US262077A - Office - Google Patents
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- Publication number
- US262077A US262077A US262077DA US262077A US 262077 A US262077 A US 262077A US 262077D A US262077D A US 262077DA US 262077 A US262077 A US 262077A
- Authority
- US
- United States
- Prior art keywords
- pyroxyline
- solvent
- compound
- cassia
- oil
- 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
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2S,3R,4S,5R,6R)-2-[(2R,3R,4S,5R,6S)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2R,3R,4S,5R,6S)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical class O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 44
- 229920001220 nitrocellulos Polymers 0.000 description 40
- 239000002904 solvent Substances 0.000 description 38
- 150000001875 compounds Chemical class 0.000 description 34
- 240000004499 Cinnamomum aromaticum Species 0.000 description 22
- 235000014489 Cinnamomum aromaticum Nutrition 0.000 description 22
- 239000003921 oil Substances 0.000 description 20
- 241000723347 Cinnamomum Species 0.000 description 18
- 235000004310 Cinnamomum zeylanicum Nutrition 0.000 description 18
- 235000017803 cinnamon Nutrition 0.000 description 18
- 239000000341 volatile oil Substances 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- 241000779819 Syncarpia glomulifera Species 0.000 description 6
- 229940036248 Turpentine Drugs 0.000 description 6
- 239000001739 pinus spp. Substances 0.000 description 6
- DSSYKIVIOFKYAU-UHFFFAOYSA-N Camphor Chemical compound C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 4
- 229960000846 Camphor Drugs 0.000 description 4
- 241000723346 Cinnamomum camphora Species 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- 229930007890 camphor Natural products 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 235000015096 spirit Nutrition 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- -1 pyroxyline compound Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D101/00—Coating compositions based on cellulose, modified cellulose, or cellulose derivatives
- C09D101/08—Cellulose derivatives
- C09D101/16—Esters of inorganic acids
- C09D101/18—Cellulose nitrate
Definitions
- This invention relates to the preparation of compounds containing pyroxyline; and it consists in combining with the pyroxyline the essential oil of cassia or cinnamon, the object being, first, to form with this oil and other ingredients a compound that will act as a latent solvent of pyroxyline to be developed by heat and pressure; second, such solvent to remain in and become a part of the resulting compound and act as a solvent of the solidified collodion at any time when it is subjected to heat and pressure; third, to form with this oil and other ingredients an active solvent of pyroxyline.
- a latent solvent of pyroxyline as follows: I use alcohol alone or alcohol in conjunction with any of the hydrocarbons, such as benzine, benzole, gasoline, 850., or such volatile products as are obtained from petroleum, coal-shale, or other bituminous substances, or spirits of turpentine, all in about equal proportions. To about eight parts of alcohol or any of the above compounds I add one part of the essential oil of cassia or cinnamon. The resulting compound is a latent solvent of pyroxyline, but will not dissolve it at ordinary temperatures. I then take of this latent solvent about one part, by weight, and add tolit one part, by weight, of pyroxyline.
- Another method I have of using my invention is to take, for instance, sulphuric ether and alcohol or any suitable active solvent of pyroxyline, and to about ten parts of this solvent I add one part of the essential oil of cassia or cinnamon, and in about four parts of the resulting compound I dissolve one part of pyroxyline, to which is added such pigments as are necessary to give it the desired weight, elasticity, and color.
- the whole is then thoroughly mixed together and then mixed with spirits of turpentine, using about two quarts of turpentine to each pound of pyroxyline, or such amount as is necessary to saturate the mixture so as to precipitate a part of the solvent.
- the whole is then placed in porous molds of any desired form, where it will drain off and harden.
- camphor in connection with some of the solvents of camphor, has been used as a solvent of pyroxyline, and that also some of the essential oils have been used for the same purpose. I do not know,
- the essential oil of cassia or cinnamon differs from all other essential oils and from all other oils of any kind in that it is a perfect solvent of pyroxyline itself without anything else; but if the pyroxylinc is dissolved in it alone it cannot be evaporated out of the compound so as to allow the pyroxyline to harden. Therefore, to make it of any practical value, it must be mixed with the other ingredients, as hereinbefore described, so that when the other fluids with which it is combined have evaporated the quantity of oil left in the compound is so small that the pyroxyline will become hard, but still retain the properties described, and have withal a permanent agreeable odor.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
UNITED STATES PATENT" intro-n7.
WILLIAM MOOAINE, OF ST. PAUL, MINNESOTA, AS SIGNOR TO HELEN J. MGOAINE, OF SAME PLACE.
* t. IPYROXYLINE COMPOUND.
SPECIFICATION forming part of Letters Patent No. 262,077, dated August 1, 1882.
' Application filed November 17, 188i. (Specimelm) To all whom it'may concern Be it known that I, WILLIAM MOGAINE, of St. Paul, in the county of Ramsey and State of Minnesota, have invented a new and useful Improvement in Pyroxyline Compounds; and I do hereby declare that the following is a full, clear, and exact description of the same.
This invention relates to the preparation of compounds containing pyroxyline; and it consists in combining with the pyroxyline the essential oil of cassia or cinnamon, the object being, first, to form with this oil and other ingredients a compound that will act as a latent solvent of pyroxyline to be developed by heat and pressure; second, such solvent to remain in and become a part of the resulting compound and act as a solvent of the solidified collodion at any time when it is subjected to heat and pressure; third, to form with this oil and other ingredients an active solvent of pyroxyline.
In carrying out my invention I first make a latent solvent of pyroxyline as follows: I use alcohol alone or alcohol in conjunction with any of the hydrocarbons, such as benzine, benzole, gasoline, 850., or such volatile products as are obtained from petroleum, coal-shale, or other bituminous substances, or spirits of turpentine, all in about equal proportions. To about eight parts of alcohol or any of the above compounds I add one part of the essential oil of cassia or cinnamon. The resulting compound is a latent solvent of pyroxyline, but will not dissolve it at ordinary temperatures. I then take of this latent solvent about one part, by weight, and add tolit one part, by weight, of pyroxyline. To this may be added such pigments as are necessary to give it the desired weight and color. The whole is then mixed or ground, either by hand or some suitable machinery, until the dift'erent ingredients are perfectly combined with each other. It is then placed in a suitable mold and subjected to a moderate degree of pressure for the purpose of bringing the particles more intimately together, and while under pressure subjected to from 150 to 200 ofhea-t. I prefer to comm unicate the heat by surrounding the mold with water heated to the proper temperature; but it may be donein this or any other convenient way. The pyroxyline will be perfectly. dis
solved as'soon as the proper degree of heat is attained. It is then removed from the mold and allowed to harden by exposure to the air. When sufli'ciently hard it is again placed in suitable molds and subjected to heat and pressure, and thus molded into any desired form. If it is desirable to make an active solvent, I take eight parts of any of the 'above compounds used in making the latent solvent and add to them two parts of the oil of cassia or cinnamon. This makes a solvent that will dissolve the pyroxyline at common temperatures.
Another method I have of using my invention is to take, for instance, sulphuric ether and alcohol or any suitable active solvent of pyroxyline, and to about ten parts of this solvent I add one part of the essential oil of cassia or cinnamon, and in about four parts of the resulting compound I dissolve one part of pyroxyline, to which is added such pigments as are necessary to give it the desired weight, elasticity, and color. The whole is then thoroughly mixed together and then mixed with spirits of turpentine, using about two quarts of turpentine to each pound of pyroxyline, or such amount as is necessary to saturate the mixture so as to precipitate a part of the solvent. The whole is then placed in porous molds of any desired form, where it will drain off and harden.
Some of the advantages of using the essential oil of cassia or cinnamon in pyroxyline compounds are the following:
First, a portion of the oil will always remain in the compound and act as a solvent of the solidified collodion at any time when exposed to heat, thus making itpracticable to take any number of separate pieces after they have become hard and under heat and pressure form them into one solid homogeneous mass.
Second, its solvent powers are sufficiently developed to dissolve the pyroxyline at so low a degree of heat that it may be imparted to it by surrounding the molds with warm water, thus making the operation perfectly safe.
I am aware of the fact that camphor, in connection with some of the solvents of camphor, has been used as a solvent of pyroxyline, and that also some of the essential oils have been used for the same purpose. I do not know,
ICO
however, that the oil of cassia or cinnamon has ever been used in this connection before. When the oil of cassia is used in the compound the nature of the compound is so changed that it can be molded by heat and pressure almost as perfectly and easily as wax. The reason that the oil of cassia produces this change in pyroxyline compounds is, first, it is a solvent of pyroxyline; secondly, it is of such a nature that it will not all evaporate out of the compound at'ter the latter becomes hard; and, third, its solventpowers are greatly increased by heat, so that when the compound is submitted to heat and pressure it may be said to be redissolved by the small amount of oil remaining in the compound. The essential oil of cassia or cinnamon differs from all other essential oils and from all other oils of any kind in that it is a perfect solvent of pyroxyline itself without anything else; but if the pyroxylinc is dissolved in it alone it cannot be evaporated out of the compound so as to allow the pyroxyline to harden. Therefore, to make it of any practical value, it must be mixed with the other ingredients, as hereinbefore described, so that when the other fluids with which it is combined have evaporated the quantity of oil left in the compound is so small that the pyroxyline will become hard, but still retain the properties described, and have withal a permanent agreeable odor.
What I claim as my invention, and desire to secure by Letters Patent, is-- 1. The use of the essential oil of cassia or cinnamon in the manufacture of compounds containing pyroxyline, substantially as herein described.
2. A pyroxyline compound containing a certain proportion of the essential oil of cassia or cinnamon, as and for the purpose described.
WILLIAM MGOAINE.
WVitnesses:
\VARREN H. MEAD, L. A. VANDERWARKER.
Publications (1)
Publication Number | Publication Date |
---|---|
US262077A true US262077A (en) | 1882-08-01 |
Family
ID=2331353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US262077D Expired - Lifetime US262077A (en) | Office |
Country Status (1)
Country | Link |
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US (1) | US262077A (en) |
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0
- US US262077D patent/US262077A/en not_active Expired - Lifetime
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