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首页> 外文期刊>Acta crystallographica. Section F, Structural biology communications >Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO4.11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy
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Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO4.11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy

机译:由中子粉末衍射和拟塑性中子谱法测定的合成式(MgSO4.11d(2)O)的正状态和高压相变的等温方程

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We have collected neutron powder diffraction data from MgSO4.11D(2)O (the deuterated analogue of meridianiite), a highly hydrated sulfate salt that is thought to be a candidate rock-forming mineral in some icy satellites of the outer solar system. Our measurements, made using the PEARL/HiPr and OSIRIS instruments at the ISIS neutron spallation source, covered the range 0.1 P 800 MPa and 150 T 280 K. The refined unit-cell volumes as a function of P and T are parameterized in the form of a Murnaghan integrated linear equation of state having a zero-pressure volume V-0 = 706.23 (8) angstrom(3), zero-pressure bulk modulus K-0 = 19.9 (4) GPa and its first pressure derivative, K-0 = 9 (1). The structure's compressibility is highly anisotropic, as expected, with the three principal directions of the unit-strain tensor having compressibilities of 9.6 x 10(-3), 3.4 x 10(-2) and 3.4 x 10(-3) GPa(-1), the most compressible direction being perpendicular to the long axis of a discrete hexadecameric water cluster, (D2O)(16). At high pressure we observed two different phase transitions. First, warming of MgSO4.11D(2)O at 545 MPa resulted in a change in the diffraction pattern at 275 K consistent with partial (peritectic) melting; quasielastic neutron spectra collected simultaneously evince the onset of the reorientational motion of D2O molecules with characteristic time-scales of 20-30 ps, longer than those found in bulk liquid water at the same temperature and commensurate with the lifetime of solvent-separated ion pairs in aqueousMgSO(4). Second, at similar to 0.9 GPa, 240 K, MgSO4.11D(2)O decomposed into high-pressure water ice phase VI and MgSO4.9D(2)O, a recently discovered phase that has hitherto only been formed at ambient pressure by quenching small droplets of MgSO4(aq) in liquid nitrogen. The fate of the high-pressure enneahydrate on further compression and warming is not clear from the neutron diffraction data, but its occurrence indicates that it ma
机译:我们从MgSO4.11d(2)O(Meridianiite的氘代类似物)中收集中子粉衍射数据,一种高度水硫酸盐盐,被认为是外太阳系统的一些冰冷卫星的候选岩石形成矿物。我们的测量,采用ISIS中子介质源的珍珠/ HIPR和OSIRIS仪器制成,覆盖0.1°10°的范围。 P& 800 MPa和150& t& 280 K.作为P和T函数的精细单元电池体积以零压积V-0 = 706.23(8)埃(3),零 - 压力堆积量K-0 = 19.9(4)GPA及其第一压力衍生物,K-0 = 9(1)。该结构的可压缩性正如预期的那样具有高度各向异性,具有4.6×10(-3),3.4×10(-2)和3.4×10(-3)GPA( - 1),最可压缩方向垂直于离散的十六分水簇的长轴(D2O)(16)。在高压下,我们观察了两种不同的相变。首先,MgSO4.11d(2)O处的MgSO4.11d(2)o在545MPa中加热导致衍射图案的变化在275k与部分(涂层)熔化一致; Quasielastic中子谱同时产生D2O分子的重新定位运动的开始,其特征时间尺度为20-30ps,比在相同温度的散装液体水中发现的那些,并与溶剂分离离子对的寿命相称AqueOUSMGSO(4)。其次,与0.9GPa,240 k,MgSO4.11d(2)o分解成高压水冰相VI和MgSO4.9D(2)O,最近发现的阶段仅在环境压力下形成迄今为止液氮中MgSO4(AQ)的小液滴。从中子衍射数据的进一步压缩和变暖上的高压奈酸的命运尚不清楚,但其发生表明它是MA

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