US2281369A - Treatment of gasolines - Google Patents
Treatment of gasolines Download PDFInfo
- Publication number
- US2281369A US2281369A US205368A US20536838A US2281369A US 2281369 A US2281369 A US 2281369A US 205368 A US205368 A US 205368A US 20536838 A US20536838 A US 20536838A US 2281369 A US2281369 A US 2281369A
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- US
- United States
- Prior art keywords
- gasoline
- valve
- line
- products
- cracked
- 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
- 238000011282 treatment Methods 0.000 title description 7
- 239000003502 gasoline Substances 0.000 description 21
- 239000000047 product Substances 0.000 description 17
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 230000000379 polymerizing effect Effects 0.000 description 10
- 150000001336 alkenes Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 6
- 238000002407 reforming Methods 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 235000015076 Shorea robusta Nutrition 0.000 description 1
- 244000166071 Shorea robusta Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- -1 carbon atom hydrocarbons Chemical class 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 229910000286 fullers earth Inorganic materials 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000005374 primary esters Chemical class 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000007420 reactivation Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 230000008016 vaporization Effects 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
- C10G59/00—Treatment of naphtha by two or more reforming processes only or by at least one reforming process and at least one process which does not substantially change the boiling range of the naphtha
- C10G59/02—Treatment of naphtha by two or more reforming processes only or by at least one reforming process and at least one process which does not substantially change the boiling range of the naphtha plural serial stages only
Definitions
- the present invention comprises a process'for improving the quality of primary cracked gasolines and particularly unstabilized cracked gasolines containing material percentages of readily polymerized olefins which consists in separating said gasoline by fractionation into a light and a heavy fraction, the light fraction being subjected to controlled contact with phosphoric acid-containing catalyst and the heavy fraction being reformed by pyrolysis.
- the products of these two separate treatments are blended'to form the final product of the process.
- the drawing shows a very simple arrangement of treaters in series although any number may be employed either in series or parallel connection.
- the vapors pass downwardly through treater l8 which contains a bed or a number of separate beds of granular material and thence through line I4 containing control valve l5 through a second treater I6 which represents the last in any series which may be employed.
- the temperature employed will vary somewhat with the relative amounts of gaseous olefins and vapors of gasoline respectively but in general they may be varied from 350-550 F. under pressures of approximately 100 to 500 lbs. per square inch.
- the vapors from separator 38 flow through line 42 containing valve 43 and enter a final fractionator 44 which is so operated that the overhead vapors contain all components of gasoline boiling range and the total fixed gases, these overhead products following a line 45 containing a valve 48 to a condenser 41, cooled and partly condensed products flowing through run-down line 48 containing a valve'49 to receiver 50 which again has a gas vent line 5
- fractionator 44 comprising the intermediate products from the reforming step heavier than gasoline but essentially nonknocking in character pass through line 55 containing valve 66 to a recycling pump 51 and are returned by way of line 58 containing valve 59 at the inlet of heating element 52 to undergo further conversion with the primary charge.
- the gasoline treated was produced by the cracking of a mixed Mid-Continent-West Texas residuum.
- This gasoline had a color of approximately 4 on the Saybolt colorimeter, a gum content of mg./ cc. by the copper dish method, and an octane number of 68 before stabilization.
- the heavier 50% was reformed at a temperature of 975 F. and a pressure of 500 lbs. per square inch with a loss of approximately 15% in heavy bottoms and fixed gases.
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- 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)
Description
Ap 8. 19 2 J. c. MoR ELL 2,281,369
TREATMENT OF GASOLINE Filed April 50, 1938 TBEATER FRACTIONATOR TREATER COOLER RECEIVER FURNACE FRACTIONATOR FURNACE INVENTOR JACQUEVC. MORRELL atented Apr. 28, 1942 TREATMENT or oasotnvas .lac ue C. Morrell, Chicago, EL, asslor-to Universal 01! Products Company, Chicago, ill a corporation of Delaware Application April 30, 1938, Serial No. 205,36
(Cl. MiG-=50) 2 Claims.
This invention relates more particularly to the treatment of gasolines produced by cracking the relatively heavy portions of petroleum oils or similar products produced by thermally decomposing' primary tars produced by the distillation of solid hydrocarbonaceous materials such as coal, and shales. It is specifically directed to improving the properties of cracked gasolines with respect to color, gum content, and antiknock value. Substantially all cracked gasolines are characterized by improved antiknock value over their straight run counter parts, but they contain undesirably high amounts of colored compounds and potential gum forming materials, the last named class being generally of the character of conjugated di-oleflns which become readily polymerized into high molecular weight resins and gummy products through the agency of accidental oxygen and catalytic con tacts.
It is recognized that many processes are in practical operation which eliminate to a greater or lesser extent the undesirable properties of cracked gasoline, the oldest of which is sulfuric acid treatment, and some of the more recent of which are characterized by the use of adsorbent material such as fullers earth which may contain in addition special chemical treating reagents or catalytic materials which tend to selectively remove gum-forming compounds as polymers which are retained mechanically. The present process is a contribution to the art of eliminating the undesirable properties ofgasoline while improving and stabilizing the more desirable properties.
In one specific embodiment the present invention comprises a process'for improving the quality of primary cracked gasolines and particularly unstabilized cracked gasolines containing material percentages of readily polymerized olefins which consists in separating said gasoline by fractionation into a light and a heavy fraction, the light fraction being subjected to controlled contact with phosphoric acid-containing catalyst and the heavy fraction being reformed by pyrolysis. The products of these two separate treatments are blended'to form the final product of the process.
In order to indicate the combination of cooperative steps which characterize the present process, a description of a characteristic process flow will be given in connection with the attached drawing which shows by the use of conventional figures in general side elevation an arrangement of interconnected units which may be employed. I
Referring to the drawing, a primary cracked naphtha of approximate gasoline-boiling range may be introduced through a line i containing a valve 2 to a charging pump 3 which discharges through a line i containing a valve 5 into and through a heating element t arranged to be heated by a furnace i. The function of this primary heating and vaporizing coil 6 is to raise the charge to the temperature necessary for separating it by fractionation into a light and heavy fraction, the heated products passing through line 8 containing a valve 9 into a primary fractionator ill. The exact point of division of difierent cracked gasolines will depend upon a variety of factors such as the amount and character of its oleiins, its boiling range, the stock from which it was produced by cracking, and various other factors. In some cases only a 25% fraction may be taken overhead for the succeeding catalytic polymerizing treatment while in other cases as high as may be thus treated. Those skilled in the refining of petroleum will appreciate the fact that only approximate rules can be given in such processes as the one at present under discussion.
The overhead vapors comprising the lighter portion of the cracked gasoline charged and the dissolved normally gaseous constituents which will ordinarily includeprincipally 3 and 4 carbon atom hydrocarbons both saturated and unsaturated pass through vapor line H containing valve It to a system of treaters containing granular material whose active constituent is an acid of phosphorus. These materials are generally known as solid phosphoric acid catalysts and are made by the general steps of incorporating a major amount of a phosphoric acid with a due principally, however, to the tendency to formpolymers from the primary esters formed by the a combination of olefins with phosphoric acid.
According to the present invention it has been determined that not only the color and gum forming properties of the lighter portions of cracked naphthas improved by the solid phosphoric acid treatment but the normally gaseous oleflns are concurrently polymerized to form additional yields of gasoline boiling range compounds having a high antiknock value so that in eflect the treatment of the light ends of the gasoline and the polymerization of the normally gaseous oleflns is effected concurrently.
The drawing shows a very simple arrangement of treaters in series although any number may be employed either in series or parallel connection. The vapors pass downwardly through treater l8 which contains a bed or a number of separate beds of granular material and thence through line I4 containing control valve l5 through a second treater I6 which represents the last in any series which may be employed. The temperature employed will vary somewhat with the relative amounts of gaseous olefins and vapors of gasoline respectively but in general they may be varied from 350-550 F. under pressures of approximately 100 to 500 lbs. per square inch. In the case of highly oleflnic mixtures there will be a tendency for a temperature rise in the first units of a series of treaters owing to the exothermic character of polymerizing and treating reactions so that it is usually best to start with a relatively low temperature and allow for the rise although cooling of the treaters or intermediate cooling between treaters may be employed.
The total products from the polymerizing and treating units pass through line H containing a valve l8, through a cooler i9 and thence through a run-down line containing a valve 2| to a receiver 22 with a conventional gas release line 23 containing. a valve 24 and a liquid draw line 25 containing valve 26. The material in receiver 22 is later blended with the cracked products separately produced by thestep to be presently described.
The treating materials may be employed in any way which effects the best overall results in the process. They will gradually become carbonized and require reactivation which may be brought about by the careful use of low oxygen content combustion gas mixtures to oxidize and remove the carbonaceous deposits at temperatures below those which have been found to be capable of causing permanent impairment of the treating reagent properties. After oxidation, steam contact may be utilized for rehydration to an optimum activity as in the case of the catalyst preparation.
The heavier fractions of the gasoline appearing as a bottoms from fractionator I0 pass through line 21 containing a valve 28 to a pump 29 which discharges through line 30 containing a valve 3| to a reforming unit which comprises a heating element 32 arranged to receive heat from a furnace 83 as its first unit. Pressures and temperatures used in reforming the heavier portions of cracked gasolines to further improve their antiknock value are relatively high, of the order. of 925-1050 F. and relatively high pressures are also employed within the safe capacity of the apparatus. The heated and partially cracked heavy fractions pass through line 34 containing valve 35 to a reaction chamber 38 which is of suitable design and capacity for permitting time for completion of the desired conversion reactions, the total cracked products following line 31 containing valve 38 to a separating chamber for further processing on account of their coke forming tendencies, these products being withdrawn through line 40 containing valve 4| to any suitable use such as fuel or a charge to a coking plant. a
The vapors from separator 38 flow through line 42 containing valve 43 and enter a final fractionator 44 which is so operated that the overhead vapors contain all components of gasoline boiling range and the total fixed gases, these overhead products following a line 45 containing a valve 48 to a condenser 41, cooled and partly condensed products flowing through run-down line 48 containing a valve'49 to receiver 50 which again has a gas vent line 5| containing a valve 52 and a liquid draw line 63 containing a valve 54. The gas mixture withdrawn from this receiver may be returned in its entirety by means of line 5| provided with valves 52' and 53' and pump 54', to the primary polymerizing and treating step to utilize its oleflnic content for the production of further yields of, good antiknock gasoline or it may be subjected to fractionation and the three and four carbon atom fraction returned. The liquid products are preferably blended with the polymerized and treated lighter fraction to form the final product of the process.
The bottoms from fractionator 44 comprising the intermediate products from the reforming step heavier than gasoline but essentially nonknocking in character pass through line 55 containing valve 66 to a recycling pump 51 and are returned by way of line 58 containing valve 59 at the inlet of heating element 52 to undergo further conversion with the primary charge.
The following example of operation is given to indicate the type of results to be expected from the practical application of the present process although its scope is not intended to be thereby precisely limited.
The gasoline treated was produced by the cracking of a mixed Mid-Continent-West Texas residuum. This gasoline had a color of approximately 4 on the Saybolt colorimeter, a gum content of mg./ cc. by the copper dish method, and an octane number of 68 before stabilization.
The gasoline was fractionated into approximately equal portions and the lighter vaporized products were passed through a series of three treaters containing solid phosphoric acid catalyst at an average temperature of 400 F. under a pressure of 250 lbs. per square inch.
The heavier 50% was reformed at a temperature of 975 F. and a pressure of 500 lbs. per square inch with a loss of approximately 15% in heavy bottoms and fixed gases.
The final products obtained by blending the stocks produced by the combined polymerizing and treating and the reforming operations respectively equalled 92% of the original gasoline and had an octane number of .73. It was found that the gum content was approximately 40 mgs. which was readily reduced to 5 mgs. by the addition of 0.01% of commercial inhibitor. The color of the final blended product was 25 on the Saybolt scale.
I claim as my invention:
1. A process which comprises separating cracked gasoline into a light fraction and a with a polymerizing agent under polymerizing conditions to produce gasoline boiling hydro= carbons from the gaseous oleiins and to free said light gasoline fraction of objectionable gum= head product containing the gaseous olefins and a substantial portion of the normally liquid fractions of the gasoline, contacting the overhead product with a polymerizing agent under poly merizing conditions to convert normally gaseous olefins contained therein into normally liquid hydrocarbons and to free said liquid fractions of the gasoline of objectionable gum-forming olefins, subjecting the bottom product of approximately gasoline end point to reforming conditions of temperature and pressure for enhancement of its anti-knock value under conditions such that a portion thereof is decomposed into normally gaseous olefins, and supplying normally gaseous olefins produced in the reforming step to the aforesaidv polymerizing step.
moon's CQMORRELL,
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US205368A US2281369A (en) | 1938-04-30 | 1938-04-30 | Treatment of gasolines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US205368A US2281369A (en) | 1938-04-30 | 1938-04-30 | Treatment of gasolines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2281369A true US2281369A (en) | 1942-04-28 |
Family
ID=22761915
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US205368A Expired - Lifetime US2281369A (en) | 1938-04-30 | 1938-04-30 | Treatment of gasolines |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2281369A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2748061A (en) * | 1951-08-18 | 1956-05-29 | Shell Dev | Thermal treatment and separation process |
-
1938
- 1938-04-30 US US205368A patent/US2281369A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2748061A (en) * | 1951-08-18 | 1956-05-29 | Shell Dev | Thermal treatment and separation process |
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