The invention pertains to pigment compositions comprising from 70 to 93%, preferably from 81 to 93%, of &egr; copper phthalocyanine, from 5 to 18% of an aminomethyl-substituted phthalocyanine, from 2 to 15% of an ammonium sulfonato phthalocyanine and less than 2% of other phthalocyanine compounds, preferably made by wet-milling a mixture of α copper phthalocyanine and &egr; copper phthalocyanine together with the aminomethyl-substituted phthalocyanine and a milling aid in an organic liquid and adding the ammonium sulfonato phthalocyanine before the milling aid and the organic liquid are separated from the wet-milled mixture.
C09B 67/22 - Mélanges de pigments ou de colorants différents, ou de solutions solides de pigments ou de colorants
G03F 7/00 - Production par voie photomécanique, p. ex. photolithographique, de surfaces texturées, p. ex. surfaces impriméesMatériaux à cet effet, p. ex. comportant des photoréservesAppareillages spécialement adaptés à cet effet
C09B 67/50 - Modifications cristallines de colorants ou de pigments de phtalocyanines
Subject matter of the present invention is a lubricant composition comprising a) A lubricant; b) A triazole metal deactivator; c) A borate ester; and, optionally, d) An amine phosphate. The invention allows for the formulation of engine lubricants that can protect copper, lead, iron and zinc from corrosion for the life of the lubricant.
C10M 133/44 - Cycle à cinq chaînons ne contenant que du carbone et de l'azote
C10M 139/00 - Compositions lubrifiantes caractérisées en ce que l'additif est un composé organique non macromoléculaire contenant des atomes d'éléments non prévus dans l'un des groupes
C10M 141/12 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'au moins deux composés couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé organique contenant des atomes d'éléments non prévus par les groupes
This invention encompasses novel amphiphilic block copolymers comprising polysiloxane blocks and polycationic blocks. The polycationic blocks are formed from diallyldialkylammonium derivatives. The formed block copolymers are particularly useful for treating or conditioning keratinous substances, such as hair or skin.
Disclosed are dyes of Formula (I) wherein D is the radical of anthraquinone, acridine, azo, azomethine, hydrazomethine, benzodifuranone, coumarine, diketopyrrolopyrrol, dioxaxine, diphenylmethane, formazane, indigoid, indophenol, naphtalimide, naphthaquinone, nitroaryl, merocyanine, methine, oxazine,perinone, perylene, pyrenequinone, phtalocyanine, phenazine, quinoneimine, quinacridone, quinophtalone, stilbene, styryl, triphenylmethane, xanthene, thiazine dye and thioxanthene dye; Q is C 1-C 30alkylene, -C 2-C 12alkenylene, C 5-C 10arylene-, C 5-C 10cycloalkylene-or -C 1- C 10alkylene(C5-C10arylene)-which may be interrupted and/or terminated at one or both ends by one or more than one -O-, -S-, -N=, -N(R 1)-, SO 2, -(CH 2CH 2-O) 1-5-, -(CH 2CH 2CH 2-O) 1-5-, -C(O)-, -C(O)-C1-C12alkenylene, -C(O)O-, -OCO-, AN+ R 1 R 2, -CON(R 1)-, -C(NR1R2) 2-, -(R 1)NC(O)-, -CSR1-or an optionally substituted, saturated or unsaturated, fused or non-fused aromatic or nonaromatic (hetero)cyclic) bivalent radical optionally comprising at least one heteroatom; -O-; -S-; -N(R1)-; SO2; -(CH2CH2-O) 1-5-; -C(O)-; -C(O)-C1-C12alkenylene; -C(O)O-, -OCO-;B N+ R 1 R 2; -CON(R1)-; -C(NR1R 2) 2-; -(R1)NC(O)-; CSR1; saturated or unsaturated, fused or non-fused aromatic or nonaro- matic bivalent radical optionally comprising at least one heteroatom; which is optionally substituted by C1-C30alkyl, C1-C30alkoxy, -C2-C12alkenyl, C5-C10aryl, C5-C10cycloalkyl, C1- C10alkyl(C5-C10arylene), hydroxy or D+; R1and R2 independently from each other are hydrogen; or unsubstituted or substituted, straight-chain or branched, monocyclic or polycyclic, interrupted or uninterrupted C1- C14alkyl; C1-C14hydroxyalkyl; C1-C14 aminoalkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl-C1- C10alkyl; or C 5-C 10alkyl(C5-C10aryl).
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 5/10 - Préparations pour la teinture permanente des cheveux ou des poils
C09B 69/00 - Colorants non prévus par un seul groupe de la présente sous-classe
The present invention is aimed at a method of providing wettability to polyester fibers or filaments, to woven or nonwoven fabrics made therefrom and to resultant articles of manufacture. The method comprises melt extruding a mixture comprising a polyester and one or more additives selected from the group consisting of phenylalkyl-oxy-alkyl metal sulfonates, alkyl-oxy-alkyl metal sulfonates,polyethyleneoxy-alkyl metal sulfonates,alkyl-polyethylene-oxy-alkyl metal sulfonatesandalkyl-1,2-disulfonate metal sulfonates into a plurality of fibers or filaments and cooling the fibers or filaments.
D01F 1/10 - Autres agents modifiant les propriétés de ces filaments
D01F 6/62 - Filaments, ou similaires, faits par l’homme, à un seul composant, formés de polymères synthétiquesLeur fabrication à partir de produits d'homopolycondensation à partir de polyesters
D01F 6/92 - Filaments, ou similaires, faits par l’homme, à un seul composant, formés de polymères synthétiquesLeur fabrication à partir de mélanges de produits de polycondensation comme constituant majeur avec d'autres polymères ou des composés de bas poids moléculaire de polyesters
D01F 8/14 - Filaments, ou similaires, faits par l’homme, conjugués, c.-à-d. à plusieurs composantsLeur fabrication à partir de polymères synthétiques avec au moins un polyester comme constituant
A61K 8/44 - Acides aminocarboxyliques ou leurs dérivés, p. ex. acides aminocarboxyliques contenant du soufreLeurs sels, esters ou dérivés N-acylés
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
7.
TINTED CLEAR COATINGS UV STABILI ZED WITH 2-HYDROXY PHENYL TRIAZINE
The present invention pertains to tinted clear coating compositions comprising (a) a 2- hydroxy phenyl triazine UV absorber, (b) a pigment, and (c) a binder and to coatings obtained by applying such compositions to a substrate.
C07D 251/24 - Composés hétérocycliques contenant des cycles triazine-1, 3, 5 non condensés avec d'autres cycles comportant trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des atomes d'hydrogène ou de carbone liés directement à au moins un atome de carbone du cycle à trois atomes de carbone du cycle
C09K 15/30 - Compositions anti-oxydantesCompositions inhibant les modifications chimiques contenant des composés organiques contenant un hétérocycle avec au moins un azote comme membre du cycle
The invention relates to the use of compounds of formulae (I) and/or (II) as colorless IR absorbers wherein M is Ni, Pd, Pt, Au, Ir, Fe, Zn, W, Cu, Mo, In, Mn, Co, Mg, V, Cr or Ti, X1, X2 and X3 are each independently of the others sulfur or oxygen, R1, R2, R3, R4, R5 and R6 are each independently of the others hydrogen, NR7R8, unsubstituted or substituted C1-C18alkyl, C1-C18 alkyl wherein the alkylene chain is interrupted with oxygen, unsubstituted or substituted C1-C18alkenyl, unsubstituted or substituted aryl, unsubstituted or substituted arylalkyl or unsubstituted or substituted heteroarylalkyl, R7 and R8, each independently of the other, being unsubstituted or substituted C1-C18alkyl, unsubstituted or substituted aryl, unsubstituted or substituted arylalkyl or unsubstituted or substituted heteroarylalkyl, a further IR absorber optionally being added to the compounds of formulae (I) and (II). The invention relates also to novel dithiolene compounds of formulae (I) and (II) wherein X1 is oxygen and X2 and X3 are oxygen or sulfur. The invention relates furthermore to novel dithiolene compounds of formulae (I) and (II) wherein R1 to R6 are NR7R8.
C07D 239/22 - Composés hétérocycliques contenant des cycles diazine-1, 3 ou diazine-1, 3 hydrogéné non condensés avec d'autres cycles comportant deux liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des hétéro-atomes liés directement aux atomes de carbone du cycle
C07F 15/00 - Composés contenant des éléments des groupes 8, 9, 10 ou 18 du tableau périodique
The instant invention relates to novel phthalocyanines and their use as IR-absorbers, in particular in transparent thermoplastic or crosslinkable polymers. A further aspect of the invention is a composition of these phthalocyanines and thermoplastic or crosslinkable polymers and an architectural or automotive glazing containing these phthatolcyanines.
The present invention is directed to a premoistened, disposable, cleaning substrate to improve dirt pick-up and to retard redeposition of the dirt back onto the cleaned leather surface. The said substrate is incorporated therein with a cleaning composition to improve cleaning and impart protection and/or preservation of the leather surface or article. The said substrate is further incorporated therein with UV absorbers to further protect the leather surface, improve appearance and durability. The impregnated substrate can be employed to clean leather surfaces such as furniture, clothing, shoes, belts, automobile upholstery and the like. In addition, a method of preserving a leather surface or article by contacting said surface with said substrate is disclosed.
The present invention relates to novel pigment mixtures comprising at least two different particulate components A and B. The first component A comprises titanium suboxide(s), a titanium oxynitride or a titanium nitride species. Component B particle comprises inorganic, or organic pigments. The titanium suboxide particles display a bluish metallic luster, are new and form a further aspect of the present invention. When combined with particles from component B such as variously coated micas, for example, the bluish or bluish/black metallic color effect from component A leads to special color effects in the various mixtures.
The invention relates to a time temperature indicator comprising a) at least one photo-chromic colorant introduced into and/or atop a matrix substrate and charged by exposure to UV light; b) at least a transparent colorless or a transparent colored light absorbing protecting layer adhered to the underlying layer a) which contains the photo-chromic colorant; characterized in that the light absorbing protecting layer comprises 1 -50 wt% of an UV light absorber or an UV light absorber mixture and 0.1 -10 wt% of an optical brightener wherein the weight ratio of the UV light absorber and optical brightener is 0.1 -10.
The present invention provides coating compositions comprising (i) a) a compound containing a free carbonyl group and b) a nucleophile or (ii) a compound containing a free carbonyl group, which compound is substituted with one or more nucleophilic groups. The present invention also provides a process for the preparation of these compositions, substrates coated with these compositions and a process for their preparation, a process for preparing marked substrates using these compositions, and marked substrates obtainable by the latter process.
A pigment composition comprising an intimate mixture of an organic pigment and fumed silica is prepared which exhibit improved coloristic characteristics including excellent chroma, color strength and enhanced color flop when incorporated into in polymeric systems, such as plastics or surface coatings, for example inks and paints. Also provided are coating compositions and plastic articles that are pigmented with a tinctorially effective amount of the inventive pigment composition. A particular embodiment of the invention relates to pigments useful in automotive coatings.
C09B 67/08 - Colorants ou pigments particulaires enrobés
C09B 67/20 - Préparations à base de pigments organiques
C09D 5/00 - Compositions de revêtement, p. ex. peintures, vernis ou vernis-laques, caractérisées par leur nature physique ou par les effets produitsApprêts en pâte
Disclosed is a UV filter composition comprising (a) an organic UV absorber of formula (1), wherein R1 and R2, independently of one another, are C3-C18alkyl; C2-C18alkenyl; a radical of the formula -CH2-CH(OH)-CH2-O-T1; or R1 and R2 are a radical of the formula (4a); R7 is a direct bond; a straight-chain or branched C1-C4alkylene radical or a radical of the formula (I) or (II); R8, R9 and R10, independently of one another, are C1-C18alkyl; C1-C18alkoxy or a radical of the formula (III); R11 is C1-C5 alkyl; m1 is a number from 1 to 4; p1 is 0; or a number from 1 to 5; A1 is a radical of the formula (1b), (1c) or (1d); R3 is hydrogen; C1-C10alkyl; -(C H2 C H R5-O) n1-T2; or -CH2-CH(-OH)-CH2-O-T2; R4 is hydrogen; M; C1-C5alkyl; or -(C H2)m2 -O-T3; R5 is hydrogen; or methyl; T1, T2 and T3 independently from each other are hydrogen; or C1-C18alkyl; Q1 is C1-C18alkyl, M is a metal cation; m2 is 1 to 4; and n1 is 1-16, (b) dimethyl capramide, (c) a cosmetically acceptable carrier; and water.
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
Disclosed are merocyanine derivatives which correspond to the formula (I), wherein L1, L2 and L3 independently of each other are hydrogen; or L1 and L3 may be linked together to form a carbocyclic ring; R3 and R4 independently of each other are CN; -COR5; -COOR5; -CONR5R6; C1-C22alkyl; C2- C22alkenyl; C2-C22alkinyl; C3-C12cycloalkyl; C3-C12cycloalkenyl; C7-C20aralkyl; C1- C20heteroalkyl; C3-C12cycloheteroalkyl; C3-C18heteroaralkyl; C6-C20 aryl; C1- C12alkylcarbonylamino-C6-C20aryl; C2-C12heteroaryl; or -X2-Sil2; n is a number from 1 to 4; the meaning of R1 and R2 depends on the definition of n. The compounds are useful as UV absorbers for cosmetic applications.
C09B 23/10 - Colorants méthiniques ou polyméthiniques, p. ex. du type cyanine caractérisés par la chaîne méthinique contenant un nombre pair de groupes CH
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
C07F 7/18 - Composés comportant une ou plusieurs liaisons C—Si ainsi qu'une ou plusieurs liaisons C—O—Si
A multifilament, a monofilament, a non-woven or a tape, each having 1 to 2000 Denier per filament and a draw ratio of 1 :2 to 1 :11 and each made of a composition containing the components (A) a polyolefin, (B) for example a compound of the formula (B-1-a-1), (C) for example a compound of the formula (C-1-b-1), wherein b1 is a number from 2 to 20, and optionally (D) one or more inorganic and/or organic pigments.
D01F 1/10 - Autres agents modifiant les propriétés de ces filaments
D01F 6/04 - Filaments, ou similaires, faits par l’homme, à un seul composant, formés de polymères synthétiquesLeur fabrication à partir d'homopolymères obtenus par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone à partir des polyoléfines
D01F 6/06 - Filaments, ou similaires, faits par l’homme, à un seul composant, formés de polymères synthétiquesLeur fabrication à partir d'homopolymères obtenus par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone à partir des polyoléfines à partir de polypropylène
D01F 6/30 - Filaments, ou similaires, faits par l’homme, à un seul composant, formés de polymères synthétiquesLeur fabrication à partir de copolymères obtenus par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone comportant des oléfines comme constituant majeur
D01F 6/46 - Filaments, ou similaires, faits par l’homme, à un seul composant, formés de polymères synthétiquesLeur fabrication à partir de mélanges de polymères obtenus par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone comme constituant majeur avec d'autres polymères ou des composés de bas poids moléculaire de polyoléfines
The invention provides an emulsion comprising an organic discontinuous phase which is distributed throughout a continuous aqueous phase, wherein the organic phase comprises, a) An organic solvent and/or, b) An organic phase stabilising material that comprises hydrophobic moieties and is a material which is more soluble in the organic phase than the aqueous phase, and the emulsion further comprises an encapsulated fragrance encapsulated in microparticles.
A61K 8/81 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons insaturées carbone-carbone
A61Q 13/00 - Formulations ou additifs pour les préparations de parfums
The invention relates to a product as obtained by reaction of: a) At least one polyol selected from the group consisting of a linear or branched, trihydric or tetrahydric alcohol and a linear pentahydric or hexahydric alcohol; b) At least one melamine comprising compound; and c) At least one dendritic polymer substituted by hydroxy groups; and to flame retardant compositions comprising these products.
The present invention is directed to a new C.I. Pigment Violet 37 in rod-like form, a process for its preparation and its use for coloring high molecular weight organic material. The C.I. Pigment Violet 37 in rod-like form having a length of 0.5 to 30 쎽m, a width of 0.05 to 1 쎽m, especially 0.100 to 0.500 쎽m and an average thickness of 0.01 to 0.200 쎽m, especially 0.03 to 0.100 쎽m.
The invention relates to pigment based on (multiple) coated platelet-shaped substrates comprising an outer layer which is obtained by treatment with a metal oxide/hydroxide and then a phosphate ester, or phosphonate, or a salt thereof, with the proviso that the phosphate ester, or phosphonate do not contain fluorine, to a method for producing said pigments and the use thereof. The outer layer provides a very good photo-stabilisation of the TiO2 coated platelet-shaped substrates, such as mica, combined with a good water resistance and an anti-yellowing performance.
A process for modifying the surface of an inorganic or organic substrate with strongly adherent nanoparticles is described, providing to the surface modified substrate durable effects like hydrophobicity, hydrophilicity, electrical conductivity, magnetic properties, flame retardance, color, adhesion, roughness, scratch resistance, UV-absorbance, antimicrobial properties, antifouling properties, antiprotein properties, antistatic properties, antifog properties, release properties. In this process, an optional first step a) a low-temperature plasma, ozonization, high energy irradiation, corona discharge or a flame is caused to act on the inorganic or organic substrate, and in a second step b) one or more defined nanoparticles or mixtures of defined nanoparticles with monomers, containing at least one ethylenically unsaturated group, or solutions, suspensions or emulsions of the afore-mentioned substances, are applied, preferably at normal pressure, to the inorganic or organic substrate. In a third step c) suitable methods are applied to dry or cure those afore-mentioned substances and, optionally, in a fourth step d) a further coating is applied on the substrate so pretreated.
B05D 5/00 - Procédés pour appliquer des liquides ou d'autres matériaux fluides aux surfaces pour obtenir des effets, finis ou des structures de surface particuliers
B29C 70/64 - Façonnage de matières composites, c.-à-d. de matières plastiques comprenant des renforcements, des matières de remplissage ou des parties préformées, p. ex. des inserts comprenant uniquement des matières de remplissage les matières de remplissage ayant une influence sur les caractéristiques de surface du matériau, p. ex. en se concentrant près de la surface ou en étant enfoncées de force dans la surface
C09C 3/00 - Traitement, en général, de substances inorganiques, autres que des charges fibreuses, pour améliorer leurs propriétés de pigmentation ou de charge
C09C 3/08 - Traitement par des composés organiques de bas poids moléculaire
C09C 3/12 - Traitement par des composés organiques du silicium
C09D 5/00 - Compositions de revêtement, p. ex. peintures, vernis ou vernis-laques, caractérisées par leur nature physique ou par les effets produitsApprêts en pâte
The invention relates to stabilized biodiesel fuel compositions, which compositions comprise a biodiesel fuel and a combination of i) one or more compounds selected from the group consisting of the sterically hindered phenolic antioxidants and ii) one or more compounds selected from the group consisting of the triazole metal deactivators.
Asphalt or bitumen compositions are effectively stabilized against the deleterious effects of heat, light and oxygen, by incorporation therein of at least one sterically hindered amine compound. Representative sterically hindered amines are the cyclic condenstates of N,N'- bis(2,2,6,6-tetramethyl-4-piperidyl)-hexamethylenediamine and 4-tert-octylamino-2,6-di- chloro-1,3,5-triazine, of N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-hexamethylenediamine and 4-cyclohexylamino-2,6-dichloro-1,3,5-triazine, or of N,N'-bis-(2,2,6,6-tetramethyl-4-piperidyl)- hexamethylenediamine and 4-morpholino-2,6-dichloro-1,3,5-triazine.
C08L 95/00 - Compositions contenant des matières bitumeuses, p. ex. asphalte, goudron ou brai
C08L 79/04 - Polycondensats possédant des hétérocycles contenant de l'azote dans la chaîne principalePolyhydrazidesPolyamide-acides ou précurseurs similaires de polyimides
25.
PROCESS FOR THE PREPARATION OF TERTIARY N-ALLYL STERICALLY HINDERED AMINES
The instant invention discloses a process for the preparation of compounds of the formula (I), wherein the general symbols are as defined in claim 1, which process comprises reacting a sterically hindered amine of the formula (II), wherein the general symbols are as defined in claim 1, with a compound of the formula (III) wherein the general symbols are as defined in claim 1, in the presence of a catalyst. The compounds of the formula (I) are useful as stabilizers for protecting organic materials, in particular synthetic polymers, reprographic materials or coating materials against oxidative, thermal or light-induced degradation.
C07D 401/14 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant au moins trois hétérocycles
26.
APPARATUS AND METHOD FOR MANUFACTURING A SECURITY PRODUCT
The present invention relates to a method of printing, an apparatus for printing and to products obtained therefrom. In particular, the present invention relates to optically variable images, or devices applied to a substrate, such as a hologram, kinegram and the like. More particularly, the present invention concerns sub-microscopic, holographic, electron beam, mechanically ruled or other diffraction or straight line gratings.
B41F 11/02 - Presses ou machines rotatives dont les cylindres de clichés portent plusieurs surfaces d'impression ou pour la mise en œuvre de procédés typographiques, lithographiques ou d'impression en creux, sélectivement ou en combinaison pour les papiers-valeurs
The invention is based on the finding that impregnating a cleaning substrate with a non-ionic, linear polymer unexpectedly improves the cleaning efficacy of the article and prevents redeposition of soil and dirt onto the cleaned hard or soft surface. The non-ionic, linear polymer is, for example, polyacrylamide. In addition, the invention relates to a method of incorporation of a cleaning composition into said substrate.
A method for producing fluorescent markings on a substrate which method comprises exposing parts of a composition comprising a polymer and an organic pigment to a heat source, such as laser radiation, to produce a fluorescent 5 markings which are are not discernable when viewed under ambient visible light but readily apparent under UV light is disclosed. The method produces novel compositions wherein a fluorescent form of a pigment is present at a higher concentration in defined domains relative to the remainder of the composition. The novel polymer composition is particularly useful in security marking applications.
B41M 5/28 - Thermographie utilisant des composés thermochromes ou des couches contenant des cristaux liquides, des microcapsules, des colorants blanchissables ou des composés thermodégradables, p. ex. libérant un gaz
B42D 15/00 - Cartes ou imprimés d'un format ou d'un type particulier non prévu ailleurs
B42D 15/10 - Cartes d'identité, cartes de crédit, cartes bancaires ou cartes analogues portant des informations (supports d'enregistrement, p.ex. cartes d'identité ou cartes de crédit, pour utilisation avec des machines et avec au moins une partie prévue pour supporter des marques numériques G06K 19/00)
The invention relates to a process for process for stabilizing polymers by addition of phenolic antioxidants in the form of a concentrated fluid, which comprises cooling, dosing in suitable containers and storing the fluid under the exclusion of oxygen and light, optionally remelting and adding the fluid under the optional addition of further polymer additives to the polymer to be stabilized.
Polymethacrylate copolymers are disclosed which comprise from about 60 - about 96 wt.-% of a C12-C16 alkyl methacrylate and from about 40 - about 4 weight percent of a C18-C30 alkyl methacrylate and provide excellent low temperature properties to lubricating oils.
C08F 220/18 - Esters des alcools ou des phénols monohydriques des phénols ou des alcools contenant plusieurs atomes de carbone avec l'acide acrylique ou l'acide méthacrylique
The present invention is directed to a new 2,9-dichloroquinacridone in platelet form, a process for its preparation and its use for coloring high molecular weight organic material. The 2,9-dichloroquinacridone in platelet form has a length of 1 to 45 쎽m, a width of 0.1 to 20 쎽m and an average thickness of 0.01 to 5 쎽m and is characterized in that the hue-value h in remission is ≤31 and/or the lightness L* in transmission is ≥20 and/or a decreasing b* value and an increasing a* value from an illuminating and viewing angle (aspecular angle) 45°/110° (+25°) to 45°/90° (+45°).
A process for mass-colouring high molecular weight material, in which process a compound of formula (I) or a tautomer thereof, wherein M1 is H, 1/2 M2, 1/3 M3 or NR4R5R6R7, preferably H, 1/2 M2 or NR4R5R6R7, especially H, M2 is an alkaline earth or transition metal in oxidation state II or an oxo-metal in oxidation state IV, M3 is Al (III), a transition metal in oxidation state III or an oxo-metal in oxidation state V, R1 is H or a non-ionic substituent, R2 is H or, independently of R1, a further non-ionic substituent, R3 is H, C1-C6alkyl, phenyl, CO-C1-C6alkyl or CO-phenyl, preferably H or CO-C1 -Cealkyl, especially H, and R4, R5, R6 and R7 are each independently of the others H or phenyl, benzyl or C1-C6alkyl, which are unsubstituted or may be substituted by hydroxy or by halogen and in the case of C3-C6alkyl is uninterrupted or interrupted by O, is incorporated into the high molecular weight material before or during shaping. The colorations obtained have good light stability and thermal stability, especially in polyolefins.
Color fast or non-yellowing aromatic polyurethane compositions comprising a combination of benzotriazole ultraviolet light absorbers and hindered amine light stabilizer and a method for maintaining the color fastness of aromatic polyurethane compositions by incorporating the ultraviolet light absorber and hindered amine light stabilizer into an aromatic polyurethane composition are provided.
D06N 3/00 - Cuir artificiel, toile cirée ou matériau similaire obtenu par enduction de nappes fibreuses avec une substance macromoléculaire, p. ex. avec des résines, du caoutchouc ou leurs dérivés
D06N 3/14 - Cuir artificiel, toile cirée ou matériau similaire obtenu par enduction de nappes fibreuses avec une substance macromoléculaire, p. ex. avec des résines, du caoutchouc ou leurs dérivés avec des composés macromoléculaires obtenus autrement que par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone avec des polyuréthanes
The present invention provides a process for preparing a paper or paper board of improved strength which comprises the steps of i) providing a cellulosic thick stock, ii) diluting the thick stock of step i) to form a thin stock, iii) draining the thin stock of step ii) on a wire to form a web, and iv) drying the web of step iii) to form paper or paper board, wherein the cellulosic thick stock of step (i) comprises organic polymeric microparticles, as well as paper obtainable by above process.
The present invention provides a process for the preparation of an aqueous composition comprising polysilicate coated mineral particles, wherein the process comprises subjecting an aqueous composition comprising gelled polysilicate and a mineral to shear of at least 5'000 rpm for at least 30 seconds. The present invention also provides polysilicate coated mineral particles obtainable by this process as well as paper filled with these particles.
C09C 3/06 - Traitement par des composés inorganiques
D21H 17/68 - Composés insolubles dans l'eau, p. ex. charges ou pigments siliceux, p. ex. argiles
D21H 17/69 - Composés insolubles dans l'eau, p. ex. charges ou pigments modifiés, p. ex. par association avec d'autres compositions préalablement à l'incorporation dans la pâte ou le papier
The invention relates to a cationic photocurable composition comprising at least one cationically polymerizable compound, at least one onium salt photoinitiator, at least a moisture scavenger, and at least a stabilizer selected from the group consisting of sterically hindered nitroxyl stabilizers, sterically hindered phenolic antioxidants, organic phosphorous stabilizers and mixtures thereof.
Engineering plastics, especially polyamide, are coloured with improved fastness and stability properties using pigment compositions comprising an organic pigment wholly overlaid with a crosslinked (meth)acrylic resin or copolymer thereof. Preference is given to the use of diketopyrrolopyrrole, azo, pteridine, isoindoline and isoindolinone pigments. Processes for the preparation of the pigment compositions are also claimed.
A composition which comprises a light absorbing layer adhered to an underlying layer containing a photo-chromic colorant, which photo-chromic colorant has been activated by exposure to UV light to undergo a reversible color change, and wherein the rate of color reversion is dependent on temperature, is provided. The ultraviolet light and/or visible light absorbing layer can be conveniently applied via thermal transfer or ink jet to a substrate comprising the photo-chromic colorant to protect it from unwanted exposure to UV and/or certain wavelengths visible light. The composition is conveniently employed in a temperature time indicator (TTI).
G01K 3/04 - Thermomètres donnant une indication autre que la valeur instantanée de la température fournissant des valeurs moyennesThermomètres donnant une indication autre que la valeur instantanée de la température fournissant des valeurs intégrées par rapport au temps
B41M 5/46 - Thermographie caractérisée par les couches de support, les couches intermédiaires ou les couches de couvertureMoyens ou couches de filtrage ou d'absorption de la chaleur ou du rayonnementThermographie combinée avec des couches ou des compositions appropriées à d'autres procédés d'enregistrement d'imagesOriginaux particuliers pour la reproduction thermographique caractérisés par les moyens pour convertir la lumière en chaleurThermographie caractérisée par les couches de support, les couches intermédiaires ou les couches de couvertureMoyens ou couches de filtrage ou d'absorption de la chaleur ou du rayonnementThermographie combinée avec des couches ou des compositions appropriées à d'autres procédés d'enregistrement d'imagesOriginaux particuliers pour la reproduction thermographique caractérisés par les moyens ou les couches de filtrage ou d'adsorption de la chaleur ou du rayonnement
B41M 5/385 - Procédés de transfert ou de sublimation par contact caractérisés par les colorants ou les pigments transférables
39.
STABILIZED MEDIUM AND HIGH VOLTAGE INSULATION COMPOSITION
The invention describes a composition comprising a) a polyethylene, b) a sulfur-containing phenolic antioxidant, c) a migrating antistatic agent, and d) an organic peroxide. The composition is useful for the preparation of a crosslinked polyethylene as cable insulation of medium and high voltage cables with improved water tree resistance.
C08K 5/375 - Sulfures contenant des cycles aromatiques à six chaînons
H01B 3/44 - Isolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques matières plastiquesIsolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques résinesIsolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques cires résines vinyliquesIsolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques matières plastiquesIsolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques résinesIsolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques cires résines acryliques
H01B 7/28 - Protection contre les dommages provoqués par des facteurs extérieurs, p. ex. gaines ou armatures par l'humidité, la corrosion, les attaques chimiques ou les conditions atmosphériques
C08L 23/04 - Homopolymères ou copolymères de l'éthylène
40.
PACKING ELEMENTS FOR EVAPORATIVE COOLERS WITH RESISTANCE TO BIOFILM FORMATION
Disclosed is a polyvinyl chloride packing material for evaporative coolers, which packing material has incorporated therein an amount effective to prevent biofilm formation of one or more antimicrobials selected from the group consisting of the metal containing zeolites and the supported metals, where the metal of the metal containing zeolites is silver, copper, zinc, mercury, tin, lead, bismuth, cadmium, chromium, cobalt, nickel, zirconium or a combination of two or more of these metals and where in the supported metals the metal is silver, a silver compound a silver complex or a combination of silver with copper, zinc or zirconium and where the support is SiO2, TiO2 or glass.
Synthetic thermoplastic polymer articles are effectively protected from infestation by mites such as house dust mites or bedmites, by incorporation of an agent selected from Propiconazole, Cyproconazole, Difenoconazole, Fludioxonil, Thiabendazole, Tebuconazole, Zinc Pyrithione, 2-n-Octyl-4-isothiazolin-3-on, 4,5-Di-chlor-N-n-octyl-isothiazolin-3-on, certain 2,4-bis(alkylamino)pyrimidines or silvers as given in claim 1, Carbendazim, 10,10'-oxy-bis- phenoxyarsene, and/or n-butyl-1,2-benzisothiazolin-3-on and optionally an antimicrobial agent into the bulk of the resin. Final articles may be filters, bed clothes and fillings, mattresses, covers, pillowcases, upholstery fabrics and foams, textiles, and floor coverings including carpets, backing material like backing for flooring, underlays.
A01N 43/36 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec un atome d'azote comme unique hétéro-atome du cycle des cycles à cinq chaînons
A01N 43/40 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec un atome d'azote comme unique hétéro-atome du cycle des cycles à six chaînons
A01N 43/80 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec des atomes d'azote et des atomes d'oxygène ou de soufre, comme hétéro-atomes du cycle des cycles à cinq chaînons avec un atome d'azote et soit un atome d'oxygène, soit un atome de soufre, en positions 1,2
A01N 47/18 - Dérivés de l'acide carbamique, c.-à-d. contenant le groupe —O—CO—NLeurs thio-analogues contenant un groupe —O—CO—N, ou un de ses thio-analogues, lié directement à un hétérocycle ou à un cycle cycloaliphatique
A01N 55/02 - Biocides, produits repoussant ou attirant les animaux nuisibles ou régulateurs de croissance des végétaux, contenant des composés organiques comportant des éléments autres que le carbone, l'hydrogène, les halogènes, l'oxygène, l'azote et le soufre contenant des atomes de métal
Compounds of the formula (I), wherein L1, L2, L3 and L4 independently of one another are hydrogen or an organic substituent; R is for example C1-C20alkyl, C5-C12cycloalkyl, C2-C20alkenyl, substituted C1-C20alkyl; X is O, S, NRa or NCORa; Ra is for example hydrogen or C1-C20alkyl; and Y is an inorganic or organic anion; are suitable as photolatent acid generators.
The invention provides a uv-curable colored composition, comprising (a) at least one selected ethylenically unsaturated photopolymerizable compound; (b) at least one selected curing agent of the phenylglyoxylate type; and (c) at least one selected colorant.
C07C 59/205 - Composés saturés ne comportant qu'un groupe carboxyle et contenant des groupes cétone contenant des cycles
C08F 2/50 - Polymérisation amorcée par énergie ondulatoire ou par rayonnement corpusculaire par la lumière ultraviolette ou visible avec des agents sensibilisants
G03F 7/00 - Production par voie photomécanique, p. ex. photolithographique, de surfaces texturées, p. ex. surfaces impriméesMatériaux à cet effet, p. ex. comportant des photoréservesAppareillages spécialement adaptés à cet effet
G03F 7/038 - Composés macromoléculaires rendus insolubles ou sélectivement mouillables
44.
METHOD FOR THE HYDROPHOBIC TREATMENT OF PIGMENT PARTICLES AND THE PERSONAL CARE COMPOSITIONS COMPRISING SAID PIGMENT PARTICLES
The present invention provides a method for the hydrophobic treatment of pigment particles comprising contacting said pigment particles with one or more silicone-based materials, that are substantially free of silicon-hydrogen bonds and fluorine, producing hydrophobic, non- covalently bound, modified pigment particles. Additionally, the present invention provides personal care compositions comprising said modified or coated pigment particles.
The invention relates to a liquid dispersant of the Formula (I) wherein T is selected from a polyethylene imine (PEI) or modified PEI moiety, polyvinylamine (PVA) or modified PVA, or polyallylamine (PAA) or modified PAA. B is a branched monomer selected from a monofunctional carboxylic acid moiety having at least two hydroxyl groups or a monofunctional carboxylic acid moiety having at least two hydroxyl groups wherein one or more of the hydroxyl groups are hydroxyalkyl substituted, R1 and R2 independently of one another are hydrophobic groups selected from a saturated or unsaturated fatty acid moiety with 3-24 carbon atoms, a monofunctional carboxylic acid moiety or a polymer moiety containing C3-C24 alkyl (hydroxyl)carboxylic acid moieties with MW ranges from 100 to 10,000g/mol, X is B with -OH terminal group, or R1 or R2, q is a number between 5 - 2000, with the proviso that q is less than the sum of all amine groups of PEI,PVA, PAA. n is a number of 1 - 6.
B01F 17/00 - Utilisation de substances comme agents émulsifiants, humidifiants, dispersants ou générateurs de mousse
B01J 13/00 - Chimie des colloïdes, p. ex. production de substances colloïdales ou de leurs solutions, non prévue ailleursFabrication de microcapsules ou de microbilles
C08G 83/00 - Composés macromoléculaires non prévus dans les groupes
C09B 67/00 - Traitements, sans réaction chimique, influençant les propriétés physiques, p. ex. de teintures ou d'impression, des matières colorantes, p. ex. traitement par des solvantsCaractéristiques du procédé de fabrication des préparations tinctorialesPréparations tinctoriales ayant un aspect physique particulier, p. ex. tablettes, feuilles
C09C 3/08 - Traitement par des composés organiques de bas poids moléculaire
C09C 3/10 - Traitement par des composés organiques macromoléculaires
C09D 17/00 - Pigments en pâtes, p. ex. pour pigmenter les peintures
The present invention pertains to a composition comprising (a) a photolatent base; (b) a blocked isocyanate or blocked isothiocyanate and (c) a hydrogen donor compound; and its applications.
Disclosed is a method for the preparation of a polyester, which method comprises in a first step, reacting a dicarboxylic acid or a C1-C4 dicarboxylic diester with a diol at a suitable temperature and pressure to effect esterification or transesterification to prepare a precondensate and in a second step, reacting the precondensate to effect polycondensation at a suitable temperature and pressure to prepare a high molecular weight polyester, where a metal phosphonic acid complex compound of the formula (I) is employed in the first step, in the second step or in both the first and second steps as a reaction catalyst; and wherein n is 0, 1, 2, 3, 4, 5 or 6; p is an integer from 1 to 30; M is a metal selected from the group consisting of Li, Na, K, Cs, Be, Ca, Mg, Sr, Ba, Al, Sb, Cd, Mn, Fe, Co, Ni, Cu and Zn; v is the valency of the metal M and is 1, 2 or 3; q is an integer from 1 to 20 where q = 2p/v; and R1 is hydrogen, straight or branched chain alkyl of 1 to 36 carbon atoms, straight or branched chain alkenyl of 1 to 36 carbon atoms, cycloalkyl of 5 to 8 carbon atoms or aryl of 6 to 10 carbon atoms; or is said alkyl, alkenyl, cycloalkyl or aryl substituted by one to four hydroxyl, halogen, straight or branched chain alkoxy of 1 to 8 carbon atoms, straight or branched chain alkyl of 1 to 8 carbon atoms or amino groups.
The invention relates to a an electrical energy storage device, such as a capacitor or a secondary battery, utilizing as active element the oxidation and reduction cycle of a sterically hindered imidazolidinone nitroxide radical. Further aspects of the invention are a method for providing such an energy storage device, the use of the respective compounds as active elements in energy storage devices and selected novel imidazolidinone nitroxide compounds.
The present invention relates electroluminescent devices, comprising a compound of the formula (I), especially as host for phosphorescent compounds. The hosts may function with phosphorescent materials to provide improved efficiency, stability, manufacturability, or spectral characteristics of electroluminescent devices.
C07D 235/18 - BenzimidazolesBenzimidazoles hydrogénés avec des radicaux aryle liés directement en position 2
C07D 241/42 - Benzopyrazines avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone de l'hétérocycle
C07D 263/56 - BenzoxazolesBenzoxazoles hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement en position 2
C07D 209/58 - Systèmes cycliques contenant au moins trois cycles condensés en [b] ou en [c]
C07D 403/14 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant au moins trois hétérocycles
C07D 413/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes d'azote et d'oxygène comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07F 7/10 - Composés comportant une ou plusieurs liaisons C—Si azotés
C07F 9/53 - Oxydes des organo-phospinesSulfures des organo-phosphines
Novel liquid polymeric compounds of the formula (I) wherein the general symbols are as defined in claim 1, are disclosed as stabilizers for protecting organic materials against oxidative, thermal or light-induced degradation.
C08G 79/02 - Composés macromoléculaires obtenus par des réactions créant dans la chaîne principale de la macromolécule une liaison contenant des atomes autres que le silicium, le soufre, l'azote, l'oxygène et le carbone, avec ou sans ces derniers éléments créant une liaison contenant du phosphore
C08G 79/04 - Phosphore lié soit à l'oxygène, soit à un oxygène et à un carbone
C08L 85/02 - Compositions contenant des composés macromoléculaires obtenus par des réactions créant dans la chaîne principale de la macromolécule une liaison contenant des atomes autres que le silicium, le soufre, l'azote, l'oxygène et le carboneCompositions contenant des dérivés de tels polymères contenant du phosphore
C08K 5/529 - Esters contenant des hétérocycles ne représentant pas des esters cycliques des acides phosphoriques ou phosphoreux
C08K 5/5373 - Esters des acides phosphoniques contenant des hétérocycles ne représentant pas des esters cycliques des acides phosphoniques
The instant invention relates to a composition comprising a) an organic material which is susceptible to oxidative, thermal or light-induced degra- dation, and b) at least one compound of the formula (I) wherein the general symbols are as defined in claim 1; especially wherein at least one of the radicals R2, R3 or R4 is is -CH2-CH(CH3)-S(O)p-R12, -CH2-CH2-CH2-S(O)p-R12, -CH2-CH(R11)-CH2-R12 or -CH2-CH=CH-R12, R11 is hydrogen or halogen, R12 is a monovalent perfluorinated alkyl or alkenyl, linear or branched organic radical having four to twenty fully fluorinated carbon atoms; or -CH2CH2(CF2)mCF3, m is 3 to 12, and p is 0, 1 or 2. The compounds of the formula I are useful as reducers of surface energy for organic mat- erials, for example synthetic polymer. Polymers with such a reduced surface energy possess an 'easy-to-clean', 'self-cleaning' 'antisoiling', 'soil-release' 'antigraffiti', 'oil resistance', 'solvent resistance', 'chemical resistance', 'self lubricating', 'scratch resistance', 'low moi- sture absorption', 'dirt pickup resistance', 'slip properties' and 'hydrophobic surface'; and anti-adhesion properties against proteins and against microorganism such as for example bacteria, fungi and algae.
C07C 43/205 - Éthers une liaison sur l'oxygène de la fonction éther étant sur un atome de carbone d'un cycle aromatique à six chaînons le cycle aromatique n'étant pas condensé
C07C 43/225 - Éthers une liaison sur l'oxygène de la fonction éther étant sur un atome de carbone d'un cycle aromatique à six chaînons contenant des atomes d'halogène
C07C 69/63 - Esters contenant des atomes d'halogène d'acides saturés
C07C 69/712 - Éthers le groupe hydroxyle de l'ester étant éthérifié par un composé hydroxylé dont le groupe hydroxyle est lié à un atome de carbone d'un cycle aromatique à six chaînons
C07C 271/44 - Esters des acides carbamiques ayant des atomes d'oxygène de groupes carbamate liés à des atomes de carbone de cycles aromatiques à six chaînons avec les atomes d'azote des groupes carbamate liés à des atomes d'hydrogène ou à des atomes de carbone acycliques à des atomes d'hydrogène ou à des atomes de carbone de radicaux hydrocarbonés non substitués
C07C 271/58 - Esters des acides carbamiques ayant des atomes d'oxygène de groupes carbamate liés à des atomes de carbone de cycles aromatiques à six chaînons avec l'atome d'azote d'au moins un des groupes carbamate lié à un atome de carbone d'un cycle aromatique à six chaînons
C07C 323/16 - Thiols, sulfures, hydropolysulfures ou polysulfures substitués par des halogènes, des atomes d'oxygène ou d'azote ou par des atomes de soufre ne faisant pas partie de groupes thio contenant des groupes thio et des atomes d'oxygène, liés par des liaisons simples, liés au même squelette carboné ayant les atomes de soufre des groupes thio liés à des atomes de carbone acycliques du squelette carboné le squelette carboné contenant des cycles aromatiques à six chaînons
52.
PROCESS FOR THE PREPARATION OF AN ANTISTATIC COMPOSITION
The invention relates to the preparation of an antistatic composition comprising adding a liquid or a dissolved ionic substance to a porous polymer and processing the porous polymer together with further additives and further thermoplastic polymers in the melt. The invention relates also to the antistatic composition itself and to its use for rendering polymers antistatic.
The present application provides a composition showing a color change depending on the absorbed radiation-dose, comprising (a) an acid responsive colorant; (b) a photolatent acid; characterized in that (b) is a sulfonyloxime ester compound; and its use as a radiation dose indicator.
Disclosed are thiol dyes of formula (1) wherein L1 is hydrogen; C1-C12alkyl; or phenyl-C1-C4alkyl; X is C1-C12alkylene, C2-C12alkenylene, C5-C10cycloalkylene, C5-C10arylene, or C5-C10arylene-C1-C10alkylene, which may by interrupted by -O-, -NH-, -S-, -CO-, o -SO2-; Y is the residue of an organic dye Z is a group of formula (1b) or -CⓎN; wherein A is O; S; or N-L2; B is L3; -OL3; -NL3L4; or -SL3; and L2, L3 and L4, indepently from other are are hydrogen; C1-C12alkyl; C5-C12aryl-C1-C12alkyl. The compounds are useful for the dyeing of organic materials, such as keratin fibers, preferably human hair.
Novel fluorescent polyhedral oligomeric silsesquioxane (POSS) colorants are provided. The colorants are strongly fluorescing and long lasting with excellent light stability. The novel colorants can be prepared from chromophores found in common pigments and provide a simple way to convert an insoluble pigment into a soluble fluorescent colorant.
C09B 67/00 - Traitements, sans réaction chimique, influençant les propriétés physiques, p. ex. de teintures ou d'impression, des matières colorantes, p. ex. traitement par des solvantsCaractéristiques du procédé de fabrication des préparations tinctorialesPréparations tinctoriales ayant un aspect physique particulier, p. ex. tablettes, feuilles
Certain NH sterically hindered amine compounds of the formula where R is a straight or branched alkyl group of from 7 to 17 carbon atoms and where n is a numeral from 6 to 18 are suitable for use as stabilizers in lubricant compositions. The sterically hindered amines are non-aggressive towards fluoroelastomer O-rings or seals.
C10M 133/06 - Amines, p. ex. polyalkylènepolyaminesAmines quaternaires comportant des groupes amine liés à des atomes de carbone acycliques ou cycloaliphatiques
C10N 30/10 - Inhibition de l'oxydation, p. ex. anti-oxydants
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
57.
BLOCK COPOLYMERS OF DIALLYLDIALKYLAMMONIUM DERIVATIVES
The invention encompasses novel amphiphilic block copolymers comprising a hydrophobic block and a hydrophilic block wherein the hydrophilic block is formed from diallyldialkylammonium salt and the hydrophobic block comprises a polyolefin. Furthermore, convenient methods of preparing the amphiphilic block copolymers are disclosed. The amphiphilic block copolymer may be used to increase the wettability and printability of a plastic surface. The amphiphilic block copolymer may also be melt blended with a thermoplastic to form an anti-statically finished polymeric.
C08F 293/00 - Composés macromoléculaires obtenus par polymérisation sur une macromolécule contenant des groupes capables d'amorcer la formation de nouvelles chaînes polymères rattachées exclusivement à une ou aux deux extrémités de la macromolécule de départ
C08F 297/04 - Composés macromoléculaires obtenus en polymérisant successivement des systèmes différents de monomère utilisant un catalyseur de type ionique ou du type de coordination sans désactivation du polymère intermédiaire utilisant un catalyseur du type anionique en polymérisant des monomères vinylaromatiques et des diènes conjugués
C08F 297/08 - Composés macromoléculaires obtenus en polymérisant successivement des systèmes différents de monomère utilisant un catalyseur de type ionique ou du type de coordination sans désactivation du polymère intermédiaire utilisant un catalyseur du type de coordination en polymérisant des mono-oléfines
The invention is directed to a method for improving the wettability/hydrophilicity of hydrophobic substrates by applying block copolymers to said substrates wherein the block copolymers comprise a quaternary ammonium polymer block and a hydrophobic block. The method of the invention is especially advantageous when used to improve the wettability of nonwovens and in the treatment of hydrophobic surfaces encountered in the home to prevent the buildup of soil residues.
C09D 153/00 - Compositions de revêtement à base de copolymères séquencés possédant au moins une séquence d'un polymère obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carboneCompositions de revêtement à base de dérivés de tels polymères
The present invention relates to polymers comprising repeating unit(s) of the formula (I), and their use in electronic devices. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In addition, high charge carrier mobilities and high temperature stability of the emission color are observed, if the polymers according to the invention are used in polymer light emitting diodes (PLEDs).
C07C 25/22 - Hydrocarbures halogénés aromatiques polycycliques à cycles condensés
C08G 61/10 - Composés macromoléculaires contenant uniquement des atomes de carbone dans la chaîne principale de la molécule, p. ex. polyxylylènes uniquement des atomes de carbone aromatiques, p. ex. polyphénylènes
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H05B 33/14 - Sources lumineuses avec des éléments radiants ayant essentiellement deux dimensions caractérisées par la composition chimique ou physique ou la disposition du matériau électroluminescent
H01L 51/00 - Dispositifs à l'état solide qui utilisent des matériaux organiques comme partie active, ou qui utilisent comme partie active une combinaison de matériaux organiques et d'autres matériaux; Procédés ou appareils spécialement adaptés à la fabrication ou au traitement de tels dispositifs ou de leurs parties constitutives
60.
USE OF AMINOPHENYLBENZOTRIAZOLE DERIVATIVES FOR PROTECTING HUMAN AND ANIMAL SKIN AND HAIR FROM THE HARMFUL EFFECTS OF UV RADIATION AND COSMETIC COMPOSITIONS THEREOF
Disclosed are-(2'-Hydroxy-4'-aminophenyl)benzotriazole derivatives of formula (1), wherein R1 and R4 independently of each other are hydrogen; C1-C28alkyl; C1-C28alkoxy; C2-C28al- kenyl; C2-C28alkinyl; C3-C12cycloalkyl; C3-C12cycloalkenyl; C7-C28 aralkyl; C1-C20hetero- alkyl; C3-C12cycloheteroalkyl; or C5-C16 heteroaralkyl; and wherein C1-C28alkyl, C1-C28al- koxy, C2-C28alkenyl and C2-C28alkinyl are unsubstituted or may be substituted by at least one C1-C5alkyl, C1-C5alkoxy or hydroxy; R2 and R3 independently of each other are hydrogen; C1-C28alkyl; C2-C28 alkenyl; C2-C22alki- nyl; C3-C12cycloalkyl; C3-C12cycloalkenyl; C7-C28 aralkyl; C1-C20 heteroalkyl; C3-C12cyclo- heteroalkyl; C5-C16heteroaralkyl; and wherein C1-C28alkyl, C1-C28alkoxy, C2-C28alkenyl and C2-C28alkinyl are unsubstituted or may be substituted by at least one C1-C5alkyl, C1- C5alkoxy or hydroxy; or CO-R5; or R2 and R3 together together with the linking nitrogen form a 5- to 7-membered, monocyclic, carbocyclic or heterocyclic ring; R5 is C1-C28alkyl; C2-C28alkenyl; C2-C28alkinyl; C3-C12cycloalkyl; C3-C12cycloalkenyl; C7-C20aralkyl; C1-C20 heteroalkyl; C3-C12 cycloheteroalkyl; C1-C5alkoxycarbonyl-C1- C5alkyl; or C5-C16heteroaralkyl; for protecting human and animal hair and skin from harmful effects of UV radiation.
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 5/00 - Préparations pour les soins des cheveux
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
61.
BINARY FLUORESCENT PIGMENT COMPOSITION AND ITS USE FOR FORGERY AND COUNTERFEIT PREVENTION
The present invention relates to binary fluorescent pigment compositions, products containing them and their use for forgery and counterfeit prevention. Especially, the invention relates to a luminous ink comprising two fluorescent pigments that emit light upon irradiation by ultraviolet light and an ink vehicle, wherein the first fluorescent pigment emits light of a first wavelength in a visible light range upon irradiation by an ultraviolet light of a first wavelength and is substantially transparent to visible light, and the second fluorescent substance that emits light of a second wavelength in a visible light range being different from the first wavelength in a visible light range upon irradiation by an ultraviolet light of a second wavelength and is substantially transparent to visible light. The fluorescent luminous ink is difficult to identify by sight in the presence of visible light and becomes identifiable by sight by emitting light in a visible light range upon irradiation by ultraviolet light.
C09K 11/64 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances inorganiques luminescentes contenant de l'aluminium
C09K 11/83 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances inorganiques luminescentes contenant des métaux des terres rares contenant du vanadium et du phosphore
A new process for enhancing the hydrophilicity of the surface of a polyolefin or polyolefin copolymer article is characterized in that the surface is treated with an enzyme selected from oxidoreductases, especially of the cytochrome P450 family or enzymes classified as EC 1.13 or EC 1.14. The process is especially useful for the treatment of polypropylene films, fibres, or fabrics, inter alia for use in sanitary articles, threads, yarns, fabrics, textiles, garments, technical or household articles, printed or dyed cover films or packaging films.
Disclosed are polymeric dyes of formula (1a); (1b); or (1c); wherein A and B, independently from each other represent a polymer backbone; X1 and X2 independently from each other are a linkage group selected from -C1-C10alkylene-; -C2-C12alkenylene-; -C5-C10cycloalkylene-; C5-C10arylene; -C5-C10arylene-(C1-C10alkylene)-; -C(O)-; -(CH2CH2-O)1-5-; -C(O)O-; -OCO-; -N(R1)-; -CON(R1)-; -(R1)NC(O)-; -0-; -S-; -S(O)-; -S(O)2-; -S(O)2-N(R1R2); or the direct bond; R1 and R2 independently from each other are hydrogen; or unsubstituted or substituted, straight-chain or branched, monocyclic or polycyclic, interrupted or uninterrupted C1- C14alkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl-C1-C10alkyl; or C5-C10alky(C5-C10aryl); Y1 and Y2 independently from each other are a residue of an organic dye; or hydrogen; wherein at least one of Y1 and Y2 is a residue of an organic dye; An1, An2 and An3, independently from each other are an anion; a and b independently from each other are a number from 1 to 3; m is a number from O to 1000; n is a number from O to 1000; and p is a number from 1 to 1000; wherein the sum of m + n + p ≥ 3.
C09B 69/10 - Colorants polymèresProduits de réactions de colorants avec des monomères ou avec des composés macromoléculaires
A61K 8/72 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires
The invention relates to a first method of bonding a first substrate to a second substrate, comprising the steps of a) applying an UV-curable adhesive resin composition comprising a photolatent base to at least one transparent surface of at least one of said first and second substrates, b) bringing said first and second substrates together with said adhesive composition there between, c) exposing said adhesive composition to actinic radiation to effect curing or alternatively to a second method of bonding a first substrate to a second substrate, comprising the steps of a) applying a UV-curable adhesive resin composition comprising a photolatent base to one surface, b) exposing said adhesive composition to actinic radiation to effect curing, c) bringing said first and second substrates together with said adhesive composition there between.
Disclosed are oligo- or polysiloxanes, which are characterized by containing at least 3, for example 4 - 3000, Si atoms in the main chain, and wherein at least one thereof is contained in a moiety of the formula (I) whose open bond of the O atom is linked to another Si atom of the oligo- or polysiloxane main chain, and whose open bond of the Si atom is linked either to another O atom of the oligo- or polysiloxane main chain or to R'1, where R1 and R'1 independently are C1-C10alkyl, R2 and R3 independently are C1-C18alkylene, X is a divalent spacer group selected from O, NR4, N(COR'5), CONR'4, OCONR'4;.Y is selected from OCOR5, NHCOR5, NHR4, COOR5, CONHR4, NR'4R4; R4 is selected from C6-C18 organic residues containing at least one aryl moiety; R'4 is as defined for R4; or is selected from H, C1-C20alkyl, C7-C20phenylalkyl, C4- C12cycloalkyl; R5 is R7-Z; R'5 is as defined for R5; or is selected from H, C1-C20alkyl, C7-C20phenylalkyl, C4- C12cycloalkyl; R7 is C1-C20alkylene, which may be interrupted by phenylene, C4-C12cycloalkylene, O, NR'4; or is unsubstituted or substituted phenylene or C4-C12cycloalkylene; Z is halogen or N+R8R9R10; R8, R9 and R10 independently are selected from C1-C20alkyl, C7-C20phenylalkyl, C4- C12cycloalkyl, unsubstituted or substituted aryl; or 2 of R8, R9 and R10 are linked together to form a quaternized aliphatic, substituted or unsubstituted N-heterocyclic ring of 4-6 carbon atoms such as a piperidine ring; or all of R8, R9 and R10 are linked together to form, together with the nitrogen atom they are bonding to, a substituted or unsubstituted N-heterocyclic ring system of 4-7 carbon atoms. The novel compounds are effective as antimicrobials.
A01N 55/10 - Biocides, produits repoussant ou attirant les animaux nuisibles ou régulateurs de croissance des végétaux, contenant des composés organiques comportant des éléments autres que le carbone, l'hydrogène, les halogènes, l'oxygène, l'azote et le soufre contenant du silicium
A01P 1/00 - DésinfectantsComposés antimicrobiens ou leurs mélanges
C07F 7/08 - Composés comportant une ou plusieurs liaisons C—Si
C08G 77/38 - Polysiloxanes modifiés par post-traitement chimique
C08G 77/388 - Polysiloxanes modifiés par post-traitement chimique contenant des atomes autres que le carbone, l'hydrogène, l'oxygène ou le silicium contenant de l'azote
The present invention relates to a method of protecting organic material, especially from the pharmaceuticals and foodstuffs sectors, against light, wherein at least one pigment of formula (1), (2), (3), (4), (5), (6) and (7) and (8) as defined in claim 1 and optionally a UV absorber as well as optionally further pigments and/or colorants is applied to or incorporated in a carrier material and the carrier material so treated is positioned between the light source and the organic material to be protected.
The invention relates to a color filter composition comprising a) a photoresist binder, b) a transparent pigment, c) optionally a solvent and/or optionally a photoinitiator or a photolatent catalyst, d) a dispersant which is a polymer or copolymer obtainable by a process comprising the steps of a1) polymerizing in a first step one or more ethylenically unsaturated monomers in the presence of at least one nitroxylether having the structural element wherein X represents a group having at least one carbon atom and is such that the free radical X derived from X is capable of initiating polymerization; or a2) polymerizing in a first step one or more ethylenically unsaturated monomers in the presence of at least one stable free nitroxyl radical and a free radical initiator; wherein at least one monomer used in the steps a1) or a2) is a C1-C6 alkyl or hydroxy C1-C6 alkyl ester of acrylic or methacrylic acid; and a second step b) comprising the modification of the polymer or copolymer prepared under a1) or a2) by a transesterification reaction, an amidation, hydrolysis or anhydride modification or a combination thereof, and optionally in addition by quaternization.
G03F 7/00 - Production par voie photomécanique, p. ex. photolithographique, de surfaces texturées, p. ex. surfaces impriméesMatériaux à cet effet, p. ex. comportant des photoréservesAppareillages spécialement adaptés à cet effet
C09B 67/00 - Traitements, sans réaction chimique, influençant les propriétés physiques, p. ex. de teintures ou d'impression, des matières colorantes, p. ex. traitement par des solvantsCaractéristiques du procédé de fabrication des préparations tinctorialesPréparations tinctoriales ayant un aspect physique particulier, p. ex. tablettes, feuilles
68.
NOVEL ELECTROLUMINESCENT POLYMERS FOR ELECTRONIC APPLICATIONS
The present invention relates to novel polymers comprising a repeating unit(s) of the formula (I) wherein at least one of the substituents R1, R2, R3, R4, R5, R6, and R7 is a group -(Sp)x1-HEI, wherein Sp is a spacer unit, HE1 is a group (HE1I), which increases the hole-injection and/or hole-transport properties of the polymers; or a group (HE1II), which increases the electron- injection and/or electron-transport properties of the polymers, or a group (HE1III), which increases the hole-injection and/or hole-transport properties of the polymers and the electron-injection and/or electron-transport properties of the polymers, x1 is 0, or 1, and their use in electronic devices. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In addition, high charge carrier mobilities and high temperature stability of the emission color can be observed, if the polymers according to the invention are used in polymer light emitting diodes (PLEDs).
C08G 61/00 - Composés macromoléculaires obtenus par des réactions créant une liaison carbone-carbone dans la chaîne principale de la macromolécule
C08G 61/12 - Composés macromoléculaires contenant d'autres atomes que le carbone dans la chaîne principale de la macromolécule
C08L 65/00 - Compositions contenant des composés macromoléculaires obtenus par des réactions créant une liaison carbone-carbone dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H01L 51/00 - Dispositifs à l'état solide qui utilisent des matériaux organiques comme partie active, ou qui utilisent comme partie active une combinaison de matériaux organiques et d'autres matériaux; Procédés ou appareils spécialement adaptés à la fabrication ou au traitement de tels dispositifs ou de leurs parties constitutives
H01L 51/42 - Dispositifs à l'état solide qui utilisent des matériaux organiques comme partie active, ou qui utilisent comme partie active une combinaison de matériaux organiques et d'autres matériaux; Procédés ou appareils spécialement adaptés à la fabrication ou au traitement de tels dispositifs ou de leurs parties constitutives spécialement adaptés, soit comme convertisseurs de l'énergie dudit rayonnement en énergie électrique, soit comme dispositifs de commande de l'énergie électrique par ledit rayonnement
69.
PROCESS FOR THE PREPARATION OF STERICALLY HINDERED NITROXYL ETHERS
The present invention relates to a novel process for the preparation of a sterically hindered nitroxyl ether from the corresponding sterically hindered nitroxyl radical by reacting it with a carbonyl compound and a hydroperoxide. The compounds prepared by this process are effective stabilizers for polymers against harmful effects of light, oxygen and/or heat, as flame-retardants for polymers and as polymerization regulators.
The present invention relates to a novel process for the preparation of specific sterically hindered nitroxyl ethers from their corresponding sterically hindered nitroxyl radicals by reacting it with an aldehyde and a hydroperoxide. This nitroxyl ether formation may be carried out from different starting nitroxyl radicals, which are subsequently further reacted to the desired compounds. The compounds prepared by this process are effective as stabilizers for polymers against harmful effects of light, oxygen and/or heat and as flame-retardants for polymers.
The invention relates to a concentrated aqueous polymer dispersion with an average particle size of less than 1000 nm comprising a) a polymer carrier prepared by heterophase radical polymerization of at least one ethylenically unsaturated monomer in the presence of b) a photoinitiator and / or photolatent catalyst and c) optionally a non-ionic, cationic or anionic surfactant, wherein the weight ratio of the photoinitiator and / or photolatent catalyst to the polymer carrier is greater than 20 parts of photoinitiator and / or photolatent catalyst per 100 parts of polymer carrier, preferably equal or greater than 35 parts of photoinitiator and / or photolatent catalyst per 100 parts of polymer carrier.
The present invention relates to the preparation and use of (colored) organic particles carrying electric charge as electrophoretic (image) displaying particles, to electrophoretic dispersions comprising the organic particles carrying electric charge, electrophoretic (image) devices (especially displays) comprising the colored organic particles carrying electric charge, to the novel functionalized particles, and to their use. The particles are obtainable according to a method represented by the reaction scheme as given in Figure 1.
C09B 69/10 - Colorants polymèresProduits de réactions de colorants avec des monomères ou avec des composés macromoléculaires
G02F 1/167 - Dispositifs ou dispositions pour la commande de l'intensité, de la couleur, de la phase, de la polarisation ou de la direction de la lumière arrivant d'une source lumineuse indépendante, p. ex. commutation, ouverture de porte ou modulationOptique non linéaire pour la commande de l'intensité, de la phase, de la polarisation ou de la couleur basés sur le mouvement de translation des particules dans un fluide sous l’influence de l’application d’un champ caractérisés par l’effet électro-optique ou magnéto-optique par électrophorèse
73.
DIHALOGENO-HYDROXYDIPHENYLETHER AS ANTIMICROBIALS IN WATER TREATMENT
The use of dihalogeno-hydroxydiphenyl ethers as antimicrobial agents in water treatment processes, such as in purification and decontamination of drinking or waste water, is claimed. Preferably the water treatment is performed in a membrane filtration system. The antimicrobial agents protect the membrane system against bacterial and/or algal decay and assist in maintaining a high efficiency of the membrane filtration process. Methods of maintaining membrane filtration efficiency using dihalogeno- hydroxydiphenylethers as well as aqueous antimicrobial rinsing liquors comprising dihalogeno-hydroxydiphenylethers are also claimed.
The invention relates to an electrophoretic display, comprising electrodes and cells containing at least one kind of ionic, monochrome particles, a non-polar liquid and a dispersant, wherein the ionic, monochrome particles of at least one kind are essentially aggregates consisting of a carbon containing pigment and an anionic pigment or anionic pigment derivative, and the dispersant is selected from the group consisting of polyacrylates, polyesters, polyurethanes and copolymers. In general, the whole quantity of the pigment and the main part, preferably at least 80%, most preferred from 95% to 100%, of the whole anionic pigment or anionic pigment derivative present within the cells is comprised in the aggregates, with essentially no pigment and only a minor part of the anionic pigment or anionic pigment derivative physically distinct from the aggregates.
G02F 1/167 - Dispositifs ou dispositions pour la commande de l'intensité, de la couleur, de la phase, de la polarisation ou de la direction de la lumière arrivant d'une source lumineuse indépendante, p. ex. commutation, ouverture de porte ou modulationOptique non linéaire pour la commande de l'intensité, de la phase, de la polarisation ou de la couleur basés sur le mouvement de translation des particules dans un fluide sous l’influence de l’application d’un champ caractérisés par l’effet électro-optique ou magnéto-optique par électrophorèse
75.
LONG WAVELENGTH SHIFTED BENZOTRIAZOLE UV-ABSORBERS AND THEIR USE
The instant invention relates to novel benzotriazole UV-absorbers having a long wavelength shifted absorption spectrum with significant absorbance up to 410-420 nm. Further aspects of the invention are a process for their preparation, a UV stabilized composition containing the new UV-absorbers and the use of the new compounds as UV-light stabilizers for organic materials.
The present invention relates to polymers comprising a repeating unit of the formula (l) and their use as organic semiconductor in organic devices, especially a diode, an organic field effect transistor and/or a solar cell, or a device containing a diode and/or an organic field effect transistor, and/or a solar cell. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In addition, high efficiency of energy conversion, excellent field-effect mobility, good on/off current ratios and/or excellent stability can be observed, when the polymers according to the invention are used in semiconductor devices or organic photovoltaic (PV) devices (solar cells).
C08G 61/12 - Composés macromoléculaires contenant d'autres atomes que le carbone dans la chaîne principale de la macromolécule
C08G 73/06 - Polycondensats possédant des hétérocycles contenant de l'azote dans la chaîne principale de la macromoléculePolyhydrazidesPolyamide-acides ou précurseurs similaires de polyimides
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H01L 27/32 - Dispositifs consistant en une pluralité de composants semi-conducteurs ou d'autres composants à l'état solide formés dans ou sur un substrat commun comprenant des composants qui utilisent des matériaux organiques comme partie active, ou qui utilisent comme partie active une combinaison de matériaux organiques et d'autres matériaux avec des composants spécialement adaptés pour l'émission de lumière, p.ex. panneaux d'affichage plats utilisant des diodes émettrices de lumière organiques
H01L 51/00 - Dispositifs à l'état solide qui utilisent des matériaux organiques comme partie active, ou qui utilisent comme partie active une combinaison de matériaux organiques et d'autres matériaux; Procédés ou appareils spécialement adaptés à la fabrication ou au traitement de tels dispositifs ou de leurs parties constitutives
77.
PROCESS FOR REMOVING ETHENE FROM BIOLOGICAL SOURCES USING METAL EXCHANGED TITANIUM ZEOLITES
The instant invention relates to a process for removing ethene from biological sources using metal ion exchanged titanium zeolites. Further aspects of the invention are polymer compositions containing these zeolites, their use as efficient ethene removing additives and the modified titanium zeolites self.
C01B 39/06 - Préparation de zéolites isomorphes caractérisée par les mesures prises pour le remplacement des atomes d'aluminium ou de silicium dans la charpente du réseau par des atomes d'autres éléments
C01B 39/08 - Préparation de zéolites isomorphes caractérisée par les mesures prises pour le remplacement des atomes d'aluminium ou de silicium dans la charpente du réseau par des atomes d'autres éléments les atomes d'aluminium étant entièrement remplacés
The invention relates to an actinic radiation-curable coating composition comprising a compound having at least two isocyanate groups, a compound having at least two hydroxyl groups, and a photolatent catalyst for the isocyanate-hydroxyl addition reaction, wherein the photolatent catalyst is an organic metal compound comprising a latent catalytically active metal, and wherein the latent catalytically active metal atom in the organic metal compound has no bonds to other metal atoms. The invention further relates to a process for forming a coating on a substrate.
The invention relates tp dye-functionalized silsesquioxane clusters, a process for their manufature and their use as colorants, wherein the compounds (functionalized clusters or nano-particles) are characterized by the general formula (I) wherein CAGE is a moiety of the formula (IA) D is a chromophoric moiety, and the other symbols have the meanings as defined in the specification, or salts thereof.
The instant invention relates to a process for removing ethene from biological sources using iodine doped titaniumdioxide. Further aspects of the invention are polymer compositions containing this iodine doped titanium dioxide, its use as efficient ethene removing additive and the iodine doped titaniumdioxide itself.
A23B 7/152 - Conservation ou mûrissement à l'aide de produits chimiques non couverts par les groupes ou sous forme de gaz, p. ex. fumigationCompositions ou appareils à cet effet en atmosphère contrôlée comportant d'autres gaz en plus des gaz suivants: CO2, N2, O2 ou H2O
A method of hand-washing of laundry is provided which comprises treating the laundry with a washing liquor containing a detergent composition comprising a surfactant and a metal complexing agent as an indicator compound indicating the current effective activity of the washing liquor. Consequently, the washing liquor can be always maintained at its optimal cleaning strength so that good washing results are obtained.
The instant invention relates to a process for enhancing plant growth in greenhouses or plant tunnels or over mulches by incorporating one or more yellow pigments or dyes into a greenhouse, mulch film or glazing and exposing the plants through or over such film to solar radiation so that specific and defined ratios of the light transmitted, emitted or reflected between 410 to 450 nm, 380 to 410 nm and 450 to 500 nm are obtained. A further aspect of the invention is the use of one or more yellow pigments or dyes as plant growth enhancing additive in polymeric films for greenhouses, plant tunnels or mulches or a coating for greenhouse glazing so that specific and defined ratios of the light transmitted, emitted or reflected between 410 to 450 nm, 380 to 410 nm and 450 to 500 nm are obtained.
Compounds of the formula (I), (Il) or (III), wherein R1 is for example C1-C18alkylsulfonyl, C1-C10haloalkylsulfonyl, camphorylsulfonyl, phenyl-C1-C3alkylsulfonyl, phenylsulfonyl, naphthylsulfonyl, anthrylsulfonyl, phenanthrylsulfonyl or heteroarylsulfonyl, R'1 is for example phenylenedisulfonyl, R2 is for example CN, C1-C10haloalkyl or C1-C10haloalkyl which is substituted by (IV); Ar1 is for example phenyl optinally substituted by a group of formula (IV); Ar'1 is for example phenylene which optionally is substituted by a group of formula (IV); A1, A2 and A3 independently of each other are for example hydrogen, halogen, CN, or C1-C18alkyl; D2 is for example a direct bond, O, (CO)O, (CO)S, SO2, OSO2 or C1-C18alkylene; or A3 and D2 together form C3-C30cycloalkenyl; or A2 and D2 together with the carbon of the ethylenically unsaturated double bond to which they are attached form C3-C30cycloalkyl; D3 and D4 for example independently of each other are a direct bond, O, S, C1-C18alkylene or C3-C30cycloalkylene provided that at least one of the radicals R2, Ar1 or Ar1' comprises a group of the formula (IV); are suitable as photolatent acid donors and for the preparation of corresponding polymers to be employed in chemically amplified photoresists.
A reversible thermochromic system comprising a) a compound of the formula (I) or a tautomer thereof (I) wherein R1 is C1-C18alkyl, C2-C18alkenyl, C3-C12cycloalkyl, C3-C12cycloalkyl substituted by 1, 2 or 3 C1-C4alkyl; or C7-C12phenylalkyl; R2 and R3 are hydrogen or R2 and R3 together form a group -CH=CH-CH=CH-; and R4 is hydrogen, -NO2, -SO2-R1 or (4-nitrophenyl)azo; and b) a compound containing a group of the formula (II).
B41M 5/28 - Thermographie utilisant des composés thermochromes ou des couches contenant des cristaux liquides, des microcapsules, des colorants blanchissables ou des composés thermodégradables, p. ex. libérant un gaz
C09B 29/01 - Colorants monoazoïques préparés par diazotation et copulation caractérisés par le composant diazo
C09B 29/15 - Colorants monoazoïques préparés par diazotation et copulation à partir de copulants ne contenant comme groupe orienteur qu'un groupe hydroxyle de la série du naphtalène
C09B 29/12 - Colorants monoazoïques préparés par diazotation et copulation à partir de copulants ne contenant comme groupe orienteur qu'un groupe hydroxyle des séries benzéniques
A reversible thermochromic system comprising a) a compound of the formula (IA) or a tautomer thereof or a compound of the formula (IB) or a tautomer thereof (IA) (IB) wherein R1 is C1-C18alkyl, C2-C18alkenyl, C3-C12cycloalkyl, C3-C12cycloalkyl substituted by 1, 2 or 3 C1-C4alkyl; phenyl, phenyl substituted by 1, 2 or 3 C1-C4alkyl; or C7-C12phenylalkyl; R2 is hydrogen or a group -SO2-R; R3 and R4 independently of one another are hydrogen, C1-C18alkyl, C2-C18alkenyl, C3-C12cycloalkyl, C3-C12cycloalkyl substituted by 1, 2 or 3 C1-C4alkyl; phenyl, phenyl substituted by 1, 2 or 3 C1-C4alkyl; or C7-C12phenylalkyl; and R is C1-C18alkyl, C2-C18alkenyl, C3-C12cycloalkyl, C3-C12cycloalkyl substituted by 1, 2 or 3 C1-C4alkyl; phenyl, phenyl substituted by 1, 2 or 3 C1-C4alkyl; or C7-C12phenylalkyl; and b) a compound containing a group of the formula (III).
C09B 1/06 - HydroxyanthraquinonesLeurs éthers ou esters préparation à partir de substances contenant déjà le noyau anthracène
C09B 69/02 - Matières colorantes sous forme de sel, p. ex. sels de colorants basiques avec des colorants acides
C09B 69/04 - Matières colorantes sous forme de sel, p. ex. sels de colorants basiques avec des colorants acides de colorants anioniques avec des composés contenant de l'azote
C09B 1/12 - Colorants contenant des groupes acide sulfonique
Disclosed are compounds of formula (I); wherein D is an aromatic or a cationic heteroaromatic group, which is optionally substituted by C1-C14alkyl, C1-C14alkoxy, hydroxy-C1-C14alkyl, C3-C8cycloalkyl, -CN, NO2, -NR3R4, halogen, C6-C10aryl, which is optionally substituted or C1-C14alkyl, or by one or more groups Z; E1 and E2 independently from each other are =CH; or =N-; K is an aromatic or heteroaromatic group which is optionally substituted by C1-C14alkyl, C1-C14alkoxy, C3-C8cycloalkyl, C6-C10aryl, halogen, hydroxy, NO2, -NR3R4, -N(R3)(CO)R4, -SO2NR1R2, -SONR1R2 or by one or more Z; or a radical of formula -NR1R2; R1 and R2 independently from each other are hydrogen; C1-C14alkyl; cyclo-C1-C14alkyl; C6- C10aryl; an aromatic or heteroaromatic group which is optionally substituted by C1- C14alkyl, C1-C14alkoxy, C3-C8cycloalkyl, C6-C10aryl, halogen, hydroxy, -NR5R6, -N(R5)-(CO)R5 or by Z; Z is a group of the formula (1 a) *- X1-Y1-W1, wherein X1 is the direct bond; -NR7-; -0-; -NR7(C=O)-; -(CO)NR7-; -0(C=O)-; -(CO)O-; or -(C=O)-; Y1 is the direct bond; C1-C12alkylene, which is optionally interrupted by -0-, -NR8, -S-, -(C=O)-, -0(C=O)-, (C=O)O-, -NR7(C=O)-, -(C=O)NR7-, and which may substituted by C1-C14alkyl, hydroxy-C1-C14alkyl, hydroxy, -NR9R10 or halogen; or C6-C10arylene, which may substituted by C1-C14alkyl, hydroxy-C1-C14alkyl, hydroxy, amino or halogen; W1 is a cationic group; and R3, R4, R5, R6, R7, R8, R9 and R10 independently from each other are hydrogen; C1-C14alkyl; or Z; and An1-, An2- and An3- independently from each other are an anion. The compounds are useful for dyeing of organic materials, such as keratin-containing fibers, wool, leather, silk, cellulose or polyamides, especially keratin-containing fibers, cotton or nylon, more preferably human hair.
C09B 44/00 - Colorants azoïques contenant des groupes onium
C09B 44/08 - Colorants azoïques contenant des groupes onium contenant des groupes ammonium non directement kiés à un groupe azo à partir de copulants comportant des hétérocycles
C09B 44/12 - Colorants azoïques contenant des groupes onium contenant des groupes cyclo-ammonium liés à un groupe azo par un atome de carbone du cycle contenant un atome d'azote comme unique hétéro-atome du cycle
C09B 44/16 - Diazoles-1, 3 ou diazoles-1, 3 hydrogénés
C09B 69/00 - Colorants non prévus par un seul groupe de la présente sous-classe
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 5/10 - Préparations pour la teinture permanente des cheveux ou des poils
87.
S-PERFLUOROALKYL SUBSTITUTED HYDROXYBENZYLTHIOETHERS AND DERIVATIVES AS SURFACE MODIFIERS
The invention describes a process for reducing the surface energy of organic materials such as for example increasing the oil and water repellency and stain release of organic materials, which comprises treating the organic material with at least a compound of the formula I wherein the general symbols are as defined in claim 1; especially wherein at least one of the radicals R2, R3 or R4 is -CH(R11)-S(O)p-R12; R11 is hydrogen, C1-C8alkyl, unsubstituted or with C1-C4alkyl substituted phenyl; R12 is a monovalent perfluorinated alkyl or alkenyl, linear or branched organic radical having four to twenty fully fluorinated carbon atoms, and p is 0, 1 or 2.
Anti-microbial compositions comprising certain imidazolium ionic liquids and non-ionic or anionic surfactants and methods of using said compositions in the preservation of personal care and cosmetic applications are provided.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 19/00 - Préparations pour les soins de la peau
89.
COMPOSITION FOR IMPROVING THE PRINTABILITY OF COATED PAPER
The present invention relates to improvement in printability of coated paper by adding composition comprising granular starch onto the paper, said composition being essentially free of mineral or synthetic pigment.
The present invention describes bleed-resistant microparticles comprising at least one colorant, a process to produce them, compositions containing them and their use in cosmetics applications to produce a natural, textured tone effect.
A61K 8/81 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons insaturées carbone-carbone
A61Q 1/02 - Préparations contenant des colorants cutanés, p. ex. pigments
The invention relates to novel acidic siloxane derivatives, the use, methods of use or processes making use of siloxane derivatives of this type, especially to achieve an anti- microbial, preservative and/or antiadhesive effect, for the protection of articles and/or materials, and a process for the manufacture of the novel compounds. The siloxane acids (which may also be in salt form) have the formula (I), formula (II) and/or formula (III), wherein the symbols have the meanings given in the specification.
C08G 77/14 - Polysiloxanes contenant du silicium lié à des groupes contenant de l'oxygène
C08G 77/28 - Polysiloxanes contenant du silicium lié à des groupes organiques contenant des atomes autres que le carbone, l'hydrogène et l'oxygène groupes contenant du soufre
C08G 77/30 - Polysiloxanes contenant du silicium lié à des groupes organiques contenant des atomes autres que le carbone, l'hydrogène et l'oxygène groupes contenant du phosphore
A01N 41/02 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de soufre lié à un hétéro-atome comportant une liaison double soufre-oxygène
A01N 37/02 - Acides carboxyliques saturés ou leurs thio-analoguesLeurs dérivés
A01N 57/12 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-oxygène ou des liaisons phosphore-soufre contenant des radicaux acycliques ou cycloaliphatiques
Disclosed is a method for the colouration of skin or a keratinic fibre, characterized in that the skin or keratinic fibre is contacted with a formulation containing a dispersion of solid particles of a tanning substance selected from a compound of the formula (I) wherein i is 0 or 1 and each of R1, R2, R3, R4, R5, R6, R7, R8 independently of each other is selected from group consisting of hydrogen, OH, C1-C6alkyl, C1-C6hydroxyalkyl and C2-C6al- kenyl; in an organic liquid of low polarity or non-polar organic liquid.
A61K 8/19 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés inorganiques
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 19/04 - Préparations pour les soins de la peau pour colorer chimiquement la peau
The invention relates to a new modified polyacrylate comprising fluorinated oxetane (FOX) polymer units functionalized with an unsaturated dicarboxylic acid and siloxane units and to its use as slip-and leveling agent and anti-cratering agent for a variety of applications.Thus, the invention relates to a slip- and leveling agent characterized in that it comprises a copolymer which is obtained by copolymerizing A at least one unit of a fluorinated oxetane polymer functionalized with an unsaturated dicarboxylic acid; B at least one terminal reactive polysiloxane unit; C at least one alkyl(meth)acrylate unit or cycloalkyl(meth)acrylate unit and/or (meth)acrylic acid and/or other units originating from vinylic compounds that can form radicals.
C08L 51/08 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères greffés sur des composés macromoléculaires obtenus autrement que par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone
C09D 151/08 - Compositions de revêtement à base de polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions de revêtement à base de dérivés de tels polymères greffés sur des composés macromoléculaires obtenus autrement que par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone
94.
A DETERGENT COMPOSITION FOR TEXTILE FIBRE MATERIALS
A detergent composition comprising i) 1-70% of an anionic or nonionic surfactant, ii) 1-75% of a builder, iii) 0.001-5% of at least one compound of Formula (1) wherein R represents a C1-C4alkyl residue and M represents hydrogen or an alkali metal cation, optionally with further FWA's, iv) 0-30% of a peroxide, v) 0-10% of a peroxide activator, vi) 0-5% of a bleaching catalyst and vii) 0-5% of an enzyme, each component by weight, based on the total weight of the detergent composition, use thereof for domestic washing of textile fibre materials and a process for the fluorescent whitening of textile materials.
The invention relates an additive composition for use as a metal working fluid and a process for protection of metals, particularly zinc or aluminum, against corrosion or oxidative degradation. The composition comprises an additive mixture of an alkenyl succinic half ester, a substituted imidazoline compound and amine phosphate partial ester in a functional fluid.
C10M 141/10 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'au moins deux composés couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé organique contenant du phosphore
C10M 161/00 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'un composé macromoléculaire et d'un composé non macromoléculaire, chacun de ces composés étant un composé essentiel
C10N 30/12 - Inhibition de la corrosion, p. ex. agents antirouille, agents anticorrosifs
96.
N-SUBSTITUTED PERFLUOROALKYLATED PYRROLIDINES AS SURFACE MODIFIERS
The invention describes a composition comprising comprising a) a natural, semi-synthetic or synthetic polymer which is susceptible to oxidative, ther- mal or light-induced degradation, and b) a compound of the formula (I) wherein RF, R, Q and q are as defined herein, and are prepared from diallylamine, a perfluoroalkyl iodide and an amino-reactive compound selected from the group of carboxylic acids, anhydrides, acid chlorides, oxiranes, haloalkanes, isocyanates and ureas. The compounds of the formula I are useful as reducers of surface energy for natural, semi- synthetic or synthetic polymers, for example, for increasing the oil and water repellency and stain release of natural, semi-synthetic or synthetic polymers.
Optical recording medium suitable for optical recording with a laser of wavelength from 350 to 500 nm, especially about 405 nm, wherein the recording track comprises a compound of formula ⏧(L1)M1(L2)]m- Z1+ (I), or a mesomeric or tautomeric form thereof, wherein L1 and L2 independently of one another are divalent, heterocyclic azo ligands of the formula (I) M1 is a metal cation in the oxidation state +3, a hydroxy or halogeno metal group wherein the metal is in the oxidation state +4, or an oxo metal group wherein the metal is in the oxidation state +5; m is 1 ; n is an integer 1 , 2 or 3; and Z1 is a cation of the formula (a), (b) or (c).
G11B 7/246 - Supports d’enregistrement caractérisés par le choix du matériau des couches d'enregistrement comprenant seulement des matériaux organiques contenant des colorants
G11B 7/249 - Supports d’enregistrement caractérisés par le choix du matériau des couches d'enregistrement comprenant seulement des matériaux organiques contenant des composés organométalliques
C09B 45/00 - Composés métalliques complexes des colorants
C09B 69/02 - Matières colorantes sous forme de sel, p. ex. sels de colorants basiques avec des colorants acides
98.
Use of a high performance water vapor barrier coating for paper under tropical conditions
This invention provides the use of a water vapor barrier as coating for paper or paperboard as substrate for lowering the water vapor transmission rate (WVTR) of the substrate under tropical conditions, for example 37.8°C and 90% relative humidity, wherein the barrier improvement factor (BIF), which is the ratio of WVTR uncoated substrate/WVTR coated substrate, is at least 80.
D21H 21/14 - Matériaux non fibreux ajoutés à la pâte, caractérisés par leur fonction, leur forme ou leurs propriétésMatériaux d'imprégnation ou de revêtement du papier, caractérisés par leur fonction, leur forme ou leurs propriétés caractérisés par leur fonction ou leurs propriétés dans, ou sur, le papier
D21H 19/72 - Papier couché caractérisé par le substrat de papier
99.
POLYMER ARTICLE MODIFIED WITH A METAL CATION CONTAINING COMPOUND
An agricultural article made of a composition containing (a) an organic polymer, and (b-I) a polyacrylic acid sodium salt or a sodium salt of ethylene/methacrylic acid copolymer, and (b-II) manganese stearate.
A non-agricultural article, which is different from a golf ball or golf ball cover and which is made of a composition containing (a) an organic polymer, and (b-I) a polyacrylic acid sodium salt or a sodium salt of ethylene/methacrylic acid copolymer, and (b-II) manganese stearate.
