Abstract: Manufacturing a spun-dyed para-aramid filament yarn includes (a) preparing a spin dope comprising a para-aramid polymer, at least one dyestuff and concentrated sulfuric acid, (b) spinning the spin dope through a spinneret to obtain spun filaments, (c) coagulating the spun filaments to obtain coagulated filaments, (d) neutralizing the coagulated filaments to obtain neutralized filaments, (e) washing the neutralized filaments to obtain washed filaments, and (f) drying the washed filaments to obtain dried filaments. In step a) the spin dope includes 17.5 to 18.5% by weight of a para-aramid polymer with respect to the weight of the spin dope, and 4 to 15% by weight of the at least one dyestuff with respect to the weight of the para-aramid polymer plus the at least one dyestuff. In step f) the filaments are hold under a tension in a range from 0.2 to 0.8 cN/dtex.

Abstract: Manufacturing a spun-dyed para-aramid filament yarn includes (a) preparing a spin dope comprising a para-aramid polymer, at least one dyestuff and concentrated sulfuric acid, (b) spinning the spin dope through a spinneret to obtain spun filaments, (c) coagulating the spun filaments to obtain coagulated filaments, (d) neutralizing the coagulated filaments to obtain neutralized filaments, (e) washing the neutralized filaments to obtain washed filaments, and (f) drying the washed filaments to obtain dried filaments. In step a) the spin dope includes 17.5 to 18.5% by weight of a para-aramid polymer with respect to the weight of the spin dope, and 4 to 15% by weight of the at least one dyestuff with respect to the weight of the para-aramid polymer plus the at least one dyestuff. In step f) the filaments are hold under a tension in a range from 0.2 to 0.8 cN/dtex.

Abstract: Spun-dyed aramid fibers, wherein spun-dyeing was performed with a completely organic pigment exhibiting the chemical structure of formula (I): wherein, independently from one another, R1 represents a substituent of formula Xa or a substituent of formula Xb: wherein Xa is linked via the group NH having two bonds in the structure represented by Xa, while Xb is linked via the carbon atom, which is in a para relationship with the NH2-group of Xb; and R2 represents H or NH2. The spun-dyed aramid fibers exhibit constant coloristic properties and wash proof properties.

Abstract: A method for dosing a powder into a kneader is provided, wherein the powder is fed via a feeder-mechanism into a feeding hole of the kneader. The powder falls from an additional feeding device of the feeder-mechanism into one of at least four segments of a rotary valve of the feeder-mechanism.

Abstract: Spun-dyed aramid fibers, wherein spun-dyeing was performed with a completely organic pigment exhibiting the chemical structure of formula (I): wherein, independently from one another, R1 represents a substituent of formula Xa or a substituent of formula Xb: wherein Xa is linked via the group NH having two bonds in the structure represented by Xa, whilst Xb is linked via the carbon atom, which is in a para relationship with the NH2-group of Xb; and R2 represents H or NH2. The spun-dyed aramid fibers exhibit constant colouristic properties and wash proof properties.

Abstract: A process is disclosed for preparing an organically modified layered double hydroxide having a distance between the individual layers of the layered double hydroxide of about 1.5 nm and comprising an organic anion as charge-balancing anion, the process comprising the steps of: (a) preparing a precursor suspension comprising a divalent metal ion source and a trivalent metal ion source; (b) solvothermally treating the precursor suspension to obtain a double layered hydroxide, wherein an organic anion is added before or during the formation of the layered double hydroxide of step (b), or following the formation of the layered double hydroxide, so as to obtain the organically modified layered double hydroxide, with the proviso that deoxycholic acid is not the sole organic anion.

Abstract: Process for the preparation of a polymer-containing composition comprising the steps of: a) preparing a mixture of at least one cyclic monomer selected from glycolide and lactide and a layered double hydroxide comprising as charge-balancing anions 10 to 100% of an organic anion and 0 to 90% of hydroxide, based on the total amount of charge-balancing anions, and b) polymerising said monomer, optionally in the presence of a polymerisation initiator or catalyst.

Abstract: The invention relates to a process for preparing a layered double hydroxide comprising a charge-balancing anion, the process comprising the steps of: (a) preparing a precursor suspension or solution comprising a divalent metal ion source, a trivalent metal ion source, water, and a solvent which is miscible with water and in which at least 5 g/l of a charge-balancing anion precursor can be dissolved; (b) treating the precursor suspension or solution to obtain the layered double hydroxide, wherein the charge-balancing anion precursor is added to the suspension or solution before, during or after step (b), and wherein, if the charge-balancing anion is an organic anion, less than 50 wt % of the charge-balancing anion precursors, based on the total weight of charge-balancing anion precursors, is a salt, with the proviso that the charge-balancing anion is not carbonate. The invention further pertains to a layered double hydroxide obtainable by this process.

Abstract: The invention relates to a layered double hydroxide having a distance between the individual layers of the layered double hydroxide of above 1.5 nm and comprising 2 or more charge-balancing organic anions having 8 or more carbon atoms, wherein at least 2 of the organic anions have a different number of carbon atoms, and wherein less than 10% of the total of charge-balancing anions are charge-balancing organic anions having 2 or more anionic groups.

Abstract: The invention relates to a process for preparing a layered double hydroxide comprising a charge-balancing anion, the process comprising the steps of: (a) preparing a precursor suspension or solution comprising a divalent metal ion source, a trivalent metal ion source, water, and a solvent which is miscible with water and in which at least 5 g/l of a charge-balancing anion precursor can be dissolved; (b) treating the precursor suspension or solution to obtain the layered double hydroxide, wherein the charge-balancing anion precursor is added to the suspension or solution before, during or after step (b), and wherein, if the charge-balancing anion is an organic anion, less than 50 wt % of the charge-balancing anion precursors, based on the total weight of charge-balancing anion precursors, is a salt, with the proviso that the charge-balancing anion is not carbonate. The invention further pertains to a layered double hydroxide obtainable by this process.

Abstract: The present invention pertains to a nanocomposite material comprising rubber and a modified layered double hydroxide comprising: a charge-balancing organic ion having a first functional group and a second functional group, wherein at least part of the organic anions is chemically linked to the rubber through the second functional group; and/or a silane coupling agent having at least one alkoxysilane group and at least one reactive group, at least one alkoxysilane group being chemically linked to the layered double hydroxide, at least one reactive group being chemically linked to the rubber. The invention further pertains to a process for preparing the nanocomposite material or a precursor thereof.

Abstract: The invention relates to a process for preparing an organically modified layered double hydroxide having a distance between the individual layers of the layered double hydroxide of above 1.5 nm and comprising an organic anion as charge-balancing anion, the process comprising the steps of: (a) preparing a precursor suspension comprising a divalent metal ion source and a trivalent metal ion source; (b) solvothermally treating the precursor suspension to obtain the layered double hydroxide, wherein an organic anion is added before or during the formation of the layered double hydroxide of step (b), or following the formation of the layered double hydroxide, so as to obtain the organically modified layered double hydroxide, with the proviso that deoxycholic acid is not the sole organic anion. The invention further pertains to a process for preparing an organically modified layered double hydroxide having a distance between the individual layers of the layered double hydroxide of above 1.

Abstract: The invention relates to clays comprising charge-balancing organic ions wherein at least part of the organic ions are rosin-based ions. The invention further pertains to a hybrid organic-inorganic composite material comprising a polymer matrix and a clay comprising charge-balancing organic ions wherein at least part of the organic ions are rosin-based ions.

Abstract: The present invention refers to a resin composition comprising an ester compound and a polymer, wherein the ester compound and the polymer are obtainable by reacting a diene, a dienophile and a carboxylic acid. The invention also refers to adhesive compositions comprising the resin composition.

Abstract: The present invention relates to a process for preparing a polyester resin having a gel content of less than 0.45 wt %, based on the total weight of the polyester resin, and a glass transition temperature of between 40 and 70° C., comprising the step of reacting a polyester resin precursor with a chain extender which is different from the building blocks of the polyester precursor resin, optionally in the presence of a catalyst, at a temperature between 170 and 300° C. in a continuous reactor, wherein the polyester resin precursor comprises a functional group present as end group selected from hydroxyl or carboxyl, and optionally a functional group in the polyester resin precursor backbone selected from hydroxyl, carboxyl, amine, and carbonate, and the molar ratio of the functional group in the polyester resin precursor backbone to the functional group present as end group is at most 10:1. The invention further pertains to a polyester resin having a gel content of less than 0.

Abstract: The present invention refers to a resin composition comprising an ester compound and a polymer, wherein the ester compound and the polymer are obtainable by reacting a diene, a dienophile and a carboxylic acid. The invention also refers to adhesive compositions comprising the resin composition.