Dataset Information

Degradation of Plastics in Simulated Landfill Conditions.

ABSTRACT: Different degradable plastics have been promoted as a solution for the accumulation of waste in landfills and the natural environment; in Mexico, the most popular options are oxo-degradable, which degrade in a sequential abiotic-biotic process, and compostable plastics. In this research, high-density polyethylene, oxo-degradable high-density polyethylene, and certified compostable plastic were exposed to simulated landfill conditions in an 854-day-long experiment to assess their degradation. High-density polyethylene showed limited degradation, due mainly to surface erosion, evidenced by a 13% decrease in elongation at break. The pro-oxidant additive in the oxo-degradable plastic increased this loss of mechanical properties to 27%. However, both plastic films kept their physical integrity and high molecular weight by the end of the experiment, evidencing degradation but no biodegradation. While the compostable film fragmented, had a lower molecular weight at the end of the experiment, and decreased the presence of C=O bonds, this degradation took place remarkably slower than expected from a composting process. Results show that oxo-degradable and compostable plastics will not biodegrade readily in landfills. This fact should be known and understood for decision-makers to match the characteristics of the materials to the features of the waste management systems.

SUBMITTER: Xochitl QP

PROVIDER: S-EPMC8037001 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

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Degradation of Plastics in Simulated Landfill Conditions.

Xochitl Quecholac-Piña QP María Del Consuelo Hernández-Berriel HB María Del Consuelo Mañón-Salas MS Rosa María Espinosa-Valdemar EV Alethia Vázquez-Morillas VM

Polymers 20210325 7

Different degradable plastics have been promoted as a solution for the accumulation of waste in landfills and the natural environment; in Mexico, the most popular options are oxo-degradable, which degrade in a sequential abiotic-biotic process, and compostable plastics. In this research, high-density polyethylene, oxo-degradable high-density polyethylene, and certified compostable plastic were exposed to simulated landfill conditions in an 854-day-long experiment to assess their degradation. Hig ...[more]

PMID: 33805998

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Project description:The OH-initiated photo-oxidation of piperidine and the photolysis of 1-nitrosopiperidine were investigated in a large atmospheric simulation chamber and in theoretical calculations based on CCSD(T*)-F12a/aug-cc-pVTZ//M062X/aug-cc-pVTZ quantum chemistry results and master equation modeling of the pivotal reaction steps. The rate coefficient for the reaction of piperidine with OH radicals was determined by the relative rate method to be kOH-piperidine = (1.19 ± 0.27) × 10-10 cm3 molecule-1 s-1 at 304 ± 2 K and 1014 ± 2 hPa. Product studies show the piperidine + OH reaction to proceed via H-abstraction from both CH2 and NH groups, resulting in the formation of the corresponding imine (2,3,4,5-tetrahydropyridine) as the major product and in the nitramine (1-nitropiperidine) and nitrosamine (1-nitrosopiperidine) as minor products. Analysis of 1-nitrosopiperidine photolysis experiments under natural sunlight conditions gave the relative rates jrel = j1-nitrosoperidine/jNO2 = 0.342 ± 0.007, k3/k4a = 0.53 ± 0.05 and k2/k4a = (7.66 ± 0.18) × 10-8 that were subsequently employed in modeling the piperidine photo-oxidation experiments, from which the initial branchings between H-abstraction from the NH and CH2 groups, kN-H/ktot = 0.38 ± 0.08 and kC2-H/ktot = 0.49 ± 0.19, were derived. All photo-oxidation experiments were accompanied by particle formation that was initiated by the acid-base reaction of piperidine with nitric acid. Primary photo-oxidation products including both 1-nitrosopiperidine and 1-nitropiperidine were detected in the particles formed. Quantum chemistry calculations on the OH initiated atmospheric photo-oxidation of piperidine suggest the branching in the initial H-abstraction routes to be ∼35% N1, ∼50% C2, ∼13% C3, and ∼2% C4. The theoretical study produced an atmospheric photo-oxidation mechanism, according to which H-abstraction from the C2 position predominantly leads to 2,3,4,5-tetrahydropyridine and H-abstraction from the C3 position results in ring opening followed by a complex autoxidation, of which the first few steps are mapped in detail. H-abstraction from the C4 position is shown to result mainly in the formation of piperidin-4-one and 2,3,4,5-tetrahydropyridin-4-ol, whereas H-abstraction from N1 under atmospheric conditions primarily leads to 2,3,4,5-tetrahydropyridine and in minor amounts of 1-nitrosopiperidine and 1-nitropiperidine. The calculated rate coefficient for the piperidine + OH reaction agrees with the experimental value within 35%, and aligning the theoretical numbers to the experimental value results in k(T) = 2.46 × 10-12 × exp(486 K/T) cm3 molecule-1 s-1 (200-400 K).

Dataset Information

Degradation of Plastics in Simulated Landfill Conditions.

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Degradation of Plastics in Simulated Landfill Conditions.

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