Abstract:
Die Erfindung betrifft ein Verfahren zur Herstellung von Isocyanaten durch Carbamatspaltung, wobei flüssiges Carbamat (3) und ein gasförmiger Hilfsstoff (11) in einen Reaktor (1) eingebracht werden, so dass eine kontinuierliche Flüssigphase gebildet wird, in der der gasförmige Hilfsstoff dispergiert ist und in der das Carbamat zu Isocyanat und Alkohol umgesetzt wird, und sich oberhalb der kontinuierlichen Flüssigphase eine kontinuierliche Gasphase bildet. Jede Phasengrenze zwischen kontinuierlicher Flüssigphase und kontinuierlicher Gasphase ist an einer Position, an der die Temperatur kleiner ist als 260°C und/oder die Konzentration an Isocyanatgruppen in der Flüssigphase an allen Phasengrenzen zwischen der kontinuierlichen Flüssigphase und der kontinuierlichen Gasphase kleiner ist als 1 Gew.-%, wobei die Konzentration an Isocyanatgruppen als NCO nach DIN EN ISO 14896 : 2009, bestimmt wird.
Abstract translation:本发明涉及一种方法,用于使用液体氨基甲酸酯(3),并在反应器的气态副(11)氨基甲酸叔丁酯的裂解的异氰酸酯的制备(1)被引入,从而形成一个连续的液体相,其中所述气态赋形剂被分散和 其中氨基甲酸酯异氰酸酯和醇进行反应,并形成连续液相上方的连续气相。 连续液相和连续气相之间的各相边界处时的温度低于260℃和/或在所述连续液相和连续气相之间的所有相位的边界在液相中的异氰酸酯基团的浓度的位置上设置比第一重量少 在2009,确定: - 异氰酸酯基团的浓度NCO根据DIN EN ISO 14896%。
Abstract:
The invention relates to a process for a continuous production of polyetherols comprising the steps of reacting of an alcohol (3) with a starter (5) or an alkoxylated precursor to give a mixture comprising an alcoholate and water, removing the water from the mixture by distillation,if appropriate feeding the alcoholate into a bubble column (23), having an inclination of from 0 to 90 to the horizontal, the bubble column (23)being divided into at least two compartments (25), wherein the compartments (25) are divided from each other by a dividing wall (27), the dividing wall (27) having a height, that liquid can flow over the dividing wall (27) from one compartment (25) into an adjacent compartment, feeding of alkylene oxide into at least one compartment (25) at the bottom of the compartment such that the alkylene oxide rises in the alcoholate, reacting of the alkylene oxide with the alcoholate or a secondary product being formed by the reaction of the alcoholate with alkylene oxide to give the polyetherol, discharging the reaction product from the bubble column (23).
Abstract:
Die Erfindung betrifft ein Verfahren zur Herstellung von aromatischen Aminen durch Hydrierung von entsprechenden Nitroaromaten mit Wasserstoff, sowie eine dafür geeignete Vorrichtung. Insbesondere betrifft die Erfindung ein Verfahren zur Herstellung von Toluylendiamin (TDA) durch Hydrierung von Dinitrotoluol (DNT).
Abstract:
The invention relates to a process for decomposing nitrous oxide from a gas stream (1), com- prising: (a) heating the gas stream (1) and splitting the gas stream (1) into at least two partial streams (3, 5) or splitting the gas stream (1) into at least two partial streams (3, 5) and heating the partial streams (3, 5); (b) feeding each of the partial streams (3, 5) into a separate decomposition reactor, wherein each reactor (31) comprises a catalyst; (c) decomposing the nitrous oxide into nitrogen and oxygen in the decomposition reactors to obtain purified streams (13, 15); (d) optionally feeding each purified stream (13, 15) into a unit (11) for decomposing nitrogen dioxide and/or nitrogen monoxide or combining at least two purified streams (13, 15) and feeding the combined purifed streams into a unit (11) for decomposing nitrogen dioxide and/or nitrogen monoxide, wherein the catalysts of the decomposition reactors (31) are changed alternatingly and wherein one of the catalysts is changed when the arithmetic mean of the lifetime of the catalysts in the other reactors has reached 25 to 75 % of the lifetime of one catalyst.
Abstract:
The invention relates on a process for working-up a nitrous oxide comprising off-gas stream from a production process of adipic acid by decomposing the nitrous oxide contained in the off- gas stream into nitrogen and oxygen in a fixed bed reactor (21) of a N2O decomposition unit (9) at a temperature in the range from 430 to 800°C to obtain a purified gas, wherein for controlling the N2O decomposition unit (9) a nonlinear model predictive control is used which is based on a reactor model of the fixed bed reactor based on equations of energy transport and species transport for nitrogen, oxygen and N2O.
Abstract:
Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung von biuretgruppenhaltigen Polyisocyanaten aus Di- oder Polyisocyanaten mit Diaminen.
Abstract:
The invention relates to a process for starting up a plant for removing isobutene from an isobutene-containing C4-hydrocarbon mixture, the plant comprising an etherification unit containing moist acidic ion exchange resin, a first distillation unit, an ether cleavage unit, and a second distillation unit. The invention further relates to a process for shutting down the plant from a stationary operation mode.
Abstract:
The invention relates to a process for obtaining isobutene from an isobutene containing C4-hydrocarbon mixture (1) in a plant comprising an etherification unit (3), a first distillation unit (5), an ether cleavage unit (8) and a second distillation unit (10), the process comprising: (a) contacting the C4-hydrocarbon mixture (1) with a primary alcohol (2) and reacting the mixture with the primary alcohol in the presence of an acidic catalyst to form the corresponding alkyl tert-butyl ether as an intermediate product and diisobutene as a by-product in the etherification unit (3); (b) distilling the reaction mixture (4) from the etherification unit (3) in the first distillation unit (5), a C4-hydrocarbon raffinate being withdrawn as the overhead product (6), the alkyl tert-butyl ether and diisobutene being withdrawn as the liquid or vaporous bottom product (7), and vaporizing the bottom product (7) if it is withdrawn as a liquid; (c) reacting the vaporous bottom product (7) in the presence of an acidic catalyst obtaining isobutene and the primary alcohol as reaction products in the ether cleavage unit (8); (d) distilling the reaction mixture (9) from the ether cleavage unit (8) in the second distillation unit (10), isobutene being withdrawn as the overhead product (11), the primary alcohol and diisobutene being withdrawn as the bottom product (12) and being recycled to the etherification unit (3); the plant further comprising a byproduct separation unit (15) being fed by a bottom purge stream (13) of the first distillation unit (5) and/or by a part of the bottom product of the second distillation unit (10), wherein a diisobutene product stream rich in diisobutene is separated from this feed stream (13, 14).
Abstract:
Die Erfindung betrifft ein Verfahren zur Herstellung reaktiven Zinks durch elektrochemische Reduktion, wobei als Kathodenmaterial Eisen oder Stahl verwendet wird.
Abstract:
The invention relates to a process for obtaining isobutene from an isobutene containing C4-hydrocarbon mixture (1) in a plant comprising an etherification unit (3), a first distillation unit (5), an ether cleavage unit (10) and a second distillation unit (12), the process comprising:(a) contacting the C4-hydrocarbon mixture (1) with a primary alcohol (2) and reacting the mixture with the primary alcohol in the presence of an acidic catalyst to form the corresponding alkyl tert-butyl ether in the etherification unit (3); (b) distilling the reaction mixture (4) from the etherification unit (3) in the first distillation unit (5), a C4-hydrocarbon raffinate being withdrawn as the overhead product (6), and the alkyl tert-butyl ether being withdrawn as the bottom product (7);(c) vaporizing the bottom product from the first distillation unit (5) in an evaporator (8) obtaining a vapor stream (9);(d) reacting the vapor stream (9) of step (c) in the presence of an acidic catalyst obtaining isobutene and the primary alcohol as reaction products in the ether cleavage unit (10);(e) distilling the reaction mixture (11) from the ether cleavage unit (10) in the second distillation unit (12), isobutene being withdrawn as the overhead product (13), the primary alcohol and diisobutene being withdrawn as the bottom product (14) and being recycled to the etherification unit (3); wherein a purge stream (15) containing high boiling components with a normal boiling point higher than that of the alkyl tert-butyl ether is withdrawn from the evaporator (8) in step (c).