Abstract: A process for preparing oligo ethylene glycol methyl ether borate involves feeding boric acid and oligo ethylene glycol monomethyl ether into a reactor, and reacting to obtain a raw product containing oligo ethylene glycol methyl ether borate, water, and unreacted boric acid and oligo ethylene glycol monomethyl ether. The raw product is fed to a reactive distillation device and boric acid is reacted with oligo ethylene glycmonomethyl ether for full conversion of boric acid. A distillate stream containing water is transferred from the top of the reactive distillation device to a condenser, and a condensed liquid stream is recycled to the top of the reactive distillation device. A bottom product stream containing oligo ethylene glycol methyl ether borate is withdrawn from the reactive distillation device. The bottom product stream is partially recycled to a reboiler. The resulting vapor stream is recycled to the bottom of the reactive distillation device.

Abstract: Low-pressure hydroformylation of diisobutene A hydroformylation process for preparing 3,5,5-trimethylhexanal comprising reacting 2,4,4-tri-methylpent-2-ene with H2 and CO in a reaction zone in the presence of one or more free organ-ophosphite ligands of the general formula (1) wherein R1, R2, R3, R4 and R5 are each independently H, C1- to C9-alkyl or C1- to C9-alkoxy and R1, R2, R3, R4 and R5 are not H at the same time, and R6, R7, R8, R9 and R10 are each independently H, C1- to C9-alkyl or C1- to C9-alkoxy and R6, R7, R8, R9 and R10 are not H at the same time, and R11, R12, R13, R14 and R15 are each independently H, C1- to C9-alkyl or C1- to C9-alkoxy and R11, R12, R13, R14 and R15 are not H at the same time, and a homogeneous rhodium catalyst complexed with one or more organophosphite ligands of the general formula (I) at a pressure of 1 to 100 bar abs and a temperature of from 50 to 200° C.

Abstract: Process for hydroformylation of olefins having 6 to 20 carbon atoms in the presence of a cobalt catalyst in the presence of an aqueous phase with thorough mixing in a reactor wherein a hydroformylation products-containing first stream is withdrawn at the top of the reactor and an aqueous phase-containing second stream is withdrawn from the bottom of the reactor via at least one line leading out of the bottom of the reactor, which process comprises controlling one or more mass flow parameters of the second stream in accordance with the density of the second stream.

Abstract: A process for preparing oligo ethylene glycol methyl ether borate involves feeding boric acid and oligo ethylene glycol monomethyl ether into a reactor, and reacting to obtain a raw product containing oligo ethylene glycol methyl ether borate, water, and unreacted boric acid and oligo ethylene glycol monomethyl ether. The raw product is fed to a reactive distillation device and boric acid is reacted with oligo ethylene glycmonomethyl ether for full conversion of boric acid. A distillate stream containing water is transferred from the top of the reactive distillation device to a condenser, and a condensed liquid stream is recycled to the top of the reactive distillation device. A bottom product stream containing oligo ethylene glycol methyl ether borate is withdrawn from the reactive distillation device. The bottom product stream is partially recycled to a reboiler. The resulting vapor stream is recycled to the bottom of the reactive distillation device.

Abstract: The present invention relates to a lubricant comprising a polyacrylate which contains a C13/15 acrylate in polymerized form, where the C13/15 acrylate comprises at least 70 wt % of linear and branched C13 and C15 alkyl (meth)acrylates. It further relates to the polyacrylate, to the C13/15 acrylate, to a method for preparing the polyacrylate by free-radical polymerization of the C13/15 acrylate, and to a method for preparing a lubricant by contacting the polyacrylate to a base oil.

Abstract: A process for preparing C4 to C13 monohydroxy compounds from a bottom fraction arising in the distillation of a crude mixture of C4 to C13 oxo-process aldehydes from cobalt-catalyzed or rhodium-catalyzed hydroformylation, or in the distillation of a crude mixture of C4 to C13 oxo-process alcohols, which comprises contacting the bottom fraction in the presence of hydrogen with a catalyst comprising copper oxide and aluminum oxide, at a temperature of 150° C. to 300° C. and a pressure of 20 bar to 300 bar and subjecting the resulting crude hydrogenation product to distillation, and the amount of C4 to C13 monohydroxy compounds present in the crude hydrogenation product after the hydrogenation being greater than the amount of C4 to C13 monohydroxy compounds given stoichiometrically from the hydrogenation of the ester and aldehyde compounds present in the bottom fraction, including the C4 to C13 monohydroxy compounds still present in the bottom fraction before the hydrogenation.

Abstract: A process for preparing C4 to C10 monohydroxy compounds from a bottom fraction arising in the distillation of a crude mixture of C4 to C10 oxo-process aldehydes from cobalt-catalyzed or rhodium-catalyzed hydroformylation, or in the distillation of a crude mixture of C4 to C10 oxo-process alcohols, which comprises contacting the bottom fraction in the presence of hydrogen with a catalyst comprising copper oxide and aluminum oxide, at a temperature of 150° C. to 300° C. and a pressure of 20 bar to 300 bar and subjecting the resulting crude hydrogenation product to distillation, and the amount of C4 to C10 monohydroxy compounds present in the crude hydrogenation product after the hydrogenation being greater than the amount of C4 to C10 monohydroxy compounds given stoichiometrically from the hydrogenation of the ester and aldehyde compounds present in the bottom fraction, including the C4 to C10 monohydroxy compounds still present in the bottom fraction before the hydrogenation.

Abstract: Method of removing cobalt deposits in a reactor for the cobalt-catalyzed high-pressure hydroformylation of olefins by treatment with aqueous nitric acid, wherein the reactor is at least partly filled with aqueous nitric acid and the temperature of the aqueous nitric acid is increased during the treatment.

Abstract: Proposed is a cylindrical reactor (1) having a vertical longitudinal axis for continuous hydroformylation of a C6-C20-olefin or a mixture of C6-C20-olefins with synthesis gas in the presence of a homogeneously dissolved metal carbonyl complex catalyst, having a multiplicity of Field tubes (2) which are oriented parallel to the longitudinal axis of the reactor (1) and welded into a tube plate at the upper end of the reactor (1), having a circulation tube (3) open at both ends which envelops the Field tubes (2) and at its lower end projects beyond said tubes, having a jet nozzle (4) at the bottom of the reactor (1) for injecting the reactant mixture comprising the C6-C20-olefin, the synthesis gas and the metal carbonyl complex catalyst, wherein the Field tubes (2) are configured in terms of their number and their dimensions such that the total heat exchanger area of said tubes per unit internal volume of the reactor is in the range from 1 m2/m3 to 11 m2/m3 and the cross sectional area occupied by the Field t

Abstract: Proposed is a cylindrical reactor (1) having a vertical longitudinal axis for continuous hydroformylation of a C6-C20-olefin or a mixture of C6-C20-olefins with synthesis gas in the presence of a homogeneously dissolved metal carbonyl complex catalyst, having a multiplicity of Field tubes (2) which are oriented parallel to the longitudinal axis of the reactor (1) and welded into a tube plate at the upper end of the reactor (1), having a circulation tube (3) open at both ends which envelops the Field tubes (2) and at its lower end projects beyond said tubes, having a jet nozzle (4) at the bottom of the reactor (1) for injecting the reactant mixture comprising the C6-C20-olefin, the synthesis gas and the metal carbonyl complex catalyst, wherein the Field tubes (2) are configured in terms of their number and their dimensions such that the total heat exchanger area of said tubes per unit internal volume of the reactor is in the range from 1 m2/m3 to 11 m2/m3 and the cross sectional area occupied by the Field t

Abstract: Method of removing cobalt deposits in a reactor for the cobalt-catalyzed high-pressure hydroformylation of olefins by treatment with aqueous nitric acid, wherein the reactor is at least partly filled with aqueous nitric acid and the temperature of the aqueous nitric acid is increased during the treatment.

Abstract: The present invention relates to a process for preparing hydroformylation products of olefins having at least four carbon atoms, in which a high proportion of both the linear Ci-olefins having a terminal double bond comprised in the olefin-comprising feed used and of the linear Ci-olefins having an internal double bond is converted into hydroformylation products. Furthermore, the invention relates to a process for preparing 2-propylheptanol which comprises such a hydroformylation process.

Abstract: In the hydroformylation of olefins having 6 to 20 carbon atoms in the presence of a cobalt catalyst in the presence of an aqueous phase with thorough mixing in a reactor, a hydroformylation products-containing first stream is withdrawn at the top of the reactor and an aqueous phase-containing second stream is withdrawn from the bottom of the reactor. The flow rate of the second stream is controlled in accordance with a temperature which is measured at a point in the bottom of the reactor or in a line leading out of the bottom of the reactor. The yield of crude hydroformylation product is increased as a result of stable sustained operation.

Abstract: In the hydroformylation of olefins having 6 to 20 carbon atoms in the presence of a cobalt catalyst in the presence of an aqueous phase with thorough mixing in a reactor, a hydroformylation products-containing first stream is withdrawn at the top of the reactor and an aqueous phase-containing second stream is withdrawn from the bottom of the reactor. The flow rate of the second stream is controlled in accordance with a temperature which is measured at a point in the bottom of the reactor or in a line leading out of the bottom of the reactor. The yield of crude hydroformylation product is increased as a result of stable sustained operation.

Abstract: The present invention relates to a process for the catalytic aldol condensation of aldehydes, in particular for preparing ?,?-unsaturated aldehydes, in a multiphase reactor.

Abstract: The present invention relates to a process for the catalytic aldol condensation of aldehydes, in particular for preparing ?,?-unsaturated aldehydes, in a multiphase reactor.

Abstract: A process for preparing oligomers by continuous oligomerization of butenes is described, wherein a) a feed stream 1) comprising 1-butene and 2-butene in a total concentration of from 10 to 70% by weight and from 10 to 60% by weight of isobutane is reacted until more than 60% by weight of the 1-butene comprised in the feed stream 1 but less than 50% by weight of the 2-butene comprised in feed stream 1 have been converted into oligomers. b) The oligomers obtained in a) are separated off and optionally passed to a further work-up and the remaining residual stream is fed to work-up by distillation. c) Isobutane is separated off by distillation from the residual stream, and d) the isobutane-depleted stream obtained after the work-up by distillation c) is reacted to form oligomers.

Abstract: Process for preparing oligomers by continuous oligomerization of butenes, wherein a) a feed stream comprising 1-butene and 2-butene in a total concentration of from 10 to 70% by weight and from 10 to 60% by weight of isobutane is used (hereinafter referred to as feed stream 1), b) this feed stream 1 is reacted until more than 60% by weight of the 1-butene comprised in the feed stream 1 but less than 50% by weight of the 2-butene comprised in feed stream 1 have been converted into oligomers, c) the oligomers obtained in b) are separated off and optionally passed to a further work-up and the remaining residual stream is fed to work-up by distillation, d) isobutane is separated off by distillation from the residual stream, e) the isobutane-depleted stream obtained after the work-up by distillation d) (hereinafter referred to as feed stream 2) is reacted to form oligomers.

Abstract: A process of controlling heavies in a recycle catalyst stream, particularly, for use in a continuous hydroformylation process of converting an olefin with synthesis gas in the presence of a hydroformylation catalyst to form an aldehyde product stream with subsequent separation of the catalyst for recycle to the hydroformylation step. Heavies are controlled, and preferably reduced, by means of feeding a recycle gas stream, taken as a portion of an over-head stream from a condenser, back to a vaporizer wherein the aldehyde product stream is separated.

Abstract: The present invention relates to the use of isoalkane mixtures for reducing or minimizing the dust emission during the handling of pulverulent construction chemistry products, a process for the preparation of the pulverulent construction chemistry products, and hydraulically setting materials comprising the isoalkane mixtures according to the invention.