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1.
Clayey subgrade soil requires treatment in order to make the subgrade stable for pavement structures. Treatment of clayey soil i.e. stabilization of clayey soil by cement, lime, and fly ash are established techniques used in geotechnical and highway engineering. Stabilization by alkali activation of fly ash is reported recently but literatures are limited. Present study investigates the stress strain behavior, peak stress and ultimate strain of clayey soil stabilized by slag and slag-fly ash blending by alkali activation. The peak stress as high as 25.0 N/mm2 may be obtained at 50% slags content when 12 molar sodium hydroxide solutions were used. Peak stress, ultimate strain and slope of stress–strain curve of stabilized clay are controlled by Na/Al and Si/Al ratios. Stress–strain response and peak stress of slag and fly ash blended specimen are not governed by Na/Al and Si/Al ratios; rather the behavior is dependent predominantly on slag content.  相似文献   

2.
《Applied Geochemistry》2005,20(7):1357-1367
Cancrinite, sodalite, and zeolite A have been found to form upon contacting hyperalkaline simulated tank waste (STW) with vadose zone sediments from the Hanford Reservation. Here, soluble silica and STW are used to study mineral formation and transformation. Two Hanford sediment fractions (diameters <50 and >50 μm instead of soluble silica) are also used as silica sources for comparison. A series of batch experiments at 50 °C and 25 days duration were conducted by reacting 0.026 mol/kg soluble Si with 6 different STW solutions. The STW solutions differed in NaOH and Al concentrations. Cancrinite, sodalite, and zeolite A formed when soluble Si was used as the Si source. The minerals were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and 27Al and 29Si magic-angle spinning nuclear magnetic resonance (MAS-NMR). Larger NaOH and Al concentrations favored formation of the more compact structures of cancrinite and sodalite. At larger NaOH concentration more Al for Si substitution occurred in the tetrahedral sites. A greater Al(4)/Al(6) ratio in the solids was found for the higher Si/Al ratio solutions based on NMR results. Mixtures of cancrinite and sodalite were characterized by particles with lepispheric morphology. At low Al concentration, increasing NaOH resulted in distinct hexagonal, prismatic particles common to crystalline cancrinite. At low Al/Si ratio, the characteristic cubic morphology of zeolite was observed in addition to cancrinite and sodalite.  相似文献   

3.
The bulk of fly ash (an inorganic waste of coal-fired power generation) produced is deposited in disposal areas where it needs to be revegetated. The effects of addition of three conventional organic amendments (biosolids, poultry manure, green waste compost), or poultry manure-derived biochar, to coal fly ash (at two rates) on some key chemical, physical and microbial properties and on growth of Rhodes grass (Chloris gayana) was studied in a laboratory incubation/greenhouse study. Addition of all amendments, including biochar, increased concentrations of extractable Mg, K, Na and P and CEC(pH 7.0). Additions of poultry manure, and particularly biosolids, also greatly increased levels of extractable NH4 + and NO3 −-N. Addition of biosolids, green waste compost and biochar resulted in a decrease in macroporosity, a concomitant increase in mesoporosity and, at the high rate of addition, an increase in available water-holding capacity. Basal respiration was very low in fly ash and was increased by addition of all amendments; metabolic quotient was markedly greater in control than amended treatments. Biosolids, poultry manure and green waste compost additions all increased microbial biomass C. Growth of Rhodes grass was extremely low under unfertilized conditions in control, biochar and, to a lesser extent, green waste compost treatments but addition of poultry manure and the lower rate of biosolids resulted in large increases in yields. Although biochar additions increased extractable Ca, K, P, Cu, Zn and Mn, CEC, mesoporosity and water-holding capacity, they had a little or no stimulatory effect on the size of the soil microbial community, N fertility or plant growth. This was attributable to the lack of metabolisable C and an insignificant N-supplying capacity.  相似文献   

4.
Zeolite Na–X (FAU type) was synthesized from F-class fly ash in simple and economical way. Several months of storage of fly ash in NaOH solution, at room temperature, without any prior treatment, results in the production of material with ca. 50% content of Na–X zeolite. The most efficient reaction takes place at (OH)− activity of 0.1–0.15 mol (OH)−/g of ash and at S/L ratio of 33 to 67 g/dm3. Higher S/L value causes an accelerating dissolution–crystallization equilibrium attainment. Cl− ion acts as the inhibitor of this reaction.  相似文献   

5.
粉煤灰基地聚物作为一种低碳胶凝材料,在地基处理中的应用越来越受到关注。但是目前关于碱激发胶凝材料加固土在冻融极端气候条件下的工程特性尚不清楚,有必要进一步开展冻融循环条件下加固土的强度、变形特征及其影响因素研究。通过室内试验研究了原材料硅铝比、碱激发剂模数及碱溶液浓度对粉煤灰基地聚物固化土的强度与抗冻融性能的影响及微观...  相似文献   

6.
Systematic changes in mineralogy, enrichment and depletion of selected elements, and mineralogical speciation of selected elements in fly ash and bottom ash samples from the Lingan Power Plant were compared to run-of-mine and pulverized feed coal from the Sydney coalfield, Nova Scotia, eastern Canada. The analytical techniques used were an electron microprobe equipped with energy and wavelength X-ray dispersive spectrometers, X-ray diffraction, neutron activation, scanning electron microscopy with energy dispersive X-ray and incident light petrography. Three types of glasses (Fe/O-rich, Fe/Al/Si/O-rich and or Al/Si/O-rich) were identified in the combustion residues; they were formed as a result of the interaction of melted pyrite and clay minerals. Compared to the feed coal, most elements were enriched 10 to20 times in the fly ash. The concentration of the elements in both the fly ash and bottom ash are comparable to coal ash that is generated by the low temperature asher in the laboratory. Some chalcophile elements such as arsenic and lead occurred as a solid solution in pyrite in the feed coal and were concentrated in the float fraction (density: <2.81 g/cm3) of the fly ash with non-crystalline Fe-oxides. X-ray mapping of arsenic in the fly ash and bottom ash indicates that arsenic was evenly distributed as oxide within the Fe/O- and Fe/Al/Si/O-rich glass and crystalline phases in the fly ash, possibly in solid solution. Arsenic is associated with Fe/O and Fe/S crystalline phases in the bottom ash.  相似文献   

7.
Adsorption of H2O, NH3 and C6H6 on H- and alkali metal-exchanged structures of mordenite and on corresponding cations on the smectite layer is investigated by ab initio density-functional calculations. Proton or an alkali metal cation compensates one Al/Si framework substitution and resides in the extra-framework position of zeolite or above flat smectite layer close to the Al/Si substitution. Pronounced similarities between zeolite and smectite are observed in changes of the adsorption energies and location of the external cation with changing character of the external cation. Calculated adsorption energies exhibit the following trend: E(NH3) > E(H2O) > E(C6H6). Because of looser contact with the framework, zeolitic cations are stronger adsorption centers and calculated adsorption energies of zeolites are by ~20–30% larger than cations of smectites. The highest adsorption energy is calculated for H-exchanged structures and down the group of alkali metal cations a decrease of the adsorption energy is observed. Deviations from the smooth variation of the adsorption energy are caused by: (1) formation of strong hydrogen bonds in H-exchanged structures, (2) adsorption induced migration of the external Li+ cation, and (3) steric hindrances of the flat C6H6 molecule adsorbed on the cation in the cage of zeolite.  相似文献   

8.
Results are reported of an experimental study which examined the effect of solution composition on the composition, structure, and crystallization path of phillipsite and merlinoite in the system Na2OK2O-Al2O3-SiO2H2O at 80°C and pH = 13.34–13.71.At a fixed 3.5 M total dissolved silica concentration, zeolite Si/Al ratio was found to be a linear function of pH within the pH range of the experiments.29Si NMR spectra of the initial solutions show that pH determines the distribution of aqueous aluminosilicate species and, as a result, the precipitated zeolite Si/Al ratio. SEM observations reveal that zeolites may precipitate with or without the presence of an intermediary gel phase, depending on solution composition. The growth rate of the zeolites was found to be dependent upon solution pH and total dissolved aluminum concentration. These observations are discussed in terms of their possible applications to natural zeolite paragenesis and serve to delineate the framework of a comprehensive theory for the mechanism of zeolite crystallization from highly alkaline solutions.  相似文献   

9.
The clinoptilolite rich zeolite from Bigadiç which was formed from alteration of volcanic glass were treated with acidic (HCl, H3BO3, H3PO4), alkaline (KOH, NaOH) solutions. Hydrothermally treated and untreated samples were heat treated at 400, 550 and 700°C. XRD, ICP-MS and N2 gas adsorption were used for physicochemical characterization of zeolites. Considering the Si/Al > 4 and Na+K/Ca+Mg < 1 ratios, zeolite sample is included to earth alkali clinoptilolite class (Heu II) which is also revealed by thermal treatments. Since zeolite structure contains low alkalies it was at collapsed 550°C. The removal of oxide elements efficiency of acids and alkalies were in the order of HCl > H3PO4 > HBO3 > KOH > NaOH. XRD analysis indicated that the structure of zeolite was not altered with acids and alkali treatments. The structure of zeolite treated with HCl and other acids started to deform at 400 and 550°C respectively. In treatment with HCl, Si/Al ratio increases with significant a decrease in K content which resulted in a decrease in the heat stability of zeolite. No change was observed in the structure and thermal stability of clinoptilolite after alkali treatments. The fact that although significant amount of Na is removed with H3BO3 acid and Na is increased with NaOH but the thermal stability remains the same indicates that Na cation is not an important parameter as much as K. HCl and H3PO4 acid treatments increased the surface area depending on the dissolution of amorphous material and H3PO4 was found to be more effective. However, the total pore size decreased due to formation of new micropores.  相似文献   

10.
The major element and Sr isotope systematics and geochemistry of coal fly ash and its interactions with environmental waters were investigated using laboratory flow-through column leaching experiments (sodium carbonate, acetic acid, nitric acid) and sequential batch leaching experiments (water, acetic acid, hydrochloric acid). Column leaching of Class F fly ash samples shows rapid release of most major elements early in the leaching procedure, suggesting an association of these elements with soluble and surface bound phases. Delayed release of certain elements (e.g., Al, Fe, Si) signals gradual dissolution of more resistant silicate or glass phases as leaching continues. Strontium isotope results from both column and batch leaching experiments show a marked increase in 87Sr/86Sr ratio with continued leaching, yielding a total range of values from 0.7107 to 0.7138. For comparison, the isotopic composition of fluid output from a fly ash impoundment in West Virginia falls in a narrow range around 0.7124. The experimental data suggest the presence of a more resistant, highly radiogenic silicate phase that survives the combustion process and is leached after the more soluble minerals are removed. Strontium isotopic homogenization of minerals in coal does not always occur during the combustion process, despite the high temperatures encountered in the boiler. Early-released Sr tends to be isotopically uniform; thus the Sr isotopic composition of fly ash could be distinguishable from other sources and is a useful tool for quantifying the possible contribution of fly ash leaching to the total dissolved load in natural surface and ground waters.  相似文献   

11.
Structural interaction between dissolved fluorine and silicate glass (25°C) and melt (to 1400°C) has been examined with 19F and 29Si MAS NMR and with Raman spectroscopy in the system Na2O-Al2O3-SiO2 as a function of Al2O3 content. Approximately 3 mol.% F calculated as NaF dissolved in these glasses and melts. From 19F NMR spectroscopy, four different fluoride complexes were identified. These are (1) Na-F complexes (NF), (2) Na-Al-F complexes with Al in 4-fold coordination (NAF), (3) Na-Al-F complexes with Al in 6-fold coordination with F (CF), and (4) Al-F complexes with Al in 6-fold, and possibly also 4-fold coordination (TF). The latter three types of complexes may be linked to the aluminosilicate network via Al-O-Si bridges.The abundance of sodium fluoride complexes (NF) decreases with increasing Al/(Al + Si) of the glasses and melts. The NF complexes were not detected in meta-aluminosilicate glasses and melts. The NAF, CF, and TF complexes coexist in peralkaline and meta-aluminosilicate glasses and melts.From 29Si-NMR spectra of glasses and Raman spectra of glasses and melts, the silicate structure of Al-free and Al-poor compositions becomes polymerized by dissolution of F because NF complexes scavenge network-modifying Na from the silicate. Solution of F in Al-rich peralkaline and meta-aluminous glasses and melts results in Al-F bonding and aluminosilicate depolymerization.Temperature (above that of the glass transition) affects the Qn-speciation reaction in the melts, 2Q3 ⇔ Q4 + Q2, in a manner similar to other alkali silicate and alkali aluminosilicate melts. Dissolved F at the concentration level used in this study does not affect the temperature-dependence of this speciation reaction.  相似文献   

12.
文章以穆棱沸石矿床为例，探讨了天然沸石矿矿化分带特征与矿石物化性能的空间变化规律。研究表明：矿床不同部位沸石矿化类型的差异变化与碱金属K、Na元素的分异富集特征关系密切；若两者分异富集明显，易形成单一的斜发沸石或丝光沸石矿；反之，则形成混合型沸石矿。由矿体浅部往深部，矿石物化性能的差异变化总体表现为：NH4^ 和K^ 的交换容量、最大热失重值、吸湿率及气体吸附容量等渐趋增大；而矿石的耐酸性和热稳定性却有相反的变化趋势。  相似文献   

13.
《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   

14.
碱渣与饱和卤水混合制成浆体回填到盐矿废弃盐腔可同时解决碱渣处理问题和地下废弃盐腔存在的地质隐患。回填碱渣强度是影响充填效果的重要因素。因此,为了提高回填碱渣强度,采用掺入粉煤灰制成复合碱渣对其强度特性进行改良。针对不同粉煤灰掺合比的碱渣开展了组成、力学和细观试验。研究结果表明：（1）掺入粉煤灰能明显改善碱渣的强度,使其黏聚力、内摩擦角都大幅提高,抗剪强度大幅增加;（2）粉煤灰掺合比越大,增强效果越明显,但强度并非随掺合比呈线性变化,对黏聚力而言,在0～20%内的掺合比下增加速度最快,而对内摩擦角则在20%～30%的掺合比区间增加最快,对抗剪强度而言,0～20%的掺合比内增加最明显;（3）粉煤灰掺入还可显著改善碱渣的压缩固结特性,使其固结系数大幅提高,从而提高碱渣固结速度,缩短充填工期,其中在0～10%的掺合比内对压缩固结特性改善最显著;（4）矿物组成分析表明,粉煤灰掺入改变了矿物组成,使得亲水性矿物含量急剧锐减,进而改变了其沉积特性。而细观分析则表明,粉煤灰掺入使碱渣从絮凝团细观结构变成了粉煤灰充当骨架的充填结构,且粒间支撑和拉联效应明显。从增强效果提高、压缩固结特性增强、控制成本和工期综合分析表明,最优掺合比为20%左右,建议工程中以不高于20%的掺合比作为实用掺合比即可取得较为理想的充填增强效果。该研究为揭示碱渣增强机制及废弃盐腔碱渣充填工艺优化提供了有益参考。  相似文献   

15.
《Applied Geochemistry》2002,17(2):93-103
Mimicking geochemical processes to solve environmental problems was implemented in dealing with waste acidic jarosite and alkaline coal fly ash. By placing these two chemically different materials adjacent to one another, a self-sealing layer was formed at the interface between both wastes, isolating and immobilizing chemical constituents in the process. A series of leaching experiments were performed on each material separately to study the release behavior of the principal constituents. Radiotracer experiments were conducted to explore diffusion and reaction of constituents such as Fe3+ in a combined jarosite/fly ash system. A model has been developed to simulate the coupled processes of diffusion and precipitation taking into account porosity change due to pore filling by precipitates. The formation of a self-sealing isolation layer in a hypothetical jarosite/fly ash disposal site was modelled. Leaching results indicate that the release of elements from jarosite is much larger than that from fly ash, and that the highly pH dependent release of Fe, Al, and Zn was controlled by the solubility of their hydroxides. Leaching results also suggest that precipitation reactions can be expected to occur at the interface between jarosite and alkaline coal fly ash where a large pH gradient exists. Radiotracer experiments showed that accumulation of constituents occurred at the interface. Modeled Fe3+ profiles in layered jarosite/fly ash were well validated by experiments. Modeling results also showed that with the accumulation of constituents at the interface, a new layer with low porosity was formed. Application of this model suggests that there is a potential use to form a self-sealing layer in jarosite/fly ash co-disposal sites.  相似文献   

16.
Ca-bentonite can be converted into zeolites A through hydrothermal alkaline treatment by varying the synthetic parameters. This study focuses on the effect of initial Si/Al molar ratio, NaOH concentration on the type of formed zeolite A. The Ca-bentonite (China, Fuxin)were mixed with an aqueous NaOH solution, Al(OH)3 powder and hydrothermally treated at about 90 ℃,12 h. Different types of zeolites (zeolite X, P, and A),sodalite were synthesized after the treatment. Zeolites were characterized and quantified by means of XRD and SEM analysis. Zeolite A predominantly formed with 0.5≤Si/Al≤2.0 was produced and zeolite X, P formed with Si/Al>2.0 under the 2.2mol/LNaOH concentration; Sodalite was also formed under high NaOH molarities. Shape of zeolite A is show the cube by the SEM micrograph.  相似文献   

17.
Structural energetics of the alkali feldspars have been studied using a “lattice” or structure energy model. Electrostatic energies, U e,for 20 well-refined, non-intergrown alkali feldspars were calculated using Bertaut's (1952) summation procedure and average about ?13,400 kcal/mol; the repulsive energies of the alkali site in each structure (～15 kcal/mol) were calculated using repulsive parameters for K-O and Na-O interactions estimated from bulk modulus data for NaF and KF and the exponential form of the repulsive potential. Using a procedure in which the position of the alkali cation was varied while the oxygen cage was kept fixed, structure energy gradients for the alkali sites of high albite and a hypersolvus Ab42Or58 structure were computed. In both cases, a broad structure energy well, elongated approximately parallel to c and subparallel to the observed split Na positions, was found. In both structures there is a single energy minimum corresponding closely with the observed single alkali positions. Comparison of U e values for the alkali feldspars with different K/Na ratios shows that intermediate compositions are predicted to be less “stable” than either endmember and that the potassic end-member is predicted to be less “stable” than the sodic one, assuming that all other factors contributiong to the free energies of each phase are approximately the same. Comparison of U e values for the high albite and low sanidine structures with different Al/Si distributions and a fixed tetrahedral framework indicates that the ordered charge distributions are 63.0 and 54.8 kcal/mol, respectively, more “stable” than the disordered distributions. Smaller, more realistic energy differences were obtained by using U evalues averaged from four separate calculations with a +3 charge on a different T site in each and with +4 charges on the other T sites. If, in addition, the charges on cations and oxygen are reduced to half their nominal formal charges, in agreement with Pauling's electroneutrality principle and the results of recent molecular orbital calculations on silicates, the predicted electrostatic energy differences are reduced to 3.6 and 1.6 kcal/mol, respectively. These calculations also indicate that the T1O site in the high albite structure energetically favors Al and that the Al/Si distribution determines the Na position within the alkali site.  相似文献   

18.
The effects of elevated pH, ionic strength, and temperature on sediments in the vadose zone are of primary importance in modeling contaminant transport and understanding the environmental impact of tank leakage at nuclear waste storage facilities like those of the Hanford site. This study was designed to investigate biotite dissolution under simulated high level waste (HLW) conditions and its impact on Cr(VI) reduction and immobilization. Biotite dissolution increased with NaOH concentrations in the range of 0.1 to 2 mol L-1. There was a corresponding release of K, Fe, Si, and Al to solution, with Si and Al showing a complex pattern due to the formation of secondary zeolite minerals. Dissolved Fe concentrations were an order of magnitude lower than the other elements, possibly due to the formation of green rust and Fe(OH)2. The reduction of Cr(VI) to Cr(III) also increased with increased NaOH concentration. A homogeneous reduction of chromate by Fe(II)aq released through biotite dissolution was probably the primary pathway responsible for this reaction. Greater ionic strengths increased biotite dissolution and consequently increased Fe(II)aq release and Cr(VI) removal. The results indicated that HLW would cause phyllosilicate dissolution and the formation of secondary precipitates that would have a major impact on radionuclide and contaminant transport in the vadose zone at the Hanford site.  相似文献   

19.
Suzanne Y. Wass 《Lithos》1979,12(2):115-132
Geochemical and textural data on clinopyroxenes in individual alkali basaltic flows from provinces in eastern Australia and the Massif Central can be used to differentiate four different modes of origin (three at high pressure) for these clinopyroxenes. Many single flows from the two provinces contain clinopyroxenes of three, or even four, of these origins. Rare flows contain core clinopyroxene with overgrowths of clinopyroxenes of two distinct generation. Each of the overgrowth is compositionally analogous to clinopyroxenes occurring in xenoliths or as discrete crystals in the same host lava. Such rimming relationships provide evidence that the host magma has undergone high pressure crystallisation and confirm that some xenoliths and megacrysts are cognate. With decreasing pressure the major changes in clinopyroxene chemistry are an increase in the ratio Allv/Alvi, a linear increase of atomic proportions of Ti and Al with decreasing Si, and an increase in the Ti: (100 Mg/(Mg + Σ Fe)) ratio of the pyroxenes. Al2O2 wt, % is an unreliable potential geobarometric indicator; consideration of tetrahedral and octahedral site occupancies by Al (Allv/Alvl ratio) is necessary. High-pressure fractionation dominated by clinopyroxene is postulated for some basaltic-composition, resulting in SiO2 depletion, alkali enrichment and decrease in the Mg/(Mg + Fe2+) value of the host magma.  相似文献   

20.
水热条件下利用微波加热从粉煤灰合成沸石研究   总被引：14，自引：0，他引：14  
着重选用NaOH水溶液为反应前驱物, 通过改变反应温度、NaOH浓度与合成时间等参数, 在水热条件下利用微波加热直接对粉煤灰进行晶化, 合成得到了浊沸石、菱沸石、NaP1沸石3种沸石.粉煤灰转化为沸石率约15%~40%.研究表明: (1) 反应体系在15min左右即有合成沸石产生, 30min左右合成沸石转化率达到最佳; (2) 为保证沸石晶核生成和晶体的生长, 反应体系的溶液/粉煤灰比不应低于2.5; (3) 在溶液/粉煤灰比为2.5时, 应控制加热时间在30min左右.   相似文献   

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