COVID-19: Performance study of microplastic inhalation risk posed by wearing masks.

Wearing face masks has become the new normal worldwide due to the global spread of the coronavirus disease 2019. The inhalation of microplastics due to the wearing of masks has rarely been reported. The present study used different types of commonly used masks to conduct breathing simulation experiments and investigate microplastic inhalation risk. Microplastic inhalation caused by reusing masks that underwent various treatment processes was also tested. Results implied that wearing masks considerably reduces the inhalation risk of particles (e.g., granular microplastics and unknown particles) even when they are worn continuously for 720 h. Surgical, cotton, fashion, and activated carbon masks wearing pose higher fiber-like microplastic inhalation risk, while all masks generally reduced exposure when used under their supposed time (<4 h). N95 poses less fiber-like microplastic inhalation risk. Reusing masks after they underwent different disinfection pretreatment processes can increase the risk of particle (e.g., granular microplastics) and fiber-like microplastic inhalation. Ultraviolet disinfection exerts a relatively weak effect on fiber-like microplastic inhalation, and thus, it can be recommended as a treatment process for reusing masks if proven effective from microbiological standpoint. Wearing an N95 mask reduces the inhalation risk of spherical-type microplastics by 25.5 times compared with not wearing a mask.

Effect of microplastic particle size to the nutrients removal in activated sludge system.

Microplastics as emerging environmental pollutants, its effect to the bioprocess of water and wastewater treatment has aroused concern. This study investigated the effects of microplastic polystyrene (PS) particle size to the activated sludge nutrient removal process. The ammonia, nitrite, nitrate and phosphorus removal under various PS particle size during nitrification and denitrification process was tested. The results indicated that with PS particle size 150-300 µm, the ammonia oxidation during nitrification process was inhibited to 71%, 92%, and 80% as compared with the blank reactor, for PS concentration at 0.01 g/L, 0.05 g/L and 0.10 g/L, respectively. The nitrite accumulation during nitrification process was also high at PS particle size 150-300 µm and concentration no less than 0.05 g/L. The nitrate reduction during the denitrification process was all inhibited to 69%-94% as compared with the blank, except for reactor No.4. The phosphate removal during nitrification process was not affected by the existence of microplastics PS, the average removal rate was over 80% after 2 h and over 95% after 3 h, respectively. The microplastics particle size plays important role in affecting the activated sludge nutrient removal process.

Effect of microplastic on anaerobic digestion of wasted activated sludge.

Over 90% of microplastics that enter wastewater treatment plants end in the wasted activated sludge. The effect of microplastic abundance on the activated sludge anaerobic digestion has been rarely reported. This study investigated the methane production performance during anaerobic digestion with different abundance of microplastic doses (0, 1,000, 3,000, 6,000, 10,000, 30,000, 60,000, 100,000 and 200,000 polyester particle/kg activated sludge). The methane production was reduced to 88.53 ± 0.5%, 90.09 ± 1.2%, 89.95 ± 4.7%, 95.08 ± 0.5%, 90.29 ± 0.5%, 93.16 ± 0.8%, 92.92 ± 1.3%, and 92.72 ± 0.6% as compared with control after digestion for 59 days. The methane production of all conditions was fitted with the logarithm model (R2 > 0.95) and one-substrate model (R2 > 0.99). The predicted and actual methane production values of digestion for 59 days had high correlation in all conditions with R2 > 0.95. The analysis based on the biochemical methane potential test model indicated that the methane production potential (B0) and hydrolysis coefficient (k) decreased at nearly all tested conditions. The reactor digestate with microplastics retained higher organic matter and nutrient concentration and had slightly lower dewaterability than the control. The inhibition of methane production potential could be attributed to the incomplete digestion with the existence of microplastics. The microbial community showed no significant difference with and without microplastics.

Evaluation of partial nitrification efficiency as a response to cadmium concentration and microplastic polyvinylchloride abundance during landfill leachate treatment.

The partial nitrification efficiency response to the presence of cadmium (Cd2+) and microplastics was investigated. Microplastics polyvinylchloride (PVC) abundance was 0-10,000 particles/L, and Cd2+ concentration was 0-10 mg/L. Cd-only inhibited the NH4+-N oxidation rate 1.21, 1.23, and 1.18 times with concentrations at 1, 5, and 10 mg/L, respectively. PVC-only inhibited NH4+-N oxidation rate 1.01, 1.21 and 1.05 times with PVC abundance at 1000, 5000 and 10,000 particles/L, respectively. The ammonia oxidation rate was improved with the co-existence of PVC and Cd2+ at the conditions PVC1000 and PVC5000, which could be attributed to the PVC. PVC at 1000 particles/L could act as carrier and mitigate the negative effect of Cd2+ to the partial nitrification process. Moreover, the partial nitrification process was largely inhibited with PVC abundance at 10,000 particles/L. First-order kinetic models could simulate the NH4+-N, NO2-N, and NO3--N changes in the partial nitrification process.

Evaluation of microplastic polyvinylchloride and antibiotics tetracycline co-effect on the partial nitrification process.

This study investigated the co-effect of microplastic polyvinylchloride and antibiotics tetracycline to partial nitrification process in treating high ammonia wastewater. The average ammonia oxidation rate of all reactors was 53.58, 56.17 and 42.08 mg·N/L·h in round 1, round 7 and round 13, respectively. The ammonia oxidation rate was reduced to 89.40%, 79.08%, 80.60%, 73.37%, 69.50%, 75.72%, 98.93% and 66.04% from 1st round of test to 13th round of test at reactor R1 to R8. The average nitrosation rate was always over 80% in all conditions tested. Tetracycline removal rate was attributed to sludge adsorption in all reactors and was increased continuously with the increment of tetracycline concentration. The nitrous oxide emission was keep decreasing from round 1 to round 13 in all reactors tested. The microbial community results revealed that with the existence of tetracycline and microplastics, the relative abundance of Bacteroidetes were reduced and Proteobacteria were increased.

Novel imidazole fluorescent poly(ionic liquid) nanoparticles for selective and sensitive determination of pyrogallol.

This paper reports novel imidazole fluorescent poly(ionic liquid) nanoparticles (FPILNs) of poly(1-[(4-methyphenyl)methyl]-3-vinyl-imidazolium bromide (poly([MVI]Br) for selective and sensitive determination of pyrogallol. An imidazole ionic liquid of 1-[(4-methyphenyl)methyl]-3-vinyl-imidazolium bromide ([MVI]Br) was synthesized and used as the only monomer to obtain poly([MVI]Br) possessing phenyl fluorophores using a radical polymerization technique. The obtained poly([MVI]Br) can form nanoparticles in water. Scanning electron microscopy and dynamic light scattering results revealed majority of poly([MVI]Br) FPILNs with diameters ranging from 40 to 400nm. Although [MVI]Br showed weak fluorescence intensity, poly([MVI]Br) FPILNs exhibited strong fluorescence intensity with a quantum yield of 0.192, which is attributed to the presence of significant number of phenyl fluorophores and rigid construction. The selective and sensitive determination of pyrogallol was achieved through fluorescence quenching of poly([MVI]Br) FPILNs, and the quenching was attributed to the oxidation of poly([MVI]Br) FPILNs by O2˙¯ produced by pyrogallol autoxidation. The poly([MVI]Br) FPILNs-based sensor demonstrated a good linear relationship between the extent of fluorescence quenching and the concentration of pyrogallol in a range of 0.05 - 10.0µM, achieving a detection limit of 0.01µM. Furthermore, the poly([MVI]Br) FPILNs-based assay detected pyrogallol in environmental water samples, suggesting its potential to be applied for practical purposes.