Tagged: engineering

The Influence of Lubricant Selection on Degradation

Guidelines should always be followed when selecting a lubricant for a particular application. OEMs will have specific criteria ranges for specialty applications that must be satisfied. Some general guidelines which should be considered can be summarized in the table below based on the listed mechanisms above.

Based on the three listed mechanisms above, one can identify that choosing a lubricant can impact the type of degradation which occurs during its lifetime. As such, when selecting lubricants, it is critical to note their applications and the conditions they will endure.

Having a history of lubricant failures for particular equipment can also assist in this regard by informing users of past failure trends. Therefore, when selecting a lubricant, operators can be more mindful of the properties which should not be compromised during the selection process.

The process of troubleshooting degradation in lubricants has been covered in detail in the book, “Lubrication Degradation – Getting Into the Root Causes” by Bob Latino and myself, published by CRC Press, Taylor and Francis.

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

Which Degradation Mechanism Is Affected?

My previous article published in Precision Lubrication covered six degradation mechanisms: oxidation, thermal degradation, microdieseling, electrostatic spark discharge, additive depletion, and contamination.

Upon further investigation, there are only three mechanisms where selecting the correct lubricant will impact the degradation mode. These are; oxidation, microdieseling, and electrostatic spark discharge. The properties of the lubricant can easily influence each of these degradation mechanisms.

When selecting a lubricant, especially for rotating equipment, one of the critical areas of importance is the performance of the antioxidants. When formulated, oils must be balanced to protect the components in various aspects.

Thus, some oils that boast a high level of antioxidants may suffer from low levels of antiwear, or these increased levels can react with other components to reduce the performance of the oil. During oxidation, antioxidants are depleted at an accelerated rate which can lead to lube oil varnish. Hence, the choice of lubricant can influence this degradation mechanism.

A good trending test, in this case, would be the RULER test to accurately quantify and trend the remaining useful antioxidants for the oil. This test can easily distinguish and quantify the type of antioxidant rather than providing an estimate of the oxidation, as with the RPVOT test.

It has been noted that oils with an RPVOT of more than 1000 mins have a low reproducibility value which can mislead users during trending of lubricant degradation. Corrosion inhibitors, not just antioxidants, have also influenced the RPVOT values. Thus, there are better tests for monitoring the presence of antioxidants and helping operators to detect the onset of possible lube oil varnish.

On the other hand, during microdieseling, entrained air can lead to pitting the equipment’s internals and eventually the production of sludge or tars depending on whether the entrained air experiences a high or low implosion pressure.

If bubbles become entrained in the lubricant and do not rise to the surface, this can directly result from the lubricant’s antifoaming property. The antifoaming property is essential when selecting an oil, especially for gearboxes. Typically, OEMs will have recommendations for their components that should be followed.

Another degradation mechanism that can be influenced by lubricant selection is electrostatic spark discharge. This mechanism occurs when the lubricant accumulates static electricity after passing through tight clearances. These then discharge at the filters or other components inside the equipment, providing sharp points or ideal areas to allow static discharge.

This is frequently seen in hydraulic oils due to the very tight clearances within the equipment. If fluid conductivity is above 100 pS/m, the risk of static being produced is reduced. Some OEMs also provide particular values the lubricant should meet for this property.

 

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

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!

How Do Lubricant Additives Work?

Each additive works differently to produce its function on the base oil and the overall finished lubricant. This section will explore how each of the lubricant additives works and some of the challenges they may experience.

Pour Point Depressants

As noted above, the pour point depressants help control the flow of the lubricant. This is achieved by modifying the wax crystals present in the lubricant’s base oil. At lower temperatures, the liquid usually has trouble being poured due to the presence of wax molecules in the base oil1.

There are two main types of pour point depressants, namely;

  • Alkylaromatic polymers adsorb on the wax crystals as they form, thus preventing them from growing and adhering to each other. This effectively controls the crystallization process and ensures the lubricant can be poured.
  • Polymethacrylates co-crystallize with wax to prevent crystal growth.

While these additives do not entirely prevent wax crystal growth, they lower the temperature at which these rigid structures are formed. These additives can achieve a pour point depression of up to 28°C (50°F); however, the common range is typically between 11-17°C (20-30°F).

Solubility thresholds may limit the use of this type of additive to achieve the desired effect on the base oil.

VI Improvers

These additives are typically long-chain, high-molecular-weight polymers that change their configuration in the lubricant based on temperature4. When the lubricant is in a cold environment, these polymers adopt a coiled form to minimize the effect on viscosity. On the other hand, in a hot environment, they will straighten out, allowing the oil to produce a thickening effect.

While it is more desirable to use high molecular weight polymers (since they provide a better thickening effect), these long-chain molecules are also subject to degradation due to mechanical shearing. Therefore, a balance must be reached between the molecular weight and shear stable service condition.

Another challenge for formulators is to balance the polymer’s tendency to shear with the expected viscosity thickening due to oxidative processes and the viscosity thinning due to the dilution of fuel1.

Friction Modifiers

These usually compete with the antiwear and extreme pressure additives (and other polar compounds) for surface room. However, they become activated at temperatures when the AW and EP additives are not yet active. Thus, they form thin mono-molecular layers of physically adsorbed polar soluble products or tribochemical friction-reducing carbon layers, which exhibit a lower friction behavior than AW and EP additives2.

There are different groups of friction modifiers based on their function. Some are mechanically working FMs (solid lubricating compounds, e.g., Molybdenum disulfide, graphite, PTFE, etc.), adsorption layers forming FMs (e.g., fatty acid ester, etc.), tribochemical reaction layers forming FMs, friction polymer forming FMs and organometallic compounds.

Defoamants (Antifoam)

When foam forms in the lubricant, tiny air bubbles become trapped either at the surface or on the inside (called inner foam). Defoamants work by adsorbing on the foam bubble and affecting the bubble surface tension. This causes coalescence and breaks the bubble on the lubricant’s surface1.

For the foam that forms at the surface, called surface foam, defoamants with a lower surface tension are used. They are usually not soluble in base oil and must be finely dispersed to be sufficiently stable even after long-term storage or use.

On the other hand, inner foam, which is finely dispersed air bubbles in the lubricant, can form stable dispersions. Common defoamants are designed to control surface foam but stabilize inner foam2.

Oxidation Inhibitors

As noted above, antioxidants are usually deployed during the propagation phase to neutralize the scavenging radicals or decompose the hydroperoxides3. There are two main forms of antioxidants: primary and secondary antioxidants.

Primary antioxidants, also known as radical scavengers, remove radicals from oil. The most common types are amines and phenols.

Secondary antioxidants are designed to eliminate peroxides and form non-reactive products in the lubricant. Some examples include zinc dithiophosphate (ZDDP) and sulphurized phenols.

Mixed antioxidant systems also exist where two antioxidants have a synergistic relationship. One example is the relationship between phenols and amines, where phenols deplete early during oxidation while amines deplete later. Another example is using primary and secondary antioxidants to remove radicals and hydroperoxides.

Rust and Corrosion Inhibitors

Rust and Corrosion inhibitors are usually long alkyl chains and polar groups that can be adsorbed on the metal surface in a densely packed formation of hydrophobic layers.

However, this is a surface-active additive, and as such, it competes with other surface-active additives (such as antiwear or extreme pressure additives) for the metal surface. There are two main groups for corrosion additives: antirust additives (to protect ferrous metals) and metal passivators (for non-ferrous metals2).

Rus inhibitors have a high polar attraction to metal surfaces. They form a tenacious, continuous film that prevents water from reaching the metal surface. It must also be noted that contaminants can introduce corrosion into an oil, just as organic acids are produced.

Detergents and Dispersants

Detergents are polar molecules that remove substances from the metal surface, similar to a cleaning action. However, some detergents also provide antioxidant properties. The nature of a detergent is particularly important as metal-containing detergents produce ash (typically calcium, lithium, potassium, and sodium)1.

On the other hand, dispersants are also polar, and they keep contaminants and insoluble oil components suspended in the lubricant. They minimize particle agglomeration, which in turn maintains the oil’s viscosity (compared to particle coalescing, which leads to thickening). Unlike detergents, dispersants are considered ashless. They typically work at low operating temperatures.

Antiwear Additives

These are typically polar with long chain molecules that adsorb onto the metal surfaces to form a protective layer. This can reduce friction and wear under mild sliding conditions. Usually, these additives are formed from esters, fatty oils, or acids, which can only work at low or moderate levels of stress within the system.

The most common form of antiwear is ZDDP, which is used in engine or hydraulic oils. On the other hand, an ashless phosphorus type of antiwear also exists for systems that require that characteristic, and tricreysl phosphate is the usual choice.

Extreme Pressure Additives

Since extreme pressure additives only become active when higher temperatures or heavier loads are on a system, they have earned the name “Anti-scuffing additives.”

Unlike antiwear additives, extreme pressure additives react chemically with the sliding metal surfaces to form relatively insoluble surface films. This reaction only occurs at higher temperatures, sometimes between 180-1000°C, depending on the type of EP additive used1.

It must be noted that even with the presence of EP additives in a lubricant, there will still be some wear during the break-in period as the additives have yet to form their protective layers on the surfaces.

EP additives must also be designed for the system they protect as different metals have varying reactivity (EP additives designed for steel-on-steel systems may not be appropriate for bronze systems as they are not as reactive with bronze).

EP additives also contribute to polishing the sliding surfaces as they experience the most significant chemical reaction when the asperities are in contact and the localized temperatures are at their highest. They tend to be created from compounds containing sulphur, phosphorus, borate, chlorine, or other metals4.

Do Lubricant Additives Degrade Over Time?

As noted earlier, most additives can deplete over time as they get used up in their various functions. Antiwear and rust protection additives continuously coat the surfaces of the interfacing metals.

This can cause their initial concentrations to decrease over time until it reaches a point where the concentration of the additive is too low to offer any protection. In this case, it has not degraded but depleted.

In earlier years, there used to be prevalent issues with the separation of additives from the finished lubricant due to filtration. However, with the evolution of technology and better practices, this is no longer a common problem operators face.

In the past, operators would notice frequent clogging of their filters and subsequent reduction of additive concentrations, rendering the oil unprotected. It was common to notice additives settling to the bottom of a drum of oil after standing still for some time.

In essence, lubricant additives do not really degrade over time; rather, their concentrations get depleted, which assists in the lubricant degrading faster than a finished lubricant with higher additive concentrations.

Innovation and Future Trends for Additives

What does the future look like for additives within our industry? Will they go away completely?

From my estimations, we’re a long way from that happening. The lubricant industry has evolved over the years, with many advances from the chemical side, which has developed better-suited additives, and the OEM side, which has pushed the chemists to develop lubricant additives that can adapt to equipment changes.

OEMs are creating more components that can withstand higher temperatures, increased pressures, and more demanding environments. Lubricants must also be developed for this specific use, and additive technology will continue to evolve as these boundaries are pushed.

We are also being driven towards more environmentally friendly products, and additives are also on that list. Most of the metals used in the production of additives (such as EP or AW additives) are toxic to the environment, and alternatives are being discovered.

In the field of tribology, there has also been continued research into ways of reducing friction and wear. This is coupled with research into the interaction of varying surfaces and ways lubricants can effectively reduce the coefficient of friction, leading to increased energy efficiency and fuel efficiency in some cases.

Lubricant additives will be around for some time as everything that moves needs to be lubricated, and base oils do not have all the required properties to handle varying temperatures and other conditions that the machine encounters.

While their structure will change to adapt to provide a more environmentally friendly impact, their functions will also evolve based on their future requirements.

References

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

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

3 Livingstone, G., Wooton, D., & Ameye, J. (2015). Antioxidant Monitoring as Part of Lubricant Diagnostics – A Luxury or a Necessity?

4 Pirro, D. M., Webster, M., & Daschner, E. (2016). Lubrication Fundamentals – Third Edition Revised and Explained. Boca Raton: CRC Press.

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!

Measuring Oil Viscosity

The viscosity of oil is one of its most essential characteristics. Thus, it is important to understand how this is measured and quantified. There are two main types of viscosity, dynamic (or absolute) and kinematic viscosity.

The dynamic viscosity measures the force required to overcome fluid friction in a film and is reported in centipoise (cP) or in SI units Pascal Seconds (Pa s) where 1 Pa s = 10 P (Poise). It can also be considered the internal friction of a fluid. This is usually used for calculating elastohydrodynamic lubrication related to rolling element bearings and gears.

On the other hand, the kinematic viscosity of a fluid is the relative flow of a fluid under the influence of gravity. Its unit of measure is centistokes (cSt) which in SI units is mm2/s, 1cSt = 1 mm2/s. (Mang & Dresel, 2007).

Kinematic Viscosity = Dynamic Viscosity / Density

Other units of measure for viscosity include; Saybolt, Redwood, and Engler, but these are less widely used than the cSt or cP, especially for lubricants.

Oil Viscosity Grades and Standards

One of the best-kept secrets about viscosity is that a particular grade often represents a range. When oils are classified, one may see an ISO 32 or ISO 220 and believe that the oil will have this exact viscosity (32 cSt or 220 cSt). However, this is not the case.

There are three general classifications where viscosity grades have particular ranges based on the fluid type. The fluid may behave differently in each application, hence the need for these three scales. However, there is a chart that allows users to convert the various scales into the one needed.

Engine Oil Classification (SAE J300)

As per the Society of Automotive Engineers (SAE), the SAE J300 standard classifies oils for use in automotive engines by viscosities determined at low shear rates and high temperature (100°C), high shear rate and high temperature (150°C) and both low and high shear rates at low temperature (-5°C to -40°C) (Pirro, Webster, & Daschner, 2016).

Engine manufacturers have widely used this system to aid in designing lubricants suited for these applications. As such, oil formulators also adhere to these classifications when engineering lubricants.

One will note the use of the suffix letter “W” in some of the grades below. These oils are intended for low ambient conditions, whereas those without the “W” are intended for oils that will not encounter low ambient conditions.

These are commonly described as multigrade (where the “W” is found between two numbers) and monograde oils (where the “W” is at the end or the grade is identified by a number only) in the table below.

The table shows that the viscosities must fall within a particular range to be classified. For instance, a 5W30 oil should meet the specifications of:

  • Low temperature, Cranking viscosity of 6600 cP at -30°C
  • Low temperature, Pumping Viscosity Max with No Yield Stress of 60,000 cP at -35°C
  • Low shear rate Kinematic viscosity at 100°C should be between 9.3 -12.5 cSt
  • High Shear rate viscosity at 150°C Max at 2.9 cP

One will notice the range of 9.3 to 12.5 cSt (at 100°C). This is where oils can be blended to either end of this scale but still achieve the classification of a 5w30 oil.

Axle and Manual Transmission Lubricant Viscosity Classification (SAE J306)

As per the SAE recommended practice J306, automotive manual transmissions and drive axles are classified by viscosity, measured at 100°C (212°F), and by the maximum temperature at which they reach the viscosity of 150,000 cP (150 Pa s) when cooled and measured in accordance to ASTM D2983 (Method of Test for Apparent Viscosity at Low Temperature Using Brookfield Viscometer). (Pirro, Webster, & Daschner, 2016).

The table below shows that for an SAE grade of 190, the kinematic viscosity must fall within the range of 13.5 to 18.5 cSt at 100°C. While most viscosities tend to fall mid-range of these values, it also indicates that if the lubricant achieves 18 cSt at 100°C, it can still be classified at an SAE grade 90.

The most common multigrade lubricants within this grade fall within the 80w90 or 75w140 classifications.

Another factor for these types of lubricants is API GL4 or GL5 ratings. It must be noted that a GL5 lubricant is recommended for hypoid gears operating under high-speed, high-load conditions.

On the other hand, a GL4 lubricant is usually recommended for the helical and spur gears in manual transmissions and transaxles operating under moderate speeds or loads. These should not be used interchangeably as the GL5 lubricants tend to adhere to the surfaces and may cause more damage in a GL4 application.

Figure 5: Automotive Gear Lubricant Viscosity Classification. Source: Lubrication Fundamentals, Third Edition Revised and Expanded by Pirro D. M., Webster M., and Daschner E. pg 52

Viscosity System for Industrial Fluid Lubricants

This classification was jointly developed by the ASTM and STLE (Society for Tribologists and Lubrication Engineers). Initially, the system was based on viscosities measured at 100°F but converted to viscosities measured at 40°C.

ASTM D2422 and ISO 3448 are the references for this system. In this system, it is clearer to see the variances in the ranges of viscosities. In this case, the mid-point of the range is used as the ISO viscosity. To determine the range of any ISO viscosity, one can calculate ±10% of the mid-point value to get the minimum and maximum values of the range.

Figure 6: Viscosity System for Industrial Fluid Lubricants. Source: Lubrication Fundamentals, Third Edition Revised and Expanded by Pirro D. M., Webster M., and Daschner E. pg 52

All of these systems can be represented in the figure below, where it is easy to calculate the oil viscosity using another system:

Figure 7: Various viscosity systems in one chart.

Can Lube Oil Varnish be Eliminated? 

Varnish can be likened to cholesterol in the human body. It can build up in our arteries and eventually clog those, causing restrictions in blood flow to our heart which may lead to a heart attack.

Humans cannot simply change their blood to remove the cholesterol build-up. However, cholesterol is controlled through proper diet, exercise, and with some condition monitoring in the form of blood tests to help gauge the presence of it in the bloodstream. Similarly, a couple of approaches can be used to reduce the varnish build-up or eliminate it.

As per Livingstone et al. (2011), the lifecycle of varnish is critical. Particular attention should be paid to the double arrows between the stages of Solubility to Varnish formation in the figure below.

This means that even after varnish has been deposited, it can be solubilized back into the oil. This can only occur if conditions are met per Hansen’s Solubility principles where the solvent and degradation products meet using the three parameters of Polarity, Hydrogen Bonding, and Dispersive Forces as discussed in “The Hansen Solubility Principles and Its Relation to Varnish” (2022).

mechanisms-oil-varnish-formation

The Varnish Lifecycle as per Livingstone et al. (2011)

Varnish exists in various forms and can consist of differing compositions. Hence, it is essential to understand the characteristics of the varnish being formed in a system before attempting to eliminate it.

There are certain technologies, such as solubility enhancers or specifically engineered filtration media, which can be effective at removing lube oil varnish. However, this technology is heavily reliant on the type of varnish being formed and can be customized as per the system accordingly.

Solubility enhancers can solubilize the varnish back into the oil solution. When these deposits are reintroduced into the oil, they can be removed using resin-based filtration. In this method, the media is specifically designed to allow for the adsorption and removal of the varnish which presently exists in the oil.

When these methods are used together, they can prove quite effective and prevent manufacturing plants from experiencing unwanted downtime.

To summarize, it is of utmost importance to first understand the characteristics of the varnish being produced in your equipment before attempting to remove it from your system.

There is no cookie-cutter method to eliminate varnish from a system as it is a complex deposit. Similar to practices we observe with our bodies in the instances of cholesterol build-up, we can employ methods of dissolving the varnish and removing it while monitoring for possible recurrences in the future.

 

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

 

References:

Livingstone, Ameye, & Wooton. (2015.). Antioxidant Monitoring as Part of Lubricant Diagnostics – A Luxury or a Necessity? OilDoc, Rosenheim, Germany.

Livingstone, Overgaag, & Ameye. (2011). Advanced removal Techniques for Turbine oil Degradation Products. Powergen Milan.

Mathura, S. (2020). Lubrication Degradation Mechanisms (CRC Press Focus Shortform Book Program) (1st ed.). CRC Press.

The Hansen Solubility Principles and its Relation to Varnish. (2022, July 31). Fluitec International. https://www.fluitec.com/the-hansen-solubility-principles-and-its-relation-to-varnish/

What is varnish or oil degradation?

Varnish is a type of deposit that forms on the surface of equipment in lubrication systems. It is caused by the oxidation of the base oil and the buildup of additives in the oil over time, forming a sticky, varnish-like substance. Lube oil varnish can cause problems in equipment operation by clogging filters, reducing oil flow, and leading to valve sticking and pump failures.

Lube oil varnish is no stranger to the manufacturing industry. It constitutes the substance of most operators’ worst nightmares and plant managers’ ultimate fears. For those who have been in the industry for the last decade, varnish is the sticky subject that unites all facility departments.

It can cause an entire manufacturing plant to shut down while sending the finance department into a frenzy trying to balance production loss with incoming repair costs. In the fight against lube oil varnish, all teams need to work together to ensure that it can be managed and possibly eliminated from the system.

 

What Is Oil Degradation?

Before diving into the world of varnish, one must first understand how it forms and the circumstances which have led to its existence. Within the industry, the term varnish is used loosely to define any form of lubricant-derived deposit found in industrial.

However, oil can degrade by several mechanisms, which require various conditions for degradation—as such, using the term varnish to describe any deposit formed within a machine does not suggest its mechanism of formation.

The lubricant begins its degradation journey from the moment the lubricant enters the machine.

A lubricant is composed of base oil and additives, of which infinite combinations exist. Additives are carefully engineered to protect the base oil and the equipment. As such, they can become depleted over time, leading to the degradation of the lubricant.

This becomes concerning when the additive levels have depleted to a threshold where they can no longer protect the base oil or the machine. At this stage, degradation is the most serious concern because its rate is greatly accelerated.

According to Mathura (2020), there are six major forms of degradation under which a lubricant can undergo. While some may argue that these can be grouped, some characteristics set these mechanisms apart.

Each mechanism has unique environmental factors which contribute to producing different types of deposits. It is critical to note that identification of the type of mechanism can assist operators in performing remedial works on their equipment to aid in preventing the formation of varnish.

Want to read the full article? Check it out here in the Precision Lubrication Magazine.

Varnish Badges of Honour

Varnish Badges_honour

Varnish is widely known as a primary culprit of equipment failure. This sticky enemy effectively finds its way into most of our equipment and causes operators, maintenance personnel and plant managers a series of nightmares. From unplanned shutdowns costing millions of dollars to sticking of servo valves on startup, or increases in bearing temperature, varnish usually announces its arrival. Once it has been found, there is typically a cause for panic but perhaps it just needs to be understood rather than feared?

 

The ICML VPR & VIM Badges

Recently (August, 2021), the International Council for Machinery Lubrication launched two new badges. These badges are, VIM (Varnish & Deposit Identification and Measurement) & VPR (Varnish & Deposit Prevention & Removal). These were created after the culmination of 3 years of work from the global varnish test development committee. It has been designed for those involved in all aspects of managing or advising lubricant programs especially those with the responsibility of recommending, selling or installing appropriate deposit control equipment or other mitigation strategies.

Most of the readers will already be familiar with my enthusiasm for understanding lubricant degradation. Thus, when these badges came out, I knew I had to secure them! While the requirements for taking the test suggest the possession of the MLT I or MLA I certification or 1 year of experience, I figured that my MLE certification would be an asset (as I haven’t gotten my MLT I certification yet, it’s on the list!). However, I wanted to make sure that I covered all of the elements in the BoK for both the VIM & VPR badges, so naturally I turned to the varnish guru himself, Greg Livingstone!

 

Fluid Learning – All the way!

Greg is the CIO at Fluitec but he’s also the facilitator for the ICML VPR & VIM badges. What a treat! If you’ve never heard the name Greg Livingstone then you’re obviously not in the lubrication field. Greg has penned hundreds of papers on varnish and can be thought of as the varnish guru since he has extensive experience in this area. It’s a no brainer that I chose Fluid Learning to get me up to speed on what I needed to know for these exams!

Greg was an amazing facilitator and not only covered information relevant to the BoK for the exams but gave students a full overview about everything you needed to know about varnish. These on demand sessions kept me scribbling notes and nodding to myself and saying, “Oh that’s what really happens!” He presents the information clearly and adds some much needed humour into the sessions. It was an absolute privilege having him as my tutor for these badges.

 

VPR & VIM- What you need to know!

Varnish Badges_need-to-know

VPR - Varnish & Deposit Prevention and Removal

The VPR badge ensures that candidates understand proactive methods and technologies which can be employed to reduce the degree of degradation. It is also designed to confirm that they can sufficiently evaluate combinations of technologies to prevent and remove varnish including the proper steps to set up and implement an effective varnish removal system.

The topics covered in the VPR include:

  • Problems associated with Varnish & Deposits (20%)
  • Factors affecting Breakdown (28%)
  • Proactive Methods that can be used to minimize oil breakdown (16%)
  • Methods / Technologies that can be used to remove oil breakdown products and/or prevent deposits (36%)

The complete BoK for the VPR badge can be found here.

 

VIM (Varnish & Deposit Identification & Measurement)

The VIM badge on the other hand is more ideally suited for personnel responsible for recommending suitable oil analysis tests and mitigation efforts related to the deposit tendencies of various in-service fluids (application dependent). They would also be responsible for monitoring and adjusting these strategies accordingly.

The topics covered in VIM include:

  • Problems associated with Varnish and Deposits (20%)
  • Varnish and Deposit Composition (24%)
  • How Breakdown Products / Contaminants become Deposits (24%)
  • Oil Analysis Techniques that can be used to gauge Breakdown and Propensity towards Deposit Formation (32%)

The complete BoK for the VIM badge can be found here.

 

Exam tips!

Varnish Badges_exam_tips

The actual exams for both the VPR & VIM are set at 45 minutes with 25 multiple choice questions. Candidates must achieve 70% grade to attain the badges. Currently, the fee for the exam is USD75. Since there were overlaps of the content and the exam durations weren’t that long, I decided to sit both exams in one day. I will only advise this for those who are comfortable with doing this as exam anxiety and all that comes along with it can be stressful!

Here are a couple tips for taking these exams:

  • Log into the system 30 minutes prior to your scheduled exam time. This allows you to clear your mind, settle yourself and gives you an extra 15 minutes to figure out where the email is with your credentials! If you can’t remember your password to login to the system, this also gives you enough time to get that reset and sorted before the actual exam time.
  • The session only opens 15 minutes before the appointed time. During this time, you will converse with the moderator as they do the checks of the room and your National Identification. The moderators will engage with you and ensure that you are sitting the correct exam.
  • Ensure you have your National Identification on hand (your passport can be used as well). As long as it has your picture and the expiration date on the same side, it will be acceptable. For the Trinidadians, do not use your National ID card as we have our pictures on the front with the information on the back (I used my Driver’s permit).
  • Candidates have the option of “Flagging” questions to come back to them later. This is a great tool to help you to mark those questions you want to return to or double check.
  • There is a timer in the screen layout which helps you to keep track of your time. 45 minutes passes very quickly when you’re running through the questions!
  • Exam results for these badges come back very quickly as much as within a few hours or one day depending on the time of your exam.

Why do you need these badges?

Varnish Badges_need-badges

As long as you work within the lubrication sector or interface with machines requiring lubrication, then you need to get these badges! Oil degradation occurs throughout the life of the lubricant whether it’s a small or large operation. By understanding how it degrades and ways to mitigate that degradation, you can save your equipment and avoid unwanted downtime. These badges were designed for the personnel in the field to allow them to make decisions regarding the lubricant and to empower them in taking steps to avoid degradation or mitigate it should the need arise. Consider it as getting your passport stamped by the ICML!

The courses offered by Fluid Learning are perfect for those seeking to understand lubrication deposits, what causes them and how they can be mitigated. While the content covered during these sessions align with the ICML VPR & VIM badges, they also add to a more holistic approach to varnish and deposits. Fluid Learning is an official ICML Training Partner and is currently the only one (of which I am aware) offering training prep for these badges. I highly recommend them for anyone seeking to learn more about or avoid sticky varnish situations. 

At the moment of writing this article, there are only 8 people globally who have acquired these badges from ICML. I am the first female in the world to attain these badges but I will not be the only female for very long. Varnish is an issue which affects us all and we need to understand it, so we can prevent it and keep our equipment safe. I hope to see many more candidates with these badges in the near future!

EALs?

EALs

Q: What makes a lubricant Environmentally Friendly?

There are many definitions of environmentally friendly. For instance, a lubricant can be environmentally friendly if it doesn’t pollute the environment which can either be understood as low toxicity or a reduced number of times that the oil is disposed.

However, there are three main factors which are considered when deeming a lubricant environmentally friendly2;

  1. Speed at which the lubricant biodegrades if introduced into nature
  2. Toxicity characteristics that may affect bacteria or aquatic life
  3. Bioaccumulation potential

Biodegradability

Biodegradability is defined as the measure of the breakdown of a chemical or chemical mixture by micro-organisms. It is considered at two levels namely;

  1. Primary biodegradation - loss of one or more active groups renders the molecule inactive with respect to a particular function
  2. Ultimate degradation – complete breakdown to carbon dioxide, water and mineral salts (known as mineralisation)3

Biodegradability is also defined by two other operational characteristics known as:

  1. Ready Biodegradability – occurs where the compound must achieve a pass level on one of the five named tests either, OECD, Strum, AFNOR, MITI or Closed Bottle3
  2. Inherent Biodegradability – occurs when the compound shows evidence in any biodegradability test.3

 

Toxicity

The toxicity of a lubricant is measured by the concentration of the test material required to kill 50% of the aquatic specimens after 96 hours of exposure (also called the LC50)1

 

Bioaccumulation

The term bioaccumulation refers to the build-up of chemicals within the tissues of an organism over time. Compounds can accumulate to such levels that they lead to adverse biological effects on the organism. Bioaccumulation is directly related to water solubility in that the accumulations can be easily soluble in water and not move into the fatty tissues where they become lodged.

 

Common Base Oils

There are three of the most common base oils that are Environmentally Acceptable2:

  1. Vegetable Oils
  2. Synthetic Esters
  3. Polyalkylene Glycols (PAGs)

These all have low toxicities and when blended with additives or thickeners for the finished lubricant, they should be retested to ensure that the additives / thickeners have not compromised the environmentally acceptable limits.

 

Labelling

Some lubricants can carry the “German Blue Angel Label” if all major components meet OECD ready biodegradability criteria and all minor components are inherently biodegradable.

Based on the requirements by Marpol, the International Maritime Organization (IMO) and current legislation from the European Inventory of Existing Commercial Chemical Substances (EINECS), a product may be considered acceptable if it meets the following requirements:

  • Aquatic toxicity >1000ppm (50% min survival of rainbow trout)
  • Ready biodegradability > 60% conversion of test material carbon to CO2 in 28 days, using unacclimated inoculum in the shake flask or ASTM D5846 test 1.

 

References:

  1. Lubrication Fundamentals Second Edition, Revised and Expanded. D.M. Pirro (Exxon Mobil Corporation Fairfax, Virginia), A.A. Wessol (Lubricant Consultant Manassas, Virginia). 2001.
  2. United States Environmental Protection Agency Office of Wastewater Management Washington, DC 20460. Environmentally Acceptable Lubricants. https://www3.epa.gov/npdes/pubs/vgp_environmentally_acceptable_lubricants.pdf
  3. Chemistry and Technology of Lubricants 3rd Edition, Chapter 1, R.M. Mortier, M.F. Fox, S.T. Orszulik)