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利用水力空化作用对模型燃料和实际燃料中的硫污染物进行氧化

Oxidation of Sulphur pollutants in model and real fuels using hydrodynamic cavitation.

作者信息

Delaney Peter, Sarvothaman Varaha P, Nagarajan Sanjay, Rooney David, Robertson Peter K J, Ranade Vivek V

机构信息

School of Chemistry and Chemical Engineering, Queen's University Belfast, Belfast BT9 5AG, UK.

School of Chemistry and Chemical Engineering, Queen's University Belfast, Belfast BT9 5AG, UK; Clean Combustion Research Center, King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia.

出版信息

Ultrason Sonochem. 2023 May;95:106405. doi: 10.1016/j.ultsonch.2023.106405. Epub 2023 Apr 14.

Abstract

Hydrodynamic Cavitation (HC) offers an attractive platform for intensifying oxidative desulphurization of fuels. In the first part of this work, we present new results on oxidising single ring thiophene in a model fuel over the extended range of volume fraction of organic phase from 2.5 to 80 v/v %. We also present influence of type and scale of HC device on performance of oxidative desulphurization. Further experiments revealed that oxidising radicals generated in-situ by HC alone were not able to oxidise dual ring thiophenes. External catalyst (formic acid) and oxidising agents (hydrogen peroxide, HO) were therefore used with HC. Based on our prior work with acoustic cavitation (AC), the volumetric ratios for HO and formic acid were identified as 0.95 v/v % and 6.25 v/v % respectively. The data of oxidation of dual ring thiophenes with n-dodecane and n-hexane as model fuels and typical transport fuels (diesel, kerosene, and petrol) using these oxidant and catalyst is presented. The observed performance with HC was compared with results obtained from a stirred tank and AC set-up. The presented data indicates that HC is able to intensify oxidation of sulphur species. The presented results provide a sound basis for further developments on HC based oxidative desulphurization processes.

摘要

水力空化(HC)为强化燃料的氧化脱硫提供了一个有吸引力的平台。在本工作的第一部分,我们展示了在有机相体积分数从2.5到80 v/v%的扩展范围内,在模型燃料中氧化单环噻吩的新结果。我们还展示了HC装置的类型和规模对氧化脱硫性能的影响。进一步的实验表明,仅由HC原位产生的氧化自由基无法氧化双环噻吩。因此,外部催化剂(甲酸)和氧化剂(过氧化氢,HO)与HC一起使用。基于我们之前关于声空化(AC)的工作,HO和甲酸的体积比分别确定为0.95 v/v%和6.25 v/v%。给出了以正十二烷和正己烷作为模型燃料以及典型运输燃料(柴油、煤油和汽油),使用这些氧化剂和催化剂氧化双环噻吩的数据。将观察到的HC性能与搅拌槽和AC装置获得的结果进行了比较。给出的数据表明HC能够强化硫物种的氧化。给出的结果为基于HC的氧化脱硫工艺的进一步发展提供了坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0120/10148227/70d75a625422/gr1.jpg

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