WO1993010897A1 - Hydrophobierte erdalkaliphosphate - Google Patents
Hydrophobierte erdalkaliphosphate Download PDFInfo
- Publication number
- WO1993010897A1 WO1993010897A1 PCT/EP1992/002632 EP9202632W WO9310897A1 WO 1993010897 A1 WO1993010897 A1 WO 1993010897A1 EP 9202632 W EP9202632 W EP 9202632W WO 9310897 A1 WO9310897 A1 WO 9310897A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkaline earth
- earth metal
- metal phosphates
- fatty acids
- acid
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J33/00—Protection of catalysts, e.g. by coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/16—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr
- B01J27/18—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr with metals other than Al or Zr
- B01J27/1802—Salts or mixtures of anhydrides with compounds of other metals than V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, e.g. phosphates, thiophosphates
- B01J27/1806—Salts or mixtures of anhydrides with compounds of other metals than V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, e.g. phosphates, thiophosphates with alkaline or alkaline earth metals
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B41/00—Formation or introduction of functional groups containing oxygen
- C07B41/04—Formation or introduction of functional groups containing oxygen of ether, acetal or ketal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/02—Preparation of ethers from oxiranes
- C07C41/03—Preparation of ethers from oxiranes by reaction of oxirane rings with hydroxy groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
- B01J2231/48—Ring-opening reactions
Definitions
- the invention relates to hydrophobized alkaline earth metal phosphates obtainable by reacting alkaline earth metal phosphates with fatty acids, a process for their preparation and their use as catalysts for the alkoxylation of compounds with active oxygen atoms and fatty acid esters.
- German Patent Application DE 38 43 713 AI and US Pat. No. 4,962,237 describe processes for the alkoxylation of compounds with active hydrogen atoms which are carried out in the presence of hydrotalcites.
- the hydrotalcites must first be converted into a calcined ("activated") form suitable for catalytic purposes by heating at temperatures from 400 to 600 ° C. for several hours.
- the narrowing of the homolog distribution of the nonionic surfactants obtainable by this process can be regarded as satisfactory, the preparation of the catalyst, particularly with regard to the calcination, is associated with a high expenditure of energy and time and is therefore disadvantageous.
- calcined compounds are susceptible to traces of water and the carbon dioxide in the air (back-reaction of the calcination), so that their area of application and their storage stability are limited as a result of the loss of activity.
- sparingly soluble alkaline earth metal phosphates are also suitable as heterogeneous catalysts for the alkoxylation.
- the narrowing of the homogeneous distribution achieved with them is not sufficient for a number of fields of application.
- the object of the invention was therefore to develop new heterogeneous alkoxylation catalysts which are free from the disadvantages described.
- the invention relates to a process for the preparation of hydrophobized alkaline earth metal phosphates, which is characterized in that alkaline earth metal phosphates are reacted with fatty acids.
- Alkaline earth metal phosphates are to be understood as the calcium, magnesium, strontium or barium salts of orthophosphoric acid or phosphorous acid.
- Typical examples are calcium phosphate, calcium hydrogen phosphate, magnesium phosphate, magnesium hydrogen phosphate, strontium phosphate, strontium hydrogen phosphate, barium phosphate, barium hydrogen phosphate and the mixed salts of the phosphates mentioned with the corresponding alkaline earth metal hydroxides (“basic phosphates”).
- basic phosphates the alkaline earth metal phosphates can be used alone or in a mixture, it being immaterial whether mixtures of different alkaline earth metal phosphates are hydrophobicized together or whether a mixture of different hydrophobicized alkaline earth metal phosphates is used.
- Suitable fatty acids are carboxylic acids of the formula (I)
- R ⁇ CO for a linear or branched, aliphatic, optionally hydroxy-substituted acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds and
- X represents hydrogen or an alkali metal
- Typical examples are caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, oleic acid, elaidic acid, petroselinic acid, ricinoleic acid, 12-hydroxystearic acid, linoleic acid, linolenic acid, arachic acid, and galenic acid, behenic acid, behenic acid .
- Fatty acids with 12 to 18 carbon atoms in particular lauric acid and stearic acid and their sodium or potassium salts, are preferred.
- fatty acids such as those used in the pressure splitting of natural fats and oils, for example coconut oil, palm oil, palm kernel oil, cottonseed oil, peanut oil, soybean oil, rape oil, sunflower oil, linseed oil, coriander oil, castor oil , Beef tallow or fish oil.
- Technical C12 / I8 "ke- relationship as Ci2 / 14 ⁇ fat are preferred äuregemische based on coconut oil.
- the alkaline earth metal phosphates and the fatty acids can be used in a molar ratio of 10: 1 to 1: 5, preferably 5: 1 to 1: 2.
- the production can take place according to different methods:
- the alkaline earth metal phosphates and the fatty acids are reacted in the absence of water in a homogenizer, for example a kneader or an extruder, and then at a temperature over a period of 0.5 to 5, preferably 1 to 2, hours heated from 150 to 200 ° C.
- a homogenizer for example a kneader or an extruder
- the alkaline earth metal phosphates and the fatty acids are initially introduced in aqueous suspension and reacted at a temperature of 50 to 100 ° C. with stirring over a period of 1 to 10, preferably 2 to 5 hours.
- the reaction products are then filtered off and dried to constant weight.
- hydrophobized alkaline earth metal phosphates are prepared in accordance with the embodiments of process B) or C) according to the invention, it is necessary to maintain the products to constant weight, ie. H. to dewater to a residual water content of less than 1% by weight, based on the resulting solid. In a preferred embodiment, it is recommended to spread the filtered solid on tray trays and to dry it at temperatures from 100 to 200 ° C., if appropriate under reduced pressure.
- the invention further relates to hydrophobized alkaline earth metal phosphates which are obtained by using alkaline earth metal phosphates which are selected from the group formed by calcium, magnesium, strontium and barium salts of orthophosphoric acid and phosphorous acid Implement fatty acids of formula (I), RiCO-OX (I)
- R ⁇ -CO for a linear or branched, aliphatic, optionally hydroxy-substituted acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds and
- X represents hydrogen or an alkali metal
- Another object of the invention relates to the use of hydrophobized alkaline earth metal phosphates as catalysts for the alkoxylation of compounds having active hydrogen atoms and fatty acid esters.
- hydrophobicized alkaline earth phosphates prepared according to the invention allows the alkoxylation of compounds with active hydrogen atoms and of fatty acid esters in short reaction times and high yields.
- the reaction products have an advantageous narrowed homolog distribution, the distribution curve coming close to the ideal Poisson distribution.
- the reaction products are also characterized by low levels of unreacted starting materials and dioxane.
- the hydrophobized alkaline earth phosphates prepared according to the invention can easily be incorporated into the reaction mixture. Since they do not dissolve in the mixture, their separation, for example by filtration, is straightforward. However, they can also remain in the reaction mixture if their Presence does not impair the further use of the products.
- Examples of compounds with active hydrogens which can be alkoxylated in the presence of the hydrophobized alkaline earth metal phosphates obtainable by the process according to the invention are fatty acids, hydroxyfatty acids, fatty acid amides, fatty alcohols, alkylphenols, polyglycols, fatty amines, fatty acid alkanolamides and vicinal hydroxy- or alkoxy- substituted alkanes.
- the alkoxylation is a known industrial process which is carried out at temperatures from 120 to 220, preferably 150 to 190 ° C. and pressures of 1 to 6 bar.
- the hydrophobized alkaline earth metal phosphates can be used in amounts of 0.1 to 10, preferably 0.5 to 5% by weight, based on the end product of the alkoxylation.
- Example 2 Analogously to Example 1, an aqueous solution of 110 g (0.49 mol) of sodium laurate in 600 ml of water was added to 70 g (0.51 mol) of calcium hydrogenphosphate and the mixture was heated to about 85 ° C. for 3 hours with stirrers. The suspension was then filtered, the residue washed with water and dried.
- Decanol / dodecanol-7E0 Analogously to Examples 8 to 11, a mixture of 170 g (1.1 mol) decanol (Lorol ( R ) C10, Henkel KGaA, Düsseldorf, FRG) and 55 g (0.3 mol) dodecanol (Lorol ( R ) C12, Fa. Henkel KGaA, Düsseldorf, FRG) with 6.3 of the catalyst from Example 1. The reaction mixture was then reacted with 413 g (9.4 mol) of ethylene oxide.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP92923729A EP0618841A1 (de) | 1991-11-25 | 1992-11-16 | Hydrophobierte erdalkaliphosphate |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19914138631 DE4138631A1 (de) | 1991-11-25 | 1991-11-25 | Hydrophobierte erdalkaliphosphate |
DEP4138631.0 | 1991-11-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993010897A1 true WO1993010897A1 (de) | 1993-06-10 |
Family
ID=6445481
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1992/002632 WO1993010897A1 (de) | 1991-11-25 | 1992-11-16 | Hydrophobierte erdalkaliphosphate |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0618841A1 (de) |
DE (1) | DE4138631A1 (de) |
WO (1) | WO1993010897A1 (de) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0085167A1 (de) * | 1981-12-24 | 1983-08-10 | Conoco Phillips Company | Alkoxylierung mit Calcium- und Magnesiumsalzen |
WO1991012220A1 (de) * | 1990-02-07 | 1991-08-22 | Henkel Kommanditgesellschaft Auf Aktien | Verfahren zur herstellung von nichtionischen oberflächenaktiven verbindungen |
DE4010606A1 (de) * | 1990-04-02 | 1991-10-10 | Henkel Kgaa | Verwendung von hydrophobierten hydrotalciten als katalysatoren fuer die ethoxylierung bzw. propoxylierung |
-
1991
- 1991-11-25 DE DE19914138631 patent/DE4138631A1/de not_active Withdrawn
-
1992
- 1992-11-16 EP EP92923729A patent/EP0618841A1/de not_active Ceased
- 1992-11-16 WO PCT/EP1992/002632 patent/WO1993010897A1/de not_active Application Discontinuation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0085167A1 (de) * | 1981-12-24 | 1983-08-10 | Conoco Phillips Company | Alkoxylierung mit Calcium- und Magnesiumsalzen |
WO1991012220A1 (de) * | 1990-02-07 | 1991-08-22 | Henkel Kommanditgesellschaft Auf Aktien | Verfahren zur herstellung von nichtionischen oberflächenaktiven verbindungen |
DE4010606A1 (de) * | 1990-04-02 | 1991-10-10 | Henkel Kgaa | Verwendung von hydrophobierten hydrotalciten als katalysatoren fuer die ethoxylierung bzw. propoxylierung |
Also Published As
Publication number | Publication date |
---|---|
EP0618841A1 (de) | 1994-10-12 |
DE4138631A1 (de) | 1993-05-27 |
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