US585347A - Julius stockhausen - Google Patents
Julius stockhausen Download PDFInfo
- Publication number
- US585347A US585347A US585347DA US585347A US 585347 A US585347 A US 585347A US 585347D A US585347D A US 585347DA US 585347 A US585347 A US 585347A
- Authority
- US
- United States
- Prior art keywords
- soap
- glycerin
- acid
- fats
- gelatinous
- 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
Links
- 239000000344 soap Substances 0.000 description 42
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 28
- 238000000034 method Methods 0.000 description 18
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 17
- 235000011187 glycerol Nutrition 0.000 description 15
- 239000003921 oil Substances 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000003925 fat Substances 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- 235000011121 sodium hydroxide Nutrition 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 239000003513 alkali Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 235000021313 oleic acid Nutrition 0.000 description 6
- 238000007127 saponification reaction Methods 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 150000002889 oleic acids Chemical class 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000003518 caustics Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 235000009001 Quillaja saponaria Nutrition 0.000 description 3
- 241001454523 Quillaja saponaria Species 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 150000002314 glycerols Chemical class 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- DICYJGINWGVIOA-UHFFFAOYSA-N 1,2,3-trihydroxypropane-1-sulfonic acid Chemical compound OCC(O)C(O)S(O)(=O)=O DICYJGINWGVIOA-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- 239000000006 Nitroglycerin Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- -1 alkaline earths Inorganic materials 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 229960001777 castor oil Drugs 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229960003711 glyceryl trinitrate Drugs 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000002316 solid fats Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
- C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C309/17—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing carboxyl groups bound to the carbon skeleton
Definitions
- the soap can be used to its greatest advantages in the hardest waters without requiring a previous softening of the water. By addinga comparatively small quantity of the soap the bath becomes as clear'as crystal in a few minutes when warmed.
- soap-baths used in dyeing have become decomposed, through any circumstances whatever, they are revivified to full usefulness by the addition of a small quantity of the gelatinous soap produced by my process. Even such baths which show separations of fatty acids produced by common soap are rendered entirely useful by the addition of a small qu antity of the new soap produced by the new process, whereas a dyeing-bath prepared solely with the new soap remains clear from beginning to end.
- soap-bark soap heretofore required in silk-dyeing will no longer be necessary if the gelatinous soap of my process is used.
- Such methods of dyeing in which the soap-bark soap was essential on account of its acid reaction produce much better results with the gelatinous soap and without the soapbark soap, and the baths never show any inj urious decomposition, which is of still greater importance.
- Baths prepared with the soap in question further have the property of fixing the coloring-matter added to the bath clearly and intensely on the fabrics and yarns.
- For coloring silks black the soap-bath produced by means of the gelatinous soap is of a value heretofore not attained.
- the separation of the sulfuric acid is accomplished best by neutralization and crystallization of the sulfates or by converting the sulfurized fats or oils into salts.
- this acid soap can be converted intoa neutral or basic soap by a corresponding addition of alkalies.
- my improved process is carried out as follows: One hundred parts, by weight, of castor-oil (or oleic acid, fluid oils, or solid fats) are separated into four to six lots, and in intervals of from one to four hours are mixed with thirty parts, by weight, of sulfuric acid of 66 Baum under constant stirring, but care must be taken to prevent the formation of sulfurous acid. This mixture is permitted to remain in a cool place for one to two days and during this time is stirred several times.
- the sulfurization of the oil or fat can also be accomplished by means of sulfoacids. Out of thispreparation the new gelatinous soap is made in the following manner:
- Second process To one hundred parts of the above-mentioned preparation one hundred to two hundred parts of alukewarm solution of common salt of 25 to 30 Baum are added for the purpose of eliminating any surplus free sulfuric acid or dirt or impurities. The mixture is stirred until the salt water has absorbed the above-named impurities and then the mixture is permitted to stand for one or two days, if necessary. Then the salt-lye and impurities are drawn off. To each one hundred parts of the cleaned preparation thirty-nine parts of caustic soda-lye of 36 to 37 Baum, as free as possible of carbonic acid, are added in one lot. The mixture is then heated to to 100 centigrade for obtaining a better chemical combination. The soap obtained is also acid and of gelatinous consistency. This soap can also be converted into a neutral or alkaline soap by the addition of lye, and it can be thinned by the addition of water.
- the soaps obtained by the first and second processes can be mixedwith each other or with suitable quantities of other neutral or alkaline soaps, according to the different branches of industry.
- the saponification of the above-mentioned preparation or other sulfonated oils, fats,- or oleic acids can be accomplished by means of caustic potash, caustic ammonia, carbonate of soda, carbonate of potash, carbonate of ammonia, alkaline earths, metal oxids, hydrates, or carbonates.
- the described process may be also used for softening hard water or for the purpose of preventing the formation of boiler-scale.
- the glycerin has been preserved in the soap by preventing it from entering the lye, with no other purpose than to increase the weight, and by the presence of this glycerin the action of the soap is not at all altered, nor is the soap improved; but this old method does not pay now that the glycerin has obtained a great importance, (e. g., in the manufacture of nitroglycerin, &.,)
- To-day big companies have grown up for making the costly glycerin by means of disassociating all sorts of fats and oils, and only afterward the oleic acids produced by the disassociation of fats and oils are saponified.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Description
UNITED STATES PATENT OFFICE.
JULIUS STOCKHAUSEN, OF OREFELD, GERMANY.
PROCESS OF MAKING SOAP.
SPECIFICATION forming part of Letters Patent No. 585,347, dated June 29, 1897.
Application filed February 26, 1896. Serial No. 580,507. (No specimens.)
T0 aZZ whom it may concern.-
Be it known that I, JULIUS STooKHAUsEN, a subject of the King of Prussia,Emperor of Germany, residing at Orei'eld, in the Kingdom of Prussia and German Empire, have invented certain new and useful Improvem cuts in Processes of Making Soap, of which the following is a specification.
The gelatinous soap made according to my improved process now to be described presents the following great technical advantages which are of special interest to the textile industries and dyeing: I
The soap can be used to its greatest advantages in the hardest waters without requiring a previous softening of the water. By addinga comparatively small quantity of the soap the bath becomes as clear'as crystal in a few minutes when warmed.
If the soap-baths used in dyeing have become decomposed, through any circumstances whatever, they are revivified to full usefulness by the addition of a small quantity of the gelatinous soap produced by my process. Even such baths which show separations of fatty acids produced by common soap are rendered entirely useful by the addition of a small qu antity of the new soap produced by the new process, whereas a dyeing-bath prepared solely with the new soap remains clear from beginning to end.
The use of soap-bark soap heretofore required in silk-dyeing will no longer be necessary if the gelatinous soap of my process is used. Such methods of dyeing in which the soap-bark soap was essential on account of its acid reaction produce much better results with the gelatinous soap and without the soapbark soap, and the baths never show any inj urious decomposition, which is of still greater importance. Baths prepared with the soap in question further have the property of fixing the coloring-matter added to the bath clearly and intensely on the fabrics and yarns. For coloring silks black the soap-bath produced by means of the gelatinous soap is of a value heretofore not attained.
The defect which always appears and removal of which has always been unsuccessfully attempted, that the fresh appearance of black and other colors has been marred by turbidities from a slight shade to crystalline not injuriously affected in the least by the use of this soap, but on the contrary a rich body of the threadthat is, a swelling of the same is attained with an uncommon flexibility. All these technical advantages are essentially attained by sulfurizing fats, oils, fatty acids, and oleic acids, the surplus of sulfuric acid being separated and the mass obtained being saponified, so that a gelatinous soap of acid reaction is obtained. This soap may be used for all purposes, but presents special advantages for technical uses, and among these for the purposes of dyeing, bleaching, and printing.
The separation of the sulfuric acid is accomplished best by neutralization and crystallization of the sulfates or by converting the sulfurized fats or oils into salts. According to the requirements of the industry this acid soap can be converted intoa neutral or basic soap by a corresponding addition of alkalies. In practice my improved process is carried out as follows: One hundred parts, by weight, of castor-oil (or oleic acid, fluid oils, or solid fats) are separated into four to six lots, and in intervals of from one to four hours are mixed with thirty parts, by weight, of sulfuric acid of 66 Baum under constant stirring, but care must be taken to prevent the formation of sulfurous acid. This mixture is permitted to remain in a cool place for one to two days and during this time is stirred several times. The sulfurization of the oil or fat can also be accomplished by means of sulfoacids. Out of thispreparation the new gelatinous soap is made in the following manner:
First process. To one hundred parts of this preparation sixty parts of caustic sodalye of 36 to 37 Baum, as free as possible of carbonic acid, are added in one lot either hotor cold, and the mixture is thoroughly and constantly stirred. This mixture is permitted to stand for from four to eight days until crystallization is completed or the completed soap has separated from the crystals. An acid soap is thus obtained which heretofore has not been possible in the industries. To neutralize this acid soap according to the requirements of the respective industries, a further quantity of the above mentioned caustic soda-lye of 36 to 37 is added and further addition of the lye produces an alkaline soap. In this manner acid, neutral, or alkaline soaps can be made by this process. The soap produced consists of a gelatinous mass. If for any reason it is desired to have the soap in a moreliquid state, this can easily be accomplished by adding water.
Second process. To one hundred parts of the above-mentioned preparation one hundred to two hundred parts of alukewarm solution of common salt of 25 to 30 Baum are added for the purpose of eliminating any surplus free sulfuric acid or dirt or impurities. The mixture is stirred until the salt water has absorbed the above-named impurities and then the mixture is permitted to stand for one or two days, if necessary. Then the salt-lye and impurities are drawn off. To each one hundred parts of the cleaned preparation thirty-nine parts of caustic soda-lye of 36 to 37 Baum, as free as possible of carbonic acid, are added in one lot. The mixture is then heated to to 100 centigrade for obtaining a better chemical combination. The soap obtained is also acid and of gelatinous consistency. This soap can also be converted into a neutral or alkaline soap by the addition of lye, and it can be thinned by the addition of water.
The soaps obtained by the first and second processes can be mixedwith each other or with suitable quantities of other neutral or alkaline soaps, according to the different branches of industry. The saponification of the above-mentioned preparation or other sulfonated oils, fats,- or oleic acids can be accomplished by means of caustic potash, caustic ammonia, carbonate of soda, carbonate of potash, carbonate of ammonia, alkaline earths, metal oxids, hydrates, or carbonates.
The described process may be also used for softening hard water or for the purpose of preventing the formation of boiler-scale.
The proportions of ingredients above given are by weight,
I am aware that it has been proposed to alter, by treatment with sulfuric acids, the glycerin contained in the oils and fats into a substance which combines with alkali and thus enters into the process of saponification. In the common process of saponification the glycerin produced out of the oils and fats by the saponification is separated, namely, up to five per cent. of glycerin, according to the nature of the fats. In olden times, when the value of glycerin was not yet known, this glycerin was judged to be offal or loss. By the addition of six parts of sulfuric acid of 66 Baum to one thousand parts of oil or fat, as heretofore proposed,'the glycerin contained in the oil would be'transformed into sulfoglycerin acid. In my process, however, I transform all the oil or fat, by an addition of thirty parts sulfuric acid at 66 Baum to one hundred parts of oil or fat, into a homogeneous completely-sulfonated mass, and it is not my intention to saponify the glycerin. The object of my invention is, on the contrary, to create by'the saponification of a perfectly-sulfonized oil a soap of an acid reaction and a gelatinous consistency which will be of great importance to the whole textile industry. Heretofore the glycerin has been preserved in the soap by preventing it from entering the lye, with no other purpose than to increase the weight, and by the presence of this glycerin the action of the soap is not at all altered, nor is the soap improved; but this old method does not pay now that the glycerin has obtained a great importance, (e. g., in the manufacture of nitroglycerin, &.,) To-day big companies have grown up for making the costly glycerin by means of disassociating all sorts of fats and oils, and only afterward the oleic acids produced by the disassociation of fats and oils are saponified.
In all important soap-houses where no previous disassociation of fats takes place the glycerin coming out after saponification is obtained by evaporating the remaining lye. For this purpose great chemical works have been established to obtain the glycerin from the remaining lye. Therefore in no soaphouses today is glycerin saponified, but everywhere the glycerin is recuperated.
Having thus described my invention, What I claim, and desire to secure by Letters Patent, is
1. The process for making soap of an acid reaction and a gelatinous consistency, which consists in completely sulfonizing fats, oils, fatty acids or oleic acids, separating the obtained product from the remaining sulfuric acid, and perfectly saponifying the sulfonized mass by a quantity of alkali equivalent to the existing fatty acids, freeing the produced soap from fatty acids and alkali, as set forth.
2. The process for making soap of a gelatinous consistency, which consists in com pletely sulfonizing fat-s, oils, fatty acids or oleic acids, separating the obtained product from the remaining sulfuric acid, perfectly saponifying the sulfonized mass by a quantity of alkali equivalent to the existing fatty acids, and finally transforming the acid soap produced into neutral or alkaline soap by a corresponding addition of alkali, as set forth.
In witnesswhereof I have hereunto set my hand in presence of two witnesses.
JULIUS STOCKHAUSEN.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US585347A true US585347A (en) | 1897-06-29 |
Family
ID=2654017
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US585347D Expired - Lifetime US585347A (en) | Julius stockhausen |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US585347A (en) |
-
0
- US US585347D patent/US585347A/en not_active Expired - Lifetime
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