CA1139295A

CA1139295A - Rotary screw compressor lubricants

Info

Publication number: CA1139295A
Application number: CA000347784A
Authority: CA
Inventors: Robert Carswell
Original assignee: Dow Chemical Co
Current assignee: Dow Chemical Co
Priority date: 1979-04-02
Filing date: 1980-03-17
Publication date: 1983-01-11
Also published as: AU5670880A; JPS55133489A; JPH0329837B2; DE3064007D1; EP0017072B1; AU536786B2; EP0017072A3; EP0017072A2

Abstract

ABSTRACT OF THE DISCLOSURE
Synthetic lubricants containing (A) 15 to 45 weight percent of an ester of a hindered polyhydric alco-hol having 3 to 6 hydroxy groups and 5 to 10 carbon atoms with one or more alkanoic acids having 4 to 18 carbon atoms blended with (B) 85 to 55 weight percent of one or more polyoxyalkylene glycols or their mono- or dialkyl ethers having a 400-5000 number average molecular weight.
The blends are compounded with antioxidants, corrosion inhibitors, and metal deactivators to produce a superior lubricant for rotary screw compressors that has a long life.

Description

2r~

WATER-RESISTANT LUBRICANT FOR
COMPRESSORS AND MARINE ENGINES

This invention relates to water-resistant l~bricants for compressors and marine engines, especially for use in rotary screw compressors.

Rotary screw air compressors are well-known in the art as can be seen from U.S. Patent 3,073,513, issued to Bailey, January 15, 1963.

It is well-known to use hydrocarbon lubricat-ing oils to seal the rotors of the foregoing rotary screw air compressors, lubricate the bearing and cool the com-pressed gases. Due to the high temperature and pressureof the air, it has be~n found that these hydrocarbon oils break down and create a sludge in a relatively short time, i.e., about 1000 hours or less.

In attempts to increase the intervals between changes of the lubricants, silicone fluids have been used.
However, these fluids are very expensive and represent a considerable capital investment because a new compressor unit with different bearings and seals is required.

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-2-It is known that synthetic esters made from dicarboxylic acids have been used in an attempt to develop a relatively inexpensive and long-lasting lubricant. How-ever, it has been found that these synthetic esters are not hydrolytically stable, and therefore do not have the long life required for use in air compressors.

Synthetic lubricants comprising a major amount of a po]yester and a minor amount of a monocapped poly-glycol are known from British Patent 1,162,818, I.C.I., August, 1969. However, these compositions are disclosed to be only useful in aircraft gas turbines where gross contamination with water is not a problem.

It now has been found that a suitably inhib-ited blend of hindered alkanoic esters of aliphatic poly-~5 hydric alcohols having 3 to 6 hydroxyl groups and 5 to10 carbon atoms with polyoxyalkylene glycols and their mono or dialkyl ethers has the required high temperature viscosity and stability to oxygen and water.

The present invention is a lubricant composi-tion characteri~ed in that it contains - (A) 15 to 45 weight percent of an ester of a hindered polyhydric alcohol having 3 to 6 hydroxyl groups and from 5 to 10 carbon atoms with one or more alkanoic acids having 4 to 18 carbon atoms, and (B) 85 to 55 weight percent of one or more compositions having a flash point greater than 191C
and having the formula R--(O-CH2-CH)n--OR

3~ R' 27,947-F ~2-4Y~5 where R is hydrogen or an alkyl group of 1-6 carbon atoms, R' is hydrogen or methyl, and n is a number having an average value which will give a molecular weight range from 400 to 5000.

An additional aspect of the present invention comprises the above base lubricant with the addition of effective amounts of oxidation inhibitors, corrosion inhibitors, and metal or copper deactivators.

While the lubricants of this invention are use-ful in rotary screw, sliding vane, and reciprocation pis-ton compressors, they are also useful in other mechanical devices where hydrolytic stability is desired or necessary, such as outboard motors or marine engines in general.

The combination of the foregoing polyoxyal-kylene glycols and esters with and without additives can also find utility in industry for other lubricating appli-cat.ions, such as mold release agents, lubricants for glass making machinery, gears, gasoline or diesel engines, tex-tile machinery, fiber lubricants and metal working fluids.

The neutral esters used in this invention are commercially available. Examples of suitable hindered esters are esters of trimethylol ethane with alkanoic acids of 4-18 carbon atoms, esters of trimethylol pro-pane with alkanoic acids of 4-18 carbon atoms, esters of trimethylol butane with alkanoic acids of ~-18 carbon atoms, and esters of pentaerythritol or dipentaerythritol with alkanoic acids of 4-18 carbon atoms.

27,947-F -3-Specific examples of these esters are tri-methylolethane tricaproate, trimethylolpropane trivaler-ate, trimethylolpropane tri n-heptanoate, trimethylolpro-pane tripelargonate, trimethylolpropane tricaprate, pen-taerythxitol tetracaproate, dipentaerythritol hexabuty-rate, pentaerythritol tetrastearate and the related esters with mixed acid moieties.

Examples of the polyoxyalkylene glycols used in this invention are those derived from ethylene, propyl-ene, 1-2, or 2-3 butylene oxide. The above oxides may be polymerized alone or in combination. The combined oxides may also be combined in a random or block addition. While some of the above compounds may be of a hydrophyllic nature, those of a hydrophobic nature are preferred, such as those derived ~rom propylene oxide, butylene oxides or combinations thereof.

Examples of suitable capped polyoxyalkylene glycols are those derived from ethylene, propylene, and butylene oxides wherein the alkylene oxides are initiated from monofunctional alkanols having 1-6 carbon atoms in a known manner. The above monoalkyl ethers of polyoxyalkyl-ene glycols can be further modified in a known manner to give the dialkyl ethers.

The foregoing glycols should have a flash point greater than 191C and preferably greater than 232C. They also should have a number average molecu-lar weight range from about 400 to 5000 and preferably in the range 700 to 2500.

27,947-F -4-The foregoing esters and glycols are blended to give a base lubricant composition containing 15 to 45 wei~ht percent of the esters and ~5 to 55 weight percent of the glycol with the ranges 22 to 35 and 78 to 65 being the preferred ranges, respectively.

The compositions of this invention are selected so as to have a viscosity in the range of 5 to 25 centi-stokes at 99C and preferably 6 to 16 centistokes at 99C
and a pour point in the range of -17.8~ to -54C.

1~ The final lubricant compositions of this invention contain effective amounts of conventional anti-oxidants, corrosion inhibitors and metal or copper deac-tivators.

Examples of useful antioxidants which can be used herein are phenyl naphthylamines, i.e., both alpha-and beta-naphthyl amines, diphenyl amine, iminodibenzyl, p,p'-dioctyl-diphenylamine, and related aromatic amines.
Other suitable antioxidants are hindered phenolics such as 6-t-butyl phPnol, 2,6-di-t-butyl phenol and 4-methyl--2,6-di-t-butyl phenol.

Examples of suitable corrosion inhibitors are the metal sulfonates such as calcium petroleum sulfonate, barium dinonylnaphthalene sulfonate and basic barium dinonylnaphthalene sulfonate (carbonated or noncarbonated).

Examples of suitable N-heterocyclic metal or copper deactivators are imidazole, benzimidazole, pyra-zole, benzotriazole, tolutriazole, 2-methyl benzimidazole, 3,5-dimethyl pyrazole, and methylene bisbenzotriazole.

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An effective amount of the foregoing addi-tives is generally in the range from 0.1 to 5.0 percent by weight for the antioxidants, 0.1 to 5.0 percent by weight for the corrosion inhibitors, and 0.001 to 0.5 percent by weight for the metal deactivators, all percen-tages being based on the total weight of the esters and the glycols. It is to be understood that more or less of the additives may be used depending upon the circum-stances ~or which the final composition is to be used.

The following examples illustrate the inven-tion.

Example 1 The following composition was prepared.

175 Pounds (79.4 kg) polyprop~lene glycol (number average molecular weight 1200), 75 pounds (34.0 kg) pentaerythritol tetraester o~ alkanoic acids, 3.75 pounds (1.70 kg) p,p'-dioctyl diphenylamine, 1.25 pounds (0.57 kg) basic barium dinonylnaphthalene sulfonate in mineral oil, and 0.125 pound (0.28 kg) benzotriazole.

The polyglycol and the ester were weighed into a 30 U.S. gallon (114 l) stainless steel mixing vessel, equipped with a paddle stirrer and a controllable electric heating element. The temperature was raised to 45-55C
with stirring. The additives were then weighed in, in the order given above.

The above 25 U.S. gallon (94.5 1) mixture was allowed to sti~ with the heating maintained at 45-55C
until a clear solution was obtained. A clear light brown 27,947~F -6 solution was obtained and was drained from the mixing ves-sel by opening a valve situated in the base of the vessel.
The blend was collected into 5 U.S. gallon (1.89 l) con-tainers. The fluid was retained for testing as described in the following manner. This example illustrates the preparation of a blend of 70 weight percent polyglycol and 30 weight percent of a polyester.

50 Grams of fluid prepared above was sealed in a rotary bomb and tested for oxidation resistance in accordance with A~erican Society for Testing Materials (ASTM) Test D-2272. The fluid gave 18.5 hours in the oxidation test.

It is to be noted in this example and the fol-lowing examples that the number of hours in the oxidation test can vary about two hours over and under the given numbers because the test procedure is not exactly repro-ducible.

300 ml of the above fluid was tested for cor-rosion resistance in accordance with ASTM Test D-665 (pro-cedure A). The fluid passed the test.

Four and one-half U.S. gallons (17.0 1) of the above fluid was placed in a 100 cubic feet (2.83 m3) per minute rotary screw air compressor and the compressor was run for 6000 continuous hours with periodic shutdowns at 1000-hour intervals to take a 4-ounce (113 g) sample for analysis. Four ounces (113 g) of new fluid replaced the withdrawn sample. The test was terminated at 6000 hours due to a breakdown of the compressor which was not asso-ciated with the lubricant. Upon examination the fluid 27,947-F 7-~8~

withdrawn from the compressor was found to be in exc~l-lent condition. Similar results will be obtained with the corresponding dibuty~ ether or butyl ether of poly-propylene glycol having a similar molecular weight.

Example 2 Following the procedures set forth in Example 1, a blend of 76 weight percent of the polypropylene glycol and 24 weight percent of trimethylolpropane tripelargonate was prepared with the same percentages of the additives.
This formulation when tested by the above oxidation test gave 16 hours and 50 minutes and passed the corrosion test.

Example 3 Following the procedures set forth in Exam-ple 1 with the same additives, a blend of 20 weight per-cent of the polypropylene glycol and 80 weight percentof a trimethylolpropane fatty acid ester was prepared.
This formulation gave 15 hours and lO minutes in the above oxidation test and passed the corrosion test.

Controls 1-3 Following the oxidation test of Example 1, a hydrocarbon lubricant (Control #l), a petroleum oil (Con-trol #2) and a synthetic fluid based on a dicarboxylic acid ester (Control #3) were tested. The above three lubricants have been recommended for use in rotary screw compressors by lubrication engineers. The results are shown in Table I.

27,947-F -8-~9_ TABLE I

Control Oxidation Test 1 2 hours 12 minutes 2 1 hour 5 minutes 3 9 hours 50 minutes From the foregoing, it is indicated that lubri-cating oils have a relatively short life span and that while dicarboxylic acid esters are better than lubricating oils they are less effective than the compositions of this invention. Furthermore, the compositions containing tri-methylolpropane esters of Example 2 are vastly improved over the known esters of Control 3. Likewise, the compo-sitions containing esters of Example 1 are even more improved over Example 2 and Control 1.

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Claims

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS.

1. A lubricant composition characterized in that it contains (A) 15 to 45 weight percent of an ester of a hindered polyhydric alcohol having 3 to 6 hydroxyl groups and from 5 to 10 carbon atoms with one or more alkanoic acids having 4 to 18 carbon atoms, and (B) 85 to 55 weight percent of one or more compositions having a flash point greater than 191°C
and having the formula where R is hydrogen or an alkyl group of 1-6 carbon atoms, R' is hydrogen or methyl, and n is a number having an average value which will give a molecular weight range from 400 to 5000.

2. The lubricant composition of Claim 1 and further characterized in that the weight percent of the ester ranges from 22 to 35 and the weight percent of the glycol ranges from 78 to 65.

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3. A lubricant composition characterized in that it contains (A) 15 to 45 weight percent of an ester of pentaerythritol with one or more alkanoic acids hav-ing 4 to 18 carbon atoms, and (B) 85 to 55 weight percent of one or more polyoxyalkylene glycols having a flash point greater than 191°C and having a number molecular weight range from 700 to 2500 and mixtures thereof.

4. The lubricant composition of Claim 3 and further characterized in that the weight percent of the ester ranges from 22 to 35 and the weight percent of the polyglycol ranges from 78 to 65.

5. The lubricant composition of Claim 4 wherein the glycol is polypropylene glycol having a number average molecular weight of 1200.

6. The lubricant composition of Claim 5 which comprises 30 weight percent of said ester and 70 weight percent of said polypropylene glycol.

7. The composition of Claim 1 and further characterized in that it also contains (A) an effective amount of an antioxidant, (B) an effective amount of a ferrous metal corrosion inhibitor, and (C) an effective amount of a metal deacti-vator.

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8. The composition of Claim 1 and further characterized in that it also contains (A) 0.1 to 5.0 weight percent of an aromatic amine antioxidant, (B) 0.1 to 5.0 weight percent of a metal salt of an aromatic sulfonic acid, and (C) 0.001 to 0.5 weight percent of a N-hetero cyclic metal deactivator.

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