[go: up one dir, main page]

US1568349A - Process of obtaining absolute propyl alcohol - Google Patents

Process of obtaining absolute propyl alcohol Download PDF

Info

Publication number
US1568349A
US1568349A US458835A US45883521A US1568349A US 1568349 A US1568349 A US 1568349A US 458835 A US458835 A US 458835A US 45883521 A US45883521 A US 45883521A US 1568349 A US1568349 A US 1568349A
Authority
US
United States
Prior art keywords
propyl alcohol
column
liquid
water
benzol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US458835A
Inventor
John A Steffens
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
US Industrial Alcohol Co
Original Assignee
US Industrial Alcohol Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by US Industrial Alcohol Co filed Critical US Industrial Alcohol Co
Priority to US458835A priority Critical patent/US1568349A/en
Application granted granted Critical
Publication of US1568349A publication Critical patent/US1568349A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/76Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
    • C07C29/80Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/76Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
    • C07C29/80Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
    • C07C29/82Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation by azeotropic distillation

Definitions

  • My invention relates particularly to a process of removing water from propyl alcohols but it has reference especially to the production of absolute propyl alcohol.
  • the object of my invention is to provide aprocess whereby the propyl alcohols, that is to say normal propyl alcohol or isop-ropyl alcohol, may be separated from the water contained therein and so that, if desired, ab-
  • solute propyl alcohol may be obtained in accordance with a commercially practicable system.
  • the object of my invention is to provide a process based upon the utilization of a third liquid which is miscible with the propyl alcohol but substa tially immiscible with water and which is of such a character that when the three constituents are present vapors of the same are evolved by distillation, containing a considerable percentage of water and the third liquid so that all of the water and the third liquid may be removed in this Way from the residual constituent which is the alcohol.
  • the evolved vapors are comprised of a ternary mixture of the three constituents.
  • This third liquid may be any one of a number of diiferentcompounds, such, for example, as benzol, carbon tetrachloride, hexane, etc., but I prefer to use benzol.
  • One of the objects of my invention is to avoid the necessity of using a large amount of benzol in carrying out the process.
  • a further object is to so arrange the process as to enable a close regulation thereof to be obtained, inasmuch as in my process the dehydration of the propyl alcohol is carried out in a column, the upper portion of which is fed continually with a quantity of the condensatev of fixed composition passing out of the top of the tower, and as a condensate rich in water is obtained with a comparatively small load being placed upon the auxiliary apparatus and as the propyl alcohol evolved in the form of vapor is re turned to the tower continually in the fornr of 'a liquid having a fixed composition obtained by a uniform rectification of the recovered propyl alcohol.
  • a further object is to so arrange the system as to enable the several operations to be carried out continuously, but so that the several operations may be carried out largely independently of the remaining operations, thus enabling the operator of the system to recover-Vin case at any time any one of the operations does not function. By reason of these features in my process the system may be operated continuously.
  • valved inlet pipe 1 for feeding continuously into the apparatus isopropyl alcohol and which may, for example, have a strength of 88%.
  • valved supply pipe 2 for sup-plying initially the desired quantity of the third liquid, as, for example, benzol, and for supplying to the system additional amounts of benzol to replace the small quantities thereof which are lost by evaporation therefrom.
  • the propyl alcohol and benzol ar fed to the system in proportions such that in the system, at any given time, there would be approximately equal parts by weight of propyl alcohol and benzol therein but preferably a slightly smaller quantity of the benzol than of the propyl alcohol.
  • the valved pipe 1 leads into a tail-box 3 which is connected by a liquid sealed pipe 4 to a dehydrating column 5 which is constructed in any suitable man? ner but which may have, for example, a plurality of plates the same as in the case of the usual ethyl alcohol rectifying column.
  • the column 5 has at the bottom an inlet 6 for steam for heating the column indirectly.
  • Vapors are evolved from the column com: prising approximately 12% by weight of propyl alcohol, 8% by weight of water and 73% by weight of benzol, and absolute propyl alcohol flows from the liquid sealed drain pipe 7.
  • the evolved vapors pass out by means of a pipe 8 into a dephlegmator 9 which is connected by a liquid sealed pipe 10 to the top plate of the column.
  • T e dephlegmator is cooled in the usual way with the aid of water inlet and outlet pipes 11 and 12.
  • the uncondensed vapors from the dephlegmator 9 pass into a condenser 13 through a pipe 13, the temperature in which is at approximately 665 (1., said condenser being cooled by Water passing through lnlet and outlet pipes 14 and 15 and-the condensate therefrom enters a vented sight-glass 16 from which a portion of the condensate passes through a valved pipe 17 to the plpe l0 and thence to the top of the column 5.
  • the main portion of the condensat is conducted by a pipe 18 to a tail-box 19 and thence by a plpe 20 to a separating chamber 21.
  • the liquld received in the separatlng chamber immediately separates into two layers, the upper layer of which is rich in benzol but poor in propyl alcohol and water, while the lower layer is rich in propyl alcohol and Water but poor in benzol.
  • the composition of the respectlve layers 1s approximately as follows: The upper layer contains approximately 79% by welght of benzol, 3% by weight of water, and 18% by weight of propyl alcohol, while the lower layer contains approximately by weight of benzol, 73.5% by weight of water, and 26% by weight of propyl alcohol.
  • Th upper layer is conveyed by a vented pipe 22, having a liquid seal 23, back to the tower 5 while the lower layer passes by a vented plpe 24 to a propyl alcohol rectifying column 25 having a steam inlet pipe 26 in the usual way for indirect heating and a liquid sealed drawofi' pipe 27 for water at the bottom of the column.
  • Th lower portion of the column 25 is maintained at a temperature of just above 100 C.
  • the evolved propyl alcohol vapors containing some water pass out of the top of the column through a pipe 28 to a dephlegmator 29, constructed substantially the same as th dephlegmator 9 and which is arranged to return the condensate therein to the top of the column 25 by a liquid sealed pipe 30.
  • the vapors from the dephlegmator 29 pass through a pip 31, the vapors in which are at a temperature of approximately 0., to a condenser 32 constructedthe same as the condenser 13.
  • the condensate from the condenser 32 which comprises approximately 88% propyl alcohol enters'a vented sight-glass 33 and a portion of the same passes back through a valved pipe 34 to th liquid sealed pipe 38 and thence to the top of the column 25,
  • the apparatus While the remainder thereof enters a tailbox 35 and is conveyed therefrom by a valved pipe 36 direct to the liquid sealed pipe 23 and thence to the column 5.
  • the apparatus is also arranged in an elfective 70 manner in that the portions thereof requiring observation are located upon an operating floor 37.
  • the propyl alcohol containing water and benzol is fed into the column 5, the lower portion of which is maintained at a temperature slightly below 825 C.
  • the vapors of propyl alcohol, water and benzol will be distilled from the top of the column 5 thus leaving behind absolute propyl alcohol which passes out of thebottom of the column through the pipe 7.
  • the evolved vapors pass into the dephlegmator 9, whence some of the condensate is returned to the topmost plate in the column 5, and at the same time a small portion of the condensate from the condenser 13 is also conveyed into the tower at the same point, thus sealing the uppermost plates in the column with a liquid of a constant composition and which is very close to the composition of the evolved vapors.
  • This column is required merely to rectify the propyl alcohol, said column at its lower portion being maintained at a temperature of approximately 100 C., the water from which passes out from the bottom of the column, while the propyl alhool is collected as a condensate having a fixed composition which is returned to the column 5.
  • the propyl alcohol returned to the column 5 has a definite composition and temperature, and as the benzol has been substantially entirely removed therefrom, the conditions in the upper portion of the column 5 are comparatively uni- 129 form so far as the character of the incoming propyl alcohol is concerned.
  • the process which comprises cont-inuously rectifying a propyl alcohol, water and benzol, separating the condensate obtained from the evolved vapors so as to remove therefrom the benzol, returning the benzolto the rectifier, rectifying the residue of the condensate, obtaining therefrom a propyl alcohol of a fixed composition and returning the same to the first mentioned rectifier, thereby obtaining an absolute propyl alcohol.
  • the process which comprises continuously rectifying a propyl alcohol, water and benzol, separating t e bulk of the'condensate obtained from the evolved vapors so to remove therefrom the benzol, returning the benzol to the rectifier, rectifying the residue of the condensate, obtaining therefrom a propyl alcohol of a fixed composition and returnin the same to the first mentioned rectifier, t e unseparated portion of the condensate being returned to the top of the first mentioned rectifier, thereby obtainit in liquid form to the column near the top thereof.
  • substantially anhydrous propyl alcohol which comprises rectifying in a column a mixture. of a propyl alcohol. water and a third liquid which is miscible with the alcohol but substantially immiscible with water, condensing the vapors evolved and returning part thereof to the top of the column, separating the alcohol and the third liquid from the remaining condensate, rectifying the alcohol, and returning it in liquid form with the third liquid to the column at a point below the point of introduction of the aforesaid condensate.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Jan. 5 1926. 1,568,349
- J. A. STEFFENS' PROCESS OF OBTAINING ABSOLUTE PROPYL ALCOHOL Filed April 5, 1921 5 z 11 1/ I Z Patented Jan. 5, 1926.
UNITED STATES PATENT OFFICE.
JOHN A. STEFFENS, OF BALTIMORE, MARYLAND, ASSIGNOR TO U. S. INDUSTRIAL ALCOHOL 00., A CORPORATION OF WEST VIRGINIA.
PROCESS OF OBTAINING ABSOLUTE PROPYL ALCOHOL.
Application filed April 5, 1921. Serial No. 458,835.
To all whom it may concern:
Be it known that I, JOHN A. STEFFENS, a citizen of the United States, residing at Baltimore, State of Maryland, have invented .a certain new and useful Improvement in Processes of Obtaining Absolute Propyl Alcohol, of which the following is a specification.
My invention relates particularly to a process of removing water from propyl alcohols but it has reference especially to the production of absolute propyl alcohol.
The object of my invention is to provide aprocess whereby the propyl alcohols, that is to say normal propyl alcohol or isop-ropyl alcohol, may be separated from the water contained therein and so that, if desired, ab-
solute propyl alcohol may be obtained in accordance with a commercially practicable system.
More particularly, the object of my invention is to provide a process based upon the utilization of a third liquid which is miscible with the propyl alcohol but substa tially immiscible with water and which is of such a character that when the three constituents are present vapors of the same are evolved by distillation, containing a considerable percentage of water and the third liquid so that all of the water and the third liquid may be removed in this Way from the residual constituent which is the alcohol. The evolved vapors are comprised of a ternary mixture of the three constituents. This third liquid may be any one of a number of diiferentcompounds, such, for example, as benzol, carbon tetrachloride, hexane, etc., but I prefer to use benzol.
One of the objects of my invention is to avoid the necessity of using a large amount of benzol in carrying out the process.
A further object is to so arrange the process as to enable a close regulation thereof to be obtained, inasmuch as in my process the dehydration of the propyl alcohol is carried out in a column, the upper portion of which is fed continually with a quantity of the condensatev of fixed composition passing out of the top of the tower, and as a condensate rich in water is obtained with a comparatively small load being placed upon the auxiliary apparatus and as the propyl alcohol evolved in the form of vapor is re turned to the tower continually in the fornr of 'a liquid having a fixed composition obtained by a uniform rectification of the recovered propyl alcohol.
A further object is to so arrange the system as to enable the several operations to be carried out continuously, but so that the several operations may be carried out largely independently of the remaining operations, thus enabling the operator of the system to recover-Vin case at any time any one of the operations does not function. By reason of these features in my process the system may be operated continuously.
Further objects will appear from the detailed description thereof contained hereinafter.
While my invention is capable of embodiment in many different forms, for the purpose of illustration I shall describe only certain ways in which my invention may be carried out, and while my invention is capable of being carried out in connection with many different types of apparatus, I have shown only one form of the same in the accompanying drawings, in which- The figure is a diagrammatic representation of an apparatus which may be used in connection with my invention.
In the drawings, I have shown a valved inlet pipe 1 for feeding continuously into the apparatus isopropyl alcohol and which may, for example, have a strength of 88%. Leading into the pipe 1 there is a valved supply pipe 2 for sup-plying initially the desired quantity of the third liquid, as, for example, benzol, and for supplying to the system additional amounts of benzol to replace the small quantities thereof which are lost by evaporation therefrom. The propyl alcohol and benzol ar fed to the system in proportions such that in the system, at any given time, there would be approximately equal parts by weight of propyl alcohol and benzol therein but preferably a slightly smaller quantity of the benzol than of the propyl alcohol. The valved pipe 1 leads into a tail-box 3 which is connected by a liquid sealed pipe 4 to a dehydrating column 5 which is constructed in any suitable man? ner but which may have, for example, a plurality of plates the same as in the case of the usual ethyl alcohol rectifying column. The column 5 has at the bottom an inlet 6 for steam for heating the column indirectly.
' Vapors are evolved from the column com: prising approximately 12% by weight of propyl alcohol, 8% by weight of water and 73% by weight of benzol, and absolute propyl alcohol flows from the liquid sealed drain pipe 7. The evolved vapors pass out by means of a pipe 8 into a dephlegmator 9 which is connected by a liquid sealed pipe 10 to the top plate of the column. T e dephlegmator is cooled in the usual way with the aid of water inlet and outlet pipes 11 and 12. The uncondensed vapors from the dephlegmator 9 pass into a condenser 13 through a pipe 13, the temperature in which is at approximately 665 (1., said condenser being cooled by Water passing through lnlet and outlet pipes 14 and 15 and-the condensate therefrom enters a vented sight-glass 16 from which a portion of the condensate passes through a valved pipe 17 to the plpe l0 and thence to the top of the column 5. The main portion of the condensat is conducted by a pipe 18 to a tail-box 19 and thence by a plpe 20 to a separating chamber 21. The liquld received in the separatlng chamber immediately separates into two layers, the upper layer of which is rich in benzol but poor in propyl alcohol and water, while the lower layer is rich in propyl alcohol and Water but poor in benzol. The composition of the respectlve layers 1s approximately as follows: The upper layer contains approximately 79% by welght of benzol, 3% by weight of water, and 18% by weight of propyl alcohol, while the lower layer contains approximately by weight of benzol, 73.5% by weight of water, and 26% by weight of propyl alcohol. Th upper layer is conveyed by a vented pipe 22, having a liquid seal 23, back to the tower 5 while the lower layer passes by a vented plpe 24 to a propyl alcohol rectifying column 25 having a steam inlet pipe 26 in the usual way for indirect heating and a liquid sealed drawofi' pipe 27 for water at the bottom of the column. Th lower portion of the column 25 is maintained at a temperature of just above 100 C. The evolved propyl alcohol vapors containing some water pass out of the top of the column through a pipe 28 to a dephlegmator 29, constructed substantially the same as th dephlegmator 9 and which is arranged to return the condensate therein to the top of the column 25 by a liquid sealed pipe 30. The vapors from the dephlegmator 29 pass through a pip 31, the vapors in which are at a temperature of approximately 0., to a condenser 32 constructedthe same as the condenser 13. The condensate from the condenser 32, which comprises approximately 88% propyl alcohol enters'a vented sight-glass 33 and a portion of the same passes back through a valved pipe 34 to th liquid sealed pipe 38 and thence to the top of the column 25,
While the remainder thereof enters a tailbox 35 and is conveyed therefrom by a valved pipe 36 direct to the liquid sealed pipe 23 and thence to the column 5. The apparatus is also arranged in an elfective 70 manner in that the portions thereof requiring observation are located upon an operating floor 37.
In carrying out my invention the propyl alcohol containing water and benzol is fed into the column 5, the lower portion of which is maintained at a temperature slightly below 825 C. The vapors of propyl alcohol, water and benzol will be distilled from the top of the column 5 thus leaving behind absolute propyl alcohol which passes out of thebottom of the column through the pipe 7. The evolved vapors pass into the dephlegmator 9, whence some of the condensate is returned to the topmost plate in the column 5, and at the same time a small portion of the condensate from the condenser 13 is also conveyed into the tower at the same point, thus sealing the uppermost plates in the column with a liquid of a constant composition and which is very close to the composition of the evolved vapors. This not only provides uniform conditions at the top of the tower but enables the process to be conducted with a comparatively small quantity of benzol so that the condensate reaching the separating chamber 21 will be rich in the water to be removed. When the liquid condensate reaches the separating chamber 21 it immediately divides into two liquid phases forming layers, the upper layer, comprised principally of benzol, being conveyed back to the tower 5, while the lower layer, comprised principally of propyl alcohol and water but containing some benzol, is conducted to the propy alcohol rectifying column 25. This column is required merely to rectify the propyl alcohol, said column at its lower portion being maintained at a temperature of approximately 100 C., the water from which passes out from the bottom of the column, while the propyl alhool is collected as a condensate having a fixed composition which is returned to the column 5. Inasmuch as the propyl alcohol returned to the column 5 has a definite composition and temperature, and as the benzol has been substantially entirely removed therefrom, the conditions in the upper portion of the column 5 are comparatively uni- 129 form so far as the character of the incoming propyl alcohol is concerned. By prowriding a system of this character in which the several parts of the system operate without a great degree of dependence upon one another it is possible to conduct the process with great uniformity of results and in such a way that the failure of any portion of the system to function temporarily would not interfere with the elfective'operation of the 130 system as a whole. For these reasons, fur thermore, it is practicable to obtain absolute propyl alcohol with the process conT tinuously.
While I have described my invention above in detail I wish it to be understood that many changes may be made therein without departing from the spirit of the same.
I claim:
1. The process of obtaining absolute propyl alcohol from aqueous propyl alcohol, which consists in adding a third liquid thereto, miscible with the alcohol but substantially immiscible" with water; distilling the mixture to evolve a ternary constant boiling mixture and leave absolute propyl alcohol as a residue; returning to the top of the rectifier a portion of the evolved distillate as a reflux; condensing the remainder of the distillate and allowing it to separate into two layers; returning to the first named liquid undergoing distillation the layer richer in said third liquid; rectifying the alcoholic layer and'returning to said first named liquid the rectified alcohol.
2. The invention of claim 1 wherein the alcohol is continuously returned with a constant aqueous content.
39The process which comprises continuously rectifying a propyl alcohol, water and a third liquid, miscible with the propyl alcohol but substantially immiscible with water, separating the condensate obtained from the evolved vapors so as to remove therefrom the third liquid, returning the third liquid to the rectifier, rectifying the residue of the condensate, obtaining therefrom a propyl alcohol of a fixed composition and returning the same to the first mentioned rectifier.
4. The process which comprises continuously rectifying a propyl alcohol, water and a third liquid, miscible with the propyl alcohol but substantially immiscible with water, separating the bulk of the condensate obtained from the evolved vapors so as to remove therefrom the third liquid, returning the third liquid to the rectifier, rectifying the residue of the condensate, obtaining therefrom a propyl alcohol of a fixed composition and returning-the same to the first mentioned rectifier, the unseparated ortion of the condensate being returne to the top of the first'mentioned rectifier.
5. The processwhich comprises cont-inuously rectifying a propyl alcohol, water and benzol, separating the condensate obtained from the evolved vapors so as to remove therefrom the benzol, returning the benzolto the rectifier, rectifying the residue of the condensate, obtaining therefrom a propyl alcohol of a fixed composition and returning the same to the first mentioned rectifier, thereby obtaining an absolute propyl alcohol.
6. The process which comprises continuously rectifying a propyl alcohol, water and benzol, separating t e bulk of the'condensate obtained from the evolved vapors so to remove therefrom the benzol, returning the benzol to the rectifier, rectifying the residue of the condensate, obtaining therefrom a propyl alcohol of a fixed composition and returnin the same to the first mentioned rectifier, t e unseparated portion of the condensate being returned to the top of the first mentioned rectifier, thereby obtainit in liquid form to the column near the top thereof.
9. The process which comprises rectifying in a column a propyl alcohol, water, and a third liquid which is miscible with the a1 cohol but substantially immiscible with water, condensing the vapors evolved and returning part thereof to the top of the column, separating the alcohol from the remaining condensate, rectifying it, and returning it to the column below the point of introduction of the aforesaid condensed vapors.
10. The process of manufacturing substantially anhydrous propyl alcohol which comprises rectifying in a column a mixture. of a propyl alcohol. water and a third liquid which is miscible with the alcohol but substantially immiscible with water, condensing the vapors evolved and returning part thereof to the top of the column, separating the alcohol and the third liquid from the remaining condensate, rectifying the alcohol, and returning it in liquid form with the third liquid to the column at a point below the point of introduction of the aforesaid condensate.
11. The process which comprises rectifying propyl alcohol, water, and benzol, separating the alcohol from the vapors evolved, rectifying it, and returning it in liquid form to the rectification process.
In testimony that I claim the foregoing, I have hereunto set my hand this 26th day of January, 1921.
. JOHN A. STEFFENS.
US458835A 1921-04-05 1921-04-05 Process of obtaining absolute propyl alcohol Expired - Lifetime US1568349A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US458835A US1568349A (en) 1921-04-05 1921-04-05 Process of obtaining absolute propyl alcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US458835A US1568349A (en) 1921-04-05 1921-04-05 Process of obtaining absolute propyl alcohol

Publications (1)

Publication Number Publication Date
US1568349A true US1568349A (en) 1926-01-05

Family

ID=23822257

Family Applications (1)

Application Number Title Priority Date Filing Date
US458835A Expired - Lifetime US1568349A (en) 1921-04-05 1921-04-05 Process of obtaining absolute propyl alcohol

Country Status (1)

Country Link
US (1) US1568349A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2489619A (en) * 1948-08-23 1949-11-29 Standard Oil Dev Co Recovery of normal propyl alcohol from oxygenated compounds
US3052731A (en) * 1962-09-04 Process for purifying higher alcohols obtained
US4204915A (en) * 1977-03-19 1980-05-27 Mitsui Petrochemical Industries, Ltd. Process for azeotropic distillation

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3052731A (en) * 1962-09-04 Process for purifying higher alcohols obtained
US2489619A (en) * 1948-08-23 1949-11-29 Standard Oil Dev Co Recovery of normal propyl alcohol from oxygenated compounds
US4204915A (en) * 1977-03-19 1980-05-27 Mitsui Petrochemical Industries, Ltd. Process for azeotropic distillation

Similar Documents

Publication Publication Date Title
US2591671A (en) Dehydration of alcohols by extractive distillation
US2551593A (en) Extractive distillation of alcohols from close-boiling aqueous mixtures
US2595805A (en) Extractive distillation of closeboiling alcohols having partial immiscibility with water
US1676735A (en) Process of obtaining absolute alcohol
US2679472A (en) Separation of hydrocarbons by azeotropic distillation
US2555939A (en) Distillation of styrene from polymers
US2591712A (en) Extractive distillation of closeboiling organic compounds from their liquid mixtures
US2722506A (en) Separation of cumene or cymene from its respective hydroperoxide by distillation
US1911832A (en) Process for separating mixtures of substances only partially miscible
US1568349A (en) Process of obtaining absolute propyl alcohol
US2434796A (en) Process for the extractive distilla
US1524192A (en) Method for dehydrating organic liquids
US2017067A (en) Process and apparatus for dehydrating liquids
US2635992A (en) Separation and purification of alcohols by extractive distillation
US2461346A (en) Separation of hydrocarbons
US2388040A (en) Process for recovering toluene
US3575818A (en) Manufacture of absolute ethanol using pentane as azeotroping agent
US1586718A (en) Apparatus for obtaining absolute alcohol
US1508436A (en) Apparatus for recovering absolute alcohol free from foreign materials
US1830469A (en) Absolute alcohol process
US1586717A (en) Process of obtaining absolute alcohol
US2080194A (en) Apparatus and process for the continuous distillation-rectification of musts containing acetone, ethyl alcohol, and butyl-alcohol
US2095347A (en) Method of and apparatus for preparing in the pure state acetone, ethyl alcohol, and butyl alcohol from watery solutions
US2556248A (en) Ether purification by distillation and adsorption
US1508435A (en) Process of recovering absolute alcohol