Excitation-emission Matrix Analysis Research Articles

Fluorescence spectrometric analysis for diagnosing compositional variations in effluent organic matter by chlorination and ozonation

Analyzing the reactivity of organic matter to oxidants such as chlorination and ozonation is crucial for evaluating the effectiveness of water treatment systems and their potential impacts on environmental safety and human health. This study explored the changes in organic substances, specifically bovine serum albumin (BSA), humic acid sodium salt (HA), and effluent organic matter (EfOM) from a wastewater treatment facility during chlorination and ozonation. Four spectrometric techniques were employed: ultraviolet absorbance at 254 nm (UVA254), fluorescent excitation-emission matrix (EEM), synchronous fluorescence two-dimensional correlation spectroscopy (SF-2DCOS), and EEM-parallel factor integrated 2DCOS (EEM-PARAFAC-2DCOS). The findings revealed that ozone possesses superior oxidizing properties compared to chlorine, as evidenced by UVA254 and EEM analyses, resulting in more diverse structural modifications in EfOM. SF-2DCOS and EEM-PARAFAC-2DCOS provided comprehensive details on the direction and sequence of these changes, with EEM-PARAFAC-2DCOS delivering clear and intuitive insights. Protein-like and fulvic-like substances were susceptible to chlorination and ozonation, exhibiting different reaction sequences with each oxidant. Furthermore, variations in protein-like and humic-like components in actual EfOM samples may not align precisely with those in model substances, emphasizing the importance of considering specific organic matter variations in real EfOM samples compared to model substances. This research offered a deeper understanding of the reactivity and transformation of organic matter in wastewater treatment processes through simple and rapid spectroscopic methods, potentially improving the management and mitigation of undesired byproducts.

Photochemical reactivity of dissolved organic carbon in subarctic lakes along a color gradient

ABSTRACT Lake–atmosphere carbon exchanges can be significantly affected by photochemical dissolved organic matter (DOM) mineralization. However, our understanding of how increasing allochthonous organic carbon input affects the photoreactivity of DOM per unit of absorbed incoming light is incomplete. Here, we measured the absorption of ultraviolet (UV) light and subsequent photochemical DOM decay in 148 lakes within the subarctic region of Abisko, Sweden. These lakes range from brown-water lakes with allochthonous input from mires to tundra clear-water lakes with relatively more autochthonous input. We used fluorescence excitation–emission matrix analysis to assess the DOM chemical composition to determine how increasing colored DOM (CDOM) affects photomineralization. We found that the photo decay rates in absolute values were positively correlated to CDOM. However, the photo decay per unit of absorbed light energy did not increase with increasing CDOM; rather, it showed a weak decreasing trend. Fluorescence analyses helped explain these patterns; humic-like fluorescent DOM, presumably of terrestrial origin, was associated with high absolute photo decay rates, but not generally with higher photoreactivity per unit of absorbed light energy than other types of DOM. The results suggest that even though increasing inputs of terrestrial substances lead to a higher abundance of photodegradable materials, CO2 emissions do not necessarily increase in lakes where browning limits the ability of light to penetrate deeper water.

Occurrence and mechanism of sulfamethoxazole in alginate-like extracellular polymers from excess sludge

The recovery of biopolymers, particularly alginate-like extracellular polymers, from municipal sludge represents a promising step toward sustainable sludge treatment practices. Originating from wastewater plants in complexly polluted environments, alginate-like extracellular polymers carry potential environmental risks concerning their reuse. This study employs ultrahigh-performance liquid chromatography–tandem mass spectrometry to investigate the distribution coefficients and occurrence of alginate-like extracellular polymers and sulfamethoxazole. Results demonstrate a negative distribution coefficient, suggesting an inhibitory effect on sulfamethoxazole dissolution. The ethanol-extracted alginate-like extracellular polymers exhibits higher sulfamethoxazole levels (approximately 52%) than those obtained via dialysis extraction. Three-dimensional excitation-emission matrix analysis and adsorption studies indicate the absence of tyrosine-like substances in the alginate-like extracellular polymers, unlike in other extracellular polymeric substances. This absence diminishes hydrophobic interactions, highlighting that electrostatic interactions play a more important role. These insights are crucial for understanding the adsorption behavior of alginate-like extracellular polymers and optimizing their large-scale extraction processes.

The effects of different electrode materials on the electric field-assisted co-composting system for the soil remediation of heavy metal pollution

The electric field-assisted composting system (EACS) is an emerging technology that can enhance composting efficiency, but little attention has been given to electrode materials. Herein, an EACS was established to investigate the effects of electrode materials on humic substance formation and heavy metal speciation. Excitation-emission matrix analysis showed that carbon-felt and stainless-steel electrodes increased humic acid (HA) by 48.57 % and 47.53 %, respectively. In the EACS with the carbon-felt electrode, the bioavailability factors (BF) of Cu and Cr decreased by 18.00 % and 7.61 %, respectively. Despite that the stainless-steel electrodes decreased the BF of As by 11.26 %, the leaching of Cr, Ni, Cu, and Fe from the electrode itself is an inevitable concern. Microbial community analyses indicated that the electric field increased the abundance of Actinobacteria and stimulated the multiplication of heavy metal-tolerant bacteria. Redundancy analysis indicates that OM, pH, and current significantly affect the evolution of heavy metal speciation in the EACS. This study first evaluated the metal leaching risk of stainless-steel electrode, and confirmed that carbon-felt electrode is environment-friendly material with high performance and low risk in future research with EACS.

Rainfall-induced changes in aquatic microbial communities and stability of dissolved organic matter: Insight from a Fen river analysis

Microbial communities are pivotal in aquatic ecosystems, as they affect water quality, energy dynamics, nutrient cycling, and hydrological stability. This study explored the effects of rainfall on hydrological and photosynthetic parameters, microbial composition, and functional gene profiles in the Fen River. Our results demonstrated that rainfall-induced decreases in stream temperature, dissolved oxygen, pH, total phosphorus, chemical oxygen demand, and dissolved organic carbon concentrations. In contrast, rainfall increased total dissolved solids, salinity, and ammonia-nitrogen concentrations. A detailed microbial community structure analysis revealed that Cyanobacteria was the dominant microbial taxon in the Fen River, accounting for approximately 75% and 25% of the microalgal and bacterial communities, respectively. The abundance of Chlorophyta and Bacillariophyta increased by 47.66% and 29.92%, respectively, whereas the relative abundance of Bacteroidetes decreased by 37.55% under rainfall conditions. Stochastic processes predominantly affected the assembly of the bacterial community on rainy days. Functional gene analysis revealed variations in bacterial functions between sunny (Sun) and rainy (Rain) conditions, particularly in genes associated with the carbon cycle. The 3-oxoacyl-[acyl-carrier-protein] reductase gene was more abundant in the Fen River bacterial community. Particular genes involved in metabolism and environmental information processing, including the acetyl-CoA C-acetyltransferase (atoB), enoyl-CoA hydratase (paaF), and branched-chain amino acid transport system gene (livK), which are integral to environmental information processing, were more abundant in Sun than the Rain conditions. In contrast, the phosphate transport system gene, the galactose metabolic gene, and the pyruvate metabolic gene were more abundant in Rain. The excitation-emission matrix analysis with parallel factor analysis identified four fluorescence components (C1–C4) in the river, which were predominantly protein- (C1) and humic-like (C2–C4) substances. Rainfall affected organic matter production and transport, leading to changes in the degradation and stability of dissolved organic matter. Overall, this study offers insight into how rainfall affects aquatic ecosystems.

Effects of BC on metal uptake by crops (availability) and the vertical migration behavior in soil: A 3-year field experiments of crop rotation

Biochar (BC) has been substantiated to effectively reduce the available content of heavy metals (HMs) in soil-plant system; however, the risk of biochar (BC)derived dissolved organic matter (DOM) induced metal vertical migration has not been well documented, especially in the long-term field conditions. Therefore, this study investigated HM vertical migration ecological risks and the long-term effectiveness of the amendment of biochar in the three successive years of field trials during the rotation system. The results revealed that biochar application could increase soil pH and DOM with a decrease in soil CaCl2 extractable pool for Pb, Cu, and Cd. Furthermore, the results indicated a significant decrease in acid phosphatase activities and an increase in urease and catalase activities in the soil. Cucumber was shown to be safe during a three-year rotation system in the field. These results suggest that BC has the potential to enhance soil environment and crop yields. BC derived DOM-specific substances were identified using parallel factor analysis of excitation-emission matrix in deep soil (0–60 cm). The study incorporated HM concentration fluctuations in deep soils, providing an additional interpretation of DOM and co-migration of HMs.The environmental risk associated with the increase in DOM hydrophobicity should not be ignored by employing BC for soil HM remediation applications. The study enhances understanding of biochar-derived DOM's migration and stabilization mechanisms on heavy metals, providing guidelines for its use as a soil amendment.

Gravity driven ceramic membrane loaded birnessite functional layer for manganese removal from groundwater: The significance of disinfection on biofilm

Gravity-Driven Ceramic Membrane (GDCM) technology has gained popularity and recognition in water purification on account of its low energy consumption and convenient operation. This study aimed to comprehensively assess the effects of different disinfectants, including hydrogen peroxide (H2O2) and sodium hypochlorite (NaClO), on GDCM performance. It focused on the change in manganese removal and structure of the powdered activated carbon (PAC) - manganese oxides (MnOx) pre-deposited at the membrane interface and as well membrane fouling mitigation. The results showed that after the first two disinfection cycles, the flux recovery was 15 LMH for H2O2, while using NaClO only achieved an average recovery of 2 LMH and increased the effluent manganese, exceeding 0.1 mg/L within a short period of time. During the disinfection process, H2O2 exhibited better performance in mitigating membrane fouling compared to NaClO in the GDCM system. Additionally, by observing the recovery time of Mn2+ after disinfection, it can be deduced that the initial manganese removal mainly resulted from biological action of manganese-oxidizing bacteria (MnOB), while the later stage relied primarily on the catalytic oxidation action of birnessite. Fluorescence excitation–emission matrix analysis (EEM) indicated that most organic compounds dissolved in the disinfectant solution after disinfection, with some permeating through the membrane, while the remaining portion continued to accumulate in the filter cake layer. This accumulation was further confirmed by the enhanced absorbance peaks of functional groups (–NH and –OH) in the Fourier-transform infrared spectroscopy (FTIR). Scanning electron microscope - energy dispersive x-ray spectroscopy (SEM-EDS) mapping analysis revealed that MnOx formed more lamellar structures between nano-flower balls after disinfection. This increased the number of active sites and opened up water flow channels, contributing to improved flux. X-ray photoelectron spectroscopy (XPS) analysis demonstrated that Mn3+ as the dominant valence in MnOx exhibited excellent catalytic oxidation ability. Raman analysis and X-ray diffraction (XRD) indicated that MnOx showed consistent Raman spectra with birnessite before and after disinfection, and the oxidative effect of disinfection did not alter the crystal structure of MnOx. This result demonstrates the importance of applying effective disinfection in the GDCMs.

Heteroatom-Doped Carbon Quantum Dots and Polymer Composite as Dual-Mode Nanoprobe for Fluorometric and Colorimetric Determination of Picric Acid.

Oxygen- and nitrogen-heteroatom-doped, water-dispersible, and bright blue-fluorescent carbon dots (ON-CDs) were prepared for the selective and sensitive determination of 2,4,6-trinitrophenol (picric acid, PA). ON-CDs with 49.7% quantum yield were one-pot manufactured by the reflux method using citric acid, d-glucose, and ethylenediamine precursors. The surface morphology of ON-CDs was determined by scanning transmission electron microscopy, high-resolution transmission electron microscopy, dynamic light scattering, Raman, infrared, and X-ray photoelectron spectroscopy techniques, and their photophysical properties were estimated by fluorescence spectroscopy, UV-vis spectroscopy, fluorescence lifetime measurement, and 3D-fluorescence excitation-emission matrix analysis. ON-CDs at an average particle size of 3.0 nm had excitation/emission wavelengths of 355 and 455 nm, respectively. With the dominant inner-filter effect- and hydrogen-bonding interaction-based static fluorescence quenching phenomena supported by ground-state charge-transfer complexation (CTC), the fluorescence of ON-CDs was selectively quenched with PA in the presence of various types of explosives (i.e., 2,4,6-trinitrotoluene, tetryl, 1,3,5-trinitroperhydro-1,3,5-triazine, 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane, pentaerythritol tetranitrate, 3-nitro-1,2,4-triazole-5-one, and TATP-hydrolyzed H2O2). The analytical results showed that the emission intensity varied linearly with a correlation coefficient of 0.9987 over a PA concentration range from 1.0 × 10-9 to 11.0 × 10-9 M. As a result of ground-state interaction (H-bonding and CTC) of ON-CDs with PA, an orange-colored complex was formed different from the characteristic yellow color of PA in an aqueous medium, allowing naked-eye detection of PA. The detection limits for PA with ON-CDs were 12.5 × 10-12 M (12.5 pM) by emission measurement and 9.0 × 10-10 M (0.9 nM) by absorption measurement. In the presence of synthetic explosive mixtures, common soil cations/anions, and camouflage materials, PA was recovered in the range of 95.2 and 102.5%. The developed method was statistically validated against a reference liquid chromatography coupled to tandem mass spectrometry method applied to PA-contaminated soil. In addition, a poly(vinyl alcohol)-based polymer composite film {PF(ON-CDs)} was prepared by incorporating ON-CDs, enabling the smartphone-assisted fluorometric detection of PA.

Insights into the Responses of the Partial Denitrification Process to Elevated Perfluorooctanoic Acid Stress: Performance, EPS Characteristic and Microbial Community

This study aimed at investigating the potential impacts of perfluorooctanoic acid (PFOA) exposure on the partial denitrification (PD) system. Our results indicated that nitrite accumulation rates were significantly decreased to 67.94 ± 1.25%–69.52 ± 3.13% after long-term PFOA exposure (0.5–20 mg/L), while the nitrate transformation ratio was slightly impacted. The PFOA removal efficiency gradually decreased from 67.42 ± 3.39% to 6.56 ± 5.25% with an increasing PFOA dosage, indicating that the main PFOA removal pathway was biosorption. The average EPS contents increased by two folds, which suggested that exposure to PFOA significantly stimulated EPS secretion. Excitation emission matrix analysis revealed that PFOA exposure promoted the secretion of tryptophan protein-like, humic acid-like, and aromatic protein II-like substances, which may act as a protective barrier against PFOA toxicity. Moreover, significant changes in characteristic peaks after PFOA exposure were shown as indicated by Fourier transform infrared spectroscopy. High-throughput sequencing suggested that PFOA significantly decreased bacterial richness and increased evenness, indicating that toxicity effects of PFOA were more pronounced for abundant species (e.g., Thauera) than rare species. Thauera was the most dominant genus responsible for nitrite accumulation, whose abundance significantly decreased from 35.99 ± 2.67% to 18.60 ± 2.18% after PFOA exposure. In comparison, the abundances of common denitrifiers, such as Denitratisoma, Bdellovibrio, and OLB8, significantly increased, suggesting that these genera were potential PFOA-resistant bacteria. This study presents new insights into the effect of PFOA on a PD system.

Remediation potential of magnetic biochar in lead smelting sites: Insight from the complexation of dissolved organic matter with potentially toxic elements

Magnetic biochar has been widely used in potentially toxic elements (PTEs) polluted soils due to its magnetic separation capability and synchronous immobilization for multiple metals. However, the contribution of magnetic biochar to soil dissolve organic material (SDOM) and its binding behavior with PTEs needs to be further clarified prior to its remediation application on lead smelting sites. In this study, multi-spectral techniques of excitation-emission matrix (EEM) fluorescence spectroscopy and two-dimensional FTIR correlation spectroscopy (2D-FTIR-COS) were used to explore the evolution characteristics of SDOM in the lead smelting site under the remediation of magnetic biochar, and to further analyze its affinity and binding behavior with Pb and As. Results showed that magnetic biochar significantly increased SDOM content and decreased Pb and As available content. EEM and parallel factor analysis (EEM-PARAFAC) and Self-Organizing map analysis showed that humus-like and aromatic DOM increased and microbial-derived SDOM decreased after magnetic biochar cultivation. Furthermore, 2D-FTIR-COS correlation spectroscopy analysis indicated that BDOM had a stronger binding affinity to Pb, while SDOM has a stronger binding affinity to As. The binding sequences of different DOMs to PTEs varied greatly, the carboxyl and amide groups of SDOM and BDOM showed a remarkable and rapid response. Our results enhance the insights of magnetic biochar on soil function and PTEs remediation potential, providing novel information for its environmental remediation application.

Effects of raw water quality on the adsorptive removal of 2-methylisoborneol by powdered activated carbon under non-equilibrium conditions

Abstract Natural organic matter contained in natural water inhibits the adsorptive removal of 2-methylisoborneol (2-MIB) by powdered activated carbon (PAC). We investigated the relationship between water-quality indices and the adsorptive removal of 2-MIB by PAC. We collected three different raw water (i.e., two lake water and one river water) samples twice per month for 10 months. We characterized the raw water using total organic carbon concentration, ultraviolet absorption at 254 nm, electrical conductivity, and excitation–emission matrix analysis. The results were compared with 2-MIB removal rates evaluated from PAC adsorption experiments and revealed that there was no universal indicator that could explain the trends of the 2-MIB removal rate during the overall experimental period. The correlation trends between 2-MIB removal rates and water-quality indices differed significantly between the high and low water-temperature periods. Several water-quality indices related to the organic matter associated with biological processes, especially algal activities (i.e., soluble microbial products, chlorophylls, and phycocyanin), exhibited significant correlations with the 2-MIB removal rates (|R| > 0.7) under certain conditions (e.g., high lake-water temperature). Both the parallel factor (PARAFAC) analysis and fluorescence regional integration (FRI) method could evaluate such behaviors after including the regions associated with algal organic matter in the calculation.

Geochemical Features of Ground Ice from the Faddeevsky Peninsula Eastern Coast (Kotelny Island, East Siberian Arctic) as a Key to Understand Paleoenvironmental Conditions of Its Formation

Understanding paleoenvironmental conditions of the permafrost formation allows us to estimate the permafrost carbon pool and its behavior upon thawing in a changing climate. In order to classify different types of ground ice and to reconstruct paleoenvironments, we examined geochemical data of ice wedges (IWs), tabular ground ice (TGI), and lens ice from the eastern coast of the Faddeevsky Peninsula (East Siberian Arctic). We analyzed isotope and ion composition, molecular composition of the gas phase, bulk biogeochemical parameters and dissolved organic matter (DOM) composition in ground ice samples. IWs formed in the Late Pleistocene under the coldest winter conditions and in the Holocene in proximity to the sea. The Holocene IWs have the highest mean d-excess (11–13‰) and a heavier isotope composition by an average of 6‰ compared with the Late Pleistocene IWs. We observe predominance of sea-salt fractions in ion composition of the Holocene IWs, while the Late Pleistocene IW shows enrichment in non-sea-salt component of SO42− (nssSO42−), which is probably associated with mineral leaching of deposits. Higher dissolved organic carbon (DOC) content in the Late Pleistocene IW (to 17.7 mg/L) may indicate more favorable vegetation conditions or lower degree of organic matter mineralization compared to Holocene IWs and TGI. CH4 concentrations were relatively low with a maximum value of 2.27 μmol/L. DOM composition, supposed to record the paleoenvironment of the freezing process, was for the first time tried as a biomarker for paleoenvironmental reconstructions of ground ice formation. Parallel factor (PARAFAC) analysis of EEM (Excitation-Emission matrix) of fluorescent DOM decomposes four components: P1–P3, which are related to allochthonous humic-like constituents, and P4, which is relevant to autochthonous fraction associated with microbial activity. The distribution of fluorescent DOM tracked the variability in both paleoclimate conditions of the IW formation (discriminating the Holocene and the Late Pleistocene IWs) and types of ground ice (IW and TGI), which demonstrates the potential of the used approach.

Insight into humification of mushroom residues under addition of Rich-N sources: Comparing key molecular evolution processes using EEM-PARAFAC and 2D-FTIR-COS analysis

Accelerating the humification of organic solid waste is one of the most important issues in composting. This present study aims to study and compare the humification process of different rich-N sources (chicken manure, cattle manure, and urea) addition during the composting of mushroom residues, from macro physicochemical properties to micro humic molecular structure evolution process. The physicochemical elements and humic components were determined for evaluating the compost quality and humification degree as composting proceed. The coupled analysis of excitation-emission matrix with parallel factor analysis (EEM-PARAFAC) and two-dimensional correlation with Fourier transform infrared spectrum (2D-FTIR-COS) were used to characterize the functional molecular structure evolution of dissolved organic matter during humification process. The results indicated that the rank order for humification level were the treatments of chicken manure (HM), urea (UM), cattle manure (CM), and single mushroom residue treatment (CK), with their humification index of 22.18%, 22.05%, 18.47%, and 16.52%, respectively. Humic substance, humic acid, and fulvic acid were obtained the highest in HM treatment with contents of 35.41 ± 0.86%, 23.32 ± 1.57%, and 10.97 ± 0.52%, respectively. The rich-N source addition enhanced the degradation of protein-like and polysaccharides-like substances in dissolved organic matter, thus accelerating the humification process of mushroom residues. The key structure evolution of dissolved organic matter in the HM treatment, in which the CO and CC stretching of quinone, amide, or ketone, and the C–O stretching of polysaccharides may be responsible for the faster formation of humus compared to the other nitrogen treatments. In this study, redundancy analysis indicated that the total nitrogen (TN) and nitrate nitrogen (NO3−-N) may be the potential indicators for determining the humification level as composting proceed. The result provides significant insight into the humification mechanism of mushroom residue under different types of nitrogen sources at the molecular level, and will be reference for improving the composting technique in practical field.

Investigation of electrochemical properties, leachate purification, organic matter characteristics, and microbial diversity in a sludge treatment wetland- microbial fuel cell

Sludge treatment wetland-microbial fuel cell (STW-MFC) is a unique sludge treatment process that produces bioelectricity, but its technology is still in its infancy. This study investigated the electrochemical properties, organic matter characteristics, leachate purification, and microbial community structure of STW-MFCs as affected by electrode location. When electrodes were placed in the filler layer, the STW-MFC system presented a higher power generation capacity (maximum output power density: 0.498 W/m3; peak cell voltage: 0.879 V) and organic matter degradation efficiency. The hydrophilic fraction was the main dissolved organic carbon fraction in sludge extracellular biological organic matter (EBOM) and leachate dissolved organic matter (DOM). Aromatics were mainly concentrated in the hydrophobic acid fraction. The UV-254 content of sludge EBOM decreased mainly in the hydrophilic and transphilic acid fractions. The excitation-emission matrix analysis showed that tryptophan-like protein was more easily eliminated than tyrosine-like protein. In addition, there was a strong correlation between voltage and NH4+ removal efficiency; a negative correlation between total chemical oxygen demand (TCOD), total nitrogen (TN), and total phosphorus (TP) removal efficiency, and a negative correlation between pH and TN, TP, and NH4+ removal efficiencies. High-throughput sequencing showed that the system was most abundant in Thermomonas, Geothrix and Geobacter when the electrodes were placed in the filled layer, while the levels of genes for membrane transport, carbohydrate metabolism and energy metabolism functions were higher than in other systems. This work will support STW- MFC widespread implementation by illuminating the underlying mechanics of different anode positions.

Accelerated stabilization of high solid sludge by thermal hydrolysis pretreatment in autothermal thermophilic aerobic digestion (ATAD) process.

Autothermal thermophilic aerobic digestion (ATAD) is a rapid biological treatment technology for sludge stabilization. To improve digestion efficiency and shorten stabilization time, thermal hydrolysis pretreatment was employed before ATAD of high solid sludge. The results showed that accelerated stabilization of high solid sludge (total solid=10.1%) was achieved by thermal hydrolysis pretreatment with volatile solid removal efficiency of 40.3% after 8 days of ATAD, 11 days earlier than unpretreated sludge. The enhanced release and hydrolysis of intracellular organics resulted in a solubilization degree of 45.3%. The reduced sludge viscosity and improved fluidity after thermal hydrolysis facilitated mixing, aeration and organics degradation during ATAD. Excitation emission matrix analysis indicated that the fluorescence intensity of soluble microbial byproduct and tyrosine-like protein increased markedly after thermal hydrolysis and decreased after ATAD. The proportion of high molecular weight (MW>10kDa) substances in the supernatant increased significantly after thermal hydrolysis, while the low MW (MW<1kDa) substances decreased after ATAD. The significant difference in microbial composition between the pretreatment and control groups elucidated the accelerated sludge stabilization under thermal hydrolysis. This work provides an efficient and practical strategy to achieve rapid stabilization of high solid sludge.

Organic matter removal performance, pathway and microbial community succession during the construction of high-ammonia anaerobic biosystems treating anaerobic digestate food waste effluent.

This study aimed to establish anaerobic biosystems which could tolerate high ammonia, and investigate the microbial community structure in these reactors. High-ammonia anaerobic biosystems that could tolerate 3600mgL-1 total ammonia nitrogen (TAN) and 1000mgL-1 free ammonia nitrogen (FAN) were successfully established. The removal efficiencies of COD and total volatile fatty acids (TVFAs) in R1 with dewatered sludge as inoculum were 68.8% and 69.2%, respectively. The maximum methane production rate reached 71.7±1.0mL CH4 L-1 d-1 at a TAN concentration of 3600mgL-1. The three-dimension excitation-emission matrix analysis indicated that both easily degradable organics and refractory organics were removed from ADFE in R1 and R2. Functional microorganisms which could bear high ammonia were gradually enriched as TAN stress was elevated. Lysinibacillus, Coprothermobacter and Sporosarcina dominated the final bacterial community. Archaeal community transformed to hydrogenotrophic methanogen. The synergy of Coprothermobacter and Methanothermobacter undertook the organic matter degradation, and was enhanced by increasing TAN stress. This study offers new insights into anaerobic bioremediation of ammonia-rich wastewater.

Identifying biotic and abiotic processes of reversing biochar-induced soil phosphorus leaching through biochar modification with MgAl layered (hydr)oxides

Biochar (BC) as a increasing widely adopted soil amendments showed potential threat to soil P leaching, but the relevant mechanisms were not clear enough and relevant strategy should be proposed to address the P leaching induced by BC application. In this study, effects of ordinary corn straw BC, and a fabricated Mg/Al-LDHs modified biochar (LBC) on soil P availability, adsorption, fraction and mobility were compared and investigated by conducting the column and incubation experiments at biochar to soil rate of 1 %, 2 % and 4 % (w/w). Chemical sequential extraction methods and various solid-state method (i.e., three-dimensional excitation emission matrix (EEM), x-ray diffraction (XRD), scanning electron micrograph (SEM) and P K-edge X-ray absorption near edge structure (XANES)) were utilized to give deep insights into the P mobilization and immobilization mechanisms by respectively applying the BC and LBC. Results of incubation experiments showed that applying the LBC reduced the labile P with significant CaP transformation to Al-retained P, while ordinary BC promoted the Fe/Al-P transformation to labile dibasic calcium phosphate and monobasic calcium phosphate evidenced by the EEM analysis, in-situ XANES investigation and chemical sequential extraction methods. Results of phosphatase and microbial analyses indicated that the decreased labile P after 30 days' incubation and the mitigated P leaching in LBC treatment were dominantly ascribed to abiotic processes of inorganic P transformation and (de)sorption. This research gave deep insights into abiotic and biotic processes of ordinary biochar promoting soil P leaching, and important implications for applying engineered biochar in reducing P leaching and improving soil productivity.

Integrating 16S rRNA amplicon metagenomics and selective culture for developing thermophilic bacterial inoculants to enhance manure composting

Composting is an important method for treating and recycling organic waste, and the use of microbial inoculants can increase the efficiency of composting. Herein, we illustrate an approach that integrate 16S rRNA amplicon metagenomics and selective culture of thermophilic bacteria for the development of inoculants to improve manure composting. The 16S rRNA amplicon sequencing analysis revealed that Firmicutes and Actinobacteria were dominant in the composting mixture, and that different microbial hubs succeeded during the thermophilic stage. All isolated thermophilic bacteria were affiliated with the order Bacillales, such as Geobacillus, Bacillus, and Aeribacillus. These isolated thermophilic bacteria were grouped into 11 phylotypes, which shared ＞99% sequence identity to 0.15% to 5.32% of 16S rRNA reads by the amplicon sequencing. Three of these phylotypes transiently enriched during the thermophilic stage. Six thermophilic bacteria were selected from the three phylotypes to obtain seven microbial inoculants. Five out of seven of the microbial inoculants enhanced the thermophilic stage of composting by 16.9% to 52.2%. Three-dimensional excitation emission matrix analysis further revealed that two inoculants (Thermoactinomyces intermedius and Ureibacillus thermophilus) stimulated humification. Additionally, the 16S rRNA amplicon sequencing analysis revealed that inoculation with thermophilic bacteria enhanced the succession of the microbial community during composting. In conclusion, 16S rRNA amplicon metagenomics is a useful tool for the development of microbial inoculants to enhance manure composting.

Comparison of Relationship between Solubilization and Methane Productivity on Anaerobic Digestion of Pre-treated Waste Activated Sludge

Objectives : Various pre-treatment methods have been applied to waste activated sludge(WAS) to improve the efficiency of anaerobic digestion(AD) by enhancing hydrolysis. The objective of this study was to find out the relationship between increased solubilization and AD efficiency in response to the application of different pretreatment methods(Acid+Heat and Alkali+Heat) to WAS.Methods : Acid+Heat(pH 2+130℃) and Alkali+Heat(pH 10+130℃) pretreatment processes were performed by adding HCl and KOH, respectively. A biochemical methane potential(BMP) test was subsequently conducted to determine the AD efficiency of pretreated WAS. Finally, the physicochemical characteristics in the effluent of AD of WAS, done by excitation-emission matrix(EEM) and size exclusion chromatography(SEC), were analyzed to investigate the degree of changed intermediates during microbial degradation of organic compounds.Results : Both Acid+Heat and Alkali+Heat pretreatments resulted in similar solubilization of WAS, reaching 34.1 and 36.3%, respectively. Meanwhile, it was found that the CH4 yield obtained from the Alkali+Heat pretreated sample was lower than the sample of Acid+Heat. The results of EEM analysis showed that the Alkali+Heat pretreated WAS had a higher portion of less biodegradable organic compounds with high- molecular weight in the soluble sample than that of the Alkali+Heat pretreated sample.Conclusion : This study was conducted to clarify the relationship by comparing the hydrolysis rate and AD efficiency according to the application of Acid+Heat and Alkali+Heat pretreatment. It was found that the amount of methane generated could vary depending on the properties of the dissolved substances in response to different pretreatment approaches.

Study on anaerobic co-digestion of municipal sewage sludge and fruit and vegetable wastes: Methane production, microbial community and three-dimension fluorescence excitation-emission matrix analysis

Constantly increased sewage sludge (SS) and fruit and vegetable wastes (FVW) are becoming the major organic solid wastes in human society. Thus, anaerobic digestion is employed as a low carbon energy strategy to reduce their environmental pollution risk. Anaerobic co-digestion system was developed based on the carbon to nitrogen ratio strategy. Results showed that the daily biogas production was higher in co-digester, and the volumetric biogas production rate (VBPR) significantly enhanced for 1.3 ∼ 3 folds, and the highest VBPR was 2.04 L/L • day with optimal OLR of 2.083 Kg L-1 d-1. Analytic results indicated that co-digestion could improve the biodegradable of feedstocks, which transforming to more VFAs and biogas. Compared with mono SS digester, mixed substrates relieved ammonia nitrogen inhibition and enhanced the hydrolytic acidification and methanogenesis. Meanwhile, the excessive humification of organics was suppressed. This study supported the concepts of improving carbon recovery from SS and FVW.