Author
Listed:
- Hajar El Haddaj
(Materials and Environmental Process Engineering Research Team, GeMaPE Laboratory, Higher School of Technology, Hassan II University of Casablanca, Casablanca 20360, Morocco)
- Salma El Meziani
(Materials and Environmental Process Engineering Research Team, GeMaPE Laboratory, Higher School of Technology, Hassan II University of Casablanca, Casablanca 20360, Morocco)
- Wafaa Boumya
(Multidisciplinary Research and Innovation Laboratory, FP Khouribga, Sultan Moulay Slimane University of Beni Mellal, BP. 145, Khouribga 25000, Morocco)
- Zohra Farid
(Materials and Environmental Process Engineering Research Team, GeMaPE Laboratory, Higher School of Technology, Hassan II University of Casablanca, Casablanca 20360, Morocco)
- Ahmed Errami
(Materials and Environmental Process Engineering Research Team, GeMaPE Laboratory, Higher School of Technology, Hassan II University of Casablanca, Casablanca 20360, Morocco)
- Abdelhafid Essadki
(Materials and Environmental Process Engineering Research Team, GeMaPE Laboratory, Higher School of Technology, Hassan II University of Casablanca, Casablanca 20360, Morocco)
- Noureddine Barka
(Multidisciplinary Research and Innovation Laboratory, FP Khouribga, Sultan Moulay Slimane University of Beni Mellal, BP. 145, Khouribga 25000, Morocco)
- Alaâeddine Elhalil
(Materials and Environmental Process Engineering Research Team, GeMaPE Laboratory, Higher School of Technology, Hassan II University of Casablanca, Casablanca 20360, Morocco)
Abstract
The uncontrolled discharge of synthetic azo dyes such as methyl orange (MO) into water bodies has become a major environmental concern because of their strong chemical stability, limited biodegradability, and harmful effects on aquatic ecosystems. In this study, MgNiFe layered double hydroxides (LDHs) were synthesized through a co-precipitation route using a molar ratio of (Mg + Ni)/Fe equal to 3, and their adsorption ability toward MO in aqueous media was investigated. The prepared materials were characterized by X-ray diffraction (XRD), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDX), Fourier-transform infrared spectroscopy (FTIR), and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The characterization results revealed the successful formation of a hydrotalcite-like layered structure with good crystallinity, a relatively uniform distribution of metallic species, and the incorporation of carbonate anions within the interlayer galleries. In addition, the adsorption performance was evaluated by studying the effects of several operational factors, namely adsorbent dosage, initial pH, and contact time. To better understand the interaction between these parameters and identify the optimum operating conditions, a Box–Behnken response surface design was applied. The results indicate solution pH is the most influential parameter in the adsorption process. Under optimized conditions, a maximum removal efficiency of 86.86% was obtained, corresponding to an adsorption capacity of approximately ~86.86 mg·g −1 (based on 100 mL solution volume). The enhanced adsorption performance may be attributed to the combined effect of the multivalent metal cations (Mg 2+ , Ni 2+ , and Fe 3+ ), likely increases the surface positive charge density of the LDH and promotes interactions with anionic dye molecules. These interactions are suggested to involve electrostatic attraction and possible surface adsorption processes. However, in the absence of post-adsorption characterization, the exact adsorption mechanism remains hypothetical. Overall, the results demonstrate the promising potential of MgNiFe LDHs as efficient adsorbent materials for the treatment of dye-contaminated wastewater.
Suggested Citation
Hajar El Haddaj & Salma El Meziani & Wafaa Boumya & Zohra Farid & Ahmed Errami & Abdelhafid Essadki & Noureddine Barka & Alaâeddine Elhalil, 2026.
"Synthesis, Characterization and Optimization of MgNiFe-CO 3 Layered Double Hydroxide Material for Textile Dye Removal,"
Sustainability, MDPI, vol. 18(10), pages 1-19, May.
Handle:
RePEc:gam:jsusta:v:18:y:2026:i:10:p:5111-:d:1946151
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jsusta:v:18:y:2026:i:10:p:5111-:d:1946151. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager The email address of this maintainer does not seem to be valid anymore. Please ask MDPI Indexing Manager to update the entry or send us the correct address
(email available below). General contact details of provider: https://www.mdpi.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.