Anissa Somrani

Anissa Somrani

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Anissa Somrani has a total of 27 co-authors. Here are the top co-authors by number of shared publications:

  • Maxime Pontié

    Group of Analysis and Processes (GA&P), Department of Chemistry, University of Angers, 49045 Angers, Cedex 01, France

    2 shared publications
  • Zaineb Mohamed

    Physics Department, College of Sciences, Jouf University, Sakaka, Saudi Arabia

    2 shared publications
  • A. H. Hamzaoui

    LVMU, National Center for Research in Materials Sciences, Soliman, Tunisia

    1 shared publication
  • A. M’NIf

    LVMU, National Center for Research in Materials Sciences, Soliman, Tunisia

    1 shared publication
  • Abdelbasset Ben Dkhil

    Department of Chemistry, Higher Institute of Sciences and Technologies of Environment, University of Carthage, Borj Cedria, P.B. no 1003, 2050 Hammam Lif, Tunisia

    1 shared publication
  • Ahmed Hannachi

    Laboratory of Engineering Processes and Industrial Systems, Chemical Engineering Department, National School of Engineers of Gabes, University of Gabes, St Omar Ibn El-Khattab, 6029 Gabes, Tunisia

    1 shared publication

Latest Publications

  • Open Access

    Efficient nitrate removal from water by biosorption onto a southern Mediterranean Sea native plant Posidonia oceanica (L.) powder

    by Abdelbasset Ben Dkhil, Haitham Elleuch, Anissa Somrani, Amor Hafiane

    An efficient method for nitrate removal from water was developed using the sea plant Posidonia oceanica (L.) as a biosorbent. Never used previously for this purpose, this plant was applied in its natural form without any chemical modification or cross-linking with another material. The nitrate biosorption was carried out in batch experiment at room temperature and under the optimum conditions of agitation time, biosorbent dose, and pH. The Langmuir model fits the experimental biosorption isotherm data better than the Freundlich one, confirming a monolayer adsorption process onto homogeneous surface and giving a relatively high maximum biosorption capacity 41.6 mg · g - 1 of nitrate nitrogen, thus demonstrating a good efficiency of the biosorbent. The thermodynamic study shows not only that the biosorption process is spontaneous and endothermic in nature, but also that increasing temperature enhances the nitrate uptake. Furthermore, the Dubinin–Radushkevich modeling gives a mean free energy of 15.81 kJ · mol - 1 , indicating that nitrate was chemisorbed. The same result was confirmed by kinetic modeling, which showed that the pseudo-second-order model fits the experimental data better than the pseudo-first order. The characterization by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) revealed that nitrate was mainly retained on the biosorbent surface through electrostatic forces with protonated amines ( RNH 3 + ; R 2 NH 2 + and R 3 NH + ). However, ion exchange with hydroxide ions and intraparticle diffusion may play an important role in the biosorption process.

  • Open Access

    A Mini Review of Reused End-of-Life Reverse Osmosis (EoL RO) Membranes

    by Anissa Somrani, Kholoud Abohelal, Maxime Pontié

    As sensitive parts of the water treatment process, reverse osmosis (RO) membranes are the most important for desalination and wastewater treatment. But the performance of RO membranes deteriorates over time due to fouling, necessitating frequent replacements. One of the environmental challenges is the disposal of End-of-Life (EoL) RO membranes, which are made of non-biodegradable polymers. The reuse of EoL membranes as a sustainable approach for waste saving and resource efficiency has recently attracted considerable attention. The present work provides a comprehensive overview of the strategies for reusing EoL RO membranes as sustainable alternatives to conventional disposal methods. Furthermore, the fundamental principles of RO technology, the primary types and impacts of membrane fouling, and advanced cleaning and regeneration techniques are discussed. The conversion of EoL membranes into nanofiltration (NF), ultrafiltration (UF), and forward osmosis (FO) membranes is also covered in this review, as well as their uses in brackish water desalination, dye/salt separation, groundwater treatment, and household wastewater reuse. Environmental and economic benefits, as well as technical, social, and regulatory challenges, are also discussed. Finally, the review highlights innovative approaches and future directions for incorporating EoL membrane reuse into circular economy models, outlining its potential to improve sustainability and reduce operational costs in water treatment systems.


  • Open Access

    Transforming end-of-life SWRO desalination membranes into nanofiltration membranes for the treatment of brackish water and wastewater

    by Anissa Somrani, Zaineb Mohamed, Kholoud Abohelal, Sara Larhrib, Noreddine Ghaffour, Maxime Pontié

    In this study, we explore the possibility of reusing end-of-life seawater reverse osmosis (RO) membranes to treat brackish water and industrial effluent. Prior to cleaning the end-of-life RO membranes, we conducted several autopsies in order to assess the extent of degradation. Based on these results, three cleaning protocols were tested and Ultrasil10 and/or chlorine solution were selected for further investigation. The cleaning capacity of the chlorine treatment at 4000 ppm.h was tested but proved inefficient as it leads to a denser cake and a significant decrease in hydraulic permeability. Therefore, we recommend commencing chemical cleaning with Ultrasil10 to remove foulants, thereby reconditioning the end-of-life RO membranes to meet nanofiltration membrane specifications. The cleaned end-of-life RO membranes exhibited enhanced hydraulic permeability (1.97 L·h⁻¹·m⁻²·bar⁻¹) and achieved a salt rejection of 85% for brackish water (6 g/L NaCl). With a molecular weight cutoff of 86 Da, these membranes effectively reduced brackish water conductivity to below 1000 µS/cm at 10 bars, complying with Tunisian drinking water standards (300–2500 µS/cm). Additionally, they demonstrated high efficiency in treating industrial effluents, achieving turbidity levels below 2 NTU and conductivity of 180 µS/cm. Operating at lower pressures, these membranes provided cost-effective, sustainable solutions and performed comparably to commercial new NF membranes, validating their potential for reuse in brackish water and wastewater treatment applications.


  • Open Access

    Dual Repurposing of End-of-Life BWRO Membranes: Ultrafiltration Membranes for Advanced Wastewater Treatment and Cation Exchange Membranes for Fungal Microbial Fuel Cells

    by Anissa Somrani, Mehri Shabani, Zaineb Mohamed, Kholoud Abohelal, Salam S. Alsharari, Ahmed Hannachi, Noreddine Ghaffour, Maxime Pontié

    The objective of this study is to evaluate the degradation of end-of-life BWRO membranes sourced from a factory in France by analyzing their water permeability, roughness, and chemical composition in order to diagnose the level of degradation incurred during their first life cycle in water softening. Following this, two new applications for the end-of-life BWRO membranes were investigated: (i) as ultrafiltration membranes (UF) for domestic effluent treatment and (ii) as cation exchange membranes (CEM) for use in fungal microbial fuel cells (FMFC). The UF membrane was renovated with an acetic acid treatment and, subsequently, used for domestic effluent filtration. The cation exchange membrane was developed in two steps: (i) chlorine treatment and (ii) the deposition of an Amer Sil layer, a functional coating formed by an interpenetrating polymer network (IPN) made of sulfonated polyether sulfone (S-PES) in a cross-linked matrix of acrylic acid and divinylbenzene.


  • Study on Lithium Extraction from Salt Lake Brines

    by A. Somrani, Z. Mohamed, A. H. Hamzaoui, A. M’NIf

    The purpose of the present study is to investigate the extraction of lithium from southern Tunisian brines. Density and concentration of Lithium in those brines were reported. Also, pondered rates of Lithium and the major elements in brines were investigated. Obtained results indicate that Lithium exist in those brines as traces. The optimization of certain parameters is required in this study. To extract Lithium from natural brines two steps were investigated. Firstly, we have used Ammonium Oxalate ((NH4)2(C2O4)⋅2H2O) to precipitate only Magnesium ion: in this procedure, three parameters were investigated (Mg/Oxalate, T (°C) and tstirring). The maximum values were found to be Mg/Ox = 0.66, T = Treflux = 100°C and tstirring ≥ 30 min. Secondly, we have used Aluminum Chloride (AlCl3⋅6H2O) in order to adsorbing lithium ions by Aluminum hydroxide. In this procedure, four parameters were investigated (pH, Al/Li, tstirring and T (°C)). Maximum values of these parameters are 7.2, 4.7, 3 h and 25°C respectively. Finally, to separate Lithium from Aluminum solution, we have used an exchange ion resin. This solution including two ions under cationic form (Al3+ and Li+). Al3+ was complexed into [Al(C2O4)3]3– using Ammonium Oxalate ions (\({{{\text{C}}}_{{\text{2}}}}{\text{O}}_{4}^{{2 - }}\)) and removed from solution using an anion exchange resin (Amberlite IRA-402). Thus, a theoretical study was carried out to determine the appropriate pH for separation. After Aluminum ions complexation by ammonium oxalate, Ox/Al molar ratio and pH was studied. Optimal values of these parameters are 3 and 4 respectively and the recovery of Li+ is set to be 98.5%.


  • Removal of Aluminium from (Li+‒Al3+) Aqueous Solutions by Adsorption onto Chitosan

    by Anissa Somrani, Zaineb Mohamed, Mounir Hajji, Ahmed Hichem Hamzaoui

    We have investigated the use of chitosan for aluminium removing from (Li+–Al3+) aqueous solutions. The isotherms and kinetics of adsorption with respect of initial aluminium concentration and pH were investigated. The optimum pH value for quantitative adsorption is 4. Langmuir and Freundlich adsorption models were applied to describe the experimental isotherms. Three simplified kinetics models, based on first-order, pseudo second-order and Elovich equations, were tested to describe the adsorption mechanism.