 In contrast to acrylates, backbiting of head radicals is shown to be kinetically insignificant in VAc PLP, further highlighting the chemical difference between both vinyl monomer types. Please click Additional Files below to see the full abstract

Surfactant-Free Peroxidase-Mediated Enzymatic Polymerization of a Biorenewable Butyrolactone Monomer via a Green Approach:Synthesis of Sustainable Biobased Latexes

A green surfactant-free one-pot horseradish peroxidase-mediated enzymatic polymerization is successfully applied to produce a sustainable and thermally stable biobased high average molar mass poly(α-methylene-γ-butyrolactone) (PMBL) at ambient conditions in water for the first time. The initiation step required only very low concentrations of hydrogen peroxide and 2,4-pentanedione water-soluble initiator to generate the keto-enoxy radicals responsible for forming the primary latex particles. The polymer nanoparticles can be seen as monodisperse, and the biobased latexes are colloidally stable and likely stabilized by the adsorption of 2,4-pentanedione moieties on the particle surfaces. Polymerizations in air produced a 98% yield of PMBL after only 3 h, highlighting the relevance of molecular oxygen. An array of characterization techniques such as dynamic light scattering (DLS), Fourier transform infrared (FTIR), 1H, 13C, and HSQC two-dimensional (2D) nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and size-exclusion chromatography (SEC) are used to confirm the properties of the synthesized latexes. The PMBL exhibited high thermal stability, with only a 5% weight loss at 340 °C and a glass-transition temperature of 200 °C, which is double that of polymethyl methacrylate (PMMA). This research provides an interesting pathway for the synthesis of sustainable biobased latexes via enzymes in a green environment using just water at ambient conditions and the potential use of the polymer in high-temperature applications.</p

Surfactant-Free Peroxidase-Mediated Enzymatic Polymerization of a Biorenewable Butyrolactone Monomer via a Green Approach:Synthesis of Sustainable Biobased Latexes

A green surfactant-free one-pot horseradish peroxidase-mediated enzymatic polymerization is successfully applied to produce a sustainable and thermally stable biobased high average molar mass poly(α-methylene-γ-butyrolactone) (PMBL) at ambient conditions in water for the first time. The initiation step required only very low concentrations of hydrogen peroxide and 2,4-pentanedione water-soluble initiator to generate the keto-enoxy radicals responsible for forming the primary latex particles. The polymer nanoparticles can be seen as monodisperse, and the biobased latexes are colloidally stable and likely stabilized by the adsorption of 2,4-pentanedione moieties on the particle surfaces. Polymerizations in air produced a 98% yield of PMBL after only 3 h, highlighting the relevance of molecular oxygen. An array of characterization techniques such as dynamic light scattering (DLS), Fourier transform infrared (FTIR), 1H, 13C, and HSQC two-dimensional (2D) nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and size-exclusion chromatography (SEC) are used to confirm the properties of the synthesized latexes. The PMBL exhibited high thermal stability, with only a 5% weight loss at 340 °C and a glass-transition temperature of 200 °C, which is double that of polymethyl methacrylate (PMMA). This research provides an interesting pathway for the synthesis of sustainable biobased latexes via enzymes in a green environment using just water at ambient conditions and the potential use of the polymer in high-temperature applications.</p