THE ROLE OF COMBINED MOLTEN SALTS IN SODIUM-CERIUM (III) ORTHOPHOSPHATE CRYSTALLIZATION

К. Klymyshyna, К. Тerebilenko, N. Strutynska, M. Slobodyanik
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Abstract

The efficient crystallization conditions for high temperature synthesis of sodium-cerium(III) orthophosphate from binary molten salts have been investigated in a light of influence of the inert reaction media addition. Taking into consideration NaF and Na2MoO4 as an addictives to a convention phosphate melt the crystallization regions of CePO4 and Na3Ce(PO4)2 have been identified by means of IR spectroscopy and powder X-Ray diffraction methods. The initial Na/P ratio in the melt has been shown to play the key role in pure Na3Ce(PO4)2 phase formation. The concentration of NaF has been chosen as 20–60 mol. % and MoO3 in a range of 30–60 mol. %, while the cerium(III) content has been maintained equal to 10 mol. %. Additional application of NaF or Na2MoO4 lowers the temperature from 1400 in comparison to Na4P2O7 flux to 1000°C and homogenization time from 12 to 1h., respectively. Thus, the optimal conditions for the high-temperature growth has been found to be Na/P = 1.67 and NaF content equal to 30–45% mol. in case of fluoride-containing systems, and Na/P> 4,00 with MoO3 content of 25–36% mol for a molybdate one. In case of both fluoride and molybdate addition the crystallization region of the target compound has been bordered by a wide area of CePO4 phase. Three crystallization regions has been estimated during crystallization process: CePO4, Na3Ce(PO4)2 and a wide field of their co-crystallization. With Na/P ratio in the binary melt there is a simultaneous change in the solids structure prepared. Thus, when CePO4 possesses highly condensed CeO8 polyhadra in the framework and crystallizes at lower Na/P ratio, Na3Ce(PO4)2 corresponds to isolated CeO8 moieties that are stabilized under higher Na/P values. Within the synthetic conditions investigated, the melts have shown to play a depolymerizing role for the phosphate chains found in the melt, leading to crystallization temperature lowering in initial melt. The approach proposed for the of Na3Ce(PO4)2 synthesis allows to expand the temperature range of its formation and to carry out its uniform doping with fluorescent activators to modify its characteristic spectrum for the needs of modern inorganic LEDs.
复合熔盐在正磷酸盐钠-铈结晶中的作用
研究了二元熔盐高温合成正磷酸钠-铈(III)的有效结晶条件,考察了惰性反应介质添加量的影响。以NaF和Na2MoO4作为常规磷酸盐熔体的助剂,用红外光谱和粉末x射线衍射方法确定了CePO4和Na3Ce(PO4)2的结晶区域。熔体中初始Na/P比值是形成纯Na3Ce(PO4)2相的关键因素。NaF的浓度选择在20 ~ 60 mol. %, MoO3的浓度选择在30 ~ 60 mol. %,而铈(III)的含量保持在10 mol. %。与Na4P2O7相比,NaF或Na2MoO4的额外应用将温度从1400℃降低到1000℃,均质时间从12℃降低到1h。,分别。结果表明,含氟体系的最佳生长条件为Na/P = 1.67, NaF含量为30-45% mol.;钼酸盐体系的最佳生长条件为Na/P bbb4000, MoO3含量为25-36% mol.。在氟化物和钼酸盐同时加入的情况下,目标化合物的结晶区被大面积的CePO4相包围。在结晶过程中估计了三个结晶区域:CePO4、Na3Ce(PO4)2及其共结晶的广阔领域。随着二元熔体中Na/P比的增加,所制备的固体结构也发生了变化。因此,当CePO4在骨架中具有高度凝聚的CeO8多晶体并在较低的Na/P比下结晶时,Na3Ce(PO4)2对应于在较高Na/P值下稳定的分离的CeO8部分。在所研究的合成条件下,熔体显示出对熔体中发现的磷酸盐链起解聚作用,导致初始熔体的结晶温度降低。提出的合成Na3Ce(PO4)2的方法可以扩大其形成的温度范围,并通过荧光激活剂对其进行均匀掺杂,以修改其特征光谱以满足现代无机led的需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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