Synthesis of Ion-Imprinted Alginate Based Beads: Selective Adsorption Behavior of Nickel (II) Ions

Ni(II) imprinted and non-imprinted bioadsorbent alginate beads were prepared, and utilized in the selective adsorption of Ni(II) ions. The optimum adsorption capacity were 6.00 mmol g^?1 at 500 ppm initial metal ion concentration at pH 7 for Ni(II) imprinted alginate beads (IIP). The equilibrium data were applied to Langmuir and Freundlich adsorption isotherms, and it fitted both isotherm models. Thermodynamic parameters showed favorable and endothermic nature of adsorption. Ni(II) imprinted bead showed the strong ability to selective adsorption from Cu(II), Co(II) and Zn(II) ions. In conclusion, Ni(II) ion imprinted alginate beads could be used repeatedly without any significant reduce of adsorption capacity.     

Hydrometallurgical processing of Nd–Fe–B magnets for Nd purification

An evaluation of various metal purification processes subsequent to the leaching processing of the neodymium (Nd) product from neodymium–iron–boron (Nd–Fe–B) magnets has been conducted. These post-leaching purification processes included precipitation; replacement and electrolysis were studied in order to check the purity of the recovered neodymium. A hydrometallurgical investigation was adopted to digest the metal content of the scrap Nd–Fe–B magnets for the recovery of valuable Nd metal and other metals such as Fe, B, Co and Ni. The effect of leaching conditions such as solid-to-liquid ratio and temperature were optimized and 100 % Nd, 100 % Fe, 100 % B and 85.87 % Co leaching efficiencies were achieved under these conditions. The coating material of the magnet, Ni, achieved 50 % impregnation after increasing the reaction temperature to 70 °C. The metals present in the optimal leaching solution were recovered 99 % by pH adjustment. However, the replacement had the highest separation efficiency for the recovery of Nd metal. Further, the optimal leaching Nd–Fe–B solution was subjected to the electrolysis processes in order to verify the recovery efficiency for all metals.     

Sequential extraction of metals from mixed and digested sludge from aerobic WWTPs sited in the south of Spain

The content of heavy metals is the major limitation to the application of sewage sludge in soil. However, assessment of the pollution by total metal determination does not reveal the true environmental impact. It is necessary to apply sequential extraction techniques to obtain suitable information about their bioavailability or toxicity. In this paper, sequential extraction of metals from sludge before and after aerobic digestion was applied to sludge from five WWTPs in southern Spain to obtain information about the influence of the digestion treatment in the concentration of the metals. The percentage of each metal as residual, oxidizable, reducible and exchangeable form was calculated. For this purpose, sludge samples were collected from two different points of the plants, namely, sludge from the mixture (primary and secondary sludge) tank (mixed sludge, MS) and the digested-dewatered sludge (final sludge, FS). Heavy metals, Al, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Ti and Zn, were extracted following the sequential extraction scheme proposed by the Standards, Measurements and Testing Programme of the European Commission and determined by inductively-coupled plasma atomic emission spectrometry. The total concentration of heavy metals in the measured sludge samples did not exceed the limits set out by European legislation and were mainly associated with the two less-available fractions (27-28% as oxidizable metal and 44-50% as residual metal). However, metals as Co (64% in MS and 52% in FS samples), Mn (82% in MS and 79% in FS), Ni (32% in MS and 26% in FS) and Zn (79% in MS and 62% in FS) were present at important percentages as available forms. In addition, results showed a clear increase of the concentration of metals after sludge treatment in the proportion of two less-available fractions (oxidizable and residual metal).     

Heavy metals in source-separated compost and digestates

The production of compost and digestate from source-separated organic residues is well established in Europe. However, these products may be a source of pollutants when applied to soils. In order to assess this issue, composts, solid and liquid digestates from Switzerland were analyzed for heavy metals (Cd, Co, Cr, Cu, Ni, Pb and Zn) addressing factors which may influence the concentration levels: the treatment process, the composition, origin, particle size and impurity content of input materials, the season of input materials collection or the degree of organic matter degradation.Composts (n = 81) showed mean contents being at 60% or less of the legal threshold values. Solid digestates (n = 20) had 20–50% lower values for Cd, Co, Pb and Zn but similar values for Cr, Cu and Ni. Liquid digestates (n = 5) exhibited mean concentrations which were approximately twice the values measured in compost for most elements. Statistical analyses did not reveal clear relationships between influencing factors and heavy metal contents. This suggests that the contamination was rather driven by factors not addressed in the present study.According to mass balance calculations related to Switzerland, the annual loads to agricultural soils resulting from the application of compost and digestates ranged between 2% (Cd) and 22% (Pb) of total heavy metal loads. At regional scale, composts and digestates are therefore minor sources of pollution compared to manure (Co, Cu, Ni, Zn), mineral fertilizer (Cd, Cr) and aerial deposition (Pb). However, for individual fields, fertilization with compost or digestates results in higher heavy metal loads than application of equivalent nutrient inputs through manure or mineral fertilizer.     

Bioleaching of metals from spent lithium ion secondary batteries using Acidithiobacillus ferrooxidans

Bioleaching of spent lithium ion secondary batteries, containing LiCoO2, was attempted in this investigation. The present study was carried out using chemolithotrophic and acidophilic bacteria Acidithiobacillus ferrooxidans, which utilized elemental sulfur and ferrous ion as the energy source to produce metabolites like sulfuric acids and ferric ion in the leaching medium. These metabolites helped dissolve metals from spent batteries. Bio-dissolution of cobalt was found to be faster than lithium. The effect of initial Fe(II) concentration, initial pH and solid/liquid (w/v) ratio during bioleaching of spent battery wastes were studied in detail. Higher Fe(II) concentration showed a decrease in dissolution due co-precipitation of Fe(III) with the metals in the residues. The higher solid/liquid ratio (w/v) also affected the metal dissolution by arresting the cell growth due to increased metal concentration in the waste sample. An EDXA mapping was carried out to compare the solubility of both cobalt and lithium, and the slow dissolution rate was clearly found from the figures.     

Synthesis,Characterization and Environmental Applications of a New Bio-Composite Gelatin-Zr(IV) Phosphate

Gelatin-Zr(IV) phosphate composite (GT/ZPC) was synthesized by sol–gel method. Different techniques viz. Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray powdered diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used for the characterisation of GT/ZPC composite ion exchanger. The ion exchange capacity (IEC) of GT/ZPC was observed to be better (1.04 meq g^?1) than its inorganic counterpart (0.64 meq g^?1). The pH studies revealed the monofunctional nature of GT/ZPC with one inflection point. The distribution studies showed that the GT/ZPC was highly selective for Cd²⁺ as compare to other metal ions. The environmental applicability of ion exchanger has been analysed for binary separations of metal ions using column method. Cd²⁺ was effectively removed from synthetic mixture of metal ions (Zn²⁺, Pb²⁺, Ni²⁺, Co²⁺ and Cu²⁺).     

磁性离子印迹聚合物的制备及其对水中Pb(Ⅱ)的吸附

以铅离子为模板离子、乙二醇二甲基丙烯酸酯和偶氮二异丁腈为交联剂和引发剂、稀盐酸为洗脱剂,采用微波辅助反相乳液悬浮聚合法,制备了磁性离子印迹聚合物(MIIP),通过SEM、FTIR、XRD和BET技术对其进行了表征,并将其用于水中Pb(Ⅱ)的吸附.在初始质量浓度60 mg/L、溶液pH 6、吸附温度303 K、吸附时间6...     

Extraction of heavy metal ions from waste colored glass through phase separation

A new method utilizing phase separation phenomena for the extraction of heavy metal ions used as colorants in colored glass is proposed. Colored soda-lime-silica glass containing Co or Cr as a colorant was remelted with B2O3 to yield soda-lime-borosilicate glass. The soda-lime-borosilicate glass thus obtained was leached in 1M nitric acid at 90 degrees C to dissolve the borate phase. All cations (Na, Ca, Cr and Co) concentrated in the borate phase are successfully leached out with the dissolution of the borate phase, when the amount of the B2O3 added to the glass and heat treatment conditions are properly chosen. Porous silicate glass powders with high SiO2 purity are obtained as the result of the leaching. Porous glass can also be formed as bulk material by controlling the composition of additives during the remelting.     

Electro-dissolution of metal scrap anodes for nickel ion removal from metal finishing effluent

This contribution reports a novel and cost efficient strategy for nickel ion removal from metal finishing effluents by electro-dissolution of scrap aluminium and iron sacrificial anodes. Electro-coagulation of effluent was carried out at 30 mA/cm² current density for 60 min. The nickel ion concentration of electroplating effluent was analysed by Atomic Absorption Spectroscopy. SEM images of iron and aluminium scrap anodes were critically analysed. Parameters such as heavy metal removal, anode dissolution rate with respect to heavy metal removal, reaction kinetics and cost estimation have been elaborately studied. Electro-coagulation at 30 mA/cm² for 60 min using iron and aluminium scrap anodes resulted in 95.9 and 94.1 % nickel ion reduction, respectively, with 0.0094 and 0.0053 g/ppm dissolution rates. The energy consumption for scrap aluminium and iron anodes was 0.0547 kWh/L. Loose internal bonding and spongy surface morphology of used metal scrap render high porosity and active surface area, enhancing reaction rate. Low cost and ready availability of waste scrap makes the process of electro-coagulation economically viable. Thus, the findings from this contribution point decisively at the superiority of waste metal scrap-based anodes for economic and environmentally sustainable heavy metal ion removal from metal finishing effluent.     

Synthesis of Chitosan@activated Carbon Beads with Abundant Amino Groups for Capture of Cu(II) and Cd(II) from Aqueous Solutions

In this study, chitosan and bio-based activated carbon obtained from sugarcane bagasse biowaste were used for the synthesis of efficient sorbent for Cu(II) and Cd(II) ion via precipitation method. The prepared material was enriched with amino groups through grafting tetraethylenepentamine and tested for heavy metal remediation from water samples. The influence of pH was investigated showing optimum sorption at pH 6 for Cu(II) and Cd(II). Sorption tests, explained by means of the most common sorption models, evidenced that the best performances were reached pointing out the promising application of the prepared sorbent for water purification treatments: Uptake kinetics are relatively fast: the equilibrium was reached within 140 min; and the kinetic profiles were preferentially fitted by the pseudo-second order rate equation. Sorption isotherms are fitted by Langmuir equation. The sorbent showed high metal ion sorption capacity with negligible influence of ion strength. The maximum sorption capacities reached 3.44 and 2.38 mmol g^??1 for Cu(II) and Cd(II), respectively at 298 K. Thermodynamic parameters were evaluated through variation of temperature. The sorption is unfavorable at elevated temperatures. Metal ions were successfully desorbed using 1 M HNO₃ solution.     

Treatment of electronic waste to recover metal values using thermal plasma coupled with acid leaching--a response surface modeling approach

The global crisis of the hazardous electronic waste (E-waste) is on the rise due to increasing usage and disposal of electronic devices. A process was developed to treat E-waste in an environmentally benign process. The process consisted of thermal plasma treatment followed by recovery of metal values through mineral acid leaching. In the thermal process, the E-waste was melted to recover the metal values as a metallic mixture. The metallic mixture was subjected to acid leaching in presence of depolarizer. The leached liquor mainly contained copper as the other elements like Al and Fe were mostly in alloy form as per the XRD and phase diagram studies. Response surface model was used to optimize the conditions for leaching. More than 90% leaching efficiency at room temperature was observed for Cu, Ni and Co with HCl as the solvent, whereas Fe and Al showed less than 40% efficiency.     

New Methods for the Preparation Nanosized Metal Coordination Polymers

Transition-metal coordination polymers [M(ndc)(bpy)·(H₂O)m]·xH₂O (where M = Co(II), Ni(II), Cu(II) and Zn(II), ndc = 1,4-naphthalenedicarboxylate, bpy = 4,4′-bipyridine; m = 0 or 1; x = 1 or 2) were prepared by reacting the ligands and metal ions at room temperature with the aid of microwave irradiation and sonication methods. The structure of the coordination polymers was assigned based on elemental analysis, FT-IR and electronic spectral studies, thermal analysis, scanning electron microscope and X-ray powder diffraction. Thermogravimetric analysis was also used to follow up the possible thermal decomposition steps and to calculate the thermodynamic parameters of the nano-sized metal complexes. The kinetic parameters were calculated making use of the Coats–Redfern and Horowitz–Metzger equations. All obtained results of the different technics used in our study stated the ability to synthesis the metal coordination polymers of our interest using both microwave irradiation and sonication methods.     

强化混凝法处理煤气冷凝水

以包头钢铁(集团)有限责任公司高炉煤气冷凝水为处理对象,采用强化混凝法进行静态混凝沉淀对比实验。实验结果表明,当聚合氯化铝加入量为20mg/L、高分子纳米除氯剂加入量为2.0mL/L时,处理后出水SS小于10mg/L,浊度小于10NTU,氯离子去除率在80%以上,而且对废水中的其他离子也有一定的去除效果,出水水质基本接近工业冷却循环水回用指标。     

Fractionation of heavy metals in sludge from anaerobic wastewater stabilization ponds in southern Spain

The analysis of heavy metals is a very important task to assess the potential environmental and health risk associated with the sludge coming from wastewater treatment plants (WWTPs). However, it is necessary to apply sequential extraction techniques to obtain suitable information about their bioavailability or toxicity. In this paper, a sequential extraction scheme according to the Standard, Measurements and Testing Programme of the European Commission was applied to sludge samples collected from ten anaerobic wastewater stabilization ponds (WSPs) located in southern Spain. Al, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Ti and Zn were determined in the sludge extracts by inductively coupled plasma atomic emission spectrometry. In relation to current international legislation for the use of sludge for agricultural purposes, none of the metal concentrations exceeded maximum permitted levels. Overall, heavy metals were mainly associated with the two less-available fractions (34% oxidizable metal and 55% residual metal). Only Mn and Zn showed the highest share of the available (exchangeable and reducible) fractions (25-48%).     

Leachability and metal-binding capacity in ageing landfill material

In order to study the stability of landfilled heavy metals, landfill material from a combined household and industrial waste landfill was aerated for 14 months to simulate the natural ageing processes as air slowly begins to penetrate the landfill mass. During aeration, the pH of the landfill material decreased from around 8.6 to 8.1 and the carbon content also decreased. In order to investigate the possible fate of metals in ageing landfills, a four-stage sequential extraction technique was applied. The ability of the materials to bind metal ions by electrostatic attractions and to form stronger complexes was studied separately. The amount of exchangeable cations, the capacity to bind metal ions by electrostatic attraction and the capacity of the landfill material to complex copper ions were increased by the aeration process. However, results from the sequential analysis showed an increased solubility of sulphur and some metals (Cd, Co, Cu, Ni and Zn). Equilibrium speciation models (Medusa) indicated that the organic matter deposit had a significant capacity to bind metal ions provided that pH was sufficiently high. However, as carbonates are consumed over time, the risk for metal mobility increases. Therefore, the landfills can become an environmental risk, depending on variations in the solubility of metal ions due to changes in pH, redox status and the availability of organic material.     

堇青石负载Pd和过渡金属氧化物催化剂的表征及其对CO的催化氧化活性

以堇青石蜂窝陶瓷(CC)为载体,采用浸渍法制备了堇青石负载Pd和过渡金属混合氧化物催化剂,记作Pd-M-Mn(M=Cu,Co,Fe,Ni)/CC。实验结果表明:Pd-Co-Mn/CC催化剂的催化活性最高;随着Pd负载量的增加,CO转化率提高;当Pd负载量为1.00%时,反应温度为150℃时CO转化率达到98%,200℃时CO转化率达到100%;在反应温度150℃条件下,Pd-Co-Mn/CC催化剂(Pd负载量1.00%)的CO转化率在前30h内小幅度下降,随后稳定在90%以上,反应100h后,催化剂表面颜色由黑色变为棕褐色。     

Thermodynamic estimation of minor element distribution between immiscible liquids in Fe-Cu-based metal phase generated in melting treatment of municipal solid wastes

Waste electrical and electronic equipment (WEEE) has become an important target in managing material cycles from the viewpoint of not only waste management and control of environmental pollution but also resource conservation. This study investigated the distribution tendency of trace elements in municipal solid waste (MSW) or incinerator ash, including valuable non-ferrous metals (Ni, Co, Cr, Mn, Mo, Ti, V, W, Zr), precious group metals (PGMs) originated from WEEE (Ag, Au, Pd, Pt), and others (Al, B, Pb, Si), between Fe-rich and Cu-rich metal phases by means of simple thermodynamic calculations. Most of the typical alloying elements for steel (Co, Cr, Mo, Nb, Ni, Si, Ti, V, and W) and Rh were preferentially distributed into the Fe-rich phase. PGMs, such as Au, Ag, and Pd, were enriched in the Cu-rich phase, whereas Pt was almost equally distributed into both phases. Since the primary metallurgical processing of Cu is followed by an electrolysis for refining, and since PGMs in crude copper have been industrially recovered from the resulting anode slime, our results indicated that Ag, Au, and Pd could be effectively recovered from MSW if the Cu-rich phase could be selectively collected.     

芳香烃清洁硝化催化剂

综述了国内外有关芳香烃硝化过程中替代硫酸的催化剂的研究进展;介绍了沸石类催化剂、粘土类催化剂、离子交换树脂催化剂、固载化液体酸催化剂、金属氧化物及金属盐催化剂、杂多酸催化剂以及固体超强酸催化剂的合成及催化效率与优缺点.     

Evaluation of Active Cap Materials for Metal Retention in Sediments

This study evaluated chemically active amendments used to construct active caps for remediating contaminated sediments. Three experiments assessed the effects of apatite, organoclay, zeolite, and biopolymers (chitosan and xanthan) on metal mobility, retention, and speciation. The first showed that the amendments individually and in mixtures (2 percent dry weight) reduced the concentrations of Cr, Co, Ni, and Pb in water extracts from reduced sediment. The second experiment, which used sequential extraction procedures to evaluate the effects of the amendments on metal speciation, showed that the amendments reduced the potentially mobile fractions of Pb, Zn, Ni, Cr, and Cd that are likely to be bioavailable. Last, column studies showed that active caps composed of the amendments prevented the diffusive transport of metals from contaminated sediment over six months. In addition, there was a “zone of influence” beneath the caps in which water extractable concentrations of metals declined substantially compared with untreated sediment. © 2014 Wiley Periodicals, Inc.     

Heavy Metals in Stockholm Groundwater – Concentrations and Fluxes

Sampling of groundwater in theQuaternary deposits was carried out at 70 sitesin Stockholm for, among other things, metalanalyses. The objectives were to get a notion of the metal content and to get a basis for anestimation of the order of magnitude of thegroundwater transported metal contribution to themain surface water bodies in comparison to otherroutes. Thus, in three watershed areaswithin the Stockholm Town, groundwater flow andmetal concentration propagation were simulatedand metal fluxes were calculated. Theconcentrations of heavy metals were in generalfound to be very high in comparison withgroundwater in forested areas. This was mostpronounced for mercury (Hg) and copper (Cu). Themost remarkable result was a Hg concentration of4.57 g L^-1 in the vicinity of a closed downhospital. The annual contribution of heavy metals(kg) by groundwater to the main surface waterbodies was estimated to: As (2.2), Cd (0.20), Co(4.9), Cr (3.1), Cu (34), Hg (0.06), Ni (28), Pb(2.2) Zn (118). These fluxes are much smallerthan those in forest ecosystems, due to lowergroundwater recharge in urban areas, where agreat part of the runoff is diverted bylandsealing, drainage, tunnels etc. The modelingresults emphasize the importance of the sorptionprocesses indicating that the modeled areas arein a non-steady state condition. It also showsthat the sources generating elevatedconcentrations of the high adsorptive metals Pband Hg are likely to be nearby.