EP1527120A1

EP1527120A1 - Demulsifiers

Info

Publication number: EP1527120A1
Application number: EP03735403A
Authority: EP
Inventors: Dirk Leinweber; Michael Feustel; Heidi Grundner
Original assignee: Clariant GmbH
Current assignee: Clariant Produkte Deutschland GmbH
Priority date: 2002-05-31
Filing date: 2003-05-16
Publication date: 2005-05-04
Also published as: WO2003102047A8; NO20044816L; US20050203193A1; DE10224275B4; WO2003102047A9; DE10224275A1; WO2003102047A1

Abstract

The invention relates to polymers that can be obtained by: A) reacting an epoxidized ester, which is selected from one or more unsaturated fatty acids having 8 to 26 C atoms and a polyol having 2 to 6 OH groups, with a monoamine, diamine or polyamine; B) alkoxylating the polyamine obtained hereby with a C2 to C4 alkylene oxide in molar excess so that the average degree of alkoxylation per OH group ranges from 1 to 100. The polymers have a numerical average molecular weight ranging from 500 to 100,000 g/mol. The invention also relates to the use of these polymers in quantities ranging from 0.0001 to 5 % by weight with regard to the oil as demulsifiers for oil-in-water emulsions.

Description

demulsifiers

The present invention relates to the use of polymers which can be prepared by reacting epoxidized fatty acid esters with amines and subsequent alkoxylation for splitting water-oil emulsions, in particular in crude oil production.

Crude oil is produced as an emulsion with water. Before the

Further processing of the crude oil, these crude oil emulsions have to be split into the oil and water components. This is generally done using so-called petroleum splitters. Petroleum fissures are surface-active compounds that are able to bring about the required separation of the emulsion components within a short time.

Among other things, alkylphenol-aldehyde resins, which are disclosed, for example, in US Pat. No. 4,032,514, are used as petroleum splitters. These resins are available from the condensation of a p-alkylphenol with an aldehyde, mostly formaldehyde. The resins are often used in alkoxylated form, as disclosed for example in DE-A-2445 873. For this purpose, the free phenolic OH groups are reacted with an alkylene oxide.

Alkylphenol-free demulsifiers are described in WO-A-99/07808. Epoxidized fatty acid esters are opened with alcohols or carboxylic acids and the resulting OH function is reacted with alkylene oxides. The compounds produced therefrom have good properties as an emulsion splitter.

The different properties (such as asphaltene and paraffin content) and the water content of different crude oils make it necessary to further develop the existing oil emulsion splitters. In particular, the focus is on a low metering rate of the emulsion splitter to be used, in addition to the desired higher effectiveness from an economic and ecological perspective. The task thus arose to develop new petroleum splitters which are more effective than the known products and can be used in even lower doses.

It was surprisingly found that products which are based on ring opening products of epoxidized fatty acid esters with amines, diamines or polyamines, after subsequent alkoxylation, have an excellent cleavage effect, even at very low doses, compared to known emulsion splitters.

The invention relates to polymers obtainable from

A) reaction of an epoxidized ester from one or more unsaturated fatty acids with 8 to 26 carbon atoms and a polyol with 2 to 6 OH groups with a mono-, di- or polyamine

B) Alkoxylation of the polyamine thus obtained with a C ₂ to C ₄ alkylene oxide in molar excess, so that the average degree of alkoxylation per OH group is between 1 and 100, the polymers having number average molecular weights of 500 to 100,000 g / mol.

Another object of the invention is the use of the polymers according to the invention in amounts of 0.0001 to 5 wt .-%, based on the oil, as a splitter for oil / water emulsions.

The invention further relates to a process for splitting oil / water emulsions by adding the polymers according to the invention in amounts of 0.0001 to 5% by weight to the emulsion.

The first step (step A) for the preparation of the polymers according to the invention consists in the reaction of an ^" epoxidized fatty acid polyol ester with a mono-, di- or polyamine.

Epoxidized fatty acid polyol esters generally correspond to Formula 1 O

R ¹ (O - C - R ² ) _x (1)

wherein

R ^{1 is} a hydrocarbon group with 2 to 6 carbon atoms which has a total of x valences,

R ^{2 is} a polymethylene group with 11 to 25 carbon atoms which carries at least one epoxy group and x is a number from 2 to 6.

The esters of formula 1 can be prepared by esterification of a polyol of formula R ¹ (OH) _x with one or more carboxylic acids of formula R ² COOH. R ¹ , x and R ² have the meaning given above.

The esters are preferably full esters, but they can also have free OH groups. They are preferably based on naturally occurring glycerides such as e.g. Soybean oil, olive oil, sunflower oil or linseed oil.

x is preferably 2 or 3.

R ¹ is preferably derived from ethylene glycol, propylene glycol, diethylene glycol, pentaerythritol, trimethylolpropane or glycerin. Ethylene glycol and glycerin are particularly preferred.

R ² preferably stands for a polymethylene group with 9 to 21 carbon atoms, so it is preferably derived from a C-io to C ₂₂ carboxylic acid. R ² can carry 1, 2 or 3 epoxy groups. The molecular weight of the polymers according to the invention is preferably at least 1000, for example 2000 g / mol, in particular from 1000 to - 50,000 g / mol. Formula 2 illustrates the ester structure using an example derived from glycerol

R stands for a hydrocarbon group to complete the fatty acid residue.

The epoxy ring opening can be carried out uncatalyzed (high nucleophilicity of the amines), acid or base catalyzed. Base catalysis using sodium methoxide or potassium te / t-butoxide has proven to be particularly preferred, since it leads to more uniform products with significantly shorter reaction times.

Suitable amines preferably correspond to formulas 3 to 5

R ³ NH R ³ R NH

H ₂ NF

NH, (3) (4) (5)

R ³ and R ⁴ independently of one another are C to C ₀ alkyl, C ₂ to C ₄₀ alkenyl, C ₆ to C 18 aryl or C ₇ to C ₃₀ alkylaryl, in particular C ₆ to C ₂₂ - Specifically for C1 ₀ to C ₈ alkyl or alkenyl, which can be straight-chain or branched. , , , - --- -

Z stands for - (CH ₂ ) _n - with n = 0 to 10 or - (CH ₂ NHCH ₂ ) _m - with m = 1 to 20.

Formulas 7 and 8 show particularly preferred compounds based on Soybean oil epoxide. Soybean oil epoxy is the epoxidized form of the natural substance soybean oil, which is the triglyceride of a polyunsaturated C ₆ -C ₈ fatty acid. An idealized chemical structure is shown in Formula 6. On average, soybean oil epoxide has 6 to 7 epoxy groups.

If R ³ and R ^{4 represent} an alkylaryl radical, alkylaryl preferably means a radical bonded via the aromatic nucleus, the aromatic nucleus of which preferably comprises 6 carbon atoms, and which, in the o-, m- or p-position to the abovementioned bond, is an alkyl radical with a Chain length of preferably 1 to 18, particularly preferably 4 to 16, in particular 6 to 12 carbon atoms.

(AO) yO stands for an alkoxylated OH radical, (AO) _y N stands for an alkoxylated NH radical, in which AO represents the alkylene oxide unit, and y indicates the degree of alkoxylation, y is preferably between 2 and 80.

For use as a petroleum emulsion splitter, the polymers are added to the water-oil emulsions, which is preferably done in solution. Paraffinic or aromatic solvents are preferred as solvents for the polymers. The polymers are used in amounts of 0.0001 to 5, preferably 0.0005 to 2, in particular 0.0008 to 1 and especially 0.001 to 0.1% by weight of polymer, based on the oil content of the emulsion to be split.

As is known in the prior art, the alkoxylation is carried out by reacting the ring-opening products with an alkylene oxide (preferably: ethylene oxide, propylene oxide or butylene oxide) under elevated pressure of generally 1.1 to 20 bar at temperatures from 50 to 200.degree. Examples

Conversion of soybean oil epoxide with coconut fatty amine (uncatalyzed)

194 g (1 mol) of coconut fatty amine were heated to 160 ° C. under a nitrogen atmosphere. 235 g of soybean oil epoxide (1 eq. Epoxy / mol amine) added dropwise. For the reaction, the mixture was left to react at 150 ° C. for 10 h. A clear-yellow, slightly viscous product was obtained, which was analyzed by means of NMR and GPC.

Implementation of soybean oil epoxide with coconut fatty amine (NaOMe-catalyzed)

(1 mol) coconut fatty amine and 1.8 g sodium methoxide (1 mol%, 30% in mol) were heated to 160 ° C. under a nitrogen atmosphere. With stirring; n, 235 g of soybean oil epoxide (1 eq.-epoxide / mol amine) is knocked out within one hour. For the reaction, the mixture was left to react at 150 ° C. for 4 h. A clear-yellow, slightly viscous product was obtained, which was analyzed by means of NMR and.

Conversion of soybean oil epoxide with dicocos fatty amine (NaOMe-catalyzed)

(1 mol) dicocos fatty amine and 4.5 g sodium methoxide (2.5 mol%, 30% in anol) were heated to 170 ° C. under a nitrogen atmosphere. While stirring, 235 g of soybean oil epoxide (1 eq.-epoxide / mol amine) is released within one hour. For the reaction, the mixture was left to react at 170 ° C. for 8 h. 3 A clear yellow, slightly viscous product was obtained, which was analyzed by means of NMR and.

Reaction of soybean oil epoxide with triethylene tetramine (NaOMe-catalyzed)

3 (1 mol) triethylenetetramine and 1.8 g sodium methoxide (1 mol%, 30% in anol) were heated to 80 ° C. under a nitrogen atmosphere. With stirring, 235 g of soybean oil epoxide (1 eq. Epoxide / mol amine) drips within one hour. The reaction was allowed to continue to react at 80 ° C. for 7 h. This gave lar-yellow product which was solid at room temperature and was analyzed by means of NMR 3PC. 5. Reaction of soybean oil epoxide with tetraethylene pentamine (NaOMe-catalyzed)

222 g (1 mol) of tetraethylene pentamine and 1.8 g of sodium methoxide (1 mol%, 30% in methanol) were heated to 80 ° C. under a nitrogen atmosphere. 235 g of soybean oil epoxide (1 eq.-epoxide / mol amine) were added dropwise with stirring over the course of one hour. The reaction was allowed to continue to react at 80 ° C. for 7 h. A clear yellow product was obtained which was solid at room temperature and was analyzed by means of NMR and GPC.

Alkoxylation of the amine-opened epoxidized carboxylic acid esters

ethylene oxide

The ring opening products described above were introduced into a 1L glass autoclave and the pressure in the autoclave was adjusted to about 0.2 bar excess pressure with nitrogen. The mixture was slowly heated to 140 ° C. and, after this temperature had been reached, the pressure was again set to 0.2 bar gauge pressure. The desired amount of EO was then metered in at 140 ° C., the pressure should not exceed 4.5 bar. After the EO addition had ended, the mixture was left to react at 140 ° C. for a further 30 minutes.

propylene oxide

The ring opening products described above were introduced into a 1L glass autoclave and the pressure in the autoclave was adjusted to about 0.2 bar excess pressure with nitrogen. The mixture was slowly heated to 130 ° C. and, once this temperature had been reached, the pressure was again set to 0.2 bar gauge pressure. The desired amount of EO was then metered in at 130 ° C., the pressure should not exceed 4.0 bar. After the EO addition had ended, the mixture was left to react at 130 ° C. for a further 30 minutes. Determination of the splitting effectiveness of petroleum emulsion splitters

To determine the effectiveness of an emulsion splitter, the water separation from a crude oil emulsion per time and the dewatering and desalination of the oil were determined. For this purpose, 100 ml each of the crude oil emulsion was poured into splitter glasses (conical, screwable, graduated glass bottles), a defined amount of the emulsion splitter was metered in with a micropipette just below the surface of the oil emulsion and the splitter was mixed into the emulsion by intensive shaking. The splitter glasses were then placed in a tempering bath (30 ° C and 50 ° C) and the water separation was monitored.

During and after the end of the emulsion splitting, samples of the oil were taken from the upper part of the splitter glass (so-called top oil) and the water content according to Karl Fischer and the salt content were determined by conductometry. In this way, the new splitters could be assessed after water separation, drainage and desalination of the oil.

Splitting effect of the emulsion breakers described

Origin of the crude oil emulsion: Holzkirchen Sonde 3, Germany Water content of the emulsion: 46% Salt content of the emulsion: 5% Demulsification temperature: 50 ° C Dosage: 20 ppm

Claims

claims:

1. Polymers available through

B) Alkoxylation of the polyamine thus obtained with a C ₂ to C alkylene oxide in molar excess, so that the average degree of alkoxylation per OH group is between 1 and 100, the polymers having number average molecular weights of 500 to 100,000 g / mol.

2. Polymers according to claim 1, characterized in that the polyol is ethylene glycol, propylene glycol, diethylene glycol, pentaerythritol, trimethylolpropane or glycerin.

3. Polymers according to claim 1 and / or 2, characterized in that the epoxidized esters are derived from naturally occurring glycerides, preferably soybean oil, olive oil, sunflower oil or linseed oil.

4. Polymers according to one or more of claims 1 to 3, characterized in that they have a number average molecular weight of 1000 to 50,000 g / mol.

5. Polymers according to one or more of claims 1 to 4, characterized in that the carboxylic acid ester ₂₂ derived from a C 10 to C.

6. Use of the polymers according to one or more of claims 1 to 5 in amounts of 0.0001 to 5 wt .-%, based on the oil, as a splitter for oil / water emulsions.