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International audience; Additive manufacturing is a powerful tool to design materials with original properties. An innovative design of poly (Ethylene Vinyl Acetate) (EVA) containing 30 wt.-% of Aluminum TriHydroxide (ATH) was reported in a previous paper and liquids (water or potassium carbonate aqueous solution) were incorporated in the 3D printed structure. These multi-materials showing interesting properties, but stability, control and processing of these liquid-containing systems were an issue due to porosity of the polymeric matrix. To overcome this issue, the use of hydrogels is considered in this study: being either solid or highly viscous, hydrogels can retain water in the design, despite the high porosity of the EVA/ATH matrix. In this paper, the liquid phase was substituted by flame retardant hydrogels (based on agar, alginate or poly (vinyl alcohol) - PVA), containing in particular vermiculite platelets and for the hydrogel based on alginate, K2CO3 as flame retardant fillers. Excellent behavior under a 50 kW/m2 heat flux during a cone calorimeter test was obtained, with fast extinguishment of the flame and a low peak of Heat Release Rate (pHRR) and Total Heat Release (THR). The physical barrier formed by vermiculite platelets during the test, as well as the condensed phase mechanism of K2CO3 were found to be responsible for these excellent results, as found by confocal microscopy observations, electron probe micro analysis and X-Ray diffraction experiments.

This work aims at presenting and comparing the antifouling and antibacterial behaviour of three biomimetic surfaces targeting dairy fouling reduction, namely atmospheric plasma-sprayed silane-based thin films, lubricated slippery surfaces and femtosecond laser textured lotus-like surfaces. Fouling tests were conducted on a pilot-scale pasteurization plant fed with a model whey protein and calcium foulant solution and tested samples were placed in isothermal holding-like conditions. Detailed characterizations of the substrates before and after fouling test allowed connecting their surface properties to their antifouling performances. The best result was obtained with the nano-rough plasma coatings which led to a substantial fouling reduction for two consecutive pasteurisation runs. These surfaces were subsequently tested towards bacterial adhesion with three different foodborne pathogenic strains, again demonstrating better performances than bare stainless steel.

Whatever the dairy derived fluids that are heat processed, many studies have demonstrated the key role of beta-lactoglobulin (β-lg) denaturation in the initiation of a dairy fouling and mentioned that interactions between β-lg, phosphate and calcium ions are essential in fouling growth. However only few authors have reported the influence of the phosphate/calcium molar ratio on fouling mechanisms. To partly fill this gap, various whey protein solutions (composed mainly of β-lg) having different phosphate:calcium molar ratios were prepared by rehydrating a whey protein isolate powder and by adding calcium chloride and various amounts of soluble inorganic phosphate (noted Pi). Fouling experiments were carried out at pilot scale using a plate heat exchanger (PHE) at a fixed temperature profile and the deposited mass per channel was measured. Finally, the chemical composition and structure of the proteinaceous fouling layer were observed using an Electron Probe Micro Analyser. Results clearly demonstrated that the phosphate:calcium molar ratio modified the deposit structure and influenced substantially the amount of fouling. These results suggest that the relative proportion of calcium phosphate and calcium ions governs the mechanism of fouling build-up and also sets, to a certain extent, the fouling ability of the whey protein solutions.

Lowering fire hazard raised by combustible materials such as plastics may be achieved by the use of suitable flame retardant treatments, like fire protective coatings. However, exposure to long-term environmental conditions can cause loss of their functional properties, thus reducing their effectiveness over time. This is why two or three different layers with specific properties (e.g. adhesive, fire retardant and hydrophobic) are generally needed to provide durable fire retardancy. Effective and economical self-layering coatings can be developed to reduce the number of layers without compromising the advantages of the actual system. In this work, the efficiency of applying a silicone based coating to fire retard polycarbonate and the modification of the behaviors of the system, using a mixture of epoxy/silicone resins, a curing agent and either iron oxide or calcium carbonate as fire retardant filler is investigated. Self-stratification and fillers dispersion were evidenced by microscopic analyses coupled with chemical detection, the flame retardant properties using Limiting Oxygen Index (LOI), UL-94, Mass Loss Calorimetry (MLC), Thermogravimetric analyses (TGA) and a tubular furnace, and aging resistance by accelerated thermal, humidity and UV exposure. It appears that the selected fillers have no negative effect on the layering process when introduced from 2.5 to 10 vol.%: perfect stratification is obtained, with the silicone layer being the top layer. The best improvements in terms of fire retardant properties, adhesion and fillers dispersion were obtained by incorporating 2.5 vol.%: V0 rating at UL-94 and 33 and 35 vol.% at LOI with Fe2O3 and CaCO3 respectively were measured when a 200 μm wet thick coating was applied. The coating containing iron oxide was unaffected by weathering conditions. Finally, the application of those coatings on polycarbonate allows the formation of a protective barrier which limits substrate/flame mass transfers. It therefore results in (i) a delay of the time to ignition, (ii) the inhibition of the flame spread and of dripping when submitted to a flame, and (iii) a reduction of the combustibility of polycarbonate. A modification of the structure of the silica network formed by the particles which enhances the barrier effect of the silicone-based layer would be the most probable assumption to explain these excellent results.

International audience; Because of its widespread use in furniture upholstery, buildings, and transportation, the flame retardancy of flexible polyurethane foam is a matter of great concern. In an effort to impart fire resistance in an environmentally benign manner, hexagonal boron nitride (h-BN) nanosheets were dispersed by an aqueous route and deposited as a single bilayer with polyethylenimine (PEI) on flexible polyurethane foam by using layer-by-layer assembly. Butane torch exposure and cone calorimetry show that the nanocoating performs similarly to vermiculite clay (VMT), while in situ quantitative gas phase analysis reveals that carbon monoxide emissions are lower with h-BN. The PEI/h-BN system also maintains foam flexibility and protects against weathering, preventing yellowing. These combined properties make the use of h-BN nanoplatelets an interesting alternative for the protection of polyurethane foam (and perhaps other flammable substrates).

Epoxy-based intumescent coatings are effective solutions for protecting steel against fire. To design a successful product, it is, however, of primary importance to investigate its long-term durability. Some of these coatings do not resist accelerated aging conditions such as contact with salted water. One solution to overcome this drawback consists of applying a specific topcoat. In this work, various topcoats were applied on a model intumescent coating. Topcoats were shown to impact, under heating, the char expansion, char morphology, and char strength. The general trend is that the topcoats, before any aging exposure, improve the fire resistance behavior of the intumescent coatings. Most topcoats, however, do not limit penetration of salted water into the coating, thus affecting the intumescent properties. Only a silane-based topcoat was reported to trap or limit the diffusion of sodium and chlorine ions, thus protecting the underlying intumescent coating.

Lignin is an abundant polyphenol biopolymeric material. Due to its aromatic structure it develops a char under fire conditions. Lignin was used as flame retardant in acrylonitrile-butadiene-styrene (ABS). Enhancement of flame retardancy was observed, and the lignin was then phosphorylated to achieve highest performance. For the first time, characterization of FR phosphorylated lignin (P-LIG) was undertaken in detail. Grafting phosphorus onto lignin significantly increases the amount of residue from the polymer blend at high temperature. At 30 wt.%, P-LIG is well dispersed in ABS and leads to a significant reduction of the peak of heat release rate. It is shown that P-LIG promotes char formation by reacting with ABS during thermal decomposition. The char is therefore more cohesive and acts as a protective layer, such that less fuel from ABS degradation is released to the flame. Thus phosphorylated lignin is as a promising bio-based flame retardant for ABS.

Effect of accelerated ageing on neat and flame retarded (FR) polylactide (PLA) has been investigated. The influence of temperature and relative humidity on (i) the visual aspect, (ii) the fire performances, (iii) the molecular mass and (iv) the thermal properties of the formulations has been evaluated. The flame retardant (FR) properties of samples before and after ageing were compared using Limiting Oxygen Index (LOI) and Mass Loss Calorimetry (MLC). It was reported that degradation of PLA, mainly driven by hydrolysis phenomenon, is accelerated in presence of FR fillers (melamine and ammonium polyphosphate). This is even more pronounced when an organomodified montmorillonite is added. However the FR properties are enhanced after ageing due to the physicochemical of the flame retarded materials (e.g. migration of the flame retardants, decrease of the molecular mass…).

The aim of this work was to study the photocatalytic degradation of Methylene Blue and phenol by nano-particles coated on diatomite as a new nano-composite catalyst. Titanium dioxide (Degussa P25) was immobilized on diatomite powder at different compositions by a very simple and low cost technique. Diatomite powder (also called Kieselguhr) is an Algerian substance with a snow-white color and porosity greater than 72%. High porosity allowed the diatomite powder to float on the surface of water providing a means for the treatment process that enabled separation from water without any need for pumping as well as the exposure to solar radiation when supported beneath titanium dioxide (TiO2) during photocatalysis. The morphology characterization of the prepared catalysts was carried out by X-ray diffraction analysis, scanning electron microscopy and infrared spectroscopy (IR). Photocatalytic activity was initially tested in a single reactor followed by pH, conductivity and absorbance analyses. Photocat...

International audience; Self-stratification is an innovative one-step process used to design multi-functional coatings gathering simultaneously in a one-pot formulation the primer, the intermediate layer and the top coat properties. Many selfstratifying coatings contain oil-based epoxy resins but the literature is scarce in the development of “greener” solutions. In this work, silicone resins and bio-based epoxy resins were dissolved in various solvent blends, applied on a composite substrate and cured under different conditions to obtain stratified coatings. To reach aperfect stratification, the influence of various parameters including (i) the surface tension and the polarity of the resins, (ii) the solvents volatility, (iii) the curing temperature and (iv) the reactivity of the epoxy/amine reaction was studied by a systematic approach. In accordance with the literature, it was demonstrated that a large difference in surface energy and polarity favors resins separation. The volatility of the solvent blend was also shown to be a key factor in the stratification process. However, the predominant parameter, rarely taken into account, isthe curing temperature, which impacts the cross-linking reaction of the epoxy resin. The increase in molecular weight (MW) of epoxy resins due to the cross-linking reaction favors the incompatibility between resins by increasing the difference in MW between epoxy and silicone resins. Thus, optimization of process conditions allowed the design of perfectly stratified bio-based epoxy/silicone coatings. The mechanism of film stratification was also elucidated thanks to in-situ analyses.

International audience; This work aims at studying the impact of silane-based coatings, generated by atmospheric pressure plasma spraying (APPS) of a liquid precursor (hexamethydisiloxane – HMDSO), on dairy antifouling and antibacterial properties of food-grade 316L stainless steel. The influence of the manufacturing parameters (precursor flow rate, nozzle-to-substrate distance and scanning speed) on the coatings properties was investigated using a wide range of characterization techniques (drop shape analysis, X-Ray Mappings, Scanning Electron Microscopy, Fourier-Transformed Infrared Spectroscopy, Atomic Force Microscopy). Coating’s roughness in particular was shown to strongly increase when precursor flow rate increases. A pilot pasteurizer, fed with a model foulant solution (whey protein and calcium), allowed performing two consecutive industrial-like isothermal dairy fouling tests, revealing the promising anti-fouling properties of the HMDSO-coated steel. A fouling reduction of up to 90% compared to bare stainless steel was achieved after first cycle for all samples. The second fouling run allowed to select the best-performing sample, which kept the same antifouling properties as in the first test. Its mechanism of action was investigated, which revealed that a nanostructured, Si-O-Si rich surface was efficient to prevent isothermal dairy fouling. The adhesion of the pathogenic bacterium Staphylococcus aureus also proved to be impacted by this plasma coating, with a significant decrease of adhered cells (−30% compared to native stainless steel).

This paper aims at developing an innovative approach to characterize the char residue of an intumescent coating obtained after a UL1709 furnace test. The intumescent formulation is based on an epoxy resin and contains numerous additives including zinc borate, ammonium polyphosphate and silicate fibers. The purpose is to characterize the numerous reactions that can occur upon burning using crossed methods including Electron Probe Micro-Analysis (EPMA), X-ray diffraction (XRD) and 1D/2D solid state Nuclear Magnetic Resonance (NMR). In particular, it emphasizes the potential of the advanced NMR technique namely two-dimensional Dipolar Heteronuclear Multiple Quantum Correlation (2D D-HMQC) NMR. As a result, EPMA evidenced that B/P and B/Si are located in the same domain suggesting the formation of boron-phosphorus and/or boron-silicone containing compounds on the sample surface. H3BO3 was identified by XRD as a main crystalline specie, additional species (e.g. SiO2, Zn4O(BO2)6) were also identified. The borate, silicate and phosphate chemical species were then characterized using 1D NMR but no definitive assignments could be given. To specify those assignments, 2D D-HMQC NMR was performed and the formation of amorphous borophosphates and borosilicates was evidenced emphasizing the chemical reactivity between the ingredients of the formulation. It was suggested that these species allow reinforcing the char and improving the fire protective properties of the coatings. This work highlights the particular interest of advanced NMR technique, which provides unique information on the characterization of intumescent char.

Flexible polyurethane foam is one of the most versatile materials used in upholstered products; however, untreated polyurethane flexible foams are prone to rapid fire growth. In order to overcome issues encountered by the addition of flame retardant additives during the manufacturing process, the sol–gel process was evaluated to make flexible polyurethane foams flame retardant. Various formulations using different catalysts and monomers were prepared and deposited on flexible polyurethane foams by an impregnation process. Coating morphology was assessed by scanning electron microscopy analyses to optimize the formulation and to obtain a homogenous crack-free coating. Flame retardant properties were measured by mass loss calorimeter and UL 94, and thermal degradation was evaluated by thermogravimetric analysis. Chemical and structural analyses were carried out using attenuated total reflectance Fourier transformed infra-red spectroscopy and electron probe microanalysis. It appears that when a mixture of an appropriate ratio of 3-amino propyl triethoxysilane and diethyl phosphate is prepared in association with tetraethoxysilicate and methyltriethoxysilicate and deposited on flexible polyurethane foam, the coating shows an intumescent behavior when exposed to a flame. The foam also self-extinguishes after 30 seconds of flame application during UL94 test and a 60% reduction of the peak of heat release rate is obtained under mass loss calorimeter conditions.

A new, efficient and fast process was developed to coat poly(ethylene terephthalate) (PET) fabrics with acrylic acid (AA) and this novel eco-friendly material was designed to be used as a filtration medium for complexing heavy metals from aqueous media. PET is impregnated with acrylic acid, and directly polymerized using a KrF excimer laser. The conditions of irradiation were optimized using the experimental design technique: a 40 mm × 3.5 mm surface was irradiated per pulse, and 24 mJ/cm 2 and 700 pulses were necessary to obtain a good coating without degrading the textile structure. For industrial purpose, these conditions were extended to treat larger surfaces (40 mm × 11.5 mm pulse) using a fluence of 24 mJ/cm 2 and 700 pulses. Scanning Electron Microscopy (SEM) and X-ray Photoelectron Spectroscopy (XPS) were carried out to characterize the functionalized surfaces. A thick coating, resistant to low-temperature-washing was obtained. Finally, the efficiency of this coated textile was evaluated with copper sulfate solutions: 0.131 mg copper was trapped per cm 2 of PET, which is a promising result.

This paper investigates the flame retardant (FR) mechanism of action of a flexible PU foam, flame retarded with a sol-gel coating made of a mixture of tetraethoxysilane (TEOS), methyl triethoxysilane (MTES), 3-amino propyl triethoxysilane (APTES) and diethyl phosphite (DEP) in an ethanol/water solution. To build a mechanism of action, the coating as well as the residues obtained after fire testing were analyzed using solid state nuclear magnetic resonance (NMR), rheology, thermogravimetric analyses coupled with infrared detection (TGA-FTIR), microcalorimetry of combustion (MCC), smoke box and Pyrolysis Gas chromatography coupled with mass spectrometry (Py-GCMS). The coating shows an intumescent behavior upon burning exhibiting significant expansion and bubbling. The expansion occurs in two steps: a first step around 190 °C, related to the release of ethanol, and a second one around 380 °C, related to the release of non-degraded DEP, ammonia and propylene during degradation of the PU matrix. The flame retardant effect occurs (i) in the condensed phase by intumescence, which yields a thermal insulating layer made of a SiO2 and Si-O-P network mixed with orthophosphate at the surface of the PU foam, but also (ii) in the gas phase by the release of non-degraded DEP, which acts as free radical scavenger. The coating allows the protection of the underlying PU foam during burning as well as the reduction of the amount of smoke released.

International audience; In this report, indium-tin-oxide (ITO)-layer extraction from end-of-life (EOL) Liquid Crystal Displays (LCDs) was discussed by sulfuric acid leaching with simultaneous application of ultrasonication on the ITO-side of glass/ITO panels, exhibiting various dimensions. Applying this technique presents several advantages compared to the traditional leaching process such as fast and controllable kinetics, high extraction yield of indium and tin, selective recovery of these two metals possible, and the opportunity to recycle the neat glass separately avoiding additional separation processes. ITO-dissolution kinetics from EOL LCD panels were investigated as function of leaching time and acidity of sulfuric acid. At a temperature of 60°C, a nearly quantitative indium yield was obtained using an acid concentration of 18 mol/L by simultaneous application of ultrasonication, whereas only 70 % were recovered in the absence of ultrasound. Results from ICP-AES agreed well with SEM/BSE observations demonstrating the high efficiency of the ultrasound assisted process since only 3-4 min were required to obtain maximum ITO recovery.

Pasteurization of dairy products is plagued by fouling, which induces significant economic, environmental and microbiological safety concerns. Herein, an amphiphilic silicone coating was evaluated for its efficacy against fouling by a model dairy fluid in a pilot pasteurizer and against foodborne bacterial adhesion. The coating was formed by modifying an RTV silicone with a PEO-silane amphiphile comprised of a PEO segment and flexible siloxane tether ([(EtO)3Si-(CH2)2-oligodimethylsiloxanem-block-(OCH2CH2)n-OCH3]). Contact angle analysis of the coating revealed that the PEO segments were able to migrate to the aqueous interface. The PEO-modified silicone coating applied to pretreated stainless steel was exceptionally resistant to fouling. After five cycles of pasteurization, these coated substrata were subjected to a standard clean-in-place process and exhibited a minor reduction in fouling resistance in subsequent tests. However, the lack of fouling prior to cleaning indicates that harsh cleaning is not necessary. PEO-modified silicone coatings also showed exceptional resistance to adhesion by foodborne pathogenic bacteria.

A classical Schiff base N,N′-bis(4-hydroxysalicylidene)ethylenediamine (L2), a member of the Salen group that has been introduced as a non-phosphorus and non-halogen flame retardant in thermoplastic polyurethane (TPU) is found to operate in an intriguing way to fire retard the material. L2 blended with TPU significantly improves the inherent flammability of TPU without a synergist. A plausible mechanism including intermediates in the reinforcement of this elastomer towards flame retardancy is elaborated in line with the char forming abilities of this β-resorcylaldehyde based Schiff base. Conclusions were drawn based on the input from thermal, spectroscopic, microscopic and operando spectroscopic techniques. While its un-substituted counterpart, N,N′-bis(salicylidene)ethylenediamine (L1) lags behind in performance, its structural isomer N,N′-bis(5-hydroxysalicylidene)ethylenediamine (L3) is equally efficient but exhibits another mechanism of action. The performance of L2-TPU is found to be mainly in a condensed phase and is due to decoding of intrinsic cross-linking ability of the key building block of the additive i.e. resorcinol via structural transformation over a range of temperature. This results in the methylene bridged phenolic resin type material having high temperature stability. The process is also found to interfere with TPU unzipping process delaying its thermal degradation and favoring extensive cross-linking promoting char formation with insulative properties.

Flame retardancy of flexible polyurethane foams has become an issue due to very severe regulations. To overcome the challenge of incorporating flame retardant (FR) additives during the foaming process without altering the foam properties, a plasma surface treatment was used for the first time in this work: a cold plasma induced graft-polymerization of phosphonate containing precursors (diethylvinylphosphonate-DEVP) with or without a crosslinking agent (1,4 butanedioldiacrylate) was applied on open cell flexible polyurethane foams (PUF). The flame retardant properties of these foams, before and after further rinsing, were evaluated using horizontal UL-94 test for 10 s and 60 s. One of the tested systems (DEVP + crosslinker), even after sonication, completely stops the melt dripping of the foams when exposed to the flame of the butane torch and charring occurs. This efficient surface treatment was characterized before and after burning by Scanning Electron Microscopy (SEM), electron probe microanalysis (EPMA), 31P solid state NMR and X-ray Photoelectron Spectroscopy (XPS). Its FR mechanism of action was then further investigated using microscale combustion calorimetry (MCC), thermogravimetric analyses coupled with infrared Fourier transform spectroscopy (TGA-FTIR), pyrolysis gas-chromatography coupled with mass spectrometry (GC-MS pyrolysis) and 31P solid state NMR. The results obtained show that it is necessary (i) to use the crosslinking agent, as DEVP mainly reacts with this crosslinker and (ii) to activate the PU foam before graft-polymerization to promote further reaction with the crosslinker. The characterizations also proved that before sonication, non-reacted DEVP precursors mainly act in the gas phase, preventing ignition, whereas after sonication the covalently grafted phosphorus containing species mainly act in the condensed phase to form phosphonic acid which will promote charring and thus will limit dripping and flame spread.

The self-stratification is an eco-efficient process since it reduces solvent emission, time of implementation and labor cost. Moreover it could lead to the development of a large range of new products for extensive application fields. For self-stratification to occur, liquid coatings must contain at least two incompatible resins, giving rise in “one pot” to a two-phases mixture after the formation of the solid film. In this work, an innovative self-stratifying coating, based on an epoxy/silicone blend, has been developed and applied on a plastic substrate (Polycarbonate). The perfect self-stratification of this system was evidenced by microscopic analysis coupled with X-ray mappings. The influence of solvents and a curing agent on the stratification process has been investigated. It is shown that the system diluted in butylacetate:xylene (at a 1:1 ratio) leads to the best stratification pattern, with the silicone phase located on the top of the coating. Three pigments (red iron oxide, calcium carbonate and zinc phosphate) were also incorporated in this epoxy/silicone system. They do not affect stratification, whereas visual appearance and adhesion are strongly dependent on the phase in which pigments are dispersed, as well as on the solvent used.

Glass-fiber reinforced polyamide 66 is flame retarded with a mixture of melamine-poly(zinc phosphate), (Safire®400) and diethyl aluminium phosphinate. The performance of this synergistic combination of additives is multi-modal and a comprehensive investigation is undertaken to elucidate the underlying flame retardancy mechanism. The strategy was to characterize the different chemical species responsible for flame retardancy that are generated in gas and condensed phases under different fire scenarios. Following heat release rate (HRR) curve of flame retarded polyamide formulations obtained by mass loss calorimeter, samples in different stages of degradation are collected and investigated. Further flame retardants and formulations were degraded in tubular furnace whose temperature protocol relied on thermal degradation profile obtained from thermogravimetric analysis (TGA). In either case, species generated in condensed phase were studied by solid state nuclear magnetic resonance spectroscopy (magic angle spinning (MAS) NMR; 27Al, 31P and 13C), Fourier transform Infra-red spectroscopy (FTIR), X-ray powder diffraction (XRD), electron probe microanalysis (EPMA), scanning electron microscopy (SEM), and optical microscopy, whereas TGA coupled FTIR, and pyrolysis gas chromatography mass spectrometry (Py/GC/MS) were utilised to investigate species released in gas phase. Flame retardancy mechanism is elaborated based on the identification of the chemical species in both gas and condensed phases and their specific contributing role.

A higher analogue in the melamine polyphosphate family, melamine-poly(aluminium phosphate) (Safire®200), that has shown flame retardancy along with aluminium phosphinate in glass-fibre reinforced polyamide 66 was investigated to elucidate their mode of action. The mechanistic investigation is based on examining the chemical species formed in the condensed and gas phase under different fire scenarios. Samples at different stages of degradation were collected based on the heat release rate (HRR) curve of cone calorimetry and further analysed. Additionally, formulations and flame retardants were also pyrolysed at characteristic temperatures in a tubular furnace based on their thermogravimetric analysis (TGA) profile and investigated. A fire retardancy-quenching mechanism is mapped out on the basis of input from solid state nuclear magnetic resonance spectroscopy (MAS NMR; 27Al, 31P and 13C), Fourier transform Infra-red spectroscopy (FTIR), X-ray powder diffraction (XRD), electron probe microanalysis (EPMA), scanning electron microscopy (SEM), and optical microscopy on degraded samples. Gas phase analysis was studied by TGA coupled FTIR.

The aim of this work was to prepare a nonwoven polypropylene (PP) textile functionalized with bioactive molecules in order to improve simultaneously anticoagulation and antibacterial properties. The immobilization of either heparin (anticoagulation agent) or gentamicin (aminoglycoside class antibiotic) alone has already been proven to be effective on PP nonwoven textiles. In this work, we managed to go further, by immobilizing both heparin and gentamicin at the same time on one unique textile. A successive immersion in different heparin and gentamicin bathes successfully led to a dual drug coated textile, as confirmed by several characterization techniques (Fourier transform infrared-attenuated total reflectance, X-ray photoelectron spectroscopy, and scanning electron microscopy). The immobilization times were varied in order to determine the best compromise between cytocompatibility, anticoagulant effect, and antimicrobial activity. Short immersion times in gentamicin solutions confer very good antimicrobial activity to the textile and avoid cytotoxicity, whereas long immersion times in heparin solution were necessary to observe a significant anticoagulant effect.

The fire performance of a curable-silicone based coatings containing expandable graphite (EG) and an organoclay is evaluated in hydrocarbon fire scenario (standard UL1709) using a lab-scale furnace test. It is shown that the use of organoclay allows achieving better performance. The influence of the clay as additional filler is investigated on the fire performance and on the mechanical properties of the char. It is shown that the clay increases significantly the mechanical properties of the char and hence, the fire performance of the silicone based coating. In a next part, the silicone/clay material was characterized by electron microscopy, wide-angle X-ray scattering and solid state 29 Si nuclear magnetic resonance (NMR). It evidences the nanodispersion of the clay into the silicone matrix and two main interactions: (i) intercalation of some silicate layers and (ii) chemical reactions between the hydroxyl groups of the clay and the silicone matrix. Finally, X-ray fluorescence of the residue after fire testing shows the organoclay is present uniformly throughout the thickness of the char, due to the previous interaction, and hence increasing the cohesion of the char.

The fire performance of two curable-silicone based coatings containing 25% expandable graphite (EG) are evaluated in hydrocarbon fire scenario (standard UL1709) using a lab-scale furnace test. In this paper, the influence of the catalyst on the fire performance are investigated. Two organometallic titanium based- and tin based catalyst are used to make the curable silicone crosslink. When titanium based catalyst is used, the fire performance are higher and the mechanical properties of the char is better than that when tin is used as catalyst. To explain this surprising different fire behavior, the two residues after the furnace test were analyzed by X-ray photospectroscopy. It has been demonstrated that in the case of titanium based catalyst, the char is composed of graphite embedded by crosslinked silicone structure compare to linear silicone structure in the case of tin based catalyst. The two silicone resins were characterized by Fourier Transform Infrared spectroscopy, 29Si NMR, thermogravimetric analyses, EPMA (electron probe microanalyses). It was highlighted that the tin migrates into the surface during the crosslinking of the matrix leading to a low thermal stability and, thus, low fire performances. Whereas, when titanium based catalyst is used, it participates to the silicone network with the formation of Si–O–Ti bounds increasing the thermal stability of the matrix and so enhancing the fire performance of the silicone/EG based coating.

The present study assesses the formation of an interfacial oxide layer on aluminum alloys concomitant to the electrodeposition of an anaphoretic coating. The morphology, size, chemical composition and corrosion resistance properties are investigated for 2024-T3 clad aluminum substrate. The morphology and thickness of the oxide layer was examined using TEM. On the other hand, a ToF-SIMS method combining depth profiling and high resolution imaging has been developed as a new approach to determine simultaneously the chemical composition, the thickness and the homogeneity of the oxide layer. The results obtained with this method are validated through comparison with those from the TEM standard approach. Finally the two complementary methods have been used to investigate the growing mechanism of the oxide layer.

The self-stratifying approach is a one step process allowing the formation of a complex laminated coating structure at the surface of plastics or other substrates, combining optimized surface and adhesion properties. These coatings have already been developed for various application fields but have never been considered for fire retardant purposes, whatever the substrate involved. In this work, the self-layering concept has been used to make polycarbonate fire retardant, using a mixture of epoxy and fluoropolymer resins, and iron oxide as flame retardant additive (10 wt%). Self-stratification was evidenced by microscopic analyses. The flame retardant properties were evaluated according to Limiting Oxygen Index (LOI), UL-94 and Mass Loss Calorimetry (MLC). Weathering resistance by accelerated UV, thermal and humidity exposure was also considered. In the first part, the effect of solvent on the self-layering process was investigated. It was shown that the system diluted in a blend of butylacetate : xylene (1 : 1 ratio) exhibits a perfect stratification and excellent adhesion onto polycarbonate. In such a system, an outstanding improvement of the fire retardant properties (V0 rating at UL-94 and 32 vol% at LOI), unaffected by weathering (both UV and temperature/humidity exposure), was observed when a 200 μm wet thick coating was applied. The coating allows the formation of a protective barrier and the presence of metal particles avoids dripping and promotes a charring effect.

International audience; Three different accelerated ageing scenarios were applied on flame retarded polylactic acid (FR-PLA). The influence of (i) Temperature and UV-light exposure (T/UV), (ii) Temperature and relative humidity exposure (T/RH) and (iii) combined Temperature, UV-light and relative humidity (T/UV/RH) exposure on (i) the morphology, (ii) the physico-chemical properties and (iii) the fire performances of FR-PLA were evaluated. The influence of FR fillers (melamine, ammonium polyphosphate and organomodified montmorillonite) as well as the associated mechanisms of degradation (i.e. photo-degradation under T/UV, hydrolysis under T/RH and a combination of both phenomena under T/UV/RH) were explained. The flame retardant properties of FR-PLA before and after ageing were compared using Limiting Oxygen Index (LOI) and Mass Loss Calorimetry (MLC). It was reported that FR-PLA aged under T/UV/RH conditions is more degraded compared to FR-PLA exposed to T/RH or T/UV. Surprisingly, the FR properties are enhanced after ageing, even if the degradation of the samples is observed.

Lignin is an abundant polyphenol biopolymeric material. Lignin was phosphorylated thanks to the presence of reactive hydroxyl groups in its structure. A detailed characterization allowed us to prove that phosphate groups are covalently bonded to the lignin's structure. The thermal stability of lignin was improved with the presence of phosphorus and was evaluated at 3% w/w. The thermal decomposition of lignin was deeply investigated through gas and condensed phases analyzes. The phosphorus was found to promote dehydration and decarboxylation reactions, thus increasing the amount of carbonaceous residue which was more stable at high temperature. The combustibility of lignin was also lowered when phosphorylated. Finally, even if half of the initial amount was released in the gas phase, the phosphorus mainly acts in the condensed phase by forming different species, which prevents the residue from oxidation.

Intumescent coatings, mainly composed of ammonium polyphosphate, pentaerythritol and melamine, are widely used in the field of fire protection of steel structures. The objective of this study was to investigate how the presence of two different inorganic fillers (titanium dioxide and mineral fibres) will affect the fire performance of an acrylic-based intumescent coating. In both cases, it was observed that the inorganic filler enabled improvement of the fire-protective behaviour of intumescent paints, maintaining their performance for a longer time. The mode of action was attributed to reinforcement of the char due to the presence of the fillers.

Functionalized polypropylene nonwoven (PP) geotextiles can be used as a new eco-friendly way to trap heavy metals in sediments. Chitosan was chosen as sorbent because of its ability to trap heavy metals, its natural origin (from shells) and its low cost. PP was first functionalized with acrylic acid using a low pressure cold plasma process, in order to bring reactive carboxylic functions onto the surface. Chitosan was then covalently grafted on the acrylic acid modified PP. The functionalized surfaces were characterized by Fourier Transform Infrared Spectroscopy–Attenuated Total Reflectance (FTIR–ATR) and X-ray Photoelectron Spectroscopy (XPS) and evidence of chitosan grafting was given. The ability of the functionalized geotextile to trap heavy metals was then investigated. Copper was chosen as a model heavy metal, and artificial solutions of CuSO 4 were prepared for the experiments. Sorption studies were carried out at 20 °C with Polypropylene-grafted-Acrylic acid-Chitosan (PP-g-AA-chitosan) varying the concentration of copper in polluted solutions to evaluate the maximum of adsorption of the surface: the textile can chelate copper increasingly as a function of the initial copper concentration until 830 ppm. At this concentration, it reaches a plateau at about 30 mg of trapped copper per gram of geotextile. The effects of pH and of the ionic strength (adsorption in a NaCl containing solution) were finally investigated. The trapping of Cu 2+ decreases slowly when the ionic strength increases. When there are 30 g/L NaCl in the artificial polluted solution (like in seawater), only 20 mg of Cu 2+ can be trapped per g of geotextile. Finally, the optimum pH to trap the maximum amount of copper was determined to be 4.8, which corresponds to the optimum pH for the chitosan solubility.

Layer-by-layer (LbL) assembly of nanocoatings on fabric substrates has been very successful in terms of reduction of flammability. In particular, an LbL system comprised ammonium polyphosphate as the polyanion and chitosan as the polycation, applied to cotton fabric, dramatically reduced cotton flammability. At this point, the fire-retardant (FR) mechanism of action of this system has never been fully elucidated. Sonicated and nonsonicated coated cotton fabrics were evaluated using a vertical flame test and mass loss calorimeter. Coating morphology was investigated before and after burning. Thermal analyses and chemical analyses in the condensed phase (and in the gas phase) were conducted to reveal the FR mechanism of action. At the cotton surface, a combination of both condensed (formation of aromatic char) and gas phase (release of water and highly flammable gases) mechanisms impart the FR behavior, promoting a kind of “microintumescence” phenomenon. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 43783.

A polyhedral oligomeric silsesquioxane (POSS) tethered imidazolium surfactant was used to exchange montmorillonite for the preparation of polymer nanocomposites in polystyrene, poly(ethylene-co-vinyl acetate), and polyamide-6 using a melt blending technique. Simultaneous temperature resolved small angle X-ray scattering and wide angle X-ray diffraction was used to monitor the surfactant stability and phase behavior of the polyamide-6 nanocomposites. Good thermal stability of the surfactant was in agreement with thermogravimetric analysis. Transmission electron microscopy revealed a mixed intercalated/exfoliated structure, with the presence of small tactoids exhibiting gallery spacings greater than 3.8 nm in all three polymers. Fluorescently tagged organically exchanged montomorillonite was used to assess the quality of nanoparticle dispersion. Exchanging the montmorillonite with lower loadings of the POSS surfactant slightly increased the size of clay tactoids, but did not significantly alter the gallery spacing or overall dispersion. The results suggest that the bulky and rigid structure of POSS, as well as its tendency to aggregate into ordered crystals, form a bilayer structure in the clay galleries and prevent montmorillonite from completely exfoliating, even in polyamide-6.

Aliphatic polyesters such as polylactide (PLA) currently deserve particular attention in the area of environmentally degradable polymer materials. PLA is produced via polymerization of renewable products, namely lactic acid or lactide. In this work, the synthesis of PLA is done by reactive extrusion via ring opening polymerization of L,L-lactide using a continuous single-stage process which is a fast and an easy method. The resulting PLA is fully characterized by solid state NMR. It is shown that it exhibits properties similar to those of PLA synthesized by the traditional methods. A kinetic model based on a phenomenological approach permits one to describe the polymerization of L,L-lactide. PLA nanocomposites containing multi-wall carbon nanotube (MWNT) are also prepared by reactive extrusion. Reaction to fire of PLA nanocomposite shows a slight improvement of the flame retardancy. The nanodispersion characterized by transmission electronic microscopy (TEM) is acceptable but should be improved to obtain the best flame retardancy. Copyright © 2010 John Wiley & Sons, Ltd.

In this article, we study the behaviour of common and low cost mineral fillers into a polyethylene matrix when exposed to mass loss calorimeter conditions. The different systems are made of linear low-density polyethylene (LLDPE), with 50 wt% of calcium carbonate (CaCO3), magnesium carbonate or talc treated with stearic acid or nontreated. These systems were exposed to an external heat flux of 50 kW/m 2 and their burning behaviours were compared. Significant decrease of heat release rate peaks (PkHRR) was obtained with all these mineral fillers; however, even better results were obtained when particles were treated with stearic acid. Indeed, the system with CaCO3-treated stearic acid leads to a surprising intumescent behaviour. A rheological study showed no impact of stearic acid on the viscosity of the system and did not explain the appearance of the intumescent phenomenon. However, scanning electron microscopy (SEM) shows that stearic acid enhances the dispersion of particles into the polymer and acts as a dispersive agent. The results also show that the aspect ratio of the particles, the cation nature of the carbonates and the polarity of the polymer matrix have an effect on the appearance or not on the intumescent phenomenon. Copyright © 2010 John Wiley & Sons, Ltd.

The aim of this work consisted in improving the heat barrier efficiency of different nonwovens (NW) to protect metallic substrates. The degradation of NW based on phenolic, melamine, polyacrylate, meta-aramid and polyimide fibers has been investigated by thermogravimetric analyses while the heat resistance of the NW has been evaluated by measuring temperature profiles in a heat radiator test. In order to decrease the surface emissivity and protect the fibers, a tetramethyldisiloxane (TMDSO) based plasma polymer has been coated on the NW surfaces using a Plasma Enhanced Chemical Vapor Deposition (PECVD) treatment. The plasma polymer has been characterized: it is composed of polysiloxanes, and the deposit coats homogeneously the surface fibers. Heat radiator tests carried out on the coated NW show that the organosilicon coating allows in most of the cases (phenolic, polyacrylate, meta-aramid and melamine NW) an effective improvement of the heat barrier effect under a radiative heat flux. The structural integrity of the NW under heating is improved as well, except in the case of polyimide based NW fabrics.

In this work, the reaction to fire of thermoplastic polyurethane (TPU) containing polyhedral oligomeric silsesquioxanes (or POSSs) was investigated by mass loss calorimetry. This composite exhibits a large reduction of peak of heat release rate (PHRR) compared to virgin TPU. The protection occurs via an intumescent mechanism. Mechanism of protection is examined in chemical and physical ways. Solid state NMR of carbon and silicon on heat-treated materials reveals that there is no significant chemical interaction between TPU and POSS. Nevertheless the intumescent char is characterized as ceramified char made of silicon network in a polyaromatic structure. The expansion occurs because of the partial volatilization of the organic part of POSS and because of the evolving degrading products of TPU. The formation of this intumescent structure makes an efficient insulating material at the surface of the substrate limiting heat and mass transfer and then decreasing heat release rate.

In this work, we have investigated the intumescent behaviour of linear low-density polyethylene (LLDPE) containing calcium carbonate (chalk) treated by stearic acid. This system swells during burning and creates a protective layer when exposed to an external heat flux of 50 kW/m 2 in a mass loss calorimeter. This system has been fully characterized by FTIR, XRD, TGA and SEM. The carbonation/decarbonation temperatures, the swelling phenomenon and the effect of the thermal stress on the swelling have been examined. The residue is composed of a smooth surface made of chalk and CaO and a bulk of only chalk. Stearic acid allows a good dispersion of chalk particles into the LLDPE matrix, and contributes to form a cohesive network during burning when the thermal stress is high enough. A governing parameter of the intumescent effect is the particle size, which permits the formation of an insulating and cohesive mineral network during burning.

Flame retardant nanocomposites have attracted many research efforts because they combine the advantages of a conventional flame retardant polymer with that of polymer nanocomposite. However the properties obtained depend on the dispersion of the nanoparticles. In this study, three types of polymer flame retarded nanocomposites based on different matrices (polypropylene (PP), polybutadiene terephtalate (PBT) and polyamide 6 (PA6)) have been prepared by extrusion. In order to investigate the dispersion of nanoparticles in the polymer containing flame retardant, conventional methods used to characterise the morphology of composites have been applied to FR composites containing nanoclays. XRD, TEM and melt rheology give useful information to describe the dispersion of the nanofiller in the flame retarded nanocomposite. In the PA6-OP1311 (phosphorus based flame retardant) materials, the clay is well dispersed unlike in PBT and PP materials where microcomposites are obtained with some intercalation. The poor dispersion is also highlighted by NMR measurements but the presence of flame retardant particles interferes in the quantitative evaluation of nanoclay dispersion and underestimations are made.

In this work, the nanodispersion of organomodified montmorillonite (MMT) in polylactide (PLA), prepared by varying the processing conditions, is investigated by solid-state nuclear magnetic resonance (NMR). The method is based on T1H (proton longitudinal relaxation time) measurement as a quantitative indicator of the dispersion. It permits extraction of two parameters: (i) f is the fraction of the potentially available clay surface, which has been transformed into polymer/clay interfaces and (ii) e is a relative measure of the homogeneity of the dispersion of these actual polymer/clay interfaces. The NMR approach is consistent with transmission electron microscopy (TEM) results but, as a bonus, NMR allows providing of a quantitative view of the whole sample, while TEM is mainly qualitative and looks only at a tiny volume of the material. This critical advantage is used, for the first time, to quantitatively investigate the influence of the processing conditions on the nanomorphology of PLA/MMT nanocomposite. It is revealed that high mechanical energy for a short time (∼1 min) followed by low shear stress for a reasonable residence time (∼5 min) results in the delamination of the clay platelets (high f value) associated with a very high degree of homogeneity (e=97%). Longer times and higher shear lead to the reagglomeration of the platelets.

Silk is one of the most desirable textile fibers due to its unprecedented flexibility, strength, and chemical resistance. Recent work has shown that ionic liquids possess great potential for dissolving and processing silk. Furthermore, ionic liquids have been shown to improve dispersion of nanoparticles throughout conventional polymer networks. In our current work, we have used imidazolium based ionic liquids to dissolve silk and disperse clay, carbon nanotubes, and chitin using film casting, wet spinning, and electrospinning techniques. The structural characteristics and morphology were determined using x-ray diffraction, Raman spectroscopy, laser scanning confocal microscopy, and scanning electron microscopy. Thermogravimetric analysis and differential scanning calorimetry were used to assess the potential benefits of adding nanocomposites to silk fibers and films. It was determined that carbon nanotubes offer the best potential for improving the thermal properties of silk.

A broad spectrum of applications of "Salen"-based Schiff bases tagged them as versatile multifunctional materials. However, their applicability is often bounded by a temperature threshold and, thus, they have rarely been used for high temperature applications. Our investigation of a classical Schiff base, N,N'-bis(4-hydroxysalicylidene)ethylenediamine (L2), reveals that it displays an intriguingly combative response to an elevated temperature/fire scenario. L2 resists and regulates thermal degradation by forming an ablative surface, and acts as a thermal shield. A polycondensation via covalent cross-linking, which forms a hyperbranched cross-linked resin is found to constitute the origin of the ablative surface. This is a unique example of a resin formation produced with a Schiff base, that mimicks the operational strategy of a high-heat resistant phenolic resin. Further applicability of L2, as a flame retardant, was tested in an engineering polymer, polyamide-6. It was found that it reinforces the polymer against fire risks by the formation of an intumescent coating. This paves the way for a new strategic avenue in safeguarding polymeric materials toward fire risks. Further, this material represents a promising start for thermal protective applications.

Luminescent ionogels were prepared by doping an europium(III) tetrakis β-diketonate complex into an imidazolium ionic liquid, followed by immobilization of the ionic liquid by confinement in a silica network. The ionogels were obtained by a non-hydrolytic method as perfect monoliths featuring both the transparency of silica and the ionic conductivity performances of ionic liquids. The ionogels contain 80 vol % of ionic liquid. The organic−inorganic hybrid materials showed a very intense red photoluminescence under ultraviolet irradiation. The red emission has a very high coloric purity.

Considerable research has been conducted in improving the performance characteristics of nanocomposites, however, relatively few attempts have been made to address the thermal stability of nanocomposites. An attempt is being made to improve the thermal properties of nanocomposites by synthesizing imidazolium salts from 2-methyl imidazole and ion exchanging the salts with clay minerals. This study focuses on the role of the chemistry of imidazolium salt(s) used in functionalizing clay and processing conditions in the formulation of epoxy nanocomposites. The nanodispersion of clay in an epoxy matrix is evaluated qualitatively by X-ray diffraction (XRD), transmission electronic microscopy (TEM), and laser scanning confocal microscopy (LSCM). We demonstrate the use of LCSM for quantitative image analysis and to study the dispersion of clay layers, tagged with a fluorescent dye in the epoxy matrix. XRD and TEM results reveal that the hand mixed nanocomposite has tactoid morphology, while ultrasonicated organoclay (without hydroxyl group) epoxy nanocomposite exhibits a mixed morphology, and an ultrasonicated organoclay (with hydroxyl group) epoxy nanocomposite had well dispersed clay distribution in the epoxy matrix. Results from the three complimentary techniques enable the characterization of the clay platelets over several length scales ranging from the micrometer to the nanometer scale.

A simple nonaqueous sol−gel processing led to ionogels, resulting in the confinement of an ionic liquid within a silica-like network. In the case of a non-water-soluble ionic liquid, ionogels were made stable toward water immersion by the presence of hydrophobic methyl groups in the solid network. A set of ionogels with different ionic liquid content was studied by DSC and 1H NMR spectroscopy. The nanometric level of the confinement of the ionic liquid turned out to significantly modify the phase transitions, while still allowing some molecular mobility. Moreover, ionogels were found to keep the high conducting performances of the ionic liquid.

Well-dispersed multiwalled carbon nanotube (MWNT)/polystyrene nanocomposites have been prepared via melt extrusion, using trialkylimidazolium tetrafluoroborate-compatibilized MWNTs. Quantification of the improvement is realized via transmission electron microscopy and laser scanning confocal microscopy image analysis. Differential scanning calorimetry and Fourier-transform infrared and X-ray diffraction analysis show evidence for a π-cation, nanotube-imidazolium interaction and the conversion from an interdigitated bilayer, for the imidazolium salt, to an ordered lamellar structure, for the imidazolium on the surface of the MWNTs.

This work investigates the melt-processing of styrene–acrylonitrile copolymer (SAN) with organo-modified montmorillonite (MMT) clays and the influence of the clay on mechanical properties and on fire performance of SAN. The nanodispersion of MMT is evaluated qualitatively by X-ray diffraction (XRD) and transmission electronic microscopy (TEM), and quantitatively by solid state nuclear magnetic resonance (NMR). SAN/MMT nanocomposites reveal an intermediate morphology, an intercalated structure with some exfoliation and with the presence of small tactoids, whatever the loading in MMT is. The polymer–clay interfacial area is estimated at 0.5 and the degree of homogeneity characterizing the distribution of MMT platelets is about 40%. The presence of clay in SAN-25 leads to a ‘filler effect’ increasing the stiffness but decreasing tensile strength of the nanocomposites. It also leads to a significant decrease of peak of heat release rate measured by mass loss calorimetry.

Summary: Laser-induced fluorescence spectroscopy of the optical probe Nile Blue A in polymer clay nanocomposites is described. Concentration quenching of the fluorescence dominates the probe behavior until the clay platelets are physically separated by polymer intercalation. Further separation into an exfoliated structure results in an intense increase in probe fluorescence. Preliminary results indicate the ability to discriminate between intercalated and exfoliated structures in nanocomposites formed by melt processing. Polyamide 6 nanocomposites: Purple, 1 minute processing (left). Red, 7 minute processing (right).

The development of an antifouling coating for 316L 2B stainless steel pipes used in heat exchangers for milk products was studied in this paper. The coating was obtained using hexamethyldisiloxane (HMDSO) as precursor applied by atmospheric plasma on stainless steel. The stainless steel plates were first pre-treated using nitrogen or air atmospheric pressure plasma to improve the surface properties before coating. Various conditions (distance between plasma source and substrate, aging time and number of passes) were tested to study the influence of these parameters on the surface energy of stainless steel. The HMDSO based coating was then deposited by atmospheric plasma on the pre-treated steel plates and the plates obtained were tested to fouling in a pilot heat-exchanger. Surface response methodology (experimental design) was used in order to identify the optimized coating conditions to minimize the fouling. Mechanical profilometry, Atomic Force Microscopy (AFM), Electron Probe Micro Analyzis (EPMA), Flight-Secondary Ion Mass Spectroscopy (ToF-SIMS), X-Ray Photoelectron Spectrometry (XPS) and goniometry were used to evaluate the coating roughness, morphology, surface energy and chemical composition.

This work describes the development of an environmental friendly functionalized polypropylene nonwoven geotextile (PP) in order to trap heavy metals in sediments and sludges. Chitosan was chosen as the sorbent because of its ability to trap heavy metals, of its natural origin (from shells), and of its low cost. PP was first functionalized with acrylic acid using a cold plasma process, in order to bring some reactive carboxylic functions onto the surface. Chitosan was then covalently grafted on the acrylic acid modified polypropylene. The functionalized surfaces were characterized by FTIR (Fourier Transform InfraRed) and chitosan was thus proven to be grafted. The ability of the functionalized textile to trap heavy metals was then investigated. Copper was chosen as the model heavy metal, and artificial solutions of CuSO4 were prepared for the experiments. Sorption studies among the concentration of copper in polluted solutions at 20°C were carried out with PP-g-AA-chitosan (Polypropylene-grafted-Acrylic acid-chitosan) in order to evaluate the maximum of absorption of this surface: the textile can chelate copper increasingly with the initial copper concentration until 800 ppm where it reaches a plateau at about 30 mg/L. The effects of pH and of the ionic strength (absorption in a NaCl containing solution) were finally investigated. The trapping of Cu 2+ decreases slowly when the ionic strength increases. For a seawater-like NaCl concentration of 30g/L, the textile still chelates about 20 mg/L of Cu 2+ . Finally, the optimum pH to trap the maximum amount of copper was determined to be 4.75, which corresponds to the optimum pH for the solubility of the chitosan.