Classifications

• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M175/00—Working-up used lubricants to recover useful products ; Cleaning
  • C10M175/005—Working-up used lubricants to recover useful products ; Cleaning using extraction processes; apparatus therefor

Definitions

• Hydrocarbon lubricating oil compositions used as lubricants in internal combustion engines contain additives which serve as dispersants so that accumulated impurities such as metallic salts particularly lead salts remain dispersed in the oil rather than settling as a sludge in the crankcase.
• the function of the dispersants is a distinct advantage when the hydrocarbonoil composition is employed as a lubricating agent, it becomes a distinct hindrance in the disposal of the used oil composition or the reclaiming thereof, in that it prevents the ready separation of lead from the used oil.
• Used oil such as that accumulated from the automobile service stations is sometimes disposed of by burning.
• the removal of lead prior to disposal is desirable for ecological reasons, for during burning, lead if not removed, is volatilized into the atmosphere in substantial quantities, the remainder entering the soil, both outlets being undesirable.
• lead must be removed therefrom in order to render it commercially saleable.
• the invention comprises contacting a hydrocarbon lubricating oil having a dispersed lead content of at least about 0.5 wt. percent, normally between about 0.5 and 1.5 wt. percent with methylethylketone (MEK) under anhydrous and mixing conditions at a temperature between about 65 and 95F. utilizing a volume ratio of methylethylketone to hydrocarbon oil of at least about 2: l preferably between about 2:1 and 3:l, separating the resultant mixture into an upper layer of clarifiedlubricating oil and methylethylketone and a bottom coagulated, insoluble layer containing the bulk of the lead impurities under said anhydrous and temperature conditions.
• MEK methylethylketone
• Separation can be effected, for example, by either gravity separation which is normally conducted for a period of between about 4 and 10 hours or centrifuging, either means followed by decanting or filtering to spatially separate the layers.
• the methylethylketone is readily recovered from the separated oil-methylethylketone layer by standard means such as distillation, leaving essentially a lead free (less than about 0.1 wt. percent) clarified dark oil.
• the recovered methylethylketone is either forwarded to storage for eventual reuse or recycled directly to the mixing stage for immediate reuse.
• Another means of sepa rating the clarified oil-methylethylketone layer from the coagulated insoluble would be employing a high speed centrifuge and then upon the completion of centrifuging spatially separating the layers, and recycling the recovered methylethylketone for reuse or storage.
• the separated lead containing sludge is normally deoiled by extraction with solvent, for example, additional methylethylketone, pentane or heptane to yield a dry powder of relatively high lead content, e.g., 20-40 wt. percent.
• solvent for example, additional methylethylketone, pentane or heptane to yield a dry powder of relatively high lead content, e.g., 20-40 wt. percent.
• the thus recovered lead can be containerized and the resultant lead filled container can be employed as land fill or the lead can be accumulated and reprocessed for industrial use.
• anhydrous denotes water content less than about 0.5 wt. percent.
• this can be accomplished by standard means such as in line" blending, paddle mixing, etc., and is normally conducted for only that period of time which is required to insure thorough contact of the oil and ketone, e.g., 0.5-10 minutes.
• the process of the invention may be conducted on a batch or continuous basis.
• An example of a continuous operation would be to employ initial in line blending using adjustable proportioning pumps to provide the proper used oil-methylethylketone mix and introducing the mixture into a series of settling vessels. At least two separation vessels are employed in the continuous procedure with the flow of the mix, for example, being alternated between settling vessels, e.g., one being filled while recovering the separated layer from the other.
• Another approach would be to connect a number of settling vessels in series, introducing the mix into the first of the series and withdrawing the clarified oilketone layer from the last of the series.
• Still another approach would I be to feed the used oilmethylethylketone mix directly into a number of high speed centrifuges and alternating such feed between the centrifuges.
• the methylethylketone functions to solubilize a yet unidentified resin, said resin believed to provide a chemical bond between the lead impurity and lube oil dispersants, the latter maintaining the lead impurity in the dispersed state. Once this bond is broken via solubilization the lead and other metallic materials become desolubilized, coagulate and separate from the oilmethylethylketone layer.
• Another surprising material feature of the invention is that normally in purifying processes elevated temperatures of the order of 100 to 300F., preferably above l50F., are employed.
• our procedure preferably employs ambient temperatures, that is, of the order of 65 to F., and therefore, affords a substantial saving in process costs since normally heat does not have to be supplied to the desolubilizing reaction. Temperatures above about 95F. in our procedure result in somewhat reduced lead removal.
• volume ratio of methylethylketone to used oil of at least about 2:1 is advantageous. Volume ratios substantially below 2:1 such as 1:1, except when high speed centrifuge separation is employed, result in a treated oil have an unsatisfactory high lead content, that is, above about 0.1 wt. percent.
• Still another material feature is the requirement that the desolubilization be conducted under anhydrous conditions, i.e., the initial oil-ketone mixture have a water content below about 0.5 wt. percent. Higher water contents prevent separation of.the lead impurity layer. If the oil to be treated has a water content which would bring the oil-ketone mixture above the aforementioned maximum value, it is subjected to a dehydration pretreatment. Such dehydration can be accomplished by standard means such as by passing used oil over a hot surface to flash off the water, by blowing with hot air or with steam above about 250F. or by vacuum treatment at ambient or elevated temperatures, preferably at about 150F.
• hydrocarbon lubricating oil it is intended to mean oils removed from the crankcases after extended use in operating internal combustion engines, wherein the lead therein has been solubilized by dispersant additive(s) in said oil and the initial lead content therein is at least about 0.5 wt. percent.
• hydrocarbon lubricating oil compositions contemplated herein are derived from the hydrocarbon lubricating compositions, normally lead free, comprising between about 85 and 99 wt. percent hydrocarbon lubricating oil and between about 1 and wt. percent additives.
• additives in addition to the aforementioned dispersants normally comprise one or more of the following: pour depressors, anti thickening agents, antioxidants, corrosion inhibitors, VI improvers, and oiliness agents.
• lube oil dispersants are overbased calcium alkylsulfonates, overbased sulfurized calcium alkyl-phenolates and polyisobutylene (e.g. 50 to 200 carbons) succinimide of tetraethylenepentamine.
• the base oils employed in formulating the initial lubricating oil compositions from which the used oils are derived include a wide variety of hydrocarbon lubricating oils such as naphthenic base, paraffinic base and mixed base mineral oils or other hydrocarbon lubricating oils such as derived from coal products, synthetic oils, e.g., alkylene polymers such as polypropylene, polyisobutylene, of a molecular weight between 250 and 2500.
• the lubricating base oils employed have an SUS viscosity at 100F. between about 50 and 2000.
• the used crankcase lubricating oil employed in the following procedure was obtained from the waste oil disposal tank at a service station catering to automobiles. It was derived-from motor oils which initially contained no lead. The used oil was introduced into a mixing kettle where it was stirred at ambient temperature to assure uniform distribution of materials therein and then stored in l-gallon cans. Before use, the gallon cans- Used crankcase oil results Lead as Pb, wt. l.25 Sulfated ash, wt. 2.95 Viscosity at l00F., SUS 3
• Table I represents the procedure of the invention utilizing gravity separation and demonstrates in Run E the gravity separation of 1:1 volume ratio is ineffective.
• Table 11 represents the method of the invention utilizing centrifugal separation and gravity separation.
• Table II further demonstrates in comparative Run F the ineffectiveness of comparative known lube oil solvent materials.
• Table III shows the property difference between the untreated used oiland the clarified oil resulting from treatment of the used oil via the method of the invention.
• EXAMPLE II This example illustrates the method of invention as practiced as a continuous process.
• EXAMPLE III This example illustrates the ineffectiveness of closely related materials to methylethylketone in separating lead from used crankcase oil.
• Example I gravity separation
• Example IV This example illustrates the importance of conducting the reaction under essentially anhydrous conditions.
• the procedure of Example I was employed utilizing a 10 volume percent water content in a 1:2 volume ratio of used oil to methylethylketone. An emulsion was formed which was stable for several days with no significant sludge coagulation being evidenced.
• a method of reducing dispersed lead impurities in a used hydrocarbon lubricating oil composition having dispersed lead content of at least about 0.5 wt. percent consisting essentially of mixing under anhydrous conditions said composition with methylethylketone utilizing a methylethylketone to used oil composition volume ratio of at least about 2:1, forming a methylethylketone-clarified oil upper layer and a lead containing insoluble lower layer, separating the resultant methylethylketone-oil upper layer from said lead containing insoluble lower layer, and recovering from said methylethylketone-clarified oil upper layer, a lubricating oil composition of reduced lead content, said mixing, said forming, and said separating conducted at a temperature of between about 65 and F.
• a method in accordance with claim 1 wherein said forming comprises passing the used oilmethylethylketone mixture to a settling tank and maintaining said mixture in said tank until said methylethylketone-clarified oil layer is formed as an upper layer and said lead containing insoluble layer is formed as a lower layer, said separating comprising subsequently decanting from said tank said methylethylketone-clarified oil upper layer, and. said recovering comprising passing the decanted methylethylketoneclarified oil upper layer to a distillation zone, recovering methylethylketone as distillation overhead, recovering a lubricating oil composition of reduced lead content as a distillation residue, and recycling the recovered methylethylketone to said mixing step.
• a method in accordance with claim 1 wherein said forming comprises centrifuging the used oilmethylethylketone mixture to separate methylethylketone-clarified oil solution as an upper layer and lead containing coagulated insolubles as a lower layer, decanting said methylethylketone-clarified oil upper layer from the centrifuge, said recovering comprising passing the decanted methylethylketone-clarified oil upper layer to a distillation zone, recovering methylethylketone as distillation overhead, recovering a lubricating oil composition of reduced lead content as distillation residue, and recycling the recovered methylethylketone to said mixing step.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Combustion & Propulsion (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Organic Chemistry (AREA)
• Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
• Lubricants (AREA)

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Cited By (13)

Citations (3)

• 0
  • BE BE794876D patent/BE794876A/xx unknown
• 1972
  • 1972-02-07 US US00224222A patent/US3763036A/en not_active Expired - Lifetime
• 1973
  • 1973-01-15 CA CA161,280A patent/CA1005007A/en not_active Expired
  • 1973-01-18 AU AU51215/73A patent/AU469320B2/en not_active Expired
  • 1973-01-19 NL NL7300786A patent/NL7300786A/xx not_active Application Discontinuation
  • 1973-01-30 JP JP48011638A patent/JPS4891107A/ja active Pending
  • 1973-01-30 FR FR7303164A patent/FR2171106B1/fr not_active Expired
  • 1973-02-05 DK DK59673AA patent/DK139074B/da unknown
  • 1973-02-06 SE SE7301629A patent/SE390976B/xx unknown
  • 1973-02-06 IT IT20065/73A patent/IT978839B/it active

Patent Citations (3)

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