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1.
The optimization for poly-β-hydroxyalkanoate production was carried out with nutrient removal efficiency for total organic carbon (TOC), phosphate, and nitrate from palm oil mill effluent waste. The experiment was conducted in a fabricated fed-batch reactor and the data obtained was analyzed using central composite rotatable design and factorial design for response surface methodology as a systematic approach for designing the experiment statistically to obtain valid results with minimum effort, time, and resources. The analysis of numerical optimization with propagation of error showed that 66 % of poly-β-hydroxyalkanoate production can be obtained with nutrient removal of TOC and nitrate by 19 and 3 %, respectively. However, phosphate removal efficiency was not found to be much effective. More over, the chemical oxygen demand: nitrogen phosphate (509 g/g N), chemical oxygen demand: phosphate (200 g/g P), air flow rate (0.59 L/min), substrate feeding rate (20 mL/min), and cycle length (20 h) were the optimized variables for maximum poly-β-hydroxyalkanoate production and nutrient removal.  相似文献   

2.
In this study, sepiolite-nano zero valent iron composite was synthesized and applied for its potential adsorption to remove phosphates from aqueous solution. This composite was characterized by different techniques. For optimization of independent parameters (pH = 3–9; initial phosphate concentration = 5–100 mg/L; adsorbent dosage = 0.2–1 g/L; and contact time = 5–100 min), response surface methodology based on central composite design was used. Adsorption isotherms and kinetic models were done under optimum conditions. The results indicated that maximum adsorption efficiency of 99.43 and 92% for synthetic solution and real surface water sample, respectively, were achieved at optimum conditions of pH 4.5, initial phosphate concentration of 25 mg/L, adsorbent dosage of 0.8 g/L, and 46.26 min contact time. The interaction between adsorbent and adsorbate is better described with the Freundlich isotherm (R 2 = 0.9537), and the kinetic of adsorption process followed pseudo-second-order model. Electrostatic interaction was the major mechanisms of the removal of phosphates from aqueous solution. The findings of this study showed that there is an effective adsorbent for removal of phosphates from aqueous solutions.  相似文献   

3.
Addis Ababa is one of the fastest growing cities where high urbanization has become a challenge. Consequently, housing shortage is a big problem of the city. The municipality has launched a huge Condominium Housing Programme in response to the problem. However, sanitary wastewater and solid waste management are the critical problems to those houses. The wastes were collected and evaluated for its biogas production and fertilizer potential to solve the foreseen waste management problems. The physicochemical characteristics of the collected wastes were determined. A laboratory scale batch anaerobic co-digestion of both wastes with different mix ratio of 100:0, 75:25, 50:50, 25:75, and 0:100 by volume [sanitary wastewater (TS = 7,068 mg/L):kitchen organic solid waste (TS = 56, 084 mg/L)]were carried out at ambient temperature for 30 days. The amount of biogas and methane produced over the digestion period for those mixing ratios were compared. The highest biogas yield obtained from a mix ratio of 25:75 was 65.6 L, and the lowest from a mix ratio of 100:0 was 9.5 L. The percentage of methane gas in the biogas was between 19.8 and 52.8 %. From the study results, it is evidenced that the mixing ratio 25:75 produced the maximum quantity of biogas and methane. With regard to the fertilizer potential of the digested sludge, composting and sun drying process were helpful for land application by inactivating the pathogen.  相似文献   

4.
The reuse of waste materials as soil additives could be a welcome development in soil remediation. The mobility of Cd, Pb and As in a contaminated soil was investigated using natural and calcined poultry wastes (eggshell and chicken bone), CaCO3 and CaO at different application rates (0, 1, 3 and 5 %). The chemical composition accompanied with mineralogical composition indicated that CaCO3 and CaO were the major components in natural and calcined eggshells, respectively, while hydroxyapatite (HAP) dominated the natural and calcined chicken bones. The results showed that soil pH tended to increase in response to increasing application rates of all soil additives. The effectiveness of the additives in reducing Cd, Pb and As mobility was assessed by means of chemical extractions with 0.1 N HCl for Cd and Pb or 1 N HCl for As, according to Korean Standard Test (KST) method. Both calcined eggshell and chicken bone were equally effective with CaO or CaCO3 in reducing the concentration of 0.1 N HCl-extractable Cd from 6.17 mg kg?1 to below warning level of 1.5 mg kg?1, especially at the highest application rate. The application of calcined eggshell, CaO and CaCO3 also decreased the concentration of 0.1 N HCl-extractable Pb from 1,012 mg kg?1 to below warning level of 100 mg kg?1. The Pb concentration decreased significantly with an increasing application rate of chicken bone, but remained above warning level even at the highest application rate. On the contrary, natural and calcined chicken bones led to a significant increase in the mobility of As when compared with the control soil. These findings illustrate that calcined eggshell in particular is equally effective as pure chemical additives in stabilizing Cd and Pb in a contaminated agricultural soil. The presence of As in metal-contaminated soils should be taken into consideration when applying phosphate-containing materials as soil additives, because phosphate can compete with arsenate on adsorption sites and result in As mobilization.  相似文献   

5.
Oil-based drilling cuttings comprise a large and hazardous waste stream generated by oil and gas wells drilling operations. Oil-based cuttings are muddy materials with high contents of salts and hydrocarbons. Composting strategies have shown to be effective in the biodegradation of petroleum hydrocarbons, and it offers numerous advantages in comparison with other bioremediation methods. In order to assess the effectiveness of drilling cuttings bioremediation by composting with food and garden wastes, an experiment was conducted in 60-L reactors for 151 days. Four treatments were carried out: only oil-based cuttings, two proportions (in a volume basis) of organic wastes to drilling cuttings (33 and 75 %) and only organic wastes (as a traditional composting reference), with pine-tree woodchips as bulking agent. High degradation percentages of total hydrocarbons (≈82 %), n-alkanes (≈96 %) and the 16 USEPA-listed polycyclic aromatic hydrocarbons (≈93 %) were reached in the treatment with 75 % of organic wastes, and applying 33 % of organic wastes was not more effective than not applying organic wastes for the drilling cuttings hydrocarbons biodegradation. Furthermore, in the treatment with 75 % of organic wastes, alkanes half-life and polycyclic aromatic hydrocarbons half-life were about 10 times and four times lower, respectively, than those in the treatment with 33 % of organic wastes. Possibly, lower hydrocarbons and salts initial concentrations (i.e., lower toxicity), higher microbial counts, adequate nutrient proportions and water content supported a high biological activity with a consequent elevated biodegradation rate in the treatment with 75 % of organic wastes.  相似文献   

6.
A total of 113 samples of waste and soil were collected from a site in the state of San Luis Potosi, Mexico, that was occupied for several years by the metallurgical industry. Specific magnetic susceptibility (MS), electrical conductivity (EC) and pH were determined, as well as the total and available concentrations of potentially toxic elements (PTEs) such as As, Cd, Cu, Fe, Pb and Zn, which may cause a health risk for humans, animals and ecosystems, and the concentrations of major ions in aqueous extracts of soils and wastes. The solid phases of the samples were also characterized. The results revealed that the soils and wastes exhibited elevated values of PTEs, MS and EC. For soils these values decreased with increasing distance from the waste storage sites. The MS values were elevated primarily due to the presence of Fe-oxyhydroxides, such as magnetite, hematite and goethite, which contain PTEs in their structure leading to a high correlation between the value of MS and the As, Cd, Fe and Pb contents (r = 0.57–0.91) as well as between the PTEs values (r = 0.68–0.92). The elevated EC values measured in the metallurgical wastes were the result of presence of the sulfate minerals of Ca, Mg and Fe. The pollution index, which indicates the levels of simultaneous toxicity from elements such as As, Cd and Pb, was determined, with extreme hazard zones corresponding to areas that exhibit high MS values (0.91 correlation). In conclusion, MS measurements can be used as an indirect indicator to evaluate the PTE contamination in metallurgical areas, and EC measurements can aid in the identification of pollution sources.  相似文献   

7.
The use of agricultural wastes as biosorbents is gaining importance in bioremediation of heavy metal-polluted water and soils, due to their effectiveness and low cost. This work assesses the Cd, Pb and Cu adsorption capacity of the raw materials used in the production of substrates for mushroom production (Agaricus bisporus and Pleurotus ostreatus) and the spent mushroom composted (SMC), based on the functional groups of their organic carbon. The raw materials studied included agricultural wastes (wheat straw, wheat and rice poultry litter, grape pomace) and inorganic substances (gypsum and calcareous sand). Organic carbon from wastes and their composting products were characterized by CP-MAS 13C NMR. Langmuir adsorption isotherms of metals were plotted for each raw material, composting step, spent A. bisporus and P. ostreatus substrates and the final SMC. The maximum adsorption capacities of SMC were 40.43, 15.16 and 36.2 mg g?1 for Cd, Pb and Cu, respectively. The composting process modified the adsorption properties of raw materials because of the enhanced adsorption of Cd and Cu and decreased adsorption capacity of Pb. CP-MAS 13C NMR and potentiometric titration were used to identify the functional groups of the organic carbon responsible for the metal adsorption. The content of cellulose was correlated with Pb adsorption (p < 0.001), alkyl and carboxyl carbon with Cd adsorption (p < 0.001), and N-alkyl (p < 0.001) and carboxyl (p < 0.010) groups with Cu adsorption. These results are valuable to develop new biosorbents based on agricultural wastes and demonstrate the high potential of SMC to adsorb heavy metals from polluted environments.  相似文献   

8.
In recent years, the need for safe and economical methods to eliminate heavy metals from contaminated waters has necessitated research on the production of low-cost alternatives to commercially available activated carbon. In the present work, in order to enhance the removal of heavy metals from contaminated water, Zizyphus vulgaris wastes were modified chemically to produce an adsorbent rich in carboxylic groups to enhance the removal of heavy metals from contaminated water. Adsorption of Zn(II) ions on the produced adsorbent was then optimized. The optimal ratio for esterification involved the treatment of Z. vulgaris wastes (1 g) with 0.0037 mmol malic acid in the presence of a very small amount of water for 2 h at 140 °C. The maximum values for adsorption capacity, q max, were 28.7 and 164.6 mg/g on native and modified Z. vulgaris wastes, respectively, at pH 5 and 30 °C with a contact time 2 h and an initial metal ion concentration of 400 mg/L. The equilibrium data were well fitted by the Langmuir and Freundlich adsorption models and demonstrated the significant capacity for Z. vulgaris wastes in the removal of Zn(II) ions from aqueous solutions.  相似文献   

9.
Amorphous tin(VI) hydrogen phosphate (ATHP) was synthesized using the liquid phase precipitation method and served as an adsorbent to remove Pb(II), Cu(II), and Zn(II) from aqueous solutions. The ATHP was characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption–desorption techniques. Adsorption properties were evaluated as a function of pH, reaction time, concentration of reactants, and salinity. Their equilibrium adsorption data were modeled using Freundlich, Langmuir, and Dubinin–Kaganer–Radushkevich isotherms, respectively. The results revealed that adsorption equilibrium reached within 180 min. ATHP indicated good adsorption even below the pHZPC, and best adsorption at pH 5 for Pb(II) and Cu(II) and at pH 5.5 for Zn(II) was observed. Equilibrium data fitted better to the Langmuir model for Pb(II) and Cu(II) and fitted better to the Freundlich model for Zn(II). The saturated adsorption capacities deduced from the Langmuir model were 2.425, 1.801, and 0.600 mmol/g for Cu(II), Pb(II), and Zn(II), respectively, indicating an adsorption affinity order of Cu > Pb > Zn. There is a negative correlation between the concentration of NaCl and adsorption capacity of ATHP, yet ATHP still exhibited excellent adsorption having an adsorption capacity of 19.35, 15.16, 6.425 mg/g when the concentration of NaCl was 0.6 mol/L. The free energy (E) was 12.33, 10.70, and 14.74 kJ/mol for Pb(II), Cu(II), and Zn(II), respectively. An adsorption mechanism based on ion exchange between heavy metal ions and H+ in the ATHP is proposed. Furthermore, the used ATHP was regenerated by HCl solution and the adsorbent was used repeatedly.  相似文献   

10.
The phosphate content of ancient alkali-glass has been tested as an indicator for biogenic ash, used in glass production. The living tissue of plants and vertebrates accumulates phosphate that remains in native ash as a main component (1 to over 10 wt%) forming together with biologically essential element oxides a complex chemical fingerprint that characterises any glass made with it. If, instead of native plant ash its alkali extract is used, soluble oxides are concentrated in the extract whilst insoluble oxides get depleted, leading to a different elemental fingerprint of the glass. Geogenic raw-materials for glass production like quartz-rich sand, evaporitic natron, or limestone are virtually phosphate free (below detection limit up to ≈0.15 wt%). Several collections of ancient glass stemming from different archaeological excavations, regions and times have been analysed by instrumental methods (WD-XFA, ED-XFA, thermal techniques), i.e. flat- and hollow K–Ca glass dated 1699/1714 N = 340, Na–Ca glass 13th/14th cy N = 94, Na–Ca glass 7th/9th cy N = 110, and alkali-Ca glass La Tène N = 395. Although the phosphate content of native alkali plant ash gets diluted with quartz sand by a factor of roughly two in glass production, it remains a main component of the product glass. Wood-ash glass contains 1–3 wt% phosphate, whilst glass manufactured from halophyte ash contains around 0.2–1 wt%. When processed wood-ash is used, the phosphate content in glass sinks below 1 wt%, the depletion factor amounting to roughly 8–15. Glass made from evaporitic soda displays phosphate contents below 0.2 wt% in the cases examined. The phosphate content of ancient alkali glass thus indicates whether virtually phosphate-free evaporitic soda has been used as a flux, or native ash of halophile plants. Ternary melting diagrams reveal at least three groups of alkali glass: Naturally coloured forest glass displays a broad distributional pattern with minimum melting temperatures ranging from 1200 to ≥1450 °C, colourless potash-extract glass from 900 to ≈1200 °C, and the typical, tight cluster of Roman sodium-calcium glass ranges from 800 to ≈900 °C. The wide-spread sodium-lime glass made with native halophytic ash, contains besides Na2O as the chemical main component always some K2O, and melting temperatures range from 800 to ≈1000 °C.  相似文献   

11.
One of the key challenges in water treatment industry is the removal of organic compounds by cost-effective methods. This study evaluated the adsorptive removal of dissolved organic carbon (DOC) from reservoir water using fuller’s earth (FE) in comparison with natural (SQ) and modified quartz (MSQ) sands. The removal capacities of FE at different contact times, pH levels, adsorbent dosages and initial DOC concentrations were compared with both the quartz sands. The optimum DOC removals by FE and SQs were achieved at contact time of 60 and 30 min, pH level of 6 and 4, and at adsorbent dose of 1.5 g/150 mL and 10 g/100 mL, respectively. The adsorption capacity of FE (1.05 mg/g) was much higher compared to the MSQ (0.04 mg/g) and SQ (0.01 mg/g). Adsorption equilibrium data better fitted to the Freundlich model than to the Langmuir model, suggesting that adsorption occurred primarily through multilayer formation onto the surfaces of FE and SQ. The pseudo-second-order model described the uptake kinetics more effectively than the pseudo-first-order and intra-particle diffusion models, indicating that the mechanism was primarily governed by chemisorption. These observations were well supported by the physiochemical characteristics and charge behaviour of the adsorbents. In mass-transfer study, the results of liquid film diffusion model showed that the adsorption of DOC on FE was not controlled by film diffusion, but other mechanisms also played an essential role. This study demonstrates that FE is an effective adsorbent for the removal of DOC in surface water treatment.  相似文献   

12.
Polycyclic aromatic hydrocarbon (PAH) and nitrated PAH (NPAH) products are toxic. Thus, determination of their concentrations is of great interest to researchers of soil and water pollution control. In this work, soil samples, surface water samples, and groundwater samples were collected, and the concentrations of 16 priority PAHs and 15 NPAHs were determined using an HPLC-ultraviolet detector. Results showed that the total PAH concentrations ranged within 489.69–1,670.11 ng/g (average = 905.89 ng/g) in soil samples, 4.00–23.4 μg/l (average = 9.84 μg/l) in surface water samples, and 2.14–22.3 μg/l (average = 8.37 μg/l) in groundwater samples. The NPAH concentrations were one to two orders of magnitude lower than the PAH concentrations and ranged within 22.72–128.70 ng/g (average = 63.88 ng/g) in soil samples. 2-Nitropyrene and 6-nitrochrysene were the most abundant compounds, accounting for about 14.3 and 26.5 %, respectively. Source analysis revealed that most PAHs originated from coal combustion around the study area, whereas NPAH studies suggested that the primary emission of gasoline engines and daytime OH reactions were the dominant sources of these compounds.  相似文献   

13.
The concentrations of uranium, iron and the major constituents were determined in groundwater samples from aquifer containing uranyl phosphate minerals (meta-autunite, meta-torbernite and torbernite) in the Köprüba?? area. Groundwater samples from wells located at shallow depths (0.5–6 m) show usually near neutral pH values (6.2–7.1) and oxidizing conditions (Eh = 119–275 mV). Electrical conductivity (EC) values of samples are between 87 and 329 μS/cm?1. They are mostly characterized by mixed cationic Ca dominating bicarbonate types. The main hydrogeochemical process is weathering of the silicates in the shallow groundwater system. All groundwater in the study area are considered undersaturated with respect to torbernite and autunite. PHREEQC predicted UO2(HPO4) 2 2? as the unique species. The excellent positive correlation coefficient (r = 0.99) between U and PO4 indicates the dissolved uranium in groundwater would be associated with the dissolution of uranyl phosphate minerals. The groundwater show U content in the range 1.71–70.45 μg/l but they are mostly lower than US EPA (2003) maximum contaminant level of 30 μg/l. This low U concentrations in oxic groundwater samples is attributed to the low solubility of U(VI) phosphate minerals under near neutral pH and low bicarbonate conditions. Iron closely associated with studied sediments, were also detected in groundwater. The maximum concentration of Fe in groundwater samples was 2837 μg/l, while the drinking water guidelines of Turkish (TSE 1997) and US EPA (2003) were suggested 200 and 300 μg/l, respectively. Furthermore, iron and uranium showed a significant correlation to each other with a correlation coefficient (r) of 0.94. This high correlation is probably related to the iron-rich sediments which contain also significant amounts of uranium mineralization. In addition to pH and bicarbonate controlling dissolution of uranyl phosphates, association of uranyl phosphates with iron (hydr) oxides seems to play important role in the amount of dissolved U in shallow groundwater.  相似文献   

14.
The mineralogical and morphological characteristics, concentration of major and trace elements, and sulfur isotopic composition of three pyrite and two coal samples in the Upper Permian high-sulfur coals from Xingren, Zhijin, and Hefeng mining area, South China, were investigated, by using optical microscopy, field emission-scanning electron microscopy in conjunction with an energy-dispersive X-ray spectrometer (FE SEM-EDS), X-ray powder diffraction (XRD), X-ray fluorescence (XRF), inductively coupled plasma mass spectrometry (ICP-MS), cold vapor atomic absorption spectrometry (CVAAS), and isotopic ratio mass spectrometer. The pyrite in Xingren and Zhijin coals mainly occurs as nodular, lens-shaped, thin-layer, and massive forms, and it occurs mainly as fine vein fillings in the Hefeng coals. Microscopically, pyrite in the coals from Xingren, Zhijin, and Hefeng mainly occurs as framboidal, cell-filling, and vein-filling forms, respectively. There is a distinct difference in X-ray powder diffractogram and diffraction data of the three pyrite samples. There is a maximum diffraction peak (2.709 Å) in pyrite in the coals from Xingren and (2.707 Å) in pyrite in the coals from Zhijin; however, the maximum diffraction peak is 3.343 Å in pyrite in the coals from Hefeng. The average unit cell length (a 0) is 5.4169 Å for the Xingren pyrite, 5.4159 Å for the Zhijin pyrite, and 5.4170 Å for the Hefeng pyrite. The ratio of S/Fe is 2.16 for the Xingren pyrite, 2.09 for the Zhijin pyrite, and 2.01 for the Hefeng pyrite. Copper (701 μg/g), Ni (369 μg/g), and Co (29.6 μg/g) concentrated in the Hefeng pyrite. The concentration of As is 126, 19.6, and 19.1 μg/g in the Hefeng, Zhijin, and Xingren pyrite, respectively. Mercury is 11.7 μg/g in the Xingren pyrite, 2.79 μg/g in the Zhijin pyrite, and 0.512 μg/g in the Hefeng pyrite. There is a clear tendency that elements Cu, Ni, Co, Cr, Se, Mo, and As are significantly enriched in the Hefeng pyrite. Mercury is greatly enriched in the Xingren pyrite, and Zn is enriched in Zhijin pyrite. Rare earth elements and yttrium (REY) are not abundant (8.276 μg/g) in the Hefeng pyrite and are characterized by maximum positive anomaly of Eu (Eu/Eu* = 6.54). The δ34S value is ?26.9 ‰ in the Xingren pyrite, +3.8 ‰ in the Zhijin pyrite, and +3.7 ‰ in the Hefeng pyrite. The trace elements in the Hefeng pyrite and coal are As (126 and 6.1 μg/g), Hg (0.512 and 0.158 μg/g), Zn (276 and 56.7 μg/g), Se (16.5 and 1.07 μg/g), Mo (45.5 and 9.93 μg/g), Cu (701 and 37.8 μg/g), Ni (369 and 16.9 μg/g), Co (29.6 and 8.63 μg/g), Sb (2.64 and 0.742 μg/g), Cd (3.49 and 0.366 μg/g), and Pb (62.8 and 33.5 μg/g), demonstrating that these potentially toxic trace elements were mainly concentrated in pyrites. The strongly positive Eu anomaly (Eu/Eu* = 6.54) in the netted pyrite vein filled in the cleats of the Hefeng coal may be the product of epigenetic hydrothermal fluid.  相似文献   

15.
The adsorption behaviors of ammonium from aqueous solutions were investigated for three solid coal wastes, slag, honeycomb-cinder and coal gangue. The ammonium sorption processes were well modeled by the pseudo second-order model (R 2 > 0.99). The experimental data were fitted to both the Langmuir model and the Freundlich model, with the Langmuir model better representing the data. The maximum ammonium sorption capacities calculated from the Langmuir model were 3.1, 5.0 and 6.0 mg/g for the slag, honeycomb-cinder and coal gangue samples, respectively. The pH value of the solution affected the ammonium removal, and the higher uptakes found in either neutral or alkaline conditions for the three materials. The thermodynamic parameters, ΔH, were calculated to be 29.75, 25.21 and 17.91 kJ/mol for the SL, HC and CG samples, respectively, with the positive values indicating that the ammonium sorption processes were endothermic. Based on the results, it can be concluded that coal gangue may have more potential for being used as a sorbent for the ammonium removal from wastewater among the three coal by-products.  相似文献   

16.
Sized aggregates of glasses (47–84 wt% SiO2) were fused from igneous-derived cohesive fault rock and igneous rock, and step-heated from ~400 to >1,200 °C to obtain their 39Ar diffusion properties (average E=33,400 cal mol?1; D o=4.63×10?3 cm2 s?1). At T<~1,000 °C, glasses containing <~69 wt% SiO2 and abundant network-forming cations (Ca, Fe, Mg) reveal moderate to strong non-linear increases in D and E, reflecting structural modifications as the solid transitions to melt. Extrapolation of these Arrhenius properties down to typical geologic T-t conditions could result in a 1.5 log10 unit underestimation in the diffusion rate of Ar in similar materials. Numerical simulations based upon the diffusion results caution that some common geologic glasses will likely yield 40Ar/39Ar cooling ages rather than formation ages. However, if cooling rates are sufficiently high, ambient temperatures are sufficiently low (e.g., <65–175 °C), and coarse particles (e.g., radius (r) >~1 mm) are analyzed, glasses with compositions similar to ours may preserve their formation ages.  相似文献   

17.
Sludge samples taken from different sources and times may have different characteristics that could affect dewatering performance. In this study, 20 sludge samples from five wastewater treatment plants and different seasons in 1 year were characterized. Pearson correlation analysis indicated that solid content (SC), total suspended solid (TSS), polysaccharides and proteins contents had positive correlations with the capillary suction time (CST), whereas volatile suspended–solid/total suspended solid (VSS/TSS) exhibited negative correlations with CST. Moreover, no correlations between CST and specific resistance to filtration were found among these different sludge samples. The principal component analysis confirmed that only two group variables could represent most of the sludge characteristic parameters. The first set of variables represents the particulate nature of the biotic factors (SC, VSS/TSS, SCOD, TSS, polysaccharides and proteins), and the second set is the pH. CST could not be a reasonable indicator of dewaterability in sludge deep dewatering by Fe2+/S2O8 2?-phosphogypsum composite conditioning. Furthermore, the results of diaphragm filter press dewatering showed that initial SC and VSS/TSS were the most dominant sludge characteristics affecting the solid content of dewatered cake (R p = 0.610, p = 0.016; R p = ?0.838, p = 0.000, respectively) with Fe2+/S2O8 2?-phosphogypsum composite conditioning. Results from this study suggest that dewatering performance is predictable by sludge characteristics parameters for Fe2+/S2O8 2?-phosphogypsum conditioning.  相似文献   

18.
Adsorptive separation of Pb(II) and Cu(II) using modified waste Lyocell fiber adsorbent was investigated in this research. The waste Lyocell fiber was functionalized through carboxymethylation of the hydroxyl moieties using sodium chloroacetate as modifying agent and was crosslinked with epichlorohydrin to provide water stability. The maximum equilibrium batch uptake in single metal system was 353.45 mg/g for Pb(II) and 98.33 mg/g for Cu(II), according to the Langmuir isotherm model. The adsorption rates were very fast and reached equilibrium within 3 and 5?10 min for Cu(II) and Pb(II), respectively. In competitive binary metal system, the uptake of Cu(II) largely decreased to 38.40 mg/g, and Pb(II) selectivity was observed. Elemental and functional characterization suggested that the adsorption proceeded by ion exchange between the adsorbent and metal ions. In a flow-through column system, adsorption followed by desorption aided in effectively eluting ~260 mg of Pb(II) (out of ~300 mg total adsorbed) from the Pb(II)–Cu(II) binary solution. Finally, the adsorbent was very effective in four successive adsorption–desorption cycles with over 99 % uptake and 94 % desorption efficiencies. The present study may provide an alternative option for waste fiber recycling and could be useful in recovering heavy metal ions from aqueous sources to complement their depleting reserves.  相似文献   

19.
A pot culture experiment was conducted to study impact and interaction of multi-metals on growth, yield and metals uptake by spinach (variety All Green). Three levels of each chromium (0, 50 and 100 mg/kg), cadmium (0, 1 and 2 mg/kg) and zinc (0, 10 and 20 mg/kg) in combinations (total treatments 3 × 3 × 3 = 27) were applied in a Vertisol (5 kg). The results showed that increasing the concentration of chromium, cadmium and zinc in soil enhanced the respective metal concentrations in spinach root and shoot. When cadmium at 2 mg/kg along with chromium at 100 mg/kg soil was applied, chromium concentration and uptake were decreased in root and shoot. Meanwhile, zinc application had no significant effect on chromium uptake and concentration in spinach biomass. From the results, it was concluded that cadmium at higher dose had an antagonistic effect over chromium. On the other hand, in chromium, cadmium and zinc combinations particularly at their higher levels, a competition among each other was found. Therefore, the findings could be used as guidelines for controlling and management of heavy metals pollution in farmland.  相似文献   

20.
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