SYNTHESIS OF COMPLEX OXIDES OF COBALT-NEODYMIUM FROM HETEROCOMPLEXES AND THEIR CATALYTIC ACTIVITY IN THE DE­COM­POSITION OF HYDROGEN PEROXIDE

L. Sliusarchuk, L. Zheleznova, S. Kuleshov, O. Rohovtsov, O. Trunova, Borys Khomenko
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Abstract

New heterometallic complexes of Сo(II) and Nd(III) with carboxylic acids (succinic, oxalic) and acetylacetone in the presence of phenanthroline or α,α'-dipyridyl have been synthesized. Their thermal properties and the ability to form complex oxides during thermal degradation have been studied. In the process of thermolysis of heterocomplexes, neodymium cobaltate NdCoO3 was obtained, which is confirmed by the results of X-ray powder diffraction. The research has established that the X-ray powder diffraction patterns of the products obtained by thermolysis of heterocomplex [Сo2Nd2(C4Н4O4)5·2Phen]·4Н2О to 1000 °С exhibits peaks at (2θ): 23.40, 33.74, 41.42, 48.32, 54.52, 59.94, 70.58°. This corresponds to the neodymium cobaltate NdCoO3. Neodymium cobaltate crystallizes in the cubic crystal system. The sample was obtained without extraneous phases inclusions. For the samples obtained by the termolysis of he­te­rocomplexes [Сo2Nd2(C2O4)5·2Phen]·4Н2О and NdCo(AA)5·2α,α'-dipy, in addition to the complex oxide NdCoO3, peaks of Nd2O3 were recorded, which crystallizes in the hexa­gonal crystal system. The X-ray powder diffraction patterns show peaks with 2θ values: 26.92, 29.75, 30.77, 40.54, 47.53, 53.63, 57.08°. The phase ratio of NdCoO3/Nd2O3 after termolysis for the sample of CoNd(AA)5·2α,α'-dipy is ~ 68.9/31.1%; for the sample of [Сo2Nd2(C2O4)5·2Phen]·4Н2О is ~ 50/50%; for the sample of [Сo2Nd2(C4Н4O4)5·2Phen]·4Н2О is NdCoO3 ~ 100%. The average crystallites size of complex oxides was calculated using the Scherer formula. It has been showed that neodymium cobaltate has an average particle size of ~33 nm, regardless of the complex precursor from which it was formed during thermolysis. The catalytic effect of neodymium cobaltates in the hydrogen peroxide decomposition reaction was studied. It was shown that all samples of complex oxides showed a quite high cataly­tic activity in the all of experiments in the hydro­gen peroxide decomposition reactions.
钴-钕络合物的合成及其对过氧化氢分解的催化活性
在邻菲罗啉或α,α′-二吡啶存在下,合成了Сo(II)和Nd(III)与羧酸(琥珀酸、草酸)和乙酰丙酮的异金属配合物。研究了它们的热性能和在热降解过程中形成复合氧化物的能力。在异质配合物的热分解过程中,得到了钴酸钕NdCoO3, x射线粉末衍射结果证实了这一点。研究发现,异质络合物[Сo2Nd2(C4Н4O4)5·2Phen]·4Н2О ~ 1000°С的x射线粉末衍射图在(2θ): 23.40、33.74、41.42、48.32、54.52、59.94、70.58°处出现峰值。这对应于钴酸钕NdCoO3。钴酸钕在立方晶系中结晶。样品没有外来相夹杂物。通过热裂解得到的fe - te配合物[Сo2Nd2(C2O4)5·2Phen]·4Н2О和NdCo(AA)5·2α,α′-dipy,除了配合物氧化物NdCoO3外,还记录到了Nd2O3的峰,并呈六角形结晶体系结晶。x射线粉末衍射图显示出2θ值为26.92°、29.75°、30.77°、40.54°、47.53°、53.63°、57.08°的峰。CoNd(AA)5·2α,α′-dipy样品经热裂解后,NdCoO3/Nd2O3的相比为~ 68.9/31.1%;对于[Сo2Nd2(C2O4)5·2Phen]·4Н2О样品为~ 50/50%;对于[Сo2Nd2(C4Н4O4)5·2Phen]·4Н2О样品,NdCoO3 ~ 100%。用Scherer公式计算了复合氧化物的平均晶粒尺寸。结果表明,无论在热裂解过程中形成的复合前驱体是什么,钴酸钕的平均粒径均为~33 nm。研究了钴酸钕在过氧化氢分解反应中的催化作用。结果表明,所有的复合氧化物样品在过氧化氢分解反应中都表现出较高的催化活性。
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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