Yongpeng Ma , Jianghui Du , Haobing Yan , Chaobin Shi
{"title":"Controlling morphology and doping tungsten to regulate sulfur species on molybdenum disulfide for removing Hg0 from flue gas","authors":"Yongpeng Ma , Jianghui Du , Haobing Yan , Chaobin Shi","doi":"10.1080/17415993.2025.2453751","DOIUrl":null,"url":null,"abstract":"<div><div>Molybdenum disulfide (MoS<sub>2</sub>) is considered a favorable absorbent for removing heavy metals. However, due to its various morphologies, MoS<sub>2</sub> exhibits significant differences in its performance for removing mercury from flue gas. In the present study, the flower-like, spherical MoS<sub>2</sub> and W-MoS<sub>2</sub> were prepared by regulating the interlayer spacing and doping tungsten (W) in MoS<sub>2</sub> for removing gaseous mercury (Hg<sup>0</sup>). The results show that the number of active sulfur sites (S<sup>2-</sup> and S<sub>2</sub><sup>2-</sup>) was critical to the adsorption performance of MoS<sub>2</sub> for Hg<sup>0</sup>. The flower-like MoS<sub>2</sub> demonstrated optimum properties below 125°C which attributed to the presence of dominated S<sup>2-</sup> sites, while spherical MoS<sub>2</sub> and W-MoS<sub>2</sub> showed a wider application temperature range (up to 175°C) during Hg<sup>0</sup> removal which attributed to the unsaturated sulfur S<sub>2</sub><sup>2-</sup> and active oxygen. In terms of the mechanism, Hg<sup>0</sup> is directly inserted into the Mo-S bond of MoS<sub>2</sub> to form a transition state [Hg·Mo]-S, and then the original Mo-S is interrupted to form a new β-Hg-S bond, or combine with surface oxidation to form HgO. The oxygen in the flue gas can supplement the surface active oxygen on the MoS<sub>2</sub>, which enables the circulation of Mo<sup>5+</sup>. Hg<sup>0</sup> also reacted with S<sub>2</sub><sup>2-</sup> to form α-HgS.</div></div>","PeriodicalId":17081,"journal":{"name":"Journal of Sulfur Chemistry","volume":"46 3","pages":"Pages 435-454"},"PeriodicalIF":2.1000,"publicationDate":"2025-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Sulfur Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1741599325000029","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Molybdenum disulfide (MoS2) is considered a favorable absorbent for removing heavy metals. However, due to its various morphologies, MoS2 exhibits significant differences in its performance for removing mercury from flue gas. In the present study, the flower-like, spherical MoS2 and W-MoS2 were prepared by regulating the interlayer spacing and doping tungsten (W) in MoS2 for removing gaseous mercury (Hg0). The results show that the number of active sulfur sites (S2- and S22-) was critical to the adsorption performance of MoS2 for Hg0. The flower-like MoS2 demonstrated optimum properties below 125°C which attributed to the presence of dominated S2- sites, while spherical MoS2 and W-MoS2 showed a wider application temperature range (up to 175°C) during Hg0 removal which attributed to the unsaturated sulfur S22- and active oxygen. In terms of the mechanism, Hg0 is directly inserted into the Mo-S bond of MoS2 to form a transition state [Hg·Mo]-S, and then the original Mo-S is interrupted to form a new β-Hg-S bond, or combine with surface oxidation to form HgO. The oxygen in the flue gas can supplement the surface active oxygen on the MoS2, which enables the circulation of Mo5+. Hg0 also reacted with S22- to form α-HgS.
期刊介绍:
The Journal of Sulfur Chemistry is an international journal for the dissemination of scientific results in the rapidly expanding realm of sulfur chemistry. The journal publishes high quality reviews, full papers and communications in the following areas: organic and inorganic chemistry, industrial chemistry, materials and polymer chemistry, biological chemistry and interdisciplinary studies directly related to sulfur science.
Papers outlining theoretical, physical, mechanistic or synthetic studies pertaining to sulfur chemistry are welcome. Hence the target audience is made up of academic and industrial chemists with peripheral or focused interests in sulfur chemistry. Manuscripts that truly define the aims of the journal include, but are not limited to, those that offer: a) innovative use of sulfur reagents; b) new synthetic approaches to sulfur-containing biomolecules, materials or organic and organometallic compounds; c) theoretical and physical studies that facilitate the understanding of sulfur structure, bonding or reactivity; d) catalytic, selective, synthetically useful or noteworthy transformations of sulfur containing molecules; e) industrial applications of sulfur chemistry; f) unique sulfur atom or molecule involvement in interfacial phenomena; g) descriptions of solid phase or combinatorial methods involving sulfur containing substrates. Submissions pertaining to related atoms such as selenium and tellurium are also welcome. Articles offering routine heterocycle formation through established reactions of sulfur containing substrates are outside the scope of the journal.