Gromilov Sergey A, Chepurov Anatoly I, Volodin Alexander M, Vedyagin Aleksey A
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Pr. Lavrentieva 3, 630090 Novosibirsk, Russia.
V.S. Sobolev Institute of Geology and Mineralogy, Siberian Branch of the Russian Academy of Sciences, Pr. Akademika Koptyuga 3, 630090 Novosibirsk, Russia.
Materials (Basel). 2023 Mar 3;16(5):2083. doi: 10.3390/ma16052083.
Calcium aluminate of a mayenite structure, 12CaO∙7AlO (C12A7), is widely applicable in many fields of modern science and technology. Therefore, its behavior under various experimental conditions is of special interest. The present research aimed to estimate the possible impact of the carbon shell in core-shell materials of C12A7@C type on the proceeding of solid-state reactions of mayenite with graphite and magnesium oxide under High Pressure, High Temperature (HPHT) conditions. The phase composition of the solid-state products formed at a pressure of 4 GPa and temperature of 1450 °C was studied. As is found, the interaction of mayenite with graphite under such conditions is accompanied by the formation of an aluminum-rich phase of the CaO∙6AlO composition, while in the case of core-shell structure (C12A7@C), the same interaction does not lead to the formation of such a single phase. For this system, a number of hardly identified calcium aluminate phases along with the carbide-like phrases have appeared. The main product of the interaction of mayenite and C12A7@C with MgO under HPHT conditions is the spinel phase AlMgO. This indicates that, in the case of the C12A7@C structure, the carbon shell is not able to prevent the interaction of the oxide mayenite core with magnesium oxide located outside the carbon shell. Nevertheless, the other solid-state products accompanying the spinel formation are significantly different for the cases of pure C12A7 and C12A7@C core-shell structure. The obtained results clearly illustrate that the HPHT conditions used in these experiments lead to the complete destruction of the mayenite structure and the formation of new phases, which compositions differ noticeably depending on the precursor used-pure mayenite or C12A7@C core-shell structure.
具有钙钛矿结构的铝酸钙,12CaO∙7AlO(C12A7),在现代科学技术的许多领域都有广泛应用。因此,其在各种实验条件下的行为备受关注。本研究旨在评估C12A7@C型核壳材料中的碳壳对钙钛矿与石墨和氧化镁在高压高温(HPHT)条件下固态反应进程的可能影响。研究了在4 GPa压力和1450 °C温度下形成的固态产物的相组成。结果发现,在这种条件下钙钛矿与石墨的相互作用伴随着形成CaO∙6AlO组成的富铝相,而在核壳结构(C12A7@C)的情况下,相同的相互作用不会导致形成这样的单相。对于该体系,出现了一些难以鉴定的铝酸钙相以及类碳化物相。在高压高温条件下,钙钛矿与C12A7@C与MgO相互作用的主要产物是尖晶石相AlMgO。这表明,在C12A7@C结构的情况下,碳壳无法阻止氧化物钙钛矿核与位于碳壳外部的氧化镁发生相互作用。然而,对于纯C12A7和C12A7@C核壳结构的情况,伴随尖晶石形成的其他固态产物有显著差异。所得结果清楚地表明,这些实验中使用的高压高温条件导致钙钛矿结构完全破坏并形成新相,其组成根据所使用的前驱体——纯钙钛矿或C12A7@C核壳结构——而有明显不同。