The pervasive discharge of antibiotics like oxytetracycline (OTC) into aquatic systems poses escalating ecological and public health risks due to incomplete metabolic assimilation and environmental persistence [
1–
3]. Conventional wastewater treatments exhibit limited removal efficiencies and risks of secondary pollution, necessitating advanced oxidation processes (AOPs) for contaminant mineralization [
4]. PMS-based AOPs, distinguished by robust oxidation capacity and broad pH adaptability, outperform ozone- or H
2O
2-driven systems [
5,
6] However, traditional PMS activation methods relying on UV irradiation, thermal energy, or transition metals face challenges including energy inefficiency and metal leaching, underscoring the imperative for sustainable metal-free catalysts [
7,
8].
Carbonaceous materials, particularly biochar derived from agro-industrial waste, offer promise due to their tunable porosity, surface functionality, and environmental compatibility [
9]. Nitrogen (N) doping enhances PMS activation by modulating electron density and creating defect-mediated active sites, improving adsorption and catalytic efficiency. In contrast, single-atom doping with oxygen (O), sulfur (S), or boron (B) yields limited improvements, primarily altering surface polarity without establishing stable catalytic centers [
10]. To enhance the performance of N-doped biochar catalysts, metal-N co-doped catalysts (
e.g., Fe/N, Co/N, Mn/N) have been developed [
11,
12]. However, this approach introduces risks of metal leaching and increases production and disposal costs, despite improving catalytic activity. Critically, oxygen's high electronegativity and lone-pair electrons theoretically synergize with nitrogen's electron-donating properties, optimizing sp
2 carbon lattice polarity and generating dual-active centers [
13]. Such N, O co-doping could mitigate the limitations of single dopants by enhancing interfacial electron transfer kinetics and stabilizing metastable radical intermediates, which is a hypothesis that requires rigorous validation through both experimental and computational methods.
Importantly, while heteroatom-doped carbons typically activate PMS
via radical pathways (SO
4•−,
•OH, O
2•−), non-radical mechanisms (
1O
2 generation, electron transfer) demonstrate superior selectivity and resistance to environmental interference, making them ideal for complex matrices [
14]. Tailoring catalysts to favor non-radical pathways demands precise control over dopant configurations (
e.g., type, coordination) and defect engineering. However, the interplay between multi-heteroatom doping, surface defects, and PMS activation mechanisms remains poorly resolved, particularly regarding
1O
2 generation pathways [
15]. Addressing these gaps is critical for designing catalysts that balance high reactivity with environmental adaptability, guiding practical applications in real-world water remediation [
16]. Furthermore, current research predominantly evaluates catalytic performance through short-term (< 1 h) static batch experiments, emphasizing initial kinetics but neglecting hydrodynamic effects on mass transfer and long-term stability [
17]. These idealized conditions poorly replicate natural aquatic environments, where turbulent flows govern pollutant-catalyst interactions.
To address these research gaps, we developed a nonmetallic N, O-doped biochar catalyst (NOBCBM) using wheat straw as a precursor to facilitate green synthesis and in-situ heteroatom doping. This study aims to: (1) Demonstrate that N, O co-doping overcomes the limitations of single N-doped biomass catalysts to achieve efficient OTC degradation; (2) elucidate non-radical degradation mechanisms, reactive sites, and pollutant degradation pathways, demonstrating system resilience to environmental perturbations; (3) simulate the real water flow conditions and consider the influence of time factors on the degradation process; (4) study the impact of purified water on plant growth and evaluate the ecological safety and environmental friendliness of the catalyst. By exploring the synergistic effects of N, O co-doping and employing holistic evaluation methods, this work not only enhances understanding of heteroatom-engineered biochar catalysis but also offers a scalable, sustainable strategy for mitigating antibiotic pollution in aquatic ecosystems, thereby advancing the field toward practical, environmentally responsible solutions.
Following ball milling, NSBC
BM displayed fragmented flake-like graphite structures (
Fig. 1a), indicative of mechanical shear forces disrupting the original biomass architecture. The synergistic combination of ball milling and N/O co-doping in NOBC
BM resulted in a highly porous, irregular microstructure (
Fig. 1b). This structural evolution arises from two key processes: (1) thermal decomposition of dicyandiamide (DCD) during pyrolysis generated gaseous byproducts that fracture the carbon matrix, and (2) oxygen atom incorporation induced lattice strain, creating interconnected pores and surface defects [
18]. Elemental mapping confirmed homogeneous distribution of carbon, nitrogen (22.8%), and oxygen (25.3%) throughout NOBC
BM (
Fig. 1c, Fig. S1a in Supporting information), ensuring uniform active site accessibility. Fig. S1b (Supporting information) displayed N
2 adsorption-desorption isotherms for NSBC
BM and NOBC
BM, revealing type Ⅳ curves with H3 hysteresis loops characteristic of mesoporous materials. Structural parameters in Table S1 (Supporting information) showed that NOBC
BM possessed enhanced textural properties relative to NSBC
BM, including the larger BET surface area (105.55
vs. 99.26 m
2/g) and the higher mesopore volume (0.59
vs. 0.48 cm
3/g). These improvements correlated with superior dispersity, accelerated mass transfer, and elevated OTC adsorption capacity.
Surface functionalization was systematically characterized through X-ray photoelectron spectroscopy (XPS) and FTIR spectroscopy. FTIR spectra (
Fig. 1d) revealed the enhanced oxygen-containing functionalities in NOBC
BM compared to NSBC
BM, particularly intensified C–O (1220 cm
−1) and C═O (1560 cm
−1) stretching vibrations [
19]. These observations aligned with XPS quantification: C 1s deconvolution showed that C–O and C═O contributions increased from 17% and 7% in NSBC
BM to 28% and 17% in NOBCBM, respectively (
Fig. 1f). Concurrently, N 1s spectra demonstrated a doubling of oxidized nitrogen species (6%
vs. 3% in N 1s XPS,
Fig. 1g), confirming oxygen doping's role in modifying chemical environments. These oxygen-rich functional groups enhanced PMS adsorption and electron transfer kinetics [
20].
Raman spectroscopy data from
Fig. 1e showed two characteristic bands: The D band at 1360 cm
−1 and the G band at 1571 cm
−1. The intensity ratio of the D and G bands (
SD1/
SG) is a well-established indicator for evaluating defect concentration in biochar materials [
21]. Notably, the
SD1/
SG value of NOBC
BM (5.49) was higher than that of NSBC
BM (2.32), indicating that O doping increased the defect density in the composite. The unique structure of NOBC
BM significantly enhances its targeting of PMS and OTC through a series of synergistic mechanisms. In terms of electronic modulation of N, O doping, the pyridine nitrogen atom in the NOBC
BM structure significantly enhances the adsorption capacity of PMS, allowing PMS molecules to be adsorbed onto the catalyst surface more efficiently (The proof is presented in DFT calculations) [
21]. Meanwhile, the presence of graphitic nitrogen atoms enhanced the electron conduction efficiency, ensuring smooth and unobstructed electron transfer during the catalytic reaction. In addition, the carbonyl oxygen atom in the structure further promoted the directional activation of PMS through surface dipole polarization, which enables the PMS molecules to be more efficiently converted into active oxide species on the catalyst surface (
Figs. 1d,
f,
h).
The catalytic performance of catalysts with varying N/O doping ratios was evaluated for OTC degradation (20 mg/L) (
Fig. 2a). Single oxygen-doped catalysts (OSBC
BM) exhibited markedly inferior activity compared to N-doped counterparts (NSBC
BM), confirming nitrogen doping sites as primary active centers. Notably, dual N/O doping achieved a 2.3-fold enhancement in
kobs (0.1523 min
−1) over single N-doped catalysts (0.0664 min
−1), demonstrating the critical role of synergistic non-metal interactions in amplifying catalytic efficiency (
Fig. 2b). While low oxygen content optimized activity by fine-tuning electronic structures and defect density, excessive oxygen loading suppressed performance, likely due to pore blockage at active sites. The catalyst synthesized at a 1:1:10 mass ratio (straw: MCHP: DCD) demonstrated peak efficiency (94% degradation;
kobs = 0.1523 min
−1), outperforming other formulations (
Fig. 2b). This breakthrough highlights the transformative potential of dual heteroatom engineering in overcoming the limitations of single-dopant systems, providing a scalable strategy for advanced water purification technologies.
The NOBC
BM/PMS system's OTC removal efficiency was systematically evaluated under varying PMS doses (0–0.5 mmol/L) (
Fig. 2c). OTC removal efficiency exhibited a dose-dependent increase, rising from 32% at 0 mmol/L PMS (adsorption-only phase) to 94% at 0.2 mmol/L PMS, with
kobs reaching 0.1833 min
−1 (
Fig. 2d). Notably, NOBC
BM achieved higher removal efficiency than NSBC
BM at all tested PMS concentrations, even surpassing NSBC
BM's performance at 0.5 mmol/L PMS when using only 0.2 mmol/L PMS. This stark contrast underscores dual N/O doping's ability to amplify catalytic performance while minimizing oxidant consumption, justifying the economic selection of 0.2 mmol/L PMS for subsequent studies. Adsorption equilibrium occurred rapidly within 40 min (
Figs. 2c and
e). NOBC
BM demonstrated a 32 mg/g adsorption capacity, exceeding NSBC
BM's 30 mg/g, directly attributable to oxygen doping-induced surface area expansion and adsorption site proliferation. In catalytic systems,
kobs values showed a linear correlation with PMS concentration (
Fig. 2f), driven by enhanced electron transfer and reactive oxygen species (ROS) generation at elevated oxidant levels. Standardized analysis (normalized to unit PMS/catalyst dosage) revealed NOBC
BM's
kN values (up to 91.45 min
−1 g
−2 L
2) were 2.2-fold higher than NSBC
BM's (up to 41.29 min
−1 g
−2 L
2) (
Fig. 2g), highlighting dual doping's synergistic role in optimizing active site accessibility and PMS utilization efficiency. Compared with the
kN values of the other non-metallic doped catalysts reported in the literature, the superior performance of NOBC
BM was further verified, achieving a standardized degradation rate increase of 2 to 12 times under the same conditions (
Fig. 2h, Tables S2 and S3 in Supporting information). These findings collectively demonstrate the transformative potential of N/O co-doping in advancing metal-free catalytic systems for sustainable water remediation.
The catalytic performance of NOBCBM was dose-dependent (Figs. S2a and b in Supporting information). At 0.05 g/L, OTC degradation reached equilibrium within 30 min (92.3% removal). Increasing the dosage to 0.1 g/L enhanced removal efficiency to 98.7% (kobs = 0.1917 min−1), demonstrating dual N/O doping's ability to amplify active site availability and PMS utilization. Compared to NSBCBM, NOBCBM's superior performance stems from synergistic effects: oxygen doping introduces additional defect sites, while nitrogen optimizes electron transfer, collectively increasing ROS generation per unit catalyst. The OTC concentration significantly influenced system performance (Figs. S2c and d in Supporting information). In NSBCBM/PMS systems, increasing OTC from 10 mg/L to 30 mg/L reduced removal efficiency from 91% to 62% (kobs = 0.1520–0.0479 min−1). In contrast, NOBCBM/PMS maintained higher stability under identical conditions (86%–97%), attributable to enhanced active site density and PMS activation efficiency from N/O co-doping. This dual doping strategy minimizes catalyst deactivation at elevated pollutant concentrations by preventing active site saturation.
To elucidate the degradation pathway of OTC in the NOBC
BM/PMS system, researchers employed free radical quenchers to characterize the contribution of ROS to OTC oxidation [
22]. From
Figs. 3a-
c, at PMS = 0.05 mmol/L, the inhibitory effect of adding EtOH and TBA on SO
4•‒ and
•OH was ~9%. This inhibitory effect weakened as the PMS concentration increased. As free radical trapping agents, EtOH and TBA have limited radical capturing ability. When the radical generation rate exceeds the trapping agent's capacity, some radicals escape and participate in the target reaction, weakening the inhibition. The minimal inhibition observed from quencher addition indicated that SO
4•‒ and
•OH did not serve as dominant oxidants in this system. To evaluate the role of O
2•−, SOD was introduced as a specific scavenger [
23]. Experimental results revealed negligible effects of O
2•− on OTC degradation, confirming its minor role as a reactive intermediate during the reaction.
The electron paramagnetic resonance (EPR) technique with DMPO spin trapping reagent showed weak signals of SO
4•‒,
•OH, and O
2•− in the NOBC
BM/PMS system (
Fig. 3d) [
24]. This indicated the catalytic system generates free radicals by oxidizing DMPO to DMPOX. However, free radicals have short lifetimes (usually microseconds or nanoseconds). They may rapidly decompose after generation. In EPR assays, radicals can be detected with a capture agent, but in the actual reaction, they may be quickly consumed and unable to effectively participate in the target reaction. The
1O
2 is commonly generated in PMS-based AOPs. TEMP was selected as the
1O
2 spin trapping reagent [
25].
Fig. 3d clearly shows a large amount of
1O
2 generated in the NOBC
BM/PMS system. TEMP also verified the role of
1O
2. In the NOBC
BM/PMS system, OTC removal decreased from 94.1% to 41.8% (
Fig. 3e). This means 0.03 mol/L TEMP inhibited OTC degradation by up to 52.3%, confirming
1O
2 as an effective reactive species for OTC removal [
26]. The oxidation of 9,10-diphenylanthracene (DPA) by
1O
2 produces a unique peak near 378 nm, which can detect
1O
2 [
27]. In the NOBC
BM/PMS system, the absorption peak intensity near 378 nm decreased over 10 min, furtherly indicating continuous
1O
2 consumption (
Fig. 3f). Furthermore, the accelerated OTC degradation observed upon replacing H
2O with D
2O (Fig. S3 in Supporting information), resulted in complete removal and an increase in
kobs from 0.206 min
−1 to 0.277 min
−1. This rate enhancement confirms the significant contribution of
1O
2.
A premix experiment was designed to investigate the electron transfer mechanism driving OTC degradation in the NOBC
BM/PMS system. NOBC
BM and PMS were premixed for 5, 10, and 15 min before OTC addition [
28]. As shown in Fig. S4a (Supporting information), OTC degradation efficiency decreased by only ~10% after 15 min of pre-mixing. This minimal reduction confirms that non-radical pathways dominate the reaction. The open circuit potential (OCP) measures electrode potential without current flow, reflecting material stability and reaction tendency under specific conditions. A higher OCP allows catalysts to reach the required reaction potential more easily, reducing overpotential and enhancing efficiency [
29]. Fig. S4b (Supporting information) showed NOBC
BM had an initial OCP of 0.2389 V, significantly higher than NSBC
BM (0.1338 V), confirming superior catalytic performance. Introducing PMS and OTC alters the catalyst's surface electronic state, affecting active sites and OCP values. This provided insights into electron transfer processes during pollutant oxidation [
30]. It can be seen that the OCP value decreases when OTC is added, indicating that electrons play a role in the degradation of OTC. In electrochemical impedance spectroscopy (EIS), the diameter of the semicircular arc reflects electron transfer resistance, with smaller radii indicating higher conductivity [
31]. As depicted in Fig. S4c (Supporting information), the radius followed the order NSBC
BM > NOBC
BM, demonstrating superior electrical conductivity in NOBC
BM. Tafel polarization curves (Fig. S4d in Supporting information) showed a corrosion potential order of NOBC
BM > NSBC
BM, suggesting from a thermodynamic perspective that NOBC
BM electrodes exhibit greater resistance to corrosion compared to NSBC
BM [
32].
XPS analysis identified catalytic active sites in NOBC
BM through chemical state evolution of carbon, nitrogen, and oxygen. Deconvolution of the C 1s spectrum revealed three characteristic peaks (
Fig. 1f): C–C/C═C (284.6 eV), C–O (286.0 eV), and C═O/C–N (288.7 eV). A marked decrease in C–/C═C (from 55% to 51%) and C═O/C–N (from 17% to 7%) contents suggested graphitic structure disruption, implicating these sites in non-radical mechanisms such as electron transport and singlet oxygen generation. The N 1s spectrum (
Fig. 2g) resolved four coordination states: Pyridinic N (397.9 eV), pyrrolic N (399.4 eV), graphitic N (400.5 eV), and oxidized N (403.6 eV). Pyridinic and graphitic N, due to nitrogen's higher electronegativity, modified nearby carbon charge distributions. Post-reaction, pyridinic and pyrrolic N contents decreased from 46% to 44% and 31% to 29%, likely from PMS/contaminant conversion
via adjacent activated carbon. Concurrent O 1s analysis (
Fig. 1h) demonstrated surface oxidation through intensified oxygen functionality signals, consistent with reactive species formation during catalysis. Complementary FTIR analysis (Fig. S5 in Supporting information) tracked functional group evolution across reaction cycles. Pre-catalysis spectra exhibited prominent C═O stretching (1553 cm
−1) and C–O vibrations (1235 cm
−1). After reaction, the intensity of oxygen-containing functional group stretching vibrations in NOBC
BM decreased, particularly for C═O groups, which aligned with the XPS analysis results (
Figs. 1f and
h) and suggested these groups serve as active sites in the reaction.
Additionally, in the NOBC
BM system, PMS activation began with chemisorption. N/O co-doping induced electronic modulation, forming localized electron-deficient regions. Pyridine nitrogen's lone pairs coordinated with PMS's terminal O atom, weakening the O–O bond (bond length increased from 1.471 Å to 1.472 Å
via DFT calculations) (
Fig. 4a). The high electronegativity of carbonyl oxygen (C═O) polarizes adjacent carbon atoms, creating localized electron-deficient regions that asymmetrically redistribute charge. This dipole polarization weakens the PMS O–O bond, elongating it from 1.472 Å to 1.476 Å and reducing bond strength. Consequently, the polarized carbon framework facilitates heterolytic O–O cleavage through electron transfer, preferentially generating
1O
2-dominated non-radical species rather than radical pathways, as conclusively validated through EPR and quenching experiments. Defect structures from ball milling (
e.g., five-membered rings, edge carbons) acted as electron transfer channels, enhancing electron flow from NOBC
BM to PMS. EIS showed NOBC
BM had a lower transfer resistance compared with that of NSBC
BM, confirming superior electron transfer. DFT calculations were performed to explore the activation of PMS by N/O co-doped biochar and material defects. As shown in
Fig. 4a, PMS adsorption on NOBC
BM exhibited an energy (
Ead) of -3.154 eV, which was more negative than that on BC and NSBC
BM. This stronger adsorption facilitates the formation of NOBC
BM/PMS* complexes, promotes PMS activation, and induces the generation of
1O
2, which were the key steps in the non-radical degradation pathway. Additionally, this non-metal doping was also confirmed to result in a longer O–O bond in the catalyst, which is favorable for the production of reactive species from PMS. The
Fig. 4b displayed the molecular electrostatic potential (ESP) of the materials, where positive and negative potential regions are represented by blue and red, respectively. Nitrogen atoms, with higher electronegativity, created localized potential wells by lowering the electrostatic potential around them, which enhanced the adsorption of PMS and contaminant. Oxygen atoms, with even stronger electronegativity, further reduced the potential around nitrogen atoms, improving adsorption capacity for PMS and contaminants and boosting catalytic activity. Consequently, NOBC
BM exhibited higher electron density than NSBC
BM. This finding suggests that OTC may be more effectively adsorbed onto the NOBC
BM material.
The Fukui function f − is associated with a molecule's ability to lose electrons. In chemical reactions, a higher f − value indicates the molecule is more prone to electron loss, favoring electrophilic reactions. f + relates to the molecule's capacity to accept electrons. A higher f + value signifies greater readiness for nucleophilic reactions. f 0 reflects changes in the molecule's electron cloud, indicating the influence of free radicals on reactivity without significant electron gain or loss. Analysis of f −, f +, and f 0 revealed that O2, N8, and N32 were favorable for electrophilic reactions; C11, C17, and C20 were prone to nucleophilic reactions; and N8 was susceptible to radical reactions (Figs. S6 and S7, Table S4 in Supporting information). These atomic sites were thus likely the most reactive during the degradation process.
By integrating identified intermediates, Fukui function results, and HPLC-MS data, the potential degradation pathways of OTC in the NOBC
BM/PMS system were discussed. Three distinct OTC removal pathways were proposed in
Fig. 5a. Pathways 1 and 2 involved hydroxylation and demethylation, leading to the formation of
P1 (
m/
z 476) and
P2 (
m/
z 433), respectively, which was consistent with result of Fukui function. Subsequently,
P1 and
P2 were transformed into
P4 and then
P5. In the third pathway, the OTC molecule lost H
2O to form
P3 (
m/
z 443), which then underwent decarbonylation to produce
P6 (
m/
z 415). These intermediates further transformed into
P7 and
P8. Finally, intermediates
P9, P10, P11, P12, and
P13 were formed and further oxidized to smaller molecules such as CO
2 and H
2O. The toxicological profiles of OTC and its degradation intermediates, including oral LD
50 (rats) and LC
50 (blackhead fish), were computationally modeled using T.E.S.T. software (Table S5 in Supporting information). Initial toxicity assessments revealed significant acute risks. OTC exhibited an oral LD50 of 1165.80 mg/kg in rats (
Fig. 5b) and an LC
50 of 1.12 mg/kg in blackhead fish (
Fig. 5c). Post-degradation intermediates demonstrated reduced toxicity, with LD
50 and LC
50 values exceeding those of parent OTC for most species. Notably, stable intermediates
P2, P5, P9-
P12 showed markedly diminished toxicity. While developmental toxicity increased for select intermediates (
P3, P6, P8), the majority displayed nontoxic characteristics. These findings suggest extended reaction cycles could enhance detoxification, as terminal intermediates exhibit lower toxic potential than initial products.
Three-dimensional fluorescence techniques were utilized to characterize the degradation of OTC molecules. Fluorescence spectra were classified into five regions: aromatic protein (Ⅰ and Ⅱ), xanthate (Ⅲ), soluble microbial by-product (Ⅳ), and humic acid (Ⅴ) fluorescence. As shown in
Figs. 5d–
g and Table S6 (Supporting information), the pre-reaction OTC solution displayed dominant fluorescence intensity in the V region, corresponding to humic acid-like substances with molecular structures containing aromatic rings, polycyclic compounds, and functional groups (amide, phenolic hydroxyl, carboxyl) at molecular edges. However, after 50 min of reaction, most fluorescent substances vanished, indicating decomposition of OTC molecules during catalysis. This process involved complete mineralization of benzene rings and carbonyl groups into H
2O and CO
2.
The NOBC
BM/PMS system maintained robust OTC degradation efficiency (96%–98%) across pH 3–11 (
Fig. 6a). Enhanced activity under acidic conditions (pH 5
vs. 11) correlated with PMS's preferential generation of SO
4•− (oxidation potential: 2.5–3.1 V) over
•OH in low-pH environments. Alkaline conditions promoted surface-bound
•OH formation but reduced overall reactivity. The system's pH resilience stems from its non-radical-dominated mechanism, which minimizes pH sensitivity compared to radical-dependent pathways. In aquatic ecosystems, inorganic anions often react with free radicals, potentially compromising the efficiency of pollutant degradation. To assess their influence, experimental trials were conducted to investigate how coexisting anions affect OTC degradation within the NOBC
BM/PMS system. As shown in
Fig. 6b, only HCO
3− caused minimal inhibition within 30 min, possibly due to its hydrolysis altering solution pH. Other coexisting anions had no significant inhibitory effect, indicating they did not substantially affect efficiency. These results validated the non-radical degradation pathway, aligning with earlier findings and underscoring the system's resilience to anion interference.
The system's performance was further evaluated using real water samples (tap water, Jiazi Lake water on campus, and Daming Lake water in the city) to assess interfering substances. As shown in
Fig. 6c, OTC degradation efficiency remained high in all samples, confirming the non-radical pathway was dominant and less affected by natural water constituents, ensuring stable removal efficiency. As shown in
Fig. 6d, NOBC
BM stability was tested over four recycling cycles. The NOBC
BM/PMS system maintained 88.4% OTC removal efficiency after four cycles, indicating significant
in situ recoverability despite slight performance decline. Catalysts were loaded onto different reactors to systematically investigate the degradation of pollutants by the NOBC
BM/PMS system under dynamic flow conditions, simulating real water flow and assessing the impact of reaction time. Detailed schematics of the experimental setups were shown in
Figs. 6e,
g and
i. As shown in
Fig. 6f, the NOBC
BM/PTFE membrane achieved approximately 90.9% OTC removal, maintaining 86.8% efficiency after 8 h of continuous operation, indicating high stability. The slight efficiency decline may result from uneven thickness and pore size distribution during catalyst loading, causing heterogeneous degradation across different membrane regions. NOBC
BM was embedded in absorbent cotton for column experiments.
Fig. 6h showed that OTC degradation initially increased to 96.1% as the catalyst-solution contact area expanded. The system retained 91.7% removal efficiency after 8 hours, demonstrating NOBC
BM stability and the column's practical potential. Two NOBC
BM sponges were placed in a beaker, with PMS-OTC solution pumped in and treated solution pumped out
via peristaltic pumps; samples were taken every 120 min. As shown in
Fig. 6j, OTC degradation stabilized above 80% over three days, though slightly lower than other reactors, likely due to catalyst detachment from floater movement.
Wheat and mung bean growth experiments evaluated purified water's effects and catalyst eco-safety. Long-term tests assessed NOBC
BM/PMS system stability for engineering applications. OTC-contaminated water caused high germination but unhealthy seedlings of wheat (short/yellow/bent stems, death/abnormalities;
Fig. 7a, Fig. S8 in Supporting information). Purified water enhanced growth. Rhizome lengths differed significantly between control and contaminated groups, but not control
vs. purified (
Fig. 7b). Contaminated-group wet weight (2.63 g) was significantly lower; dry weight differences were minor, suggesting impaired water uptake (
Fig. 7c). Contaminated water induced stunted growth, weak stems, and deformities of mung bean growth (
Fig. 7d, Fig. S9 in Supporting information). Purified water improved plant height/leaf expansion. Rhizome development differed significantly between control and contaminated groups, but not control
vs. purified (
Fig. 7e). Contaminated-group wet weight (5.26 g) was lower than control (6.31 g); its lowest dry weight indicated biomass disruption, while purified water matched control levels (
Fig. 7f). Microbial toxicity assessment revealed higher toxicity and reduced
E. coli density in solutions treated with OTC-contaminated water. In contrast,
E. coli growth in the NOBC
BM/PMS-treated solution matched the control group (Fig. S10 in Supporting information), indicating minimal toxicity from its degradation products. Biochar catalyst/PMS systems had lower environmental impact than PMS alone due to better efficiency, reduced energy, and renewable biomass (
Fig. 7g). N/O doping further reduced impacts by enhancing active sites/PMS activation, but increased marine eutrophication risk from nitrogen compounds (
e.g., C
2H
4N
4) during pyrolysis.
In summary, N/O co-doped biochar (NOBCBM) was synthesized via mechanical ball milling and pyrolysis. SEM, FTIR, and Raman analyses showed NOBCBM had a porous structure with high defect density. Degradation tests revealed NOBCBM removed 94% of OTC (20 mg/L) in 30 min, with a kinetic constant (kobs = 0.1523 min−1) over twice that of NSBCBM (0.0664 min−1). Its high PMS adsorption energy (−3.154 eV) promoted preferential O-site binding, accelerating electron transfer to PMS and generating 1O2. EPR, quenching, and electrochemical experiments confirmed 1O2 and e− as the main reactive species for OTC degradation. DFT calculations showed O-doping increased electrostatic potential, redistributed electron density at doping sites, and enhanced N-doped catalytic activity. LCA indicated favorable environmental performance. Dynamic flow tests on NOBCBM/PTFE membranes and packed columns showed > 90% OTC removal after 8 h of continuous operation. Seven-day plant growth experiments with wheat and mung bean demonstrated significantly higher morphological parameters (plant height, rhizome) in purified water vs. OTC-contaminated water. Statistical analysis showed no differences between purified water and control groups, confirming effective toxicity removal. These results highlight NOBCBM's long-term application potential, ecological safety, and environmental friendliness.
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