Selective Oxidation of Cyclohexane Using Iron, Manganese, Nickel and Vanadium Doped ZrO2 in the Presence of Ozone

IF 3.7 3区 化学 Q2 CHEMISTRY, APPLIED
Siphumelele Thandokwazi Mkhondwane, Viswanadha Srirama Rajasekhar Pullabhotla
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引用次数: 0

Abstract

In this study, 2.5 wt% of iron (Fe), manganese (Mn), nickel (Ni) and vanadium (V) doped zirconium oxide (ZrO2) were used as catalysts for selective oxidation of cyclohexane in the presence of ozone. The catalysts were prepared using wet impregnation method. The catalysts were characterized using various spectroscopic and microscopic techniques. Cyclohexane (25 mL) was oxidized in an impinger glass reactor using 0.2 g of the catalysts at pH 3, 7 and 11. The reaction products were identified using gas chromatograph-mass spectrometry (GC–MS) and Fourier transform infrared spectroscopy (FT-IR). Fe/ZrO2 outperformed all the catalysts with conversion of 36%. V/ZrO2 was the least active catalyst at pH 3 with 14% cyclohexane conversion, whereas Mn/ZrO2 was the least active catalyst at pH 7 and 11 with conversions of 21 and 28%, respectively. Cyclohexanol and cyclohexanone were only reaction products identified after 30 min at pH 3, 7 and 11. After 60 min only cyclohexanone was identified as reaction product. The results showed that Fe, Mn, Ni and V doped ZrO2 coupled with ozone is the potential prospect for oxidation of cyclohexane.

臭氧存在下,铁、锰、镍、钒掺杂ZrO2选择性氧化环己烷
本研究以2.5 wt%的铁(Fe)、锰(Mn)、镍(Ni)和钒(V)掺杂氧化锆(ZrO2)为催化剂,在臭氧存在下选择性氧化环己烷。采用湿浸渍法制备催化剂。采用各种光谱和显微技术对催化剂进行了表征。环己烷(25 mL)在冲击玻璃反应器中氧化,催化剂用量为0.2 g, pH值为3、7和11。采用气相色谱-质谱(GC-MS)和傅里叶变换红外光谱(FT-IR)对反应产物进行鉴定。Fe/ZrO2催化剂的转化率最高,达到36%。pH = 3时,V/ZrO2催化剂活性最低,环己烷转化率为14%;pH = 7和pH = 11时,Mn/ZrO2催化剂活性最低,环己烷转化率分别为21%和28%。环己醇和环己酮在pH为3、7和11的条件下反应30 min后才被鉴定出来。60 min后,仅鉴定出环己酮为反应产物。结果表明,Fe, Mn, Ni和V掺杂ZrO2与臭氧耦合是环己烷氧化的潜在前景。
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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来源期刊
Topics in Catalysis
Topics in Catalysis 化学-物理化学
CiteScore
5.70
自引率
5.60%
发文量
197
审稿时长
2 months
期刊介绍: Topics in Catalysis publishes topical collections in all fields of catalysis which are composed only of invited articles from leading authors. The journal documents today’s emerging and critical trends in all branches of catalysis. Each themed issue is organized by renowned Guest Editors in collaboration with the Editors-in-Chief. Proposals for new topics are welcome and should be submitted directly to the Editors-in-Chief. The publication of individual uninvited original research articles can be sent to our sister journal Catalysis Letters. This journal aims for rapid publication of high-impact original research articles in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
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