Patent Application
20050049153
Not applicable.
There is always a need to develop biodegradable lubricants for use in applications which might result in the leakage of such lubricants into the soil and into waterways, such as rivers, oceans and lakes. Base stocks for biodegradable lubricant applications such as two-cycle engine oils, catapult oils, hydraulic fluids, drilling fluids, water turbine oils, greases, gear lubricants, shock absorber fluids, plasticizers, internal lubricants, and the like have to meet increasingly stringent criteria such as enhanced biodegradability, higher viscosity index, better lubricity, better demulsibility, better additive solubility, lower density, etc. than existing lubricants.
One class of compounds that have the potential of meeting the above requirements are complex esters which are polyol esters of dicarboxylic acids and polyols, especially trifunctional polyols. Examples of such polyols are described in U.S. Pat. No. 5,912,214, the entire contents of which are incorporated herein by reference.
However, it has been found that complex polyol esters which contain short chain dicarboxylic acid residues, such as adipic acid, often exhibit diminished biodegradability, demulsibility, lubricity and additive solubility in the higher viscosity (higher average molecular weight) versions. It has also been observed that complex polyol esters which contain longer chain dicarboxylic acid residues such as “dimer” acid (C36-54 difunctional) often exhibit diminished biodegradability and demulsibility in the higher viscosity (higher average molecular weight) versions.
A lubricant base stock is comprised of a complex polyol ester having a polyfunctional alcohol residue and a saturated or unsaturated dicarboxylic acid residue having from about 9 to about 22 carbon atoms. Such esters are high viscosity esters exhibiting improved biodegradability and viscosity index.
Not applicable.
Other than in the operating examples, or where otherwise indicated, all numbers expressing quantities of ingredients or reaction conditions are understood as being modified in all instances by the term “about”.
The term residue, as used herein, means the portion of a polyol or dicarboxylic acid that remains in the polymer after reaction of the polyol or dicarboxylic acid in the esterification reaction.
Polyols which can be used to make the complex esters according to the invention are those having 2 or more hydroxyl groups. Examples of suitable polyols include, but are not limited to, ethylene glycol, propylene glycol, trimethylol propane, neopentyl glycol, pentaerythritol, dipentaerythritol, and glycerol. A particularly preferred polyol for use in the present invention is trimethylol propane.
Suitable saturated or unsaturated diacids which may be employed include those having from about 9 to about 22 carbon atoms. A particularly preferred diacid for use in the present invention is a saturated or unsaturated C18 dicarboxylic acid which can be made from oleic acid by the biooxidation process described in U.S. Pat. No. 5,254,466, the entire contents of which is incorporated herein by reference.
The polyols and diacids are typically employed in a molar ratio of about 0.001-1000: 1, preferably about 0.1-800: 1, and most preferably about 1-500 : 1.
The complex polyol esters according to the invention can be made by the processes described in U.S. Pat. No. 5,912,214, the entire contents of which is incorporated herein by reference. Typically an esterification is carried out in a 4-neck, round bottom flask at 240° C. at atmospheric pressure with overhead stirring, sub-surface nitrogen purge, and a temperature programmed heat source. Water of reaction was drawn off continuously at atmospheric pressure until the reaction was close to completion. Additional water of reaction was drawn off with vacuum at approximately 600 torr. Residual acids were stripped under vacuum at less than 2 torr. Crude esters were produced with an acid value around 3, then optionally refined to an acid value below 0.5 by reaction of the residual acid with a glycidyl ester such as glycidyl neodecanoate. More specifically, an amount of glycidyl ester based on the acid number of the crude ester product is heated to a temperature of about 200° C. for one hour after which the excess glycidyl ester is stripped out of the reaction mixture. The esters according to the invention can also contain mono-carboxylic acid residues and mono-alcohol residues.
The complex polyol esters of the present invention will typically be present in lubricant compositions in an amount of from about 0.1 to about 100% by weight, preferably from about 25 to about 100% by weight, and most preferably from about 50 to about 100% by weight, based on the weight of the lubricant composition.
Various additives may also be employed in the lubricant composition of the present invention. Examples thereof include, but are not limited to, extreme pressure additives, anti-foaming agents, pour point depressants, rust or corrosion prevention agents, oxidation inhibitors, detergents, dispersants, smoke-suppression agents, hydrocarbon diluents, stabilizers, dyes, pigments, and mixtures thereof. These additives, if employed, will typically be present in the lubricant composition in an amount of from about 0.1 to about 90% by weight, preferably from about 0.1 to about 60% by weight, and most preferably from about 0.1 to about 30% by weight, based on the weight of the lubricant composition.
The present invention will be better understood from the examples which follow, all of which are intended for illustrative purposes only, and are not meant to limit the invention in any way.
Complex polyol esters were prepared and tested for the properties set forth in the tables below. The abbreviation diacid C 18:1 stands for an acid which is primarily a mono-unsaturated C18 dicarboxylic acid, specifically Δ-9octadecenedioic acid. The abbreviation diacid C 18 stands for an acid which is primarily a saturated C18 dicarboxylic acid, specifically octadecanedioic acid. The abbreviation diacid C 9 stands for an acid which is primarily a saturated C9 dicarboxylic acid, specifically nonanedioic (azelaic) acid. TMP is trimethylol propane.
As can be seen from the above-disclosed data, complex polyol esters corresponding to the present invention exhibit a significantly improved biodegradability profile as compared to currently available products.
This application claims the benefit of copending provisional application Ser. No. 60/496,535 filed on Aug. 20, 2003
| Number | Date | Country | |
|---|---|---|---|
| 60496535 | Aug 2003 | US |
