Synergetic Bioproduction of Short-Chain Fatty Acids from Waste Activated Sludge Intensified by the Combined Use of Potassium Ferrate and Biosurfactants

The synergetic effect and underlying mechanism of potassium ferrate(PF)with tea saponin(TS,a biosurfactant)in producing short chain fatty acids(SCFAs)from anaerobic fermentation of waste activated sludge(WAS)were explored in this work.Experimental results showed that 0.2 g PF(g TSS)^(-1)(total suspended solid)combined with 0.02 g TS(g TSS)^(-1) could further improve SCFAs’production,and the maximum SCFAs content reached 2008.7 mg COD L^(-1),which is 1.2 and 4.5 times higher than those with PF and TS individually added,respectively,and 5.3 times higher than that of blank WAS on Day 12.In the model substrates experiments,the degradation rates of bovine serum albumin and dextran with combination of PF and TS were 41.3%±0.1% and 48.5%±0.06%,respectively,on Day 3,which are lower than those in blank WAS(with degradation rates of 72.3%±0.5%and 90.3%±0.3%).It was revealed that the oxidative effect of PF and the solubilization of TS caused more organic matters to be dissolved out from WAS,providing a large number of biodegradable substances for subsequent SCFAs production.While WAS pretreated with the combination of PF and TS,the relative abundances of Firmicutes increased from 6.4%(blank)to 38.6%,and that of Proteobacteria decreased from 41.8%(blank)to 21.8%.The combination of PF and TS promoted the hydrolysis process of WAS by enriching Firmicutes,and then increased acetic acid production by inhibiting Proteobacteria that consumed SCFAs.Meanwhile,at the genus level,acidogenesis bacteria(e.g.,Proteiniclasticum and Petrimonas)were enriched whereas SCFAs consuming bacteria(e.g.,Dokdonella)were inhibited.

Flotation behaviors of chalcopyrite and galena using ferrate(Ⅵ) as a depressant

This paper investigated the effects of potassium ferrate(PF)on the flotation performances of chalcopyrite and galena.The flotation results showed that PF obviously depressed galena,but had little effects on the floatability of chalcopyrite within pH range of 4.0–12.0.Zeta potential tests showed that the addition of PF induced the formation of more amounts of hydrophilic species on the surface of galena under an alkaline environment.Industrial grade O-isopropyl-N-ethyl thionocarbamate(IPETC)chemically adsorbed on the surface of the PF-treated chalcopyrite and galena after its addition.Contact angle measurements showed that with the addition of PF,the contact angle of the galena surface significantly decreased compared with the chalcopyrite surface.Localized electrochemical impedance spectroscopy(LEIS)tests showed that the addition of PF increased the impedance of the galena surface.X-ray photoelectron spectroscopy(XPS)analyses revealed that the formation of hydrophilic species,namely lead sulfite,lead hydroxide and ferric hydroxide,on the galena surface,decreased its floatability in the presence of PF,while the formation of hydrophobic species,namely copper disulfide and elemental sulfur,on the chalcopyrite surface,maintained its floatability.Finally,a descriptive model for the reaction of PF with chalcopyrite and galena was proposed.

Effects of Potassium Ferrate and Low-Temperature Thermal Hydrolysis Co-Pretreatment on the Hydrolysis and Anaerobic Digestion Process of Waste Activated Sludge

This study evaluated the effect of potassium ferrate(PF)and low-temperature thermal hydrolysis co-pretreatment on the promotion of sludge hydrolysis process and the impact on acid production in the subsequent anaerobic digestion process.The analytical investigations showed that co-pretreatment significantly facilitated the hydrolysis process of the sludge and contributed to the accumulation of short-chain fatty acids(SCFAs).The pretreatment conditions under the optimal leaching of organic matter from sludge were hydrothermal temperature of 75℃,hydrothermal treatment time of 12 h,and PF dosage of 0.25 g g^(−1)TSS(total suspended solids),according to the results of orthogonal experiments.By pretreatment under proper conditions,the removal rate of soluble chemical oxygen demand(SCOD)achieved 71.8%at the end of fermentation and the removal rate of total phosphorus(TP)was 69.1%.The maximum yield of SCFAs was 750.3 mg L^(−1),7.45 times greater than that of the blank group.Based on the analysis of the anaerobic digestion mechanism,it was indicated that the co-pretreatment could destroy the floc structure on the sludge surface and improve organic matter dissolving,resulting in more soluble organic substances for the acidification process.Furthermore,microbial community research revealed that the main cause of enhanced SCFAs generation was an increase in acidogenic bacteria and a reduction of methanogenic bacteria.

Application of ferrate(VI) in the treatment of industrial wastes containing metal-complexed cyanides : A green treatment

Ferrate（VI） was employed for the oxidation of cyanide （CN） and simultaneous removal of copper or nickel in the mixed/complexed systems of CN-Cu, CN-Ni, or CN-Cu-Ni. The degradation of CN （1.00 mmol/L） and removal of Cu （0.095 mmol/L） were investigated as a function of Fe（Ⅵ） doses from 0.3-2.00 mmol/L at pH 10.0. It was found that Fe（Ⅵ） could readily oxidize CN and the reduction of Fe（Ⅵ） into Fe（Ⅲ） might serve efficiently for the removal of free copper ions. The increase in Fe（Ⅵ） dose apparently favoured the CN oxidation as well as Cu removal. Moreover, the pH dependence study （pH 10.0-13.0） revealed that the oxidation of CN was almost unaffected in the studied pH range （10.0-13.0）, however, the maximum removal efficiency of Cu was obtained at pH 13.0. Similarly, treatment was carded out for CN-Ni system having the initial Ni concentration of 0.170 mmol/L and CN concentration of 1.00 mmol with Fe（Ⅵ） dose 2.00 mmol at various pH values （10.0-12.0）. Results showed a partial oxidation of CN and partial removal of Ni. It can be observed that Fe（Ⅵ） can partially degrade the CN-Ni complex in this pH range. Further, Fe（Ⅵ） was applied for the treatment of simulated industrial waste/effluent waters treatment containing CN, Cu, and Ni.

Double catholyte electrochemical approach for preparing ferrate-aluminum: a compound oxidant-coagulant for water purification

Ferrate is an excellent water treatment agent for its multi functions in oxidation, disinfection, coagulation and adsorption, but its coagulation ability depends on its dosage and is after its oxidation. This paper focuses on preparing a new kind of ferrate combined with alum to enhance its coagulation function for water purification. An effective electrolysis reactor was designed and employed in the test. Some key parameters in the process of electrolysis concerning the preparation efficiency, such as the current density, temperature and alkalinity were also investigated. The proper conditions for ferrate alum preparation were determined. Under the condition of 5V given voltage, 6h electrolyzing interval, below 2% alum concentration (in weight), a combined liquid ferrate alum products was successfully prepared, which contained 0.0294 mol/L FeO 2- 4 and 0.0302 mol/L total soluble ferron with 2% Al 2O 3. There was no insoluble ferron produced by controlling an optimum electrochemical condition.

Versatile Functionalization of Carbon Nanomaterials by Ferrate(Ⅵ)

As a high-valent iron compound with Fe in the highest accessible oxidation state,ferrate(VI)brings unique opportunities for a number of areas where chemical oxidation is essential.Recently,it is emerging as a novel oxidizing agent for materials chemistry,especially for the oxidation of carbon materials.However,the reported reactivity in liquid phase(H2SO4 medium)is confusing,which ranges from aggressive to moderate,and even incompetent.Meanwhile,the solid-state reactivity underlying the“dry”chemistry of ferrate(VI)remains poorly understood.Herein,we scrutinize the reactivity of K2FeO4 using fullerene C60 and various nanocarbons as substrates.The results unravel a modest reactivity in liquid phase that only oxidizes the active defects on carbon surface and a powerful oxidizing ability in solid state that can open the inert C=C bonds in carbon lattice.We also discuss respective benefit and limitation of the wet and dry approaches.Our work provides a rational understanding on the oxidizing ability of ferrate(VI)and can guide its application in functionalization/transformation of carbons and also other kinds of materials.

Synthesis and Characterization of Ferrate(VI) Alkali Metal by Electrochemical Method

This works aims at preparing at room stable Na2FeO4 and tracking its degradation over time. The synthetic, during this step, was carried out by electrochemical method. The latter was given maximum focus because of its simplicity and the high degree of purity of the resulting product with respect to wet and dry method. This paper reviews the development of the electrochemical method applied to the synthesis of stable at room Na2FeO4, optimizing the parameters impacting the performance of the oxidation of iron(II) in to iron(VI) in alkaline NaOH, saturated at a temperature of 61°C and a current density of 1.4 A/dm2, in order to simplify the synthesis process, to minimize the cost and to improve the production of iron(VI) to meet the growing demand of ferrate(VI) useful for water treatment. The supervision of the degradation of synthesized Na2FeO4 shows its stability over a period of 10 months, which makes storage and transport easier. The phases obtained were characterized by IR spectrometry, X-ray, M?ssbauer, spectroscopy and thermogravimeric analysis.

Effect of Degree of ClO‾Hypochlorite on the Wet Synthesis of Ferrate (VI)

This work is a result of previously done studies on the synthesis of A2FeVIO4 wet ferrate (VI) formula, using chlorine as an oxidant. The major problem of these ferrates is related to their stability over time. This brings us to identify and optimize the critical parameters influencing the preparation of the Na2FeO4 at room stable phase with acceptable performance. The use of water bleach (hypochlorite ClO‾) at a chlorometric degree of 50°F in the synthesis of the Na2FeO4 ambient stable phase promotes the oxidation of iron (II) iron to (VI) in a concentrated NaOH alkaline medium. The synthesis reaction is in the presence of FeSO4 7H2O hydrated iron sulfate at a temperature of about 55°C in order to simplify the synthesis process, to enhance the production of the Fe (VI) and to meet the growing demand of ferrates (VI) for their interest in the treatment of water. Monitoring the degradation of synthesized Na2FeO4 shows its stability up to 12 months, which facilitates storage and transportation. The phases obtained were characterized by IR spectroscopy, and RX by UV spectrophotometer, measuring the optical density at 507 nm.

Electrogeneration of ferrate (Ⅵ) in low concentration NaOH solution for flow-injection-chemiluminescence detection

The possibility of direct analytical applications of ferrate（Ⅵ） solution,which was freshly electrogenerated in low-concentration NaOH electrolyte,was studied by a flow-injection-chemiluminescence（FI-CL） system.It was found that some inorganic ions, organic molecule and biomolecule could enhance the chemiluminescence emission caused by ferrate（Ⅵ）-luminol reaction.V（Ⅴ）, Ca（Ⅱ）,Mg（Ⅱ）,phloroglucinol,and bovine hemoglobin（Hb） chosen as samples were successfully detected by this developed method.The analytical characteristics of the system for the analytes determination including linear ranges,correlation coefficients, limits of detection combined with FI analysis were studied.

Process for the Synthesis of Ferrate (VI) Alkali Metal Dry

The iron compounds in the oxidation state (VI) have the specific advantage of being powerful oxidants and bactericides. This feature explains their particular interest in the treatment of water. The aim of this work is to prepare Na2FeO4 stable at ambient in order to optimize the key parameters influencing the performance of the oxidation of iron (II) to iron (VI), as well as to monitor its degradation over time. The synthesis of this phase has been carried out by using the dry reaction Na2O2 with Fe2O3 with a temperature of 700°C for a reaction time of 13 hours with a Na/Fe ratio of 4 to make it possible to simplify the synthesis procedure, to minimize the cost and enhance the production of iron (VI) to meet the growing demand of ferrate (VI) for its interest in water treatment. The obtained phase was characterized by UV spectrophotometer by measuring the optical density at a wavelength of 507 nm.

Effects of operating conditions on iron(hydr)oxides evolution and ciprofloxacin degradation in potassium ferrate-ozone stepwise oxidation system

In this study,a stepwise oxidation system of potassium ferrate(K_(2)FeO_(4))combined with ozone(O+3)was used to degrade ciprofloxacin(CIP).The effects of pH and pre-oxidation time of K_(2)FeO_(4) on the evolution of K_(2)FeO_(4) reduction products(iron(hydr)oxides)and CIP degradation were investigated.It was found that in addition to its own oxidation capacity,K_(2)FeO_(4) can also influence the treatment effect of CIP by changing the catalyst content.The presence of iron(hydr)oxides effectively enhanced the mineralization rate of CIP by catalyzing ozonation.The pH value can influence the content and types of the components with catalytic ozonation effect in iron(hydr)oxides.The K_(2)FeO_(4) pre-oxidation stage can produce more iron(hydr)oxides with catalytic components for subsequent ozonation,but the evolution of iron(hydr)oxides components was influenced by O_(3) treatment.It can also avoid the waste of oxidation capacity owing to the oxidation of iron(hydr)oxides by O_(3) and free radicals.The intermediate degradation products were identified by Fourier transform ion cyclotron resonance mass spectrometry(FT-ICR-MS).Besides,the degradation pathways were proposed.Among the degradation products of CIP,the product with broken quinolone ring structure only appeared in the stepwise oxidation system.

Transformation and migration of phosphorus in excess sludge reduction pretreatment by alkaline ferrate oxidation combined with anaerobic digestion

Recently,more and more attention has been paid to the strong oxidation ability of newly prepared potassium ferrate(NAPF) in sludge reduction process,but less attention has been paid to the change of phosphorus in this process.The feasibility of phosphorus migration and transformation during excess sludge reduction pretre atment using NAPF pre-oxidation combined with anaerobic digestion was investigated.After 70 mg/g suspended solids NAPF pretreatment and 16 days anaerobic digestion,the solid-phase volatile suspended solids decreased by 44.2%,and much organic matter had been released into the liquid-phase and then degraded during digestion by indigenous microorganisms.As the sludge pre-oxidation process was performed,solid-phase organic phosphorus and chemically combined phosphorus also released into the liquid-phase as PO4^3-,peaking at 100 mg/L.During anaerobic digestion,the Fe3+in the liquid-phase was gradually reduced to Fe2+,and then formed Fe^2+-PO4^3- compound crystals and re-migrated to the solid-phase.The concentration of PO4^3- decreased to 17.08± 1.1 mg/L in the liquid-phase after anaerobic digestion.Finally,the phosphorus in the Fe^2+-PO4^3- compound accounts for 80% of the total phosphorus in the solid-phase.A large number of vivianite crystals in sludge were observed.Therefore,this technology not only effectively reduces sludge,but also increases the proportion of PO43-in the sludge in the form of Vivianite.

Potassium ferrate pretreatment promotes short chain fatty acids yield and antibiotics reduction in acidogenic fermentation of sewage sludge

During the acidogenic fermentation converting waste activated sludge (WAS) into shortchain fatty acids (SCFA), hydrolysis of complex organic polymers is a limiting step and the transformation of harmful substances (such as antibiotics) during acidogenic fermentation is unknown. In this study, potassium ferrate (KFeO) oxidation was used as a pretreatment strategy for WAS acidogenic fermentation to increase the hydrolysis of sludge and destruct the harmful antibiotics. Pretreatment with KFeOcan effectively increase the SCFA production during acidogenic fermentation and change the distribution of SCFA components.With the dosage of 0.2 g/g TS, the maximum SCFA yield was 4823 mg COD/L, which is 28.3times that of the control group;acetic acid accounts for more than 90% of the total SCFA. The higher dosage (0.5 g/g TS) can further increase the proportion of acetic acid, but inhibit the overall performance of SCFA production. Apart from the promotion of hydrolysis and acidogenesis, KFeOpretreatment can also simultaneously oxidizes and degrades part of the antibiotics in the sludge. When the dosage is 0.5 g/g TS, the degradation efficacy of antibiotics is the most significant, and the contents of ofloxacin, azithromycin, and tetracycline in the sludge are reduced by 69%, 42%, and 50%, respectively. In addition, KFeOpretreatment can also promote the release of antibiotics from sludge flocs, which is conducive to the simultaneous degradation of antibiotics in the subsequent biological treatment process.

Spontaneous polarization enhanced bismuth ferrate photoelectrode:fabrication and boosted photoelectrochemical water splitting property

In this paper,the fabrication of a highly orientated Bi_(2)Fe_(4)O_(9)(BFO)photoelectrode in the presence of two-dimensional(2D)graphene oxide(GO)was reported.It was found that the GO can be used as a template for controlling the growth of BFO,and the nanoplate composites of BFO/reduced graphene oxide(RGO)with a high orientation can be fabricated.The thickness of the nanoplates became thinner as the ratio of GO increased.As a result,the ferroelectric spontaneous polarization unit arranges itself in the space in a periodic manner,leading to the formation of a polarization field along a special direction.Therefore,the created built-in electric field of the nanoplate composites of BFO/RGO is improved upon the increase of the amount of RGO.As expected,carrier separation is enhanced by the built-in electric field,therefore substantially enhancing the photoelectrochemical(PEC)activity of water splitting compared to pure BFO under the irradiation of visible-light.

On-line batch production of ferrate with an chemical method and its potential application for greywater recycling with Al(Ⅲ) salt

Ferrate（Ⅵ ） salt is an oxidant and coagulant for water and wastewater treatment. It is considered as a possible alternative method in greywater treatment. However, challenges have existed in putting ferrate（Ⅵ ） technology into full-scale practice in water and wastewater treatment due to the instability of ferrate solution and high production cost of solid ferrate products. This study demonstrated a new approach of greywater treatment with on-line batch production of Fe（Ⅵ ） to which Fe（Ⅲ ） salt was oxidized at a weak acidity solution. A series of experiments were conducted to investigate the effect of Fe（Ⅵ ） on light greywater（total organic carbon（TOC） = 19.5 mg/L） and dark greywater（TOC = 55 mg/L）treatment under different conditions with varying p H and Fe（Ⅵ ） doses. In addition, the combination use of Fe（Ⅵ ） and Al（Ⅲ ） salts was proved to be more efficient than using the Fe（Ⅵ ） salts alone at greywater recycling. The optimum dosage of Fe（Ⅵ ）/Al（Ⅲ ） salts was 25/25 mg/L for light greywater, 90/60 mg/L for dark greywater, respectively. The TOC values of both light greywater and dark greywater were reduced to less than 3 mg/L with the dosages.The cost for treating greywater was 0.06–0.2 $/ton at ferrate（Ⅵ ） dosage of 25–90 mg/L and0.008–0.024 $/ton at AlCl3 dosage of 25–60 mg/L. The full operating cost needs further assessment before the Fe（Ⅵ ）/Al（Ⅲ ） technology could be implemented in greywater treatment.

Modeling the aqueous reaction kinetics of estriol with ferrate

In this study the aqueous oxidation kinetics of estriol(E3)by potassium ferrate(K_(2)FeO_(4)),a chemical for its strong oxidizing power and for producing a coagulant from its reduced state(i.e.Fe(III)),was evaluated in the range of pH 8–12 with different molar ratios of the reactants.As the degree of Fe(VI)protonation varies with the solution pH,it was found that afirst order model was not suitable to describe the oxidation reaction.This paper describes a theoretical representation that closely models the reaction kinetics of E3 and ferrate.From this modeling,the reaction rates of HFeO_(4)^(-) and FeO_(4)^(2-) with E3 have been determined.The results show that the reactivity of HFeO–with dissociated and undissociated E3 is greater than that4 of FeO_(4)^(2-),and that E3 is more reactive in its dissociated state.

Nitric oxide removal from flue gas by ferrate(Ⅵ)/urea solutions

In this work,nitric oxide absorption process by using ferrate(Ⅵ)/urea was proposed.The respective influences of the four factors including pH value,ferrate(Ⅵ) concentration,urea concentration,and the temperature and the interactive function of them on nitric oxide absorption were investigated with the response surface methodology(RSM) by central composite design(CCD).The proposed model system showed good consistency with the experiment results,by a correlated coefficient(R^(2)) of 0.9875.In addition,the interactive influences between any two variables were elaborated through analysis of response surface.The optimal parameters were found at pH of 7.1,reaction temperature of 43.8C,urea concentration of 6.3 wt%,ferrate(Ⅵ) concentration of 4.4 mmol/L for 85.2% NO absorption.Finally,Ncontaining product analysis shows that nitric oxide was primarily transformed to N2 and NO_(3)^(-).

Efficient iodination of aromatic compounds using potassium ferrate supported on montmorillonite

Potassium ferrate impregnated on montmorillonite is a mild,cheap,and non-toxic reagent for the iodination of phenols, including naphthol,aromatic amines,and heterocyclic substrates in fair to excellent yields by a simple isolation procedure.

Comparative study on the removal technologies of 2-methylisoborneol(MIB) in drinking water

Removal of 2-methylisoborneol （MIB） in drinking water by ozone, powdered activated carbon （PAC）, potassium permanganate and potassium ferrate was investigated. The adsorption kinetics of MIB by both wood-based and coat-based PACs show that main removal of MIB occurs within contact time of 1 h. Compared with the wood-based PAC, the coat-based PAC evidently improved the removal efficiency of MIB. The removal percentage of trace MIB at any given time for a particular carbon dosage was irrelative to the initial concentration of MIB. A series of experiments were performed to determine the effect of pH on the ozonation of MIB. The results show that pH has a significant effect on the ozonation of MIB. It is conclusive that potassium permanganate and potassium ferrate are ineffective in removing the MIB in drinking water.