Related Experiment Video
Updated: Sep 30, 2025

Facile Preparation of Ultrafine Aluminum Hydroxide Particles with or without Mesoporous MCM-41 in Ambient Environments
Published on: May 11, 2017
The Performance and Mechanism of a Mg-Al Double-Layer Oxide in Chloride ion Removal from an Aqueous Solution
Xueqin Xu1, Peng Li2, Shichong Yang2
1Henan Province Industrial Technology Research Institution of Resources and Materials, Zhengzhou University, Zhengzhou 450001, China.
Abstract:
The increasing threat of chloride ions (Cl-) has led researchers to explore efficient removal technologies. Sewage treatment with a double-layer hydroxide/oxide (LDH/LDO) is receiving increasing attention. In this work, Mg-Al LDO adsorbents were produced by the calcination of the Mg-Al LDH precursor, which was constituted by improved coprecipitation. The influence of calcination temperature, calcination time, adsorbent dosage, Cl- initial concentration, contact time, and adsorption temperature on Cl- elimination was investigated systematically. The experimental results showed that a better porous structure endowed the Mg-Al LDO with outstanding adsorption properties for Cl-. The adsorption process was well matched to the pseudo-second-order kinetics model and the Freundlich model. Under optimal conditions, more than 97% of the Cl- could be eliminated. Moreover, the removal efficiency was greater than 90% even after 11 adsorption-desorption cycles. It was found that the electrostatic interaction between Cl- and the positively charged Mg-Al LDO laminate, coupled with the reconstruction of the layer structure, was what dominated the Cl- removal process.
Related Concept Videos
Extraction: Advanced Methods
Common Ion Effect
Electrolysis
Chemical Reactions in Aqueous Solutions
Acid Halides to Ketones: Gilman Reagent
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
Ion Exchange

