Method for removal of oder from poly alpha-olefins

Abstract
This invention provides a facile method for removing odor-causing species from lubricants. In this method, such species are removed by contacting the lubricant composition with at least one zeolite. Preferred zeolites include the type 13X Molecular Sieve, i.e., Na86[(AlO2)86(SiO2)106].276 H2O.
Description


FIELD OF THE INVENTION

[0001] This invention belongs to the field of synthetic lubricants. More particularly, this invention relates to a method for removing odor from synthetic lubricants derived from poly α-olefins.



BACKGROUND OF THE INVENTION

[0002] Poly α-olefins comprise one class of synthetic hydrocarbon lubricants which have achieved importance in the lubricating oil market. These materials are typically produced by the polymerization (the term “oligomerization” is often use for the lower molecular weight products which are used as low viscosity basestocks) of α-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. Pat. No. 4,956,122 and the patents referred to therein. The poly α-olefin (PAO) products may be obtained with a wide range of viscosities varying from highly mobile fluids of about 2 cSt at 100° C. to higher molecular weight, viscous materials which have viscosities exceeding 100 cSt at 100° C. The PAO's are conventionally produced by the polymerization of olefin feed in the presence of a catalyst such as AlCl3, BF3, or BF3 complexes. Processes for the production of PAO lubricants are disclosed, for example, in the following patents: U.S. Pat. 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 bromine number of the lubricant is reduced from typical values of about or higher for low viscosity PAO's and 5 to 15 for high viscosity PAO's to a value of not more than about 2 or even lower.


[0003] Low viscosity PAO's (i.e., 2-10 cSt at 100° C.) generally contain odor-causing species which are believed to be low boiling oxygenates. This odor problem in low viscosity PAO's renders these lubricants unacceptable for use in many applications. A typical method for removal of such odor-causing species is steam distillation.



SUMMARY OF THE INVENTION

[0004] This invention provides a facile method for removing odor-causing species from lubricants. In this method, such species are removed by contacting the lubricant composition with at least one zeolite. Preferred zeolites include the type 13X Molecular Sieve, such as that sold by UOP, Inc., and W. R. Grace, i.e., Na86[(AlO2)86(SiO2)106].276 H2O, as well as the type 4A Molecular Sieve, Na12(AlO2)12(SiO2)12.27 H2O



DETAILED DESCRIPTION OF THE INVENTION

[0005] The present invention provides a method for removing odor-causing species from a lubricant composition, which comprises contacting said composition with at least one zeolite.


[0006] In the practice of the invention, it is preferred that the zeolite utilized is a Molecular Sieve of Type 4A or 13X. Especially preferred is Molecular Sieve of Type 13X, in the form of beads of clay/zeolite blends of a diameter of {fraction (1/16)} to ⅛ inch. In the examples below, a bed of Molecular Sieves of diameter of {fraction (1/16)} inch were placed in a glass column of a diameter of about 1 inch, and the lubricant composition fed to the bottom of the column under sufficient pressure to move the material to the top of the column where it was removed. While the present invention contemplates the feeding of the lubricant composition to either the top or bottom of such a column, it is preferred that it be fed from the bottom in order to minimize or eliminate channeling within the packed Molecular Sieves.


[0007] It is further preferred that the lubricant composition be contacted with such zeolites at a temperature of about 40° F. to 130° F., most preferably 70° F. to 100° F., and at pressures of about 0 psig to 5.0 psig, most preferably 0 psig to 2.0 psig.


[0008] In a further aspect of the invention, there is provided a method for removing odor-causing species from a lubricant composition which comprises feeding said lubricant to a column packed with Type 13X Molecular Sieve or Type 4A Molecular Sieve, preferably Type 13X, at a temperature of about 40 to 130° F., preferably about 70° F. to 100° F., at a pressure of about 0 psig to 5.0 psig, preferably about 0 psig to 3.0 psig, for an average residence time of about 0.15 hours to 3.5 hours. In a preferred embodiment, the lubricant composition is comprised of at least one poly α-olefin derived lubricant having a viscosity of from about 2-10 cSt at 100° C. In a further preferred embodiment, the temperature is about 70° F. to about 95° F., and the pressure is about 0 psig to about 2.0 psig. In the practice of this aspect of the invention, it is further preferred that the average residence time in said column is about 1.0 hour to about 3.5 hours, most preferably about 1.5 hours to about 2.0 hours.


[0009] Once utilized according to the method of the present invention, the Molecular Sieves may be regenerated by utilizing the following procedure which was utilized in the examples below:


[0010] 1. The Molecular Sieves are regenerated at 660 F for 2.5 hours at lmm Hg absolute pressure.


[0011] 2. A N2 purge at 5 cc/minute (100 cc bed) is sent through the bed for 30 minutes at 660° F.


[0012] 3. The heat is turned off and N2 purge continued to cool the bed to room temperature.


[0013] 4. The amount of oil recovered from the sieves during regeneration is ˜20 grams.







EXPERIMENTAL SECTION


Example 1

[0014] 2 cSt PAO was treated over a 100 cc volume of 13X molecular sieve bed, packed in a glass column, at temperatures from 50° F. to 95° F. and at liquid hourly space velocities (LHSV's) ranging from 3.0 to 6.0 hours. Table-1 compares molecular sieve treatment to the industry accepted steam distillation for odor removal.
1TABLE 1ProductTreatmentOdor Level2 cSt PAONone5 (strong odor)2 cSt PAOSteam distillation0 (No odor)2 cSt PAOMolecular Sieve0 (No odor)


[0015] Table-2 compares the effect of residence time on the adsorption capacity of molecular sieves. The longer the residence time the higher the capacity in grams of oil processed with zero odor.
2TABLE 2LHSVOdorBed Life: GramsProduct(hours)TemperatureLevelOf Oil Processed2 cSt PAO6.077° F.060292 cSt PAO3.077° F.08816



Example 2

[0016] 4 cSt PAO was treated over a 100 cc volume of 13X molecular sieve bed, packed in a glass column, at temperatures from 50° F. to 95° F. and at liquid hourly space velocities ranging from 1.8 to 3.0 hours. Table-3 compares molecular sieve treatment to the industry accepted steam distillation for odor removal
3TABLE 3ProductTreatmentOdor Level4 cSt PAONone5 (strong odor)4 cSt PAOSteam distillation0 (No odor)4 cSt PAOMolecular Sieve0 (No odor)


[0017] Table-4 compares the adsorption capacity of 13X molecular sieves as a function of residence time for 4 cSt PAO. The adsorption capacity increases with the higher residence time.
4TABLE 4LHSVOdorBed Life: GramsProducthoursTemperatureLevelOf Oil Processed2 cSt PAO6.077° F.060292 cSt PAO3.077° F.08816



Example 3

[0018] 6 cSt PAO was treated over a 100 cc volume of 13X molecular sieve, in a glass column, bed at temperatures from 50° F. to 95° F. and at liquid space velocities ranging from 0.6 to 3.0 hours. Table-5 compares Molecular Sieve treatment to the industry accepted steam distillation for odor removal.
5TABLE 5ProductTreatmentOdor Level6 cSt PAONone5 (strong odor)6 cSt PAOSteam distillation.0 (No odor)6 cSt PAOMolecular Sieve0 (No odor)


[0019] Table-6 compares the adsorption capacity of 13X molecular sieves as a function of residence time for 6 cSt PAO. The adsorption capacity increases with the higher residence time.
6TABLE 6LHSVOdorBed Life: GramsProducthoursTemperatureLevelOf Oil Processed6 cSt PAO3.077° F.07656 cSt PAO1.877° F.013206 cSt PAO0.677° F.02400


[0020]

7





TABLE 7










6 cSt Deodorization Using 13X Molecular Sieve Packed Column

















Oil

Ratio






Absorbed

PAO:Mol




Total

in Molecular

Sieve



Temp
Flow
LHSV
Sieve
%
Weight


Run #
F.
gms
(hours)
(grams)
Loss
Basis
















PureSyn ® 6*








1
95
1638
0.6
50.9
3.1
27.25


2
77
2263
0.6
46.9
2.1
38.1


3
50
2564
0.6
29.6
1.15
41.0






*PureSyn ® 6 is a C10 based 6cSt PAO sold by ExxonMobil Chemical.




Note:




Run numbers 1 and 2 could have been extended to give total throughput close to 2500 grams. We believe that these experiments were prematurely terminated. The end of run is when a distinct odor is detected on repeated smelling.








[0021]

8





TABLE 8










2 cSt Deodorization Using 13X Mol Sieve Packed Column




















Ratio







Oil

PAO






Absorbed

Mol




Total

in Mol

Sieve


Run
Temp.
Flow

Sieve
%
Weight


#
° F.
gms
LHSV
gms
Loss
Basis
Comments





1
95
9360
3.0
33.0
0.35
139.7



2
77
8816
3.0
33.2
0.37
137.8


3
50
8500
3.0
33.0
0.39
133.0


4
77
8696
3.0
25.0
0.29
127.5
One









regenera-









tion


5
77
8326
3.0
28.0
0.33
128.0
Two









regenera-









tions


6
77
8300
3.0
27.8
0.33
126.0
Three









regenera-









tions










[0022]

9










TABLE 9












Bed Life:
Ratio






Grams of
PAO:Mol



LHSV

Odor
Oil
Sieve


Product
(hours)
Temperature
Level
Processed
Weight Basis







2 cSt PAO
6.0
77° F.
0
6029
 97:1


2 cSt PAO
3.0
77° F.
0
8816
142:1


2 cSt PAO
1.5
77° F.
0
12300 
198:1










[0023]

10










TABLE 10












Bed Life:







Grams of
Ratio PAO



LHSV

Odor
Oil
Mol Sieve


Product
(hours)
Temperature
Level
Processed
Weight Basis







4 cSt PAO
3.0
77° F.
0
 900
14.5:1


4 cSt PAO
1.8
77° F.
0
3400
  55:1










[0024]

11










TABLE 11












Bed Life:
Ratio






Grams of
PAO:Mol.



LHSV

Odor
Oil
Sieve


Product
(hours)
Temperature
Level
Processed
Weight Basis







6 cSt PAO
3.0
77° F.
0
 765
12.3:1  


6 cSt PAO
1.8
77° F.
0
1320
21:1


6 cSt PAO
0.6
77° F.
0
2400
39:1










[0025]

12





TABLE 12










Effect of In-Situ Regeneration On Bed Life


2 cSt PAO*


















Oil Ab-

Ratio







sorbed

PAO:Mol




Total

in Mol

Sieve


Run
Temp.
Flow

Sieve
%
Weight
Com-


#
° F.
(Grams)
LHSV
Gms
Loss
Basis
ments*





1
77°
8816
3.0
33.2
0.37
137.8
Base









Case


2
77°
8696
3.0
25.0
0.29
127.5
One









regen-









eration


3
77°
8326
3.0
28.0
0.33
128.0
Two









regen-









erations


4
77°
8300
3.0
27.8
0.33
126.0
Three









regen-









erations






*(Regeneration At 650° F. and full vacuum)








Claims
  • 1. A method for removing odor-causing species from a lubricant composition, which comprises contacting said composition with at least one zeolite.
  • 2. The method of claim 1, wherein said zeolite is a Type 4A or Type 13X Molecular Sieve.
  • 3. The method of claim 1, wherein said zeolite is a Type 13X Molecular Sieve.
  • 4. The method of claim 2, wherein said Molecular Sieve has been pre-treated by heating at a temperature of at least about 300° F. and a pressure of less than about 3 psig for a period of time sufficient to remove traces of water.
  • 5. The method of claim 1, wherein said lubricant composition is comprised of a 2-10 cSt poly α-olefin derived lubricant.
  • 6. A method for removing odor-causing species from a lubricant composition which comprises feeding said lubricant to a column packed with Type 13X Molecular Sieve at a temperature of about 40° F. to 130° F., at a pressure of about 0 psig to 5 psig, for an average residence time of about 0.15 hours to 3.5 hours.
  • 7. The method of claim 6, wherein said lubricant composition is comprised of at least one poly α-olefin derived lubricant having a viscosity of from about 2-10 cSt at 100° C.
  • 8. The method of claim 6, wherein the pressure is about 0 psig to about 3.0 psig.
  • 9. The method of claim 6, wherein the residence time is about 1 hour to about 3.5 hours.
  • 10. The method of claim 6, wherein the temperature is about 70-100° F.
  • 11. The method of claim 6, wherein the temperature is about 70 to 95 F and the residence time is abut 1.5-2.0 hours.