US2049059A - Dewaxing hydrocarbon oils - Google Patents

Dewaxing hydrocarbon oils Download PDF

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US2049059A
US2049059A US631332A US63133232A US2049059A US 2049059 A US2049059 A US 2049059A US 631332 A US631332 A US 631332A US 63133232 A US63133232 A US 63133232A US 2049059 A US2049059 A US 2049059A
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wax
flux
oil
line
chilling
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US631332A
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Goss Henry Frank
Opryshek John
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Standard Oil Development Co
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Standard Oil Development Co
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    • 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
    • C10G73/06Recovery of petroleum waxes from hydrocarbon oils; Dewaxing of hydrocarbon oils with the use of solvents

Definitions

  • This invention therefore has for itsprincipal object the provision of an improved method for substantially lowering the pour points of suchoilsf 1
  • the improvement comprises carrying out the dewaxing process in a series of stages, with alternate chilling and reheating of the flux between stages, 1 Y a 1 1
  • the dewaxing is done in naphthasolution and the precipitated wax is removed between stages by centrifugal means.
  • numeral I designates oil to be dewaxed is first diluted while maina pump which draws the flux of oil and diluent at a temperature well-above the wax separation point through line 2 and forces it through line 3 into a heat interchanging means 4 wherein it is partiallycooled by interchange of heat with cold fiux from the chillersf From the heat interchangerv 4 the partially cooled flux flows through line 5 into the first stage chillers denoted by numerals 6, I and 8.
  • The'fiux passes from chiller 6 to chiller I through line 9 and-from-chillerto chiller8 through line --l0.-- The-"thoroughly chilled; flux 'fiows out of the last chiller 8 through line H and is passed into a series of centrifuges denoted by the numerals l2, l3 and l4wherein as much as possible of the separated wax is removed.
  • the partially dewaxd' flux leaves the centrifuges through line l5 and collects in drum Hi from which it is withdrawn by pump I! through line I8 I and forced through line l9 into heat interchanging means 4 wherein it serves partially to cool the entering warm flux and at the same time is reheated to a temperature at which finely divided particles of wax not removed in the centrifuges are redissolved. From the heat interchanging means 4 the reheated partially dewaxed flux flows through line 20 into a second series of chillers denoted by the numerals 2
  • the rechilled flux passes out of the last chiller 23 through line 26 and is introduced into a second series of centrifuges denoted by the numerals 21, 28 and 29 wherein separated wax is again removed and from I which the dewaxed fiux is withdrawn through line 30 and collected in drum 3
  • the dewaxed fiux is removed through line 31 and is then passed to suitable means (not shown) for removing the diluent from the dewaxed oil.
  • the chilling medium used in the second stage chillers may be introduced into chiller 23 through line 38 and will fiow from one chiller to another through lines 39 and 40, leaving the last chiller through line 4
  • Any suitable chilling medium may be used, such as for example cold brine.
  • chilling stages Although only two chilling stages have been shown in the drawing, it will be understood that as many additional chilling and centrifuging stages may be used as are found necessary to lower the pour point of the oil to the desired degree. It will also be understood that the temperature to which the chilled fiux is reheated between stages fmay be suitably regulated by the provision of additional heating means (not shown), such as steam coils.
  • the chilled flux is then centrifuged at this temperature in order to separate as much wax as possible from the flux.
  • the partially dewaxed flux is then reheated to a temperature well above the wax separation point thereof in order to redissolve any small particles of wax that remain in the flux after centrifuging.
  • the reheating may be conveniently effected by 60 interchange of heat with the warm entering flux.
  • the reheated flux is again chilled, this time to a lower temperature than in the first chilling.
  • the precipitated wax is again removed by centrifuging and the cycle of reheating and rechilling is repeated as many times as is found necessary to obtain a final oil of the desired low pour point. Chilling may be carried to 30 F.,- --0 ,F.,
  • solvents other than naphtha may be used.
  • Alcohols such as propyl and isopropyl alcohol, ketones such as methyl ketone, methyl ethyl ketone, esters such as secondary butyl acetate, liquefied hydrocarbons such as liquid ethane, propane and butane, and miscellaneous solvents such as benzol, toluol,
  • acetone methylene chloride, ethylene dichloride and so forth, or mixtures of any two or more of these may be used.
  • the chilling may be conveniently effected by auto-refrigeration, that is bydirect vaporization of the propane from the flux by release of pressure.
  • a wax-containing oil comprising a blend of oils obtained from Panhandle, Reagan and Salt Flat crudes' and having the following characteristics:
  • the flux then reheated to a temperature of .F. and then rechilled to 10 F. and
  • Saybolt viscosity at F 1560 seconds 104 seconds Saybolt viscosity at 210 F V 7 As another example, a treated wax-containing.
  • the flux is then heated to a temperature of 100 F. and then rechilled to -50 F. and again centrifuged.
  • the dewaxed oil so obtained has the following inspection:
  • An improved process for dewaxing hydrocarbon oils which comprises diluting the oil with a suitable solvent, chilling the mixture to a temperature at which at least a portion of the wax is caused to precipitate, removing the precipitated wax by centrifugal means, reheating the partially dewaxed mixture to a temperature at which any unseparated wax is caused to redissolve, rechilling the mixture to a temperature at which wax is again caused to precipitate, removing this wax and recovering the dewaxed oil from the remaining mixture.
  • Process according partially dewaxed mixture is rechilled to a temperature lower than that at which the mixture was chilled in the preceding step.

Description

y 1936- H. F. 6088 ET AL 2,049,059
DEWAXING HYDROCARBON OILS Filed Sept. 1, 1952 Patented July 28, 1936 :i 1 1 UNITED STATES PATENT OFFICE DEWAXING HYDROCARBON OILS Henry Frank Goss and John Opryshek, Baytown,
Tex., assignors to Standard Oil Development Company, a corporation of Delaware Application September 1, 1932, Serial No. 631,332
" 2 claims (01. 19618) ture to which the flux is chilled is determined by the pour point and cloud point desired in the final dewaxed oil. s
We have found that with .certain types of oils, especially those. containing substantial amounts of the so-called amorphous waxes, removal of sufiici'ent wax totlower the' pour point-to. about 0 F. or below is difficult to accomplish by the usual methods of dewaxing. This invention therefore has for itsprincipal object the provision of an improved method for substantially lowering the pour points of suchoilsf 1 The improvement comprises carrying out the dewaxing process in a series of stages, with alternate chilling and reheating of the flux between stages, 1 Y a 1 1 In the preferred embodiment of the invention the dewaxing is done in naphthasolution and the precipitated wax is removed between stages by centrifugal means. It should be understood, however, that the process is not limited .to this diluent and method of removing precipitated wax, but that any other suitable means may be used. The method ofcarrying out the process will be fully understood. from. the following. description read with reference to the accompanying drawing which is a semi-diagrammatic 'view'in sectional elevation of a suitable type of apparatus that may be used.
Referring to the drawing, numeral I designates oil to be dewaxed is first diluted while maina pump which draws the flux of oil and diluent at a temperature well-above the wax separation point through line 2 and forces it through line 3 into a heat interchanging means 4 wherein it is partiallycooled by interchange of heat with cold fiux from the chillersf From the heat interchangerv 4 the partially cooled flux flows through line 5 into the first stage chillers denoted by numerals 6, I and 8. The'fiux passes from chiller 6 to chiller I through line 9 and-from-chillerto chiller8 through line --l0.-- The-"thoroughly chilled; flux 'fiows out of the last chiller 8 through line H and is passed into a series of centrifuges denoted by the numerals l2, l3 and l4wherein as much as possible of the separated wax is removed. I
The partially dewaxd' flux leaves the centrifuges through line l5 and collects in drum Hi from which it is withdrawn by pump I! through line I8 I and forced through line l9 into heat interchanging means 4 wherein it serves partially to cool the entering warm flux and at the same time is reheated to a temperature at which finely divided particles of wax not removed in the centrifuges are redissolved. From the heat interchanging means 4 the reheated partially dewaxed flux flows through line 20 into a second series of chillers denoted by the numerals 2|, 22, and 23 which are connected by means of lines 24 and 25. The rechilled flux passes out of the last chiller 23 through line 26 and is introduced into a second series of centrifuges denoted by the numerals 21, 28 and 29 wherein separated wax is again removed and from I which the dewaxed fiux is withdrawn through line 30 and collected in drum 3| from which it is withdrawn by pump 32 through line 33 and forced through line 34 into and through the first stage 20 chillerswhere it serves as the cooling medium,
1 flowing from chiller 8 to chiller I through line 35 ,and from chiller l to chiller 6 through line 36.
From the last chiller the dewaxed fiux is removed through line 31 and is then passed to suitable means (not shown) for removing the diluent from the dewaxed oil.
The chilling medium used in the second stage chillers may be introduced into chiller 23 through line 38 and will fiow from one chiller to another through lines 39 and 40, leaving the last chiller through line 4|. Any suitable chilling medium may be used, such as for example cold brine.
Although only two chilling stages have been shown in the drawing, it will be understood that as many additional chilling and centrifuging stages may be used as are found necessary to lower the pour point of the oil to the desired degree. It will also be understood that the temperature to which the chilled fiux is reheated between stages fmay be suitably regulated by the provision of additional heating means (not shown), such as steam coils.
In the operation of our improved process the tained at a temperature well above the wax separation, point, say about to F., with from 1 to 4 volumes of a suitable diluent such as depending upon the wax content and type of wax'in the particular oil. The chilled flux is then centrifuged at this temperature in order to separate as much wax as possible from the flux. The partially dewaxed flux is then reheated to a temperature well above the wax separation point thereof in order to redissolve any small particles of wax that remain in the flux after centrifuging.
The reheating may be conveniently effected by 60 interchange of heat with the warm entering flux. The reheated flux is again chilled, this time to a lower temperature than in the first chilling. The precipitated wax is again removed by centrifuging and the cycle of reheating and rechilling is repeated as many times as is found necessary to obtain a final oil of the desired low pour point. Chilling may be carried to 30 F.,- --0 ,F.,
50 F., F., and even lower in the successive steps and reheating may be carried to properature and the chilled flux then centrifuged, .fine particles or crystals of wax remain in the 'fiux'and cannot be separated even by prolonged centrifuging. These fine particles cannot be removed by further chilling and centrifuging but appear to form a wax gel which favors the formation of additional fine gel-forming particles from the remainder of the wax. A further undesirable feature of the fine wax particles is that they decrease markedly the rate of heat transfer through the fiux and this results in a loss of heat exchange efiiciency.
The difficulties incident to the formation of the fine particles of wax are substantially avoided by the practice of the present improvement. 'Reheating of the flux after centrifuging causes the fine particles to redissolve and then upon rechillingthe remaining waxis again precipitated ina form in which at least a substantial portion of it may be removed by centrifuging. As indicated above, the chilling may be carried to increasingly lower temperatures in each step. It is possible by this method to remove a greater proportion of the wax and to obtain oils of lower pour points and cloud points than can be accomplished by chilling to a very low temperature in a single step or in a series of termediate reheating.
The increased cost due to reheating and rechilling between stages is largely offset by the fact that a smaller quantity of diluent may be used than ordinarily, thus increasing the oil throughput of the centrifuges and decreasing the cost of refrigeration per gallon of oil, and
steps without inalso by the fact that much better heat transfer is obtained when the fine particles of wax are not present in the flux.
Various modifications of our improved process may be made without departing from the scope of the invention. Thus for example solvents other than naphtha may be used. Alcohols such as propyl and isopropyl alcohol, ketones such as methyl ketone, methyl ethyl ketone, esters such as secondary butyl acetate, liquefied hydrocarbons such as liquid ethane, propane and butane, and miscellaneous solvents such as benzol, toluol,
acetone, methylene chloride, ethylene dichloride and so forth, or mixtures of any two or more of these may be used.
When using liquefied hydrocarbons such as propane, the chilling may be conveniently effected by auto-refrigeration, that is bydirect vaporization of the propane from the flux by release of pressure.
Other methods of separating the precipitated wax may also be used such as those mentioned s aver. W en. working. with oi s containin s b- -;Sa-ybolt viscosity at 210 stantial amounts of amorphous waxes, however, centrifuging is the preferred method of wax separation. Various filter aids such as finely divided clay, fullers earth, silica and the like may be useful in facilitating the separation of .the wax.
The following examples illustrate the application of our improved dewaxing method:
A wax-containing oil comprising a blend of oils obtained from Panhandle, Reagan and Salt Flat crudes' and having the following characteristics:
Gravity; A. P. I 26.8 Pour point 115 F. Flash point 515 F. Saybolt viscosity at 100F 1130 seconds Saybolt viscosity at 210 .F 84 seconds is diluted with a naphtha having a gravity (A. P. I.) of 58", so that the resulting blend comprises 30% oil and naphtha. This flux is chilled tor50 F. and the chilled flux is then centrifuged at 50 F. in order to remove as much wax as'possible. The partially dewaxed oil has a pour point of F. V
The fluxis then reheated to a temperature of .F. and then rechilled to 10 F. and
again centrifuged. The oil so obtained has a.
' pour point of 55. F.
Again theremaining flux is reheated to 60 F. or higher and rechilled to 50 F. The oil now has a pounpoint of 0 F. It is reheated to 50 F. or higher and rechilled this time to --60 F.
and the oil finallyobtained has a pour point of I -109.F.. e. final dewaxed oil has the following inspectionr Gravity, A. P. I 23.9 'Cloud point 0 to 10 F. Pour point --10F.
Saybolt viscosity at F 1560 seconds 104 seconds Saybolt viscosity at 210 F V 7 As another example, a treated wax-containing.
from Panhaving the following characoil comprising a blend of'oils obtained handle crude and teristics:
Gravity, A. P. I 272, .Pour point F. Flash point 1. 500 F. Saybolt viscosity at 100 F 725 seconds 70 seconds Saybolt viscosity at 210 F is diluted with naphtha having a gravity of 57.2
Gravity, A. P. I 245 Pour 'pOint 0 F. Cloud point -1 0 Saybolt viscosity at 100 F 1044 seconds F 82.6 seconds In another experiment an untreated wax-con- F. in order to remove as much wax 2 id l ig 9. QQ PP WBS'B. b end M pbbai 76 from Panhandle crude and having the following characteristics Gravity, A. P. I 26.8 Pour point 120 F. Flash point 525 F. Saybolt viscosity at 100 F 850 seconds Saybolt viscosity at 210 F 73.2 seconds is diluted with naphtha having a gravity of 5'7.2 A. P. I., so that the resulting blend comprises 33% oil and 67% naphtha. This flux is chilled to 30 F. and the chilled flux is then centrifuged at 30 F. in order to remove as much wax as possible. The partially dewaxed oil has a pour point of 65 F.
The flux is then heated to a temperature of 100 F. and then rechilled to -50 F. and again centrifuged. The dewaxed oil so obtained has the following inspection:
Saybolt viscosity at 210F 91.6 seconds This invention is not limited by any theory of the mechanism of the dewaxing nor by any details which have been given merely for purposes of illustration, but is limited only in and by the following claims in which we wish to claim all novelty inherent in the process.
We claim:
1. An improved process for dewaxing hydrocarbon oils which comprises diluting the oil with a suitable solvent, chilling the mixture to a temperature at which at least a portion of the wax is caused to precipitate, removing the precipitated wax by centrifugal means, reheating the partially dewaxed mixture to a temperature at which any unseparated wax is caused to redissolve, rechilling the mixture to a temperature at which wax is again caused to precipitate, removing this wax and recovering the dewaxed oil from the remaining mixture.
2. Process according partially dewaxed mixture is rechilled to a temperature lower than that at which the mixture was chilled in the preceding step.
. HENRY FRANK GOSS.
JOHN OPRYSHEK.
to claim 1 in which the 2d
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2453933A (en) * 1945-02-10 1948-11-16 Union Oil Co Refining of wax
US2578685A (en) * 1949-11-10 1951-12-18 Karl A Fischer Method of dewaxing petroleum products with monobromo-monochloromethane
US2625502A (en) * 1948-07-24 1953-01-13 Union Oil Co Wax-oil separation
US2712519A (en) * 1953-11-03 1955-07-05 Edeleanu Gmbh Process for evaporating and drying chlorinated hydrocarbons used in the dewaxing of mineral oils
US2773803A (en) * 1954-10-22 1956-12-11 Sun Oil Co Combination adsorption and dewaxing process
US5474668A (en) * 1991-02-11 1995-12-12 University Of Arkansas Petroleum-wax separation
US5853564A (en) * 1991-02-11 1998-12-29 University Of Arkansas Petroleum-wax separation

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2453933A (en) * 1945-02-10 1948-11-16 Union Oil Co Refining of wax
US2625502A (en) * 1948-07-24 1953-01-13 Union Oil Co Wax-oil separation
US2578685A (en) * 1949-11-10 1951-12-18 Karl A Fischer Method of dewaxing petroleum products with monobromo-monochloromethane
US2712519A (en) * 1953-11-03 1955-07-05 Edeleanu Gmbh Process for evaporating and drying chlorinated hydrocarbons used in the dewaxing of mineral oils
US2773803A (en) * 1954-10-22 1956-12-11 Sun Oil Co Combination adsorption and dewaxing process
US5474668A (en) * 1991-02-11 1995-12-12 University Of Arkansas Petroleum-wax separation
US5853564A (en) * 1991-02-11 1998-12-29 University Of Arkansas Petroleum-wax separation
US6024862A (en) * 1991-02-11 2000-02-15 Advanced Refining Technologies, Inc. Petroleum-wax separation

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