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1.
Cost-effective oil absorbents for the remediation of oil spills have been developed following a facile process involving the modification of polyurethane foam surfaces with mixtures of silicon oxide nanoparticles and polydimethylsiloxane. Polyurethane foams with different pore sizes and connectivity are tested, and it was found that the proposed treatment, applied by dip coating and spray coating, strongly improves the intrinsic foams’ performance in terms of selectivity and oil absorption capacity. The modified foams reach oil absorption capacities up to 60 g/g and simultaneous negligible water uptake. The treatment is stable after multiple absorption cycles, and therefore, the foams can be reused without significant decrease in their performance, being possible, after five cycles of absorption and recovery of oil, to reach overall oil absorption capacities up to 250 g/g.  相似文献   

2.
In the present work, an attempt was made to provide an efficient, easily deployable method of cleaning up oil spills and recovering of the oil. Carbonized pith bagasse, a relatively abundant and inexpensive material is currently being investigated as an adsorbent to remove contaminants “oil” from water. Fibers extracted from bagasse and carbonized at 300 °C were found to have a high performance for sorption and recovery of light, heavy oils and even the viscous ones. The physical properties of pith bagasse were investigated using scanning electronic microscope to show the inner and the outer surface and the cross section area of the pith bagasse and thermo gravimetric analyzer to investigate the degradation profile of the pith bagasse. The carbonized pith bagasse was packed into a polypropylene bag and its sorption behavior was studied. A comparison was made between the prepared pad and the commercial sorbents show that the pad containing carbonized pith bagasse has higher sorption capacity in comparison to the commercial sorbents. The pad exhibited high oil retention ability and a high selectivity for the oils over the water. The pad showed a possibility of reuse for eight times. The sorption capacity of the pads containing carbonized pith bagasse was found to increase with increasing the time of sorption till it reaches the maximum value at the time of sorption equal to 60 min.  相似文献   

3.
Availability of barley straw application on oil spill clean up   总被引：1，自引：0，他引：1  
Oil spills are a global concern due to the environmental and economical impact. Various commercial systems have been developed to control these spills, including the use of fibers as sorbents. However, most sorbents end up in landfills or in cineration after single use. These options either produce another source of pollution or increase the oil recovery cost. Plant biomass is renewable resource that can be converted into useful materials and energy. Barley straw, an agricultural waste, was used as sorbent material. The present study examines the absorption capacity of raw barley straw for different petroleum products and water pick up. The investigate revealed that the capacity of fibers to remove crude oil from sea water was related to the surface properties of the fibers, concentration of the oil, size of the fiber, amount of the fibers, as well as the temperature of the crude oil. Cyclic sorption / desorption studies indicated that a simple squeezing operation was enough to remove most of the oil sorbed and that recycling was feasible.  相似文献   

4.
In present work, fabrication of functionally tailored nanobiomaterials paraben-modified nanocellulose (PNC) and (2,3-epoxypropyl) trimethylammonium chloride-modified nanocellulose (EPTMAC-NC) for the remediation of trivalent and hexavalent chromium, respectively, from water streams has been done. The resulting PNC and EPTMAC-NC were characterized before and after sorption of chromium using spectroscopic and microscopic techniques. The sorption performance of PNC (23.92 mg/g; 95.67 %) and EPTMAC-NC (23.99 mg/g; 95.94 %) was evaluated for trivalent and hexavalent chromium, respectively, at 0.5 g biosorbent dose; 500 mL sample volume; 25 mg/L chromium conc.; 40 min kinetic time; pH (6.5 for trivalent and 2.5 for hexavalent chromium) and 298 K temperature. From isothermic, kinetic and thermodynamic modeling, the sorption of trivalent and hexavalent chromium was physisorption, spontaneous, feasible and endothermic in nature. These findings expose new path in the line of high performance, scalable and economic nanobiomaterials for the abatement of toxic metals from water streams.  相似文献   

5.
Biochars generated at various temperatures might show significant differences in sorption for organic contaminants. In this study, a series of biochars, generated from pyrolyzing maize straws at different temperatures, were systematically characterized. The characterization results showed that with increasing pyrolysis temperature, the surface areas, micropore areas and aromaticity of biochars were enhanced. Batch experiments were conducted to study methyl tert-butyl ether (MTBE) and benzene sorption to biochars. The results indicated that the sorption capacity of benzene to biochars was higher than that of MTBE. The higher pyrolyzed temperature of biochars resulted in a stronger sorption affinity for target compounds, and the dominant sorption mechanisms varied for biochars pyrolyzed at different temperatures. The sorption to biochars pyrolyzed at 700 and 800 °C performed a high adsorption capacity, which indicated that they might be a promising sorbent to remove MTBE and benzene from water. Biochar pyrolyzed at 400 °C showed transitional sorption mechanisms from partition to adsorption for MTBE and benzene. Pore-filling was a possible sorption mechanism to biochars pyrolyzed at high temperature.  相似文献   

6.
Investigations on how desiccation changes sorption of organic compounds by salt marsh sediments provide insight into the physical and chemical properties of these wide-spread coastal sediments. We measured sorption of compounds with different polarities (lysine, tyrosine, naphthalene and aniline) onto natural sediments and sediments that were dried and rewetted. Sorption of lysine by marsh sediment decreased significantly when the sediment was dried using a freeze-drier, oven, or desiccator, and sorption capacity was not restored when sediments were rewetted. In contrast to lysine, the sorption capacity of more hydrophobic compounds (tyrosine, aniline and naphthalene) increased significantly after salt marsh sediment was dried. These results suggest that drying greatly increased sediment hydrophobicity. Consistently, water drop penetration time, an index of hydrophobicity, was significantly lower for combusted sediments than for those that were simply dried. Sediments treated with EDTA, or boiled in seawater, exhibited a similar or even greater reduction in lysine sorption capacity compared with sediments that were dried. Water retention capacity of salt marsh sediment decreased 50% after sediment was dried. The effects of pH and salinity on lysine sorption in wet and dry sediments suggest that carboxyl groups play a major role in lysine sorption through cation ion exchange, and drying may reduce access to carboxyl groups. We hypothesize that the three-dimensional (3D) structure of organic matter, originating mainly from Spartina alterniflora, is an important factor controlling sorption capacity in salt marsh sediment. The drying process makes sedimentary organic matter change conformation, shrink in volume, and expose hydrophobic groups, thus becoming more hydrophobic. In environments with wet and dry cycles, the distribution of hydrophobic or hydrophilic compounds between solution and particulate phases could thus be influenced by the 3D structure and polarity of organic matter.  相似文献   

7.
The present study attempted to identify the efficient hazardous metal-removing sorbent from specific types of soil, upper and middle layer shirasu, shell fossil, tuff, akadama and kanuma soils of Japan by physico-chemical and metal (arsenic, cadmium and lead) removal characterizations. The physico-chemical characteristics of soil were evaluated using X-ray diffraction and scanning electron microscopy with energy dispersive spectroscopy techniques, whereas metal removal properties of soil were characterized by analyzing removal capacity and sorption kinetics of potential metal-removing soils. The chemical characteristics revealed that all soils are prevalently constituted of silicon dioxide (21.83–78.58 %), aluminum oxide (4.13–38 %) and ferrous oxide (0.835–7.7 %), whereas calcium oxide showed the highest percentage (65.36 %) followed by silicon dioxide (21.83 %) in tuff soil. The results demonstrated that arsenic removal efficiency was higher in elevated aluminum oxide-containing akadama (0.00452 mg/L/g/h) and kanuma (0.00225 mg/L/g/h) soils, whereas cadmium (0.00634 mg/L/g/h) and lead (0.00693 mg/L/g/h) removal efficiencies were maximum in elevated calcium oxide-containing tuff soil. Physico-chemical sorption and ion exchange processes are the metal removal mechanisms. The critical appraisal of three metal removal data also clearly revealed cadmium > lead > arsenic order of removal efficiency in different soils, except in tuff and akadama soils followed by lead > cadmium > arsenic. It clearly signified that each type of soil had a specific metal adsorption affinity which was regulated by the specific chemical composition. It may be concluded that akadama would be potential arsenic-removing and tuff would be efficient cadmium and lead-removing soil sorbents.  相似文献   

8.
Due to the severity of arsenic contamination of soil and water resources around the world, finding new adsorbents for arsenic removal from the water is of high importance. The present study investigates the possible use and effectiveness of starch-stabilized Fe/Cu nanoparticles for adsorption of arsenic from aqueous solutions. First, Fe/Cu nanoparticles at various starch concentrations of 0, 0.02, 0.04 and 0.06 wt% were synthesized and characterized by X-ray diffraction, transmission electron microscopy and zeta potential/particle size analyzer. Then 0.04 wt% stabilized Fe/Cu nanoparticles were tested for the sorption of As(III) and As(V) from synthetic arsenic-contaminated water. To have an understanding about the arsenic adsorption mechanism of nanoparticles, X-ray photoelectron spectroscopy (XPS) was performed before and after adsorption. The results showed that starch provides nanoparticles with a neutral surface and stabilization of nanoparticles is possible with 0.04 wt% or higher concentrations of starch. For 0.04 wt% starch-stabilized Fe/Cu nanoparticles, the adsorption isotherms fit well within the Langmuir equation, with maximum sorption capacities of 90.1 mg/g for As(III) and 126.58 mg/g for As(V) at a pH of 7.0 from the aqueous arsenic solutions. Examining the XPS spectra of nanoparticles before and after adsorption showed that arsenic adsorption by this nanoparticle can be due to the formation of inner-sphere arsenic complexes on the particle surface, and the surface oxygen-containing functional groups involved in adsorption. The high sorption capacity suggests the potential for applying starch-stabilized Fe/Cu nanoparticles to the contaminated waters for removal of arsenic.  相似文献   

9.
The biosorption of ammoniacal nitrogen (N-NH4 +) from aqueous solutions by dead biomass of brown seaweed Cystoseira indica and Jatropha oil cake (JOC), which is generated in the process of biodiesel recovery from its seeds, was studied under diverse experimental conditions. The N-NH4 + biosorption was strictly pH dependent, and maximum uptake capacity of C. indica (15.21 mg/g) and JOC (13.59 mg/g) was observed at initial pH 7 and 3, respectively. For each biosorbent–N-NH4 + system, kinetic models were applied to the experimental data to examine the mechanisms of sorption and potential rate-controlling steps. The generalized rate model and pseudo-second-order kinetic models described the biosorption kinetics accurately, and the sorption process was found to be controlled by pore and surface diffusion for these biosorbents. Results of four-stage batch biosorber design analysis revealed that the required time for the 99 % efficiency removal of 40 mg/L N-NH4 + from 500 L of aqueous solution were 76 and 96 min for C. indica and JOC, respectively. The Fourier transform infrared spectroscopy analysis before and after biosorption of ammonium onto C. indica and JOC revealed involvement of carboxylic and hydroxyl functional groups.  相似文献   

10.
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   

11.
The aim of this study was to evaluate the biosorption capacity of selected strains of microscopic fungi. We optimized the biosorption process and used the Freundlich isotherm for three strains: H. haematococca BwIII43, K37 and T. harzianum BsIII33 to describe the biosorption equilibrium of anthraquinone dye, Alizarin Blue Black B (ABBB) and alkali lignin (AL). In optimal conditions (1 g of mycelium biomass, pH = 7.0, 28 °C) for ABBB and AL sorption, the live biomass of H. haematococca BwIII43 was characterized by a higher sorption capacity, amounting to 247.47 and 161.00 mg g?1, respectively. The highest sorption properties toward anthraquinone dye (K F = 19.96 mg g?1) were shown for the biomass of H. haematococca K37. In the presence of alkali lignin, the highest sorption capacity and bond strength exhibited the biomass of H. haematococca BwIII43 (K F = 28.20 mg g?1, n = 3.46). Effective decolorization of ABBB and AL by the selected strains of microscopic fungi indicated that the biosorption process additionally enhanced the removal of color compounds from the solution.  相似文献   

12.
The objective of this work was to study sorption–desorption and/or precipitation–dissolution processes of Hg(II) compounds considering an eventual contact of soils with Hg-bearing wastes. In addition, this study contributes new data about Hg(II) chemistry in alkaline systems. Saline and alkaline soils with low organic matter (<1 %) and high clay content (60–70 %) were obtained near a chlor-alkali plant. Batch techniques were used to perform the experiments using 0.1 M NaNO3 solutions. Total Hg(II) concentrations ranged from 6.2 × 10?8 to 6.3 × 10?3 M. Sorption of Hg(II) was evaluated at two concentration ranges: (a) 6.2 × 10?8 to 1.1 × 10?4 M, and (b) 6.4 × 10?4 to 6.3 × 10?3 M. At low Hg(II) concentrations, adsorption occurred with a maximum sorption capacity ranging from 4 to 5 mmol/kg. At high Hg(II) concentrations, sorption–precipitation reactions occurred and maximum sorption capacity ranged from 17 to 31 mmol/kg. The distribution of Hg(II) hydrolysis products showed that Hg(OH)2 was the predominant species under soil conditions. According to sorption experiments, X-ray diffraction and chemical speciation modelling, the presence of Hg(OH)2 in the interlayer of the interstratified clay minerals can be proposed. Hg(OH)2 was partially desorbed by repeated equilibrations in 0.1 M NaNO3 solution. Desorption ranged from 0.1 to 0.9 mmol/kg for soils treated with 5.8 × 10?5 M Hg(II), whereas 2.1–3.8 mmol/kg was desorbed from soils treated with 6.3 × 10?3 M Hg(II). Formation of soluble Hg(II) complexes was limited by low organic matter content, whereas neutral Hg(OH)2 was retained by adsorption on clay mineral surfaces.  相似文献   

13.
Gaza central seawater desalination plant is a promising solution to alleviate the problem of water crisis in the Gaza Strip. The plant in the short term, phase (I), will desalinate seawater for potable uses with a capacity of 55 million cubic meters per year, while in the long term, phase (II), the plant capacity will be doubled to 110 million cubic meters per year of freshwater. As a product from the reverse osmosis process, a huge amount of brine with salinity reaches to 75,000 mg/L will be redirected to seawater; nearly 12,200 m3/h of brine will be rejected from phase (I) while in the long term, a brine flow rate of 24,400 m3/h will be disposed from phase (II). In order to minimize the negative impacts of the rejected brine on the marine environment, it is urgent to modeling numerically the impact of the discharged brine through various disposal systems to define the most environmental system. Various scenarios were defined and simulated using CORMIX model to study the efficiencies of onshore surface open channel, offshore submerged single port as well as offshore submerged multiport outfalls taking salinity variations as an indicator. Sensitivity analysis was conducted to identify the most influencing input parameters on the simulation results as well as to evaluate the optimal environmental disposal system which can mitigate the adverse impacts of brine on the marine ecosystem as much as possible in the worst seawater conditions. The simulation results showed that the discharge via surface open channel is not environmentally feasible where the seawater salinity rose by more than 2000 mg/L at RMZ. The single-port scenario can meet the regulations at RMZ but the standard at GMZ was not met, where the rejected brine from phase (I) through single port at 1500 m offshore raises the seawater salinity at GMZ by more than 600  mg/L. The staged multiport outfall, capped by 24 ports, achieves acceptable brine dilution at seawater depth of about 7.5  m, and in the worst ambient conditions in the case of phase (II) in operation, the brine’s excess salinity was 536, 497, and 379 mg/L above the salinity of seawater at RMZ, GMZ, and ROI, respectively.  相似文献   

14.
This study describes the development of scallop shell synthesized ceramic biomaterial for phosphorus removal from water. The synthesized biomaterial was characterized by scanning electron microscope, Brunauer–Emmett–Teller and X-ray diffractometer methods. The influences of contact time, initial phosphate concentration, initial solution pH, co-existing ions and temperature for phosphorus removal were investigated by batch experiments. The results indicated that the equilibrium data can be fitted by the Langmuir isotherm model at temperatures ranging from 15 to 55 °C, with the maximum sorption capacity of 13.6 mg/g. Sorption kinetics followed a pseudo-second-order kinetic equation model. The sorption process was optimal at a wide range of solution pH (above 2.4), with a relatively high sorption capacity level. Phosphorus sorption was slightly impeded by the presence of F?, HCO3 ? and NH4 + ions, and significantly inhibited by Cl?, SO4 2? and NO3 ? ions. Sorption process appeared to be controlled by a chemical precipitation processes. The mechanism may be attributed to ion complexation during subsequent sorption of phosphorus on scallop shell synthesized ceramic biomaterial.  相似文献   

15.
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   

16.
Cation and anion concentrations and oxygen and hydrogen isotopic ratios of brines in the Asmari Formation (Oligocene–early Miocene) from the Marun oil field of southwest Iran were measured to identify the origin of these brines (e.g. salt dissolution vs. seawater evaporation) as well as the involvement of water–rock reaction processes in their evolution. Marun brines are characterized by having higher concentrations of calcium (11 000–20 000 mg/L), chlorine (120 000–160 000 mg/L) and bromide (600–1000 mg/L) compared to modern seawater. Samples are also enriched in 18O relative to seawater, fall to the right of the Global Meteoric Water Line and local rain water, and plot close to the halite brine trajectory on the δD versus δ18O diagram. Geochemical characteristics of Marun brines are inconsistent with a meteoric origin, but instead correspond to residual evaporated seawater modified by water–rock interaction, most significantly dolomitization. In addition, anhydrite precipitation or sulphate reduction appears to be important in chemical modification of the Marun brines, as indicated by lower sulphate contents relative to evaporated seawater. Extensive dolomitization, the presence of anhydrite nodules and high salinity fluid inclusions in the upper parts of the Asmari Formation fit a model whereby the Marun brines likely originated from the seepage reflux of concentrated seawater during the deposition of the overlying Gachsaran Formation evaporites in the Miocene. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

17.
Naturally occurring pyroclastic materials, quartz-rich tuffs (Qz) and stellerite tuffs, were evaluated for their capacities to remove As(V) from aqueous solutions. The mechanism of As(V) uptake was evaluated using sequential extraction of As(V)-loaded adsorbent which entailed that the plausible removal mechanism is sorption to short-range ordered hydrous oxides of iron and aluminum. In addition, buffering effects of adsorbents could form favorable charges upon them through hydrolysis of amphoteric oxides, enhancing the performance of sorption. The influence of anions co-existing with As(V) in water such as carbonate, bicarbonate, nitrate, chloride, phosphate, and sulfate was studied in a batch sorption process. The impact of most anions on As(V) removal was found to be negligible except phosphate. The sorption behavior well fitted to Langmuir and Freundlich models. Estimated maximum sorption capacities of 0.42 and 0.23 mg/L were observed using quartz-rich tuffs and stellerite tuffs, respectively. As(V) concentration of 0.8 mg/L was easily decreased to below the drinking water standard of 0.01 mg/L using Qz adsorbent, whereas 0.1 mg/L As(V) decreased to below this limit upon the use of stellerite tuffs under similar conditions. The buffering capacity of quartz-rich tuffs and stellerite tuffs induced a pH increase to 5.76 and 5.40, respectively, from initial pH of 3.50, which will incur an important asset in real applications.  相似文献   

18.
Cation and anion concentrations and boron isotopic ratio of brines in the Mishrif Formation (U. Campanian-Tuoronian) from North Rumaila, South Rumaila, Majnoon, Zubair, and West Qurna oilfields southern Iraq were investigated. The aims of this study are to define the type, origin of the oilfield waters, and its flow model in the subsurface oil traps. Mishrif brines are characterized by having higher concentrations of sodium (50,500–84,200 ppm), chlorine (102,100–161,500 ppm), and boron (21.9–31.1 ppm) with lower sulfate contents (187–1350 ppm) relative to the modern seawater. Samples have slightly depleted in δ 11B (35.4‰) relative to seawater fall near the seawater intrusion of the diagram Cl/Br Vs δ 11B and occupied the field of evaporated seawater on the diagrams of Cl vs B and 1/Br vs δ 11B. The brine of Na-chloride type is characteristics of the Mishrif reservoir in all oilfields except WQ which defined by facies of Na-Ca-chloride type. A weak acidic brine of a salinity six-time greater than seawater plays a role in generating the formation pressure and controlling the fluid flow. The reservoir rock-fluid interactions were interpreted using boron isotopes which eventually reveal an ongoing dilution process by the present seawater intrusion and injection water used for the secondary production under conditions of high-temperature digenetic reactions. The 11B in the oilfield water is resulted from uptake of the tetrahedral borate after precipitation of calcium carbonate, while 10B is sourced from the thermal maturation of organic matters.  相似文献   

19.
In this work, the studies on the formation of zeolites from expanded perlite waste and their use in the sorption process of Cd2+ ions will be reported. Such approach is innovative and has not been investigated elsewhere. The results of the synthesis of zeolites from aluminosilicate waste using hydrothermal method were presented. By-product from the process production of expanded perlite was used as the starting material. Theoretical and practical aspects of Cd2+ ions sorption process onto material synthesized in selected conditions (a material with good sorption capacity can be obtained by 24 h reaction of 1 g of perlite waste in 10 mL of 4.0 M NaOH solution with at 70 °C) will be presented. The atomic absorption spectroscopy has been used as the main method, from which the effective cation exchange capacity as well as the proportion of ion exchange to chemisorption in the sorption process have been determined. Structural analyses of the sample before and after sorption process have been also carried out by the mid-infrared spectra measurement, especially pseudolattice range of the spectra was analyzed in detail in which changes caused by ion exchange of non-tetrahedral ions have been observed.  相似文献   

20.
In many petroleum-producing regions, there are not adequate controls to prevent pipeline breaks and spills, and thus soil is frequently contaminated with petroleum hydrocarbons. Different petroleum oil compounds may produce negative impacts on soil fertility. In this study, four fresh crudes, a weathered petroleum, and oils from bioremediated and burned sites were investigated (specific gravities 0.83–1.27). Fourier transform infrared spectroscopy revealed three predominant polar functional groups to be more plentiful in the heavier crudes. The relative abundance of these groups was used to calculate an index that was directly correlated with specific gravity (R 2 = 0.9960) and the percent of asphaltene plus (polars + resins) fractions in the oil (R 2 = 0.9643). This index correlated exponentially to the water repellency caused by petroleum in an alluvial soil (R 2 = 0.9928). Furthermore, extra-heavy oil at a concentration of 10,000 ppm, the maximum allowable oil concentration in the soil that is within regulatory norms in many US states and other countries, and with a specific gravity >1.002, showed severe water repellency. This study presents an alternative for determining soil remediation criteria based on the API gravity of the oil rather than the C-range of the hydrocarbon mixtures, simplifying analytical methods and systematically studying the interaction between the kinds of petroleum mixtures and potential impacts to soil fertility.  相似文献   

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