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1.
By using the diamond-anvil pressure cell coupled with laser heating, Ca2GeO4 in the K2NiF4-type structure has been found to decompose into the mixture Ca3Ge2O7 plus CaO at pressures greater than 200 kbar and at about 1000°C, and the same type of structure for Ca2MnO4 has been found to decompose into the mixture CaMnO3 (perovskite) plus CaO at pressures greater than 100 kbar and at about 1400°C. The decomposition product of Ca3Ge2O7 is a new compound which is isostructural with Sr3Ti2O7 and has the lattice parameters of a = 3.72 ± 0.01 and c = 19.32 ± 0.05 A? at room temperature and 1 bar pressure. The results of the study of Ca2GeO4 and Ca2MnO4 (both with the K2NiF4-type structure) strongly support the view that compounds possessing the K2NiF4-type structure are unstable relative to corresponding mixtures possessing the perovskite and rocksalt structures. It is concluded that, in the earth's mantle, the K2NiF4-type Ca2SiO4 would ultimately decompose into the mixture CaSiO3 (perovskite) + CaO or would otherwise transform to other as-yet-unknown phase(s), and that the mixture of MgSiO3 (perovskite) + MgO (the post-spinel phase of Mg2SiO4) would not adopt the K2NiF4-type structure.  相似文献   

2.

In the processes of discrimination between oil-cracked gases and kerogen-cracked gases, Behar and Pinzgofer et al.’s results were adopted in the former researches, in which the ratio of C2/C3 is basically a constant while the ratio of C1/C2 gradually increases in the course of primary cracking of kerogen. Otherwise in the course of secondary cracking of oil, the ratio of C2/C3 increases rapidly while C1/C2 keeps relatively stable. Our study on analogue experiment shows that, whether it is oil or kerogen, in its process of gas generating by cracking, the ratios of C2/C3, C1/C2 or C1/C3 will all be increased with the growth of thermal conditions. In comparison, the ratio of C2/C3, which is affected by genetic type to some comparatively less extent, mainly responds to the maturity of gases, while the value of C2/C3 is about 2, and that of C2/iC4 is about 10, and the corresponding value of R o is about 1.5%–1.6%. The influence of gas source on C2/C3 is less than that of gas maturity, otherwise C1/C2 (or C1/C3) is obviously affected by cracking matrices. The ratios of C1/C2, C1/C3 of oil-cracked gases are less than that of kerogen-cracked gases, under the condition that the ratios of C2/C3 are similar in value, so are the value of dryness indexes. There exists wide diffidence between this view and the former discrimination method in theory. The analysis of the spot sample indicates that we can apply the above basic view to dealing efficiently with the problem of the discrimination between oil-cracked gas and kerogen-cracked gas.

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3.
Extraterrestrial calcium phosphates (“whitlockites”) have the anhydrous β-Ca3(PO4)2 structure, which is different from that of hydrous terrestrial whitlockite. This has been confirmed by X-ray refinement of the structure of a phosphate from the achondrite Angra dos Reis. In the β-Ca3(PO4)2 structure, there is one crystallographic site, Ca(IIA), which is half-occupied by calcium, and which seems to have an energetically unfavorable configuration; natural phosphates with this configuration (including Angra dos Reis) have composition Ca19(Mg,Fe)2(PO4)14. Stability of the structure is probably increased by substitution of Na for Ca in Ca(IIA) giving composition Ca18 (Mg,Fe)2Na2(PO4)14, which occurs in chondrites; by vacancy of Ca(IIA), with rare earths and yttrium substituting for calcium in other sites for charge balance, giving composition Ca16(Y,RE)2(Mg,Fe)2(PO4)14, found in lunar rocks; or by replacing Ca with hydrogen, giving composition Ca18(Mg,Fe)2H2(PO4)14, which is terrestrial whitlockite. Lack of the favorable substitutions of Na, (Y, RE) or H in Angra dos Reis phosphate implies that these elements were relatively scarce in its environment of formation.  相似文献   

4.
Pyroxene-garnet solid-solution equilibria have been studied in the pressure range 41–200 kbar and over the temperature range 850–1,450°C for the system Mg4Si4O12Mg3Al2Si3O12, and in the pressure range 30–105 kbar and over the temperature range 1,000–1,300°C for the system Fe4Si4O12Fe3Al2Si3O12. At 1,000°C, the solid solubility of enstatite (MgSiO3) in pyrope (Mg3Al2Si3O12) increases gradually to 140 kbar and then increases suddenly in the pressure range 140–175 kbar, resulting in the formation of a homogeneous garnet with composition Mg3(Al0.8Mg0.6Si0.6)Si3O12. In the MgSiO3-rich field, the three-phase assemblage of β- or γ-Mg2SiO4, stishovite and a garnet solid solution is stable at pressures above 175 kbar at 1,000°C. The system Fe4Si4O12Fe3Al2Si3O12 shows a similar trend of high-pressure transformations: the maximum solubility of ferrosilite (FeSiO3) in almandine (Fe3Al2Si3O12) forming a homogeneous garnet solid solution is 40 mol% at 93 kbar and 1,000°C.If a pyrolite mantle is assumed, from the present results, the following transformation scheme is suggested for the pyroxene-garnet assemblage in the mantle. Pyroxenes begin to react with the already present pyrope-rich garnet at depths around 150 km. Although the pyroxene-garnet transformation is spread over more than 400 km in depth, the most effective transition to a complex garnet solid solution takes place at depths between 450 and 540 km. The complex garnet solid solution is expected to be stable at depths between 540 and 590 km. At greater depths, it will decompose to a mixture of modified spinel or spinel, stishovite and garnet solid solutions with smaller amounts of a pyroxene component in solution.  相似文献   

5.
A variety of electrolytes FeCl3, CaCl2, CuSO4, Al2(SO4)3, and LaCl3 was investigated for their efficiency in removing biostimulants (phosphorous and nitrogen) to improve the water quality. Results show that the removal of PO43– was achieved below the detection limit (BDL) by two electrolytes, CuSO4 and Al2(SO4)3, and up to 1.0 ± 0.0 mg/L by LaCl3 from a value of 15.0 mg/L, of the concentration of PO43– in amended water. The turbidity was found to be removed significantly by FeCl3, CuSO4, and Al2(SO4)3 by about 5.8 ± 2.6, 9.7 ± 1.0, and 5.4 ± 1.1 nephalometric turbidity unit (NTU), respectively. The removal of the members of Enterobacteriaceae viz., Escherichia coli, Enterobacter spp. Pseudomonas fluorescence, and Pseudomonas spp. was found almost in all the chemical precipitants but their removal was more significant in the water samples treated with CuSO4, Al2(SO4)3, and LaCl3. To achieve a complete removal and to sustain the after effects of precipitation, such as recurrence of algal growth, the combination of CuSO4 and Al2(SO4)3 was investigated. Reduction in the turbidity from 30.83 to <2 NTU, phosphate ion from a value of 1.28 mg/L to BDL and ammonia ion from a value of 44.71 to 36.48 mg/L of natural pond water were observed after the treatment with CuSO4 and Al2(SO4)3 in combination.  相似文献   

6.
Samples from the surface of lava flows discharged by the 2012–2013 Tolbachik Fissure Eruption were found to contain oxysulfates of copper, sodium, and potassium: K2Cu3O(SO4)2 (fedotovite), NaKCu2O(SO4)2, and Na3K5Cu8O4(SO4)8. The last two phases have no naturally occurring or synthetic analogues that we are aware of. They form flattened crystals of prismatic to long-prismatic habits. The crystals of Na3K5Cu8O4(SO4)8 have a chemical composition corresponding to the empirical formula Na2.22K5.47Cu8.02S8.05O36. An X-ray analysis of this compound showed that it has a monoclinic symmetry, P2/c, a = 13.909(4), b = 4.977(1), c = 23.525(6) Å, β = 90.021(5)°, V = 1628.3(7) Å3. The crystal structure was determined by direct techniques and refined to yield R 1 for 3955 reflexes//web// with F 2 > 4σF. The compound NaKCu2O(SO4)2 also belongs to the monoclinic system, P2/c, a = 14.111(4), b = 4.946(1), c = 23.673(6) Å, β = 92.052(6)°, V = 1651.1(8) Å3. The structure was determined by direct techniques to yield a tentative structural model that has been refined up to R 1 = 0.135 for 4088 reflexes with F 2 > 4σF. The crystal structure of Na3K5Cu8O4(SO4)8 is based on chains of [O2Cu4]4+ consisting of rib-coupled oxy-centered tetrahedrons of (OCu4)6+. The chains are surrounded by sulfate radicals, resulting in columns of {[O2Cu4](SO4)4}4? aligned along the b axis. The interchain space contains completely ordered positions of Na+ and K+ cations. The principle underlying the connection of NaKCu2O(SO4)2 columns in the crystal structure of {[O2Cu4](SO4)4}4? is different, in view of the relation Na:K = 1 as contrasted with 3:5 for the compound Na3K5Cu8O4(SO4)8. The presence of oxy-centered tetrahedrons in the structure of these new compounds furnishes an indirect hint at the importance of polynuclear copper-oxygen radicals with centering oxygen atoms as forms of transport of copper by volcanic gases.  相似文献   

7.
Toxic effects of five commonly used pesticides on the biomass of a municipal activated sludge system were determined on the basis of the reduction in the oxygen uptake rate (OUR) and specific oxygen uptake rate (SOUR). Toxicity levels of the selected pesticides were determined by employing a modified OECD 209 (Organisation for Economic Cooperation and Development) method which was performed as batch experiments using a respirometer. Copper sulphate (CuSO4 · 5 H2O), copper oxychloride (Cu2Cl(OH)3), copper calcium oxychloride (CaCu3Cl2(OH)6) as copper‐based pesticides and chlorsulphuron (C12H12ClN5O4S), 2,4‐dichlorophenoxyacetic acid (2,4‐D) (C8H6Cl2O3) as synthetic organic pesticides were selected for the experiments. The EC50 values were determined to be 78, 249 and 281 mg/L for CuSO4 · 5 H2O, Cu2Cl(OH)3 and CaCu3Cl2(OH)6, respectively. Corresponding values for C12H12ClN5O4S and 2,4‐D were 860 and 3664 mg/L, respectively. Results indicated that toxicity effects of copper‐based pesticides were higher than that of synthetic organic pesticides. CuSO4 · 5 H2O was found to exert the highest toxicity among the copper‐based pesticides, whereas, C12H12ClN5O4S was determined to be the most toxic among the organic pesticides on activated sludge biomass.  相似文献   

8.
《Continental Shelf Research》1987,7(10):1181-1209
The quadratic law of bottom friction demands an increased frictional coefficient for the S2 and N2 tides with respect to a dominant M2 tidal signal. A numerical model of the semidiurnal tides in the northeast Atlantic gives an increase in friction of ∼35% for the N2, S2 and K2 tides with respect to the M2 tide and this value is close to a theoretically derived estimate for the region, providing confirmation of the general widescale applicability of the quadratic friction law. Small differences in friction also occur for the N2, S2 and K2 tides and this is attributed to the interaction of the L2 and μ2 tides with the M2 tide in the presence of quadratic friction. Energy dissipation relationships, anomalous K2/S2 amplitude ratios and the role of quadratic friction on 18.6 year variations of semidiurnal forcing are examined.  相似文献   

9.
Ibitira meteorite is interpreted as a strongly metamorphosed, unbrecciated, vesicular eucrite with a primary variolitic and secondary hornfelsic texture dominated by 60% pyroxene (bulk composition En37Fs48Wo15 exsolved into lamellae several micrometers wide of augite En32Fs27Wo41 and pigeonite En40Fs56Wo4) and 30% plagioclase An94 (mosaic extinction and variable structural state). Minor phases are 5% tridymite plates one-quarter occupied by plagioclase (An94) inclusions; several percent intergrowths of ilmenite and Ti-chromite with trace kamacite Fe99Co0.5Ni0.2 and narrow olivine (Fa83) rims; one grain of low-Ti-chromite enclosed in tridymite; trace troilite with kamacite Fe98Co1.0Ni0.9. Euhedral ilmenite, Ti-chromite, plagioclase and merrillite in vesicles indicate vapor deposition. These properties can be explained by a series of processes including at least the following: (1) igneous crystallization under pressure low enough to allow vesiculation, (2) prolonged metamorphism, perhaps associated with vapor deposition and reduction, to produce the coarse exsolution of the pyroxene and the coarse ilmenite-chromite intergrowths, (3) strong shock which affected the plagioclase and tridymite but not the pyroxene, (4) sufficient annealing to allow recrystallization of the plagioclase and tridymite, and partial conversion to the low structural state of the former.  相似文献   

10.
Two synthetic pyroxenes (FeSiO3, MgSiO3) and five natural pyroxenes with compositions of about Fs80En20, Fs60En40, Fs50En50, Fs40En60, and Fs20En80 have been subjected to pressures up to250 ± 50kbars at a temperature of about1500 ± 200°C in a diamond anvil cell heated by an infrared laser beam. After quenching and unloading X-ray data analysis indicates that (1) those with Mg less than 50% undergo the following reactions: 2(Mg,Fe)SiO3 (pyroxene) → (Mg,Fe)2SiO4 (spinel) + SiO2 (stishovite) → 2(Mg,Fe)O (magnesiowu¨stite) + SiO2 (stishovite) with increase of pressure, and (2) those with Mg higher than 60%, undergo the following reactions: 2(Mg,Fe)SiO3 (pyroxene) → (Mg,Fe)2SiO4 (spinel) + SiO2 (stishovite) → 2(Mg,Fe)SiO3 (hexagonal phase) → 2(Mg,Fe)O (magnesiowu¨stite) + SiO2 (stishovite) with increase of pressure.  相似文献   

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