US2306484A - Process for the distillation of oil containing salts of hydrochloric acid - Google Patents
Process for the distillation of oil containing salts of hydrochloric acid Download PDFInfo
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- US2306484A US2306484A US320293A US32029340A US2306484A US 2306484 A US2306484 A US 2306484A US 320293 A US320293 A US 320293A US 32029340 A US32029340 A US 32029340A US 2306484 A US2306484 A US 2306484A
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- Prior art keywords
- oil
- sulfide
- sodium
- distillation
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- 238000004821 distillation Methods 0.000 title description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 title description 14
- 238000000034 method Methods 0.000 title description 11
- 150000003839 salts Chemical class 0.000 title description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 54
- 239000003921 oil Substances 0.000 description 33
- 239000000243 solution Substances 0.000 description 26
- 238000009835 boiling Methods 0.000 description 19
- 239000003208 petroleum Substances 0.000 description 16
- 229910052979 sodium sulfide Inorganic materials 0.000 description 14
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 14
- 239000000470 constituent Substances 0.000 description 10
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 8
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 239000000446 fuel Substances 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 6
- 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 6
- 239000001110 calcium chloride Substances 0.000 description 6
- 229960002713 calcium chloride Drugs 0.000 description 6
- 229910001628 calcium chloride Inorganic materials 0.000 description 6
- 235000011148 calcium chloride Nutrition 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 239000010779 crude oil Substances 0.000 description 5
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
- 229910001629 magnesium chloride Inorganic materials 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 150000004763 sulfides Chemical class 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- DPLVEEXVKBWGHE-UHFFFAOYSA-N potassium sulfide Chemical compound [S-2].[K+].[K+] DPLVEEXVKBWGHE-UHFFFAOYSA-N 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 150000003464 sulfur compounds Chemical class 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 229910052977 alkali metal sulfide Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000011179 visual inspection 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
- C10G19/00—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
Definitions
- the present invention relates to the refiningv of mineral oils...
- the invention is moreparticularly concerned with a method forthe prevention of corrosion of the refining equipment.
- petroleum oils which tend'to cause excessive corrosionare distilled in the presence of a reagent 'whichserves to substantially' completely'v eliminate prohibitive corrosion'of the equipment.
- a special modification of the invention is directed to an improvedV process for the productionof hydrogen sulfidefree 'petroleum oilsboiling in themotor fuel boiling range'l 'from' petroleum crude oils containing acid-formingl constituents,
- petroleum oils containing vacid-forming constituents are distilled in the presence of a sulfide ⁇ selected fromv the classof suliides which are characterized by' the fact that they form stable salts whichdo .noty decompose under distillation conditions into'harmful acidic substances',
- Subst'aifees'V of this type areyfor example, am-
- nonium'fs'ulde, sodium sulfide and potassium sulfide Ap'referred'modification of my inven- Ain'g'"nsulfurcompounds vand ⁇ acidic forming materialsV asfo'r example, relatively unstable salts of hydrochloricjacid suchy tas magesium chloride, calciumchloride and iron chloride.
- the lower lboiling constituents preferably boil inthe motor My lrecess maybe readilyv understood by refdrawing illustrating 'modifications of the samer-#For 'purposes of description itjis assumed-:that the feed oil is an un- Vrefined petroleum roil containing appreciable quantitiesr of acidic forming substances such as magnesiumiand calcium chloride.
- the feed oil is introduced into 'distillation tower l by means of 'feedf line 2-.n Prior to introducingthefeed oil "intodistillationtower l it is mixed with asuliide 'jsolutionwwhich is introducedintodfeed line y2 by irieagns'ofqline.
- the sulfide solution is an aqueous sodium sulfide solution.
- Efficient mixing of the feed eiland-reagent is secured by -meansofmixer ⁇ 4.
- - ,-V'Iemperature and ⁇ pressure conditions are A -maintained inr distillation tower I, adapted to revove overhead by means ofv line Blower boiling ydrocarbon fractions preferably boiling inthe otorfuel boiling range.
- oil and reduced crude streams may be -handled in any manner desirable.
- 'I 'he cracked products are v.then refined vbyvarious lrefining operations such ooi as ⁇ debutanization. stabilization, acid treating yand the ylikein.. order to produce finished products.
- 'I'he distillate fraction removed overhead from distillation tower I by means of line 5 is condensed in condenser 9 and passed to distillate drum IIJ. moved from distillate drum I by means of line II and handled in any desired manner.
- the mixture is withdrawn from treating plant I3 by means of line I5 and passed to settling unit I6, in which the spent sodium hydroxide solution comprising a sodium sulfide solution substantially free of sodium hydroxide separates from theV treated oil.
- Hydrogen sulfide-free oil is withdrawn from settling unit I6 by means of line I'I and passed into storage tank I8.
- the oil is withdrawn from storage tank I8 by means of line I9 and handled in any manner desirable. erally the oil is sweetened and blended into a finished refined product.
- the spent sodium hydroxide solution comprising sodium sulfide and substantially free of sodium hydroxide is Withdrawn from settling drums I6 and 23 by means of lines 21 and 28 respectively. These solutions are passed into sodium sulfide storage 29 by means of line 3D from which it is withdrawn by means of line 3 and introduced into the unrened feed oil. Excess solution may be withdrawn from storage tank 29 by means of line 3
- the present invention may be widely varied.
- the process may be applied to any distillation operation utilized in the refining of mineral oils containing sulfur and acid forming compounds.
- the process is particularly adapt-ed for the production of hydrogen sulfide-free refined oil produces boiling in the motor fuel boiling range from sulfur-containing crude oils which also contain acid-forming salts, such as magnesium chloride and calcium chloride.
- acid-forming salts such as magnesium chloride and calcium chloride.
- any sulfide which has the abilityto prevent the formation vof or to neutralize the free acids Uncondensed and fixed gases are reformed may be used.
- the preferred sulfides are the alkali metal sulfides particularly sodium sulfide.
- the amount of the sulfide added to the un- Arened oil will be a function to a large extent of the characteristic of the unrefined oil and of the particular sulfide employed.
- the quantity added should be at least suflicient to completely neutralize the acid-forming constituents present. vIn general, it is preferred that the quantity added should be several times the amount equivalent to secure theoretical complete neutralization.
- the concentration of the sulde solutions may also vary considerably depending upon the various factors. For example, when employing spent sodium hydroxide solution the concentrations will vary depending upon the relative proportions of sodium sulfide 'and sodium hydrogen sulfide present. We have found, for example, that sodium sulfide solutions comprising from 0.01 1b. to 0.1 lb.
- the spent sodium hydroxide solution may be processed or concentrated prior to introducing the same into the oil feed.
- the spent sodium hydroxide solution should comprise sodium sulfide and sodium acid sulfide and should preferably be substantially completelyV free of sodium hydroxide.
- Example 1 Operations were conducted on West Texas crude oils and the quantities of hydrochloric acid evolved per unit quantity of oil determined. In one operationvno'sulde was added to the oil. In a second operation a spent sodium hydroxide solution free Vof sodium hydroxideV and secured from a plant operated for the removal of hydrogen sulfide from petroleum, hydrocarbons boiling in the motor fuel boiling range was employed. In a third operation sodium sulfide was utilized. The amounts of the solutions utilized were controlled to theoretically neutralize of the acidity. The quantities of acidicvapors evolved in the respective operations were Vas follows:v V-
- a process for the distillation of oil containing salts of hydrochloric acid of the class consisting of magnesium chloride, calcium chloride and iron chloride comprising distilling said oil in the presence of an added solution containing a sulfide salt selected from the class consisting of sodium sulfide and potassium sulfide.
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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
1942. J. H. MccLlNTocK 2,306,484
PROCESS FOR THE DISTILLATION OF- OIL CONTAINING SALTS OF HYDROCHLORIC ACID Dec. 29,
Filed Feb. 23', 1940 QN NN III 4 "uga Y It is'known in L111'@.Selmef` l .c A suldes' which 'are characterized by the-fact that Patented Dec. 29, 1942 asoaieij vAcmr JohnH. McClintockfCranford, NQJ'.;assi-giuri'.to".4v I,
" Standard Oil DevelopmentCompany, a corporation of Delaware lApplication February 23, 19,40;
(Cl. Y. stable l nder the temperature and pressure condi- A3 Claims.
The present invention relates to the refiningv of mineral oils... The invention is moreparticularly concerned with a method forthe prevention of corrosion of the refining equipment. In accordance with Vthe present process, petroleum oils which tend'to cause excessive corrosionare distilled in the presence of a reagent 'whichserves to substantially' completely'v eliminate prohibitive corrosion'of the equipment. A special modification of the inventionis directed to an improvedV process for the productionof hydrogen sulfidefree 'petroleum oilsboiling in themotor fuel boiling range'l 'from' petroleum crude oils containing acid-formingl constituents, In accordance -with .thev present fpjrocess, petroleum oils containing vacid-forming constituents are distilled in the presence of a sulfide `selected fromv the classof suliides which are characterized by' the fact that they form stable salts whichdo .noty decompose under distillation conditions into'harmful acidic substances',
theY art thatyarious petroleum crude oils contain appreciable l'amounts of,v constituents which, upon distillation of the oil, form corrosive acids which materially decrease the f life of the distillation and'related equipment, re- ,sulting in a substantial increase in operating costs. Particularly harmful acidic-forming 'constituents v`contained! inv unreflned petroleum oils arexrelatively unstable salts ofhydrochloric acid,
`as for example, magnesium, `calcium and iron chloride which hydroliz'ejtoj jform free hydrochloric acid. Thus'numeroussuggestions have been made that various reagents be addedfto petroleum oils prior 'toi distilling the same in A order tosprevent the formation ofr or to neutralize freeacidswhich may be formed. lSubstanceswhich have been employed for this purposeara'for example, aqueous solutions of sodium, hydroxide and sodium'carbonate. These materials due'in Iv'have now discovered a process by which it is troleum oils containing acid-forming constituents utilizing a reagent whichwill substantially entirely prevent corrosionof ther equipment and which will not fuse with the metallic surfaces of the same. lMyprocess comprises distillingrmineral oilswhich'tend 'to cause `excessive corrosion of the distillation andi related equipmentY in the 'a sulfide-selected from the class of they form salts which are entirely substantially,
part to their cost are not entirely satisfactoryggoV "erncelf'to' the attachedtions v.prevailing in 'the distillation operation.
Subst'aifees'V of this type areyfor example, am-
nonium'fs'ulde, sodium sulfide and potassium sulfide., Ap'referred'modification of my inven- Ain'g'"nsulfurcompounds vand `acidic forming materialsV asfo'r example, relatively unstable salts of hydrochloricjacid suchy tas magesium chloride, calciumchloride and iron chloride., In accordlnce with'my preferred adaptation of the invention, -these` unrened crude'oils -are distilled in the-:presence of-sodium; suliide solutions vwhich argl-secured; iri the removal of hydrogen sulde irorrrthe lower boiling constituents of said crude oilsbyftreating said lower-boiling constituents 'with a sodium hydroxide solution. 4The lower lboiling constituents preferably boil inthe motor My lrecess maybe readilyv understood by refdrawing illustrating 'modifications of the samer-#For 'purposes of description itjis assumed-:that the feed oil is an un- Vrefined petroleum roil containing appreciable quantitiesr of acidic forming substances such as magnesiumiand calcium chloride. [The feed oil is introduced into 'distillation tower l by means of 'feedf line 2-.n Prior to introducingthefeed oil "intodistillationtower l it is mixed with asuliide 'jsolutionwwhich is introducedintodfeed line y2 by irieagns'ofqline. For purposes of description it isassumed'the sulfide solution is an aqueous sodium sulfide solution. Efficient mixing of the feed eiland-reagent is secured by -meansofmixer `4.- ,-V'Iemperature and` pressure conditions are A -maintained inr distillation tower I, adapted to revove overhead by means ofv line Blower boiling ydrocarbon fractions preferably boiling inthe otorfuel boiling range. Under certain condiitfmay berdesirable to withdrawV as a side y 45fhfsr'trjream bymeansl'of line`6 a; relatively high boiling l fraction of hydrocarbons boiling substantially in possible to efficiently*andeconomically distill -pethe'y motor fuel boiling lrange.A If this*V operation be employed the boiling k,range of -this stream will be, from abouty 250 to 4202 Intermediate and higher boilingrangeY streams, `as for example Vgas il'fractifons and jreduce'd crude fractions are withdrawal by-means of lines 1 and 8 respectively.
oil and reduced crude streams may be -handled in any manner desirable. Generally 'theyare processed by various cracking operations Afor the production of cracked motor fuels, heaty ingoils andthe like. 'I 'he cracked products are v.then refined vbyvarious lrefining operations such ooi as `debutanization. stabilization, acid treating yand the ylikein.. order to produce finished products. 'I'he distillate fraction removed overhead from distillation tower I by means of line 5 is condensed in condenser 9 and passed to distillate drum IIJ. moved from distillate drum I by means of line II and handled in any desired manner. These gases may be processed for the recovery of valuable hydrocarbons which may be included in motor fuels or may be passed to a burning line. The condensed distillate containing various sulfur compounds, as for example hydrogen sulfide, is removed from distillate drum Ill by means of line I2, and passed through treating plant I3, in which it is contacted with an alkaline solution preferably a solution of sodium hydroxide. Treating plant I3 may comprise any number of stages arranged in any desirable manner. The sodium hydroxide solution is introduced into treating plant I3 by means of line I4. The mixture is withdrawn from treating plant I3 by means of line I5 and passed to settling unit I6, in which the spent sodium hydroxide solution comprising a sodium sulfide solution substantially free of sodium hydroxide separates from theV treated oil. Hydrogen sulfide-free oil is withdrawn from settling unit I6 by means of line I'I and passed into storage tank I8. The oil is withdrawn from storage tank I8 by means of line I9 and handled in any manner desirable. erally the oil is sweetened and blended into a finished refined product. If the operation be conducted under conditions to remove a relatively higher boiling fraction of hydrocarbons boiling in the motor fuel boiling range by means of line 6 this fraction is cooled in cooler 1 and passed to treating plant 20, which may comprise any suitable number of units arranged in any desirable manner.. This oil in treating plant 20 is thoroughly contacted with an alkaline solution preferably with a sodium hydroxide solution which is introduced by means of line 2|. The mixture is withdrawn from treating unit 20 by means of line 22 and passed to settling drum 23 from which a hydrogen sulfide-free oil is Withdrawn by means of line 24 and passed to storage tank 25. The oil withdrawn from tank 25 by means of line 26 may be acid treated or reformed or further processed in any manner desired. The spent sodium hydroxide solution comprising sodium sulfide and substantially free of sodium hydroxide is Withdrawn from settling drums I6 and 23 by means of lines 21 and 28 respectively. These solutions are passed into sodium sulfide storage 29 by means of line 3D from which it is withdrawn by means of line 3 and introduced into the unrened feed oil. Excess solution may be withdrawn from storage tank 29 by means of line 3| and disposed of as desired. Under certain conditions it may be desirable to utilize or to employ in part, a sodium sulfide not produced in the manner described in which casefthe solution is introduced into the feed oil by means of line 32.
The present invention may be widely varied. The process may be applied to any distillation operation utilized in the refining of mineral oils containing sulfur and acid forming compounds. The process, however, is particularly adapt-ed for the production of hydrogen sulfide-free refined oil produces boiling in the motor fuel boiling range from sulfur-containing crude oils which also contain acid-forming salts, such as magnesium chloride and calcium chloride. Although any sulfide which has the abilityto prevent the formation vof or to neutralize the free acids Uncondensed and fixed gases are reformed may be used. I have found that the preferred sulfides are the alkali metal sulfides particularly sodium sulfide.
The amount of the sulfide added to the un- Arened oil will be a function to a large extent of the characteristic of the unrefined oil and of the particular sulfide employed. The quantity added should be at least suflicient to completely neutralize the acid-forming constituents present. vIn general, it is preferred that the quantity added should be several times the amount equivalent to secure theoretical complete neutralization. The concentration of the sulde solutions may also vary considerably depending upon the various factors. For example, when employing spent sodium hydroxide solution the concentrations will vary depending upon the relative proportions of sodium sulfide 'and sodium hydrogen sulfide present. We have found, for example, that sodium sulfide solutions comprising from 0.01 1b. to 0.1 lb. of sodium sulfide and from 0.1 to 0.5 lb. of sodium hydrogen sulfide er gallon are very satisfactory. When employing the preferredv modication of the invention in order to secure the desired concentration of sodium sulfide and sodium vhydrogen sulfide and to substantially completely eliminate freesodium hydroxide, the spent sodium hydroxide solution may be processed or concentrated prior to introducing the same into the oil feed. The spent sodium hydroxide solution should comprise sodium sulfide and sodium acid sulfide and should preferably be substantially completelyV free of sodium hydroxide.
In order to further illustrate the invention, the following examples are given which should not be construed as limiting the invention in any manner whatsoever.
Example 1 Operations were conducted on West Texas crude oils and the quantities of hydrochloric acid evolved per unit quantity of oil determined. In one operationvno'sulde was added to the oil. In a second operation a spent sodium hydroxide solution free Vof sodium hydroxideV and secured from a plant operated for the removal of hydrogen sulfide from petroleum, hydrocarbons boiling in the motor fuel boiling range was employed. In a third operation sodium sulfide was utilized. The amounts of the solutions utilized were controlled to theoretically neutralize of the acidity. The quantities of acidicvapors evolved in the respective operations were Vas follows:v V-
sulfides were particularly leffective and that by utilizingvasomewhat greater quantity than the theoretical amount needed, substantially complete removal of the acidic `constituents will Vbe effected.
Example 2 n a commercial distillation operation when processing East Texas crude oil a visual inspection disclosed that considerable corrosion of the distillation equipment occurred. This corrosion was substantially completely prevented by employing a spent sodium hydroxide solution which Was essentially free of sodium hydroxide and comprised about 0.1 lb. of sodium sulflde and about 0.1 lb. of sodium hydrogen sulde per gallon.
What I claim as new and Wish to protect by Letters Patent is: n
1. Process for the distillation lof petroleum oils containing salts of hydrochloric acid of the class consisting of magnesium chloride, calcium chloride and iron chloride comprising distilling said oils in the presence of a spent sodium hydroxide solution secured in the removal of hydrogen sulfide from petroleum oils said spent sodium hydroxide solution being substantially completely free of sodium hydroxide.
2. Process for the production of a hydrogen sulfide free rened petroleum oil boiling substantially in the motor `fuel boiling range from an unrened petroleum oil containing sulfur compounds and salts of hydrochloric acid selected from the class consisting of magnesium chloride, calcium chloride and iron chloride comprising distilling said unrened petroleum oil in the presencerof a spent alkali metal hydroxide solution secured in the removal of hydrogen sulde from said refined petroleum oil derived from said unrened petroleum oil, said spent alkali metal hydroxide solution being substantially completely free of alkali metal hydroxide constituents.
3. A process for the distillation of oil containing salts of hydrochloric acid of the class consisting of magnesium chloride, calcium chloride and iron chloride, comprising distilling said oil in the presence of an added solution containing a sulfide salt selected from the class consisting of sodium sulfide and potassium sulfide.
JOHN H. MCCLINTOCK.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US320293A US2306484A (en) | 1940-02-23 | 1940-02-23 | Process for the distillation of oil containing salts of hydrochloric acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US320293A US2306484A (en) | 1940-02-23 | 1940-02-23 | Process for the distillation of oil containing salts of hydrochloric acid |
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| Publication Number | Publication Date |
|---|---|
| US2306484A true US2306484A (en) | 1942-12-29 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US320293A Expired - Lifetime US2306484A (en) | 1940-02-23 | 1940-02-23 | Process for the distillation of oil containing salts of hydrochloric acid |
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| Country | Link |
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| US (1) | US2306484A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3294678A (en) * | 1964-01-29 | 1966-12-27 | Universal Oil Prod Co | Process for deasphaltening heavy petroleum crude oil |
| US4468316A (en) | 1983-03-03 | 1984-08-28 | Chemroll Enterprises, Inc. | Hydrogenation of asphaltenes and the like |
| US4606812A (en) * | 1980-04-15 | 1986-08-19 | Chemroll Enterprises, Inc. | Hydrotreating of carbonaceous materials |
-
1940
- 1940-02-23 US US320293A patent/US2306484A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3294678A (en) * | 1964-01-29 | 1966-12-27 | Universal Oil Prod Co | Process for deasphaltening heavy petroleum crude oil |
| US4606812A (en) * | 1980-04-15 | 1986-08-19 | Chemroll Enterprises, Inc. | Hydrotreating of carbonaceous materials |
| US4468316A (en) | 1983-03-03 | 1984-08-28 | Chemroll Enterprises, Inc. | Hydrogenation of asphaltenes and the like |
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