US2035610A - Process of purifying and refining hydrocarbon oils with aluminum salts - Google Patents
Process of purifying and refining hydrocarbon oils with aluminum salts Download PDFInfo
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- US2035610A US2035610A US637424A US63742432A US2035610A US 2035610 A US2035610 A US 2035610A US 637424 A US637424 A US 637424A US 63742432 A US63742432 A US 63742432A US 2035610 A US2035610 A US 2035610A
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- 238000000034 method Methods 0.000 title description 29
- 239000003921 oil Substances 0.000 title description 19
- 229930195733 hydrocarbon Natural products 0.000 title description 15
- 150000002430 hydrocarbons Chemical class 0.000 title description 15
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 title description 13
- 239000004215 Carbon black (E152) Substances 0.000 title description 9
- 238000007670 refining Methods 0.000 title description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 67
- 150000003839 salts Chemical class 0.000 description 49
- 239000000243 solution Substances 0.000 description 44
- 239000000047 product Substances 0.000 description 32
- 239000003208 petroleum Substances 0.000 description 27
- 238000006243 chemical reaction Methods 0.000 description 26
- 230000008016 vaporization Effects 0.000 description 26
- 238000004821 distillation Methods 0.000 description 24
- 239000000203 mixture Substances 0.000 description 20
- 238000010438 heat treatment Methods 0.000 description 19
- 238000011282 treatment Methods 0.000 description 18
- 238000009834 vaporization Methods 0.000 description 18
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 238000009835 boiling Methods 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 10
- 235000011149 sulphuric acid Nutrition 0.000 description 10
- 239000001117 sulphuric acid Substances 0.000 description 10
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 230000003578 releasing effect Effects 0.000 description 8
- 238000009833 condensation Methods 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- 238000005336 cracking Methods 0.000 description 6
- 238000005194 fractionation Methods 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-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
- 238000000354 decomposition reaction Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- VNDYJBBGRKZCSX-UHFFFAOYSA-L zinc bromide Chemical compound Br[Zn]Br VNDYJBBGRKZCSX-UHFFFAOYSA-L 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 description 4
- 239000005864 Sulphur Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000010924 continuous production Methods 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical group S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- SAXCKUIOAKKRAS-UHFFFAOYSA-N cobalt;hydrate Chemical compound O.[Co] SAXCKUIOAKKRAS-UHFFFAOYSA-N 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229940102001 zinc bromide Drugs 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- -1 cadmercury Chemical compound 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000012809 cooling fluid Substances 0.000 description 1
- 125000002534 ethynyl group Chemical class [H]C#C* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011874 heated mixture Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 239000012476 oxidizable substance Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000005406 washing Methods 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
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/06—Metal salts, or metal salts deposited on a carrier
Definitions
- This invention relates to an improved process of purifying and refining hydrocarbon oils obtained by distillation or cracking of mineral oils such as lubricating oil stocks, lamp oil distill'ates, gasoline or naphtha stocks, or distillates derived from shale oil, and more specifically refers to the treatment of gasoline or naphtha stock produced by cracking crude petroleum oils or distillates derived from relatively high sulphur bearing mineral oils, in which hydrogen sulphide, mercaptans and other sulphur bearing compounds, as well as varying percentages of oxygenated hydrocarbons and unstable hydrocarbons (such as diolefines and acetylenes) may be present or formed during said distillation or cracking operation.
- mineral oils such as lubricating oil stocks, lamp oil distill'ates, gasoline or naphtha stocks, or distillates derived from shale oil
- Crude gasoline stocks obtained by distillation or cracking petroleum oils consist of a mi ture of saturated and unsaturated hydrocarbons, together with sulphur compounds, nitrogen bases and other substances of an undefined nature. These latter substances are readily oxidizable at ordinary temperature and are usually responsible for the change of color which takes place when refined gasoline is stored. These oxidizable substances are removed with dimculty when gasoline stocks are treated by the methods 51 known in the art.
- crude gasoline stocks obtained by distillation of crude petroleum oil, or by cracking a higher boiling petroleum oil are customarily treated with approximately from 1 per cent to as high as 8 per cent or higher by weight, sulphuric acid, the quantity of sulphuric acid depending upon the nature of the gasoline stock to be treated and the degree of refinement desired.
- This acid treatment usually consists in commingling the gasoline stock with the required amount of sulphuric acid necessary to obtain the desired extraction, either by the well-known batch or continuous treatment, after which the prodnets of the acid reaction are permitted to settle and are then withdrawn from the treated gasoline stock.
- the acid treated gasoline stock is then neutralized by washing with a water solution of an alkali and finally with water.
- This treatment removes most of the impurities, but subsequent treatments are usually necessary to deodorize and remove or convert corrosive sulphur compounds into noncorrosive bodies.
- a water solution of sodium plumbite or sodium hypochlorite is usually employed to render the gasoline stock sweet to the doctor test.
- chlorinated hydrocarbons may be formed to a small extent, which may be converted into corrosive compounds during a subsequent distillation.
- sulphuric acid normally used to treat crude gasoline stocks may be reduced to a great extent, and in many cases may be entirely eliminated by the employment of a water solution of certain metallic salts, or mixtures of the same, which may be zinc, copper, cadmium, mercury, iron, chromium, manganese, aluminum, nickel, or cobalt
- Water soluble salts such as the chloride, bromide, iodide, sulphate, sulphite, nitrate, nitrite, and also any of the water soluble salts of the above named metals of organic acids, such as the sulphonic acids of benzol, toluol and xylol, or the sulphonic acid salts derived from the treatment of petroleum oils with sulphuric acid.
- the process consists in'passing the hydrocarbon 011 product, such as gasoline stock, in a liquid phase, commingled with a substantially concentrated water solution of any of the above named salts or mixtures thereof, through a heating coil under a pressure sufficient to prevent any substantial vaporization therein, at temperatures of approximately 300 to 600 degrees F., and then immediately releasing the pressure and separating by distillation the purified hydrocarbon oil product from the water solution of the metallic salt or salts, the extracted impurities and products of polymerization or condensation; or, as shown in Figure II, the gasoline stock and water solution of metallic salt or salts may be first separately heated and then commingled under a pressure.
- hydrocarbon oil stock to be treated by my invention may or may not have had a preliminary treatment With sulphuric acid, or other agents to partly purify the same, or may be first partly purified by my invention and the purification completed by methods known in the art,
- One of the principal objects of this invention is to accomplish a purification of gasoline or naphtha stocks produced by thermo molecular decomposition of high boiling petroleum oils, by a treatment with a substantially concentrated water solution of a metal salt, under a pressure sufiicientto prevent any substantial vaporization thereof, and at a temperature of approximately 300 to 600 degrees F., followed by a distillation and fractionation operation to separate the products of reaction and higher boiling polymerized products from the purified gasoline or naphtha stocks.
- Another object of the invention is to provide a continuous, rapid and economical process for purifying gasoline stocks produced by the thermo decomposition of higher boiling petroleum oils, by treating the same, under superatmospheric pressure sufiicient to maintain a liquid phase, with a substantially concentrated water solution of a metallic salt, at temperatures of approximately 300 to 600 degrees F., to polymerize substantially all the unstable hydrocarbons contained therein, and at the same time remove oxygenated hydrocarbons and render the gasoline sweet to the doctor test.
- Another object of the invention is to provide a continuous, economical method for improving the color and removing gums and gum forming material from gasoline or naphtha stock, so that top to condenser coil 3
- a I I the same may be kept in storage for relatively long periods of time without changing color or quality by the formation of polymerized bodies.
- Figure I represents one form of an apparatus for carrying out the invention, in which the pe-' troleum oil product to be treated is first commingled with the water solution of a metallic salt and thereafter heated to a reaction temperature, by causing the same to pass through a heating coil under pressure.
- Figure II represents another form of apparatus in which the pertoleum oil product and the water solution of a metallic salt are separately heated to a reaction temperature, and are thereafter commingled by means of a jet mixer.
- FIG. 1 represents generally a tank for holding a supply of gasoline or other petroleum oil stock to be processed.
- Pipe I controlled by valve 2, connects the gasoline stock tank 3 .near
- Pipe 4 controlled by valve 5 connects gasoline stock tank 3' to the inlet side of pump 6.
- Pipe 40 controlled by valve 4
- Pipe 1 connects pump 6 to jet mixer 8.
- I3 represents generally a tank for holding a concentrated water solution of a metallic salt, such as zinc chloride, zinc bromide, zinc iodide, etc., or any of the other metal salts heretofore enumerated.
- Pipe l4 controlled by valve [5, connects tank I3 near the top to a source of supply not shown.
- Pipe ll controlled by valve l2, connects tank I3 near the bottom to the inlet side of pump l0.
- Pipe 9 connects the discharge side of pump 10 to jet mixer 8.
- Pipe l6 connects jet mixer 8 to heater coil 38. I1.
- Furnace I1 is provided with a burner l8 which leads to a supply of fuel not shown.
- Pipe 39 controlled by pressure release valve l9, connects heater coil 38 to distillation tower 29.
- Distillation tower 20 is provided with bubble trays 2 I.
- Pipe 22, controlled by valve 23, connects distillation tower 20 near the bottom to a source of water supply not shown.
- Pipe 25, controlled by valve 24, connects distillation tower 20 at the bottom to tank 25.
- Pipe 28, controlled by valve 27, connects tank 26 to a storage not shown.
- Pipe 29 connects distillation tower 20 at the Condenser coil 3
- Pipe 32 leads to a source of water supply not shown, and pipe 31 leads to a waste receiver not shown.
- Pipe 33 connects condenser coil 3
- Pipe 36 controlled by valve 35, connects the treated gasoline tank near the bottom to a storage not shown.
- 3 represents generally a tank for holding a supply of gasoline or other petroleum controlled by valve 4
- Pipe 1 connects pump 6 to heater coil 38.
- Heater coil 38 is stationed in a furnace I1.
- Furnace H is provided with a burner l8 which leads to a fuel supply not shown.
- [3 represents generally a tank for holding a concentrated water solution of a metallic salt, such as zinc chloride, zinc bromide, zinc iodide, etc., or any of the other metallic salts heretofore enumerated.
- Pipe [4, controlled by valve 15, connects tank [3 near the top to a source of supply not shown.
- Pipe ll, controlled by valve l2, connects tank l3 near the bottom to the inlet side of pump I0.
- Pipe 9 connects the discharge side of pump I!) to heater coil 44.
- Heater @1144 is stationed in furnace 42. Furnace 42 is provided with a burner 43 which leads to a fuel supply not shown.
- Pipe 45 connects heater coil 44 to jet mixer 8.
- Pipe 39 connects heater coil 38 to jet mixer 8.
- Pipe l6 connects jet mixer 8 to reaction chamber 46.
- Pipe 41 controlled by pressure release valve l9, connects reaction chamber 46 to distillation tower 20.
- Distillation tower 20 is provided with bubble trays 2
- Pipe 22, controlled by valve 23, connects distillation tower 20 to a source of water supply not shown.
- Pipe 25, controlled by valve 24, connects the bottom of distillation tower 29 to tank 26.
- Pipe 28, controlled by valve 21, connects tank 26 to a storage not shown.
- Pipe 29 connects distillation tower 20 at the top to condenser coil 3
- Condenser coil Si is situated in condenser box 30, which is provided with a water inlet pipe 32 and a water outlet pipe 31.
- Pipe 32 leads to a source of water supply not shown, and pipe 3'! leads to a waste receiver not shown.
- Pipe 33 connects condenser box 30 to treated gasoline tank 34.
- Pipe 36 controlled by valve 35, connects treated gasoline tank 34 near the bottom to a storage not shown.
- Tank 3 is filled with the petroleum oil product to be treated by operation of valve 2.
- Petroleum oil distillate, such as gasoline stock, contained in tank 3, is permitted to flow through pipe 4 and into the inlet side of pump 6, the rate of flow being governed by operation of valve 5.
- Pump 6 continuously discharges the gasoline stock, under a pressure of approximately 100 to 1,000 pounds gauge, into jet mixer 8, wherein the gasoline" stock is continuously commingled with the necessary quantity of a substantially concentrated water solution of a metallic salt such as aluminum chloride from the supply tank l3.
- the water solution of metallic salt contained in supply tank I 3 is permitted to flow through pipe H and into the inlet side of pump l0, which discharges the same under a pressure ranging from approximately 100 to 1000 pounds gauge through pipe 9 and into said jet mixer 8, the rate of fiow being governed by operation of valve l2.
- the quantity of water solution of metallic salt may range from as low as 1 per cent to as high as 10 per cent or higher, by volume, depending upon the stock to be treated. For example, if a crude gasoline stock contains a high percentage of impurities to be extracted, as high as 10 per cent by volume or more of a concentrated water solution of any of the aforesaid metallic salts or mixtures of the same may be employed.
- the presimingled mixture of the water solution of metallic salt or salts and gasoline stock under treat- -ment, passing through coil 38, will be maintained in a substantially liquid phase, such pressure depending upon the boiling point of the gasoline stock and the temperature employed.
- the gasoline stock, commingled with the water solution of the metallic salt or salts passes through heater coil 38, pipe 39 and pressure release valve l9, where the pressure is reduced to atmospheric or approximately atmospheric, and then passes into distillation tower 28.
- the commingled mixture passing through heater coil 38 is heated to the reaction temperature.
- a temperature ranging from approximately 300 to 400 degrees F. is suitable to employ in treating ordinary gasoline stocks.
- some grades of petroleum oil distillates as high as 600 degrees F. or a little higher may be employed.
- distillation tower 20 the purified gasoline stock, at a temperature ranging from approximately 300 to 400 degrees F., together with a portion of the water content of the salt solution, are
- the purified gasoline stock, mixed with water vapor, passes out of distillation tower 20, through pipe 29, into condenser coil 3i, stationed in condenser box 30, wherein the said purified gasoline stock and water vapor are condensed to a liquid, passing through pipe 33 and into the treated gasoline tank 34.
- a cooling fluid such as water is employed to condense the gasoline vapors passing through condenser coil 3
- the metallic salts and products of reaction which separate in the bottom of distillation tower 28 are intermittently or continuously drawn into tank 26 through pipe 25, the flow being controlled by valve 24, water being continuously or intermittently introduced into the lower section of distillation tower 20 through pipe 22, controlled by valve 23, in quantities sufiicient to replace the vaporized water from the metallic salt water solution, so as to maintain the used metallic salts or compounds and products of reaction in a fluid condition.
- valve is closed and valve 4! is opened, which permits the gasoline stock coming from a source not shown, in a vapor or semi-vapor state, to flow through pipe 48 and into the inlet side of pump 6, wherein the gasoline stock is completely condensed to a liquid by the applied pressure maintained on the system and the introduction of the cool water solution of a metallic salt or salts.
- a process of purifying a petroleum oil product which comprises, causing the said product to vaporize from a heatedicommingled mixture of the product and a maintained water solution of an aluminum salt at a reaction temperature.
- a process of purifying a petroleum oil product which comprises, heating and commingling said product with a Water solution of an aluminum salt, under pressure sufficient to prevent substantial vaporization, thereafter releasing the .pressure and causing the product to vaporize from the heated commingled mixture at a reaction temperature while maintaining the aluminum salt in solution by the addition of water.
- a process of purifying petroleum oil products comprising, commingling a petroleum oil product with a substantially concentrated water solution of an aluminum salt, passing the commingled mixture through a heating coil and heating the mixture to a reaction temperature, under pressure sufficient to prevent substantial vaporization, releasing the pressure and separating by vaporization, fractionation and condensation a purified petroleum oil product from products of reaction and excess treat-ing agent.
- a process of purifying petroleum oil comprising, commingling the petroleum oil with a substantially concentrated water solution of aluminum salt, passing the commingled mixture through a heating coil andheating the mixture to a temperature of approximately 300-600 F., under pressure sufficient to prevent substantial vaporization, releasing the pressure and separating by vaporization, fractionation and condensation a purified'petroleum oil product from products of reaction and excess treating agent.
- a continuous process for purifying gasoline stocks comprising, continuously commingling gasthe commingled mixture through a heating element and heating the mixture to a temperature of approximately, 300-600 F., under pressure sufii cient to prevent substantial vaporization, releas ing the pressure and. separating by vaporization, fractionation and condensation a purified gasoline stock from products of reaction and, excess treating agent.
- a process of removing gum forming constituents from cracked gasoline stock comprising, commingling cracked gasoline stock with a water solution of aluminum'salt, and heating the commingled mixture to a temperature of approximately 300-600 F., under a pressure sufiicient to prevent substantial vaporization, while passing through a heating zone, for a period of time sufficient to cause the unstable hydrocarbons contained in the cracked gasoline stock to polymerize with the formation of gums, then reducing the pressure to approximately atmospheric, and separating by vaporization, fractionation and condensation a purified gasoline stock from products of reaction and polymerization, and excess treating agent.
- a continuous process for purifying gasoline or naphtha derived by thermo decomposition of higher boiling petroleum oils comprising, continuously commingling the gasoline or naphtha with a. water solution of aluminum chloride, continuously passing the commingled mixture through a heating zone and heating the commingled gasoline or naphtha and water solution of aluminum chloride to a temperature of approximately 300-600 F., under a pressure sufiicient to prevent substantial vaporization, continuously releasing the pressure after the commingled mixture of gasoline or naphtha and water solution of aluminum chloride has passed through said heating zone, continuously passing the treated gasoline or naphtha, products of reaction and excess treating agent into a vaporizing zone, continuously vaporizing, fractionating and separating a purified gasoline or naphtha and water vapor from higher boiling reaction products and excess treating agent.
- a continuous process of purifying gasoline or naphtha derived by the thermo-molecular decomposition of higher boiling mineral oils comprising, continuously commingling the gasoline or naphtha with a water solution of aluminum salt, continuously passing the commingled mixture through-a heating zone and heating the commingled gasoline or naphtha and water solution of aluminumsalt to a temperature of approximately 300-600 F., under a pressure sufficient to prevent substantial vaporization, continuously releasing the pressure and continuously passing the heated mixture of gasoline or Y naphtha, water solution of aluminum salt and products of reaction into a vaporizing zone, continuously vaporizing and separating by fractionation and condensation a purified gasoline or naphtha mixed with water from higher boiling products of reaction and excess treating agent, continuously introducing water into the vaporizing zone in quantities sufiicient to replace the water of vaporization, continuously withdrawing products of reaction and introduced water containing excess treating agent, substantially as described.
- a process of purifying gasoline or naphtha comprising, contacting the gasoline or naphtha with a water solution of aluminum salt while passing through a heating zone, under a pressure suflicient to prevent substantial vaporization, and
Description
March 31, 1936. LAHMAN 2,035,619
PROCESS OF PURIFYING AND REFINING HYDROCARBON OILS wn'n ALUMINUM SALTS Original Filed July-26, 1929 2 Sheets-Sheet J,
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co/vos/vss/z 24 I F/ST/LLfiT/O/f ram/Ea ATTORN EY March 31, 1936. MA I 2,035,610
PROCESS OF PURIF'YING AND REFINING HYDRCCARBO N OILS WITH ALUMINUM SALTS Original Filed July 26, 1929 2 shets-sheet 2 EffiCT/O/V CHHMBER Patented Mar. 31, 1936 STATES ATENT FFlCE PROCESS OF PURIFYING AND REFINING HYDROCARBON OILS WITH ALUIVHNUM SALTS Arthur Lachman, Berkeley, Oalif., assignor to Vapor Treating Processes, Inc., Los Angeles, Calif., a corporation of California 10 Claims.
This invention relates to an improved process of purifying and refining hydrocarbon oils obtained by distillation or cracking of mineral oils such as lubricating oil stocks, lamp oil distill'ates, gasoline or naphtha stocks, or distillates derived from shale oil, and more specifically refers to the treatment of gasoline or naphtha stock produced by cracking crude petroleum oils or distillates derived from relatively high sulphur bearing mineral oils, in which hydrogen sulphide, mercaptans and other sulphur bearing compounds, as well as varying percentages of oxygenated hydrocarbons and unstable hydrocarbons (such as diolefines and acetylenes) may be present or formed during said distillation or cracking operation.
This application is a division of my application Serial Number 381,305, filed July 26, 1929, for Process of purifying and refining hydrocarbon oils.
Reference is made to United States Patent Number 1,899,170, granted June 9, 1931 to Arthur Lac'nman, Serial Number 361,513, filed May 8,.
29, for Process of refining hydrocarbon oils, which discloses a vapor phase method or process for purifying and refining mineral oil products with a water solution of certain metallic salts, or
"tires of he same, such as zinc, copper, cadmercury, iron, chromium, manganese, aluminum, nickel or cobalt water soluble salts which may be the chloride, bromide, iodide, sulphate, sulphite, nitrate and also any of the water soluble salts of the above named metals of organic acids, such as the sulphonic acids of henzol, toluol xylol, or the sulphonic acids derived from the treatment of petroleum oil with sulphuric acid.
For the purposes of simplifying the description of my invention, reference will be made mainly to gasoline stock. Crude gasoline stocks obtained by distillation or cracking petroleum oils consist of a mi ture of saturated and unsaturated hydrocarbons, together with sulphur compounds, nitrogen bases and other substances of an undefined nature. These latter substances are readily oxidizable at ordinary temperature and are usually responsible for the change of color which takes place when refined gasoline is stored. These oxidizable substances are removed with dimculty when gasoline stocks are treated by the methods 51 known in the art.
By well-known methods, crude gasoline stocks obtained by distillation of crude petroleum oil, or by cracking a higher boiling petroleum oil, are customarily treated with approximately from 1 per cent to as high as 8 per cent or higher by weight, sulphuric acid, the quantity of sulphuric acid depending upon the nature of the gasoline stock to be treated and the degree of refinement desired. This acid treatment usually consists in commingling the gasoline stock with the required amount of sulphuric acid necessary to obtain the desired extraction, either by the well-known batch or continuous treatment, after which the prodnets of the acid reaction are permitted to settle and are then withdrawn from the treated gasoline stock. The acid treated gasoline stock is then neutralized by washing with a water solution of an alkali and finally with water. This treatment removes most of the impurities, but subsequent treatments are usually necessary to deodorize and remove or convert corrosive sulphur compounds into noncorrosive bodies.
For this purpose, a water solution of sodium plumbite or sodium hypochlorite is usually employed to render the gasoline stock sweet to the doctor test. In these treatments, particularly where hypochlorite of soda is employed, chlorinated hydrocarbons may be formed to a small extent, which may be converted into corrosive compounds during a subsequent distillation.
The general objections to a treatment of this character are as follows: (1) Gasoline purified by this method frequently becomes discolored when stored for a period of time; (2) considerable quantities of sulphuric acid are required, which are difficult to recover; (3) as high as per cent of the valuable unstable hydrocarbons contained in the gasoline stock may be lost; and (4) the treatment must frequently be followed by a sweetening process, such as that heretofore described.
Now, I have discovered that the sulphuric acid normally used to treat crude gasoline stocks may be reduced to a great extent, and in many cases may be entirely eliminated by the employment of a water solution of certain metallic salts, or mixtures of the same, which may be zinc, copper, cadmium, mercury, iron, chromium, manganese, aluminum, nickel, or cobalt Water soluble salts such as the chloride, bromide, iodide, sulphate, sulphite, nitrate, nitrite, and also any of the water soluble salts of the above named metals of organic acids, such as the sulphonic acids of benzol, toluol and xylol, or the sulphonic acid salts derived from the treatment of petroleum oils with sulphuric acid.
The process, described briefly, consists in'passing the hydrocarbon 011 product, such as gasoline stock, in a liquid phase, commingled with a substantially concentrated water solution of any of the above named salts or mixtures thereof, through a heating coil under a pressure sufficient to prevent any substantial vaporization therein, at temperatures of approximately 300 to 600 degrees F., and then immediately releasing the pressure and separating by distillation the purified hydrocarbon oil product from the water solution of the metallic salt or salts, the extracted impurities and products of polymerization or condensation; or, as shown in Figure II, the gasoline stock and water solution of metallic salt or salts may be first separately heated and then commingled under a pressure.
The hydrocarbon oil stock to be treated by my invention may or may not have had a preliminary treatment With sulphuric acid, or other agents to partly purify the same, or may be first partly purified by my invention and the purification completed by methods known in the art,
suchas treatment with caustic alkali, sulphuric acid, etc.
In the case of gasoline stocks produced by cracking high sulphur bearing crude petroleum oil or residuums, it may be advantageous to treat such gasoline stocks with sulphuric acid or sulphuric anhydride at low temperatures,
. ranging from approximately to 30 degrees F.,
before the treatment witha concentrated Water solution of any of the aforesaid water soluble metallic salts at the elevated temperatures and pressures heretofore stated, and this treatment i may also be followed by treatment with an alkaline water solution of sodium, potassium, or calwater solution of the metallic salt or mixtures 'of' salts employed is preferably a substantially Y concentrated solution, and the temperature employed for the treatment is preferably approxi- ,mately 300 to 600 degrees F., this temperature depending upon the vaporizing temperature of the oil under treatment.
One of the principal objects of this invention is to accomplish a purification of gasoline or naphtha stocks produced by thermo molecular decomposition of high boiling petroleum oils, by a treatment with a substantially concentrated water solution of a metal salt, under a pressure sufiicientto prevent any substantial vaporization thereof, and at a temperature of approximately 300 to 600 degrees F., followed by a distillation and fractionation operation to separate the products of reaction and higher boiling polymerized products from the purified gasoline or naphtha stocks.
Another object of the invention is to provide a continuous, rapid and economical process for purifying gasoline stocks produced by the thermo decomposition of higher boiling petroleum oils, by treating the same, under superatmospheric pressure sufiicient to maintain a liquid phase, with a substantially concentrated water solution of a metallic salt, at temperatures of approximately 300 to 600 degrees F., to polymerize substantially all the unstable hydrocarbons contained therein, and at the same time remove oxygenated hydrocarbons and render the gasoline sweet to the doctor test.
Another object of the invention is to provide a continuous, economical method for improving the color and removing gums and gum forming material from gasoline or naphtha stock, so that top to condenser coil 3|.
a I I the same may be kept in storage for relatively long periods of time without changing color or quality by the formation of polymerized bodies.
Various other objects and advantages of the present invention will be apparent from the description of the preferred form or example of 'the process embodying the invention. For this purpose, reference is made to the accompanying drawings, in which there are illustrated two forms of apparatus in which the invention may be performed.
' Figure I represents one form of an apparatus for carrying out the invention, in which the pe-' troleum oil product to be treated is first commingled with the water solution of a metallic salt and thereafter heated to a reaction temperature, by causing the same to pass through a heating coil under pressure.
Figure II represents another form of apparatus in which the pertoleum oil product and the water solution of a metallic salt are separately heated to a reaction temperature, and are thereafter commingled by means of a jet mixer.
In Figure I, 3 represents generally a tank for holding a supply of gasoline or other petroleum oil stock to be processed. Pipe I, controlled by valve 2, connects the gasoline stock tank 3 .near
the top to a source of supply not shown.
Pipe 4, controlled by valve 5, connects gasoline stock tank 3' to the inlet side of pump 6. Pipe 40, controlled by valve 4|, connects pipe 4 to a fractionating tower not shown. Pipe 1 connects pump 6 to jet mixer 8.
I3 represents generally a tank for holding a concentrated water solution of a metallic salt, such as zinc chloride, zinc bromide, zinc iodide, etc., or any of the other metal salts heretofore enumerated. Pipe l4, controlled by valve [5, connects tank I3 near the top to a source of supply not shown. Pipe ll, controlled by valve l2, connects tank I3 near the bottom to the inlet side of pump l0. Pipe 9 connects the discharge side of pump 10 to jet mixer 8.
Pipe l6 connects jet mixer 8 to heater coil 38. I1. Furnace I1 is provided with a burner l8 which leads to a supply of fuel not shown. Pipe 39, controlled by pressure release valve l9, connects heater coil 38 to distillation tower 29. Distillation tower 20 is provided with bubble trays 2 I. Pipe 22, controlled by valve 23, connects distillation tower 20 near the bottom to a source of water supply not shown. Pipe 25, controlled by valve 24, connects distillation tower 20 at the bottom to tank 25. Pipe 28, controlled by valve 27, connects tank 26 to a storage not shown.
Pipe 29 connects distillation tower 20 at the Condenser coil 3| is stationed in condenser box 30, which is provided with a water inlet pipe 32 and a water outlet pipe 31. Pipe 32 leads to a source of water supply not shown, and pipe 31 leads to a waste receiver not shown.
Pipe 33 connects condenser coil 3| to treated gasoline tank 34. Pipe 36, controlled by valve 35, connects the treated gasoline tank near the bottom to a storage not shown.
In Figure II, 3 represents generally a tank for holding a supply of gasoline or other petroleum controlled by valve 4|, connects pipe 4 to a I-Ieater'coil 38 is stationed in the furnacefractionating tower not shown. Pipe 1 connects pump 6 to heater coil 38.
[3 represents generally a tank for holding a concentrated water solution of a metallic salt, such as zinc chloride, zinc bromide, zinc iodide, etc., or any of the other metallic salts heretofore enumerated. Pipe [4, controlled by valve 15, connects tank [3 near the top to a source of supply not shown. Pipe ll, controlled by valve l2, connects tank l3 near the bottom to the inlet side of pump I0. Pipe 9 connects the discharge side of pump I!) to heater coil 44. Heater @1144 is stationed in furnace 42. Furnace 42 is provided with a burner 43 which leads to a fuel supply not shown.
Pipe 29 connects distillation tower 20 at the top to condenser coil 3|. Condenser coil Si is situated in condenser box 30, which is provided with a water inlet pipe 32 and a water outlet pipe 31. Pipe 32 leads to a source of water supply not shown, and pipe 3'! leads to a waste receiver not shown. Pipe 33 connects condenser box 30 to treated gasoline tank 34. Pipe 36, controlled by valve 35, connects treated gasoline tank 34 near the bottom to a storage not shown.
The process as carried out in the apparatus described in Figure I is as follows:
The water solution of metallic salt contained in supply tank I 3 is permitted to flow through pipe H and into the inlet side of pump l0, which discharges the same under a pressure ranging from approximately 100 to 1000 pounds gauge through pipe 9 and into said jet mixer 8, the rate of fiow being governed by operation of valve l2.
The quantity of water solution of metallic salt may range from as low as 1 per cent to as high as 10 per cent or higher, by volume, depending upon the stock to be treated. For example, if a crude gasoline stock contains a high percentage of impurities to be extracted, as high as 10 per cent by volume or more of a concentrated water solution of any of the aforesaid metallic salts or mixtures of the same may be employed. The presimingled mixture of the water solution of metallic salt or salts and gasoline stock under treat- -ment, passing through coil 38, will be maintained in a substantially liquid phase, such pressure depending upon the boiling point of the gasoline stock and the temperature employed.
From jet mixer 8, the gasoline stock, commingled with the water solution of the metallic salt or salts, passes through heater coil 38, pipe 39 and pressure release valve l9, where the pressure is reduced to atmospheric or approximately atmospheric, and then passes into distillation tower 28. The commingled mixture passing through heater coil 38 is heated to the reaction temperature. Preferably, a temperature ranging from approximately 300 to 400 degrees F. is suitable to employ in treating ordinary gasoline stocks. However, with some grades of petroleum oil distillates, as high as 600 degrees F. or a little higher may be employed.
In distillation tower 20, the purified gasoline stock, at a temperature ranging from approximately 300 to 400 degrees F., together with a portion of the water content of the salt solution, are
vaporized and separated from the products of the reaction and the metallic salt or salts employed. The purified gasoline stock, mixed with water vapor, passes out of distillation tower 20, through pipe 29, into condenser coil 3i, stationed in condenser box 30, wherein the said purified gasoline stock and water vapor are condensed to a liquid, passing through pipe 33 and into the treated gasoline tank 34. A cooling fluid such as water is employed to condense the gasoline vapors passing through condenser coil 3|, coming from a source' The metallic salts and products of reaction which separate in the bottom of distillation tower 28 are intermittently or continuously drawn into tank 26 through pipe 25, the flow being controlled by valve 24, water being continuously or intermittently introduced into the lower section of distillation tower 20 through pipe 22, controlled by valve 23, in quantities sufiicient to replace the vaporized water from the metallic salt water solution, so as to maintain the used metallic salts or compounds and products of reaction in a fluid condition.
From tank 26 the excess water solution of metallic salt or salts and products of reaction are conducted to a storage not shown through pipe 28, controlled by valve 21, and the metallic salts or compounds are separated from the reaction products and purified for re-use.
As illustrated in Figures I and II, if it is desired to treat a gasoline stock coming directly from a fractionating tower or other distillation apparatus, in a vapor or semi-vapor state, valve is closed and valve 4! is opened, which permits the gasoline stock coming from a source not shown, in a vapor or semi-vapor state, to flow through pipe 48 and into the inlet side of pump 6, wherein the gasoline stock is completely condensed to a liquid by the applied pressure maintained on the system and the introduction of the cool water solution of a metallic salt or salts. in
The
Figure. I, and by the application of' pressure in Figure 11. V
The process as carried out in the apparatus described in Figure II is substantially the same as the process heretofore described for Figure I, except that the petroleum oil or gasoline stock to be treated and the water solution of a metallic salt or salts are first separately heated to the reaction temperature by heating coils 38 and 44, at a pressure sufficient to prevent any substantial vaporization therein, after which the heated gasoline stock and heated water solution of a metallic salt or salts, as heretofore enumerated, are commingled in jet mixer 8 andpass through pipe I 6, reaction chamber 46, pipe 41, pressure release valve l9, and into distillation tower 20.
While the process herein described is well adapted for carrying out the objects of the present invention, it is to be understood that various modifications and changes may be made without departing from the invention, such for example, as the use of centrifugal or other mechanical mixers, or the employment of any of the well known contact towers wherein a water solution of a metallic salt or mixtures of metallic salts, either organic or inorganic, heretofore enumerated, may becommingled with or brought into contact with a petroleum oil at a pressure sufficient to prevent substantial vaporization at the reacting temperature, and the invention includes all such modifications and changes as come within the scope of the appended claims.
I claim:
1. A process of purifying a petroleum oil product which comprises, causing the said product to vaporize from a heatedicommingled mixture of the product and a maintained water solution of an aluminum salt at a reaction temperature.
2. A process of purifying a petroleum oil product which comprises, heating and commingling said product with a Water solution of an aluminum salt, under pressure sufficient to prevent substantial vaporization, thereafter releasing the .pressure and causing the product to vaporize from the heated commingled mixture at a reaction temperature while maintaining the aluminum salt in solution by the addition of water.
3. A process of purifying petroleum oil products, comprising, commingling a petroleum oil product with a substantially concentrated water solution of an aluminum salt, passing the commingled mixture through a heating coil and heating the mixture to a reaction temperature, under pressure sufficient to prevent substantial vaporization, releasing the pressure and separating by vaporization, fractionation and condensation a purified petroleum oil product from products of reaction and excess treat-ing agent.
4. A process of purifying petroleum oil, comprising, commingling the petroleum oil with a substantially concentrated water solution of aluminum salt, passing the commingled mixture through a heating coil andheating the mixture to a temperature of approximately 300-600 F., under pressure sufficient to prevent substantial vaporization, releasing the pressure and separating by vaporization, fractionation and condensation a purified'petroleum oil product from products of reaction and excess treating agent.
5. A continuous process for purifying gasoline stocks, comprising, continuously commingling gasthe commingled mixture through a heating element and heating the mixture to a temperature of approximately, 300-600 F., under pressure sufii cient to prevent substantial vaporization, releas ing the pressure and. separating by vaporization, fractionation and condensation a purified gasoline stock from products of reaction and, excess treating agent.
6. A process of removing gum forming constituents from cracked gasoline stock, comprising, commingling cracked gasoline stock with a water solution of aluminum'salt, and heating the commingled mixture to a temperature of approximately 300-600 F., under a pressure sufiicient to prevent substantial vaporization, while passing through a heating zone, for a period of time sufficient to cause the unstable hydrocarbons contained in the cracked gasoline stock to polymerize with the formation of gums, then reducing the pressure to approximately atmospheric, and separating by vaporization, fractionation and condensation a purified gasoline stock from products of reaction and polymerization, and excess treating agent.
7. A continuous process for purifying gasoline or naphtha derived by thermo decomposition of higher boiling petroleum oils, comprising, continuously commingling the gasoline or naphtha with a. water solution of aluminum chloride, continuously passing the commingled mixture through a heating zone and heating the commingled gasoline or naphtha and water solution of aluminum chloride to a temperature of approximately 300-600 F., under a pressure sufiicient to prevent substantial vaporization, continuously releasing the pressure after the commingled mixture of gasoline or naphtha and water solution of aluminum chloride has passed through said heating zone, continuously passing the treated gasoline or naphtha, products of reaction and excess treating agent into a vaporizing zone, continuously vaporizing, fractionating and separating a purified gasoline or naphtha and water vapor from higher boiling reaction products and excess treating agent.
8. A continuous process of purifying gasoline or naphtha derived by the thermo-molecular decomposition of higher boiling mineral oils, comprising, continuously commingling the gasoline or naphtha with a water solution of aluminum salt, continuously passing the commingled mixture through-a heating zone and heating the commingled gasoline or naphtha and water solution of aluminumsalt to a temperature of approximately 300-600 F., under a pressure sufficient to prevent substantial vaporization, continuously releasing the pressure and continuously passing the heated mixture of gasoline or Y naphtha, water solution of aluminum salt and products of reaction into a vaporizing zone, continuously vaporizing and separating by fractionation and condensation a purified gasoline or naphtha mixed with water from higher boiling products of reaction and excess treating agent, continuously introducing water into the vaporizing zone in quantities sufiicient to replace the water of vaporization, continuously withdrawing products of reaction and introduced water containing excess treating agent, substantially as described.
9. A process of purifying gasoline or naphtha, comprising, contacting the gasoline or naphtha with a water solution of aluminum salt while passing through a heating zone, under a pressure suflicient to prevent substantial vaporization, and
heating the mixed gasoline or naphtha and water solution of aluminum salt to a temperature of heating the commingled mixture to a reaction temperature, under a pressure sufiicient to prevent substantial vaporization, releasing the pressure and passing the treated petroleum oil, products of reaction and Water solution of aluminum salt into a vaporizing zone, maintaining thealuminum salt in a fluid condition by the addition of water, vaporizing, fractionating and separating a purified petroleum oil mixed with water vapor fromhigher boiling reaction products and 10 excess treating agent.
ARTHUR LACHMAN.
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US637424A US2035610A (en) | 1929-07-26 | 1932-10-12 | Process of purifying and refining hydrocarbon oils with aluminum salts |
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US381305A US2035607A (en) | 1929-07-26 | 1929-07-26 | Process of purifying and refining hydrocarbon oils |
US637424A US2035610A (en) | 1929-07-26 | 1932-10-12 | Process of purifying and refining hydrocarbon oils with aluminum salts |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2526963A (en) * | 1946-07-11 | 1950-10-24 | Phillips Petroleum Co | Process for stabilizing hydrocarbons |
US2711990A (en) * | 1951-03-03 | 1955-06-28 | Sumner E Campbell | Refining of lubricating oils |
-
1932
- 1932-10-12 US US637424A patent/US2035610A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2526963A (en) * | 1946-07-11 | 1950-10-24 | Phillips Petroleum Co | Process for stabilizing hydrocarbons |
US2711990A (en) * | 1951-03-03 | 1955-06-28 | Sumner E Campbell | Refining of lubricating oils |
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