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1.
Mechanism and kinetics of hydrothermal replacement of magnetite by hematite   总被引：1，自引：1，他引：0  
The replacement of magnetite by hematite was studied through a series of experiments under mild hydrothermal conditions(140 -220℃, vapour saturated pressures) to quantify the kinetics of the transformation and the relative effects of redox and non-redox processes on the transformation. The results indicate that oxygen is not an essential factor in the replacement reaction of magnetite by hematite, but the addition of excess oxidant does trigger the oxidation reaction, and increases the kinetics of the transformation. However, even under high O_2(aq) environments, some of the replacement still occurred via Fe2+ leaching from magnetite. The kinetics of the replacement reaction depends upon temperature and solution parameters such as pH and the concentrations of ligands, all of which are factors that control the solubility of magnetite and affect the transport of Fe2+ (and the oxidant) to and from the reaction front. Reaction rates are fast at ~200℃, and in nature transport properties of Fe and,in the case of the redox-controlled replacement, the oxidant will be the rate-limiting control on the reaction progress. Using an Avrami treatment of the kinetic data and the Arrhenius equation, the activation energy for the transformation under non-redox conditions was calculated to be 26 ± 6 kJ mol-1.This value is in agreement with the reported activation energy for the dissolution of magnetite, which is the rate-limiting process for the transformation under non-redox conditions.  相似文献   

2.
This study investigated the potential application of heavy oil burning fly ash as a precursor to prepare activated carbon. The raw fly ash obtained from a power plant is cleaned by nitric acid/hydrochloric acid and activated at 550–800 °C with hold times of 30 and 60 min to obtain fly ash activated carbon. The phosphoric acid is used as a chemical agent to improve the surface characteristics of the cleaned fly ash. The effects of process variables such as amount of chemical reagents, activation time and temperature were investigated according to two-levels full factorial design. The resultant activated carbons were characterized in terms of Brunauer, Emmett and Teller surface area and total and pore volume. The maximum specific surface area was found of 148.30 m2/g at 800 °C temperatures with 60 min holding time. The test showed that the surface area and pore volumes of the material are also significantly enhanced by the activation process.  相似文献   

3.
At present, nearly 100 million tonnes of fly ash is being generated annually in India posing serious health and environmental problems. To control these problems, the most commonly used method is addition of fly ash as a stabilizing agent usually used in combination with soils. In the present study, high-calcium (ASTM Class C—Neyveli fly) and low-calcium (ASTM Class F—Badarpur fly ash) fly ashes in different proportions by weight (10, 20, 40, 60 and 80 %) were added to a highly expansive soil [known as black cotton (BC) soil] from India. Laboratory tests involved determination of physical properties, compaction characteristics and swell potential. The test results show that the consistency limits, compaction characteristics and swelling potential of expansive soil–fly ash mixtures are significantly modified and improved. It is seen that 40 % fly ash content is the optimum quantity to improve the plasticity characteristics of BC soil. The fly ashes exhibit low dry unit weight compared to BC soil. With the addition of fly ash to BC soil the maximum dry unit weight (γdmax) of the soil–fly ash mixtures decreases with increase in optimum moisture content (OMC), which can be mainly attributed to the improvement in gradation of the fly ash. It is also observed that 10 % of Neyveli fly ash is the optimum amount required to minimize the swell potential compared to 40 % of Badarpur fly ash. Therefore, the main objective of the study was to study the effect of fly ashes on the physical, compaction, and swelling potential of BC soils, and bulk utilization of industrial waste by-product without adversely affecting the environment.  相似文献   

4.
Thermal treatment of waste from the meat industry in high scale rotary kiln   总被引：1，自引：0，他引：1  
Recently there has been an increase in consumption of meat, especially poultry. This results in an increase in the quantity of waste, including waste feathers. Waste from the meat industry are hazardous, which must be disposed of in accordance with the law. Wastes from the meat industry normally consist of valuable elements such as phosphorus, calcium, potassium, magnesium (macronutrients), and iron, copper, zinc, manganese (micronutrients), which after suitable processing can be used for the purposes of fertilization. The paper presents the results of thermal treatment of feathers with meat and bone meal and feathers with poultry litter in a high scale rotary kiln. Mixtures of wastes were incinerated in temperature range from 600 to 900 °C for about 20–25 min. The resulting ashes were characterized by a high content of phosphorus (4–17%), calcium (17–30%) and potassium (0.6–3.6%). The study revealed that the selection of process parameters allows for obtaining ash with controlled and desired composition of macro and micronutrients, moreover, it is safe in terms of sanitary.  相似文献   

5.
One of the effective utilization strategies for fly ash and waste sludge is to use it as a fill material to raise low lying areas. Bearing capacity and settlement are the required input for the design of foundations on such fills. To determine the bearing capacity, plate load tests were carried out on the compacted beds of fly ash, fly ash-waste sludge and fly ash-waste sludge–cement. The tests were conducted by keeping 90, 95 and 100 % relative compaction, fresh and fresh submerged conditions, aged (28 days) and aged (28 days) submerged conditions as variables of the tests. The load-settlement curves were plotted for fly ash and mix blends. The minimum load was obtained for fly ash under submerged condition, further the test results show that the fly ash becomes flowable on submergence. On the other hand when the fly ash was mixed with waste sludge and cement, the load carrying capacity was found to improve to a greater extent. Test beds prepared with fly ash–cement-waste sludge under as compacted condition (fresh) show very high load carrying capacity (1600–2180 kN/m2). An analytical method has also been validated for fly ash–cement-waste sludge mix which was developed to estimate the settlement of footing resting on fly ash taking into account the pre-consolidation stresses. The non linearity of load-settlement behavior was appropriately modeled, on the basis of available plate load test data incorporated in the method. The method requires as input, the pre-consolidation stress and Young’s modulus of compacted mix of fly ash-waste sludge–cement. A comparison of load-settlement values observed in plate load tests and predicted values for the mix 47 %FA + 45 %S + 8 %C, using the proposed method shows good agreement. Hence, this relationship may also be useful to the field engineers to check the reported load-settlement values for such types of mixes in the field.  相似文献   

6.
In this paper, an experimental study was conducted in order to test the feasibility of sintering mullite directly from the high-alumina fly ash, without adding any extra material. The results show that the mullite contents in most sintered samples are over 70%. The samples sintered from the beneficiated fly ash have a higher content of mullite than those from the as-received fly ash under the same synthetic conditions. To obtain an equal amount of mullite, a higher sintering temperature is needed for the beneficiated fly ash than for the as-received fly ash. Considering the physical properties of sintered mullite, the favorable sintering temperature is 1400℃ for the as-received fly ash and 1500℃ for the beneficiated fly ash. A higher sintering temperature and a shorter holding time are profitable to sintering mullite. The orthogonal test confirmed that the dominant factor affecting mullite synthesis is sintering temperature, and that the most profitable matching conditions are 200 MPa-1500℃-3 h for the as-received fly ash and 200 MPa-1500 ℃-4 h for the beneficiated fly ash.  相似文献   

7.
Impacts of subsurface heat storage on aquifer hydrogeochemistry   总被引：3，自引：3，他引：0  
The use of shallow aquifers for subsurface heat storage in terms of energy management and building climatisation can lead to a temperature rise in the aquifer to 70 °C and above. The influence of temperature changes on individual mineral and sorption equilibria, reaction kinetics and microbial activity is largely known. However, the impact of heating to temperatures as high as 70 °C on the aquifer overall system has not been quantified yet. Temperature-related changes in sediment ion exchange behaviour, dimension and rates of mineral dissolution and precipitation as well as microbially enhanced redox processes were studied in column experiments using aquifer sediment and tap water at 10, 25, 40, and 70 °C. At 70 °C, a change in sediment sorption behaviour for cations and organic acids was postulated based on temporal changes in pH, magnesium, and potassium concentration in the experimental solution. No clear changes of pH, TIC and major cations were found at 10–40 °C. Redox zoning shifted from oxic conditions towards nitrate and iron(III) reducing conditions at 25 and 40 °C and sulphate reducing conditions at 70 °C. This was attributed to (a) a temperature-related increase in microbial reduction activity, and (b) three times higher release of organic carbon from the sediment at 70 °C compared to the lower temperatures. The findings of this study predict that a temperature increase in the subsurface up to 25 °C and above can impair the usability of ground water as drinking and process water, by reducing metal oxides and thus possibly releasing heavy metals from the sediment. Generally, at 70 °C, where clear cation and organic carbon desorption processes were observed and sulphate reducing conditions could be achieved, a site-specific assessment of temperature effects is required, especially for long-term operations of subsurface heat storage facilities.  相似文献   

8.
Coal, a fossil fuel, is the largest source of energy for the generation of electricity in India. In order to study the potential environmental hazards by coal based power plants, particulate matters were collected using Stack Monitoring Kit and gaseous pollutants by Automatic Flue Gas Analyzer. The morphological and chemical properties, mineralogical composition and particle size distributions have been determined by SEM–EDX, XRD and CILAS. The data revealed the presence of particulate matters, SO2, NOx in the range of 236–315, 162–238, 173–222 mg/Nm3 respectively. The emission of CO2 was in the range of 43,004–60,115 Nm3/h with an average of 52,830 Nm3/h. Among the elements, Fe > Mn > Al > Zn > B > Ni > Cr > Cu were present in substantially higher proportion than Pb > Mo > Cd > Se > As > Hg. It was found that most of the elements were concentrated on fly ash surface rather than coal, bottom ash and pond ash. This variation may be attributed to the fineness of fly ash particles with large surface ratio to mass. Mineralogical studies of coal and fly ash by X-ray diffraction revealed the presence of mullite, quartz, cristobalite and maghemite. Presence of mullite and quartz found in fly ash indicate the conversion of complex minerals to mullite and quartz at high temperature. Transfer Coefficient was calculated to determine the ratio of the enrichment of trace elements in fly or bottom ash with respect to coal and pond ash.  相似文献   

9.
《Applied Geochemistry》2002,17(8):1143-1148
Finding means of utilising waste products is a very important field of research at the moment. In this study, fly ash, a waste product of the electricity and petrochemical industries, was investigated as a basic ingredient of a new geopolymeric material. The similarity of fly ash to natural pozzolans has encouraged the use of this waste product in the synthesis of geopolymers, which, in turn, can best be viewed as consisting of a polymeric Si–O–Al framework. Manufacturing of the geopolymers was conducted by mixing fly ash, kaolinite, sodium silicate solution, NaOH and water. The samples were cured at 40, 50, 60 and 70 °C for different time intervals (6, 24, 48 and 72 h). The optimum condition was found to be at 60 °C for a period of 48 h. Compressive strength measurements show a maximum strength of almost 8 MPa after 28 days. Infrared spectroscopic measurements were obtained of the samples after 7 and 28 days. X-ray diffraction measurements show quartz as the main constituent with the largest part of the geopolymer structure being amorphous and glass-like.  相似文献   

10.
Aquifer thermal energy storage in urban and industrial areas can lead to an increase in subsurface temperature to 70 °C and more. Besides its impacts on mineral and sorption equilibria and chemical reaction kinetics in an aquifer, temperature sensitively influences microbial activity and thus redox processes, such as sulphate reduction. Microorganism species can only operate within limited temperature ranges and their adaptability to temperature is a crucial point for the assessment of the environmental consequences of subsurface heat storage. Column experiments with aquifer sediment and tap water at 10, 25, 40, and 70 °C showed that under the constant addition of acetate sulphate reduction could be initiated after 26–63 pore volumes exchanged at all temperatures. Fastest initiation of sulphate reduction with the highest reduction rates was found at 40 °C. Maximum rate constants during experimental run-time were 0.56 h?1 at 40 °C and 0.33, 0.36, and 0.25 h?1 at 10 and, 25, and 70 °C, respectively. Hence, microbial activity was enhanced by a temperature increase to 40 °C but was significantly lowered at 70 °C. At 25 °C methane was found in solution, indicating the presence of fermenting organisms; at 10, 40, and 70 °C no methane production was observed. It could be shown that redox processes in an aquifer generally can adapt to temperatures significantly higher than in situ temperature and that the efficiency of the reduction process can be enhanced by temperature increase to a certain limit. Enhancement of sulphate reduction in an aquifer due to temperature increase could also allow enhanced degradation of organic ground water contaminants such as BTEX, where sulphate is an important electron acceptor.  相似文献   

11.
The thermal behaviour of silica rocks upon heat treatment is dependent on the constituent minerals and petrographic texture types. These constituents can be shown to be mainly quartz in the form of two types of chalcedony (Length-fast (LF) chalcedony and Length-slow (LS) chalcedony, the latter also being termed quartzine) and moganite. Even though the thermal behaviour of LF-chalcedony is well understood, major uncertainties persist concerning the high-temperature behaviour of LS-chalcedony and moganite. We present here a comparative study of these three constituents of common silica rocks. Our results show that the chemical reaction is the same in all three, Si–OH + HO–Si → Si–O–Si + H2O, but that the reaction kinetics and activation temperatures are very different. LS-chalcedony begins to react from 200 °C upwards, that is at temperatures 50 °C below the ones observed in LF-chalcedony, and shows the fastest reaction kinetics of this ‘water’ loss. Chemically bound water (SiOH) in moganite is more stable at high temperatures and no specific activation temperature is necessary for triggering the temperature-induced ‘water’ loss. Moganite is also found to act as a stabilizer in silica rocks preventing them from temperature-induced fracturing. These findings have implications for the study of potential heat treatment temperatures of silica rocks (in industry and heritage studies), but they also shed light on the different structures of SiO2 minerals and the role of OH impurities therein.  相似文献   

12.
A set of experiments have been performed on volcanic materials from Etna, Stromboli and Vesuvius in order to evaluate how the exposure to thermal and redox conditions close to that of active craters affects the texture and composition of juvenile pyroclasts. Selected samples were placed within a quartz tube, in presence of air or under vacuum, and kept at T between 700 and 1,130 °C, for variable time (40 min to 12 h). Results show that reheating reactivates the melt, which, through processes of chemical and thermal diffusion, reaches new equilibrium conditions. In all the experiments performed at T = 700–750 °C, a large number of crystal nuclei and spherulites grows in the groundmass, suggesting conditions of high undercooling. This process creates textural heterogeneities at the scale of few microns but only limited changes of groundmass composition, which remains clustered around that of the natural glasses. Reheating at T = 1,000–1,050 °C promotes massive groundmass crystallization, with a different mineral assemblage as a function of the redox conditions. Morphological modifications of clasts, from softening to sintering as temperature increases, occur under these conditions, accompanied by progressive smoothing of external surfaces, and a reduction in size and abundance of vesicles, until the complete obliteration of the pre-existing vesicularity. The transition from sintering to welding, characteristic of high temperature, is influenced by redox conditions. Experiments at T = 1,100–1,130 °C and under vacuum produce groundmass textures and glass compositions similar to that of the respective starting material. Collapse and welding of the clasts cause significant densification of the whole charge. At the same temperature, but in presence of air, experimental products at least result sintered and show holocrystalline groundmass. In all experiments, sublimates grow on the external surfaces of the clasts or form a lining on the bubble walls. Their shape and composition is a function of temperature and fO2 and the abundance of sublimates shows a peak at 1,000 °C. The identification of the features recorded by pyroclasts during complex heating–cooling cycles allows reconstructing the complete clasts history before their final emplacement, during weakly explosive volcanic activity. This has a strong implication on the characterization of primary juvenile material and on the interpretation of eruption dynamics.  相似文献   

13.
Iron oxide nanoparticles (nano-Fe) have been widely used in environmental remediation, including that of emerging contaminants, such as antibiotics. Magnetite nanoparticles (nano-Fe3O4) have been reported to form on the outer surface of nano-Fe and have the potential to be a good sorbent for certain antibiotics. This study reports, for the first time, the kinetics and thermodynamics of adsorption of a common tetracycline group antibiotic, oxytetracycline (OTC), on nano-Fe3O4. Batch sorption kinetics were evaluated by varying initial OTC concentration (0.25–2 mM), nano-Fe3O4 concentration (2.5–20 g L?1), pH (3.8–7.6), temperature (5, 15, 35 °C), and ionic strength (0.01–0.5 M KCl) to derive thermodynamic and kinetic constants. Results show that OTC sorption kinetics is rapid and increases with increasing temperature. The derived thermodynamic constants suggest a surface chemical-controlled reaction that proceeds via an associative mechanism. Results indicate the potential of developing a nano-magnetite-based remediation system for tetracycline group of antibiotics.  相似文献   

14.
Swelling behavior of expansive soil has always created problems in the field of geotechnical engineering. Generally, the method used to assess the swelling potential of expansive soil from its plasticity index, shrinkage limit and colloidal content. Alternative way to evaluate swelling behavior is from its expansive index (EI) and swelling pressure value. The present study investigates the reduction of EI and swelling pressure for kaolinite and bentonite clay when mixed with various percentages of Ottawa sand and Class C fly ash. The percentages of Ottawa sand and Class C fly ash used were 0–50 % by weight. The results show that there is a significant reduction in the swelling properties of expansive soil with the addition of Ottawa sand and Class C fly ash. The reduction in EI ranged approximately from 10 to 50 and 4 to 49 % for kaolinite and bentonite clay, respectively. Also the maximum swelling pressure of kaolinite and bentonite clay decreased approximately 93 and 64 %, respectively with the addition of various percentages of Ottawa sand and Class C fly ash. Standard index properties test viz., liquid limit, plastic limit and linear shrinkage test were conducted to see the characteristics of expansive soil when mixed with less expansive sand and fly ash. Also, for these expansive soils one dimensional consolidation test have been conducted with sand and fly ash mixtures and the results were compared with pure kaolinite and bentonite clay.  相似文献   

15.
The aim of this research was to evaluate the feasibility of using the vitrification process as an alternative solution to the disposal of a coal fly ash and metallurgical slags in landfills. The starting wastes were characterised in terms of chemical, granulometric, mineralogical, and microstructural analysis. A selected batch composition composed by 58.5% fly ash, 31.5% metallurgical slag and 10.0 Na2O% (wt%) was melted at 1450 °C and poured to obtain monolithic glass samples. The environmental behaviour of the starting wastes and the resulting glass was evaluated by standard leaching tests, which shows that vitrification leads to a stabilisation process in which the inorganic components of the wastes are immobilised throughout their incorporation into the glass structure. Moreover, vitrification transforms those hazardous wastes into a new non-hazardous glass. A preliminary study shows that the new glass is suitable for developing glass–ceramic tiles appropriate for floor pavement and wall covering.  相似文献   

16.
The objective of this study was to evaluate the effect of fly ash amendment on the compression behavior of mine tailings. Natural and synthetic (i.e., laboratory prepared) mine tailings were used to assess the effects of tailings composition and tailings solids content on compressibility. Three types of off-specification fly ashes and Type I–II Portland cement were used as cementitious binders. Tailings-fly ash mixtures were prepared at solids content of 60–75% (water content = 33–67%), water-to-binder ratios of 2.5 and 5, and were cured for 0.1 days (2 h), 7, and 28 days. Bi-linear compression curves on semi-log plots were observed in most of the binder-amended tailings specimens. The break in slope on the compression curve was identified as the breaking stress, whereupon cementitious bonds were broken. The breaking stress increased with an increase in fly ash content, which was attributed to a lower water-to-binder ratio and void volume-to-binder volume ratio that produced more effective particle bonding. Breaking stress also increased with an increase in CaO content and CaO-to-SiO2 ratio of fly ash, which resulted in more effective bonding between particles. The effect of curing time on the breaking stress of fly ash amended specimens was characterized by (1) an increase in breaking stress via increase in curing time and cementitious bond formation or (2) a constant breaking stress with curing time due to competing mechanisms during loading. Specimens cured under a vertical stress showed an increase in breakings stress with applied load water removal prior to cementitious bond formation that reduced the water-to-binder ratio and led to more effective cementation.  相似文献   

17.
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   

18.
Differentiation of mantle-derived, hydrous, basaltic magmas is a fundamental process to produce evolved intermediate to SiO2-rich magmas that form the bulk of the middle to shallow continental and island arc crust. This study reports the results of fractional crystallization experiments conducted in a piston cylinder apparatus at 0.7 GPa for hydrous, calc-alkaline to arc tholeiitic magmas. Fractional crystallization was approached by synthesis of starting materials representing the liquid composition of the previous, higher temperature experiment. Temperatures ranged from near-liquidus at 1,170 °C to near-solidus conditions at 700 °C. H2O contents varied from 3.0 to more than 10 wt%. The liquid line of descent covers the entire compositional range from olivine–tholeiite (1,170 °C) to high-silica rhyolite (700 °C) and evolves from metaluminous to peraluminous compositions. The following crystallization sequence has been established: olivine → clinopyroxene → plagioclase, spinel → orthopyroxene, amphibole, titanomagnetite → apatite → quartz, biotite. Anorthite-rich plagioclase and spinel are responsible for a marked increase in SiO2-content (from 51 to 53 wt%) at 1,040 °C. At lower temperatures, fractionation of amphibole, plagioclase and Fe–Ti oxide over a temperature interval of 280 °C drives the SiO2 content continuously from 53 to 78 wt%. Largest crystallization steps were recorded around 1,040 °C and at 700 °C. About 40 % of ultramafic plutonic rocks have to crystallize to generate basaltic–andesitic liquids, and an additional 40 % of amphibole–gabbroic cumulate to produce granitic melts. Andesitic liquids with a liquidus temperature of 1,010 °C only crystallize 50 % over an 280 °C wide range to 730 °C implying that such liquids form mobile crystal mushes (<50 % crystals) in long-lived magmatic systems in the middle crust, allowing for extensive fractionation, assimilation and hybridization with periodic replenishment of more mafic magmas from deeper magma reservoirs.  相似文献   

19.
In the present study, the waste coral was utilized as a source of calcium oxide for transesterification of soybean oil into biodiesel (methyl esters). Characterization results revealed that the main component of the waste coral is calcium carbonate which transformed into calcium oxide when calcined above 700 °C. The Box–Behnken design of experiment was carried out, and the results were analyzed using response surface methodology. Calcination temperature, methanol– soybean oil molar ratio and catalyst concentration were chosen as variables. The methyl ester content (wt%) was response which must be maximized. A second-order model was obtained to predict methyl ester content as a function of these variables. Each variable was placed in the three low, medium and high levels (calcination temperature of 700, 800 and 900 °C; catalyst concentration of 3, 6 and 9 wt%; methanol-to-oil ratios of 12:1, 18:1 and 24:1). The optimum conditions from the experiment were found that the calcination temperature of 900 °C, catalyst concentration of 6 wt% and methanol-to-oil ratio of 12:1. Under these conditions, methyl ester content reached to 100 wt%. The waste catalyst was capable of being reused up to 4 times without much loss in the activity.  相似文献   

20.
Fly ash is a product arising from coal combustion in thermal power plants. It represents a major source of environmental pollution. It is well known by its chemical composition rich of SiO2 and Al2O3. With the aim of preserving the environment against this contamination, fly ash was used along with the starting materials for producing glass cordierite (2MgO, 2Al2O3, 5SiO2). Four formulations were developed by mixing the silica gel, magnesium chloride (MgCl2.6H2O) and fly ash in the percentages enclosing the stoichiometry of cordierite (2MgO, 2Al2O3, 5SiO2). Different experimental techniques (DTA/TGA, X-ray diffraction, FTIR and SEM) were used to characterise the prepared formulations. The results shown that for all formulations, a cordierite phase was obtained at 1200 °C along with several secondary phases such as mullite, cristobalite, silicon oxide, enstatite and spinel. At 1300 °C, pure indialite (α-cordierite) was obtained along with a small amount of spinel. The four formulations sintered at 1200 °C exhibit a homogenous morphology and high porosity. The acicular-shaped indialite grains were observed in both formulations with excess of alumina and excess of magnesia.  相似文献   

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