Hydrated lanthanum oxide-modified diatomite as highly efficient adsorbent for low-concentration phosphate removal from secondary effluents.

The requirement to the phosphorus (P) emission from wastewater treatment plants (WWTPs) is becoming increasingly strict, which makes an advanced treatment for the low-concentration phosphate removal from secondary effluents indispensable. In present work, hydrated lanthanum (La) oxide-modified diatomite composites (La-diatomite) were fabricated by a facile method and employed as the highly efficient adsorbent for the low-concentration phosphate removal from simulating secondary effluents. Comparative experiments indicated that the La-diatomite treated by 0.1 mol/L LaCl3 exhibited the highest La availability (P/La molar ratio of 2.30) and performed good selectivity to phosphate adsorption even with the coexistence of competing anions and humic acid. The maximum P adsorption capacity reached to 58.7 mg P/g and the 96% P was removed quickly within 30 min at initial phosphate concentration 2 mg P/L. Insignificant La leaching was observed during the process due to the La stabilization by macroporous diatomite. Eight cycles of adsorption-desorption experiments revealed that the excellent repeated use property of La-diatomite. At the column test, La-diatomite showed superior treatment capacities of 3455 kg water/kg La-diatomite for simulated secondary effluents. The La-diatomite maintained high and stable adsorption effectiveness in wide pH range, which should be attributed to the synergistic effect of electrostatic interactions, ligand exchange and Lewis acid-based interaction. This work might provide a candidate for low-concentration phosphate removal from secondary effluent to alleviate the eutrophication.

The fate of cyanuric acid in biological wastewater treatment system and its impact on biological nutrient removal.

Cyanuric acid (CA) is widely used in living and production. It is a kind of environmental priority pollutants which exists chronically in soil and water, but is difficult to be chemically hydrolyzed or oxidized. The behavior of CA at different levels of 0, 0.01, 0.10 and 1.00 mg L-1 in biological wastewater treatment process was investigated in this paper. Experimental results showed that CA (0.01 and 0.10 mg L-1) was removed in biological wastewater treatment process, which was mainly achieved by biodegradation of particular species (Acidovorax and Pseudomonas) in the anaerobic condition. However, 1.00 mg L-1 CA was reluctant to be degraded in biological wastewater treatment system. With the CA level increase from 0 to 1.00 mg L-1, total nitrogen removal efficiency decreased from 97.23 to 74.72%. The presence of CA promoted both the synthesis and decomposition metabolisms of poly-hydroxyalkanoates and glycogen, thereby providing the advantage for phosphorus removal. CA could inhibit nitrification process because of inhibition to nitrite oxidizing bacteria (NOB). Moreover, the microbial community of activated sludge was changed by the exposure of CA. Polyphosphate accumulating organisms, such as Bacteroidetes, Chloroflexi and Saccharibacteria increased, but the abundance of Nitrospirae was decreased.

Efficient degradation of bisphenol A via peroxydisulfate activation using in-situ N-doped carbon nanoparticles: Structure-function relationship and reaction mechanism.

A novel in-situ N-doped carbon nanoparticles (NCNs) was prepared through direct pyrolysis of N-rich polyaniline (PANI) without using external N-containing precursor and the as-prepared materials were employed as metal-free peroxydisulfate (PDS) activator for bisphenol A (BPA) degradation. The catalyst derived from PANI carbonization at 900 °C (NCNs-9) displayed the excellent catalytic activity to activate PDS, resulting in 96.0% BPA degradation efficiency within 20 min. The catalytic activity of NCNs was closely related to their structure-composition, and higher graphitic N content and larger BET surface area were beneficial to the generation of reactive oxygen species (ROS). The quenching tests and electron paramagnetic resonance (EPR) demonstrated that BPA degradation in PDS/NCNs system was accomplished via non-radical (1O2) and radical ( ·OH, SO4·-, and O2·-) pathways, in which O2·- was the main ROS. The origin of O2·- was the conversion of dissolved oxygen and the activation of PDS. The possible degradation pathways of BPA were also proposed. This study might provide inspirations to design in-situ N-doped carbon nanoparticles as the PDS activator for efficient degradation of persistent organic compound via advanced oxidation processes (AOPs).

The effects of thiosulfinates on methane production from anaerobic co-digestion of waste activated sludge and food waste and mitigate method.

Thiosulfinates, a natural antibiotic, existed in all parts of Allium, therefore might be accumulated in large amounts in food waste (FW). FW was often added into waste activated sludge (WAS) anaerobic digestion process as a kind of supplement for nutrition balance. However, the impact of thiosulfinates on methane production and the possible approach to mitigate its inhibition on the co-digestion process could be available in few literatures. This work was carried out in a series of batch experiment at pH 7.0 ±â€¯0.2 and 35 ±â€¯1.0 ℃ to promote the further understanding of this process. The experimental results showed that the methane accumulation decreased from 270.6 ±â€¯13.4 to 16.7 ±â€¯7.0 mL/g VSS (volatile suspended solids) when the initial concentration of thiosulfinates increased from 0 to 2.5 µg/g VSS. The activities of functional enzymes (F420 and CoM) were inhibited by 99.06% and 99.82% compared with control group when reactor contained 2.5 µg/g VSS thiosulfinates. Furthermore, different temperature, pH, and combination pretreat were applied to impair the inhibition of thiosulfinate. Compared with no pretreatment group, methane yield was increased by 2.26, 32.18 and 42.2-fold, respectively which group was under pretreatment method of heat (100 ℃), alkali (pH 9) and combination.

The inhibitory effect of thiosulfinate on volatile fatty acid and hydrogen production from anaerobic co-fermentation of food waste and waste activated sludge.

Thiosulfinate, a nature antibiotic, existed in all parts of Allium thereby accumulating in kitchen waste vastly. However, few literatures were available related to its influence on volatile fatty acids (VFA) and hydrogen production when kitchen waste digestion technology was applied. This study aimed to explore the inhibitory effect and the relevant mechanism. Experimental results showed that the hydrogen accumulation decreased from 23.2 ± 0.8 to 8.2 ± 0.1 mL/g VSS (volatile suspended solid) and maximal total VFA yield decreased from 765.7 ± 21.2 to 376.4 ± 21.7 mg COD (chemical oxygen demand)/g VSS when the dosage of thiosulfinate increased from 0 to 12.5 µg/g VSS. The mechanism study indicated, compared with control group, that the butyric acid decreased from 59% to 20.1% of total VFA yield when reactor in present of 12.5 µg/g VSS thiosulfinate. Moreover, the relative activities of functional enzymes were inhibited 73.4% (butyryl-CoA) and 72.7% (NADH), respectively.

Influence of low voltage electric field stimulation on hydrogen generation from anaerobic digestion of waste activated sludge.

Low voltage electric field is an important stimulation condition for biochemical metabolic of microorganism. But few literatures were available related to the effect of low voltage electric field on hydrogen production from anaerobic digestion of waste activated sludge (WAS). This study aims to explore such influencing thus carried a series experiments under 35 ± 1 °C and pH 7.0 ± 0.2. The experimental results showed that the hydrogen production increased from 28.1 to 32.5 mL/g VSS with electric field strengthening from 0 to 40 V/m. The mechanism explorations revealed that the yield of volatile fatty acids (VFAs) yield could reach 1.16-fold of control group when the highest-level electric field (40 V/m) forced in the anaerobic fermentation system with dextran as model substrate. Further analysis of relative activities of functional enzymes, such as NADH, acetate kinase, butyrate kinase and OAATC, showed that it was promoted by electric field stimulation as 2.09, 1.52, 1.28 and 1.16-fold of the control test, respectively. Meanwhile, the conductivity of fermentation liquor in presence of low voltage electric field stimulation increased 83% compared with the control group. This work verified the promotion of low voltage electric field stimulation on hydrogen production from anaerobic digestion of WAS and might provide a new sight for the green energy generation.

Enhanced anaerobic co-digestion of waste activated sludge and food waste by sulfidated microscale zerovalent iron: Insights in direct interspecies electron transfer mechanism.

The enhancement of zerovalent iron (ZVI) on anaerobic digestion (AD) has been proved, but there are still some problems that constrain the large-scale application of ZVI, such as the destruction of cell membrane and the inhibition of methanogenesis led by rapid H2 accumulation. Aiming at these problems, sulfidated microscale zerovalent iron (S-mZVI) was employed to evaluate its effect on anaerobic co-digestion (AcoD) of waste activated sludge (WAS) and food waste (FW). Experimental results showed that S-mZVI promoted the direct interspecies electron transfer (DIET) between specific bacteria and methanogens, resulting in higher methane yield. At S-mZVI 10 g/L, the cumulative methane yield and ETS activity reached 264.78 mL/g-VS and 24.62 mg INTF/(g-TS h), which was 1.33 and 1.83 times that of blank. Microbiological analysis demonstrated that the abundance of DIET-related microorganisms such as Syntrophomonas, Methanosarcina and Methanobacterium increased with the increasing dosage of S-mZVI.

Heterogeneous activation of persulfate by Ag doped BiFeO3 composites for tetracycline degradation.

Persulfate (PS) activation have been extensively considered as a promising technology for removing recalcitrant pollutants, due to their production of radicals with superior oxidation reactivity. However, a catalyst with high reactive and convenient recovery for PS activation still remains to be developed. In this work, the silver-doped bismuth ferrite (Agx-BiFeO3, x = 0.1, 0.2, 0.3 and 0.4) catalysts with variable Ag content were synthesized via a facile sol-gel method and applied as heterogeneous catalyst in PS activation for tetracycline (TC) degradation. Ag0.4-BiFeO3 presented the best catalytic activity compared with other Ag doped BiFeO3 composites, 91% TC could be efficiently removed within 60 min under optimized conditions and the reaction rate constant was 0.0338 min-1. On the basis of the characterization analysis and catalytic test results, Ag could be the effective active site in PS activation and had a significant effect on PS activation. Moreover, the initial pH has negligible effect on the catalytic performance, indicating that Ag0.4-BiFeO3/PS system could work in a wide pH range. The results of electron spin-resonance spectroscopy and radical quenching tests suggested that both SO4- and OH radicals were involved in the Ag0.4-BiFeO3/PS system. The possible mechanism of Ag0.4-BiFeO3 activating PS and the major degradation pathway of TC degradation were proposed. At last, the reusability experiment results proved that Ag0.4-BiFeO3 catalyst still has a high catalytic performance after 4 times used.

Effect of citric acid on extracellular polymeric substances disruption and cell lysis in the waste activated sludge by pH regulation.

This paper investigated the effects of citric acid (CA) on extracellular polymer destruction and cell lysis in sludge at different initial pH by measuring capillary suction time (CST), extracellular polymeric substances (EPS) and intracellular bound water. The results indicated that under CA concentration at 0.05 g/g suspended solids (SS) and initial pH 4, the CST value decreased from 175.5 s to 112.3 s, slime extracellular polymeric substances (S-EPS) and loosely bound EPS (LB-EPS) content respectively to increase from 4.92 to 41.43, 2.27 to 5.49 mg/g volatile suspended solids (Vss), while tightly bound EPS (TB-EPS) content to decrease from 12.35 to 5.01 mg/g (Vss), which suggested CA could disrupt outer EPS effectively. Intracellular bound water content decreased from 1.23 g/g to 0.41 g/g dry solid (DS). As a result, CA could release intracellular bound water effectively, thereby improving sludge dewatering degree.

Sulfate radical-mediated degradation of phenol and methylene blue by manganese oxide octahedral molecular sieve (OMS-2) activation of peroxymonosulfate.

Activation of peroxymonosulfate (PMS) has been concentrated on degrading refractory organic pollutants owing to the generation of sulfate radical ([Formula: see text]) with high standard redox potential. In this study, manganese oxide octahedral molecular sieve (OMS-2) with cryptomelane type was synthesized by a new hydrothermal method to activate PMS for the degradation of phenol and methylene blue (MB) in water. The as-prepared composites were fully characterized, and the effects of PMS dosage, OMS-2 dosage, initial pollutant concentration, pH, and chloride on the degradation of phenol were elaborately investigated. Moreover, the phenol degradation was evaluated through the variations of total organic carbon (TOC) and three-dimensional excitation emission matrix (3D-EEM), and reaction intermediates were also investigated. Both electron spin resonance (ESR) spectra and comparative experiments suggested [Formula: see text] and hydroxyl radical (HO•) took part in the phenol degradation and [Formula: see text] was more significant than HO•. The fine degradation efficiency of phenol in different water source, as well as the stability after continuous use, indicated the possible application of PMS/OMS-2 in real wastewater treatment.

Enhanced volatile fatty acids production from waste activated sludge anaerobic fermentation by adding tofu residue.

In this study, an economical and eco-friendly strategy (i.e., adding tofu residue (TR) into waste activated sludge (WAS)) to enhance volatile fatty acid (VFA) production was reported. Experimental results indicated that the maximal VFA yield at T/W ratio (TR/WAS, the ratio of the volatile suspended solids (VSS)) of 0.64 on 5 d was 240.8 mg COD/g VSS, which was 10.2 and 1.1-fold of that in sole WAS and sole TR, respectively. The feasible fermentation time was shortened by 2 days, as compared with sole WAS or sole TR. Mechanism investigation showed that the addition of TR promoted solubilization, hydrolysis, and acidogenesis processes. The synergistic effect of microorganisms contained in TR and WAS may be responsible for the enhancement of lignocellulose hydrolysis and VFA generation. Appropriate amounts of mineral elements in TR benefited solubilization, the soluble iron and calcium in TR could contribute to the phosphorus removal in fermentation liquor.