Ultrasound‒induced facile synthesis of spinel CoFe2O4‒PAC magnetic nanocatalyst for remediation of hypersaline petrochemical wastewater: Degradation mechanism, biodegradability enhancement and phytotoxicity mitigation.

In this study, magnetic CoFe2O4-PAC nanocatalysts were synthesized through facile hydrothermal and co‒precipitation approaches with ultrasonic irradiation, which were used for the treatment of hypersaline petrochemical wastewater (HPCW). When an ultrasound‒induced synthesis process (US@CoFe2O4‒PAC) was used, a more efficient and stable magnetic spinel CoFe2O4‒PAC nanocatalyst was developed. The application of this nanocatalyst as a PMS activator, not only caused eradication of 90.4% of chemical oxygen demand (COD) of a HPCW after 90 min reaction time under the optimum conditions (pH 5-6, catalyst dose 1.0 g/L and 1.0 mM PMS), but also led to marginal leaching of iron (314 µg/L) and cobalt (95 µg/L) from the nanocatalyst. Recycling experiments over five consecutive runs showed a negligible decrease (7.2%) in COD removal efficiency which proved the stability and reusability of magnetic US@CoFe2O4-PAC. Two main mechanisms of adsorption and catalytic oxidation processes (homogeneous and heterogeneous PMS) are involved simultaneously in the PMS/US@CoFe2O4-PAC system, which are responsible for the destruction of refractory contaminants of HPCW through the generation of SO4•‒ and OH• radicals. COD of HPCW was mainly removed through SO4•- radical attack (73.6%) and the biodegradability of HPCW was enhanced dramatically after 90 min reaction time. The germination index (GI) of raw HPCW was increased 17.1 ± 4.2% and 24.3 ± 8.8% after 15 and 90 min reaction time, respectively, even PMS/US@CoFe2O4-PAC system showed less impact on phytotoxicity mitigation. Hence, it can be recommended to dilute the effluent before using for irrigational purpose. The findings of this study present practical significance of spinel US@CoFe2O4-PAC, which is an environment‒friendly catalyst, easy to handle and can sustain long‒term operation for the treatment of recalcitrant hypersaline wastewater and the other potential practical applications.

Xylanase treatment of eucalypt kraft pulps: effect of carryover.

The influence of pulp carryover on the efficiency of the xylanase (X) treatment of industrial unbleached and oxygen-delignified eucalypt kraft pulps (A1 and A2 pulps, with kappa number (KN) values of 16 and 10, respectively), collected at the same pulp mill, was studied regarding the consumption of bleaching chemicals and pulp bleachability. Another non-oxygen-delignified eucalyptus kraft pulp of KN 13 was received after the extended cooking from a different pulp mill (pulp B). The assays were performed with both lab-washed (carryover-free) and unwashed (carryover-rich) pulps. Both lab-washed and unwashed pulps with carryover were subjected to X treatment, the former being demonstrating considerably higher ClO2 savings than the pulps containing carryover. The savings of bleaching reagents were higher when the X stage was applied to the A1 pulp than to the A2 pulp. This advantage of A1 pulp, however, was not confirmed when using unwashed pulps. In contrast, the gains obtained from the X treatment of unwashed pulp A2 were practically as high as those observed for the lab-washed A2 pulp. Furthermore, a similar effect in X stage was recorded for unwashed pulps having close KN: oxygen-delignified A2 pulp and non-oxygen-delignified B pulp. The results suggest that pulp carryover and initial pH were the key factors relating to the effectiveness of X treatment. The application of X treatment to the A2 unwashed pulp (after the oxygen stage) not only saved 20% of the ClO2 and 10% of the sodium hydroxide, but also improved the brightness stability of the bleached pulp without affecting its papermaking properties. KEY POINTS: • Xylanase treatment boosts kraft pulp bleaching • Pulp carryover hinders the xylanase treatment • Nearly 20% of ClO2 and 10% NaOH savings can be reached using xylanase.

Oxidation and mineralization rates of harmful organic chemicals in hydroxyl radical induced reactions.

In most of advanced oxidation processes (AOPs) used to destroy harmful organic chemicals in water/wastewater hydroxyl radical (•OH) reactions oxidize (increasing the oxygen/carbon ratio in the molecules) and mineralize (transforming them to inorganic molecules, H2O, CO2, etc.) these contaminants. In this paper, we used the radiolysis of water to produce •OH and characterised the rate of oxidation and mineralization by the dose dependences of the Chemical Oxygen Demand (COD) and Total Organic Carbon (TOC) content values. Analysis of the dose dependences for 34 harmful organic compounds showed large differences in the oxidation and mineralization rates and these parameters are characteristic to the given group of chemicals. E.g., the rate of oxidation is relatively low for fluoroquinolone antibiotics; it is high for ß-blocker medicines. Mineralization rates are low for both fluoroquinolones and ß-blockers. The one-electron-oxidant •OH in most cases induces two - four-electron-oxidations. Most of the degradation takes place gradually, through several stable molecule intermediates. However, based on the results it is likely, that some part of the oxidation and mineralization takes place parallel. The organic radicals formed in •OH reactions react with several O2 molecules and release several inorganic fragments during the radical life cycle.

An integrated smartphone-based electrochemical detection system for highly sensitive and on-site detection of chemical oxygen demand by copper-cobalt bimetallic oxide-modified electrode.

A portable and integrated electrochemical detection system has been constructed for on-site and real-time detection of chemical oxygen demand (COD). The system mainly consists of four parts: (i) sensing electrode with a copper-cobalt bimetallic oxide (CuCoOx)-modified screen-printed electrode; (ii) an integrated electrochemical detector for the conversion, amplification, and transmission of weak signals; (iii) a smartphone installed with a self-developed Android application (APP) for issuing commands, receiving, and displaying detection results; and (iv) a 3D-printed microfluidic cell for the continuous input of water samples. Benefiting from the superior catalytic capability of CuCoOx, the developed system shows a high detection sensitivity with 0.335 µA/(mg/L) and a low detection limit of 5.957 mg/L for COD determination and possessing high anti-interference ability to chloride ions. Moreover, this system presents good consistency with the traditional dichromate method in COD detection of actual water samples. Due to the advantages of cost effectiveness, portability, and point-of-care testing, the system shows great potential for water quality monitoring, especially in resource-limited remote areas.

Wastewater treatment in lagoons: A systematic review and a meta-analysis.

This study has carried out a systematic review of 36 scientific papers (reporting 63 case studies) published in the last 15 years about the treatment of industrial, agri-food and municipal wastewater in lagoons. A concentration of studies from a few countries (Italy, Algeria and Iran) and about municipal wastewater (70% of papers) was revealed by the bibliographic analysis. Aeration was supplied in more than 50% of case studies; the storage capacity of lagoons (adopted as a measure of size) was extremely variable (over seven orders of magnitude), while their depth was generally lower than a few metres. The efficiency of lagoon treatments at removing COD was in a wide range (25-98%). Very few studies analysed the energy intensity of treatments in lagoons. The meta-analysis applied to a further selection of 10 papers with 29 case studies revealed significant differences in pH and dissolved oxygen concentration, due to aeration or type of treated wastewater. Treatment efficiency was higher in aerated lagoons compared to non-aerated systems, and did not depend on the type of treated wastewater. Based on the analysis of the reviewed papers, an urgent research need on this topic arises, mainly due to the oldness of most analysed studies. Practical suggestions are given to optimise the depuration performances of lagoons: (i) application of intermittent and night aeration; (ii) reduced air flow rates; (iii) adaptation of microbial biomass to high contents of inhibiting compounds in wastewater; (iv) construction of baffles to keep the planned hydraulic retention time avoiding short-circuit; (v) integration of lagoons with other treatments (e.g., constructed wetlands); (vi) ferti-irrigation of crops with lagoon effluents rather than disposal into water bodies.

Sustainable power production from petrochemical industrial effluent using dual chambered microbial fuel cell.

Dual chambered microbial fuel cell (DMFC) is an advanced and effective treatment technology in wastewater treatment. The current work has made an effort to treat petrochemical industrial wastewater (PWW) as a DMFC substrate for power generation and organic substance removal. Investigating the impact of organic load (OL) on organic reduction and electricity generation is the main objective of this study. At the OL of 1.5 g COD/L, the highest total chemical oxygen demand (TCOD) removal efficiency of 88%, soluble oxygen demand (SCOD) removal efficiency of 80% and total suspended solids (TSS) removal efficiency of 71% were seen, respectively. In the same optimum condition of 1.5 g COD/L, the highest current and power density of about 270 mW/m2 and 376 mA/m2 were also observed. According to the results of this study, using high-strength organic wastewater in DMFC can assist in addressing the issue of the petrochemical industries and minimize the energy demand.

Wastewater Characterization: Chemical Oxygen Demand or Total Organic Carbon Content Measurement?

The long time (2 h) required for measurement, expensive chemicals (Ag2SO4), and toxic reagents (K2Cr2O7, HgSO4) limit the application of the standard method for measuring the oxygen equivalent of organic content in wastewater (chemical oxygen demand, COD). In recent years, the COD has increasingly been replaced by the total organic carbon (TOC) parameter. Since the limit values of the pollution levels are usually given in terms of the COD, efforts are being made to find the correlation between these parameters. Several papers have published correlation analyses of COD and TOC for industrial and municipal wastewater, but the relationship has not been discussed for individual chemicals. Here, this relationship was investigated using 70 contaminants (laboratory chemicals, pharmaceuticals, and pesticides). The calculated COD values, in most cases, agreed, within ~10%, with the experimental ones; for tetracyclines and some chloroaromatic molecules, the measured values were 20-50% lower than the calculated values. The COD/TOC ratios were between 2 and 3: for macrolides, they were ~3; for fluoroquinolones and tetracyclines, they were ~2. The molecular structure dependence of the ratio necessitates the establishing of the correlation on an individual basis. In advanced oxidation processes (AOPs), the ratio changes during degradation, limiting the application of TOC instead of COD.

Determination of seawater COD spectra using double-loop contraction and sorted frog optimization.

This study develops a novel double-loop contraction and C value sorting selection-based shrinkage frog-leaping algorithm (double-contractive cognitive random field [DC-CRF]) to mitigate the interference of complex salts and ions in seawater on the ultraviolet-visible (UV-Vis) absorbance spectra for chemical oxygen demand (COD) quantification. The key innovations of DC-CRF are introducing variable importance evaluation via C value to guide wavelength selection and accelerate convergence; a double-loop structure integrating random frog (RF) leaping and contraction attenuation to dynamically balance convergence speed and efficiency. Utilizing seawater samples from Jiaozhou Bay, DC-CRF-partial least squares regression (PLSR) reduced the input variables by 97.5% after 1,600 iterations relative to full-spectrum PLSR, RF-PLSR, and CRF-PLSR. It achieved a test R2 of 0.943 and root mean square error of 1.603, markedly improving prediction accuracy and efficiency. This work demonstrates the efficacy of DC-CRF-PLSR in enhancing UV-Vis spectroscopy for rapid COD analysis in intricate seawater matrices, providing an efficient solution for optimizing seawater spectra.

Evolving tolerance of Yarrowia lipolytica to hydrothermal liquefaction aqueous phase waste.

Hydrothermal liquefaction (HTL) is an emerging method for thermochemical conversion of wet organic waste and biomass into renewable biocrude. HTL also produces an aqueous phase (HTL-AP) side stream containing 2-4% light organic compounds that require treatment. Although anaerobic digestion (AD) of HTL-AP has shown promise, lengthy time periods were required for AD microbial communities to adapt to metabolic inhibitors in HTL-AP. An alternative for HTL-AP valorization was recently demonstrated using two engineered strains of Yarrowia lipolytica, E26 and Diploid TAL, for the overproduction of lipids and the polyketide triacetic acid lactone (TAL) respectively. These strains tolerated up to 10% HTL-AP (v/v) in defined media and up to 25% (v/v) HTL-AP in rich media. In this work, adaptive laboratory evolution (ALE) of these strains increased the bulk population tolerance for HTL-AP to up to 30% (v/v) in defined media and up to 35% (v/v) for individual isolates in rich media. The predominate organic acids within HTL-AP (acetic, butyric, and propionic) were rapidly consumed by the evolved Y. lipolytica strains. A TAL-producing isolate (strain 144-3) achieved a nearly 3-fold increase in TAL titer over the parent strain while simultaneously reducing the chemical oxygen demand (COD) of HTL-AP containing media. Fermentation with HTL-AP as the sole nutrient source demonstrated direct conversion of waste into TAL at 10% theoretical yield. Potential genetic mutations of evolved TAL production strains that could be imparting tolerance were explored. This work advances the potential of Y. lipolytica to biologically treat and simultaneously extract value from HTL wastewater. KEY POINTS: • Adaptive evolution of two Y. lipolytica strains enhanced their tolerance to waste. • Y. lipolytica reduces chemical oxygen demand in media containing waste. • Y. lipolytica can produce triacetic acid lactone directly from wastewater.

Removal of chemical oxygen demand and ammonia nitrogen from high salinity tungsten smelting wastewater by one-step electrochemical oxidation: From bench-scale test, pilot-scale test, to industrial test.

In recent years, electrochemical oxidation (EO) shows the characteristics of green and high efficiency in removing chemical oxygen demand (COD) and ammonia nitrogen (NH3-N) from wastewater, which has been favored by researchers. However, at present, most of current studies on EO remain in laboratory stage, reports about pilot-scale or even industrial tests with large treatment capacity are few, which slowing down the use of the advanced technology to practical application. In this study, bench-scale tests, pilot-scale tests (treatment capacity 200-500 L/h), and industrial tests (treatment capacity 100 m3/h) were carried out by EO technology in view of the characteristics of tungsten smelting wastewater (TSW) with high salinity (NaCl), COD, and NH3-N. Results showed that the removal of COD and NH3-N was a competitive reaction in the EO process, and COD could be removed more preferentially than NH3-N. When NH3-N content was low, the influent pH had a minimal effect on its removal, and when NH3-N content was high, increasing the influent pH was beneficial to its removal. Industrial tests showed that the one-step removal of COD and NH3-N in TSW met the standard, and the power consumption per cubic meter of wastewater was only 4.2 kW h, and the treatment cost was much lower than the two-step process of "breaking point chlorination to remove NH3-N and adding oxidant to remove COD". This study has successfully realized industrial application of EO technology in TSW treatment for the first time and provided a successful case, which is helpful to accelerate the popularization and application of this technology in the field of high salinity organic ammonia nitrogen wastewater treatment.

Application of a membrane-less air cathode microbial fuel cell to treat municipal waste composting leachate.

The adverse effects of high strength wastewaters on the microbial activities have created a challenge to biological treatments. Microbial fuel cell has been considered as a promising process because the electrical potential generation can stimulate microorganisms and overcome the inhibitory effect. However, several issues (e.g., scalability, high costs and maintenance) have prevented the process from the industrial applications. Elimination of the proton exchange membrane has been suggested as a remedy to the mentioned problems. In this work, a membrane-less microbial fuel cell was modified by putting the cathode within a thin sand layer (instead of the proton exchange membrane) to treat a high strength wastewater sample. The influences of the feed organic load and time of treatment in the modified system were studied in batch and continuous operations. It was revealed that the batch operation efficiency was higher for the lower feed loadings as a 5-day batch treatment removed 66 ± 4% of the 15,000 ± 500 mg/L initial chemical oxygen demand while the continuous process efficiency with 9-day hydraulic residence time was slightly more than 50%. However, the efficiency of the continuous operation for treatment of higher initial loading values was better than the batch mode with the removal efficiency of 41 ± 2% versus 12 ± 2% for a more concentrated leachate feed (45,000 ± 1000 mg/L). Finally, it was disclosed that the modified membrane-less MFC employed in this work can be effective in treatment of high strength wastewaters in larger scales with lower costs.

BaTiO3 Functional Perovskite as Photocathode in Microbial Fuel Cells for Energy Production and Wastewater Treatment.

Microbial fuel cells (MFCs) provide new opportunities for the sustainable production of energy, converting organic matter into electricity through microorganisms. Moreover, MFCs play an important role in remediation of environmental pollutants from wastewater with power generation. This work focuses on the evaluation of ferroelectric perovskite materials as a new class of non-precious photocatalysts for MFC cathode construction. Nanoparticles of BaTiO3 (BT) were prepared and tested in a microbial fuel cell (MFC) as photocathode catalytic components. The catalyst phases were synthesized, identified and characterized by XRD, SEM, UV-Vis absorption spectroscopy, P-E hysteresis and dielectric measurements. The maximum absorption of BT nanoparticles was recorded at 285 nm and the energy gap (Eg) was estimated to be 3.77 eV. Photocatalytic performance of cathodes coated with BaTiO3 was measured in a dark environment and then in the presence of a UV-visible (UV-Vis) light source, using a mixture of dairy industry and domestic wastewater as a feedstock for the MFCs. The performance of the BT cathodic component is strongly dependent on the presence of UV-Vis irradiation. The BT-based cathode functioning under UV-visible light improves the maximum power densities and the open circuit voltage (OCV) of the MFC system. The values increased from 64 mW m-2 to 498 mW m-2 and from 280 mV to 387 mV, respectively, showing that the presence of light effectively improved the photocatalytic activity of this ceramic. Furthermore, the MFCs operating under optimal conditions were able to reduce the chemical oxygen demand load in wastewater by 90% (initial COD = 2500 mg L-1).

Sensing of chemical oxygen demand (COD) by amperometric detection-dependence of current signal on concentration and type of organic species.

The standard method to determine chemical oxygen demand (COD) with K2Cr2O6 uses harmful chemicals, has a long analysis time, and cannot be used for on-site online monitoring. It is therefore necessary to find a fast, cheap, and harmless alternative. The amperometric determination of COD on boron-doped diamond (BDD) electrodes is a promising approach. However, to be a suitable alternative, the electrochemical method must at least be able to determine the COD of water samples independently of the contained substances. Therefore, the current signal as a function of various organic materials was investigated for the first time. It was shown that the height of the signal current depended on the type of organic matter in single-substance solutions and that this substance dependency increases with the amount of COD. Those findings could be explained by the mechanism proposed for this reaction, showing that the selectivity of the reaction depends on the ratio of the concentration of hydroxyl radicals and organic species. We give an outlook on how to improve the method in order to increase the linear working range and avoid signal variance and how to further explain the signal variance.

Characterizing and optimizing adsorption for olive mill wastewater processing in Loukkos, Morocco.

The present research consists of studying the characterization and treatment of the olive mill wastewater (OMWW) resulting from the olive industries of the region of Loukkos, Morocco. According to the national plan for green Morocco, the annual volumes of OMWW discharges increase with the expansion of the areas of olive plantations compared to agricultural activities. The study of the organic, mineral, and microbiological composition of the obtained OMWW showed that they are rich in microbiological (FMAT, Let M., and B.L.), mineral (total Kjeldhal nitrogen, orthophosphate, total phosphorus, sodium, potassium, calcium, copper, iron, zinc, manganese, and lead ions), and organic (COD, BOD5, and polyphenols) micropollutants with very high percentages that are higher than the standards in force. The treatment used in this study is the combined process of aerated lagooning/adsorption using powdered activated carbon after optimization of the experimental parameters (mass concentration of activated carbon (AC) and agitation rapidity (Ar)) by experiment design method. The obtained physicochemical parameters, such as pH, total suspended solids (TSS), chemical oxygen demand (COD), rate of discoloration, and polyphenol content of raw OMWW, were 4.87, 0.63, 80.3, 0.8, and 1.45 g/l, respectively. The results of these parameters for the treated OMWW were obtained in the order of 6.10, 0.22, 28, 0.28, and 0.44 g/l for pH, TSS, COD, discoloration rate, and polyphenol content, respectively. These results show that the proposed treatment significantly reduced acidity, TSS, COD, discoloration rate, and polyphenol contents, with a performance of about 25.26, 65, 65.13, 65, and 69.65%, respectively. This indicates that there is significant performance in the processing of exploited OMWW.

Simultaneous reuse and treatment of sugar-sweetened beverage wastes for citric acid production.

This study aimed to evaluate the feasibility of using sugar-sweetened beverages (SSB) for citric acid (CA) production and its impact on chemical oxygen demand (COD) of SSB. Five types of SSB were used as a carbon source for CA production by A. niger, and the COD of each SSB was measured before and after the bioprocess. Results showed that all tested SSB were suitable for CA production, with maximum yields ranging from 13.01 to 56.62 g L- 1. The COD was reduced from 53 to 75.64%, indicating that the bioprocess effectively treated SSB wastes. The use of SSB as a substrate for CA production provides an alternative to traditional feedstocks, such as sugarcane and beet molasses. The low-cost and high availability of SSB makes it an attractive option for CA production. Moreover, the study demonstrated the potential of the bioprocess to simultaneously treat and reuse SSB wastes, reducing the environmental impact of the beverage industry. Supplementary Information: The online version contains supplementary material available at 10.1007/s13197-023-05761-9.

Correlating black soldier fly larvae growths with soluble nutrients derived from thermally pre-treated waste activated sludge.

Black soldier fly larvae (BSFL) have been deployed to valorize various organic wastes. Nonetheless, its growth rate whilst being offered with waste activated sludge (WAS) is not promising, likely by virtue of the presence of extracellular polymeric substances' structure in WAS. In this work, the WAS were first thermally pre-treated under different treatment temperatures and durations before being administered as the feeding substrates for BSFL. The results showed the thermal pre-treatment could improve WAS palatability and subsequently, enhance the growth of BSFL especially after the pre-treatments at 75 °C and above. The highest larva weight gained was recorded at 2.16 mg/larva for the WAS sample being pre-treated at 90 °C and 16 h. Furthermore, the samples pre-treated above 75 °C also achieved higher degradation rates, indicating that the 75 °C was a threshold temperature to effectively hydrolyze the WAS. The changes of WAS characteristics, namely, (i) soluble chemical oxygen demand (SCOD), (ii) soluble carbohydrate, (iii) soluble protein, (iv) humic substances and (v) total soluble protein and humic substances, after the thermal pre-treatments were also studied in correlating with the BSFL growth. Accordingly, a model was successfully developed with the highest R2 value attained at 0.95, evidencing the SCOD was the most suitable WAS characteristic to accurately predict the BSFL growth behavior.

Improved water quality monitoring indicators may increase carbon storage in the oceans.

Indicators related to organic matter are important when assessing aquatic environment quality. The chemical oxygen demand (COD) is widely used as a water quality reference. However, oxidizing agents used to determine the COD can oxidize refractory organic matter that is not pollutant and can persist in the ocean for thousands of years. This means the COD can misrepresent the water quality. The actual water quality can be indicated better by the biochemical oxygen demand (BOD) than the COD, but determining the BOD is time-consuming and gives variable results. In this study, the optical properties of dissolved organic matter in water samples from the Chinese coast that had been incubated for a long time or directly oxidized using COD oxidant were analyzed. The results indicated that the oxidizing agent rapidly oxidized 22.93% ± 4.96% of refractory dissolved organic matter (RDOM) that was resistant to microbial degradation, implying that RDOM made a marked contribution to the COD. Meanwhile, size-fractional fluorescence spectroscopy and COD measurements indicated that the COD of the >0.7 µm fraction and the fluorescence intensity of the protein-like component significantly positively correlated with the BOD of the bulk sample. This indicated that, for monitoring organic pollutants in coastal waters, the COD of the >0.7 µm fraction could be used as a proxy for the standard COD and that the fluorescence intensity of the protein-like component could be used as a convenient proxy for the BOD. The method can help retain recalcitrant organic matter in seawater to act as a carbon sink.

Estimation of chemical oxygen demand in different water systems by near-infrared spectroscopy.

To monitor environmental water pollution effectively and meet human water needs, it is crucial to develop a fast, simple, and accurate method for monitoring chemical oxygen demand (COD) in various water systems. In this study, COD prediction models for different water systems were developed by combining near-infrared (NIR) spectroscopy with partial least squares regression (PLSR). Samples of wastewater, surface water, and seawater were collected from Guangzhou, Guangdong Province, China. Three pretreatment methods were used to preprocess the spectra in order to improve the accuracy and minimalism of the model. We investigate the performance of two variable selection algorithms, namely, binary gray wolf optimization (BGWO) and competitive adaptive reweighting sampling (CARS). The results show that both BGWO and CARS improved the performance of the model in terms of higher accuracy and less wavelength input; both of the combined model performances were better than that of PLSR alone, and CARS-PLSR achieved the best results. Using CARS-PLSR, surface water, wastewater, and seawater model inputs were reduced by 96 %, 96 %, and 82 % as compared to the PLSR results, respectively, and the testing sets R2 reached 0.860, 0.815, and 0.692, respectively. The spectral variable selection algorithm could identify the important spectral variables between COD content and NIR spectra in three water systems, thereby improving the accuracy and simplicity of the PLSR model for COD prediction. Our results have important practical value for predicting COD content in different water systems by NIR spectroscopy.

Controlling the formation of halogenated byproducts in the chlorination of source waters by oxidative pre-treatment with the Fe(II)/Fe(III)-S(IV)-air system.

Breakpoint chlorination is a generally accepted method for removing ammonium ion from source waters in drinking water treatment technologies. This process is often accompanied by the formation of halogenated organic byproducts. The presence of these compounds in potable water is of primary concern. In this paper, we demonstrate that the concentration of the precursors of the halogenated species can sufficiently be decreased by oxidizing the organic pollutants with the Fe(II)/Fe(III) - S(IV) - air system. Pre-oxidative treatment of the source waters results in a substantial reduction of chemical oxygen demand, while the ammonium ion concentration remains unaffected. The breakpoint chlorination produces substantially less trihalomethanes (THMs) and adsorbable halogenated organic compounds (AOXs) in oxidatively pre-treated source waters than in raw waters. These results offer a possibility to improve drinking water treatment technologies for better controlling the formation of antagonistic byproducts. It is demonstrated that reaching the regulated concentration levels of THMs is feasible with this method even in source waters containing organic pollutants at relatively high concentration levels. The main advantage of the procedure is that the reagents used for the oxidative pre-treatment are converted into non-toxic products (Fe(III) and SO42-) by the end of the process.

Synchronous bio-degradation and bio-electricity generation in a Microbial Fuel Cell with aged and fresh leachate from the identical subtropical area.

Seasonal leachate from both sealed and operating landfill in the identical district were employed as the sole substrate in the Microbial Fuel Cell (MFC) to evaluate the power output performance and aqueous organic waste disposal. The electrical performance was characterized to study the power generation, while the Chemical Oxygen Demand (COD) removal ratio and Coulombic Efficiency (CE) were calculated to illustrate the substrate disposal effect. In addition, Scanning Electron Microscope (SEM) on the operated anode was conducted to preliminarily explain the microbial community difference, and the phylogenetic tree constructed on the cultivated microorganism was an insight into the dominant bacteria suitable for leachate degradation. It was found that the MFCs inoculated with seasonal leachate from both sealed and operating landfill could generate electricity successfully. Although the fresh leachate-inoculated MFCs had better electrical output performance (22.7-25.6 W/m3 versus 6.61-7.48 W/m3) and COD removal efficiency (55.8%∼61.7% versus 47.7%∼51.4%), the CEs were only 4.3%∼7.6%, which were lower than the aged leachate inoculated group (5.9%∼11.3%). Based on the SEM images and the phylogenetic tree of the operated anode, the composition impacts on the microbial community and power output performance were verified, which was instructive for the leachate disposal in the MFC.