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Activation of Peroxymonosulfate and Persulfate by Metal Loaded Mesoporous Catalysts for Orange G Dye Degradation

机译:金属负载的介孔催化剂活化过氧单硫酸盐和过硫酸盐以降解橙G染料

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The main objective of this research was to study the catalytic activation of two different oxidants (potassium persulfate, PS and peroxymonosulfate, PMS) employing sulfate-based Advanced Oxidation Processes (AOPs). For this purpose, heterogeneous copper and cobalt catalysts were synthesized supported on MCM-41 mesoporous material. These catalysts were characterized by means of Atomic Absorption Spectroscopy (AA), X-ray diffraction (XRD), and Transmission Electron Microscopy (TEM). The metal charge of the catalysts ranged from 5% to 18%. The mesoporous arrangement was held after the metal loading and calcination, as shown by XRD patterns and TEM micrographs. The catalytic degradation of Orange G azo dye (Orange G: OG, disodium 7-hydroxy-8-[(E)-phenyldiazenyl]-l,3-naphthalenedisulfonate) was analysed, and the catalyst activities were determined in a batch reactor. The combination of PMS and higher metal-content Co-supported catalyst attained the best efficiency. In these conditions, the complete decolourization (100%) of the dye was achieved in the first minutes of reaction, while its mineral-ization reached after 4 h was 49%. Additionally, the catalytic activity of the Co/PMS system (a measure of the catalyst's reusability) remained constant after three cycles of usage.
机译:这项研究的主要目的是研究基于硫酸盐的高级氧化工艺(AOP)对两种不同氧化剂(过硫酸钾,PS和过一硫酸氢盐,PMS)的催化活化。为此,合成了负载在MCM-41中孔材料上的多相铜和钴催化剂。这些催化剂通过原子吸收光谱(AA),X射线衍射(XRD)和透射电子显微镜(TEM)进行表征。催化剂的金属装料量为5%至18%。 X射线衍射图谱和TEM显微照片显示,在金属负载和煅烧后,介孔结构得以保持。分析了橙色G偶氮染料(橙色G:OG,7-羟基-8-[(E)-苯基二氮烯基] -1,3-萘二磺酸二钠二钠)的催化降解,并在间歇反应器中确定了催化剂活性。 PMS和较高金属含量的Co负载型催化剂的组合获得了最佳效率。在这些条件下,染料在反应的最初几分钟内完全脱色(100%),而4小时后达到的矿化度为49%。另外,在使用了三个循环之后,Co / PMS系统的催化活性(衡量催化剂可重复使用性的指标)保持恒定。

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