Abstract: The present invention relates to a dimensionally stable adhesive compound which is formulated so as to be largely water- and solvent-free and can be brought into contact with the substrate to be bonded by being wiped on in the form of a thin adhesive film that is suitable in particular for bonding materials obtained from plant fibers. The organic constituent of the adhesive compound according to the invention consists predominantly of polyester polyurethanes, at least some of which are based on semi-crystalline polyester polyols. The invention also relates to a method for applying a tacky film to a planar substrate, preferably to paper, by wiping the adhesive compound onto the point of contact with the substrate.

Abstract: The present invention relates to a dimensionally stable adhesive compound which is formulated so as to be largely water- and solvent-free and can be brought into contact with the substrate to be bonded by being wiped on in the form of a thin adhesive film that is suitable in particular for bonding materials obtained from plant fibers. The organic constituent of the adhesive compound according to the invention consists predominantly of a mixture of polyether polyurethanes which are end-capped with at least two monohydric aliphatic alcohols of different chain lengths. The invention also relates to a method for applying a tacky film to a planar substrate, preferably to paper, by wiping the adhesive compound onto the point of contact with the substrate.

Abstract: The subject of the present disclosure is a process for the preparation and storage of an agent for the treatment of keratinous material, in particular human hair, comprising the following steps: (1) mixing one or more organic C1-C6 alkoxy silanes with water, (2) optionally, partial, or complete removal from the reaction mixture of the C1-C6 alcohols liberated by the reaction in step (1), (3) if necessary, addition of one or more cosmetic ingredients, (4) filling of the preparation into a packaging unit, and (5) storage of the preparation in the packaging unit, wherein at least one of steps (1), (2), (3), (4) and/or (5) is carried out under an atmosphere having a water vapor content of less than about 10 g/m3.

Abstract: The subject of the present application is a process for the preparation of an agent for the treatment of keratinous material, in particular human hair, comprising the following steps: (1) reaction of one or more organic C1-C6 alkoxy silanes with water at a temperature of from about 20 to about 70° C. to give a reaction mixture, (2) complete or partial removal of C1-C6 alcohols released by a reaction in step (1) from the reaction mixture at a temperature of from about 20 to about 70° C., (3) optionally, addition of one or more cosmetic ingredients to the reaction mixture, thereby giving a preparation, and (4) filling the preparation into a packaging unit.

Abstract: The subject of the present application is a method for the preparation and use of an agent for the treatment of keratinous material, in particular human hair, comprising the following steps: (1) Mixing one or more organic C1-C6 alkoxy silanes with water, (2) optionally, partial, or complete removal from the reaction mixture of the C1-C6 alcohols liberated by the reaction in step (1), (3) if necessary, addition of one or more cosmetic ingredients, (4) Filling of the preparation into a packaging unit, (5) Storage of the preparation in the packaging unit for a period of at least about 5 days; and (6) Application of the preparation on the keratinous material.

Abstract: The subject of the present application is a process for the preparation of an agent for the treatment of keratinous material, in particular human hair, comprising the following steps: (1) Mixing one or more organic C1-C6 alkoxy silanes with water, (2) partial or complete removal from the reaction mixture of the C1-C6 alcohols released by the reaction in step (1), (3) optionally addition of one or more cosmetic ingredients, and (4) Filling of the preparation into a packaging unit, exemplified in that the total content of C1-C6 alcohols in the preparation obtained in step (4)—based on the total weight of the preparation—is below about 10.0% by weight.

Abstract: The present disclosure provides improved dye transfer inhibition in the washing of textiles by the use of urea derivatives comprising sulfonic or carboxylic acid groups.

Abstract: The present invention describes reaction products from 2,4?-diphenylmethane diisocyanate with a content of at least 95 wt. % of 2,4? isomer with at least one polyether-polyol and/or polyalkylene glycol with a molecular weight of less than 1,000 and/or one crystalline or partly crystalline or vitreously amorphous polyester-polyol and optionally polyester-polyols and/or polyether-polyols which are liquid at room temperature and have molecular weights of greater than 1,000 can be converted into adhesive compositions which have a very low content of monomeric diisocyanate of less than 0.5, preferably less than 0.25 wt. %. Such hot melt adhesive compositions have a high melt stability and a low viscosity, in addition to the low content of monomeric diisocyanate.

Abstract: Cross-linkable foamable composition with low content of monomeric isocyanates, containing a pre-polymer of polyester diols and/or polyether dials reacted i) with asymmetric aromatic diisocyanates to form a reaction product with OH and NCO groups, ii) subsequent addition of and reaction with symmetric aromatic diisocyanate in a quantity at least equivalent to the available OH-groups, 0.1 to 30 wt % additives, at least one propellant, wherein the polyols have a molar mass (MN) of less than 5000 g/mol, and the reaction product has a content of less than 0.1 wt % monomeric asymmetric isocyanate and less than 2 wt % monomeric symmetric isocyanate.

Abstract: Cross-linkable foamable composition with low content of monomeric isocyanates, containing a pre-polymer of polyester diols and/or polyether dials reacted i) with asymmetric aromatic diisocyanates to form a reaction product with OH and NCO groups, ii) subsequent addition of and reaction with symmetric aromatic diisocyanate in a quantity at least equivalent to the available OH-groups, 0.1 to 30 wt % additives, at least one propellant, wherein the polyols have a molar mass (MN) of less than 5000 g/mol, and the reaction product has a content of less than 0.1 wt % monomeric asymmetric isocyanate and less than 2 wt % monomeric symmetric isocyanate.

Abstract: The invention relates to the use of a solvent-free, 2 component adhesive for adhering sterilizable composite films, wherein the adhesive comprises a component A made from at least one pre-polymer comprised of NCO groups, said pre-polymer produced from low molecular weight polyether alcohols, polyester alcohols and/or polyalkylene alcohols having a functionality of 2 or 3, implemented having a high molar excess of TDI and removal of the unimplemented monomer diisocyanate, and a component B comprising at least one 2 or 3 functional polyesterpolyol, produced from diols and/or triols on the basis of polyethers or polyalkylene diols implemented having dicarboxylic acids and derivatives thereof, wherein at least 10 to 40 wt % must be comprised of aliphatic C8 to C20 dicarboxylic acids, and auxiliary and additive materials in at least one component A or B.

Abstract: The invention relates to the use of a solvent-free, 2 component adhesive for adhering sterilizable composite films, wherein the adhesive comprises a component A made from at least one pre-polymer comprised of NCO groups, said pre-polymer produced from low molecular weight polyether alcohols, polyester alcohols and/or polyalkylene alcohols having a functionality of 2 or 3, implemented having a high molar excess of TDI and removal of the unimplemented monomer diisocyanate, and a component B comprising at least one 2 or 3 functional polyesterpolyol, produced from diols and/or triols on the basis of polyethers or polyalkylene diols implemented having dicarboxylic acids and derivatives thereof, wherein at least 10 to 40 wt % must be comprised of aliphatic C8 to C20 dicarboxylic acids, and auxiliary and additive materials in at least one component A or B.

Abstract: Polyurethane compositions are produced in a two-stage method. In a first step, a diol component with a molecular weight of less than 2000 is reacted with a monomeric diisocyanate with a molecular weight of less than 500 and the unreacted monomeric diisocyanate is removed from this reaction product. In a second step, the resulting high-molecular diisocyanate is reacted with a polyol to produce a reactive prepolymer with isocyanate and groups. The addition of polyisocyanates which are capable of migration and which have a substantially lower vapor pressure than diphenylmethanediisocyanate, improves the addition behavior of the invention polyurethane compositions. Reactive polyurethane compositions of this type are suitable for using as binding agents for reactive one or two component adhesives/sealants, which may optionally contain solvents. These compositions are also suitable for producing reactive hot melt adhesives when suitable polyols are selected.

Abstract: The invention relates to a polymer dispersion which contains water, at least one polymer that has been produced by emulsion polymerisation, at least one protective colloid, at least one water-soluble acidic metallic salt and at least one cross-linking resin that is based on phenol-formaldehyde condensation products, hydroxymethyl-substituted imidazolidinones, such as 1,3-dimethylol-4,5-dihydroxy-imidazolidinone (4,5-dihydroxy-N,N?-dimethylolethylene urea), hydroxymethyl-substituted pyrimidinones, or hydroxymethyl-substituted triazinones or their auto-condensation products, or mixed condensates from two or more of the aforementioned compounds, or a mixture of two or more of the aforementioned compounds.

Abstract: A reactive hotmelt adhesive is prepared which contains a reaction product of a stoichiometric excess of a polyisocyanate with a hydroxyl-functional polyester-ether block copolymer based on aromatic dicarboxylic acids. The adhesive additionally contains a reaction product of a polyisocyanate and at least one of either a polyether polyol or a polyester polyol. A thermoplastic polymer may also be present.

Abstract: The present invention relates to compositions comprising reaction products of a polyisocyanate with a polyester block copolymer and a process for the preparation thereof. These are suitable as a moisture-curing hot melt adhesive. The hot melt adhesive composition may optionally also comprise a reaction product of a polyisocyanate with a polyester polyol and/or a reaction product of a polyisocyanate with a polyether polyol. Such polyurethane hot melt adhesive compositions have good creep resistance and interfacial adhesion values on plastics and show very high strength values.

Abstract: The present invention describes reaction products from 2,4?-diphenylmethane diisocyanate with a content of at least 95 wt. % of 2,4? isomer with at least one polyether-polyol and/or polyalkylene glycol with a molecular weight of less than 1,000 and/or one crystalline or partly crystalline or vitreously amorphous polyester-polyol and optionally polyester-polyols and/or polyether-polyols which are liquid at room temperature and have molecular weights of greater than 1,000 can be converted into adhesive compositions which have a very low content of monomeric diisocyanate of less than 0.5, preferably less than 0.25 wt. %. Such hot melt adhesive compositions have a high melt stability and a low viscosity, in addition to the low content of monomeric diisocyanate.

Abstract: The invention relates to a polymer dispersion which contains water, at least one polymer that has been produced by emulsion polymerisation, at least one protective colloid, at least one water-soluble acidic metallic salt and at least one cross-linking resin that is based on phenol-formaldehyde condensation products, hydroxymethyl-substituted imidazolidinones, such as 1,3-dimethylol-4,5-dihydroxy-imidazolidinone (4,5-dihydroxy-N,N′-dimethylolethylene urea), hydroxymethyl-substituted pyrimidinones, or hydroxymethyl-substituted triazinones or their auto-condensation products, or mixed condensates from two or more of the aforementioned compounds, or a mixture of two or more of the aforementioned compounds.

Abstract: A cleaning composition effective for removing reactive polyurethane hotmelts and reaction products thereof is presented containing (a) a non-volatile monohydroxy compound having a boiling point at normal pressure of greater than 140° C., a secondary monoamine, or mixtures thereof, and (b) a catalyst for the production of a polyurethane or a depolymerization catalyst selected from the group consisting of an alkali metal alcoholate, an alkaline earth metal alcoholate, an aluminum alcoholate, a tertiary amine and mixtures thereof. The cleaning composition removes both residues of the reactive uncrosslinked hotmelt and also adhering deposits of already reacted, crosslinked or cracked, infusible hotmelt.

Abstract: A cleaning composition effective for removing reactive polyurethane hotmelts and reaction products thereof is presented containing (a) a non-volatile monohydroxy compound having a boiling point at normal pressure of greater than 140° C., a monoamine, or mixtures thereof, and (b) a catalyst for the production of a polyurethane or a depolymerization catalyst selected from the group consisting of an alkali metal alcoholate, an alkaline earth metal alcoholate, an aluminum alcoholate, a tertiary amine and mixtures thereof. The cleaning composition removes both residues of the reactive uncrosslinked hotmelt and also adhering deposits of already reacted, crosslinked or cracked, infusible hotmelt.