Abstract: Superabsorbents are produced by polymerization in the presence of at least one unsaturated polyetherol selected from the group consisting of polyetherols having the following structural formulae (1), (2), (3) and (4): where n is 0 or 1, m is 1, 2, 3, 4, 5 or 6, o is a natural number from 1 to 200, and A is —(H2C—CHR1—O)— or —(R1HC—CH2—O)—, where R1 in each occurrence is independently hydrogen or an organic radical.

Abstract: The present invention relates to copolymers which are obtainable from the free radical copolymerization of at least (a) a monoethylenically unsaturated carboxylic acid having 3 to 6 carbon atoms or the anhydride thereof with (b) a reaction mixture comprising a component of the general structural formula where R1, R2, R3, R4, independently of one another, are H or C1- to C4-alkyl, n and m, independently of one another, are an integer from 1 to 100 and R5 is H or methyl, a process for the preparation of the polymer according to the invention and the use thereof as a scale inhibitor.

Abstract: Superabsorbents are produced by polymerization in the presence of at least one unsaturated polyetherol selected from the group consisting of polyetherols having the following structural formulae (1), (2), (3) and (4): where n is 0 or 1, m is 1, 2, 3, 4, 5 or 6, o is a natural number from 1 to 200, and A is —(H2C—CHR1—O)— or —(R1HC—CH2—O)—, where R1 in each occurrence is independently hydrogen or an organic radical.

Abstract: A process for preparing polyether polyols by reaction of the following starting materials: a) one or more alkylene oxides and, if appropriate, carbon dioxide and also b) one or more H-functional starter substances, in the presence of a catalyst, in a reaction unit having a plurality of parallel layers A, B which are microstructured so that each layer has a multiplicity of channels which are arranged parallel to one another and form a continuous flow path from one side of the plate to the opposite side of this, wherein a distribution device for introduction of the starting materials and the catalyst is provided at one end of the channels of the layers A and a collection device for the reaction mixture is provided at the other end of these is proposed.

Abstract: Process for preparing double metal cyanide catalysts of the general formula (I) M2a[M1(CN)rXt]b ??(I) where M2 is preferably Co(III) or Fe(III), and M1 is preferably Zn(II), X is a group other than cyanide which forms a coordinate bond to M1 and is selected from the group consisting of carbonyl, cyanate, isocyanate, nitrile, thiocyanate and nitrosyl, a, b, r, t are integers which are selected so that the compound is electrically neutral, by reacting a) a cyanometallic acid of the general formula (II) Hw[M1(CN)r(X)t] where M1 and X are as defined above, r and t are as defined above and w is selected so that the compound is electrically neutral, with b) a readily protolyzable metal compound (IIIa) M2Rw and/or (IIIb) M2RuYv, where M2 is as defined above, the groups R are identical or different and are each the anion of a very weak protic acid having a pKa of ?20, and Y is the anion of an inorganic mineral acid or a moderately strong to strong organic acid having a pKa of from ?10 to +10, w correspon

Abstract: The present invention relates to a process for the preparation of at least one alkoxylate comprising the bringing into contact of an alkylene oxide mixture at least comprising ethylene oxide with at least one starter compound in the presence of at least one double-metal cyanide compound, where, during the induction phase, the sum of inert gas partial pressure and ethylene oxide partial pressure is 1.5 bar to 6.0 bar, to the alkoxylates obtainable by such a process, and to the use of such alkoxylates as emulsifier, foam regulator or as wetting agent for hard surfaces.

Abstract: A process for preparing polyether polyols includes a precipitation step, a recrystallization step, and a reaction step. In the precipitation step, a multimetal cyanide compound is precipitated by reaction of a metal salt with a cyanometalate compound. In the recrystallization step, the multimetal cyanide compound precipitated above is recrystallized by adding further metal salt and/or further cyanometalate compound. The recrystallization forms a multimetal cyanide catalyst compound. In the reaction step, an initiator and one or more alkylene oxide are reacted in the presence of the multimetal cyanide catalyst compound.

Abstract: The present invention relates to a process for preparing at least one alkoxylate, which comprises bringing at least one alkylene oxide selected from the group consisting of ethylene oxide, propylene oxide, butylene oxide, pentylene oxide and decene oxide into contact with at least one starter compound in the presence of at least one double metal cyanide compound, with the reaction being carried out at a temperature of from 130° C. to 155° C., to the alkoxylates, in particular ethoxylates, themselves and to the use of such ethoxylates as emulsifier, foam regulator or as wetting agents for hard surfaces.

Abstract: The present invention relates to a process for the preparation of at least one alkoxylate comprising the bringing into contact of an alkylene oxide mixture at least comprising ethylene oxide with at least one starter compound in the presence of at least one double-metal cyanide compound, where, during the induction phase, the sum of inert gas partial pressure and ethylene oxide partial pressure is 1.5 bar to 6.0 bar, to the alkoxylates obtainable by such a process, and to the use of such alkoxylates as emulsifier, foam regulator or as wetting agent for hard surfaces.

Abstract: The present invention relates to compositions at least comprising one alkoxylate of the formula RO(A)n(B)mH, to processes for the preparation of such compositions, in particular in the presence of double-metal cyanide compounds as catalyst, and their use as emulsifier, foam regulator or as wetting agents for hard surfaces. Moreover, the present invention also relates to the use of such compositions in detergents and surfactant formulations.

Abstract: The invention relates to a process for preparing polyether alcohols by addition of alkylene oxides onto H-functional starter substances using multimetal cyanide compounds as catalysts, wherein the multimetal cyanide compound is prepared by a process comprising the steps: a) adding a metal salt solution to a cyanometalate solution at a specific stirring power ? in the range from 0.05 to 10 W/l, preferably from 0.4 to 4 W/l, a temperature in the range from 0° C. to 100° C., preferably from 20° C. to 60° C., and an addition time of from 5 to 120 minutes, b) reducing the specific stirring power ? to a value in the range from 0.03 to 0.8 W/l and at the same time adding a surface-active agent, c) heating the solution while stirring at a specific stirring power ? of from 0.03 to 0.8 W/l, to a temperature of not more than 100° C., preferably in the range from 55° C. to 75° C., d) adding further metal salt solution while stirring at a specific stirring power ? of from 0.03 to 0.

Abstract: The present invention relates to a process for reacting epoxides with an initiator compound in the presence of a double metal cyanide compound as a catalyst, said process having a shortened induction period, and the double metal cyanide compound being activated by adding the epoxide to a mixture of double metal cyanide compound and initiator compound at an internal reactor pressure of less than 1 bar, and also to the polyethers themselves obtainable by such a process.

Abstract: The present invention relates to polyethers which are obtainable from 1-butene oxide and an alcohol using a double metal cyanide compound as a catalyst and have a content of unsaturated components of 6 mol % or more, to a process for preparing such a polyether and also to the use of a polyether according to the invention as a carrier oil or in a carrier oil formulation, in particular in additive packages for gasoline fuels, and furthermore also to carrier oil formulations and also to fuels comprising a polyether according to the invention.

Abstract: A process for preparing an organometallic framework material comprising reacting at least one metal salt with at least one at least bidentate compound capable of coordination to the metal ion of said metal salt, in the presence of an aqueous solvent system and at least one base wherein at least one bidentate compound comprises at least carboxy group and at least one further group which is not a carboxy group and which is capable of forming a hydrogen bridge linkage.

Abstract: Hydraulic fluids, in particular brake fluids for motor vehicles, comprising from 0.01 to 50 wt % of one or more cyclic carboxylates, or cyclic carboxamides, which can carry a linear or branched C1-bis C20 alkyl group on the nitrogen atom.

Abstract: A process for preparing multimetal cyanide compounds by reacting a metal salt with a cyanometalate compound comprises the steps

Abstract: The invention relates to DMC catalysts which comprise at least 10% by weight, based on the weight of the DMC catalysts, of a crystalline multimetal cyanide compound whose X-ray diffractogram shows sharp reflections at least at the d values of 11.4 ű0.5 Å 8.9 ű0.5 Å 6.3 ű0.5 Å 5.8 ű0.5 Å 5.5 ű0.5 Å 4.5 ű0.5 Å 4.4 ű0.5 Å 3.9 ű0.4 Å 3.7 ű0.4 Å 3.4 ű0.4 Å.

Abstract: In a process for working up polyether monools which have been prepared by ring-opening polymerization of epoxides by means of OH-functional starters using at least one heterogeneous catalyst, the heterogeneous catalyst or catalysts is/are separated off from the polyether monool by means of a membrane separation process.

Abstract: The invention relates to DMC catalysts which comprise at least 10% by weight, based on the weight of the DMC catalysts, of a crystalline multimetal cyanide compound whose X-ray diffractogram shows sharp reflections at least at the d values of

Abstract: A process for preparing multimetal cyanide compounds by reacting a metal salt with a cyanometalate compound comprises the steps a) precipitation of the multimetal cyanide compound by reaction of a metal salt with a cyanometalate compound and b) recrystallization of the multimetal cyanide compound precipitated in step a).