US269345A - John h - Google Patents
John h Download PDFInfo
- Publication number
- US269345A US269345A US269345DA US269345A US 269345 A US269345 A US 269345A US 269345D A US269345D A US 269345DA US 269345 A US269345 A US 269345A
- Authority
- US
- United States
- Prior art keywords
- oil
- alcohol
- new
- ordinary
- john
- 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
- 239000003921 oil Substances 0.000 description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 38
- 229920001220 nitrocellulos Polymers 0.000 description 24
- 229940079938 Nitrocellulose Drugs 0.000 description 16
- 239000000020 Nitrocellulose Substances 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- 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 compound 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 14
- 150000001875 compounds Chemical class 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 240000000662 Anethum graveolens Species 0.000 description 2
- 235000007639 Anthemis cotula Nutrition 0.000 description 2
- 238000003339 Best practice Methods 0.000 description 2
- 240000004183 Bongardia chrysogonum Species 0.000 description 2
- DSSYKIVIOFKYAU-UHFFFAOYSA-N Camphor Chemical compound C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 2
- 229960000846 Camphor Drugs 0.000 description 2
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 2
- 241000723346 Cinnamomum camphora Species 0.000 description 2
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 2
- 235000004310 Cinnamomum zeylanicum Nutrition 0.000 description 2
- 240000004559 Cuminum cyminum Species 0.000 description 2
- 235000007129 Cuminum cyminum Nutrition 0.000 description 2
- 240000002776 Cymbopogon martinii Species 0.000 description 2
- 229960000935 Dehydrated Alcohol Drugs 0.000 description 2
- 241000132521 Erigeron Species 0.000 description 2
- 235000004694 Eucalyptus leucoxylon Nutrition 0.000 description 2
- 244000004281 Eucalyptus maculata Species 0.000 description 2
- 235000010705 Eucalyptus maculata Nutrition 0.000 description 2
- 235000009683 Eucalyptus polybractea Nutrition 0.000 description 2
- 235000009687 Eucalyptus sargentii Nutrition 0.000 description 2
- 240000006223 Matricaria chamomilla Species 0.000 description 2
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 2
- 240000006217 Mentha pulegium Species 0.000 description 2
- 235000016257 Mentha pulegium Nutrition 0.000 description 2
- 244000227633 Ocotea pretiosa Species 0.000 description 2
- 235000004263 Ocotea pretiosa Nutrition 0.000 description 2
- 240000000783 Origanum majorana Species 0.000 description 2
- 235000006297 Origanum majorana Nutrition 0.000 description 2
- 240000003136 Rosmarinus officinalis Species 0.000 description 2
- 235000017304 Ruaghas Nutrition 0.000 description 2
- 235000000914 Solidago virgaurea Nutrition 0.000 description 2
- 240000006745 Valeriana officinalis Species 0.000 description 2
- 235000013832 Valeriana officinalis Nutrition 0.000 description 2
- NNJVILVZKWQKPM-UHFFFAOYSA-N Xylocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 description 2
- 239000001264 anethum graveolens Substances 0.000 description 2
- 229930007890 camphor Natural products 0.000 description 2
- 235000001544 chamomile Nutrition 0.000 description 2
- 235000017803 cinnamon Nutrition 0.000 description 2
- KHLVKKOJDHCJMG-QDBORUFSSA-L disodium;(2E)-3-oxo-2-(3-oxo-5-sulfonato-1H-indol-2-ylidene)-1H-indole-5-sulfonate Chemical compound [Na+].[Na+].N/1C2=CC=C(S([O-])(=O)=O)C=C2C(=O)C\1=C1/NC2=CC=C(S(=O)(=O)[O-])C=C2C1=O KHLVKKOJDHCJMG-QDBORUFSSA-L 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 235000001612 eucalyptus Nutrition 0.000 description 2
- 235000001617 eucalyptus Nutrition 0.000 description 2
- 235000001621 eucalyptus Nutrition 0.000 description 2
- 235000006356 eucalyptus Nutrition 0.000 description 2
- 235000001050 hortel pimenta Nutrition 0.000 description 2
- 238000000034 method Methods 0.000 description 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 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- 235000006678 peppermint Nutrition 0.000 description 2
- 235000007735 peppermint Nutrition 0.000 description 2
- 235000015132 peppermint Nutrition 0.000 description 2
- 235000005227 red mallee Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000016788 valerian Nutrition 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
- alcohol is of itself a solvent of nitrocellulose under certain conditions-that is to say, ordinary alcohol, (such as is known as ninety-five per cent) when heated to about 160 or 1700 Fahrenheit, will readily dissolve the ordinary soluble forms of nitro-cellulose; or, if the nitrocellulose is made extra soluble, it can be converted into a solid compound with ordinary alcohol by the use of heated rolls; or, again, with a sufficient quantity of absolute alcohol or dehydrated alcohol, the ordinary forms of soluble nitrocellulose, such as are used in these compounds, can be readily converted in open rolls; but it is only with such qualifications that alcohol can be termed a solvent of nitrocellulose, and as the necessary conditions are difficult of attainment in the practical manufacture of these compounds alcohol alone is not used as a solvent, and, in a practical sense, is not classed with the solv- 0 cuts of pyroxyline.
- the best practice in using these ingredients in conjunction with alcohol is to add the alcohol to the nitro-cellulose,incorporatingin this mixture the coloring- 6 matters and other inert substances to be included in the product, and then to add the new menstruum, which may be any one of those enumerated above, or a mixture of any two or moreofthem.
- Thecompound shouldbeallowed to stand after the addition of the menstruum for about twelve hours in a closed vessel, and then be masticated in heated rolls in the usual manner, and the product should be formed into shapes before it has hardened or seasoned with time.
- YVood-spirit may be usedin conjunction with alcohol and with my new menstrua; but in such case the menstruum should be first mixed with the nitro-cellulose and other ingreo hists, and the alcohol and wood-spirit mixed separately and added last. In other respects the treatment is the same as already described. With wood-spirit good proportions would be:
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Medicines Containing Plant Substances (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
UNITED STATES .ATENT FFICE.
JOHN H. STEVENS, OF NEWARK, NEW JERSEY, ASSIGNOR TO THE CELLU- LOID MANUFACTURING COMPANY, OF NEW YORK, N. Y.
MANUFACTURE OF COMPOUNDS F PYROXYLINE OR NlTRO-CELLULOSE.
SPECIFICATION forming part of Letters Patent No. 269,345, dated December 19, 1882.
Application filed June 24, 1882. (No specimens.)
To an whom it may concern Be it known that I, JOHN H. STEVENS, of the city 01' Newark, in the county of Essex and State of New Jersey, have invented cer- 5 tain new and useful Improvements in the Mannfacture of Compounds of Pyro'xyline or Nitro- Oellulose, of which improvements the following is a specification.
It is well known to those skilled in this manu- IO 'facture that alcohol is of itself a solvent of nitrocellulose under certain conditions-that is to say, ordinary alcohol, (such as is known as ninety-five per cent) when heated to about 160 or 1700 Fahrenheit, will readily dissolve the ordinary soluble forms of nitro-cellulose; or, if the nitrocellulose is made extra soluble, it can be converted into a solid compound with ordinary alcohol by the use of heated rolls; or, again, with a sufficient quantity of absolute alcohol or dehydrated alcohol, the ordinary forms of soluble nitrocellulose, such as are used in these compounds, can be readily converted in open rolls; but it is only with such qualifications that alcohol can be termed a solvent of nitrocellulose, and as the necessary conditions are difficult of attainment in the practical manufacture of these compounds alcohol alone is not used as a solvent, and, in a practical sense, is not classed with the solv- 0 cuts of pyroxyline. It is, however, a valuable ingredient of such compounds, and it is the object of my invention to render it available in the ordinary processes by employing in conjunction with it certain other ingredi- 5 cuts, which, as I have discovered, when combinedwith ordinary alcohol, constitute or form solvents of nitrocellulose under ordinary conditions.
It has long been known that, as above ex- 0 plained, while alcohol is not of itself an active or positive solvent of nitrocellulose under ordinary conditions, yet in conjunction with camphor or with ether and with several other substances it forms such an active solvent. The
4 5 category of these substances has heretofore been limited, and l have, by experiment, ascertained that while in themselves like alcohol not solvents of pyroxyline, yet in conjunction with alcohol the following new menstrua constitute active solvents under ordinary condi- 5o tions, to wit racetal, nitrate of amyl, nitrite of aniyl, oil of chamomile, oil of valerian, oil of golden-rod, oil of sassafras, oil ofanise, light oil of cinnamon, oil of cumin, oil ofcynaa ether, oil of dill, oil otelecampane, oil offennel-seed,0il of eucalyptus, oil of fennel-chaff, oil of wine, (heavy,)oilofworm-seed,oilofmyrtle,oiloflaurel, oil of marjoram, oil of peppermint, oil ofrue, oil of cinnamon-leaves, oil of palmarosa, oil of rosemary, (that from French flowers preferred.) oil of erigeron, and these are what I herein refer to as new menstrua. The best practice in using these ingredients in conjunction with alcohol is to add the alcohol to the nitro-cellulose,incorporatingin this mixture the coloring- 6 matters and other inert substances to be included in the product, and then to add the new menstruum, which may be any one of those enumerated above, or a mixture of any two or moreofthem. Thecompound shouldbeallowed to stand after the addition of the menstruum for about twelve hours in a closed vessel, and then be masticated in heated rolls in the usual manner, and the product should be formed into shapes before it has hardened or seasoned with time. Varying between the extremes given according as the menstruum selected is less or more volatile-the less volatile, as the oils, requiring the smaller proportion, and the more volatile, as the ethers, requiring the greater proportion-the proportions used will be about as follows: of pyroxyline, say, four parts, by weight; alcohol, three to four parts, by weight; any of the above-enumerated menstrna, (or mixtures of the same,') two to three 8 parts, by weight.
YVood-spirit may be usedin conjunction with alcohol and with my new menstrua; but in such case the menstruum should be first mixed with the nitro-cellulose and other ingreo dients, and the alcohol and wood-spirit mixed separately and added last. In other respects the treatment is the same as already described. With wood-spirit good proportions would be:
pyr0xyline,tw0 parts, by Weight; alcohol,one part; menstruum, one part; wood-spirit, one part, all by weight;
Having thus described the nature and 0h- 5 jects of my invention, What I claim as new,
and desire to secure by Letters .Patent, is-
As an improvement in the manufacture ofl compounds of pyroxyline, the employment, in
conjunction with alcohol, (ethylic or methylic,) of the hereinbefore-specified new menstrua or to mixtures of the same, substantially as described.
JOHN H. STEVENS. \Vitnesses AB RAIIAM: MANNEns, J. O. FORGE.
Publications (1)
Publication Number | Publication Date |
---|---|
US269345A true US269345A (en) | 1882-12-19 |
Family
ID=2338590
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US269345D Expired - Lifetime US269345A (en) | John h |
Country Status (1)
Country | Link |
---|---|
US (1) | US269345A (en) |
-
0
- US US269345D patent/US269345A/en not_active Expired - Lifetime
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