Rapid and long-effective removal of broad-spectrum pollutants from aqueous system by ZVI/oxidants

• The coupling of oxidants with ZVI overcome the impedance of ZVI passive layer. • ZVI/oxidants system achieved fast and long-effective removal of contaminants. • Multiple mechanisms are involved in contaminants removal by ZVI/oxidant system. • ZVI/Oxidants did not change the reducing property of ORP in the fixed-bed system. Zero-valent iron (ZVI) technology has recently gained significant interest in the efficient sequestration of a wide variety of contaminants. However, surface passivation of ZVI because of its intrinsic passive layer would lead to the inferior reactivity of ZVI and its lower efficacy in contaminant removal. Therefore, to activate the ZVI surface cheaply, continuously, and efficiently is an important challenge that ZVI technology must overcome before its wide-scale application. To date, several physical and chemical approaches have been extensively applied to increase the reactivity of the ZVI surface toward the elimination of broad-spectrum pollutants. Nevertheless, these techniques have several limitations such as low efficacy, narrow working pH, eco-toxicity, and high installation cost. The objective of this mini-review paper is to identify the critical role of oxygen in determining the reactivity of ZVI toward contaminant removal. Subsequently, the effect of three typical oxidants (H₂O₂, KMnO₄, and NaClO) on broad-spectrum contaminants removal by ZVI has been documented and discussed. The reaction mechanism and sequestration efficacies of the ZVI/oxidant system were evaluated and reviewed. The technical basis of the ZVI/oxidant approach is based on the half-reaction of the cathodic reduction of the oxidants. The oxidants commonly used in the water treatment industry, i.e., NaClO, O₃, and H₂O₂, can be served as an ideal coupling electron receptor. With the combination of these oxidants, the surface corrosion of ZVI can be continuously driven. The ZVI/oxidants technology has been compared with other conventional technologies and conclusions have been drawn.     

Synthesis of vinasse-dolomite nanocomposite biochar via a novel developed functionalization method to recover phosphate as a potential fertilizer substitute

• Nanocomposites were prepared by adding dolomite to vinasse at different ratio. • Textural and morphological features of adsorbents were studied in detail. • CCD based RSM was used for investigation of P ion removal by nanocomposite. • The q_m based on Langmuir model for modified vinasse biochar was 178.57 mg/g. • P loaded nanocomposite improved plant growth and could be utilized as P-fertilizer. The effectiveness of phosphate (P) removal from aqueous solutions was investigated by novel low-cost biochars synthesized from vinasse and functionalized with calcined dolomite. The vinasse-derived biochar, synthesized via pyrolysis at different temperatures, showed easy preparation and a large surface area. The novel vinasse biochar nanocomposites were prepared by adding dolomite to the vinasse biochars with different weight percentages (10, 20 and 30%). The characteristics of the prepared materials were identified for further understanding of the inherent adsorption mechanism between P ions and vinasse biochars. Vinasse-dolomite nanocomposite was very effective in the adsorption of P species from aqueous media. The effect of the operational factors on Vinasse-dolomite nanocomposite was explored by applying response surface methodology (RSM). According to RSM results, the optimum condition was achieved to be contact time 90 (min), 250 (mg/L) of P concentration and pH 7. Thermodynamic isotherm and kinetic studies were applied on experimental data to understand the adsorption behavior. The Vinasse-dolomite nanocomposite revealed preferential P species adsorption in the presence of co-existing anions. The P species could be recovered by 1.0 M HCl where the efficiency was not affected up to the fifth cycle. The P-loaded Vinasse-dolomite nanocomposite was successfully tested on a plant; it significantly improved its growth and proved its potency as a P-based fertilizer substitute.     

Products and stability of phosphate reactions with lead under freeze-thaw cycling in simple systems

Orthophosphate fixation of metal contaminated soils in environments that undergo freeze-thaw cycles is understudied. Freeze-thaw cycling potentially influences the reaction rate, mineral chemical stability and physical breakdown of particles during fixation. This study determines what products form when phosphate (triple superphosphate [Ca(H₂PO₄)₂] or sodium phosphate [Na₃PO₄]) reacts with lead (PbSO₄ or PbCl₂) in simple chemical systems in vitro, and assesses potential changes in formation during freeze-thaw cycles. Systems were subjected to multiple freeze-thaw cycles from +10 °C to −20 °C and then analysed by X-ray diffractometry. Pyromorphite formed in all systems and was stable over multiple freeze-thaw cycles. Low temperature lead orthophosphate reaction efficiency varied according to both phosphate and lead source; the most time-efficient pyromorphite formation was observed when PbSO₄ and Na₃PO₄ were present together. These findings have implications for the manner in which metal contaminated materials in freezing ground can be treated with phosphate.     

Phosphate enrichment in the northern Gulf of Aqaba: Regulation by carbonate sediments and impact on nitrogen elevation

The effect of carbonate sediment in regulating phosphate concentrations in sea water was investigated by laboratory incubation experiments using different sediment types. Incubation experiments were made with two types of sediments: uncontaminated sediment from a marine reserve and contaminated sediment with deposited phosphate powders. Fluxes of inorganic nitrogen and phosphate were estimated from linear regressions of solute concentrations over incubation periods. Ammonium and phosphate fluxes were about twofold higher in the uncontaminated sediment that had significantly lower organic carbon and total phosphate concentrations than in the phosphate-contaminated sediment. To test the effect of dissolved phosphate on increasing nitrogen fixation, additional incubation experiments were carried out using treated carbonate and silicate sediments with added dissolved phosphate (20 μM). Incubations were made under sterile conditions with HgCl₂ added to distinguish between biologically enhanced processes and pure physicochemical processes. The adsorption rate of phosphate onto carbonate sediment was about twice that onto silicate sediments. No nitrogen elevation either as ammonium or as nitrate was observed in the soluble phosphate enrichment incubations. In conclusion, this study demonstrates the importance of the regulation of soluble phosphate concentrations in carbonate sediment environments where the carbonate sediment acts as a buffering system keeping soluble phosphate concentrations at certain steady-state levels. The study also demonstrates the lack of evidence on enhancement of nitrogen concentrations due to the increase phosphate concentrations.     

Phosphorus sorption on marine carbonate sediment: phosphonate as model organic compounds

Organophosphonate, characterized by the presence of a stable, covalent, carbon to phosphorus (C-P) bond, is a group of synthetic or biogenic organophosphorus compounds. The fate of these organic phosphorus compounds in the environment is not well studied. This study presents the first investigation on the sorption of phosphorus (P) in the presence of two model phosphonate compounds, 2-aminothylphosphonoic acid (2-AEP) and phosphonoformic acid (PFA), on marine carbonate sediments. In contrast to other organic P compounds, no significant inorganic phosphate exchange was observed in seawater. P was found to adsorb on the sediment only in the presence of PFA, not 2-AEP. This indicated that sorption of P from phosphonate on marine sediment was compound specific. Compared with inorganic phosphate sorption on the same sediments, P sorption from organic phosphorus is much less in the marine environment. Further study is needed to understand the potential role of the organophosphonate compounds in biogeochemical cycle of phosphorus in the environment.     

Building future nuclear power fleets: The available uranium resources constraint

According to almost all forward-looking studies, the world′s energy consumption will increase in the future decades, mostly because of the growing world population and the long-term development of emerging countries. The effort to contain global warming makes it hard to exclude nuclear energy from the global energy mix.     

Recovery of phosphate from calcinated bone by dissolution in hydrochloric acid solutions

In this study, the optimum conditions of dissolution of calcinated bone in HCl solutions with different concentrations are investigated. Recovery of phosphate from calcinated bone by dissolution with hydrochloric acid solutions was investigated in a batch reactor, it was observed that a 32% hydrochloric acid solution can dissolve the calcinated bone effectively. Using the Taguchi fractional design method, it was found that the optimum process conditions, at which 67.2% P₂O₅ dissolution was reached, were as follows: Reaction temperature: 318 K, solid-to-liquid ratio: 1/5 (g ml⁻¹), acid concentrations:32 (% w/v), stirring speed:400 min⁻¹ and reaction time: 60 min.     

Inoculation of plant growth promoting bacterium Achromobacter xylosoxidans strain Ax10 for the improvement of copper phytoextraction by Brassica juncea

In this study, a copper-resistant plant growth promoting bacterial (PGPB) strain Ax10 was isolated from a Cu mine soil to assess its plant growth promotion and copper uptake in Brassica juncea. The strain Ax10 tolerated concentrations up to 600 mg CuL(-1) on a Luria-Bertani (LB) agar medium and utilized 1-aminocyclopropane-1-carboxylic acid (ACC) as a sole N source in DF salts minimal medium. The strain Ax10 was characterized as Achromobacter xylosoxidans based on its 16S rDNA sequence homology (99%). The bacterium A. xylosoxidans Ax10 has also exhibited the capability of producing indole acetic acid (IAA) (6.4 microg mL(-1)), and solubilizing inorganic phosphate (89.6 microg mL(-1)) in specific culture media. In pot experiments, inoculation of A. xylosoxidans Ax10 significantly increased the root length, shoot length, fresh weight and dry weight of B. juncea plants compared to the control. This effect can be attributed to the utilization of ACC, production of IAA and solubilization of phosphate. Furthermore, A. xylosoxidans Ax10 inoculation significantly improved Cu uptake by B. juncea. Owing to its wide action spectrum, the Cu-resistant A. xylosoxidans Ax10 could serve as an effective metal sequestering and growth promoting bioinoculant for plants in Cu-stressed soil. The present study has provided a new insight into the phytoremediation of Cu-contaminated soil.     

Effect of application of phosphate and organic manure-based fertilizers on arsenic transformation in soil columns

The mobility of arsenic in Cambisol under the influence of added barnyard manure and application of a phosphate solution to the soil was described on the basis of column experiments. A soil sample containing 126 mg/kg total As and 3.72 mg/kg specifically-sorbed As was extracted using demineralized water (DIW) or a 28 μmol/l phosphate solution in a column containing untreated soil and in a column with added barnyard fertilizer. The pH, Eh, alkalinity, main components, including DOC, and selected trace elements (Al, Mn, Pb, Cu, Zn, Cd, Cr, Co, Ni, Ba and As) were determined in the extracts. Hydrodynamic tests of the flow and transport of the substances in the columns were carried out. The addition of barnyard manure was manifested in elevated concentrations of the main inorganic components, DOC and Al and a decrease in the Eh value and Mn concentration. Application of a phosphate solution was manifested in a decrease in the NO₃ and SO₄ concentrations, probably as a result of the effect of increased biological fixation. The As concentration in extracts varied from 8.8 to 15.5 μg/l and was not dependent on the composition of the extracting solution or the addition of barnyard fertilizer.     

纳米氢氧化钛及焙烧产物对磷酸根的吸附特性研究

以纳米氢氧化钛(NTH)作为吸附水溶液中磷酸根的吸附剂,考察了NTH不同焙烧温度下的分子式及其对PO43-吸附效果的影响.选择PO43-初始浓度为50 mg/L,通过正交试验确定在pH=2、吸附剂用量为0.1g、吸附时间为40min、温度25℃时,NTH吸附效果达到最佳,吸附量为55.5 mg/g,经200、300、400及500℃焙烧后的NTH对磷酸根的吸附量逐渐减小;吸附量分别为494、40.6、25.5及16.8 mg/g;NTH经800℃焙烧后,焙烧产物TiO2不具有吸附性.TG、XRD分析表明随着焙烧温度的升高,NTH的表面活性基团(-OH)数量逐渐减少.结果表明,吸附剂的吸附性与吸附剂表面羟基的数量有直接关系.