US2053485A - Process for refining mineral oil - Google Patents
Process for refining mineral oil Download PDFInfo
- Publication number
- US2053485A US2053485A US740286A US74028634A US2053485A US 2053485 A US2053485 A US 2053485A US 740286 A US740286 A US 740286A US 74028634 A US74028634 A US 74028634A US 2053485 A US2053485 A US 2053485A
- Authority
- US
- United States
- Prior art keywords
- solvent
- extraction
- mixture
- aromatic
- diluent
- 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
Links
- 238000000034 method Methods 0.000 title description 22
- 239000002480 mineral oil Substances 0.000 title description 13
- 238000007670 refining Methods 0.000 title description 11
- 235000010446 mineral oil Nutrition 0.000 title description 6
- 239000002904 solvent Substances 0.000 description 93
- 239000000203 mixture Substances 0.000 description 66
- 238000000605 extraction Methods 0.000 description 52
- 239000003085 diluting agent Substances 0.000 description 41
- 229930195733 hydrocarbon Natural products 0.000 description 41
- 150000002430 hydrocarbons Chemical class 0.000 description 35
- -1 monocyclic aromatic hydrocarbons Chemical class 0.000 description 34
- 239000004215 Carbon black (E152) Substances 0.000 description 30
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 28
- 125000003118 aryl group Chemical group 0.000 description 27
- 239000000284 extract Substances 0.000 description 27
- 239000012071 phase Substances 0.000 description 23
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 22
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 19
- 239000003921 oil Substances 0.000 description 17
- 239000007791 liquid phase Substances 0.000 description 15
- 235000010290 biphenyl Nutrition 0.000 description 13
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 12
- 125000002619 bicyclic group Chemical group 0.000 description 12
- 239000004305 biphenyl Substances 0.000 description 11
- 230000005484 gravity Effects 0.000 description 11
- 239000007788 liquid Substances 0.000 description 11
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 10
- 238000009835 boiling Methods 0.000 description 10
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 10
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 10
- 125000003367 polycyclic group Chemical group 0.000 description 9
- 125000006267 biphenyl group Chemical group 0.000 description 8
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000012046 mixed solvent Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 239000003208 petroleum Substances 0.000 description 5
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 4
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- SXWIAEOZZQADEY-UHFFFAOYSA-N 1,3,5-triphenylbenzene Chemical compound C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=C1 SXWIAEOZZQADEY-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003350 kerosene Substances 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000000638 solvent extraction Methods 0.000 description 3
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical class CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 2
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical class CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- BDUPRNVPXOHWIL-UHFFFAOYSA-N dimethyl sulfite Chemical compound COS(=O)OC BDUPRNVPXOHWIL-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical compound C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 2
- NXLOLUFNDSBYTP-UHFFFAOYSA-N retene Chemical compound C1=CC=C2C3=CC=C(C(C)C)C=C3C=CC2=C1C NXLOLUFNDSBYTP-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- SXQXMKMHOFIAHT-UHFFFAOYSA-N 1,1-dichloro-2-(2,2-dichloroethoxy)ethane Chemical compound ClC(Cl)COCC(Cl)Cl SXQXMKMHOFIAHT-UHFFFAOYSA-N 0.000 description 1
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- GUPIKZAAELPHQW-UHFFFAOYSA-N 1-ethylanthracene Chemical compound C1=CC=C2C=C3C(CC)=CC=CC3=CC2=C1 GUPIKZAAELPHQW-UHFFFAOYSA-N 0.000 description 1
- LOCGAKKLRVLQAM-UHFFFAOYSA-N 4-methylphenanthrene Chemical compound C1=CC=CC2=C3C(C)=CC=CC3=CC=C21 LOCGAKKLRVLQAM-UHFFFAOYSA-N 0.000 description 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- JUTIJVADGQDBGY-UHFFFAOYSA-N anthracene photodimer Chemical compound C12=CC=CC=C2C2C(C3=CC=CC=C33)C4=CC=CC=C4C3C1C1=CC=CC=C12 JUTIJVADGQDBGY-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical compound C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004434 industrial solvent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING 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
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
Definitions
- Our invention relates to a process for separating normally liquid hydrocarbon mixtures by extraction with selective solvents. More particularly, the invention relates to the improving of 5 the extraction methods by the use of polycyclic aromatic hydrocarbons as an auxiliary solvent in connection with a selective solvent.
- suitable selective solvents can be used to extract various types of hydrocarbon mixtures, such as crude petroleum oils, lubricating, transformer and spindle oils, heavy or light naphthas, etc., either natural or synthetic.
- the extraction process of our invention has as its main object an eflicient separation of'hydrocarl5 bon mixtures into 'so called aromatic and nonaromatic groups of components. It consists, briefly, in bringing the hydrocarbon mixture into contact with a selective solvent in the presence of an effective quantity of polycyclic aromatic hydrocarbons, thereby causing two layers to form.
- the raflinate layer contains mainly the non-aromatic constituents of the mixture and/or certain impurities which may be present in mineral oils. Each of the layers may then be treated to separate its hydrocarbon portion from the solvents.
- I s:s,Th'e present invention is basedon the discovery '35 that polycyclic hydrocarbons containing aromatic rings, and particularly bicyclic aromatic hydrocarbons are even more effective than monocyclic hydrocarbons when used as a solvent diluent in extracting hydrocarbon mixtures.
- polycyclic hydrocarbons and polycyclic aromatic hydrocarbons are used to designate compounds having an aromatic, i. e., a six membered ring, in addition to at least one other ring, which may or may not be an aromatic ring.
- naphthalene and its homologues, such as monoor poly-alkyl naphthalenes, as a-methyl naphthalene, other monoor poly-methyl naphthalenes, monoor poly-ethyl naphthalenes, diphenyl, its homologues, such as ditolyl, monoor poly-'alkyl diphenyl or methylor poly-methyl, ethylor poly-ethyl diphenyls,
- diphenyl alkanes such as diphenyl methane, di-
- phenyl ethane, stilbene, tolane, etc. all partially hydrogenated or not; among the tricyclic compounds: anthracene and its homologues, as alkyl-' or poly-alkyl anthracene. as methylor polymethyl anthracene, ethylor poly-ethyl anthracene, phenanthrene and its homologues, such as alkylor poly-alkyl phenanthrene, as retene, monoor poly-methyl phenanthrene, triphenyl methane, triphenyl benzene; among other polycyclic compounds: indene, monoor poly-alkyl indene, polyphenyl alkanes, dianthracene, etc., 5 all partially hydrogenated or not; or mixtures of any of the above polycyclic compounds, or their solutions in aliphatic hydrocarbons, as light naphthas, and preferably in cyclic hydrocarbons, such as benzol or toluol
- solul0 tions may be used as: benzol and naphthalene; benzol and diphenyl; benzol, diphenyl and naphthalene; an aromatic portion of a mineral oil distillate containing considerable quantities of polyor bicyclic aromatic hydrocarbons, such as an ex- 15 tract wherein bicyclic aromatic hydrocarbons have been concentrated beyond a certain critical concentration by intensive solvent extraction, etc.
- extracts when they are used as solvent diluents, is usually greatly impeded by relatively high contents of aliphatic and naphthenic components.
- extracts can be subjected to further refining treatments, such as intensive solvent extraction, whereby their non-aromatic components are substantially removed and the concentration of the total and'bicyclic aromatic hydrocarbons is 35 made sufiiciently high to make such treated extracts even more eflective as solvent diluents than pure benzol, the latter being one of the most effective diluents among monocyclic aromatics.
- naphthalene, dipheny1, other p lycyclic hydrocarbons, and many of their alkyl sub tituted derivatives boil within the range of 00 C.
- any mixed base or 55 naphthenic base crude or cracked distillate or residue containing a substantial fraction boiling between about 180 C..-300 C. can be used as a source of the desirable concentrated bicyclic extract.
- bicyclic aro- 60 matic hydrocarbons Since the specific gravity of bicyclic aro- 60 matic hydrocarbons is substantially higher than the specific gravity of the monocyclic or aliphatic hydrocarbons boiling at the same temperatures, such concentrated bicyclic extracts would, due to their high total aromatic content, possess considerably higher specific gravity than pure benzol or ordinary naphthenic extracts obtained by Boiling range "C 180 -300 Gravity A. P. I 8.0- 25.0 Total aromatics, by vol 90 100%
- the bicyclic aromatic diluents boiling above 300 C. may also be used, the above range stating only the preferred type of the diluent.
- the bicyclic aromatics may also be dissolved in non-aromatic hydrocarbons or other solvents to produce the auxiliary solvent of our invention. In this case the gravity and other characteristics will not necessarily fall within the limits recited, but will depend on the nature of the non-aromatic hydrocarbon used.
- concentrated bicyclic extract is used in this specification, it is to be understood to include aromatic portions'of mineral oil fractions containing effective concentrations of bicyclic aromatic hydrocarbons as discussed above and particularly the bicyclic concentrates possessing above mentioned physical and chemical properties.
- selective solvents which may be used singly or mixed as extracting agents in the refining of mineral oils or other hydrocarbon mixtures are sulfur dioxide, furfu'ral, ppdichlorethylether, acetone, nitromethane, nitrobenzene, propionitrile, dimethyl sulphate, dimethyl sulphite, methyl formate, phenols, aromatic or allphatic amines, pyridine, isoquinoline, quinoline, quinaldine, picolines, lutidines, and other substantially pure or industrial solvents, such as petroleum nitrogen bases, various alcohols, esters, etc.
- auxiliary solvents whose presence in the extraction mixtures improves the efilciency of extraction, are merely represented by the specific polycyclic hydrocarbons, 'or the various mixtures or solutions recited, and may be selected from a number of other polycyclic hydrocarbons containing one six membered ring and at least one additional ring which may or may not be six membered, which produce the desired efiect, and which can be separated relatively easily from the material being treated. for example, by distillation, and have no detrimental effect on the refined products.
- the present invention is to include within its scope the extraction processes for extracting mineral oils or other hydrocarbon mixtures employing a selective solvent in the presence of an auxiliary solvent having a high content of polycyclic aromatic hydrocarbons.
- the eificiency of extraction is determined by the solvent power and the selectivity of the solvent (or solvent mixture) with regard to the components of the mixture being extracted. This efilciency may be expressed in terms of the quantity or quality of the rafiinate.
- the quality of the raflinate may be taken as a measure of the efiiciency of the extraction.
- the maximum quantity of the raffinate of a specified purity may be produced by the maximum quantity of the raffinate of a specified purity, while keeping the mass or volume of the main or selective solvent constant. Under these conditions the quantity of the rafiinate may be taken as a measure of the efliciency.
- the efliciency of the various extractions may also be measured by comparing the extent to which the solvent is conserved when the same rafiinate is made with or without the use of the auxiliary solvent described in this specification.
- Themethod of this invention also. makes it possible to improve mineral oils having relatively low contents of n'aphthenic or aromatic components, which contents it is difiicult or impossible to reduce by extraction'with the main solvent alone or in the presence of a monocyclic aromatic diluent only, like benzol.
- the increased extraction efiiciency of the mixed solvent process employing polycyclic aromatics in the auxiliary solvents, as compared withthe efliciency of the corresponding single solvent process or with the mixed solvent process employing only benzene or compositions other than those of the present invention for the auxiliary solvent, is apparently due to the favorable effect of the mixed solvent of this invention on the distribution ratios of the nonparaflinic and parafllnic components of the oil being treated in the extract and rafiinatephases.
- the relative content of the preferentially soluble components in the selective solvent as compared with that in the raillnate phase is increased in the presence 01' the auxiliary polycyclic aromatics, so that when such a mixed solvent is.
- the extraction temperature is so selected as to create optimum conditions from the viewpoints of economy of operation, yield, purity of product, conservation of solvents, etc.
- auxiliary solvent may be mixed with the hydrocarbon mixture undergoing treatment either before or at the time the hydrocarbon mixture is contacted with the main solvent; or the whole or a part of the auxiliary solvent may be mixed with the main solvent prior to contacting it with the hydrocarbon mixture.
- the process is carried out by conducting the mixed solvent, 1. e. a selective solvent containing polycyclic aromatics, countercurrently to and in contact with the hydrocarbon mixture being treated.
- the main solvent usually together with the auxiliary solvent, or diluent, is caused to pass countercurrently toand in contact with the hydrocarbon mixture being extracted through a mixingsettling or extraction zone, which may consist of a contact column or a series of alternate mixing and phase-separating
- a mixingsettling or extraction zone which may consist of a contact column or a series of alternate mixing and phase-separating
- the resulting extract and raflinate phases are separated, usually by gravity, or centrifugin'g, and withdrawn at the opposite ends of the zone; the main and auxiliary solvents are then removed from each of the phases, either together or in separate stages, by any suitable means, as by distillation, absorption, etc.
- the recovered solvents may be reused repeatedly.
- auxiliary solvent or a portion thereof may be left only ineffective amounts of teristicsf gravity 18.l A. P. 1..
- the process of this invention is effective not only with oils which may be viscous at extraction temperatures, but-also with hydrocarbon mixtures which are easy flowing or non-viscous at such temperatures, e. g. gasolines.
- oils which may be regarded as being viscous at ordinary temperatures would become easy flowing at the slightly elevated temperatures of extraction with furfural, for example, 0r phenol, or some other selective solvent, so that their dilution for the purpose of reducing their viscosity would be unnecessary.
- the refining treatment consisted of (1) Two extractions with 200% of a mixture of 75 parts of S02 and 25 parts of the auxiliary solvent: (2) one extraction with 100% of mixture of 65 parts of S02 and 35 parts of the auxiliary solvent; the percentages express quantities of mixed solvents based on the primary Edeleanu rafiinate.
- the treating temperature was between 45 and F.
- These finished railinates obtained in each treatment were then fractionated, and the viscosity index for each cut determined. From these cuts an oil was blended to meet S.
- A. E. 40 viscosity speci- These results indicate that the substitution of concentrated bicyclic extract for benzol produces material increase in the yield when the quality is unaltered. If'the extraction with concentrated kerosene extract as a diluent were carried out under conditions to produce a lower yield, the quality of the product would be materially increased.
- Example I A COalinga bulk distillate was treated twice with 200% S02. Five samples of the resulting primary raflinate were separately treated, each being successively subjected to the same steps, but using different auxiliary solvents in each instance, these solvents being, respectively, ((1) benzene; (b) concentrated extract used in Example I; (c) a methyl naphthalene; (d) a mixture containing 71% benzol and 29% naphthalene; (e) a mixture containing 31% benzol, 42% diphenyl, and 27% naphthalene.
- the treatment steps were (1) two extractions were 200% of a mixture of 75 parts of S02 and 25 parts of auxiliary solvent; (2) one extraction with 100% of a mixture of 67 parts of S02 and 33 parts of the auxiliary solvent.
- auxiliary solvent necessary to improve the extraction efliciency will vary with the nature of the oil being extracted, the main solvent used, etc., and no general figure can be stated, although it was found from experience that the ratio of the selective solvent to the diluent usually should be between one and four.
- effective quantity as used.
- polycyclic aromatic hydrocarbons are selected from the group: naphthalene, alkyl' naphthalenes, diphenyl, alkyl diphenyls, diphenyl alkanes, anthracene, alkyl anthracenes, phenanthrene, alkyl phenanthrene, triphenyl benzene, triphenyl alkanes, indene, alkyl indenes, and partially hydrogenated homologues of said compounds.
- the diluent is a mixture selected from the group consisting of a mixture of benzol, diphenyl and naphthalene, a mixture of benzol and naphthalene, a mixture of benzol and a methyl naphthalene.
- a process for extracting a liquid hydrocar bon mixture containing aromatic constituents comprising flowing said mixture countercurrent- 1y to and in contact with a stream of a selective solvent containing an effective quantity of polycyclic aromatic hydrocarbons to produce two liquid phases, and subsequently separating said liquid phases.
- a process for refining petroleum lubricating oil comprising extracting the oil with a' solvent selected from the group: liquid sulfur dioxide, dichlorethylether, acetone, nitromethane, nitrobenzene, propionitrile, dimethyl sulphate, dimethyl sulphite, methyl formate, phenols, aromatic and aliphatic amines, nitriles and thionitriles, pyridine, qui'nolines, picolines, lutidines,
- a process for refining petroleum lubricating oil comprising extracting-the Joilf'at'least once with a selective solventto ⁇ produce almanac containing smaller amounts of aromatics, and then further reducing the aromatic content of said rafiinate by extracting said raflinatewith a selective solvent plus an aromatic diluent containing an effective quantity of polycyclic aromatic hydrocarbons to produce two liquid phases, and subsequently separating said liquid phases.
- a process for refining hydrocarbon mixtures comprising extracting said mixture with a'selective solvent in the presence of an aromatic diluent containing an efiective quantity of polycyclic aromatic hydrocarbons, said diluent being present in such amounts that the ratio of the main solvent to the diluent is between one and four to produce two liquid phases, and subsequently separating said liquid phases.
- the aromatic diluent is the aromatic portion of' a mineral oil distillate having a gravity between 8.0" A. P. 1. and 24.0 A. P. I. and boiling between about 180 C. and 300 C. t q
- polycyclic hydrocarbons are selected from the groups naphthalene, alkyl naphthalenes, di-
- phenyl alkyl diphenyls diphen'yl alkanes, anthracene, alkyl anthracene, phenanthrene, alkyl phenanthrene, triphenylbenzene, triphenyl al-- kanes, indene and alkyl indenes, and partially hydrogenated homologues of said compounds.
- a process for refining a hydrocarbonmix- I ture containing aromatic'constituents comprising extracting said mixture at least once with a selective solvent to produce a primary liquid raflinate containing smaller amounts of aromatics than the original mixture, and treating said primary raflinate at least once with a selective solvent containing an aromatic diluent containing an effective quantity oi polycyclicaromatics, the
- ratio of the selective solvent to the aromatic diluent being between one and four, to produce a secondary rafiinate having a lower aromatic content than said first rafflnate.
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented Sept. 8, 1936 UNITED STATES 2,053,485 I PROCESS FOR REFINING 'MINERAL 01L Hans Friedrich Lindeke and Bernard -Sutro Greensfelder, Martinez, CaliL, Shell Development Company,
assignors to San Francisco,
Calif., a corporation of Delaware Application August 17, 1934, Serial No. 740,286
' 20 Claims. (01. 196-13) Our invention relates to a process for separating normally liquid hydrocarbon mixtures by extraction with selective solvents. More particularly, the invention relates to the improving of 5 the extraction methods by the use of polycyclic aromatic hydrocarbons as an auxiliary solvent in connection with a selective solvent.
It is known that suitable selective solvents can be used to extract various types of hydrocarbon mixtures, such as crude petroleum oils, lubricating, transformer and spindle oils, heavy or light naphthas, etc., either natural or synthetic. The extraction process of our invention has as its main object an eflicient separation of'hydrocarl5 bon mixtures into 'so called aromatic and nonaromatic groups of components. It consists, briefly, in bringing the hydrocarbon mixture into contact with a selective solvent in the presence of an effective quantity of polycyclic aromatic hydrocarbons, thereby causing two layers to form.
The raflinate layer contains mainly the non-aromatic constituents of the mixture and/or certain impurities which may be present in mineral oils. Each of the layers may then be treated to separate its hydrocarbon portion from the solvents.
The use of benzol or toluol or similar monocyclic aromatic hydrocarbons as an auxiliary solvent or solvent diluent in extracting hydrocarbon mixtures isknow n, the advantage of such extraction processes being an improved eillciency of separation of the components of the mixtureunder suitable temperature conditions.
I s:s,Th'e present invention is basedon the discovery '35 that polycyclic hydrocarbons containing aromatic rings, and particularly bicyclic aromatic hydrocarbons are even more effective than monocyclic hydrocarbons when used as a solvent diluent in extracting hydrocarbon mixtures. As used in 40 the present specification and claims, the terms polycyclic hydrocarbons and polycyclic aromatic hydrocarbons are used to designate compounds having an aromatic, i. e., a six membered ring, in addition to at least one other ring, which may or may not be an aromatic ring. Among such diluents may be mentioned, for example, among the bicyclic compounds: naphthalene, and its homologues, such as monoor poly-alkyl naphthalenes, as a-methyl naphthalene, other monoor poly-methyl naphthalenes, monoor poly-ethyl naphthalenes, diphenyl, its homologues, such as ditolyl, monoor poly-'alkyl diphenyl or methylor poly-methyl, ethylor poly-ethyl diphenyls,
1 diphenyl alkanes, such as diphenyl methane, di-
phenyl ethane, stilbene, tolane, etc., all partially hydrogenated or not; among the tricyclic compounds: anthracene and its homologues, as alkyl-' or poly-alkyl anthracene. as methylor polymethyl anthracene, ethylor poly-ethyl anthracene, phenanthrene and its homologues, such as alkylor poly-alkyl phenanthrene, as retene, monoor poly-methyl phenanthrene, triphenyl methane, triphenyl benzene; among other polycyclic compounds: indene, monoor poly-alkyl indene, polyphenyl alkanes, dianthracene, etc., 5 all partially hydrogenated or not; or mixtures of any of the above polycyclic compounds, or their solutions in aliphatic hydrocarbons, as light naphthas, and preferably in cyclic hydrocarbons, such as benzol or toluol. For example, such solul0 tions may be used as: benzol and naphthalene; benzol and diphenyl; benzol, diphenyl and naphthalene; an aromatic portion of a mineral oil distillate containing considerable quantities of polyor bicyclic aromatic hydrocarbons, such as an ex- 15 tract wherein bicyclic aromatic hydrocarbons have been concentrated beyond a certain critical concentration by intensive solvent extraction, etc. It should be noted, however, that while some of such solutions, like ordinary Edeleanu kerosene 20 extracts, for example, may contain a certain quantity of bicyclic aromatics, this quantity is generally toosmall to be effective in causing an improvement in the efiiciency of the solvent extraction, when the extract is substituted, for 25 benzol as an auxiliary solvent.
Moreover, the efiectiveness of such extracts,
when they are used as solvent diluents, is usually greatly impeded by relatively high contents of aliphatic and naphthenic components. How- 30 ever, extracts can be subjected to further refining treatments, such as intensive solvent extraction, whereby their non-aromatic components are substantially removed and the concentration of the total and'bicyclic aromatic hydrocarbons is 35 made sufiiciently high to make such treated extracts even more eflective as solvent diluents than pure benzol, the latter being one of the most effective diluents among monocyclic aromatics.
From experience it has been found that in order, 40 to be so effective such concentrated bicyclic extracts must contain at least total-aromatic components (preferably over of which at least an appreciable portion should be bicyclic aromatic hydrocarbons. 45
Since naphthalene, dipheny1, other p lycyclic hydrocarbons, and many of their alkyl sub tituted derivatives boil within the range of 00 C., it was ,often found particularly advantageous from the practical viewpoint to obtain the desired 50 concentrated extracts from that portion of the hydrocarbon oil, which is usually known as kerosene distillate, and which boils substantially within the range of about 180" C.-300 C. It should be understood, however, that any mixed base or 55 naphthenic base crude or cracked distillate or residue containing a substantial fraction boiling between about 180 C..-300 C. can be used as a source of the desirable concentrated bicyclic extract. Since the specific gravity of bicyclic aro- 60 matic hydrocarbons is substantially higher than the specific gravity of the monocyclic or aliphatic hydrocarbons boiling at the same temperatures, such concentrated bicyclic extracts would, due to their high total aromatic content, possess considerably higher specific gravity than pure benzol or ordinary naphthenic extracts obtained by Boiling range "C 180 -300 Gravity A. P. I 8.0- 25.0 Total aromatics, by vol 90 100% As stated hereinbefore, the bicyclic aromatic diluents boiling above 300 C., may also be used, the above range stating only the preferred type of the diluent. The bicyclic aromatics may also be dissolved in non-aromatic hydrocarbons or other solvents to produce the auxiliary solvent of our invention. In this case the gravity and other characteristics will not necessarily fall within the limits recited, but will depend on the nature of the non-aromatic hydrocarbon used.
Where the term concentrated bicyclic extract is used in this specification, it is to be understood to include aromatic portions'of mineral oil fractions containing effective concentrations of bicyclic aromatic hydrocarbons as discussed above and particularly the bicyclic concentrates possessing above mentioned physical and chemical properties.
.Among the selective solvents which may be used singly or mixed as extracting agents in the refining of mineral oils or other hydrocarbon mixtures are sulfur dioxide, furfu'ral, ppdichlorethylether, acetone, nitromethane, nitrobenzene, propionitrile, dimethyl sulphate, dimethyl sulphite, methyl formate, phenols, aromatic or allphatic amines, pyridine, isoquinoline, quinoline, quinaldine, picolines, lutidines, and other substantially pure or industrial solvents, such as petroleum nitrogen bases, various alcohols, esters, etc. These specific solvents represent, however, only typical examples of a large number of known selective solvents capable of separating mineral oils or hydrocarbon mixtures into aromatic and non-aromatic components (sometimes referred to as naphthenic and parafilnic or as non-parailinic and parafllnic), which solvents arelntended to be within the scope of this invention. These main solvents used for extracting hydrocarbon mixtures have the common characteristic that, at the extraction temperatures, they are only partly miscible with the mixture being extracted and act as preferential, solvents for both nonparafiinic hydrocarbons and polar organic compounds containing sulfur, nitrogen, oxygen, etc. With the paraillnic hydrocarbons they are miscible only to a lesser extent.
Likewise, the auxiliary solvents, whose presence in the extraction mixtures improves the efilciency of extraction, are merely represented by the specific polycyclic hydrocarbons, 'or the various mixtures or solutions recited, and may be selected from a number of other polycyclic hydrocarbons containing one six membered ring and at least one additional ring which may or may not be six membered, which produce the desired efiect, and which can be separated relatively easily from the material being treated. for example, by distillation, and have no detrimental effect on the refined products.
It will be understood, therefore, that the present invention is to include within its scope the extraction processes for extracting mineral oils or other hydrocarbon mixtures employing a selective solvent in the presence of an auxiliary solvent having a high content of polycyclic aromatic hydrocarbons.
Generally speaking, the eificiency of extraction is determined by the solvent power and the selectivity of the solvent (or solvent mixture) with regard to the components of the mixture being extracted. This efilciency may be expressed in terms of the quantity or quality of the rafiinate.
Thus, if the masses or volumes of the relative yield and of the main or selective solvent are kept constant, the quality of the raflinate may be taken as a measure of the efiiciency of the extraction.
Alternatively, it may be desired to produce the maximum quantity of the raffinate of a specified purity, while keeping the mass or volume of the main or selective solvent constant. Under these conditions the quantity of the rafiinate may be taken as a measure of the efliciency.
The efliciency of the various extractions may also be measured by comparing the extent to which the solvent is conserved when the same rafiinate is made with or without the use of the auxiliary solvent described in this specification.
By conducting the extraction in accordance with the present invention, i. e., by using a main selective solvent in the presence of polycyclic aromatic hydrocarbons, it becomes possible to improve the quality and/or quantity of the mineral oil rafiinate, and/or to conserve the main solvent.
Themethod of this invention also. makes it possible to improve mineral oils having relatively low contents of n'aphthenic or aromatic components, which contents it is difiicult or impossible to reduce by extraction'with the main solvent alone or in the presence of a monocyclic aromatic diluent only, like benzol.
The increased extraction efiiciency of the mixed solvent process employing polycyclic aromatics in the auxiliary solvents, as compared withthe efliciency of the corresponding single solvent process or with the mixed solvent process employing only benzene or compositions other than those of the present invention for the auxiliary solvent, is apparently due to the favorable effect of the mixed solvent of this invention on the distribution ratios of the nonparaflinic and parafllnic components of the oil being treated in the extract and rafiinatephases. In other-words, the relative content of the preferentially soluble components in the selective solvent as compared with that in the raillnate phase is increased in the presence 01' the auxiliary polycyclic aromatics, so that when such a mixed solvent is. used it becomes possible, under suitable temperature conditions, to produce a greater quantity of raflinate from a given quantityaf oil, and this rafiinate often will be richer in parafiin'ic components than it would have been possible to obtain if the extraction were conducted in the absence of these polycyclic aromatics.
Since the addition of these auxiliary solvents selectivity will be restored, thereby increasing the v yield of the raflinate and further increasing the eiiiciency. In general, the extraction temperature is so selected as to create optimum conditions from the viewpoints of economy of operation, yield, purity of product, conservation of solvents, etc.
The manipulative details of practicing the invention may vary widely to suit local conditions and specific properties of the substances used in each case. For example, in a so-called batch extraction system the auxiliary solvent may be mixed with the hydrocarbon mixture undergoing treatment either before or at the time the hydrocarbon mixture is contacted with the main solvent; or the whole or a part of the auxiliary solvent may be mixed with the main solvent prior to contacting it with the hydrocarbon mixture.
However, in its preferred form, the process is carried out by conducting the mixed solvent, 1. e. a selective solvent containing polycyclic aromatics, countercurrently to and in contact with the hydrocarbon mixture being treated.
It has heretofore been proposed to dilute certain lubricating oils with low boiling hydrocarbons and/or low boiling hydrocarbon raflinates or extractives prior to treatment with sulfur dioxide for the purpose of reducing the viscosity of the oil and of obtaining a more facile separation of the extract and ramnate layers. The dilution of the phases was the only effect previously expected from the use of light diluents. For that reason the diluents selected for this purpose were either entirely free of bicyclic aromatic hydrocarbons, such as low boiling distillates of gasoline type, .or contained bicyclic aromatic hydrocarbons, likeunextractedkerosene distillates or ordinary Edeleanu kerodevices seneextracts or raifinates.
It was recognized that, when such diluents are used for reducing the viscosity of an extraction mixture, particularly in so called batch processes, it is immaterial whether the diluent is added either to the oil or the solvent, or to the mixture of the two.
However, in the present method of extraction, where the solvent diluent is used to cause a more advantageous separation of parafiinic and nonparafiinic oil components in the 'raflinate and extract phases, it is preferable to employ counter-'- current method of extraction, in which case introducing a diluent of this invention into an extraction zone together with the solvent, or, in general, near the point where the raifinate phase is withdrawn from the extraction zone, becomes essential.
In practicing this invention, the main solvent usually together with the auxiliary solvent, or diluent, is caused to pass countercurrently toand in contact with the hydrocarbon mixture being extracted through a mixingsettling or extraction zone, which may consist of a contact column or a series of alternate mixing and phase-separating The resulting extract and raflinate phases are separated, usually by gravity, or centrifugin'g, and withdrawn at the opposite ends of the zone; the main and auxiliary solvents are then removed from each of the phases, either together or in separate stages, by any suitable means, as by distillation, absorption, etc. The recovered solventsmay be reused repeatedly. The
auxiliary solvent or a portion thereof may be left only ineffective amounts of teristicsf gravity 18.l A. P. 1..
return the residual portion of the withdrawn phase to the extraction zone near the point where the said phase was withdrawn. By repeating this operation at successive points of the extraction zone, the effect of having a progressively decreasing concentration of the auxiliary solvent in the direction of flow of the extract phase can be obtained, which often may further improve the extraction efliciency of our process.
While it is practical and may be desirable in some cases to carry out the extraction of mineral oils by means of the main and auxiliary solvents at such temperatures, at which the auxiliary solvent is only partially soluble in either the main solvent or the oil being extracted, or inboth, it should be noted that the extraction process of this invention is usually operated at the temperatures at which the auxiliary solvent becomes miscible in all proportions with either the main (selective) solvent, or theoil, or both.
The process of this invention is effective not only with oils which may be viscous at extraction temperatures, but-also with hydrocarbon mixtures which are easy flowing or non-viscous at such temperatures, e. g. gasolines. In many cases, the oils which may be regarded as being viscous at ordinary temperatures (say, over 80 seconds at 100 FjSaybolt Universal) would become easy flowing at the slightly elevated temperatures of extraction with furfural, for example, 0r phenol, or some other selective solvent, so that their dilution for the purpose of reducing their viscosity would be unnecessary. The use of auxiliary solvent, or diluents, in these cases would serve only the purpose of improving the extraction efliciency through the effect of such diluents on the distribution of the components being extracted between the extract and rafdnate phases, no dilution Example I A Coalinga bulk distillate was extracted with 200% S0: and a primary raflinate obtained, having a gravity of 23 AP. 1., and a viscosity of 457 seconds S. U. at 100 F. Three samples of this primary Edeleanu raflinate were refined separately with liquid- S02, using as the auxiliary solvent: benzol for the first sample, a concentrated bicyclic extract of the following characboiling range 198-275" C., and containing 47% by wt. bicyclie aromatics, :for the second sample, and a mixture of 31% benzol, 42% diphenyl and 27% naphthalene for the third sample. The refining treatment consisted of (1) Two extractions with 200% of a mixture of 75 parts of S02 and 25 parts of the auxiliary solvent: (2) one extraction with 100% of mixture of 65 parts of S02 and 35 parts of the auxiliary solvent; the percentages express quantities of mixed solvents based on the primary Edeleanu rafiinate. The treating temperature was between 45 and F. These finished railinates obtained in each treatment were then fractionated, and the viscosity index for each cut determined. From these cuts an oil was blended to meet S. A. E. 40 viscosity speci- These results indicate that the substitution of concentrated bicyclic extract for benzol produces material increase in the yield when the quality is unaltered. If'the extraction with concentrated kerosene extract as a diluent were carried out under conditions to produce a lower yield, the quality of the product would be materially increased.
When using the benzol-naphthalene-diphenyl mixture as a diluent, such an improvement in the quality was achieved.
Example I! A COalinga bulk distillate was treated twice with 200% S02. Five samples of the resulting primary raflinate were separately treated, each being successively subjected to the same steps, but using different auxiliary solvents in each instance, these solvents being, respectively, ((1) benzene; (b) concentrated extract used in Example I; (c) a methyl naphthalene; (d) a mixture containing 71% benzol and 29% naphthalene; (e) a mixture containing 31% benzol, 42% diphenyl, and 27% naphthalene. The treatment steps were (1) two extractions were 200% of a mixture of 75 parts of S02 and 25 parts of auxiliary solvent; (2) one extraction with 100% of a mixture of 67 parts of S02 and 33 parts of the auxiliary solvent.
The resulting raffinate obtained in each treatmcnt was fractionated, and the viscosity index forqeach cut determined. The viscosity indices were plotted, and are shown in the drawing. The comparable yields of S. A. E. 40 blends based on distillate for each of the auxiliary solvents were as follows:
These data demonstrate that the degree of refinement and/or the yield are substantially improved by-the use of the auxiliary solvents which contain bicyclic aromatics. viscosity indices of the valuable cuts above 60 In every C859 the.
seconds, S. U. at 210 F. have been improved by the substitution of the diluents containing polycyclic aromatics for benzol, and the yields were improved in every case, except when the benzol-naphthalene mixture was used, which, however, resulted in an unusually high V. 1. product.
The general method of refining mineral oils as illustrated by the above examples was found very useful in many cases. In general, it consists of subjecting an oil to extraction with a selective solvent to remove the most soluble oil components, and then refining the resulting raffinate, or the raflinate phase (oil plus solvent),
by extracting it with thesame or different sol vents in the presence of a polycyclic aromatic diluent, as described.
While we have illustrated our invention by using certain specific auxiliary solvents, our invention is not limited thereto. bon mixture, a substantial portion of which consists of polycyclic aromatic hydrocarbons, can be used as auxiliary solvent.
The amounts of the auxiliary solvent necessary to improve the extraction efliciency will vary with the nature of the oil being extracted, the main solvent used, etc., and no general figure can be stated, although it was found from experience that the ratio of the selective solvent to the diluent usually should be between one and four. By the term effective quantity, as used.
in the claims, we mean such a quantity of polycyclic aromatic hydrocarbons as will substantially improve the extraction characteristics for the particular conditions encountered, it being understood that this quantity may-be determined readily by one skilled in the art. More specifically, when such polycyclics are used alone or in mixtures with diluents other than and less effective than benzol this term may designate such concentrations of polycyclics in the extraction mixtures which improve the efliciency of extraction beyond that attainable with benzol.
We claim as our invention:
1. In an extraction process for separating liquid hydrocarbon mixtures into their component groups, the steps of extracting the mixture with Any hydrocara selective solvent in the presence of an effective quantity of a polycyclic aromatic hydrocarbon diluent to produce two liquid phases, and subsequently separating said liquid phases.
2. The process of claim 1, wherein the polycyclic aromatic hydrocarbons are selected from the group: naphthalene, alkyl' naphthalenes, diphenyl, alkyl diphenyls, diphenyl alkanes, anthracene, alkyl anthracenes, phenanthrene, alkyl phenanthrene, triphenyl benzene, triphenyl alkanes, indene, alkyl indenes, and partially hydrogenated homologues of said compounds.
3. In an extraction process for separating liquid hydrocarbon mixtures into their component groups, the steps of extracting the mixture with a selective solvent in the presence of an efi'ective quantity of a bicyclic aromatic hydrocarbon diluent to produce two liquid phases, and subsequently separating said liquid phases.
4. The process of claim 3, wherein the diluent is a mixture selected from the group consisting of a mixture of benzol, diphenyl and naphthalene, a mixture of benzol and naphthalene, a mixture of benzol and a methyl naphthalene.
5. In an extraction process for separating liquid hydrocarbon mixtures into their component groups, the steps of extracting the mixture with a selective solvent in the presence of an arcmatic hydrocarbon diluent having a gravity between 8.0 A. P. I. and 24.0" A. P. I. and boiling between about 180 C. and 300 C. to produce two liquid phases, and subsequently separating said liquid phases.
6. A process for extracting a liquid hydrocar bon mixture containing aromatic constituents comprising flowing said mixture countercurrent- 1y to and in contact with a stream of a selective solvent containing an effective quantity of polycyclic aromatic hydrocarbons to produce two liquid phases, and subsequently separating said liquid phases.
7. A process for refining petroleum lubricating oil comprising extracting the oil with a' solvent selected from the group: liquid sulfur dioxide, dichlorethylether, acetone, nitromethane, nitrobenzene, propionitrile, dimethyl sulphate, dimethyl sulphite, methyl formate, phenols, aromatic and aliphatic amines, nitriles and thionitriles, pyridine, qui'nolines, picolines, lutidines,
and petroleum nitrogen bases, in the presence of an aromatic diluent containing an efiective quan tity of polycyclic aromatic hydrocarbons to produce two liquid phases, and subsequently separating said liquid phases.
8. A process for refining petroleum lubricating oil comprising extracting-the Joilf'at'least once with a selective solventto{produce almanac containing smaller amounts of aromatics, and then further reducing the aromatic content of said rafiinate by extracting said raflinatewith a selective solvent plus an aromatic diluent containing an effective quantity of polycyclic aromatic hydrocarbons to produce two liquid phases, and subsequently separating said liquid phases.
9. A process for refining hydrocarbon mixtures comprising extracting said mixture with a'selective solvent in the presence of an aromatic diluent containing an efiective quantity of polycyclic aromatic hydrocarbons, said diluent being present in such amounts that the ratio of the main solvent to the diluent is between one and four to produce two liquid phases, and subsequently separating said liquid phases.
'10. The process according to claim 9,in which the aromatic diluent is the aromatic portion of' a mineral oil distillate having a gravity between 8.0" A. P. 1. and 24.0 A. P. I. and boiling between about 180 C. and 300 C. t q
' 11. The process according to claim 9 in which the polycyclic hydrocarbons are selected from the groups naphthalene, alkyl naphthalenes, di-
phenyl, alkyl diphenyls diphen'yl alkanes, anthracene, alkyl anthracene, phenanthrene, alkyl phenanthrene, triphenylbenzene, triphenyl al-- kanes, indene and alkyl indenes, and partially hydrogenated homologues of said compounds.
12. A process for refining a hydrocarbonmix- I ture containing aromatic'constituents comprising extracting said mixture at least once with a selective solvent to produce a primary liquid raflinate containing smaller amounts of aromatics than the original mixture, and treating said primary raflinate at least once with a selective solvent containing an aromatic diluent containing an effective quantity oi polycyclicaromatics, the
ratio of the selective solvent to the aromatic diluent being between one and four, to produce a secondary rafiinate having a lower aromatic content than said first rafflnate.
13. The process according to claim 12, in which the aromatic diluent is the aromatic portion of a mineral oil distillate having a gravity between through the zone 8.0 A. P. I. and 24.0 A. P. I. and boiling between about 180 C. and 300 C.
14. In an extraction process for treating hydrocarbon mixtures the steps of counterflowing under extracting conditions a stream of the hydrocarbon mixture and concurrent streams of a selective solvent and a diluent containing an cf fective quantity of polycyclic aromatic hydrocarbons, thereby producing liquid extract and rathnate phases, and separating said two phases.
15. In an extraction process for treating laydrocarbon mixtures the steps of introducing at one point of an extraction zone the said mixture, introducing at another point of the zone a selective solvent containing an efiective quantity of polycyclic aromatic hydrocarbon, counterflowing the mixture and the solvent through the zone while in contact with each other,-,:thereby producing liquid extract and raflinatei'phases, and i 20 separating said two phases.
carrying out said extracting process in the presence of an effective amount of polycyclic aromatic. hydrocarbon.
17. In a process of extracting hydrocarbon mixtures by forming two liquid phases by means of a selective solvent diluted with benzol the steps of carrying out said,extracting process in thepresence of an eifective amount of polycyclic aromatic hydrocarbon.
18. In an extraction process drocarbon mixtures, the steps of introducing at one point of an extraction zone the saidxmixture, introducing at another point of the zone aselective solventcontaining benzol and an effective amount of polycyclic aromatic hydrocarbon, counterflowing the mixture and the, solvent while in contact with each other, thereby producing liquid extract and raflie nate phases, and separating said two phases.
19. In an extraction process for treating hyfor treating hyzone the said mixture, introducingEat la secondpoint of the zone a selective solvent; counterflowing the mixture and the solventthrough, the zone in contact 7 ing liquid extract and raflinate phases, withdrawing the raihnate phase at a point near said second extract phase at a point and withdrawing the third point of the zone, the
improvement which consists of introducing near said second'point. of
the zone a diluent containing an effective quantity of polycyclic aromatic hydrocarbons. I
20. In an extraction process for treating hydrocarbon mixtures, the steps of counterflowing in an extraction zone a stream of the hydrocarbon mixture and a stream of a selective solvent with each other, ther'eby-produm and a diluent containing an eflective'quantity of phase was' withdrawn, and separating the-extract and raflinate phases. v 1 j HANS FRIEDRICH LINDEKE. BERNARD SUTRO GREENSFEIDER.
. polycyclic aromatic hydrocarbons thereby proa raflinate phase withthe diluent fromthe with- I returning the residual]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US740286A US2053485A (en) | 1934-08-17 | 1934-08-17 | Process for refining mineral oil |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US740286A US2053485A (en) | 1934-08-17 | 1934-08-17 | Process for refining mineral oil |
Publications (1)
Publication Number | Publication Date |
---|---|
US2053485A true US2053485A (en) | 1936-09-08 |
Family
ID=24975852
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US740286A Expired - Lifetime US2053485A (en) | 1934-08-17 | 1934-08-17 | Process for refining mineral oil |
Country Status (1)
Country | Link |
---|---|
US (1) | US2053485A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2441827A (en) * | 1943-10-27 | 1948-05-18 | Union Oil Co | Extraction process |
US2793167A (en) * | 1954-09-20 | 1957-05-21 | Exxon Research Engineering Co | Solvent deasphalting of residual oils with wash oil to remove metal contaminants |
US2793168A (en) * | 1954-10-15 | 1957-05-21 | Exxon Research Engineering Co | Method for solvent deasphalting of residual oil |
US2853426A (en) * | 1955-03-10 | 1958-09-23 | Exxon Research Engineering Co | Solvent deasphalting of residual oils with wash oil to remove metal contaminants |
US2922760A (en) * | 1955-01-28 | 1960-01-26 | Exxon Research Engineering Co | Extraction of metals from heavy petroleum oils utilizing pyridine containing 10-40 percent water |
US2928788A (en) * | 1957-05-08 | 1960-03-15 | Sun Oil Co | Viscosity index and oxidation stability of lubricating oil |
US2935470A (en) * | 1955-03-11 | 1960-05-03 | Standard Oil Co | Extraction process for recovery of aromatic hydrocarbons utilizing pyridine-bf3 or picoline-bf3 as the solvent |
US4395324A (en) * | 1981-11-02 | 1983-07-26 | Mobil Oil Corporation | Thermal cracking with hydrogen donor diluent |
-
1934
- 1934-08-17 US US740286A patent/US2053485A/en not_active Expired - Lifetime
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2441827A (en) * | 1943-10-27 | 1948-05-18 | Union Oil Co | Extraction process |
US2793167A (en) * | 1954-09-20 | 1957-05-21 | Exxon Research Engineering Co | Solvent deasphalting of residual oils with wash oil to remove metal contaminants |
US2793168A (en) * | 1954-10-15 | 1957-05-21 | Exxon Research Engineering Co | Method for solvent deasphalting of residual oil |
US2922760A (en) * | 1955-01-28 | 1960-01-26 | Exxon Research Engineering Co | Extraction of metals from heavy petroleum oils utilizing pyridine containing 10-40 percent water |
US2853426A (en) * | 1955-03-10 | 1958-09-23 | Exxon Research Engineering Co | Solvent deasphalting of residual oils with wash oil to remove metal contaminants |
US2935470A (en) * | 1955-03-11 | 1960-05-03 | Standard Oil Co | Extraction process for recovery of aromatic hydrocarbons utilizing pyridine-bf3 or picoline-bf3 as the solvent |
US2928788A (en) * | 1957-05-08 | 1960-03-15 | Sun Oil Co | Viscosity index and oxidation stability of lubricating oil |
US4395324A (en) * | 1981-11-02 | 1983-07-26 | Mobil Oil Corporation | Thermal cracking with hydrogen donor diluent |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2114524A (en) | Extraction process | |
US2188013A (en) | Method of separating high molecular mixtures | |
US2053485A (en) | Process for refining mineral oil | |
US2035102A (en) | Treating residual oils with a selective solvent | |
US2257086A (en) | Treating hydrocarbon fluids | |
US2023375A (en) | Process of manufacturing refined products from mineral oils | |
US2087455A (en) | Recovering aromatic constituents from mineral oil | |
US2582197A (en) | Solvent extraction process | |
USRE19763E (en) | Process for separation of | |
US2109476A (en) | Hydrocarbon oil treatment | |
US2440258A (en) | Refining of petroleum distillates | |
US2086484A (en) | Solvent refining oil | |
US2115960A (en) | Method of treating mineral oils | |
US1998399A (en) | Solvent refining of hydrocarbon oil | |
US2160607A (en) | Extraction process | |
US1988793A (en) | Process for the production of lubricating oil | |
US2054050A (en) | Solvent refining oil | |
US2111968A (en) | Hydrocarbon oil treatment | |
US1885524A (en) | Process for treating hydrocarbon oils | |
US2342362A (en) | Solvent refining of lubricating oils | |
US2228507A (en) | Solvent refining of hydrocarbon oil | |
US2124606A (en) | Process for refining mineral oil | |
US2026729A (en) | Process for production of lubricating oil | |
US1908646A (en) | Treatment of mineral oils with liquid sulphur dioxide | |
US3017346A (en) | Solvent extraction process using dimethyl hydrogen phosphite |