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Effective removal of organic dyes using the ultrasonic-assisted hydrothermal synthesis of NaP zeolite doping Cu or Fe in Fenton-like oxidation systems

沸石 结晶度 亚甲蓝 热液循环 吸附 水热合成 材料科学 结晶 结晶紫 核化学 化学 催化作用 光催化 化学工程 有机化学 结晶学 病理 工程类 医学
作者
Yanan Zhang,Zhenli Zhang,Hongjing Han,Mei Zhang,Haiying Wang,Hua Song,Yanguang Chen
出处
期刊:Separation and Purification Technology [Elsevier]
卷期号:299: 121767-121767 被引量:15
标识
DOI:10.1016/j.seppur.2022.121767
摘要

NaP zeolite was successfully synthesized via ultrasonic-assisted hydrothermal synthesis. The approaches for Cu or Fe doping were screened. Additionally, the oxidation process of methylene blue (MB) and methyl violet-6B (MV-6B) by the doped NaPultra zeolites was surveyed. NaPultra zeolite exhibited higher crystallinity (94.99%), while the crystallization temperature and duration decreased from 120 °C to 90 °C and from 8 h to 4 h with the n(SiO2)/n(Al2O3) increasing from 2.0 to 4.0, compared to the hydrothermal synthesis. At the ultrasonic power intensity of 30% and the density of 60 mL/W, the conversion rates of Si and Al rosed from 66.46% to 84.68% and from 73.75% to 95.25%, respectively. Comparatively, the complexation approach demonstrated superior findings in the crystallinity (Fe-NaPultra: 92.37% and Cu-NaPultra: 94.14%) at the n(Fe(NO3)3):n(Al2O3) ratio of 1:4 and the n(Cu(NO3)2):n(Al2O3) ratio of 1:6. The ultrasonic resulted in the smaller crystal sizes for Fe-NaPultra (1.90 μm) and Cu-NaPultra (1.80 μm). Cu-NaPultra displayed better oxidation performance in the elimination of MB (93.22%) and MV-6B (98.71%) via the HO at the condition of pH = 5.0, 30 min, 2.5 g/L, 50 mg/L, and 25 °C. Through the combined action of adsorption and Fenton-like oxidation, the rapid enrichment of organic dyes by the zeolite was realized, and the dyes were removed efficiently. Cu-NaPultra was capable of retaining good removal performance throughout four cycles, suggesting that it is a promising catalyst for Fenton-like oxidation reactions and may help to pave the way for the removal of organic dyes.
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