合成豪斯曼铁矿在臭氧分解反应中的催化性能

A. Truba, T. L. Rakitskaya
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引用次数: 0

摘要

合成了IS-Mn和IS-Mn样品,并用x射线衍射、红外光谱和ph法对其进行了表征。x射线衍射法显示两种样品均为晶体和单相。IS-Mn样品中含有一种高斯锰矿相(Mn3O4),其晶格参数为四方对称,晶粒尺寸为43 nm。Mn3O4样品在空气中600℃下煅烧4小时得到的IIS-Mn样品含有立方晶格的bixbyite Mn2O3相,晶粒尺寸为66 nm。Mn3O4和Mn2O3样品在Mn-OH和Mn-O价振动区域的光谱差异较大。在631 cm-1的td配位上Mn2+的吸收带,在523和407cm-1的oh配位上Mn3+的吸收带清晰可见。在碳化物的红外光谱中,674处有多条强吸收带;658;606和542 cm-1,与文献数据相关,对应于Mn2O3中Mn-O的价态振荡。合成样品的水悬浮液pH值测定表明,Mn3O4与水分子接触后形成碱性介质,Mn2O3 -弱酸性介质。对初始浓度为100 mg/m3的臭氧分解反应中Mn3O4和Mn2O3样品的动力学曲线分布进行了测试,结果表明,动力学曲线分布由相组成决定。样品的测试已完成,并确定臭氧分解程度相同,即50%,达到。豪斯曼尼体的臭氧半衰期(t1/2)和实验结束时发生反应的臭氧量(Qexp)均大于Mn2O3样品。Mn3O4结构中锰以Mn2+和Mn3+两种氧化态的存在促进了氧化还原过程,碱性介质有利于自由基链反应,影响了反应的t1/2和Qexp值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CATALYTIC PROPERTIES OF SYNTHETIC HAUSMANNITE IN THE OZONE DECOMPOSITION REACTION
Samples of IS-Mn and IIS-Mn were synthesized and characterized by X-ray diffraction, IR spectroscopy and pH-metry. The X-ray diffraction method revealed both samples to be crystalline and single-phase. IS-Mn sample contains a phase of gausmannite (Mn3O4) with the parameters of the crystal lattice of tetragonal symmetry and the crystallites sized 43 nm. IIS-Mn sample, obtained by calcination of Mn3O4 sample in air under the condition of 600 oC for 4 hours, contains a phase of bixbyite Mn2O3 with a cubic crystal lattice and the crystallites sized 66 nm. The spectra of the Mn3O4 and Mn2O3 samples are particularly different in the region of Mn-OH and Mn-O valence vibrations. For gausmannite, the absorption band for Mn2+ in Td-coordination at 631 cm-1 and the absorption band for Mn3+ in Oh-coordination at 523 and 407cm-1 were clearly shown. In the IR spectrum of bixbyite, several intense absorption bands were observed at 674; 658; 606 and 542 cm-1, which correlate with the literature data and correspond to the valence oscillations of Mn-O in Mn2O3. The pH measurement of the aqueous suspension of the synthesized samples showed that Mn3O4 forms an alkaline medium, and Mn2O3 –weakly acidic upon contact with water molecules. Testing of Mn3O4 and Mn2O3 samples in the ozone decomposition reaction at the initial concentration of 100 mg/m3 showed that the kinetic curves profiles were determined by the phase composition. The testing of the samples was completed and it was established that the same degree of ozone decomposition, namely 50%, was achieved. For hausmannite, the values of the ozone half-life (t1/2) and the amount of ozone (Qexp), which reacted at the end of the experiment, are greater than Mn2O3 sample. The presence of manganese in two oxidation states Mn2+ and Mn3+ in the Mn3O4 structure promotes the redox process, and the alkaline medium contributes to the radical-chain reaction, which affects values t1/2 of and Qexp, which reacted.
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