Abstract: A delivery device for a sheet-processing machine, comprises at least one deposition station and a conveyer station, by the use of which, upstream-processed sheets of printed material can be picked up in a transfer location, and can be conveyed through the deposition station via a first conveying system, where they can be deposited optionally to form a stack, or can be conveyed beyond that stack. A holding device, which holds down the uppermost sheet of the stack during the transfer of a sheet to be conveyed against an entrainment or a lifting, is provided with one or with a plurality of holding assemblies which are spaced apart from each other transversely to the transport direction. A sheet-guiding element may be provided, which adjoins the deposition station and which is variable in its vertical position with at least its upstream end by the use of an actuating drive.

Abstract: Please add the Abstract of the Disclosure, as set forth on the separate accompanying sheet. This Abstract of the Disclosure is essentially the same, in content, as the Abstract which is a part of the published PCT application, WO 2017/202762A1. No new matter is being presented by the addition of this Abstract of the Disclosure.

Abstract: An arrangement for correcting registration during guiding of sheets in a multi-color rotary sheet printing press including a plurality of printing units, each having a printing cylinder, a transfer cylinder connected between printing cylinders of two adjacent printing units for transfer sheets between the printing units, and a plurality of gear drives for driving the printing and transfer cylinders, includes a plurality of adjusting devices arranged within gear drives. Each adjusting device has two conical sleeves fixedly mounted within a gear drive, two conical bushings cooperating with the two conical sleeves, and an adjusting spindle for supporting the two conical bushings for linear displacement toward and away from each other.

Abstract: Sulphonamide compounds of the formula ##STR1## are prepared by condensation of sulphonamides of the formulaR.sup.1 --SO.sub.2 --NH.sub.2-m-p R.sup.2.sub.m (--CH.sub.2 OH).sub.pwith formaldehyde and diols or diol monoethers of the formula ##STR2## in a molar ratio of sulphonamide: formaldehyde: diol or diol monether of 1:(1-p):0.5 to 1:(4-p):6 in the presence of a catalyst which splits off water and at temperatures of 80.degree. to 250.degree. C.,whereinR.sup.1 is phenyl, phenyl substituted phenyl, or alkyl substituted phenyl having 1 to 4 alkyl carbon atoms,R.sup.2 is alkyl having 1 to 4 carbon atoms,R.sup.3 is hydrogen or alkyl having 1 to 4 carbon atoms,R.sup.4 is hydrogen or alkyl having 1 to 18 carbon atoms,R.sup.5 is hydrogen, R.sup.2, ##STR3## R.sup.6 is R.sup.4 or ##STR4## m is zero or one, p is zero, one or two with the sum of m and p ranging from 0 to 2, andn is a number from 2 to 19q is one, two or threeand the compounds so obtained are used as modifying agents for melamine resins.

Abstract: Modified aminoplast resin comprising:(a) 60 to 99.5% by weight of an aminoplast precondensate which has been etherified with a lower alkanol to an extent not exceeding 10% and(b) 0.5 to 40% by weight of a modifying agent which comprises a mixture of (i) a water-soluble polyester prepared from carboxylic acids with at least one carboxyl and dihydric or polyhydric alcohols, and (ii) sufficient free diol or polyol whereby the mixture has a ratio of the sum of free and esterified hydroxyls of 0.8 to 4.5 moles for each mole of the sum of free and esterified carboxyls which resins are useful in impregnating webs for producing laminates and panels of wood-based materials.

Abstract: The present invention relates to macromolecular compositions crosslinked by a novel bridge having the formula --NR.sup.x --CH.dbd.N--CO--. This novel bridge is obtained by reacting a macro-molecule, preferably a polymer, having at least two amidocarbonyl groups with a compound having at least two formylamido groups in an aqueous medium under highly acidic conditions. The crosslinking bridge formed by the reaction of this invention is produced in accord with the following formula: ##STR1## Compositions containing macromolecules having at least two amidocarbonyl groups and a compound having at least two formylamido groups can act as viscosifying or gelling agents for aqueous acids where when added to aqueous acids, crosslinking occurs. Acids gelled in this manner have important use in the recovery of oil and natural gas from subterranean formations.

Abstract: The present invention relates to macromolecular compositions crosslinked by a novel bridge having the formula --NR.sup.x --CH.dbd.N--CO--. This novel bridge is obtained by reacting a macro-molecule, preferably a polymer, having at least two amidocarbonyl groups with a compound having at least two formylamido groups in an aqueous medium under highly acidic conditions. The crosslinking bridge formed by the reaction of this invention is produced in accord with the following formula: ##STR1## Compositions containing macromolecules having at least two amidocarbonyl groups and a compound having at least two formylamido groups can act as viscosifying or gelling agents for aqueous acids where when added to aqueous acids, crosslinking occurs. Acids gelled in this manner have important use in the recovery of oil and natural gas from subterranean formations.

Abstract: Diethanolammonium sulphamate is a curing agent for modified aminoplast resins.

Abstract: A bonded structure of textile materials bonded by a melamine-formaldehyde precondensate is produced by applying to a textile material a melamine-formaldehyde precondensate with a molar ratio of melamine to formaldehyde of 1:(0.8 to 1.26) to form a composite and then compressing the composite with an overpressure of 1 to 200 bars at temperature of from 130.degree. to 220.degree. C.

Abstract: Modified melamine-formaldehyde resins having a melamine:formaldehyde molar ratio of 1:(1.27 to 0.7) are prepared by heating melamine in an aqueous solution or suspension with formaldehyde in a melamine:formaldehyde molar ratio of 1:(1.27 to 0.7) at a pH value of 8 to 11 and at temperatures of 105.degree. to 160.degree. C. until the finished resin has reached a dilutability with water of 1:(0.1 to 4) at 20.degree. C., and, before, during or after the condensation reaction, adding less than 25% by weight of a glycol ether of the formulaR(OCH.sub.2 CH.sub.2).sub.n OHin which R denotes alkyl having 1 to 4 C atoms and n denotes an integer from 1 to 5, and/or of p-toluenesulfonamide. The resins are used in particular for the production of molding compositions.

Abstract: Low viscosity, aqueous impregnating resin solution with improved stability containing 30-70% by weight of solid resin which comprises:(A) 80-98% by weight of a melamine-formaldehyde precondensate and(B) 2-20% by weight of a water soluble copolymer.

Abstract: Carbazoleazomethines are prepared and sulfur dyestuffs are prepared by sulphurizing a carbazoleazomethine of the formula ##STR1## wherein R.sup.1 is hydrogen, hydroxyl, halogen, nitro, alkyl having 1 to 8 carbon atoms, alkoxy having 1 to 8 carbon atoms, dialkylamino having 1 to 4 carbon atoms per alkyl, alkanoyloxy having 1 to 8 carbon atoms, benzoyloxy, alkanoylamino having 1 to 8 carbon atoms or benzoylamino;R.sup.2 is hydrogen, hydroxyl, halogen, alkyl having 1 to 8 carbon atoms or alkoxy having 1 to 8 carbon atoms;R.sup.3 is hydrogen or alkyl having 1 to 7 carbon atoms;R.sup.4 is hydrogen or halogen; andR.sup.5 is hydrogen or alkyl having 1 to 8 carbon atoms.

Abstract: Partially etherified melamine-formaldehyde resins having a melamine:formaldehyde molar ratio of 1:(1.25 to 1) can be prepared by a condensation reaction under neutral or weakly alkaline conditions if the condensation reaction is carried out in the presence of a glycol monoether of the general formula IR(OCH.sub.2 CH.sub.2).sub.n OH (I)wherein R denotes alkyl having 1 to 4 C atoms and n denotes a number from 1 to 5. The partially etherified melamine-formaldehyde resins are suitable for the production of compression moulding compositions having a high flow and minimal processing shrinkage and after-shrinkage.

Abstract: The process for the preparation of a 3-(4-hydroxyanilino)carbazole of the formula ##STR1## wherein R is hydrogen, alkyl having 1 to 8 carbon atoms or halogenoalkyl having 1 to 8 carbon atoms, comprising reacting a 3-aminocarbazole of the formula ##STR2## with p-hydroquinone or p-aminophenol or a mixture of p-hydroquinone and p-aminophenol in at least stoichiometric amounts by heating to a temperature of 150.degree. to 300.degree. C. with exclusion of oxygen.

Abstract: Partially etherified melamine-formaldehyde resins having a melamine: formaldehyde molar ratio of 1:(1.25 to 1) can be prepared by a condensation reaction under neutral or weakly alkaline conditions if the condensation reaction is carried out in the presence of a glycol monoether of the general formula IR (OCH.sub.2 CH.sub.2).sub.n OH (I)wherein R denotes alkyl having 1 to 4 C atoms and n denotes a number from 1 to 5. The partially etherified melamine-formaldehyde resins are suitable for the production of compression moulding compositions having a high flow and minimal processing shrinkage and after-shrinkage.

Abstract: A latent curing agent for aminoplast resins produced by reacting diethanolamine with glycidol in a molar ratio of 1:(1 to 1.2) at 0.degree. to 90.degree. C. and then reacting the product with 0.5 to 1 mole of sulfur dioxide per mole of diethanolamine at 0.degree. to 90.degree. C.

Abstract: The present invention relates to new, pharmacologically-valuable antidepressants, which are 2,4,5,6-tetrahydro-1H-pyrazino-[3,2,1-jk]-carbazoles substituted in the 8-position and having the formula I ##STR1## wherein R stands for an alkyl or alkoxy group having 1 to 4 carbon atoms or a fluorine, chlorine or bromine atom, and a method for making them by reacting with ammonia a 6,9-disubstituted 1,2,3,4-tetrahydrocarbazol-1-one of the formula II ##STR2## wherein X denotes a bromine, chlorine or iodine atom or a radical of the formula --O--SO.sub.2 --R', and R' is an alkyl radical having 1 to 3 carbon atoms, phenyl or tolyl.

Abstract: A melamine-formaldehyde resin useful for making coated wood-based materials and laminates and having a prolonged pot life comprises (a) melamine-formaldehyde precondensation product wherein the molar ratio of melamine:formaldehyde is 1:1.4 to 1:2.6 and (b) 0.1 to 1.0% by weight based on total solids, of an amine of the formula ##STR1## wherein R.sup.1 and R.sup.2 are each identical or different alkyl having 1 to 4 carbon atoms and R.sup.3 is 2-hydroxyethyl, 2-(2-hydroxyethoxy)-ethyl, 3-hydroxy-1-propyl, 3-hydroxy-2-propyl, 2,3-dihydroxypropyl or--CH.sub.2 CH.sub.2 --NR.sup.1 R.sup.2,wherein said amine may be present entirely or partially in the form of its reaction product with the melamine-formaldehyde pre-condensation product.

Abstract: Condensation products of .epsilon.-caprolactam, formaldehyde and formamide, especially N-(formylaminomethyl)-.epsilon.-caprolactam and N-(N'-formyl-N'-hydroxymethyl-aminomethyl)-.epsilon.-caprolactam, are prepared by reacting formamide and formaldehyde in the presence of a base and in the presence or absence of .epsilon.-caprolactam at temperatures of 70.degree. to 90.degree. C. for 4 to 15 hours, then acidifying the reaction batch and, if no .epsilon.-caprolactam is present, adding .epsilon.-caprolactam, and distilling off water at 100.degree. to 135.degree. C.The condensation products are valuable modifiers for use in the manufacture of aminoplast resins employed for impregnating paper and fabrics which are used for the manufacture of coated wood-based materials and laminates.

Abstract: A melamine-formaldehyde resin useful for making coated wood-based materials and laminates and having a prolonged pot life comprises (a) melamine-formaldehyde precondensation product wherein the molar ratio of melamine:formaldehyde is 1:1.4 to 1:2.6 (b) 0.1 to 1.0% by weight based on total solids, of an amine of the formula ##STR1## wherein R.sup.1 and R.sup.2 are each identical or different alkyl having 1 to 4 carbon atoms and R.sup.3 is 2-hydroxyethyl, 2-(2-hydroxyethoxy)-ethyl, 3-hydroxy-1-propyl, 3-hydroxy-2-propyl, 2,3-dihydroxypropyl or--CH.sub.2 CH.sub.2 --NR.sup.1 R.sup.2,wherein said amine may be present entirely or partially in the form of its reaction product with the melamine-formaldehyde pre-condensation product.