Chao Chai
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Chao Chai has a total of 62 co-authors. Here are the top co-authors by number of shared publications:
Wei Ge
School of Life Sciences, Shandong Province Key Laboratory of Applied Mycology, Qingdao Agricultural University, Qingdao, China
23 shared publicationsJuan Wu
School of Resources and Environment, Qingdao Engineering Research Center for Rural Environment, Qingdao Agricultural University, Qingdao, China
16 shared publicationsNingning Song
School of Resources and Environment, Qingdao Engineering Research Center for Rural Environment, Qingdao Agricultural University, Qingdao, China
8 shared publicationsTao Jiang
School of Ocean, Yantai University, Yantai 264005, China
7 shared publicationsDong Ma
Qingdao Engineering Research Center for Rural Environment, Qingdao Agricultural University, Qingdao, 266109, China
6 shared publicationsHao Liang
School of Engineering, China Pharmaceutical University, Nanjing, China
6 shared publications
Latest Publications
- 26 April 2024
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 31 (22) , 33047-33057
Exploring the release mechanism of micro/nanoplastics from different layers of masks in water: towards reduction of plastic contamination in masks
During the COVID-19 pandemic, a substantial quantity of disposable face masks was discarded, consisting of three layers of nonwoven fabric. However, their improper disposal led to the release of microplastics (MPs) and nanoplastics (NPs) when they ended up in aquatic environments. To analyze the release kinetics and size characteristics of these masks, release experiments were performed on commercially available disposable masks over a period of 7 days and micro- and nanoplastic releases were detected using fiber counting and nanoparticle tracking analysis. The study’s findings revealed that there was no significant difference (p > 0.05) in the quantity of MPs released among the layers of the masks. However, the quantity of NPs released from the middle layer of the mask was 25.9 ± 1.3 × 108 to 81.3 ± 5.3 × 108 particles/piece, significantly higher than the inner and outer layers (p < 0.05). The release process of micro/nanoplastics (M/NPs) from each layer of the mask followed the Elovich equation and the power function equation, indicating that the release was divided into two stages. MPs in the range of 1–500 µm and NPs in the range of 100–300 nm dominated the release from each layer of the mask, accounting for an average of 93.81% and 67.52%, respectively. Based on these findings, recommendations are proposed to reduce the release of M/NPs from masks during subsequent use.
- 26 April 2024
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 31 (22) , 33047-33057
Exploring the release mechanism of micro/nanoplastics from different layers of masks in water: towards reduction of plastic contamination in masks
During the COVID-19 pandemic, a substantial quantity of disposable face masks was discarded, consisting of three layers of nonwoven fabric. However, their improper disposal led to the release of microplastics (MPs) and nanoplastics (NPs) when they ended up in aquatic environments. To analyze the release kinetics and size characteristics of these masks, release experiments were performed on commercially available disposable masks over a period of 7 days and micro- and nanoplastic releases were detected using fiber counting and nanoparticle tracking analysis. The study’s findings revealed that there was no significant difference (p > 0.05) in the quantity of MPs released among the layers of the masks. However, the quantity of NPs released from the middle layer of the mask was 25.9 ± 1.3 × 108 to 81.3 ± 5.3 × 108 particles/piece, significantly higher than the inner and outer layers (p < 0.05). The release process of micro/nanoplastics (M/NPs) from each layer of the mask followed the Elovich equation and the power function equation, indicating that the release was divided into two stages. MPs in the range of 1–500 µm and NPs in the range of 100–300 nm dominated the release from each layer of the mask, accounting for an average of 93.81% and 67.52%, respectively. Based on these findings, recommendations are proposed to reduce the release of M/NPs from masks during subsequent use.
- 13 November 2023
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 30 (58) , 121702-121712
Photocatalytic degradation of polyethylene and polystyrene microplastics by α-Fe2O3/g-C3N4
- 13 November 2023
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 30 (58) , 121702-121712
Photocatalytic degradation of polyethylene and polystyrene microplastics by α-Fe2O3/g-C3N4
- Open Access
- 24 August 2023
- Published by Springer Nature in Research Square
Photocatalytic degradation of polyethylene and polystyrene microplastics by α-Fe2O3/g-C3N4
This study investigated the photodegradation of microplastics (MPs) by α-Fe2O3/g-C3N4. The effects of α-Fe2O3/g-C3N4 on MPs' surface were investigated through various techniques. With the addition of α-Fe2O3/g-C3N4 and under visible light irradiation, cracks and folds were observed on the MP films and particles. Compared to the treatment without photocatalyst addition, the mass loss of MPs increased with irradiation time when α-Fe2O3/g-C3N4 was added. Specifically, polystyrene films and particles in water showed 9.94% and 7.81% increased mass loss, respectively. The degradation of MPs using α-Fe2O3/g-C3N4 demonstrated the behavior consistent with the pseudo-first-order kinetic model. The presence of α-Fe2O3/g-C3N4 led to an increase in surface oxygen-containing functional groups and crystallinity while decreasing the average molecular weight of MPs. After 30 days of irradiation, the characteristic tensile bands of MPs with α-Fe2O3/g-C3N4 significantly increased, and the detection of carboxyl bands indicated the formation of carboxylic acid, ketones, and lactones as degradation products.
- 24 August 2023
- Published by Springer Nature in Research Square
Open AccessPhotocatalytic degradation of polyethylene and polystyrene microplastics by α-Fe2O3/g-C3N4
This study investigated the photodegradation of microplastics (MPs) by α-Fe2O3/g-C3N4. The effects of α-Fe2O3/g-C3N4 on MPs' surface were investigated through various techniques. With the addition of α-Fe2O3/g-C3N4 and under visible light irradiation, cracks and folds were observed on the MP films and particles. Compared to the treatment without photocatalyst addition, the mass loss of MPs increased with irradiation time when α-Fe2O3/g-C3N4 was added. Specifically, polystyrene films and particles in water showed 9.94% and 7.81% increased mass loss, respectively. The degradation of MPs using α-Fe2O3/g-C3N4 demonstrated the behavior consistent with the pseudo-first-order kinetic model. The presence of α-Fe2O3/g-C3N4 led to an increase in surface oxygen-containing functional groups and crystallinity while decreasing the average molecular weight of MPs. After 30 days of irradiation, the characteristic tensile bands of MPs with α-Fe2O3/g-C3N4 significantly increased, and the detection of carboxyl bands indicated the formation of carboxylic acid, ketones, and lactones as degradation products.
- 26 May 2023
- Published by Elsevier in Science of The Total Environment
- Vol. 891, 164361
The behavior of microplastics and nanoplastics release from UV-aged masks in the water
- 26 May 2023
- Published by Elsevier in Science of The Total Environment
- Vol. 891, 164361
The behavior of microplastics and nanoplastics release from UV-aged masks in the water
- 10 November 2022
- Published by Springer Nature in Journal of Soils and Sediments
- Vol. 23 (3) , 1511-1523
Remediation of polycyclic aromatic hydrocarbons in aged agricultural soil using spent Pleurotus eryngii mushroom substrate
- 10 November 2022
- Published by Springer Nature in Journal of Soils and Sediments
- Vol. 23 (3) , 1511-1523
Remediation of polycyclic aromatic hydrocarbons in aged agricultural soil using spent Pleurotus eryngii mushroom substrate
- 29 September 2022
- Published by Elsevier in Marine Pollution Bulletin
- Vol. 184, 114184
Release of microplastics and nanoplastics in water from disposable surgical masks after disinfection
- 29 September 2022
- Published by Elsevier in Marine Pollution Bulletin
- Vol. 184, 114184
Release of microplastics and nanoplastics in water from disposable surgical masks after disinfection
- 13 November 2021
- Published by Elsevier in Science of The Total Environment
- Vol. 816, 151650
Release kinetics of microplastics from disposable face masks into the aqueous environment
- 13 November 2021
- Published by Elsevier in Science of The Total Environment
- Vol. 816, 151650
Release kinetics of microplastics from disposable face masks into the aqueous environment
- 1 October 2021
- Published by Elsevier in Marine Pollution Bulletin
- Vol. 171, 112782
Phthalate esters in surface sediments from fishing ports in Circum-Bohai-Sea region, China
- 1 October 2021
- Published by Elsevier in Marine Pollution Bulletin
- Vol. 171, 112782
Phthalate esters in surface sediments from fishing ports in Circum-Bohai-Sea region, China
- 15 September 2021
- Published by Taylor & Francis in Bioremediation Journal
- Vol. 26 (4) , 305-317
Bioremediation of polycyclic aromatic hydrocarbons from an aged contaminated agricultural soil using degrading bacteria and soil amendments
The combined effects of degrading bacteria (Paracoccus sp. LXC), humic acid (HA), and soil amendments, including chicken manure, biochar, and wormcast, were investigated through 84 d of incubation in order to improve the remediation of polycyclic aromatic hydrocarbon (PAH) in aged contaminated agricultural soil. PAH concentrations and dissipation kinetics were analyzed, and the biomass and communities of microorganisms and soil enzyme activities were examined to clarify the possible mechanism. The highest removal efficiency of PAHs was 42.1% when treated with Paracoccus sp. LXC combined with biochar and HA. PAH dissipation was consistent with the first-order kinetics model and the half-life of PAHs decreased from 2323.3 d in the natural attenuation to 103–277 d in the amended microcosms. Soil amendments and HA promoted the development of PAH-degrading bacteria and diversity of bacterial communities in soil but not that of fungi. The removal efficiency of PAHs was positively correlated with the density of PAH-degrading bacteria and soil urease (Ure), dehydrogenase (Deh), and manganese-dependent peroxidase (Mnp) activities (r = 0.824–0.941, p < .01). The Paracoccus sp. LXC apparently removed 2–4-ring PAHs, and biochar and wormcast were effective in removing 2–4-ring and 5–6-ring PAHs, respectively. The combined bioremediation strategy using degrading bacteria with soil amendments and HA has high potential for PAH removal in aged contaminated agricultural soil and the possible mechanism was the combination of bioaugmentation with Paracoccus sp. LXC and biostimulation with HA and soil amendments.
- 15 September 2021
- Published by Taylor & Francis in Bioremediation Journal
- Vol. 26 (4) , 305-317
Bioremediation of polycyclic aromatic hydrocarbons from an aged contaminated agricultural soil using degrading bacteria and soil amendments
The combined effects of degrading bacteria (Paracoccus sp. LXC), humic acid (HA), and soil amendments, including chicken manure, biochar, and wormcast, were investigated through 84 d of incubation in order to improve the remediation of polycyclic aromatic hydrocarbon (PAH) in aged contaminated agricultural soil. PAH concentrations and dissipation kinetics were analyzed, and the biomass and communities of microorganisms and soil enzyme activities were examined to clarify the possible mechanism. The highest removal efficiency of PAHs was 42.1% when treated with Paracoccus sp. LXC combined with biochar and HA. PAH dissipation was consistent with the first-order kinetics model and the half-life of PAHs decreased from 2323.3 d in the natural attenuation to 103–277 d in the amended microcosms. Soil amendments and HA promoted the development of PAH-degrading bacteria and diversity of bacterial communities in soil but not that of fungi. The removal efficiency of PAHs was positively correlated with the density of PAH-degrading bacteria and soil urease (Ure), dehydrogenase (Deh), and manganese-dependent peroxidase (Mnp) activities (r = 0.824–0.941, p < .01). The Paracoccus sp. LXC apparently removed 2–4-ring PAHs, and biochar and wormcast were effective in removing 2–4-ring and 5–6-ring PAHs, respectively. The combined bioremediation strategy using degrading bacteria with soil amendments and HA has high potential for PAH removal in aged contaminated agricultural soil and the possible mechanism was the combination of bioaugmentation with Paracoccus sp. LXC and biostimulation with HA and soil amendments.
- 1 March 2021
- Published by Elsevier in Marine Pollution Bulletin
- Vol. 164, 112037
Polybrominated diphenyl ethers in surface sediments from fishing ports along the coast of Bohai Sea, China
- 1 March 2021
- Published by Elsevier in Marine Pollution Bulletin
- Vol. 164, 112037
Polybrominated diphenyl ethers in surface sediments from fishing ports along the coast of Bohai Sea, China