Philippe Namour
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Philippe Namour has a total of 108 co-authors. Here are the top co-authors by number of shared publications:
Nicole Jaffrezic-Renault
Institut des Sciences Analytiques UMR CNRS 5280, Université de Lyon, 5 rue de la Doua, 69100, Villeurbanne, France
10 shared publicationsAbdesslem Ben Haj Amara
Laboratoire de Physique des Matériaux Lamellaires et Nanomatériaux Hybrides (Université de Carthage, Faculté des Sciences de Bizerte, 7021 Zarzouna - Tunisia)
7 shared publications- Mohamed Amine Djebbi
Laboratory of Resources, Materials & Ecosystem (RME), University of Carthage, Faculty of Sciences of Bizerte, Zarzouna, 7021, Tunisia
7 shared publications - Nicole Jaffrezic-Renault
Institut UTINAM (UMR CNRS 6213), Université Marie et Louis Pasteur, F-25000 Besançon, France
6 shared publications - Pascal Breil
Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Unité de Recherche RiverLy, 69625 Villeurbanne, France
6 shared publications Zaineb Bouaziz
IEM - Institut Européen des membranes (1919, route de Mende - BP 5051 - 34293 Montpellier cedex 5 - France)
5 shared publications
Latest Publications
- Open Access
- 22 July 2022
- Published by Elsevier in Journal of Hazardous Materials Advances
- Vol. 7
The biogeochemical origin of sewage gases and control of their generation
- 22 July 2022
- Published by Elsevier in Journal of Hazardous Materials Advances
- Vol. 7
Open AccessThe biogeochemical origin of sewage gases and control of their generation
- 1 September 2018
- Published by Elsevier in Microporous and Mesoporous Materials
- Vol. 267, 43-52
Extended-release of chlorpromazine intercalated into montmorillonite clays
- 1 September 2018
- Published by Elsevier in Microporous and Mesoporous Materials
- Vol. 267, 43-52
Extended-release of chlorpromazine intercalated into montmorillonite clays
- 6 June 2018
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 25 (24) , 23817-23832
Removal of two anionic reactive textile dyes by adsorption into MgAl-layered double hydroxide in aqueous solutions
Textile dyes pose a significant challenge for water pollution due to the poor degradability of their complex aromatic structures (e.g., RR-120 and RBB-150). In order to minimize the harmful effects of RR-120 and RBB-150, the capacity of MgAl-layered double hydroxide for removing of these contaminants was studied herein. Batch adsorption experiments were conducted to investigate the effect of various operating parameters, such as solution pH, contact time, dye concentration, and temperature in order to provide optimal conditions for removal. Structural and morphological analyses were used to highlight the assembly and/or interaction LDH-dye. The state of equilibrium of RR-120 and RBB-150 adsorption was pH- and temperature-dependent and followed the pseudo-second-order rate model. Also, the equilibrium adsorption data of both dyes were found to adopt the Langmuir type isotherm model, which assumes a monolayer arrangement in LDH-dye. Furthermore, the effects of four major coexisting and competing mono- and divalent interlayer anions, such as NO3−, Cl−, CO32−, and SO42−, on the uptakes of RR-120 and RBB-150 were studied and the results showed that NO3− anions had insignificant effect on the uptakes of RR-120 and RBB-150 by MgAl. An equivalent study on the presence of both dyes in competitive trial adsorption/desorption from binary aqueous solution was investigated. And finally, the reuse operation of recovered material after dye adsorption was tested in up to 5 cycles of recyclability.
- 6 June 2018
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 25 (24) , 23817-23832
Removal of two anionic reactive textile dyes by adsorption into MgAl-layered double hydroxide in aqueous solutions
Textile dyes pose a significant challenge for water pollution due to the poor degradability of their complex aromatic structures (e.g., RR-120 and RBB-150). In order to minimize the harmful effects of RR-120 and RBB-150, the capacity of MgAl-layered double hydroxide for removing of these contaminants was studied herein. Batch adsorption experiments were conducted to investigate the effect of various operating parameters, such as solution pH, contact time, dye concentration, and temperature in order to provide optimal conditions for removal. Structural and morphological analyses were used to highlight the assembly and/or interaction LDH-dye. The state of equilibrium of RR-120 and RBB-150 adsorption was pH- and temperature-dependent and followed the pseudo-second-order rate model. Also, the equilibrium adsorption data of both dyes were found to adopt the Langmuir type isotherm model, which assumes a monolayer arrangement in LDH-dye. Furthermore, the effects of four major coexisting and competing mono- and divalent interlayer anions, such as NO3−, Cl−, CO32−, and SO42−, on the uptakes of RR-120 and RBB-150 were studied and the results showed that NO3− anions had insignificant effect on the uptakes of RR-120 and RBB-150 by MgAl. An equivalent study on the presence of both dyes in competitive trial adsorption/desorption from binary aqueous solution was investigated. And finally, the reuse operation of recovered material after dye adsorption was tested in up to 5 cycles of recyclability.
- 1 February 2018
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 6 (1) , 803-810
Methanogenesis control in bioelectrochemical systems: A carbon footprint reduction assessment
- 1 February 2018
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 6 (1) , 803-810
Methanogenesis control in bioelectrochemical systems: A carbon footprint reduction assessment
- 13 December 2017
- Published by Springer Nature
- p. 145-147
Biodegradation of Urban Stromwater Pollution in a Sequence of Constructed Porous Riffles in a Mediterranean Creek
- 13 December 2017
- Published by Springer Nature
- p. 145-147
Biodegradation of Urban Stromwater Pollution in a Sequence of Constructed Porous Riffles in a Mediterranean Creek
- 7 October 2017
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 24 (36) , 27879-27896
Nanoscale zero-valent iron functionalized Posidonia oceanica marine biomass for heavy metal removal from water
Because of the excellent reducing capacity of nanoscale zero-valent iron (NZVI), it can be used as alternative materials for the removal of a variety of reducible water contaminants including toxic metals. The current paper reports the research results obtained for self-prepared biosorbent, Posidonia oceanica biomass, activated in alkaline medium and functionalized with NZVI particles. The structural characteristics, surface morphology, and binding properties of the resulting nanobiosorbent are presented. Batch comparative adsorption trials including adsorption kinetics and isothermals onto raw Posidonia, Posidonia–OH and Posidonia–OH–NZVI were investigated on three heavy metal ions: Cd(II), Pb(II), and Cu(II). The nanobiosorbent showed better properties, such as high reactivity and high uptake rate through the sorption process. The toxic metal removal has been monitored in terms of pseudo-first- and pseudo-second-order kinetics, and both Langmuir- and Freundlich-type isotherm models have been used to describe the sorption mechanism. The experimental data of all studied systems showed that the uptake kinetics follow the pseudo-second-order kinetic model and the equilibrium uptake can adopt the Langmuir-type isotherm model which assumes a monolayer coverage as the adsorption saturates and no further adsorption occurs. The thermodynamic results confirm that all sorption processes were feasible, spontaneous and thermodynamically favorable. Zeta potential data displayed that Cd(II), Pb(II), and Cu(II) tend to be reduced after exposure on the Posidonia–OH–NZVI surface. Furthermore, sorption competitions of the metals from binary and ternary systems were carried out onto Posidonia–OH–NZVI in order to gain further insight into the sorption efficiency of this material. Therefore, as a result, the proposed new nanobiosorbent could offer potential benefits in remediation of heavy metal-contaminated water as a green and environmentally friendly bionanocomposite.
- 7 October 2017
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 24 (36) , 27879-27896
Nanoscale zero-valent iron functionalized Posidonia oceanica marine biomass for heavy metal removal from water
Because of the excellent reducing capacity of nanoscale zero-valent iron (NZVI), it can be used as alternative materials for the removal of a variety of reducible water contaminants including toxic metals. The current paper reports the research results obtained for self-prepared biosorbent, Posidonia oceanica biomass, activated in alkaline medium and functionalized with NZVI particles. The structural characteristics, surface morphology, and binding properties of the resulting nanobiosorbent are presented. Batch comparative adsorption trials including adsorption kinetics and isothermals onto raw Posidonia, Posidonia–OH and Posidonia–OH–NZVI were investigated on three heavy metal ions: Cd(II), Pb(II), and Cu(II). The nanobiosorbent showed better properties, such as high reactivity and high uptake rate through the sorption process. The toxic metal removal has been monitored in terms of pseudo-first- and pseudo-second-order kinetics, and both Langmuir- and Freundlich-type isotherm models have been used to describe the sorption mechanism. The experimental data of all studied systems showed that the uptake kinetics follow the pseudo-second-order kinetic model and the equilibrium uptake can adopt the Langmuir-type isotherm model which assumes a monolayer coverage as the adsorption saturates and no further adsorption occurs. The thermodynamic results confirm that all sorption processes were feasible, spontaneous and thermodynamically favorable. Zeta potential data displayed that Cd(II), Pb(II), and Cu(II) tend to be reduced after exposure on the Posidonia–OH–NZVI surface. Furthermore, sorption competitions of the metals from binary and ternary systems were carried out onto Posidonia–OH–NZVI in order to gain further insight into the sorption efficiency of this material. Therefore, as a result, the proposed new nanobiosorbent could offer potential benefits in remediation of heavy metal-contaminated water as a green and environmentally friendly bionanocomposite.
- 30 December 2016
- Published by International Information and Engineering Technology Association in Instrumentation Mesure Métrologie
- Vol. 15 (3-4)
Influence des faciès hydro-morphologiques sur la répartition des polluants dans les sédiments d’une rivière périurbaine. La Chaudanne (France)
Influence des faciès hydro-morphologiques sur la répartition des polluants dans les sédiments d’une rivière périurbaine. La Chaudanne (France) Influence of instream geomorphic units on the spatial distribution of pollutants in suburban river sediments. Case of the Chaudanne (France
- 30 December 2016
- Published by International Information and Engineering Technology Association in Instrumentation Mesure Métrologie
- Vol. 15 (3-4)
Influence des faciès hydro-morphologiques sur la répartition des polluants dans les sédiments d’une rivière périurbaine. La Chaudanne (France)
Influence des faciès hydro-morphologiques sur la répartition des polluants dans les sédiments d’une rivière périurbaine. La Chaudanne (France) Influence of instream geomorphic units on the spatial distribution of pollutants in suburban river sediments. Case of the Chaudanne (France
- 1 November 2016
- Published by Elsevier in Applied Surface Science
- Vol. 386, 352-363
Layered double hydroxide materials coated carbon electrode: New challenge to future electrochemical power devices
- 1 November 2016
- Published by Elsevier in Applied Surface Science
- Vol. 386, 352-363
Layered double hydroxide materials coated carbon electrode: New challenge to future electrochemical power devices