Removal of heavy metals in rinsing wastewater from plating factory by adsorption with economical viable materials

The removal of heavy metals from plating factory wastewater with economical materials was investigated by the column method. Montmorillonite, kaolin, tobermorite, magnetite, silica gel and alumina were used as the economical adsorbents to wastewater containing Cd(II), Cr(VI), Cu(II) and Pb(II). This removal method of heavy metals proved highly effective as removal efficiency tended to increase with increasing pH and decrease with increasing metal concentration. The removal percentages by adsorption onto montmorillonite, tobermorite, magnetite, and silica gel showed high values for all metals. From the results for the heat of adsorption, the adsorption process in the present study might be chemisorption. The proposed method was successfully applied to the removal of Cd(II), Cr(VI) and Cu(II) in rinsing wastewater from plating factory in Nagoya City, Aichi Prefecture, Japan. Since the economical adsorbents used can be obtained commercially because they are easily synthesized, the wastewater treatment system developed is rapid, simple and cheap for the removal of heavy metals.     

Adsorption of cadmium, copper, nickel, and zinc to a poly(tetrafluorethene) porous soil solution sampler

Suction cups made of poly(tetrafluorethene) (PTFE) are widely used for sampling of soil solution. A brand (Prenart) of PTFE cups was tested for adsorption of Cd, Cu, Ni, and Zn at low concentrations under different conditions. In a laboratory experiment adsorption from a 10 microg L(-1) heavy metal solution with a 0.01 M NaCl background electrolyte was investigated at pH 3.6, 4.5, and 5.8 by pumping the solutions through the cups. The effect of three different ionic compositions was also investigated using 0.01 M CaCl2, 0.01 M NaCl, and no background electrolyte at pH 4.5. In 0.01 M NaCl electrolyte at pH 5.8 the cups acted as effective filters. At pH 3.6 after 300 mL of solution had passed through the cup, equivalence between the Cd and Ni concentrations in influent and effluent was found. No equivalence between effluent and influent concentrations was found for Zn and Cu at pH 4.5 and 5.8. With Ca as the electrolyte, no adsorption of Cd, Ni, or Zn was found. In Na electrolyte, equivalence between influent and effluent concentrations for Cd, Ni, and Zn was reached. The difference between effluent and influent concentrations of Zn, Ni, and Cd remained significant in the absence of electrolyte. For all pH values and electrolytes the difference between effluent and influent concentrations of Cu was significant. It is concluded that PTFE cups affect the concentrations of heavy metals sampled at low soil solution concentrations. Cadmium, Cu, Ni, and Zn adsorb to the cup at pH > 4.5 and low ionic strength.     

Adsorption of Pb and Cd on the natural surface coatings (NSCs) in the presence of organochlorine pesticides: a preliminary investigation

Adsorption of Pb and Cd in the presence and absence of organochlorine pesticides (OCPs) on natural surface coatings (NSCs), which were collected in the Nanhu Lake in Changchun, China, was measured in order to investigate the effect of the OCPs on the adsorption of heavy metals on the NSCs. Adsorption of Pb/Cd was carried out under controlled laboratory conditions (mineral salt solution with defined species, ionic strength 0.05 mol/l, 25 degrees C and pH 6.0) with initial Pb and Cd concentrations ranging from 0.2 to 2.5 mol/l. The classical Langmuir adsorption isotherm was applied to estimate the equilibrium coefficients of the adsorption of Pb and Cd on the NSCs. Adsorption interference between Pb/Cd and the OCPs on the NSCs indicated that the adsorption of Pb/Cd on the NSCs was influenced by the OCPs, and competitive adsorption between Pb and the OCPs was observed while adsorption of Cd was enhanced by addition of the OCPs. Adsorption data fit the Langmuir isotherm well for the NSCs treated with the OCPs at different equilibrium concentrations. The results showed that the amount of adsorbed Pb decreased by more than 40% while the amount of adsorbed Cd increased by over 60% with an increase in the initial concentrations of the OCPs ranging from 0 to 5.0 microg/l and that adsorption of Pb/Cd on the NSCs was strongly affected by the OCPs. This preliminary study highlights the importance of the OCPs on the NSCs in controlling the transport, fate, biogeochemistry, bioavailability and toxicity of trace metals in aquatic environments.     

Transport of Escherichia coli in sand columns with constant and changing water contents

Understanding how changes in volumetric water content (theta) affect bacterial adsorption could help reduce transport of pathogenic and indicator bacteria that may be present in infiltrating wastewater. Three flow regimes that simulated infiltration from a household septic system were evaluated: saturated, unsaturated with a constant volumetric water content theta (constant unsaturated flow), and unsaturated with cyclic changes in theta (variable unsaturated flow). Escherichia coli was suspended in artificial sewage (AS) and applied as step inputs to sand columns, with regular interruptions in input for variable unsaturated flow. A transport model was fit to the saturated and constant unsaturated flow breakthrough curves to determine retardation (R), the first-order filtration coefficient (mu), and the maximum outflow relative concentration (Cmax). The total cells transported as a fraction of input (tau) in all three flow regimes was calculated. Constant unsaturated flow resulted in a significantly lower Cmax (0.633) in comparison with saturated flow (0.803, P < or = 0.05), although unsaturated mu (0.0693 h(-1)) was not significantly different from saturated mu (0.0259 h(-1)). Constant unsaturated flow also resulted in a significantly smaller tau (0.617) than saturated (0.806) or variable unsaturated flow (0.734). In variable unsaturated flow, cell concentrations were out of phase with theta--as the column drained, cell concentrations in the outflow increased; and when a pulse of suspension was applied, cell concentrations decreased. Constant unsaturated flow is probably the best for removal of pathogenic bacteria because this regime resulted in lower maximum concentrations of E. coli and greater cell removal, in comparison with saturated and variable unsaturated flow.     

Metal pollution in sediments of Jamaica Bay,New York,USA—An urban estuary

Calculations of the annual input of heavy metals to Jamaica Bay, New York, USA, reveal that sewage effluent carries the largest quantities of Ni, Zn, Cu, and Cd to the bay. Storm sewers and atmospheric fallout are the main sources of Pb. Atmospheric fallout of Zn, Cu, and Cd, although smaller than the combined input from sewers, contributes a significant fraction of these metals. The metal input from landfill leachate is far smaller than that from other sources. Analysis of available data shows that metal concentrations in the sediment of the bay correlate with each other and with percent total organic carbon (%TOC). This is consistent with the observation that the input of metals is predominantly associated with sewage. It is demonstrated that metal-TOC ratios, rather than metal concentrations, must be used in efforts to detect local intensive sources of metals in solution; metal-TOC ratios in intertidal sediment adjacent to these landfills are elevated by the adsorption of leachate metals, while metal concentrations are not. Subtidal sediment within a few hundred meters from two landfills shows no evidence of the addition of metals from that source, which is consistent with the small input of metals estimated for these landfills. The evidence cited in this study sharply contradicts the implication made in a widely publicized report issued by an environmental advocacy group that a significant link exists between metals found in subtidal sediment of Jamaica Bay and landfill leachate.     

An assessment of stream water quality of the Rio San Juan,Nuevo Leon,Mexico, 1995-1996

Good water quality of the Rio San Juan is critical for economic development of northeastern Mexico. However, water quality of the river has rapidly degraded during the last few decades. Societal concerns include indications of contamination problems and increased water diversions for agriculture, residential, and industrial water supplies. Eight sampling sites were selected along the river where water samples were collected monthly for 10 mo (October 1995-July 1996). The concentration of heavy metals and chemical constituents and measurements of bacteriological and physical parameters were determined on water samples. In addition, river discharge was recorded. Constituent concentrations in 18.7% of all samples exceeded at least one water quality standard. In particular, concentrations of fecal and total coliform bacteria, sulfate, detergent, dissolved solids, Al, Ba, Cr, Fe, and Cd, exceeded several water quality standards. Pollution showed spatial and temporal variations and trends. These variations were statistically explained by spatial and temporal changes of constituent inputs and discharge. Samples collected from the site upstream of El Cuchillo reservoir had large constituent concentrations when discharge was small; this reservoir supplies domestic and industrial water to the city of Monterrey.     

Influence of organic waste type and soil structure on the bacterial filtration rates in unsaturated intact soil columns

Organic wastes are considered to be a source for the potentially pathogenic microorganisms found in surface and sub-surface water resources. Following their release from the organic waste matrix, bacteria often infiltrate into soil and may be transported to significant depths contaminating aquifers. We investigated the influence of soil texture and structure and most importantly the organic waste properties on the transport and filtration coefficients of Escherichia coli and total bacteria in undisturbed soil columns. Intact soil columns (diameter 16 cm and height 25 cm) were collected from two soils: sandy clay loam (SCL) and loamy sand (LS) in Hamadan, western Iran. The cores were amended with cow manure, poultry manure and sewage sludge at a rate of 10 Mg ha(-1) (dry basis). The amended soil cores were leached at a steady-state flux of 4.8 cm h(-1) (i.e. 0.12 of saturated hydraulic conductivity of the SCL) to a total volume of up to 4 times the pore volume of the columns. The influent (C(0)) and effluent (C) were sampled at similar time intervals during the experiments and bacterial concentrations were measured by the plate count method. Cumulative numbers of the leached bacteria, filtration coefficient (lambda(f)), and relative adsorption index (S(R)) were calculated. The preferential pathways and stable structure of the SCL facilitated the rapid transport and early appearance of the bacteria in the effluent. The LS filtered more bacteria when compared with the SCL. The effluent contamination of poultry manure-treated columns was greater than the cow manure- and sewage sludge-treated ones. The difference between cow manure and sewage sludge was negligible. The lambda(f) and S(R) values for E. coli and total bacteria were greater in the LS than in the SCL. This indicates a predominant role for the physical pore-obstruction filtration mechanisms as present in the poorly structured LS vs. the retention at adsorptive sites (chemical filtration) more likely in the better structured SCL. While the results confirmed the significant role of soil structure and preferential (macroporous) pathways, manure type was proven to have a major role in determining the maximum penetration risk of bacteria by governing filtration of bacteria. Thus while the numbers of bacteria in waste may be of significance for shallow aquifers, the type of waste may determine the risk for microbial contamination of deep aquifers.     

Characteristic levels of heavy metals in soil profiles of automobile mechanic waste dumps in Nigeria

The characteristic levels of heavy metals (Cd, Cr, Cu, Pb, Ni and Zn) of soil profiles of automobile mechanic waste dumps were studied. The concentration of heavy metals decreased with the depth of the profile and lateral distance from the dumpsites. The levels found in this study exceeded background concentrations and limits for agricultural and residential purposes. The distribution pattern of heavy metals in the soil profiles were in the following order Pb > Zn > Cu > Cd > Ni > Cr. The mechanic waste dumps represent potential sources of heavy metal pollution to environment. The elevated levels of heavy metals in these soil profiles constitute a serious threat to both surface and groundwater.     

Determination of model parameters for zinc (II) ion biosorption onto powdered waste sludge (PWS) in a fed-batch system

Biosorption of zinc (II) ions onto pre-treated powdered waste sludge (PWS) was investigated using a completely mixed tank operating in fed-batch mode instead of an adsorption column. Experiments with variable feed flow rate (0.05-0.5 L h(-1)), feed Zn(II) ion concentrations (37.5-275 mg L(-1)) and amount of adsorbent (1-6 g PWS) were performed using fed-batch operation at pH 5 and room temperature (20-25 degrees C). Break-through curves describing variations of aqueous (effluent) zinc ion concentrations with time were determined for different operating conditions. Percent zinc removal from the aqueous phase decreased, but the biosorbed (solid phase) zinc ion concentration increased with increasing feed flow rate and zinc concentration. A modified Bohart-Adams equation was used to determine the biosorption capacity of PWS (q'(s)) and the rate constant (K) for zinc ion biosorption. Biosorption capacity (q'(s)=57.7 g Zn kg(-1) PWS) of PWS in fed-batch operation was found to be comparable with powdered activated carbon (PAC) in column operations. However, the adsorption rate constant (K=9.17 m(3) kg(-1) h(-1)) in fed-batch operation was an order of magnitude larger than those obtained in adsorption columns because of elimination of mass transfer limitations encountered in the column operations. Therefore, a completely mixed tank operated in fed-batch mode was proven to be more advantageous as compared to adsorption columns due to better contact between the phases yielding faster adsorption rates.     

Phosphorus leaching from cow manure patches on soil columns

The loss of P in overland flow or leachate from manure patches can impair surface water quality. We studied leaching of P from 10-cm-high lysimeters filled with intact grassland soil or with acid-washed sand. A manure patch was created on two grassland and two sand-filled lysimeters, and an additional two grass lysimeters served as blanks. Lysimeters were leached in the laboratory during 234 d with a diluted salt solution, and column effluent was passed through a 0.45-microm filter, analyzed for pH, dissolved reactive P (DRP), and total dissolved P (TDP). At the end of the experiment lysimeter soil was sampled and analyzed for pH, available P, and oxalate-extractable P, Fe, and Al. The concentration of TDP in the effluent from the sand column increased to 25 mg L-1 during the first weeks and remained above 10 mg L-1 during the rest of the percolation. In effluent from grass + patch lysimeters TDP gradually increased to 4 mg L-1. Both in the manure and in the effluent of the sand lysimeter P was found mainly in the form of DRP, but in the effluent from the grass lysimeters was found mainly as dissolved unreactive P (DUP=TDP-DRP). Earthworm activity was responsible for decomposition of the manure patch on the grass lysimeters. Manure patches and their remains were found to be a long-term source of high concentrations of P in leachates. Spreading of patches after a grazing period could reduce their possible negative impacts on the environment.     

Bacterial pretreatment enhances removal of heavy metals during treatment of post-methanated distillery effluent by Typha angustata L

A combination of bacterial pretreatment followed by free water surface flow through wetland plants was investigated to determine its effect on removal of heavy metals in bioremediation of post-methanated distillery effluent (PMDE). The bacterial pretreatment was intended to transform the metal complexes and organic pollutants into simpler, biologically assimilable molecules. The 10% and 30% v/v concentrations of PMDE favored luxuriant bacterial growth; the 50% concentration supported less growth, whereas the undiluted effluent (i.e., 100%) supported very little bacterial growth. The use of bacterial pretreatment combined with the constructed wetland system greatly increase the overall bioaccumulation of all heavy metals by the plants compared with the control treatment. However, the integration of bacterial pretreatment of PMDE with the Typha angustata resulted in enhanced removal of Cd (34.02–61.50% increase), Cr (35.90–57.60% increase), Cu (32.88–54.22% increase), Fe (32.50–51.26% increase), Mn (35.99–82.85% increase), Ni (35.85–59.24% increase), Pb (33.45–59.51% increase) and Zn (31.95–53.70% increase) compared with a control that lacked this pretreatment. In addition to the bioaccumulation of these heavy metals, several physico-chemical parameters also improved at the 30% effluent concentration: color, BOD, COD, phenol and total nitrogen decreased by 98.33%, 98.89%, 98.50%, 93.75% and 82.39%, respectively, after 7 days of free water surface flow treatment. The results suggest that bacterial pretreatment of PMDE, integrated with phytoremediation will improve the treatment process of PMDE and promote safer disposal of this waste.     

FACTORS INFLUENCING ACUTE TOXICfrY OF COAL ASH TO RAINBOW TROUT (SALMO GAIRDNERI) AND BLUEGILL SUNFISH (LEPOMIS MACROCHIRUS)1

ABSTRACT: The potentially toxic components in coal ash (ash particles, heavy metals) were evaluated in laboratory static, acute (96 hr) bioassays, both separately and in various combinations with extreme pH (5.0 and 8.5), using rainbow trout (Salmo gairdneri) and bluegifi sunfish (Lepomis macrochirus). Ash particle morphology and metal distribution anlaysis, using electron microscopy and surface-subsurface analysis by ion microscopy, showed that metals could be either clumped or evenly distributed on the surface of fly ash. Surface enrichment on fly ash particles from electrostatic precipitators, as measured by ion microscopy, was found for cadmium, copper, chromium, nickel, lead, mercury, titanium, arsenic, and selenium. Bottom (heavy) ash was not acutely toxic to either fish species at concentrations of up to 1500 mg/l total suspended solids (TSS) at pH 5.0, 7.5, or 8.5. Fly ash particles were not acutely toxic to blue-gill at levels up to 1360 mg/l TSS. Rainbow trout were highly sensitive to fly ash (25 to 60 percent mortality) at concentrations of 4.3 to 20.5 mg/I TSS when dissolved metal availability was high but were not sensitive at higher particulate concentrations (58 to 638 mg/I TSS) when dissolved metals were low. When metals were acid-leached from fly ash prior to testing, no rainbow trout mortality occurred at TSS concentrations of up to 2,350 mg/l TSS. When the percent of dissolved metal was high (e.g., 50–90 percent of the total), fish mortality was increased. Rainbow trout were nearly two orders of magnitude more sensitive than bluegill when subjected to a blend of cadmium, chromium, copper, nickel, lead, and zinc. The two species were similar in their acute sensitivity to acidic pH at levels at or below 4.0 and alkaline pH of 9.1. If the pH of coal ash effluent is contained within the range 6.0 to 9.0, acute toxicity to fish can be attributed to trace element availability from fly ash but not heavy ash. Control of holding pond and effluent pH and maximizing pond residence time are important strategies for minimizing effects of ash pond discharges on fish.     

The fate of heavy metals in green waste composting

It has long been known that heavy metals, when in high enough concentration, have the potential to be both phytotoxic and zootoxic. Heavy metals are frequently found as contaminants in green waste. Any such waste that is subsequently segregated for composting theoretically has the potential to retain that possible contamination. To date, there have been a limited number of publications addressing this issue. Most reports have concentrated on the types of heavy metals found in compost and their acceptable levels, rather than the fate of heavy metal contaminants throughout the composting process. This investigation was aimed to identify the fate of cadmium (Cd), copper (Cu), chromium (Cr), lead (Pb) and zinc (Zn) concentrations throughout a fourteen week composting cycle. The results of this study showed a general increase in the removal of Pb, Cu, Cr, and to a much smaller extent Zn, manifested by a decrease in their overall concentrations within the solid fraction of the final product, by 93, 49, 43, and 20 percent respectively. By contrast, there was no decrease in the overall concentration of Cd.     

柴窝堡湖表层底泥重金属污染评价

研究了乌鲁木齐市柴窝堡湖表层底泥的重金属含量,并采用Hakanson潜在生态危害指数法对底泥中的重金属潜在生态风险进行评价。结果表明:底泥中Cu、Zn、Pb、Cd含量均超出乌鲁木齐市土壤背景值。除湖心区外,Cd在5个监测区域中的潜在生态危害均为中等;其它重金属在5个采样点的潜在生态危害均为轻微。各重金属间的相关性分析表明,Zn与Cu,Pb与Cd、Cu呈显著正相关,说明这4种元素污染源可能相同。柴窝堡湖表层底泥受到Cu、Zn、Pb、Cd污染,需采取相应措施防止重金属由底泥进入水相。     

鲫鱼对铜和锌的吸收蓄积研究

用原子吸收分光光度法研究铜和锌在鲫鱼体内积累行为，结果表明，溶解态和颗粒态铜和锌在鱼鳃、肌肉中的积累量随其浓度的增加而增加。铜和锌积累能力的大小顺序为锌〉铜。鱼鳃和肌肉对溶解态和颗粒态重金属的积累能力为鱼鳃大于肌肉，蓄积曲线表现为逐渐趋向平缓的形式。颗粒态鱼鳃积累尤其大于肌肉，说明鱼在对颗粒态铜和锌的积累过程中，部分颗粒态金属是吸附在鱼鳃上的。由于生理功能不同，鲫鱼对锌需要量比铜多。     

Fecal contamination of pastoral wetlands

Near-channel hill-country wetlands draining steep pastoral land in New Zealand exhibit high levels of fecal contamination at a range of flows. This contamination is attributed to both the transport of bacteria into a wetland from the surrounding catchment and the direct excretion of fecal material onto wetlands by grazing cattle. E. coli concentrations observed at low to moderate flow at 20 sites varied between 0.5 x 10(1) and 2 x 10(4) most probable number (MPN) 100 mL(-1). High flow concentrations measured at two wetlands ranged up to 6 x 10(6) MPN 100 mL(-1) and yielded storm period bacterial loads of between 1 x 10(6) and 3 x 10(10) MPN per event. Given the disproportionately large fraction of surface and subsurface flow from the catchment that passes through the wetlands, these yields represent a large proportion of the total loss of bacteria from steep grazed hillsides, across a range of storm events. Cattle are attracted to the smaller, shallower wetlands for grazing in both summer and winter. Excluding stock from shallow wetlands may therefore yield improvements in bacterial water quality, although accurately quantifying this improvement is difficult without long-term studies. Cattle are not attracted to larger, deeper wetlands, presumably for fear of entrapment, and fencing them is unlikely to realize significant improvements in bacterial water quality. A statistical model incorporating solar radiation and flow explains 87% of the variance in E. coli concentrations across five monitored rainfall events. A positive correlation was found between solar radiation and E. coli concentration. The study was conducted in winter when clear, sunny days are relatively cold. Solar radiation on these days appears to be too weak to promote die-off but the colder temperatures aid survival.     

GOLD-MINING EFFECTS ON HEAVY METALS IN STREAMS,CIRCLE QUADRANGLE,ALASKA1

Placer gold mining, which extracts gold from buried or exposed alluvia, is often conducted on or near streams. Such mining has the potential to adversely affect water quality. Other heavy metals associated with the gold (such as arsenic, cadmium, lead, zinc, and copper) may be freed to enter streams. Mercury may also enter streams if miners are using it to recover fine particles of gold. These heavy metals are toxic and thus may be harmful to the aquatic life of the streams receiving effluent or runoff from placer mines. In 1982 we sampled two streams intensively - one heavily mined and one unmined - for total recoverable arsenic, mercury, lead, zinc, and copper. Only mercury was not significantly higher in concentration in the mined streams. In 1983 we sampled two stream pairs three times, and 10 other sites at least once, for total and dissolved arsenic, cadmium, mercury, lead, zinc, and copper. Mercury and cadmium were not significantly elevated in mined streams, but the concentrations of total arsenic, lead, zinc, and copper, and dissolved arsenic and zinc were significantly higher in streams below active placer mining sites than in these that were not being mined or those that had never been mined. Additionally, total arsenic, lead, zinc, and copper and dissolved arsenic and copper became elevated after mining began in 1983 on a previously unmined stream.     

Heavy metal release from contaminated soils: comparison of column leaching and batch extraction results

Heavy metals in soils may adversely affect environmental quality. In this study, we investigated the release of Zn, Cd, Pb, and Cu from four contaminated soils by column leaching and single and sequential batch extractions. Homogeneously packed soil columns were leached with 67 mL/g 10(-2) M CaCl2 to investigate the exchangeable metal pool and subsequently with 1400 mL/g 10(-2) M CaCl2 adjusted to pH 3 to study the potential of metal release in response to soil acidification. In two noncalcareous soils (pH 5.7 and 5.1), exchange by Ca resulted in pronounced release peaks for Zn and Cd that were coupled to the exchange of Mg by Ca, and 40 to 70% of total Zn and Cd contents were rapidly mobilized. These amounts compared well with exchangeable pools determined in single and sequential batch extractions. In two soils with near-neutral pH, the effluent concentrations of Zn and Cd were several orders of magnitude lower and no pronounced elution peaks were observed. This behavior was also observed for Cu and Pb in all four soils. When the soils were leached at pH 3, the column effluent patterns reflected the coupling of CaCO3 dissolution (if present) and other proton buffering reactions, proton-induced metal release, and metal-specific readsorption within the soil column. Varying the flow rate by a factor of five had only minor effects on the release patterns. Overall, Ca exchange and subsequent acidification to pH 3 removed between 65 and 90% of total Zn, Cd, Pb, and Cu from the four contaminated soils.     

Natural materials for treatment of industrial effluents: comparative study of the retention of Cd, Zn and Co by calcite and hydroxyapatite. Part I: batch experiments

This work explores the heavy metal retention capacity of materials developed from minerals that are abundant in nature, with low cost and minimum environmental impact. To accomplish this objective we have: (a) characterized commercial samples of calcite (CA) and hydroxyapatite (HAP)--including their surface properties (BET area, electrophoretic mobility, SEM, and X-ray energy dispersive spectroscopy); and, (b) qualified and quantified the interaction of Cd, Zn and Co with calcite (CaCO3) and hydroxyapatite [Ca5(PO4)3OH] through batch experiments, in a range of metal concentrations (4Zn>Co and Cd>Zn approximately Co, respectively. Retention increased with pCa and pH and could be modeled by: (a) a non-ideal ion exchange mechanism (Me/Ca) for the adsorption of Cd, Zn and Co onto CA; and, (b) a mechanism of non-ideal ion exchange and specific adsorption (Me/Ca and identical with PO4O-Me) in the case of HAP. The pH dependence is indirect in CA and is related to its solubility changes (pCa increases with pH, and so does sorption of Cd, Zn and Co). Both materials, HAP and CA, can be used for heavy metal retention. The former has better performance for water treatment due to its greater efficiency for the retention of Cd, Zn and Co (over two orders of magnitude per gram of material) and its lower solubility in a wide range of pH (6相似文献   

A review and experimental verification of using chitosan and its derivatives as adsorbents for selected heavy metals

A literature survey on liquid-phase adsorption of selected heavy metals including Cu(II), Zn(II), Ni(II), Cd(II), Pb(II), Hg(II), and Cr(VI) on chitosan (CTS) and its derivatives was made from the viewpoint of adsorption capacity. This parameter was obtained from the Langmuir fit of isotherm data. The magnitude of adsorption capacity of heavy metals on pristine CTS was also used to discuss the mechanism of adsorption; that is, how many amino groups in CTS chains would coordinate with one heavy metal ion. Furthermore, a newly defined parameter, the approaching equilibrium factor R_L, was proposed to quantitatively indicate the favorability of the related adsorption process and to judge the correctness of adsorption capacity determined by the Langmuir equation.