提高Cr降解和Fe3O4吸附的效率,使用通过各种方法制备的ZSM-5热岩支
Nichapha Senamart1, Worapol Yingyuen1, Waranya Obrom1
1Materials Chemistry Research Center, Department of Chemistry, Faculty of Science, Khon Kaen University Khon Kaen 40002 Thailand sirilo@kku.ac.th.
RSC advances
|February 21, 2025
概括
合成了磁铁 (Fe3O4) 纳米颗粒和以热为支的Fe3O4,以有效地去除. 石支显著增强了吸附能力,创造了稳定的物种用于水处理.
科学领域:
- 环境科学 环境科学
- 材料科学 材料科学 材料科学
- 化学 化学 化学
背景情况:
- (VI) 是水中的有毒污染物.
- 需要有效的吸附剂进行修复.
研究的目的:
- 为了合成和表征磁铁 (Fe3O4) 和以焦石为支的Fe3O4 (Fe/Z) 吸附剂.
- 评估它们在从水中去除 (VI) 的效率.
- 了解合成方法对吸附剂性能和性能的影响.
主要方法:
- 联合降水 (COP) 和水热 (HYD) 合成方法.
- 用于结构分析的X射线衍射 (XRD).
- 用于物种识别的X射线光电子光谱 (XPS) 和X射线吸收光谱 (XAS).
主要成果:
- 无论是COP还是HYD方法都能产生有效的Fe3O4吸附剂.
- HYD方法产生了更高的结晶度和均的球形Fe3O4颗粒 (400-500nm).
- 石支持显著提高Fe3O4吸附能力 (2.33 mg/g Fe) 和吸附的Cr.物种的稳定性.
结论:
- 铁3O4 / ZSM-5焦石是Cr6修复的一个有前途的材料.
- 合成方法对吸附剂形态,结晶性和性能产生了重大影响.
- 在Fe/Z_HYD上形成的稳定Cr物种包括离子交换格子结构.
相关概念视频
Redox Titration: Other Oxidizing and Reducing Agents
224
Besides iodine, other oxidizing or reducing agents can serve as titrants in redox titrations. Common oxidizing titrants include KMnO4, cerium(IV), and K2Cr2O7. The choice of oxidizing titrants depends on factors like stability, cost, analyte strength, and reaction rate between the analyte and titrant. KMnO4 is a strong oxidizing titrant that reduces from Mn(VII) to Mn(II) in a highly acidic solution, simultaneously oxidizing the analyte to a higher oxidation state. In this case, KMnO4 acts as a...
224
Precipitation and Co-precipitation
1.7K
Precipitation and coprecipitation methods can be used to separate a mixture of ions in a solution. In qualitative inorganic analysis, ions that form sparingly soluble precipitates with the same reagent are separated based on the differences in solubility products. For example, consider the separation of Cu(II) and Fe(II) ions by precipitation as insoluble sulfides. First, copper(II) sulfide is precipitated by the addition of acidic H2S, where the dissociation of H2S is suppressed. Adding H2S...
1.7K
Extraction: Advanced Methods
401
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
401
Voltammetry: Stripping Methods
164
Anodic Stripping Voltammetry (ASV), Cathodic Stripping Voltammetry (CSV), and Adsorptive Stripping Voltammetry (AdSV) are electrochemical techniques used to determine trace amounts of analytes in solution. These methods involve applying a potential to an electrode and measuring the resulting current.
Anodic Stripping Voltammetry (ASV)
ASV is used to determine metals and metalloids at trace levels. It involves two steps: deposition and stripping. First, a negative potential is applied to the...
Anodic Stripping Voltammetry (ASV)
ASV is used to determine metals and metalloids at trace levels. It involves two steps: deposition and stripping. First, a negative potential is applied to the...
164
Formation of Complex Ions
23.2K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
23.2K
Colloidal precipitates
481
The high insolubility of some precipitates can result in an unfavorable relative supersaturation. This can lead to colloidal particles with a large surface-to-mass ratio, where adsorption is promoted. For instance, in the precipitation of silver chloride, silver ions are adsorbed on the surface of the colloidal particles, forming a primary layer. This layer attracts ions of opposite charge (such as nitrate ions), forming a diffuse secondary layer of adsorbed ions. This electric double layer...
481


