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1.
Experimente zur Zeolithbildung durch hydrothermale Umwandlung   总被引：1，自引：0，他引：1  
The formation of zeolites by hydrothermal alteration has been investigated by taking trass from the Laach volcanic area as a sample. Zeolites to be found are chabazite, phillipsite and analcime, all of which originated from the same phonolitic glass. This paper aims at explaining the formation of zeolites by means of experimental alteration of the pumice with various solutions. NaOH and KOH solutions were used in the experiments, these limited the formation conditions of chabazite, phillipsite, analcime in alkaline environments. Moreover, experiments were carried out with H2O dist and with solutions that formed during the alteration of pumice by reacting with H2O. These experiments were conducted to supply clues concerning the formation of zeolites in the Laach volcanic area. With NaOH solutions zeolites were formed from pumice within a temperature range of 70 to 250° C and a concentration range of 0.001 to 1.0 n; with KOH solutions they were formed in the same concentration range within a temperature range of 100 to 250° C. The formation of zeolites proved to depend much on temperature and concentration: At low temperatures high concentrations are necessary, higher temperatures need lower concentrations. With NaOH solutions the zeolites are formed in the succession, chabazite, phillipsite, analcime at increasing temperatures and increasing concentrations. With KOH solutions the same succession is to be found with rising temperature. With rising concentration, however, this succession is changed at higher temperatures: Phillipsite appears in place of analcime at high temperatures and concentrations. By the alteration of pumice with H2O, zeolites are formed from 200° C onward. With solutions that had been formed during the alteration of pumice by reacting with H2O, the minimum temperature for the formation of zeolites was 180° C. Concerning the genesis of zeolites in the Laach volcanic area, the experiments showed that the temperature for the formation of analcime was about 250° C; for the formation of chabazite and phillipsite it was between 150 and 190° C. The pH of the reacting solutions may have been between 7 and 8. Thus the experiments proved that from the same material different zeolites, chabazite, phillipsite, analcime may be formed by temperature change of the reacting solutions (H2O to slightly alkaline solutions).  相似文献   

2.
《Applied Geochemistry》2005,20(1):89-99
The reaction of the clay fraction of the Callovo–Oxfordian hard shale formation hosting the French underground laboratory site, with high pH NaOH, KOH and Ca(OH)2 solutions has been investigated through closed system experiments at 60, 90 and 120 °C over 6, 24 and 168 h. The mineralogical composition of the run samples has been determined using X-ray diffraction (XRD) of randomly oriented powders showing the formation of different species of zeolites (analcime, chabazite, phillipsite) and Ca silicates (tobermorite, katoite). The phyllosilicates were studied using XRD of oriented preparations and cation exchange capacity measurements. Detrital or diagenetic mica and chlorite in the <2 μm fraction remain unchanged. On the contrary, the smectite and random illite–smectite mixed layer minerals are strongly reactive. The expandable layers of montmorillonite type are selectively dissolved while beidellitic ones survive or are transitionally formed.  相似文献   

3.
The incorporation of the molecular species of C-H-N fluid (ammonium, methane, and propane) into the structural cavities of natrolite and scolecite was experimentally studied at t = 200°C, P = 20 MPa, and an experiment duration of 192 h. The zeolites were modified without ion exchange by the exposure of a preliminarily dehydrated mineral to the appropriate gas. The presence of ammonium and light hydrocarbons in the crystal matrix of zeolites was confirmed by IR and Raman spectroscopy and gas chromatography. The data of differential thermogravimetry revealed differences in the behavior of CH4- and NH3-zeolites during heating. The X-ray diffraction patterns and IR and Raman spectra of zeolites in the region of framework vibration indicate deformations in the matrix structure after the experiments. The interaction of dehydrated scolecite with “dry” propane resulted in amorphization under the experimental parameters. The maximum methane contents in the freshly synthesized zeolites determined by gas chromatography are 4.12 wt % for CH4-scolecite and 8.96 wt % for CH4-natrolite. The synthetic C3H8-natrolite contains 4.45 wt % C3H8. In the zeolites saturated with respect to dry ammonium, the highest NH3 contents were observed in the 0.4–0.25 mm scolecite fraction (12.86 wt %), 0.25–0.05 mm scolecite fraction (11.43 wt %), and NH3-natrolite (9.28 wt %).  相似文献   

4.
 The exchange and release properties of the natural phillipsite tuff from the Aritain area in Jordan were evaluated by studying the exchange properties of this natural zeolite in the NH4 +–Na+ system. Exchange isotherms at 18, 35, and 50  °C showed that phillipsite exchanged NH4 + preferably over Na+ at all temperatures. However, the selectivity coefficient for NH4 + decreased with decreasing temperature. The release of NH4 + from phillipsite saturated with ammonium sulfate took place in two stages characterized by different SO4 2– : NH4 + ratios. Aritain phillipsite from NE Jordan could be processed and used as NH4 + slow-release fertilizers. The use of NH4 +-phillipsite tuff offers an option to the widely used soluble NH4-fertilizers in agciculture to avoid environmental problems associated with nitrogen contamination of surface water and groundwater. Received: 19 December 1996 · Accepted: 13 May 1997  相似文献   

5.
In the formation of zeolites by hydrothermal alteration volcanic glasses are the starting material in most cases. The experiments aimed at demonstrating in what way the chemistry of the volcanic glass influences:
  1. the alteration rate of the volcanic glass to zeolites,
  2. the kind of zeolites being formed and their formation conditions.
Three volcanic glasses were used, a basaltic, a phonolitic, and a rhyolitic one. The experimental conditions were as similar as possible to the natural alteration conditions. Solutions being used: H2O dist (pH ～5.5), 0.01 n NaOH (pH ～10.5), and solutions of similar chemistry to the natural ones. The temperatures were 180 °, 200 °, 250 ° C. The experiments were carried out both in closed and in open systems. The experimental results show a difference in the alteration rate and in the zeolites being formed between the basaltic and the phonolitic glasses on the one hand and the rhyolitic one on the other. In case of the closed system the SiO2-poor volcanic glasses react more rapidly than the SiO2-rich one. The zeolites being formed are chabazite, phillipsite, analcime respectively mordenite, analcime. In case of the open system the influence of the chemistry of the volcanic glass on the alteration rate and the zeolite being formed is less significant. Which zeolite is formed at a given temperature depends on: the chemistry of the starting material, the chemistry of the reacting solution and wether there is a closed or an open system.  相似文献   

6.
Results of structural transformation studies in the natural fibrous zeolites natrolite and edingtonite are presented. The minerals were studied in situ in a wide range of temperatures, pressures and compositions by differential scanning microcalorimetry, thermogravimetry, dilatometry, X-ray diffractometry, nuclear magnetic resonance (NMR)and Raman-spectroscopy. The high-pressure experiments were done in diamond anvil cell and Be-bronze bomb for NMR using liquids with various dimensions of molecules as pressure-transmitting media. A number of structural transformations in natrolites and edingtonite have been found with constant or changing water content during transformation. Under high water pressures, some additional H2O molecules entered the framework channels causing a framework deformation and an anisotropic “swelling” of the crystal. Under compression in nonpenetrating liquids no transformations were detected and above 70 kbar amorphization of the minerals was observed. The same displacive-tilt transformations were observed in zeolites at elevated temperatures as a result of the dehydration, e.g. natrolite ? α-metanatrolite at 280° C. Fully reversible phase transitions at constant H2O content were observed in natrolites and edingtonite at low temperatures (down to -120° C). These are connected with a variation in the mobility and position of exchange cations and water molecules within the framework channels and are followed by significant volume and thermal effects. In dehydrated zeolites, the transformations were found to be similar to the α ? β transition in quartz (α-metanatrolite ? β-metanatrolite). Heating of fibrous zeolites above 500 ÷ 700° C causes their amorphization and formation of porous quasiglass. The principal difference in structural behaviour of microporous crystals under compression in penetrating and nonpenetrating media has essential geochemical implications. Structural transformations of zeolites in P-T-X space demonstrate crystal chemical analogy of these parameters. Some deviations from this analogy depend on complex interactions between channel “filling”, H2O and cations, and the [(Al,Si)-O4/2] framework.  相似文献   

7.
Characterization of zeolitic tuff from Jabal Hannoun (HN) and Mukawir (MR) was carried out to examine the ability of using low-cost natural materials in domestic wastewater treatment. The grain size between 0.3 and 1 mm (0.3–1 mm) of the HN and MR has the highest total zeolite grade (faujasite–phillipsite and phillipsite–chabazite) and suitable cation exchange capacity. They were used as fixed-bed ion exchangers and adsorbents. The zeolitic tuff efficiently removed the organic and nitrogen compounds, Pb and Zn from the effluent. One bed volume (1 BV) of the zeolitic tuff is capable to remove up to 95 % of total organic carbon form 500 BV of the effluent. The removal percent of total nitrogen by HN and MR is close to 95 and 90 %, respectively. The zeolitic tuff has an excellent efficiency to remove Pb and Zn from the effluent. 1 BV of HN completely cleans Zn and Pb from 680 and 730 BV of the effluent, respectively, whereas 1 BV of MR is able to clean completely Zn and Pb from 500 and 685 BV of the effluent, respectively. The greater performance of the HN compared with the MR may be explained by its higher zeolites grade and presence of faujasite.  相似文献   

8.
The authors have studied alterations of Cenozoic and Mesozoic pyroclastic rocks of Japan, which contain several kinds of zeolites in abundance. This paper summarizes zeolites in sedimentary rocks, with reference to the depositional environments and zonal distribution, by a survey of the literature in addition to the authors’ data. The zonal distribution of zeolites is recognized in buried sedimentary rocks as follows: The zeolites in syngenetic or early diagenetic origin depend strongly upon a specific sedimentary environment. Phillipsite occurs largely in pelagic sediments of the younger geologic age. Analcime is found in saline-lake and terrestrial sediments in a warm, rather arid region, frequently associated with phillipsite, chabazite and natrolite. The zeolites are not influenced by the sedimentary environments but depend upon the depth of burial, i.e., increasing temperature and pressure. Most of clinop- tilolite, mordenite and erionite, forming at a relatively shallow depth, occur only as an alteration product of acidic to intermediate volcanic glass and cement of the post- Jurassic pyroclastic rocks. Laumontite, forming at a greater depth, on the other hand, is widely distributed in the pre-Pliocene various sedimentary rocks.  相似文献   

9.
Six different Ca‐zeolite minerals are widespread in various assemblages in late fissures and fractures in granites and gneisses of the Swiss Alps. The zeolites formed as a result of water–rock interaction at relatively low temperatures (<250 °C) in the continental upper crust. The zeolites typically overgrow earlier minerals of the fissure assemblages, but zeolites also occur as monomineralic fissure fillings. They represent the youngest fissure minerals formed during uplift and exhumation of the Alpine orogen. A systematic study of zeolite samples showed that the majority of finds originate from three regions particularity rich in zeolite‐bearing fissures: (i) in the central and eastern part of the Aar‐ and Gotthard Massifs; (2) Gibelsbach/Fiesch, in a fissure breccia located at the boundary of Aar Massif and Permian sedimentary rocks; and (3) in Penninic gneisses of the Simano nappe at Arvigo (Val Calanca). Rail and road tunnel construction across the Aar‐ and Gotthard Massif provided excellent data on zeolite frequency in Alpine fissures. It was found that 32% (Gotthard NEAT rail base tunnel, Amsteg section) and 18% (Gotthard road tunnel) of all studied fissures are filled with zeolites. The number of different zeolites is limited to six species: laumontite, stilbite and scolecite are abundant and common, whereas heulandite, chabazite and epistilbite occur occasionally. Calcium is the dominant extra‐framework cation, with minor K and Na. Heulandite and chabazite contain Sr up to 29 and 10 mol.% extra‐framework cations respectively. Na and K contents in zeolites tend to increase during growth as a result of changes in fluid composition and/or temperature. The K enrichment of stilbite found in surface outcrops compared to subsurface samples may indicate late stage cation exchange with surface water. Texture data, relative age sequences derived from fissure assemblages and equilibrium calculations show that the Ca‐dominated zeolites precipitated from fluid with decreasing temperature in the order (old to young = hot to cold): scolecite, laumontite, heulandite, chabazite and stilbite. The necessary components for zeolite formation are derived from dissolving primary granite and gneiss minerals. The nature of these minerals depends, among other factors, on the metamorphic history of the host rock. Zeolites in the Aar Massif derived from the dissolution of epidote, secondary calcite and albite that were originally formed during Alpine greenschist metamorphism from primary granite and gneiss assemblages. Zeolite fissures occur in areas of H2O‐dominated fluids. This is consistent with equilibrium calculations that predict a low CO2 tolerance of zeolite assemblages, particularly at low temperature.  相似文献   

10.
Zeolites from the most important volcanoclastic deposits of Italy include: (1) phillipsite and heulandite from the cinerite of the central northern Apennines; (2) chabazite and phillipsite from the phonolitic tephritic ignimbrite with black pumices; (3) phillipsite from the “tufo lionato” of Vulcano Laziale; (4) chabazite and phillipsite from the Campanian ignimbrite; (5) phillipsite from the Neapolitan yellow tuff; and (6) chabazite and phillipsite from the pyroclastics of Monte Vulture. Compared with sedimentary phillipsites and chabazites described in the literature, the chabazites and phillipsites studied here have lower Si/Al ratios and higher K contents. These chemical peculiarities are correlated with both the K-rich vesuvitic-leucititic, latitic-phonolitic, and potassic alkali-trachytic chemistry of the ash from which they were derived and, very likely, with the character of the hydrologically open system environment in which they formed. The zeolite of the heulandite-clinoptilolite group from the cinerite of the central northern Apennines is classified as a true heulandite on the basis of its chemical composition and thermal behavior.  相似文献   

11.
Diagenetic transformation of clay minerals, zeolites and silica minerals in Cretaceous and Tertiary argillaceous rocks from deeply drilled wells in Japan were studied. Transformations of these minerals during diagenesis were as follows: in clay minerals, montmorillonite → montmorillonite-illite mixed-layer mineral → illite; in zeolites, volcanic glass → clinoptilolite → heulandite and/or analcite → laumontite and/or albite; in silica minerals, amorphous silica → low-cristobalite → low-quartz. Maximum overburden pressures and geothermal temperatures corresponding to these transformations in each well studied were calculated. For clay minerals, a pressure of approximately 900 kg cm?2 and a temperature of about 100°C are necessary for the transformation from montmorillonite to mixed-layer mineral and 920 kg cm?2 and 140°C for mixed-layer mineral to illite. Transformation from kaolinite to other minerals requires much higher pressures and temperatures than from montmorillonite to mixed-layer mineral. For zeolites, 330 kg cm?2 and 60°C are required for the transformation from volcanic glass to clinoptilolite, 860 kg cm?2 and 120°C for clinoptilolite to heulandite and/or analcite, and 930 kg cm?2 and 140°C for heulandite and/or analcite to laumontite and/or albite. For silica minerals, 250 kg cm?2 and 50°C are necessary for the transformation from amorphous silica to low-cristobalite and 660 kg cm?2 and 70°C for low-cristobalite to low-quartz. Based on these diagenetic mineral transformations, seven mineral zones are recognized in argillaceous sediments. On the other hand, from the porosity studies of argillaceous sediments in Japan, the process of diagenesis is classified into the following three stages. The early compaction stage is marked by shallow burial and viscous rocks with more than 30% porosity. The late compaction stage is characterized by intermediate burial and plastic rocks with 30-10% porosities. The transformation stage is marked by deep burial and elastic rocks with less than 10% porosity.  相似文献   

12.
Large areas of Italian territory are covered by thick and widespread deposits of zeolite-bearing volcaniclastic products. The main zeolites are phillipsite and chabazite spread over the whole peninsula, and clinoptilolite recorded only in Sardinia. A trachytic to phonolitic glassy precursor accounts for the formation of the former zeolites characterized by low Si/Al ratios (3.00), while clinoptilolite is related to more acidic volcanism. The genesis of most of these zeolitized deposits is linked to pyroclastic flow emplacement mechanisms characterized by quite high temperatures and by the presence of abundant fluids. The main utilization of these materials has been and still is as dimension stones in the building industry. Currently, limited amounts are also employed in animal farming (dietary supplement, pet litter and manure deodorizer) and in agriculture as soil improvement and slow-release fertilizers. New fields of application have been proposed for these products on account of their easy availability, very low cost, their high-grade zeolites (50–70%), and good technological features such as high cation exchange capacities and adsorption properties.  相似文献   

13.
Hydrothermal investigation of the bulk composition CaO·Al2O3·4SiO2 + excess H2O has been conducted using conventional techniques over the temperature range 200–500° C and 500–5,000 bars P fluid. The fully ordered wairakite was synthesized unequivocally in the laboratory, probably for the first time.The gradual, sluggish and continuous transformation from disordered to ordered wairakite evidently accounts for failure by previous investigators to synthesize ordered wairakite in runs of week-long duration. The dehydration of metastable disordered wairakite to metastable hexagonal anorthite, quartz and H2O has been determined; this reaction takes place at temperatures exceeding 400° C, even at fluid pressures of 500 bars or less. The upper P fluid-T boundary of the disordered phase is equivalent to the maximum temperature curve of synthetic wairakite presented by previous investigators. The hydrothermal breakdown of natural wairakite above its stability limit appears to be a very slow process.The equilibrium dehydration of wairakite to anorthite, quartz and H2O occurs at 330±5° C at 500 bars, 348±5° C at 1,000 bars, 372±5° C at 2,000 bars and 385±5° C at 3,000 bars. Where fluid pressure equals total pressure, the thermal stability range of wairakite is about 100° C wide. At lower temperatures wairakite reacts with H2O to form laumontite. Reconnaissance experiments dealing with the effect of CO2 on stabilities of calcium zeolites suggest that wairakite or laumontite may be replaced by the assemblage calcite + montmorillonite in the presence of a CO2-bearing fluid phase.The determined P fluid -T field of wairakite is compatible with field observations in some metamorphic terrains where it is related to the shallow emplacement of granitic magma and with direct pressure-temperature measurements in certain active geothermal areas. Under inferred conditions of higher CO2/H2O ratios, essentially unmetamorphosed rocks grade directly into those characteristic of the greenschist facies; moderately high values of CO2 in carbonate-bearing rocks result in the downgrade extension of the greenschist facies at the expense of zeolite-bearing assemblages.  相似文献   

14.
The water tracer diffusion in single crystals of natrolite, scolecite, mesolite, heulandite, and chabazite has been studied by Raman micro-spectroscopy. A model of water tracer diffusion is proposed. The H2O, HDO, and D2O molecule concentrations are calculated for a crystal of orthorhombic symmetry on deuteration of the initial H2O-sample. A way is shown to find the diffusion coefficients, the constant of equilibrium, and the deuteron-proton exchange rate from experimental data. The water diffusion coefficients for natrolite placed in liquid D2O appeared to be 1.5–2 times higher than those for a sample in vaporous D2O. For natrolite at room temperature, 1.5–1.6 times higher water diffusion occurs along [001] than along [110].  相似文献   

15.
Harmotome-rich scorias and indurated tuffaceous mudstones occur in sediments west of the Society Ridge, South Pacific. Diagenetic alteration of mafic palagonite produces the following authigenic minerals: harmotome, phillipsite, goethite, limonite and montmorillonite. A major mode of induration of pyroclastic-rich marine sediments is the devitrification of mafic palagonite producing the following diagenetic cementing minerals: phillipsite, harmotome, limonite, and to some extent, manganese and ferromanganese oxides.  相似文献   

16.
LIOU  J. G. 《Journal of Petrology》1971,12(2):379-411
Hydrothermal investigation of the bulk composition CaO.Al2O3.4SiO2+excessH2O has been conducted using conventional techniques over thetemperature ranges 200–450 °C and 500–6000 barsPfluid. A number of reactions have been studied by employingmineral mixtures consisting of reactants and products in about9: 1 and 1: 9 ratios. The phase relations were deduced fromrelatively long experiments by observing which seeded assemblagedisappeared or decreased markedly in one of the paired run charges. Laumontite was synthesized in the laboratory, probably for thefirst time. Laumontite was grown from seeded wairakite to over99 per cent using a weak NaCl solution. The refractive indicesof the synthetic material are about = 1.504 and = 1.514. Theaverage unit cell dimensions are a0 = 14.761±0.005 Å;b0 = 13.077±0.005 Å; c0 = 7.561±0.003 Å;and ß = 112.02°±0.04°. Within the errorof measurement, the optical properties and cell parameters arein good agreement with those of natural laumontite. The equilibriumdehydration of laumontite involves two reactions: (1) laumontite= wairakite+2H2O, passing through about 230 °C at 0.5 kb,255±5 °C at 1 kb, 282±5 °C at 2 kb, 297±5°C at 3 kb and 325±5 °C at 6 kb; and (2) laumontite= lawsonite+2 quartz+2H2O, taking place at about 210 °Cat 3 kb and 275 °C at 3.2 kb. Above 300 °C, the equilibriumcurve for the solid-solid reaction (3) lawsonite+2 quartz =wairakite passes through 305 °C, 3.4 kb and 390 °C,4.4 kb. Equilibrium has been demonstrated unambiguously forthe above three reactions. The hydrothermal decomposition ofnatural laumontite above its own stability limit appears tobe a very slow process. Combined with previously published equilibria determined hydrothermallyfor wairakite, the phase relations are further investigatedby chemographic analysis interrelating the phases, laumontite,wairakite, lawsonite, anorthite, prehnite+kaolinite, and 2 pumpellyite+kaolinitein the system CaAl2Si2O8-SiO2-H2O. This synthesis allowed theconstruction of a semiquantitative petrogenetic grid applicableto natural parageneses and the delineation of the physical conditionsfor the various low-grade metamorphic facies in low µCO2environments. The similar stratigraphic zonations, consistentlyfound in a variety of environments, are recognized to be a functionof burial depth, geothermal gradient, and mineralogical andchemical composition of the parental rocks. Departures fromthe normal sequences are believed to be due to the combinationsof mineralogical variations, availability of H2O, differencesin the ratio µCO2/µH2O, and the rate of reaction.The possible P-T boundaries for diagenesis, the zeolite facies,the lawsonite-albite facies, the prehnite-pumpellyite facies,and the adjacent metamorphic facies are illustrated diagrammatically.  相似文献   

17.
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18.
 Two MgAl2O4 stoichiometric spinel crystals, one natural and one synthetic, were heated from 25 to 950 °C and studied in situ by single-crystal X-ray diffraction. The natural crystal, quenched from 850 °C, was further heated and cooled. Thermal expansion was characterized, and cation partitioning at the various temperatures was determined according to a model purposely constructed for high-temperature bond lengths. It was found that the structural evolution of the samples with temperature depended on order–disorder at room temperature. At the temperatures lower than the beginning of cation exchange, thermal expansion was completely reversible and the oxygen coordinate remained stable in spite of varying temperatures. At the temperature at which cation exchange starts, the disordered samples first tend to order and then to disorder at higher temperatures, at variance with the ordered sample, which tends to disorder steadily. In general, the evolution of the spinel structural state on cooling and heating over the same temperature range and the same time intervals does not follow the same path. In particular, in the 600–950 °C range, only partially reversible order–disorder processes occurred in the time span used for the experiments. Received: 16 July 2001 / Accepted: 8 January 2002  相似文献   

19.
《Chemical Geology》2006,225(3-4):373-387
Rock-forming zeolites often exhibit complex solid solutions reflecting isomorphous substitutions between Si and Al in tetrahedral framework sites, between charge-balancing extraframework cations, and between water molecules and vacancies. Although the number of moles of charge on extraframework cations in a zeolite must equal the moles of Al in order to maintain charge balance, the relationships between Si–Al and extraframework substitutions vary considerably across this mineral group. Review of available compositional data suggests that there are three main modes of Si–Al substitution in zeolites: 1) coupled CaAl–NaSi substitution; 2) coupled substitution of a single extraframework cation plus Al for Si; and 3) completely uncoupled substitution among extraframework cations and Si and Al on tetrahedral sites. Among zeolites that exhibit the latter two modes of solid solution, Si–Al substitution can be described by an SiO2 (± H2O) compositional exchange vector from a hypothetical, pure-silica endmember composition. Recent calorimetric, structural, and theoretical investigations suggest that Si–Al substitution follows a non-ideal, athermal solution model characterized by no excess enthalpies of mixing and negative excess entropies of mixing. Because Si–Al exchange in these minerals can be explicitly or implicitly described by exchange of an SiO2 component, the Si/Al ratio in their framework can be predicted solely as a function of temperature, pressure, and the chemical potential of SiO2. Application of this model leads to calculated Si/Al ratios in stilbite (coexisting with albite), analcime, and chabazite consistent with observed mineral compositions and parageneses in very low-grade metamorphic environments. Coexistence of silica polymorphs with zeolites containing SiO2·nH2O exchange vectors potentially provides a means of performing thermobarometric calculations in very low-grade metamorphic and diagenetic environments.  相似文献   

20.
Three reactions limiting the stability field of the di-trioctahedral chlorite cookeite in the presence of quartz, in the system Li2O−Al2O3−SiO2−H2O (LASH) have been reversed in the range 290–480°C, 0.8–14 kbar, using natural material close to the end member composition. Combining our results with known and estimated thermodynamic properties of the other minerals belonging to the LASH system, the enthalpy (-8512200 J/mol) and the entropy (504.8 J/mol*K) of cookeite are calculated by a feasible solution space approach. The knowledge of these values allowed us to draw the first P−T phase diagram involving both the hydrated Li-aluminosilicates cookeite and bikitaite, which is applicable to a large variety of natural rock systems. The low thermal extent of the stability field of cookeite+quartz (260–480°C) makes cookeite a valuable indicator of low temperature conditions within a wide range of pressure (1–14 kbar).  相似文献   

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