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1.
The present state and the trends of the recovery of heavy metals from wastewaters are presented. The classical precipitation techniques are insatisfactory due to increases of solubility in the presence of impurity ions and/or complexing agents. At present, ion-exchange processes constitute the most frequently used method of metal recycling with an effective enrichment of metal ions. For the effective separation of metals from solutions of a low concentration the electrolytic reduction demands large electrode surface areas. In cells with fixed-bed or fluidized cathodes one can obtain specific electrode surface areas of some 103 m2/mm3. For the future, processes of extraction and especially membrane separation will gain in importance. In the past few years, a large number of highly selective metal extracting agents as well as the liquid membrane permeation with suitable carriers were developed. Combinations of membrane separation processes with chemical reactions may attain the same importance, as e.g. ultrafiltration in connection with the fixation of metal ions to watersoluble polymers. In the long run, especially techniques will prevail which will not only result in metal enrichment but also in the recovery of the raw material water. 相似文献
2.
The separation of heavy metals from wastewater may be improved by precipitation/flocculation with iron- or aluminium salts. Often, the resulting products are voluminous, water-containing, amorphous hydroxides which show only limited flocculation properties and may possibly pose problems with the technical separation from the aqueous phase. The application of magnetite could be advantageous because magnetite is ferromagnetic and can be separated very quickly in a magnetic field. First of all, a simple preparation method for magnetite was studied. Pure magnetite could be prepared by mixing an iron(II) salt solution with an equivalent amount of sodium hydroxide at room temperature without oxidation by air. The required reaction time was only 3 hours. For the precipitation of heavy metals from an electroplating wastewater, a better metal elimination and smaller sludge volumes resulted with that artificially produced magnetite in comparison with a precipitation by NaOH. Thereby not only the adsorption of metals was established but also coagulation effects of the magnetite sludge with small metal hydroxide particles. By means of the experimental results. sorption of nickel and chromium was compiled as function of pH and precipitation time. Because freshly precipitated magnetite shows very good sorption and flocculation properties, and pH of precipitation may be lower, its use in high gradient magnetic separation (HGMS) could be more effective for metal elimination than magnetite powder. 相似文献
3.
Conditions of the Formation of Zinc-bearing Ferrites in Regard of Heavy Metal Removal from Wastewater by Magnetic Separation Magnetic separation techniques can be applied for heavy metal removal from wastewater if it is reached to link together the heavy metals with a substance which is sufficiently influenced by a magnetic field. Such a substance is the ferrimagnetic magnetite which can be prepared under special conditions – by oxidation of ferrous hydroxide – in wastewater. In this paper, zinc was chosen as an example for technically relevant, diamagnetic heavy metals. The investigations deal with the influence of zinc onto the structure and the magnetic properties of the reaction products produced by oxidation of zink-bearing ferrous hydroxide in aqueous solutions at room temperature. The oxidation was caused by synthetic air passing through the suspension. During the reaction, the parameters pH value, redox potential, and concentration of dissolved oxygen were observed continuously. The plots of these parameters versus time yield typical courses which can be used as measurement for the progress of the reaction. The results show that magnet ite can only be prepared if the molar ferrous concentration at the beginning is four times higher than the concentration of the dissolved oxygen. Furthermore, the oxidation rate must be slow, a condition which could be achieved by mass transfer controlled kinetics. The products of the oxidation of zinc-bearing ferrous hydroxide show a colour between black and brown. They consist of magnetite, zinc-bearing ferrite and amorphous iron hydroxide. It can be observed that with increasing initial zinc concentrations, increasing amounts of zinc-bearing ferrite but also of amorphous iron hydroxide are produced. Therefore, it seems that the impact of zinc on the reaction is in such a way that more amorphous compounds instead of the thermodynamically stabile ferrite are formed; The magnetic properties show also a dependence on the initial zinc concentration: The saturation magnetization decreases with an increase of the zinc concentration. The reaction product which results from the experiment with an initial mole ratio of Zn:Fe = 1:1 points out only paramagnetic behaviour. 相似文献
4.
In static laboratory experiments there are determined quantities influencing the adsorption of selected metal ions on different surfaces (base metals, glass of instruments, quartz glass, plastic materials, precious metals). A great dependence on pH, ionic species, ionic concentration, material as well as temperature and presence of complexing agents is observed. Processes are proposed or confirmed by which the losses of material during the trace analysis are reduced. 相似文献
5.
This paper describes relations between the degree of complexation calculated with a mathematical model (FISCHER and REISSIG, 1984) and the ion-exchange and migration behaviour of iron(II, III)-compounds in a simulated aquifer. In general, the bonding of the complexes to the soil matrix becomes stronger with increasing positive charge. Negatively charged or neutral complex compounds do not show any, or show only slight interactions with the soil matrix. By complexation it is possible to achieve great differences in the migration behaviour of a particular metal. In the course of migration in the deposit there was found a separation of the complex mixture in accordance with charge. The break-through curves are characterized by a stepped shape, for this case. If weak acids or weak bases act as complex-forming ligands, the pH-dependent dissociation of the complexing species has to be taken into account in the complex calculation; this is represented by the example of the iron(III)-citrate system in this paper. Moreover, experimental results concerning the migration behaviour of iron(II, III)-fulvic acid complexes are given 相似文献
6.
The distribution of organic carbon (OC) and of some metals (Cu, Mn) amongst the particulate (>0·2 μm), colloidal (10 kDa–0·2 μm) and the truly dissolved (<10 kDa) fractions of the River Marne was investigated during the phytoplankton spring bloom. A tangential ultrafiltration (UF) device was utilized to separate the colloidal fraction. On average, 22% of the OC, 31% of the Cu and 53% of the Mn, usually assigned to the so‐called dissolved fraction, were found in the colloidal fraction. The colloidal fraction exhibited a behaviour different from that of the particulate and truly dissolved fractions. Autochthonous production led to enrichment in the colloidal and particulate OC pools: up to 47% of the total dissolved OC was in the colloidal fraction. An increase in the colloidal metal fraction, concomitant with a fall in the truly dissolved fraction, coincided with peaks in phytoplankton during the bloom. These phenomena might be related either to an increase in pH associated with photosynthetic activity, resulting in the precipitation of truly dissolved forms into the colloidal fraction, or to scavenging of the truly dissolved metals by the algal species of colloidal size. The interaction between the colloidal and the truly dissolved phases was very important. The partition coefficients of the Cu and Mn between the colloidal and truly dissolved fractions were higher than between the particulate and the truly dissolved fractions. This pattern is consistent with a greater specific surface area of colloids than macroparticles. Consequently, the adsorption and complexation capacities are enhanced in the colloidal fraction of the particulate matter. The extraction of hydrophobic complexes with Cu using C18 Sep‐Pak columns, showed that the Cu occurring in colloidal, total dissolved or truly dissolved forms was significantly complexed by the organic matter. The truly dissolved fraction might be complexed up to 100% during a phytoplankton bloom. Copyright © 1999 John Wiley & Sons, Ltd. 相似文献
7.
Zinc remediation of aqueous streams is of special concern due to its highly toxic and persistent nature. Conventional treatment technologies for the removal of zinc are not economical and further generate huge quantity of toxic chemical sludge. Biosorption is emerging as a potential alternative to the existing conventional technologies for the removal of metal ions from aqueous solutions. Mechanisms involved in the biosorption process include chemisorption, complexation, adsorption–complexation on surface and pores, ion exchange, microprecipitation, heavy metal hydroxide condensation onto the bio surface, and surface adsorption. Biosorption largely depends on parameters such as pH, the initial metal ion concentration, biomass concentration, presence of various competitive metal ions in solution, and to a limited extent on temperature. Biosorption using biomass such as agricultural wastes, industrial residues, municipal solid waste, biosolids, food processing waste, aquatic plants, animal wastes, etc., is regarded as a cost‐effective technique for the treatment of high volume and low concentration complex wastewaters containing zinc metal. Very few reviews are available where readers can get an overview of the sorption capacities of agro based biomasses used for zinc remediation together with the traditional remediation methods. The purpose of this review article is to provide the scattered available information on various aspects of utilization of the agro based biomasses for zinc metal ions removal. An extensive table summarizes the sorption capacities of various adsorbents. These biosorbents can be modified using various methods for better efficiency and multiple reuses to enhance their applicability at industrial scale. We have incorporated most of the valuable available literature on zinc removal from waste water using agro based biomasses in this review. 相似文献
8.
Sorption of Heavy Metals from Acetic Acid Extracts by Ferric Phosphate Colloids A conceivable procedure to remedy heavy metal contaminated soil materials is given with extraction of organic acids, i. e. by the use of a biological degradable extraction agent. The following concentration step of heavy metal extracts should be carried out to a great extent without a change of the low pH values. A conventional precipitation of the heavy metals by rising the pH should be avoided in order to introduce no large amounts of salts into the wastewaters of the process and furthermore, to reduce the amount of sludge to be deposited. The process scheme developed with the objective of heavy metals recycling consists of the following steps: the extraction of the heavy metal contaminated soils with weak organic acids like acetic acid or citric acid, the electrolysis of the extract, and a concentration step in order to treat metal concentrations not fully removed by electrolysis. This third step, e.g. could contain sorption on iron phosphate colloids and precipitation within the acidic environment. It has been examined whether a removal of the heavy metals Pb, Cd, Cu, Sb, Cr, Ni and Zn from acetic aqueous solutions of pH between 2 and 3 can be carried out. 相似文献
9.
New aspects on the chemistry of aluminum in soils 总被引：2，自引：0，他引：2
Gerhard Furrer 《Aquatic Sciences - Research Across Boundaries》1993,55(4):281-290
Dissolution kinetics of minerals can be significantly inhibited by re-adsorbed aluminum. As a consequence of neutralization, polynuclear Al species may be formed in soil solutions. While re-acidification leads to decomposition of the polymers, further neutralization induces the formation of aggregates. The complexation of heavy metal ions with dissolved and aggregated Al polymers is illustrated as a potential factor influencing the chemical speciation of heavy metals in soils. 相似文献
10.
Alain C.M. Bourg 《Continental Shelf Research》1987,7(11-12)
A brief, critical review of empirical and conceptual metal adsorption models is presented. This covers models conditional to seawater chemistry, as well as models applicable to estuaries or other systems of variable solution chemistry. The conceptual surface complexation approach is used to show why desorption of trace metals does not necessarily occur readily in estuaries, and why in some cases adsorption can even take place. The relevance and weaknesses of this model for the understanding of the mobility and fate of heavy metals in turbid environments, as related to particle dynamics, is discussed using the macrotidal Gironde Estuary, France, as the example. 相似文献
11.
Comparison of Selected Elution Procedures for the Valuation of the Mobility of Metals from Sediment and Sewage Sludge Several methods of extraction are generally used to evaluate environmental or ecological toxicity and deposition of waste material. In this paper, the application of the German standard methods DIN 38414-S7, DIN 38414-S4, pHstat method, “Schweizer method” (elution test, Switzerland), and some variants of the pHstat method on two very different samples are described. A rudimental sediment and a municipal sewage sludge are chosen as sample materials. The metal contents of extract solutions are determined by ICP-OES. The results of the DIN-S4 extractions depend definitely on the mechanic way of movement, i.e. the amount of heavy metals which are mobilized out of the samples differs considerably. In fact, DIN-S7 in combination with DIN-S4 is not sufficient to estimate the mobility of heavy metals. Solid samples should only be evaluated by applying a combination of several methods of extraction. The usefulness of the pHstat method for an evaluation is discussed. 相似文献
12.
H. Waeschke 《洁净——土壤、空气、水》1991,19(4):435-451
Possible formulae of complex compounds of copper and polyacrylic acid as well as polysulfonic acid are demonstrated. The formal complex dissociation constants of the complexes with copper and acrylic acid are developed. The actual concentration of unbonded copper ions under different media conditions are calculated in terms of the formal complex dissociation constants of the most important complex compound for ultrafiltration consisting of one copper ion and two acrylic acid monomer units. As a result follows the theoretical retention capacity of membranes and the underlying limit of the concentration of metal ions for the economical application of ultrafiltration. Most of the experimental findings in the first part have been given their theoretical foundation. 相似文献
13.
14.
This investigation had the purpose of evaluating the reliability of a sequential extraction procedure according to Zeien and Brümmer (1989) which is performed routinely to analyse the distribution of heavy metals to different soil phases. Reliability was tested by two hypotheses. According to the first hypothesis an error propagation increased during a morefold extraction of heavy metals from a single soil sample to such an extend that it does not allow a statistical comparison of different analyses. This assumption was confirmed in an interlaboratory study of five participants applying the sequential extraction scheme on two different soils. The heavy metal amounts extracted by the different partners were of the same magnitude, but from the results no statistical correspondence at the 95% confidence level could be observed. The second hypothesis stated that also weak extraction agents were able to release metals from the more immobile soil fractions, especially if the amount of easily soluble metals was comparatively small. To answer this question the sequential extraction was modified by carrying out selected weak extraction steps several times. As expected the intensified extraction conditions caused a decrease of the element content within the more resistant phases. However, the additional release in the first four extraction steps of Pb, Mn, Fe, and Zn was only in the range of 5 to 10%. Furthermore, it was observed that a single EDTA extraction (step four within the sequential extraction scheme) was capable to extract the same amount of metals as the first four extraction steps of the original scheme at a variation of about 15%. From these results it was concluded that the EDTA step alone already represents a reliable pool of mobilisable metals. Thus it can be maintained that such a simple single EDTA extraction can be used to assess the environmental risk from heavy metal contaminated soils or to predict the potential heavy metal release of soil remediation processes. 相似文献
15.
Concentrations of heavy metals (Cd, Cu, Pb and Zn) on suspended sediments during a flood event at Thwaite Mills, River Aire, were analysed using a five step sequential extraction technique to determine their major chemical associations (exchangeable, surface oxide and carbonate, Fe and Mn oxides, organic and residual metal ions). Total metal concentrations were lowest at higher discharges, resulting from dilution by clean sediment. The major transport fractions are the Fe and Mn oxides, which carry 29% of the total metals. Knowledge of the chemical forms of heavy metals on suspended sediment is essential for estimating their biological availability and physicochemical reactivity. © 1998 John Wiley & Sons, Ltd. 相似文献
16.
Intermittent anoxia in the Saanich Inlet water column provides an easily accessible marine O2/H2S interface to study the response of metals to both a steep redox gradient and the availability of reactive reduced sulfur species. Our study indicates a strong anoxic zone sink for copper and cadmium and the characteristically enhanced solubility of manganese and iron. Thiosulfate and sulfite are below detection limits (1 μM and 0.1 μM, respectively) and thus not important in metal complexation. Elemental sulfur concentrations are high at the oxic/anoxic interface and throughout the anoxic zone, indicating the potential for metal complexation by polysulfides. A thermodynamic approach employing metal sulfide formation and class specific sulfidic ligand complexation to generate equilibrium profiles adequately describes the solubility of iron, copper, and cadmium. The extension of this scheme to other transition and class B metals in other marine environments with redox fronts is suggested. 相似文献
17.
Long‐term Assessment for the Leachate Release of Heavy Metals from Municipal Solid Waste Incineration Bottom Ash Monofills Municipal solid waste incineration (MSWI) bottom ash was investigated by chemical, mineralogical, and microbiological methods as well as leaching‐ and laboratory lysimeter tests. Compared to geological material bottom ash shows a high content of soluble salts, organic carbon, and heavy metals. The heavy metals are mainly bound in alloys and glas. Addition of oxic and acetic solutions quickly oxigenize the metal‐phases and alloys. Only fixation in newly formed phases like carbonates or hydroxides prevents heavy metal release till pH 7 in case of pH‐reduce. In the long‐term the acid buffer is reduced by the environmental acid input in combination with the release of buffering phases (mostly calcite). Internal acid producing processes like decay of organic matter or oxidation of sulfides are not important for the pH‐decrease. Cu, Ni, and Zn are first released between pH 7 and 6 (mainly Zn) and a second time at pH values below 5 (mainly Cu). Pb is significantly released at pH values below 5, Cr only at pH < 4. Mainly metals, alloys, and the rims of glas are destroyed by leaching. Phases like metal hydroxides (mainly Fe‐phases) or amorphous, water bearing Fe‐Al‐Si‐oxides are finally formed. Long‐term leaching by acetic fluids increases the total availability of heavy metals (except Cr) with increasing time. Kinetic effects including changing of metal binding forms seem to be responsible for this development. Within deposit conditions of limited gas exchange (closed system) the pH of the carbonate buffering zone can drop below pH 7 in case of very strong acid input and quickly cause an enhanced metal release. But in reality such a strong acid input is not to be expected. Calcite will buffer between pH 8 and 7 for a long time. Depending on the environmental conditions (water balance, acidity of rain) and landfill design (compaction, permeability, cover, thickness) it can take hundreds till thousands of years until metal release will start. The long‐term metal release of matter with an acid buffer like carbonates can be approximately determined only by short‐term tests with powder (e.g. pHstatic tests at pH 4). 相似文献
18.
This study aims to remove of Cu2+, Cd2+, and Pb2+ ions from solution and to investigate the adsorption isotherms, adsorption kinetics, and ion‐exchange affinities of these metals using waste activated sludge (AS) biomass. The adsorptions of the metals on biomass were optimal at an acidic pH value of 6.0 based on its monolayer capacities. Maximum monolayer capacities of AS biomass (qmax) were calculated as 0.478, 0.358, and 0.280 mmol g?1 for Cu2+, Cd2+, and Pb2+, respectively, and the adsorption equilibrium time was found as 60 min for each metal. The adsorbed amount of metal rose with increasing of initial metal ion concentration. The equilibrium adsorption capacity of AS for initial 0.25 mmol L?1 metal concentration was determined as 0.200, 0.167, and 0.155 mmol g?1 for Cu2+, Cd2+, and Pb2+ ions, respectively. These relevant values were determined as 0.420, 0.305, and 0.282 mmol g?1 for Cu2+, Cd2+, and Pb2+ ions, respectively, when initial metal concentration was 0.50 mmol L?1. In the multi‐metal sorption system, the adsorption capacity of AS biomass was observed in the order of Cu2+ > Cd2+ > Pb2+. In the presence of 100 mmol L?1 H+ ion, the order of ion‐exchange affinity with H+ was found as Cu2+ > Cd2+ > Pb2+. The adsorption kinetics were also found to be well described by the pseudo‐second‐order and intraparticle diffusion models. Two different rate constants were obtained as ki1 and ki2 and ki1 (first stage) was found to be higher than ki2 (second stage). 相似文献
19.
Ponnusamy Senthil Kumar Subramaniam Ramalingam Ramasundaram Vijayakumar Abhinaya Selvaraj Dinesh Kirupha Arukkani Murugesan Subramanian Sivanesan 《洁净——土壤、空气、水》2012,40(2):188-197
This paper discusses about the adsorption of metal ions such as Cu(II), Cd(II), Zn(II), and Ni(II) from aqueous solution by sulfuric acid treated cashew nut shell (STCNS). The adsorption process depends on the solution pH, adsorbent dose, contact time, initial metal ions concentration, and temperature. The adsorption kinetics was relatively fast and equilibrium was reached at 30 min. The adsorption equilibrium follows Langmuir adsorption isotherm model. The maximum adsorption capacity values of the modified cashew nut shell (CNS) for metal ions were 406.6 mg/g for Cu(II), 436.7 mg/g for Cd(II), 455.7 mg/g for Zn(II), and 456.3 mg/g for Ni(II). The thermodynamic study shows the adsorption of metal ions onto the STCNS was spontaneous and exothermic in nature. The kinetics of metal ions adsorption onto the STCNS followed a pseudo‐second‐order kinetic model. The external mass transfer controlled metal ions removal at the earlier stages and intraparticle diffusion at the later stages of adsorption. A Boyd kinetic plot confirms that the external mass transfer was the slowest step involved in the adsorption of metal ions onto the STCNS. A single‐stage batch adsorber was designed using the Langmuir adsorption isotherm equation. 相似文献
20.
H. Waeschke 《洁净——土壤、空气、水》1989,17(5):583-592
Fundamental experimental experience on the concentration of metal ions was gathered by ultrafiltration at 0.3 MPa pressure by using membranes with pores in a laboratory cell with stirrer. The potentiality of retention against the metal ions R and the stream density of filtration IF were measured for model liquids of CuSO4, NiSO4, ZnSO4 and AgNO3. The experimental results involve the influence of the membran materials, the role of several tested additives for complex formation and pH, and the influence of strange electrolytes, respectively, on the membrane characteristics R and IF. 相似文献