GB694795A - Improvements in or relating to a process of treating steep liquor and the product resulting therefrom - Google Patents
Improvements in or relating to a process of treating steep liquor and the product resulting therefromInfo
- Publication number
- GB694795A GB694795A GB25363/50A GB2536350A GB694795A GB 694795 A GB694795 A GB 694795A GB 25363/50 A GB25363/50 A GB 25363/50A GB 2536350 A GB2536350 A GB 2536350A GB 694795 A GB694795 A GB 694795A
- Authority
- GB
- United Kingdom
- Prior art keywords
- steep liquor
- lactic acid
- calcium
- water
- steam
- 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
Links
- 238000000034 method Methods 0.000 title abstract 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 abstract 28
- 239000004310 lactic acid Substances 0.000 abstract 14
- 235000014655 lactic acid Nutrition 0.000 abstract 14
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 10
- 239000000463 material Substances 0.000 abstract 10
- 235000015097 nutrients Nutrition 0.000 abstract 7
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 abstract 6
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 abstract 5
- WPEXVRDUEAJUGY-UHFFFAOYSA-B hexacalcium;(2,3,4,5,6-pentaphosphonatooxycyclohexyl) phosphate Chemical compound [Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])(=O)OC1C(OP([O-])([O-])=O)C(OP([O-])([O-])=O)C(OP([O-])([O-])=O)C(OP([O-])([O-])=O)C1OP([O-])([O-])=O WPEXVRDUEAJUGY-UHFFFAOYSA-B 0.000 abstract 5
- 239000000203 mixture Substances 0.000 abstract 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- 240000008042 Zea mays Species 0.000 abstract 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 abstract 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 4
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 abstract 4
- 239000000920 calcium hydroxide Substances 0.000 abstract 4
- 229910001861 calcium hydroxide Inorganic materials 0.000 abstract 4
- 235000005822 corn Nutrition 0.000 abstract 4
- 238000000605 extraction Methods 0.000 abstract 4
- 239000007791 liquid phase Substances 0.000 abstract 4
- 239000001175 calcium sulphate Substances 0.000 abstract 3
- 235000011132 calcium sulphate Nutrition 0.000 abstract 3
- 238000011084 recovery Methods 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- 240000006394 Sorghum bicolor Species 0.000 abstract 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 150000001720 carbohydrates Chemical class 0.000 abstract 2
- 235000014633 carbohydrates Nutrition 0.000 abstract 2
- 238000005119 centrifugation Methods 0.000 abstract 2
- 235000013339 cereals Nutrition 0.000 abstract 2
- 238000001035 drying Methods 0.000 abstract 2
- 238000001704 evaporation Methods 0.000 abstract 2
- 239000012065 filter cake Substances 0.000 abstract 2
- -1 hexyl alcohols Chemical class 0.000 abstract 2
- 229910010272 inorganic material Inorganic materials 0.000 abstract 2
- 239000011147 inorganic material Substances 0.000 abstract 2
- 244000005700 microbiome Species 0.000 abstract 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 238000010992 reflux Methods 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000007790 solid phase Substances 0.000 abstract 2
- 239000007921 spray Substances 0.000 abstract 2
- 239000001117 sulphuric acid Substances 0.000 abstract 2
- 235000011149 sulphuric acid Nutrition 0.000 abstract 2
- 239000000725 suspension Substances 0.000 abstract 2
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 abstract 1
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000000706 filtrate Substances 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 238000004508 fractional distillation Methods 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 150000003903 lactic acid esters Chemical class 0.000 abstract 1
- 239000012071 phase Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/02—Preparation of carboxylic acids or their salts, halides or anhydrides from salts of carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process of treating corn steep liquor or sorghum grain steep liquor comprises incubating the steep liquor to form lactic acid therein, adding sulphuric acid to decrease the pH to a value not exceeding 2.0, removing the lactic acid, adding an alkaline earth metal hydroxide to adjust the pH to about 5.5 to 7.5, autoclaving the entire mixture at about 10 to 20 pounds per square inch steam pressure, separating the liquid and solid phases and drying the liquid phase. Either light steep liquor, i.e. that drawn directly from the steeps, or heavy steep liquor, i.e. that concentrated to about 30 DEG B<\>e, is satisfactory. The lactic acid may be removed by extraction with butanol or any alcohol selected from butyl, amyl or hexyl alcohols, thus butanol may be added to the acidified steep liquor and the mixture agitated to extract the lactic acid or the extraction may be effected in continuous countercurrent manner. The extracting alcohol may be anhydrous or water-laden. The extract containing the lactic acid is then separated and treated to convert the lactic acid therein to the ester, e.g. by concentrating under vacuum and then refluxing, or by evaporating at atmospheric pressure until essentially all of the water is removed and then either evaporating or refluxing at atmospheric pressure to complete the esterification. The esterified liquor is then cooled and the pH adjusted to 4.5 to 6.0 to prevent hydrolysis and steam is then passed through rapidly until the distillate layer no longer separates into two phases; the lactic acid ester is recovered from the upper layer of the distillate by fractional distillation. The acidified steep liquor is then treated for the recovery of a nutrient for micro-organisms by first removing residual extract by means of steam and then adding an alkaline earth metal hydroxide, especially calcium hydroxide, to adjust the pH to 5.5 to 7.5 and the material is then autoclaved as with steam as described above. The autoclaved material is then filtered, e.g. by centrifugation, preferably at 80-90 DEG C., and the cake obtained consisting mainly of calcium phytate and calcium sulphate is washed with water and the centrifugates combined and spray dried to yield a nutrient soluble in water and containing nitrogeneous materials, together with inorganic material and small amounts of carbohydrates and salts of lactic acid. The filter cake containing calcium phytate and calcium sulphate is then treated for recovery of purified calcium phytate by dissolving the latter in hydrochloric acid at a pH of about 1.0 to 2.0 and filtering or centrifuging the suspension to leave the undissolved calcium sulphate as filter cake. The filtrate is then treated with calcium hydroxide suspension to adjust the pH to 5.0 to 5.5 so as to precipitate the calcium phytate which is then separated and dried. An example is given in which corn steep liquor is employed as starting material, and butanol is used as the lactic acid extractant, butyl lactate, calcium phytate and nutrient material being recovered as above.ALSO:Nitrogenous materials useful as nutrients for certain micro organisms are recovered from corn steep liquor or sorghum grain steep liquor by incubating the steep liquor to form lactic acid therein, adding sulphuric acid to decrease the pH to a value not exceeding 2.0, removing the lactic acid, adding an alkaline earth metal hydroxide to adjust the pH to about 5.5 to 7.5, autoclaving the entire mixture at about 10 to 20 pounds per square inch steam pressure, separating the liquid and solid phases and drying the liquid phase. Either light steep liquor, i.e. that drawn directly from the steeps, or heavy steep liquor, i.e. that concentrated to about 30 DEG B<\>ae. is satisfactory. The lactic acid may be removed by extraction with an alcohol selected from butyl, amyl, or hexyl alcohols; thus butanol may be added to the acidified steep liquor and the mixture agitated to extract the lactic acid. The extraction may also be effected in continuous countercurrent manner. The extracting alcohol may be anhydrous or water-laden. The acidified steep liquor is then treated for the recovery of the nutrient material by first removing any residual extractant by passing steam through the liquor, adding an alkaline earth metal hydroxide especially calcium hydroxide to adjust the pH to 5.5 to 7.5 and then autoclaving the entire mixture with steam as described above. The autoclaved material is then filtered, e.g. by centrifugation, preferably at 80-90 DEG C., and the cake obtained is washed with water and the centrifugates washed and spray dried to yield the nutrient material which is soluble in water and contains nitrogenous materials together with inorganic material and small amounts of carbohydrates and salts of lactic acid. An example is given in which nutrient material is recovered from corn steep liquor, butanol being employed as the lactic acid extractant and calcium hydroxide as the alkaline earth metal hydroxide.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US694795XA | 1950-06-17 | 1950-06-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB694795A true GB694795A (en) | 1953-07-29 |
Family
ID=22089262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB25363/50A Expired GB694795A (en) | 1950-06-17 | 1950-10-18 | Improvements in or relating to a process of treating steep liquor and the product resulting therefrom |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB694795A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0711269A4 (en) * | 1993-07-26 | 1996-05-29 | ||
| US5766439A (en) * | 1996-10-10 | 1998-06-16 | A. E. Staley Manufacturing Co. | Production and recovery of organic acids |
-
1950
- 1950-10-18 GB GB25363/50A patent/GB694795A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0711269A4 (en) * | 1993-07-26 | 1996-05-29 | ||
| US5766439A (en) * | 1996-10-10 | 1998-06-16 | A. E. Staley Manufacturing Co. | Production and recovery of organic acids |
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