Ionic strength effect on copper biosorption by Sphaerotilus natans: equilibrium study and dynamic modelling in membrane reactor

Biosorption of copper by Sphaerotilus natans in different conditions of ionic strength and pH was studied by performing sorption tests in batch and membrane reactors. Equilibrium batch tests evidenced the negative effect of ionic strength and the positive effect of pH on biosorption performances: the highest determined value for copper specific uptake, q, was about 60 mg/g at pH 6 and about 15 mg/g at pH 4. A competitive equilibrium model was successfully fitted to experimental data at different ionic strength levels to account for copper-sodium competition. In membrane reactor tests, experimental profiles of copper concentration in the permeate vs. time did not evidence a significant effect of ionic strength at low pH values (4 and 5). On the other hand a more remarkable effect of ionic strength on copper concentration in the permeate was observed at pH 6. Experimental profiles of continuous biosorption in the membrane reactors were successfully simulated by developing a dynamic model accounting for Cu-Na competition and for binding ability of cells fragments.     

Biosorption of binary heavy metal systems onto Sphaerotilus natans cells confined in an UF/MF membrane reactor: dynamic simulations by different Langmuir-type competitive models

Continuous heavy metal biosorption in membrane reactor apparatus using binary metal solutions was here considered. A dynamic model was developed to simulate biosorption performances on the base of metal mass balances in the system considering biosorption as an equilibrium process. The effect of three Langmuir-type competitive models on dynamic simulations of biosorption was then studied by using predictive equilibrium models (whose adjustable parameters were determined only by single metal system biosorption data) and not predictive equilibrium models (adjustable parameters directly by binary biosorption data). Predictive competitive models can give simulation profiles that are different from those obtained using non-predictive models. This detachment is due to the non-ideal competition among metals in solution which cannot be predicted only on the base of biosorption data in single metal systems. The dynamic model for multi-component biosorption here proposed was compared with experimental results reported in the literature and obtained using a biomass in a similar membrane reactor apparatus with ternary metal systems. The simulated profiles (obtained by using predictive equilibrium models) can reproduce qualitatively the specific adsorbent selectivity and the overshoot regions in the permeate concentrations of the metals with the minor affinity.     

Influence of pH and TOC concentration on Cu,Zn, Cd,and Al speciation in rivers

Dissolved ( < approximately 4 nm, dialysis in situ), colloidal ( < 0.45 microm filtered, minus dissolved) and particulate (total, minus < 0.45 microm filtered) concentrations of Cu, Zn, Cd, (Al) in eight (three) mining polluted rivers were determined by atomic absorption spectrometry (flame and graphite furnace). The metal size distribution in the rivers was compared to pH, Ca concentration, alkalinity, conductivity, and total organic carbon (TOC). Data plots based on the present and other studies also yielded information about the interrelations between TOC, pH and metal adsorption in rivers and lakes. Less than 10% of Cu, Zn, and Cd were sorbed on particles or colloids in two rivers with average pH at 3.1 and 5.1, whereas 46%, 21%, and 21% of Cu, Zn, and Cd, respectively, occurred in sorbed form in six pH neutral rivers. In three pH neutral rivers, on average 55% of Al was in colloidal form, whereas the dissolved and particulate fractions were 21% and 23%, respectively. Our data combined with data from similar studies support conclusions from other research suggesting that the percent fraction of metals adsorbed on particles rises steeply from almost zero to nearly 100% within a narrow and element specific pH range. Changes in TOC concentration seem capable of shifting the pH to % metal absorption curves in the order of one pH unit.     

Sources of Cd,Cu, Pb and Zn in biowaste

Biowaste, the separately collected organic fraction of municipal solid waste, can be reused for soil conditioning after composting. In this way, environmentally harmful waste management strategies, such as landfilling or incineration, can be reduced. However, frequent application of composts to soil systems may lead to the accumulation of heavy metals in soils, and therefore legal criteria were laid down in a decree to guarantee the safe use of composts. The heavy metal content of biowaste-composts frequently exceeds the legal standards, and thus raises a conflict between two governmental policies: the recycling of solid waste on the one hand, and the protection of natural ecosystems and public health on the other hand. In this study, the heavy metal content (Cd, Cu, Pb and Zn) of biowaste was compared with the natural background content of Cd, Cu, Pb and Zn in the different constituents of biowaste. For this, the physical entities of biowaste were physically fractionated by wet-sieving and subsequent water-elutriation. In this way, organic and inorganic fractions of different particle sizes were obtained and the content of Cd, Cu, Pb and Zn and the organic matter content of the different fractions were determined. On the basis of particle size, density and visual appearance, the particle-size fractions were assigned to various indoor and outdoor origins of the biowaste. It was found that a large amount of biowaste was not organic, but over 50% was made up of soil minerals due to the collection of biowaste constituents from gardens. The heavy metal content of the various fractions in biowaste was compared with the natural background contents of heavy metals in the constituents of biowaste, i.e. food products, plant material, soil organic matter and soil minerals, by collecting literature data. The heavy metal content in the fractionated physical entities of biowaste corresponded with the natural background concentration of its constituents and indicated that biowaste was not contaminated by other sources. However, the natural background content of biowaste constituents will result in heavy metal contents for biowaste-compost that will exceed the legal standards. It is advised that the legal standards for composts should be critically re-examined. The protection of soil systems could be better guaranteed if the input of heavy metals was evaluated for all inputs of fertilisers and soil conditioners, i.e. animal manures, various types of compost and artificial fertilisers.     

超声消解-ICP-AES法测定土壤中的Co、Cu、Mn、Pb、Zn

采用正交试验对超声波消解土壤中Co、Cu、Mn、Pb、Zn的影响因素进行研究,并与微波消解试验结果进行比对分析.结果表明,影响超声波消解土壤样品的因素依次为:超声功率>固液比>超声时间>反应温度;最佳消解条件为:100%W_(max)超声波功率,固液比1: 16,超声时间40 min,反应温度45 ℃.ICP-AES对Co和Mn的测试结果分别为微波消解测试结果的81.79%～98.15%.     

Development of multimetal binding model and application to binary metal biosorption onto peat biomass

Biosorption of Cr(3+), Cu(2+) and Cd(2+) from binary metal solutions onto peat in the batch systems was investigated at pH 4. The order of maximum uptake was Cr>or=Cu>Cd and maximum uptake levels of ca. 0.4 mmol/g were observed for chromium and copper while cadmium was taken up to a maximum of ca. 0.2 mmol/g. Co-ion competition resulted in up to 70 percent decrease of primary metal uptake. A novel approach to multicomponent sorption modelling involving regression to the total metal taken up was adopted. Two extended Langmuir-type models were found to exhibit good fit to the experimental data. Using the simpler model of these, three-dimensional sorption surfaces were generated which describe the metal uptake as a function of equilibrium concentrations of both metals. These methods allow prediction of metal uptakes over a continuum of concentrations of both metals in binary systems.     

A comparison of the properties of polyurethane immobilised Sphagnum moss, seaweed, sunflower waste and maize for the biosorption of Cu, Pb, Zn and Ni in continuous flow packed columns

The biosorption of Cu, Pb, Zn and Ni from a mixed solution of the metals was investigated in continuous flow packed columns containing polyurethane immobilised biomass. The characteristics and biosorption properties of Sphagnum moss, the brown seaweed Ascophyllum nodosum, waste biomass from the preparation of sunflower oil, and whole plant maize were compared. All the biomass types showed a preference for the sequestration of Pb followed by Cu, with Ni and Zn having roughly equal affinity. With continuous metal loading to the column there was an initial binding of all metals and then a displacement of the lower affinity metals by those with a high affinity. This led to a chromatographic effect in the column with breakthrough concentrations for low-affinity metals higher than the concentration in the feed. A similar phenomenon was found on desorption using acidic solutions where low-affinity metals were desorbed preferentially. The results also indicated that despite competitive displacement of one metal species by another the biomass appeared to succeed in retaining some low-affinity metal species indicating that there may be selective sites present with different affinity characteristics. When using a multi-metal solution with Cu, Pb, Zn and Ni at equal 10 mgl(-1) concentrations as column influent, the total quantities of metal sequestered were: seaweed, 117.3 mg g(-1); sunflower waste, 33.2 mg g(-1); Sphagnum moss, 32.5 mg g(-1); and maize, 2.3 mg g(-1). The use of an acid base potentiometric titration showed a relationship between the number of acid functional groups and biosorption capacity, although this was not proportional for the biomass types studied. It can, however, be used in conjunction with a simple classification of metals into high and low-affinity bands to make a preliminary assessment of a biosorption system.     

Adsorption of Cu(II) and Pb(II) onto a grafted silica: isotherms and kinetic models

The isotherms and kinetics of adsorption of lead(II) and copper(II) onto a grafted silica are studied at 20 degrees C. A commercial silica is grafted with an ethylediamine derivative, N-[3-(trimethoxysilyl)propyl]-ethylenediamine. From the Langmuir isotherms, maximum adsorption capacities of the grafted silica towards Pb(II) and Cu(II) are determined (0.184 mmol Pb(II)g-1 and 0.261 mmol Cu(II)g-1) and compared to those of non-modified silica (respectively, 0.019 and 0.036 mmol g-1). Four kinetic models, i.e., pseudo-first order, pseudo-second order, Langmuir and double-exponential are applied to fit the experimental kinetic data. The kinetic parameters are determined which allow to calculate the theoretical metal uptake as a function of time. The results are discussed and indicate the best fit is obtained with the double-exponential model. A discussion on the adsorption mechanism with respect to the double-exponential model leads to two possible interpretations: the metal uptake may follow a diffusion-controlled mechanism or a two-site adsorption process.     

Uncertainty-based calibration and prediction with a stormwater surface accumulation-washoff model based on coverage of sampled Zn, Cu, Pb and Cd field data

A dynamic conceptual and lumped accumulation wash-off model (SEWSYS) is uncertainty-calibrated with Zn, Cu, Pb and Cd field data from an intensive, detailed monitoring campaign. We use the generalized linear uncertainty estimation (GLUE) technique in combination with the Metropolis algorithm, which allows identifying a range of behavioral model parameter sets. The small catchment size and nearness of the rain gauge justified excluding the hydrological model parameters from the uncertainty assessment. Uniform, closed prior distributions were heuristically specified for the dry and wet removal parameters, which allowed using an open not specified uniform prior for the dry deposition parameter. We used an exponential likelihood function based on the sum of squared errors between observed and simulated event masses and adjusted a scaling factor to cover 95% of the observations within the empirical 95% model prediction bounds. A positive correlation between the dry deposition and the dry (wind) removal rates was revealed as well as a negative correlation between the wet removal (wash-off) rate and the ratio between the dry deposition and wind removal rates, which determines the maximum pool of accumulated metal available on the conceptual catchment surface. Forward Monte Carlo analysis based on the posterior parameter sets covered 95% of the observed event mean concentrations, and 95% prediction quantiles for site mean concentrations were estimated to 470 μg/l ±20% for Zn, 295 μg/l ±40% for Cu, 20 μg/l ±80% for Pb and 0.6 μg/l ±35% for Cd. This uncertainty-based calibration procedure adequately describes the prediction uncertainty conditioned on the used model and data, but seasonal and site-to-site variation is not considered, i.e. predicting metal concentrations in stormwater runoff from gauged as well as ungauged catchments with the SEWSYS model is generally more uncertain than the indicated numbers.     

Cu(II) binding by dried biomass of red, green and brown macroalgae

Dried biomass of the marine macroalgae Fucus spiralis and Fucus vesiculosus (brown), Ulva spp. (comprising Ulva linza, Ulva compressa and Ulva intestinalis) and Ulva lactuca (green), Palmaria palmata and Polysiphonia lanosa (red) were studied in terms of their Cu(II) biosorption performance. This is the first study of its kind to compare Cu(II) uptake by these seaweeds in the South-East of Ireland. Potentiometric and conductimetric titrations revealed a variety of functionalities on the seaweed surface including carboxyl and amino groups, which are capable of metal binding. It was also found that, of the seaweeds investigated, F. vesiculosus contained the greatest number of acidic surface binding sites while Palmaria palmata contained the least. The metal uptake capacities of the seaweeds increased with increasing pH and kinetic behaviour followed a similar pattern for all seaweeds: a rapid initial sorption period followed by a longer equilibrium period. P. palmata reached equilibrium within 10min of exposure while F. vesiculosus required 60min. Correlation was found between the total number of acidic binding sites and the time taken to reach equilibrium. Fourier transform infra-red (FTIR) analysis of the seaweeds revealed the interaction of carboxyl, amino, sulphonate and hydroxyl groups on the seaweed surface with Cu(2+) ions while time course studies established the relative contribution of each of these groups in metal binding.     

Trace metals: Cd, Cu, Pb and Zn in gelatinous macroplankton from the Northwestern Mediterranean

Gelatinous macroplankton organisms were collected in May 1984 in Villefranche-sur-Mer Bay and analysed for cadmium, copper, lead and zinc. Analyses were carried out by polarography for Cd, Cu and Pb and by flame atomic absorption for Zn. Phosphorus was also measured in the samples as a biomass parameter due to difficulties inherent in measuring dry weight of gelatinous organisms. The samples belong to the Tunicates, the Cnidarians (Hydromedusae, Siphonophores and Scyphomedusae), the Ctenophores and the Molluscs. Crustaceans living on some Tunicates were also sampled.As regards cadmium, copper and lead, mean concentrations did not show significant differences among the phyla studied: especially for Tunicates with mean values of 0.1 ng Cd μg P⁻¹, 2.0 ng Cu μg P⁻¹ and 0.9 ng Pb μg P⁻¹ and for Cnidarians with mean values of 0.5 ng Cd μg P⁻¹, 2.0 ng Cu μg P⁻¹ and 0.9 ng Pb μg P⁻¹ and for Cnidarians with mean values of 0.5 ng Cd μg P⁻¹, 2.0 ng Cu μg P⁻¹, 1.0 ng Pb μg P⁻¹. On the other hand, mean zinc concentrations were significantly lower in Tunicates (7.9 ng Zn μg P⁻¹) than in Cnidarians (36.8 ng Zn μg P⁻¹).Zinc seems to be preferentially concentrated in organisms which are rich in collagen, constituting the mesoglea, such as the Cnidarians, the Ctenophore and the gelatinous Mollusc studied, rather than in organisms rich in tunicin such as the Tunicates.     

Total metal concentrations and partitioning of Cd, Cr, Cu, Fe, Ni and Zn in sewage sludge

Application of the BCR three-step sequential extraction procedure to sewage sludge samples collected at an urban wastewater treatment plant (Dom ale, Slovenia) is reported. The total concentrations of Cd, Cr, Cu, Fe, Ni and Zn and their concentrations in fractions after extraction were determined by flame or electrothermal atomic absorption spectrometry (FAAS, ETAAS) under optimised measurement conditions. Total acid digestion including hydrofluoric acid (HF) treatment and aqua regia extraction were compared in order to estimate the efficiency of aqua regia extraction for determination of total metal concentrations in sewage sludge. It was found experimentally that aqua regia quantitatively leached these heavy metals from the sewage sludge and could therefore be applied in analysis of total heavy metal concentrations. The total concentrations of 856 mg kg⁻¹ Cr, 621 mg kg⁻¹ Ni and 2032 mg kg⁻¹ Zn were higher than those set by Slovenian legislation for sludge to be used in agriculture. Total concentrations of 2.78 mg kg⁻¹ Cd, 433 mg kg⁻¹ Cu and 126 mg kg⁻¹ Pb were below those permitted in the relevant legislation. CRM 146R reference material was used to follow the quality of the analytical process. The results of the BCR three-step sequential extraction procedure indicate high Ni and Zn mobility in the sludge analysed. The other heavy metals were primarily in sparingly soluble fractions and hence poorly mobile. Due to the high total Ni concentration and its high mobility the investigated sewage sludge could not be used in agriculture.     

Simultaneous removal of As, Cd, Cr, Cu, Ni and Zn from stormwater: experimental comparison of 11 different sorbents

The potential of using alumina, activated bauxsol-coated sand (ABCS), bark, bauxsol-coated sand (BCS), fly ash (FA), granulated activated carbon (GAC), granulated ferric hydroxide (GFH), iron oxide-coated sand (IOCS), natural zeolite (NZ), sand, and spinel (MgAl(2)O(4)) as sorbents for removing heavy metals from stormwater are investigated in the present study. The ability of the sorbents to remove a mixture of As, Cd, Cr, Cu, Ni and Zn from synthetic stormwater samples were evaluated in batch tests at a starting pH of 6.5. The metal speciation and saturation data is obtained using the PHREEQ-C geochemical model and used to elucidate the sorption data. It is found that BCS, FA, and spinel have significantly higher affinity towards heavy metals mainly present as cationic or non-charged species (i.e. Cd, Cu, Ni and Zn) compared to those present as anionic species (i.e. As and Cr). However, IOCS, NZ and sand have higher affinity towards As and Cr, while alumina has equally high affinity to all tested heavy metals. The Freundlich isotherm model is found to fit the data in many cases, but ill fitted results are also observed, especially for FA, BCS and GAC, possibly due to leaching of some metals from the sorbents (i.e. for FA) and oversaturated conditions making precipitation the dominant removal mechanism over sorption in batches with high heavy metal concentrations and pH. Calculated sorption constants (i.e. K(d)) are used to compare the overall heavy metal removal efficiency of the sorbents, which in a decreasing order are found to be: alumina, BCS, GFH, FA, GAC, spinel, ABCS, IOCS, NZ, bark, and sand. These findings are significant for future development of secondary filters for removal of dissolved heavy metals from stormwater runoff under realistic competitive conditions in terms of initial heavy metal concentrations, pH and ionic strength.     

Short-term temporal variations in speciation of Pb, Cu, Zn and Sb in a shooting range runoff stream

This study was designed to explore the changes in physico-chemical forms of Pb, Cu, Zn and Sb in a stream draining a contaminated shooting range, located at Steinsjøen in the South-Eastern part of Norway, during a period of 21 days. To obtain information on the element species distribution, an interphased size and charge fractionation system was applied, where membrane filtration (0.45 µm) and ultrafiltration using hollow fibre (nominal cut off 10 kDa) were performed prior to charge fractionation using chromatography (cationic and anionic exchange resins). The results show that Pb mainly was present as particulate and colloidal high molecular mass (HMM) species, Cu as colloidal (HMM) and low molecular mass (LMM) species, while Sb and Zn were mainly present as LMM species. The total element concentrations of Pb, Cu, Zn and Sb were positively correlated to water flow and dissolved organic carbon (DOC), suggesting these are important factors in controlling the run-off of the investigated elements in this catchment. During episodes of higher water flow, the increase in element concentration was mainly in the colloidal fraction. Partial redundancy analysis (pRDA) revealed that variations in pH, HMM organic carbon (HMM OC) and LMM organic carbon (LMM OC) explained 47% of the variation in size distribution of the elements, while variations in precipitation and water flow explained 48% of the variation in the charge distribution of the elements. The variation in concentrations during the period varied by a factor of 4, also stressing the importance of frequent sampling opposed to spot sampling in environmental surveys and risk assessments.     

Blood lead and its effect on Cd, Cu, Zn, Fe and hemoglobin levels of children

The levels of heavy metals, such as Pb, Cd, Cu, Zn and Fe, in whole blood samples of Mumbai and Hyderabad children have been determined. In the present study, 576 blood samples of children (3-6 years old) were collected during 1996-1998 and analyzed for heavy metal contents by anodic stripping voltammetry and atomic absorption spectrometry. The geometric mean concentrations of Pb, Cd, Cu and Zn in blood of Mumbai children were 8.0, 0.10, 86.5 and 398.9 microg dl(-1), while those for Hyderabad children were 13.3, 0.13, 100.6 and 483.4 microg dl(-1) respectively. The geometric mean concentrations of Fe in the blood of Mumbai and Hyderabad children were 21.9 and 34.5 mg dl(-1), respectively. Of the Mumbai children, 61.8% were found to have a blood lead concentration lcss than 10 microg dl(-1), while the corresponding proportion of Hyderabad children was 27.4%. Higher concentrations of Pb in the children's blood were observed at high traffic areas in both cities. A decreasing trend in the hemoglobin content with increasing blood lead levels was observed for Mumbai children. A good negative correlation (-0.61) between the blood lead and iron has been observed for Mumbai children The hemoglobin content of 85% of the study population was found to vary between 8 and 14 g%.     

The physicochemical speciation of Cd, Pb, Cu, Fe and Mn in the final effluent of a sewage treatment works and its impact on speciation in the receiving river

A scheme for the speciation of metals in freshwaters has been applied to the analysis of the final effluent from a sewage treatment plant and to the receiving river upstream and downstream of the effluent outfall. The treatment plant was selected because of the high influent and effluent concentrations of Cd. The metal speciation patterns in the effluent are interpreted primarily in terms of organic interactions, which appear to be exerting a solubilizing effect on Cd and Cu, but not on the Pb and Fe which are principally associated with the particulate size fraction (> 12 μm). The influx of metals with the sewage effluent alters the speciation pattern in the river. A large part of the Cd is added to the smallest size fraction (< 0.015 μm). However, the major part of each metal, with the exception of Mn, is associated with the colloidal and particulate size fractions, thus minimising the immediate toxic significance to aquatic life.     

Influence of surfactants on the determination of Cu, Pb and Cd by ASV

In anodic stripping voltammetric studies using a thin film Hg electrode and an acetate buffered base solution containing NaCl, peak currents were found to be influenced by the presence of surfactants of different charge types. The addition of mg l⁻¹ amounts of di-stearyl dimethyl ammonium chloride, lauryl dimethyl-benzyl ammonium chloride, sodium alkyl-benzene sulfonate, sodium salt of sulfonated lauryl alcohol polyoxyethylene condensate, coconut mono-ethanol-amide ethoxylate or octa-decylamine ethoxylate caused enhancement of Cu (20%) and Pb (10%) peaks and suppression of Cd response. The magnitude of the induced changes was not directly related to surfactant type, or experimental parameters, and as a result it is recommended that when analysing waters suspected of containing surfactants, extra care should be taken in the calibration stage.     

关于黄菖蒲和再力花固定西湖底泥中重金属Cd和Pb能力的研究

利用植物对重金属元素的累积和固定能力来修复和净化污染水体是一种环境友好的生态修复方式,黄菖蒲和再力花作为一种观赏价值较高、生物量较大、适应性很强的多年生挺水草本植物被广泛应用于湿地景观设计中。为了验证黄菖蒲和再力花固定水体Cd和Pb的能力,本研究通过探索盆栽试验和野外试验,分析了黄菖蒲和再力花地上部分和地下部分中Cd和Pb的累积浓度,结果表明,黄菖蒲地上和地下部分吸收Cd的能力都较强,具有净化和固定底泥中Cd的能力;而再力花地下部分吸收固定Pb的能力较强,具有净化和固定底泥中Pb的能力。因此,可以在湿地景观设计中配置一定比例的黄菖蒲和再力花,成熟期后收割地上部分进行适当处理,能够起到净化水体、固定底泥中重金属Cd和Pb的作用。     

Geochemical signals and source contributions to heavy metal (Cd, Zn, Pb, Cu) fluxes into the Gironde Estuary via its major tributaries

Daily measurements of water discharges and suspended particulate matter (SPM) concentrations and monthly sampling for trace element analyses (Cd, Zn, Pb and Cu) were conducted from 1999 to 2002 on the Garonne, Dordogne and Isle Rivers, the three main tributaries of the Gironde Estuary, France. Dissolved and particulate Cd, Zn, Pb and Cu concentrations in the Isle River were generally higher than those in the Garonne River, despite the known historical polymetallic pollution affecting the Lot-Garonne River system. Even if the relatively high dissolved metal concentrations in the Isle River may be of importance for the local ecosystem, metal inputs into the estuarine and coastal zones are mainly controlled by fluvial transport via the Garonne River. Characteristic element concentration ratios (e.g., Zn/Pb) in SPM and stream sediments from the Dordogne and Isle Rivers suggest two different metal source areas with distinct geochemical signals. Low Zn/Pb ratios (<8) and low Cu/Pb ratios (<0.8) have been attributed to upstream source zones in the Massif Central, featuring various ore deposits and mining areas. High Zn/Pb ratios were assigned to downstream sources (e.g., vineyards), partly explaining high Zn and Cu concentrations and high Cu/Pb ratios (>0.8) in SPM. Although SPM derived from the upstream parts of the studied watersheds may greatly contribute to the observed fluvial metal transport (up to approximately 80% for Pb), the results suggest that intensive agriculture also considerably influences gross metal (e.g., Zn, Cu) fluxes into the Gironde Estuary. Relative contributions of upstream and downstream source zones may vary from one year to another reflecting hydrological variations and/or reservoir management. Monitoring fluxes and identifying distinct geochemical signals from source areas in heterogeneous watersheds may greatly improve understanding of contaminant transport to the coast.     

Influences of pH, heavy metals and phosphate and their co-influences on the sorption of pentachlorophenol on cyanobacterial biomass

Influences of pH, two types of ions of transition metals (Cu²⁺, Cd²⁺), Na₃PO₄ and their co-influences on the sorption of pentachlorophenol (PCP) on cyanobacterial biomass derived from natural bloom were studied. Sorption of PCP significantly decreases with pH in the range of 3.25-9.00. Although sorption coefficient of ionized PCP is 8.51 times lower than that of neutral species, it is the dominant species at environmentally relevant pH and contributes more to the total sorption of PCP. In the presence of low concentration of Cu²⁺ (≤40 μmol L⁻¹), sorption of PCP was much lower than that of the blank. However, it increased gradually with Cu²⁺, and overpassed the blank when concentration of Cu²⁺ was higher than 50 μmol L⁻¹. Compared with the sole influence of pH, coexisted Cu²⁺ inhibited the sorption of PCP at pH of 3.25 and 4.35, but enhanced it in the pH range of 5.00-9.00. In the presence of Cd²⁺, sorption of PCP first increased then decreased rapidly and finally increased slightly again with Cd²⁺. Except for at pH of 9.00, sorption of PCP at other pH in the presence of Cd²⁺ was much lower than that solely affected by pH. In the presence of Na₃PO₄, sorption of PCP increased rapidly then maintained with Na₃PO₄. Under the influence of both Na₃PO₄ and pH, sorption of PCP at pH from 3.25 to 5.00 was lower than that solely affected by pH, while it increased with pH in the range of 5.00-9.00 and was higher than that solely affected by pH in the range of 6.00-9.00. Ion pairs of pentachlorophenolate-metal facilitated the sorption of PCP, which was largely dependent on pH illustrated by UV-visible and FTIR spectra. Speciations of metals and PCP and the stability constants of ion pairs of pentachlorophenolate-metal greatly affected the sorption. Ionic strength also played an important role for the sorption of PCP.