US2096188A - Process for manufacturing soap and for recovering unsaponifiable ingredients including glycerine, alcohols, gases, water vapors, and other impurities - Google Patents
Process for manufacturing soap and for recovering unsaponifiable ingredients including glycerine, alcohols, gases, water vapors, and other impurities Download PDFInfo
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- US2096188A US2096188A US27672A US2767235A US2096188A US 2096188 A US2096188 A US 2096188A US 27672 A US27672 A US 27672A US 2767235 A US2767235 A US 2767235A US 2096188 A US2096188 A US 2096188A
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- United States
- Prior art keywords
- glycerine
- soap
- oil
- recovering
- gases
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D13/00—Making of soap or soap solutions in general; Apparatus therefor
- C11D13/02—Boiling soap; Refining
- C11D13/04—Continuous methods therefor
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D19/00—Recovery of glycerol from a saponification liquor
Definitions
- This invention relates to the process and apparatus for manufacturing chemical products, e. g. soap and glycerine from oils and fats, by means of spraying chemically interactive substances into steam.
- chemical products e. g. soap and glycerine from oils and fats
- the object of this invention is to produce a processior bringing about chemical reactions with steam, superheated or saturated, in such a manner that the reaction product, if non-volatile, results as a more or less dry and pulverulent mass, or as a more orless dry liquid. If there are formed both volatile and non-volatile substances, the two are readily separated in the process; the general purpose being to render a chemical process more expeditious and considerably cheaper than when carried out by present methods.
- saponifiable oils and fats can be saponified, with caustic alkali, primarily into soap and glycerine with. superheated steam.
- the drawing illustrates schematically a preferred form, of apparatus which may be employed for carrying out our improved process.
- the process contemplates the spraying and heating of the soap-making materials in such a manner that the water condensed from the caustic solution and from the superheated steam, the 'glycerine liberated from the oil or fat, and the small percentage of the volatile matter of an oily nature, are drawn off and collected. During the operation the proper amount of a current of superheated steam, is maintained.
- the oil and alkali in intimate mixture or emulsion can be done by the usual methods, or by sprayingthe oil into the alkali or the alkali in the oil, etc.
- the oil and alkali solution can be sprayed separately, in proper proportions, into the reaction chamber, in such a way that the two sprays are intimately mixed, preferably at a point of entering the chamber.
- the resultant soap is, of course, anhydrous, and within the range .of temperatures above stated and even at temperatures considerably below said range, the anhydrous soap is in a molten or semi-liquid or even in a liquid condition. All soaps when heated to temperaturesrangingfrom 150 C. to 250 C. are dry.
- the melting temperatures of anhydrous soap lie generally between about 200 C. and 300 C. and these melting points are dependent upon the nature of materials employed.
- the salts of the pure fatty acids have melting points ranging from 220 C. to 270 C., and inasmuch as all com-.dorfal .soaps contain impurities and mixtures of salts of diiferent fatty acids, the anhydrous soaps have melting points at temperatures below the melting point of that ofthe highest melting. point.
- the point at which glycerineboils at atmospheric pressure is around 290 C. We therefore preferably employ temperatures high enough to produce a distillation of all of the glycerine formed during the hydrolysis of the fatty acids.
- the volatile oil (floating on the surface) can be readily separated from the glycerine-water solution, the latter evaporated down to any consistency required. It is also understood, that through suitable apparatus the glycerine can be evaporated down to proper concentration in'one and the same set. of apparatus.
- An inert salt such as sodium silicate, borax,
- sodium-perborate, sodium carbonate, trisodium dium carbonate, trisodium phosphate also other suitable additions in the form of other substances .
- suitable additions in the form of other substances such as waxes, heavy mineral oils, can be either added to the mixture to be sprayed, before spraying, or can be sprayed into the reaction chamber separately. this substance in intimate mixture.
- the resultant soap then contains volatile product and calcium carbonate, which ing the precipitated matter formed during the operation.
- the process canbe applied to a large variety of chemical reactionsby thus spraying chemically reactive substances into steam, ordinary, or superheated.
- the steam itself can be the carrier of one or more of the chemically reactive substances, with which the chemicals sprayed react.
- the sprayed substances need not be liquids, they may be gases or solids, the latter preferably in'a flnely divided state, or colloidal in nature. Again, they may be mixtures of gases, of gases and liquids, of gases, liquids and solids solids and gases, etc.. .etc.
- a and B are tanks, C a steam superheater, D aheating device, E a reaction chamber,
- F a condenser and GG' and HH' pumps.
- l is a pipe and 2
- I, 0, I, II, II, I, I4 and 20 are valves
- 22 is an oil burner
- 24 a spraying device.
- valve 6 leading-to theheating device D and exit 5 valves I are also opened, as is valve leading to the reaction chamber E.
- Valves l0 and H on pipes I! and I8 are now opened and the pumps GG and HH started.
- the oil and alkali are now pumped through-pipes i9 and 20 through the heater D, valves 28 and 29 being opened and so regulated that equimolecular quantities-of oil and alkali can enter through the spraying device 24, projecting into reaction chamber E as shown at 23.
- the soap formed in chamber E can be removed through the door 2
- 21 represents the flue extending from the steam superheater C.
- 26 represents the inlet for the cooling water for condenser F.
- 25 represents the outlet for same.
- a process of producing an anhydrous soap and glycerine in a reaction chamber through which continuously flows a stream of super-heated steam which consists in spraying an unsaponified mixture of fat or oil and a caustic alkali solution in commingling relationship in'said stream of super-heated steam, thereby effecting immediate and complete saponification of the saponifiable constituents of said fat or oil and removal of the glycerine, moisture and other unsaponifiable constituents, and then recovering the anhydrous soap and glycerine.
Description
Oct. 19, 1937. H. w. F. LORENZ ET AL 2,096,188 PROCESS FOR MANUFACTURING SOAP AND FOR RECOVERING UNSAPONIFIABLE INGREDIENTS INCLUDING GLYCERINE, ALCOHOLSK, GASES, WATER VAPORS, AND OTHER IMPURITHES Original Filed April 15. 1920 INVENTORS v Henry 1 1/ F L orenz Hederick F r0 2?. Y
ATTORNEY.
Patented Oct. 19, 1937 1 PROCESS FOR MANUFACTURING SOAPv AND FOR RECOVERING UNSAPONIFIABLE IN- GREDIENTS INCLUDING GLYCERINE, AL- COHOLS, GASES, WATER VAPORS, AND- OTHER IMPURITIES Henry W. F. Lorenz, Jersey City, N. J., and Frederick W. Brown, New York, N. Y., assignors, by direct and mesne assignments, of thirty-three and one-third per cent to said Lorenz, thirtythree and one-third percent to Theodore M. Sewar'ds, and thirty-three and one-third .per cent to Charles H. Wilson, both of New York,
Reflled for application Serial No. 374,179,'April 15, 1920. This application June.21, 1935, Serial 6 Claims.
This invention relates to the process and apparatus for manufacturing chemical products, e. g. soap and glycerine from oils and fats, by means of spraying chemically interactive substances into steam.
The object of this invention is to produce a processior bringing about chemical reactions with steam, superheated or saturated, in such a manner that the reaction product, if non-volatile, results as a more or less dry and pulverulent mass, or as a more orless dry liquid. If there are formed both volatile and non-volatile substances, the two are readily separated in the process; the general purpose being to render a chemical process more expeditious and considerably cheaper than when carried out by present methods. Thus saponifiable oils and fats can be saponified, with caustic alkali, primarily into soap and glycerine with. superheated steam.
' The process and apparatus invented by us can be very well illustrated by the example of producing soap and glycerine, as will be described below: In soap 'manufacture in the usual way the oils or fats are mixed with an excess of caustic alkali and boiled in an enclosed or open kettle until saponiflcation is complete. The soap lye is salted out and the glycerine extracted and re fined. By our process an excess of alkali is not needed, in fact, only the exact amount of alkali required for neutralizing the fatty acids need be used, a neutral soap being obtained in one operation. Again, we obtain a practically pure grade of glycerine, free from caustic alkali, salt, or other inorganic impurities; Also, practically all the glycerine is nicely and smoothly separated from the soap residue.
The invention consists in the process, to be more fully described hereinafter and particularly set forth in the claims. Said invention may have the apparatus modified to suit'the nature of the reacting substances. v
The process can be carried out in a. number of ways and with a variety of apparatus without departing from the spirit of our invention.
Other objectives and aims of the invention,
more or less specific than those referred to above, will be in part obvious and in part pointed out in. the course of the following description of the various steps of our process, and the relation of one or moreof said steps to the others thereof,
constituting the invention; and the scope of protection contemplated will be indicated in the appended drawing wherein we have illustrated schematically, a form of apparatus which may be employed to carry out our invention; The figure illustrates in vertical section and in elevation, said apparatus.
The drawing illustrates schematically a preferred form, of apparatus which may be employed for carrying out our improved process.
Before proceeding to a detailed description of the parts of the apparatus-and the manner of carrying out the process, it may facilitate the disclosure to state that the process contemplates the spraying and heating of the soap-making materials in such a manner that the water condensed from the caustic solution and from the superheated steam, the 'glycerine liberated from the oil or fat, and the small percentage of the volatile matter of an oily nature, are drawn off and collected. During the operation the proper amount of a current of superheated steam, is maintained.
Referring more particularly to the parts, and describing the process more fully, we may say that one method of carrying out our process is to mix, or emulsify, the oil or fat with a suitable oil and caustic alkali striking the current of.
superheated steam' in the reaction chamber causes the instant saponificationo-f the oil with (1) the formation of a dry precipitate of soap on the bottom of said chamber, (2) the liberation of glycerine and some volatile oil which pass 0115 with the steam and are condensed in the receiver. Thus, for every one hundred pounds of the fat or oil, approximately thirteen and onehalf pounds of caustic soda, or twenty pounds of caustic potash, dissolved in twenty-five to thirty pounds of water would be required to form the spraying mixture.
Obviously, to obtain a high yield of glycerine and to ensure the immediate and complete saponification of the oil or fat the temperature of the superheated steam must be sufliciently high to bring this about. We have found that a temperature of about 250-300 degrees, centigrade,
to have the oil and alkali in intimate mixture or emulsion. This latter can be done by the usual methods, or by sprayingthe oil into the alkali or the alkali in the oil, etc. Again, the oil and alkali solution can be sprayed separately, in proper proportions, into the reaction chamber, in such a way that the two sprays are intimately mixed, preferably at a point of entering the chamber.
While the spraying can also be accomplished with air, or better with an indifferent gas, we prefer to use .steam, ordinary or superheated, for the purpose. For instance, to prepare soap and glycerine from cottonseed oil we may proceed as follows:-.-
Emulsify' four hundred and thirty pounds of cottonseed oil and fifty-eight pounds of caustic soda dissolved in one hundred pounds of water.
Spray this mixture with superheated steam into a receptacle or chamber heated to 250-290 degrees, centigrade. By means .of superheated steam which is passed into and through said chamber, the latter having an outlet connected with a condensing system for the glycerine, water, and a small quantity of a volatile alcohol (probably cholesterin and phytosterin).
Within the range of temperatures above set forth to which the sprayed material or materials are heated in the current or in the atmosphere of super-heated steam, the resultant soap is, of course, anhydrous, and within the range .of temperatures above stated and even at temperatures considerably below said range, the anhydrous soap is in a molten or semi-liquid or even in a liquid condition. All soaps when heated to temperaturesrangingfrom 150 C. to 250 C. are dry. The melting temperatures of anhydrous soap lie generally between about 200 C. and 300 C. and these melting points are dependent upon the nature of materials employed. The salts of the pure fatty acids have melting points ranging from 220 C. to 270 C., and inasmuch as all com-. mercial .soaps contain impurities and mixtures of salts of diiferent fatty acids, the anhydrous soaps have melting points at temperatures below the melting point of that ofthe highest melting. point.
of the constituent. The impurities always present in soaps also tendto lower the melting points thereof. f
The point at which glycerineboils at atmospheric pressure is around 290 C. We therefore preferably employ temperatures high enough to produce a distillation of all of the glycerine formed during the hydrolysis of the fatty acids.
Obviously, we can saponify an oil or fat first in the usual way and spray the mixture into the reaction chamber through which is passing super-'- heated steam, and thus distill oil the glycerine.
In the distillate, the volatile oil (floating on the surface) can be readily separated from the glycerine-water solution, the latter evaporated down to any consistency required. It is also understood, that through suitable apparatus the glycerine can be evaporated down to proper concentration in'one and the same set. of apparatus.
An inert salt (such as sodium silicate, borax,
sodium-perborate, sodium carbonate, trisodium dium carbonate, trisodium phosphate, also other suitable additions in the form of other substances .such as waxes, heavy mineral oils, can be either added to the mixture to be sprayed, before spraying, or can be sprayed into the reaction chamber separately. this substance in intimate mixture.
It is understood that in carrying out other reactions (above described more particularly for soap making), by the method of spraying the chemically reactive substances into superheated steam, e. g. a current of superheated steam, the process and apparatus are modified to suit'the particular object in view. Two or more chemically reactive substances may be mixed before spraying (or sprayed separately) and dissolved in one another, or by emulsions Thus calcium acetate and calcium benzoate in admixture may be sprayed with superheated steam into a retort through which superheated steam is passing,
resulting in the formation of acetophenene, a
The resultant soap then contains volatile product and calcium carbonate, which ing the precipitated matter formed during the operation.
The process canbe applied to a large variety of chemical reactionsby thus spraying chemically reactive substances into steam, ordinary, or superheated. The steam itself can be the carrier of one or more of the chemically reactive substances, with which the chemicals sprayed react. Again, the sprayed substances need not be liquids, they may be gases or solids, the latter preferably in'a flnely divided state, or colloidal in nature. Again, they may be mixtures of gases, of gases and liquids, of gases, liquids and solids solids and gases, etc.. .etc.
The drawing, which is an elevation, repre-v sents one of various methods of carrying out our process. A and B are tanks, C a steam superheater, D aheating device, E a reaction chamber,
F a condenser and GG' and HH' pumps. l is a pipe and 2, I, 0, I, II, II, I, I4 and 20 are valves, 22 is an oil burner, 24 a spraying device.
In operation, a properquantity of saponiflable oil is introduced into tank A through pipe l5.
Into tank B, a strong caustic alkali solution just sufllcient for saponifying the oil in tank A, is
introduced through pipe Ii. Steam, obtained from any source, through pipe I is nowpermitted to enter the superheater C by opening valve 2,
valve 6 leading-to theheating device D and exit 5 valves I are also opened, as is valve leading to the reaction chamber E. Valves l0 and H on pipes I! and I8 are now opened and the pumps GG and HH started. The oil and alkali are now pumped through-pipes i9 and 20 through the heater D, valves 28 and 29 being opened and so regulated that equimolecular quantities-of oil and alkali can enter through the spraying device 24, projecting into reaction chamber E as shown at 23. The soap formed in chamber E can be removed through the door 2|. i. e. steam, glycerine, and volatile oil, pass from chamber E to condenser F and are collected through the outlet 9. 21 represents the flue extending from the steam superheater C. 26 represents the inlet for the cooling water for condenser F. 25 represents the outlet for same.
It will accordingly be seen that we have provided a process well adapted to attain, among others, all of the ends and objectives above pointed out, in an extremely facile manner; and that we have provided a better process for manufacturing soap and recovering the unsaponifiable products than haspbtained in processes. hitherto carried out. v
As many changes could be made in this construction without departing from the scope of the following claims, it is intended that all matter contained in the above description or shown in the accompanying drawing shall be interpreted as illustrative only and not in a limiting sense.
Having thus described our invention, what we claim as new and desire to secure by Letters Patent is: v
1. A process of producing an anhydrous soap and glycerine in a reaction chamber through which continuously flows a stream of super-heated steam, which consists in spraying an unsaponified mixture of fat or oil and a caustic alkali solution in commingling relationship in'said stream of super-heated steam, thereby effecting immediate and complete saponification of the saponifiable constituents of said fat or oil and removal of the glycerine, moisture and other unsaponifiable constituents, and then recovering the anhydrous soap and glycerine.
2. A process of producing an anhydrous soap and glycerine in a reaction chamber through which continuously flows a stream of super-heated steam, which consists in spraying separate streams of saponifiable fat or oil and a caustic alkali solution in commingling relationship in said stream of super-heated steam, thereby efl'ecting immediate and complete saponiflcation of the saponifiable constituent of said fat or oil and The volatile matter,
removal of the glycerine, moisture and other dasaponifiable constituents, and'then recovering the [I anhydrous soap and glycerine.
3. A process ofproducing an anhydrous soap and glycerine ina reaction chamber through which continuously flows a stream of super-heated steam, which consists in spraying saponifiable fat or oil and a caustic alkali solution in commingling relationship in said stream of superheated steam, thereby effecting immediate and complete saponification of the saponifiable constituents of said fat or oil and removal of the glycerine, moisture and other unsaponifl'able constituents, and then recovering the anhydrous soap and glycerine.
4. A process of producing an anhydrous soap and glycerine in a reaction chamber through which continuously flows a stream of super-heated steam' heated to a temperature ranging from 250 C. to 290 C., which consists in spraying saponifiable fat or oil and a caustic alkali solution in commingling relationship in said stream of super-heated steam, thereby effecting immediate v and complete saponification of the saponifiable caustic alkali solution in commingling relationship in said stream of super-heated steam, thereby efiecting immediate and complete saponification of the saponifiable constituents of .said fat or oil and removal of the glycerine, moisture and other unsaponifiable constituents, and then recovering'the anhydrous soap and glycerine.
6. A process of producing an anhydrous soap and. glycerine in a reaction chamber through which continuously flows a stream of super-heated steam heated to a temperature ranging from 250 C. to 300 0., which consists in spraying separate streams of saponifiable fat or oil and a caustic alkali solution in commingling relationship in said stream of super-heated steam, thereby efiecting immediate and complete saponification of the saponifiable constituents of said fat or oil and removal of the glycerine, moisture and other unsaponifiable constituents, and then recovering the anhydrous soap and glycerine.
HENRY W. F. LORENZ. FREDERICK W. BlItOWN.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27672A US2096188A (en) | 1935-06-21 | 1935-06-21 | Process for manufacturing soap and for recovering unsaponifiable ingredients including glycerine, alcohols, gases, water vapors, and other impurities |
GB28134/37A GB504117A (en) | 1935-06-21 | 1937-10-15 | Improvements in process of producing an anhydrous soap and glycerine |
FR828022D FR828022A (en) | 1935-06-21 | 1937-10-18 | Improvements to the process for the manufacture of anhydrous soap and glycerin |
BE424155D BE424155A (en) | 1935-06-21 | 1937-10-19 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27672A US2096188A (en) | 1935-06-21 | 1935-06-21 | Process for manufacturing soap and for recovering unsaponifiable ingredients including glycerine, alcohols, gases, water vapors, and other impurities |
GB28134/37A GB504117A (en) | 1935-06-21 | 1937-10-15 | Improvements in process of producing an anhydrous soap and glycerine |
FR828022T | 1937-10-18 | ||
BE424155T | 1937-10-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2096188A true US2096188A (en) | 1937-10-19 |
Family
ID=41347790
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US27672A Expired - Lifetime US2096188A (en) | 1935-06-21 | 1935-06-21 | Process for manufacturing soap and for recovering unsaponifiable ingredients including glycerine, alcohols, gases, water vapors, and other impurities |
Country Status (4)
Country | Link |
---|---|
US (1) | US2096188A (en) |
BE (1) | BE424155A (en) |
FR (1) | FR828022A (en) |
GB (1) | GB504117A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2422128A (en) * | 1941-08-09 | 1947-06-10 | Colgate Palmolive Peet Co | Process of preparing purified organic sulphonates |
ITUA20162615A1 (en) * | 2016-04-14 | 2017-10-14 | Desmet Ballestra S P A | CONTINUOUS SAPONIFICATION AND APPARATUS PROCESS |
ITUA20162614A1 (en) * | 2016-04-14 | 2017-10-14 | Desmet Ballestra S P A In Breve Ballestra S P A | REACTOR NOZZLE SAPONIFICATION METHOD |
-
1935
- 1935-06-21 US US27672A patent/US2096188A/en not_active Expired - Lifetime
-
1937
- 1937-10-15 GB GB28134/37A patent/GB504117A/en not_active Expired
- 1937-10-18 FR FR828022D patent/FR828022A/en not_active Expired
- 1937-10-19 BE BE424155D patent/BE424155A/xx unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2422128A (en) * | 1941-08-09 | 1947-06-10 | Colgate Palmolive Peet Co | Process of preparing purified organic sulphonates |
ITUA20162615A1 (en) * | 2016-04-14 | 2017-10-14 | Desmet Ballestra S P A | CONTINUOUS SAPONIFICATION AND APPARATUS PROCESS |
ITUA20162614A1 (en) * | 2016-04-14 | 2017-10-14 | Desmet Ballestra S P A In Breve Ballestra S P A | REACTOR NOZZLE SAPONIFICATION METHOD |
Also Published As
Publication number | Publication date |
---|---|
FR828022A (en) | 1938-05-09 |
BE424155A (en) | 1937-11-30 |
GB504117A (en) | 1939-04-17 |
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