Abstract: An improved reactive dyestuff mixture comprises at least one monochlorotriazine dyestuff 1 and at least one monofluorotriazine dyestuff 2 and/or fluorochloropyrimidine dyestuff 3, and if appropriate additional dyestuffs having the formulae given in the description.

Abstract: The gasification apparatus for gasification of finely divided combustible material under pressure includes a gasification reactor which produces a crude gas, a quenching pipe and a convection-heated boiler with a boiler housing, all mounted inside a pressurized vessel. A gas flow guiding device is provided above the quenching pipe for conducting a mixed gas flow containing the crude gas and a quenching gas from the quenching pipe into the convection-heated boiler which surrounds the quenching pipe concentrically. A gas outlet device is provided for the gas flow from the convection-heated boiler and from the pressurized vessel. The gasification reactor is supported at its bottom end in the pressurized vessel at anchoring points. The convection-heated surface elements of the convection-heated boiler are supported by the quenching pipe and the boiler housing but in a stress-free manner.

Abstract: The gasification process includes providing a gasification reactor for gasifying a finely divided combustible material under pressure to form a crude gas with cinder and ash components, a quenching pipe positioned concentrically above the gasification reactor, a convection-heated boiler concentrically surrounding the quenching pipe and a gas flow guide device above the quenching pipe, the gas flow guide device being rotationally symmetric with respect to a longitudinal axis of the quenching pipe; conducting the crude gas with the cinder and ash components from the gasification reactor into the quenching pipe; feeding a quenching gas into the quenching pipe during the gasifying to form a mixed flow including the crude gas, the cinder and ash components and the quenching gas; guiding the mixed flow about a 180.degree.

Abstract: A reactive dyestuff mixture contains at least one vinylsulphonylphthalocyanine dyestuff, at least one Ni fluoro-chloropyrimidenyl phthalocyanine dyestuff and/or one Ni chlorotriazinyl-phthalocyanine dyestuff.

Abstract: Improved reactive dyestuff red mixtures comprise in each case at least one component of the formula 1 ##STR1## and one component of the formula 2 ##STR2## wherein the substituents have the meaning given in the description.

Abstract: A reactive dyestuff mixture showing improved compatibility contains at least one vinylsulphonyltriazine dyestuff 1, at least one monofluorotriazine dyestuff 2 or fluorochloropyrimidine dyestuff 3 together with, if desired, additional dyestuffs.

Abstract: Improved reactive dyestuff mixtures comprise a reactive dyestuff of the formula (I) ##STR1## and a chlorotriazine dyestuff of the formula ##STR2## wherein the substituents have the meaning given in the description.

Abstract: A phthalocyanine reactive dyestuff mixture having an improved dyeing levelness and combination properties comprises at least one phthalocyanine vinylsulphonyl reactive dyestuff 1, at least one phthalocyanine fluorochloropyrimidinyl reactive dyestuff 2 and/or a phthalocyanine monochlorotriazinyl reactive dyestuff 3.

Abstract: New dyestuff mixtures contain in each case at least one fluoropyrimidine dyestuff of the general formula (I) ##STR1## and a vinylsulfonyl dyestuff of the formula (II) ##STR2## in which the substituents have the meaning given in the description.

Abstract: Solid dyestuff preparations of reactive phthalocyanine dyestuffs of the formula ##STR1## in which the substituents have the meaning given in the description, have improved solubility in water if they contain 5 to 15% by weight of an acid-binding agent.

Abstract: Dyestuffs of the formula ##STR1## in which the substituents have the meanings given in the description are suitable for the dyeing and printing of hydroxy-containing and amido-containing materials. They produce blue dyeings having high color density and high light fastness and wet fastness properties.

Abstract: Azo dyes are obtained by diazotizing an aromatic amine and combining the resulting diazonium salt solution with a sulpho-containing coupling component when the sole acid donor used for the diazotization reaction--instead of the otherwise customary mineral or fatty acids--is a low molecular weight, nonsurfactantlike aromatic sulphonic acid.

Abstract: Ultrafiltered solutions of the dyestuff of the formula ##STR1## (Me=cation) such as is obtained directly on synthesis, are distinguished by an increased tinctorial strength in pad-steam dyeing of cellulose fibres.

Abstract: A new method of diazotization consists in using as the diazotizing agent in an aqueous, aqueous organic or organic medium the system comprising salt of nitrous acid+acid insoluble in the reaction medium, in particular organic or inorganic cation exchangers having acid groups. The diazonium salt solutions thus prepared are immediately reacted with coupling components to give azo dyestuffs, the insoluble acid and/or its salt being separated off before or after the coupling.

Abstract: Liquid water-containing concentrated reactive dye-stuff preparations of monofluorotriazinyl reactive dye-stuffs with a pH value of at least 8, preferably 8.5-10, are stable on storage and display no noticeable hydrolysis, even after prolonged storage.

Abstract: Stable, concentrated aqueous solutions of, in particular, anionic reactive dyestuffs are obtained in a comparatively simple manner by freeing from salts, preferably by means of membrane separation processes, solutions of these substances just as they are obtained in the course of synthesis, and by replacing, with the aid of ion exchangers, the cations which cause sparing solubility.

Abstract: Concentrated aqueous solutions of dyestuffs having water-solubilizing groups which contain cyanamides of the formula ##STR1## wherein R.sub.1 =NHCN, NHCONH.sub.2 or NHCONHCH.sub.3 where n=0 andm=1 or n=1 and m=0,have a long shelf life, in particular also in the case of reactive dyestuffs.

Abstract: A new storage-stable solution of the reactive dyestuff of the formula ##STR1## wherein CuPc=the radical of a Cu phthalocyanine dyestuff,m=1, 2 or 3,n=1, 2 or 3,m+n=3 to 4 andM.sup..sym. =H.sup..sym., an alkali metal cation or an ammonium ion,is provided.The storage-stable solution according to the invention is characterized in that it contains 10-35% by weight of reactive dyestuff (1), 10-30% by weight of solubilizing agent, 0-10% by weight of anionic dispersing agent, 0-7% by weight of inorganic salts, such as Na.sub.2 SO.sub.4, Li.sub.2 SO.sub.4 and the like, and 0.1-3% by weight of buffer (pH 4-7), the remainder to make up to 100% by weight being water.

Abstract: The lyotropic, liquid-crystalline, aqueous phase of a reactive dyestuff of the formula ##STR1## wherein M.sym. represents H.sym. or an alkali metal cation (preferably Na.sym., K.sym. or Li.sym.) andR is a fibre-reactive groupingpresent in water at room temperature in a concentration of 10-25%, if appropriate in the presence of concentration-increasing additives and/or buffer substances, is highly suitable for preparing dyebaths and print pastes for application to natural and synthetic substrates, in particular cotton, wool, regenerated cellulose, paper and leather.

Abstract: The present disclosure is concerned with storage stable concentrated fluid aqueous dispersions of water soluble cold dyeing fiber reactive dyes. These dispersions contain anionic or polyvinyl dispersants to provide resistance against settling or agglomeration and water soluble electrolytes to provide resistance against hydrolysis of the fiber reactive groups. The dispersions have an average particle size of less than 100 microns and in a preferred embodiment sufficient buffering agent to stabilize the pH at between about 5 and 8.