Wildner Manfred, Zakharov Boris A, Bogdanov Nikita E, Talla Dominik, Boldyreva Elena V, Miletich Ronald
Department of Mineralogy and Crystallography, University of Vienna, Althanstraße 14, A-1090 Wien, Austria.
Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Lavrentieva Avenue 5, Novosibirsk 630090, Russian Federation.
IUCrJ. 2022 Jan 11;9(Pt 2):194-203. doi: 10.1107/S2052252521012720. eCollection 2022 Mar 1.
Monohydrate sulfate kieserites ( SO·HO) and their solid solutions are essential constituents on the surface of Mars and most likely also on Galilean icy moons in our solar system. Phase stabilities of end-member representatives ( = Mg, Fe, Co, Ni) have been examined crystallographically using single-crystal X-ray diffraction at 1 bar and temperatures down to 15 K, by means of applying open He cryojet techniques at in-house laboratory instrumentation. All four representative phases show a comparable, highly anisotropic thermal expansion behavior with a remarkable negative thermal expansion along the monoclinic axis and a pronounced anisotropic expansion perpendicular to it. The lattice changes down to 15 K correspond to an 'inverse thermal pressure' of approximately 0.7 GPa, which is far below the critical pressures of transition under hydro-static compression ( ≥ 2.40 GPa). Consequently, no equivalent structural phase transition was observed for any compound, and neither dehydration nor rearrangements of the hydrogen bonding schemes have been observed. The SO·HO ( = Mg, Fe, Co, Ni) end-member phases preserve the kieserite-type 2/ symmetry; hydrogen bonds and other structural details were found to vary smoothly down to the lowest experimental temperature. These findings serve as an important basis for the assignment of sulfate-related signals in remote-sensing data obtained from orbiters at celestial bodies, as well as for thermodynamic considerations and modeling of properties of kieserite-type sulfate monohydrates relevant to extraterrestrial sulfate associations at very low temperatures.
一水合硫酸镁钾(MgSO₄·H₂O)及其固溶体是火星表面的重要成分,在我们太阳系的伽利略冰卫星表面很可能也是如此。通过在内部实验室仪器上应用开放式氦低温喷射技术,利用单晶X射线衍射在1巴和低至15K的温度下对端元代表物(M = Mg、Fe、Co、Ni)的相稳定性进行了晶体学研究。所有四个代表性相都表现出类似的高度各向异性的热膨胀行为,沿单斜b轴有显著的负热膨胀,垂直于该轴有明显的各向异性膨胀。降至15K时的晶格变化对应于约0.7GPa的“逆热压力”,这远低于静水压缩下的临界转变压力(≥2.40GPa)。因此,未观察到任何化合物发生等效的结构相变,也未观察到氢键方案的脱水或重排。MgSO₄·H₂O(M = Mg、Fe、Co、Ni)端元相保持了水镁矾型2/m对称性;发现氢键和其他结构细节在最低实验温度下都有平滑变化。这些发现为从天体轨道器获得的遥感数据中硫酸盐相关信号的识别提供了重要依据,也为与极低温下的外星硫酸盐组合相关的水镁矾型硫酸盐水合物的性质进行热力学考虑和建模提供了重要依据。