Phosphate Removal Efficiency Research Articles

Boron-doping tunes nitrogen species to abundant edge-N and B-N matrix for efficient phosphate removal in capacitive deionization: Additional accessible sites and defective centers

The elimination of eutrophication necessitates the implement of a clean and efficient phosphate removal strategy. Capacitive deionization (CDI) is recently regarded a promising approach for removing pollutants from aqueous environment with high-efficiency, facile operation, and low-energy consumption. Development of electrode materials with good properties is crucial for CDI. In this study, novel edge-N-modified boron-doped hierarchical carbon composites (MBCNs) were prepared via a hard template strategy for phosphate electrosorption. According to the pseudo-second-order kinetic, the MBCN2 electrode exhibited a dynamic capacity of 196.02 mg PO43− g−1 in 150 min with an initial concentration of 100 mg PO43− L−1 at 1.2 V. And it also demonstrated an exceptional saturation capacity of 399.70 mg PO43− g−1 under the Langmuir model. Based on theoretical analysis and experimental results, the incorporation of boron atoms in the carbon framework indicated a dual reinforcement. This included an enhanced proportion of edge-N modifications for defective centers and sufficient high-polarity B-N matrix for additional available active sites. The joint contribution of edge-N and B-N matrix revealed favorable electrical double layer capacitance, which resulted in good phosphate removal performance. This work disclosed the synergistic impact of dual nonmetallic atom doping, providing insights into the efficient phosphate removal anode for CDI.

Thauera enriched granular activated carbon-assisted aerobic granular sludge performs enhanced biological nitrogen and phosphate removal via propionate utilization

Propionate constituting up to 25 % of volatile fatty acids in municipal wastewater, presents metabolic challenges for microorganisms. This study investigated the combined use of propionate along with granular activated carbon (GAC) for aerobic granular sludge (AGS) development and biological nutrient removal (BNR), particularly bio-P removal in granular reactors. GAC addition decreased granulation time and facilitated stable BNR pathways with propionate. AGS demonstrated robust settling properties (≥1 mm, 6 g/L MLSS, 40 mL/g SVI) with increased alginate-like exopolysaccharide (ALE) content up to 400 mgALE/gSS, indicating stable granule formation. Effective ammonium removal via simultaneous nitrification and denitrification was achieved. By day 90, phosphate removals reached 89 %, due to enrichment of polyphosphate accumulating organisms (PAOs) in GAC-containing AGS. The sludge fraction (>0.5 mm) comprised of granules and GAC-biofilms showed efficient phosphate removal through enhanced biological phosphate removal (EBPR). Enrichment of denitrifying PAO, Thauera sp., contributed to enhanced granulation, granular stability and nutrient removals.

Highly efficient removal of aqueous phosphate via iron-manganese fabricated biochar: Performance and mechanism

Biochar (BC) has emerged as a potential solution to phosphate removal from wastewater primarily resulting from global overuse of fertilizers. Further modification by embedment of iron (Fe)-manganese (Mn) oxides on BC can enhance phosphate removal; however, the modification method serves as a vital factor underlying distinctive removal performances and mechanisms, which have yet been systematically examined. Herein, two Fe–Mn modified BC, Fe/MnBC (comprised of Fe3O4 and MnO2) and Fe–MnBC (comprised of MnFe2O4), were comprehensively investigated for gaining insights into the unsolved perspectives. The results indicated that Fe–MnBC exhibited a markedly greater maximum phosphate adsorption capacity of 135.88 mg g−1 than that of Fe/MnBC with 17.93 mg g−1. The comparative results based on microstructure and spectroscopic analyses suggested that different Fe and Mn oxides were successfully loaded, which played a distinctive role in phosphate removal. Further characterizations unveiled that the key mechanisms for phosphate removal by Fe/MnBC are inner-sphere complexation and precipitation, while electrostatic interaction and outer-sphere complexation are the dominant mechanisms underlying the notable performance of Fe–MnBC. The delicately designed Fe–MnBC with special structure and property also enabled a superior regeneration capacity, which presented a promisingly high phosphate removal efficacy of over 81.34% after five cycles. These results enhance comprehension regarding the impact of biochar modification techniques on phosphate removal, offering positive indications for the remediation of excessive phosphate and other pollutant-containing water through feasible design and green chemicals.

Simultaneous removal of Cd(II) and phosphate by nanoscale zero-valent iron from solution: Co-sorption and implication of corrosion

Nanoscale zero-valent iron (nZVI) has been extensively utilized in environmental remediation, but its reactivity in the presence of co-contaminants requires further investigation for effective application in complex environments. Here, we conducted batch removal experiments to systematically investigate the co-removal behaviors of Cd(II) and phosphate by nZVI. Results showed that nZVI can synergistically remove Cd(II) and phosphate in solution, with the removal efficiency of Cd(II) and phosphate in the binary system being approximately 2 and 5 times higher than those in the single system, respectively. Sequential removal experiments combined with characterization analysis revealed the co-sorption of Cd(II) and phosphate onto the corrosion product of nZVI mainly by forming the ternary complexes (≡Fe–P–Cd). The Fe(OH)2 formed as the initial nZVI corrosion product provides numerous active sites for immobilization of Cd(II) and phosphate. Such effective co-sorption of Fe(OH)2 inhibits its subsequent phase transformation to Fe3O4. Overall, our work sheds light on how nZVI, Cd(II), and phosphate interact in solution as well as highlights the influence of phase transformation on co-removal, which can broaden the potential applications of nZVI in the practical environment.

The Efficiency of Phosphate Removal via Shallow Wastewater Injection into a Saline Carbonate Aquifer.

Wastewater-derived phosphate contributes to eutrophication if the phosphate is not efficiently removed before it is discharged to surface waters. In the Florida Keys (USA), shallow injection of treated wastewater into saline limestone aquifers is a common mode of wastewater disposal. We assessed the possibility of efficient and permanent phosphate removal following injection at a wastewater treatment facility in Marathon, Florida. The concentrations of nutrients, dissolved ions, and anthropogenic compounds in groundwater and nearshore waters were monitored over two years, as was the progression of a patch of fluorescent dye emplaced by the wastewater injection well. The density contrast between the wastewater effluent and saline groundwater caused the effluent plume to buoy to the shallow subsurface near the injection well. Soluble reactive phosphorus (SRP) and sucralose were both detected in nearshore waters, indicating incomplete removal of contaminants. However, ∼75% of the SRP is removed from the plume in the first 10 days of transit by adsorption followed by a slower removal mechanism, bringing the P removal efficiency above 90%. A positive relationship between excess calcium and phosphate removal efficiency, together with high levels of calcium phosphate mineral supersaturation, supports calcite dissolution followed by calcium phosphate mineralization as this slower removal process.

Selective and efficient removal of phosphate from aqueous solution using activated carbon‐supported Mg–Fe layered double oxide nanocomposites

Selective and efficient removal of phosphate from aqueous solution using activated carbon‐supported Mg–Fe layered double oxide nanocomposites

Treatment of real carwash wastewater using high-efficiency and energy-saving electrocoagulation technique

This study focused on the treatment of actual wastewater from a car wash facility using electrocoagulation. The primary objective was to decrease chemical oxygen demand (COD) and eliminate turbidity by employing various electrodes such as Stainless Steel (SS) 304, Galvanized Iron (GI), and aluminum foil (α-Al) in a batch configuration. Several factors including contact time, current density, initial pH, and electrode material were examined to optimize process efficiency. The sludge generated during electrocoagulation was analyzed using Scanning Electron Microscopy/Energy-Dispersive X-ray Spectrometry (SEM-EDS). The results indicated that COD removal efficiency initially decreased between 30 and 60 min before improving. The data for COD, turbidity, and total phosphate reduction aligned well with the pseudo-first-order kinetic model, with R2 values of 0.275, 0.898, and 0.522, respectively. Minor variations were observed in pH, Total Dissolved Solids (TDS), Electrical Conductivity (EC), and alkalinity, while the temperature increased from 12 to 18.6 °C. Optimal removal efficiency for turbidity, total phosphate, and COD was achieved at pH = 6. The study demonstrated that higher current density resulted in enhanced COD reduction and turbidity removal. Chloride levels decreased with increasing applied current. The α-Al electrode exhibited superior performance compared to SS 304 and GI electrodes, with notable pH fluctuations during the process. UV–visible absorption spectra indicated differences in treated wastewater patterns based on the electrode utilized. SEM analysis revealed distinct characteristics of sludge produced by different electrodes. Energy and electrode consumption varied among the electrodes, with SS 304 displaying the lowest values.

Synergistic effects of defect engineering and functionalizing ionic liquids within UiO-66(Zr)-NH2 frameworks towards improving removal efficiency of phosphate and methyl orange

In this study, novel ionic liquid (IL)-entrapped UiO-66(Zr)-NH2 frameworks are proposed as efficient adsorbents to remove phosphate and methyl orange (MO). First, cetyltrimethylammonium bromide (CTAB) surfactant-defected UiO-66(Zr)-NH2 with tuned ligand deficiencies was produced using the continuous tubular reactor under microwave irradiation, making it a fast and scalable process. Upon changing the CTAB/ligand molar ratio from 0.5 to 1.5 and 2.5, the reaction yield deminised from ∼72–68 and 59 %, while the linker deficiency per Zr6 unit increased from ∼ 0.54–1.72 and 2.01, respectively. Defect-contained UiO-66(Zr)-NH2 was favourably entrapped with 1-butyl-3-methylimidazoliumbromide ([Bmim]+[Br]-) ionic liquid using a ship-in-bottle method to obtain host-guest [Bmim]+[Br]-@UiO-66(Zr)-NH2 composites, named Bmim@UN. Results revealed that IL-functionalized UiO-66(Zr)-NH2 comprised N-heteroaromatic rings and NH2 groups, creating a synergetic effect that enhanced the phosphate and MO adsorptions. At pH 4.5 and 27 °C, the Bmim@UN loaded 12 wt% IL had the equilibrium adsorbing capacity for phosphate and MO of ∼ 197 and ∼ 98 mg/g, respectively, and their corresponding adsorption rate constant of ∼ 0.0036 g mg−1min−1 and 0.0022 g mg−1min−1. Notably, the harvested Bmim@UN exhibited good simultaneous decontamination of phosphate and MO in their binary solution, where MO further accelerated the phosphate adsorption. The mechanism studies revealed that electrostatic interactions, hydrogen bonds, cation-π, and π-π interactions drove these adsorptions. The study demonstrates that combining defect engineering and IL-functionalizing of MOF has constructed efficient materials for wastewater remediation.

Synthesis of a novel magnetic calcium-rich biochar nanocomposite for efficient removal of phosphate from aqueous solution.

Phosphorus (P) scarcity and eutrophication have triggered the development of new materials for P recovery. In this work, a novel magnetic calcium-rich biochar nanocomposite (MCRB) was prepared through co-precipitation of crab shell derived biochar, Fe2+ and Fe3+. Characteristics of the material demonstrated that the MCRB was rich in calcite and that the Fe3O4 NPs with a diameter range of 18-22nanometers were uniformly adhered on the biochar surface by strong ether linking (C-O-Fe). Batch tests demonstrated that the removal of P was pH dependent with an optimal pH of 3-7. The MCRB exhibited a superior P removal performance, with a maximum removal capacity of 105.6mgg-1, which was even higher than the majority lanthanum containing compounds. Study of the removal mechanisms revealed that the P removal by MCRB involved the formation of hydroxyapatite (HAP-Ca5(PO4)3OH), electrostatic attraction and ligand exchange. The recyclability test demonstrated that a certain level (approximately 60%) was still maintained even after the six adsorption-desorption process, suggesting that MCRB is a promising material for P removal from wastewater.

Selective, Efficient Removal and Recovery of Phosphate from Wastewater by Promoting the Mass Transfer with Anion Exchange Resin in Redox Flow Deionization Cell

Selective, Efficient Removal and Recovery of Phosphate from Wastewater by Promoting the Mass Transfer with Anion Exchange Resin in Redox Flow Deionization Cell

Selective phosphate removal with manganese oxide composite anion exchange membranes in membrane capacitive deionization

The discharge of excessive phosphorous into water bodies can lead to serious eutrophication threatening aquatic ecosystem. Membrane capacitive deionization (MCDI) is an effective platform for deionizing aqueous streams; however, conventional MCDI is unable to selectively remove targeted ions from a liquid mixture. In this work, we fabricated manganese oxide composite anion exchange membranes (AEMs) for MCDI to enhance phosphate removal selectivity from sodium chloride-sodium dihydrogen phosphate (10:1 M ratio) aqueous mixtures. We systematically investigated several critical factors, such as constant current or voltage operation, applied voltage amount, process stream pH, and manganese oxide (Mn2O3) content in the AEM, on phosphate removal efficiency and phosphate selectivity. A trade-off was observed between phosphate removal and selectivity when increasing the cell voltage. Under the best conditions, a MCDI unit with a 20 wt% Mn2O3 composite AEM and a bipolar membrane facilitated high phosphate removal efficiency of ≥ 31.8 % and a phosphate over chloride selectivity of 1.1 while showing stability for at least 30 cycles. To help understand how Mn2O3 composite AEM boosts phosphate selectivity, static electronic structure calculations were performed, and they revelated that hydrogen phosphate absorption on Mn2O3 composite AEM was 314 kcal/mol more exothermic than that on pristine AEM while chloride adsorption on Mn2O3 composite AEM was 2.2 kcal/mol less exothermic than that on a pristine AEM. Overall, this work presents an effective strategy for selectively removing phosphate from model wastewater solutions and the mechanistic understanding that governs ion selectivity in composite ion-exchange membranes used in MCDI.

Determination of operation parameters for magnesium-air fuel cell to recover nitrogen and phosphorus from wastewater

Recovering phosphorus (P) and nitrogen (N) from wastewater not only contributes to environmental protection but also aligns with sustainable development goals. This study employed a magnesium-air fuel cell (Mg-O2-FC) to extract P and N from wastewater in the form of struvite (MgNH4·6H2O), based on the removal efficiency of ammonia and phosphate, electricity generation capacity and struvite purity to determine the optimal operation parameters. These parameters included hydraulic retention time (HRT), service life of magnesium sheet, and precipitation discharge frequency. The results showed that the removal efficiency of ammonia from 0 to 4h was 55.99%, and that from 4 to 12h was only 15.74%. The phosphate removal efficiency in the initial cycle was 97.68% but decreased to 63.25% after 24h. The phosphate removal rate in 2 min increased by 145% when the precipitation discharge frequency increased from 4 h/time to 24 h/time. Consequently, the HRT, service life of the magnesium sheet, and precipitation discharge frequency were selected as 4 h, 24 h, and 24 h/time. These optimized conditions provide valuable insights for the practical implementation of Mg-O2-FC in recovering N and P from wastewater.

Preparation of a novel LC@MWCNTs membrane and its application for enhanced phosphate removal and fouling control

To control the eutrophication originating from phosphate discharge, a novel adsorptive membrane was prepared by vacuum filtrating lanthanum carbonate modified multi-walled carbon nanotubes (LC@MWCNTs) on the UF membrane. The LC@MWCNTs were firstly made using an in-situ method by adding MWCNTs to LaCl3·7H2O solution and forming lanthanum carbonate under alkaline conditions. The adsorption experiments exhibited that the maximum adsorption capacity of LC@MWCNTs was 77.58 mg P/g at pH 5. And the phosphate adsorption by LC@MWCNTs was not predominantly reliant on electrostatic interaction, but rather achieved through chemical interactions. Then, the prepared LC@MWCNTs membrane was systematically evaluated for its phosphate removal efficiency and anti-fouling performance during filtration. With the initial phosphate concentration of 1 mg P/L and membrane flux of 378 L·m−2 h−1, the phosphate removal by LC@MWCNTs membrane approached almost 100 %. Moreover, the LC@MWCNTs membrane exhibited higher permeability (281.6 L·m−2h−1bar−1) and effectiveness for humic acid (HA) removal (75 %), and LC@MWCNTs membrane mitigated the fouling caused by HA. XPS, FTIR and XRD elucidated that phosphate removal by LC@MWCNTs membrane primarily through the formation of La-O-P inner-sphere complexes via ligand exchange, resulting in the formation of adsorption product LaPO4·0.5H2O. Under strong alkaline conditions, the LC@MWCNTs membrane rapidly restored its phosphate removal performance (30 min) with no significant detachment of the LC@MWCNTs layer, indicating its good recovery and reusability performance. Additionally, the LC@MWCNTs membrane could continuously remove phosphate from actual water, confirming its potential for future practical applications.

Efficient removal of phosphate and fluoride from phosphogypsum leachate by lanthanum-modified zeolite: Synchronous adsorption behavior and mechanism

Phosphogypsum is a common large-tonnage by–product in phosphorous chemicals industry, its stacking not only causes severe environmental problems, but also leads to a serious waste of phosphate and fluoride resources. The objective of this study was to tackle the recycling treatment of phosphogypsum leachate by using a highly efficient adsorbent lanthanum hydroxide-modified zeolite (LMZ). The adsorption behaviors of phosphate and fluoride by LMZ in the coexisting system under static and dynamic conditions were studied. And further, the competitive adsorption mechanism involved was analyzed. The results showed that LMZ possessed excellent adsorption performance toward both phosphate and fluoride in the single system, but the fluoride adsorption capacity decreased by 57.9 % in the coexisting system, with no change in phosphate adsorption. In the competitive adsorption process, ligand exchange interaction on La active sites contributed most to phosphate adsorption, while fluoride could be adsorbed onto LMZ via electrostatic attraction, surface precipitation with Al sites, and hydrogen bonds with hydroxyl groups in La−OH and P−OH. In actual phosphogypsum leachate, the removal of phosphate had priority over the removal of fluorine. Under continuous adsorption condition, the concentration of phosphorus and fluoride could be decreased to below 0.5 and 1.0 mg/L, respectively, meeting the safe concentration in drinking water. This study promotes the application of La–based adsorbents in the treatment of phosphogypsum leachate, and provides a green and sustainable strategy toward practical phosphorus and fluorine recovery.

Mesopore-rich La-based metal organic framework derivatives for phosphorus removal from mariculture tailwater

Deep dephosphorization of mariculture tailwater, a typical high-salinity and weakly alkaline wastewater, is difficult but essential for meeting ever-stricter stringent emission standards. Herein, we developed an alkaline-conversion method to prepare lanthanum-based metal organic framework (La–MOF) derivatives for efficient phosphate removal from mariculture tailwater. During the templated alkaline-conversion process, the strong-alkaline regent gradually broke the coordination bonds of La–MOF while maintained its macrostructure, and the La nodes liberated from the framework were then crystallized into La(OH)3. The universality of this conversion method was verified on other La–MOF precursors with different benzoic multicarboxylate ligands. Importantly, numerous mesopores were formed in the derivative interior, increasing the number of exposed active La sites and accessible transfer channels. Therefore, the derivative exhibited superior phosphate-adsorption performance with a high adsorption capacity (Langmuir Q0: 155.7 mg P/g) and a rapid adsorption rate. The obtained La–MOF derivative with stable structure had broad neutral–alkaline pH range adaptability, which was demonstrated satisfactory dephosphorization selectivity and high cyclic performance under different seawater conditions (coexisting anions, cations, H3BO3 and natural organic matter). Finally, the obtained mesopore-rich La–MOF derivative exhibited an excellent deep dephosphorization capacity for actual mariculture tailwaters collected from seven mariculture ponds. The reactive phosphate level was quickly reduced to an ultra-low effluent concentration (<0.05 mg P/L), demonstrating the promising application potential of the La–MOF derivative.

Biodegradable chelator GLDA intercalated magnesium/aluminum layered double hydroxides for efficient phosphate capture and removal from wastewater

Phosphate removal and recovery from wastewater play a vital role in controlling water eutrophication and facilitating resource recycling. Adsorbents of layered double hydroxides (LDHs) exhibit promising potential in the removal of phosphate; however, the removal efficiency often suffers insufficient as easy aggregation and inevitable loss of LDHs. Herein, a novel N, N–bis (carboxymethyl)–L–glutamic acid intercalated magnesium–aluminum LDH (GLDA@MgAl–LDH) were successfully synthesized. Intercalating with GLDA spawned dual functionality, i.e., the layer spacing expansion elevated the loading of phosphate, while GLDA also acted as additional binding sites toward phosphate. A higher phosphate capture (＞90%) was obtained in pH 5.0–8.0. Phosphate uptake was predominantly observed within the first1h, reaching equilibrium in approximately 4 h. The maximum adsorption capacity of 44.17 mg g–1 was attained for GLDA@MgAl–LDH at pH 6.70, which are far higher than that of pristine MgAl–LDH. GLDA@MgAl–LDH also had the excellent stability and reusability in five adsorption/desorption experiments. The GLDA@MgAl–LDH demonstrated significant efficacy in treating actual phosphate-containing wastewater in the fixed–bed adsorption column. Spectroscopic analysis, in conjunction with density functional theory, elucidated that GLDA intercalation enhanced the adsorption efficiency of MgAl–LDH. The key mechanisms facilitating phosphate removal included electrostatic attraction, anion and ligand exchange, and surface complexation. The above results highlight that GLDA@MgAl–LDH could serve as a promising and environmentally friendly candidate for phosphate treatment from the real wastewater.

Highly Efficient Clay Based Degumming Aid for Phosphorous Removal from Crude Palm Oil

The removal of phosphorous from crude oil is a complex and necessary step to enhance the oxidative stability and shelf life of edible oil. In this aspect, the current work proposed clay based degumming aid for the removal of phosphorous from the crude palm oil during the bleaching process. The state of art qualitative and quantitative techniques was adopted for the study of physical and chemical properties of different raw materials and oil. A profound study on the stability of the degumming aid is based on the assessment of phosphorous removal efficiency with time (up to 6 months) and bleachability. The results of current work revealed that clay based degumming aid is highly effective in removing phosphorous up to 96%. Additionally, the bleaching performance of clay-based aid is also palpable (around 45%), which influences the deodorization process of the crude palm oil positively. The clay based degumming aid eliminate separate degumming process with acids, which directly impact the oil processing time and cost. Overall, proposed clay based degumming aid is highly efficient, stable for long time and cost effective as well, for the removal of undesired phosphorous from the crude palm oil during the bleaching process.

A comparative study on the treatment of kitchen grey water using microalgae consortia and microalgae-synthesized silver nanoparticles.

Comparative study on the potential of microalgae consortia and green-synthesized silver nanoparticles using microalgae (M-AgNP) consortia for the treatment of kitchen grey water was investigated in this study. The microalgae consortia consisting of four species, viz., Chlorella sp., Scenedesmus sp., Coelastrum sp., and Pediastrum sp. were isolated from a local fish pond and the silver nanoparticles were synthesized with the same. Thus, synthesized silver nanoparticles exhibited a distinctive yellowish-brown colour and spherical morphology. Extensive qualitative and quantitative characterization techniques were employed to determine their size and morphology. Both microalgae consortia and M-AgNP were used separately for the treatment of kitchen grey water under experimental conditions. The synthesized silver nanoparticles demonstrated promising potential for domestic wastewater treatment, leading to substantial reductions in various parameters: total dissolved solids (29.6%), conductivity (49.4%), chemical oxygen demand (64.6%), and heavy metals (arsenic-63.5%, zinc-45.6%, cadmium-88%, copper-60.52%, and lead-80.82%). Notably, microalgae exhibited superior removal efficiency for nitrate (83.1%), sulphate (70.3%), and phosphate (96.5%) compared to microalgae-synthesized silver nanoparticles. This study underscores the effective utilization of both microalgae and microalgae-synthesized silver nanoparticles for wastewater treatment applications.

Hydrothermal-enhanced pyrolysis for efficient NOX reduction and biochar valorization from food waste digestate

Pyrolysis has emerged as a promising technology for valorizing digestate resulting from the anaerobic digestion of food waste. However, the high NOX emissions during pyrolysis limit its application. This study proposed a hydrothermal coupled pyrolysis process to control the element transfer in digestate during biochar production. The efficient reduction of NOX emissions and the improvement of biochar adsorbability were realized. The hydrothermal process reduced the nitrogen content in solid digestate by 49.10 %–81.79 %, thus reducing the NOX precursors in syngas and the N-containing substances in bio-oil. Additionally, the specific surface area and the total pore volume of biochar were enhanced from 25 m2/g to 60–73 m2/g and 0.06 cm3/g to 0.12–0.14 cm3/g, respectively. More defects, oxygen-containing functional groups, and doped Ca on the biochar resulted in a high phosphate removal efficiency of 94 %. The proposed technology provides an efficient and environmentally friendly way to utilize the digestate.

Efficient phosphate and hydrogen recovery from sludge fermentation liquid by sacrificial iron anode in electro-fermentation system

Electro-fermentation (EF) has been extensively studied for recovering hydrogen and phosphorus from waste activated sludge (WAS), while was limited for the further application due to the low hydrogen yield and phosphorus recovery efficiency. This study proposed an efficient strategy for hydrogen and vivianite recovery from the simulated sludge fermentation liquid by sacrificial iron anode in EF. The optimum hydrogen productivity and the utilization efficiency of short chain fatty acids (SCFAs) reached 45.2 mmol/g COD and 77.6% at 5 d in pH 8. Phosphate removal efficiency achieved at 90.8% at 2 d and the high crystallinity and weight percentage of vivianite (84.8%) was obtained. The functional microbes, i.e., anaerobic fermentative bacteria, electrochemical active bacteria, homo-acetogens and iron-reducing bacteria were highly enriched and the inherent interaction between the microbial consortia and environmental variables was thoroughly explored. This work may provide a theoretical basis for energy/resource recovery from WAS in the further implementation.