If the health community had a problem as large as turbine oil varnish it would be classed as an epidemic. Predicting and understanding lubricating oil degradation like human health, is not only an art but also a science. Numerous articles have been published revealing the various diseases within lubrication oil systems. The motivation for writing this paper is to deal with this highly published epidemic and prescribe a control for the disease.
As with human health, lubricating oil health should be looked upon and respected like the components that keep the body healthy. There are many analogies that relate to the human body and lubrication oil systems, heart (the pump), lungs, (system breathing), kidneys/liver (filters), veins (oil lines).
Machines are used to clean not cure body functions, such as kidney dialysis. A similar application is used to clean not cure lubrication oil functions, hot oil flushing/filtration. As with the human body various medications are used to control not cure health problems. The same holds true for lubrication oil systems, various additives are prescribed, and sometimes the side affects are worse than the problem.
As with the health of the human body there are a number of lubrication oil disease's that must be diagnosed; oxidation, varnish formation, peroxide, water, particle contamination additive depletion.
Oxidation is one of the most detrimental processes causing degradation of turbine oils during service. Oil oxidation leads to formation of acidic products, insoluble materials, and sludge, depletion of additives, loss of dispersancy, increase of viscosity, etc. All of these undesirable changes are, however, also affected by other concurrent processes occurring in an operating turbine oil system such as thermal degradation, mechanical, chemical reactions, metal catalysis, and interactions with other products, which result in nitration and hydrolysis. Contributions of such processes to degradation are the main reason that correlation of turbine oil test results with results of laboratory oxidation tests is not always successful.
Oxidation properties of a turbine oil are determined by its composition. In this respect, contributing factors are compositions of base oils, additives, and additive diluent oils. Particularly important are the presence and anti¬oxidant properties of synthetic antioxidant additives and of natural inhibitors in base and diluent oils. Conse¬quently, antioxidant capability is one of the most impor¬tant technological parameters determining the oxidation stability of turbine oils.
Turbine oil oxidation is initiated by free radicals, which are derived either from temperature or from decomposition of primary oxidation products such as hydroperoxides. These free radicals react with the oil, to abstract hydrogen and form alkyl radicals, which in the presence of oxygen form peroxy radicals. In the absence of antioxidants, peroxy radicals further react with additional oil to form hydroperoxides and alkyl radicals. This continues in a chain reaction process, which can result in the formation of a high concentration of hydroperoxides. Adding radical-trapping antioxidants to the oil can inhibit the chain reaction process.
Varnish
Varnish is a hard, sometimes brittle, veneer-like coating that covers metallic components inside lubrication systems. Varnish and sludge are terms that are interchangeable as they proliferate from the same degradation processes. To distinguish between the two, sludge is less dense than varnish and acts as a predecessor to varnish. Sludge will have higher water content, whereas varnish is moisture-free. Prolonged elevated temperatures will evaporate the moisture from the sludge increasing its density. Although they basically come from the same source, varnish as it forms on metal components, is a much more difficult problem to address. It's a sticky, gooey substance that can cause serious stiction and seizure problems in valves and other close tolerance system components. Combustion turbines in particular are very sensitive to varnish formation. Varnish with its sticky, gooey adhesive properties will combine with debris particles producing a slurry of oxidation wear contaminants.
The human health analogy to varnish is plaque that gradually builds-up in blood streams and attaches to the lining of veins and heart valves and varnish that attaches to the lining of piping and system valves. If not corrected both will eventually die. The human prescription to control or prevent this problem; medication, diet, exercise and other life style changes. The industry's prescription now used to control varnish that builds-up in lubrication oil streams; oil replacement and hot oil filtration/flushing.
Oxidation States
Before we go further in prescribing a cure for varnish, we must understand oxidation states. The oxidation state or oxidation number is defined as the sum of negative and positive charges in an atom, which indirectly indicates the number of electrons it has accepted or donated. The rules for oxidation states are in some ways arbitrary and unnatural, but need to be reviewed.
- All free (unattached) elements without a charge has the oxidation state of zero.
- All compounds have a net oxidation state of zero.
- The oxidation state of all of the atoms adds up to zero
- Polyatomic ions (radicals) have an oxidation states for the whole ion that is the charge on that ion.
- Oxygen has an oxidation state of minus two, except for oxygen as peroxide, which is minus one.
- Hydrogen has an oxidation state of plus one, except for hydrogen as hydride, which is minus one.
- Radicals or small covalent molecules, the element with the greatest electronegativity has its natural ion charge asits oxidation state.
In organic chemistry, oxidation of a hydrocarbon produces water and successively, an alcohol, an aldehyde or a ketone, carboxylic acid, and then a peroxide.
Oxygen will normally take in two electrons when it is not a free element therefore the combined form of oxygen (oxide) has an oxidation state of minus two. The exception of oxygen taking two electrons is peroxide.
Antioxidants
An antioxidant is any substance that retards or prevents deterioration, damage or destruction by oxidation. Free radicals act by oxidation. Oxidation is always damaging to whatever is oxidized, although often it is very useful-indeed, it is the source of all our energy, and our bodies could not work without it.
Chemists have known that free radical oxidation action can be controlled or even prevented by a range of antioxidant substances. It is, for instance, vital that lubricating oils should remain stable and liquid and should not dry up like paints. For this reason, such oils usually have small quantities of antioxidants, such as phenol or amine derivatives, added to them.
Peroxide
Peroxides are powerful oxidizers, and usually fairly unstable. Ionic peroxides react with water and diluted acids to form hydrogen peroxide. Organic compounds are oxidized to carbonates, even at normal temperatures. A peroxide ion contains two electrons more than an oxygen molecule and is diamagnetic (repelled by a magnet).
Diagnosing Lubricating Oil Problems
Oxidation is a chemical reaction promulgated by moisture, additive depletion. and lack of negative ions promoting the build-up of sludge. Varnish is a by-product.
Chain propagation and branching reactions in thermal failure produces organic, soluble compounds. The process continues until insoluble species are generated forming polymers and other compounds of high molecular weight. These insolubles have a sticky characteristic and easily bond to particles, depleted additives and water.
Varnish forms when the solubility limit for the high molecular weight insolubles is exceeded. Temperature is a key factor in the solvency of a lubricant, and is a determinant for the creation of varnish. Studies have shown that insoluble compounds are more resistant to dropping out of solution at temperatures above 68°C. This explains why varnish will first start to form in cooler spots in the system, such as strainers and the splash area immediate above the fluid capacity in the reservoir. At extreme temperatures, thermal failure has the potential to produce black carbon particles, which can fall out of solution immediately.
The Varnish Detection Challenge
It is not possible to monitor thermal and oxidative degradation on the molecular level, but it is possible to observe the products formed at the termination of the degradation process. Employing oil analysis as a tool to monitor thermal and oxidative degradation to predict the formation of varnish can be a powerful addition to a predictive maintenance program. In many applications, routine oil analysis tests such as viscosity and acid number will alert the user of increases levels of thermal failure and oxidation. Measuring a fluid's resistance to oxidation (RPVOT - ASTM D2272) can also assess the health of a lubricant and indicate the fluid's potential to oxidize and produce varnish.
Once acid numbers become elevated, signifying thermal failure and oxidation, there exist sufficient levels of insolubles in the lubricant to justify varnishing concerns. Emptying reservoirs of thermally damaged lubricants will reveal sludge and varnish accumulation. Strainers will be covered in a brown, resinous material and sight-glasses may be hazy.
Ideally, detection of a fluid's varnish potential would occur when the thermal and oxidative degradation process initiates the production of soluble and quasi-soluble contaminants, well prior to the creation of varnish. Unfortunately, there are no known analytical procedures with the sensitivity to measure these minute organic compounds in this state. However, there are several oil analysis tests that have the ability to detect varnish pre-cursors and are suitable to be part of a predictive maintenance program.
High molecular weight by-products are the pre-cursor to varnish. They are polar in nature and have an inclination to precipitate out of the non-polar lubricant onto dipolar metallic surfaces. They can affect several of the lubricants properties including viscosity, foaming, demulsibility characteristics and cause interference with polar additives such as Extreme Pressure (EP), Anti Wear (A W) and corrosion inhibitors.
Thermal failure occurs in one or more of the following conditions. A hot spot in the system elevates the lubricant to a very high temperature causing localized thermal failure. Pressure-Induced Thermal Failure is a rapid adiabatic compression of air bubbles in a system that creates excessive high temperatures, causing thermal failure. Static electricity sometimes is generated between oil and mechanical filtration, creating high temperatures and free-radical generation.
Thermal Failure and Oxidation
Thermal failure and oxidation are similar lubricant destructive mechanisms involving free¬ radical chain proliferation. Thermal failure occurs in the absence of oxygen where as the process of oxidation uses an oxygen molecule as a catalyst to the reaction. Both degradation processes generate similar by-products. Analytical methods to measure thermal and oxidative degradation processes are also similar.
Following are some of the differences between thermal failure and oxidation: Thermal failure can occur in a lubricant prior to the anti-oxidants being depleted. Thermal failure can happen before elevations in acid number. Thermal failure can occur in new products I caused by improper storage practices.
Most lubricants are formulated with anti-oxidants designed to retard the thermal and oxidative process. Primary anti-oxidants are free-radicals scavengers, bringing an abrupt end to the self-accelerating degradation process. The key types of primary anti-oxidants are hindered phenols and aromatic amines. Secondary anti-oxidants decompose hydro-peroxides, another by-product in oxidation. Finally, oils are formulated with metal deactivators that render metallic oxidation catalysts inert.
Varnish Detection
When acid numbers become elevated, this is a signal that thermal failure and oxidation must be appraised for products of oxidation and varnish. Reservoirs bottoms and walls are a good source for discovery of sludge and varnish accumulation. Strainers may be coated in a brown, resinous material and sight-glasses may be also coated.
The challenge with combustion turbine applications and other sensitive applications is the amount of varnish that can cause serious consequences, in most cases it is extremely low. The formation of damaging varnish may be progressing well before typical routine oil analysis detects signs of degradation.
There are six tests that have the ability to detect varnish pre-cursors. These tests can help to trend the increase of insolubles and will indicate early detection of oxidation.
- Colorimetric Analysis
- Gravimetric Patch Test
- Ultracentrifuge
- Fourier Transform Infrared (FTIR)
- Interfacial Tension
- RULER™
Combining the test results will provide valuable information that positively correlates to the oils potential to produce varnish.
Oxidation-Reduction (REDOX)
The term redox comes from the two concepts of REDuction and OXidation. Oxidation describes the loss of an electron by a molecule, atom, or ion. It also means an increase in oxidation number. Reduction describes the uptake of an electron by a molecule, atom, or ion. It also means a decrease in oxidation number. These two terms go together, because in a chemical reaction, one cannot occur without the other; electrons lost by one compound must be gained by another. Reduction can also be considered to be the reducing of an atom's positive charge, and oxidation its opposite (gaining positive charge).
The logical starting point in the discussion of oxidation-reduction reactions is the atom, and the terms and conventions used by chemists in describing this phenomenon. All atoms are electrically neutral even though they are comprised of charged, subatomic particles.
Atoms and Subatomic Particles
Atoms can be visualized, as spherical, electrically neutral particles comprised of many subatomic particles. As far as the topic of oxidation-reduction is concerned, we shall consider only two of these particles, the proton and the electron. Protons are positively charged particles, which are always found in the dense core or nucleus of the atom. According to theory, the electrons, or negatively charged particle, are located somewhere outside of the nucleus and surrounding it in spherical fashion as shown in the sketch below.
Each proton is arbitrarily assigned a charge of "+1″; and each electron, a charge of "-1″. In every atom there is always the same number of protons (p) as there are electrons (e). Hence, every atom is electrically neutral, as the positive charges of the protons always cancel the negative charge of the electrons. In other words, the net electrical charge of any atom is always zero.
The terms, oxidation state or oxidation number, have been developed to describe this "electrical state" of the atom. The oxidation state or oxidation number of an atom is simply defined as the sum of the negative and positive charges in an atom. Since every atom contains equal numbers of positive and negative charges, the oxidation state or oxidation number of any atom is always zero.
Some Atoms attract electrons more strongly than others. This attraction for electrons shared in covalent bonds is called electronegativity. Strong attractions create electronegativity of the atom. When an electronegativity atom, such as oxygen, shares electrons with hydrogen to form water there is an unequal pull on the shared electrons. Oxygen pulls them harder than does hydrogen.
It is well known scientifically, that atoms and molecules are electrically neutral, and the number of negatively charged electrons is exactly equal to the number of positively charged protons. Much of the "normal matter" that we find around us is in this form. However, particularly when there are energy sources available, atoms or molecules can gain or loose electrons and acquire a net electrical charge. This process is called ionization. To use electrostatics and ionization energy (IE) to cure a disease, we must understand the importance of ionization.
Ionization
Ionization energy (IE) is the amount of energy required to remove one electron from an atom. It is measured by how strong the outermost electron is attached to the atom. Some atoms my have one or more ionization energies. If this is the case it's referred to as the "first ionization energy" or "i", second ionization energy" or "h" and so on. As stated earlier the ionization energy is the amount of energy it takes to detach one electron from a neutral atom. Ionization is endothermic meaning that the atom or molecule increases its internal energy (receiving energy from an outside source).
The ionization energy of an atom is equal to the amount of energy given off when an electron is added to an atom. Electrons added to an atom and the energy given off is called electron affinity (EA). For most atoms the initial electron affinity is exothermic meaning energy is given off. However when adding a second, third etc. electron you are working with a negative ion. Therefore it takes greater energy to add the extra electron.
Electrons
Electrons can be moved from atoms by heat, light, electric energy, or bombardment with high-energy particles. Electronegativity is a parameter, which describes, on a relative basis, the power of an atom to attract electrons. A free radical is a molecule fragment having one or more unpaired electrons, usually short-lived and highly reactive. They can be produced by proteolysis (hydrolytic breakdown) or pyrolysis (decomposition) in which a bond is broken without forming ions. Free radicals are known to be formed by ionizing radiation and thus play a part in deleterious degradation effects that occur in irradiated tissue. They also act as initiators or intermediates in oxidation, combustion, photolysis (chemical decomposition induced by light) and polymerization (bonding two or more monomers). Free radicals are highly reactive molecules or atoms with an unpaired electron.
Polar Molecules
Chemical bonding is the result of elements sharing or taking electrons in the outer orbits of the element with which it is bonding. Normally, an atom has an even distribution of electrons in the orbits or shells, but if more end up on one side than the other in a molecule, there can be a resulting electrical field in that area. Water molecules are polar, with positive charges on one side and negative charges on the other side.
Polar Covalent bonds
A polar bond is a covalent bond (electrostatic force of attraction when one or more pairs of electrons are shared between atoms) in which there is a separation of charge between one end and the other, one end is slightly positive and the other end slightly negative.
Non Polar Molecules
Oil is a non-polar molecule, with electrons distributed more symmetrically, but do not have and abundance of charges at the opposite sides, thus canceling out each other.
Rule Polar and Non Polar Molecules
Polar molecules will mix to form solutions and non-polar molecules will mix to form solutions, but polar and non-polar combinations will not form a solution.
So far we have covered the basics of ionization energy. Now we need to look at the more advanced methods of discovery. Two characteristics of an atom that are very important to scientists are the Highest Occupied Molecular Orbital (HOMD) and the Lowest Unoccupied Molecular Orbital (LUMO). Together these two orbital are referred to as frontier orbitals. The HOMO can be found by locating the outer most orbital containing an electron. The LUMO is the first orbital that does not contain an electron. The frontier orbitals also give some insight into various aspects of the molecule such as hardness, aromatics and electronegativity.
Electronegativity
Electronegativity has an affinity for electrons and is a measure of the tendency of an atom to attract a bonding pair of electrons. If atoms are equally electronegative, both have the same tendency to attract the bonding pair of electrons, and so it will be found on average half way between the two atoms.
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A+ B-
•
To get a bond like this, A and B would usually have to be the same atom. This sort of bond could be thought of as being a "pure" covalent bond - where the electrons are shared evenly between the two atoms. If B is slightly more electronegative than A, B will attract the electron pair more than A. That means that the B end of the bond has more than its fair share of electron density and so becomes slightly negative. At the same time, the A end (rather short of electrons) becomes slightly positive.
•
A+ B-
•
A redox reaction, also known as an oxidation-reduction reaction, is a type of chemical reaction where one of the reactants is oxidized and one of the reactants is reduced. Oxidation of a compound can be defined in several ways, one of which is that it is the gain of bonds to oxygen, another of which is that it is the loss of electrons. Similarly, two useful definitions of reduction, (the opposite of oxidation), are the gain of hydrogen or the gain of electrons.
The mnemonic OIL RIG can help you remember these definitions: Oxidation Is Loss (of electrons), Reduction Is Gain (of electrons).
Oxidation and reduction reactions always occur together, because the electrons that are donated from one compound, must be received by another compound. This is why redox reactions are said to be the product of two half reactions, the oxidation half reaction and the reduction half reaction. Each half reaction has a measurable reduction potential E0, which is a measure in volts of how easily the compound is reduced (how easily it gains electrons). Remember, the reduction potential is how much a species "wants" to get reduced, and the higher the number, the greater the potential.
Redox reactions play an important part in our lives. Combustion reactions that generate heat and electricity, such as the burning of natural gas, oil, gasoline or wood, are redox reactions, and in our bodies, redox reactions are needed to generate ATP to power our metabolism and our muscles.
Redox involves the transfer of electron density from one atom to another. For example, the electron density reaction of hydrogen and oxygen to produce water: The H2 and O2 both carry a charge of zero because they are nonpolar. But the product, water, is polar and hydrogen has a partial positive charge and the oxygen has a partial negative charge. During the reaction, the hydrogen atoms lose some electron density and the oxygen atoms gain. Many chemical reactions involve a shift of electron density and are called redox reactions. Reduction and oxidation always occur together. If one thing is reduced, another thing is oxidized. The reactant that is reduced is called the oxidizing agent and accepts electrons. The reactant that is oxidized is called the reducing agent and supplies electrons.
Redox reactions include all chemical processes in which atoms have their oxidation number (oxidation state) changed. This can be a simple redox process, such as the combustion of carbon to yield carbon dioxide, it could be the reduction of carbon by hydrogen to yield methane, or it could be the oxidation of sugar in the human body, through a series of very complex electron transfer processes.
One of the primary questions is: How can an object be charged and what effect does that charge have upon other objects in its vicinity? The answer to this question begins with an understanding of the structure of matter. Understanding charge as a fundamental quantity demands that we have an understanding of the structure of an atom.
One sure truth of this unit is that the protons and neutrons will remain within the nucleus of the atom; the movement of protons can never explain electrostatic phenomenon.
Nature of the Ionic Bond
An ionic bond is an electrical attraction between two oppositely charged atoms or groups of atoms. Normally, atoms are neutral and have no charge. However, in order to gain stability they will sacrifice their neutrality by either losing one or more of its outermost electrons thus becoming a positive ion (cation) or they will gain one or more electrons thus becoming a negative ion (anion). Elements that are described as "metallic" tend to lose electrons and elements that are described as "non-metallic" tend to gain electrons. Once this has happened the resulting charged atoms will attract each other. That electrical attraction between two oppositely charged ions is referred to as an ionic bond. Most salts are ionic. Any metal will combine chemically with any non-metal to form ionic bonds that hold the molecule together
Polarity of the Ionic Bond
Because the bonding electrons are literally under the domain of the non-metal in an ionic bond, the bond is said to be polar. Polar bonds generate a dipole moment. A dipole moment is an electrical force that is generated because of the unequal distribution of the bonding electrons between the two bonded atoms. In the case of an ionic bond that unequal distribution is extreme. The dipole moment that is generated is quite large compared to polar bonds of the co-valent bond.
A dipole moment is a vector measurement. A vector is a measurement that has a magnitude and a directional component. Any force (mechanical, electrical, magnetic, etc.) will be vector measurement. Examples would be velocity and forces. The other type of measurement is scalar measurement. These are measurements that have only a magnitude component but no directional one. Examples would be temperature, mass, speed, etc. Scalar measurements are handled differently than vector measurements when it comes to math operations. For example when you add or subtract scalar measurements you pay no attention to direction. With vector forces, you must pay attention to the direction and the angle between the vectors. Often the use of trigonometry is called for in order to resolve vectors.
Characteristics of Ionic Compounds
- Crystalline solids at room temperature
- Have higher melting points and boiling points compared to co-valent compounds
- Conduct electrical current in molten or solution state
- Are extremely polar bonds
- Most are soluble in water but not soluble in non-polar solvents
Controlling Turbine Oil Varnish
Controlling turbine oil varnish is analogous to controlling disease in the human body. One example, the substance that attaches to the lining of veins and heart valves and varnish that attaches to the lining of piping and system valves. If not corrected both will eventually die. The most efficient and effective means to control turbine oil varnish is with electrostatic charging of atoms and ions in combination with filtration. Electrostatic fundamentally is a phenomenon and must rely on theory in some cases. Therefore to help accomplish the task of controlling varnish requires some understanding of Electron Transfer Rules, Theory, Forces and Electrostatic Chemistry.
Electrostatic Chemistry
Bonding
The following are terms used to refer to bonding force between particles to remove solid particles and varnish:
Intermolecular
Force of attraction between atoms and molecules.
Ionic
Electrostatic force of attraction between two oppositely charged Ions.
Covalent
Electrostatic force of attraction when 1 or more pairs of electrons is shared between atoms.
Dative
- A covalent bond in which the pairs of electrons involved in the bond is donated entirely from one of the atoms.
- A bond in which both electrons come from a single donator atom.
Metallic
The attraction of free-floating valence electrons for the positively charged metal ions.
Hydrogen
Attractive forces in which hydrogen that is covalently bonded to a very electronegative atom is also weakly bonded to an unshared electron pair of an electronegative atom in the molecule or in a nearby molecule. The hydrogen bonding in water has about 5% of the strength of an average covalent bond.
Pi
In a pi bond, the bonding electrons are most likely to be found in sausage-shaped regions above and below the bond axis of the bonded atoms.
Sigma
A bond formed when two atomic orbitals combine to form a molecular orbital that is symmetrical along the axis connecting two atomic nuclei.
Bond Length
A measure of the distance between the centers of two bonded atoms.
Bond Enthalpy
The energy required to break a bond in standard conditions. (The condition of a substance at 25°C and 1 atm pressure).
Electrostatic Theory
VSEPRT (Valance Shell Electron Pair Repulsion) states that because electron pairs repel, molecules adjust their shapes so that the valance electron pairs are as far apart from possible.
Kinetic Theory
A theory stating that tiny particles in all forms of matter are in constant motion.
Van der Waals
The weakest of all attractions. Also known as Dispersion forces: generally thought to be caused by the motion of electrons, the strength of dispersion forces increases as the number of electrons in a molecule increases. As the electrons move about the molecule, temporary dipoles will be created that attracts the molecules to each other. Generally larger molecules exhibit larger Van der Waals forces.
Diffusion
The tendency of molecules and ions to move toward areas of lower concentration until the concentration is uniform throughout the system.
Brownian Motion
Brownian motion is the continuous random movement of small particles suspended in a fluid, which arise from collision with the fluid molecules. First observed when studying pollen particles. The effect is also visible in particles of smoke suspended in a still gas.
Laws
Coulomb's
The statement that force F between two electrical charges q1 and q2 separated by a distance r.
Force
Any two charged objects will create a force on each other. Opposite charges will produce an attractive force while similar charges will produce a repulsive force. The greater the electric charge the greater the force. The greater the distance between the two charges, the smaller the force.
Conservation of Charge
The Law of conservation of charge states that the net charge of an isolated system remains constant. If a system starts out with an equal number of positive and negative charges, there's nothing we can do to create an excess of one kind of charge in that system unless we bring in a charge from outside the system (or remove some charge from the system). Likewise, if something starts out with a certain net charge, say +100 e, it will always have +100 e unless it is allowed to interact with something external to it.
Charge can be created and destroyed, but only in positive-negative pairs.
Electrostatic Charging of Objects
Electrostatics
The study of electrostatic charges at rest:
There are two kinds of electrical charges, positive (+) and negative (-). Like charges repel and unlike charges attract. Thus, electrical charges exert a force on other electrical charges. This electrostatic force is directly proportional to the product of the charges and inversely proportional to the square of the distance of separation (another inverse square relationship).
Charged Object Created By The Separation Of Charges
- An atom is electrically neutral; it has the same number of protons (positive charges) as it does electrons (negative charges)
- Objects are charged by adding or removing electrons
- A positive charge occurs when there are fewer electrons than protons; its classical definition is the charge accumulated by a glass rod rubbed with silk or wool
- A negative charge occurs when there are more electrons than protons; it's classical definition is the charge accumulated by a hard, rubber rod rubbed with fur.
The choice of which name went with which charge was arbitrary. Benjamin Franklin set the convention. Franklin called the charge accumulation by the rubbed glass rod to be positive and that the rubber rod negative. Franklin also argued that whenever a certain amount of charge was produced on one-body in a process, an equal amount of the opposite charge was produced on another body. In any process, the net charge in the amount of charge produced is zero.
Electrostatic Field
When two objects in each other's vicinity have different electrical charges, an electrostatic field exists between them. An electrostatic field also forms around any single object that is electrically charged with respect to its environment. An object is negatively charged (-) if it has an excess of electrons relative to its surroundings. An object is positively charged (+) if it is deficient in electrons with respect to its surroundings.
Electrostatic fields bear some similarity to magnetic fields. Objects attract if their charges are opposite polarity (+/-); objects repel if their charges are of the same polarity (+/+ or -/-). The lines of electrostatic flux in the vicinity of a pair of oppositely charged objects are similar to lines of magnetic flux between and around a pair of opposite magnetic poles.
Conduction
A charged object touches another object; the amount of charge equally divides between the two objects; each object acquires the same sign charge.
Induction
A charged object is brought near, but not touching, another object; it attracts charges opposite to it and repels charges like it; when a ground is used, the opposite charge is acquired on the other object; it is thus charged without being touched. Of course, the net charge is still zero. Charges have merely been separated.
The idea by some that ions must be balanced to successfully remove debris from oil electrostatically is not a scientific fact. For example an electrostatic filtration system having one line that branches into two lines. With line A charged internally positive and line B charged internally negative, ion distribution in each line would have to be the same to balance the charge.
Electrostatic filtration the charging of atoms/ions has a distinct advantage over generic type mechanical filtration. Angstrom sized debris can be efficiently and effectively removed from turbine oil. The angstrom-sized particles are electrostatically attracted to one another forming large bundles of debris large enough to be captured in an open pore filter media.
Varnish Adhesive Theory
The basis of the electrostatic theory of adhesion is the difference in electonegativities of adhering materials. Adhesive force is attributed to the transfer of electrons across the interface creating positive and negative charges that attract one another. For example, when an organic polymer is brought into contact with metal, electrons are transferred from metal into the polymer, creating an attracting electrical double layer (EDL). The electrostatic theory tells us that these electrostatic forces at the interface (i.e. in the EDL), account for resistance to separation of the adhesive and the substrate.