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Title:
COPOLYMERS OF 1-DECENE AND 1-DODECENE AS LUBRICANTS
Document Type and Number:
WIPO Patent Application WO/2002/092729
Kind Code:
A1
Abstract:
The present invention relates to poly $g(a)-olefins (PAO's) which exhibit superior Noack volatility at low pour points. Mixtures of 1-decene and 1-dodecene are polymerized using an alcohol pronoted BF¿3? in conjunction with a combination of cocatalysts. The reaction mixture is distilled to remove the unreacted monomeric and dimeric species. The resulting products is then hydrogenated to saturate the oligomers to provide a hydrogenated prodcts which has a viscosity of 5 cSt. This product is distilled to provide PAO's of varying viscosity grades. The 4 cSt PAO is comprised mostly of trimers and tetramers while the 6cSt product is comprised of trimers, tetramers, and pentamers.

Inventors:
Goze, Maria Caridad B. (90 Morgan Place East Brunswick, NJ, 08816, US)
Yang, Norman (2 Normandy Drive Westfield, NJ, 07090, US)
Application Number:
PCT/US2002/011808
Publication Date:
November 21, 2002
Filing Date:
April 16, 2002
Export Citation:
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Assignee:
EXXONMOBIL CHEMICAL PATENTS, INC. (5200 Bayway Drive Baytown, TX, 77520-5200, US)
International Classes:
C10G45/00; C10G50/00; C10G50/02; C10G69/12; C10M105/04; C10M107/10; C10M107/12; C10M109/02; C10M111/04; C10M111/06; C10M177/00; C10N20/00; C10N30/00; C10N30/02; C10N40/25; C10N60/02; C10N70/00; (IPC1-7): C10G50/02; C07C2/22; C10M107/10
Foreign References:
US4032591A1977-06-28
US3780128A1973-12-18
US4045507A1977-08-30
US3576898A1971-04-27
US4172855A1979-10-30
US3149178A1964-09-15
Other References:
None
Attorney, Agent or Firm:
Moreno, Louis N. (ExxonMobil Chemical Company P.O. Box 2149 Baytown, TX _, 77522-2149, US)
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Claims:
CLAIMS : We claim:
1. A process for preparing a lubricant, which comprises (a) oligomerizing an aolefin feed, wherein said feed is comprised of 50 to 80 weight percent of 1decene and 50 to 20 weight percent of 1 dodecene, in the presence of BF3 and at least two different cocatalysts, wherein said cocatalysts are selected from groups (i) and (ii): (i) alcohols and (ii) alkyl acetates, provided that at least one cocatalyst is from group (i) and at least one cocatalyst is from group (ii); followed by (b) hydrogenation of at least a portion of residual unsaturation.
2. The process of claim 1, wherein groups (i) and (ii) are selected from CiCio alcohols and ClClo alkyl acetates.
3. The process of claim 1, wherein groups (i) and/or (ii) are selected from C1C6 alcohols and C1C6 alkyl acetates.
4. The process of claim 1, wherein the Clcalo alcohols are selected from ethanol, npropanol, nbutanol, npentanol, and nhexanol.
5. The process of claim 1, wherein the cocatalyst is comprised of ethanol and ethyl acetate.
6. The process of claim 1, wherein the cocatalyst is comprised of n butanol and nbutyl acetate.
7. The process of claim 1, wherein the lubricant possesses a Noack volatility of about 4 to 12 % weight loss, as determined by a modified ASTM D5800 method, and a pour point of about40° C to65° C, as determined by a modified ASTM D5950 method; wherein said modified ASTM D5800 method is an ASTM D5800 method with the exception that thermometer calibration is performed annually; and wherein said modified ASTM D5950 method is an ASTM D5950 method with the exception that the lubricant to be tested is not heated prior to performing said method.
8. The process of claim 7, wherein the Noack volatility is 5 to 11 % weight loss.
9. The process of claim 7, wherein the pour point is45° C to60° C.
10. The process of claim 1, wherein the feed is comprised of 55 to 75 weight percent of 1decene and 1dodecene and 45 to 25 weight percent 1 dodecene.
11. The process of claim 1, further comprising the step of subjecting said lubricant to distillation to afford a fraction having a viscosity of about 4 cSt and/or a fraction having a viscosity of about 6 cSt.
12. The process of claim 11, wherein the 4cSt fraction possesses a Noack volatility of 9 to 15% weight loss.
13. The process of claim 11, wherein the 4 cSt fraction exhibits a pour point of45° C to65° C.
14. The process of claim 11, wherein the 6 cSt fraction possesses a Noack volatility of 3 to 10 % weight loss.
15. The process of claim 11, wherein the 6 cSt fraction exhibits a pour point of40° C to60° C.
16. The process of claim 1, wherein the cocatalyst is used in an amount of from about 0.01 to about 10 weight percent, based on the weight of the aolefin feed, and wherein the ratio of the group (i) cocatalyst to group (ii) cocatalyst ranges from about 0.2 to 15.
17. A process for preparing a lubricant, which comprises (a) oligomerizing an aolefin feed, wherein said feed consists essentially of about 50 to 80 weight percent of 1decene and 1dodecene and 50 to 20 weight percent 1dodecene, in the presence of BF3 and at least two different cocatalysts, wherein said cocatalysts are selected from the groups (i) and (ii): (i) alcohols and (ii) alkyl acetates, provided that at least one cocatalyst is from group (i) and at least one cocatalyst is from group (ii); followed by (b) hydrogenation of at least a portion of residual unsaturation.
18. The process of claim 17, wherein at least 90 percent of residual unsaturation is hydrogenated.
19. The process of claim 17, wherein groups (i) and (ii) are selected from ClCl0 alcohols and ClClo alkyl acetates.
20. The process of claim 17, wherein groups (i) and (ii) are selected from ClC6 alcohols and ClC6 alkyl acetates.
21. The process of claim 17, wherein the ClC6 alcohols are selected from ethanol, npropanol, nbutanol, npentanol, and nhexanol.
22. The process of claim 17, wherein the cocatalyst is comprised of ethanol and ethyl acetate.
23. The process of claim 17, wherein the cocatalyst is comprised of n butanol and nbutyl acetate.
24. The process of claim 17, wherein the lubricant possesses a Noack volatility of about 6 to 10 % weight loss, as determined by a modified ASTM D5800 method, and a pour point of about50°C to58°, as determined by a modified ASTM D5950 method; wherein said modified ASTM D5800 method is an ASTM D5800 method with the exception that thermometer calibration is performed annually; and wherein said modified ASTM D5950 method is an ASTM D5950 method with the exception that the lubricant to be tested is not heated prior to performing said method.
25. The process of claim 17, wherein the feed consists essentially of 55 to 75 weight percent of 1decene and 1dodecene and 45 to 25 weight percent 1 dodecene.
26. A lubricant comprised of an oligomerized aolefin which has been subjected to hydrogenation, wherein said oligomerized aolefin is prepared from an olefin feed comprised of 50 to 80 weight percent of 1decene and 50 to 20 weight percent 1dodecene, wherein said oligomerized aolefin exhibits a Noack volatility of about 4 to 12 % weight loss, as determined by as determined by a modified ASTM D5800 method, and a pour point of about40° C to65° C as determined by a modified ASTM D5950 method; wherein said modified ASTM D5800 method is an ASTM D5800 method with the exception that thermometer calibration is performed annually; and wherein said modified ASTM D5950 method is an ASTM D5950 method with the exception that the lubricant to be tested is not heated prior to performing said method.
27. The lubricant of claim 26, wherein the Noack volatility is 5.0 to 11.0 % weight loss.
28. The lubricant of claim 26, wherein the pour point is45° C to65° C.
29. The lubricant of claim 26, wherein said lubricant has a viscosity of about 5 cSt.
30. The lubricant of claim 26, wherein said lubricant has a viscosity of about 4 cSt.
31. The lubricant of claim 26, wherein said lubricant has a viscosity of about 6 cSt.
32. The lubricant of claim 26, wherein the feed consists essentially of 55 to 75 weight percent of 1decene and 45 to 35 weight percent 1dodecene.
33. The lubricant of claim 26, wherein said lubricant is prepared by oligomerization in the presence of BF3 and at least two different cocatalysts, wherein said cocatalysts are selected from the groups (i) and (ii): (i) alcohols and (ii) alkyl acetates, provided that at least one cocatalyst is from group (i) and at least one cocatalyst is from group (ii).
34. The lubricant of claim 26, wherein at least 90 percent of residual unsaturation is hydrogenated.
35. The lubricant of claim 26, wherein groups (i) and/or (ii) are selected from ClCl0 alcohols and C1Clo alkyl acetates.
36. The lubricant of claim 26, wherein groups (i) and/or (ii) are selected from CiC6 alcohols and C1C6 alkyl acetates.
37. The lubricant of claim 26, wherein the C1C6 alcohols are selected from ethanol, npropanol, nbutanol, npentanol, and nhexanol.
38. The lubricant of claim 26, wherein the cocatalyst is comprised of ethanol and ethyl acetate.
39. The lubricant of claim 26, wherein the cocatalyst is comprised of n butanol and nbutyl acetate.
40. A lubricant composition comprising (a) a conventional lubricant ; and (b) at least one lubricant comprised of an oligomerized aolefin which has been subjected to hydrogenation, wherein said oligomerized aolefin is prepared from an olefin feed comprised of 50 to 80 weight percent of 1decene and 50 to 20 weight percent 1dodecene, wherein said oligomerized aolefin exhibits a Noack volatility of about 4 to 12 % weight loss, as determined by as determined by a modified ASTM D5800 method, and a pour point of about40° C to65° C as determined by a modified ASTM D5950 method; wherein said modified ASTM D5800 method is an ASTM D5800 method with the exception that thermometer calibration is performed annually ; and wherein said modified ASTM D5950 method is an ASTM D5950 method with the exception that the lubricant to be tested is not heated prior to performing said method.
Description:
COPOLYMERS OF 1-DECENE AND 1-DODECEN AS LUBRICANTS Field of the Invention This invention belongs to the field of lubricants. More particularly, this invention relates to certain improved poly a-olefins prepared from a mixed feed of olefins.

Background Of The Invention Poly a-olefins comprise one class of hydrocarbon lubricants which has achieved importance in the lubricating oil market. These materials are typically produced by the polymerization of a-olefins typically ranging from 1-octene to 1- dodecene, with 1-decene being a preferred material, although polymers of lower olefins such as ethylene and propylene may also be used, including copolymers of ethylene with higher olefins, as described in U. S. Patent No. 4,956,122 and the patents referred to therein. The poly a-olefin (PAO) products may be obtained with a wide range of viscosities varying from highly mobile fluids of about 2cSt at 100° C to higher molecular weight, viscous materials which have viscosities exceeding 100 cSt at 100° C. The PAO's may be produced by the polymerization of olefin feed in the presence of a catalyst such as Aids, BF3, or BF3 complexes.

Processes for the production of PAO lubricants are disclosed, for example, in the following patents: U. S. Patent Nos: 3,382,291; 4,172,855; 3,742,082; 3,780,128; 3,149,178; and 4,956,122. The PAO lubricants are also discussed in Lubrication Fundamentals, J. G. Wills, Marcel Dekker Inc., (New York, 1980). Subsequent to the polymerization, the lubricant range products are hydrogenated in order to reduce the residual unsaturation. In the course of this reaction, the amount of unsaturation is generally reduced by greater than 90%.

A major trend in passenger car engine oil usage is the extension of oil drain intervals. Thus, a need exists for low viscosity PAO's which exhibit low Noack volatility. (See ASTM D 5800 Standard Test Method for Evaporation Loss of Lubricating Oils by the Noack Method.) The properties of a particular grade of PAO are greatly dependent on the a-olefin used to make that product. In general, the higher the carbon number of

the a-olefin, the lower the Noack volatility and the higher the pour point of the product.

PAO's having a viscosity of 4cSt are typically made from 1-decene and have a Noack volatility of 13-14% and pour point of <-60°C. PAO's having a viscosity of 6cSt are typically prepared from 1-decene or a blend of a-olefins and have a Noack volatility of about 7.0% and pour point of about-60°C.

Summary Of The Invention The present invention relates to poly a-olefins (PAO's) which exhibit superior Noack volatility, while maintaining good low temperature properties.

Mixtures of 1-decene and 1-dodecene are polymerized using BF3 promoted alcohol/ester mixture. The reaction mixture is distilled to remove the unreacted monomeric and dimeric species. The resulting product is hydrogenated to saturate the oligomers, to provide a product having a viscosity of 5cSt. This product is distilled and distillation cuts blended to provide PAO's of varying viscosity grades. The 4 cSt PAO is comprised mostly of trimers and tetramers while the 6cSt is comprised of trimers, tetramers, and pentamers.

Detailed Description Of The Invention In one aspect, the present invention provides a process for preparing a lubricant, which comprises (a) oligomerizing an a-olefin feed, wherein said feed is comprised of 50 to 80 weight percent of 1-decene and 50 to 20 weight percent of 1- dodecene, in the presence of BF3 and at least two different cocatalysts, wherein said cocatalysts are selected from groups (i) and (ii): (i) alcohols and (ii) alkyl acetates, provided that at least one cocatalyst is from group (i) and at least one cocatalyst is from group (ii); followed by (b) hydrogenation of at least a portion of residual unsaturation.

In the above process, it is preferred that the a-olefin feed consists essentially of 50 to 80 weight percent of 1-decene and 50 to 20 weight percent of

1-dodecene, with 55 to 75 weight percent of 1-decene and 45 to 25 weight percent of 1-dodecene being more preferred. We have found that a combination of cocatalysts (or promoters), one cocatalyst selected from the class of alcohols, i. e., compounds having one hydroxyl functional group, preferably Cl-Cl0 alcohols, more preferably Cl-C6 alcohols, and at least one cocatalyst selected from alkyl acetates, preferably Cl-Cl0 alkyl acetates, more preferably C1-C6 alkyl acetates, provides oligomers which possess desired distributions and physical properties.

In this regard, we have found that PAO's prepared from either group (i) or (ii) alone exhibit low product yields.

In this process, it is preferred that the ratio of the group (i) cocatalysts to group (ii) cocatalysts range from about 0.2 to 15, (i. e., (i): (ii)) with 0.5 to 7 being preferred.

Preferred C1-C6 alcohols include methanol, ethanol, n-propanol, n-butanol, n-pentanol, and n-hexanol.

Preferred C1-C6 alkyl acetates include methyl acetate, ethyl acetate, n- propyl acetate, n-butyl acetate, and the like.

We have found that, surprisingly, the products of this process possess a good balance of properties, especially low Noack volatility and pour point. Thus, in a preferred embodiment, the present invention provides a lubricant which possesses a Noack volatility of about 4 to 12 % weight loss, alternatively 6 to 10% weight loss, as determined by a modified ASTM D5800 method, and a pour point of about-40° C to-65° C, alternatively-50° to-58° C, as determined by a modified ASTM D5950 method; wherein said modified ASTM D5800 method is an ASTM D5800 method with the exception that thermometer calibration is performed annually; and wherein said modified ASTM D5950 method is an ASTM D5950 method with the exception that the sample to be tested is not heated prior to performing said method.

In this regard, the modified ASTM D5800 method is the same as the ASTM D5800 method, with the exception that the thermometer calibration is performed annually rather than biannually. The modified ASTM D5950 method is the same as the ASTM D5950 method with the exception that the sample to be

tested is not heated prior to performing said method. In particular, the preliminary preheat of the test specimen, as set forth in 11.3.1 and 11.3.2, in ASTM D 5950, is not followed.

The oligomerized a-olefins of the present invention are preferably subjected to hydrogenation using conventional hydrogenation methodology to reduce at least a portion of the residual unsaturation which remains after the oligomerization. In this regard, typical hydrogenation catalysts such as Pd, Pt, Ni, etc., can be utilized. In the hydrogenation step, it is preferred that at least about 90% of the residual unsaturation be reduced. The lubricants thus provided may be utilized as is in lubricant applications or may be formulated with other conventional lubricants. Accordingly, in another aspect, the present invention provides a lubricant composition comprising (a) a conventional lubricant; and (b) at least one lubricant comprised of an oligomerized a-olefin which has been subjected to hydrogenation, wherein said oligomerized a-olefin is prepared from an olefin feed comprised of 50 to 80 weight percent of 1-decene and 50 to 20 weight percent 1-dodecene, wherein said oligomerized a-olefin exhibits a Noack volatility of about 4 to 12 % weight loss, as determined by as determined by a modified ASTM D5800 method, and a pour point of about-40° C to-65° C as determined by a modified ASTM D5950 method ; wherein said modified ASTM D5800 method is an ASTM D5800 method with the exception that thermometer calibration is performed annually ; and wherein said modified ASTM D5950 method is an ASTM D5950 method with the exception that the lubricant to be tested is not heated prior to performing said method.

In the above lubricant compositions, suitable conventional lubricants include known synthetic and natural lubricants which may form a major or minor portion of the overall lubricant composition and their choice and quantity can be tailored to meet desired end-use criteria. (See, for example, Synthetic Lubricants and High-Performance Functional Fluids, Ed. Ronald L. Shubkin, Marcel Dekker, Inc., (New York, 1993).

The oligomerization reaction can be conducted in a single or multiple stage process to produce a mixture of dimer, trimer, tetramer, and pentamer products. As is shown below in the experimental section, the product of the oligomerization reaction is desirably subjected to fractional distillation to afford products via blending having 4,5, and 6 cSt.

Boron trifluoride is used as the catalyst in the process of the present invention along with a combination of cocatalysts. As noted above, we have found that surprisingly, when one selects at least one catalyst from the classes of alcohols and at least one selected from alkyl acetates, followed by conventional hydrogenation, a lubricant having a superior balance of properties results. The cocatalyst complexes with the boron trifluoride to form a coordination compound which is catalytically active. In a preferred embodiment, the cocatalyst is used in an amount of from about 0.01 to about 10 weight percent, based on the weight of the a-olefin feed, most preferably about 0.1 to 6 weight percent.

As to the boron trifluoride, it is preferred that it be introduced into the reactor simultaneously with cocatalysts and olefin feed. It is further preferred that the reaction zone contains an excess of boron trifluoride, which is governed by the pressure and partial pressure of the boron trifluoride. In this regard, it is preferred that the boron trifluoride be maintained in the reaction zone at a pressure of about 2 to about 500 psig, preferably about 2 to 50 psig. Alternatively, the boron trifluoride can be sparged into the reaction mixture, along with other known methods for introducing the boron trifluoride to the reaction zone.

Suitable temperatures for the reaction are also conventional and can vary from about-20° C to about 90° C, with a range of about 15° to 70° C being preferred.

Further details regarding suitable conventional processing methodologies can be found in U. S. Patent No. 4,045,507, incorporated herein by reference, and in Synthetic Lubricants and High-Performance Functional Fluids, Ed. Ronald L.

Shubkin, Marcel Dekker, Inc., (New York, 1993).

Experimental Section Example 1.

A 1-decene and 1-dodecene mixture containing 70 weight percent 1- decene and 30 weight percent 1-dodecene was oligomerized in two continuous stirred-tank reactors in series at 18° C and 5psig using BF3 promoted with a 12: 1 mole ratio mixture of ethanol and ethyl acetate at a total catalyst concentration of 3.5 weight percent. When a steady-state condition was attained, a sample was distilled to remove the monomers and dimers. The bottoms stream was hydrogenated to saturate the trimers/oligomers. The hydrogenated product is 5cSt PAO. A sample of this hydrogenated product was distilled and distillation cuts blended to produce different viscosities of PAO. The 4cSt PAO contained mostly trimers and tetramers while the 6cSt PAO trimers, tetramers, and pentamers. The properties of the final 4cSt, 5cSt and 6cSt PAO products as well as those of the 1- decene and 1-dodecene based references are shown in Tables 1, 2, and 3 below.

The Noack volatility of each product is significantly lower than that of the Clo based reference oil. However, the pour points are higher than those of the corresponding C1o-based reference oils but are well within desired specifications. Both the 1-dodecene based 5cSt and 6cSt PAO's have pour points that do not meet desired specifications.

Example 2.

Similar to Example 1, except that the olefin mixture contained 60 weight percent 1-decene and 40 weight percent 1-dodecene was oligomerized using BF3 promoted with a 3.5: 1 mole ratio mixture of butanol and n-butyl acetate, at a total catalyst concentration of 5.3 weight percent. With the incorporation of more 1- dodecene in the feed mixture, the Noack volatility of each product was further reduced. The pour points are either the same or higher than those of the products made from 70/30 1-decene/1-dodecene mix.

Example 3.

Similar to Example 1, except that the olefin mixture contained 50 weight percent 1-decene and 50 weight percent 1-dodecene was oligomerized using BF3

promoted with a 4: 1 mole ratio mixture of n-butanol and n-butyl acetate at a total catalyst concentration of 1.8 weight percent. Again, the Noack volatility of each product decreased with the increase of 1-dodecene content of the feed mixture.

Table 1: Properties of 4cSt PAO Example No. Feed 100°C Vis.-40°C Vis VI Noack Pour CIO : Ci2 CSt cSt Vol. wt% Point °C Reference A 100: 0 4.10 2850 122 13. 5 <-60 170 : 30 4.10 2899 128 11.7-60 260 : 40 4.09 2680 130 10.6-60 3 50 : 50 4. 15 2930 134 9. 9 Table 2: Properties of 5cSt PAO Example No. Feed 100°C Vis.-40°C Vis VI Noack Pour CIO : C12 CSt cSt Vol. wt% Point °C Reference B 100: 0 5.05 4911 135 8.9 <-56 1 70 : 30 5.10 5272 136 7.7-56 2 60 : 40 5. 00 4520 139 7.5-54 3 50 : 50 5. 00 4346 140 6. 4 Reference C 0: 100 5. 25 4647 148 4. 8-45 Table 3 Properties of 6 cSt PAO Example No. Feed 100°C Vis. -40°C Vis VI Noack Pour CIO : CI2 CSt cSt Vol. wt% Point °C Reference D 100: 0 5.9 7906 138 6.8-59 1 70:30 5.89 7817 140 5.3-56 2 60 : 40 5.90 7400 140 5.0-54 3 50 : 50 5. 86 6607 143 4. 3 Reference E 0 : 100 6. 20 8150 146 4. 0-42 While the invention has been described and illustrated with reference to certain preferred embodiments thereof, those skilled in the art will appreciate that various changes, modifications and substitutions can be made therein without departing from the spirit and scope of the invention.