Insight into the Structure and Redox Chemistry of [Carbonatotetraamminecobalt(III)] Permanganate and Its Monohydrate as Co-Mn-Oxide Catalyst Precursors of the Fischer-Tropsch Synthesis

K. Béres, Z. Dürvanger, Zoltán Homonnay, L. Bereczki, Berta Barta Holló, A. Farkas, V. Petruševski, László Kótai
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Abstract

[Carbonatotetraamminecobalt(III)] permanganate monohydrate was synthesized first in the metathesis reaction of [Co(NH3)4CO3]NO3 and NaMnO4 in aqueous solution. Its thermal dehydration at 100 °C resulted in phase-pure [Co(NH3)4CO3]MnO4 (compound 1). Compounds 1 and 2 (i.e., the hydrated form) were studied with IR, far-IR, and low-temperature Raman spectroscopies, and their vibrational modes were assigned. The lattice parameters were determined by powder X-ray diffraction (PXRD) and single crystal X-ray diffraction (SXRD) methods for the triclinic and orthorhombic compounds 1 and 2, respectively. The detailed structure of compound 2 was determined, and the role of hydrogen bonds in the structural motifs was clarified. UV studies on compounds 1 and 2 showed the distortion of the octahedral geometry of the complex cation during dehydration because of the partial loss of the hydrogen bonds between the crystal water and the ligands of the complex cation. The thermal decomposition consists of a solid phase quasi-intramolecular redox reaction between the ammonia ligands and permanganate anions with the formation of ammonia oxidation products (H2O, NO, N2O, and CO2). The solid phase reaction product is amorphous cobalt manganese oxide containing ammonium, carbonate (and nitrate) anions. The temperature-controlled thermal decomposition of compound 2 in toluene at 110 °C showed that one of the decomposition intermediates is ammonium nitrate. The decomposition intermediates are transformed into Co1.5Mn1.5O4 spinel with MnCo2O4 structure upon further heating. Solid compound 2 gave the spinel at 500 °C both in an inert and air atmosphere, whereas the sample pre-treated in toluene at 110 °C without and with the removal of ammonium nitrate by aqueous washing, gave the spinel already at 300 and 400 °C, respectively. The molten NH4NO3 is a medium to start spinel crystallization, but its decomposition stops further crystal growth of the spinel phase. By this procedure, the particle size of the spinel product as low as ~4.0 nm could be achieved for the treatments at 300 and 400 °C, and it increased only to 5.7 nm at 500 °C. The nano-sized mixed cobalt manganese oxides are potential candidates as Fischer-Tropsch catalysts.
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洞察作为费托合成钴氧化物催化剂前驱体的 [碳四胺钴(III)] 高锰酸盐及其一水合物的结构和氧化还原化学性质
[碳四胺钴(III)]高锰酸钾一水合物首先是在[Co(NH3)4CO3]NO3 和 NaMnO4 的水溶液中通过偏析反应合成的。在 100 °C下进行热脱水,得到相纯的[Co(NH3)4CO3]MnO4(化合物 1)。利用红外光谱、远红外光谱和低温拉曼光谱对化合物 1 和 2(即水合形式)进行了研究,并分配了它们的振动模式。通过粉末 X 射线衍射 (PXRD) 和单晶 X 射线衍射 (SXRD) 方法,分别测定了三菱形和正方形化合物 1 和 2 的晶格参数。确定了化合物 2 的详细结构,并阐明了氢键在结构基团中的作用。对化合物 1 和 2 的紫外研究表明,在脱水过程中,由于晶体水与络合阳离子配体之间的氢键部分消失,络合阳离子的八面体几何形状发生了畸变。热分解包括氨配体和高锰酸根阴离子之间的固相准分子内氧化还原反应,并形成氨氧化产物(H2O、NO、N2O 和 CO2)。固相反应产物是含有铵、碳酸盐(和硝酸盐)阴离子的无定形钴锰氧化物。化合物 2 在 110 °C 的甲苯中的温控热分解显示,分解中间产物之一是硝酸铵。分解中间产物在进一步加热后转化为具有 MnCo2O4 结构的 Co1.5Mn1.5O4 尖晶石。固体化合物 2 在惰性气氛和空气中均于 500 ℃ 时生成尖晶石,而在 110 ℃ 的甲苯中进行预处理的样品,在不去除硝酸铵的情况下和通过水洗去除硝酸铵的情况下,分别于 300 ℃ 和 400 ℃ 时生成尖晶石。熔融 NH4NO3 是开始尖晶石结晶的介质,但它的分解会阻止尖晶石相晶体的进一步生长。通过这种方法,在 300 ℃ 和 400 ℃ 处理时,尖晶石产品的粒度可低至 ~4.0 nm,而在 500 ℃ 时,粒度仅增至 5.7 nm。纳米级混合钴锰氧化物有望成为费托催化剂。
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