Metagenomics insights into the effect of co-landfill of incineration fly ash and refuse for bacterial community succession and metabolism pathway of VFAs production.

With the development of incineration technologies, incineration has become the most common treatment method of municipal solid waste in China. However, stabilized fly ash may enter landfills during the transition from landfill to incineration, which caused uncertain impact on landfill waste stabilization. Two simulated co-landfill columns were constructed based on different co-landfill methods (layer co-landfill and mixed co-landfill) to investigate the effect of stabilized fly ash co-landfilled municipal solid waste for bacterial community succession and change in metabolic pathways during hydrolysis-acidogenesis stage. The mixed co-landfill method resulted in higher degree of organic matter degradation, and the concentrations of volatile fatty acids (VFA) and chemical oxygen demand (COD) in leachate were higher. The dominant phyla were Firmicutes in the layered co-landfill column and Bacteroidetes in mixed co-landfill column. The dominant genera for the total bacterial composition and VFA production were different, Pseudomonas and Propionibacterium, Proteiniphilum and unclassified Bacteroides were the dominant genera responsible for VFA generation in the layered and mixed co-landfill columns. The genes for butyrate production were enriched in the layered co-landfill column, whereas those related to acetate production were enriched in mixed co-landfill column. However, the layered co-landfill inhibited the microbial metabolic activity at the end of the co-landfill process.

Stability evaluation of potentially toxic elements in MSWI fly ash during carbonation in view of two leaching scenarios.

Carbonation treatment (CT) by alkaline fly ash (FA) affects the stability of potentially toxic elements (PTEs). This study investigated the leachability and environmental risk of six PTEs contained in FA during natural and accelerated carbonation (NC, AC) using two typical leaching scenarios with distilled water (DW) and acetic acid (AA). The leaching of Pb/Cu/Cr/Ni in solidified/stabilized FA decreased due to CT in DW leaching, but the leaching of Pb/Zn/Cu/Cd increased due to CT in AA leaching. The leaching of the six PTEs (especially Pb/Cd) in AA leaching was significantly higher than that in DW leaching. CT was a promoting factor to increase the environmental risk level of PTEs in FA leachate, especially in AA leaching with H+ input. In the early stage of NC, under DW leaching tests, the environmental risk level of PTEs in FA leachate can be weakened due to the formation of carbonate minerals in the FA matrix. However, excessive NC increases the environmental risk of leached PTEs due to the decalcification of carbonate minerals. Both NC and AC increased the potential environmental risk of PTEs contained in the carbonated FA matrix. The nucleation and dissolution of carbonate minerals were interdependent with the immobilization and leaching of PTEs, which played a dominant role in the CT and leaching tests respectively. They jointly affected the occurrence behavior of PTEs in the FA matrix in CT tests and the leachability of PTEs in leaching tests. This study demonstrates that it is more scientific to evaluate the leachability of PTEs in carbonated FA according to the actual disposal scenarios.

Mechanisms of emerging pollutant Dechlorane Plus on the production of short-chain fatty acids from sludge anaerobic fermentation.

The effect of emerging pollutant Dechlorane Plus (DPs), an organochlorine aliphatic flame retardant, on waste-activated sludge anaerobic fermentation was investigated, and the related mechanisms were revealed for the first time. The results of this experiment suggested that the presence of DPs had a significant inhibitory effect on sludge anaerobic fermentation to generate the intermediate valuable product short-chain fatty acids (SCFA), and when the DP content was 3034.1±101.7 mg/kg total suspended solids (TSS), the maximal output of SCFA was only 215.04 mg/g, which was 0.47 times of that in the blank. The underlying mechanism investigation indicated DPs promoted the disintegration of sludge, but inhibited the process of hydrolysis and acidification. DPs inhibited the release of soluble bound extracellular polymers (SB-EPS) in sludge. The analysis of microbial community characteristics indicated that DPs reduced the level of Firmicutes and Actinobacteriathe, which were the key acid producing bacteria. At the genus level, DPs reduced the relative abundance of Proteiniclasticum and Mycobacteriumwas.

Leaching behavior and environmental risk assessment of toxic metals in municipal solid waste incineration fly ash exposed to mature landfill leachate environment.

Solidification/stabilization pretreatment + landfill disposal in municipal solid waste (MSW) landfill sites is a widely accepted MSW incineration (MSWI) fly ash (FA) management strategy in China. However, in reality, the stability of FA disposed in MSW landfill sites may be affected by the organic landfill leachate environment. The purpose of this study was to explore the mobility and environmental risks of six toxic metals (Mn+, Pb/Zn/Cu/Cd/Cr/Ni), from raw and solidified/stabilized FA, by simulating a leaching environment with mature landfill leachate (MLL). The leaching of Mn+ mainly occurred in the early leaching stage, and their leaching behavior was controlled by the diffusion of surface Mn+ in the FA matrix. The destructive effect of dissolved organic matter (DOM) on the local precipitation-dissolution equilibrium of FA-leachate interface, the formation of non-adsorptive DOM-Mn+ complex (easy to migrate), and the competitive effect of DOM on the binding sites of Mn+ on the surface of the FA matrix may play an important role in increasing the leaching level of most Mn+. By contrast, the potential of solidified FA in reducing the environmental risk level of leached Mn+ was better than that of stabilized FA. However, the immobilization capability of solidification/stabilization pretreatment on various types of Mn+ in FA should be judged according to their practical disposal environment. Compared to MLL leaching tests, Acetic Acid Buffer Solution Method (HJ/T300-2007) can effectively strengthen the exposure environment and provide a reliable reference level of environmental risk for MSWI FA disposed in MSW landfill sites.

Municipal solid waste incineration fly ash exposed to carbonation and acid rain corrosion scenarios: Release behavior, environmental risk, and dissolution mechanism of toxic metals.

This study investigated the leaching behavior, environmental risk, and dissolution mechanism of toxic metals (TMs) in solidified/stabilized municipal solid waste incineration fly ash (MSWI FA) exposed to alternative "carbonation + acid rain corrosion" disposal scenarios. The content of TMs (mg/kg) showed a trend of Zn (12,187.10 ± 168.60) > Pb (3374.43 ± 66.12) > Cu (1055.14 ± 32.52) > Cr (127.95 ± 8.12) > Cd (119.05 ± 6.26) > Ni (49.50 ± 3.20). Initial leaching of CO2-saturated water (CSW) and replacement of simulated acid rain (SAR) increased the environmental risk of leached TMs. The results of "average release rate" (mg/(kg·d)) of TMs indicated that Zn (0.8307)/Cu (0.0278)/Cd (0.0109) and Cu (0.0581)/Cr (0.001176)/Ni (0.004339) in phosphoric acid stabilized FA and Pb (0.0753)/Cr (0.001921)/Ni (0.00111) and Pb (0.0656)/Zn (1.0560)/Cd (0.0050) in Portland cement solidified FA were the key "problem TMs" during carbonation and acid rain corrosion, respectively. CSW leaching increased the independent environmental risk of most TMs in residual FA (especially Zn/Cd) due to the increased carbonate-bound fraction. Compared with independent carbonation, alternative "carbonation + acid rain corrosion" contributed to a higher comprehensive environmental risk for TMs in residual FA. CSW leaching system was an indirect carbonation based on CO2-water and FA matrix, in which "nucleation and dissolution" of carbonates and "immobilization and dissolution" of TMs coexisted. The dissolution mechanism of TMs was mainly controlled by reaction equilibrium of nucleation and dissolution of carbonates containing TMs. Dissolution and nucleation were the dominant mechanism in the early and later periods of CSW leaching, respectively. Carbonate layer dissolution, H+ corrosion/displacement, and counter-ion effect (SO42- > NO3- > Cl-) were the main mechanisms affecting TM dissolution during SAR leaching.

Diclofenac inhibited the biological phosphorus removal: Performance and mechanism.

This work aims to evaluate the effect of new contaminant diclofenac (DCF) in sewage on the performance of Enhanced Biological Phosphorus Removal (EBPR) and its mechanism. The results showed that low-level DCF had no significant effect on EBPR. However, when the concentration of DCF was 2.0 mg/L, the removal efficiencies of chemical oxygen demand (COD), NH4+-N and soluble orthophosphate (SOP) decreased significantly to 71.2 ± 4.2%, 78.6 ± 2.9%, and 64.3 ± 4.2%, respectively. Mechanisms revealed that DCF promoted the ratio of protein to polysaccharide in activated sludge extracellular polymers and inhibited anaerobic phosphorus release and oxic phosphorus uptake. Intracellular polymer analysis showed that when the DCF content was 2.0 mg/L, the maximum content of polyhydroxyalkanoates (PHA) was only 2.5 ± 0.4 mmol-C/g VSS, which was significantly lower than that in the blank. Analysis of key enzyme activities indicated that the presence of DCF reduced the activities of exopolyphosphatase and polyphosphate kinase.