Iron Flocculation Research Articles

Optimization of iron flocculation for enrichment of CyHV-2 in aquaculture water

Cyprinid herpesvirus 2 (CyHV-2) is an important infectious virus endangering the farmed Carassius species industry. The enrichment and identification of CyHV-2 in the water is a vital means of early warning diagnostics, which is helpful to aquatic diseases prevention and control. In this study, we employed and optimized iron flocculation to enrich the concentrations of CyHV-2 in aquaculture water. Different Fe3+ concentrations (0.5, 1.0, and 10.0 mg/L), various membrane filters (mixed cellulose ester, glass fiber, nylon microporous filter membrane), different elution buffers containing reductants (ascorbate, citrate, DL-malate, and their combinations with EDTA or TE buffer) were compared to check the recovery yield of CyHV-2. Viral genome quantitation was determined using quantitative real-time PCR. The results showed that Fe3+ concentration of 1.0 mg/L, the glass fiber and citrate-TE were determined to have high efficiency and stable recovery yield. To evaluate infectious CyHV-2 viral titres, crucian carps (Carassius auratus) were intraperitoneally injected with CyHV-2. The mortality rate was 100 % at 9 days postinoculation (dpi) with the 96.7 % detection of CyHV-2 in the pooled tissues. The histopathological phenotype showed necrotic cell death in the liver, spleen and kidney. The CyHV-2 genome was ranging from 101.1 to 107.5 copies/μl in the deceased fish, and 101.4 to 103.0 copies/μl in the feeding water at various stages from latent infection to onset of disease. The field samples from Huzhou, Zhejiang Province on June 4th and 7th had higher detection rates, 87.5 % and 100 % respectively, corresponding to higher CyHV-2 detected in the aquaculture water. CyHV-2 viral load in cultured waters tends to increase prior to fish death, which provides a new indicator for the prediction of fish diseases. In summary, we have established a unified operational standard for enrichment of CyHV-2 in the aqueous environment by iron flocculation.

Photochemical Origins of Iron Flocculation in Acid Mine Drainage.

Acid mine drainage (AMD) raises a global environmental concern impacting the iron cycle. Although the formation of Fe(III) minerals in AMD-impacted waters has previously been reported to be regulated by biological processes, the role of abiotic processes remains largely unknown. This study first reported that a photochemical reaction coupled with O2 significantly accelerated the formation of Fe(III) flocculates (i.e., schwertmannite) in the AMD, as evidenced by the comparison of samples from contaminated sites across different natural conditions at latitudes 24-29° N. Combined with experimental and modeling results, it is further discovered that the intramolecular oxidation of photogenerated Fe(II) with a five-coordinative pyramidal configuration (i.e., [(H2O)5Fe]2+) by O2 was the key in enhancing the photooxidation of Fe(II) in the simulated AMD. The in situ attenuated total reflectance-Fourier transform infrared spectrometry (ATR-FTIR), UV-vis spectroscopy, solvent substitution, and quantum yield analyses indicated that, acting as a precursor for flocculation, [(H2O)5Fe]2+ likely originated from both the dissolved and colloidal forms of Fe(III) through homogeneous and surface ligand-to-metal charge transfers. Density functional theory calculations and X-ray absorption spectroscopy results further suggested that the specific oxidation pathways of Fe(II) produced the highly reactive iron species and triggered the hydrolysis and formation of transient dihydroxo dimers. The proposed new pathways of Fe cycle are crucial in controlling the mobility of heavy metal anions in acidic waters and enhance the understanding of complicated iron biochemistry that is related to the fate of contaminants and nutrients.

Inhibiting effects of humic acid on iron flocculation hindered As removal by electro-flocculation on air cathode iron anode

Activated carbon air cathode combined with iron anode oxidation-flocculation synergistic Arsenic (As) removal was a new groundwater purification technology with low energy consumption and high efficiency for groundwater with high As concentration. The presence of organic matter such as humic acid (HA) had ambiguous effects on formation of organic colloids in the system. The effects of the particle size distribution characteristics of these colloids on the formation characteristics of flocs and the efficiency of As purification was not clear. In this work, we used five different pore size alumina filter membranes to separate mixed phase solutions and studied the corresponding changes in iron and arsenic concentrations in the presence and absence of humic acid conditions. In the presence of HA, the arsenic concentration of < 0.05 µm particle size components was 1.01, 1.28, 3.07, 7.69, 2.85 and 1.24 times of that in the absence of HA. At the same time, the arsenic content in 0.05–0.1 µm and 0.1–0.45 µm particle size components was also higher than that in the system without HA, which revealed that the presence of HA hindered the flocculation behavior of As distribution to higher particle sizes in the early stage of the reaction. The presence of HA affected the flocculation rate of iron flocs from small to large particle size fractions and it had limited effect on the behavior of large-size flocs in adsorption of As. These results provide a theoretical basis for targeted, rapid, and low consumption synergistic removal of arsenic and organic compounds in high arsenic groundwater.

Utilizing CaCl2 to promote the enrichment and bioavailability of phosphorus in incinerated sludge ash.

Recovering phosphorus from incineration sludge sewage ash (ISSA) is a well-established technology, with a greater recovery potential than that of supernatant or sludge. ISSA can be utilized as a secondary raw material in the fertilizer industry, or as a fertilizer if heavy metal concentrations do not exceed permissible limits, thus reducing the cost of phosphorus recovery. Increasing the temperature to produce ISSA with higher solubility and plant availability of phosphorus is advantageous for both pathways. But a decrease in the extraction of phosphorus is also observed at high temperatures, thereby diminishing the overall economic benefits. In this study, CaCl2 was utilized to mitigate the decrease in the extraction rate and also to promote the bioavailability of phosphorus. The addition of CaCl2 (80 g/kg of dry sludge) effectively promoted the conversion of non-apatite inorganic phosphorus to apatite inorganic phosphorus at a rate of 87.73% at 750 °C. Furthermore, the decrease in the extraction rate of phosphorus at 1,050 °C was comparatively smaller in the presence of CaCl2. If iron flocculants are used to capture P in wastewater management, it may be necessary to pay special attention to the amount of addition and incineration temperature to maximize the economic potential of recycling.

Establishing environmental DNA and RNA protocols for the simultaneous detection of fish viruses from seawater

AbstractAquatic viruses are major threats to global aquacultural productivity. While conventional diagnostic methods for disease investigation are laborious, time‐consuming, and often involve the sacrifice of animals, environmental DNA and RNA (eDNA/eRNA) tools have the potential in being non‐invasive alternatives for the effective and early detection of various pathogens simultaneously. In this study, three seawater filtration methods—Sterivex syringe filtration, centrifugal ultrafiltration, and vacuum pump filtration with iron flocculation—were assessed for the recovery rates in co‐detecting fish virus eDNA/eRNA from natural seawater that was spiked with fish red seabream iridovirus (RSIV, DNA virus) and nervous necrosis virus (NNV, RNA virus). The centrifugal ultrafiltration method was the most effective for the capture of small‐sized viruses like NNV with a recovery rate of 63.23%, while the method of vacuum pump filtration with iron flocculation and chloroform disintegration of filter membranes had the highest RSIV recovery rate of 32.61%. We also optimized both automated and manual nucleic acid extraction methods and found comparable eDNA/eRNA extraction efficiencies. Our findings from the systematic comparison of seawater filtration and extraction methods suggest that each seawater filtration/nucleic acid extraction method can cater to different aquatic animal virus surveillance and disease investigation scenarios. These highlight the potential of virus eDNA/eRNA approaches for advancing the field of disease ecology and safeguarding aquatic animal health.

In Vitro Viral Recovery Yields under Different Re-Suspension Buffers in Iron Flocculation to Concentrate Viral Hemorrhagic Septicemia Virus Genotype IVa in Seawater.

Iron flocculation is widely used to concentrate viruses in water, followed by Fe-virus flocculate formation, collection, and elution. In the elution stage, an oxalic or ascorbic acid re-suspension buffer dissolved iron hydroxide. After the concentration of viral hemorrhagic septicemia virus (VHSV) in seawater (1 × 101 to 1 × 105 viral genome copies or plaque-forming unit (PFU)/mL), the recovery yield of the viral genome using quantitative real-time PCR (qRT-PCR) and viral infectivity using the plaque assay were investigated to evaluate the validity of the two re-suspension buffers to concentrate VHSV. The mean viral genome recovery yield with oxalic and ascorbic acid was 71.2 ± 12.3% and 81.4 ± 9.5%, respectively. The mean viral infective recovery yields based on the PFU were significantly different between the two buffers at 23.8 ± 22.7% (oxalic acid) and 4.4 ± 2.7% (ascorbic acid). Notably, although oxalic acid maintains viral infectivity over 60% at a viral concentration above 105 PFU/mL, the infective VHSVs were not sufficiently recovered at a low viral concentration (102 PFU/mL, <10%). To support this result, concentrated VHSV was inoculated in Epithelioma papulosum cyprini (EPC) cells to confirm cell viability, viral gene expression, and extracellular viral titer. All results demonstrated that oxalic acid buffer was superior to ascorbic acid buffer in preserving viral infectivity.

Salt‐Induced Flocculation of Dissolved Organic Matter and Iron Is Controlled by Their Concentration and Ratio in Boreal Coastal Systems

AbstractRivers and estuaries are important conduits and reactors for organic matter (OM). Despite the substantial export of terrestrial OM by rivers, only a small proportion of this material reaches the open ocean. One potentially important mechanism contributing to the removal of terrestrial dissolved OM (DOM) is flocculation; a process that transforms DOM into larger size fractions that can settle into sediment pools. Here we investigate the role of flocculation in adjacent boreal coastal systems over three consecutive seasons. Flocculation experiments, which include the artificial salting of freshwater DOM to mid (12 psu) and high salinity (25 psu), and a 1:1 mixture of freshwater DOM with their respective saline endmember, highlight a potentially important source of particulate carbon (PC) in boreal estuaries. Along with a 3.5% ± 1.0% removal of dissolved organic carbon (DOC) and 44% ± 16% dissolved iron (DFe), the potential for flocculation of these constituents significantly increased with increasing salinity from 12 to 25 psu. The particulate matter (PM) produced by salt‐induced flocculation was comparable to in situ PC concentrations (in situ PC = 27.5 μmol L−1 and flocculated PC = 15.0 μmol L−1) and stable carbon isotopic signatures (in situ PM = −28.8‰ and flocculated PM = −28.3‰). DFe:DOC and Sr were the only parameters that could significantly explain the degree of carbon and iron flocculation. This demonstrates the importance of DOC, DFe, and optical properties, and the predictive value of DFe:DOC for understanding DOM susceptibility to flocculation and its relevance and contribution to regional and global carbon budgets.

Combination of iron flocculation and qPCR for quantitative evaluation of virus-shedding intensity of goldfish Carassius auratus infected with cyprinid herpesvirus 2 in the water and the effect of sodium chlorite powder in blocking waterborne horizontal viral transmission

Cyprinid herpesvirus 2 (CyHV-2), a member of the Alloherpesviridae family belonging to the genus Cyprinivirus, was initially isolated from goldfish (Carassius auratus) and has been recently emerging as a virulent pathogen for cultured prussian carp (Carassius auratus gibelio) world-wide. In this study, a novel and effective method for concentration and quantification of live CyHV-2 virions from water was successfully established through coupling the iron flocculation with real time qPCR assay. Then, the shedding intensity of CyHV-2 in fish-tank water from artificially-challenged goldfish (25 fish/20 L) was monitored continuously for 7 days on a daily basis through quantitating viral genomic copy numbers by qPCR, and the maximum shedding level was determined to be 105 copies/L. Horizontal transmission research system was established by inoculating healthy goldfish in water spiked with serial dilution of CyHV-2 virions ranging from 107 to 103 copies/L. Our results indicated that water-borne CyHV-2 efficiently caused the infection of tested goldfish even in a concentration of 103 copies/L, and the overall transmission efficacy was not linearly correlated with the level of input virus in the fish tank. Commercial disinfectant Composite Sodium Chlorite Powder (CSCP) has been widely applied in aquaculture to control microbial infection through direct spill in the water, and its effect in inactivating the CyHV-2 infectivity remains unknown. We further determined that the EC50 of CSCP against 3.89 TCID50/mL CyHV-2 was close to 15.625 μg/mL in vitro, and application of CSCP in a level as high as 60 μg/mL (the safety concentration of CSCP for goldfish) couldn't protect goldfish from CyHV-2 challenge through immersion. Thus, the disinfectant CSCP was regarded as none-effective for blocking CyHV-2 transmission in water during epidemic. Overall, our data provided quantitative data to demonstrate the shedding intensity of CyHV-2 in water, and CSCP was shown to be not effective in blocking water-borne horizontal transmission of CyHV-2 in goldfish. The virus-concentration protocol and virus-inhibition assay established here also paved the way for evaluating more commercial disinfectants in their effects in blocking water-borne horizontal transmission of CyHV-2.

In-situ production of iron flocculation and reactive oxygen species by electrochemically decomposing siderite: An innovative Fe-EC route to remove trivalent arsenic

The removal of trivalent arsenic (As (III)) from water has received extensive attention from researchers. Iron electrocoagulation (Fe-EC) is an efficient technology for arsenic removal. However, electrode passivation hinders the development and application of Fe-EC. In this work, an innovative Fe-EC route was developed to remove As (III) through an electrochemical-siderite packed column (ESC). Ferrous ions were produced from siderite near the anode, and hydroxide was generated near the cathode during the electrochemical decomposition of siderite. As a result, an effect of Fe-EC-like was obtained. The results showed that an excellent removal performance of As (III) (>99%) was obtained by adjusting the parameters (As (III) concentration at 10 mg/L, pH at 7, Na2SO4 at 10 mM and the hydraulic retention time at 30 min) and the oxidation rate of As (III) reached 84.12%. The mechanism analysis indicated that As (III) was oxidized to As (Ⅴ) by the produced active oxide species and electrode, and then was removed by capturing on the iron oxide precipitates. As (III) was likely to be oxidized in two ways, one by the reactive oxygen species (possibly •OH, Fe(IV) and •O2- species), and another directly by the anode. The long-term effectiveness of arsenic removal demonstrated that ESC process based on the electrochemical-siderite packed column was an appropriate candidate for treating As (III) pollution.

Application of iron flocculation to concentrate white spot syndrome virus in seawater

The iron flocculation method, which comprises the Fe-virus flocculate formation-filtration-resuspension steps, is extensively used to concentrate and precipitate viruses distributed in water. To apply this method to concentrate white spot syndrome virus (WSSV) in seawater, viral genomic and infective recovery yields were compared between polyethylene sulfone (PES) and polycarbonate (PC) membrane filters and two types of resuspension buffers (oxalate and ascorbate). Viral genome quantitation was determined above a 95 % limit of detection (11.48 viral DNA copies/μL) using quantitative real-time PCR. From WSSV-spiked seawater (100–106 viral DNA copies/mL), the viral genomic recovery yields of the PES-Oxalate, PC-Oxalate, PES-Ascorbate, and PC-Ascorbate conditions were 78.67 % ± 12.90 %, 84.53 % ± 24.30 %, 85.59 % ± 16.98 %, and 93.74 % ± 7.44 %, respectively. The detectable Fe-virus flocculates collected by the PC membrane were approximately 101 WSSV DNA copies/mL of seawater, a value more than 10-fold higher than that compared to the PES membrane filter (102 WSSV DNA copies/mL), regardless of the resuspension buffer types. WSSV resuspended with oxalate buffer caused mass mortality among whiteleg shrimp (Litopenaeus vannamei), inducing the expression of the virus envelope protein, VP28, similar to that of a native virus, suggesting stable viral activity during the resuspension process. Based on the PES-Ascorbate, WSSV particles could be successfully concentrated in seawater from shrimp farms with white spot disease outbreaks (approximately 102 WSSV DNA copies/mL). Collectively, these findings indicate that the simple and efficient method of iron flocculation is sufficient to concentrate WSSV in seawater and could be used as a non-invasive approach and one of the reasonable diagnostic processes for white spot disease surveillance.

Concentration and quantification of Tilapia tilapinevirus from water using a simple iron flocculation coupled with probe-based RT-qPCR.

BackgroundTilapia tilapinevirus, also known as tilapia lake virus (TiLV), is a significant virus that is responsible for the die-off of farmed tilapia across the globe. The detection and quantification of the virus using environmental RNA (eRNA) from pond water samples represents a potentially non-invasive and routine strategy for monitoring pathogens and early disease forecasting in aquaculture systems.MethodsHere, we report a simple iron flocculation method for concentrating viruses in water, together with a newly-developed hydrolysis probe quantitative RT-qPCR method for the detection and quantification of TiLV.ResultsThe RT-qPCR method designed to target a conserved region of the TiLV genome segment 9 has a detection limit of 10 viral copies per µL of template. The method had a 100% analytical specificity and sensitivity for TiLV. The optimized iron flocculation method was able to recover 16.11 ± 3.3% of the virus from water samples spiked with viral cultures. Tilapia and water samples were collected for use in the detection and quantification of TiLV disease during outbreaks in an open-caged river farming system and two earthen fish farms. TiLV was detected from both clinically sick and asymptomatic fish. Most importantly, the virus was successfully detected from water samples collected from different locations in the affected farms (i.e., river water samples from affected cages (8.50 × 103 to 2.79 × 105 copies/L) and fish-rearing water samples, sewage, and reservoir (4.29 × 103 to 3.53 × 104 copies/L)). By contrast, TiLV was not detected in fish or water samples collected from two farms that had previously experienced TiLV outbreaks and from one farm that had never experienced a TiLV outbreak. In summary, this study suggests that the eRNA detection system using iron flocculation, coupled with probe based-RT-qPCR, is feasible for use in the concentration and quantification of TiLV from water. This approach may be useful for the non-invasive monitoring of TiLV in tilapia aquaculture systems and may support evidence-based decisions on biosecurity interventions needed.

Stable and efficient sulfamethoxazole and phosphorus removal by an electrolysis-integrated bio-rack constructed wetland system

Pollution of sulfamethoxazole (SMX) in rural domestic sewage are a great challenge for ecological security because of limited treatment. In this study, an electrolysis-integrated bio-rack constructed wetland system (EC-CW-P) without substrates was developed for enhancing SMX removal in rural domestic sewage. The dynamic performance and mechanism of SMX (1 mg L-1) removal, occurrence of antibiotic resistance genes (ARGs) and microbial community composition at 4 ~ 24℃ were assessed. Meanwhile, the simultaneous removal performance of phosphorus in EC-CW-P was also analyzed due to key role of substrate adsorption and iron flocculation. The results revealed that the removal efficiency of SMX could reach 97.13% at 4 ~ 24℃ in the EC-CW-P by the electrocatalysis and adsorption of a ferric iron coagulant and biodegradation. Moreover, efficient removal of 74.12%~99.52% total phosphorus (TP) was obtained through electrocoagulation because of the formation of ferric ions. The occurrence of SMX had no effect on TP removal because of the different removal pathway. Itshouldbeemphasizedthat the removal efficiency of SMX owing to high microbial and plant activity which may be due to the formation of iron film and micro current stimulation and TP owing to adsorption of iron mud remained high (>80%) when the electrode was gradually passivated. Overall, the performance of bio-rack CW system was intensified by electrolysis (iron electrode) with higher bacterial abundance and plant activity in the EC-CW-P. However, the high relative abundance of sul ARGs (from 2.15 × 10-1 to 2.41 × 101 copies 16S rRNA-1) in the influent of the EC-CW-P may pose a severe threat to ecosystem. These results provide a novel perspective for enhancing SMX and phosphorus removal by bio-rack constructed wetland system.

Comparison of ultrafiltration and iron chloride flocculation in the preparation of aquatic viromes from contrasting sample types.

Viral metagenomes (viromes) are a valuable untargeted tool for studying viral diversity and the central roles viruses play in host disease, ecology, and evolution. Establishing effective methods to concentrate and purify viral genomes prior to sequencing is essential for high quality viromes. Using virus spike-and-recovery experiments, we stepwise compared two common approaches for virus concentration, ultrafiltration and iron chloride flocculation, across diverse matrices: wastewater influent, wastewater secondary effluent, river water, and seawater. Viral DNA was purified by removing cellular DNA via chloroform cell lysis, filtration, and enzymatic degradation of extra-viral DNA. We found that viral genomes were concentrated 1-2 orders of magnitude more with ultrafiltration than iron chloride flocculation for all matrices and resulted in higher quality DNA suitable for amplification-free and long-read sequencing. Given its widespread use and utility as an inexpensive field method for virome sampling, we nonetheless sought to optimize iron flocculation. We found viruses were best concentrated in seawater with five-fold higher iron concentrations than the standard used, inhibition of DNase activity reduced purification effectiveness, and five-fold more iron was needed to flocculate viruses from freshwater than seawater—critical knowledge for those seeking to apply this broadly used method to freshwater virome samples. Overall, our results demonstrated that ultrafiltration and purification performed better than iron chloride flocculation and purification in the tested matrices. Given that the method performance depended on the solids content and salinity of the samples, we suggest spike-and-recovery experiments be applied when concentrating and purifying sample types that diverge from those tested here.

High-level waste activated sludge dewaterability using Fenton-like process based on pretreated zero valent scrap iron as an in-situ cycle iron donator

A novel, recyclable, and rapid pre-ultrasound-thermal-acid-washed zero valent scrap iron/hydrogen peroxide (UTA-ZVSI/H2O2) method has been developed to effectively enhance waste activated sludge (WAS) dewaterability. The effects of UTA ultrasound densities, UTA temperature, newly generated iron solution, H2O2 concentrations, and WAS conditioning time on the WAS dewaterability were investigated using a bench-scale system. Results indicated that the UTA-ZVSI/H2O2 treatment significantly improved the WAS dewaterability. The water content of the dewatered cake decreased to 44.15 ± 0.98 wt% during optimal operational conditions, which was significantly lower than that achieved using Fenton-based processes. Based on this outcome, a three-step treatment mechanism involving UTA-ZVSI/H2O2 has been developed, including iron flocculation, hydroxyl radical oxidation, and skeleton building. The dewatering efficiencies of three types of representative WAS were consistently effective in the UTA-ZVSI/H2O2 reactor for up to 15 cycles. Efficiencies levels were significantly higher than those achieved with Fenton-based processes. Economic analysis illustrated that the developed UTA-ZVSI/H2O2 system was the most cost-effective among other WAS dewatering treatments. In addition, the treatment system significantly alleviated toxicity of heavy metals and phytotoxicity in the dewatered sludge. This supported subsequent agricultural use. In summary, this study provided a comprehensive and useful basis for improving WAS dewatering and subsequent disposal.

Fluorescent carbon dots for ratiometric detection of curcumin and ferric ion based on inner filter effect, cell imaging and PVDF membrane fouling research of iron flocculants in wastewater treatment

The CDs were used as the ratiometric probe for detection of curcumin and Fe3+. The fluorescence of CDs at 420 nm was quenched through inner filter effect (IFE) while the fluorescence of curcumin at 525 nm was enhanced after adding curcumin. The value of ln(I525/I420) increased linearly with the curcumin concentration in the range of 5–30 μM, the limit of detection was 21.79 nM. After adding Fe3+ into the system of CDs-curcumin, curcumin complexed with Fe3+ leading to the quenching of the fluorescence of curcumin at 525 nm, which declined the spectra overlap between curcumin and CDs. The process of IFE was inhibited, the fluorescence of CDs at 420 nm was recovered. The value of ln(I525/I420) linearly decreased with the increasing of Fe3+ in the range of 2-14 μM, the limit of detection is 18.11 nM. The CDs-curcumin system was successfully applied for H1299 cell imaging and has potential applications in the fields of fluorescent labeling and inhibition of tumor cells. The CDs-curcumin system was furtherly used for PVDF membrane fouling research of iron flocculants in wastewater treatment.

Sulfate radical oxidation combined with iron flocculation for upgrading biological effluent of coking wastewater.

Because the components of the coking wastewater was biologically toxic and hence inhibit the actions of microorganisms in conventional biological treatment processes,the biological effluent of coking wastewater (BECW) still remains much recalcitrant pollutants. In the current work, we set out to explore the feasibility of using a proposed advanced oxidation method, involving the persulfate-activated zero-valent iron system (PS/ZVI), to realize a deep treatment of BECW. The efficiency levels at which sulfate radical oxidation combined with iron flocculation removed pollutants, specifically TOC, phenolic compounds (PCs), cyanide, and suspended solids (SSs), as well as removing colour were investigated in batch tests. Increasing the persulfate concentration generally resulted in improved pollutant removal, with maximum removal efficiency levels of 58.5%, 68.4%, 61% 99.9% and 91.04% for TOC, PCs, SS, cyanide and colour, respectively. Note that the coexisting inorganic ions CO32− and HCO3− were strong competitors of the radical consumption of TOC, but this interference was eliminated by adjusting the pH to 4.5. Also, flocculation of the generated Fe3+ ions from the radical reaction significantly enhanced SS removal. GC-MS analysis showed that the compositional diversity of the BECW decreased after oxidation. Meanwhile its biodegradability increased, indicating less bio-toxicity reaching the natural water body. This study suggests that the PS/ZVI system may be an alternative safer and more efficient method than Fenton's method for carrying out an advanced treatment of coking wastewater.

Influence of particle properties on iron flocculation

Abstract In this study, the importance of charge interactions during flocculation of Fe3+ in the presence of particles and anions/cations at various pH values was investigated. SiO2, (s) and ZnO(s) were dosed as particles to promote charge interactions and/or serve as a nucleus to accelerate floc formation. In the pH range 6–9, SiO2, (s) is negatively charged, while ZnO(s) carries a positive charge. Ca2+ and HPO42− were selected to investigate charge interactions in the water phase. A significant delay in floc growth due to charge repulsion between negatively charged iron species was observed at pHini 9. For positively charged species at pHini 6, a delay in floc growth was observed as well, but to a lesser degree. These effects could be neutralized by either dosing (positively charged) ZnO(s) or Ca2+ at pHini 9, or (negatively charged) SiO2, (s) at pHini 6. The addition of phosphate did not hinder floc growth at pHini 6. While phosphate completely inhibited floc growth at pHini 7–9 in the presence of negatively charged SiO2, (s), the presence of positively charged ZnO(s) partly neutralized the detrimental influence of phosphate on floc growth. Similarly, dosing Ca2+ partly neutralized the effect of phosphate.

Iron Chloride Flocculation of Bacteriophages from Seawater.

Viruses influence ecosystem dynamics by modulating microbial host population dynamics, evolutionary trajectories and metabolic outputs. While they are ecologically important across diverse ecosystems, viruses are challenging to study due to minimal biomass often obtained when sampling natural communities. Here we describe a technique using chemical flocculation, filtration and resuspension to recover bacteriophages from seawater and other natural waters. The method uses iron to precipitate viruses which are recovered by filtration onto large-pore size membranes and then resuspended using a buffer containing magnesium and a reductant (ascorbic acid or oxalic acid) at slightly acid pH (6-6.5). The recovery of bacteriophages using iron flocculation is efficient (>90%), inexpensive and reliable, resulting in preparations that are amenable to downstream analysis by next generation DNA sequencing, proteomics and, in some cases, can be used to study virus-host interactions.

Influence of iron precipitated condition and light intensity on microalgae activated sludge based wastewater remediation

The indigenous microalgae-activated sludge (MAAS) process during remediation of municipal wastewater was investigated by studying the influence of iron flocculation step and light intensity. In addition, availability of total phosphorous (P) and photosynthetic activity was examined in fed-batch and batch mode under northern climatic conditions and limited lighting. This was followed by a semi-continuous operation with 4 d of hydraulic retention time and mean cell residence time of 6.75 d in a photo-bioreactor (PBR) with varying P availability. The fed-batch condition showed that P concentrations of 3–4 mg L−1 were effective for photosynthetic chl. a development in iron flocculated conditions. In the PBR, the oxygen evolution rate increased with increase in the concentration of MAAS (from 258 to 573 mg TSS L−1) at higher surface photosynthetic active radiation (250 and 500 μmol m−2 s−1). Additionally, the rate approached a saturation phase at low MAAS (110 mg L−1) with higher light intensities. Semi-continuous operation with luxury P uptake and effective P condition showed stable average total nitrogen removal of 88 and 92% respectively, with residual concentrations of 3.77 and 2.21 mg L−1. The corresponding average P removal was 68 and 59% with residual concentrations of 2.32 and 1.75 mg L−1. The semi-continuous operation produced a rapidly settleable MAAS under iron flocculated condition with a settling velocity of 92–106 m h−1 and sludge volume index of 31–43 ml g−1 in the studied cases.

Development of red sea bream iridovirus concentration method in seawater by iron flocculation

Pathogen dynamics in environmental water are considered to be highly associated with the prevalence of fish disease. To examine the dynamics of red sea bream iridovirus (RSIV), which has caused serious damage in marine aquacultures in Japan, we developed a highly sensitive and quantitative method by combining the viral concentration and real-time PCR to detect the virus in seawater. The iron flocculation method employed here successfully concentrated 500mL of artificial seawater spiked with RSIV in a 0.1-mL DNA solution at a 5000 concentration magnification, and the recovery rate of the RSIV genome by real-time PCR was higher than 80%. The detection limit of this method was approximately 8.0×101RSIVcopiesL−1 of sample water, which is a more than 1000 times improvement compared to the conventional DNA extraction method without concentration of water sample. Using this method, we detected the RSIV genome from the rearing water for experimentally infected Japanese amberjack Seriola quinqueradiata at ranges from 102.1 to 105.5copiesL−1. The RSIV copy number in the rearing water was increased more than 5days before mortality started and it might become an indicator of disease prediction. These results indicate that the iron flocculation method coupled with PCR detection is useful for monitoring RSIV dynamics in the aquaculture setting. Statement of relevanceMonitoring of RSIV in environmental water.