US2150757A - Film drier - Google Patents
Film drier Download PDFInfo
- Publication number
- US2150757A US2150757A US149696A US14969637A US2150757A US 2150757 A US2150757 A US 2150757A US 149696 A US149696 A US 149696A US 14969637 A US14969637 A US 14969637A US 2150757 A US2150757 A US 2150757A
- Authority
- US
- United States
- Prior art keywords
- film
- composition
- alcohol
- formaldehyde
- drier
- 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
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 23
- 239000000203 mixture Substances 0.000 description 23
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 235000019441 ethanol Nutrition 0.000 description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000001828 Gelatine Substances 0.000 description 5
- 229940072049 amyl acetate Drugs 0.000 description 5
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229920000159 gelatin Polymers 0.000 description 5
- 235000019322 gelatine Nutrition 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 5
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 5
- 150000005846 sugar alcohols Polymers 0.000 description 5
- 239000003921 oil Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000012024 dehydrating agents Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- 241001479434 Agfa Species 0.000 description 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- 241000498779 Myristica Species 0.000 description 1
- 235000009421 Myristica fragrans Nutrition 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000017803 cinnamon Nutrition 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000001702 nutmeg Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- RBNWAMSGVWEHFP-UHFFFAOYSA-N trans-p-Menthane-1,8-diol Chemical compound CC(C)(O)C1CCC(C)(O)CC1 RBNWAMSGVWEHFP-UHFFFAOYSA-N 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
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
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C11/00—Auxiliary processes in photography
- G03C11/16—Drying
Definitions
- the present invention relates to a composition for effecting the rapid drying of photographic films.
- Methyl alcohol has the drawback that it has a solvent action on the film base and thereby causes a softening and a permanent swelling of the base, which imparts a decided It is, therefore, manifest that methyl alcohol does not measure up to the practical requirements of the photographic art.
- the object of the present invention is to provide a film drier which will cause a rapid drying of the film without a streaking of the film and without imparting any substantial softening or curling propensities to the film.
- My rapid film drier is a composition essentially comprising a. dehydrating and a hardening agent to which the film and emulsion are inert, such as a low molecular weight aliphatic alcohol and a substance capable of hardening the gelatine layer.
- a hardening agent such as a low molecular weight aliphatic alcohol and a substance capable of hardening the gelatine layer.
- a low molecular weight alcohol which has the function of removing the water as by forming an azeotropic mixture therewith
- I may use such alcohols as ethyl alcohol, isopropyl alcohol and the like either alone or in admixture with each other.
- Different hardening agents for gelatine such as formaldehyde, acetaldehyde, tannic acid, synthetic tanning agents, for example those comprising thiophenol such as that sold under the trade name Katanol and the like may be utilized, but for best results I recommend the utilization of formaldehyde.
- formaldehyde is employed in the form of a 40% solution in water.
- my drier While the principal and essential components of my drier are a dehydrating agent and a hardening agent, I find it advantageous to also include with said components a polyhydric alcohol or another softening agent such as glycerine, glycol, diethylene glycol and the like.
- a polyhydric alcohol or another softening agent such as glycerine, glycol, diethylene glycol and the like.
- the action of the polyhydric alcohol is not only to increase the flexibility of the hardened gelatine layer but it has been found that its presence in the film drier counteracts the tendency of the film to show blushing or to become cloudy, especially if the drying is carried on in an atmosphere of low relative humidity or at higher temperature.
- compositions may also be incorporated in the composition. For instance it is often found desirable to cover the objectionable odor of formaldehyde and therefore to impart to the composition a pleasant odor by adding thereto a substance such as amyl acetate, essential oils and the like. Water may also be added to the composition, if desired. The quantity of water in no case, however, should exceed the quantity of dehydrating agent in the composition.
- Parts are by Parts Methyl alcohol 100 Formaldehyde 40% 10 Glycerine C. P 1,2
- Methyl alcohol 100 Water 9 Formaldehyde 40%-"--. 4.5 Glycerine C. P 1.2 Amyl acetate .6
- the treatment baths of the present invention are used according to the conventional practice of the art, that is the film, after a thorough washing to remove salts carried over from the fixing bath, is placed in a receptacle containing the rapid drying solution. 'The ,fllmis permitted to remain in said solution for a period varying from 1 to 5 minutes. The film is then subjected to the action of theatmosphere whereupon the residual moisture and drying agents are evaporated. If desired, the evaporation of the moisture may be considerably accelerated by subjecting the film to the action of hot air.
- Treatment baths according'to the present invention havebeenfound to very rapidly remove moisture carried by the film without the film suffering anyinjuries as theresult of being suby it can'be seen that said compositions possess par ticularadvantages especially when compared to jected to said treatment baths.
- the film is not streaked as is the case when ethyl alcohol in a concentrated state is employed per se as a I drier.
- compositions of the present invention may be made up by the very simple expedient of mixing. the components thereof, and inasmuch as they produce the de- Nordo'es the film show brittleness or any sired result without injury to the film in any way,
- a rapid film drier containing as its three essential components a volatile low -molecular' weight aliphatic alcohol, an aliphatic polyhydric alcohol and an agent capable of hardening or tanning gelatine, said first alcohol being the predominant component of the composition any waterimmiscible oil in the composition being present in very small amounts, said composition remaining homogeneous after extended use.
- a rapid film drier containingas its three essential components ethyl alcohol, a polyhydric alcohol and aqucousformaldehyde, the ethyl alcohol being the predominant component of said composition any water-immiscible oilin the. composition being present in very small amounts, said composition remaining homogeneous after extended use.
- a rapid film drier consisting of ethyl alcohol
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- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- General Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Paints Or Removers (AREA)
Description
.tendency to the film to curl.
Patented Mar. 14, 1939 UNITED STATES PATENT OFFICE Agfa Ansco Corporation, Binghamton, corporation of New York N. Y., a
No Drawing. Application June 22, 1937, Serial No. 149,696
6 Claims.
The present invention relates to a composition for effecting the rapid drying of photographic films.
It has been found advantageous to rapidly dry photographic negatives after the washing treatment designed to remove substances carried over from the fixing bath as such drying has the effect to lessen the duration of treatment. Rapid drying by the application of elevated temperatures is, of course, more or less hazardous because of the susceptibility of the emulsion to injuries and to the liquification of the gelatine layer at elevated temperatures. The practice has, therefore, been developed of using low boiling, water miscible solvents for removing the water carried by the film. Ethyl alcohol was originally used as such a solvent. Ethyl alcohol, however, has the disadvantage that it causes streaking or clouding of the film. Methy alcohol is less open to this objection and for this reason ethyl alcohol has to a great extent been supplanted by methyl alcohol. Methyl alcohol, on the other hand, has the drawback that it has a solvent action on the film base and thereby causes a softening and a permanent swelling of the base, which imparts a decided It is, therefore, manifest that methyl alcohol does not measure up to the practical requirements of the photographic art.
The object of the present invention is to provide a film drier which will cause a rapid drying of the film without a streaking of the film and without imparting any substantial softening or curling propensities to the film.
My rapid film drier is a composition essentially comprising a. dehydrating and a hardening agent to which the film and emulsion are inert, such as a low molecular weight aliphatic alcohol and a substance capable of hardening the gelatine layer. As the low molecular weight alcohol, which has the function of removing the water as by forming an azeotropic mixture therewith, I may use such alcohols as ethyl alcohol, isopropyl alcohol and the like either alone or in admixture with each other. Different hardening agents for gelatine such as formaldehyde, acetaldehyde, tannic acid, synthetic tanning agents, for example those comprising thiophenol such as that sold under the trade name Katanol and the like may be utilized, but for best results I recommend the utilization of formaldehyde. Generally the formaldehyde is employed in the form of a 40% solution in water.
While the principal and essential components of my drier are a dehydrating agent and a hardening agent, I find it advantageous to also include with said components a polyhydric alcohol or another softening agent such as glycerine, glycol, diethylene glycol and the like. The action of the polyhydric alcohol is not only to increase the flexibility of the hardened gelatine layer but it has been found that its presence in the film drier counteracts the tendency of the film to show blushing or to become cloudy, especially if the drying is carried on in an atmosphere of low relative humidity or at higher temperature.
Other components may also be incorporated in the composition. For instance it is often found desirable to cover the objectionable odor of formaldehyde and therefore to impart to the composition a pleasant odor by adding thereto a substance such as amyl acetate, essential oils and the like. Water may also be added to the composition, if desired. The quantity of water in no case, however, should exceed the quantity of dehydrating agent in the composition.
My invention is further illustrated by the following examples although it is to be understood that my invention is not restricted to these examples. Parts are by Parts Methyl alcohol 100 Formaldehyde 40% 10 Glycerine C. P 1,2
2 Methyl alcohol 67 Isopropyl alcohol 99% 33 Diethylene glycol 1.8 Formaldehyde 40% 10 Oil cinnamon .005 Oil nutmeg .005 Terpinol .02
Methyl alcohol 100 Water 9 Formaldehyde 40%-"--. 4.5 Glycerine C. P 1.2 Amyl acetate .6
4 Ethyl alcohol 100 Formaldehyde 40% 5 Ethylene glycol l0 Amyl acetate .5
The treatment baths of the present invention are used according to the conventional practice of the art, that is the film, after a thorough washing to remove salts carried over from the fixing bath, is placed in a receptacle containing the rapid drying solution. 'The ,fllmis permitted to remain in said solution for a period varying from 1 to 5 minutes. The film is then subjected to the action of theatmosphere whereupon the residual moisture and drying agents are evaporated. If desired, the evaporation of the moisture may be considerably accelerated by subjecting the film to the action of hot air.
Treatment baths according'to the present invention havebeenfound to very rapidly remove moisture carried by the film without the film suffering anyinjuries as theresult of being suby it can'be seen that said compositions possess par ticularadvantages especially when compared to jected to said treatment baths. Thus the film is not streaked as is the case when ethyl alcohol in a concentrated state is employed per se as a I drier.
tendency to curl. Inasmuch as the compositions of the present invention may be made up by the very simple expedient of mixing. the components thereof, and inasmuch as they produce the de- Nordo'es the film show brittleness or any sired result without injury to the film in any way,
the treating baths usedheretofore.
What I claim is:
l. A rapid film drier containing as its three essential components a volatile low -molecular' weight aliphatic alcohol, an aliphatic polyhydric alcohol and an agent capable of hardening or tanning gelatine, said first alcohol being the predominant component of the composition any waterimmiscible oil in the composition being present in very small amounts, said composition remaining homogeneous after extended use.
2. A rapid film drier containingas its three essential components ethyl alcohol, a polyhydric alcohol and aqucousformaldehyde, the ethyl alcohol being the predominant component of said composition any water-immiscible oilin the. composition being present in very small amounts, said composition remaining homogeneous after extended use.
3. A rapid film drier consisting of ethyl alcohol,
a polyhydric alcohol selected from the class con-,
sisting of 'a'glycerine and glycol, aqueous formaldehyde and a substance for imparting a pleasant odor to the composition, the ethyl alcohol being the predominant component or the. composition any water-immiscible oil in the composition being present in very small amounts, said i composition remaining homogeneous after exsaid composition remaining homogeneous after extended use. l l 5. A rapid film drier composition, consisting of 7 Parts Methyl alcohol 100 Water 9 Formaldehyde 40% 4.5 I Glycerine C. P y 1.2 Amyl acetate .6
said: composition remaining, homogeneous after 1 extended use. I
' 6'.-A rapid film drier compositiomconsisting of Parts Ethyl o ol I 100 Formaldehyde 40% 5 Ethylene glycol e 10 g y Amyl acetate .5
said composition remaining homogeneousafter extended use; I
HOWARD O. BODINE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US149696A US2150757A (en) | 1937-06-22 | 1937-06-22 | Film drier |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US149696A US2150757A (en) | 1937-06-22 | 1937-06-22 | Film drier |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2150757A true US2150757A (en) | 1939-03-14 |
Family
ID=22531420
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US149696A Expired - Lifetime US2150757A (en) | 1937-06-22 | 1937-06-22 | Film drier |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2150757A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2472794A (en) * | 1944-09-15 | 1949-06-14 | M W Engleman | Removal of surface moisture from wet articles |
| US2490760A (en) * | 1946-04-15 | 1949-12-06 | Eastman Kodak Co | Water spot prevention in photographic film |
| US2517201A (en) * | 1945-03-01 | 1950-08-01 | Klar Film A G | Liquid for treating motion-picture film |
| US2518686A (en) * | 1945-11-08 | 1950-08-15 | Gen Aniline & Film Corp | Aldehyde antistain baths for developed color photographic material |
| US2556540A (en) * | 1946-04-15 | 1951-06-12 | Eastman Kodak Co | Water spot prevention in photographic film |
| US2684925A (en) * | 1949-03-16 | 1954-07-27 | Technicon Chemical Company Inc | Liquid for treating tissue in histologic processing |
| US3384971A (en) * | 1965-06-11 | 1968-05-28 | Eastman Kodak Co | Non-evaporative drying method |
| US3448528A (en) * | 1967-12-26 | 1969-06-10 | Eastman Kodak Co | Process and apparatus for removing diffusible liquid from a permeable solid |
| US3617274A (en) * | 1968-03-29 | 1971-11-02 | Bell Telephone Labor Inc | Hardened gelatin holographic recording medium |
| US6586713B2 (en) | 1997-08-20 | 2003-07-01 | The University Of Miami | Apparatus for high quality, continuous throughput, tissue fixation-dehydration-fat removal-impregnation |
| US6793890B2 (en) | 1997-08-20 | 2004-09-21 | The University Of Miami | Rapid tissue processor |
| US20050090017A1 (en) * | 2003-10-24 | 2005-04-28 | Morales Azorides R. | Simplified tissue processing |
| US20090298172A1 (en) * | 2008-05-28 | 2009-12-03 | Steven Paul Wheeler | Histological specimen treatment apparatus and method |
| US10365189B2 (en) | 2015-05-07 | 2019-07-30 | Steven Wheeler | Histological specimen treatment |
-
1937
- 1937-06-22 US US149696A patent/US2150757A/en not_active Expired - Lifetime
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2472794A (en) * | 1944-09-15 | 1949-06-14 | M W Engleman | Removal of surface moisture from wet articles |
| US2517201A (en) * | 1945-03-01 | 1950-08-01 | Klar Film A G | Liquid for treating motion-picture film |
| US2518686A (en) * | 1945-11-08 | 1950-08-15 | Gen Aniline & Film Corp | Aldehyde antistain baths for developed color photographic material |
| US2490760A (en) * | 1946-04-15 | 1949-12-06 | Eastman Kodak Co | Water spot prevention in photographic film |
| US2556540A (en) * | 1946-04-15 | 1951-06-12 | Eastman Kodak Co | Water spot prevention in photographic film |
| US2684925A (en) * | 1949-03-16 | 1954-07-27 | Technicon Chemical Company Inc | Liquid for treating tissue in histologic processing |
| US3384971A (en) * | 1965-06-11 | 1968-05-28 | Eastman Kodak Co | Non-evaporative drying method |
| US3448528A (en) * | 1967-12-26 | 1969-06-10 | Eastman Kodak Co | Process and apparatus for removing diffusible liquid from a permeable solid |
| US3617274A (en) * | 1968-03-29 | 1971-11-02 | Bell Telephone Labor Inc | Hardened gelatin holographic recording medium |
| US8221996B2 (en) | 1997-08-20 | 2012-07-17 | The University Of Miami | High quality, continuous throughput, tissue processing |
| US7547538B2 (en) | 1997-08-20 | 2009-06-16 | The University Of Miami | High quality, continuous throughput, tissue processing |
| US6793890B2 (en) | 1997-08-20 | 2004-09-21 | The University Of Miami | Rapid tissue processor |
| US6586713B2 (en) | 1997-08-20 | 2003-07-01 | The University Of Miami | Apparatus for high quality, continuous throughput, tissue fixation-dehydration-fat removal-impregnation |
| US20080153127A1 (en) * | 1997-08-20 | 2008-06-26 | University Of Miami | High quality, continuous throughput, tissue processing |
| US20040004075A1 (en) * | 1997-08-20 | 2004-01-08 | The University Of Miami, Harold Essenfeld | High quality, continuous throughput, tissue processing |
| US20090136992A1 (en) * | 2003-10-24 | 2009-05-28 | The University Of Miami | Simplified tissue processing |
| US7470401B2 (en) | 2003-10-24 | 2008-12-30 | The University Of Miami | Simplified tissue processing |
| US20050090017A1 (en) * | 2003-10-24 | 2005-04-28 | Morales Azorides R. | Simplified tissue processing |
| US8288168B2 (en) | 2003-10-24 | 2012-10-16 | The University Of Miami | Simplified tissue processing |
| US20090298172A1 (en) * | 2008-05-28 | 2009-12-03 | Steven Paul Wheeler | Histological specimen treatment apparatus and method |
| US9366605B2 (en) | 2008-05-28 | 2016-06-14 | Steven Paul Wheeler | Histological specimen treatment apparatus and method |
| US10365189B2 (en) | 2015-05-07 | 2019-07-30 | Steven Wheeler | Histological specimen treatment |
| US10641688B2 (en) | 2015-05-07 | 2020-05-05 | Steven Wheeler | Histological specimen treatment |
| US11885723B2 (en) | 2015-05-07 | 2024-01-30 | Steven Wheeler | Histological specimen treatment |
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