EP2323778A1 - Method for bonding active molecules onto a carrier, active element obtained by said method, and chemical composition for implementing said method - Google Patents
Method for bonding active molecules onto a carrier, active element obtained by said method, and chemical composition for implementing said methodInfo
- Publication number
- EP2323778A1 EP2323778A1 EP08875642A EP08875642A EP2323778A1 EP 2323778 A1 EP2323778 A1 EP 2323778A1 EP 08875642 A EP08875642 A EP 08875642A EP 08875642 A EP08875642 A EP 08875642A EP 2323778 A1 EP2323778 A1 EP 2323778A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cationic
- active
- micelles
- support
- active molecules
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
- C04B41/48—Macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
- C04B41/61—Coating or impregnation
- C04B41/62—Coating or impregnation with organic materials
- C04B41/63—Macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/46—Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic System; Titanates; Zirconates; Stannates; Plumbates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/005—Compositions containing perfumes; Compositions containing deodorants
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
- D06M13/463—Compounds containing quaternary nitrogen atoms derived from monoamines
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/0004—General aspects of dyeing
- D06P1/0012—Effecting dyeing to obtain luminescent or phosphorescent dyeings
Definitions
- the present invention relates to a method for fixing, on a support, active molecules exhibiting an activity, in particular physical, physicochemical, chemical, biochemical or biological activity, either against unwanted organisms or phenomena, or in favor of of a desired phenomenon.
- This invention also relates to an active element comprising a support as well as to such active molecules, fixed on this support.
- the invention relates to a chemical composition for the implementation of this process and / or for producing this active support.
- the invention relates to the field of media processing and will find an application when it comes to producing an active element comprising a support provided with active molecules fixed on this support, so that this active element has specific properties, more particularly against an undesirable effect or, conversely, in favor of a desired effect.
- WO2004065024 discloses a method of treating a support with a chemical composition containing, on the one hand, a binder consisting of polymerizable and / or crosslinkable chemical compounds and, on the other hand, a chemical compound having a strong ionic character. This treatment is intended to provide an ionic charge to the support by fixing the ionic chemical compound on the support by polymerization and / or crosslinking of the binder at high temperature.
- US-5,631,072 relates to a method of attaching an insecticide to a fabric.
- Such a process consists, first of all, in making a paste containing an insecticide dispersion, a thickening agent, a polymer and a crosslinking agent.
- This method then consists in coating a support with this paste before polymerization of the polymer and crosslinking of the crosslinking agent. This polymerization and crosslinking has the effect of trapping the insecticide molecules in the crystalline mass of the polymer so that these molecules lose their effectiveness considerably.
- the present invention is intended to overcome the disadvantages of the methods of the state of the art.
- the invention relates to a method for fixing, on a support, active molecules having an activity, in particular physical, physicochemical, chemical, biochemical or biological activity, either against organisms or undesirable phenomena, or in favor of a desired phenomenon, this method being characterized in that:
- a chemical composition is produced containing at least cationic micelles each comprising at least one active molecule;
- the support is impregnated with the chemical composition of cationic micelles
- the active molecules are fixed on the support by producing at least one electrostatic type bond between the cationic micelles and this support.
- the invention also relates to an active element comprising, on the one hand, a support and, on the other hand, active molecules, fixed on this support, and having an activity, in particular physical, physicochemical, chemical, biochemical or biological, either against organisms or undesirable phenomena, or in favor of a desired phenomenon, characterized in that the active element comprises cationic micelles, on the one hand, fixed on the support by on least one electrostatic type bond and, on the other hand, each having at least one active molecule.
- This invention further relates to a chemical composition for carrying out the above-mentioned method and / or for producing the above-mentioned active element.
- This chemical composition is characterized in that it contains at least cationic micelles each comprising at least one active molecule having an activity, in particular a physical, physicochemical, chemical, biochemical or biological activity, or against organisms or undesirable phenomena, either in favor of a desired phenomenon.
- the advantages of the present invention consist in that the fixing of the active molecules on the support is ensured by performing at least one electrostatic type bond between this support and cationic micelles each comprising at least one such active molecule.
- Such a type of bond makes it possible to optimize the quantity of molecules fixed on a support, to guarantee a high level of fixation as well as a significant remanence over time.
- Such a connection allows, again, good weather resistance (this for externally implanted supports) as well as washes (this for washable media, especially textiles).
- Another advantage is that the process according to the present invention makes it possible to treat any type of support, in particular polar, apolar or anionic.
- FIG. 1 is a schematic representation of the electrostatic fixation, on a polar support, of a micelle containing an active molecule
- FIG. 2 is a schematic representation of the electrostatic fixation, on an anionic support, of a micelle containing an active molecule
- FIG. 3 is a schematic representation of the electrostatic attachment, on an apolar support, of a micelle containing an active molecule
- FIG. 4 is a diagrammatic representation of an electrostatic fixation and by polymerization and / or crosslinking, on a support, of micelles containing an active molecule.
- the present invention relates to the field of the treatment of supports 2 and will find an application when it comes to producing an active element 1 comprising a support 2 provided with active molecules 30, on the one hand, fixed on this support 2 and, d on the other hand, presenting an activity, in particular physical, physicochemical, chemical, biochemical or biological activity,
- This invention relates, more particularly, to a process for fixing such active molecules on such a support 2.
- Such a process consists in: - producing a chemical composition containing at least cationic micelles 3 each comprising at least one active molecule 30;
- the support 2 is impregnated with this chemical composition of cationic micelles 3; the active molecules 30 are immobilized on the support 2 by producing at least one type of binding electrostatic between the cationic micelles 3 and this support 2.
- the method comprises making a chemical composition of cationic micelles 3 each having a plurality of polarized active molecules.
- a micellar solution containing micelles 3 each consisting of an assembly of a plurality of polarized active molecules, is produced first and from polarized active molecules. The method then consists in adding to this micellar solution chemical compounds intended to cationize these micelles 3.
- the process consists in producing a chemical composition of cationic micelles 3, each comprising at least one such cationic active molecule. .
- the production of such a composition is ensured by producing a micellar solution containing, on the one hand, cationic active molecules and, on the other hand, chemical compounds 31 intended to form cationic micelles with these cationic active molecules. .
- the process consists in producing a chemical composition of cationic micelles 3 each comprising at least one active molecule. neutral or cationic, this by realizing, firstly and from such active molecules 30 and chemical compounds 31 intended to form micelles 3 with such active molecules 30, a micellar solution containing micelles 3 each constituted by an assembly of at least one such active molecule 30 and at least one such chemical compound 31.
- the method then consists in adding to this micellar solution chemical compounds intended to cationize these micelles 3.
- a chemical composition of cationic micelles 3, each comprising at least one such anionic active molecule is carried out, this:
- micellar solution containing micelles 3 each constituted by an assembly of at least one such anionic active molecule and at least one such chemical compound 31;
- micellar solution by then adding, to this micellar solution, chemical compounds intended to cationise these micelles 3.
- the anionic active molecules are neutralized by means of specific chemical compounds incorporated in the chemical composition (more particularly in the micellar solution). .
- the anionic active molecules are neutralized by chemical compounds 31 intended to form micelles with such anionic active molecules, these chemical compounds being chosen from cationic ensure such neutralization.
- the process according to the invention consists, when a chemical composition is made, of producing, first of all, a micellar solution.
- a micellar solution when such a micellar solution is produced, in fact, a solution containing, on the one hand, a solvent of the organic type (oil, alcohol, ketone or the like) and / or mineral (water or the like) and, on the other hand, active molecules solubilized in this solvent.
- a solvent of the organic type oil, alcohol, ketone or the like
- mineral water or the like
- active molecules solubilized in this solvent.
- such active molecules can also be in an emulsifiable or dispersible form in such a solvent.
- the process according to the invention consists, then and where appropriate, in introducing into this solution chemical compounds 31 intended to form micelles 3 with such active molecules 30.
- Another characteristic of the process according to the invention is that, if appropriate, at least one acidic substance or at least one acid, especially a mixture, is added to the cationic micellar composition (more particularly to the micellar solution). of acids.
- such an addition advantageously makes it possible to neutralize the pH of the chemical composition (more particularly that of the micellar solution) as well as that of the support 2 to be treated.
- such an addition makes it possible to neutralize the alkalis present in this composition (more particularly in the micellar solution) and on this support 2 which, in the absence of such an addition, are capable of reacting with the chemical compounds intended to to cationize these micelles.
- the process consists in the fact that the support 2 is impregnated with the chemical composition of cationic micelles 3.
- Such impregnation is ensured by immersion (more particularly inside a tank, a bacholle, a washing machine or the like), by spraying (more particularly by means of at least one spray nozzle) or by coating (more particularly by means of a doctor blade, a brush, a roller or similar) .
- An additional feature of this process is that after impregnation of the support 2 with the cationic micellar composition, the drying of the impregnated support 2 is ensured.
- drying is more particularly suitable after impregnation of this support 2 by immersion.
- drying is preferably provided after a spin of the impregnated support 2.
- this is ensured at a temperature of between 20 and 200 ° C., preferably between 20 and 180 ° C., in particular between 20 and 150 ° C.
- this drying is ensured inside an oven, preferably before cooling of the active element 1, either by passing it through a cooling zone of the air-flow type, or by direct cooling of the on cooling cylinders or the like.
- the active molecules 30 are immobilized on the support 2 by producing at least one electrostatic-type bond between the cationic micelles 3 and this support 2.
- this support 2 when this support is of the polar type as illustrated in FIG. 1, this support 2 has, in fact (and more particularly at its surface), permanent dipoles which make it possible to create, between the dipoles of this support 2 and the cationic micelles 3 to be fixed on this support 2, strong electrostatic bonds of the "ion-dipole" type.
- polar-type supports 2 consisting of: cellulosic supports such as paper, wood, flax, viscose, hemp, ramie, jute, or rayon;
- an ester for example a polyester
- an amide for example a polyamide
- PVC polyvinyl chloride
- supports 2 having, naturally, a strong ionic polarity of anionic type as shown in FIG.
- the fixing of the cationic micelles 3 on such a support 2 is ensured by producing, between this support 2 and the cationic micelles 3 to be fixed on the support 2, a strong electrostatic bond of the ionic type, more particularly of the type " ion-ion ".
- supports 2 apolar type as shown in Figure 3, more particularly constituted by supports 2 having apolar groups.
- the process according to the present invention also makes it possible to fix cationic micelles on supports 2 of this type.
- cationic micelles 3 in the vicinity of such a non-charged apolar support 2, cause a deformation of the electron cloud of this support 2 (polarizing field caused by the highly cationic charge of the micelle 3) and the creation of an induced dipole.
- the fixing of such a cationic micelle (comprising at least one active molecule 30) is ensured by providing, between this support 2 and the cationic micelles 3 to be fixed on the support 2, a strong electrostatic bond of the " induced ion-dipole ".
- supports 2 of polyolefin type more particularly polyethylene, polypropylene or the like.
- the fixing of a cationic micelle 3 is carried out on a support 2 of polar, apolar or anionic type, except however a support 2 of cationic type.
- Such fixing is ensured by performing an electrostatic bonding, in a particularly advantageous manner, on the one hand, to fix effectively and perennially almost all the active molecules 30 on such a support 2 and, on the other hand, to retain the properties (physical, chemical, biological) of the active molecules without altering them.
- such chemical compounds 31 may be composed of polymerizable and / or crosslinkable compounds.
- the electrostatic fixation of the cationic micelles (more particularly the active molecules 30) on the support 2 can be completed by carrying out a fixation by polymerization and / or crosslinking of the chemical compounds 31 intended to form cationic micelles with these active molecules 30 as illustrated in FIG.
- an active element 1 comprising, on the one hand, a support 2 and, on the other hand, active molecules (30, more particularly arranged within at least one cationic micelle 3) fixed on this support 2.
- the active element 1 comprises cationic micelles 3, on the one hand, fixed on the support 2 by at least one electrostatic type connection and, on the other hand, each comprising at least one an active molecule 30.
- the active molecules may be of the polarized type.
- the cationic micelles 3 each comprise at least a plurality of polarized active molecules.
- each cationic micelle 3 comprises a plurality of polarized active molecules 30 which can be in the form of a micelle 3, naturally and in the absence of any additional chemical compound capable of forming such a micelle 3 with such an active molecule 30.
- the active molecules can also be neutral or cationic.
- the cationic micelles 3 each comprise, on the one hand, at least one such neutral or cationic active molecule and, on the other hand, at least one chemical compound 31, of nonionic or cationic type, forming a cationic micelle 3 with at least one such active molecule 30.
- these active molecules can, again, be of the anionic type.
- the cationic micelles 3 each then comprise, on the one hand, at least one anionic active molecule 30 and, on the other hand, at least one chemical compound 31, preferably of cationic type, forming a cationic micelle 3 with at least one such anionic active molecule 30 and, if appropriate (more particularly when the chemical compound 31 forming a micelle 3 with the active molecule 30 is not of cationic type or is not capable of electrically neutralizing such a molecule), at least a chemical compound for electrically neutralizing such anionic active molecule.
- a cationic micelle 3 may comprise at least one chemical compound 31 forming such a micelle 3 with at least one active molecule 30 (anionic, neutral or cationic).
- a chemical compound 31 may consist of a surfactant.
- such a chemical compound 31 may consist of a polymerizable and / or crosslinkable type compound.
- the active element 1 in accordance with the invention comprises a support 2 as well as active molecules 30 fixed to this support 2.
- a support 2 may, then and as described above, be polar type (FIG. 1), apolar (FIG. 3) or anionic (FIG. 2), whereas the electrostatic bond between a cationic micelle 3 and this support 2 is of the ion-dipole, ion-dipole-induced or ionic type, respectively ( ion-ion).
- the invention has a particularly versatile character so that the implementation of the aforementioned method makes it possible to obtain a plurality of singularly different active elements 1 comprising different active molecules having an activity, in particular physical, physicochemical, chemical, biochemical or biologically, either against unwanted organisms or phenomena, or in favor of a desired phenomenon.
- the active molecules may have an activity in the prophylactic or curative treatment of a disease.
- such active molecules 30 may be associated with a support 2 constituted by a protective element (more particularly a dressing) or by a clothing element (more particularly a garment, in particular called “intelligent").
- the active molecules may exhibit activity against pathogenic elements and / or microorganisms, in particular viruses, bacteria, microbes or the like.
- pathogenic elements and / or microorganisms in particular viruses, bacteria, microbes or the like.
- active molecules having such a The activity may then consist of isothiazolinone derivatives, silver salts, triclosan, titanium dioxide or the like.
- a third embodiment consists in the fact that the active molecules have an activity in favor of a visual phenomenon associated with this support 2.
- a visual phenomenon can be a photoluminescence, a fluorescence or a coloration of this support 2.
- the active molecules having an activity against parasites (especially animals) or animals, more particularly mites or insects.
- Such activity may be repulsive, annoying or lethal. More particularly, such active molecules may be of the pesticide, insecticide, insect repellent or the like type.
- pesticide-type active molecules such as permethrin, deltamethrin, fenitrothion, cyfluthrin, geraniol,
- a fifth embodiment consists in that the active molecules have an activity against the fixation of staining products on said support 2.
- the active molecules have an activity against radiation, especially ultraviolet radiation.
- Such molecules may, more particularly, be titanium dioxide.
- a seventh embodiment is that the active molecules can exhibit an activity against fungi (these active molecules then being of the fungicidal type) or plants, especially weeds (these active molecules then being of the herbicide type). ), mosses, plant pests (these active molecules then being of the pesticide type) or the like.
- the active molecules can have an activity against olfactory nuisances, more particularly those caused by substances produced by the human or animal body (sweat, urine, excrement), by waste (garbage, wastewater) or by organic or plant residues.
- Such active molecules can be used to treat all foci that generate such odor nuisances and preferably exhibit activity as part of the odor neutralization treatment.
- active molecules chosen from the following compounds: aliphatic alcohols (such as decanol, citronelol, geraniol), aldehydes (such as normal or branched dodecanal), phenols (such as eugenol and isoeugenol).
- aliphatic alcohols such as decanol, citronelol, geraniol
- aldehydes such as normal or branched dodecanal
- phenols such as eugenol and isoeugenol
- these active molecules can be attached to at least one type of support 2 determined.
- such a support 2 may then be constituted, at least in part, by: - an item of clothing (garment, especially trellis);
- shelter element (tent); - a protective element (dressing, tarpaulin, blind, mosquito net).
- the support 2 can be made, at least in part, of a textile material (natural or synthetic).
- a textile material may be of the knitted, woven, nonwoven or other type and be constituted by fibers and / or natural, artificial or synthetic filaments, such as, for example, polyester, viscose, cotton, wool, polyamide, aramid, silk, polypropylene, polyethylene or a mixture of different fibers and / or filaments.
- the elements described above can then receive active molecules as described above and having an activity, either in favor of a visual phenomenon, or against: pathogenic elements and / or microorganisms;
- Another type of embodiment may consist in that the support 2 is constituted by:
- a storage element bin, bucket
- an item of equipment sanitary, including urinal
- a protection element (shutter, shutter, blind, mosquito net) that includes a building, including a residential building, storage, livestock, public utility (including public toilets).
- a protection element can then be made of any material such as wood, concrete, textile, metal, leather, ceramic, stone, paper, cardboard, plastic or other.
- a type of embodiment consists, again, in that the support 2 is constituted by an element of an installation for storing, conveying and / or treating waste.
- such an element can then be constituted by an element of a conveyor system (skips, pipes, sewers) and / or treatment (wastewater treatment plants) of waste, more particularly wastewater.
- the invention relates, on the one hand, to a method for binding active molecules to a support 2 and, on the other hand, to an active element 1 comprising such a support 1 and to such molecules 30.
- the invention also relates to a chemical composition for the implementation of this process and / or for the production of this active element 1.
- this chemical composition contains at least cationic micelles comprising each having at least one active molecule having an activity, in particular physical, physicochemical, chemical, biochemical or biological activity, either against unwanted organisms or phenomena or in favor of a desired phenomenon.
- such a chemical composition contains micelles 3 each comprising at least one active molecule 30 of polarized type and each consisting, and preferably, of an assembly of a plurality of these polarized active molecules.
- this chemical composition also comprises at least one chemical compound intended to cationize such a micelle 3.
- a second embodiment is that the chemical composition contains cationic micelles each having at least one cationic active molecule, more particularly a cationic active molecule having a strong cationic polarity.
- This cationic micelle 3 then also comprises at least one chemical compound 31 forming a cationic micelle with at least one such cationic active molecule.
- the chemical composition contains micelles 3 each comprising, on the one hand, at least one neutral or cationic active molecule (more particularly one molecule having a low cationic polarity) and, on the other hand, at least one chemical compound 31 forming a micelle 3 with at least one such neutral or cationic active molecule.
- Such a chemical composition also contains at least one chemical compound for cationizing such a micelle 3.
- a fourth embodiment relates to a chemical composition containing, on the one hand, micelles 3 comprising at least one anionic active molecule, at least one chemical compound 31 (preferably of the cationic type) forming a micelle 3 with at least one such anionic active molecule and, where appropriate (more particularly when the chemical compound forming a micelle 3 with the active molecule 30 is not of cationic type or is not capable of electrically neutralizing such an anionic active molecule), less a chemical compound (preferably cationic type) for electrically neutralizing such an anionic active molecule.
- the chemical compound for electrically neutralizing an anionic active molecule is constituted by a chemical compound (preferably of cationic type, especially a cationic polymer) distinct from that forming a micelle 3 with at least such an anionic active molecule.
- the chemical compound for electrically neutralizing such an anionic active molecule is constituted by the chemical compound 31 (preferably cationic) forming a micelle 3 with at least one such anionic active molecule (such as compound being, more particularly, constituted by a cationic polymer).
- the chemical composition also contains at least one chemical compound intended to cationize such a micelle 3.
- this chemical composition may, depending on the type of active molecule 30 considered, contain at least one chemical compound 31 forming a micelle 3 with at least one active molecule 30.
- such a chemical compound 31 may consist of a polymerizable and / or crosslinkable compound, in particular of nonionic or cationic type.
- the concentration of such a polymerizable and / or crosslinkable nonionic compound preferably varies between 0.1% and 30% (which corresponds to a quantity of compound of between Ig and 300g per liter of composition).
- such a chemical compound 31 forming a micelle may, again, be constituted by a surfactant, in particular of nonionic or cationic type.
- the chemical composition may, depending on the type of active molecule 30 considered, contain at least one chemical compound for cationizing a micelle 3.
- Such a chemical compound is constituted by a chemical compound having a strong cationic polarity, more particularly a molecule comprising at least one atom having at least one cationic charge.
- a chemical compound intended to cationize a micelle 3 may consist of a quaternary ammonium derivative or of a molecule having at least one quaternized nitrogen atom.
- a chemical compound may consist of a cationic surfactant, more particularly chosen from alkyltrimethylammonium halides, benzethonium halides and cationic derivatives of nitrogenous heterocycles.
- Such a cationic chemical compound can also be derived from monomers chosen from the following monomers:
- N, N-dimethyldiallyl ammonium chloride - Dimethylaminopropylmethacrylamide chloride, N- (3-chloro-2-hydroxypropyl) trimethylammonium ...
- the concentration of such a compound intended to cationize a micelle 3 varies, preferably, between 5% and 10% (which corresponds to a quantity of compound of between 50 g and 100 g per liter of composition).
- the chemical composition also contains at least one acidic substance or at least one acid, especially a mixture of acids, in order to neutralize the pH of the composition and the support 2 (more particularly to neutralize the alkalis present in the medium and on the support 2).
- this composition contains a solvent of the organic type (oil, alcohol, ketone or the like) and / or mineral (water or the like).
- the treatment consists of applying a chemical composition containing permethrin-based insecticidal active molecules to a textile support consisting of a 100% polyester knit with a basis weight of 35 g / m 2 .
- the target amount of permethrin to be fixed on the support is 1000 mg / m2.
- the effective concentration of permethrin on the support depends on the concentration of insecticide in the bath and the transport rate
- the fixing process consists of:
- an insecticidal chemical composition containing: 1. 98 g / liter of a permethrin formulation in a 50% emulsion;
- a textile support is treated by impregnating this support on a beaker; the active element is dried on a train at a temperature of 120 ° C.
- Mosquitoes of a susceptible strain of Anopheles gambiae ss are exposed for 3 minutes to the tissue to be tested.
- Geigy cages are used for this purpose.
- Females three to five days old, not siphoned, are introduced in sets of 11 in the cages.
- a total of 44 females are used to test each sample.
- the tests are conducted at a temperature of between 23 ° C. and 25 ° C. at 50% to 70% relative humidity.
- the observation made during the 24 hours following the introduction of mosquitoes into the cage is carried out at a temperature of 28 ° C. at 70% relative humidity.
- KD is the number of mosquitoes that respond to the effect of the insecticide. The latter show signs of weakening and are unable to sting.
- the treatment consists in applying a chemical composition containing active molecules intended for neutralization odors based on a mixture of geraniol and eugenol on a concrete support.
- the effective concentration of the mixture of geraniol and eugenol to be fixed on the support depends on the concentration of the mixture in the bath, the level of odor to be neutralized and the amount of bath deposited on the support.
- the fixing process consists of:
- a chemical odor neutralization composition is prepared containing: 1. 739 g / liter of a formulation of a mixture of geraniol and eugenol in emulsion at 30%;
- the active element is dried at ambient temperature (between 20 ° C. and 25 ° C.).
- Odor neutralization treatment has been effective for up to 10 weeks.
- the odor neutralization treatment is effective for a maximum duration of 4 to 5 days.
Abstract
Description
Claims
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/FR2008/051493 WO2010018311A1 (en) | 2008-08-13 | 2008-08-13 | Method for bonding active molecules onto a carrier, active element obtained by said method, and chemical composition for implementing said method |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2323778A1 true EP2323778A1 (en) | 2011-05-25 |
Family
ID=40647165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08875642A Withdrawn EP2323778A1 (en) | 2008-08-13 | 2008-08-13 | Method for bonding active molecules onto a carrier, active element obtained by said method, and chemical composition for implementing said method |
Country Status (9)
Country | Link |
---|---|
US (1) | US8940840B2 (en) |
EP (1) | EP2323778A1 (en) |
CN (1) | CN102131593A (en) |
AP (1) | AP3026A (en) |
CA (1) | CA2734294A1 (en) |
MX (1) | MX2011001575A (en) |
RU (1) | RU2470718C2 (en) |
WO (2) | WO2010018311A1 (en) |
ZA (1) | ZA201101846B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105442359B (en) * | 2014-09-01 | 2018-01-05 | 香港理工大学 | A kind of non-aqueous dyeing process methods of bafta and the reactive dye liquid of reverse micelle encapsulating |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1519326A1 (en) | 1964-02-17 | 1970-03-19 | Ransburg Electro Coating Corp | Preparations for the surface treatment of insulating materials |
JP2677618B2 (en) * | 1988-07-11 | 1997-11-17 | 日本ペイント株式会社 | Aqueous paint composition |
US5145518A (en) * | 1990-06-27 | 1992-09-08 | Xerox Corporation | Inks containing block copolymer micelles |
DE29819745U1 (en) * | 1998-11-05 | 2000-03-09 | Spreng Thomas | 2-component textile paint |
US6475974B1 (en) * | 2000-09-01 | 2002-11-05 | Dow Corning Corporation | Mechanical microemulsions of blended silicones |
KR20040054612A (en) * | 2001-03-30 | 2004-06-25 | 에스지티 테크놀로지 홀딩스, 엘엘씨 | Process and composition for treating wood |
JP3935363B2 (en) * | 2001-06-26 | 2007-06-20 | サカタインクス株式会社 | Method for producing aqueous pigment dispersion and aqueous pigment dispersion obtained from the method |
TW200304385A (en) * | 2002-03-13 | 2003-10-01 | Novartis Ag | Materials containing multiple layers of vesicles |
WO2004065024A1 (en) | 2002-12-20 | 2004-08-05 | Fafet Jean-Francois | Support for active molecules, method for fixing active molecules on said support and composition for implementing said method |
MD2401G2 (en) * | 2003-06-27 | 2004-11-30 | Хелибрасас С.Р.Л. | Process for powdery coating of wooden articles |
WO2006111399A2 (en) | 2005-04-22 | 2006-10-26 | Dsm Ip Assets B.V. | Highly porous polymeric materials comprising biologically active molecules via covalent grafting |
EP1954795B8 (en) * | 2005-11-29 | 2009-08-26 | Basf Se | Capsules |
BRPI0921099A2 (en) | 2008-11-17 | 2017-07-11 | Dsm Ip Assets Bv | SURFACE MODIFICATION OF POLYMERS THROUGH REACTIVE AND SURFACE ACTIVE TERMINAL GROUPS |
-
2008
- 2008-08-13 CA CA2734294A patent/CA2734294A1/en not_active Abandoned
- 2008-08-13 US US13/058,993 patent/US8940840B2/en not_active Expired - Fee Related
- 2008-08-13 MX MX2011001575A patent/MX2011001575A/en not_active Application Discontinuation
- 2008-08-13 WO PCT/FR2008/051493 patent/WO2010018311A1/en active Application Filing
- 2008-08-13 CN CN200880130878.XA patent/CN102131593A/en active Pending
- 2008-08-13 EP EP08875642A patent/EP2323778A1/en not_active Withdrawn
- 2008-08-13 RU RU2011108836/04A patent/RU2470718C2/en not_active IP Right Cessation
- 2008-08-13 AP AP2011005584A patent/AP3026A/en active
-
2009
- 2009-01-22 WO PCT/FR2009/050090 patent/WO2010018330A2/en active Application Filing
-
2011
- 2011-03-11 ZA ZA2011/01846A patent/ZA201101846B/en unknown
Non-Patent Citations (2)
Title |
---|
None * |
See also references of WO2010018311A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2010018330A4 (en) | 2010-07-22 |
RU2011108836A (en) | 2012-09-20 |
CA2734294A1 (en) | 2010-02-18 |
WO2010018311A1 (en) | 2010-02-18 |
ZA201101846B (en) | 2011-11-30 |
AP2011005584A0 (en) | 2011-02-28 |
RU2470718C2 (en) | 2012-12-27 |
AP3026A (en) | 2014-11-30 |
MX2011001575A (en) | 2011-05-31 |
WO2010018330A2 (en) | 2010-02-18 |
US20110190452A1 (en) | 2011-08-04 |
US8940840B2 (en) | 2015-01-27 |
WO2010018330A3 (en) | 2010-05-27 |
CN102131593A (en) | 2011-07-20 |
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