[go: up one dir, main page]

US1901240A - Method of dewaxing oils - Google Patents

Method of dewaxing oils Download PDF

Info

Publication number
US1901240A
US1901240A US421815A US42181530A US1901240A US 1901240 A US1901240 A US 1901240A US 421815 A US421815 A US 421815A US 42181530 A US42181530 A US 42181530A US 1901240 A US1901240 A US 1901240A
Authority
US
United States
Prior art keywords
wax
centrifuge
stock
oil
chilling
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US421815A
Inventor
Henriksen Alfred
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ConocoPhillips Co
Original Assignee
Continental Oil Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Continental Oil Co filed Critical Continental Oil Co
Priority to US421815A priority Critical patent/US1901240A/en
Application granted granted Critical
Publication of US1901240A publication Critical patent/US1901240A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G73/00Recovery or refining of mineral waxes, e.g. montan wax
    • C10G73/02Recovery of petroleum waxes from hydrocarbon oils; Dewaxing of hydrocarbon oils
    • C10G73/04Recovery of petroleum waxes from hydrocarbon oils; Dewaxing of hydrocarbon oils with the use of filter aids

Definitions

  • waxes In the production of lubricating oils, one 'of the troublesome group of compounds en'- countered is the waxes. These waxes'vary from low melting point amorphous wax to highlmelting crystalline Wax-and are com- Lubricating pounds of the paraffin series. I oils to be used at low temperatures must have these waxes removed in order to obtain free movement of the lubricating medium; moreover, the waxes themselves are of very poor lubricating value and act as a detriment to the lubricating qualities of the oil. High wax content oils, being solid at relatively high temperatures, give considerable trouble in refining practice because they cannot be pumped or require heated tanks for cold weather storage.
  • Oil refiners have developed three general methods of wax separation:
  • Lubricating stock dilution with naphtha 2. Lubricating stock dilution with naphtha, chilling and cold settling. 3. Lubricating stock dilution with naph tha, chilling and centrifuging.
  • the amount of crystalline-amorphous wax separation depends on the nature-of the crude and control of the refining process.
  • the wax distillate is either chilled and pressed directly or given a heating treatment with a small amount of steam, called cracking wax distillate, then chilled and cold pressed.
  • the steamrefined cylinder stock requires other treatment to obtain high class lubricating oil price.
  • This further refining includes acid treating and/or clay treating, which treating causes the waxes to be less soluble and a higher pour point results on the finished stock.
  • a steam refined stock may have a 40 F. pour point before treating with acid and/or clay for color and removal of impurities, and an 80 F. pour point after treatment.
  • the wax separates from the oil and is held by the finely divided solid material suspended in the oil;'alsothe finely divided material forms a mat with the wax and aids in holding the wax from assing through the filter cloth.
  • the finely divided solid and wax form such a thick bed on the filter cloth that the process must be stopped and the filter cloth cleaned. This process is a batch process and the regular required cleaning of the filter cloth is costly and cuts down the unit volume throughput.
  • the wax must be in a specific form. Some oils will not give up their wax by this process.
  • the present invention provides an improved method of separation of wax from cold' type stock mixtures, or from crude petrolatum stock produced by present dewaxing methods, or form other fractions from which separation of wax is desired.
  • Objects of the present invention are:
  • the stock to be dewaxed is diluted with a suitable solvent, such as naphtha, any of the heavy alcohols, benzol, acetone and similar organic solvents, or any other solvent which will give a wax-solution density differential, and remain liquid at the temperatures used.
  • a suitable solvent such as naphtha, any of the heavy alcohols, benzol, acetone and similar organic solvents, or any other solvent which will give a wax-solution density differential, and remain liquid at the temperatures used.
  • a suitable solvent such as naphtha, any of the heavy alcohols, benzol, acetone and similar organic solvents, or any other solvent which will give a wax-solution density differential, and remain liquid at the temperatures used.
  • a suitable solvent such as naphtha, any of the heavy alcohols, benzol, acetone and similar organic solvents, or any other solvent which will give a wax-solution density differential, and remain liquid at the temperatures used.
  • a substance which will give a colloidal solution Such substances as bitumen
  • the chilled stock-naphtha blend with the centrifuge aid added is now charged to'the centrifuge where the wax and centrifuge aid are easily thrown out of the oil naphtha solution.
  • the nature of the centrifuge aid allows it to be easily washed out of the centrifuge with the wax without obstructing or clogging the system.- This advantage is not present in finely divided or inorganic pulverized solids which would not flow from a high speed centrifuge.
  • the de-waxed stock-solvent' solution is drawn off the top of the centrifuge from which the de-waxed tha being the class of substances intermediate between asphalt and petroleum.
  • centrifuge-aid is used to include substances which allow better operation of the centrifuge, substances which in any way
  • the solvent in 'which the colloidal solute is converted to a colloidal solution may be the same or dif alter the nature of the wax particles and more easily precipitated at the temperatures and dilutionsused.
  • centrifuge-aid required for de-waxing one stock may be found in another stockwhich is to be de-waxed and in such cases the centrifuge-aid naturally existing in one stockmay be utilized by blending with the other.
  • the material or centrifuge-aid thought to be bitumen or the constitutents thereof may be:
  • (a) An example of (a) is as follows: A cylinder stock produced from Tonkawa crude after acid treating and neutralizing was dissolved or blended in the proportion of 2 parts naphtha to 1 part oil, chilled to minus 15 F. and centrifuged, giving good wax separation and a finished oil having pour test of 15 F. The above indicates that. oil from this source contains at least sufiicient centrifuge-aid to give satisfactory wax separation.
  • (b) is a cylinder stock made by distillation overhead from dark .of this overhead distillate Mid-Continent oil was blended with 3parts of the Tonkawa cylinder stock or flux from this cylinder stock in smaller quantities mentioned under (a) and the mixture blended, .chilled and centrifuged as above, there was asatisfactory wax separation with a resulting pour test on the finished-oil of 20 F. A residue,
  • Example 1 Overhead lube treated with 30# sulfuric acid per barrel and 15% clay showing on the treated oil Gravity Vicos ity Pour point Gn Fl. Fr. Vis. Pour pt. Color 23.7 490 F. 565 F. 80 100 F. 2-Tag.Robinson was blended with 68.5% of 57 .4 gravity naphtha, to which was added 0.025% California bitumen and 2% petrolatum. This was chilled at 6 F. per hour to minus 40 F. and gave at the centrifuge after finishing a lubricating stock of pour point 8 F., filtered through clay 200 bbls/ton.
  • Example 3 A commercial product known as Grahamite to an amount of 0.1% was used with success lowering the pour point on the finished oil 50 F. By use of 0.1% Grahamite and 2% petrolatum, the pour point was lowered on the'finished stock 65 F.
  • Example 4 A treated overhead lube stock was diluted
  • a method for removing wax from waxcontaining oils comprising the steps of adding a suitable solvent and a colloidal asphaltite, chilling the mixture to the desired temperature, and subjecting the chilled mixture to a centrifugal action.
  • a method for removing wax from W axcontaining'oils comprising the steps of adding a suitable solvent and Grahamite, chilling the mixture to the desired temperature and subjecting the chilled mixture to a centrifugal action.v
  • a method ing a suitable solvent and amixture of Grahamite and petrolatum, chilling the resulting mixture to the desired temperature, and subjecting the chilled mixture to a centrifugal action.
  • a method for removing wax from waxcontaining oils comprising the steps of adding a suitable solvent and on asphaltite capable of forming a dispersoid in the solution, chilling the mixture to the desired temperature and subjecting the chilled oil to a centrifugal action.

Landscapes

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

Description

Patented Mar. 14,- 1933 UNITED STATES PATENT OFFICE 'ALERED HENRIKSEN, F PONCA CITY, OKLAHOMA, ASSIGNOR TO CONTINENTAL OIL I COMPANY, OF PONCA CITY, OKLAHOMA, A CORPORATION OF DELAWARE METHOD OF DEWAXING OILS No Drawing.
a continuous centrifuge process.
In the production of lubricating oils, one 'of the troublesome group of compounds en'- countered is the waxes. These waxes'vary from low melting point amorphous wax to highlmelting crystalline Wax-and are com- Lubricating pounds of the paraffin series. I oils to be used at low temperatures must have these waxes removed in order to obtain free movement of the lubricating medium; moreover, the waxes themselves are of very poor lubricating value and act as a detriment to the lubricating qualities of the oil. High wax content oils, being solid at relatively high temperatures, give considerable trouble in refining practice because they cannot be pumped or require heated tanks for cold weather storage.
Oil refiners have developed three general methods of wax separation:
-l. Lubricating stock dilution with naphtha, chilling and pressing.
2. Lubricating stock dilution with naphtha, chilling and cold settling. 3. Lubricating stock dilution with naph tha, chilling and centrifuging.
These general methods have taken on various modifications in an effort to solvethe dewaxing problem.
A brief outline of the refinery practice on parafiin base crudes will show the essentials of Wax separation methods. The-ordinary break-up of crude in the "refinery is: 1,'
naphtha; 2, kerosene; 3, gas oil; 4, wax distillate; 5, residue-steam refined cylindertemperature, rate of distillation, amount of steam, etc. are regulated to prevent injury of the residue. 'The Wax distillate is removed at as low still temperature as pos sible, using large amounts of steam. This gives the crystalline waxes in the overhead Application filed January 18, 1930. Serial No. 421,815,
wax distillate and the amorphous waxes in r the residue.
' The amount of crystalline-amorphous wax separation depends on the nature-of the crude and control of the refining process. The wax distillate is either chilled and pressed directly or given a heating treatment with a small amount of steam, called cracking wax distillate, then chilled and cold pressed. I
The steamrefined cylinder stock requires other treatment to obtain high class lubricating oil price. This further refining includes acid treating and/or clay treating, which treating causes the waxes to be less soluble and a higher pour point results on the finished stock. For example, a steam refined stock may have a 40 F. pour point before treating with acid and/or clay for color and removal of impurities, and an 80 F. pour point after treatment.
It is, therefore, necessary to dewax the finished oil. Ifthe stock is diluted with naphtha and chilled, the wax crystals will form and settle to the bottom of the container. This is a very slow'pnocess requiring severaldays for completion, and gives a rather poor separation and a large loss of stock in the settled wax solvent solution. The chilling is done slowly at the top of the container and the wax crystals start flowing to the bottom, care being taken that no external agitation is obtained; therefore, the process could not be continuous. This process maybe more successfully operated if a heavy finely divided substance, that is wax .adherent, is 'added'to give'a greater gravity difference between the oil and the wax.
chilling, the wax separates from the oil and is held by the finely divided solid material suspended in the oil;'alsothe finely divided material forms a mat with the wax and aids in holding the wax from assing through the filter cloth. After the 'lter has been in operation for a short period, the finely divided solid and wax form such a thick bed on the filter cloth that the process must be stopped and the filter cloth cleaned. This process is a batch process and the regular required cleaning of the filter cloth is costly and cuts down the unit volume throughput. To process an oil by this method, the wax must be in a specific form. Some oils will not give up their wax by this process.
When a lubricating stock is diluted with naphtha and chilled, the wax crystals that separate out have a slightly higher specific gravity than the solvent oil mixture. Advantage is taken of this characteristic in wax removal by high speed centrifuge. I The wax bodies are thrown out by'the centrifugal action into the outer compartment of a special apparatus from which they are removed by a warmer solution. The partly dewaxed lube oil stocknaphtha solution passes onup and out of the centrifuge. The density of the wax is so near that of the mother liquorthat separation of wax is rather poor. Under the best operating conditions, one obtains a pour point on the finished oil of about 35 F to 40 F. higher than the temperature at which the solution goes to the centrifuge.
To dewax stocks with the centrifuge, they I must be very carefully blended to the proper gravity with the solvent used. Another disadvantage of this process is the time and required regularity of cooling. After the careful blending, the solution must be chilled at a slow rate requiring, as a rule, nearly twenty four hours for chilling; the chilling rate usually is from 3 F. to 6 F. per hour, depending on the stock, solvent and result required.
Some stocks cannot be dewaxed by the centrifuge process, 'even though all known disturbing factors are controlled.
The present invention provides an improved method of separation of wax from cold' type stock mixtures, or from crude petrolatum stock produced by present dewaxing methods, or form other fractions from which separation of wax is desired. Objects of the present invention are:
1. More nearly complete wax separation by centrifugal action.
2. Wax removal in centrifuge with the aid of collodial substances in the stock naphtha solution.
3. Continuous wax removal in the centri- 4. Continuous wax removal in the centrifuge by' the addition of bituminous colloidal centrifuge aids.
5. Centrifugal continuous wax removal using substances capable of forming a dispersoid in the solvent used.
6. Wax removal which allows the shockchilling of the stock naptha solution without the detrimental effects obtained in other methods by shock-chilling.
In the operation of this method, the stock to be dewaxed is diluted with a suitable solvent, such as naphtha, any of the heavy alcohols, benzol, acetone and similar organic solvents, or any other solvent which will give a wax-solution density differential, and remain liquid at the temperatures used. To this solution is added a substance which will give a colloidal solution. Such substances as bitumen, Grahamite and the like, which are not soluble or are only partly soluble in the solution, are desirable. This material may be added before chilling, during chilling, or after the chilling period. In actual practice the most satisfactory method for adding the centrifuging aid to the oil to be treated is to preparethe colloidal solution of the centrifuging aid in a suitable medium and add the colloidal solution at any point in the chilling process prior to centrifuging.
ferent from the diluent used for the oil.
The chilled stock-naphtha blend with the centrifuge aid added is now charged to'the centrifuge where the wax and centrifuge aid are easily thrown out of the oil naphtha solution. The nature of the centrifuge aid allows it to be easily washed out of the centrifuge with the wax without obstructing or clogging the system.- This advantage is not present in finely divided or inorganic pulverized solids which would not flow from a high speed centrifuge. As in other centrifugal processes, the de-waxed stock-solvent' solution is drawn off the top of the centrifuge from which the de-waxed tha being the class of substances intermediate between asphalt and petroleum.
The definition of the term centrifuge-aid is apparent from the context ofthespecification. The term centrifuge-aid is used to include substances which allow better operation of the centrifuge, substances which in any way The solvent in 'which the colloidal solute is converted to a colloidal solution may be the same or dif alter the nature of the wax particles and more easily precipitated at the temperatures and dilutionsused.
In the application of the process many comparisons of the merits of our process and the other type processes have been made. For example, two stocks can be chosen, one of which may be de-waxed at the centrifuge and not de-waxed by the cold pressing with filter-aid process; the other being de-waxed by the cold pressing with a filter-aid process and not de-waxed at thecentrifuge. By conditioning these two stocks for my process, that is, by adding a centrifuge-aid, I can de-wax both at the centrifuge.
Numerous colloidal agents have been found that have given satisfactory commercial results. In the practice of this process it has been found that the centrifuge-aid required for de-waxing one stock may be found in another stockwhich is to be de-waxed and in such cases the centrifuge-aid naturally existing in one stockmay be utilized by blending with the other.
The material or centrifuge-aid thought to be bitumen or the constitutents thereof may be:
(a) Naturally present in the oil or its residues to be processed;
(6) Present in excess of requirement in one stock and deficient in another, so blended will give proper percentage;
(0) A product of addition.
An example of (a) is as follows: A cylinder stock produced from Tonkawa crude after acid treating and neutralizing was dissolved or blended in the proportion of 2 parts naphtha to 1 part oil, chilled to minus 15 F. and centrifuged, giving good wax separation and a finished oil having pour test of 15 F. The above indicates that. oil from this source contains at least sufiicient centrifuge-aid to give satisfactory wax separation.
An example of (b) is a cylinder stock made by distillation overhead from dark .of this overhead distillate Mid-Continent oil was blended with 3parts of the Tonkawa cylinder stock or flux from this cylinder stock in smaller quantities mentioned under (a) and the mixture blended, .chilled and centrifuged as above, there was asatisfactory wax separation with a resulting pour test on the finished-oil of 20 F. A residue,
flux or extract from distillation of some oils contain the centrifuge aid contemplated herein.
The following examples, which include examples of (c), are not to be considered a limitation of the invention, it being understood that these are just a few examples given to make clear the operation of the process. Some of the examples also disclose the-use of a bitumen in combination with petrolatum. Example 1 Overhead lube treated with 30# sulfuric acid per barrel and 15% clay showing on the treated oil Gravity Vicos ity Pour point Gn Fl. Fr. Vis. Pour pt. Color 23.7 490 F. 565 F. 80 100 F. 2-Tag.Robinson was blended with 68.5% of 57 .4 gravity naphtha, to which was added 0.025% California bitumen and 2% petrolatum. This was chilled at 6 F. per hour to minus 40 F. and gave at the centrifuge after finishing a lubricating stock of pour point 8 F., filtered through clay 200 bbls/ton.
Gr. F1. Fr. Vis. Pour point Color 22.0 500 580 90 7 F. 1% T.R
Example 3 A commercial product known as Grahamite to an amount of 0.1% was used with success lowering the pour point on the finished oil 50 F. By use of 0.1% Grahamite and 2% petrolatum, the pour point was lowered on the'finished stock 65 F.
Example 4 A treated overhead lube stock was diluted,
chilled and centrifuged yielding a finished stock of 44 F. pour point. The centrifuged stock was blended with 56.9% of 54.6 gravity naphtha and 0.2% Montan wax, chilled at 6 F. per hour to F.; then centrifuged yielding a finished product of F. pour point; operating same as above with the addition of 0.05% bitumen gave a finished product of 15 F. pour point.
By extensive actual tests, I have found that any bituminous substance that is not soluble or partly soluble at centrifuging temperatures used proves satisfactory in the operation of this process. I have further found that substances which give a dispersoid solution of naptha and lubricating oil understood that this proves satisfactory. I believe that the dispersoid gives a nucleus around which the wax gathers, forming a body of greater density than the solutionfrom which the Wax came. The centrifuge can then make a better a separation. It is to be clearly patent is independent of any theory oifered.
I claim as my invention:
1. A method for removing wax from waxcontaining oils comprising the steps of adding a suitable solvent and a colloidal asphaltite, chilling the mixture to the desired temperature, and subjecting the chilled mixture to a centrifugal action.
2. A method for removing wax from W axcontaining'oilscomprising the steps of adding a suitable solvent and Grahamite, chilling the mixture to the desired temperature and subjecting the chilled mixture to a centrifugal action.v
3. A method ing a suitable solvent and amixture of Grahamite and petrolatum, chilling the resulting mixture to the desired temperature, and subjecting the chilled mixture to a centrifugal action.
4. A method for removing wax from waxcontaining oils comprising the steps of adding a suitable solvent and on asphaltite capable of forming a dispersoid in the solution, chilling the mixture to the desired temperature and subjecting the chilled oil to a centrifugal action. a
In testimony whereof I aflix my signature.
ALFRED HENRIKSEN.
for removing wax from waxcontamlng olls comprising the steps of add-.
US421815A 1930-01-18 1930-01-18 Method of dewaxing oils Expired - Lifetime US1901240A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US421815A US1901240A (en) 1930-01-18 1930-01-18 Method of dewaxing oils

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US421815A US1901240A (en) 1930-01-18 1930-01-18 Method of dewaxing oils

Publications (1)

Publication Number Publication Date
US1901240A true US1901240A (en) 1933-03-14

Family

ID=23672156

Family Applications (1)

Application Number Title Priority Date Filing Date
US421815A Expired - Lifetime US1901240A (en) 1930-01-18 1930-01-18 Method of dewaxing oils

Country Status (1)

Country Link
US (1) US1901240A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2674578A (en) * 1950-09-26 1954-04-06 Johnson & Co A Process for preventing cloudiness in refined lubricating oils
US2833815A (en) * 1958-05-06 Treatment of naphthenic acids

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2833815A (en) * 1958-05-06 Treatment of naphthenic acids
US2674578A (en) * 1950-09-26 1954-04-06 Johnson & Co A Process for preventing cloudiness in refined lubricating oils

Similar Documents

Publication Publication Date Title
US2229658A (en) Process for separating wax from oil
US1901240A (en) Method of dewaxing oils
US2248498A (en) Dewaxing hydrocarbon oil
US2261108A (en) Process for deasphalting oil
US2123833A (en) Dewaxing wax-bearing mineral oil
US3006839A (en) Dewaxing hydrocarbon oil
US2193767A (en) Dewaxing hydrocarbon oil
US2115846A (en) Process for obtaining valuable products from petroleum residues
US1930479A (en) Dewaxing of oil
US1881643A (en) Dewaxing of petroleum oils
US2036188A (en) Art of dewaxing hydrocarbon oils
US2137207A (en) Removing wax and asphaltic constituents from oil
US1857404A (en) Removal of wax from oil
US1820645A (en) Process of separating wax from mineral oils
US1968239A (en) Art of dewaxing hydrocarbon oils
US2161569A (en) Dewaxing hydrocarbon oil
US2200534A (en) Low pour point lubricating oil
US2132354A (en) Dewaxing wax-bearing oil
US2091640A (en) Process of dewaxing mineral oil
US2134336A (en) Dewaxing mineral oil
USRE19303E (en) Dewaxing of petroleum oils
US2044722A (en) Manufacture of lubricating oil
US2034175A (en) Settling aid
US2178328A (en) Method of dewaxing petroleum oils
US1963175A (en) Removal of wax from oil