Synthetic Base Oils and Discussion from One Perspective

By MolaKule

Section I: Group I through 3 base oils.

In order to set the stage for this discussion, let us first review the basic API Groups of base oils and discuss basic refining and crude oil processing.

Solvent Refining

[Definition of Wax: Wax is a large hydrocarbon molecule that prevents oil from
flowing at colder temperatures; paraffin, a flammable, whitish, translucent, waxy solid consisting of a mixture of saturated hydrocarbons, obtained by distillation from petroleum or shale and used in candles, cosmetics, polishes, and sealing and waterproofing compounds; In chemistry, paraffin is used synonymously with alkane, indicating hydrocarbons with the general formula CnH2n+2].

[Definition of Catalyst: A substance that participates in chemical reactions by increasing the rate of reaction, yet the catalyst remains intact after the reaction is complete].

In the past, two-thirds of the base oil in North America was manufactured using solvent refining. Solvent refined base oils are commonly called Group I base oils which are characterized as those having less than 90% saturates (>10% aromatics) and more than 300 ppm sulfur.

The solvents and hardware used to manufacture solvent-refined base oils have
changed over time, but the basic strategy has not changed since 1930. The two main
processing steps are:

1. Remove aromatics by solvent extraction.
2. Remove wax by chilling and precipitation in the presence of a different solvent.

Aromatics are removed by solvent extraction to improve the lubricating quality
of the oil. Aromatics make good solvents but they make poor quality base oils because
they are among the most reactive components in the natural lube boiling range.

Oxidation of aromatics can start a chain reaction that can dramatically shorten the useful
life of a base oil.

The viscosity of aromatic components in a base oil also responds relatively
poorly to changes in temperature. Lubricants are often designed to provide a viscosity
that is low enough for good cold weather starting and high enough to provide adequate
film thickness and lubricity in hot, high-severity service. Therefore, when hot and cold
performance is required, a small response to changes in temperature is desired.

The lubricants industry expresses this response as the viscosity index (V.I.). A higher V.I.
indicates a smaller, more favorable response to temperature. Correspondingly, many
turbine manufacturers have a minimum V.I. specification for their turbine oils. Base oil
selection is key for meeting this specification because turbine oil additives do not
normally contribute positively to the V.I. in turbine oil formulations.

Aromatics are removed by feeding the raw lube distillate (vacuum gas oil) into a
solvent extractor where it is contacted countercurrently with a solvent. Popular choices
of solvent are furfural, n-methyl pyrrolidone (NMP), and DUO-SOL™. Phenol was
another popular solvent but it is rarely used today due to environmental concerns.
Solvent extraction typically removes 50-80% of the impurities (aromatics, polars, sulfur
and nitrogen containing species).

The resulting product of solvent extraction is usually referred to as a raffinate. The second step is solvent dewaxing. Wax is removed from the oil to keep it from freezing. Wax is removed by first diluting the raffinate with a solvent to lower its viscosity to improve low-temperature filterability.

Popular dewaxing solvents are methyl-ethyl ketone (MEK)/toluene, MEK/methyl-isobutyl ketone, or (rarely) propane. The diluted oil is then chilled to -10 to -20_C. Wax crystals form, precipitate, and are removed by filtration.

Hydrotreating (Predominately Group I)

Hydrotreating was developed in the 1950s and first used in base oil
manufacturing in the 1960s by Amoco and others. It was used as an additional
“cleanup” step added to the end of a conventional solvent refining process.

Hydrotreating is a process for adding hydrogen to the base oil at elevated temperatures
in the presence of catalyst to stabilize the most reactive components in the base oil,
improve color, and increase the useful life of the base oil. This process removed some
of the nitrogen and sulfur containing molecules but was not severe enough to remove a
significant amount of aromatic molecules. Hydrotreating was a small improvement in
base oil technology that would become more important later.

Hydrocracking (Predominately Group II)

Hydrocracking is a more severe form of hydroprocessing. It is done by adding
hydrogen to the base oil feed at even higher temperatures and pressures than simple
hydrotreating. Feed molecules are reshaped and often cracked into smaller molecules.
A great majority of the sulfur, nitrogen, and aromatics are removed. Molecular
reshaping of the remaining saturated species occurs as naphthenic rings are opened and
paraffin isomers are redistributed, driven by thermodynamics with reaction rates
facilitated by catalysts. Clean fuels are byproducts of this process.

Chevron commercialized this technology for fuels production in the late 1950’s. In 1969 the first hydrocracker for Base Oil Manufacturing was commercialized in Idemitsu Kosan Company’s Chiba Refinery using technology licensed by Gulf. This was followed by Sun Oil Company’s Yabucoa Refinery in Puerto Rico in 1971, also using Gulf technology.

Group II base oils are differentiated from Group I base oils because they contain significantly lower levels of impurities (<10% aromatics, <300 ppm S). They also look different. Group II oils are so pure that they have almost no color at all. From a performance standpoint, improved purity means that the base oil and the additives in the finished product can last much longer. More specifically, the oil is more inert and forms less oxidation byproducts that increase base oil viscosity and react with additives.

Catalytic Dewaxing and Wax Hydroisomerization Group III

[Definition: ISODEWAXING™: A patented process developed by Chevron which includes the catalytic hydroprocessing steps of Hydrocracking, Hydroisomerization, and Hydrotreating to produce Group III oils].

The first catalytic dewaxing and wax hydroisomerization technologies were commercialized in the 1970s. Shell used wax hydroisomerization technology coupled with solvent dewaxing to manufacture extra high V.I. base oils in Europe. Exxon and others built similar plants in the 1990s. In the U.S., Mobil used catalytic dewaxing in place of solvent dewaxing, but still coupled it with solvent extraction to manufacture conventional oils.

Catalytic dewaxing was a desirable alternative to solvent dewaxing especially for conventional neutral oils, because it removed n-paraffins and waxy side chains from other molecules by catalytically cracking them into smaller molecules. This process lowered the pour point of the base oil so that it flowed at low temperatures, like solvent dewaxed oils. Hydroisomerization also saturated the majority of remaining aromatics and removed the majority of remaining sulfur and nitrogen species.

Chevron was the first to combine catalytic dewaxing with hydrocracking and hydrofinishing in their Richmond, California base oil plant in 1984. This was the first commercial demonstration of an all-hydroprocessing route for lube base oil manufacturing.

In 1993, the first modern wax hydroisomerization process was commercialized by Chevron. This was an improvement over earlier catalytic dewaxing because the pour point of the base oil was lowered by isomerizing (reshaping) the n-paraffins and other molecules with waxy side chains into very desirable branched compounds with superior lubricating qualities rather than cracking them away. Hydroisomerization was also an improvement over earlier wax hydroisomerization technology, because it eliminated the subsequent solvent dewaxing step, which was a requirement for earlier generation wax isomerization technologies to achieve adequate yield at standard pour points. Modern wax hydroisomerization makes products with exceptional purity and stability due to extremely high degree of saturation. They are very distinctive because, unlike other base oils, they typically have no color.

By combining three catalytic hydroprocessing steps (Hydrocracking, Hydroisomerization, Hydrotreating), molecules with poor lubricating qualities are reshaped into higher quality base oil molecules. Pour point, V.I., and oxidation stability are controlled independently.

All three steps convert undesirable molecules into desirable ones, rather than have one, two, or all three steps rely on subtraction.

Among the many benefits of this combination of processes is greater crude oil flexibility; that is, less reliance on a narrow range of crude oils from which to make high-quality base oils. In addition, the base oil performance is exceptionally favorable and substantially independent of crude source, unlike solvent-refined base oil.

So base oils with a “conventional” V.I. (80-119) are Group II. Base oils with an “unconventional” V.I. (120+) are Group III. Group III oils have also been called unconventional base oils (UCBOs) or very high V.I. (VHVI) base oils.

Modern Group III oils have greatly improved oxidation stability and low temperature performance. Consequently, many group I or II plants are now being upgraded to enable them to make the modern hydroisomerized Group III oils.

Modern Group III oils today can be designed and manufactured so that their performance closely matches PAOs in most commercially significant finished lube applications. .

From a processing standpoint, modern Group III base oils are manufactured by essentially the same processing route as modern Group II base oils. Higher V.I. is achieved by increasing the temperature or time in the hydrocracker. This is sometimes collectively referred to as the “severity.” Alternatively, the product V.I. could be increased simply by increasing the feed V.I., which is typically done by selecting the appropriate crude.

Summary of Section I: So up to this point, we see that Group I to III base oils (excepting GTL, see below) result from a succession of steps defined by the severity of processing and the catalyzation of crude oil. I.e., the “reshaping of molecules via catalytic action.”

Gas-to-Liquid (GTL) base oils:

The API officially considers GTL base oils as Group III or unofficially it has been called, “Group III+.” It is this author’s view that the GTL process results in a “synthesized” oil and should be given a separate API classification as they do PAO, or moved to the Group V classification. A separate, future debate can address this issue and will not be further discussed here in this white paper.

Section II: Synthetic Base Oils group IV and V

[Definition: Chemical Synthesis; the process of constructing complex chemical compounds from selected, simpler ones; it is applied to all types of chemical compounds, but most syntheses are of organic molecules; chemical synthesis involves the combination of two or more selected atoms (or molecules) to make a finished and predictable product].

Since many chemical substances do not occur naturally, or in enough quantity or purity for commercialization, we resort to chemical synthesis to make new products.

For example aspirin is made by synthesis using an esterification reaction. Salicylic acid is treated with acetic anhydride, an acid derivative, causing a chemical reaction that turns salicylic acid’s hydroxyl group into an ester group (R-OH → R-OCOCH3). This process yields aspirin and acetic acid, which is considered a byproduct of this reaction. Small amounts of a specific acid are always used as a catalyst. (See D. R. Palleros, Experimental Organic Chemistry. New York: John Wiley & Sons. (2000) ISBN 0-471-28250-2).

During a chemical synthesis, we refer to the starting materials as the reactants. Think of the reactants as your basic building blocks; they are your atoms (or molecules) that are absolutely required to complete any chemical synthesis reaction. The type of product made varies depending on the reactants.

When the atoms (or molecules) combine, they will form a product. What drives this ability to make a product, using reactants, is a chemical reaction, a process that is driving the formation of a product using different starting materials, or reactants. With chemical syntheses, these processes generally only go in one direction.

A synthetic chemical is then made from the ground up in the laboratory or the chemical processing plant by the process of synthesis, as differentiated from refinement or extraction.

A synthetic base oil is produced from well-defined and carefully chosen chemical compounds and by specific chemical reactions. A molecularly engineered base stock is optimized for viscosity index, pour point, volatility, oxidative stability, flash point, shear stability, and other desirable properties. Classified as API Group IV and Group V base oils.

The use of the word “synthetic” in the lubricants industry has historically been synonymous with polymerized base oils such as poly-alpha olefins (PAOs), Esters, and other synthesized base oils, such as alkylated naphthalenes (AN), which are made from selected starting atoms or molecules.

Some authors have stated that the term “synthetic” was given a special meaning by the lubricants industry because these types of oils were the only components available for high-performance lubricants at that time. This is purely an attempt to obfuscate the issue.

Since PAO and Ester base oils are synthesized base oils, what better phrase to use than, “Synthetic Lubricant?”

Other authors and marketing folks have attempted to further obfuscate the issue by using the word, “Performance,” in advertising media, as if ‘performance” somehow equaled “synthetic.” While Group III base oils approach the characteristics of Group IV base oils, “performance” is not a chemistry term, but rather an ambiguous term used by marketing.

In an attempt to further clarify the issue, finished engine oils (base oils plus additives) are NOT to be placed into any base group, as has been attempted by our beloved and uneducated marketing folks.

In the academia and in the chemical industry the term “synthetic” never meant anything different than the definition given above.

The first commercially viable process for making Group IV PAO was pioneered by Gulf Oil in 1951 using an AlCl3 catalyst. Mobil patented an improved process using a BF3/AlCl3 catalyst in the 1960s.

(See also, https://bobistheoilguy.com/forums/ubbthreads.php/topics/1252107/Synlube_Overview#Post1252107, for a review of Synthetic Lubricants).

[Definition: Polymerization; the process of forming a repeating chain molecule].

[Definition: Monomer; A monomer is a molecule that forms the basic unit for polymers; Monomers may bind to other monomers to. Monomers may be either natural or synthetic in origin and form a repeating chain molecule via a process called polymerization].

[Definition: Oligomers; Oligomers are polymers consisting of a small number (typically under one hundred) of monomer subunits].

[Definition: Oligimerization; a chemical process that converts monomers to macromolecular complexes through a finite degree of polymerization].

[Definition: Olefin; an alkene, or unsaturated hydrocarbon with the general formula CnHn. The simplest olefin is ethylene (ethane) gas, or C2H2].

PAO’s are the workhorses of synthetic and Blend lubricating oils, comprising greater than 45% of the synthetic base oil market.

For PAO synthesis, the starting olefin (see above definition) is 1-Decene, C10H20. 1-Decene is produced by the oligomerization of the simpler ethylene gas molecule. (Again, an oligomer is a molecular complex that consists of a few monomer {mono-molecular) units. For example, Dimers, Trimers, and Tetramers are oligomerss. It is one of the many linear alpha-olefins (LAOs) used in the growth process to finally yield C4 to C70 LAOs.

The 1-Decene becomes a PAO liquid by polymerization (the linking together of monomers) using the Friedel-Crafts process. This process uses a catalyst, specific temperature conditions, and specific pressures to give rise to the higher olefin oligomers, such as the C20 through C70 olefins. (A catalyst is a substance that enhances chemical reactions with very catalyst little being consumed in the process). The degree of polymerization is dependent upon the type of catalyst used. For example, a Boron Triflouride (BF3) catalyst gives low viscosity base stocks from about 2.4 to 8.0 cSt. An Aluminum Trichloride (AlCl3) catalyst will produce higher viscosity PAOs from 10 cSt on up.

The final process in the PAO synthesis is to introduce hydrogen at specific temperatures and pressures to create a fully saturated hydrocarbon. This hydrogenation process enhances the oxidation stability of the PAO.

So the PAO development process is essentially: ethylene gas >> 1-Decene gas >> Catalyzation of gas to a liquid polymer >> Hydrogenation of polymer >> Finished PAO.

Esters are synthesized by the chemical reaction of selected alcohols and acids.

Esters occur naturally in many plant and animal materials. However, virgin plant and animal oils also contain other products that tend to increase oxidation and degradation, and therefore are not suitable for lubricants in their virgin states.

Many plant and animal oils are processed such that after pressing, the acids are separated from the other products. The resulting acids are then reacted with selected alcohols to produce an ester with characteristics and qualities far superior to plant and animal oils.

Ester starting materials are also made from chemicals derived from petroleum refining processes.

(See also, https://bobistheoilguy.com/forums/ubbthreads.php/topics/729310/Esters,_General#Post729310

and,

https://bobistheoilguy.com/forums/ubbthreads.php/topics/1252272/An_Overview_of_Esters_in_Synth#Post1252272 for a review of Esters in synthetic lubricants).

For example, a very useful ester in additive chemistry is the ZDDP molecule, whose function is as an Anti-Wear (AW) and Oxidation Inhibitor (OI). Members of the zinc dialkyldithiophosphate category are substances prepared by reacting phosphorous pentasulfide (P2S5) with one or more primary or secondary C3-C10 branched or linear alcohols to form the phosphorodithioic acid ester. The only exception is the alkaryl dithiophosphate where the alcohol moiety is tetrapropenylphenol. The dithiophosphoric acid ester is further diluted with 10-15 wt-% highly refined lubricating base oil (typical CAS #s 64742-54-7 and 64741-88-4) before it is neutralized with zinc oxide. The oil acts as a solvent in the neutralization reaction, manages the viscosity of the final product and improves consistency. The zinc complex that is formed upon neutralization is not a salt in the traditional sense, since the Zn-S bond is more coordinate covalent in character than ionic. (See, American Chemistry Council Publication 210-144870. There are about 15 versions of ZDDP chemistry. In fact, many other additive chemistries are in ester or esterified forms.

Synthetic Group V base oils include esters (dibasic and polyol), alkylated benzenes (ABs), alkylated napthalenes (ANs), Polyisobutylenes (PIBs), phosphate esters, silicones, PAG’s (especially oil soluble PEGs or OSPs), and other similar synthesized lubricants not including Group IV.

One of the first companies to successfully market a majority ester-based finished oil was the Amsoil Corporation. (Remember, I said, “successfully”). This was a di-ester based finished oil that was formulated and packaged by the Hatco Corporation, a pioneer in the production of a wide range of various ester base oils.

As the price of esters increased, and reached a certain Return-on-Investment (ROI) point, Amsoil and other companies started formulating finished products containing PAO’s with esters and other Group V base oils such as AN’s.

Summary of Section II: While Group III base oils have positive characteristics that approach Group IV and V oils, Groups IV and V are truly synthesized oils using selected starting molecules (the monomer(s)) up to the finished product, with specific and predictable outcomes.

Section III: Discussion, Opinions, and Summary

[Definition: Finished lubricant; a lubricant in which a series of selected base oils have been blended with a performance improvement additive package such that the final product shows definitive improvements over the base oils alone].

Hopefully, the above sections have provided the reader with enough background information so that he or she can now make an informed decision as to what is a synthetic oil and what is not.

However, it is important to note a number of facts about modern finished lubricants.

1) todays finished lubricants are composed of various viscosities of base oils and of various Groups of base oils to exhibit targeted characteristics in specific environments and applications,
2) performance improvement additive packages are different from one specific environment and application to another,
3) it is the complete, overall package and not the specific base oil or oils, that constitute the final quality and performance of that lubricant.

Marketing propaganda and media hype will always attempt to persuade you that a certain product has an advantage over another. This is a simply a fact in terms of competition among manufactures.

Neither the NAD/BBB decision nor the PQIA stamp will solve this chaos. PQIA is going in the right direction but more needs to be done.

However, unless we come to grips with definitive statements and guidelines as to what is a synthetic lubricant is, and what is not, confusion will only continue. Standards’ groups and committees such as the API, SAE, the S.T.L.E., ILMA and others should address the goal of clarification and meet this issue head on.

As for labeling, I would suggest the following labeling standards for base oil percentages using only three categories:

Automotive Full Synthetic Lubricant: 50% Group IV OR 50% GTL WITH the remaining 25% containing any combination of Group V components. Tolerance +, – 10% for improvements in base oil technology.

Automotive Synthetic Blend: 40% of Group II WITH the remaining 35% containing any combination of Groups III, GTL, IV and V. Tolerance +, – 15% for improvements in base oil technology.

Automotive Conventional: 70% Group II WITH the remaining 15% containing any combination of Groups III, GTL, IV and V. Tolerance +, – 20% for improvements in base oil technology.

REFERENCES:

Kramer, D. C., Lok, B. K., Krug, R. R., “The Evolution of Base Oil Technology,” Turbine Lubrication in the 21st Century, ASTM STP #1407, W. R.
Herguth and T. M. Warne, Eds., American Society for Testing and Materials, West
Conshohocken, PA, 2001.

D. R. Palleros, Experimental Organic Chemistry. New York: John Wiley & Sons. (2000).
Freidel-Krafts Process, retrieved from, https://en.wikipedia.org/wiki/Friedel%E2%80%93Crafts_reaction
W. Brown, C. Foot, B. Anderson, Organic Chemistry, Thompson, (2005).
T. Engel and P. Reid, Physical Chemistry, Pearson, (2006).
American Chemistry Council, Various Publications

Esters, in organic chemistry, are compounds formed (along with water), by the reaction of acids and alcohols. Because this process is analogous to the neutralization of an acid by a base in salt formation, esters were formerly called ethereal salts. This term is misleading because esters, unlike salts, are not ionized in solution (see acids and bases).

Esters can be formed from both organic and inorganic acids. For example, the simple ester ethyl nitrate may be obtained from ethyl alcohol and nitric acid (an inorganic acid), and the ester ethyl acetate may be obtained from ethyl alcohol and acetic acid (an organic acid). Another method of preparing esters is to employ not the acid itself but its chloride. For example, ethyl acetate may be prepared by the action of alcohol upon acetyl chloride, the chloride of acetic acid. Another important method of preparation is by the reaction of the silver salts of acids with an alkyl halide (usually iodine). For example, ethyl acetate may be prepared from silver acetate and ethyl iodide.

Esters are broken up by the action of water into their component acids and alcohols, a reaction greatly speeded by the presence of acids. For example, ethyl acetate is broken up into acetic acid and ethyl alcohol. The conversion of an acid into an ester is termed esterification. The reaction between an ester and a metallic base is known as saponification (see soap). When the decomposition of an ester occurs upon its reaction with water, the ester is said to be hydrolyzed.

The esters of organic acids are usually colorless, neutral liquids, pleasant-smelling and generally insoluble in water but readily soluble in organic solvents. Many esters have a fruity odor and are prepared synthetically in large quantities for commercial use as artificial fruit essences and other flavorings and as components of perfumes (see essential oils).

All natural fats and oils (other than mineral oils) and most waxes are mixtures of esters. For example, esters are the principal constituents of beef fat (tallow), hog fat (lard), fish oils (including cod-liver oil), and flaxseed oil (linseed oil). Esters of cetyl alcohol are found in the head oil of the sperm whale, and esters of myricyl alcohol in beeswax. Nitroglycerin, an important explosive, is an ester.

Esters such as amyl acetate (banana oil), ethyl acetate, and cyclohexanol acetate are the principal solvents for lacquer preparations. Other esters, such as dibutyl phthalate and tricresyl phosphate, are used as plasticizers in lacquers. Amyl acetate is employed as odor bait in grasshopper poisons, and several of the formates are good fumigants. Esters also have an important function in organic synthesis.
Esters have important medical uses. Ethyl nitrite is a diuretic and an antipyretic. Amyl nitrite is used in the treatment of asthma and epileptic convulsions as an antispasmodic. Nitroglycerin and amyl nitrite both cause blood-vessel dilation thereby lowering blood pressure. Ethyl chaulmoograte has been used in the treatment of leprosy. Dimethyl sulfate (often used in organic synthesis as a methylating agent) and diethyl sulfate are extremely dangerous in vapor form and must be handled cautiously.

Many additives are in the form of esters when added to the formulated oil, but carboxylic acid esters (and the sub-classes di-esters and polyol esters) are contained in fully formulated synthetic oils. Most Group III oils and PAO based oils need a small amount of ester for seal swell, increased detergency, better oxidative stability, greater VI, and increased additive solubility.

The two most common polyol esters for automotive applications are TMP (trimethylpropane) and DPE (DiPentaerythritol) PE (Pentaerythritol) or similar. Some di-esters are used in non-detergent compressor fluids, and NEO-Oil uses these as bases exclusively.

There are over 175 di-esters and over 250 polyol esters of last count.

A good overall description of esters for ester lubricating fluids can be found at:
http://www.hatcocorporation.com/pages/about_esters.html

Added: Carboxylic Acid Esters

Esters are created by a process called, “esterification,” the reaction of alcohols or phenols with acids. For example, react tricresyl phosphate acid with an alcohol called n-butyl alcohol and the result is an ester product called “Neutra,” a fuel system and crankcase cleaner.

A carboxylic acid is a general term for a number of acids with a specific molecular arrangement. A carboxylic ester can be made with one of over 120 carboxylic acids. Carboxylic acids may be used to form dibasic esters (as in NEO base oils)and polyol esters such as TMP and PE, which are used in Amsoil and Redline oils, respectively.

Hydroxyalkyl Carboxylic ester is actually a “lactone,” a cyclic ester made from the salt of a hydroxy acid.

This ester is used in many motor oil formulations that contain PAO(s) and is used to increase the VI, cause a slight seal swell, adds miscibility (mixibility) for additives, increases oxidative stability, and acts as a Friction Modifier.

The relative molecular mass (sometimes called “Molecular Weight”) is the ratio of the average mass per molecule of an element or compound TO 1/12 the mass of a carbon-12 atom. I.E., it is equal to the SUM of relative atomic masses of ALL atoms that comprise a molecule.

Generally speaking, the higher molecular weight products of an oil show higher viscosities, but that only half of the story since the molecular “structure” also affects the molecular weight. Take the VII molecules of polymthylacrylates. These are high molecular weight structures that cause the formulated oil to become more viscous as temperature rises because of uncoiling at higher temperatures.

Ester may contain high or low molecular weight components as well, and may have KV’s of 2 cST to over 100 cSt at 100 C. In esters, the structures are more important than molecular weight (except of course in determining final base viscosity).

When developing esters, particular attention is paid to ester structure. Short linear chains show better oxidative stability, whereas increasing the acid chain length of the molecule improves (decreases) the coefficient of friction.

This why Di- and Pentaerithyritol esters (PE’s) are better (more stable) than Trimethylpropane (TMP) esters, and why TMP is better than Neopentylglycol (NPG) esters. The PE’s have short chains of linear acid chains with make the ester more oxidatively stable and exhibit lower coefficients of friction.

If the ester is made from linear branched acids, the ester has higher flash points; increasing the molecular weight (making the ester molecule more compact) will also increase the flash point.

Representative esters:

Phthalates – Used mainly in air compressors; short fat molecule results in VI v.s pour point tradeoff.

Trimellitates – Short, branched esters that have high flash points and low volatilities and good thermal stability. Used when you need to leave a soft film behind.

Dimerates – Made from the acid of tallow oils and an alcohol (is three-branched); Has excellent lubricity and thermal and oxidative stability; used mainly in 2-stroke oils.

Polyols – SPE’s, PE’s, TMP’s, TME’s, and NPG’s. Three or more shortchain but fat molecules. Polyols are generally more oxidative and thermally stable by 50 C over diesters and 150 C over petroleum oils. These esters have lower coefficients of friction than either diesters or PAO’s.

By adding a polyol ester at least 5-10% to a PAO or mineral oil reduces base oil friction remarkably. So esters are natural Friction Modifiers.

Advanced esters can also BE USED AS VII improvers. Unlike long-chain polymers (such as methacrylates), complex polyols do NOT EXHIBIT the temporary loss of viscosity under forces exerted by shear, as in gears. Because complex esters are shorter chain molecules, they tend not to shear into smaller molecules.

Adding amine “backbones” to ester molecules allows them to have better antioxidant capabilities.

Here are some very useful esters used in motor oils and gear lubes:

1. PHOSPHORODITHIOIC ACID, O,ODI-C1-14-ALKYL ESTERS, ZINC SALTS 68649-42-3

Also known as ZDDP

2. 2-ETHYLHEXYL SEBACATE 122-62-3

Used as a seal swell agent, base oil, and friction modifier.

Here’s another useful multifunctional ester:

1. PHOSPHORODITHIOIC ACID, O,OBIS(
2-ETHYLHEXYL) ESTER,
MOLYBDENUM COMPLEX 72030-25-2

Soluble Moly complex, AW/EP and antioxidant

Excellent point Primus.

Bio oils are indeed “natural” esters, which interest me very much as well, and presents an exciting way of weaning ourselves off petroleum-based feed stocks.

The term or prefix Bio or Bio-oil usually denotes an oil derived from living organisms, sch as plants or animals.

Some plant derived Bio-oils which may be used as lubricants are: {This list is NOT all inclusive since new bio-oils useful for lubrication are being discovered every day].

Peanut
Corn
Sesame
Soyabean
Walnut
Macadamia
Grapeseed
Sunflower
Canola (rapeseed)
Castor
Jojoba
Palm
Crambe
Coconut

BTW, canola is the term for genetically modified rape seed.