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1.
This study examines the phosphorus attenuation capacity of acid mine drainage (AMD) floc (also called ocher or sludge)—generated by neutralizing AMD with ammonia, lime, and sodium hydroxide—in the face of competition from two major organic companions, citrate and oxalate, of phosphorus in manure. Lime-treated floc (LF) was the least effective of the three flocs in attenuating both inorganic phosphorus and organic phosphorus (OP: represented by inositol hexaphosphate or phytate). Out of the remaining two flocs, ammonia-treated floc (AF) attenuated more inorganic phosphorus and less organic phosphorus than did sodium hydroxide-treated floc (SF). Increasing citrate:phosphorus molar ratio in the solution from 0:1 to 1:1 decreased the inorganic P attenuation capacity (IPAC) from 53 to 29 % in AF, 33 to 16 % in LF, and from 49 % to 27 % in SF at pH 4. The corresponding figures for organic P attenuation capacity (OPAC) were from 73 to 54 % in AF, 58 to 45 % in LF, and from 76 to 58 % in SF. Increasing oxalate:phosphorus molar ratio from 0:1 to 1:1 decreased IPAC and OPAC similarly, but to a lesser extent. The competitive influence of citrate and oxalate went on weakening with increase in pH. A likely increase in pH following prolonged manure application may undermine the competitive ability of citrate and oxalate. The study shows that manure P attenuation potential of waste of AMD treatment, notwithstanding the peer anion competition to P, warrants its effectiveness in controlling buildup of P in heavily manured soils.  相似文献   

2.
The high phosphorus levels cause the release of phosphorus from soils, thereby increasing the potential for phosphorus export to adjacent water bodies. The loss of phosphorus from soils to surface waters is a major source of water quality impairment. Therefore, soil phosphorus immobilization seems necessary. In this study, red mud (RM) was employed to immobilize phosphorus in a typical agricultural soil. It was found that phosphorus was effectively immobilized by RM. Batch leaching experiments showed that RM reduced phosphorus release from 14.38 to 2.56 mg/kg when soil was amended with 1% RM. Column leaching experiments showed that RM reduced the total amount of phosphorus released from 36.73 to 18.79 mg/kg during the investigated period. Sequential chemical extraction results indicated that RM amendment transformed H2O-P into more stable fractions. The results suggested that application of RM amendment to soils could significantly immobilize soluble phosphorus, reducing phosphorus release to the environment.  相似文献   

3.
Removal of arsenite from aqueous solution was carried out using electro-coagulation method. The experiments were conducted using copper–copper and zinc–zinc electrodes. The optimized experimental parameters were 2.0 mg/L initial concentration, 16.0-min processing time, 6.0 pH, 3.0-V applied voltage and 30 °C temperature for zinc–zinc electrodes while these values for copper–copper electrodes were 2.0 mg/L initial concentration, 20.0-min processing time, 7.0 pH, 5.0-V applied voltage and 30 °C temperature. The results demonstrated that zinc–zinc and copper–copper electrodes removed arsenite up to 99.89 and 99.56 %, respectively. The treated water was clear, colorless and odorless without any secondary contamination. There was no change in water quality after the removal of arsenite. The reported method is capable to remove arsenite from water at 6–7 pH range, which is a pH range of natural water. Therefore, this method may be the choice of arsenite removal from natural ground water.  相似文献   

4.
Red mud (RM) was produced during alumina production from bauxite known as the Bayer process. Arsenic was detected in the solid phase of RM (RMsf) which was disposed in the disposal area. This study investigates the effectiveness of using Zero-valent iron (ZVI), ferrihydrite, ferrous sulfate (FeSO4), waste acid (WA) or CO2 for immobilization of arsenic in the RMsf. To test the effect of the amendments on the arsenic leachability, the RMsf samples were amended with the iron-based materials or acidifiers at various w/w (weight/weight) ratios (1–10 %) for 30 days. The leachability of arsenic in the RMsf was evaluated by a 4-step water elusion process. After 30-day treatment of the RMsf, the leachability of As decreased from an initial (12.7 %) to (7.0 %) with a w/w ratio of 5 % ZVI (0 %) with 5 % FeSO4·7H2O, (3.4 %) with 5 % ferryhydrite, (2.0 %) with 6 % WA and (11.8 %) with 6 % CO2. FeSO4·7H2O and WA showed more effectively than other amendments for immobilizing arsenic. Arsenic fractionation with a sequential extraction procedure was used to evaluate the arsenic migration potential in the RMsf. FeSO4 and WA were effective in increasing the hydrous oxide combined arsenic in the RMsf. The leachable Cl? and SO4 2? in the RMsf increased from 2.9 to 14.1 mg/g and 19.9–44.4 mg/g with 6 % WA and 5 % FeSO4·7H2O added, respectively. The estimated cost of the FeSO4 and WA treatment was 0.47 and 0.49 USD per ton, respectively.  相似文献   

5.
Immobilization of trace elements in contaminated soils by zero-valent iron (ZVI) is a promising remediation method, but questions about its long-term performance remain unanswered. To quantify immobilization and predict possible contaminant remobilization on long timescales detailed knowledge about immobilization mechanisms is needed. This study aimed at assessing the long-term effect of ZVI amendments on dissolved copper and arsenic in contaminated soils, at exploring the immobilization mechanism(s), and at setting up a geochemical model able to estimate dissolved copper and arsenic under different scenarios. Samples from untreated and ZVI-treated plots in two field experiments where ZVI had been added 6 and 15 years ago were investigated by a combination of batch experiments, geochemical modeling and extended X-ray absorption fine structure (EXAFS) spectroscopy. Dissolved copper and arsenic concentrations were described by a multisurface geochemical model with surface complexation reactions, verified by EXAFS. The ZVI remained “reactive” after 6–15 years, i.e. the dissolved concentrations of copper and arsenic were lower in the ZVI-treated than in the untreated soils. There was a shift in copper speciation from organic matter complexes in the untreated soil to surface complexes with iron (hydr)oxides in the ZVI-treated soil. The pH value was important for copper immobilization and ZVI did not have a stabilizing effect if pH was lower than about 6. Immobilization of arsenic was slightly pH-dependent and sensitive to the competition with phosphate. If phosphate was ignored in the modeling, the dissolution of arsenate was greatly underestimated.  相似文献   

6.
Mercury, zinc and copper contamination was evaluated in soils and fluvial sediments from an abandoned gold mining site at Descoberto Municipality (southern Minas Gerais State, Brazil). Metals bioavailability and potential mobility were studied through physical, chemical and mineralogical characterization, geoaccumulation indexes calculations, mercury speciation and determination of potentially bioavailable contents of zinc and copper. Values of pH were in the neutral range, while organic matter concentrations were very low. Mineralogical characterization, in the total samples, indicated the presence of quartz, kaolinite and gibbsite for all samples. Total mercury, zinc and cooper concentrations were higher than the limits recommended by Brazilian documents. Geoaccumulations indexes revealed that most of the sediment samples were low to moderately polluted by zinc and copper, while just one sample was very strongly polluted by mercury. Mercury speciation revealed the predominance of the elementary form for all samples, and low concentrations for exchangeable, strongly bound and residual fractions. Zinc and copper behavior was strongly controlled by iron and aluminum concentrations, while their bioavailable contents were very low in comparison with the total concentrations.  相似文献   

7.
Calcareous and smectitic clay samples from the Coniacian–Lower Campanian system, Tunisia, were used as adsorbents for the removal of copper and zinc from aqueous solutions in single and binary systems. Calcareous clay sample was treated with acetic acid to obtain carbonate-free sample that was also used for metals removal. The adsorption of metal ions onto natural clay was tested in a batch method by mixing 1 g/L of each sample with a metal ion solution of zinc (300 μmol/L) and/or copper 600 μmol/L under the operating pH of 6, and agitation speed of 200 rpm within the equilibrium time of 60 min at 25 °C for single and binary systems. Our results showed that natural clay samples were mainly composed of silica, alumina, iron, and magnesium oxides. Adsorption data showed that the studied clay samples removed substantial amounts of heavy metals in single and mixed systems. Initial solution pH and carbonates contents enhanced the removal capacities of the studied clay samples, confirming their strong influencing effects. Thermodynamic parameters indicated an endothermic adsorption for metals removal by calcareous clay, but exothermic process for the smectitic sample. These results suggest that the Late Cretaceous clays, Tunisia, can be effectively used as natural adsorbents for the removal of toxic heavy metals in aqueous systems.  相似文献   

8.
To increase soil productivity, ameliorate nutrient scarcity, and reduce metal toxicity in highly weathered acidic soils usually requires fertilizer and lime application. Effects of three biochars on soil acidity, Olsen-phosphorus (P), phosphatase activities, and heavy metal availability were investigated to test potential of these biochars as soil amendments in highly weathered acidic soils. Incubation experiments were conducted for 6 weeks with three acidic soils: Alfisol, Ultisol, and Oxisol. Three biochars were derived from chicken manure (CMB), pig manure (PMB), and peat moss (PB) at 400 °C and applied at 1 or 2% (wt/wt). The addition of the three biochars increased Olsen-P in the three acidic soils in the following order: CMB?>?PMB?>?PB. Application of 2% CMB increased Olsen-P contents by 2.41-, 7.4-, and 1.78-fold in the Ultisol, Oxisol, and Alfisol compared with controls, respectively. Moreover, CMB increased the soil pH, electrical conductivity (EC), cation exchange capacity (CEC), and alkaline phosphatase activity, but reduced exchangeable acidity, acid phosphatase activity, and the availability of heavy metals—more effectively than PMB and PB. Addition of CMB increased soil pH by 0.90, 0.90, and 0.92 units for the Alfisol, Ultisol, and Oxisol, respectively, correspondingly followed by 0.80, 0.84, and 0.87 units for PMB and 0.15, 0.28, and 0.25 for PM. Changes in EC, CEC, and exchangeable acidity followed the same order for the three soils: CMB?>?PMB?>?PB. The results suggested that the magnitude of changes in soil properties and Olsen-P contents depended on biochar type and application rate. Application of CMB increased nutrient availability and reduced the availability of heavy metals more than other amendments. Due to higher pH, EC, and CEC, and greater concentrations of carbon, nitrogen, and exchangeable calcium and potassium, incorporation of CMB should be a better cost-effective method to correct soil acidity and improve fertility and Olsen-P contents in Ultisols and Oxisols from tropical and subtropical regions of the world.  相似文献   

9.
High As contents in groundwater were found in Rayen area and chosen for a detailed hydrogeochemical study. A total of 121 groundwater samples were collected from existing tube wells in the study areas in January 2012 and analyzed. Hydrogeochemical data of samples suggested that the groundwater is mostly Na–Cl type; also nearly 25.62 % of samples have arsenic concentrations above WHO permissible value (10 μg/l) for drinking waters with maximum concentration of aqueous arsenic up to 25,000 μg/l. The reducing conditions prevailing in the area and high arsenic concentration correlated with high bicarbonate and pH. Results show that arsenic is released into groundwater by two major phenomena: (1) through reduction of arsenic-bearing iron oxides/oxyhydroxides and Fe may be precipitated as iron sulfide when anoxic conditions prevail in the aquifer sediments and (2) transferring of As into the water system during water–acidic volcanic rock interactions.  相似文献   

10.
In this study, dried anaerobic digested sludge (DADS) was utilized to remove 4-chlorophenol (4-CP) from aqueous solutions. Batch biosorption experiments were carried out to investigate the effects of physicochemical parameters such as pH, contact time, biosorbent dosage, and initial concentration. Artificial neural network (ANN) was then used to predict the removal efficiency of the process. The comparison between predicted and experimental results provided a high degree of determination coefficient (R2 = 0.98), indicating that the model could predict the biosorption efficiency with reasonable accuracy. Biosorption data were successfully described by the Freundlich isotherm and pseudofirst-order model. The Weber–Morris kinetic model indicated that intraparticle diffusion was not the only rate-controlling step, and other mechanisms may be involved in the biosorption process. The optimum pH was detected to be 3 for DADS. By increasing contact time and biosorbent dosage, the removal efficiency of 4-CP increased. Also, a decreasing trend was observed when initial concentrations were increased. The findings suggested that the results predicted by ANN are very close to the experimental values, and DADS as an available adsorbent can efficiently remove 4-CP from aqueous solutions.  相似文献   

11.
Phenol is one of the aromatic hydrocarbons. Phenol and its derivatives are highly toxic. These pollutants can be observed in the effluents of many industries. This research investigates the removal of phenol by the use of activated sludge in a batch system. The effects of influencing factors on biodegradation efficiency have been evaluated. The main factors considered in this study were the volume of acclimatized activated sludge inoculation, pH, temperature, and initial concentration of phenol. The inoculation volumes of 1, 3, and 5 mL of acclimatized activated sludge were taken into account. Different pH values of 3, 5, 7, 9, and 11 were examined. The experiments were conducted for temperatures of 25, 30, 35, and 40 °C and initial phenol concentrations of 400, 800, 1,000, and 1,500 ppm. The results show that the acclimatized activated sludge has a high capacity for the removal of phenol. From a 100-mL aqueous solution was removed 1,500 ppm of phenol after 80 h. Furthermore, maximum phenol removal was observed for an inoculation volume of 5 mL for three different phenol concentrations of 100, 400, and 800 ppm. The best pH was 7 for the biodegradation process, and the optimum temperature was 30 °C. It was further found that an increase in the phenol concentration increased its removal time. Moreover, the activated sludge could effectively remove about 99.9 % of phenol from a synthetic aqueous solution in a batch system.  相似文献   

12.
This study was carried out to assess the effects of hematite nanoparticles (α-Fe2O3) on the motility and phytoavailability of arsenic in contaminated soils and corn growth. A factorial experiment was conducted using a completely randomized design and three replications. The examined factors were the application rates of hematite nanoparticles (0, 0.05, 0.1 and 0.2%) and the levels of soil arsenic (0, 6, 12, 24, 48, and 96 mg/kg). Before sowing of corn seeds, the concentrations of soil available arsenic were measured in all soil samples. Corn plant was used as a biological indicator of arsenic phytoavailability and 75 days after sowing, it was harvested, and dry weights of aerial parts and roots and concentrations of arsenic and phosphorus of these parts were measured. The results showed that the concentration of soil available arsenic and arsenic concentrations of root and aerial parts increased as the concentration of soil total arsenic increased. Contamination of soil by arsenic increased the concentration of phosphorus in root but decreased it in the aerial parts of corn. In contaminated soils, the application of hematite nanoparticles significantly decreased the concentrations of arsenic in soil and in root and aerial parts of corn and increased the dry weights of root and aerial parts. But in uncontaminated soils, the application of hematite nanoparticles decreased the concentration of phosphorus and the dry weights of root and aerial parts of corn.  相似文献   

13.
Heavy metals on tidal flats in the Yangtze Estuary, China   总被引：7，自引：0，他引：7  
 Five short cores were used to examine heavy metals on tidal flats in the Yangtze Estuary, China. Statistically insignificant trends in lead-210 and most metals with core depth are primarily due to high sedimentation rates. Metal contents are correlated with percent aluminum, which reflects the clay contents in the sediment, and they are also affected by proximity to sewage outlets and local industry. National standards for copper are exceeded in four cores, zinc in one core, and arsenic in all cores. Heavy metal contents are generally lower on the Yangtze tidal flats compared to most other estuaries because high sediment loads dilute metal inputs. Received: 1 June 1999 · Accepted: 15 August 2000  相似文献   

14.
A zinc oxide-coated nanoporous carbon sorbent was prepared by acid modification and ZnO functionalization of mesoporous carbon. The synthesized materials, such as mesoporous carbon, oxidized mesoporous carbon and zinc oxide-coated nanoporous carbon, were characterized by nitrogen adsorption–desorption analysis, Fourier transform infrared spectra, scanning electron microscopy, and transmission electron microscopy. ZnO on oxidized mesoporous carbon gradually increased with increase in the number of cycles. Furthermore, the effects of agitation time, initial metal ions concentration, adsorbent dose, temperature and pH on the efficiency of Pb(II) ion removal were investigated as the controllable factors by Taguchi method. The value of correlation coefficients showed that the equilibrium data fitted well to the Langmuir isotherm. Among the adsorbents, zinc oxide-coated nanoporous carbon showed the largest adsorption capacity of 522.8 mg/g (2.52 mmol/g) which was almost close to that of the zinc oxide-coated (2.38 mmol/g), indicating the monolayer spreading of ZnO onto the oxidized mesoporous carbon. The results of the present study suggest that ZnO-coated nanoporous carbon can be effectively used for Pb(II) adsorption from aqueous solution, whereas a part of acidic functional groups may be contributed to binding the Pb(II) for the oxidized mesoporous carbon and mesoporous carbon. Kinetic studies indicated that the overall adsorption process of Pb(II) followed the pseudo-second-order model. The ZnO-coated nanoporous carbon was regenerated and found to be suitable of reuse of the adsorbent for successive adsorption–desorption cycles without considerable loss of adsorption capacity.  相似文献   

15.
 The focus of this research was to determine the impact of abandoned mines on surface water and groundwater in the historical mining districts of the Cerbat Mountains, Arizona. The surface water in the mining areas was found to be contaminated by various combinations and concentrations of heavy metals. Elevated arsenic, cadmium, and iron concentrations were detected in most surface-water samples, while lead, copper, and zinc contamination differed from region to region, depending on the ore mined. The groundwater was seriously polluted by arsenic, cadmium, lead, zinc, iron, and manganese in the immediate vicinity of mines that processed ore on the site, such as the Tennessee Mine near Chloride. Chloride's groundwater, however, showed no evidence of contamination. Three possible explanations are discussed: immobilization of the heavy metals in the soil by chemical reactions and adsorption, dilution effects due to the rainy season in spring, or the existence of different groundwater systems. Received: 17 September 1996 · Accepted: 14 May 1997  相似文献   

16.
The batch removal of copper(II) ions from aqueous solution under different experimental conditions using alkali-leached silica and activated charcoal was investigated in this study. The copper(II) uptake was dependent on varying time, pH, copper concentration and temperature. Copper sorption was found fast reaching equilibrium within 1 h with better performance for alkali-leached silica than charcoal. Copper sorption was low at low pH values and increased with rise in initial pH-value until 6.7. Sorption fits well the Langmuir and Freundlich equations with higher uptake by increasing temperature. According to Langmuir equation, the maximum uptake of Cu(II) ions by alkali-leached SiO2 and charcoal was found to be 242.5 and 94.4 mmol/g at temperature 60 °C and pH 6. Thermodynamic studies confirm that the process was spontaneous and endothermic nature. Kinetic data for Cu(II) sorption was found to follow pseudo-second-order model.  相似文献   

17.
This Article deals with the utilization of agricultural waste such as cattle manure, swine manure, chicken manure and their mixtures. It is promising a simultaneous running of biogas processes and vermitechnology. A special biogas–vermitechnological shoulder was constructed. A special organic catalyst, which contained glucose and cellulose, was used in the biogas process, as a source of biogas bacteria and to alter C/N ratio of the fermented substrate, to C/N = 30/1. Swine manure shows a higher biogas yield and methane-in-biogas content than others. It is effective to mix different manures to increase biogas yield. Earthworms Eisenia Foetida were used in the vermitechnological stage. Using only cattle manure and in mixtures with leaves (4:1 wt) was processed to make vermicompost. The obtained biohumus was studied with a microscope. It was found to have a more homogenous and structured porosity surface. It was observed that the organic content increased in vermicompost. The ratio of humic and fulvic acids can be varied using rotted leaves as fillers. Atomic Absorption Spectrometry was used to determine the content of metals. It was observed that metals from manure (Sb, Rb, Sr) were accumulated in earthworms, therefore biohumus was purified from pollutants. The released heat from the biogas stage was used for the vermitechnology stage heating. Using the biogas heat, it is possible to conduct the vermiprocess, even in cold seasons.  相似文献   

18.
In this research, spent coffee grains were modified with citric acid solutions (0.1 and 0.6 M) to increase the quantity of carboxylic groups improving its metal adsorption capacity. Added functional groups on modified and non-modified spent coffee grains were identified and quantified by attenuated total reflection Fourier transform infrared analyses and potentiometric titrations, respectively. These adsorbents were used for the removal of lead (II) and copper (II) from aqueous solutions at 30 °C and different pH in batch systems. In addition, adsorption–desorption experiments were conducted to evaluate the possibility of re-using the modified adsorbent. Potentiometric titrations data reveal that the quantity of carboxylic groups was increased from 0.47 to 2.2 mmol/g when spent coffee grains were modified with 0.1 and 0.6 M citric acid. Spent coffee grains treated with 0.6 M citric acid, achieved a maximum adsorption capacity of 0.77 and 1.53 mmol/g for lead (II) and copper (II), respectively, whereas non-modified spent coffee grains only reached 0.24 and 0.19 mmol/g for lead (II) and copper (II), respectively. Desorption of lead (II) and copper (II) achieved around 70 % using 0.1 N HCl for non-modified and modified spent coffee grains with 0.6 M citric acid. It is suggested that lead (II) and copper (II) species were adsorbed mainly on the carboxylic groups of modified spent coffee grains and these metals may be exchanged for hydrogen and calcium (II) ions during adsorption on non-modified spent coffee grains. Finally, the adsorption equilibrium was reached after 400 min for modified spent coffee grains with 0.6 M citric acid. Modified spent coffee grains are a promising option for removing metal cations from aqueous solutions due to its low cost and high adsorption capacity (about 10 times higher than the activated carbons).  相似文献   

19.
The remobilization of iron, manganese, cobalt, cadmium, copper and zinc in the pore water of estuarine sediment cores at Yingkou was assessed using diffusive equilibrium in thin films and diffusive gradients in thin films techniques. A relatively anoxic system (+33.7 to ?224.1 mV) in the sediment cores might cause the reductive release of iron, manganese and cobalt into pore water from the estuarine sediment. High-average concentrations of iron (47.85 μg ml?1) and manganese (3.81 μg ml?1) were observed using diffusive equilibrium in thin films on the sediment core, but the concentration of cobalt (18.02 ng ml?1) was relatively low. A strong correlation between iron and cobalt was observed based on the vertical profiles of the metals. Manganese and iron were more readily released from the solid phase to the solution. The peak cobalt, copper and zinc concentrations were observed in the upper layer (2–4 cm) measured using diffusive gradients in thin films. However, the peak iron, manganese and cobalt concentrations were located in the deeper layer (≥7 cm). In addition, the concentration profiles measured using diffusive gradients in thin films of cobalt, copper and zinc were independent of the iron, manganese and cobalt distribution with respect to depth.  相似文献   

20.
综合采用地统计学、GIS和传统统计分析方法,研究了瑞安市耕作层土壤9种养分元素有效态含量空间变异特征及其影响因素。结果显示,研究区耕作层土壤碱解氮呈西高东低的分布趋势,速效钾、有效硼、有效锰、有效钼、有效铜和有效锌呈西低东高的分布趋势,有效磷呈东西高、中间低的分布趋势,有效铁分布均匀;研究区中西部耕作层有效硼较缺乏,东部碱解氮较缺乏,中部有效磷较缺乏,其他地区9种养分元素有效态含量均达到中等以上;半方差函数分析显示有效锰和有效铁为强空间相关性,碱解氮、速效钾、有效磷、有效钼、有效铜和有效锌为中等空间相关性,有效硼为弱空间相关性。研究认为,中性或是弱碱性、含盐量较高且阳离子较活跃的土壤环境有利于速效钾和有效硼富集,酸性或弱酸性和有机质含量较高的土壤有利于碱解氮和有效铁富集;速效钾、有效钼、有效硼、有效铜和有效锌含量的控制因素相似,主要受成土母质、土壤类型以及地形地貌等结构性因素和施肥、耕作等随机性因素的双重影响,而碱解氮、有效铁、有效磷和有效锰的含量分布主要受成土母质、土壤类型以及地形地貌等结构性因素的影响。  相似文献   

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