阅读说明：本技术 在用于处理金属表面的组合物中作为ep剂/腐蚀抑制剂的胺官能化有机硅烷/有机磷酸酯组合体系 (Amine functionalized organosilane/organophosphate combination system as EP agent/corrosion inhibitor in compositions for treating metal surfaces ) 是由 H·金 R·阿申佐 于 2019-06-13 设计创作，主要内容包括：根据本发明,处理金属表面的组合物,尤其是金属加工流体,其包含至少一种胺官能化有机硅烷和至少一种有机磷酸酯的反应产物和/或所述反应产物的至少一种低聚物或聚合物,其中所述至少一种胺官能化有机硅烷的氨基与所述至少一种有机磷酸酯的摩尔比为1.0:0.4至1.0:1.2,并且其中所述至少一种胺官能化有机硅烷通过至少一个磷酸/胺盐键连接到所述至少一种有机磷酸酯上。本发明还包括制备所述组合物的方法、所述组合物的用途以及处理金属表面的方法。(According to the present invention, a composition for treating metal surfaces, especially a metalworking fluid, comprises the reaction product of at least one amine-functionalized organosilane and at least one organophosphate ester and/or at least one oligomer or polymer of said reaction product, wherein the molar ratio of amino groups of the at least one amine-functionalized organosilane to the at least one organophosphate ester is from 1.0:0.4 to 1.0:1.2, and wherein the at least one amine-functionalized organosilane is linked to the at least one organophosphate ester by at least one phosphoric acid/amine salt bond. The invention also comprises a method for preparing the composition, the use of the composition and a method for treating metal surfaces.)

1. A composition, especially a metalworking fluid, for treating metal surfaces comprising the reaction product of at least one amine-functionalized organosilane and at least one organophosphate ester and/or at least one oligomer or polymer of said reaction product, wherein the molar ratio of amino groups of the at least one amine-functionalized organosilane to the at least one organophosphate ester is from 1.0:0.4 to 1.0:1.2, and wherein the at least one amine-functionalized organosilane is linked to the at least one organophosphate ester by at least one phosphoric acid/amine salt linkage.

2. The composition of claim 1, wherein: the at least one amine-functionalized organosilane comprises at least one aminoalkyl trialkoxysilane.

3. The composition according to claim 1 or 2, characterized in that: the at least one organophosphate has at least one hydrocarbon chain with at least one C ═ C double bond, more preferably at least one C ═ C double bond in the cis configuration.

4. The composition according to any one of the preceding claims, characterized in that: the at least one organophosphate ester includes at least one organophosphate ester having the structure: o ═ P (OR)₂-oh (i), wherein each of the two R moieties may be H, X- (OCH)₂CH₂)_n-or X_mPh-(OCH₂CH₂)_nProvided that at least one of the R moieties is X- (OCH)₂CH₂)_n-or X_mPh-(OCH₂CH₂)_n-, wherein X is a linear alkyl chain which may be interrupted by one or two C ═ C bonds and has from 6 to 22 carbon atoms, and wherein m is an integer from 1 to 3 and n is an integer from 0 to 12.

5. The composition of claim 4, wherein: the at least one organophosphate ester comprises at least one organophosphate ester according to formula (I) wherein each of the two R moieties may be H or X- (OCH)₂CH₂)_nProvided that at least one of the R moieties is X- (OCH)₂CH₂)_n-, wherein X is a linear alkyl chain interrupted by one or two C ═ C bonds and having 6 to 22 carbon atoms, and wherein n is an integer from 1 to 12.

6. The composition of claim 4, wherein: the at least one organophosphate ester comprises at least one organophosphate ester according to formula (I) wherein each of the two R moieties may be H or X- (OCH)₂CH₂)_nProvided that at least one of the R moieties is X- (OCH)₂CH₂)_n-, wherein X is a linear alkyl chain uninterrupted by C ═ C bonds and having 6 to 22 carbon atoms, and wherein n is an integer from 1 to 12.

7. The composition of claim 4, wherein: the at least one organophosphate ester includes at least one organophosphate ester according to formula (I) wherein each of the two R moieties may be H or X-with the proviso that at least one of the R moieties is X-wherein X is a linear alkyl chain having from 6 to 22 carbon atoms.

8. The composition of claim 7, wherein: both R moieties are X-where X is a linear alkyl chain having 6 to 22 carbon atoms.

9. The composition according to claim 7 or 8, characterized in that: each of the two R moieties may be H or X-, provided that at least one of the R moieties is X-, wherein X is a linear alkyl chain having from 8 to 12 carbon atoms.

10. The composition of claim 4, wherein: the at least one organophosphate ester comprises at least one organophosphate ester according to formula (I) wherein each of the two R moieties may be H or X_mPh-(OCH₂CH₂)_nProvided that at least one of the R moieties is X_mPh-(OCH₂CH₂)_n-, wherein X is a linear alkyl chain having 6 to 22 carbon atoms, and wherein m is an integer of 1 to 3 and n is an integer of 1 to 12.

11. The composition according to any one of the preceding claims, characterized in that: the composition comprises at least one oligomer or polymer of the reaction product of the at least one amine-functionalized organosilane and the at least one organophosphate ester.

12. A concentrate characterized by: the composition according to any of the preceding claims can be obtained by diluting the concentrate and optionally adjusting the pH.

13. A process for preparing a composition according to any one of the preceding claims, characterized in that: i) mixing at least one amine-functional organosilane (meaning an amino group) with at least one organophosphate in a molar ratio of 1.0:0.4 to 1.0:1.2 in a neat reaction or in at least one organic solvent, ii) subjecting the mixture to a temperature of at least 10 ℃ for at least 35 minutes with stirring, iii) isolating the reaction product as a viscous liquid in the case of steps i) and ii) in at least one organic solvent, and iv) then combining said reaction product with other components in order to obtain a composition for treating metal surfaces or a concentrate of the composition, wherein the mixture obtained from step i) is substantially free of water.

14. A method of treating a metal surface, characterized by: contacting the metal surface with the composition of any one of claims 1-11.

15. Use of a composition according to any one of claims 1 to 11 as a metalworking fluid, as a lubricant, in particular as a dry lubricant, as a rust inhibitor, as a cleaning agent and/or for permanently coating metal surfaces, preferably as a metalworking fluid.

Technical Field

The present invention relates to a composition for treating metal surfaces, in particular metalworking fluids, which provides improved high load carrying extreme pressure properties and corrosion inhibition, as well as to a process for preparing said composition and a process for treating metal surfaces with said composition.

Background

Modern metalworking processes are becoming increasingly demanding and complex and there is a need for metalworking fluids (MWF) with enhanced high load bearing capacity, i.e. which act as lubricants at extreme pressure, in other words, at high loads. Therefore, a great deal of technical effort and research activity has been invested in improving the lubricating properties of MWFs, especially under high pressure, heavy load and high temperature conditions, so-called boundary lubrication.

In these lines, the high load bearing, EP (extreme pressure) technology of modern MWFs relies primarily on various chlorinated paraffin, phosphate or sulfide chemicals that form tribofilms on metal surfaces through chemical reactions with metals or metal oxides during metalworking operations. The choice of a particular EP chemical depends on the severity of the metal working operation and the activation temperature of the reaction between the EP agent and the metal surface (chlorinated paraffin: about 180 ℃ C. and 420 ℃ C., phosphate: about 200 ℃ C. and 600 ℃ C., sulfide: >600 ℃ C.). At the activation temperature, the EP agent begins to form a tribofilm on the metal surface.

Among the various EP agents, Chlorinated Paraffins (CPs) are the most popular EP additive in MWF formulations due to a number of advantages, including cost-effectiveness, broad activation temperature spectrum, versatility of application, ease of formulation and stability in water, which are unparalleled. However, CP presents health and environmental issues due to the potentially toxic release upon breakdown. This is why EPA regulations may prohibit CP in the near future, in addition to very long chain CP (> C20).

Therefore, recently all MWF manufacturers are looking for CP alternatives, and most of them look at various phosphate and sulfur compounds as potential alternatives. However, phosphorus or sulfur containing compounds have the inherent disadvantage of accumulating excess nutrients in aqueous systems, causing microbial proliferation, which in turn has a detrimental effect on MWF performance.

Therefore, the development of a new EP chemical that can minimize microbial growth would be one of the most important topics in finding a new EP technology platform to replace CP in MWF formulations.

Corrosion inhibition is also an important issue in the field of MWF, since metal surfaces tend to be corroded in aqueous environments, and most modern MWF are composed mainly of water. It would therefore be very advantageous if the EP agent also exhibited corrosion inhibiting properties.

As will be explained below, the present invention describes the use of amine-functionalized organosilanes reacted with organophosphates and having a minimum phosphorus content as new CP-free EP and corrosion inhibition techniques for treating metal surfaces, particularly semi-synthetic MWF formulations.

Brief description of the invention

Compositions for treating metal surfaces, especially metalworking fluids, according to the present invention comprise the reaction product of at least one amine-functionalized organosilane and at least one organophosphate ester and/or at least one oligomer or polymer of said reaction product, wherein the molar ratio of amino groups of the at least one amine-functionalized organosilane to the at least one organophosphate ester is from 1.0:0.4 to 1.0:1.2, and wherein the at least one amine-functionalized organosilane is linked to the at least one organophosphate ester by at least one phosphoric acid/amine salt linkage.

The alkoxysilane and phosphate functional groups react with the treated metal surface and the non-polar hydrocarbon chain of the phosphate ester linked to the organosilane by salt formation serves as a barrier to prevent water, oxygen and corrosive chemicals from contacting the metal surface.

Furthermore, the hydrophobic character of the hydrocarbon chain also inhibits undesirable gel formation of the alkoxysilane groups by preventing excessive hydrolysis and subsequent condensation. The resulting barrier thickness can be controlled by varying the hydrocarbon chain length and structure.

Enhanced high load bearing capacity between metal/metal interfaces, particularly during metal processing, is achieved by the combined action of a) organophosphate functional groups that react with the metal surface under high pressure/high temperature conditions and b) aminoalkylsilane functional groups that are anchored to the metal/metal oxide surface by charge transfer interactions.

Description of The Preferred Embodiment

The following paragraphs describe preferred embodiments of the compositions of the present invention.

In the sense of the present invention, the term "composition for treating metal surfaces" does not only include metalworking fluids. For example, it also refers to lubricants such as dry lubricants, rust inhibitors, detergents and compositions for permanently coating metal surfaces. However, the use of the compositions of the present invention as metalworking fluids is particularly preferred.

The "metal surface" to be treated preferably comprises aluminum, aluminum alloys, steel and/or galvanized steel. Here, the preferred aluminum alloy contains Cu, Si, Mg and/or Zn, and the galvanized steel may be hot-dipped or electrolytically galvanized steel. More preferably, the "metal surface" comprises a mixture of different metals, such as aluminium/aluminium alloy regions and (galvanized) steel regions, as the present technique is particularly suitable for such multi-metal surfaces.

The "metallic surface" may also be a metallic surface coated with a conversion or passivation layer. Preferably, however, it is not coated with a conversion or passivation layer.

In the present invention, the term "amine-functionalized organosilane" denotes an amine-functionalized organosilane and/or oligomers and/or polymers thereof, which may be derived from the partial hydrolysis of the amine-functionalized organosilane and the subsequent (partial) condensation of the hydrolysis products (i.e. the corresponding organosilanols), respectively. The water used for the hydrolysis may be released as a by-product during the reaction of the at least one amine-functionalized organosilane and the at least one organophosphate ester, i.e. during the formation of phosphoramide bonds, and/or may be a contaminant in the educts used.

In the present invention, the term "organophosphate" denotes all protonated and deprotonated forms of the organophosphate.

The at least one amine-functionalized organosilane may be a single organosilane or a mixture of two or more different organosilanes.

The at least one amine-functionalized organosilane has at least one hydrocarbyl moiety bearing at least one amino group. As amino group, primary-NH is preferred₂. The organosilane preferably has a hydrocarbyl moiety bearing an amino group. However, it may also have two or more hydrocarbyl moieties bearing one or two or more amino groups.

As the hydrocarbyl moiety, an alkyl group is preferable, and an alkyl group having 3 or more carbon atoms is more preferable. According to one embodiment, at least one amine-functionalized organosilane having two or more alkyl groups and/or branched alkyl groups that is more stable with respect to hydrolysis may be used. However, the organosilane has low adhesion to the treated metal surface.

The at least one amine-functionalized organosilane preferably has one or more hydrocarbyloxy moieties in addition to the at least one hydrocarbyl moiety, wherein the sum of hydrocarbyl and hydrocarbyloxy moieties is preferably 4, i.e. there are no other moieties at the central silicon atom of the organosilane. As the hydrocarbyloxy moiety, an alkoxy group is preferred.

However, the at least one amine-functionalized organosilane may also have one or more-OH groups instead of one or more hydrocarbyloxy groups.

Particularly preferably, the at least one amine-functional organosilane comprises at least one aminoalkyl trialkoxysilane, most preferably 3-aminopropyltriethoxysilane.

The at least one organophosphate ester may be a single organophosphate ester or a mixture of two or more different organophosphate esters.

Each organophosphate molecule has one or two hydrocarbon chains attached to the central phosphate atom by a phosphate ester linkage (C-O-P).

The hydrocarbon chain may be interrupted by at least one heteroatom, in particular by nitrogen, oxygen and/or sulfur, preferably by oxygen. Furthermore, the hydrocarbon chain may comprise at least one aromatic or heteroaromatic moiety, in particular a phenylene moiety.

The overall hydrophobic character of the long hydrocarbon chains inhibits undesirable gel formation within the composition by preventing excessive hydrolysis and subsequent condensation. The hydrocarbon chains repel water and thus reduce the chance of water coming into contact with the amine-functionalized organosilane.

For use of the composition as a metalworking fluid, the hydrocarbon chain preferably has from 8 to 22 carbon atoms.

According to one embodiment, the at least one organophosphate has at least one branched hydrocarbon chain, preferably having at least one side chain containing at least 2 carbon atoms, more preferably having at least one side chain containing at least 4 carbon atoms. Such branched hydrocarbon chains are advantageous if the metal surface is treated with amine-functional organosilanes and/or oligomers and/or polymers thereof having a large polar head group, e.g. 3-triethoxysilylpropylamino.

The adhesion of the at least one organophosphate to metal surfaces comprising aluminum, steel, and/or galvanized steel may be enhanced by introducing at least one C ═ C double bond into the at least one hydrocarbon chain because of attractive forces between the C ═ C double bond and the corresponding metal.

The at least one organic phosphate therefore preferably has at least one hydrocarbon chain having at least one C ═ C double bond, more preferably at least one C ═ C double bond in the cis configuration, since the latter is expected to enhance adsorption, in particular, to aluminum-containing surfaces.

By using as the at least one organophosphate a mixture of at least two organophosphates having different hydrocarbon chains (number of carbon atoms, hydrophobicity/hydrophilicity, unbranched/branched, saturated/unsaturated), the properties of the composition of the present invention and the resulting barrier layer can be tailored to the intended application.

Preferably, the at least one organophosphate ester comprises at least one organophosphate ester having the structure:

O＝P(OR)₂–OH (I)

wherein each of the two R moieties may be H, X- (OCH)₂CH₂)_n-or X_mPh-(OCH₂CH₂)_n-, with the proviso that at least one R moiety is X- (OCH)₂CH₂)_n-or X_mPh-(OCH₂CH₂)_n-, wherein X is a linear alkyl chain which may be interrupted by one or two C ═ C bonds and has from 6 to 22 carbon atoms, and wherein m is an integer from 1 to 3 and n is an integer from 0 to 12.

Preferably, m is 1 or 2, n is an integer from 0 to 9, and X has from 8 to 18 carbon atoms.

According toFirst particularly preferred embodimentThe compositions of the present invention are prepared by using at least one organophosphate according to formula (I) above, wherein each of the two R moieties may be H or X- (OCH)₂CH₂)_nProvided that at least one of the R moieties is X- (OCH)₂CH₂)_n-, wherein X is a linear alkyl chain interrupted by one or two C ═ C bonds and having 6 to 22 carbon atoms, and wherein n is an integer from 1 to 12.

By controlling the value of n in addition to the EP agent function, the resulting reaction product can be a multifunctional additive that acts as an emulsifier/surfactant. As described above, C ═ C enhances adhesion to metal surfaces comprising aluminum, steel, and/or galvanized steel. X protects the surface from corrosive agents, i.e., acts as a corrosion inhibitor, while the phosphorus-containing head group improves lubricity as an EP agent.

Further preferably, one of the 3R moieties is X- (OCH)₂CH₂)_nAnd the other two R moieties are H, wherein X is a linear alkyl chain interrupted by one or two C ═ C bonds and having from 6 to 22 carbon atoms, and wherein n is an integer from 1 to 12.

Still further preferably, each of the two R moieties can be H or X- (OCH)₂CH₂)_nProvided that at least one of the R moieties is X- (OCH)₂CH₂)_n-, wherein X is a linear alkyl chain interrupted by one C ═ C bond and having 14 to 20 carbon atoms, and wherein n is an integer of 1 to 5.

Even more preferably, one of the two R moieties is X- (OCH)₂CH₂)_nAnd the other is H, wherein X is a linear alkyl chain interrupted by one C ═ C bond and having 14 to 20 carbon atoms, and wherein n is an integer from 1 to 5.

Particularly preferred examples of organophosphates according to this first preferred embodiment are:

the organic phosphate is preferably reacted with 3-aminopropyltrimethoxysilane or 3-aminopropyltriethoxysilane, in particular with 3-aminopropyltriethoxysilane.

According toSecond particularly preferred embodimentThe compositions of the present invention are prepared by using at least one organophosphate according to formula (I) above, wherein each of the two R moieties may be H or X- (OCH)₂CH₂)_nProvided that at least one of the R moieties is X- (OCH)₂CH₂)_n-, wherein X is a linear alkyl chain having 6 to 22 carbon atoms which is not interrupted by C ═ C bonds, and wherein n is an integer from 1 to 12.

The absence of C ═ C improves the oxidation stability of the resulting reaction product.

Further preferably, one of the two R moieties is X- (OCH)₂CH₂)_nAnd the other is H, wherein X is a linear alkyl chain having 6 to 22 carbon atoms, and wherein n is an integer from 1 to 12.

Still further preferably, each of the two R moieties can be H or X- (OCH)₂CH₂)_n-, with the proviso that at least one R moiety is X- (OCH)₂CH₂)_n-, wherein X is a linear alkyl chain having from 8 to 16 carbon atoms, and wherein n is an integer from 1 to 8.

Even more preferably, one of the two R moieties is X- (OCH)₂CH₂)_nAnd the other is H, wherein X is a linear alkyl chain having from 8 to 16 carbon atoms, and wherein n is an integer from 1 to 8.

Particularly preferred examples of organophosphates according to this second preferred embodiment are:

the organic phosphate is preferably reacted with 3-aminopropyltrimethoxysilane or 3-aminopropyltriethoxysilane, in particular with 3-aminopropyltriethoxysilane.

According toThird particularly preferred embodimentThe compositions of the present invention are prepared by using at least one organophosphate according to formula (I) above, wherein each of the two R moieties may be H or X-, provided that at least one of the R moieties is X-, wherein X is a linear alkyl chain having from 6 to 22 carbon atoms.

Further preferably, both R moieties are X-, wherein X is a linear alkyl chain having 6 to 22 carbon atoms.

Due to its branched structure, the resulting reaction product exhibits the best oxidation stability, excellent anti-corrosion/fouling properties, minimal pH change and better microbial control.

Still further preferably, each of the two R moieties may be H or X-, provided that at least one of the R moieties is X-, wherein X is a linear alkyl chain having from 8 to 12 carbon atoms.

Even more preferably, both R moieties are X-, wherein X is a linear alkyl chain having from 8 to 12 carbon atoms.

Particularly preferred examples of organophosphates according to this third preferred embodiment are:

the organic phosphate is preferably reacted with 3-aminopropyltrimethoxysilane or 3-aminopropyltriethoxysilane, in particular with 3-aminopropyltriethoxysilane.

According toFourth particularly preferred embodimentThe compositions of the present invention are prepared by using at least one organophosphate according to formula (I) above, wherein each of the two R moieties may be H or X_mPh-(OCH₂CH₂)_nProvided that at least one R moiety is X_mPh-(OCH₂CH₂)_n-, wherein X is a linear alkyl chain having 6 to 22 carbon atoms, and wherein m is an integer of 1 to 3 and n is an integer of 1 to 12.

The obtained reaction product shows better emulsification and microbial control.

Further preferably, one of the two R moieties is X_mPh-(OCH₂CH₂)_nAnd the other is H, wherein X is a linear alkyl chain having 6 to 22 carbon atoms, and wherein m is an integer from 1 to 3 and n is an integer from 1 to 12.

Still further preferably, each of the two R moieties may be H or X_mPh-(OCH₂CH₂)_nProvided that at least one R moiety is X_mPh-(OCH2CH2)_n-, wherein X is a linear alkyl chain having 7 to 13 carbon atoms, and wherein m is 1 or 2 and n is an integer of 2 to 11.

Even more preferably, one of the two R moieties is X_mPh-(OCH₂CH₂)_n-, and the other is H, wherein X is a linear alkyl chain having 7 to 13 carbon atoms, and wherein m is 1 or 2 and n is an integer of 2 to 11.

Particularly preferred examples of organophosphates according to this fourth preferred embodiment are:

these organic phosphates are preferably reacted with 3-aminopropyltrimethoxysilane or 3-aminopropyltriethoxysilane, in particular with 3-aminopropyltriethoxysilane.

The thickness and density of the barrier layer and the adsorption of the barrier layer on the treated metal surface depend on the length and structure of the hydrocarbon chain of the at least one organophosphate applied and the structure of the at least one amine-functionalized organosilane used. The branched tails result in a less dense and less thick membrane but show strong adsorption, while the long linear tails result in a membrane with higher density and thickness at the expense of some adsorption strength. The large head groups derived from the organosilane result in a membrane with lower density and thickness but with strong adsorption, while the small head groups result in a more dense and thicker membrane with some loss of adsorption strength.

In the composition of the present invention, the molar ratio of the amino groups of the at least one amine-functionalized organosilane and/or oligomer and/or polymer thereof to the at least one organophosphate ester is preferably from 1.0:0.4 to 1.0:0.6 or from 1.0:0.8 to 1.0: 1.2.

The compositions of the invention can be prepared by diluting a suitable concentrate with a suitable solvent, preferably deionized water, preferably 1:10 to 1:20 fold (corresponding to 5-10% by weight of the concentrate) and, if desired, subsequently adjusting the pH with a suitable pH adjuster.

In this concentrate, the concentration of the at least one amine-functionalized organosilane is preferably in the range of from 0.1 to 4.0 wt.%, more preferably in the range of from 0.2 to 2.0 wt.%, particularly preferably in the range of from 0.6 to 1.5 wt.% (based on educt), and the concentration of the at least one organic phosphate is preferably in the range of from 0.1 to 4.0 wt.%, more preferably in the range of from 0.3 to 3.0 wt.%, particularly preferably in the range of from 1.0 to 2.0 wt.% (based on educt).

Accordingly, in the compositions of the invention obtainable by diluting the concentrate, the concentration of the at least one amine-functional organosilane is preferably from 0.005 to 0.4% by weight, more preferably from 0.01 to 0.2% by weight, especially preferably from 0.03 to 0.15% by weight, based on the educts, and the concentration of the at least one organic phosphate is preferably from 0.005 to 0.4% by weight, more preferably from 0.015 to 0.3% by weight, especially preferably from 0.05 to 0.2% by weight, based on the educts.

Preferably, the above concentrate additionally comprises:

10-40% by weight of a naphthenic oil,

4-7% by weight of polyricinoleic acid,

3-6% by weight of a self-emulsifying ester,

2-4% by weight of a polymeric complex ester,

3-6% by weight of a maleated polymeric ester,

2-4% by weight of erucic acid,

3-6% by weight of diethylethanolamine,

2-4% by weight of diglycolamine,

1-2% by weight of tripropylene glycol butyl ether,

1-3% by weight of 3-amino-4-octanol,

20-40% by weight of deionized water,

2-4% by weight of triethanolamine,

4-8% by weight of a mixture of dodecanedioic acid and triethanolamine in a molar ratio of about 1:1,

1-2% by weight of a secondary alcohol ethoxylate as nonionic surfactant,

0.5 to 1.5% by weight of dicarboxylic fatty acids,

2-4% by weight of the reaction product of (3-aminopropyl) triethoxysilane and erucic acid (1:1 molar ratio), and/or

Up to 0.5% by weight of a defoamer mixture,

(provided that the sum of all components is 100 wt%).

According to a particularly preferred embodiment, the concentrate additionally comprises all the components mentioned above in the abovementioned% by weight.

Thus, the composition of the invention additionally comprises:

0.5-4 wt% naphthenic oil,

up to 0.7% by weight of polyricinoleic acid,

0.15-0.6 wt% of a self-emulsifying ester,

up to 0.4 wt% of a polymeric complex ester,

0.15 to 0.6% by weight of a maleated polymeric ester,

(ii) up to 0.4% by weight of erucic acid,

0.15-0.6% by weight of diethylethanolamine,

up to 0.4% by weight of diglycolamine,

0.05 to 0.2% by weight of tripropylene glycol butyl ether,

0.05 to 0.3% by weight of 3-amino-4-octanol,

91-95% by weight of deionized water,

up to 0.4% by weight of triethanolamine,

up to 0.8% by weight of a mixture of dodecanedioic acid and triethanolamine in a molar ratio of about 1:1,

0.05-0.2% by weight of a secondary alcohol ethoxylate as nonionic surfactant,

0.025 to 0.15% by weight of a dicarboxylic fatty acid,

up to 0.4% by weight of the reaction product of (3-aminopropyl) triethoxysilane and erucic acid (1:1 molar ratio), and/or

0.005-0.05 wt.% of a defoamer mixture

(provided that all components add up to 100 wt%).

According to a particularly preferred embodiment, the composition of the invention additionally comprises all the components mentioned above in the abovementioned% by weight.

According to a preferred embodiment, the composition is an aqueous composition, which means, for example, that when the concentrate is diluted with water as the solvent, more than 50% by weight of the solvent is water. The composition may also comprise synthetic and/or mineral oils as solvents, such as naphthenic oils. Due to the additional use of such oil, the composition has the advantage of good lubricity and high cooling capacity.

Depending on the intended metal surface treatment, the properties of the composition of the invention can be adjusted by adding different kinds of additives.

In detail, the additive may be a neutralizing agent, an emulsifier, a lubricity enhancer, a biocide, a fungicide, a metal deactivator and/or a stability enhancer for freeze/thaw cycles.

Furthermore, the additives may be used for corrosion resistance, pH adjustment, coupling, wetting, microbial control, and/or prevention of foam formation.

The pH of the composition is preferably 8.5 to 10.5, more preferably 9.0 to 10.0, and particularly preferably 9.2 to 9.7.

The invention also includes a method of making the composition of the invention. In the method, the first step of the method,

i) mixing at least one amine-functional organosilane (meaning an amino group) and at least one organophosphate in a molar ratio of 1.0:0.4 to 1.0:1.2 in a neat reaction or in at least one organic solvent,

ii) subjecting the mixture to a temperature of at least 10 ℃ for at least 35 minutes with stirring,

iii) in the case of carrying out steps i) and ii) in at least one organic solvent, the reaction product is isolated as a viscous liquid, and

iv) then, combining the reaction product with other components in order to obtain a composition for treating metal surfaces or a concentrate of the composition,

wherein the mixture obtained from step i) is substantially free of water.

Here, "substantially free of water" means water which may be contained as a contaminant in the mixture of step i) due to a corresponding contamination of the educts and/or the solvent used. Here, water is not intentionally added, and is therefore preferably contained in the mixture of step i) in a concentration of not more than 0.1% by weight.

If water is contained as a contaminant in the mixture of step i), oligomeric and/or polymeric substances are formed to some extent by partial hydrolysis of the alkoxysilane groups and subsequent condensation of the resulting silanol groups to siloxane groups. However, the water released as a by-product during the formation of phosphoramide bonds in step ii) may also cause partial hydrolysis and subsequent condensation reactions, thereby producing oligomeric and/or polymeric species.

Steps i) and ii) are preferably carried out without using any solvent, i.e. in a neat reaction. At this point step iii) is omitted. However, it is also possible to use organic solvents which are substantially free of water, for example base oils, for preparing the mixture in step i). In this case, the reaction time required in step ii) will be longer, while the exothermicity of the reaction can be better controlled, which may be particularly advantageous for large-scale production.

In step ii), the at least one amine-functionalized organosilane and the at least one organophosphate are linked by a typical acid/base reaction, i.e. by at least one phosphoric acid/amine salt bond, in the absence of any catalyst. However, a phosphoamide bond may also be formed.

Step ii) is preferably carried out at a temperature of from 20 to 55 ℃ and particularly preferably at room temperature. The reaction time required in step ii) is preferably 40 to 50 minutes.

Preferably, the composition of the present invention comprises at least one oligomer or polymer of the reaction product of at least one amine-functionalized organosilane and at least one organophosphate ester. This is particularly advantageous because such oligomeric/polymeric products will increase emulsion stability.

In step iv), the reaction product is preferably combined with other components in order to obtain a concentrate of the composition for treating metal surfaces, which is then diluted to the composition.

Furthermore, the invention also includes a method of treating a metal surface, wherein the metal surface is contacted with the composition of the invention and then optionally rinsed.

The metal surface may also be cleaned and/or rinsed prior to contact with the composition of the present invention.

Preferably, the metal surface is a multi-metal surface and is contacted with the composition of the present invention, which is a metalworking fluid, and then the metalworking process is carried out under extreme pressure/high load conditions. Here, the metal surface preferably comprises aluminum and/or aluminum alloy and steel and/or galvanized steel.

The compositions of the invention are preferably used as metalworking fluids, as lubricants, in particular as dry lubricants, as rust inhibitors, as detergents and/or for permanently coating metal surfaces. More preferably, the composition is used as a metal working fluid.

The invention is indicated by the following examples without thereby limiting the scope of the invention.

(comparative) examples

Comparative example 1(CE 1):

a concentrate of a metalworking fluid comprising 30 wt.% naphthenic oil, 20.5 wt.% deionized water, 8 wt.% 2-amino-2-methylpropanol, 4 wt.% boric acid, 7 wt.% of a mixture of dodecanedioic acid and triethanolamine in a molar ratio of about 1:1, 1 wt.% secondary alcohol ethoxylate as a nonionic surfactant, 3 wt.% branched succinic acid, 1% by weight tallow amine ethoxylate, 0.5% by weight dicarboxylic fatty acid, 0.3% by weight dipropylene glycol butyl ether, 8% by weight chlorinated fatty acid, 0.5% by weight 3-iodo-2-propylbutyl carbamate, 2% by weight oleyl alcohol, 14% by weight medium chain chlorinated paraffin and 0.2% by weight defoamer mixture (provided that the sum of all components is 100% by weight) -are prepared by mixing the components.

Comparative example 2(CE 2):

concentrate of metalworking fluid comprising 23 wt% naphthenic oil, 6 wt% polyricinoleic acid, 4 wt% self-emulsifying ester, 3 wt% polymeric complex ester, 4 wt% maleated polymeric ester, 3 wt% erucic acid, 5 wt% diethylethanolamine, 3 wt% diglycolamine, 2 wt% tripropylene glycol butyl ether, 2 wt% 3-amino-4-octanol, 30 wt% deionized water, 3 wt% triethanolamine, 6 wt% mixture of dodecanedioic acid and triethanolamine in about 1:1 molar ratio, 1.5 wt% secondary alcohol ethoxylate as a nonionic surfactant, 1 wt% dicarboxy fatty acid, 3 wt% reaction product of (3-aminopropyl) triethoxysilane and erucic acid (1:1 molar ratio), and 0.5 wt% defoamer mixture (provided that the sum of all components is 100 wt%) -mixing said concentrate with defoamer mixture Preparing the components.

Example 1 (E1):

a concentrate of a metalworking fluid comprising 22.2 wt.% naphthenic oil, 5 wt.% polyricinoleic acid, 4 wt.% self-emulsifying ester, 2.5 wt.% polymeric complex ester, 4 wt.% maleated polymeric ester, 3 wt.% erucic acid, 5 wt.% diethylethanolamine, 2.5 wt.% diglycolamine, 2 wt.% tripropylene glycol butyl ether, 2 wt.% 3-amino-4-octanol, 30 wt.% deionized water, 3 wt.% triethanolamine, 6 wt.% of a mixture of dodecanedioic acid and triethanolamine in about a 1:1 molar ratio, 1.5 wt.% secondary alcohol ethoxylate as a non-ionic surfactant, 1 wt.% dicarboxy fatty acid, 3 wt.% reaction product of (3-aminopropyl) triethoxysilane and decyloctyl phosphate (1:1 molar ratio), a metal working fluid, and a metal working fluid, 3% by weight of the reaction product of (3-aminopropyl) triethoxysilane and erucic acid (1:1 molar ratio) and 0.3% by weight of the defoamer mixture (provided that the sum of all components is 100% by weight) -was prepared by mixing the components.

Here, the reaction product of (3-aminopropyl) triethoxysilane and decyl octyl phosphate (1:1 molar ratio) was prepared by the following procedure:

(3-aminopropyl) triethoxysilane and decyl octyl phosphate were mixed in a molar ratio of 1:1 in a neat reaction without using any solvent.

The mixture was then left at room temperature for 40-50 minutes with stirring.

8 parts by volume of concentrate CE1, CE2, or E1 were added to 92 parts by volume of hard water (75 ppm calcium acetate in deionized water) and mixed. The obtained metalworking fluids CE1, CE2, and E1 were applied to 1018 steel (CRS) test plates and 6061 aluminum test plates by using a disposable pipette.

To measure the torque force, a micro tapping test was performed by a thread tapping apparatus. The results obtained are shown in table 1 below:

table 1:

it can clearly be seen that, in contrast to CE2, the metalworking fluid containing the reaction product (E1) of (3-aminopropyl) triethoxysilane and decyloctyl octyl phosphate (1:1 molar ratio) resulted in torque values on steel and aluminium that were even better than, i.e. lower than, the values obtained with the metalworking fluid containing chlorinated paraffins and chlorinated fatty acids (CE1, prior art).