Phosphorus Adsorption Research Articles

Synthesis, characterization, and phosphorus adsorption of Mg/Fe-modified biochar from cotton stalk pretreated with Coriolus versicolor.

In recent years, the research potential in utilizing biochars as adsorbents in adsorption processes has grown due to their eco-friendly and economical nature. However, biochar often possesses a negative surface charge that limits its affinity for binding anions. Nitric acid washing and pretreatment with Coriolus versicolor can break down the lignocellulosic structure in cotton stalk waste, facilitating the subsequent impregnation of Mg and Fe metal oxides. These pretreatment steps can lead to the production of diverse and functionalized biochars with higher adsorption capacities. In this study, cotton stalk waste was first washed with diluted nitric acid and then subjected to biological pretreatment by incubation with C. versicolor, followed by impregnation with Mg and Fe to obtain CV-CS/Fe and CV-CS/Mg biochars. The results showed that the applied pretreatments altered the physicochemical properties and significantly increased the phosphorus adsorption capacity. The adsorption capacities of CV-CS/Fe and CV-CS/Mg biochars were found to be 277.88 and 507.01 mg g-1, respectively. The results indicate that the incorporation of multiple metal oxide impregnates enhances P adsorption. Furthermore, in the kinetic study, pseudo-first-order and pseudo-second-order models provided a well fit, determining chemical adsorption as the main adsorption mechanism for phosphorus adsorption. The biochars demonstrated compatibility with Langmuir-Freundlich models. Overall, the findings suggest the possibility of synthesizing biochars with improved adsorptive properties through pretreatment, and these engineered biochars hold promising potential as effective adsorbents in the field. PRACTITIONER POINTS: Eco-friendly, natural, and economical biochar was synthesized. Biochar was produced via Coriolus versicolor pretreatment. High adsorption capacities of CV-PS/Mg biochars were found to be 507.01 mg g-1. Adsorption capacities of biochars can be improved by pretreatment.

Lanthanum-doped chitosan-based polyacrylamide double network hydrogels for adsorption of phosphorus from wastewater.

Excessive phosphorus in aqueous solutions can cause eutrophication, which can harm aquatic organisms and pose a risk to the safety of drinking water for humans. The Chitosan/Polyacrylamide/Lanthanum (CS/PAM/La) hydrogel was designed to get rid of phosphate from aqueous solutions. La (III) was used to enhance the capacity of adsorption of CS. Polyacrylamide was used to enhance the mechanical properties of CS. The results showed that the adsorption capacity of CS/PAM/La hydrogel for phosphate was increased compared with that of CS. When pH of 5.0, the adsorption capacity was 80.07mg-P/g. In addition, after five adsorption and desorption cycles, the adsorption efficiency remained above 90%. The mechanism of phosphate adsorption on CS/PAM/La material was analyzed using a mass transfer factor model (MTF) and the possible structure of CS/PAM/La hydrogel was calculated by density functional theory calculation (DFT). The application of CS/PAM/La composite hydrogel for removal of phosphate from actual wastewater was investigated, and the results met the requirement of national standard.

Study on vertical variation characteristics of soil phosphorus adsorption and desorption in black soil region of Northeast China.

The adsorption and desorption of phosphorus (P) in soil constitute a crucial internal cycle that is closely associated with soil fertility, exerting direct influence on the quantity, form, and availability of P within the soil. The vertical spatial variation characteristics of soil adsorption and desorption were investigated for the 0-100 cm soil layer in the northeast black soil region in this study. The maximum adsorption capacity (Qmax) and maximum adsorption buffer capacity (MBC) of black soil in the study area ranged from 313.8 to 411.9 mg kg-1 and from 3.1 to 28.8 L kg-1, respectively, within the soil layer of 0-100 cm depth, exhibiting an increasing trend with greater soil depth. The degree of P adsorption saturation (DPS) exhibited a contrasting trend with the variations in Qmax and MBC, ranging from 3.8% to 21.6%. The maximum desorption capacity (Dmax) and desorption rate (Dr) of soil P ranged from 112.8 to 215.7 mg kg-1 and 32.1% to 52.5%, respectively, while the readily desorbable P (RDP) in soil was within the range of 1.02 to 3.35 mg kg-1. Both Dmax, Dr, and RDP exhibited a decreasing trend with increasing soil depth before showing an upward trend. These research findings not only provide essential background data for the systematic investigation of soil P in the black soil region but also serve as a valuable reference for assessing soil quality in this area.

Sludge-Based Superparamagnetic Nano-Sorbent Functionalized by Lanthanum Silicate Nanorods for Phosphorus Adsorption and Fertilization

Phosphorus (P) recovery from wastewater is considered to be a positive human intervention towards sustainable P use in the global P cycle. This study investigated the feasibility of synthesizing a superparamagnetic nano-sorbent that was functionalized by lanthanum silicate nanorods (NRLa-Si) using drinking water treatment sludge (DWTS), evaluating both its P adsorption capacity and fertilization effect. The DWTS-based La-modified P nano-sorbent (P-sorbent D) exhibited complicated but single-layer-dominant adsorption for phosphate, with a maximum adsorption capacity up to 26.8 mg/g, which was superior to that of most of the similar sludge-based P-sorbent. The NRLa-Si-modified P-sorbent D was identified with several characterization techniques and the leaching metal elements from the nano-sorbent were tested, which were below the limits proposed by the Food and Agriculture Organization of the United Nations. In addition, the growth and vigorousness of Arabidopsis thaliana indicated that the exhausted P-sorbent D could be used as a potential water-soluble moderate-release P fertilizer, which was also confirmed by the well-fitted P uptake model and the P desorption pattern from the sorbent–fertilizer. The doped lanthanum silicate nanorods could play the dual role of P complexation enhancement and health/growth promotion. In light of this, this study proposed a new way of reclaiming DWTS as a P-sorbent for fertilization, offering new insights into the path toward “closing the P loop”.

Phosphorus Availability and Adsorption Kinetics of Novel DAP Encapsulated Nano Clay Polymer Composites (NCPCs)

Phosphorus Availability and Adsorption Kinetics of Novel DAP Encapsulated Nano Clay Polymer Composites (NCPCs)

Deciphering competitive interactions: Phosphate and organic matter binding on goethite through experimental and theoretical insights

The adsorption of phosphorus (P) onto active soil surfaces plays a pivotal role in immobilizing P, thereby influencing soil fertility and the filter function of soil to protect freshwater systems from eutrophication. Competitive anions, such as organic matter (OM), significantly affect the strength of this P-binding, eventually controlling P mobility and release, but surprisingly, these processes are insufficiently understood at the molecular level. In this study, we provide a molecular-level perspective on the influence of OM on P binding at the goethite-water interface using a combined experimental-theoretical approach. By examining the impact of citric acid (CIT) and histidine (HIS) on the adsorption of orthophosphate (OP), glycerol phosphate (GP), and inositol hexaphosphate (IHP) through adsorption experiments and molecular dynamics simulations, we address fundamental questions regarding P binding trends, OM interaction with the goethite surface, and the effect of OM on P adsorption. Our findings reveal the complex nature of P adsorption on goethite surfaces, where the specific OM, treatment conditions (covering the surface with OM or simultaneous co-adsorption), and initial concentrations collectively shape these interactions. P adsorption on goethite exhibits a binding strength increasing in the order of GP < OP < IHP. Crucially, this trend remains consistent across all adsorption experiments, regardless of the presence or absence of OM, CIT, or HIS, and irrespective of the specific treatment method. Notably, OP is particularly susceptible to inhibition by OM, while adsorption of GP depends on specific OM treatments. Despite being less sensitive to OM, IHP shows reduced adsorption, especially at higher initial P concentrations. Of significance is the strong inhibitory effect of CIT, particularly evident when the surface is pre-covered, resulting in a substantial 70 % reduction in OP adsorption compared to bare goethite. The sequence of goethite binding affinity to P and OM underscores a higher affinity of CIT and HIS compared to OP and GP, suggesting that OM can effectively compete with both OP and GP and replace them at the surface. In contrast, the impact of OM on IHP adsorption appears insignificant, as IHP exhibits a higher affinity than both CIT and HIS towards the goethite surface. The coverage of goethite surfaces with OM results in the blocking of active sites and the generation of an unfavorable electric potential and field, inhibiting anion adsorption and consequently reducing P binding. It is noteworthy that electrostatic interactions predominantly contribute more to the binding of P and OM to the surface compared to dispersion interactions.

Recycling of sludge residue as a coagulant for phosphorus removal from aqueous solutions.

Phosphorus pollution poses a significant challenge in addressing water contamination. The coagulant is one of the effective methods to remove phosphorus from wastewater. Abundant Al and Fe oxides in sludge residue make it have great potential to synthesize water treatment coagulants. However, the utilization of sludge residue for preparation of coagulant was seldom investigated. In this study, we fabricated a novel coagulant, polyaluminum ferric chloride (SM-PAC), using sludge residue as a raw material through acid leaching and polymerization processes. Characterization results confirm that the parameters of SM-PAC meet the specifications outlined in the national standard (GB/T 22627-2022). We investigated the effects of pH, dosage, initial phosphorus concentration, and contact time on the removal efficiency of SM-PAC. As anticipated, the prepared SM-PAC exhibited a significant efficacy in removing phosphorus, meeting the discharge standards set for municipal sewage. Furthermore, the adsorption kinetics analysis suggests that the predominant mode of phosphorus adsorption on SM-PAC is chemical adsorption. Furthermore, the SM-PAC was employed in the actual wastewater treatment plant and exhibited excellent efficiency in phosphorus removal. The utilization of SM-PAC can not only effectively address the issue of sludge disposal but also achieve the goal of "treating waste with waste." It is expected that the proposed method of reusing sludge residue as a resource can provide a sustainable way to synthesize a coagulant for phosphorus removal.

Unraveling the Phosphorus Adsorption Mechanisms in Three-dimensional Reduced Graphene Oxide Materials.

To prevent eutrophication, controlling the phosphate concentration levels is one of the most important issues in surface water management. One of the most utilized methods is phosphate adsorption. However, its application faces a bottleneck due to the unclear understanding of adsorption and interaction mechanisms. The present work unlocks the phosphorus adsorption mechanisms in three-dimensional reduced graphene oxide with different reduction levels and pore sizes to remove phosphate from water using experiments and multiscale simulations. Experiments were performed to evaluate the influence of pH, ionic strength, and temperature on the adsorption. Molecular Dynamics and Ab Initio simulations evaluated the influence of the pore size and oxidation degrees of the materials. We show that the adsorption capacity of the materials increases with increasing pH and ionic strength and decreasing temperature. It is observed that the more oxidized the material and the less compact the structure, the better the adsorption. These results are theoretically explained in terms of the interaction of functional groups and the clustering of phosphate ions, which results in better adsorption in materials with larger pores. The underlying mechanisms for the 3D-reduced graphene oxide performance were confirmed by spectroscopy analysis. All the results show that 3D-reduced graphene oxide can sorb phosphate in different complex water remediation systems with characteristics that can be modulated by changing the material synthesis method.

Removal and recovery of phosphorus by a long–term stabilized amorphous calcium carbonate

Phosphorus is a non–renewable resource that guarantees food production, while excessive phosphorus discharge leads to water eutrophication. Phosphorus removal/recovery could help improve water quality and ensure food security. In this contribution, silica–stabilized amorphous calcium carbonates (Si–ACC) were prepared and used to remove/recover phosphate in sludge and domestic sewage. The mechanisms were investigated via kinetic and isothermal adsorption studies and XRD, TEM, Raman, and FT–IR characterization. The results showed that the homogeneously distributed silica successfully inhibited ACC transformation and helped Si–ACC keep the amorphous feature within 680 d. During phosphorus adsorption, Si–ACC quickly transformed into calcite within 5 min and reacted with phosphorus to generate polycrystalline hydroxylapatite within 60 min. The recovered product possessed a maximum specific surface area (SSA) of 209 m2/g and available phosphorus content of 18.0 %, suggesting that Si–ACC was a promising phosphorus recovery material and the recovered product could be a potential phosphate fertilizer.

Soil Properties Related to Phosphorus Sorption and Prediction of Maximum Phosphorus Adsorption Capacity of Soils from Southern Brazil

Soil Properties Related to Phosphorus Sorption and Prediction of Maximum Phosphorus Adsorption Capacity of Soils from Southern Brazil

The growth and nutrient removal properties of heterotrophic microalgae Chlorella sorokiniana in simulated wastewater containing volatile fatty acids

To reduce the high cost of organic carbon sources in waste resource utilization in the cultivation of microalgae, volatile fatty acids (VFAs) derived from activated sludge were used as the sole carbon source to culture Chlorella sorokiniana under the heterotrophic cultivation. The addition of VFAs in the heterotrophic condition enhanced the total nitrogen (TN) and phosphorus (TP) removal of C. sorokiniana, which proved the advantageous microalgae in using VFAs in the heterotrophic culture after screening in the previous study. To discover the possible mechanism of nitrogen and phosphorus adsorption in heterotrophic conditions by microalgae, the effect of different ratios of VFAs (acetic acid (AA): propionic acid (PA): butyric acid (BA)) on the nutrient removal and growth properties of C. sorokiniana was studied. In the 8:1:1 group, the highest efficiency (77.19%) of VFAs assimilation, the highest biomass (0.80 g L−1) and lipid content (31.35%) were achieved, with the highest TN and TP removal efficiencies of 97.44 % and 91.02 %, respectively. Moreover, an aerobic denitrifying bacterium, Pseudomonas, was determined to be the dominant genus under this heterotrophic condition. This suggested that besides nitrate uptake and utilization by C. sorokiniana under the heterotrophy, the conduct of the denitrification process was also the main reason for obtaining high nitrogen removal efficiency.

Desalination RO reject brine as a novel-based porous geopolymer for phosphorus removal from contaminated media

Desalination reverse osmosis reject brine-based porous geopolymer (RO/GP) was produced and investigated as an improved adsorbent for phosphorus (P) removal from tainted seawater, brackish water, river water, and municipal wastewater effluent. The RO reject brine/geopolymer was produced by reacting metakaolin and fly ash with a Na-alkali activator and anhydrous RO brine as a sacrificial template. The influence of RO reject brine content on water absorption, porosity, mechanical, and structural properties were examined. The developed RO-based geopolymers exhibited the greatest porosity (58.3–84.2 % vol%), a significant ratio of open porosity to total porosity (67.7–92.1 %), and outstanding compression strength (3.6–10.4 MPa). The produced RO/GP structure has an adsorption capacity of 92.4 mg-P/g. The sequestration reaction of phosphorus by RO/GP is of pseudo-second-order kinetic behavior via Chi-squared (χ2), RMSE, and determination coefficient (R2) values. Regarding their agreement with Langmuir behavior, the phosphorus adsorption uptakes occur in homogeneous and monolayer states. The reaction is exothermic, spontaneous, and favorable. The RO/GP exhibits significant affinity for phosphorus co-existing with Cl−, Na+, SO42−, K+, HCO3−, and Ca2+. The RO/GP shows high safety during the adsorption investigation, with a total cost of 0.32 $/kg-P.

Magnesium doped biochar for simultaneous adsorption of phosphate and nitrogen ions from aqueous solution

Phosphorus (P) and Ammonium Nitrogen (N) are essential nutrients for plants and environmental stability. However, their excess in water causes eutrophication, damaging aquatic ecosystems. While adsorption is a promising solution, finding affordable and efficient adsorbents remains a challenge. In this study, magnesium (Mg), iron (Fe), and Mg/Fe doped biochars (BC) adsorbents were synthesized, and evaluated for adsorption of individual P and N and a P + N mixture from a solution and wastewater from a wastewater treatment plant. Compared to other adsorbents, Mg/BC showed excellent performance in adsorbing phosphorus (P) and ammonium nitrogen (N) from aqueous solutions. It demonstrated a large adsorption capacity of 64.65 mg/g and 62.50 mg/g from individual P and N solutions, and 30.3 mg/g and 27.67 mg/g from the P and N mixture solution, respectively. In addition, Mg/BC efficiently removed P and N from real-life wastewater. In the real wastewater, P and N removal efficiencies reached 88.30% and 59.36%, respectively. Kinetics analysis revealed that the pseudo-second-order model accurately described the adsorption of phosphorus (P) and ammonium nitrogen (N) in all solutions. The adsorbent followed the monolayer-Langmuir isotherm for N ions and the multilayer-Freundlich isotherm for P, indicating efficient adsorption processes. Thermodynamic experiments indicated that the adsorption of P and N was not only feasible but also occurred spontaneously in a natural manner. This study revealed that the strategic modification of biochar plays a crucial role in advancing effective wastewater treatment technologies designed for nutrient removal.

Phosphate recovery from urban sewage by the biofilm sequencing batch reactor process: Key factors in biofilm formation and related mechanisms

The biofilm sequencing batch reactor (BSBR) technique has been deployed in the laboratory to enrich phosphorus from simulated wastewater, but it is still not clear what its performance will be when real world sewage is used. In this work, the effluent from the multi-stage anoxic-oxic (AO) activated sludge process at a sewage plant was used as the feed water for a BSBR pilot system, which had three reactors operating at different levels of dissolved oxygen (DO). The phosphorus adsorption and release, the biofilm growth, and the extracellular polymeric substances (EPS) components and contents were examined. The microbial communities and the signaling molecules N-acyl-l-homoserine lactones (AHLs) were also analyzed. Gratifyingly, the BSBR process successfully processed the treated sewage, and the biofilm developed phosphorus accumulation capability within 40 days. After entering stable operation, the system concentrated phosphate from 2.59 ± 0.77 mg/L in the influent to as much as 81.64 mg/L in the recovery liquid. Sludge discharge had profound impacts on all aspects of BSBR, and it was carried out successfully when the phosphorus absorption capacity of the biofilm alone was comparable to that of the reactor containing the activated sludge. Shortly after the sludge discharge, the phosphate concentration of the recovery liquid surged from 50 to 140 mg/L, the biofilm thickness grew from 20.56 to 67.32 μm, and the diversity of the microbial population plunged. Sludge discharge stimulated Candidatus competibacter to produce a large amount of AHLs, which was key in culturing the biofilm. Among the AHLs, both C10-HSL and 3OC12-HSL were significantly positively correlated with EPS and the abundance of Candidatus competibacter. The current results demonstrated BSBR as a viable option to enrich phosphorus from real world sewage with low phosphorus content and fluctuating chemistry. The mechanistic explorations also provided theoretical guidance for cultivating phosphorus-accumulating biofilms.

Investigating phosphorus adsorption characteristics of sediment in a river reach receiving municipal tailwater: a response surface methodology

Investigating phosphorus adsorption characteristics of sediment in a river reach receiving municipal tailwater: a response surface methodology

Application of corn stover derived pyrolyzed hydrochars for efficient phosphorus removal from water: Influence of pyrolysis temperature

Excessive phosphorus load to surface water is undesirable since it can cause eutrophication. In this study, three different pyrolyzed hydrochars from corn stover were synthesized by applying hydrothermal carbonization (HTC) at 260 °C and then eventual pyrolysis at 400°, 600°, and 800 °C, respectively, and finally were used for phosphorus removal from aqueous solution. By linking the physicochemical properties of these pyrolyzed hydrochars investigated here, we tried to comprehend the effect of HTC and pyrolysis temperature on the hydrochar structure and phosphorus adsorption. Results show that high pyrolysis temperatures (600 °C and 800 °C) enhanced the hydrochar's phosphorus adsorption compared to low pyrolysis temperature (400 °C). HTC260P800 type hydrochar showed a fast phosphorus adsorption kinetics, while the HTC260P600 showed an overall high adsorption capacity, with the maximum phosphate adsorption capacity of 5090 mg/kg calculated using isotherm model. Three different adsorption isotherm models (Langmuir, Fruendlich, and Redlich-Peterson) were used to fit the isotherm data; among them, the Redlich-Peterson isotherm model fit the data best for all three hydrochars. pH was found to be a critical factor in terms of phosphorus removal, and the optimum pH was found to be 5, probably due to the enhanced electrostatic interaction between positively charged hydrochar and negatively charged phosphate ions. The desorption experiment showed that a small fraction of the adsorbed phosphate (15.6 % to 24.4 %) was released from the spent hydrochar samples, which might be due to the strong attachment of phosphate ions to the sorption sites. Reusing the spent pyrolyzed hydrochar showed lower phosphate adsorption capacity than the fresh ones, ranging from 423 mg/kg to 903 mg/kg.

Adsorption of phosphate over a novel magnesium-loaded sludge-based biochar.

The production of sludge-based biochar to recover phosphorus (P) from wastewater and reuse the recovered phosphorus as agricultural fertilizer is a preferred process. This article mainly studied the removal of phosphate (PO4-P) from aqueous solution by synthesizing sludge-based biochar (MgSBC-0.1) from anaerobic fermentation sludge treated with magnesium (Mg)-loading-modification, and compared it with unmodified sludge-based biochar (SBC). The physicochemical properties, adsorption efficiency, and adsorption mechanism of MgSBC-0.1 were studied. The results showed that the surface area of MgSBC-0.1 synthesized increased by 5.57 times. The material surface contained MgO, Mg(OH)2, and CaO nanoparticles. MgSBC-0.1 can effectively remove phosphate in the initial solution pH range of 3.00-7.00, with a fitted maximum phosphorus adsorption capacity of 379.52 mg·g-1. The adsorption conforms to the pseudo second-order kinetics model and Langmuir isotherm adsorption curve. The characterization of the adsorbed composite material revealed the contribution of phosphorus crystal deposition and electrostatic attraction to phosphorus absorption.

La-doped CeO2/rGO hybrid with high oxygen vacancy to enhance phosphorus adsorption by capacitive deionization

Cerium oxide is one of the most attractive electrode materials in capacitive deionization (CDI) technology for selective phosphate adsorption due to the specific interaction. However, Ce3+/Ce4+ ratio and material conductivity of cerium oxide electrode determine the adsorption performance. Herein, a dual strategy was exploited with polyol-solvothermal reaction in the presence of graphite oxide and cerium salt followed by hydrothermal La-doping to obtain the three-dimensional (3D) assembly of La-doped CeO2 at the reduced graphene oxide (La-CeO2/rGO). The as-prepared La-CeO2/rGO hybrid exhibited interconnected structure with CeO2 uniformly distributed on the rGO support. La3+, by partially replacing Ce4+ in the lattice, was evenly fused into CeO2 nanosphere, enhancing the content of Ce3+ and oxygen vacancies and inhibiting lattice distortion. As a CDI positive electrode, the La0.15-CeO2/rGO with optimal La doping achieved the maximum theoretical adsorption capacity of 118.7 mg P/g with high separation factor (αSO42-P = 13.9), superior to the CeO2/rGO (67.8 mg P/g, αSO42-P = 10.1). In addition, the La-CeO2/rGO electrode is extremely robust, with excellent adsorption performance in wide pH range and good regeneration ability, compared to CeO2/rGO. This work proves that the synergy of trace La doping and 3D rGO support effectively improves the adsorption performance of La-CeO2/rGO electrodes and enhances the cycling stability of CDI devices. The corresponding adsorption mechanism was demonstrated.

Using shell to enhance the phosphorus adsorption capability of aluminum-based drinking water treatment residue-dominant sintered ceramsite

Al-based drinking water treatment residue (DWTR) is an inevitable byproduct of potable production that can provide skeletal components to make sintered ceramsite for water treatment. However, sintering promotes Al aging and decreases its adsorption capability. This study proposes and verifies a strategy for using shell, a common natural Ca-based material, to enhance P adsorption by Al-based DWTR-dominant ceramsite. The results showed that the shell mainly acted as an expanding component, and thermolysis of CaCO3 to form CaO was the main expanding mechanism, further enhancing the coupling effect of Fe, K, and Si for sintering. This mechanism led to a reduction in the cylinder compressive strength with increasing shell proportions and an increase in the broken rate and cylinder compressive strength with increasing temperature. However, all DWTR shell-based ceramsites are non-hazardous. Importantly, the shell increased the P adsorption capacity of the ceramsite by approximately two orders of magnitude and caused the adsorbed P to remain as HCl-extractable and residual P. A logistic equation (r2 = 0.923, n = 10) was established for the cylinder compressive strength to Si, K, Fe, and Ca in ceramsite and loss on ignition in raw materials to provide a potential reference for ceramsite production.

The influence of biochar from animal and plant on the transformation of phosphorus during paper mill sludge composting.

Biochar has effect on phosphorus adsorption, release, and transformation. This study compared the influence of biochar derived from animal (AB) and plant (PB) during paper mill sludge composting. Results indicated AB not only accelerated sludge decomposition but also had significantly higher levels of available phosphorus (AP) than PB and CK (no biochar), with AP contents in the order of AB > PB > CK. Compared to CK, AB was found to increase the relative abundance of thermophilic bacteria, and PB diversified the microbial community. Based on Pearson and RDA results, TOC/TN ratio (C/N) and organic matter (OM) explained above 50% of the variance in microbial community and phosphorus fractions. Thermophilic bacteria with high levels of OM and C/N promoted the conversion among labile and moderately labile organic phosphorus, moderately labile inorganic phosphorus, and AP. Biochar could enhance the AP conversion pathway, leading to increased levels of AP.