Journal
ENVIRONMENTAL POLLUTION
Volume 298, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2022.118821
Keywords
High-density polyethylene bead; Microplastic; Hydrolytic enzyme; Model calibration; Protease; Kinetic constant
Categories
Funding
- Natural Sciences and Engineering Research Council of Canada [RGPIN-2019-06747, RGPAS-2019-00102]
- Ontario Ministry of Research and Innovation (Ontario Research Fund-Research Excellence) [RE09-077]
Ask authors/readers for more resources
Microplastic beads are an emerging contaminant that can cause serious environmental and public health problems. This study investigates the degradation of high-density polyethylene beads by hydrolytic enzymes, specifically lipase and protease, under various experimental conditions such as temperature. The results suggest that hydrolytic enzymes can be an efficient technology for large-scale polyethylene bead removal, especially in anaerobic digestion processes.
Microplastic beads are an emerging contaminant that can cause serious environmental and public health problems. Potential bypass of microplastic beads from wastewater to sludge treatment systems is a key challenge in the conventional wastewater treatment process. Moreover, there are no systematic studies on microplastic bead degradation by hydrolytic enzymes that are rich in concentration within wastewater and sludge treatment processes (e.g., anaerobic digestion (AD)). In this study, lab-scale experiments were conducted to investigate the degradation of high-density polyethylene beads by hydrolytic enzymes (e.g., lipase) under various experimental conditions (e.g., temperature). In a 3-day batch experiment, protease was most effective in polyethylene bead degradation as 4.0% of the initial bead mass was removed at an enzyme concentration of 88 mg/L under thermophilic temperature (55 degrees C). It was also found that the increasing enzyme concentration and high temperature enhanced the polyethylene bead degradation. In a separate 7-day experiment with repeated doses of protease, 23.3% of the initial mass of beads was removed at thermophilic temperature, indicating that AD with a long retention time (e.g., 20 days) and heated temperature has a significant potential for polyethylene bead degradation. A mathematical model was developed and calibrated using the experimental results to estimate the kinetic constant of the high-density polyethylene bead reduction by an enzyme (k(1,i)) and enzyme self-decay constant (k(2,ii)). The calibrated k(1,i) ranged from 5.0 to 8.1 x 10(-4) L/mg/hr while k(2,ii) was 0.44-1.10 L/mg/hr. Using the calibrated model, degradation of polyethylene beads using a mixture of cellulase and protease was simulated, considering an interactive-decay reaction between the two enzymes. The calibrated model was used to simulate the polyethylene bead degradation in AD where 70-95% of the initial bead mass was removed at typical retention time under mesophilic digestion (37.5 degrees C). Based on the experimental and simulation results, it can be concluded that hydrolytic enzymes can be an efficient technology for large-scale high-density polyethylene bead removal applications.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available