3O4磁性納米顆粒,利用SiO2、羧甲基-β-環(huán)糊精(CM-β-CD)對磁性顆粒的表面進行修飾,制備了具有高吸附性能的Fe3O4基磁性納米材料(Fe3O4@SiO2@CM-β-CD),開展了單因素優(yōu)化實驗,通過TEM、Mapping、EDS、BET等手段對磁性納米復合材料的物化特性進行表征,探討了Fe3O4@SiO2@CM-β-CD對稀土Er(Ⅲ)的吸附行為。結(jié)果表明:十二烷基苯磺酸鈉(SDBS)的投加量為1 g,正硅酸四乙酯(TEOS)的投加量6 mL,氨丙基三乙氧基硅烷(APTES)的投加量為1 mL,CM-β-CD投加量為0.5 g時,Er(Ⅲ)去除率最高,可達到95%以上。進一步探究了吸附劑投加量、溫度及轉(zhuǎn)速對Er(Ⅲ)去除率的影響。結(jié)果發(fā)現(xiàn),當接觸時間為30 min,初始Er(Ⅲ)濃度為10 mg/L,初始pH為4.5,吸附劑用量為 30 mg,溫度為298 K,轉(zhuǎn)速為150 r/min時,Er(Ⅲ)的去除率約為98%。將吸附Er(Ⅲ)后的納米材料用0.1 mol/L HNO3進行解吸,解吸20 min,Er(Ⅲ)的解吸率可達87%以上。采用XPS分析手段對Fe3O4@SiO2@CM-β-CD吸附機制進行了初步探究。結(jié)果表明,F(xiàn)e3O4@SiO2@CM-β-CD對Er(Ⅲ)的吸附以環(huán)糊精空腔的包和作用為主,靜電吸附、化學吸附為輔。本研究可為水溶液中低濃度稀土元素的高效回收提供新方法。"/>

最新色国产精品精品视频,中文字幕日韩一区二区不卡,亚洲有码转帖,夜夜躁日日躁狠狠久久av,中国凸偷窥xxxx自由视频

+高級檢索
Fe3O4@SiO2@CM-β-CD磁性納米材料制備及對Er()吸附性能的影響
作者:
作者單位:

青島理工大學 環(huán)境與市政工程學院,山東 青島 266520

作者簡介:

通訊作者:

中圖分類號:

TB383

基金項目:

國家自然科學基金(52174336,21606248);山東省重點研發(fā)計劃(2018GSF117028);山東省自然科學基金(ZR202102280404)


Preparation of Fe3O4@SiO2@CM-β-CD Magnetic Nanomaterials and Its Their Adsorption Properties on Er()
Author:
Affiliation:

School of Environmental and Municipal Engineering, Qingdao University of Technology, Qingdao 266520, China

Fund Project:

國家自然科學基金資助項目(52174336;21606248);山東省重點研發(fā)計劃(2018GSF117028);山東省自然科學基金(ZR202102280404)

  • 摘要
  • |
  • 圖/表
  • |
  • 訪問統(tǒng)計
  • |
  • 參考文獻
  • |
  • 相似文獻
  • |
  • 引證文獻
  • |
  • 資源附件
  • |
  • 文章評論
    摘要:

    采用共沉淀法制備Fe3O4磁性納米顆粒,利用SiO2、羧甲基-β-環(huán)糊精(CM-β-CD)對磁性顆粒的表面進行修飾,制備了具有高吸附性能的Fe3O4基磁性納米材料(Fe3O4@SiO2@CM-β-CD),開展了單因素優(yōu)化實驗,通過TEM、Mapping、EDS、BET等手段對磁性納米復合材料的物化特性進行表征,探討了Fe3O4@SiO2@CM-β-CD對稀土Er(Ⅲ)的吸附行為。結(jié)果表明:十二烷基苯磺酸鈉(SDBS)的投加量為1 g,正硅酸四乙酯(TEOS)的投加量6 mL,氨丙基三乙氧基硅烷(APTES)的投加量為1 mL,CM-β-CD投加量為0.5 g時,Er(Ⅲ)去除率最高,可達到95%以上。進一步探究了吸附劑投加量、溫度及轉(zhuǎn)速對Er(Ⅲ)去除率的影響。結(jié)果發(fā)現(xiàn),當接觸時間為30 min,初始Er(Ⅲ)濃度為10 mg/L,初始pH為4.5,吸附劑用量為 30 mg,溫度為298 K,轉(zhuǎn)速為150 r/min時,Er(Ⅲ)的去除率約為98%。將吸附Er(Ⅲ)后的納米材料用0.1 mol/L HNO3進行解吸,解吸20 min,Er(Ⅲ)的解吸率可達87%以上。采用XPS分析手段對Fe3O4@SiO2@CM-β-CD吸附機制進行了初步探究。結(jié)果表明,F(xiàn)e3O4@SiO2@CM-β-CD對Er(Ⅲ)的吸附以環(huán)糊精空腔的包和作用為主,靜電吸附、化學吸附為輔。本研究可為水溶液中低濃度稀土元素的高效回收提供新方法。

    Abstract:

    Fe3O4 magnetic nanoparticles were prepared by co-precipitation method, the surface of the magnetic particles was modified by SiO2 and CM-β-CD, and Fe3O4-based magnetic nanomaterials (Fe3O4@SiO2@CM-β-CD) with high adsorption properties were prepared. Single factor optimization experiments were carried out, and the physical and chemical properties of magnetic nanocomposites were characterized by TEM, EDS and BET. The adsorption behavior of Fe3O4@SiO2@CM-β-CD on rare earth Er(Ⅲ) was investigated. The effects of adsorbent dosage, temperature and rotational speed on erbium removal rate were also investigated. The results show that when the dosage of SDBS is 1 g, the dosage of TEOS is 6 mL, the dosage of APTES is 1 mL, and the dosage of CM-β-CD is 0.5 g, the adsorption rate of Er(Ⅲ) can preferably reach more than 95%. When the contact time is 30 min, the initial concentration of Er(Ⅲ) is 10 mg/L, the initial pH is 4.5, the dosage of adsorbent is 30 mg, the temperature is 298 K, and the rotational speed is 150 r/min, the removal rate of Er(Ⅲ) is about 98%. After the adsorption of erbium, the nanomaterials were desorbed with 0.1 mol/L HNO3 for 20 min, and the desorption efficiency of rare earth Er(Ⅲ) can be more than 87%. The adsorption mechanism of Fe3O4@SiO2@CM-β-CD was investigated by XPS analysis. It is found that the adsorption of Fe3O4@SiO2@CM-β-CD on Er(Ⅲ) is mainly by the inclusion of cyclodextrin cavity, supplemented by electrostatic adsorption and chemisorption. The results of this study can provide a new method for efficient recovery of rare earth elements with low concentration in aqueous solution.

    參考文獻
    相似文獻
    引證文獻
引用本文

趙玉秀,劉杰,張寧,張鑫,薛志瀟,張秋露,李倩婷.Fe3O4@SiO2@CM-β-CD磁性納米材料制備及對Er()吸附性能的影響[J].稀有金屬材料與工程,2025,54(3):730~740.[Zhao Yuxiu, Liu Jie, Zhang Ning, Zhang Xin, Xue Zhixiao, Zhang Qiulu, Li Qianting.Preparation of Fe3O4@SiO2@CM-β-CD Magnetic Nanomaterials and Its Their Adsorption Properties on Er()[J]. Rare Metal Materials and Engineering,2025,54(3):730~740.]
DOI:10.12442/j. issn.1002-185X.20230715

復制
文章指標
  • 點擊次數(shù):
  • 下載次數(shù):
  • HTML閱讀次數(shù):
  • 引用次數(shù):
歷史
  • 收稿日期:2023-11-12
  • 最后修改日期:2023-12-17
  • 錄用日期:2024-01-05
  • 在線發(fā)布日期: 2025-03-25
  • 出版日期: 2025-03-25