Use of Power Plant Ash to Remove and Solidify Heavy Metals from a Metal-finishing Wastewater

This laboratory-scale study investigated initially the potential of heavy metal removal from a metal-finishing wastewater using fly and bottom ash from a power plant as coagulants. It was found that the maximum heavy metal content in the ash–sludge mix was obtained at a fly ash-to-bottom ash ratio of 1.5:1 and a stirring time of 3 h, which resulted in heavy metal removal (i.e., Cr, Ni, Cu, Zn, Cd, and Pb) in excess of 99%, with effluent concentrations below the corresponding regulatory standards of Thailand. Furthermore, the feasibility of using fly ash as an admixture to stabilize and solidify the ash–sludge mix generated previously was explored. Results indicated that the stabilization/solidification process can achieve a high level of heavy metal removal efficiency from the ash–sludge mix. The optimum ratio regarding chromium leaching was found to be 1:0.75:0.75 (cement:fly ash:ash–sludge). In addition, the compressive strength and the chromium leaching concentration of the solidified sludge were within acceptable levels for secure landfill disposal and/or use as a construction material.     

Adsorption of Dioxin by Bag Filter + Powdered Activated Carbon

A novel bag filter + powdered activated carbon technique is here proposed to address the low utilization rate of powdered activated carbon and the low dioxin removal rate associated with the conventional activated carbon injection + bag filter technique, better known as the fly ash + activated carbon + bag technique. In this method, dibenzofuran serves as a dioxin simulant. The effect of the adsorption temperature and dibenzofuran inlet concentration on the adsorption performance of activated carbon was studied using a filter cloth adsorption device with an inner diameter of 25 mm, and the adsorption performances of fly ash, activated carbon, and fly ash +5% activated carbon were compared. The results showed that activated carbon exhibited a higher adsorption efficiency and remained highly efficient longer than fly ash +5% activated carbon. When the dibenzofuran inlet concentration was 0.0956 g/m³ (about one million times the concentration of dioxin in the flue gas of incinerated waste), the duration of the high-efficiency (>90%) adsorption of the powdered activated carbon (thickness 1.2 mm) on the filter cloth was over 7 h. These results prove that the replacement of fly ash + activated carbon + filter bag with powdered activated carbon + bag filter can significantly improve the removal efficiency of the dioxin in waste incineration flue gas and the utilization rate of activated carbon.     

Removal of Hexavalent Chromium from Water by Polyurethane�CKeratin Hybrid Membranes

The feasibility of employing a porous polyurethane?Ckeratin hybrid membrane for the removal of hexavalent chromium was investigated. Keratin was extracted from chicken feathers and incorporated onto a synthetic polyurethane polymer to synthesize a hybrid membrane. Keratin supply active sites to bioadsorb Cr(VI) and polyurethane play an important role as the support to protein. Also, polyurethane?Ckeratin biofiber membranes were synthesized. Biofibers obtained from chicken feathers were modified to activate their surface. The effective pore in membranes is less than 50 nm, which places these materials in the mesopore range. Scanning electron microscopy (SEM) was used to study the morphology of membranes, and mechanical dynamical analysis (DMA) was used to evaluate the viscoelastic properties. NH, C=O, S?CS and C?CS were determined via Fourier-transform infrared (FTIR) analysis as functional groups of keratin, which participate in the linking sorption of hexavalent chromium. Adsorption of Cr(VI) was carried out in a filtering system at low contact time in continuous flux; the maximum removal reached was 38% at neutral pH of chromium solution. Results indicate that the isoelectric point of keratin is relevant in the adsorption process. pH of keratin solution above the isoelectric point brings about higher adsorption of heavy metals, whereas lower pH causes minor adsorptions, due to the functional groups?? ion charges. Based on the results, keratin extracted from feathers is a natural biosorbent that can be incorporated onto synthetic polymers to develop novel membranes and improve its applications in the heavy metal separation process.     

Studies on the Phase Mineralogy and Leaching Characteristics of Coal Fly Ash

The phase mineralogy and leaching characteristics of some Indian coal fly ashes were studied to assess their safe disposal in abandoned coal mines. Since, fly ash contains a number of toxic trace elements, the leaching of fly ash was tested using strong acid/alkali solutions and distilled water under different conditions (solid-liquid ratio, leaching time, pH) in the temperature range of 30-100 °C. It was found that the concentration of various metals in leachates depends on their chemical nature, association with mineral phases of ash and follows the almost similar concentration profile to that of iron, especially in acidic medium. The distribution of toxic trace elements in fly ash and their leachability were found to depend on the amount of unburnt carbon and iron in fly ash. In alkaline medium, leaching of iron and toxic trace elements (except As) from fly ash was very negligible. Hence, alkali treatment of coal fly ash is desirable for its safe use in refilling of coal mines.     

Characteristics of synthetic soil aggregates produced by mixing acidic “Kunigami Mahji” soil with coal fly ash and their utilization as a medium for crop growth

Abstract

This study was carried out to examine the characteristics and potential utilization of synthetic soil aggregates (SSA) produced by mixing acidic “Kunigami Mahji” soil in Okinawa, Japan, with waste materials, such as coal fly ash, used paper and starch, as media for crop growth. A series of different SSA were produced by incorporating various percentages (i.e. 0, 20, 40, 60, 80 and 100%) of coal fly ash into the “Kunigami Mahji” soil with used paper and starch. The particle density and bulk density of the original “Kunigami Mahji” soil were 2.67 and 1.23 g cm^?3, respectively. The increased percentages of added coal fly ash, used paper and starch significantly decreased the particle and bulk densities of SSA compared with the original “Kunigami Mahji” soil because of the low particle and bulk densities of the coal fly ash (2.10 and 0.96 g cm^?3, respectively). The SSA particle density varied between 2.39 and 2.14 g cm^?3, and bulk density varied between 0.72 and 0.81 g cm^?3, depending on the additional percentages of coal ash from 20–100%. Maximum water-holding capacity and saturated hydraulic conductivity were increased with the formation of SSA with coal fly ash, used paper and starch binder compared with the original “Kunigami Mahji” soil. The saturated hydraulic conductivity values of the SSA increased because of their low bulk density compared with the original soil. The addition of coal fly ash, used paper and starch to the acidic (pH = 4.62) “Kunigami Mahji” soil to form SSA increased the pH (6.70–9.96), electrical conductivity, exchangeable cation concentration and cation exchange capacity. The addition of coal fly ash up to 60% increased the aggregate strength. The growth and yield of komatsuna and soybean crops with SSA as a crop growth medium was assessed. Both crops showed the highest growth and yield when grown with SSA containing 20% of coal fly ash. Synthetic soil aggregates containing more than 20% of coal fly ash reduced plant growth and yield. Therefore, SSA produced from “Kunigami Mahji” soil with 20% of coal fly ash, used paper and starch can be successfully used as a medium for crop growth.     

Elemental composition and release characteristics of some South African fly ashes and their potential for land application

Eight fly ash samples collected from South African power stations were evaluated for various chemical properties, liming potential and metal species release under incubation. All fly ashes had alkaline pH ranging from 10.97 to 12.75 with much wider variations of electrical conductivity (range 0.46–8.27 dS m^?1). Their total P content ranged from 553.3 to 1514 mg P kg^?1 and Olsen extractable P from 130 to 345.5 mg P kg^?1. Application of two of the fly ashes to three different soils showed a high ability to neutralize acidity, resulting in an average of 41% change in pH after 8 weeks of incubation. Across all three soils, the fly ash incorporation increased extractable P content from a P-deficient level to levels above 25 mg P kg^?1 in two of the three soils. Except for Cu, all metal species (Cr, Pb, Ni and Fe) showed significantly (P ≤ 0.05) low extractability under fly ash treated soils compared to the soil alone control. These results suggest that the South African fly ashes studied are effective liming materials and can provide essential elements such as P with minimum risk of soil contamination from metal species release.     

Adsorption-Desorption of Zinc as Influenced by Fly Ash in Inceptisols of Assam

This study investigates the influence of fly ash (FA) application on zinc adsorption-desorption in recommended chemical fertilizer (RDF) and farmyard manure (FYM) treatments of acidic Inceptisols of Assam. Zinc adsorption was better explained by Freundlich over the Langmuir adsorption equation. Adsorption was greatest in the treatment receiving FA only at 15 t ha^?1 and least in the treatment receiving RDF 50 percent + FYM 5 t ha^?1 + FA 5 t ha^?1. The zinc distribution coefficient of treatment FA 15 t ha^?1 was 40 to 31 times greater than treatments containing FA + RDF + FYM. The zinc supply parameter increased when FA was applied with RDF and FYM, and zinc desorption followed the order of exctractants CaCl₂ > MgCl₂ > DTPA > HCl. They desorbed more Zn from soils with low “b” and vice versa. Results confirm that fly ash integrated with RDF + FYM can effectively be used to maintain substantial concentrations of Zn in soil.     

Activated Biochar Prepared by Pomelo Peel Using H<Subscript>3</Subscript>PO<Subscript>4</Subscript> for the Adsorption of Hexavalent Chromium: Performance and Mechanism

Adsorption of hexavalent chromium (Cr(VI)) using pomelo peel activated biochar (PPAB) as a adsorbent was investigated. The characterization of the adsorbent was studied by Brunauer-Emmett-Teller (BET), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and zeta potentials analysis. The results showed that the PPAB had a high microporous structure and the existence of organic compounds such as hemicellulose, cellulose, and lignin. Various parameters including initial Cr(VI) concentration, pH, and adsorbent dosage were studied. The results indicated that the adsorption process was pH dependent and maximum adsorption capacity of Cr(VI) was 57.637 mg/g at pH 2.0 and 35 °C with PPAB dosage of 0.05 g. The adsorption kinetics fitted well to the pseudo-second-order model and the correlation coefficients were greater than 0.999. The adsorption isotherm data could be better described with the Langmuir model, suggesting the homogeneous and monolayer adsorption. Moreover, the scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), and Fourier transform infrared spectrum (FTIR) results showed that the surface of PPAB had plenty of developed pores after activation and the modification process was deemed to proceed between the O–H groups from pomelo peel and H₃PO₄ molecules. The main adsorption mechanism was attributed electrostatic interaction and ion exchange between the surface of PPAB and Cr(VI).     

The use of coal fly ash in sodic soil reclamation

An experiment was conducted for two years in northwest India to explore the feasibility of using coal fly ash for reclamation of waterlogged sodic soils and its resultant effects on plant growth in padi–wheat rotation. The initial pH, electrical conductivity, exchangeable sodium percentage and sodium adsorption ratio of the experimental soil were 9.07, 3.87 dS m⁻¹, 26.0 and 4.77 (me l)^−1/2, respectively. The fly ash obtained from electrostatic precipitators of thermal power plant had a pH of 5.89 and electrical conductivity of 0.88 dS m⁻¹. The treatments comprised of fly ash levels of 0.0, 1.5, 3.0, 4.5, 6.0 and 7.5 per cent, used alone as well as in combination with 100, 80, 60, 40, 20 and 10 per cent gypsum requirement of the soil, respectively. There was a slight reduction in soil pH while electrical conductivity of the soil decreased significantly with fly ash as measured after padi and wheat crops. The sodium adsorption ratio of the soil decreased with increasing fly ash levels, while gypsum treatments considerably added to its favourable effects. Fly ash application increased the available elemental status of N, K, Ca, Mg, S, Fe, Mn, B, Mo, Al, Pb, Ni, Co, but decreased Na, P and Zn in the soil. An application of fly ash to the soil also increased the concentrations of above elements except Na, P and Zn in the seeds and straw of padi and wheat crops. The available as well as elemental concentrations in the plants was maximum in the 0 per cent fly ash + 100 per cent gypsum requirement treatment except Na and heavy elements like Ni, Co, Cr. The treatment effects were greater in the fly ash + gypsum requirement combinations as compared to fly ash alone. Saturated hydraulic conductivity and soil water retention generally improved with the addition of fly ash while bulk density decreased. Application of fly ash up to 4.5 per cent level increased the straw and grain yield of padi and wheat crops significantly in both years. The results indicated that for reclaiming sodic soils of the southwest Punjab, gypsum could possibly be substituted up to 40 per cent of the gypsum requirement with 3.0 per cent acidic fly ash. Copyright © 2003 John Wiley & Sons, Ltd.     

Influence of fly ash and quicklime addition on behaviour of municipal solid wastes

Purpose

Many closed municipal solid waste landfill sites are near urban areas and there are high expectations to improve geotechnical properties of these sites for re-development. Construction on closed landfill sites is generally a challenging task due to complex behaviour of creep, settlement, high amount of moisture content and weak shear strength of waste. This study presents the experimental results for the use of fly ash and quicklime in improvement of the geotechnical properties of municipal solid wastes (MSW).

Materials and methods

The waste materials were collected from a closed landfill in the southwest of Sydney. The samples were prepared by integrating MSW with a mixture of fly ash–quicklime with a ratio of 3:1 in percentages of 5, 10, 15 and 20 of fly ash by dry weight of the MSW. An array of experimental tests has been conducted on treated and untreated MSW samples including sieve analysis, Atterberg limits, compaction and consolidated–drained triaxial tests.

Results and discussion

Results of this investigation showed a significant improvement in geotechnical properties of MSW. It has been found that by increasing fly ash–quicklime admixtures from 0 to 26.7 % (0 to 20 % fly ash), the internal friction angle increased from 29 to 39° and the cohesion intercept increased from 11 to 30 kPa. Under an effective confining pressure of 300 kPa, the peak strength, the brittleness index and the Young's modulus at failure increased from 600 to 1,150 kPa, 0.13 to 0.35 and 5.5 MPa to 28 MPa, by addition of 26.7 % fly ash–quicklime admixture, respectively. Moreover, the compression and the secondary compression indices decreased from 0.33 to 0.23 and 0.052 to 0.033, respectively.

Conclusions

It is found that the chemical stabilisation effectively increases the compressive strength, the shear strength parameters, the stiffness and the brittleness index whilst decreases the settlement of the MSW layer. It will be beneficial and effective in re-development of closed landfill sites incorporating chemical treatments. The findings of this study may facilitate the calculations of the bearing capacity and settlement as well as the slope stability analysis of chemically treated closed landfill sites.     

A Comparison of Inorganic Solid Wastes as Adsorbents of Heavy Metal Cations in Aqueous Solution and Their Capacity for Desorption and Regeneration

The adsorption capacity of seven inorganic solid wastes [air-cooled blast furnace (BF) slag, water-quenched BF slag, steel furnace slag, coal fly ash, coal bottom ash, water treatment (alum) sludge and seawater-neutralized red mud] for Cd²⁺, Cu²⁺, Pb²⁺, Zn²⁺ and Cr³⁺ was determined at two metal concentrations (10 and 100 mg?L^?1) and three equilibrium pH values (4.0, 6.0 and 8.0) in batch adsorption experiments. All materials had the ability to remove metal cations from aqueous solution (fly and bottom ash were the least effective), their relative abilities were partially pH dependant and adsorption increased greatly with increasing pH. At equimolar concentrations of added metal, the magnitude of sorption at pH 6.0 followed the general order: Cr³⁺????Pb²⁺????Cu²⁺?>?Zn²⁺?=?Cd²⁺. The amounts of previously sorbed Pb and Cd desorbed in 0.01 M NaNO₃ electrolyte were very small, but those removed with 0.01 M HNO₃, and more particularly 0.10 M HNO₃, were substantial. Water treatment sludge was shown to maintain its Pb and Cd adsorption capability (pH 6.0) over eight successive cycles of adsorption/regeneration using 0.10 M HNO₃ as a regenerating agent. By contrast, for BF slag and red mud, there was a very pronounced decline in adsorption of both Pb and Cd after only one regeneration cycle. A comparison of Pb and Cd adsorption isotherms at pH 6.0 for untreated and acid-pre-treated materials confirmed that for water treatment sludge acid pre-treatment had no significant effect, but for BF slag and red mud, adsorption was greatly reduced. This was explained in terms of residual surface alkalinity being the key factor contributing to the high adsorption capability of the latter two materials, and acid pre-treatment results in neutralization of much of this alkalinity. It was concluded that acid is not a suitable regenerating agent for slags and red mud and that further research and development with water treatment sludge as a metal adsorbent are warranted.     

Potential of Eisenia foetida for Sustainable and Efficient Vermicomposting of Fly Ash

Vermicomposting of fly ash has been attempted, using red earthworm, Eisenia foetida. Fly ash, which was obtained from thermal power station, was mixed with cowdung in different proportions (20, 40, 60 and 80%). These mixtures were used as feed for earthworms, and after 30 days, vermicast recovery, worm zoomass and numbers of juveniles produced were recorded. A total of six runs each of 30 days were conducted during the whole study. Concentrations of heavy metals in different mixtures of fly ash–cowdung, before and after vermicomposting and in the earthworms used in the study were also estimated. Results show maximum output of vermicasts and maximum number of juveniles produced was in reactors with 40% fly ash while maximum weight gain by earthworm was in 20% fly ash vermireactors. Performance of vermireactors up to 60% fly ash was more or less similar but at 80% fly ash, there is a marked reduction in overall performance of the reactors. Chemical analysis of different samples of fly ash–cowdung mixtures prior to vermicomposting revealed high concentrations of zinc, chromium, lead, nickel and copper. Chemical analysis of vermicomposted samples showed 30–50% reduction in heavy metals up to 60% fly ash and 10–30% reduction in 80% fly ash. Metal analysis of earthworms revealed considerable bioaccumulation of heavy metals in their body. The Present study indicates the feasibility of E. foetida for mitigating the toxicity of metals and up to 60% fly ash–cowdung mixtures can be used for sustainable and efficient vermicomposting.     

Hexavalent Chromium Removal by a Trichoderma inhamatum Fungal Strain Isolated from Tannery Effluent

A fungal strain possibly capable of removing hexavalent chromium was to be isolated from industrial effluent from a leather factory located in the city of Guadalajara, state of Jalisco, Mexico. The strain was identified as Trichoderma inhamatum by the D1/D2 domain sequence of the 28S rDNA gene. Batch cultures of T. inhamatum in media containing initial Cr(VI) concentrations from 0.83 to 2.43 mM Cr(VI) were prepared. Experimental results suggest that the fungus is capable of transforming hexavalent chromium to trivalent chromium; a transformation of a highly toxic contaminant to a low toxic form. The specific and volumetric rates of Cr(VI) reduction by T. inhamatum cultures decreased as the initial Cr(VI) concentration increased. The fungus exhibited a remarkable capacity to tolerate and completely reduce Cr(VI) concentrations up to 2.43 mM. These results indicate that the T. inhamatum fungal strain may have potential applications in bioremediation of Cr(VI)-contaminated wastewaters.     

Optimization of Ammonia Removal from Aqueous Solution by Microwave-Assisted Air Stripping

In this study, the optimum conditions for the ammonia removal from aqueous solution by microwave-assisted air stripping have been investigated at pH 11. Ammonia solution with five different initial ammonia concentrations was prepared synthetically. The Taguchi method was applied to optimize the ammonia removal conditions. Initial ammonia concentration, air flow rate, temperature, stirring speed, microwave radiation power, and radiation time were defined as the optimization parameters. Experiments were carried out at five different levels for each operational parameter. The results of the experiments revealed that 1800 ppm of initial ammonia concentration, 7.5 L min^?1 of air flow rate, 60 °C of temperature, 500 rpm of stirring speed, and 500 W of microwave radiation power for 180 min. of microwave radiation time are optimum conditions for complete ammonia removal. In addition to present experimental data, the optimum operational conditions predicted by the balanced characteristics of orthogonal array were confirmed experimentally. Finally, the effect of optimization parameters was discussed in detail.

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Graphical Abstract ?

     

Technogenic Magnetic Particles in Alkaline Dusts from Power and Cement Plants

During this study, we investigated the mineralogical characterization of technogenic magnetic particles (TMPs) contained in alkaline industrial dust and fly ash emitted by coal burning power plants and cement plants. The reaction of tested dust samples varied between values of pH 8 and pH 12. Their magnetic properties were characterized by measurement of magnetic susceptibility (χ), frequency dependence of magnetic susceptibility (χ_fd), and temperature dependence of magnetic susceptibility. Mineralogical and geochemical analyses included scanning electron microscopy with energy dispersive spectroscopy, microprobe analysis and X-ray diffraction. The TMPs in fly ash from hard coal combustion have the form of typical magnetic spherules with a smooth or corrugated surface as well as a skeletal morphology, composed of iron oxides (magnetite, maghemite, and magnesioferrite) that occurred in the form of incrustation on the surface of mullite, amorphous silica, or aluminosilicate particles. The TMPs observed in fly ash from lignite combustion have a similar morphological form but a different mineralogical composition. Instead of magnetite and magnesioferrite, maghemite and hematite with lower χ values were the prevailing magnetic minerals, which explains the much lower magnetic susceptibility of this kind of ash in comparison with the ash from hard coal combustion, and probably results from the lower temperature of lignite combustion. Morphology and mineralogical composition of TMPs in cement dust is more diverse. The magnetic fraction of cement dust occurs mostly in the form of angular and octahedral grains of a significantly finer granulation (<20 μm); however, spherules are also present. A very characteristic magnetic form for cement dust is calcium ferrite (CaFe₃O₅). The greatest impact on the magnetic susceptibility of cement dust results from iron-bearing additives (often waste materials from other branches of industry), which should be considered the most dangerous to the environment. Stoichiometric analysis of micro-particles confirmed the presence of heavy metals such as Pb, Mn, Cd, and Zn connected with TMPs, which are carriers of magnetic signals in atmospheric dust. Therefore, in some cases, their presence in topsoil when detected by magnetic measurement can be treated as an indicator of inorganic soil contamination.     

Combined Removal of Zinc (II) and Cadmium (II) from Aqueous Solutions by Adsorption onto High-Calcium Turkish Fly Ash

The aim of this work is the investigation of possible use of flyash in the removal of zinc (Zn²⁺) and cadmium (Cd²⁺) contained in aqueous solutions. Batch adsorption experiments wereperformed in order to evaluate the removal efficiency oflignite-based fly ash. The parameters studied include contact time, pH,temperature, initial concentration of the adsorbate and fly ashdosage. The contact time necessary to attain equilibrium was found to be two hours. Maximum adsorption occurred in the pH range of 7.0 to 7.5. The percent adsorption of Zn²⁺ and Cd²⁺ increased with an increase in concentration of Zn²⁺ and Cd²⁺, dosage of fly ash and temperature. Theapplicability of Langmuir isotherm suggests the formation ofmonolayer coverage Zn²⁺ and Cd²⁺ ions at the outer surface of the adsorbent. Thermodynamic parameters suggested the endothermic nature of the adsorption process. The fly ashwas found to be an metal adsorbent as effective as activated carbon.     

Tracking of Chromium in Plasma co-Melting of Fly Ashes and Sludges

Leachable chromium in the incineration fly ash and wastewater sludge has been thermally stabilized by plasma melting at the temperature of 1,773?K. To better understand how chromium is stabilized with the high-temperature treatment, chemical structure of the slags sampled at temperature zones of 1,100?C1,700?K has been studied by synchrotron X-ray absorption spectroscopy. The component-fitted X-ray absorption near edge structure spectra of chromium indicate that the main chromium compounds in the sludge and fly ash are Cr(OH)₃, Cr₂O₃, and CrCl₃. A small amount of toxic CrO₃ is also observed in the fly ash. In the plasma melting chamber under the reducing environment, the high-oxidation state chromium is not found. The slags in the plasma melting chamber have much less leachable chromium, which is due to chemical interactions between chromium and SiO₂ in the slags. The existence of the interconnected Cr-O-Si species is observed by refined extended X-ray absorption fine structure spectroscopy. In the Cr₂O₃ phase of the slags, their bond distances, and coordination numbers for the first (Cr-O) and second (Cr-(O)-Cr) shells have insignificant perturbation when experienced with different melting temperatures between 1,300 and 1,700?K. It seems that Cr₂O₃ and chromium encapsulated in the silicate matrix of the slags have relatively much lower leachability. With this concept, to obtain a low chromium leachability slag from the plasma melting process, the residence time of the melting chamber may be decreased, and the slag discharge temperatures may be increased to 1,300?K. This work also exemplifies utilization of molecule-scale data obtained from synchrotron X-ray absorption spectroscopy to reveal how chromium is thermally stabilized in a commercial scale plasma melting process.     

Feasibility Assessment of Chromium Removal from Groundwater for Drinking Purposes by Sorption on Granular Activated Carbon and Strong Base Anion Exchange

The goal of this study was to compare the performances of strong base anion (SBA) exchange and activated carbon adsorption in the removal of hexavalent chromium, Cr(VI), from a real groundwater matrix exploited for drinking purposes. Two SBA resins and three granular activated carbons (GAC) were tested by batch experiments for kinetics and equilibrium isotherm determination. SBA resins showed higher affinity toward Cr(VI) (present in raw water at about 20 μg L^?1) with respect to the GACs, with faster kinetics and higher equilibrium adsorption capacities. Among GACs, vegetal-based carbons showed higher Cr(VI) removal efficiencies than the mineral-based carbon, which can be related to the more developed textural properties. SBA resins also displayed relevant removal capacities towards nitrate and sulfate (present at mg L^?1 concentration levels), while boron (present at about 60 μg L^?1) was effectively removed by GACs. Batch experiment results were elaborated to estimate the chromium throughputs for the studied materials, to preliminary compare their performances in a real-scale application. The monitoring of a real-scale GAC adsorption stage permitted to validate throughputs estimation and confirmed that, despite being effective toward synthetic organics, GAC adsorption is a not feasible solution for Cr(VI) removal, with extremely early breakthrough. SBA exchange process resulted to be the most suitable solution, providing the best sorbent usage rates. However, SBA resin usage rates can strongly increase when considering the removal of nitrate and sulfate ions, requiring much shorter cycle times.     

Adsorption-desorption studies of selected herbicides in soil-Fly ash mixtures

Fly ash and soil mixtures with a range of fly ash content from 0 to 100% were used to study the adsorption and desorption of herbicides atrazine, propazine, prometryne, propanil, and molinate in batch experiments. The isotherms shapes according to Giles classification (Giles et al., 1960) were S, L, and H as the substrate changed from sandy clay loam (SCL) to fly ash, depending on the percent of fly ash in the mixture. The adsorption isotherms fit the Freundlich equation x/m = K(f) C(1/)(n)(). The K(f) values increase with the increase of the fly ash content. The mean percent amounts of herbicides, for a range of concentration 1-20 mg L(-)(1), adsorbed on the soil were 21.9% for atrazine, 50.7% for propazine, 29.04% for prometryne, 43.14% for molinate, 31.35% for propachlor, and 46.34% for propanil. Mass balance estimations show that the adsorbed amounts of the herbicides increase along with the fly ash content in the sorbent mixture and reach the 99% in the "pure" fly ash. In contrast, the amounts desorbed with water decrease as the fly ash content increases. The n values ranged from 0.82 to 3.05 indicating that the carbon content of fly ash plays a significant role during the sorption process and an increase of heterogenity of solid substrate. The increase of the amounts desorbed with acetone indicates that the sorption of organic compounds onto fly ash is believed to occur principally via the weak induction forces of London or dispersion forces which are characteristic of the physical adsorption process. The results of this research demonstrate that the fly ash shows a significant capacity for adsorption of organic compounds from aqueous solution.     

Increase of Available Phosphorus by Fly‐Ash Application in Paddy Soils

Abstract

Fly ash from the coal‐burning industry may be a potential inorganic soil amendment to increase rice productivity and to restore the soil nutrient balance in paddy soil. In this study, fly ash was applied at rates of 0, 40, 80, and 120 Mg ha^?1 in two paddy soils (silt loam in Yehari and loamy sand in Daegok). During rice cultivation, available phosphorus (P) increased significantly with fly ash application, as there was high content of P (786 mg kg^?1) in the applied fly ash. In addition, high content of silicon (Si) and high pH of fly ash contributed to increased available‐P content by ion competition between phosphate and silicate and by neutralization of soil acidity, respectively. With fly‐ash application, water‐soluble P (W‐P) content increased significantly together with increasing aluminum‐bound P (Al‐P) and calcium‐bound P (Ca‐P) fractions. By contrast, iron‐bound P (Fe‐P) decreased significantly because of reduction of iron under the flooded paddy soil during rice cultivation. The present experiment indicated that addition of fly ash had a positive benefit on increasing the P availability.