Aspects of iron and nitrogen nutrition in the red tide dinoflagellateGymnodinium sanguineum

Iron-stress-mediated effects on biochemical constituents of the red tide dinoflagellateGymnodinium sanguineum Hirasaka were examined in 1988 by comparing Fe-replete and Fe-deplete batch cultures. The influence of nitrogen source (NO₃ or NH₄) on characteristics of Fe-deplete cells was also studied [i.e., Fe-deplete/NO₃-grown (= — Fe/NO₃) vs Fe-deplete/NH₄-grown (= — Fe/NH₄)]. Common to both N sources were reductions of chlorophylla (chla) and Fe quotas (per cell volume) by 75% and ca. 1.5 orders of magnitude, respectively, under Fe depletion. The Fe requirement ofG. sanguineum exceeded those of certain neritic diatoms by one to two orders of magnitude. — Fe/NH₄ cells exhibited 30 to 50% greater N quotas and free amino acid:protein ratios than did Fe-deplete cells grown on NO₃. In vivo fluorescence:chla increased with Fe deficiency particularly in — Fe/NO₃ cultures, surpassing — Fe/NH₄ values by ca. two-fold. Effects of Fe depletion were consistent with this element's essential role in the biosynthesis of chla and components of the photosynthetic electron transport (PET) system, and also in NO₃ utilization. Fe:N ratios were larger (1.5-fold) for iron-deficient NO₃-grown than NH₄-grown cells, likely reflecting the Fe content of NO₃ assimilatory enzymes [nitrate (NR) and nitrite (NiR) reductase] and of electron transport components needed to provide reductant, coupled with a diminished capacity of — Fe/NO₃ cells to acquire and assimilate nitrogen. Indicators of PET efficiency suggested that under iron stress, supply of Fe for NR and NiR is partly at the expense of iron-containing PET components. Utilization of nitrate by NO₃-grown cells was inhibited sufficiently by Fe depletion to yield symptoms bordering on N deficiency. In an ecological context, the most important effect mediated by nitrogen source may be the determination of critical Q_Fe (i.e., Fe required to just sustain maximal growth), thereby regulating the degree of growth limitation for a given subsaturating iron concentration.     

Pollutant removal by an integrated vertical-flow constructed wetland treating simulated river water by reoxygenation

The effects and mechanism of chemical oxygen demand (COD), nitrogen, and phosphorus concentration removal by an integrated vertical-flow constructed wetland were studied in the wetland system during one inlet–outlet operating period, in two typical stages (each stage is connective 24 h, sampled once every 4 h). The concentration of ammonia decreased along the flow direction in the system, while levels of nitrate (NO₃^?-N) increased. In one operating period, total nitrogen (TN) concentration fell with rising operation time due to evacuative reoxygenation. The TN and NH₃-N removal rates in the system were 26.6% and 97.5%, respectively. COD decreased rapidly in the early stages and more gradually in the direction of water flow of the wetland system. Average total phosphorus (TP) removal rate was 20.71%. TN and NO₃^?-N levels in water of the wetland had a tendency to decline gradually with increasing operation time. Ammonia concentrations displayed only a small variation with operation time. The results also indicated that the wetland was able to maintain its temperature. The oxygen content differed during the various operating stages and exerted a marked influence on COD, TP, and TN removal.     

Optimization of denitrifying phosphorus removal in a pre-denitrification anaerobic/anoxic/post-aeration + nitrification sequence batch reactor (pre-A<Subscript>2</Subscript>NSBR) system: Nitrate recycling,carbon/nitrogen ratio and carbon source type

Because the efficiency of biological nutrient removal is always limited by the deficient carbon source for the low carbon/nitrogen (C/N) ratio in real domestic sewage, the denitrifying phosphorus removal (DNPR) was developed as a simple and efficient method to remove nitrogen and phosphorous. In addition, this method has the advantage of saving aeration energy while reducing the sludge production. In this context, a pre-denitrification anaerobic/anoxic/post-aeration + nitrification sequence batch reactor (pre-A₂NSBR) system, which could also reduce high ammonia effluent concentration in the traditional two-sludge DNPR process, is proposed in this work. The pre-A₂NSBR process was mainly composed of a DNPR SBR and a nitrifying SBR, operating as alternating anaerobic/anoxic/post-aeration + nitrification sequence. Herein, the long-term performance of different nitrate recycling ratios (0–300%) and C/N ratios (2.5–8.8), carbon source type, and functional microbial community were studied. The results showed that the removal efficiency of total inorganic nitrogen (TIN, including NH₄⁺-N, NO₂^– -N, and NO₃^– -N) gradually increased with the nitrate recycling ratios, and the system reached the highest DNPR efficiency of 94.45% at the nitrate recycling ratio of 300%. The optimum C/N ratio was around 3.9–7.3 with a nitrogen and phosphorus removal efficiency of 80.15% and 93.57%, respectively. The acetate was proved to be a high-quality carbon source for DNPR process. The results of fluorescence in situ hybridization (FISH) analysis indicated that nitrifiers and phosphorus accumulating organisms (PAOs) were accumulated with a proportion of 19.41% and 26.48%, respectively.

Open image in new window

     

Kinetics of hexavalent chromium reduction by iron metal

The kinetics of Cr(VI) reduction to Cr(III) by metallic iron (Fe⁰) was studied in batch reactors for a range of reactant concentrations, pH and temperatures. Nearly 86.8% removal efficiency for Cr(VI) was achieved when Fe⁰ concentration was 6 g/L (using commercial iron powder (< 200 mesh) in 120 min). The reduction of hexavalent chromium took place on the surface of the iron particles following pseudo-first order kinetics. The rate of Cr(VI) reduction increased with increasing Fe⁰ addition and temperature but inversely with initial pH. The pseudo-first-order rate coefficients (k _obs) were determined as 0.0024, 0.010, 0.0268 and 0.062 8 min^?1 when iron powder dosages were 2, 6, 10 and 14 g/L at 25°C and pH 5.5, respectively. According to the Arrehenius equation, the apparent activation energy of 26.5 kJ/mol and pre-exponential factor of 3 330 min^?1 were obtained at the temperature range of 288–308 K. Different Fe⁰ types were compared in this study. The reactivity was in the order starch-stabilized Fe⁰ nanoparticles > Fe⁰ nanoparticles > Fe⁰ powder > Fe⁰ filings. Electrochemical analysis of the reaction process showed that Cr(III) and Fe(III) hydroxides should be the dominant final products.     

Synthesis of nanoiron by microemulsion with Span/Tween as mixed surfactants for reduction of nitrate in water

Denitrification of nitrate in groundwater using iron nanoparticles has received increasing interest in recent years. In order to fabricate iron nanoparticles with homogeneously spherical shape and narrow size distribution, a simple and “green” method was developed to synthesize iron nanoparticles. The conventional microemulsion methods were modified by applying Span 80 and Tween 60 as mixed surfactants. The maximum content of water in the Water-in-oil (W/O) microemulsion and its appropriate forming conditions were found, and then the microemulsion system consisting of saturated Fe²⁺ solution was used to synthesize α-Fe ultrafine particles by redox reaction. The nanoparticles were characterized by using powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results show that the average diameter of the particle is about 80–90 nm. The chemical activity of the obtained iron nanoparticles was studied by the denitrification experiment of nitrate. The results show that under the experimental conditions, iron removed most of the 80 mg/L nitrate within 30 min. The mass balance of nitrate reduction with nanoscale Fe indicates that endproducts are mainly ammonia. Two possible reaction pathways for nitrate reduction by nanoscale iron particles have been proposed in this work.     

Adsorption of phosphate ions from water using a novel cellulose-based adsorbent

A novel cellulose-based adsorbent, iron(III)-coordinated amino-functionalised poly(glycidylmethacrylate)-grafted cellulose [Fe(III)–AM-PGMACell] was developed for the removal of phosphate from water and wastewater. The scanning electron micrograph showed that AM-PGMACell has a rougher surface than cellulose and the adsorption of Fe(III) on AM-PGMACell made the surface even rougher. Infrared spectroscopy revealed that amino groups on the surface of AM-PGMACell complexed with Fe(III) played an important role in the removal of phosphate from solutions. X-Ray diffraction patterns showed a decrease in crystallinity after graft copolymerisation onto cellulose. The effects of contact time, initial sorbate concentration, pH, agitation speed, dose of adsorbent and temperature on the removal process were investigated. Maximum removal of 99.1% was observed for an initial concentration of 25 mg·L ^?1 at pH 6.0 and an adsorbent dose of 2.0 g·L ^?1. A two-step pseudo-first-order kinetic model and Sips isotherm model represented the measured data very well. Complete removal of 11.6 mg·L ^?1 phosphate from fertiliser industry wastewater was achieved by 1.6 g·L ^?1 Fe(III)–AM-PGMACell. The adsorbent exhibited very high reusability for several cycles. Overall, the study demonstrated that Fe(III)–AM-PGMACell can be used as an efficient adsorbent for the removal and recovery of phosphate from water and wastewater.     

Effects of La3+, Ce3+ on nitrogen removal in sequencing batch reactor

Batch experiments were conducted to study the short-term biological effects of rare earth ions (La³⁺, Ce³⁺) and their mixture on the nitrogen removal in a sequencing batch reactor (SBR). The data showed that higher NH₄ ⁺-N removal rate, total inorganic nitrogen removal efficiency, and denitrification efficiency were achieved at lower concentrations of rare earth elements (REEs) (<1 mg/L). In the first hour of the aeration stage of SBR, the presence of REEs increased the total inorganic nitrogen removal efficiency and NH₄ ⁺-N removal efficiency by 15.7% and 10%–15%, respectively. When the concentrations of REEs were higher than 1 mg/L, the total inorganic nitrogen removal efficiency decreased, and nitrate was found to accumulate in the effluent. When the concentrations of REEs was up to 50.0 mg/L, the total inorganic nitrogen removal efficiency was less than 30% of the control efficiency with a high level of nitrate. Lower concentrations of REEs were found to accelerate the nitrogen conversion and removal in SBR.     

Kinetics of the oxidation of endocrine disruptor nonylphenol by ferrate(VI)

The kinetics of the oxidation of endocrine disruptor nonylphenol (NP) by potassium ferrate(VI) (K₂FeO₄) in water as a function of pH 8.0–10.9 at 25°C is presented. The observed second-order rate constants, k _obs, decrease with an increase in pH 269–32 M^?1 s^?1. The speciation of Fe(VI) (HFeO ₄ ^? and FeO ₄ ^2? ) and NP (NP–OH and NP–O^?) species was used to explain the pH dependence of the k _obs values. At a dose of 10 mg L^?1 (50 μM) K₂FeO₄, the half-life for the removal of NP by Fe(VI), under water treatment conditions, is less than 1 min.     

Chemically modified biochar produced from conocarpus waste increases NO<Subscript>3</Subscript> removal from aqueous solutions

Biochar has emerged as a universal sorbent for the removal of contaminants from water and soil. However, its efficiency is lower than that of commercially available sorbents. Engineering biochar by chemical modification may improve its sorption efficiency. In this study, conocarpus green waste was chemically modified with magnesium and iron oxides and then subjected to thermal pyrolysis to produce biochar. These chemically modified biochars were tested for NO₃ removal efficiency from aqueous solutions in batch sorption isothermal and kinetic experiments. The results revealed that MgO-biochar outperformed other biochars with a maximum NO₃ sorption capacity of 45.36 mmol kg^?1 predicted by the Langmuir sorption model. The kinetics data were well described by the Type 1 pseudo-second-order model, indicating chemisorption as the dominating mechanism of NO₃ sorption onto biochars. Greater efficiency of MgO-biochar was related to its high specific surface area (391.8 m² g^?1) and formation of strong ionic complexes with NO₃. At an initial pH of 2, more than 89 % NO₃ removal efficiency was observed for all of the biochars. We conclude that chemical modification can alter the surface chemistry of biochar, thereby leading to enhanced sorption capacity compared with simple biochar.     

Short-term effects of excessive anaerobic reaction time on anaerobic metabolism of denitrifying polyphosphate-accumulating organisms linked to phosphorus removal and N2O production

The short-term effect of anaerobic reaction time (AnRT) (i.e., 90, 120 and 150 min) on the denitrifying phosphorus (P) removal performance and N₂O production was examined using a denitrifying enhanced biologic phosphorus removal (EBPR) sludge acclimatized with mixed acetate (HAc) and propionate (Pro) (in the molar ratio 3:1) as carbon sources. The results showed that when the AnRT was prolonged from 90 to 150 min, the anaerobic polyhydroxyalkanoate (PHA) synthesis was decreased by 15.3%. Moreover, the ineffective PHA consumption occurred in anaerobic phases and contributed to an increased NO ₂ ^? -N accumulation and higher free nitrous acid (FNA) concentrations (?0.001–0.0011 mg HNO₂-N/L) in the subsequent anoxic phases, causing a severe inhibition on anoxic P-uptake and denitrification. Accordingly, the total nitrogen (TN) and total phosphorus (TP) removal efficiencies dropped by approximately 6.3% and 85.5%, respectively; and the ratio of anoxic N₂O-N production to TN removal increased by approximately 3.8%. The fluorescence in situ hybridization (FISH) analysis revealed that the sludge was mainly dominated by Accumulibacter (62.0% (SE_mean = 1.5%)). In conclusion, the short-term excessive anaerobic reaction time negatively impacted denitrifying P removal performance and stimulated more N₂O production, and its effect on P removal was more obvious than that on nitrogen removal.     

Circulating fluidized bed biological reactor for nutrients removal

A new biological nitrogen removal process, which is named herein “The circulating fluidized bed bioreactor (CFBBR)”, was developed for simultaneous removal of nitrogen and organic matter. This process was composed of an anaerobic bed (Riser), aerobic bed (Downer) and connecting device. Influent and nitrified liquid from the aerobic bed enters the anaerobic bed from the bottom of the anaerobic bed, completing the removal of nitrogen and organic matter. The system performance under the conditions of different inflow loadings and nitrified liquid recirculation rates ranging from 200% to 600% was examined. From a technical and economic point of view, the optimum nitrified liquid recirculation ratewas 400%. With a shortest total retention time of 2.5 h (0.8 h in the anaerobic bed and 1.5 h in the aerobic bed) and a nitrified liquid recirculation rate of 400% based on the influent flow rate, the average removal efficiencies of total nitrogen (TN) and soluble chemical oxygen demand (SCOD) were found to be 88% and 95%, respectively. The average effluent concentrations of TN and SCOD were 3.5 mg/L and 16 mg/L, respectively. The volatile suspended solid (VSS) concentration, nitrification rate and denitrification rate in the system were less than 1.0 g/L, 0.026-0.1 g NH₄ ⁺-N/g VSS·d, and 0.016–0.074 g NO_x ^?-N/g VSS·d, respectively.     

Seasonal variation in total and soluble tissue nitrogen of Pleurophycus gardneri (Phaeophyceae: Laminariales) in relation to environmental nitrate

Seasonal variations in tissue nitrogen (ethanol soluble nitrate and ninhydrin positive substances, as well as total nitrogen) of different thallus parts of Pleurophycus gardneri Setchell and Saunders were monitored simultaneously with ambient seawater nitrate from 1982 until 1984 in Bamfield, Vancouver Island, British Columbia, Canada. A trend of low, nearly zero levels in ambient nitrate typical for the area in late spring and early summer normally contrasts with average nitrate concentrations of 10 mol NO₃ ^- l^-1 in late fall and winter. Total nitrogen content was greater in the perennial thallus parts, stipe and holdfast than in the annual blade and peaked in fall and early winter. The longitudinal thallus distribution of nitrate revealed a distinct and significant concentration of nitrate in the haptera reaching at maximum 8% nitrate-N of the internal total nitrogen. Internal nitrate concentration ranged from 20 to 5 000 times the ambient nitrate concentration in the midrib, and from 40 to 3 100 times in the wing, while the range was greatest with 400 to 14 000 times in the haptera. P. gardneri contained at most about 7 mol NO₃ ^- g fresh wt^-1 in the blade, which corresponds to about 6% of total tissue nitrogen. Ninhydrin positive substances comprised the major portion of the soluble N pool in P. gardneri and showed a pronounced seasonality. Concentrations of ninhydrin positive substances ranged from 20 to 800 g N g fresh wt^-1 in the midrib and in the wing. In the stipe, ninhydrin positive substances varied from 180 to 2 200 g N g fresh wt^-1, and from 250 to 1 200 g N g fresh wt^-1 in the haptera. Evidence is given that (1) the perennial parts, stipe and haptera of P. gardneri contain the majority of nitrogen products independent of season and ontogenetic stage; (2) ninhydrin positive substances are the most abundant internal nitrogen constituents; (3) the low N values in the blade in summer suggest a nitrogen limited growth; and (4) nitrate may not be the predominant external nitrogen source.     

Duckweed: an effective tool for phyto-remediation

Effective wastewater treatment through conventional methods that rely on heavy aeration are expensive to install and operate. Duckweed is capable of recovering or extracting nutrients or pollutants and is an excellent candidate for bio-remediation of wastewaters. Such plants grow very fast, utilizing wastewater nutrients and also yield cost effective protein-rich biomass as a by-product. Duckweeds being tiny surface-floating plants are easy to harvest and have an appreciable amount of protein (15%–45% dry mass basis) and a lower fiber (7%–14% dry mass basis) content. Besides nutrient extraction, duckweeds has been found to reduce total suspended solids, biochemical oxygen demand (BOD), and chemical oxygen demand in wastewater significantly. Depending on the initial concentrations of nutrients, duckweed-covered systems can remove nitrate (NO₃^?) at daily rates of 120–590 mg NO₃^? m^?2 (73%–97% of initial concentration) and phosphate (PO₄^?) at 14–74 mg PO₄^? m^?2 (63%–99% of initial concentration). Removal efficiencies within 3 days of 96% and 99% have been reported for BOD and ammonia (NH₃). Besides several genera of duckweeds (Spirodela, Lemna, Wolffia), other surface-floating aquatic plants like water hyacinth (Eichhornia) are well known for their phyto-remediation qualities.     

Effect of humic acids,nitrate and oxygen on the photodegradation of the flubendiamide insecticide: identification of products

Flubendiamide is a ryanodine insecticide that shows a strong insecticidal activity and is relatively safe for non-target organisms. Actually only flubendiamide and its product desiodo-flubendiamide have been studied during catalytic degradation using TiO₂ and ZnO. Therefore, here we tested the photocatalytic removal of flubendiamide in the presence of nitrates or humic acids. Degradation kinetics were monitored using high-performance liquid chromatography ultraviolet–visible detector. Product identification was done using a high-resolution time-of-flight mass spectrometer coupled to a gas chromatograph (GC-HRMS). Results show that the addition of humic acids at 10 mg l^?1 increased the removal of flubendiamide more than five times. The addition of nitrate ions at 10 mg l^?1 had no influence. The removal of flubendiamide was more than ten times faster in experiments with oxygen purging. Fourteen degradation products were identified, which can be classified into three groups: phthalimide and related phthalic acid derivatives, fluorinated species related to the second amide moiety, and advanced transformation products.     

Comparison between chemical and isotopic measurements of biological nitrate utilization: further evidence of low new-production levels in the equatorial Pacific

New-production (nitrate uptake) rates in the equatorial Pacific were estimated by parallel measurements of nitrate disappearance from sea water using a colorimetric method and of ¹⁵N-labelled nitrate (¹⁵NO₃ ⁻) incorporation into particulate organic nitrogen (PON) collected on GF/F filters (net nitrate uptake, conventional ¹⁵N-tracer method) and Anopore (0.2 μm) membranes. Regression analyses of 74 sample pairs gathered during 12 and 24 h productivity experiments revealed a significant positive relationship between decreasing nitrate level and ¹⁵NO₃ ⁻ accumulation into PON retained on GF/F filters, but the slopes of Model I and Model II regression lines were 1.18 and 1.29, respectively, suggesting that 15 to 22% of ¹⁵NO₃ ⁻ removed from the dissolved fraction were lost to another N-pool. Two possible avenues for the missing ¹⁵NO₃ ⁻ have been examined: uptake by submicron particles passed through the GF/F filters, and loss as dissolved organic nitrogen (DON). Nitrate uptake by small cells not recovered on GF/F filters, could be safely eliminated as a cause of loss, since ¹⁵NO₃ ⁻ uptake rates obtained from ¹⁵N entering PON collected on GF/F filters agreed well with those obtained from ¹⁵N entering PON collected on Anopore membranes (32 sample pairs). Inspection of the DON pool of 0.2 μm filtrates for excess-¹⁵N enrichment (20 samples) revealed that in nitrate-rich waters (equatorial upwelling between 1°N and 10°S), loss of ¹⁵NO₃ ⁻ as DO¹⁵N accounted for <5% of net nitrate uptake. In samples from subtropical oligotrophic waters (from 11°S southward), however, ¹⁵NO₃ loss as DO¹⁵N represented up to 20% of net NO₃ ⁻ uptake. These results, as well as experimental considerations concerning the use of colorimetric and isotopic methods to measure new production show that: (1) earlier reported high discrepancies between nitrate decreases (ΔNO₃ ⁻) and ¹⁵NO₃ ⁻ incorporation into filterable particles (ΔNO₃ ⁻/¹⁵NO₃ ⁻ incorporation >2) were probably erroneous; (2) the use of GF/F filters does not result in an underestimation of new production, although it was found to underestimate PON concentrations by up to 60%; (3) in the equatorial upwelling area (1°N to 10°S), which has high ambient nitrate levels (>2000 nmol l⁻¹) but only slight changes in concentration (0 to 80 nmol l⁻¹ d⁻¹), new production is more accurately estimated by the isotopic method than by the chemical method; (4) in subtropical oligotrophic waters (from 11°S southward) with low ambient nitrate levels (0 to 100 nmol l⁻¹), both procedures are appropriate as long as nitrate removal per incubation period is >3 nmol l⁻¹ (lower rates are only detectable with the isotopic method); (5) the traditional ¹⁵N-tracer technique does not substantially underestimate net new-production in the equatorial Pacific, and failure to account for the loss of ¹⁵NO₃ ⁻ as DON, i.e. to estimate gross nitrate uptake (gross uptake = net uptake + ¹⁵N loss) tends to underestimate new production on an average by only 10%. Overall, the apparent low level of new production in the nitrate-rich area of the central equatorial Pacific seems to be a fact, and may be ascribable to other nutrient (macro and micro) deficiencies and/or to intense in situ recycling of ammonium and nitrate (regenerated production) rather than to inaccurate nitrate uptake rates measured with the classical ¹⁵N-tracer technique. Received: 24 November 1998 / Accepted 10 March 2000     

One-step synthesis of bentonite-supported nanoscale Fe/Ni bimetals for rapid degradation of methyl orange in water

Although nanoscale zero-valent iron (nano-Fe⁰) is used to remediate pollutants, this reagent still presents stability and reactivity issues. To solve those issues, we synthesized bentonite-supported nanoscale iron bimetals B-Fe/Ni and B-Fe/Pd. We then used those reagents to degrade the methyl orange dye in water. Results of scanning electron microscopy and X-ray diffraction showed that the presence of bentonite and bimetal decreased nanoscale iron aggregation and increased methyl orange removal efficiency. More than 90 % of methyl orange at 100 mg/L was degraded by B-Fe/Ni (0.15 g/L) in 10 min. By comparison, only 62 % of methyl orange was degraded by B-Fe, and 35 % of methyl orange was degraded by nano-Fe⁰. The degradation rate decreased with the increase of the initial concentration of methyl orange. Lower pH allowed fast removal of methyl orange. Overall our findings show that a nanoscale Fe/Ni on bentonite-supported material is more efficient than nano-Fe⁰. One-step synthesis is more convenient than current two-step-synthesized nanoscale bimetals. Bentonite-supported nanoscale bimetals could therefore be an economic competitive candidate for contaminated water remediation.     

Effects of nitrite on phosphate uptake in anaerobic-oxic process

An anaerobic-oxic (A/O) biological phosphorus removal reactor was operated to study the effect of nitrite on phosphate uptake. The phosphorus uptake profile was determined under different operating conditions. The results indicated that in addition to oxygen and nitrate (DPB_Na, nitrate denitrifying phosphorus removal), to some extent, nitrite could also serve as an electron acceptor to achieve nitrite denitrifying phosphorus removal (DPB_Ni). The quantity and rate of phosphorus uptake of DPB_Ni, however, were evidently lower than that of DPB_Na. The experiment results revealed that nitrite would bring toxic action to phosphate-accumulating organisms (PAOs) when NO₂ ^?-N ? 93.7 mg/L. The nitrite existing in the anoxic reactor made no difference to the quantity and rate of denitrifying phosphorus removal, but it could reduce the consumption of nitrate. Moreover, the data showed that the aerobic phosphate uptake of DPB_Ni was lower than that of anaerobic phosphorus-released sludge in a traditional A/O process. However, there was not much difference between these two kinds of sludge in terms of the total phosphorus uptake quantity and the effluent quality.     

Removal of acid yellow 36 using Box–Behnken designed photoelectro-Fenton: a study on removal mechanisms

Photoelectro-Fenton was applied for the removal of acid yellow 36 (AY36) from synthetic aqueous solution using iron electrodes. A Box–Behnken design was used for optimization of the effects of pH, H₂O₂ concentration, current density, and reaction time. Individual effects of these variables were more important than their interaction effects. The derived model was in good agreement with the experimental results. Total organic carbon was determined in solution and sludge in order to clarify the removal mechanism. Increase of H₂O₂ concentration and current density led to domination of oxidation and coagulation mechanisms, respectively. The effects of scavenging and inhibiting agents were also investigated: (1) presence of alcohols can reduce the efficiency through competition with dye for reaction with hydroxyl radicals; (2) anions (NO₃^?, HCO₃^?, and H₂PO₄^?) scavenged hydroxyl radicals and reduced decolorization of AY36.     

Color removal efficiency of dyes using nanozerovalent iron treatment

In this study, zerovalent iron nanoparticles (Fe⁰) were synthesized by chemical reduction method using ferric chloride hexahydrate (FeCl₃?·?6H₂O) as a starting material. Sodium borohydride (NaBH₄) was used as a reducer. The synthesized nanozerovalent iron (NZVI) was separated using magnets. The X-ray diffraction pattern of iron (Fe) nanoparticles showed that the presence of intensive diffraction peak at 2θ value of 45.33° from the lattice plane of face-centered cubic Fe unequivocally indicates that the particles are made of pure Fe. The size of the synthesized NZVI was found to be 16.64?nm. The scanning electron micrograph revealed that the particles have a hexagonal and spherical shape in nature. EDX showed the surface atomic distribution and chemical composition of NZVI. The decolorization efficiency rose with increasing concentration of nanoparticles as well as with time. Maximal color removal efficiency was 90.72% when using 0.5?g/100?mL Fe nanoparticle for acridine orange. Data revealed that the function of NZVI on color removal efficiency was statistically significant. The correlation coefficient between NZVI concentration and time showed a strong negative correlation for dyes used in the experiment.