Abstract: A process for the purification of acid-containing crude caprolactam obtained by the rearrangement of cyclohexanone oxime, wherein the crude caprolactam is mixed with from 0.8 to 2.0 equivalents of a base, from 3 to 6 parts by weight of toluene, based on caprolactam and from 2 to 10 parts by weight of water, based on inorganic constituents, separating the mixture into a toluene phase and two aqueous phases the upper of which containing all contaminants and discarding this phase.

Abstract: A process for the purification of a solution of .epsilon.-caprolactam in benzene, toluene or xylene by washing with a liquid, wherein the washing liquid is a solution of .epsilon.-caprolactam in water in a weight ratio of from 15 : 1 to 1 : 3, which is used in a quantity of from 5 to 20% by weight, based on the solution of caprolactam in benzene, toluene or xylene, and wherein there are several washing stages so that the equilibrium between the two solutions can be readjusted.

Abstract: A process for the preparation of catalyst granulates from carbon black, boric acid, water and optionally nitrogenous additives, characterized in that from 3 to 50% by weight of a finely divided catalyst, which has already been used for the preparation of caprolactam and which has optionally been regenerated, are added.

Abstract: A process for the regeneration of a granular, supported catalyst of boric acid on carbon, wherein a part of the catalyst is removed from a fluidized bed reactor, in which cyclohexanone oxime is rearranged into caprolactam on this catalyst, when the "differential content in the catalyst of organic nitrogen" is between 0.3 and 2.0% by weight and is replaced by an equal amount of regenerated catalyst so that the differential organic nitrogen content remains in the above-mentioned range, the quantity of catalyst removed is regenerated with air in a fluidized bed at a temperature of from 400.degree. to 700.degree. C. and is returned to the fluidized bed reactor used for rearrangement when a further part of the catalyst is removed therefrom for regeneration.

Abstract: Process for the removal of residues of solvent from crystallized .epsilon.-caprolactam, wherein the major quantity of solvent is removed in a first stage by distillation in the presence of water in an amount so that the water content of the residue of the first stage is from 0.5 to 6% by weight, and in a second stage by distilling water and any residues of solvent still present.

Abstract: A process for the purification of .epsilon.-caprolactam, wherein .epsilon.-caprolactam is treated with potassium permanganate in the presence of from 0.01 to 5% by weight of water, based on caprolactam, and subsequently crystallized from toluene, benzene, ethylbenzene or xylene.

Abstract: A process for the production of .epsilon.-caprolactum from cyclohexanone oxime by rearrangement in the gaseous phase on a fluid-bed catalyst containing boron oxide, wherein residues from the distillation of cyclohexanone oxime are introduced into the reaction in liquid form, and wherein from 5 to 500 times their quantity of cyclohexanone oxime in vapor form and at least 50 times their quantity of inert gas are present during the reaction.

Abstract: A process for the evaporation of cyclohexanone oxime, wherein the cyclohexanone oxime is evaporated in the presence of an inert gas at a superatmospheric pressure of at least 300 Torr at 110.degree. to 160.degree. C, the evaporation temperature being governed by the inert gas pressure or by the ratio of cyclohexanone oxime to inert gas.

Abstract: A water-insoluble condensation product of a polyalcohol, a dicarboxylic acid, from 5 to 35% by weight of a saturated monohydric alcohol having from 1 to 3 carbon atoms and, optionally, a monocarboxylic acid, said condensation product being soluble in lacquer solvents and useful for producing stoving lacquers.

Abstract: Liquid stoving-lacquer systems based on oil-free polyesters obtained by reacting polybasic carboxylic acids or their anhydrides and 2-ethylpropane diol-1.3 and optionally additional polyhydric alcohols, are highly compatible with melamine resins.