US498000A - Alfred wohl and alexander kollrepp - Google Patents
Alfred wohl and alexander kollrepp Download PDFInfo
- Publication number
- US498000A US498000A US498000DA US498000A US 498000 A US498000 A US 498000A US 498000D A US498000D A US 498000DA US 498000 A US498000 A US 498000A
- Authority
- US
- United States
- Prior art keywords
- sugar
- acid
- sirup
- centigrade
- grams
- 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 23
- 235000020357 syrup Nutrition 0.000 description 16
- 101100476962 Drosophila melanogaster Sirup gene Proteins 0.000 description 15
- 239000002253 acid Substances 0.000 description 15
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 15
- 235000002918 Fraxinus excelsior Nutrition 0.000 description 11
- 239000002956 ash Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229960004903 invert sugar Drugs 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 229930006000 Sucrose Natural products 0.000 description 5
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229960004793 sucrose Drugs 0.000 description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 3
- 230000029087 digestion Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 3
- 239000011975 tartaric acid Substances 0.000 description 3
- 235000002906 tartaric acid Nutrition 0.000 description 3
- MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 235000013736 caramel Nutrition 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 150000004677 hydrates Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- PJVXUVWGSCCGHT-ZPYZYFCMSA-N (2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanal;(3s,4r,5r)-1,3,4,5,6-pentahydroxyhexan-2-one Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O.OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO PJVXUVWGSCCGHT-ZPYZYFCMSA-N 0.000 description 1
- ORKBYCQJWQBPFG-WOMZHKBXSA-N (8r,9s,10r,13s,14s,17r)-13-ethyl-17-ethynyl-17-hydroxy-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one;(8r,9s,13s,14s,17r)-17-ethynyl-13-methyl-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthrene-3,17-diol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1.O=C1CC[C@@H]2[C@H]3CC[C@](CC)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 ORKBYCQJWQBPFG-WOMZHKBXSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000015107 ale Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K3/00—Invert sugar; Separation of glucose or fructose from invert sugar
Definitions
- invert sugar Prior to this invention the production of invert sugar has been performed as follows:- Cane sugar is dissolved in water to form a diluted solution; this solution is mixed with acid, and the mixture subjected to heat; after heating, the acid is neutralized by means of alkalies (carbonates or hydrates) and the neutralized solution carefully evaporated in a vacuum pan at the lowest temperature admissible in order to obtain the product in a merchantable form ready for use. No process, however, is known, which permits the inversion of cane sugar sirup of the same density as required for the sirup, t'. 6. without the necessity of concentration subsequent to inversion.
- the new process consists in simply melting together cane sugar and water in the proportion required by the degree of concentration of the sirup to be prepared, and digesting the mixture together with a very small quantity of acid, for instance hydrochloric acid, dependent upon the ashes contained in the sugar.
- a very small quantity of acid for instance hydrochloric acid
- the process comprises the following successive operations: first, estimation of the ashes of the sugar to be transformed into invert sugarsirup; second, melting the mixture of sugar and water; third, digesting the same with acid; fourth, neutralizingtheacid; fifth, filtering the sirup.
- the estimation of the ashes is carried out in the usual manner, viz: by heat ing a sample of the sugar to be inverted together with sulphuric acid. In case the quantity of resulting ashes is less than 0.03 per cent. of the weight of the sugar, to each one hundred kiligrams of sugar is added a watery solution containing ten grams of hydrochloric acid, (E01,) free from hydrate. In case of a greater proportion of ashes, sufficient hydrochoric acid has to be added in such excess to the above quantity that the proportion of hydrochloric acid free from hydrate (H01) is equal to 0.4 of the weight of the ashes.
- the melting of the sugar isoperated in an open pan provided with a jacketed bottom to receive steam.
- the said pan should moreover be provided with a stirrer, so as to facilitate mechanical stirring.
- To each one hundred parts by weight of sugar are added ten to fifty parts of water according to the desired degree of concentration of the invert sugar sirup to be produced.
- the mixture is heated to to 110 centigrade under constant stirring. While the proportion of water here given gives the best results, and aless amount of water will probably not be used in practice, we do not limit our to these exact figures, as it is possible that a slightly greater amount of water than fifty parts might be used under some circumstances without seriously prejudicing the result.
- the saccharine solution formed by this mixing of sugar and water must contain, however, sixty per cent. or more of sugar.
- the sirup thus obtained is passed through a fine sieve in order to remove any mechanical impurities, and cooled down, when it is ready for use.
- sirup corresponding to half the normal weight of cane sugar and dissolved in as much water as to obtain one hundred cubic centimeters, will, on observation at 20 centigrade, show a levorotation equal to twelve degrees of the saccharometer.
- the sirup contains 0.008 per cent. of free hydrochloric acid which is neutralized by the addition of 0.23 kilograms of bicarbonate of soda so that the sirup finally contains 0.013 per cent. of chloride of sodium.
- the proportion of hydrochloric acid has to be increased as fol.lows:at 80 to 90 centigrade twenty grams of hydrochloric acid per one hundred kilograms of sugar and 0.425 of the ashes; at 70 to 80 centigrade, forty grams of hydrochloric acid per one hundred kilograms of sugar and 0.45 of the ashes.
- H01 otheracids maybemade use of, such as H1312,I-INO ,H 80 ,HFI, G H O (tartaric acid), C H O (citric acid), H PO or H 80 and in such proportion that there are employed, for each ten grams of hydrochloric acid twenty grams HBr, twenty grams I INO thirty grams H 80 fifty grams HFI, ninety grams tartaric acid, one hundred and twenty grams citric acid, one hundred and fifty grams H PO two hundred grams H 80 and in respect to the ashes: in lieu of 0.4 to 0.45 hydrochloric acid 0.7 to 0.8 H 80 0.45 to 0.5 HFl, 0.95 to 1.1 H PO 0.9 to 1.0 H 80 0.7 to 0.8 HNO 1.75 to 2.0 tartaric acid, 2.0 to 2.4 citric acid. In all cases the neutralization of the acid has to be performed by the equivalent quantity of an alkali (carbonate or hydrate).
- an alkali carbonate or hydrate
- the same process may be utilized for producing highly concentrated non-crystallizable sugar-solutions by inverting only half the quantity of sugar contained in the original solution. To this end the described process is so modified as to reduce to one- .third either the time of digestion or the proportion of acid which would be necessary for completely inverting all the sugar present in the solution.
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- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Organic Chemistry (AREA)
- Saccharide Compounds (AREA)
Description
UNITED STATES PATENT OFFICE.
ALFRED WOHL AND ALEXANDER KOLLREPP, OF BERLIN, GERMANY.
PROCESSOF MAKING INVERT SUGAR.
SPECIFICATION forming; part of Letters Patent No. 498,000, dated May 23, 1893.
Application filed April 22, 1891. Serial No. 890,072.
(No specimens.) Patented in France October 18, 183 and November 15,
1889i ,406; in Belgium October 19, 1889, No. 88,121, and November 16, 1889, No. 88,481; in England October 19 1889, No. 16,540; in Italy October 21,1889, LIV, 188, and November 16, 1889, LIV, 191; in Luxemburg December 8, 1889, No. 1,217; in Spain July 12, 1890, No. 10,731, and in Austria Hungary August 16,1890,No.49,445 and No. 30,255.
To all whom it may concern.-
Be it known that we, ALFRED \VOHL and ALEXANDER KOLLREPP, doctors of philoso: phy, subjects of the King of Prussia, and residing in Berlin, Kingdom of Prussia, German Empire, have invented new and useful Improvements in the Production of Invert Sugar, (for which we have obtained patents in Belgium October 19, 1889, No. 88,121, and November 16, 1889, No. 88,481; in France October 18, 1889, and November 15, 1889, No. 201,406; in Great Britain October 19,1889, No. 16,540; in Italy October 21, 1889, No. 188, Vol. LIV, and November 16, 1889, No. 191, Vol. LIV; in Austria-Hungary August 16, 1890, No. 49,445 and No. 80,255; in Luxemburg December 8, 1889, No. 1,217, and in Spain July 12, 1890, No. 10,731,) of which the following is a specification.
Prior to this invention the production of invert sugar has been performed as follows:- Cane sugar is dissolved in water to form a diluted solution; this solution is mixed with acid, and the mixture subjected to heat; after heating, the acid is neutralized by means of alkalies (carbonates or hydrates) and the neutralized solution carefully evaporated in a vacuum pan at the lowest temperature admissible in order to obtain the product in a merchantable form ready for use. No process, however, is known, which permits the inversion of cane sugar sirup of the same density as required for the sirup, t'. 6. without the necessity of concentration subsequent to inversion.
Now, we have invented a process by means of which sugar solutions of any degree of concentration, t'. e.,up to ninety per cent, may be completely inverted at any temperature up to 110 centigrade without causing formation of caramel or coloration of the sirups.
The new process consists in simply melting together cane sugar and water in the proportion required by the degree of concentration of the sirup to be prepared, and digesting the mixture together with a very small quantity of acid, for instance hydrochloric acid, dependent upon the ashes contained in the sugar.
The process comprises the following successive operations: first, estimation of the ashes of the sugar to be transformed into invert sugarsirup; second, melting the mixture of sugar and water; third, digesting the same with acid; fourth, neutralizingtheacid; fifth, filtering the sirup.
First. The estimation of the ashes is carried out in the usual manner, viz: by heat ing a sample of the sugar to be inverted together with sulphuric acid. In case the quantity of resulting ashes is less than 0.03 per cent. of the weight of the sugar, to each one hundred kiligrams of sugar is added a watery solution containing ten grams of hydrochloric acid, (E01,) free from hydrate. In case of a greater proportion of ashes, sufficient hydrochoric acid has to be added in such excess to the above quantity that the proportion of hydrochloric acid free from hydrate (H01) is equal to 0.4 of the weight of the ashes.
Second. The melting of the sugar isoperated in an open pan provided with a jacketed bottom to receive steam. In case more than two thousand kilograms of sugar are to be transformed at a time, the said pan should moreover be provided with a stirrer, so as to facilitate mechanical stirring. To each one hundred parts by weight of sugar are added ten to fifty parts of water according to the desired degree of concentration of the invert sugar sirup to be produced. The mixture is heated to to 110 centigrade under constant stirring. While the proportion of water here given gives the best results, and aless amount of water will probably not be used in practice, we do not limit ourselves to these exact figures, as it is possible that a slightly greater amount of water than fifty parts might be used under some circumstances without seriously prejudicing the result. The saccharine solution formed by this mixing of sugar and water must contain, however, sixty per cent. or more of sugar.
Third. As soon as the mass of sugar and wa ter is heated to the desired degree of temperature, whereby it is reduced to a partly molten state, acid is added in quantity calculated as stated, and the acidulated mass is subjected to digestion. Thisprocedure is continued for one-fourth hour with a digesting temperature of 100 to 110 centigrade; one-half hour with a digesting temperature of 90 to 100 centigrade; one hour with a digesting temperature of to centigrade; two hours with a digesting temperature of 70 to 80 centigrade. Within this lapse of time the sugar will completely be transformed into invert sugar. without any formation of caramel or coloration of the sirup. The proportions of acid are given giving the best results, but we do not limit ourselves to the exact figures, as a small excess of acid especially of the weaker acids may be used without seriously prejudicing the result. a
Fourth. After digestion the acid is neutralized by means of sodic or potassic carbonates or hydrates applied in calculated quantity.
Fifth. The sirup thus obtained is passed through a fine sieve in order to remove any mechanical impurities, and cooled down, when it is ready for use.
Example: One thousand kilograms of white sugar containing 0.025 per cent. of ashes, are mixed with two .to four hectoliters of water and the mixture is heated until it shows a temperature of about centigrade, when the steam is cut off and the hot mass acidulated with 0.264 kilograms equal to 0.222 liters of hydrochloric acid having the specific gravity 1.188 e. containing one hundred grams H01), this acid having previously been diluted with 10 liters of water. The acidulated mass is exposed to the action of a temperature of 90 to 80 centigrade for one-half hour, when the sirup is removed from the pan and subjected to rapid cooling. In this manner a clear, colorless and thick sirup is obtained having eightyfive per cent. A quantity of this sirup corresponding to half the normal weight of cane sugar and dissolved in as much water as to obtain one hundred cubic centimeters, will, on observation at 20 centigrade, show a levorotation equal to twelve degrees of the saccharometer. The sirup contains 0.008 per cent. of free hydrochloric acid which is neutralized by the addition of 0.23 kilograms of bicarbonate of soda so that the sirup finally contains 0.013 per cent. of chloride of sodium.
The described process of producing invert sugar sirup may be modified as follows:
First. In order to allow the inversion to be finished in one-half hour at a lower temperature than 90 to centigrade, the proportion of hydrochloric acid has to be increased as fol.lows:at 80 to 90 centigrade twenty grams of hydrochloric acid per one hundred kilograms of sugar and 0.425 of the ashes; at 70 to 80 centigrade, forty grams of hydrochloric acid per one hundred kilograms of sugar and 0.45 of the ashes.
Second. In order to carry out the inversi n in one-half hour at 100 to 110 centigrade, the proportion of hydrochloric acid has to be reduced to five grams H01 per one hundred kilograms of sugar and 0.4 of the ashes.
Third. In lieu of H01 otheracids maybemade use of, such as H1312,I-INO ,H 80 ,HFI, G H O (tartaric acid), C H O (citric acid), H PO or H 80 and in such proportion that there are employed, for each ten grams of hydrochloric acid twenty grams HBr, twenty grams I INO thirty grams H 80 fifty grams HFI, ninety grams tartaric acid, one hundred and twenty grams citric acid, one hundred and fifty grams H PO two hundred grams H 80 and in respect to the ashes: in lieu of 0.4 to 0.45 hydrochloric acid 0.7 to 0.8 H 80 0.45 to 0.5 HFl, 0.95 to 1.1 H PO 0.9 to 1.0 H 80 0.7 to 0.8 HNO 1.75 to 2.0 tartaric acid, 2.0 to 2.4 citric acid. In all cases the neutralization of the acid has to be performed by the equivalent quantity of an alkali (carbonate or hydrate).
Fourth. The same process may be utilized for producing highly concentrated non-crystallizable sugar-solutions by inverting only half the quantity of sugar contained in the original solution. To this end the described process is so modified as to reduce to one- .third either the time of digestion or the proportion of acid which would be necessary for completely inverting all the sugar present in the solution.
WVe claim,
l'xThe process of producing concentrated invert sugar sirup which consists in mixing saccharine solutions containing sixty or more per cent. of sugar with dilute acid in proportion determinated as described, and heating, substantially as and for the purpose specified.
2. The process of producing concentrated invert sugar sirup which consists in mixing concentrated saccharine solutions containing sixty or more per cent. of sugar with dilute acid in proportion determinated as described, heating the mixture and neutralizing the acid, substantially as and for the purpose described.
In testimony whereof we have hereunto set our hands in the presence of two subscribing witnesses.
ALFRED WVOI'IL. ALEXANDER KOLLREPP. Witnesses:
HENRY SPRINGMANN, WILHELM LINDMAR.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US498000A true US498000A (en) | 1893-05-23 |
Family
ID=2566836
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US498000D Expired - Lifetime US498000A (en) | Alfred wohl and alexander kollrepp |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US498000A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2954324A (en) * | 1957-05-13 | 1960-09-27 | Brummer Ella Bache | Epilating composition and device |
| US3632446A (en) * | 1969-03-05 | 1972-01-04 | California & Hawaiian Sugar | Continuous invert sugar process |
| US4332622A (en) * | 1980-08-25 | 1982-06-01 | Savannah Foods & Industries, Inc. | Direct production of a pure sugar product from cane juice |
-
0
- US US498000D patent/US498000A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2954324A (en) * | 1957-05-13 | 1960-09-27 | Brummer Ella Bache | Epilating composition and device |
| US3632446A (en) * | 1969-03-05 | 1972-01-04 | California & Hawaiian Sugar | Continuous invert sugar process |
| US4332622A (en) * | 1980-08-25 | 1982-06-01 | Savannah Foods & Industries, Inc. | Direct production of a pure sugar product from cane juice |
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