US2170872A - Process for extracting carotinoids - Google Patents
Process for extracting carotinoids Download PDFInfo
- Publication number
- US2170872A US2170872A US51424A US5142435A US2170872A US 2170872 A US2170872 A US 2170872A US 51424 A US51424 A US 51424A US 5142435 A US5142435 A US 5142435A US 2170872 A US2170872 A US 2170872A
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- US
- United States
- Prior art keywords
- solvent
- carotinoids
- extracting
- carotene
- extraction
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/59—Compounds containing 9, 10- seco- cyclopenta[a]hydrophenanthrene ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/02—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains containing only carbon and hydrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/24—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by six-membered non-aromatic rings, e.g. beta-carotene
Definitions
- This invention relates generally to the extracpossible manufacture of vitamin concentrates at relatively low cost, and with a minimum amount of plant equipment.
- a suitable carotinoid bearing material such as fresh carrots
- a grinding or macerating operation I to form a wet ground mass.
- a suitable caustic such vas sodium hydroxide is introduced into the ground mass of material, as indicated at 2. While the process is not' critical with respect to the ⁇ amount of caustic employed, "good results v5 are secured by employing an amount of sodium hydroxide equal to about 5% oi.' the weight of the original carrots.
- the alkaline mass is now subjected to a digesting operation 3, in which it is heated to an elevated temperature.
- vThis can be accomplished by the use of a suitable closed digestor, within j,introduction of steam into the digestor at a suitable pressure, such as about 100 pounds per square inch.
- a suitable pressure such as about 100 pounds per square inch.
- the time required to effect a proper degree of digestion will depend somewhat upon the type of material being treated, but with carrots a period of about fifteen to thirty minutes will suffice.
- the resulting digested material is a slurry containing pulp like material, and can be readily blown out of the digestor, for subsequent treatment.
- the digested material is then subjected to an ⁇ extracting operation 4, which can be carried outy by the use of a solvent which can be removed by evaporation or steam distillation, such as a petroleum ether, heptane, or a petroleum solvent known as mineral spirits, which consists of a mixture of petroleum fractions intermediate with respect to kerosene and gasoline.
- a solvent which can be removed by evaporation or steam distillation
- the solvent is introduced with agitation, in order to secure a .thorough intermingling such as will enable emcient extraction of carotene by the solvent.
- This mixture is then subjected to a separating operation 5, for the removal of solids.
- This opera.- tion can be carried out by methods of gravity settling and decantatlon, orby the use of a centrifugal separator.
- the solids thus removed can be further extracted in progressive operations, until substantially all of the residual carotene has been removed.
- operationv the solids removed in the operation 5 are shown being remixed with a solvent, with solids being again removed from the mixture at 1.
- Solvent 45 removed from Vthe operation 'I is shown being utilized in the primary extracting operation 4.
- the liquor consists of hydrocarbon solvent, together with water, and possibly a certain amount of emulsion.
- This 50 mixture of solvent and water may then be subjected to a further separating operation 8, which can be carried out by the use of a suitable centrifuge, with or without heating, for removing a majority of the water and for breaking down any emulsion which may be formed.
- the resulting solvent is then subjected to steam distillation operation 9.
- a suitable antioxidant like hydroquinone
- aqueous material is then mixed with a suitable oil, like coconut, sardine, or ottonseedoil, as indicated at Il, whereby carotenes and-other fat soluble' vitamin values are extracted and dissolved by,the oil.
- a suitable oil like coconut, sardine, or ottonseedoil, as indicated at Il, whereby carotenes and-other fat soluble' vitamin values are extracted and dissolved by,the oil.
- This admixture is then subjected to a separating operation l2, which can be carried out by a suitable centrifuge, to remove the water.
- the carotene concentrate obtained as described above forms a marketable product, suitable for many purposes. fortify vitamin values contained in various food materials, such as milk products, or to supply a desired caroteneI content for other vitamin con taining materials.
- aclosed digesting chamber adapted to receive a chargefof" ,inaterial and capable of withstanding considerable internal pressure
- said method comprising macerating the material and introducing a caustic into the 1 same, introducing the macerated material into said chamber, introducing steam under pressure into the interior of the chamber whereby the material is digested at an elevated temperature in excess of 212 F. and. at a pressure substantially greater than atmospheric, causing the digested material to be blown from said chamber, and then subjecting the digested material to solvent extraction for removal of carotinoids.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Extraction Or Liquid Replacement (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Description
Aug. .29, 1939. D. D. PEEBLES 2,170,872
PROCESS FOR EXTRAGTING CAROTINOIDS Filed Nov. 25, 1935 (aro/@p conce/#rafle El@ resented aug. ze, 19,39
umrso sra'resf' PATENT oi-Flcr Davia n. Peeblesrsmka, oeuf. Application November 25, 1935, Serial No. 51,424
3 Claims.
This invention relates generally to the extracpossible manufacture of vitamin concentrates at relatively low cost, and with a minimum amount of plant equipment.
It is a further object of the invention to provide a vitamin extracting process which will be characterized Vby a relatively high percentage yield of the desired carotenes.
Further objects of the invention will appear from the following description in which the preferred embodiment of the present invention has been described in detail in conjunction with the accompanying flow sheet.
In the past, processes for the extraction of carotenes from various vegetables or like carotinoid bearing materials, have utilized direct extraction of the carotene by the use of a hydrocarbon solvent. In some instances the solvent has been contacted with `juices expressed from the vegetable material, and in other instances the vegetable material is first dried, and then contacted with a solvent. Both of these processes are relatively inefficient with respect to the percentage of carotene recovered in the ilnal product.
Where drying is employed prior to the extraction' operation, in order to reduce therbulk of material to be treated, the extraction is apt to be ineicient, due to impairment of the carotene during the drying operation, and also due to the manner in which the carotene is held with the brous `or cellular material. Furthermore, dehydrating operations are relatively expensive and require elaborate pant equipment.
The present process deviates from prior practice in that the carotinoid bearing material is,
first subjected to a digesting operation, to break down the cellular structure of the material, before the extraction operation. It has been found that such a digesting operation can be carried out without material injury to the carotene content, and that it enables relatively eilicient extraction.
In commercial operations my process can be carried out as follows:-A suitable carotinoid bearing material, such as fresh carrots, is first subjected to a grinding or macerating operation I, to form a wet ground mass. Preparatory to carrying out the digesting operation, a suitable caustic, such vas sodium hydroxide is introduced into the ground mass of material, as indicated at 2. While the process is not' critical with respect to the`amount of caustic employed, "good results v5 are secured by employing an amount of sodium hydroxide equal to about 5% oi.' the weight of the original carrots. l The alkaline mass is now subjected to a digesting operation 3, in which it is heated to an elevated temperature. vThis can be accomplished by the use of a suitable closed digestor, within j,introduction of steam into the digestor at a suitable pressure, such as about 100 pounds per square inch. The time required to effect a proper degree of digestion will depend somewhat upon the type of material being treated, but with carrots a period of about fifteen to thirty minutes will suffice. The resulting digested material is a slurry containing pulp like material, and can be readily blown out of the digestor, for subsequent treatment.
The digested material is then subjected to an `extracting operation 4, which can be carried outy by the use of a solvent which can be removed by evaporation or steam distillation, such as a petroleum ether, heptane, or a petroleum solvent known as mineral spirits, which consists of a mixture of petroleum fractions intermediate with respect to kerosene and gasoline. The solvent is introduced with agitation, in order to secure a .thorough intermingling such as will enable emcient extraction of carotene by the solvent. This mixture is then subjected to a separating operation 5, for the removal of solids. This opera.- tion can be carried out by methods of gravity settling and decantatlon, orby the use of a centrifugal separator. In order to increase the eiliciency of extraction, the solids thus removed can be further extracted in progressive operations, until substantially all of the residual carotene has been removed. For example in operationv the solids removed in the operation 5 are shown being remixed with a solvent, with solids being again removed from the mixture at 1. Solvent 45 removed from Vthe operation 'I is shown being utilized in the primary extracting operation 4.
After removal of solids at 5, the liquor consists of hydrocarbon solvent, together with water, and possibly a certain amount of emulsion. This 50 mixture of solvent and water may then be subjected to a further separating operation 8, which can be carried out by the use of a suitable centrifuge, with or without heating, for removing a majority of the water and for breaking down any emulsion which may be formed. The resulting solvent is then subjected to steam distillation operation 9. Before all of the solventhas been removed by distillation it is desirable to introduce a suitable antioxidant, like hydroquinone, into the remaining material, in order to protect the carotene against oxidation. After the solvent has been entirely removed there remains an aque- A ous material in which the carotene is suspended,
together with other vitamin values if present, which were extracted by the solvent. This aqueous material is then mixed with a suitable oil, like coconut, sardine, or ottonseedoil, as indicated at Il, whereby carotenes and-other fat soluble' vitamin values are extracted and dissolved by,the oil. This admixture is then subjected to a separating operation l2, which can be carried out by a suitable centrifuge, to remove the water. The carotene concentrate obtained as described above forms a marketable product, suitable for many purposes. fortify vitamin values contained in various food materials, such as milk products, or to supply a desired caroteneI content for other vitamin con taining materials. Y,
With respect to the eciency of my process, it makes possible recovery of about ofl the carotene contained in the material being treated. This high percentage of recovery is attributed largely to the digesting operation, which makes the material amenable to eicient extraction. With my process, large scale production of carotene concentrates at low cost is made possible, not only because of the high eiiciency, but also because relatively inexpensive plant equipment is required, with relatively low operating and maintenance costs.
I claim:
1. In a process for extracting carotinoids from cellular carotnoid-bearing materials,l macerating carotinoid-bearing materials, said process being For example, it can be used toA 2,170,872 the material, breaking down thecellular material u' 212 F., rapidly releasing the pressure upon said 5 material, and then subjecting` the digested material to solvent extraction for removal of carotinoids.
2. In a process 'for extracting carotinoids from characterized by the use.0f aclosed digesting chamber adapted to receive a chargefof" ,inaterial and capable of withstanding considerable internal pressure, said method comprising macerating the material and introducing a caustic into the 1 same, introducing the macerated material into said chamber, introducing steam under pressure into the interior of the chamber whereby the material is digested at an elevated temperature in excess of 212 F. and. at a pressure substantially greater than atmospheric, causing the digested material to be blown from said chamber, and then subjecting the digested material to solvent extraction for removal of carotinoids.
3. In a process for extracting carotinoids from materials like fresh vegetables or greens, mechanically crushing the material to form a wet divided mass, introducing a caustic into the wet divided mass whereby the mass is rendered alkaline, subjecting the alkaline mass to the action of steam :i0
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51424A US2170872A (en) | 1935-11-25 | 1935-11-25 | Process for extracting carotinoids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US51424A US2170872A (en) | 1935-11-25 | 1935-11-25 | Process for extracting carotinoids |
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US2170872A true US2170872A (en) | 1939-08-29 |
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US51424A Expired - Lifetime US2170872A (en) | 1935-11-25 | 1935-11-25 | Process for extracting carotinoids |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2440029A (en) * | 1943-10-13 | 1948-04-20 | Gen Biochemicals Inc | Method for extracting pigments |
US2460796A (en) * | 1942-05-04 | 1949-02-01 | Procter & Gamble | Process for preparing carotenoid concentrates from palm oil |
US2461300A (en) * | 1943-10-13 | 1949-02-08 | Gen Biochemicals Inc | Method of conditioning a hard soap for solvent extraction |
US2557987A (en) * | 1947-09-09 | 1951-06-26 | Alfred G Marshak | Method for extracting usnic acid |
US2567362A (en) * | 1945-05-03 | 1951-09-11 | Sophia S Berkman | Method of extracting pigments from plants |
WO1992018471A1 (en) * | 1991-04-12 | 1992-10-29 | Humanetics Corporation | Extraction of carotenoids from natural sources |
US20020082459A1 (en) * | 1997-05-28 | 2002-06-27 | Bailey David T. | High purity beta-carotene and process for obtaining same |
-
1935
- 1935-11-25 US US51424A patent/US2170872A/en not_active Expired - Lifetime
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2460796A (en) * | 1942-05-04 | 1949-02-01 | Procter & Gamble | Process for preparing carotenoid concentrates from palm oil |
US2440029A (en) * | 1943-10-13 | 1948-04-20 | Gen Biochemicals Inc | Method for extracting pigments |
US2461300A (en) * | 1943-10-13 | 1949-02-08 | Gen Biochemicals Inc | Method of conditioning a hard soap for solvent extraction |
US2567362A (en) * | 1945-05-03 | 1951-09-11 | Sophia S Berkman | Method of extracting pigments from plants |
US2557987A (en) * | 1947-09-09 | 1951-06-26 | Alfred G Marshak | Method for extracting usnic acid |
WO1992018471A1 (en) * | 1991-04-12 | 1992-10-29 | Humanetics Corporation | Extraction of carotenoids from natural sources |
US5245095A (en) * | 1991-04-12 | 1993-09-14 | Humanetics Corporation | Extraction of carotenoids from natural sources |
US5510551A (en) * | 1991-04-12 | 1996-04-23 | Humanetics Corporation | Extraction of carotenoids from natural sources |
US20020082459A1 (en) * | 1997-05-28 | 2002-06-27 | Bailey David T. | High purity beta-carotene and process for obtaining same |
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