A novel co-metabolic mode with Spirulina powder in enhancing the anaerobic degradation of typical nitrogen heterocyclic compounds.

Spirulina powder emerged as a novel and suitable co-metabolism substance significantly enhancing the anaerobic degradation of specific nitrogen heterocyclic compounds. On the addition of 1.0 mg/L of Spirulina powder, the reactor demonstrated optimal degradation efficiency for quinoline and indole, achieving ratios of 99.77 ± 1.83% and 99.57 ± 1.98%, respectively. Moreover, the incorporation of Spirulina powder resulted in increased concentrations of mixed liquor suspended solids, mixed liquor volatile suspended solids, proteins, and polysaccharides in anaerobic sludge. In addition, Spirulina powder led to reduced levels of Acinetobacter and enriched Aminicenantes genera incertae sedis, Levilinea, and Longilinea. The analysis of the archaeal community structure confirmed that the addition of Spirulina powder increased archaeal sequences, fostering greater richness and diversity in the archaeal community.

Phosphorus biorecovery from wastewater contaminated with multiple nitrogen species by a bacterial consortium.

Recovering finite and non-substitutable phosphorus from liquid waste streams through bio-mediated techniques has attracted increasing interest, but current approaches are incredibly dependent on ammonium. Herein, a process to recover phosphorus from wastewater under multiple nitrogen species conditions was developed. This study compared the effects of nitrogen species on the recovery of phosphorus resources by a bacterial consortium. It found that the consortium could not only efficiently utilize ammonium to enable phosphorus recovery but also utilize nitrate via dissimilatory nitrate reduction to ammonium (DNRA) to recover phosphorus. The characteristics of the generated phosphorus-bearing minerals, including magnesium phosphate and struvite, were evaluated. Furthermore, nitrogen loading positively influenced the stability of the bacterial community structure. The genus Acinetobacter was dominant under nitrate and ammonium conditions, with a relatively stable abundance of 89.01% and 88.54%, respectively. The finding may provide new insights into nutrient biorecovery from phosphorus-containing wastewater contaminated with multiple nitrogen species.

Effects of methanol, sodium citrate, and chlorella powder on enhanced anaerobic treatment of coal pyrolysis wastewater.

To better promote environment friendly development of the coal chemical industry, this study investigated effects of methanol, sodium citrate, and chlorella powder (a type of microalgae) as co-metabolic substances on enhanced anaerobic treatment of coal pyrolysis wastewater with anaerobic sludge. The anaerobic sludge was loaded into four 2 L anaerobic reactors for co-metabolism enhanced anaerobic experiments. Anaerobic reactor 1 (R1) as control group did not add a co-metabolic substance; anaerobic reactor 2 (R2) added methanol; anaerobic reactor 3 (R3) added sodium citrate; and anaerobic reactor 4 (R4) added chlorella powder. In the blank control group, the removal ratios of total phenol (TPh), quinoline, and indole were only 12.07%, 42.15%, and 50.47%, respectively, indicating that 50 mg/L quinoline, 50 mg/L indole, and 600 mg/L TPh produced strong toxicity inhibition function on the anaerobic microorganism in reactor. When the concentration of methanol, sodium citrate, and chlorella was 400 µg/L, the reactors with co-metabolic substances had better treatment effect on TPh. Among them, the strengthening effects of sodium citrate (TPh removal ratio: 44.87%) and chlorella (47.85%) were better than that of methanol (38.72%) and the control group (10.62%). Additionally, the reactors with co-metabolic substances had higher degradation ratios on quinoline, indole, and chemical oxygen demand (COD). The data of extracellular polymeric substances showed that with the co-metabolic substances, anaerobic microorganisms produced more humic acids by degrading phenols and nitrogen-containing heterocyclic compounds (NHCs). Compared with the control group, the reactors added with sodium citrate and chlorella had larger average particle size of sludge. Thus, sodium citrate and chlorella could improve sludge sedimentation performance by increasing the sludge particle size. The bacterial community structures of reactors were explored and the results showed that Aminicenantes genera incertae sedis, Levinea, Geobacter, Smithella, Brachymonas, and Longilinea were the main functional bacteria in reactor added with chlorella.

Efficient adsorption of dyes from aqueous solution using a novel functionalized magnetic biochar: Synthesis, kinetics, isotherms, adsorption mechanism, and reusability.

In this study, a novel adsorbent, dodecylbenzene sulfonic acid (DBSA) functionalized magnetic biochar (DBSA-Fe3O4@BC), was synthesized and used to efficiently remove dyes from aqueous solution. The results indicated that DBSA-Fe3O4@BC exhibited an excellent adsorption capacity for Rhodamine B (RhB), and the maximum adsorption capacity for RhB at 298 K was 367.67 mg/g, which was approximately 2.3-1.2 folds than that of BC, dodecylsulfonic acid functionalized biochar (DSA@BC), DBSA@BC, Fe3O4@BC, and DSA-Fe3O4@BC. The possible adsorption mechanisms for RhB adsorption by DBSA-Fe3O4@BC included pore filling, electrostatic attraction, H bond, and surface complexation. Importantly, structural control presented that the simultaneous introduction of alkyl and phenyl groups significantly enhanced RhB adsorption by DBSA-Fe3O4@BC through hydrophobic and π-π interaction. Combined ethanol (EtOH) desorption and H2O2 oxidation regeneration, DBSA-Fe3O4@BC remained high-performance for RhB adsorption after six cycles (97.44%), indicating its outstanding reusability. In summary, DBSA-Fe3O4@BC exhibited a prospective application for dyeing wastewater treatment.

Simultaneous adsorption of tetracycline, ammonium and phosphate from wastewater by iron and nitrogen modified biochar: Kinetics, isotherm, thermodynamic and mechanism.

The simultaneous removal of various pollutants in wastewater is increasingly deserved attention. In this study, an efficient adsorbent Fe/N@BC was synthesized by Fe-N co-modification. The adsorbability of Fe/N@BC was evaluated using a mixture with tetracycline (TC), NH4+-N and PO43-P. In comparison to BC, N@BC and Fe@BC, Fe/N@BC exhibited an excellent performance for simultaneously absorbing TC, NH4+-N and PO43-P. The pseudo-first-order was used to describe the adsorption process of NH4+-N and PO43-P, while the pseudo-second-order could be well fitted to TC adsorption data. The adsorption isotherms of TC, NH4+-N and PO43-P were more in line with Sips model (Adj.R2 > 0.97). The maximum adsorption capacities of Fe/N@BC towards TC, NH4+-N and PO43-P were 238.94, 111.87 and 165.02 mg g-1, respectively, which were 1.31-1.91 times than that of BC, N@BC and Fe@BC. The simultaneous adsorption mechanism mainly involved pore filling, electrostatic interaction, ion exchange, surface complexation, surface precipitation, H bond and π-π interaction. Furthermore, after six cycles, the removal efficiencies of TC, NH4+-N and PO43-P were 75.3, 66.1 and 64.5% by Fe/N@BC, highlighting its promising potential to adsorb multi-pollutants from aqueous solution.

Rapid and efficient adsorption of tetracycline from aqueous solution in a wide pH range by using iron and aminoacetic acid sequentially modified hierarchical porous biochar.

The object of this work was to synthesize an iron and aminoacetic acid sequentially modified hierarchical porous biochar (AC-Fe@HPBC) for tetracycline (TC) removal from aqueous solution. Results showed that AC-Fe@HPBC had a larger surface area (362.5370 m2/g), developed microporous structure (0.1802 cm3/g), and numerous functional groups, which provided more adsorption sites. The maximum adsorption capacity towards TC by AC-Fe@HPBC was 457.85 mg/g, 1.43, 1.29 and 1.20-fold than that of HPBC, AC@PHBC and Fe@HPBC, respectively, and the super-fast adsorptive equilibrium was achieved within 10 min. Additionally, introducing amino and carboxyl functional groups on the AC-Fe@HPBC surface significantly broadened the operation pH range (3-11). Site energy analysis indicated TC and AC-Fe@HPBC had stronger adsorption affinity at a higher temperature. The adsorption mechanism involved pore filling, surface complexation, H-bond and π-π interaction. Moreover, the reusability experiments proved AC-Fe@HPBC as an effective adsorbent for TC removal from aqueous solution.

Enhanced adsorption of rhodamine B from water by Fe-N co-modified biochar: Preparation, performance, mechanism and reusability.

To adsorb rhodamine B (RhB) in wastewater by pristine biochar was limited, while the modified biochar has shown great potential adsorption performance. Here, coconut shell mixed with FeSO4·7H2O and urea was prepared to synthesize Fe-N co-modified biochar by once pyrolysis method at 500℃. The results showed Fe-N-BC had larger surface area (972.8714 m2·g-1), higher developed porous structure (0.65016 cm3·g-1), and more oxygen-containing groups, which collectively contributed to significantly improve the adsorption performance of the Fe-N-BC towards RhB. The maximum adsorption capacity of RhB reached 12.41 mg·g-1 by Fe-N-BC which was 1.58, 1.43 and 1.26 folds than that of BC, N-BC and Fe-BC, respectively. The mechanism of adsorption for Fe-N-BC towards RhB including ion exchange, pore filling, surface complexation, H-bond and π-π interaction. This study indicates that Fe-N-BC is an excellent adsorbent for RhB removal from wastewater.

Metagenomic analysis of aromatic ring-cleavage mechanism in nano-Fe3O4@activated coke enhanced bio-system for coal pyrolysis wastewater treatment.

In current study, nano-Fe3O4@activated coke enhanced bio-system (FEBS) under limited-oxygen condition was applied for efficient treatment of aromatic organics in coal pyrolysis wastewater. Metagenomic analyses revealed functional microbiome linkages and mechanism involved in aromatic ring-cleavage. Based on biodegradation efficiency in different reactors, FEBS supplementation conferred the best organic removal (avg. 92.29%). It also showed a remarkable advantage in biodegradability maintenance (>40%) over control reactors. Metagenomics profiling revealed the degradation processes were driven by Fe3O4 redox reactions and microbial biofilm, while the suspended sludge was the principal force for aromatic mineralization. Based on the analysis of functional species and genes, most bacteria cleaved the benzene ring preferably through the aerobic pathways, mediated by catechol 1, 2-dioxygenase, catechol 2, 3-dioxygenase and protocatechuate 3, 4-dioxygenase (66-84%). Ecological network showed that Comamonas testosterone-centered microbiome and Azotobacter linked to the nitrogen (N)-heterocyclic ring-cleavage. Network linkage further demonstrated that Alicycliphilus and Acidovorax were the key tone taxa involved in benzene ring-cleavage. Finally, combined with analysis of degradation products, bacteria degraded N-heterocyclic ring containing organic aromatic compounds (quinoline) mainly through anaerobic processes, whereas cleavage of benzene ring preferred aerobic pathways. The enriched functional species were the primary reason for the enhanced biodegradation in FEBS.

Enhanced anaerobic degradation of quinoline and indole with the coupling of sodium citrate and polyurethane.

A coupling system of sodium citrate and biofilm based on polyurethane was prepared to analyse the coupling enhancement degradation on quinoline and indole. Four reactors (R1: sludge, R2: sludge + sodium citrate, R3: biofilm on polyurethane, and R4: biofilm + sodium citrate) were operated 120 days to compare the degradation efficiency. During whole running phases, R4 showed high degradation efficiency on quinoline (≥98.55%) and indole (≥95.44%). Analysis of bacterial colony showed anaerobic sludge reactors benefited the enrichment of Aminicenantes, Levilinea, and Longilinea, while anaerobic biofilm reactors benefited the enrichment of Giesbergeria and Comamonas. Furthermore, analysis of archaea colony showed acetic acid metabolism to produce methane was the main mode in anaerobic sludge reactors, while acetic acid and hydrogen metabolism to produce methane were both the main modes in biofilm reactors. This study can provide some references for the treatment of nitrogen heterocyclic wastewater.

Insights into electroactive biofilms for enhanced phenolic degradation of coal pyrolysis wastewater (CPW) by magnetic activated coke (MAC): Metagenomic analysis in attached biofilm and suspended sludge.

To investigate the role of electroactive biofilms for enhanced phenolic degradation, lignite activated coke (LAC) and MAC were used as carriers in moving-bed biofilm reactor (MBBR) for CPW treatment. In contrast to activated sludge (AS) reactor, the carriers improved degradation performance of MBBR. Although two MBBRs exerted similar degradation capacity with over 92% of COD and 93% phenols removal under the highest phenolics concentration (500 mg/L), the effluent of MAC-based MBBR remained higher biodegradability (BOD5/COD = 0.34 vs 0.18) than that of LAC-based MBBR. Metagenomic analysis revealed that electroactive biofilms determined phenolic degradation of MAC-based MBBR. Primarily, Geobacter (17.33%) started Fe redox cycle on biofilms and developed syntrophy with Syntrophorhabdus (6.47%), which fermented phenols into easily biodegradable substrates. Subsequently, Ignavibacterium (3.38% to 2.52%) and Acidovorax (0.46% to 8.83%) conducted biological electricity from electroactive biofilms to suspended sludge. They synergized with dominated genus in suspended sludge, Alicycliphilus (19.56%) that accounted for phenolic oxidation and nitrate reduction. Consequently, the significantly advantage of Geobater and Syntrophorhabdus was the keystone reason for superior biodegradability maintenance of MAC-based MBBR.

Ecological and functional research into microbiomes for targeted phenolic removal in anoxic carbon-based fluidized bed reactor (CBFBR) treating coal pyrolysis wastewater (CPW).

Powdered activated carbon (PAC), lignite activated coke (LAC) and Fe-C carriers were applied to enhance CBFBRs to degrade targeted phenolics. In start-up stage, PAC and LAC equipped CBFBRs with higher environment adaptability and phenolic degradation capacity for phenol (>96%), p-cresol (>91%) and 3, 5-dimethylphenol (>84%) in comparison to Fe-C carrier. In recovery stage, the superior performance was also identified for CBFBRs in basis of PAC and LAC than Fe-C-based reactor. However, the Fe-C carrier assisted CBFBR with more stable degradation performance under impact loading. By comparing microbiomes, significantly enriched Brachymonas (54.80%-68.81%) in CBFBRs exerted primary role for phenolic degradation, and positively contributed to microbial network. Meanwhile, Geobacter in Fe-C-based reactor induced excellent impact resistance by enhancing interspecific electron transfer among microbes. Furthermore, the investigation on functional genes related to phenolic degradation revealed that anaerobic pathway accounted for demethylation procedure, while aerobic pathways dominated the phenolic ring-cleavage process.

Effect of low-intensity electric current field and iron anode on biological nitrate removal in wastewater with low COD to nitrogen ratio from coal pyrolysis.

Mixotrophic nitrate removal in wastewater from coal pyrolysis was achieved in microbial electrolysis cell with iron anode (iron-MEC). The effect of voltage, iron anode and conductivity were investigated. The effluent TN concentration was 8.35 ± 1.94 mg/L in iron-MEC when the conductivity of the wastewater was adjusted to 3.97 ± 0.08 mS/cm, which was lower than that in no-treated reactor. The increase of current density, which was resulted from the elevation of conductivity, promoted the iron corrosion and Fe2+ ion generation. Therefore, more Fe2+ ion was utilized by nitrate reducing ferrous oxidation bacteria (NRFOB) used to reduce nitrate. The microbial community analysis demonstrated that NRFOB, including Acidovorax and Bradyrhizobium, possessed a higher abundance in iron-MEC. The enrichment of Geobacter in iron-MEC might imply that the part of Fe(III) produced by ferrous oxidation was reduced by Geobacter, which established an iron cycle. Moreover, the production of N2O was decreased by the formation of Fe2+ ion.

Enhanced anaerobic degradation of nitrogen heterocyclic compounds with methanol, sodium citrate, chlorella, spirulina, and carboxymethylcellulose as co-metabolic substances.

The aim of the study was to explore the feasibility of methanol, sodium citrate, chlorella, spirulina, and carboxymethylcellulose (CMC) as co-metabolic substances in strengthening the anaerobic degradation of selected nitrogen heterocyclic compounds (NHCs). Chlorella, spirulina, and CMC as co-metabolic substances were first introduced into the enhanced anaerobic treatment of refractory compounds. With the addition of 300 µg/L sodium citrate, chlorella, spirulina, and CMC, reactor 3, reactor 4, reactor 5, and reactor 6 had higher degradation ratios than reactor 2 with methanol as co-metabolic substance. The addition of sodium citrate, chlorella, spirulina, and CMC increased the number of bacterial sequences, promoted the richness and diversity of the bacterial community structure, and enriched the functional genera (Levilinea and Longilinea) responsible for the degradation of quinoline and indole.

The concept of anaerobic hydrolysis to produce clean and stable energy from the case study of utilization of three types of pollutants in coal pyrolysis wastewater.

The purpose of the research was to explore the feasibility of anaerobic hydrolysis in the recycling of chemical wastewater. From the case study of utilization of coal pyrolysis wastewater (CPW), the concept of anaerobic hydrolysis to produce clean and stable energy was proposed. Compared with anaerobic methane production and hydrogen production, anaerobic hydrolysis was more suitable to realize the resource utilization of chemical wastewater. Typical pollutants in CPW could be hydrolyzed into short chain alkanes (or alkane alcohol) under the action of anaerobic hydrolysis. Furthermore, element N was released during the anaerobic hydrolysis of nitrogen heterocyclic compounds. The advantages and existing problems of anaerobic hydrolysis were also discussed. The conversion mechanism of pollutants in CPW can provide a theoretical basis for the utilization of chemical wastewater.

A novel enhanced anaerobic biodegradation method using biochar and Fe(OH)3@biochar for the removal of nitrogen heterocyclic compounds from coal gasification wastewater.

Three identical lab-scale sequencing batch reactors (SBR) were operated for 120 days for raw (R1), biochar (R2), and Fe(OH)3@biochar (R3) enhanced anaerobic degradation of selected nitrogen heterocyclic compounds (NHCs). The occurrence of Fe-OH ensured the successful attachment of Fe(OH)3 to biochar as evidenced by the Fourier transform infrared (FTIR) spectra of biochar and Fe(OH)3@biochar. Acute biotoxicity experiments revealed that enhancing biochar and Fe(OH)3@biochar effectively decreased the toxicity of microorganisms. Additionally, the introduction of biochar and Fe(OH)3@biochar improved the settling performance of anaerobic sludge. Further, it was concluded that enriched Longilinea and Comamonas might be the major genera that function to degrade selected NHCs in anaerobic conditions.

Enhanced anaerobic degradation of quinoline, pyriding, and indole with polyurethane (PU), Fe3O4@PU, powdered activated carbon (PAC), Fe(OH)3@PAC, biochar, and Fe(OH)3@biochar and analysis of microbial succession in different reactors.

The study was to explore the feasibility of polyurethane (PU), Fe3O4@PU, powdered activated carbon (PAC), Fe(OH)3@PAC, biochar, and Fe(OH)3@biochar as biological carriers in strengthening anaerobic degradation of quinoline, pyridine, and indole. When the concentrations of pollutants were 25 mg/L and 50 mg/L, reactors based on PAC and Fe(OH)3@PAC had higher degradation ratios than the other reactors. However, when the concentrations of pollutants were 75 mg/L and 100 mg/L, with the addition of PU and Fe3O4@PU, reactors began to show their superiority in the degradation of the selected NHCs. Among these, the reactor based on Fe3O4@PU had the optimal degradation ratio on quinoline, pyridine, and indole. PU, PAC, Fe(OH)3@PAC, biochar, and Fe(OH)3@biochar benefited the enrichment of Acinetobacter, Comamonas, Levilinea, Longilinea, and Desulfomicrobium. The reactor with the carrier of Fe3O4@PU had some specificity, which benefited the enrichment of Zoogloea, Thiobacillus, Anaeromyxobacter, Sphingobium, Terrimonas, Parcubacteria genera incertae sedis, Bdellovibrio, Rhizobium, and Acidovorax.

Enhanced biodegradation of coal gasification wastewater with anaerobic biofilm on polyurethane (PU), powdered activated carbon (PAC), and biochar.

The primary objective was to explore the feasibility of anaerobic biofilm on polyurethane (PU), powdered activated carbon (PAC), and biochar in strengthening anaerobic degradation of phenolic compounds and selected nitrogen heterocyclic compounds (NHCs) in coal gasification wastewater (CGW). When total phenols (TPh) was less than 300 mg/L, PAC-based biofilm was more efficient. Whereas, when the TPh concentration was more than 450 mg/L, PU-based biofilm performed the optimal degradation efficiency. Furthermore, microbial community structure analysis showed that PAC and biochar had little effect on the microbial community structure after 120 days of operation, while the addition of PU could lead to the enrichment of Giesbergeria, Caldisericum, Thauera, Methanolinea, and Methanoregula.

Enhanced anaerobic degradation of selected nitrogen heterocyclic compounds with the assistance of carboxymethyl cellulose.

Carboxymethyl cellulose (CMC) is a modified cellulose compound that is dispersible in water. Microbial anaerobic degradation of nitrogen heterocyclic compounds (NHCs) in wastewater treatment may be enhanced by CMC addition, but this remains uncertain due to a lack of experimental evidence. In this study, It was demonstrated that CMC is a suitable co-metabolic matrix in an enhanced anaerobic degradation of quinoline and indole in coal gasification wastewater. When the dosage of CMC was 0.5 mg/L, a reactor exhibited a high degradation efficiency on quinoline and indole, with ratios of 95.23 ±â€¯1.99% and 94.33 ±â€¯3.45%. The addition of CMC increased the concentration of extracellular polymeric substances in anaerobic sludge and increased the particle size of the sludge, which improved the microbial stability and sedimentation of anaerobic granular sludge. Analysis of high-throughput sequencing indicated that the addition of CMC improved the richness and diversity of bacterial and archaea communities. Acetic acid metabolism was the primary mechanism to produce methane during anaerobic degradation of NHCs wastewater.

Anaerobic bioaugmentation hydrolysis of selected nitrogen heterocyclic compound in coal gasification wastewater.

Anaerobic bottle experiments were conducted in parallel for 120 consecutive days to perform the bioaugmentation hydrolysis of selected nitrogen heterocyclic compounds (NHCs) in coal gasification wastewater. Due to enhancement with PAC and Fe(OH)3@PAC, quinoline, pyridine, and indole were hydrolyzed more effectively. The addition of PAC and Fe(OH)3@PAC improved the coagulation capacity of microorganisms, which laid a solid foundation for the removal of selected NHCs and the adverse environmental conditions. Anaerobic degradation of the NHCs occurred first through hydrogenation, then through the opening of the nitrogen heterocycles, followed by the release of ammonia nitrogen and finally the opening of the benzene rings. Enriched Acinetobacter, Levilinea, Comamonas, and Longilinea were the main functional groups responsible for the anaerobic biodegradation of the selected NHCs.