Zuoyi Yang

Levels, composition profiles and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in sludge from ten textile dyeing plants

As components of synthetic dyes, polycyclic aromatic hydrocarbons (PAHs) are present as contaminants in textile dyeing sludge due to the recalcitrance in wastewater treatment process, which may pose a threat to environment in the process of sludge disposal. In order to evaluate PAHs in textile dyeing sludge, comprehensive investigation comprising 10 textile dyeing plants was undertaken. Levels, composition profiles and risk assessment of 16 EPA-priority PAHs were analyzed in this study. The total concentrations of 16 PAHs (∑16 PAHs) varied from 1463 ± 177 ng g(-1) to 16,714 ± 1,507 ng g(-1) with a mean value of 6386 ng g(-1). The composition profiles of PAHs were characterized by 3- and 4-ring PAHs, among which phenanthrene, anthracene and fluoranthene were the most dominant components. The mean benzo[a]pyrene equivalent (BaPeq) concentration of ∑16 PAHs in textile dyeing sludge was 423 ng g(-1), which was 2-3 times higher than concentrations reported for urban soil. According to ecological risk assessment, the levels of PAHs in the textile dyeing sludge may cause a significant risk to soil ecosystem after landfill or dumping on soil.

Aromatic amine contents, component distributions and risk assessment in sludge from 10 textile-dyeing plants

Aromatic amines (AAs), which are components of synthetic dyes, are recalcitrant to the wastewater treatment process and can accumulate in sludge produced by textile-dyeing, which may pose a threat to the environment. A comprehensive investigation of 10 textile-dyeing plants was undertaken in Guangdong Province in China. The contents and component distributions of AAs were evaluated in this study, and a risk assessment was performed. The total concentrations of 14 AAs (Σ14 AAs) varied from 11 μg g(-1)dw to 82.5 μg g(-1)dw, with a mean value of 25 μg g(-1)dw. The component distributions of AAs were characterized by monocyclic anilines, of which 2-methoxy-5-methylaniline and 5-nitro-o-toluidine were the most dominant components. The risk quotient (RQ) value was used to numerically evaluate the ecological risk of 14 AAs in the environment. The result showed that the 14 AAs contents in textile-dyeing sludge may pose a high risk to the soil ecosystem after being discarded on soil or in a landfill.

Fate of volatile aromatic hydrocarbons in the wastewater from six textile dyeing wastewater treatment plants

The occurrence and removal of benzene, toluene, ethylbenzene, xylenes, styrene and isopropylbenzene (BTEXSI) from 6 textile dyeing wastewater treatment plants (TDWTPs) were investigated in this study. The practical capacities of the 6 representative plants, which used the activated sludge process, ranged from 1200 to 26000 m(3) d(-1). The results indicated that BTEXSI were ubiquitous in the raw textile dyeing wastewater, except for isopropylbenzene, and that toluene and xylenes were predominant in raw wastewaters (RWs). TDWTP-E was selected to study the residual BTEXSI at different stages. The total BTEXSI reduction on the aerobic process of TDWTP-E accounted for 82.2% of the entire process. The total BTEXSI concentrations from the final effluents (FEs) were observed to be below 1 μg L(-1), except for TDWTP-F (2.12 μg L(-1)). Volatilization and biodegradation rather than sludge sorption contributed significantly to BTEXSI removal in the treatment system. BTEXSI were not found to be the main contaminants in textile dyeing wastewater.

Synthesis, physiochemical property and antibacterial activity of gemini quaternary ammonium salts with a rigid spacer

A novel series of adamantane-based gemini quaternary ammonium salts (GQASs) named as m-Ad-m (bromides, alkyl chain length, m = 12, 14, 16) are synthesized from 1,3-adamantanedicarboxylic acid. Their chemical structures are confirmed by 1H NMR, FT-IR and ESI-MS. The surface activities in aqueous solutions of m-Ad-m are evaluated by surface tension. Unlike conventional GQASs with a flexible spacer, m-Ad-m possessing a rigid adamantane spacer show lower surface tension (γCMC) values as compared to conventional GQASs bearing the same alkyl chains. The thermodynamic properties of m-Ad-m are examined by electrical conductivity measurements at different temperatures, including molecular interaction parameters (β), standard Gibbs free energy (ΔG0m), enthalpy (ΔH0m) and entropy (ΔS0m), which show that the micellization of m-Ad-m is entropy-driven. TEM study exhibits that the aggregate morphologies of m-Ad-m change from micelles and spheroidal vesicles of varying size to network aggregates and then to globular vesicles with the increase in m-Ad-m concentration. Furthermore, the antimicrobial efficacy of m-Ad-m against both Gram-positive bacteria (S. aureus and B. subtilis) and Gram-negative bacteria (E. coli, P. aeruginosa and V. parahaemolyticus) is systematically studied by minimum inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) methods, which indicates the favorable antibacterial activity of 12-Ad-12 against the studied bacteria.

Degradation of polycyclic aromatic hydrocarbons (PAHs) in textile dyeing sludge by O3/H2O2 treatment

The degradation of polycyclic aromatic hydrocarbons (PAHs) in textile dyeing sludge by O3/H2O2 treatment was investigated. Fluorene (Fl), phenanthrene (Ph), anthracene (An) and dibenz[a,h]anthracene (DBA) were selected to represent typical PAHs. The effect of radical inhibitors, H2O2, O3 flow rate, pH and reaction time on the degradation of the four types of PAHs were examined to determine the optimal conditions for degradation and to clarify the mechanism(s) of PAHs degradation. The results indicated that the combined O3/H2O2 treatment resulted in high removal rates of the selected PAHs: 89% for Fl, 66% for Ph, 71% for An and 81% for DBA. These results correspond to the optimal conditions of an O3 flow rate of 0.4 L min−1, a H2O2 concentration of 0.60 mol L−1, a reaction time of 15 min and pH 7. The removal rate (within 30 min) increased by 5% for Fl, 27% for Ph, 21% for An and 5% for DBA through the addition of H2O2 to the O3 process. The O3 flow rate, reaction time and pH were the key parameters affecting PAH degradation with multiple interacting factors (p < 0.05) by the O3/H2O2 treatment. The degradation of the PAHs can be fitted well by pseudo-first-order kinetics (R2 = 0.9656). The combined O3/H2O2 treatment is demonstrated to be an efficient approach for the degradation of PAHs in textile dyeing sludge.

Enhanced bioelectricity generation and azo dye treatment in a reversible photo-bioelectrochemical cell by using novel anthraquinone-2,6-disulfonate (AQDS)/MnOx-doped polypyrrole film electrodes.

A novel anthraquinone-2,6-disulfonate/MnOx-doped polypyrrole film (AQDS/Mn/PPy) electrode was prepared by one-step electropolymerization method and was used to improve performance of a reversible photo-bioelectrochemical cell (RPBEC). The RPBEC was operated in polarity reversion depended on dark/light reaction of alga Chlorella vulgaris by which sequential decolorization of azo dye and mineralization of decolorization products coupled with bioelectricity generation can be achieved. The results showed that formation of uniform AQDS/Mn/PPy film significantly enhanced electroactive surface area and electrocatalytic activity of carbon electrode. The RPBEC with AQDS/Mn/PPy electrodes demonstrated 77% increases in maximum power and 73% increases in Congo red decolorization rate before polarity reversion, and 198% increases in maximum power and 138% increases in decolorization products mineralization rate after polarity reversion, respectively, compared to the RPBEC with bare electrode. This was resulted from simultaneous dynamics improvement in half-reaction rate of anode and photo-biocathode due to enhanced electron transfer and algal-bacterial biofilm formation.

Decolorization and biodegradation of the azo dye Congo red by an isolated Acinetobacter baumannii YNWH 226

A strict aerobic Acinetobacter baumannii YNWH 226, isolated from an activated sludge reactor treating textile wastewater, was able to grow on Congo red as the sole carbon source under aerobic conditions. The decolorization and TOC reduction efficiency were 99.1 and 93.72%, respectively. The effects of the Congo red concentration were studied. The environmental factors (i.e., pH, temperature and agitation speed) on the biodegradation of Congo red in aqueous phase were studied and evaluated using response surface methodology. The results indicated that when the Congo red concentration was 100 mg/L, the optimal decolorization conditions were as follows: 37°C, pH 7.0 and 180 rpm. The single A. baumannii YNWH 226 was able to form aromatic amines by reductive breakage of the azo bond and then oxidize them into non-toxic metabolites.

Spent mushroom substrate biochar as a potential amendment in pig manure and rice straw composting processes

ABSTRACT Spent mushroom substrate (SMS) is a bulky waste byproduct of commercial mushroom production, which can cause serious environmental problems and, therefore, poses a significant barrier to future expansion of the mushroom industry. In the present study, we explored the use of SMS as a biochar to improve the quality of bio-fertilizer. Specifically, we performed a series of experiments using composting reactors to investigate the effects of SMS biochar on the physio-chemical properties of bio-fertilizer. Biochar was derived from dry SMS pyrolysed at 500°C and mixed with pig manure and rice straw. Results from this study demonstrate that the addition of biochar significantly reduced electrical conductivity and loss of organic matter in compost material. Nutrient analysis revealed that the SMS-derived biochar is rich in fertilizer nutrients such as P, K, Na, and N. All of these findings suggest that SMS biochar could be an excellent medium for compost.

Electrochemical and microbial community responses of electrochemically active biofilms to copper ions in bioelectrochemical systems

Heavy metals play an important role in the conductivity of solution, power generation and activity of microorganisms in bioelectrochemical systems (BESs). However, effect of heavy metal on the process of exoelectrogenesis metabolism and extracellular electron transfer of electrochemically active biofilms (EABs) was poorly understood. Herein, we investigated the impact of Cu2+ at gradually increasing concentration on the morphological and electrochemical performance and bacterial communities of anodic biofilms in mixed-culture BESs. The voltage output decreased continuously and dropped to zero at 10 mg L-1, which was attributed to the toxic inhibition that cased anodic biofilm damage and decreased secretion of outer membrane cytochromes. When stopping the introduction of Cu2+ to anodic chamber, the maximum voltage production recovered 75.1% of the voltage produced from BES and coulombic efficiency was higher but acetate removal rate was lower than that before Cu2+ addition, demonstrating the recovery capability of EABs was higher compared to nonelectroactive bacteria. Moreover, SEM-EDS and XPS suggested that most of Cu2+ was adsorbed by the anode electrode and reduced by EABs on anode. Compared to the open-circuit BES, the flow of electrons through a circuit could improve the reduction of copper. Community analysis showed a decrease in Geobacter accompanied by an increase in Stenotrophomonas in response to Cu2+ shock in anodic chamber.

Analysis of the Metabolites of Indole Degraded by an Isolated Acinetobacter pittii L1

Indole and its derivatives are typical nitrogen heterocyclic compounds and have been of immense concern since they are known for the risk of their toxic, recalcitrant, and carcinogenic properties for human and ecological environment. In this study, a Gram-negative bacterial strain of eliminating indole was isolated from a coking wastewater. The strain was confirmed as Acinetobacter pittii L1 based on the physiological and biochemical characterization and 16S ribosomal DNA (rDNA) gene sequence homology. 400 mg/L indole could be completely removed within 48 h by the strain on the optimum condition of 37°C, pH 7.4, and 150 rpm. The organic nitrogen was converted to NH3-N and then to NO3− and the organic carbon was partially transferred to CO2 during the indole biodegradation. The metabolic pathways were proposed to explain the indole degradation based on the liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis of indigo, 4-(3-Hydroxy-1H-pyrrol-2-yl)-2-oxo-but-3-enoic acid, and isatin. The toxicity of the biodegradation products was evaluated using the Microtox test, which revealed that the metabolites were more toxic than indole. Our research holds promise for the potential application of Acinetobacter pittii L1 for NHCs degradation, production of indigoids, and soil remediation as well as treatment of indole containing wastewater.