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Understanding Oxidation: The Basis for Antioxidant Use

When speaking about antioxidants, the first thing that comes to mind is oxidation. This is the primary reason that antioxidants exist: to reduce oxidation. But what is oxidation, and why should there be antioxidants?

Oxidation occurs in everything in life (not just finished lubricants). We see oxidation regularly when we leave certain fruits exposed to the atmosphere (think about cut pears or apples). After being in the elements for some time, they are no longer fresh and have degraded slightly.

A similar reaction occurs during the oxidation of finished lubricants. Greg Livingstone provides an excellent summary of the oxidation process in his article, “Varnish, Deposits in Bearings, Causes, Consequences, and Cures.” The oxidation degradation pathway begins with initiation, where free radicals are formed in the presence of heat, wear metals, water, and oxygen as shown in Figure 1.

Afterward, during propagation, the free radicals form hydroperoxides, which can create oxidation by-products (Alkoxy radicals), eventually leading to high molecular weight oxygenated by-products.

During this process, the free radicals can also react with primary antioxidants, or the hydroperoxides can react with secondary antioxidants to slow these reactions. However, they will still form the high molecular weight oxygenated by-products once depleted.

Next in the termination phase is polymerization and agglomeration, followed by the physical and chemical changes to the lubricant. It must be noted that there are various stages to oxidation, and typically, when we see sludge or varnish, oxidation has already occurred.

Figure 1: Summary of the oxidation process.
Figure 1: Summary of the oxidation process.

When oxidation occurs, the oil quickly loses its antioxidants; they can no longer protect the oil. As such, the oil begins to undergo physical changes where sludge and varnish appear, and viscosity usually increases. These oils also experience a rise in acid production after these reactions occur.

Now that we have a better understanding of oxidation, whereby the antioxidants are deployed to help reduce the oxidation rate, we can dive deeper into the world of antioxidants and how they can help fight against oxidation for the finished lubricant.

Want to read the entire article? Find it here in Precision Lubrication Magazine!

Determining the Root Causes of Oxidation in Lubricants

Finally, we’ve arrived at the point where we can effectively determine the root cause. It is critical that the analyst understands oxidation and has knowledge of the evidence needed before embarking on the root cause journey. As noted in the first part of this article, the question we should ask is, “How could?”.

We hypothesize that oxidation is occurring. In a complete root cause analysis, we should hypothesize the occurrence of all the degradation mechanisms and eliminate them with evidence-based data.

There are two main ways in which oxidation can occur either through the presence of oxygen and temperature over the normal operating temperature of the system or if there is a less-than-adequate presence of antioxidants.

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If we follow our line of questioning with the presence of oxygen and temperature and again ask, “How could?” we can get two primary responses. Either there was an air leak in the system, or the system was being pushed beyond its operating limits.

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If we further investigate the air leak into the system, we ask, “How could it?” again. There are two main ways: either there are damaged components, or a less-than-adequate system design allows air to enter the system.

If we follow the pathway of investigating “how could” the system be pushed beyond its operating limits, then we can come up with two hypotheses. Either an increase in production was required, or there was a malfunction of the components, which caused strain on the other components.

Both of these hypotheses are physical and can be investigated further, but we will focus on the lubricant aspect of this article. Hence, we will follow the questioning surrounding the less-than-adequate presence of antioxidants.

We begin with the question, “How could we have a less-than-adequate presence of antioxidants?”. From the information gathered in this article, we know this can result from free radicals or less than adequate lubricant specifications.

We will investigate the “Presence of free radicals” first.

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“How could we have the presence of free radicals?” Free radicals can emerge as a result of chemical reactions.

“How could these chemical reactions produce free radicals?” There are two main ways in which this can occur. Either the lubricant got contaminated, which introduced catalysts for these chemical reactions, or adverse operating conditions gave rise to these chemical reactions.

Then, we must ask again, “How could we have contamination?” Contamination can occur if leaks are getting into a closed lubrication system or if there is ingress of foreign material from the environment.

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Our line of questioning continues when we ask, “How could we have leaks in a closed lubrication system?”. These can result from damaged components or seals allowing leaks into the system or if the system is less than adequately designed.

These are physical attributes of the system, so we will go back to investigating the lubricant aspect.

This is where we get to ask our famous question, “How could we have ingress of foreign material from the environment?”. Ideally, this can be classified in three ways;

  1. There are openings which are allowing materials to enter the system or
  2. Wrong lubricant was placed in the system or
  3. Contaminated lubricant was placed in the system
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Let’s investigate all three aspects, starting with the openings allowing foreign material to enter the system. There are two main ways in which this can occur. Either the openings were not closed after use, or the safety latches malfunctioned.

Suppose the openings were not closed after use. In that case, there is a possibility that there were less than adequate inspections to verify that these were closed after use or a less than adequate procedure for the task being completed which required the opening of the hatch.

On the other hand, if the safety latches malfunctioned, this could result from less than adequate checks to verify the functioning of the safety latches.

In these cases, the root causes are not the physical elements but rather the systemic reasons for these procedures not being adequately performed.

Now we investigate the second central hypothesis, “How could the wrong lubricant be placed in the system?” While there are many ways in which this can occur, we have narrowed it down to two main areas.

Either there were less than adequate checks to verify that the technician received the correct lubricant, or there were less than adequate procedures to dispatch the correct lubricant from the warehouse. We will not go further into these two as they are now systemic causes that must be addressed.

Onto the third hypothesis of “How could a contaminated lubricant be placed in the system?”. There are two main avenues for this to occur. Either there were improper storage and handling procedures, or there needed to be more adequate procedures to verify the cleanliness of the lubricant before entering the system.

The other hypothesis stemming from the “less than the adequate presence of antioxidants” is having “less than adequate lubricant specifications.” Let’s investigate this one a bit further.

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“How could we have a less than adequate lubricant specification?” Typically, this can result from the lubricant not being blended properly or less than adequate antioxidant levels, which were inappropriate to protect the lubricant.

Now, the line of questioning changes to “Why?” as we have gone past the physical element and some decision-making was involved in this hypothesis. We must ask, “Why wasn’t the lubricant blended properly?”

This can result from less than adequate procedures to ensure the quality of the lubricant by the supplier or less than sufficient checks for the proper blending mix being processed.

These are factors one should consider when receiving any lubricant from their supplier.

On the other hand, if we follow the line of questioning of “How could there be a less than adequate antioxidant level to protect the lubricant?” we can come up with the following.

Either the operating environment caused the antioxidants to be depleted at a higher rate. This would be as a result of a harsh but normal operating environment. In this case, we may be unable to make those environmental changes (without the OEM’s consent).

Or the antioxidants used were not suited to the operating conditions. This is where the line of questioning again shifts to “Why were they not suited?”. This could result from inadequate information in choosing the right lubricant suited for the system.

What Is the Real Root Cause of Oxidation?

From the logic tree that we have created, we can see that there is no sole root cause for oxidation. It can stem from various causes, including physical, human, and even systemic roots. The main takeaway from this exercise is to acknowledge that root causes are not limited to physical causes, such as leaks in the system.

Instead, the actual root causes can be linked to systemic areas of concern where there may not have been enough information to guide the analyst in choosing the most ideally suited lubricant for the application. There are also root causes related to the lubricant not being appropriately blended.

It is critical to thoroughly investigate the real root causes when the lubricant becomes degraded to avoid being stuck in the loop of constantly experiencing degradation.

For more info on other methods, check out the book Bob Latino, and I authored called “Lubrication Degradation – Getting Into the Root Causes,” published by CRC Press.

 

References:

Ameye, Jo, Dave Wooton, and Greg Livingstone. 2015. Antioxidant Monitoring as Part of a Lubricant Diagnostics – A Luxury or Necessity. Rosenheim, Germany. February 2015.

Latino, Bob, Sanya Mathura. 2021. Lubrication Degradation – Getting into the Root Causes. CRC Press, Taylor & Francis.

How do I know if Oxidation is occurring?

What Evidence is needed to prove that oxidation has occurred / is occurring?

However, understanding the oxidation process is just one part of the puzzle. When performing an investigation, we also need to know what factors or characteristics should be present. Additionally, we need to prove that their presence confirms our hypothesis of whether or not oxidation is occurring. This is where the line of evidence-based questioning plays a significant role.

When oxidation occurs, it is usual to see the presence of aldehydes, ketones, hydroperoxides, and even carboxylic acids. These can be confirmed using the FTIR (Fourier Transform Infrared test).

Typically, one will also find some deposits in the system. These deposits can be further characterized and tested to determine their nature using FTIR. Their presence, however, may be confirmed using the MPC (Membrane Path Colorimetry, ASTMD7843) test.

Identifying the presence of the deposits and/or the compounds listed above can lead to the conclusion that oxidation has occurred.

Another critical characteristic of oxidation is the depletion of antioxidants. This can be easily identified by utilizing the RULER® (Remaining Useful Life Evaluation Routine) test. This test quantifies the remaining antioxidants in the oil and gives the value for the amines and phenols (which is very important, especially in synergistic mixtures).

As such, one can detect the trend in the depletion of antioxidants and implement measures to prevent this before they become depleted.

The main tests to assist in determining the presence of Oxidation include:

RULER (Remaining Useful Life Evaluation Routine) levels less than 25% compared to new oil. This value represents the level of antioxidants in the oil. Hence, low levels indicate that the antioxidants are decreasing, possibly due to oxidation. This test can accurately give information on whether oxidation is currently occurring in the oil before deposits are formed.

An increase in acid number indicates the presence of acids resulting from oxidation. However, it must be noted that this change in acid number only occurs after oxidation has taken place. Hence this test is not a good indicator to determine if oxidation is occurring; instead, it is more definitive in letting us know that oxidation has already occurred.

Rapid color changes – darkening of the oil due to the deposits being present. While color is not the best indicator, in some instances, the darkening of the oil can provide a bystander to ask whether something is occurring in the oil. It is not a definitive test for the presence of oxidation.

FTIR test (Fourier Transform Infrared) for the presence of insolubles formed during the oxidation reaction. This can accurately determine the presence of any compound to assist us in determining whether oxidation is occurring.

MPC (Membrane Patch Colorimetry) levels outside the normal range (above 20). This lets us know that insoluble deposits are present in the oil. One must note that there may be instances where the deposits might not appear in the MPC test. As such, this should not be a standalone test to determine the presence of deposits.

RPVOT (Rotating Pressure Vessel Oxidation Test) levels are less than 25% compared to new oil (this is the warning limit). This is the industry standard, but this test does not have a high repeatability value in that if the same test were performed on identical samples, the values would be different. Additionally, the value (reported in minutes) is not easily translated into the environment of the components.

These tests provide us with the evidence we need to determine the presence of oxidation when performing the root cause analysis on the component’s failure.

How Can Oxidation Occur in Lubricants?

Typically, when an oil undergoes degradation, the first culprit to be blamed is oxidation. We often hear that the oil has oxidized, producing varnish, leading to its degradation. While this simple statement may seem plausible, it is not the only way oil can degrade.

If an oil has undergone oxidation, the real question we should be asking is not how much varnish has been produced but what caused the oxidation in the first place?

In this article, we will explore the various ways in which an oil can degrade via oxidation. However, as you know from previous articles, other degradation methods exist.

How Can Oxidation Occur?

Before diving further into the root cause of oxidation, one must first fully understand how oxidation occurs. When truly investigating a root cause for a failure, we should start with the question “How could?” rather than “Why?”.

This line of questioning heavily influences the answers. The “How could?” responses stem from a more evidence-based approach.

On the contrary, if we question “Why?” this is more opinionated and can mislead the investigation towards a biased opinion rather than the facts.

This leads us to the main question, “How can oxidation occur?”.

According to Ameye, Wooton, and Livingstone, 2015, oxidation occurs when there is any reaction in which electrons are transferred from one molecule. Ideally, in oxidation, during the initiation phase, free radicals are formed, which in turn produce more free radicals.

A free radical is a molecular fragment with one or more unpaired electrons which are accessible and can easily react with other hydrocarbons, as explained by Ameye, Wooton, and Livingstone, 2015.

After the initiation phase, which has the free radicals, the propagation phase follows, in which the antioxidants react with these free radicals to make them more stable. This is part of the reaction in which there is usually a drastic depletion of antioxidants or where the oil becomes sacrificial.

The antioxidants act as a barrier to protect the base oil from oxidizing. However, they can no longer protect the base oil once they become depleted. This leads to the termination phase, where the remaining free radicals attack the base oil.

As a result, this gives rise to the condensation phase, where we begin to physically notice the changes in the oil’s viscosity and the presence of insoluble by-products. These are the deposits that are known are lube oil varnish to some but can further be defined by their chemical composition.

Understanding how oxidation occurs can assist us in determining the root cause when an oil degrades. It allows us to identify the different stages to further help us determine if it is indeed oxidation that is occurring or not.

Has the Lubricant Failed the Equipment, or Has the Equipment Failed the Lubricant?

Many lubrication engineers are faced with finding the most appropriate lubricant for an application. Therefore, they are tasked with selecting the “right” lubricant; subsequently, their decision can influence several outcomes.

A lot of the positive results are in the realm of extending the life of the oil, providing better energy efficiency, and even saving costs associated with downtime. However, can the choice of an “incorrect” lubricant impact its degradation process or lead to the presence of lube oil varnish?

Has the Lubricant Failed the Equipment, or Has the Equipment Failed the Lubricant?

Lubricants provide many different functions. These can range from moving heat or contaminants away from the components, minimizing wear and friction, improving efficiency, providing information about the status of the lubricant, or even transmitting power, as is the case with hydraulic oils.

There has been the time aged question of whether a lubricant fails the equipment or the equipment has failed the lubricant. If a deeper dive is performed into this question, one can deduce that lubricants are engineered to withstand particular conditions.

Once those conditions are met, lubricants can perform their intended functions. However, if the conditions exceed the tolerances of the lubricant, then one will notice a faster degradation. In this case, the environment and its conditions have failed the lubricant.

On the other hand, lubricants are designed to be sacrificial and are used up while in service. Hence, it is normal to see additives’ values deplete when trending oil analysis values, especially for turbine oils. Quite notably, additives responsible for antiwear or extreme pressure will decrease over time as they protect the components.

For this instance, the lubricant would have been performing its function until it could no longer do so or has reached its end of life. The conditions in the environment cannot be blamed for the lubricant failing. This is the nature of the lubricant.

Lubricant condition monitoring lets analysts detect whether a lubricant is undergoing degradation and can even help determine some areas where it has begun to fail. For instance, if the RULER® test can quantify the remaining antioxidants in an oil. Analysts can easily interpret its results to determine if the process of oxidation is occurring within that lubricant.

Similarly, an FTIR test can detect whether contaminants are present in the lubricant or if the additive packages have become severely depleted. These tests all aid in allowing analysts to successfully determine whether or not a lubricant is performing at its full functional capacity.

 

Want to read the entire article? Find it here in Precision Lubrication Magazine!

Why Do We Need Lubricant Additives?

Lubricants keep the world turning. Once something moves, a lubricant should be present to reduce friction or wear between the surfaces. But what makes lubricants so unique in our industry? Is it just the base oil?

No, this is where the power of lubricant additives truly shines, an area many overlook.

Why Do We Need Lubricant Additives?

Before getting into the world of additives, let’s step back to the basics: why are they needed? A lubricant is composed of base oil and additives. Depending on the type of oil, different ratios of additives will be used for the various applications. Additionally, each Lubricant OEM will have its unique formula for its lubricant.

To simplify this, we can think of making a cup of tea. The first thing we need is some hot water in a cup. This can be our base oil. It can be used on its own (some people drink hot water or use it for other purposes), but if we want to make a cup of tea, we must add stuff.

Depending on the purpose for which you’re drinking the tea, you may choose a particular flavor. Perhaps peppermint for improved digestion or to help improve your concentration or chamomile to keep you calm.

These flavors can represent the various types of oils: gear oils, turbine oils, or motor oils. Different blends are suited for different applications.

Now, while we’ve added the tea bag to the hot water (and some people can drink tea like this), others need to add sweetener or milk. These are the additives to the base oil (hot water).

Depending on the preference of the person drinking the tea, there will be varying amounts of sweetener (honey, stevia, or sugar) and varying amounts of milk (regular, low-fat, oat, dairy-free). The combinations are endless!

The same can be said of additives in finished lubricants. Depending on the type of oil (tea flavor, think gear or turbine oil) and its application (the person drinking the tea, with dietary preferences of being dairy-free or sugar-free), the combination of lubricant additives and their ratios will differ. The percentage of additives can vary from 0.001 to 30% based on the type of oil.

Additives have three main functions in a finished lubricant. They can;

  • Enhance – improve some of the properties of the base oil
  • Suppress – reduce some of the characteristics of the base oil
  • Add new properties – introduce new features to the base oil

The finished lubricant will have properties from the base oil and additives combined.

Want to read the entire article? Find it here in Precision Lubrication Magazine!

The Difference Between Antiwear and Extreme Pressure Additives

The terms antiwear additives and extreme pressure additives are often used interchangeably, suggesting that they provide the same functions in a lubricant. This is not exactly true. While there are many similarities in how they function, both additives have distinct functions in protecting lubricants.

Both are film-forming additives (Bruce, 2012). Their functions are to reduce wear between two contacting surfaces or reduce friction to lower the heat produced between the two rubbing surfaces.

They can also be classified as boundary additives that can be temperature-dependent (EP additives) or non-temperature-dependent (Antiwear additives). They both function to mitigate against wear, which is usually caused during boundary lubrication where higher speeds, loads, or temperatures can cause contact with the asperities.

One of the significant differences, as noted by Mang & Dresel, 2007 is that antiwear additives are designed to reduce wear when the system is exposed to moderate stress. On the other hand, EP additives are much more reactive. These are used when the system’s stress is very high to prevent the welding of moving parts.

According to (Bruce, 2012), there are four main groups of commercially available EP additives based on the structures containing phosphorus, sulphur, chlorine, and overbased sulfonates. He explains that the phosphorus, sulphur, and chlorine-containing EP additives are activated by heat over a range of temperatures.

For instance, chlorine-containing EP additives are usually activated between 180-240°C, phosphorus-containing additives are activated at higher temperatures, and sulphur-containing additives operate at 600-1,000°C.

On the other hand, overbased sulfonates contain a colloidal carbonate that reacts with iron to form a thin-film barrier layer between tribocontacts. This protects the surface from direct contact and welding.

As we can see, antiwear and EP additives protect the surfaces between which the lubricant exists. However, they are activated differently and subsequently perform two different functions.

Antiwear additives protect against wear and are not temperature dependent, while EP additives are activated by high stress to prevent the welding of moving parts.

Both functions are essential to protecting the system from additional wear and ensuring it remains operational.

 

Want to read the entire article? Find it here in Precision Lubrication Magazine!

 

References

Bloch, H. (2009). Practical lubrication for industrial facilities, Second edition. Lilburn: Fairmont Press Inc.

Bruce, R. W. (2012). Handbook of Lubrication and Tribology, Volume II, Theory and Design, Second Edition. Boca Raton: CRC Press Taylor and Francis Group.

Coyle, C. L., Greaney, M. A., Stiefel, E. I., Francis, J. N., & Beltzer, M. (1991, Feb 26). United States of America Patent No. 4,995,996.

Mang, T., & Dresel, W. (2007). Lubricants and Lubrication, Second, Completely Revised and Extended Edition. Weinheim: WILEY-VCH Verlag GmbH & Co. KGaA.

Mortier, R. M., Fox, M. F., & Orszulik, S. T. (2010). Chemistry and Technology of Lubricants, Third Edition. (C. Bovington, Ed.) Dordrecht Heidelberg: Springer Science+Business Media B.V. doi:10.1023/b105569_3

Pirro, D. M., Webster, M., & Daschner, E. (2016). ExxonMobil, Lubrication Fundamentals, Third Edition, Revised and Explained. USA: CRC Press Taylor and Francis Group.

Zhang, J., & Spikes, H. (2016). On the Mechanism of ZDDP Antiwear Film Formation. Tribol Lett, pp. 1–2.

Types Of Antiwear Additives and How They Work

There are many types of antiwear additives, but they typically all fall under the category of polar materials such as fatty oils, acids, and esters, according to Pirro, Webster & Daschner, 2016. According to Mortier, Fox, & Orszulik, 2010, several compounds can form surface films to help protect against friction and wear.

These include:

  • Oxygen-containing organic compounds (with a polar head that can adsorb to surfaces). These can include alcohols, esters, and carboxylic acids.
  • Organic compounds containing nitrogen groups
  • Organic sulphur compounds which can form reacted films at surfaces
  • Organic phosphorus compounds which can form reacted films at surfaces
  • Organic boron compounds which may form reacted films at surfaces
  • Organic molybdenum compounds which can form MoS2 film on surfaces
  • ZDDPs, which can form polymeric films on surfaces

While this is an exhaustive list, the more popular ones are listed below. In this next part of the article, we will also dive into how they function.

Organic Oxygen Compounds

According to Mortier, Fox, & Orszulik, 2010, these compounds usually include esters, alcohols and acids. These are generally responsible for improving the “oiliness” or reducing the friction for most lubricants. However, how does this work?

Carboxylic acids form metallic soaps with the contacting surfaces. According to Mortier, Fox, & Orszulik, 2010, some evidence suggests that the upper limit of friction coincides with the melting point of the metal soap. As such, when the upper limit of friction is reached, the metallic soap melts, protecting the surface and performing its antiwear function.

Interestingly, there has been a debate concerning whether these long-chain surfactant friction modifiers reduce friction by forming adsorbed films of monolayer thickness or if they form thick films equivalent to several or many multilayers.

Again, as per Mortier, Fox, & Orszulik, 2010, after experimenting, it was concluded that some of these types of additives form thick boundary films while others do not.

The thick boundary films result from the formation of insoluble iron (II) oleate on the rubbing surfaces. For metal oleates, this will only occur for metals lower than iron in the electrochemical series.

Thus, when speaking about organic oxygen compounds, they help to reduce the friction in lubricants by forming layers on the contacting surfaces.

Organophosphorus Esters

These types of esters have long been used as antiwear additives, according to Mortier, Fox, & Orszulik, 2010. There are two different types of reaction films which are typically formed:

  • Films derived from tricresyl phosphate which form thin films (0.1-2nm) consisting of low shear strength FePO4 and FePo4.2H2O
  • Films consisting of iron (III) monoalkyl/aryl phosphate oligomers are thicker (approximately 100-300nm) and polymeric.

It is important to note that for the tricresyl phosphate (TCP) to be effective, the presence of oxygen, water, and other polar impurities is necessary to form the reaction film. Typically, the hydrolysis of the ester occurs initially, which releases phosphoric acid. This is then critical in the formation of the surface oxide film.

Another noteworthy function of the ester of phosphoric acid is that it helps ensure the solubility of the product in the oil. It can also aid in rust protection by hydrolysis to the phosphoric acid.

During the formation of the film, there is a loss of an alkyl group by hydrolysis, which generates two P-O ligands for coordination. This phosphate anion, which was formed, has reduced oil solubility, which allows for the boundary layer of oil covering the metal surface.

Eventually, as the polymer continues growing, the film moves from a soft, viscous liquid to that of a glass-like solid. This glass-like solid allows the surfaces to stay separated, thus reducing wear.

Essentially, organophosphorus esters form films that can either be very thin or thicker and glass-like, depending on their nature. While they act as antiwear additives, they can also perform the function of rust inhibition in the appropriate environments.

Molybdenum Sulfur

Coyle et al., Patent No. 4,995,996, 1991 recognize Molybdenum disulphide as a lubricant additive and discuss its origins. They mention that molybdic xanthine typically decomposes under particular conditions to form the molybdenum sulfide on protected materials. The use of thiosulfenyl xanthates has also been formulated for particular ashless lubricants.

As per Mortier, Fox, & Orszulik, 2010, compounds such as MoDTC (molybdenum dithiocarbamate) or MoDDP (molybdenum dithiophosphate) typically react with the surfaces to produce the famous molybdenum disulphide. In this compound, there is an ease of shearing, which leads to unusually low coefficients of friction.

A synergistic relationship exists between MoDTC and ZDDP. While MoDTC does not form low friction layers independently, these layers are only formed when ZDDP is present. The layer of MoS2 is only formed on top of the glass of ZDDP reaction products. The ZDDP layer acts as a source of sulphur, reduces the oxidation of MoS2 and limits the diffusion of sulphur from MoS2 into the ferrous substrate.

Interestingly, Molybdenum disulphide (also commonly known as “Moly”) is extremely popular in grease applications especially in the mining industry. “Moly” is known for being a solid additive to grease thickeners for specific applications.

As seen above, it may not exactly be “Moly” added to the lubricant, but rather, it is only created when its parent compound decomposes and is formed.

Zinc Dialkyldithiophosphates (ZDDP)

These are the most commonly used antiwear additives on the market and are known by their chemical abbreviation ZDDP. Originally, ZDDP was developed as an antioxidant additive. However, it has been used in many applications, such as engine, hydraulic, and even circulating oils, as both an antiwear and antioxidant additive.

According to Bruce, 2012, The Ecole Centrale de Lyon / Shell Corporation collaboration made significant conclusions on ZDDP performance. This study shows that ZDDP produces a thin film of iron sulfide and zinc sulfide nearest to the metal surface. Next, there is a zinc polyphosphate layer, made up of long-chain zinc polyphosphates and then soluble alkylphosphates, closest to the oil layer.

According to Zhang & Spikes, 2016, at very high temperatures (above 150°C), ZDDP reacts slowly to form films on solid surfaces. This occurs despite the absence of rubbing and is called “thermal films .” However, at lower temperatures (below 25°C) in the presence of rubbing films in a ZDDP lubricant, these ZDDP films are generated more rapidly. These are called “tribofilms”. Based on analysis, it is suggested that both films have similar structures.

It has also been shown (through inelastic electron tunneling spectroscopy, IETS with Yamaguchi and Ryason) that secondary ZDDP is adsorbed much more readily than primary ZDDP. On the other hand, alkaryl ZDDP is hydrolyzed on adsorption onto aluminum oxide surfaces.

According to Mortier, Fox, & Orszulik, 2010, ZDDP reduces wear by forming relatively thick boundary lubrication films. These are usually 50-150nm thick and are based on a complex glass-like structure (as mentioned earlier). The figure below, taken from Mortier, Fox, & Orszulik, 2010, shows the structure of this ZDDP glass film.

Structure and composition of a ZDDP glass film (taken from Mortier, Fox, & Orszulik, 2010)

The strength of the ZDDP’s antiwear function lies in the structure of the alkyl groups. Chain branching and chain length have critical roles in this determination. Short-chain primary alkyl groups are more reactive than long primary alkyl groups.

As Mortier, Fox, & Orszulik, 2010, explain, the ZDDPs most efficient at antiwear film formation typically suffer depletion due to thermal effects. Under very high temperatures and/or long drain service, the most active ZDDP may not provide the best wear protection.

 

Want to read the entire article? Find it here in Precision Lubrication Magazine! 

What Are Antiwear Additives?

As the name suggests, antiwear additives help to prevent wear in one way or another. However, what makes them unique compared to other additives in lubricants? Why are they used more predominantly in specific applications than other applications? This article explores antiwear additives, why they are needed, and how they work.

What Are Antiwear Additives?

According to (Bloch, 2009), antiwear agents can also be called mild EP (Extreme Pressure) additives. In some cases, they may also act as antioxidant additives (depending on their chemical structure). In essence, antiwear additives protect against friction and wear when the surfaces experience moderate boundary conditions.

During moderate boundary conditions, the full film of the lubricant has not yet formed, and asperities on both surfaces can come into contact with each other. As such, antiwear additives can also be called boundary lubrication additives.

antiwear-addtives-work-2

Usually, these antiwear additives react chemically with the metal to form a protective layer. This layer or coating will allow the two surfaces to slide over each other with low friction and minimal metal loss. As such, antiwear additives have also adopted the nickname “anti-scuff” additives.

According to Pirro, Webster, & Daschner, 2016, the adsorbed film on metal surfaces is formed from long-chain materials. In these cases, the polar ends of the molecules attach to the metal while the projecting ends of the molecules remain between the surfaces.

Under mild sliding conditions, wear is reduced; however, under severe conditions, molecules can be rubbed off such that the wear-reducing effect is lost. When this happens, it is evident in the oil analysis data with the presence of wear metals in large quantities.

In essence, antiwear additives help protect the oil while reducing friction, protecting the surfaces, and, in some cases, enhancing the oil to be more resistant to oxidation. While they can perform these functions, it must be noted that there are many different types of antiwear additives.

 

Want to read the entire article? Find it here in Precision Lubrication Magazine!

Factors That Affect Oil Viscosity

Similar to the molasses and water examples above, different factors can affect the viscosity of a liquid. For instance, water can assume other states depending on the temperature.

If water is at its freezing point (0°C), it can turn to ice but remains liquid at room temperature (around 20-30°C). Then, at 100°C, it can turn into a vapor. Its viscosity can change depending on the influencing factors.

Four factors affect oil viscosity:

  • Temperature
  • Pressure
  • Shear rate
  • Oil type, composition, and additives

Temperature

As seen with the example of the water above, when the temperature decreases, the water can turn to ice. Similarly, for lubricants, as the temperature drops, the viscosity increases. This means the oil will get thicker or more resistant to flow at lower temperatures. Likewise, as the oil heats up, it can become thinner.

This is similar to a block of ice melting as temperatures increase. Its viscosity will decrease, and the ice will turn to water. In this case, the internal molecules gain more energy with the increase in temperature, lowering the internal friction within the fluid. As such, the viscosity also decreases.

Since the oil’s viscosity will change with temperature, most OEMs will supply a temperature–viscosity chart for their equipment to help ensure the correct viscosity is used depending on the operating temperature.

In the figure below, gear oils of varying viscosities are plotted against the temperature for a particular piece of equipment. OEMs will typically specify the optimum operational viscosity range for their equipment.

It is then up to the lubrication engineers to determine the ideal viscosity based on the conditions of their equipment (this can vary depending on the application).

Figure 1: Temperature – Viscosity chart for Shell Omala S2 G (Source: Shell Lubricants TDS)
Figure 1: Temperature – Viscosity chart for Shell Omala S2 G (Source: Shell Lubricants TDS)

From the figure above, one can see that at 40°C, most of the gear oil grades correspond with their viscosities (ISO 68 corresponds with a 68 viscosity). However, at 0°C, an ISO 68 gear oil can become 1000 cSt, while at 90°C, this same grade of oil is around 11cSt.

Interestingly, all of the oils listed here can achieve a viscosity of 100cSt but at different temperatures, as shown below:

  • 32°C – ISO 68
  • 40°C – ISO 100
  • 47°C – ISO 150
  • 55°C – ISO 220
  • 63°C – ISO 320
  • 68°C – ISO 460
  • 75°C – ISO 680

Temperature is a significant influencing factor of viscosity, but it is not the only factor.

Pressure

The effects of pressure on a lubricant’s viscosity are often overlooked. However, the viscosity-pressure behavior has become part of the calculation for elastohydrodynamic films. In these cases, oil viscosity can rapidly increase with pressure.

One such instance occurs with metal-forming lubricants, which are subjected to high pressures such that the oil’s viscosity can increase tenfold (Mang & Dresel, 2007). As the pressure increases, viscosity also increases, protecting the surface in these lubricant films.

The very definition of viscosity alludes to pressure’s impact on Newtonian and non-Newtonian fluids. For example, with Newtonian fluids (regular lubricating oils), the shear rate is proportional to the applied shear stress (pressure) at any given temperature.

As seen above, the viscosity can be determined once the temperature remains the same. However, Non-Newtonian fluids, such as greases, only flow once a shear stress exceeding the yield point is applied (Pirro, Webster, & Daschner, 2016).

Hence, this is why the observed viscosity of grease is called its apparent viscosity and should always be reported at a specific temperature and flow rate.

Shear Rate

For Newtonian fluids, viscosity does not vary with shear rate (Pirro, Webster, & Daschner, 2016). In fact, per the definition of viscosity for Newtonian fluids (regular lubricating oils), viscosity is a constant proportionality factor between the shear force and shear rate. Thus, even when subjected to greater shear forces, the viscosity will not change for Newtonian fluids.

On the other hand, for non-Newtonian fluids, the viscosity is influenced by the shear rate. Some non-Newtonian fluids can include; pseudoplastic fluids, dilatant fluids, and a Bingham solid, the effects of shear rate on these fluids are shown in the figure below.

A Bingham solid is a plastic solid such as grease that only flows above a particular yield stress. It can be seen that pseudoplastic fluids decrease viscosity with an increasing shear rate, while dilatant fluids show an increase in viscosity with an increasing shear rate. (Hamrock, Schmid, & Jacobson, 2004)

Figure 2: Characteristics of different fluids as a function of shear rate vs. viscosity (a) and shear rate vs. shear stress (b). Source: Fundamentals of Fluid Film Lubrication by Hamrock, Schmid & Jacobson, page 102.
Figure 2: Characteristics of different fluids as a function of shear rate vs. viscosity (a) and shear rate vs. shear stress (b). Source: Fundamentals of Fluid Film Lubrication by Hamrock, Schmid & Jacobson, page 102.

The shear of a lubricant can influence its shear rate. Typically, longer-chain polymer viscosity index improvers can shear over time. When this happens, it can result in a decrease in oil viscosity. Similarly, non-Newtonian fluids, such as grease, experience a decrease in viscosity as a function of shear rate (Totten, 2006).

Another essential characteristic to note is whether a material is thixotropic or rheopectic. For a thixotropic material, if it is placed under a continuous mechanical load over a period of time, the viscosity will appear to decrease over this time.

However, the original viscosity is restored after a specific rest period, as shown in the figure below. On the other hand, for rheopectic materials, continuous shearing causes the viscosity to increase. (Mang & Dresel, 2007).

Figure 3: Flow characteristics of a thixotropic lubricant (Source: Lubricants and Lubrication edited by Theo Mang and Wilfried Dresel, page 30)

Oil Type, Composition, and Additives

Various oil types, compositions, and additives can influence a lubricant’s viscosity. For instance, the five groups of base oils all have varying characteristics, as shown in the figure below. One can note the differing viscosities for the various groups.

Figure 4: Base Stock property comparison (Source: Lubricants and Lubrication edited by Theo Mang and Wilfried Dresel, page 13)
Figure 4: Base Stock property comparison (Source: Lubricants and Lubrication edited by Theo Mang and Wilfried Dresel, page 13)

When a finished lubricant is made, it usually consists of a base oil and additives. Hence, the base oil will have a significant role in determining the final viscosity of the oil. However, with the advent of Viscosity Index Improvers, desired viscosities can be engineered regardless of the base oil type being used.

 

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