Low-viscosity allophanates having actinically hardenable groupsDetrembleur, Christophe ![]() Patent (2007) Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter ... [more ▼] Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation reagierende Gruppen enthalten, ein Verfahren zu ihrer Herstellung sowie deren Verwendung in Beschichtungsmitteln. [less ▲] Detailed reference viewed: 8 (2 ULg) Low viscosity allophanates containing actinically hardenable groupsDetrembleur, Christophe ; ; et alPatent (2007) Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter ... [more ▼] Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation reagierende Gruppen enthalten, ein Verfahren zu ihrer Herstellung sowie deren Verwendung in Beschichtungsmitteln. [less ▲] Detailed reference viewed: 8 (2 ULg) METHOD FOR PURIFYING ELECTRICALLY CHARGED POLYSACCHARIDES AND POLYSACCHARIDE-PROTEIN COMPLEX FORMED DURING SAID PROCESSPaquot, Michel ; Wathelet, Bernard ; et alPatent (2007) Detailed reference viewed: 9 (0 ULg) Mucoadhesive composition comprising polyacrylate and chemoattractantHubert, Pascale ; Evrard, Brigitte ; Delattre, Luc et alPatent (2006) Detailed reference viewed: 24 (1 ULg) Production of novel radiation-hardening binding agentsDetrembleur, Christophe ; ; et alPatent (2006) Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung neuartiger Bindemittel, die unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation ... [more ▼] Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung neuartiger Bindemittel, die unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation reagierende Gruppen und gegebenenfalls auch gegenüber Isocyanaten reaktive Gruppen aufweisen, sowie deren Verwendung in Beschichtungsmitteln. [less ▲] Detailed reference viewed: 9 (5 ULg) Low viscosity allophanates containing actinically hardenable groupsDetrembleur, Christophe ; ; et alPatent (2006) The invention relates to low-viscosity conversion products of polyisocyanates containing activated groups that, under the influence of actinic radiation, react with ethylenically unsaturated compounds ... [more ▼] The invention relates to low-viscosity conversion products of polyisocyanates containing activated groups that, under the influence of actinic radiation, react with ethylenically unsaturated compounds while polymerizing, to a method for producing these conversion products, and to their use in coating agents. [less ▲] Detailed reference viewed: 5 (2 ULg) Production of novel radiation-hardening binding agentsDetrembleur, Christophe ; ; et alPatent (2006) The invention relates to a method for producing novel binding agents comprising groups reacting with polymerising ethylenically unsaturated compounds under the action of actinic radiation and optionally ... [more ▼] The invention relates to a method for producing novel binding agents comprising groups reacting with polymerising ethylenically unsaturated compounds under the action of actinic radiation and optionally also isocyanate-reactive groups. The invention also relates to the use of said binding agents in coating substances. [less ▲] Detailed reference viewed: 8 (5 ULg) The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary aminesDetrembleur, Christophe ; ; Patent (2006) The present invention relates to a new process for the preparation of well-defined random and block polymers or copolymers using hindered secondary amine-oligomers or polymers. Detailed reference viewed: 12 (4 ULg) Method and kit for the measurement of neutrophil cell activationSerteyn, Didier ; ; Franck, Thierry et alPatent (2006) The present invention is related to methods and kits (or devices) for the measurement of equine myeloperoxidase (MPO), a specific enzyme of equine neutrophils, either in total [first method], or ... [more ▼] The present invention is related to methods and kits (or devices) for the measurement of equine myeloperoxidase (MPO), a specific enzyme of equine neutrophils, either in total [first method], or specifically in its active form [second method]. Said methods and kits (or devices), used independently or in combination, find improved applications in the veterinary field and can be adapted for application in human health care. The concept of the second method is applicable to any other enzyme. [less ▲] Detailed reference viewed: 14 (1 ULg) MUCOADHESIVE PHARMACEUTICAL COMPOSITIONS COMPRISING CHEMOATTRACTANTS.Herman, Ludivine ; Hubert, Pascale ; Delvenne, Philippe et alPatent (2006) Detailed reference viewed: 25 (8 ULg) Radiation-curing binders and a process for their preparationDetrembleur, Christophe ![]() Patent (2006) The invention relates to a process for preparing binders which contain 1) allophanate groups, 2) groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic ... [more ▼] The invention relates to a process for preparing binders which contain 1) allophanate groups, 2) groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups) and 3) optionally NCO-reactive groups, by reacting at temperatures <=130 DEG C. A) one or more NCO-functional compounds containing uretdione groups with B) one or more compounds that contain isocyanate-reactive groups and groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups), and then C) with one or more saturated, hydroxyl-containing compounds other than B), at least one of these compounds having an OH functionality of >=2, in the presence of D) a catalyst containing one or more zinc compounds, the reaction with compounds C) taking place at least proportionally with the formation of allophanate groups. The present invention also relates to the binders obtained by the pro cess of the invention. [less ▲] Detailed reference viewed: 14 (5 ULg) Radiation-curing binders and a process for their preparation; ; et al Patent (2006) PROBLEM TO BE SOLVED: To provide a process for preparing a binder which contains (1) an allophanate group, (2) a group that reacts with an ethylenically unsaturated compound with polymerization on ... [more ▼] PROBLEM TO BE SOLVED: To provide a process for preparing a binder which contains (1) an allophanate group, (2) a group that reacts with an ethylenically unsaturated compound with polymerization on exposure to actinic radiation (radiation-curing group) and (3) optionally an NCO-reactive group; and to provide the binder obtained by the process. ; SOLUTION: The process comprises reacting at a temperature <=130[deg.]C, (A) one or more NCO-functional compounds containing uretdione groups with (B) one or more compounds that contain isocyanate-reactive groups and radiation-curing groups and then (C) with one or more saturated hydroxy-containing compounds other than (B), at least one of these compounds having an OH functionality of >=2, in the presence of (D) a catalyst containing one or more zinc compounds, the reaction with compounds (C) taking place at least proportionally with the formation of allophanate groups. [less ▲] Detailed reference viewed: 7 (4 ULg) Low viscosity allophanates containing actinically curable groups; Detrembleur, Christophe ; et alPatent (2006) PROBLEM TO BE SOLVED: To provide a process for producing a radiation-curing binder containing an allophanate group; and to provide the binder obtained by the process, and a coating composition containing ... [more ▼] PROBLEM TO BE SOLVED: To provide a process for producing a radiation-curing binder containing an allophanate group; and to provide the binder obtained by the process, and a coating composition containing the binder. ; SOLUTION: The process comprises reacting at a temperature of <=130[deg.]C (A) one or more compounds containing uretdione groups with (B) one or more OH-functional compounds which contain groups which react, with polymerization, with ethylenically unsaturated compounds on exposure to actinic radiation (radiation-curing groups), (C) optionally NCO-reactive compounds other than (B) in the presence of (D) a catalyst containing at least one zinc compound to form allophanate groups by opening the uretdione ring. [less ▲] Detailed reference viewed: 5 (2 ULg) Utilisation d'une nouvelle espèce de Bifidobacterium (Bifidobacterium crudilactis) à effets probiotiquesDaube, Georges ; ; Delcenserie, Véronique ![]() Patent (2006) Detailed reference viewed: 47 (8 ULg) The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary aminesDetrembleur, Christophe ; ; Patent (2006) A process for the preparation of (co)oligomers or (co)polymers is disclosed. The process entails first the preparation of a mixture that contains a monoethylenically unsaturated monomer conforming to HR<1 ... [more ▼] A process for the preparation of (co)oligomers or (co)polymers is disclosed. The process entails first the preparation of a mixture that contains a monoethylenically unsaturated monomer conforming to HR<1>C = CR<2>R<3> an oxidizing agent and at least one polymer or oligomer conforming to formula (I), <CHEM> and an optional free radical initiator and then heating the mixture at a temperature in the range of 0 DEG C to 220 DEG C. [less ▲] Detailed reference viewed: 17 (5 ULg) Radiation-curing binders and a process for their preparation; Detrembleur, Christophe ; et alPatent (2006) A binder is prepared by reacting isocyanate-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically ... [more ▼] A binder is prepared by reacting isocyanate-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically unsaturated compounds; saturated, hydroxyl-containing compound(s); and a catalyst containing ammonium salts or phosphonium salts of aliphatic or cycloaliphatic carboxylic acids. Preparation of a binder containing allophanate groups, groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups), and optionally isocyanate (NCO)-reactive groups, which comprises reacting at 130[deg]C NCO-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups); saturated, hydroxyl-containing compound(s), at least one of these compounds having an OH functionality of 2; and a catalyst containing one or more ammonium salts or phosphonium salts of aliphatic or cycloaliphatic carboxylic acids, the reaction hydroxyl-containing compounds taking place at least proportionally with the formation of allophanate groups. An independent claim is also included for a coating composition comprising: (1) binders; (2) optionally polyisocyanate(s) which contain free or blocked isocyanate groups and optionally contain groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation; (3) optionally compounds other than the polyisocyanate(s) which contain groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation and optionally contain NCO-reactive groups; (4) optionally isocyanate-reactive compound(s) which are free from groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation; and (5) initiators. [less ▲] Detailed reference viewed: 4 (3 ULg) Low-viscosity allophanates having actinically hardenable groups; Detrembleur, Christophe ; et alPatent (2006) A radiation-curing binder containing allophanate groups is prepared by reacting at =130[deg]C compound(s) containing uretdione groups with OH-functional compounds containing groups reacting with ... [more ▼] A radiation-curing binder containing allophanate groups is prepared by reacting at =130[deg]C compound(s) containing uretdione groups with OH-functional compounds containing groups reacting with polymerization with ethylenically unsaturated compounds on exposure to actinic radiation, optionally other NCO-reactive compounds, in the presence of a catalyst comprising at least one zinc compound to form allophanate groups by opening the uretdione ring. Independent claims are also included for: (A) a coating composition comprising the radiation-curing binder(s) containing allophanate groups, optionally polyisocyanate(s) containing free or blocked isocyanate groups, which are free from groups which react, with polymerization, with ethylenically unsaturated compounds on exposure to actinic radiation, optionally other compounds containing groups which react, with polymerization, with ethylenically unsaturated compounds on exposure to actinic radiation, and optionally contain free or blocked NCO groups, optionally one or more isocyanate-reactive compounds, initiator(s), and optionally solvents; and (B) a substrate coated with a coating obtained from the radiation-curing binder containing allophanate groups. [less ▲] Detailed reference viewed: 10 (3 ULg) Radiation-curing binders and a process for their preparation; Detrembleur, Christophe ![]() Patent (2006) A binder is prepared by reacting isocyanate-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically ... [more ▼] A binder is prepared by reacting isocyanate-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically unsaturated compounds; saturated, hydroxyl-containing compound(s); and a catalyst containing ammonium salts or phosphonium salts of aliphatic or cycloaliphatic carboxylic acids. Preparation of a binder containing allophanate groups, groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups), and optionally isocyanate (NCO)-reactive groups, which comprises reacting at 130[deg]C NCO-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups); saturated, hydroxyl-containing compound(s), at least one of these compounds having an OH functionality of 2; and a catalyst containing one or more ammonium salts or phosphonium salts of aliphatic or cycloaliphatic carboxylic acids, the reaction hydroxyl-containing compounds taking place at least proportionally with the formation of allophanate groups. An independent claim is also included for a coating composition comprising: (1) binders; (2) optionally polyisocyanate(s) which contain free or blocked isocyanate groups and optionally contain groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation; (3) optionally compounds other than the polyisocyanate(s) which contain groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation and optionally contain NCO-reactive groups; (4) optionally isocyanate-reactive compound(s) which are free from groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation; and (5) initiators. [less ▲] Detailed reference viewed: 5 (3 ULg) Herstellung von neuen strahlenhärtbarenden Bindemitteln; ; et al Patent (2006) A binder is prepared by reacting isocyanate-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically ... [more ▼] A binder is prepared by reacting isocyanate-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically unsaturated compounds; saturated, hydroxyl-containing compound(s); and a catalyst containing ammonium salts or phosphonium salts of aliphatic or cycloaliphatic carboxylic acids. Preparation of a binder containing allophanate groups, groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups), and optionally isocyanate (NCO)-reactive groups, which comprises reacting at 130[deg]C NCO-functional compound(s) containing uretdione groups; compounds that contain isocyanate-reactive groups and contain groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups); saturated, hydroxyl-containing compound(s), at least one of these compounds having an OH functionality of 2; and a catalyst containing one or more ammonium salts or phosphonium salts of aliphatic or cycloaliphatic carboxylic acids, the reaction hydroxyl-containing compounds taking place at least proportionally with the formation of allophanate groups. An independent claim is also included for a coating composition comprising: (1) binders; (2) optionally polyisocyanate(s) which contain free or blocked isocyanate groups and optionally contain groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation; (3) optionally compounds other than the polyisocyanate(s) which contain groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation and optionally contain NCO-reactive groups; (4) optionally isocyanate-reactive compound(s) which are free from groups which react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation; and (5) initiators. [less ▲] Detailed reference viewed: 9 (3 ULg) Low viscosity allophanates containing actinically curable groups; Detrembleur, Christophe ; et alPatent (2006) The present invention relates to a process for preparing radiation-curing binders containing allophanate groups by reacting at temperatures of <=130 DEG C. A) one or more compounds containing uretdione ... [more ▼] The present invention relates to a process for preparing radiation-curing binders containing allophanate groups by reacting at temperatures of <=130 DEG C. A) one or more compounds containing uretdione groups with B) one or more OH-functional compounds which contain groups which react, with polymerization, with ethylenically unsaturated compounds on exposure to actinic radiation (radiation-curing groups), C) optionally NCO-reactive compounds other than B), in the presence of D) a catalyst containing at least one zinc compound, to form allophanate groups by opening the uretdione ring. The present invention also relates to the binders obtained by the process of the invention and to coating compositions containing these binders. [less ▲] Detailed reference viewed: 10 (6 ULg) Radiation-curing binders and a process for their preparation; ; et al Patent (2006) The invention relates to a process for preparing binders which contain 1) allophanate groups, 2) groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic ... [more ▼] The invention relates to a process for preparing binders which contain 1) allophanate groups, 2) groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups) and 3) optionally NCO-reactive groups, by reacting at temperatures <=130 DEG C. A) one or more NCO-functional compounds containing uretdione groups with B) one or more compounds that contain isocyanate-reactive groups and groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups), and then C) with one or more saturated, hydroxyl-containing compounds other than B), at least one of these compounds having an OH functionality of >=2, in the presence of D) a catalyst containing one or more zinc compounds, the reaction with compounds C) taking place at least proportionally with the formation of allophanate groups. The present invention also relates to the binders obtained by the process of the invention. [less ▲] Detailed reference viewed: 6 (2 ULg) Radiation-curing binders and a process for their preparation; ; et al Patent (2006) The invention relates to a process for preparing binders which contain 1) allophanate groups, 2) groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic ... [more ▼] The invention relates to a process for preparing binders which contain 1) allophanate groups, 2) groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing group s) and 3) optionally NCO-reactive groups, by reacting at temperatures .ltoreq. 130.degree.C A) one or more NCO-functional compounds containing uretdione groups wit h B) one or more compounds that contain isocyanate-reactive groups and groups that react with ethylenically unsaturated compounds with polymerization on exposure to actinic radiation (radiation-curing groups), and then C) with one or more saturated, hydroxyl-containing compounds other than B ), at least one of these compounds having an OH functionality of .gtoreq. 2, in the presence of D) a catalyst containing one or more zinc compounds, the reaction with compounds C) taking place at least proportionally with the formation of allophanate groups. The present invention also relates to the binders obtained by the process of the invention. [less ▲] Detailed reference viewed: 27 (2 ULg) Low viscosity allophanates containing actinically curable groupsDetrembleur, Christophe ; ; et alPatent (2006) The present invention relates to a process for preparing radiation-curing binders containing allophanate groups by reacting at temperatures of .ltoreq.130.degree.C A) one or more compounds containing ... [more ▼] The present invention relates to a process for preparing radiation-curing binders containing allophanate groups by reacting at temperatures of .ltoreq.130.degree.C A) one or more compounds containing uretdione groups with B) one or more OH-functional compounds which contain groups which react , with polymerization, with ethylenically unsaturated compounds on exposure to actinic radiation (radiation-curing groups), C) optionally NCO-reactive compounds other than B), in the presence of D) a catalyst containing at least one zinc compound, to form allophanate groups by opening the uretdione ring. The present invention also relates to the binders obtained by the process of the invention and to coating compositions containing these binders. [less ▲] Detailed reference viewed: 6 (4 ULg) Preparation of 5-(1,1'-biphenyl)-4-yl-5-(4-(4-aminoacylphenyl)-piperazin)-1-yl-pyrimidine-2,4,6-triones and their use as inhibitors of zinc metalloendopeptidasesPirotte, Bernard ; Counerotte, Stéphane ; et alPatent (2006) Detailed reference viewed: 12 (3 ULg) Procédé et dispositif de production d'énergie en présence de circuit magnétique (page17)Lecomte-Beckers, Jacqueline ; Patent (2006) Detailed reference viewed: 7 (4 ULg) Herstellung von neuen strahlenhärtenden bindemittelnDetrembleur, Christophe ; ; et alPatent (2005) Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung neuartiger Bindemittel, die unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation ... [more ▼] Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung neuartiger Bindemittel, die unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation reagierende Gruppen und gegebenenfalls auch gegenüber Isocyanaten reaktive Gruppen aufweisen, sowie deren Verwendung in Beschichtungsmitteln. [less ▲] Detailed reference viewed: 2 (2 ULg) Niedrigviskose Allophanate mit aktinisch härtbaren GruppenDetrembleur, Christophe ; ; et alPatent (2005) Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter ... [more ▼] Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation reagierende Gruppen enthalten, ein Verfahren zu ihrer Herstellung sowie deren Verwendung in Beschichtungsmitteln. [less ▲] Detailed reference viewed: 4 (3 ULg) Low viscosity allophanates having actinically hardenable groupsDetrembleur, Christophe ; ; et alPatent (2005) The invention relates to low-viscosity conversion products of polyisocyanates containing activated groups that, under the influence of actinic radiation, react with ethylenically unsaturated compounds ... [more ▼] The invention relates to low-viscosity conversion products of polyisocyanates containing activated groups that, under the influence of actinic radiation, react with ethylenically unsaturated compounds while polymerizing, to a method for producing these conversion products, and to their use in coating agents. [less ▲] Detailed reference viewed: 12 (2 ULg) Production of novel radiation-hardening binding agentsDetrembleur, Christophe ; ; et alPatent (2005) The invention relates to a method for producing novel binding agents comprising groups reacting with polymerising ethylenically unsaturated compounds under the action of actinic radiation and optionally ... [more ▼] The invention relates to a method for producing novel binding agents comprising groups reacting with polymerising ethylenically unsaturated compounds under the action of actinic radiation and optionally also isocyanate-reactive groups. The invention also relates to the use of said binding agents in coating substances. [less ▲] Detailed reference viewed: 9 (2 ULg) Low viscosity allophanates having actinically hardenable groups; ; et al Patent (2005) Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter ... [more ▼] Die vorliegende Erfindung betrifft niedrigviskose Umsetzungsprodukte von Polyisocyanaten, die aktivierte unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation reagierende Gruppen enthalten, ein Verfahren zu ihrer Herstellung sowie deren Verwendung in Beschichtungsmitteln. [less ▲] Detailed reference viewed: 7 (2 ULg) Production of novel radiation-hardening binding agents; ; Detrembleur, Christophe et alPatent (2005) The invention relates to a method for producing novel binding agents comprising groups reacting with polymerising ethylenically unsaturated compounds under the action of actinic radiation and optionally ... [more ▼] The invention relates to a method for producing novel binding agents comprising groups reacting with polymerising ethylenically unsaturated compounds under the action of actinic radiation and optionally also isocyana te- reactive groups. The invention also relates to the use of said binding agent s in coating substances. [less ▲] Detailed reference viewed: 10 (2 ULg) Production of novel radiation-hardening binding agents; Detrembleur, Christophe ; et alPatent (2005) Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung neuartiger Bindemittel, die unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation ... [more ▼] Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung neuartiger Bindemittel, die unter Einwirkung aktinischer Strahlung mit ethylenisch ungesättigten Verbindungen unter Polymerisation reagierende Gruppen und gegebenenfalls auch gegenüber Isocyanaten reaktive Gruppen aufweisen, sowie deren Verwendung in Beschichtungsmitteln. [less ▲] Detailed reference viewed: 6 (3 ULg) Preparation of new radiation-curing bindersDetrembleur, Christophe ; ; et alPatent (2005) Process for preparing binders including reacting A) one or more NCO-functional compounds containing uretdione groups with B) one or more compounds containing groups capable of participating in ... [more ▼] Process for preparing binders including reacting A) one or more NCO-functional compounds containing uretdione groups with B) one or more compounds containing groups capable of participating in polymerization reaction with ethylenically unsaturated compounds on exposure to actinic radiation, and contain isocyanate-reactive groups, followed by C) reaction with one or more hydroxyl-containing compounds other than B), wherein at least one of these compounds has an OH functionality of >=2, D) in the presence of one or more compounds containing phenoxide groups, as catalysts, and E) optionally auxiliaries and additives, where the reaction with compounds of component C); proceeds at least proportionally with the formation of allophanate groups and where and including binders containing allophanate groups and groups capable of participating in a polymerization reaction with ethylenically unsaturated compounds on exposure to actinic radiation, and optionally also contain NCO-reactive groups. The binders are used in coating compositions used to coat substrates [less ▲] Detailed reference viewed: 5 (2 ULg) Low viscosity allophanates containing actinically curable groupsDetrembleur, Christophe ; ; et alPatent (2005) A process for preparing binders containing allophanate groups which contain, at the oxygen atom of the allophanate group that is bonded via two single bonds, organic radicals with activated groups capable ... [more ▼] A process for preparing binders containing allophanate groups which contain, at the oxygen atom of the allophanate group that is bonded via two single bonds, organic radicals with activated groups capable of participating in a polymerization reaction with ethylenically unsaturated compounds on exposure to actinic radiation; the process includes reacting A) one or more compounds containing uretdione groups with B) one or more OH-functional compounds which contain groups capable of participating in a polymerization reaction with ethylenically unsaturated compounds on exposure to actinic radiation, and C) optionally further NCO-reactive compounds, and D) in the presence of one or more compounds containing phenoxide groups, as catalysts.; The binders can be used in preparing coatings, coating materials, coating compositions, adhesives, printing inks, casting resins, dental compounds, sizes, photoresists, stereolithography systems, resins for composite materials and sealants. [less ▲] Detailed reference viewed: 5 (3 ULg) Benzopyran derivatives, method of production and use thereof; Pirotte, Bernard ; et alPatent (2005) Detailed reference viewed: 8 (1 ULg) Preparation of fluorinated benzothiadiazine derivatives and their use as AMPA receptor modulatorsFrancotte, Pierre ; Fraikin, Pierre ; De Tullio, Pascal et alPatent (2005) Detailed reference viewed: 11 (5 ULg) Fluorinated benzothiadiazine derivatives and their use as AMPA receptor modulatorsFrancotte, Pierre ; ; De Tullio, Pascal et alPatent (2005) Detailed reference viewed: 15 (9 ULg) Solar ConcentratorHabraken, Serge ; Defise, Jean-Marc ; Collette, Jean-Paul ![]() Patent (2005) A concentrator based on a combination of Fresnel lens and mirror to incresa the efficiency and uniformity Detailed reference viewed: 20 (2 ULg) Device allowing measurement of photosyntesis of a whole small plantTocquin, Pierre ; Périlleux, Claire ![]() Patent (2005) Detailed reference viewed: 10 (2 ULg) Process for depositing strong adherend polymer coating onto an electrically conductive surface; Jérôme, Robert ; et alPatent (2004) Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising an electrochemical grafting at the surface of an active monomer for forming a ... [more ▼] Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising an electrochemical grafting at the surface of an active monomer for forming a primer coating P onto said surface and having as general formula: X0 (meth)acrylate wherein X is either part of a preformed polymer or is an intermediate agent for polyaddition reaction or is an anchoring group for attachment of a molecule having at least one complementary reactive group. Such process allows formation of new primer by one-step electro-grafting of a reactive polymer called macromonomer.; Such process also allows further modification of an initial electrografted polymer (called primer coating) to increase the coating thickness by the so-called grafting-from technique i.e. polymerization of a second monomer or to introduce other types of polymers(also called top coating) via covalent attachment between the primer and the top coating through the X ester group by the so called grafting onto technique. Such process also allows to graft onto the primer coating compounds like functional polymer, peptide, protein, oligonucleotide, dyes, drugs, anti-bacterian compounds. [less ▲] Detailed reference viewed: 17 (7 ULg) DETECTION OF SPECIFIC NITRATED MARKERSReginster, Jean-Yves ; ; Henrotin, Yves et alPatent (2004) Methods are described for improving the diagnostic possibilities of diseases where oxidative NO-modifications occur, for example inflammatory conditions, cancer, Parkinson's or Alzheimer's disease, and to ... [more ▼] Methods are described for improving the diagnostic possibilities of diseases where oxidative NO-modifications occur, for example inflammatory conditions, cancer, Parkinson's or Alzheimer's disease, and to provide means of monitoring the effects of therapeutical measures taken towards such diseases. The invention enables the detection of disease specific catabolic markers related to oxidative NO-modifications, utilizing an immunoassay comprising antibodies directed against nitrated and non-nitrated epitopes characteristic of a specific protein. [less ▲] Detailed reference viewed: 10 (1 ULg) METHOD FOR MONITORING COLLAGEN TYPE II DEGRADATION IN CARTILAGEReginster, Jean-Yves ; ; Henrotin, Yves et alPatent (2004) A method for improving the diagnostic assessment of cartilage degenerative processes, and to provide means of monitoring the effects of therapeutical measures taken towards arthritic diseases in most ... [more ▼] A method for improving the diagnostic assessment of cartilage degenerative processes, and to provide means of monitoring the effects of therapeutical measures taken towards arthritic diseases in most mammals ultizes an immunoassay to detect fragments of collagen type II resulting from collagenase activity comprising an antibody directed against an epitope comprised in the amino acid sequence HRGYPGLDG, located in the helical region of collagen type II. [less ▲] Detailed reference viewed: 6 (2 ULg) (WO/2004/104211) METHOD FOR DETECTING TOXIC AND NON-TOXIC CYANOBACTERIA; ; et al Patent (2004) This invention is related to a method for detecting toxic and non-toxic cyanobacteria. The method comprises that nucleic acid from a biological sample is brought into contact with an oligonucleotide ... [more ▼] This invention is related to a method for detecting toxic and non-toxic cyanobacteria. The method comprises that nucleic acid from a biological sample is brought into contact with an oligonucleotide designed to be specific for particular regions of the mcyE gene, the mcyE in combination with mcyD, and with an oligonucleotide designed to be specific for 16SrDNA, and the presence or absence of toxic cyanobacteria is detected by a suitable molecular biology method. The invention is related also to oligonucleotides used in the method. [less ▲] Detailed reference viewed: 61 (6 ULg) Novel thiadiazine derivatives useful as AMPA receptor modulators, preparation method, and pharmaceutical compositions containing them; Francotte, Pierre ; et alPatent (2004) Detailed reference viewed: 8 (1 ULg) An illumination device formed by cutting and laminating coated plates; Habraken, Serge ![]() Patent (2004) An illumination device based on multi facet plastic optics is proposed.The fabrication principle is novative and based on specific cutting geometry and coating lamination Detailed reference viewed: 12 (2 ULg) Solar ConcentrationCollette, Jean-Paul ; Defise, Jean-Marc ; Habraken, Serge ![]() Patent (2004) We propose a solar concentrator based on a combination of Fresnel lens and reflectors. This architecture allows for a better light distribution and a thinner lighweight concentrator. Detailed reference viewed: 19 (3 ULg) Process for depositing strong adherend polymer coating onto an electrically conductive surface; Jérôme, Robert ; et alPatent (2004) Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising the step of electrochemical grafting of an active monomer for forming a ... [more ▼] Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising the step of electrochemical grafting of an active monomer for forming a primer coating P onto the surface and having as general formula: X0 (meth)acrylate wherein X is either part of a preformed polymer or is an intermediate agent for polyaddition reaction or is an anchoring group for attachment of a molecule having at least one complementary reactive group. Such process allows formation of new primer by one-step electro-grafting of a macromonomer. Such process also allows further modification of an initial electrografted polymer to increase the coating thickness by the grafting-from technique. Such process also allows to graft onto the primer coating compounds like functional polymer, peptide, protein, oligonucleotide, dyes, drugs, anti-bacterian compounds. [less ▲] Detailed reference viewed: 3 (3 ULg) Verfahren zur Veränderung des Gehalts von Speicherstoffen in PflanzenVigeolas, Hélène ; ; et alPatent (2004) (FR) L'invention concerne un procédé de modification de la teneur en réserves de plantes, pour lequel on utilise des plantes modifiées exprimant de la leghémoglobine et/ou de l'hémoglobine. L'invention ... [more ▼] (FR) L'invention concerne un procédé de modification de la teneur en réserves de plantes, pour lequel on utilise des plantes modifiées exprimant de la leghémoglobine et/ou de l'hémoglobine. L'invention concerne également les plantes correspondantes et leur utilisation. [less ▲] Detailed reference viewed: 15 (3 ULg) In-situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary aminesDetrembleur, Christophe ; ; Patent (2004) PROBLEM TO BE SOLVED: To provide a process for preparing a (co)oligomer or a (co)polymer. ; SOLUTION: The process for preparing a (co)oligomer or (co)polymer comprises forming a mixture containing a ... [more ▼] PROBLEM TO BE SOLVED: To provide a process for preparing a (co)oligomer or a (co)polymer. ; SOLUTION: The process for preparing a (co)oligomer or (co)polymer comprises forming a mixture containing a monoethylencally unsaturated monomer of formula (M): HR<SP>1</SP>C=CR<SP>2</SP>R<SP>3</SP>, an oxidizing agent, at least one polymer or oligomer of formula (I), and an optional radical initiator and heating the mixture at 0-220[deg.]C. [less ▲] Detailed reference viewed: 3 (2 ULg) In-situ polymerization of monoethylenically unsaturated monomers with secondary aminesDetrembleur, Christophe ; ; Patent (2004) PROBLEM TO BE SOLVED: To provide a novel process for producing a homopolymer, a random copolymer, or a block copolymer having a controlled molecular weight, a narrow molecular weight distribution, a high ... [more ▼] PROBLEM TO BE SOLVED: To provide a novel process for producing a homopolymer, a random copolymer, or a block copolymer having a controlled molecular weight, a narrow molecular weight distribution, a high monomer conversion ratio, and a controlled structure. ; SOLUTION: The polymer having a controlled molecular weight, a narrow polydispersibility, a high monomer conversion ratio, and a controlled structure is produced by polymerizing a vinyl monomer during the formation of a mixture of a hindered secondary amine and an oxidizing agent at a relatively low temperature in a short reaction time. It is unnecessary to add a free radical initiator before polymerization. Further, it is unnecessary to preliminarily react the secondary amine with the oxidizing agent before adding the monomer. [less ▲] Detailed reference viewed: 5 (2 ULg) Polymerization method of polymer compound by in situ polymerization of monoethylenically unsaturated monomer and secondary amineDetrembleur, Christophe ; ; Patent (2004) Provided is a method for preparing a polymer compound selected from the group consisting of an oligomer, a cooligomer, a polymer and a copolymer without using an additional free radical initiator ... [more ▼] Provided is a method for preparing a polymer compound selected from the group consisting of an oligomer, a cooligomer, a polymer and a copolymer without using an additional free radical initiator. CONSTITUTION: The method comprises the steps of mixing at least one monoethylenically unsaturated monomer represented by HR1C=CR2R3, at least one oxidant and at least one secondary amine represented by the formula 2; and heating the mixture at a polymerization temperature of 0-220 deg.C, wherein R1, R2 and R3 are independently H, a C1-C20 alkyl group, a C1-C20 cycloalkyl group, a C6-C24 aryl group, a halogen atom, a cyano group, a C1-C20 alkyl ester group, a C1-C20 cycloalkyl ester group, a C1-C20 alkylamide group, a C1-C20 cycloalkylamide group, a C6-C24 aryl ester group or a C6-C24 arylamide group; R4 and R5 are independently a C1-C18 alkyl group, a C2-C18 alkenyl group, a C2-C18 alkynyl group, a C3-C12 cycloalkyl group, a C3-C12 hetero cycloalkyl group, a C6-C24 aryl group or a C4-C12 alkanol group; and R4 and R5 can form a C2-C13 hetero cycloalkyl residue containing O, S or N together with a nitrogen atom connecting them, or a polycyclic ring-based or polycyclic heterocycloaliphatic ring-based residue containing O, S or N, and in the each case the carbon atom of the radical next to the nitrogen atom is substituted with two or three additional organic substituents. [less ▲] Detailed reference viewed: 39 (2 ULg) Preparation method of (co)oligomer or (co)polymer by in-situ polymerization of monoethylenically unsaturated monomer and oligomer or polymer secondary amine to control molecular weight and molecular structureDetrembleur, Christophe ; ; Patent (2004) PURPOSE: Provided is a method for preparing a (co)oligomer or a (co)polymer having a controlled molecular weight, a controlled molecular weight and a narrow polydispersity at a relatively low temperature ... [more ▼] PURPOSE: Provided is a method for preparing a (co)oligomer or a (co)polymer having a controlled molecular weight, a controlled molecular weight and a narrow polydispersity at a relatively low temperature and for a short time. CONSTITUTION: The method comprises the steps of mixing at least one monoethylenically unsaturated monomer represented by HR1C=CR2R3, at least one oxidant, at least one polymer or oligomer represented by the formula 1, and optionally a free radical initiator; and heating the mixture at a temperature of 0-220 deg.C, wherein R1, R2 and R3 are independently H, a C1-C20 alkyl group, a C1-C20 cycloalkyl group, a C6-C24 aryl group, a halogen atom, a cyano group, a C1-C20 alkyl ester group, a C1-C20 cycloalkyl ester group, a C1-C20 alkylamide group, a C1-C20 cycloalkylamide group, a C6-C24 aryl ester group or a C6-C24 arylamide group; Y is an organic residue based on the monomer corresponding to HR1C=CR2R3; m is an integer of 1-50; n is an integer of 1-300; I1 is an initiator; and R4 and X are a secondary or tertiary carbon atom and are independently selected from the group consisting of a C1-C18 alkyl group, a C2-C18 alkenyl group, a C2-C18 alkynyl group, a C3-C12 cycloalkyl group, a C3-C12 hetero cycloalkyl group or a C6-C24 aryl group unsubstituted or substituted with NO2, a halogen atom, an amino group, a hydroxyl group, a cyano group, a carboxyl group, a ketone group, a C1-C4 alkoxy group, a C1-C4 alkylthio group or a C1-C4 alkylamino group. [less ▲] Detailed reference viewed: 19 (2 ULg) In-situ polymerization of monoethylenically unsaturated monomers with secondary aminesDetrembleur, Christophe ; ; Patent (2004) A process for the preparation of any of well-defined homopolymers, random and block copolymers is disclosed. The process that entails forming a mixture of monomers, a hindered secondary amine and an ... [more ▼] A process for the preparation of any of well-defined homopolymers, random and block copolymers is disclosed. The process that entails forming a mixture of monomers, a hindered secondary amine and an oxidizing agent is characterized in the absence of any additional free-radical initiator. [less ▲] Detailed reference viewed: 4 (2 ULg) Situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary aminesDetrembleur, Christophe ; ; Patent (2004) A process for the preparation of (co)oligomers or (co)polymers is disclosed. The process entails first the preparation of a mixture that contains a monoethylenically unsaturated monomer conforming to HR<1 ... [more ▼] A process for the preparation of (co)oligomers or (co)polymers is disclosed. The process entails first the preparation of a mixture that contains a monoethylenically unsaturated monomer conforming to HR<1>C=CR<2>R<3> (M) an oxidizing agent and at least one polymer or oligomer conforming to formula (I), and an optional free radical initiator and then heating the mixture at a temperature in the range of 0 DEG C. to 220 DEG C. [less ▲] Detailed reference viewed: 8 (2 ULg) The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary aminesDetrembleur, Christophe ; ; Patent (2004) A process for the preparation of (co)oligomers or (co)polymers is disclosed. The process entails first the preparation of a mixture that contains a monoethylenically unsaturated monomer conforming to HR<1 ... [more ▼] A process for the preparation of (co)oligomers or (co)polymers is disclosed. The process entails first the preparation of a mixture that contains a monoethylenically unsaturated monomer conforming to HR<1>C = CR<2>R<3> an oxidizing agent and at least one polymer or oligomer conforming to formula (I), <CHEM> and an optional free radical initiator and then heating the mixture at a temperature in the range of 0 DEG C to 220 DEG C. [less ▲] Detailed reference viewed: 3 (2 ULg) In situ polymerization with monoethenoid unsaturation monomer of secondary amineDetrembleur, Christophe ; ; Patent (2004) The present invention relates to a new process for the preparation of well-defined homopolymers, random and block copolymers using a mixture of a hindered secondary amine and an oxidizing agent, without ... [more ▼] The present invention relates to a new process for the preparation of well-defined homopolymers, random and block copolymers using a mixture of a hindered secondary amine and an oxidizing agent, without any additional free-radical initiator. [less ▲] Detailed reference viewed: 5 (2 ULg) In-situ polymerization of monoethylenically unsaturated monomers with secondary aminesDetrembleur, Christophe ; ; Patent (2004) A process for the preparation of any of well-defined homopolymers, random and block copolymers is disclosed. The process that entails forming a mixture of monomers, a hindered secondary amine and an ... [more ▼] A process for the preparation of any of well-defined homopolymers, random and block copolymers is disclosed. The process that entails forming a mixture of monomers, a hindered secondary amine and an oxidizing agent is characterized in the absence of any additional free-radical initiator. [less ▲] Detailed reference viewed: 3 (2 ULg) The in-situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary aminesDetrembleur, Christophe ; ; Patent (2004) The present invention relates to a new process for the preparation of well-defined random and block polymers or copolymers using hindered secondary amine-oligomers or polymers. Detailed reference viewed: 4 (2 ULg) In-situ polymerization of monoethylenically unsaturated monomers with secondary aminesDetrembleur, Christophe ; ; Patent (2004) The present invention relates to a new process for the preparation of well-defined homopolymers, random and block copolymers using a mixture of a hindered secondary amine and an oxidizing agent, without ... [more ▼] The present invention relates to a new process for the preparation of well-defined homopolymers, random and block copolymers using a mixture of a hindered secondary amine and an oxidizing agent, without any additional free-radical initiator. [less ▲] Detailed reference viewed: 6 (2 ULg) The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines; ; Detrembleur, Christophe ![]() Patent (2004) The present invention relates to a new process for the preparation of well-defined random and block polymers or copolymers using hindered secondary amine-oligomers or polymers. Detailed reference viewed: 7 (2 ULg) In-situ polymerization of monoethylenically unsaturated monomers with secondary amines; ; Detrembleur, Christophe ![]() Patent (2004) The present invention relates to a new process for the preparation of well-defined homopolymers, random and block copolymers using a mixture of a hindered secondary amine and an oxidizing agent, without ... [more ▼] The present invention relates to a new process for the preparation of well-defined homopolymers, random and block copolymers using a mixture of a hindered secondary amine and an oxidizing agent, without any additional free-radical initiator. [less ▲] Detailed reference viewed: 21 (9 ULg) Process for depositing strong adherend polymer coating onto an electrically conductive surface; Jérôme, Robert ; et alPatent (2004) Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising an electrochemical grafting at the surface of an active monomer for forming a ... [more ▼] Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising an electrochemical grafting at the surface of an active monomer for forming a primer coating P onto said surface and having as general formula: X0 (meth)acrylate wherein X is either part of a preformed polymer or is an intermediate agent for polyaddition reaction or is an anchoring group for attachment of a molecule having at least one complementary reactive group. Such process allows formation of new primer by one-step electro-grafting of a reactive polymer called macromonomer.; Such process also allows further modification of an initial electrografted polymer (called primer coating) to increase the coating thickness by the so-called grafting-from technique i.e. polymerization of a second monomer or to introduce other types of polymers(also called top coating) via covalent attachment between the primer and the top coating through the X ester group by the so called grafting onto technique. Such process also allows to graft onto the primer coating compounds like functional polymer, peptide, protein, oligonucleotide, dyes, drugs, anti-bacterian compounds. [less ▲] Detailed reference viewed: 4 (1 ULg) Controlled free-radical polymerization products using new controlled agents; ; Detrembleur, Christophe et alPatent (2004) A process for the production of polymers by means of pseudo-living free-radical polymerization is disclosed. The process entails (i) reacting a polymerizable vinyl monomer with nitrogen monoxide and at ... [more ▼] A process for the production of polymers by means of pseudo-living free-radical polymerization is disclosed. The process entails (i) reacting a polymerizable vinyl monomer with nitrogen monoxide and at least one initiator to prepare a free-radical intermediate product, and (ii) polymerizing the intermediate product optionally together with one or more additional monomers and/or with a free-radical initiator. [less ▲] Detailed reference viewed: 12 (5 ULg) Method for producing functionalized alkoxyamine initiator and use thereofDetrembleur, Christophe ; ; Patent (2004) PROBLEM TO BE SOLVED: To provide a method for producing a functionalized alkoxyamine initiator and its use in radical polymerization process. ; SOLUTION: The invention provides a one-pot process for the ... [more ▼] PROBLEM TO BE SOLVED: To provide a method for producing a functionalized alkoxyamine initiator and its use in radical polymerization process. ; SOLUTION: The invention provides a one-pot process for the production of a functionalized alkoxyamine of general formula (I) (for example, R<SP>1</SP>and R<SP>2</SP>are each H; R<SP>3</SP>is phenyl; and R<SP>4</SP>and R<SP>5</SP>together with nitrogen atom form an alicyclic 6-membered ring). The method includes (1) the formation of an aqueous phase and nitroxyl radical by reacting an oxidizing agent with a secondary amine having steric hindrance and (2) the removal of the aqueous phase and the addition of one or more vinyl monomers to the nitroxyl radical according to the method and system for the production of the radical. The invention further provides a monomer polymerization method using the functionalized alkoxyamine. [less ▲] Detailed reference viewed: 3 (1 ULg) Use of family 8 enzymes with xylanolytic activity in baking; ; et al Patent (2004) Detailed reference viewed: 24 (3 ULg) A process for the synthesis of alkoxyamines and their use in controlled radical polymerizationDetrembleur, Christophe ; ; Patent (2004) PROBLEM TO BE SOLVED: To provide a method for synthesizing an alkoxyamine, and to provide a method for using the same in controlled radical polymerization. ; SOLUTION: This method for synthesizing the ... [more ▼] PROBLEM TO BE SOLVED: To provide a method for synthesizing an alkoxyamine, and to provide a method for using the same in controlled radical polymerization. ; SOLUTION: This method for synthesizing the alkoxyamine expressed by general formula (I) or (II) [preferably, general formula (I)] comprises a one-pot process, wherein the process includes (1) reacting an oxidizing agent (A) with a sterically hindered secondary amine of general formula (III) in a water-containing medium to form a reaction product and an aqueous phase, (2) removing the aqueous phase, and (3) adding a free radical initiator (B) to the reaction product under such a condition that decomposition of the initiator is promoted to generate free radicals. Further, a method for polymerizing a monomer, namely the method for using the alkoxyamine synthesized by the method with originality, is provided [less ▲] Detailed reference viewed: 15 (2 ULg) Solar ConcentratorCollette, Jean-Paul ; Defise, Jean-Marc ; Habraken, Serge ![]() Patent (2004) A solar concentrator based on multi V shape reflectors is proposed to reduce the PV cell area (and cost). The optimisation is for space concentration purpose but extendable to terrestrial system. Detailed reference viewed: 35 (6 ULg) Preparation of functionalized alkoxyamine initiator and its useDetrembleur, Christophe ; ; Patent (2004) A one-pot process for the preparation of functional alkoxyamines of the general formula (I),is disclosed. The process entails (1) reacting an oxidizing agent with a sterically hindered secondary amine to ... [more ▼] A one-pot process for the preparation of functional alkoxyamines of the general formula (I),is disclosed. The process entails (1) reacting an oxidizing agent with a sterically hindered secondary amine to produce an aqueous phase and a nitroxyl radical (2) removing the aqueous phase and adding to the nitroxyl radical one or more vinyl monomer(s) conforming to a formula and a system which produces free radicals. Also disclosed is a process of polymerizing monomers using the functional alkoxyamine. [less ▲] Detailed reference viewed: 9 (3 ULg) A new process for the synthesis of alkoxyamines active in controlled radical polymerizationDetrembleur, Christophe ; ; Patent (2004) The present invention relates to a new process for the preparation of alkoxyamine initiators and to a process of radical polymerization using the alkoxyamine initiators as intermediates. Detailed reference viewed: 6 (2 ULg) One-pot process for the preparation of functionalized alkoxyaminesDetrembleur, Christophe ; ; Patent (2004) The present invention relates to a new one-pot process for the preparation of functionalized alkoxyamine initiators of the formula (I) <CHEM> from amines of the formula (II) <CHEM> and to a process of ... [more ▼] The present invention relates to a new one-pot process for the preparation of functionalized alkoxyamine initiators of the formula (I) <CHEM> from amines of the formula (II) <CHEM> and to a process of controlled radical polymerization using the functionalized alkoxyamine as initiators. In the above formulae, R<1>-R<5> have the meanings given in the description. [less ▲] Detailed reference viewed: 3 (2 ULg) Process for the synthesis for alkoxy amines and their use in controlled radical polymerizationDetrembleur, Christophe ; ; Patent (2004) A one-pot process for the preparation of alkoxyamines conforming to formulae (I) or (II), preferably (I) is disclosed. The process entails (1) reacting of an oxidizing agent (A) with a sterically hindered ... [more ▼] A one-pot process for the preparation of alkoxyamines conforming to formulae (I) or (II), preferably (I) is disclosed. The process entails (1) reacting of an oxidizing agent (A) with a sterically hindered secondary amine of the general formula (III), in a water-containing medium to form a reaction product and an aqueous phase, (2) removing of the aqueous phase, and (3) (adding to the reaction product a free-radical initiator (B) under conditions that promote the decomposition of the initiator to generate free radicals. Also disclosed is a process for polymerizing monomers, the process using the alkoxyamine prepared by the inventive process. [less ▲] Detailed reference viewed: 5 (2 ULg) Preparation of functionalized alkoxyamine initiator and its useDetrembleur, Christophe ; ; Patent (2003) A one-pot process for the preparation of functional alkoxyamines of the general formula (I), is disclosed. The process entails (1) reacting an oxidizing agent with a sterically hindered secondary amine to ... [more ▼] A one-pot process for the preparation of functional alkoxyamines of the general formula (I), is disclosed. The process entails (1) reacting an oxidizing agent with a sterically hindered secondary amine to produce an aqueous phase and a nitroxyl radical (2) removing the aqueous phase and adding to the nitroxyl radical one or more vinyl monomer(s) conforming to a formula and a system which produces free radicals. Also disclosed is a process of polymerizing monomers using the functional alkoxyamine. [less ▲] Detailed reference viewed: 11 (1 ULg) The preparation of functionalized alkoxyamine initiator and its useDetrembleur, Christophe ; ; Patent (2003) A one-pot process for the preparation of functional alkoxyamines of the general formula (I), (See Formula I) is disclosed. The process entails (1) reacting an oxidizing agent with a sterically hindered ... [more ▼] A one-pot process for the preparation of functional alkoxyamines of the general formula (I), (See Formula I) is disclosed. The process entails (1) reacting an oxidizing agent with a sterically hindered secondary amine to produce an aqueous phase and a nitroxyl radical (2) removing the aqueous phase and adding to the nitroxyl radical one or more vinyl monomer(s) conforming to a formula and a system which produces free radicals . Also disclosed is a process of polymerizing monomers using the function al alkoxyamine. [less ▲] Detailed reference viewed: 4 (2 ULg) A process for the synthesis of alkoxyamines and their use in controlled radical polymerizationDetrembleur, Christophe ; ; Patent (2003) A one-pot process for the preparation of alkoxyamines conforming to formulae (I) or (II), preferably (I) (See formulas I and II) is disclosed. The process entails (1) reacting of an oxidizing agent (A ... [more ▼] A one-pot process for the preparation of alkoxyamines conforming to formulae (I) or (II), preferably (I) (See formulas I and II) is disclosed. The process entails (1) reacting of an oxidizing agent (A) with a sterically hindered secondary amine of the general formula (III), (See formula III) in a water-containing medium to form a reaction product and an aqueous phase , (2) removing of the aqueous phase, and (3) adding to the reaction product a free-radical initiator (B) under conditions that promote the decomposition of the initiator to generate free radicals. Also disclosed is a process for polymerizing monomers, the process using the alkoxyamine prepared by the inventive process. [less ▲] Detailed reference viewed: 12 (2 ULg) VERFAHREN ZUM ERHÖHEN DES ÖLGEHALTES IN PFLANZENVigeolas, Hélène ; ; et alPatent (2003) The invention relates to methods for increasing the oil content in plants, preferably in the seeds of plants, by expression of glycerol-3-phosphatdehydrogenases (G3PDH) from yeast, preferably from ... [more ▼] The invention relates to methods for increasing the oil content in plants, preferably in the seeds of plants, by expression of glycerol-3-phosphatdehydrogenases (G3PDH) from yeast, preferably from Saccharomyces cerevisiae. The invention also relates to expression constructs for the expression of G3PDH yeast in plants, preferably in the seeds of plants, transgenic plants expressing G3PDH, and to the use of said transgenic plants in the production of foodstuffs, feed, seeds, pharmaceuticals or fine chemicals, especially in the production of oils. [less ▲] Detailed reference viewed: 12 (3 ULg) Crèmes laitières reconstituéesDanthine, Sabine ; Blecker, Christophe ; Paquot, Michel et alPatent (2003) Detailed reference viewed: 7 (3 ULg) Nucleotidaktivierte Di- und Oligosaccharide sowie Verfahren zu deren HerstellungZervosen, Astrid ; ; et alPatent (2003) Detailed reference viewed: 2 (0 ULg) Portable Holographic Marking UnitHabraken, Serge ; ; Patent (2003) Detailed reference viewed: 11 (2 ULg) Light Guiding Plate With Internal Micro-PrismsHabraken, Serge ![]() Patent (2003) A guiding plate is used to split light in several beams, called fan out. In a different embodiment, the light splitting is used to produce an extraction as a uniform lighting Detailed reference viewed: 13 (3 ULg) Hydrosoluble mixtures of cyproterone and/or an ester of it, processes to obtain them and uses thereofDelattre, Luc ; ; Evrard, Brigitte ![]() Patent (2003) Detailed reference viewed: 4 (1 ULg) Hydroponic growing device adapted for the growing and scientific study of arabidopsis thaliana; Tocquin, Pierre ; Pieltain, Alexandra et alPatent (2003) Detailed reference viewed: 26 (2 ULg) Pyridinic sulfonamide derivatives, method of production and use thereof; Pirotte, Bernard ; et alPatent (2003) Detailed reference viewed: 3 (2 ULg) Solar ConcentratorCollette, Jean-Paul ; Defise, Jean-Marc ; Habraken, Serge ![]() Patent (2003) A space solar concentrator based on light weight reflectors Detailed reference viewed: 17 (3 ULg) Method for identifying animals likely to have good milk production qualities by analyzing the polymorphism of the PIT-1 and Kappa-Casein genesRenaville, Robert ; Gengler, Nicolas ![]() Patent (2003) Detailed reference viewed: 17 (0 ULg) Porous carbon materialPirard, Jean-Paul ; Pirard, René ; Job, Nathalie ![]() Patent (2003) Detailed reference viewed: 2 (0 ULg) Process for depositing strong adherend polymer coating onto an electrically conductive surfaceDetrembleur, Christophe ; ; et alPatent (2002) Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising an electrochemical grafting at the surface of an active monomer for forming a ... [more ▼] Process for depositing by electrografting a strong adherent polymer coating onto an electrically conductive surface comprising an electrochemical grafting at the surface of an active monomer for forming a primer coating P onto said surface and having as general formula: X0 (meth)acrylate wherein X is either part of a preformed polymer or is an intermediate agent for polyaddition reaction or is an anchoring group for attachment of a molecule having at least one complementary reactive group. Such process allows formation of new primer by one-step electro-grafting of a reactive polymer called macromonomer.; Such process also allows further modification of an initial electrografted polymer (called primer coating) to increase the coating thickness by the so-called grafting-from technique i.e. polymerization of a second monomer or to introduce other types of polymers(also called top coating) via covalent attachment between the primer and the top coating through the X ester group by the so called grafting onto technique. Such process also allows to graft onto the primer coating compounds like functional polymer, peptide, protein, oligonucleotide, dyes, drugs, anti-bacterian compounds. [less ▲] Detailed reference viewed: 8 (4 ULg) Process for depositing strong adherend polymer coating onto an electrically conductive surface; Jérôme, Robert ; et alPatent (2002) Detailed reference viewed: 21 (2 ULg) Controlled free-radical polymerization products using new controlled agents; ; Detrembleur, Christophe et alPatent (2002) A process for the production of polymers by means of pseudo-living free-radical polymerization is disclosed. The process entails (i) reacting a polymerizable vinyl monomer with nitrogen monoxide and at ... [more ▼] A process for the production of polymers by means of pseudo-living free-radical polymerization is disclosed. The process entails (i) reacting a polymerizable vinyl monomer with nitrogen monoxide and at least one initiator to prepare a free-radical intermediate product, and (ii) polymerizing the intermediate product optionally together with one or more additional monomers and/or with a free-radical initiator. [less ▲] Detailed reference viewed: 4 (4 ULg) Controlled free-radical polymerization products using new controlled agentsJérôme, Robert ; ; et alPatent (2002) The present invention relates to a new process for the production of polymers by means of pseudo-living free-radical polymerization using nitrogen monoxide, as well as to intermediate products and ... [more ▼] The present invention relates to a new process for the production of polymers by means of pseudo-living free-radical polymerization using nitrogen monoxide, as well as to intermediate products and polymers obtainable by the process according to the invention and the use thereof. [less ▲] Detailed reference viewed: 8 (2 ULg) Controlled free-radical polymerization products using new controlled agents; ; Detrembleur, Christophe et alPatent (2002) The present invention relates to a new process for the production of polymers by means of pseudo-living free-radical polymerization using nitrogen monoxide, as well as to intermediate products and ... [more ▼] The present invention relates to a new process for the production of polymers by means of pseudo-living free-radical polymerization using nitrogen monoxide, as well as to intermediate products and polymers obtainable by the process according to the invention and the use thereof. [less ▲] Detailed reference viewed: 10 (3 ULg) Controlled free-radical polymerization products using new controlled agents; ; Detrembleur, Christophe et alPatent (2002) The present invention relates to a new process for the production of polymers by means of pseudo-living free-radical polymerization using nitrogen monoxide, as well as to intermediate products and ... [more ▼] The present invention relates to a new process for the production of polymers by means of pseudo-living free-radical polymerization using nitrogen monoxide, as well as to intermediate products and polymers obtainable by the process according to the invention and the use thereof. [less ▲] Detailed reference viewed: 10 (5 ULg) Polypeptide inducing HIV-neutralising antibodiesBrasseur, Robert ; Charloteaux, Benoît ; et alPatent (2002) Detailed reference viewed: 8 (0 ULg) Nouvelles fractions d'inuline. Leur préparation et leur utilisation.Blecker, Christophe ; Razafindralambo, Hary ; et alPatent (2002) Detailed reference viewed: 10 (6 ULg) Optical Device For Projection Display SystemHabraken, Serge ![]() Patent (2002) An optical system to track a laser pointer in a multi media presentation. The information is used for dispaying symbols or activation of controls Detailed reference viewed: 11 (4 ULg) Cyclic esterketone compounds, processes for the synthesis thereof and process for the preparation of poly (esterketone) polymers; ; Lecomte, Philippe et alPatent (2002) Unsubstituted oxepane-diones useful as monomers for the production of polymers, process for the synthesis thereof by oxidation of unsubstituted cyclohexanediones, process for the preparation of ... [more ▼] Unsubstituted oxepane-diones useful as monomers for the production of polymers, process for the synthesis thereof by oxidation of unsubstituted cyclohexanediones, process for the preparation of polyesterketone polymers by polymerization of cyclic esterketones and polyesterketone polymers so obtained. [less ▲] Detailed reference viewed: 6 (2 ULg) USE OF COX-2 INHIBITORS FOR PREVENTING IMMUNODEFICIENCY; Moutschen, Michel ; Rahmouni, Souad et alPatent (2002) The present invention provides a method for treating or preventing a disorder typified by an immunodificiency (e.g. HIV), wherein the patient is administered a COX-2 inhibitor or derivative or ... [more ▼] The present invention provides a method for treating or preventing a disorder typified by an immunodificiency (e.g. HIV), wherein the patient is administered a COX-2 inhibitor or derivative or pharmaceutically acceptable salt thereof, preferably diisopropylfluorophasphaate, L-745337, rofecoxi, NS 398, SC 58125, etodolac, meloxicam, celecoxib flusolide or nimesulide, and compositions and products containing the same or use of the same in preparing medicaments and for treatment. [less ▲] Detailed reference viewed: 26 (8 ULg) Chanel catfish virus vaccine; Martial, Joseph ; Patent (2001) An attenuated, avirulent recombinant vaccine providing challenged protection against channel catfish virus comprises deletion of gene 50. Gene 50 encodes a secreted glycoprotein. Removal of gene 50, or ... [more ▼] An attenuated, avirulent recombinant vaccine providing challenged protection against channel catfish virus comprises deletion of gene 50. Gene 50 encodes a secreted glycoprotein. Removal of gene 50, or replacement of gene 50 with foreign genetic material, provides a vaccine with which induces virus specific immunity against CCV disease. [less ▲] Detailed reference viewed: 30 (1 ULg) Cyclic esterketone compounds and processes for the synthesis and use thereof; ; Lecomte, Philippe et alPatent (2001) Cyclic esterketone compounds, and in particular, 2-oxepane-1,5-dione, which are useful as a monomer for the production of polymers, and in particular for the production of poly(2-oxepane-1,5-dione ... [more ▼] Cyclic esterketone compounds, and in particular, 2-oxepane-1,5-dione, which are useful as a monomer for the production of polymers, and in particular for the production of poly(2-oxepane-1,5-dione). Processes are also disclosed for both the synthesis of this new compound and for the use (polymerization) thereof for the preparation of poly(2-oxepane-1,5-dione). The poly(2-oxepane-1,5-dione) polymers and copolymers which are obtained by use of the polymerization processes with the monomer compounds are also disclosed. [less ▲] Detailed reference viewed: 4 (2 ULg) Novel benzothiadiazine derivatives, preparation method and pharmaceutical compositions containing themPirotte, Bernard ; De Tullio, Pascal ; et alPatent (2001) Detailed reference viewed: 3 (1 ULg) |
||