US2464576A - Process for the removal of mercaptans from petroleum distillates with an aqueous alkaline reagent containing lignin and the regeneration of the spent alkaline reagent - Google Patents
Process for the removal of mercaptans from petroleum distillates with an aqueous alkaline reagent containing lignin and the regeneration of the spent alkaline reagent Download PDFInfo
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- US2464576A US2464576A US663237A US66323746A US2464576A US 2464576 A US2464576 A US 2464576A US 663237 A US663237 A US 663237A US 66323746 A US66323746 A US 66323746A US 2464576 A US2464576 A US 2464576A
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- mercaptans
- alkaline reagent
- lignin
- mercaptan
- hydrocarbon
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- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 title description 37
- 229920005610 lignin Polymers 0.000 title description 32
- 238000000034 method Methods 0.000 title description 29
- 239000003153 chemical reaction reagent Substances 0.000 title description 25
- 239000003209 petroleum derivative Substances 0.000 title description 6
- 230000008929 regeneration Effects 0.000 title description 2
- 238000011069 regeneration method Methods 0.000 title description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 45
- 229930195733 hydrocarbon Natural products 0.000 description 44
- 239000004215 Carbon black (E152) Substances 0.000 description 33
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 26
- 239000003518 caustics Substances 0.000 description 21
- 239000000243 solution Substances 0.000 description 21
- 239000003513 alkali Substances 0.000 description 20
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 14
- 239000001301 oxygen Substances 0.000 description 14
- 229910052760 oxygen Inorganic materials 0.000 description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 11
- 239000011593 sulfur Substances 0.000 description 10
- 229910052717 sulfur Inorganic materials 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000007791 liquid phase Substances 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000000470 constituent Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229920001131 Pulp (paper) Polymers 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 150000003464 sulfur compounds Chemical class 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- ZMWAXVAETNTVAT-UHFFFAOYSA-N 7-n,8-n,5-triphenylphenazin-5-ium-2,3,7,8-tetramine;chloride Chemical compound [Cl-].C=1C=CC=CC=1NC=1C=C2[N+](C=3C=CC=CC=3)=C3C=C(N)C(N)=CC3=NC2=CC=1NC1=CC=CC=C1 ZMWAXVAETNTVAT-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- -1 alkali metal salts Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
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
- C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
- C10G27/04—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen
Definitions
- This invention relates to the treatmentoi' hydrocarbons to remove sulfur constituents normally present, and has specific reference to the removal of mercaptans from petroleum distillates.
- Petroleum cllstillates commonly contain mercaptans in concentrations of from 0.001 to 0.1%, expressed as weight percent of mercaptan sulfur.
- the mercaptans are weakly acidic, and are often only partially removed by the alkali wash, so that the amount of mercaptans remaining present in the petroleum distillate is above the critical limit for a so-called "sweet gasoline. This may be explained by the following equilibrium equation oi mercaptans in a hydrocarbon distillate treated with an aqueous alkali solution:
- the process may be a single stage process, i. e., the hydrocarbons may be treated with the llgnincontaining alkali in the presence of oxygen.
- the presence of the iignin assists in causing the solution of mercaptans in the caustic shifting equilibrium (l) to the right.
- the presence of the lignin also assists the oxygen in converting mercaptides to oxidation products, further shifting equilibrium (2) and (3) to the right.
- the process is carried out in two steps in a coinmercial operation in which the lignin-containing caustic is contacted with the mercaptan-containing hydrocarbon, and the mercaptan-contalning and lignin-containing caustic is treated with oxygen to convert the mercaptans to oxidation products.
- the two-step process is preferred and will be referred to hereinafter in describing the invention.
- the hydrocarbon material treated may be any containing mercaptans. Generally they are from petroleum sources and the materials most commonly treated are distillates, such as naphthas, gasoline, kerosene, etb.
- Lignin is readily available as icy-products of processes involving the separation of ceilulosic from non-cellulosic substances, such as the waste liquors from chemical wood pulping processes.
- aqueous alkali solution directly, or the lignin content may be isolated from the waste liquors by acid precipitation and then added to the caustic solution.
- Lignin derivatives such as the disodlum salt or other alkali metal salts, may be employed satisfactorily. Standardized grades of llgnln are presently available commercially and it may be desirable to employ lignin of a uniform reproducible grade in carrying out the present invention.
- the alkali solution to be used may be any of those normally employed for such purposes, such as caustic soda, caustic potash, alkali metal carbonates, and other equivalent alkali compounds.
- the concentration of the caustic may be any concentration which will remove merca'ptans to the desired extent. the preferred concentration being between 5 B. to 25 as. (about 3 to 20%), the optimum strength being to in aqueous solution.
- the lignin constituent may be employed in an amount sufficient to facilitate mercaptan removal, concentrations of 0.5 to 10% being suitable, and amounts of 2 to 4% by weight of the caustic solution being optimum.
- the hydrocarbon distillate with caustic to remove the more readily removable sulfur constituents, such as free sulfur and hydrogen sulfide, thus avoiding undue sulfur contamination of the caustic containing lignin, employed in the separation of the mercaptans.
- the mercaptan extraction is eflected at temperatures at which the mercaptans pass readily to the caustic phase, temperatures between F. and 200 F. being preferred and best results being obtained with a temperature approximating 100 F.
- the mercaptan extraction with aqueous alkali solution may be accomplished in any known way.
- suillcient caustic to extract the mercaptans to the desired extent, for example, 10 to 1000 volumes oi caustic with 100 volumes of hydrocarbon distillate, carrying the liquids through a single stage or a counter current multi-stage extraction process, as desired, to effect removal of the mercaptans from the hydrocarbon distillate.
- Suitable additives to aid in solution of the mercaptans in the caustic, other than the lignin, may be employed. It has been found that advantageous results are obtained by allowing natural cresol and xylol, components normally present in the hydrocarbon, to build up in concentration in the caustic.
- Oxidation of the mercaptans in the spent caustic containing the lignin may be accomplished in any known manner, such as by passing oxygen or an oxygen-containing gas through the caustic solution.
- Advantageous results may be obtained by use of superatmospheric pressures, although the advantages of the invention are not limited to employment of this expedient. Pressures from atmospheric to 250 lbs. sq. in, have been employed satisfactorily.
- the temperature at which the mercaptan oxidation step may be carried out should be such as to accomplish removal of the mercaptans and a temperature of between 50 F. and 200 F. is satisfactory, desirable results being obtained with a temperature of 125 F.
- a method of improving hydrocarbons containing sulfur compounds comprising contacting a hydrocarbon distillate in the liquid phase with a first alkaline solution to remove free sulfur and hydrogen sulfide constituents normally present. and contacting the distillate with a second aqueous alkaline solution having liznin dissolved therein, said lignin having been obtained from av sulfate and soda pulp process.
- a method of improving hydrocarbons the step of contacting a mercaptan-containing hydrocarbon distillate in the liquid phase with an aqueous alkaline reagent having lignin dissolved therein, said lignin having been obtained from a sulfate and soda paper pulp process.
- aqueous alkaline reagent in a method of improving mercaptan-containing hydrocarbon distillate in liquid phase by treating the same with an aqueous alkaline reagent, the step of contacting a mercaptan-containing aqueous alkaline reagent with oxygen in the presence of lignin dissolved therein, said lignin having been obtained from a sulfate and soda paper pulp process, whereby the aqueous alkaline reagent may be recycled for reuse in further treating said hydrocarbon.
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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
Patented Mar. 15, 1949 PROCESS FOR THE REMOVAL OF MERCAP- TAN 8 FROM PETROLEUM DISTILLATES WITH AN AQUEOUS ALKALINE REAGENT CONTAINING LIGNIN AND THE REGENER- ATION OF THE SPENT ALKALINE REAGENT Robert R. Hibbard, Lorain, and Franklin Veatch, Cleveland, Ohio, asalgnors to The Standard Oil gohrlnpany, Cleveland, Ohio, a corporation of N o Drawing 10 Claims.
This invention relates to the treatmentoi' hydrocarbons to remove sulfur constituents normally present, and has specific reference to the removal of mercaptans from petroleum distillates.
The treatment of petroleum distillates, such as gasoline, to remove sulfur compounds stems from the objectionable character of such compounds, particularly from the standpoint of odor. It is desirable to "sweeten" the distillate by removal of sulfur constituents in the nature 01 free sulfur, hydrogen sulfide, mercaptans and thio compounds either by conversion to less objectionable suliur-containlng compounds, or by actual removal from the petroleum distillate.
It has long been known that sulfur compounds can be extracted from a hydrocarbon distillate to a great extent by washing with an aqueous solution of alkali, such as caustic soda. The more acidic compounds such as hydrogen sulfide go into solution readily, and their removal presents little problem.
Petroleum cllstillates commonly contain mercaptans in concentrations of from 0.001 to 0.1%, expressed as weight percent of mercaptan sulfur. The mercaptans are weakly acidic, and are often only partially removed by the alkali wash, so that the amount of mercaptans remaining present in the petroleum distillate is above the critical limit for a so-called "sweet gasoline. This may be explained by the following equilibrium equation oi mercaptans in a hydrocarbon distillate treated with an aqueous alkali solution:
+M H RSH RSH T: Its-+11 RSM V Dissolved in Dissolved in Ionized in Saponiiled hydrocarbon (l) alkali (2) alkali (3) in alkali It will be apparent that the concentration of m'ercaptans in the hydrocarbon phase can be kept at a desired low level if the equilibrium (1) is shifted by rendering the mercaptans more soluble in the alkali phase, or by maintaining a low concentration of mercaptans (either ionized or as mercaptides) in the alkali phase.
It has been proposed heretofore to facilitate mercaptan removal from hydrocarbon distillates by the addition of compounds to the alkali solution which renders the mercaptans more soluble therein, and then removing the dissolved mercaptans when the alkali solution is spent" or Application April 18, 1946, erlal No. 683,237
(Cl. lac-29) has absorbed mercaptans to an extent that its mercaptan-removing action is lessened. The latter has been accomplished, for example. by stripping the mercaptans from the spent alkali solution with steam, by treating the alkali solution with a solution of elemental sulfur or polysulfldes, by oxidizing the mercaptans with air, and by other known methods of mercaptan separation. The rate of oxidation of mercaptans in spent alkali solutions by treatment with air can be accelerated by adding suitable catalysts to the solution. Metallic oxidation catalysts and tannicacid have been proposed for this purpose.
In accordance with the present invention. it has been discovered that mercaptan reduction in hydrocarbons is effectively increased by using lignin in the aqueous alkali solution that is used to treat the hydrocarbon distillate, the alkali being treated with oxygen or an oxygen containing gas, such as air, at some stage during the process.
The process may be a single stage process, i. e., the hydrocarbons may be treated with the llgnincontaining alkali in the presence of oxygen. The presence of the iignin assists in causing the solution of mercaptans in the caustic shifting equilibrium (l) to the right. The presence of the lignin also assists the oxygen in converting mercaptides to oxidation products, further shifting equilibrium (2) and (3) to the right. Generally the process is carried out in two steps in a coinmercial operation in which the lignin-containing caustic is contacted with the mercaptan-containing hydrocarbon, and the mercaptan-contalning and lignin-containing caustic is treated with oxygen to convert the mercaptans to oxidation products. The two-step process is preferred and will be referred to hereinafter in describing the invention.
The hydrocarbon material treated may be any containing mercaptans. Generally they are from petroleum sources and the materials most commonly treated are distillates, such as naphthas, gasoline, kerosene, etb.
Lignin is readily available as icy-products of processes involving the separation of ceilulosic from non-cellulosic substances, such as the waste liquors from chemical wood pulping processes.
aqueous alkali solution directly, or the lignin content may be isolated from the waste liquors by acid precipitation and then added to the caustic solution. Lignin derivatives, such as the disodlum salt or other alkali metal salts, may be employed satisfactorily. Standardized grades of llgnln are presently available commercially and it may be desirable to employ lignin of a uniform reproducible grade in carrying out the present invention.
The alkali solution to be used may be any of those normally employed for such purposes, such as caustic soda, caustic potash, alkali metal carbonates, and other equivalent alkali compounds. The concentration of the caustic may be any concentration which will remove merca'ptans to the desired extent. the preferred concentration being between 5 B. to 25 as. (about 3 to 20%), the optimum strength being to in aqueous solution.
The lignin constituent may be employed in an amount sufficient to facilitate mercaptan removal, concentrations of 0.5 to 10% being suitable, and amounts of 2 to 4% by weight of the caustic solution being optimum.
In carrying out the method of the present inmention, it is preferred to prewash the hydrocarbon distillate with caustic to remove the more readily removable sulfur constituents, such as free sulfur and hydrogen sulfide, thus avoiding undue sulfur contamination of the caustic containing lignin, employed in the separation of the mercaptans. The mercaptan extraction is eflected at temperatures at which the mercaptans pass readily to the caustic phase, temperatures between F. and 200 F. being preferred and best results being obtained with a temperature approximating 100 F.
The mercaptan extraction with aqueous alkali solution, in a two-step operation, may be accomplished in any known way. In practice, it has been found desirable to employ suillcient caustic to extract the mercaptans to the desired extent, for example, 10 to 1000 volumes oi caustic with 100 volumes of hydrocarbon distillate, carrying the liquids through a single stage or a counter current multi-stage extraction process, as desired, to effect removal of the mercaptans from the hydrocarbon distillate.
Suitable additives to aid in solution of the mercaptans in the caustic, other than the lignin, may be employed. It has been found that advantageous results are obtained by allowing natural cresol and xylol, components normally present in the hydrocarbon, to build up in concentration in the caustic.
Oxidation of the mercaptans in the spent caustic containing the lignin may be accomplished in any known manner, such as by passing oxygen or an oxygen-containing gas through the caustic solution. Advantageous results may be obtained by use of superatmospheric pressures, although the advantages of the invention are not limited to employment of this expedient. Pressures from atmospheric to 250 lbs. sq. in, have been employed satisfactorily.
The temperature at which the mercaptan oxidation step may be carried out should be such as to accomplish removal of the mercaptans and a temperature of between 50 F. and 200 F. is satisfactory, desirable results being obtained with a temperature of 125 F.
The following experimental data substantiates the effectiveness of lignin to facilitate the removal of mercaptans from the caustic. In carrying out 4 the experiments, "Induiin A" is a commercially available lignln product obtained by acidifying the waste liquor from a sulfate and soda paper pulp process, whereas "Indulin C" is the disodium derivative of "Indulin A."
[All values in mine] Mercaptan Sulfur per Liter oi Caustic Liguln Additive in l5% NaOH Moral tan Initial ono. ftcr Oxidation Mercanlb Min Rate Per ton Cone. Treatment Min.
with Air None 8. 3 4. 2 27 4% "lndulin A" 8.3 1.3 .45 4% "lndulln C 8.3 0.0 .55 N one e o. 1.1 .7 .027 4% "Induiin C". I. l .18 .002
Mermptan Sulfur in Hgdrocarbon istillates Merca tan Lignln Additive in 15% Noon Initial Mercaptan Extraction Per cent Per cent None 5% "lndulin C 0. 041
The above data show the efl'ectivcness of llgnln in facilitating the action of the caustic in removing mercaptans from a hydrocarbon distillate such as gasoline.
It is not intended that the process of the resent invention be limited to certain conditions of temperature and pressure hereinbefore described, for the many variations possible in carrying out the invention will be apparent to those skilled in the art.
We claim:
1. In a method of improving hydrocarbons the step of contacting a mercaptan-containing hydrocarbon distillate in the liquid phase with an aqueous alkaline reagent having lignin dissolved therein.
2. In a'method of improving hydrocarbons the step of contacting a mercaptan-containing hydrocarbon distillate in the liquid phase with an aqueous alkaline reagent having lignin dissolved therein in the presence of oxygen.
3. In a method of improving mercaptan-containing hydrocarbon distillate in liquid phase by treating the same with an aqueous alkaline reagent, the step of contacting a mercaptan-contaming aqueous alkaline reagent with oxygen in the presence of lignin dissolved therein, whereby the aqueous alkaline reagent may be recycled ior reuse in further treating said hydrocarbon.
4. In a method oi improving hydrocarbons the steps of contacting a mercaptan-containing hydrocarbon distillate in the liquid phase with an 5 aqueous alkaline reagent having lignin dissolved therein to remove mercaptans from the hydrocarbon, and treating the mercaptan-containing and lignin-containing alkaline reagent with oxygen to remove mercaptans from the reagent. whereby the aqueous alkaline treating reagent may be recycled to the hydrocarbon treating step.
5. In a method of improving hydrocarbons the steps of contacting a mercaptan-contalning hydrocarbon distillate in the liquid phase with an aqueous alkaline reagent having lignin dissolved therein, separating the hydrocarbon from the alkaline reagent containing the mercaptan, to remove mercaptans from the hydrocarbon, and treating the mercaptan-containing and lignincontaining alkaline reagent with oxygen to remove mercaptans from the reagent, said lignin having been obtained from a sulfate and soda pulp process, whereby the aqueous alkaline treating reagent may be recycled to the hydrocarbon treating step.
6. In a method of improving hydrocarbons the steps of contacting a mercaptan-containing hydrocarbon with an aqueous caustic solution having lignin dissolved therein, separating the hydrocarbon from the caustic solution containing the mercaptan, to remove mercaptans from the hydrocarbon, and treating the mercaptan-containing and lignin-containing caustic solution with oxygen to remove mercaptans from the reagent, said lignin having been obtained from a sulfate and soda pulp process, whereby the aqueous alkaline treating reagent may be recycled to the hydrocarbon treating step.
7. In a method of improving hydrocarbons containing sulfur compounds, comprising contacting a hydrocarbon distillate in the liquid phase with a first alkaline solution to remove free sulfur and hydrogen sulfide constituents normally present. and contacting the distillate with a second aqueous alkaline solution having liznin dissolved therein, said lignin having been obtained from av sulfate and soda pulp process.
ii. In a method of improving hydrocarbons the step of contacting a mercaptan-containing hydrocarbon distillate in the liquid phase with an aqueous alkaline reagent having lignin dissolved therein, said lignin having been obtained from a sulfate and soda paper pulp process.
9. In a method of improving hydrocarbons the step of contacting a mercaptan-containing hydrocarbon distillate in the liquid phase with an aqueous alkaline reagent having lignin dissolved therein, in the presence of oxygen, said lignin having been obtained from a sulfate and soda pap r Dull process.
10. In a method of improving mercaptan-containing hydrocarbon distillate in liquid phase by treating the same with an aqueous alkaline reagent, the step of contacting a mercaptan-containing aqueous alkaline reagent with oxygen in the presence of lignin dissolved therein, said lignin having been obtained from a sulfate and soda paper pulp process, whereby the aqueous alkaline reagent may be recycled for reuse in further treating said hydrocarbon.
ROBERT R. HIBBARD. FRANKLIN VEATCH.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,015,038 Pevere Sept. 17, 1935 2,272,594 Bender Feb. 10, 1942 2,315,530 Loyd Apr. 6, 1943 2,317,054 Henderson et al. Apr. 20, 1943 2,389,771 Bond Feb. 20, 1945 2,413,945 Bolt Jan. '7, 1947 OTHER REFERENCES Gordon et al., Chlorine as a Deodorant Pulp Manufacture," Paper Trade Journal. April 28. 1938, pages 81-85.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US663237A US2464576A (en) | 1946-04-18 | 1946-04-18 | Process for the removal of mercaptans from petroleum distillates with an aqueous alkaline reagent containing lignin and the regeneration of the spent alkaline reagent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US663237A US2464576A (en) | 1946-04-18 | 1946-04-18 | Process for the removal of mercaptans from petroleum distillates with an aqueous alkaline reagent containing lignin and the regeneration of the spent alkaline reagent |
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| Publication Number | Publication Date |
|---|---|
| US2464576A true US2464576A (en) | 1949-03-15 |
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| Application Number | Title | Priority Date | Filing Date |
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| US663237A Expired - Lifetime US2464576A (en) | 1946-04-18 | 1946-04-18 | Process for the removal of mercaptans from petroleum distillates with an aqueous alkaline reagent containing lignin and the regeneration of the spent alkaline reagent |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2529670A (en) * | 1948-07-31 | 1950-11-14 | Pure Oil Co | Sweetening gasoline |
| US2616832A (en) * | 1949-10-14 | 1952-11-04 | Standard Oil Dev Co | Treatment of petroleum distillates with an alkali and an aldehyde |
| US3178260A (en) * | 1961-03-02 | 1965-04-13 | Papel Loreto & Pena Pobre | Method for the oxidation of black liquor |
| US4392947A (en) * | 1981-09-30 | 1983-07-12 | Mobil Oil Corporation | Integrated refining process |
| WO2010151361A1 (en) * | 2009-06-25 | 2010-12-29 | Bp Corporation North America Inc. | Hydrocarbon conversion process additive and related processes |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2015038A (en) * | 1932-07-23 | 1935-09-17 | Texas Co | Process of sweetening petroleum hydrocarbons |
| US2272594A (en) * | 1939-10-20 | 1942-02-10 | Sinclair Refining Co | Refining of oil |
| US2315530A (en) * | 1941-07-31 | 1943-04-06 | Socony Vacuum Oil Co Inc | Method of sweetening oils |
| US2317054A (en) * | 1940-04-06 | 1943-04-20 | Pure Oil Co | Method of treating petroleum oils |
| US2369771A (en) * | 1944-04-20 | 1945-02-20 | Pure Oil Co | Removal of sulphur compounds from hydrocarbon oils |
| US2413945A (en) * | 1944-03-09 | 1947-01-07 | Standard Oil Co | Treating petroleum distillates |
-
1946
- 1946-04-18 US US663237A patent/US2464576A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2015038A (en) * | 1932-07-23 | 1935-09-17 | Texas Co | Process of sweetening petroleum hydrocarbons |
| US2272594A (en) * | 1939-10-20 | 1942-02-10 | Sinclair Refining Co | Refining of oil |
| US2317054A (en) * | 1940-04-06 | 1943-04-20 | Pure Oil Co | Method of treating petroleum oils |
| US2315530A (en) * | 1941-07-31 | 1943-04-06 | Socony Vacuum Oil Co Inc | Method of sweetening oils |
| US2413945A (en) * | 1944-03-09 | 1947-01-07 | Standard Oil Co | Treating petroleum distillates |
| US2369771A (en) * | 1944-04-20 | 1945-02-20 | Pure Oil Co | Removal of sulphur compounds from hydrocarbon oils |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2529670A (en) * | 1948-07-31 | 1950-11-14 | Pure Oil Co | Sweetening gasoline |
| US2616832A (en) * | 1949-10-14 | 1952-11-04 | Standard Oil Dev Co | Treatment of petroleum distillates with an alkali and an aldehyde |
| US3178260A (en) * | 1961-03-02 | 1965-04-13 | Papel Loreto & Pena Pobre | Method for the oxidation of black liquor |
| US4392947A (en) * | 1981-09-30 | 1983-07-12 | Mobil Oil Corporation | Integrated refining process |
| WO2010151361A1 (en) * | 2009-06-25 | 2010-12-29 | Bp Corporation North America Inc. | Hydrocarbon conversion process additive and related processes |
| US20100326880A1 (en) * | 2009-06-25 | 2010-12-30 | Bp Corporation North America Inc. | Hydrocarbon Conversion Process Additive and Related Processes |
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