Comparative study of adsorption and slow-release performance and mechanism of phosphoric acid and ammonia-modified biochars on 2,4-dichlorophenoxyacetic acid

[Display omitted] •The prominent adsorption mechanisms of P-WBC were hydrogen bonding and P-containing groups bonding, while those of NP-WBC were pore filling and π-π interactions.•Density functional theory calculation confirmed that the main active reaction sites of P-WBC and NP-WBC were C-O-P1 and...

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Veröffentlicht in:Separation and purification technology 2025-06, Vol.358, p.130470, Article 130470
Hauptverfasser: Tang, Liangjie, Chen, Shuiqing, Wang, Ning, Jiang, Xiaoqian
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Sprache:eng
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Zusammenfassung:[Display omitted] •The prominent adsorption mechanisms of P-WBC were hydrogen bonding and P-containing groups bonding, while those of NP-WBC were pore filling and π-π interactions.•Density functional theory calculation confirmed that the main active reaction sites of P-WBC and NP-WBC were C-O-P1 and pyridinic N, respectively.•500 °C P-WBC exhibited exceptional thermal stability, high adsorption capacity (75.27 mg/g) and the most effective slow-release performance (9.34%) for 2,4-D.•500 °C P-WBC@2,4-D demonstrated equivalent herbicidal efficacy to commercially available 2,4-D. Developing slow-release pesticides and reducing the migration of pesticides are the keys to improving the utilization efficiency of pesticides. Here, phosphorus-modified (P-WBC) and subsequent ammonia-modified biochar (NP-WBC) were prepared using pine tree sawdust at different pyrolysis temperatures (300 °C, 500 °C, and 700 °C), while the adsorption and desorption capacities of P-WBC and NP-WBC on 2,4-dichlorophenoxyacetic acid (2,4-D) were compared, as well as their intrinsic mechanism disparity. It was found that pyrolysis temperature, phosphorus- and ammonia-modification all improved the adsorption and slow-release of 2,4-D from biochar significantly through enriching the surface morphology, pore structure and optimizing the composition of functional groups of biochar. The adsorption mechanisms involved pore filling, hydrogen bonding, π-π interactions and phosphorus/nitrogen (P/N)-containing groups bonding, while the release behavior was predominantly governed by Fickian diffusion. The main active reaction sites of P-WBC and NP-WBC were the edge-located phosphate-like functional groups (C-O-P1) and pyridinic N, respectively, and C-O-P1 had the highest affinity for 2,4-D, as corroborated by density functional theory (DFT) calculation. Compared to NP-WBC, P-WBC exhibited greater 2,4-D adsorption and slow-release capacities, which was attributed to the stronger hydrogen bonding and P-containing functional groups bonding of C-O-P1 with 2,4-D. In particular, 500 °C P-WBC demonstrated exceptional thermal stability, great 2,4-D adsorption capacity (75.27 mg/g), and the most effective slow-release performance (9.34%). In addition, further germination experiments showed that 500 °C P-WBC loaded with 2,4-D (500 °C P-WBC@2,4-D) exhibited equivalent herbicidal efficacy to commercially available 2,4-D while also reducing the toxicity of the pesticide to maize to a certain extent. This work offe
ISSN:1383-5866
DOI:10.1016/j.seppur.2024.130470