WO2008002349A1 - Method of blending lubricants using positive displacement liquid-handling equipment - Google Patents
Method of blending lubricants using positive displacement liquid-handling equipment Download PDFInfo
- Publication number
- WO2008002349A1 WO2008002349A1 PCT/US2007/010700 US2007010700W WO2008002349A1 WO 2008002349 A1 WO2008002349 A1 WO 2008002349A1 US 2007010700 W US2007010700 W US 2007010700W WO 2008002349 A1 WO2008002349 A1 WO 2008002349A1
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- WIPO (PCT)
- Prior art keywords
- lubricant
- positive displacement
- void volume
- displacement pipette
- low void
- Prior art date
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/80—Mixing plants; Combinations of mixers
- B01F33/84—Mixing plants with mixing receptacles receiving material dispensed from several component receptacles, e.g. paint tins
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
- B01F35/80—Forming a predetermined ratio of the substances to be mixed
- B01F35/88—Forming a predetermined ratio of the substances to be mixed by feeding the materials batchwise
- B01F35/881—Forming a predetermined ratio of the substances to be mixed by feeding the materials batchwise by weighing, e.g. with automatic discharge
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
- B01F35/80—Forming a predetermined ratio of the substances to be mixed
- B01F35/88—Forming a predetermined ratio of the substances to be mixed by feeding the materials batchwise
- B01F35/882—Forming a predetermined ratio of the substances to be mixed by feeding the materials batchwise using measuring chambers, e.g. volumetric pumps, for feeding the substances
- B01F35/8822—Forming a predetermined ratio of the substances to be mixed by feeding the materials batchwise using measuring chambers, e.g. volumetric pumps, for feeding the substances using measuring chambers of the piston or plunger type
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/02—Burettes; Pipettes
- B01L3/021—Pipettes, i.e. with only one conduit for withdrawing and redistributing liquids
- B01L3/0217—Pipettes, i.e. with only one conduit for withdrawing and redistributing liquids of the plunger pump type
Definitions
- the present invention relates to the field of lubricant blending. It more particularly relates to an improved method of accurately blending highly viscous additives into lubricants. Still more particularly, the present invention relates to a method of dispensing accurately small amounts of high viscosity lubricant components using positive-displacement pipettes.
- Lubricants are generally mixtures of several components.
- the largest fraction of the blended lubricant is a mineral oil or synthetic basestock that typically makes up more than 80 percent of the total volume.
- the remainder of the lubricant consists of various additives which impart performance improving attributes such as antioxidancy, antiwear, foam reduction and the like.
- Additional additives known as viscosity modifiers, are also sometimes added to thicken the lubricant and improve the viscosity versus temperature attributes of the lubricant.
- Viscosity modifiers are made of relatively high molecular weight polymeric molecules that can be quite viscous. Basestocks are much lower in viscosity. Consequently, lubricant blending equipment and methods usually necessitate dispensing components that span a wide viscosity range.
- Viscous liquids generate significant resistance to the applied gas pressure and gas compression may result in less liquid than desired being ejected from the pipette.
- polymeric viscosity modifiers may form stringy residue near the tip inside the pipette, resulting in less liquid dispensed in the receiving vessel.
- a further limitation of air displacement pipettes is that they require connection to a pump or vacuum system.
- a rubber bulb is typically utilized in the case of manually operated pipettes.
- tubing is typically connected to each pipette.
- a system liquid is also used to help the transfer of the pump action to the pipette tips and an air gap is used to separate the system liquid from the liquid to be transferred (a combination of air and liquid displacement).
- This can be quite cumbersome when many pipettes are used. For example, if many blend components are being used, each component requires its own pipette to avoid having to continuously clean pipettes. With air displacement or combination of air/liquid displacement pipettes, each pipette must be connected to a pump, which may not be practical.
- one pipette may be utilized, but this necessitates repeated cleaning of the pipette between each use of a different component.
- a system liquid is used, there is also a possibility of cross- contamination between the system liquid and the lubricant additives.
- High viscosity lubricant components are often derived from high molecular weight polymers. Thus, high viscosity lubricant components may degrade when subjected to high shear conditions. High shear results when a high viscosity lubricant is forced through a small orifice at high pressure, which may cause permanent rupture of molecular bonds. It is therefore desirable when pipetting high viscosity lubricant components to maintain a relatively low shear rate when ingesting them into the pipette, and also when expelling them from the pipette. In some cases, the blending process may be improved by heating high viscosity components thereby reducing their viscosity. It is desirable to minimize the need for heating components because lubricant components may degrade at elevated temperature.
- the present invention provides an advantageous method of accurately blending high viscosity lubricant components with tubeless positive displacement pipettes to form a lubricant blend comprising the following steps: providing a low void volume positive displacement pipette for each lubricant component contained within a lubricant additive reservoir, and one or more lubricant blend containers; ingesting into the low void volume positive displacement pipette from the lubricant additive reservoir an ingestion volume of a lubricant component; moving the low void volume positive displacement pipette from the lubricant additive reservoir to the one or more lubricant blend containers; ejecting into the one or more lubricant blend containers an ejection volume of the lubricant component from the low void volume positive displacement pipette; returning the low void volume positive displacement pipette from the one or more lubricant blend containers to the additive reservoir; and repeating the ingesting, the moving, the ejecting and the returning steps for each additional steps.
- the present invention provides an advantageous method of accurately blending high viscosity lubricant components with tubeless positive displacement pipettes to form a lubricant blend comprising the following steps: providing a low void volume positive displacement pipette for each lubricant component contained within a lubricant additive reservoir, a heating means for the lubricant additive reservoir, one or more lubricant blend containers, a balance for weighing a mass of the one or more lubricant blend containers, and a robotic means coupled to a computer or programmable logic controller for coordinating and controlling the following steps; heating one or more lubricant components with a high viscosity to a temperature below about HO 0 C; ingesting into the low void volume positive displacement pipette from the lubricant additive reservoir an ingestion volume of a lubricant component; moving the low void volume positive displacement pipette from the lubricant additive reservoir to the one or more lubricant blend containers; ejecting into the following steps: providing a low
- the present invention provides an advantageous method of accurately blending high viscosity lubricant components with tubeless positive displacement pipettes to form a lubricant blend comprising the following steps: providing a low void volume positive displacement pipette for each lubricant component contained within a lubricant additive reservoir, a heating means for the lubricant additive reservoir, one or more lubricant blend containers with a volume less than 10 milliliters, a balance for weighing a mass of the one or more lubricant blend containers, and a robotic arm connected to a support bridge coupled to a computer or programmable logic controller programmed with one or more lubricant blend recipes for coordinating and controlling the following steps; heating one or more lubricant components with a viscosity greater than about 500 centipoise at 100 0 C to a temperature of less than about 110 0 C; ingesting into the low void volume positive displacement pipette from the lubricant additive reservoir an ingestion volume of
- the disclosed method of blending lubricant additives using positive-displacement liquid- handling equipment provides for improved accuracy of dispensing high viscosity additives into lubricants.
- the disclosed method of blending lubricant additives using positive-displacement liquid-handling equipment provides for a method of accurately producing small lubricant blends, which may be used in high throughput experimentation type of environments.
- the disclosed method of blending lubricant additives using positive-displacement liquid-handling equipment provides for dispensing of high viscosity lubricant components without shear induced degradation of the components.
- the disclosed method of blending lubricant additives using positive-displacement liquid-handling equipment provides for less stringy residue at the pipette tip upon discharge.
- the disclosed method of blending lubricant additives using positive-displacement liquid-handling equipment provides for a means of more quickly dispensing small volumes of high viscosity lubricant components.
- the disclosed method of blending lubricant additives using positive-displacement liquid-handling equipment provides for minimal heating of lubricant additives, and therefore less degradation and discoloration prior to discharge.
- the disclosed method of blending lubricant additives using positive-displacement liquid-handling equipment provides for a means to measure in real time the density of the lubricant additive being dispensed into the lubricant.
- the disclosed method of blending lubricant additives using positive-displacement liquid- handling equipment provides for a means to measure in real time the mass of lubricant additive being dispensed into the lubricant.
- Figure 1 depicts an exemplary schematic of a low void volume positive displacement pipette of the present invention.
- Figure 2 depicts an alternative exemplary schematic of a low void volume positive displacement pipette of the present invention.
- Figure 3 depicts an exemplary schematic of a low void volume positive displacement pipette in a lubricant additive reservoir.
- Figure 4 depicts an exemplary schematic of an array of additive reservoirs.
- Figure 5 depicts an exemplary schematic of a lubricant blend station based on the use of positive-displacement pipettes.
- the present invention relates to a method of blending high viscosity lubricant components comprising the use of positive-displacement pipettes.
- the method of blending high viscosity lubricant components of the present invention are distinguishable over the prior art in disclosing the use of positive displacement pipettes to accurately meter small quantities of high viscosity lubricant additives into a lubricant formulation.
- the advantages of the disclosed method of the present invention include, inter alia, improved dispensing accuracy, lower shear rate during dispensing, lower temperature for dispensing, less residual additive on the tip of the device after dispensing, and the ability to real time monitor density and mass during dispensing.
- Blends made according to volume concentration are generally made using air displacement pipettes or air/liquid displacement liquid handling systems.
- a source of air is attached to the end of the pipette and suction is applied to draw fluid into the pipette.
- the pipette is then placed in the receiving vessel and gas is applied to eject liquid into the receiving vessel.
- the suction is provided by a pump and action is transferred through a system liquid and the air gap between the system liquid and the liquid to be transferred.
- Different pipettes can be used for each lubricant component.
- a single pipette may be used if it is cleaned between exposure to different lubricant blend components in order to avoid contamination and inaccuracies.
- HTE high throughput experimentation
- Lubricants are typically blended from several components of different molecular weight and viscosity.
- High viscosity lubricant components are sometimes used to modify the viscometric properties of the lubricant blend.
- These viscosity modifiers are typically comprised of high molecular weight polymers. It is especially difficult to accurately measure the volume of high viscosity lubricant components blended into small blends when air displacement pipettes are used in a conventional way because of two factors. One factor is that viscous liquids generate significant resistance to the applied gas pressure, and gas compression can result in less liquid being ejected from the pipette than anticipated.
- a second factor is that because high viscosity lubricant components are typically polymers, they tend to form a stringy residue inside the pipette near tip. Consequently, less liquid ends up in the receiving vessel than was expelled from the pipette, which may lead to blending inaccuracies. The error introduced by these two factors is exacerbated when making small blend quantities.
- high viscosity lubricant components are blended after heating them to a temperature sufficient to reduce their viscosity to a range where they can be handled like low viscosity liquids.
- they may be diluted with low viscosity solvents. In this way they can be easily pipetted with standard air displacement pipettes and can be accurately dispensed.
- elevated temperature can cause high viscosity lubricant components to discolor or degrade. It is therefore desirable to blend them with minimal heating.
- High viscosity lubricant components may degrade under high shear flow conditions. Shear degradation may occur when such additives are forced under pressure through a small orifice such as the exit opening on a pipette.
- High viscosity lubricant components are often comprised of high molecular weight polymers. When these polymers are forced through a small opening, the shear rate and shear stress may be sufficiently high to cause breaking of chemical bonds, which lowers the molecular weight and the associated benefits of the high molecular weight molecules in the lubricant blend.
- An object of the present invention is to improve the accuracy of small lubricant blends containing high viscosity lubricant components made in a laboratory without causing degradation of the high viscosity lubricant component.
- it is necessary to accurately monitor the concentration of each component of the blend.
- blends can be made by controlling the concentration by weight of each component or by volume of each component.
- a further object of the present invention is to provide a method for accurately producing small lubricant blends, which include high viscosity lubricant components.
- These small lubricant blends contain preferably less than 100 milliliters of total volume, more preferably less than 25 milliliters of total volume, and even more preferably less than 10 milliliters of total volume.
- the present invention relates to the discovery that accuracy of small lubricant blends containing high viscosity components can be improved by using pipettes activated by movement of a piston with a shaft all the way to the tip, which are defined as positive displacement pipettes (herein also referred to as "PDP").
- PDP positive displacement pipettes
- Such pipettes are typically gear driven and generate sufficient pressure to ensure that all liquid residing in the pipette barrel is ejected.
- PDPs improve blend accuracy because the piston displaces a constant volume of liquid regardless of liquid viscosity.
- the piston may generate high pressure in the liquid, which is particularly relevant when using pipettes with a small orifice as is necessary when making small blend quantities.
- shear rate and shear stress When using pipettes with a small orifice to dispense high viscosity lubricant components, shear rate and shear stress must be such as to not cause degradation of the lubricant components. Shear rate and shear stress are proportional to the rate of flow through an orifice, and therefore to minimize lubricant degradation, it is important to keep flow rates below certain threshold shear rates.
- the flow rate of the high viscosity component flowing through an orifice should be controlled to keep the shear rate below 5 x 10 6 sec "1 , preferably below 1 x 10 6 sec "1 , more preferably below 1 x 10 5 sec "1 , and even more preferably below 1 x 10 4 sec “1 .
- the disclosed method of blending lubricant additives using tubeless positive- displacement pipettes is particularly suitable for dispensing high viscosity lubricant components or additives.
- a high viscosity lubricant component or additive is defined as a liquid with a viscosity greater than 100 centipoise at 100 0 C.
- the method of the present invention is particularly suitable for dispensing lubricant components or additives with a viscosity of greater than 500 centipoise at 100 0 C 3 and even more particularly suitable for dispensing lubricant components or additives with a viscosity of greater than 1000 centipoise at 100 0 C.
- Lubricant additives or components include, but are not limited to, viscosity modifiers, dispersants, detergents, pour point depressants, polyisobutylenes, high molecular weight polyalphaolefins, antiwear/extreme pressure agents, antioxidants, demulsifiers, seal swelling agents, friction modifiers, corrosion inhibitors, and antifoam additives, as well as packages containing mixtures of these lubricant additives, such as for example mixtures of dispersants, detergents, antiwear/extreme pressure agents, antioxidants, demulsifiers, seal swelling agents, friction modifiers, corrosion inhibitors, antifoam additives, and pour point depressants.
- High viscosity lubricants include, but are not limited to, viscosity modifiers, pour point depressants, dispersants, polyisobutylenes, and high molecular weight polyalphaolefins and additive packages containing one or more of these high viscosity lubricants.
- the disclosed method of blending lubricant additives using positive-displacement liquid-handling equipment method also allows blending to be done with minimal chemical, thermal or physical degradation of the high viscosity lubricant components within the lubricant blend.
- Viscosity modifiers also known as VI improvers and viscosity index improvers
- Suitable viscosity index improvers include high molecular weight (polymeric) hydrocarbons, polyesters and viscosity index improver dispersants that function as both a viscosity index improver and a dispersant. Typical molecular weights of these polymers are between about 10,000 to 1,000,000, more typically about 20,000 to 500,000, and even more typically between about 50,000 and 200,000.
- suitable viscosity index improvers are polymers and copolymers of methacrylate, butadiene, olefins, or alkylated styrenes.
- Polyisobutylene is a commonly used viscosity index improver.
- Another suitable viscosity index improver is polymethacrylate (copolymers of various chain length alkyl methacrylates, for example), some formulations of which also serve as pour point depressants.
- Other suitable viscosity index improvers include copolymers of ethylene and propylene, hydrogenated block copolymers of styrene and isoprene, and polyacrylates (copolymers of various chain length acrylates, for example). Specific examples include olefin copolymer and hydrogenated styrene-isoprene copolymer of 50,000 to 200,000 molecular weight.
- Viscosity modifiers are used in an amount of about 1 to 25 wt% on an as received basis. Because viscosity modifiers are usually supplied diluted in a carrier or diluent oil and constitute about 5 to 50 wt% active ingredient in the additive concentrates as received from the manufacturer, the amount of viscosity modifiers used in the formulation can also be expressed as being in the range of about 0.20 to about 3.0 wt% active ingredient, preferably about 0.3 to 2.5 wt% active ingredient.
- the active ingredient is in the range of about 5 to 15 wt% in the additive concentrates from the manufacturer, the amount of the viscosity modifiers used in the formulation can also be expressed as being in the range of about 0.20 to 1.9 wt% active ingredient, and preferably about 0.3 to 1.5 wt% active ingredient.
- Dispersants help keep these byproducts in solution, thus diminishing their deposition on metal surfaces.
- Dispersants may be ashless or ash-forming in nature.
- the dispersant is ashless.
- So called ashless dispersants are organic materials that form substantially no ash upon combustion.
- non-metal-containing or borated metal-free dispersants are considered ashless.
- metal-containing detergents discussed above form ash upon combustion.
- Suitable dispersants typically contain a polar group attached to a relatively high molecular weight hydrocarbon chain.
- the polar group typically contains at least one element of nitrogen, oxygen, or phosphorus.
- Typical hydrocarbon chains contain 50 to 400 carbon atoms.
- dispersants may be characterized as phenates, sulfonates, sulfurized phenates, salicylates, naphthenates, stearates, carbamates, thiocarbamates, phosphorus derivatives.
- a particularly useful class of dispersants are the alkenylsuccinic derivatives, typically produced by the reaction of a long chain substituted alkenyl succinic compound, usually a substituted succinic anhydride, with a polyhydroxy or polyamino compound.
- the long chain group constituting the oleophilic portion of the molecule which confers solubility in the oil is normally a polyisobutylene group.
- Other types of dispersant are described in U.S. Patents Nos.
- Hydrocarbyl-substituted succinic acid compounds are popular dispersants.
- succinimide, succinate esters, or succinate ester amides prepared by the reaction of a hydrocarbon-substituted succinic acid compound preferably having at least 50 carbon atoms in the hydrocarbon substiruent, with at least one equivalent of an alkylene amine are particularly useful.
- Succinimides are formed by the condensation reaction between alkenyl succinic anhydrides and amines. Molar ratios can vary depending on the polyamine. For example, the molar ratio of alkenyl succinic anhydride to TEPA can vary from about 1:1 to about 5:1. Representative examples are shown in U.S. Patent Nos. 3,087,936; 3,172,892; 3,219,666; 3,272,746; 3,322,670; and 3,652,616, 3,948,800; and Canada Pat. No. 1,094,044, all of which are incorporated by reference in their entirety.
- Succinate esters are formed by the condensation reaction between alkenyl succinic anhydrides and alcohols or polyols. Molar ratios can vary depending on the alcohol or polyol used. For example, the condensation product of an alkenyl succinic anhydride and pentaerythritol is a useful dispersant.
- Succinate ester amides are formed by condensation reaction between alkenyl succinic anhydrides and alkanol amines.
- suitable alkanol amines include ethoxylated polyalkylpolyamines, propoxylated polyalkylpolyamines and polyalkenyl- polyamines such as polyethylene polyamines.
- propoxylated hexamethylenediamine Representative examples are shown in U.S. Patent No. 4,426,305, which is incorporated by reference in its entirety.
- the molecular weight of the alkenyl succinic anhydrides used in the preceding paragraphs will typically range between 800 and 2,500.
- the above products can be post-reacted with various reagents such as sulfur, oxygen, formaldehyde, carboxylic acids such as oleic acid, and boron compounds such as borate esters or highly borated dispersants.
- the dispersants can be borated with from about 0.1 to about 5 moles of boron per mole of dispersant reaction product.
- Mannich base dispersants are made from the reaction of alkylphenols, formaldehyde, and amines. See U.S. Patent No. 4,767,551, which is incorporated herein by reference. Process aids and catalysts, such as oleic acid and sulfonic acids, can also be part of the reaction mixture. Molecular weights of the alkylphenols range from 800 to 2,500. Representative examples are also shown in U.S. Patent Nos. 3,697,574; 3,703,536; 3,704,308; 3,751,365; 3,756,953; 3,798,165; and 3,803,039, all of which are herein incorporated by reference in their entirety.
- Typical high molecular weight aliphatic acid modified Mannich condensation products useful in this invention can be prepared from high molecular weight alkyl- substituted hydroxyaromatics or HN(R) 2 group-containing reactants.
- Examples of high molecular weight alkyl-substituted hydroxyaromatic compounds are polypropylphenol, polybutylphenol, and other polyalkylphenols. These polyalkylphenols can be obtained by the alkylation, in the presence of an alkylating catalyst, such as BF 3 , of phenol with high molecular weight polypropylene, polybutylene, and other polyalkylene compounds to give alkyl substituents on the benzene ring of phenol having an average 600-100,000 molecular weight.
- an alkylating catalyst such as BF 3
- HN(R) 2 group-containing reactants are alkylene polyamines, principally polyethylene polyamines.
- Other representative organic compounds containing at least one HN(R) 2 group suitable for use in the preparation of Mannich condensation products are well known and include the mono- and di-amino alkanes and their substituted analogs, e.g., ethylamine and diethanol amine; aromatic diamines, e.g., phenylene diamine, diamino naphthalenes; heterocyclic amines, e.g., morpholine, pyrrole, pyrrolidine, imidazole, imidazolidine, and piperidine; melamine and their substituted analogs.
- alkylene polyamide reactants include ethylenediamine, diethylene triamine, triethylene tetraamine, tetraethylene pentaamine, pentaethylene hexamine, hexaethylene heptaamine, heptaethylene octaamine, octaethylene nonaamine, nonaethylene decamine, and decaethylene undecamine and mixture of such amines having nitrogen contents corresponding to the alkylene polyamines, in the formula H 2 N-(Z-NH-) n H, mentioned before, Z is a divalent ethylene and n is 1 to 10 of the foregoing formula.
- propylene polyamines such as propylene diamine and di-, tri-, terra-, pentapropylene tri-, terra-, penta- and hexaamines are also suitable reactants.
- the alkylene polyamines are usually obtained by the reaction of ammonia and dihalo alkanes, such as dichloro alkanes.
- the alkylene polyamines obtained from the reaction of 2 to 11 moles of ammonia with 1 to 10 moles of dichloroalkanes having 2 to 6 carbon atoms and the chlorines on different carbons are suitable alkylene polyamine reactants.
- Aldehyde reactants useful in the preparation of the high molecular products useful in this invention include the aliphatic aldehydes such as formaldehyde (also as paraformaldehyde and formalin), acetaldehyde and aldol ( ⁇ -hydroxybutyraldehyde). Formaldehyde or a formaldehyde-yielding reactant is preferred.
- Hydrocarbyl substituted amine ashless dispersant additives are disclosed, for example, in U.S. Patent Nos. 3,275,554; 3,438,757; 3,565,804; 3,755,433; 3,822,209 and 5,084,19; all of which are herein incorporated by reference.
- Preferred dispersants include borated and non-borated succinimides, including those derivatives from mono-succinimides, bis-succinimides, and/or mixtures of mono- and bis-succinimides, wherein the hydrocarbyl succinimide is derived from a hydrocarbylene group such as polyisobutylene having a Mn of from about 500 to about 5000 or a mixture of such hydrocarbylene groups.
- Other preferred dispersants include succinic acid-esters and amides, alkylphenol-polyamine-coupled Mannich adducts, their capped derivatives, and other related components. Such additives may be used in an amount of about 0.1 to 20 wt%, preferably about 0.1 to 8 wt%.
- pour point depressants also known as lube oil flow improvers
- pour point depressants may be added to lubricating compositions of the present invention to lower the minimum temperature at which the fluid will flow or can be poured.
- suitable pour point depressants include polymethacrylates, polyacrylates, polyaryl amides, condensation products of haloparaffin waxes and aromatic compounds, vinyl carboxylate polymers, and terpolymers of dialkylfumarates, vinyl esters of fatty acids and allyl vinyl ethers.
- lubricating oil compositions contain one or more of the additives discussed above, the additive(s) are blended into the composition in an amount sufficient for it to perform its intended function.
- Exemplary amounts of such additives useful in the present invention are depicted in Table 1 below. Note that many of the additives are shipped from the manufacturer and used with a certain amount of base oil solvent in the formulation. Accordingly, the weight amounts in the table below, as well as other amounts referenced in the present disclosure, unless otherwise indicated, are directed to the amount of active ingredient (that is the non-solvent portion of the ingredient). The weight percentages indicated below are based on the total weight of the lubricating oil composition.
- Anti-wear Additive 0.01-6 0.01-4
- Anti-foam Agent 0.001-3 0.001-0.15
- Commercial additive packages usually include, but are not limited to, one or more detergents, dispersants, friction reducers, antioxidants, corrosion inhibitors, and anti-wear additives.
- An exemplary, but not limiting, engine oil formulation will contain 70-90 wt% base oil, 4-10 wt% VI improver, 4-10 wt% dispersants, 1-3 wt% anti wear/extreme pressure agents, 0.2-2 wt% antioxidants, 1-4% detergents, 0.01-0.1 wt% each of demulsifier, seal swelling agent, friction modifier, and antifoam additive, 0.1-0.5 wt% pour point depressant.
- some of these additives are packaged together by an additive supplier.
- the VI improver and dispersants are high viscosity components (13,000 - 17000 centipoise under low shear condition). When heated to about 90° C, the viscosities of these two components decrease to a viscosity from about 500 to about 2000 centipoise under low shear conditions, which are still difficult to handle with the traditional liquid handling equipment.
- the void volume is less than 1 milliliter, preferably less than 0.5 milliliter, more preferably less than 0.05 milliliter, and even more preferably less than 0.5 microliter or essentially zero to minimize the amount of liquid or air trapped between the piston and the liquid.
- a LVVPDP may be alternatively defined by the % volume of the dispensing tip or needle that is filled by the plunger.
- a LVVPDP it is one having at least 70% of the volume of the dispensing tip or needle filled by the plunger, therefore resulting in a void volume of the tip or needle of 30% or less of the total volume of the tip or needle. More preferably, a LVVPDP is one having at least 90% of the volume of the dispensing tip or needle filled by the plunger, therefore resulting in a void volume of the tip or needle of 10% or less of the total volume of the tip or needle. Even more preferably, a LVVPDP is one having at least 98% of the volume of the dispensing tip or needle filled by the plunger, therefore resulting in a void volume of the tip or needle of 2% or less of the total volume of the tip or needle.
- FIG. 1 is one exemplary embodiment of a low void volume positive displacement pipette 10 for use in the present invention.
- the LVVPDP 10 is a syringe-like injector that may be disposable or non-disposable. A non-disposable device may be reused, whereas a disposable device is intended for single use. In many applications, the pipettes might be used multiple times for the same components.
- the LVVPDP 10 includes a barrel 11, a plunger 12 fitted to the barrel 11, an actuator 13 for the plunger 12, and a dispensing tip or needle 14.
- the dispensing tip or needle 14 preferably has a tapered design.
- the high viscosity lubricant fills the volume of the barrel 11 below the plunger 12 and into the tip or needle 14.
- the actuator 13 may be moved up and down by either a manual means or via a robotic means.
- One schematic (a) of Figure 1 depicts the plunger 12 in the up or fill position, and the other schematic (b) of Figure 1 depicts the plunger in the down or dispensing position.
- Schematic (b) of Figure 1 also shows the close fit between the plunger 12 and the barrel 1 1 such as to minimize the void volume when the plunger is fully actuated.
- Figure 2 is another exemplary embodiment of a low void volume positive displacement pipette 15 for use in the present invention.
- the LWPDP 15 includes a barrel 16, a plunger 17 fitted to the barrel 16, an actuator 18 for the plunger 17, and a dispensing tip or needle 19.
- the barrel 16, plunger 17, and tip or needle 19 are of an alternative shape that minimizes the void volume between the plunger 17, and the inside of the barrel 16 and dispensing tip or needle 19. This minimizes the void volume when the plunger 12 is fully actuated.
- One schematic (a) of Figure 2 depicts the plunger 17 in the up or fill position, and the other schematic (b) of Figure 2 depicts the plunger in the down or dispensing position.
- An advantage of using a LVVPDP to dispense lubricant additives is that individual pipettes may be used for each individual additive. In the case of air- displacement or liquid/air displacement pipettes, each pipette requires a separate pump. This results in a cumbersome system when many pipettes are used. LVVPDPs do not require pumps, and therefore equipment complexity and the possibility of contamination are avoided. Correspondingly, the overall lubricant blending system is simplified when using LVVPDPs.
- FIG. 3 is an exemplary schematic of a low void volume positive displacement pipette in a lubricant additive reservoir 20.
- a LVVPDP 10 is inserted into an additive reservoir 22 containing lubricant (not shown).
- the additive reservoir 22 is surrounded by a heating block 24 so that the high viscosity lubricant component (not shown) can be heated to reduce its viscosity.
- VI improvers, pour point depressants, dispersants, polyisobutylenes, high molecular weight polyalphaolefins and other high viscosity lubricant components are typically heated from about 70 degrees C to about 100 degrees C to decrease their viscosity for ingestion into and ejection out of the LVVPDP 10.
- Additives packages containing one or more of these high viscosity lubricant components are typically heated from about 40 degrees C to about 60 degrees C to decrease their viscosity for ingestion into and ejection out of the LVVPDP 10.
- FIG 4 is an exemplary schematic of an array of additive reservoirs 30.
- Each additive reservoir 22 is surrounded by a heating block 24.
- Each additive reservoir 22 may contain a different high viscosity lubricant additive (not shown), as well as its own dedicated LVVPDP 10 to avoid issues associated with cross contamination of lubricant additives.
- There may be from 1 to a multitude of heating blocks 24 depending upon the type and number of lubricant additives.
- a heating block 24 may also control from one to a multitude of additive reservoirs 30.
- the heating blocks 24 may be controlled to a temperature ranging from room temperature to up to about 100 degrees C depending upon the type of additive.
- FIG. 5 is an exemplary schematic of a lubricant blend station 40 based on the use of LVVPDPs.
- a robotic means is used to control the movement of LVVPDPs 10, ingestion of lubricant component from the lubricant additive reservoir 22, and ejection of lubricant into a destination blend container 52.
- An exemplary, but not limiting robotic means includes a robotic arm 42 connected to a support bridge 44 as shown in Figure 5. The robotic arm 42 is used to select a LVVPDP 10 from its respective additive reservoir 22 in the LVVPDP source array 46 and transport the LVVPDP 10 to the LVVPDP destination array 48.
- the source array 46 may also include one or more heating blocks 24 to preheat the high viscosity additive in order to lower the viscosity.
- the destination array 48 includes a series of destination blend containers 52 for delivery of the high viscosity additive.
- the destination array 48 may also include a balance 54 for weighing the amount of lubricant additive deposited into a destination blend container positioned on the balance 53.
- the robotic arm 42 positions the LVVPDP 10 above the destination blend container 53 that is positioned on top of the balance 54 and injects the additive into the blend container 53.
- the robotic arm 42 may then optionally inject the additive from the same LVVPDP 10 into one or more other destination blend containers 52.
- the robotic arm 42 then moves the LVVPDP 10 back to the original additive reservoir 22 of the source array 46. No washing of the line and the tip of the LVVPDP 10 is needed between each use as the additive remains constant in each additive reservoir 22.
- Each additive reservoir 22 and/or destination blend 52 container may also have a septum (not shown) to reduce the amount of viscous additive coating the needle or tip of the LWPDP 10.
- the robotic arm 42 and support bridge 44 are controlled by a computer or a programmable logic controller (not shown) to control their movement relative to the source array 46 and the destination array 48 in order to pick-up and return LVVPDPs 10.
- the robotic arm 42 controlled by a computer or a programmable logic controller (not shown) is also used to control the amount of additive sucked into the LVVPDP 10 at the source array 46 from each additive reservoir 22 and the amount of additive dispensed at the destination array 48 into each destination blend container 52.
- the computer or programmable logic controller contains information on all the additives contained in the additive reservoirs 22. This information includes, but is not limited to, physical properties such as viscosity and density.
- the computer also has a list of blend recipes, which includes the concentration of each additive in the blend recipe.
- the computer or programmable logic controller also has a feedback control mechanism to the balance for controlling the weight of each additive component dispensed into the destination blend container 53.
- the computer or programmable logic controller includes a calibration routine for the stroke of the plunger 12 in the barrel 11 and needle 14 of the LVVPDP 10 versus the weight of a particular lubricant additive dispensed.
- the calibration routine and feedback control mechanism allows the lubricant blend station 40 of the present invention to more quickly and accurately dispense lubricant additive components into a destination blend container 53 positioned on the balance 54.
- the computer directs a LVVPDP 10 to withdraw a specific volume of high viscosity lubricant component from an additive reservoir 22 and deposit it into a destination blend container 53, it may make two or more measurements.
- the computer monitors the volume of high viscosity lubricant component withdrawn by the LVVPDP 10.
- the mass of high viscosity lubricant component deposited into the destination blend container 53 is measured by the balance 54 sitting under the destination blend container 53.
- the destination blend container for lubricants may accommodate less than 100 milliliters in volume, and preferably less than 10 milliliters in volume for producing small lubricant blends.
- the LVVPDP 10 associated with each additive reservoir 22 in the source array 46 may also be a disposable-type pipette.
- the robotic arm 42 will pick up a disposable LVVPDP 10, move it to the appropriate additive reservoir 22 depending on the additive desired, load the disposable LVVPDP 10 with additive, move to the destination blend container 52 (could be on top of a balance), and inject the lubricant additive into the blend container 52.
- the destination blend container 53 may also optionally be sitting on the balance 54 at the time of injection to measure real time the weight of lubricant additive being dispensed.
- the disposable LVVPDP 10 is discarded once the additive has been added to all the required destination blend containers 52.
- the positive displacement technology of the present invention still requires heating to handle high viscosity lubricant additives.
- the use of LVVPDPs results in more accurate blends without excessive heating of the high viscosity blend component.
- the temperature of the high viscosity blend component or additive should be below 11O 0 C, preferably below 91 0 C, and more preferably below 51 0 C.
- the accuracy of lubricant blends made with high viscosity lubricant blend components and method of the present invention may be further improved by simultaneously measuring the weight and volume delivered to the blend vessel. This may be done by comparing the volume pipetted by the LVVPDP to the volume calculated by multiplying the measured mass with the density of the high viscosity component stored in the computer. If the volume and mass measurements are not in agreement than an error condition may be reported by the computer.
- density of a high viscosity lubricant component may be accurately measured while simultaneously making lubricant blends via the computer or programmable logic controller. This is done by using the volume and mass measurements made by the computer for each high viscosity lubricant component.
- density of a high viscosity lubricant component may be measured over a range of temperatures by varying the temperature of the high viscosity lubricant components and measuring the volume and mass. The density is then calculated by the computer or programmable logic controller by dividing the mass by the volume.
- the identity of a given high viscosity lubricant component may be verified by comparing the density measured as above with an expected density stored in a computer database. If the two densities agree within a certain tolerance, than the identity of the high viscosity lubricant component is known to be correct. If the densities fall outside this tolerance than either the wrong high viscosity lubricant component has been used or its density is outside of the specification.
- the accuracy of dispensing a given amount of lubricant additives can be further improved by using a combination of a large LVVPDP or a conventional pipette with a small LVVPDP.
- the large LVVPDP or the conventional pipette is used to dispense 90-99% of the target quantity and the actual quantity added is determined by the balance.
- the computer or the programmable logic controller then calculates the remaining amount to be added by the small LVVPDP.
- An automated feedback routine can be used to further improve the dispensing of lubricant additives from LVVPDPs and conventional pipettes.
- the lubricant blend station including LVVPDPs for dispensing high viscosity additives of the present invention are suitable for laboratory applications where the blend quantities are relatively small.
- the lubricant blend station including LVVPDPs for dispensing high viscosity additives of the present invention are also suitable for high throughout experimentation (HTE) type applications. These applications do not limit the range of other applications for blending lubricants and lubricant additives where the lubricant blend station of the present invention may be utilized.
- Dispense #1 0.0078 0.0090 0.0083 Dispense #2 0.0079 0.0091 0.0080 Dispense #3 0.0081 0.0093 0.0085 Dispense #4 0.0080 0.0095 0.0081 Dispense #5 0.0080 0.0091 0.0084 Dispense #6 0.0078 0.0093 0.0084 Dispense #7 0.0080 0.0094 0.0083 Dispense #8 0.0080 0.0091 0.0083 Dispense #9 0.0079 0.0092 0.0081 Dispense #10 0.0080 v 0.0091 0.0085 Average 0.0080 0.0092 0.0083 Standard Deviation 0.00010 0.00016 0.00017 % Coefficient of Variation 1.22 1.73 2.09 [0086] Table 4: Dispensing precision of Tecan RSPlOO liquid handling System
- Dispense #1 0.00546 0.00939 0.00932
- Dispense #11 0.00616 0.01046 0.00938
- Dispense #12 0.00563 0.00981 0.00973
- Dispense #11 0.01894 0.02808 0.11596
- Table 7 Dispense of Paratone 8011 at Room Temperature, 5O 0 C, and 90 0 C using 2.5 ml Jencons Scientific pipettes with and without modifications.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Lubricants (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2654864A CA2654864C (en) | 2006-06-23 | 2007-05-01 | Method of blending lubricants using positive displacement liquid-handling equipment |
JP2009516485A JP2009541527A (en) | 2006-06-23 | 2007-05-01 | Method of blending lubricant using positive displacement liquid handling equipment |
EP07776666.5A EP2035706A4 (en) | 2006-06-23 | 2007-05-01 | Method of blending lubricants using positive displacement liquid-handling equipment |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/473,697 US7625115B2 (en) | 2006-06-23 | 2006-06-23 | Method of blending lubricants using positive displacement liquid-handling equipment |
US11/473,697 | 2006-06-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008002349A1 true WO2008002349A1 (en) | 2008-01-03 |
Family
ID=38845934
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2007/010700 WO2008002349A1 (en) | 2006-06-23 | 2007-05-01 | Method of blending lubricants using positive displacement liquid-handling equipment |
Country Status (6)
Country | Link |
---|---|
US (1) | US7625115B2 (en) |
EP (1) | EP2035706A4 (en) |
JP (1) | JP2009541527A (en) |
CN (1) | CN101479480A (en) |
CA (1) | CA2654864C (en) |
WO (1) | WO2008002349A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0606754D0 (en) * | 2006-04-04 | 2006-05-10 | Ici Plc | Sample preparation |
FR2899836B1 (en) * | 2006-04-14 | 2010-10-15 | Olilab Llc | PROCESS FOR THE CONTINUOUS PRODUCTION BY INJECTION-COMPRESSION OF PREFORMS FOR THE MANUFACTURE OF PACKAGING AND THE INSTALLATION OF IMPLEMENTATION |
US7625115B2 (en) * | 2006-06-23 | 2009-12-01 | Exxonmobil Research And Engineering Company | Method of blending lubricants using positive displacement liquid-handling equipment |
EP1947463A1 (en) * | 2007-01-16 | 2008-07-23 | Roche Diagnostics GmbH | Collection of liquid analytical samples for clinical analytical purpose |
FR2986617B1 (en) * | 2012-02-02 | 2015-03-27 | Horiba Abx Sas | DEVICE AND METHOD FOR PERFORMING HEMATOLOGICAL AND BIOCHEMICAL MEASUREMENTS FROM A BIOLOGICAL SAMPLE |
WO2020014416A1 (en) * | 2018-07-13 | 2020-01-16 | Baker Hughes, A Ge Company, Llc | Method and system for demulsifier testing |
US20220097037A1 (en) * | 2019-01-17 | 2022-03-31 | Dan Yehoshoa SHAHAR | Pipettor calibration system devices and methods thereof |
CN111889060A (en) * | 2020-04-20 | 2020-11-06 | 璧典赴 | Food detects uses quick testing platform equipment |
US20230415144A1 (en) * | 2022-06-28 | 2023-12-28 | Mettler-Toledo Rainin, LLC | Positive displacement pipette syringe with reduced fluid drag |
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2007
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- 2007-05-01 WO PCT/US2007/010700 patent/WO2008002349A1/en active Application Filing
- 2007-05-01 EP EP07776666.5A patent/EP2035706A4/en not_active Withdrawn
- 2007-05-01 JP JP2009516485A patent/JP2009541527A/en active Pending
- 2007-05-01 CN CNA2007800235310A patent/CN101479480A/en active Pending
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Also Published As
Publication number | Publication date |
---|---|
EP2035706A4 (en) | 2017-11-22 |
US20070297279A1 (en) | 2007-12-27 |
EP2035706A1 (en) | 2009-03-18 |
CN101479480A (en) | 2009-07-08 |
CA2654864C (en) | 2012-06-12 |
CA2654864A1 (en) | 2008-01-03 |
US7625115B2 (en) | 2009-12-01 |
JP2009541527A (en) | 2009-11-26 |
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