Secondary phase validation—Phase classification by polarization

A long-standing problem in operational seismology is that of reliable focal depth estimation. Standard analyst practice is to pick and identify a ‘phase’ in the P-coda. This picking will always produce a depth estimate but without any validation it cannot be trusted. In this article we ‘hunt’ for standard depth phases like pP, sP and/or PmP but unlike the analyst we use Bayes statistics for classifying the probability that polarization characteristics of pickings belong to one of the mentioned depth phases given preliminary epicenter information. In this regard we describe a general-purpose PC implementation of the Bayesian methodology that can deal with complex nonlinear models in a flexible way. The models are represented by a data-flow diagram that may be manipulated by the analyst through a graphical-programming environment. An analytic signal representation is used with the imaginary part being the Hilbert transform of the signal itself. The pickings are in terms of a plot of posterior probabilities as a function of time for pP, Sp or PmP being within the presumed azimuth and incident angle sectors for given preliminary epicenter locations. We have tested this novel focal depth estimation procedure on explosion and earthquake recordings from Cossack Ranger II stations in Karelia, NW Russia, and with encouraging results. For example, pickings deviating more than 5° off ‘true’ azimuth are rejected while Pn-incident angle estimate exhibit considerable scatter. A comprehensive test of our approach is not quite easy as recordings from so-called Ground Truth events are elusive.     

Elastic and anelastic anomalies in (Ca,Sr)TiO3 perovskites: Analogue behaviour for silicate perovskites

Values of bulk modulus (K), shear modulus (G) and mechanical quality factor (Q) have been determined for polycrystalline samples across the CaTiO₃ (CST0)–SrTiO₃ (CST100) solid solution by resonant ultrasound spectroscopy. Because of similarities with low frequency elastic and anelastic anomalies due to twin wall motion reported in previous studies, a working hypothesis is developed in which dissipation processes are interpreted in terms of twin wall displacements. At high temperatures in CST50 the stability field of the I4/mcm structure is marked by the disappearance of all resonance peaks (superattenuation). This is attributed to anelastic domain wall sliding. At room temperature the I4/mcm phase of CST70 and CST80 has values of G which are lower than those of cubic or orthorhombic phases, and a concomitant drop in Q is interpreted as implying that the domain wall pinning process reported elsewhere to occur below 400–450 K is only partial. A similar drop in G and Q was found in CST95 below the transition at 238 K. The I4/mcm ↔ Pbcm transition in CST70 at 230 K is marked by an abrupt increase in Q, suggesting that mobile twins in crystals with the I4/mcm structure become effectively immobile in antiferroelectric crystals with the Pbcm structure. The I4/mcm ↔ Pnma transition in CST50 is marked by a similarly abrupt increase in Q, consistent with twin walls becoming effectively immobile also in crystals with the Pnma structure. A fall in Q below 800 K in CST0, however, could imply that a degree of twin wall mobility might develop in Pnma crystals if the tetragonal spontaneous strain departs significantly from zero. The remarkable attenuation behaviour of crystals with the I4/mcm structure at the relatively low stress conditions which apply during resonances of a parallelepiped with edge dimensions of 2–4 mm, is consistent with the view that a characteristic signature for tetragonal CaSiO₃ in the Earth's lower mantle should be a marked attenuation of seismic waves.     

Rb2CO3-CH3CH2OH-H2O三元体系20°C相平衡的研究

研究了Rb2 CO3-CH3CH2 OH -H2 O体系在 2 0°C下的相平衡 ,绘制了相应的溶度图。发现Rb2 CO3·2 .5H2 O的新物相 ,与以往报道的结果不一致     

氯化钾与硫酸钠制硫酸钾工艺的优化

根据 K+ ,Na+∥ Cl-,SO4 2 -— H2 O体系相图 ,提出了氯化钾与芒硝制备硫酸钾工艺中新的工业化生产循环和解决钾芒硝富集问题的具体方案 ,取得良好效果。     

The crystal and magnetic structure of Li-aegirine LiFe3+Si2O6: a temperature-dependent study

Single crystals of Li-aegirine LiFe³⁺Si₂O₆ were synthesized at 1573?K and 3?GPa, and a polycrystalline sample suitable for neutron diffraction was produced by ceramic sintering at 1223?K. LiFe³⁺Si₂O₆ is monoclinic, space group C2/c, a=9.6641(2)?Å, b= 8.6612(3)?Å, c=5.2924(2)?Å, β=110.12(1)^° at 300?K as refined from powder neutron data. At 229?K Li-aegirine undergoes a phase transition from C2/c to P2₁ /c. This is indicated by strong discontinuities in the temperature variation of the lattice parameters, especially for the monoclinic angle β and by the appearance of Bragg reflections (hkl) with h+k≠2n. In the low-temperature form two non-equivalent Si-sites with 〈SiA–O〉=1.622?Å and 〈SiB–O〉=1.624?Å at 100?K are present. The bridging angles of the SiO₄ tetrahedra O3–O3–O3 are 192.55(8)° and 160.02(9)° at 100?K in the two independent tetrahedral chains in space group P2₁ /c, whereas it is 180.83(9)° at 300?K in the high-temperature C2/c phase, i.e. the chains are nearly fully expanded. Upon the phase transition the Li-coordination changes from six to five. At 100?K four Li–O bond lengths lie within 2.072(4)–2.172(3)?Å, the fifth Li–O bond length is 2.356(4)?Å, whereas the Li–O3?A bond lengths amount to 2.796(4)?Å. From ⁵⁷Fe Mössbauer spectroscopic measurements between 80 and 500?K the structural phase transition is characterized by a small discontinuity of the quadrupole splitting. Temperature-dependent neutron powder diffraction experiments show first occurrence of magnetic reflections at 16.5?K in good agreement with the point of inflection in the temperature-dependent magnetization of LiFe³⁺Si₂O₆. Distinct preordering phenomena can be observed up to 35?K. At the magnetic phase transition the unit cell parameters exhibit a pronounced magneto-striction of the lattice. Below T _N Li-aegirine shows a collinear antiferromagnetic structure. From our neutron powder diffraction experiments we extract a collinear antiferromagnetic spin arrangement within the a–c plane.     

1.0GPa和常温至1100 ℃条件下角闪石斜长片麻岩的V_p变化:实验测量与理论计算

在1．0GPa、常温至1100℃条件下测量了角闪石斜长片麻岩的纵波速度（Vp）,并统计了不同温度实验产物中各种矿物的体积百分含量。结果显示,1．0GPa下,角闪石斜长片麻岩的Vp首先随温度升高（室温至700℃）缓慢降低约6％,然后（700—850℃）快速降低约6％,再（850～950℃）转而急剧升高15％～25％,最后（T〉950℃）又快速下降。实验产物分析表明在高温高压下α-石英-β石英相变和岩石部分熔融是岩石Vp异常变化的主要因素。由取样产物的矿物含量和弹性参数,计算了各温度条件下岩石的Vp得出与实验测量相同的波速-温度变化趋势,即Vp随温度升高先缓慢降低,接着快速降低后又急剧升高,最后又快速减小。实验测量和理论计算对比研究表明,通过高温高压下岩石中的物相变化观测结果进行岩石波速的计算,是检验岩石弹性波速测量结果和研究地球内部地震波结构的一种有效方法。     

Heat capacity and phase equilibria of wadeite-type K2Si4O9

The low-temperature heat capacity (C _p) of Si-wadeite (K₂Si₄O₉) synthesized with a piston cylinder device was measured over the range of 5–303 K using the heat capacity option of a physical properties measurement system. The entropy of Si-wadeite at standard temperature and pressure calculated from the measured heat capacity data is 253.8 ± 0.6 J mol⁻¹ K⁻¹, which is considerably larger than some of the previous estimated values. The calculated phase transition boundaries in the system K₂O–Al₂O₃–SiO₂ are generally consistent with previous experimental results. Together with our calculated phase boundaries, seven multi-anvil experiments at 1,400 K and 6.0–7.7 GPa suggest that no equilibrium stability field of kalsilite + coesite intervenes between the stability field of sanidine and that of coesite + kyanite + Si-wadeite, in contrast to previous predictions. First-order approximations were undertaken to calculate the phase diagram in the system K₂Si₄O₉ at lower pressure and temperature. Large discrepancies were shown between the calculated diagram compared with previously published versions, suggesting that further experimental or/and calorimetric work is needed to better constrain the low-pressure phase relations of the K₂Si₄O₉ polymorphs. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

三元体系CaCl2?SrCl2?H2O的相平衡及其在钙锶分离中的应用

采用等温溶解平衡法研究了三元体系CaCl₂?SrCl₂?H₂O温度从323.15 K到353.15 K范围内的相平衡。基于该三元体系多温下的相平衡数据,设计开展了实验室模拟南翼山油田卤水中氯化钙和氯化锶在温度323.15 K下的分离实验。实验室模拟钙锶分离实验结果表明,在323.15 K下时分离一次固相产品中的钙锶摩尔比可以从25.46:1降至1.73:1,SrCl₂的回收率为52.47 %,所得一次固相产品在323.15 K下溶解并再次蒸发。钙和锶的摩尔比从1.73:1降至1.1:1,SrCl₂的回收率为78.67 %。     

LiMn_2O_4的溶胶─凝胶─酯化法合成及性能Ⅱ 立方尖晶石的形成及其形貌

以溶胶-凝胶-酯化法在220℃即可得到纯相的LixMn2O4（0.762＜x＜1.139）尖晶石粉体材料。它在880℃时发生立方相向四方相的转变：900℃－1000℃间,四方相渐变为正交相LiMnO2,过程中有Li2MnO3生成。应用SEM、TEM观测了材料的粘度及形貌,其粒度10－40nm,粒子间极易团聚成为1-206μm的团块。以BET法测其比表面为3.6m2／g。     

岩石圈中水的临界奇异性——大规模成矿的根源

水的临界奇异性是岩石圈中许多重大地质作用的关键和枢纽,有独特的地质意义、超乎常识。水在临界点发生二级相变,许多物理化学性质奇异性突变,特别是溶解行为和热压的突变,对成矿作用影响极大。