US2374455A - Drying of materials - Google Patents
Drying of materials Download PDFInfo
- Publication number
- US2374455A US2374455A US391518A US39151841A US2374455A US 2374455 A US2374455 A US 2374455A US 391518 A US391518 A US 391518A US 39151841 A US39151841 A US 39151841A US 2374455 A US2374455 A US 2374455A
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- Prior art keywords
- drying
- materials
- dried
- moisture
- flask
- Prior art date
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- Expired - Lifetime
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- 239000000463 material Substances 0.000 title description 54
- 238000001035 drying Methods 0.000 title description 27
- 239000007788 liquid Substances 0.000 description 23
- 238000000034 method Methods 0.000 description 22
- 230000008569 process Effects 0.000 description 18
- 239000002904 solvent Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000003925 fat Substances 0.000 description 9
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 8
- 238000004821 distillation Methods 0.000 description 8
- 239000008096 xylene Substances 0.000 description 8
- 238000013019 agitation Methods 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- 239000011368 organic material Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000470 constituent Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- 210000000941 bile Anatomy 0.000 description 3
- 230000000762 glandular Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 206010062767 Hypophysitis Diseases 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000010981 drying operation Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 210000004907 gland Anatomy 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000001817 pituitary effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 210000003635 pituitary gland Anatomy 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F26—DRYING
- F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
- F26B5/00—Drying solid materials or objects by processes not involving the application of heat
- F26B5/005—Drying solid materials or objects by processes not involving the application of heat by dipping them into or mixing them with a chemical liquid, e.g. organic; chemical, e.g. organic, dewatering aids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S159/00—Concentrating evaporators
- Y10S159/11—Biologicals
Definitions
- This invention relates to the drying of materials, and is particularly concerned with a process for drying organic material which are deleteriously afiected by high temperatures.
- a further object of our invention is to1provide processes for drying heat-labile materials in a very rapid and emcient manner.
- Another object of our invention is to preserve the colorof the starting material and to prevent darkening thereof.
- the material to be dried is immersed'in a liquid heat transfer mediumwsuch as xylene or kerosene, and preferably is' well dispersed throughout the body of this liquid medium. Then while so held in the medium the temperature and pressure are regulated to distill off the moisture from the material.
- a liquid'heat transfer medium having a'boilin g point 'above the-boiling point of water, and in this case the temperature employed may be regulated so as to distill off moisture but not to distill excessive amounts of the liquid medium. Then the medium may be separated from the material after drying.
- the invention can, however, be practiced using a heat transfer medium having a boiling point below the boiling point of water, in which case itis desirable to add further quantities of medium during the drying period.
- a heat transfer medium having a boiling point below the boiling point of water
- the apparatus includes a flask Ill, suitably of glass, which. may be 3-necked as shown.
- a shaft ll fitted with agitator blades l3 enters flask l0 through a glass tube 2
- An electric motor, or other suitable means I2 is provided to activate shaft I i.
- the receiving flask 89 also her- 25 metically fitted to condenser it has tube 20 leading to a vacuum line or to a means for reducing the pressure in the system.
- Heat or refrigeration may be imparted in any suitable way, as by placing the flask in a bath ofwater having controlled temperatures.
- Example 1 30 grams of posterior lobes of pituitary glands are minced and emulsified with cc. of a heat transfer medium consisting of xylene. 500 cc. of xylene are place in distillation'flask ill and the stirring device is started. The emulsion of minced glandular material and xylene is then allowed to flow into flask ill by way of funnel I 5 while stirring is continued. After all of the xylene has been added, stopcock it is closed and tube 20 is connected with the vacuum line, where-. upon the pressure in the system is reduced to 12 mm. of mercury. At this pressure, distillation is carried on at 25 C. for one hour.
- Example 2 I 500 cc. of fresh ox bile are thoroughly mixed with 1000 cc. of deodorized kerosene and the-resulting emulsion is placed in distilling flask l and agitation started. A pressure of 9 mmrof mercury is applied and distillation proceeds under agitation at C. for two hours. At the end of this time, the process is stopped and the contents of the flask are filtered through paper. The solid residue on the filter is washed with hexane and is recovered as-a light yellowish-green product which is easily powdered 'and is completely soluble in water, indicating that no denaturatiorf has taken place.
- a great variety of materials may be dried by the process of our invention and we find it especially advantageous for drying organic and biological substances which are unstable toward heat and which are ordinarily very difficult to dry.
- we find it especially suitable for drying glandular material such as pancreas, pituitaries, ovaries, stomachs and the like and for drying organic liquids such as bile, plasma, aqueous solutions of organic materials andthe like.
- the process is useful for drying solids and liquids of widely varying character and we do not wish to limit the invention to any kind of material to be dried.
- the material to be dried is desired in the form of a dry powder
- the material such as plant or animal organic substances is ground before being added to the liquid medium. In general, the more finely the material is ground the better for the drying procedure.
- the liquid heat transfer medium employed may be any suitable liquid other than water and where the medium is to be separated from the dry material, should preferably be aQliquidwhich is easily separated from the material and which Where material such as animal glands or other material containing delicate destructible factors is dried, care must be taken not to select a medium which will by its chemical constitution be injurious to such factors.
- the invention can be practiced using a water-miscible medium, it is much to be preferred that the liquid medium used be waterimmiscible.
- the liquid medium used be waterimmiscible.
- cohols,'ketones, halogenated hydrocarbons, and esters may also be used.
- the solvents such as toluene, xylene, kerosene, ketones, etc. are all volatile liquids and by volatile we mean they can vent and recover the fatty constituents with the other solids.
- fat solvents may be used as the liquid heat transfer medium.
- fat solvents we mean to include those liquids in which fats are soluble but do not mean to include fats themselves. These solvents dissolve fatty constituents and are removed by filtration after the distillation process. Thus the fat has,
- the liquid medium desirably should have a boiling point above that of water at the pressure at which the operations are performed. However, as shown above, a, medium having a lower boiling point than-that of water may also be used.
- suchlower boiling solvent is supplied, as needed, through the funnel it until the distillation of moisture is complete.
- a high boilingsolvent is used. the moisture will have been removed before the solvent begins to distill over, and the appearance of solvent in the condenser or receiver indicates the end of the drying process. Any solvent which distills oil may be recovered and used again.
- the temperature should not be so high as to cause distillation of substantialamounts-of liquid heat transfer medium, but in some cases it is desirable to raise the temperature" so that after distillation of the moisture the liquid medium is also separated from the dried material by distillation.
- the agitation of the material in the liquid medium during drying is an important feature of the invention.
- the agitation has been continuous throughout the drying period, but the purpose may be served, though less effectively, by intermittent agitation at frequent intervals.
- the time of drying is greatly reduced, less heat is required resulting in avoidance of the destruction of heatlabile materials, and also other unwanted chemical changes such as oxidation are avoided.
- the final dried products have an extremely low moisture content and are easily handled. Also, there is the further advantage that the products dried in the liquid medium by this method are lesshygroscopic and upon standing after drying do not readily absorb moisture from the air.
- the process is also applicable to the removal of water which is present in the form of ice crystals.
- frozenglandular material may be ground and dispersed in a liquid heat transfer medium at a temperature below the melting point of the ice present. This mixture may be subjected to a reduced pressure at a temperature of about 5 C. and the water present is removed without liquefaction in accordance with the process herein described.
- a process for treating a heat labile fatcontaining materialto dry and defat comprising dispersing said material in a liquid water-immiscible fat solvent having a boiling point higher than that of water, subjecting said material while so dispersed to a pressure less than atmospheric and a temperature high enough to distill water from said material at said pressure, subjecting said material and solvent to mechanical agitation while maintaining said pressure and temperature until moisture contained in the material is driven ofi, and separating the solvent together with fat contained therein from the remaining dried material.
- a process for drying a heat labile material in the frozen state comprising dispersing said material, while frozen, in a non-aqueous liquid heat transfer medium, subjecting said material while so dispersed to a pressure less than atmospheric and a temperature below the melting point of the frozen moisture in said mate- 'rial, subjecting said dispersed material to agitation while withdrawing the resulting vapors, and separating the heat transfer medium from the dried material.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Drying Of Solid Materials (AREA)
Description
April 24, 1 J. D. PORSCHE ET AL DRYING OF MATERIALS Filed May 2, 1941 I INVENTOR5- George-Josh; BY Jules .faraclze,
Fianna... 24, 1945 l DRYING F MATE IQIALS Jules D. Porsche, Clarendon Hills, IlL, and George Josh, Crown Point, Ind., assignors to Amour and Company, Chicago, Ill., a corporation of Illinois Application May 2, 1941 Serial No. 391,518
Claims.
This invention relates to the drying of materials, and is particularly concerned with a process for drying organic material which are deleteriously afiected by high temperatures.
In removing moisture from organic materials it is essential in many cases to do so under conditions which preserve as many of the physiologically active constituents as possible and which avoid other objectionable changes. The art has long desired a more efficient way of drying without causing destruction or rearrangement in the materials themselves, such as denaturation of protein constituents or inactivation of physiologically active substances like the active factors present in animal glandular materials.
It has been customary in the past to dry th organic materials, for example, by treating at low temperatures with air which has been previously dried, or by subjecting the materials to heat under a vacuum, or by drying them in a current of warm air. These methods have required long drying times and the roducts obtained have disadvantages. For example, when the material is spread out on trays and dried in avacuum oven, the necessary heat usually destroys at least a part of the wanted characteristics of the material. Furthermore, the color of the material, in the case'of organic substances, usually darkens greatly and objectionable bacterial action. frequently takes place. Also, in the usual drying operations considerable effort is required to scrape the dense, dried product off the trays at the end of the drying operation.
It is an important object of our invention to produce dried materials which exhibit as little change as possible, other than loss of moisture, in the starting constituents. A further object of our invention is to1provide processes for drying heat-labile materials in a very rapid and emcient manner. Another object of our invention is to preserve the colorof the starting material and to prevent darkening thereof. Many other objects and advantages will be made apparent as the description proceeds.
By the process of our invention, the material to be dried is immersed'in a liquid heat transfer mediumwsuch as xylene or kerosene, and preferably is' well dispersed throughout the body of this liquid medium. Then while so held in the medium the temperature and pressure are regulated to distill off the moisture from the material. We prefer to use a liquid'heat transfer medium having a'boilin g point 'above the-boiling point of water, and in this case the temperature employed may be regulated so as to distill off moisture but not to distill excessive amounts of the liquid medium. Then the medium may be separated from the material after drying. The invention can, however, be practiced using a heat transfer medium having a boiling point below the boiling point of water, in which case itis desirable to add further quantities of medium during the drying period. We find a marked advantage in the use of a vacuum where heat sensitive organic materials are being dried.
One typ of apparatus which may be used in practicing the invention is illustrated schematically in the accompanying drawing.
In the drawing, the apparatus includes a flask Ill, suitably of glass, which. may be 3-necked as shown. A shaft ll fitted with agitator blades l3 enters flask l0 through a glass tube 2| fitted with a stopper 22 which provides a hermetic seal for the flask. An electric motor, or other suitable means I2, is provided to activate shaft I i. A funnel i=5 serves to feed material into flask it] and maybe closed ed by the stopcock it. A tube ll, fitted with a hermetic seal to flask it, leads to the condenser 18. The receiving flask 89, also her- 25 metically fitted to condenser it has tube 20 leading to a vacuum line or to a means for reducing the pressure in the system. Heat or refrigeration may be imparted in any suitable way, as by placing the flask in a bath ofwater having controlled temperatures.
The following specific examples will serve more clearly to illustrate the process of our invention ascarried out using the type of apparatus illustrated:
Example 1 30 grams of posterior lobes of pituitary glands are minced and emulsified with cc. of a heat transfer medium consisting of xylene. 500 cc. of xylene are place in distillation'flask ill and the stirring device is started. The emulsion of minced glandular material and xylene is then allowed to flow into flask ill by way of funnel I 5 while stirring is continued. After all of the xylene has been added, stopcock it is closed and tube 20 is connected with the vacuum line, where-. upon the pressure in the system is reduced to 12 mm. of mercury. At this pressure, distillation is carried on at 25 C. for one hour. Atthe end of this time no more moisture is observed to distill over and the residual material in the flask is filtered to recover the solid residue. The residue is air-washed by maintaining a suction in the filter flask for a time to remove the odor of xylene. The powdery residue is a light pinkish will not leave an objectional odor.
color and assays 110% when compared with standard posterior pituitary powder prepared according tothe U, S. Pharmacopoeia method. 1
i Example 2 I 500 cc. of fresh ox bile are thoroughly mixed with 1000 cc. of deodorized kerosene and the-resulting emulsion is placed in distilling flask l and agitation started. A pressure of 9 mmrof mercury is applied and distillation proceeds under agitation at C. for two hours. At the end of this time, the process is stopped and the contents of the flask are filtered through paper. The solid residue on the filter is washed with hexane and is recovered as-a light yellowish-green product which is easily powdered 'and is completely soluble in water, indicating that no denaturatiorf has taken place.
A great variety of materials may be dried by the process of our invention and we find it especially advantageous for drying organic and biological substances which are unstable toward heat and which are ordinarily very difficult to dry. For example, we find it especially suitable for drying glandular material such as pancreas, pituitaries, ovaries, stomachs and the like and for drying organic liquids such as bile, plasma, aqueous solutions of organic materials andthe like. The process is useful for drying solids and liquids of widely varying character and we do not wish to limit the invention to any kind of material to be dried.
Where the material to be dried is desired in the form of a dry powder, the material such as plant or animal organic substances is ground before being added to the liquid medium. In general, the more finely the material is ground the better for the drying procedure.
The liquid heat transfer medium employed may be any suitable liquid other than water and where the medium is to be separated from the dry material, should preferably be aQliquidwhich is easily separated from the material and which Where material such as animal glands or other material containing delicate destructible factors is dried, care must be taken not to select a medium which will by its chemical constitution be injurious to such factors.
Though the invention can be practiced using a water-miscible medium, it is much to be preferred that the liquid medium used be waterimmiscible. Especially when drying organic materials like bile, glands and the like, we recommend the use of water-immiscible organic liquids, such as toluene, xylene, paraffin hydrocarbons,
such as kerosene, Skelly Solve, and the like. Al-
cohols,'ketones, halogenated hydrocarbons, and esters may also be used, The solvents such as toluene, xylene, kerosene, ketones, etc. are all volatile liquids and by volatile we mean they can vent and recover the fatty constituents with the other solids. Alternatively, we canseparate the v solvent from the solid residue and evaporate the be vaporized without chemical breakdown using heat and an ordinary vacuum such as 10 mm. of mercury.
When the material being dried contains fat desired to be removed, fat solvents may be used as the liquid heat transfer medium. By the term fat solvents" we mean to include those liquids in which fats are soluble but do not mean to include fats themselves. These solvents dissolve fatty constituents and are removed by filtration after the distillation process. Thus the fat has,
been removed without practicing any more steps than are employed in -the regular-procedure of solvent to recover separately the materials which have been dissolved therein.
The liquid medium desirably should have a boiling point above that of water at the pressure at which the operations are performed. However, as shown above, a, medium having a lower boiling point than-that of water may also be used. In carrying out the process in an apparatus such as shown, suchlower boiling solvent is supplied, as needed, through the funnel it until the distillation of moisture is complete. a high boilingsolvent is used. the moisture will have been removed before the solvent begins to distill over, and the appearance of solvent in the condenser or receiver indicates the end of the drying process. Any solvent which distills oil may be recovered and used again.
Especially when drying heat sensitive organic materials we prefer to maintain a high vacuum on the mixture during drying. We usually emmixture and in the case of heat sensitive mate-- rials should be lower than the temperature at which the materials are deleteriously affected.
In most cases the temperature should not be so high as to cause distillation of substantialamounts-of liquid heat transfer medium, but in some cases it is desirable to raise the temperature" so that after distillation of the moisture the liquid medium is also separated from the dried material by distillation.
The agitation of the material in the liquid medium during drying is an important feature of the invention. In the specific examples given, the agitation has been continuous throughout the drying period, but the purpose may be served, though less effectively, by intermittent agitation at frequent intervals.
By practicing the present invention, the time of drying is greatly reduced, less heat is required resulting in avoidance of the destruction of heatlabile materials, and also other unwanted chemical changes such as oxidation are avoided. The final dried products have an extremely low moisture content and are easily handled. Also, there is the further advantage that the products dried in the liquid medium by this method are lesshygroscopic and upon standing after drying do not readily absorb moisture from the air.
The process is also applicable to the removal of water which is present in the form of ice crystals. For example, frozenglandular material may be ground and dispersed in a liquid heat transfer medium at a temperature below the melting point of the ice present. This mixture may be subjected to a reduced pressure at a temperature of about 5 C. and the water present is removed without liquefaction in accordance with the process herein described.
It is believed that many of the advantages resulting from our process are due to having the drying material widely dispersed in the liquidmedium, thus exposing tremenduously large surfaces of the material to contact with a. heat transfer medium,- making it easier for the moisture contained to readily absorb heat for vapori-' When zation. However, we do not wish to bind ourselves to any theory of explanation.
Although in the foregoing description we have referred to the removal of water from the material being dried, the process is applicable also to the removal of other substances of this nature, such as acetone, alcohol or the like.
It is to be understood that the foregoing detailed description and specific examples have been given for explanation only. The apparatus illustrated is only one of many widely varying types which may be employed. It will be understood that many changes and modifications may be made in the practice of the processes set forth without departing from the spirit of the invention. The foregoing detailed description has been given for clearnes of understanding only and no unnecessary limitations are to be understood therefrom.
We claim:
1. A process for treating a heat labile fatcontaining materialto dry and defat the same comprising dispersing said material in a liquid water-immiscible fat solvent having a boiling point higher than that of water, subjecting said material while so dispersed to a pressure less than atmospheric and a temperature high enough to distill water from said material at said pressure, subjecting said material and solvent to mechanical agitation while maintaining said pressure and temperature until moisture contained in the material is driven ofi, and separating the solvent together with fat contained therein from the remaining dried material.
2. A process as in claim 1 where said material is animal grandular material.
3. A process for drying a heat labile material in the frozen state comprising dispersing said material, while frozen, in a non-aqueous liquid heat transfer medium, subjecting said material while so dispersed to a pressure less than atmospheric and a temperature below the melting point of the frozen moisture in said mate- 'rial, subjecting said dispersed material to agitation while withdrawing the resulting vapors, and separating the heat transfer medium from the dried material.
4. In a process for drying a heat labile material the step of applying heat and reduced pressure to said material while it is frozen and dispersed in a non-aqueous liquid heat transfer medium and at a temperature below the melting point of moisture in the material under the reduced pressure applied.
5. A process as in claim 1 and including the step of evaporating said separated solvent to separate the fat therefrom.
JU'LES D. PORSCHE. GEORGE JOSH.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US391518A US2374455A (en) | 1941-05-02 | 1941-05-02 | Drying of materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US391518A US2374455A (en) | 1941-05-02 | 1941-05-02 | Drying of materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2374455A true US2374455A (en) | 1945-04-24 |
Family
ID=23546922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US391518A Expired - Lifetime US2374455A (en) | 1941-05-02 | 1941-05-02 | Drying of materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2374455A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2602084A (en) * | 1951-01-29 | 1952-07-01 | Univ Ohio State Res Found | Preparation of 2-alkali carbohydric derivative utilizing azeotropic distillation |
| US2648475A (en) * | 1946-12-02 | 1953-08-11 | Martin Philip | Method for cleaning and filling containers |
| US2695285A (en) * | 1948-11-04 | 1954-11-23 | Distillers Co Yeast Ltd | Processes for drying streptomycin |
| US2727665A (en) * | 1952-09-24 | 1955-12-20 | Merck & Co Inc | Liquid filling of therapeutic substances |
| US2731731A (en) * | 1952-03-07 | 1956-01-24 | Cutter Lab | Method of drying heat sensitive biologically active substances |
| US3298109A (en) * | 1966-04-21 | 1967-01-17 | Sun Oil Co | Azeotropic drying process |
| US3628967A (en) * | 1969-07-07 | 1971-12-21 | Florasynth Inc | Two-stage solvent drying of foods |
-
1941
- 1941-05-02 US US391518A patent/US2374455A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2648475A (en) * | 1946-12-02 | 1953-08-11 | Martin Philip | Method for cleaning and filling containers |
| US2695285A (en) * | 1948-11-04 | 1954-11-23 | Distillers Co Yeast Ltd | Processes for drying streptomycin |
| US2602084A (en) * | 1951-01-29 | 1952-07-01 | Univ Ohio State Res Found | Preparation of 2-alkali carbohydric derivative utilizing azeotropic distillation |
| US2731731A (en) * | 1952-03-07 | 1956-01-24 | Cutter Lab | Method of drying heat sensitive biologically active substances |
| US2727665A (en) * | 1952-09-24 | 1955-12-20 | Merck & Co Inc | Liquid filling of therapeutic substances |
| US3298109A (en) * | 1966-04-21 | 1967-01-17 | Sun Oil Co | Azeotropic drying process |
| US3628967A (en) * | 1969-07-07 | 1971-12-21 | Florasynth Inc | Two-stage solvent drying of foods |
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