Treatment Of Metal-containing Wastewater Research Articles

Mitigation of biofouling in membrane bioreactors by quorum-quenching bacteria during the treatment of metal-containing wastewater.

Quorum quenching (QQ) is an efficient way to mitigate membrane biofouling in a membrane bioreactor (MBR) during wastewater treatment. A QQ bacterium, Lysinibacillus sp. A4, was isolated and used to mitigate biofouling in an MBR during the treatment of wastewater containing metals. A QQ enzyme (named AilY) was cloned from A4 and identified as a metallo-β-lactamase-like lactonase. The QQ activity of A4 and that of Escherichia coli BL21 (DE3) overexpressing AilY could be promoted by Fe2+, Mn2+, and Zn2+ while remaining unaffected by other metals tested. The two bacteria effectively mitigated biofouling by reducing the transmembrane pressure from around 30 to 20kPa without negative influence on the COD, NH4+-N, or total phosphorus of the effluent. The relative abundance of Lysinibacillus sp. A4 increased greatly from 0.04 to 8.29% in the MBR with metal-containing wastewater, suggesting that Lysinibacillus sp. A4 could multiply quickly and adapt to this environment. Taken together, the findings suggested that A4 could tolerate metal to a certain degree, and this property could allow A4 to adapt well to metal-containing wastewater, making it a valuable strain for mitigating biofouling in MBR during the treatment of metal-containing wastewater.

Prediction of heavy metal removal performance of sulfate-reducing bacteria using machine learning

A robust modeling approach for predicting heavy metal removal by sulfate-reducing bacteria (SRB) is currently missing. In this study, four machine learning models were constructed and compared to predict the removal of Cd, Cu, Pb, and Zn as individual ions by SRB. The CatBoost model exhibited the best predictive performance across the four subsets, achieving R2 values of 0.83, 0.91, 0.92, and 0.83 for the Cd, Cu, Pb, and Zn models, respectively. Feature analysis revealed that temperature, pH, sulfate concentration, and C/S (the mass ratio of chemical oxygen demand to sulfate) had significant impacts on the outcomes. These features exhibited the most effective metal removal at 35 °C and sulfate concentrations of 1000–1200 mg/L, with variations observed in pH and C/S ratios. This study introduced a new modeling approach for predicting the treatment of metal-containing wastewater by SRB, offering guidance for optimizing operational parameters in the biological sulfidogenic process.

Aerobic granular sludge for complex heavy metal-containing wastewater treatment: characterization, performance, and mechanisms analysis.

Complex heavy metal (HM)-containing wastewater discharges pose substantial risks to global water ecosystems and human health. Aerobic granular sludge (AGS) has attracted increased attention as an efficient and low-cost adsorbent in HM-containing wastewater treatment. Therefore, this study systematically evaluates the effect of Cu(II), Ni(II), and Cr(III) addition on the characteristics, performance and mechanism of AGS in complex HM-containing wastewater treatment process by means of fourier transform infrared spectroscopy, inductively coupled plasma spectrocopcy, confocal laser scanning microscopy, extracellular polymeric substances (EPS) fractions detection and scanning electron microscope-energy dispersive X-ray. The results showed that AGS efficiently eliminated Cu(II), Ni(II), and Cr(III) by the orchestrated mechanisms of ion exchange, three-layer EPS adsorption [soluble microbial products EPS (SMP-EPS), loosely bound EPS (LB-EPS), tightly bound EPS (TB-EPS)], and inner-sphere adsorption; notably, almost 100% of Ni(II) was removed. Three-layer EPS adsorption was the dominant mechanism through which the HM were removed, followed by ion exchange and inner-sphere adsorption. SMP-EPS and TB-EPS were identified as the key EPS fractions for adsorbing Cr(III) and Cu(II), respectively, while Ni(II) was adsorbed evenly on SMP-EPS, TB-EPS, and LB-EPS. Moreover, the rates at which the complex HM penetrated into the granule interior and their affinity for EPS followed the order Cu(II) > Ni(II) > Cr(III). Ultimately, addition of complex HM stimulated microorganisms to excrete massive phosphodiesterases (PDEs), leading to a pronounced decrease in cyclic diguanylate (c-di-GMP) levels, which subsequently suppressed EPS secretion due to the direct linkage between c-di-GMP and EPS. This study unveils the adaptability and removal mechanism of AGS in the treatment of complex HM-containing wastewater, which is expected to provide novel insights for addressing the challenges posed by intricate real wastewater scenarios.

APPLICATION OF COAL FLY ASH-BASED SORPTION MATERIALS IN HIGHLY MINERALIZED WASTEWATER TREATMENT

The results of the study showed that Ukrainian coal fly ash (CFA) and acid mine drainage (AMD) can be successfully processed into zeolite-like sorptive material (ZSM) to extract pollutants from AMD. This approach provides a twofold benefit: firstly, the interaction between CFA with AMD provides an alternative method of conditioning AMD. Secondly, the solid residues contain a lot of Al and Si so they can be used for the synthesis of ZSM. The synthesis was done via alkaline conversion followed by hydrothermal crystallization. ZSM can be effectively used as an ion exchanger and sorbent for the conditioning of highly saline wastewater. Mercury, which is considered a priority pollutant, can be removed to levels below the permission level. Anion species were also removed from the solution by mechanisms other than ion exchange, e. g. arsenic.
 Studies discovered the following results:
 - pH plays a key role in the formation of metal ions as well as the charge of the surface functional groups of the ZSM, thus changing the physicochemical interactions between the ZSM and pollutant ions.
 - in addition to ion exchange, other mechanisms are also suggested, including adsorption, and the formation of complex compounds that significantly contribute to the purification process.
 Given its simplicity, this technology can be implemented as the first stage in the treatment of metal-containing wastewater at an operating or decommissioned coal mining enterprise. This technology can also be implemented as part of the desalination stages at TPP treatment plants. The proposed method is based on waste utilization, so it can be considered an eco-friendly low-cost method of wastewater treatment. However, on an industrial scale, hydrothermal activation will lead to increased operating costs due to increased energy consumption. Therefore, future research should be conducted on the application of ZSM in a pilot plant.
 Since this technology can be applied to the removal of both cations and anions, it will undoubtedly attract interest, provided the synthesis technology is optimized. First of all, it is necessary to optimize the synthesis method in order to use low-temperature activation methods to lessen operating costs.

Responses of Bacillus sp. under Cu(II) stress in relation to extracellular polymeric substances and functional gene expression level.

The production and composition of extracellular polymeric substances (EPS), as well as the EPS-related functional resistance genes and metabolic levels of Bacillus sp. under Cu(II) stress, were investigated. EPS production increased by 2.73 ± 0.29 times compared to the control when the strain was treated with 30 mg L-1 Cu(II). Specifically, the polysaccharide (PS) content in EPS increased by 2.26 ± 0.28 g CDW-1 and the PN/PS (protein/polysaccharide) ratio value increased by 3.18 ± 0.33 times under 30 mg L-1 Cu(II) compared to the control. The increased EPS secretion and higher PN/PS ratio in EPS strengthened the cells' ability to resist the toxic effect of Cu(II). Differential expression of functional genes under Cu(II) stress was revealed by Gene Ontology pathway enrichment analysis and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis. The enriched genes were most obviously upregulated in the UMP biosynthesis pathway, the pyrimidine metabolism pathway, and the TCS metabolism pathway. This indicates an enhancement of EPS regulation-related metabolic levels and their role as a defense mechanism for cells to adapt to Cu(II) stress. Additionally, seven copper resistance genes were upregulated while three were downregulated. The upregulated genes were related to the heavy metal resistance, while downregulated genes were related to cell differentiation, indicating that the strain had initiated an obvious resistance to Cu(II) despite its severe cell toxicity. These results provided a basis for promoting EPS-regulated associated functional genes and the application of gene-regulated bacteria in heavy metal-containing wastewater treatment.

Feather-weight cryostructured thiourea-chitosan aerogels for highly efficient removal of heavy metal ions and bacterial pathogens

Designing of economically feasible and recyclable polysaccharide-based materials with thiourea functional groups for removal of specific metal ions such as Ag(I), Au(I), Pb(II) or Hg(II) remains a major challenge for environmental applications. Here, we introduce ultra-lightweight thiourea-chitosan (CSTU) aerogels engineered by combining successive freeze-thawing cycles with covalent formaldehyde-mediated cross-linking and lyophilization. All aerogels exhibited outstanding low densities (0.0021–0.0103 g/cm3) and remarkable high specific surface areas (416.64–447.26 m2/g), outperforming the common polysaccharide-based aerogels. Benefitting from their superior structural features (honeycomb interconnected pores and high porosity), CSTU aerogels demonstrate fast sorption rates and excellent performance in sorption of heavy metal ions from highly-concentrated single or binary-component mixtures (1.11 mmol Ag (I)/g and 0.48 mmol Pb(II)/g). A remarkable recycling stability was observed after five sorption-desorption-regeneration cycles when the removal efficiency was up to 80 %. These results support the high potential of CSTU aerogels in the treatment of metal-containing wastewater. Moreover, the Ag(I)-loaded CSTU aerogels exhibited excellent antimicrobial properties against Escherichia coli and Staphylococcus aureus bacterial strains, the killing rate being around 100 %. This data points towards the potential application of developed aerogels in circular economy, by employing the spent Ag(I)-loaded aerogels in the biological decontamination of waters.

Biosorption and removal of toxic heavy metals by metal tolerating bacteria for bioremediation of metal contamination: A comprehensive review

Heavy metal pollution caused due to the industrialization has been considered as a significant public health hazard, and these heavy metals exhibit various types of toxicological manifestations. Conventional remediation methods are expensive and also yield toxic by-products, which negatively affect the environment. Hence, a green technology employing various biological agents, predominantly bacteria, algae, yeasts, and fungi, has received more attention for heavy metal removal and recovery because of their high removal efficiency, low cost, and availability. However, bacterial biosorption is the safest treatment method for the toxic pollutants that are not readily biodegradable such as heavy metals. Metal biosorption by bacteria has received significant attention due to a safe, productive, and feasible technology for the heavy metal-containing wastewater treatment. These metal tolerating bacteria can bind the cationic toxic heavy metals with the negatively charged bacterial structures and live or dead biomass components. Due to the large surface area to volume ratio, these bacterial biomasses efficiently act as the biosorbent for metal bioremediation under multimetal conditions. This review summarizes the biosorption potentials of bacterial biomass towards different metal ions, cell wall constituent, biofilm, extracellular polymeric substances (EPS) in metal binding, and the effect of various environmental parameters influencing the metal removal. Suitable mathematical models of biosorption and their application have been discussed to understand and interpret the adsorption process. Furthermore, different desorbing agents and their utilization in heavy metals recovery and regeneration of biosorbent have been summarized.

Bioindication of the metal-containing wastewater treatment process

The influence of Nickel (II) and Chronic (VI) ions on the redox processes in activated sludge community is discussed. Toxicity definition is made on the basis of fermentation activity (measurement dehydrogenase activity of sludge)

Automation of the process of stepwise adjustment of pH and Eh parameters in the treatment of metal-containing wastewater

The system of complex multistage control of process of sewage treatment from heavy metals by stepwise regulation of parameters Еh and pH is developed. Each of the control steps consists of a series of reagent dosing periods and a stabilization period. Reagent dosing is managed by local regulators, whose tuning parameters are determined for each step and adjustment period.

Comparative study on the synthesis of magnetic ferrite adsorbent for the removal of Cd(II) from wastewater

The magnetic ferrites were synthesized at ambient temperature through the precipitation method in aqueous solution at varying pH values and were used as novel adsorbents for heavy metal-containing wastewater treatment. The magnetic ferrites were applied for the removal of Cd(II) ion from wastewater. The synthesized magnetic ferrites were characterized by settling velocity, X-ray diffraction, scanning electron microscopy, laser particles size analyzer, and vibrating sample magnetometer. The effects of pH value and contact time on the adsorption process were investigated. The magnetic ferrites had a saturation magnetization value of 82.30 emu/g and a settling velocity of 2%, indicating easy separation from aqueous solution under magnetic field. The adsorption of Cd(II) onto the magnetic ferrites followed the pseudo-second-order kinetics and the Langmuir isotherm model. The most suitable pH condition for the synthesis of magnetic ferrite with optimal Cd(II) adsorption capacity was 9.0, and a maximum adsorption capacity of 160.91 mg/g for Cd(II) ions can be achieved. Based on the cost analysis, the magnetic ferrite was a cost-effective adsorbent for Cd-containing wastewater treatment.

Enhancing peat metal sorption and settling characteristics

Peat is an excellent material for metal sorption since it naturally contains different kinds of functional groups that can sorb metal cations from water. The main objective of this work was to test low-cost treatment (acid and alkali) methods for natural peat, which would improve the settling properties of peat particles while maintaining its metal removal efficiency. Particularly, the poor settling properties of peat hinder its practical application. The study revealed that NaOH-treated peat (0.1M) had excellent settling properties and could be applied in wastewater applications having mixing and settling systems without a settling aid. The superior leaching of humic and fulvic acids in alkaline treatment caused a change in morphology, making it a harder and sticky material. Moreover, the NaOH-treated (0.1M) peat was proven to be the most efficient material for nickel removal followed by the HCl-treated (0.2M) peat, citric acid-treated (0.16M) peat and water-treated peat. A higher temperature and longer time slightly increased the Ni removal efficiency with NaOH-treated peat material. The settling of HCl-treated peat was studied further using polyacrylamide flocculants (cationic, neutral, anionic). Cationic flocculants performed best and the cationic charge density also had an effect on the flocculation performance of peat particles. This study provides further evidence that peat can be applied in the treatment of metal-containing wastewaters.

Enhanced lead and cadmium removal using biochar-supported hydrated manganese oxide (HMO) nanoparticles: Behavior and mechanism

Hydrated manganese oxide (HMO) nanoparticles were impregnated into a peanut shell-derived biochar (BC) to obtain a remarkable nanocomposite adsorbent, HMO-BC, which overcomes the technical barriers of singly applying either HMO or BC in practical heavy metal-containing wastewater treatment. HMO-BC can effectively sequestrate Pb(II) and Cd(II) in a wide pH range of 3–7 and exhibited more preferable sorption than bare BC in the presence of high-level competing cations. BC also significantly lowered the Mn leaching at acidic pH. Fixed-bed column adsorption tests showed that the effective treatment volume of HMO-BC for a simulated Pb(II)- or Cd(II)-laden wastewater is about 4–6 times higher than that of the BC host. In addition, HMO-BC was effective in removing Pb(II) from a real Pb-containing electroplating wastewater to discharge limit (0.2mgL−1) with treatable volume of 525BV, much higher than that of the bare BC (60BV). More importantly, the saturated HMO-BC can be thoroughly regenerated for repeated uses without any observable capacity loss. Such attractive results of HMO-BC were attributed to the complementary effect of its two components. The embedded HMO nanoparticles provide preferable capture of target cations through specific inner-sphere complexation, as illustrated by XPS spectra of Pb 4f7/2 and O1s, while the non-diffusive negatively charged oxygen-containing groups bound to BC facilitate the pre-enrichment and permeation of Pb(II) and Cd(II) cations into the pore channels prior to their preferable sorption through the Donnan membrane effect.

Studies of selective adsorption, desorption and reuse of chemically altered biomass produced from aquatic macrophytes for treatment of metal-containing wastewater.

The aquatic macrophytes Salvinia sp. and Pistia stratiotes have a natural capacity to adsorb various elements, including heavy metals. This capacity was enhanced with a chemical treatment using NaOH alkaline solution for Salvinia sp. and a mixture of both Salvinia sp. and Pistia stratiotes at a proportion of 1:1, whose respective biosorbents were called SSOH and MBOH. Adsorption tests were done in a ternary system containing the metals copper, lead and manganese; the parameters considered were: starting concentration, kinetics, pH and temperature. The adsorption isotherms for SSOH had a maximum adsorptive capacity of 50.20, 53.85 and 14.68 mg g-1 for Cu, Pb and Mn, respectively; for MBOH, maximum values were 44.62, 35.17 and 15.74 mg g-1 for Cu, Pb and Mn, respectively. The metals displayed different behaviors with pH variation. The results also showed an adsorption preference of Cu > Pb > Mn for SSOH. Desorption and readsorption studies were also carried out, showing 100% desorption and increased adsorption capacity in readsorption tests. Surface area and porosity analysis with the Brunauer-Emmett-Teller (BET) method indicate that after chemical modification, MBOH and SSOH biomasses had their surface increased in comparison to SS, with values of 165.5657 (MBOH), 157.4392 (SSOH) and 78.9432 m2 g-1 (SS).

Regulation of biofilm formation and cellular buoyancy through modulating intracellular cyclic di-GMP levels in engineered cyanobacteria.

The second messenger cyclic dimeric (3'→5') GMP (cyclic di-GMP or c-di-GMP) has been implicated in the transition between motile and sessile lifestyles in bacteria. In this study, we demonstrate that biofilm formation, cellular aggregation or flocculation, and cellular buoyancy are under the control of c-di-GMP in Synechocystis sp. PCC 6803 (Synechocystis) and Fremyella diplosiphon. Synechocystis is a unicellular cyanobacterium and displays lower levels of c-di-GMP; F. diplosiphon is filamentous and displays higher intracellular c-di-GMP levels. We transformed Synechocystis and F. diplosiphon with a plasmid for constitutive expression of genes encoding diguanylate cylase (DGC) and phosphodiesterase (PDE) proteins from Vibrio cholerae or Escherichia coli, respectively. These engineered strains allowed us to modulate intracellular c-di-GMP levels. Biofilm formation and cellular deposition were induced in the DGC-expressing Synechocystis strain which exhibited high intracellular levels of c-di-GMP; whereas strains expressing PDE in Synechocystis and F. diplosiphon to drive low intracellular levels of c-di-GMP exhibited enhanced cellular buoyancy. In addition, the PDE-expressing F. diplosiphon strain showed elevated chlorophyll levels. These results imply roles for coordinating c-di-GMP homeostasis in regulating native cyanobacterial phenotypes. Engineering exogenous DGC or PDE proteins to regulate intracellular c-di-GMP levels represents an effective tool for uncovering cryptic phenotypes or modulating phenotypes in cyanobacteria for practical applications in biotechnology applicable in photobioreactors and in green biotechnologies, such as energy-efficient harvesting of cellular biomass or the treatment of metal-containing wastewaters.

Integration of polyelectrolyte enhanced ultrafiltration and chemical reduction for metal-containing wastewater treatment and metal recovery.

Chemical reduction was firstly employed to treat synthetic wastewaters of various compositions prepared to simulate the retentate stream of polyelectrolyte enhanced ultrafiltration (PEUF). With fixed Cu:polyethylenimine (PEI) monomer:dithionite molar ratio, increasing copper concentration increases copper removal efficiency. Under fixed Cu:dithionite molar ratio and fixed Cu concentration, increasing PEI monomer:copper molar ratio decreases copper removal efficiency. The formation of nano-sized copper particles, which readily pass through 0.45 μm filter used for sample pretreatment before residual copper analysis, might be the reason behind the decreasing copper removal efficiency observed. Particle size analysis shows that the size of copper particles, which are formed through reduction reaction, increases with decreasing pH value and increasing reaction time. As ultrafiltration is capable of removing these nano-sized particles, integration of chemical reduction and PEUF is proposed to simultaneously achieve regeneration of polyelectrolyte and recovery of copper in one process. Results show that the proposed process could achieve almost complete copper removal without being affected by reaction pH.

Enhancement of the Stability of Biosorbents for Metal-Ion Adsorption

Biosorbents have demonstrated great potential in the treatment of metal-containing wastewater. However, one of the bottleneck issues of using biosorbents is that amounts of organic carbon release f...

Draft genome sequence of the first acid-tolerant sulfate-reducing deltaproteobacterium Desulfovibrio sp. TomC having potential for minewater treatment.

The sulfidogenic bacterium Desulfovibrio sp. TomC was isolated from acidic waste at the abandoned gold ore mining site in the Martaiga gold ore belt, Western Siberia. This bacterium, being the first reported acid-tolerant gram-negative sulfate-reducer of the order Deltaproteobacteria, is able to grow at pH as low as 2.5 and is resistant to high concentrations of metals. The draft 5.3 Mb genome sequence of Desulfovibrio sp. TomC has been established and provides the genetic basis for application of this microorganism in bioreactors and other bioremediation schemes for the treatment of metal-containing wastewater.

Application of Immobilized Fungi <i>Phanerochaete chrysosporium</i> in Removal of Heavy-Metals from Wastewater

Immobilized microbe technologies are expected to be effectively used in wastewater treatment. Removal of heavy-metals from wastewater by immobilized Phanerochaete chrysosporium (Pc) with Ca-alginate and iron oxide magnetic nanoparticles (MNPs) was studied. The results showed that a biosorbent as Pc immobilized by Ca-alginate and iron oxide magnetic nanoparticles was successfully developed. And the iron oxide magnetic nanoparticles played an important role in the increase of biosorption capacity of Pc. Energy dispersive spectrometer (EDS) analysis confirmed that metal ions adsorbed to the surface of the biosorbents were partly transmitted to the interior of biosorbents, mainly embedded with iron oxide nanoparticles and Ca-alginate. Moreover, it was found that MNPs-Ca-alginate immobilized Pc showed a good affinity to various heavy metals, such as Pb(II), Zn(II), Cd(II) or Mg(II) and so on. The results proved the high efficiency of the biosorbents for heavy-metal removal and its potential application in the treatment of metal-containing wastewater.

Utilization of calcium sulfide derived from waste gypsum board for metal-containing wastewater treatment

To achieve recycling of waste gypsum boards (CaSO4), production of calcium sulfide by reductive decomposition of CaSO4 was investigated and the decomposition product of CaS was used as a sulfuration agent in the treatment of nickel-containing simulated wastewater. At the end of the experiment, residual nickel concentration and filtration characteristics of the slurry formed by adding CaS to the nickel-containing wastewater were investigated. Regarding the reductive decomposition of CaSO4, it was found that CaS could be effectively generated by CaSO4 reductive decomposition with graphite and the CaS content in the final product was greater than 80% when the reductive decomposition was carried out for one hour at a temperature of 1273 K, under N2 atmosphere. Then, in the sulfuration treatment of nickel-containing wastewater with CaS, the applicability of CaS as a sulfuration agent was confirmed and the nickel concentration in the simulated wastewater was reduced from 100 mg-Ni l-1 to a value below 1.0 mg l-1, when the CaS was added to the simulated wastewater at CaS to Ni molar ratio of 1.3. Moreover, sulfide slurry obtained by adding CaS was characterized by lower average specific filtration resistance and compressibility coefficient, compared to hydroxide slurry formed by the conventional precipitation treatment.

High-rate sulphidogenic fluidised-bed treatment of metal-containing wastewater at high temperature

The applicability of fluidised-bed reactor (FBR) based sulphate reducing bioprocess was investigated for the treatment of iron containing (40-90 mg/L) acidic wastewater at 65 degrees C. The FBR was inoculated with sulphate-reducing bacteria (SRB) originally enriched from a hot mining environment. Ethanol or acetate was supplemented as carbon and electron source for the SRB. A rapid startup with 99.9, 46 and 29% ethanol, sulphate and acetate removals, in respective order, was observed even after 6 days. Iron was almost completely removed with a rate of 90 mg/L.d. The feed pH was decreased gradually from its initial value of 6 to around 3.7 during 100 days of operation. The wastewater pH of 4.3-4.4 was neutralised by the alkalinity produced in acetate oxidation and the average effluent pH was 7.8 +/- 0.8. Although ethanol removal was complete, acetate accumulated. Later the FBR was fed with acetate only. Although acetate was present in the reactor for 295 days, its oxidation rates did not improve, which may be due to low growth rate and poor attachment ability of acetate oxidising SRB. Hence, the oxidation of acetate is the rate limiting step in the sulphidogenic ethanol oxidation by the thermophilic SRB.