US608726A - Pyroxylin compound - Google Patents
Pyroxylin compound Download PDFInfo
- Publication number
- US608726A US608726A US608726DA US608726A US 608726 A US608726 A US 608726A US 608726D A US608726D A US 608726DA US 608726 A US608726 A US 608726A
- Authority
- US
- United States
- Prior art keywords
- pyroxylin
- lead
- acetate
- compounds
- compound
- 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
- 229920001220 nitrocellulos Polymers 0.000 title description 46
- 229940079938 Nitrocellulose Drugs 0.000 title description 44
- 229950006485 Pyroxylin Drugs 0.000 title description 44
- -1 Pyroxylin compound Chemical class 0.000 title description 4
- 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 46
- 150000003839 salts Chemical class 0.000 description 22
- 239000011780 sodium chloride Substances 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 16
- 239000002253 acid Substances 0.000 description 16
- GUWSLQUAAYEZAF-UHFFFAOYSA-L Lead(II) acetate Chemical compound O1C(C)=O[Pb]21O=C(C)O2 GUWSLQUAAYEZAF-UHFFFAOYSA-L 0.000 description 14
- 229940046892 lead acetate Drugs 0.000 description 14
- 239000002360 explosive Substances 0.000 description 12
- 239000003159 antacid agent Substances 0.000 description 10
- 230000001458 anti-acid Effects 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
- 239000003755 preservative agent Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 4
- FERIUCNNQQJTOY-UHFFFAOYSA-M butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-M methanoate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 4
- 230000001264 neutralization Effects 0.000 description 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-M valerate Chemical compound CCCCC([O-])=O NQPDZGIKBAWPEJ-UHFFFAOYSA-M 0.000 description 4
- 229940070710 valerate Drugs 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229940069428 ANTACIDS Drugs 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L Magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 229920002892 amber Polymers 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229960004756 ethanol Drugs 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- FYDIWJWWROEQCB-UHFFFAOYSA-L lead(2+);propanoate Chemical compound [Pb+2].CCC([O-])=O.CCC([O-])=O FYDIWJWWROEQCB-UHFFFAOYSA-L 0.000 description 2
- 239000006193 liquid solution Substances 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 239000011776 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002035 prolonged Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 230000001681 protective Effects 0.000 description 2
- 230000001603 reducing Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- 238000009736 wetting Methods 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
- I preferably introduce the acetate of lead dissolved in wood-spirit or grain-alcohol.
- transparent products I mean those solid homogeneous combinations which per mit the transmission of light-for instance,
- Acetate of lead is also useful in making an imitation of jet from pyroxylin, as theeffects of the salt do not interfere with the required depth of color, while the desirable depth of color or intense blackness is interfered with more or less when some of the ordinary antacid substances-like magnesium carbonate, for instance are used.
- lead acetate is only one member of a class of substances known as the lead salts of the volatile monatomic fatty acids. These acids are formic, acetic, propionic, butyric, and Valerie acids. Ihave found that all of these salts are equivalents as preserving agents for pyroxylin, although they vary in intensity of effect.
- the lead acetate is to be preferred, both on account of its gen eral properties and low price.
- the butyrate and valerate of lead are equal to the acetate as preservers and can be used in the same proportions; but they have an ofiensive odor.
- the propionate of lead is a powerful antacid and also yields transparent products.
- the formate of lead is more feeble in preserving power than the acetate and other members of this class, and 1t does not give good transparency.
- Eflicient antacid or preserving agents to be used with pyroxylin are scarce. Many substances have been proposed and used, but with more or less failure. I have found in practice that some of the proposed antacids really aid decomposition and seem to either invite the nitro elements to leave the pyroxylin or else by their presence or reducing action change the pyroxylin to a more easily decomposable condition.
- a new composition of matter consisting of pyroxylin, a solvent of the same, and a lead salt of a volatile monatomic fatty acid.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
JOHN II. STEVENS, OE NEWARK, NEW JERSEY, ASSIGNOR TO THE OELLULOID COMPANY, OF NEW YORK, N. Y., A CORPORATION OF NEW JERSEY.
pvsoxvun COMPOUND.
SPECIFICATION forming part of Letters Patent No. 608,726, dated August 9, 1898. Application filed April 1, 1898. Serial No. 676,056. (No specimens.)
To all, whom it may concern,- V
Be it known that I, JOHN H. STEVENS, of the city of Newark, county of Essex, and State of New Jersey, have invented certain new and useful Improvements in Pyroxylin Gompounds, of which the following is a specification The object of my invention is to render pyroxylin or nitrated cellulose and its compounds less liable to acid decomposition. As is well known, the nitro elements in perfectly pure or freshly-made pyroxylin are held in such close chemical combination that it is neutral to test-paper. I In the course of time and under extraordinary conditions-like high temperatures, for instance-these nitro elements are slowly evolved as free acid, which results in great danger when the dry pyroxylin is stored or transported and also injures those compounds which are made by dissolving pyroxylin for the purpose of making liquid solutions or solid products.
I have discovered that by combining pyroxylin with asmall proportion of lead acetate this tendency to a disorganization of its constituent elements is entirely prevented under ordinary conditions and is minimized under extraordinary conditions,lik'e prolonged heat mg or age.
In practicing my invention I proceed as follows: IVhen the pyroxylin is to be sold or stored in a dry state, I introduce the lead acetate by thoroughly wetting the pyroxylin with a solution of the preservingsalt in water or other menstruum which does not dissolve the pyroxylin. On evaporating or otherwise removing the water the pyroxylin is left in a more permanent condition.
In using the acetate of lead in pyroxylin compounds made with solvents I preferably introduce the acetate of lead dissolved in wood-spirit or grain-alcohol. The acetate of lead is especially suitable for materials used as explosives or pyroxylin compounds in which extreme paleness is not a necessary feature. I have, however, obtained good results byits use in a pyroxylin compound made in imitation of clear tortoiseshell and have success fully employed it in making thin trans= parent sheets. The slightly-yellow color imparted by the acetate of lead does no harm to many of these transparent products.
By. transparent products I mean those solid homogeneous combinations which per mit the transmission of light-for instance,
imitations of glass, amber, shell, &c.-and also solutions and varnishes used for pro tective purposes. Explosives, like guncotton and smokeless powder, are not classed with transparent compounds, as their form prevents theunimpeded passage of light. Be
sides, transparency in explosives is not at all required.
Acetate of lead is also useful in making an imitation of jet from pyroxylin, as theeffects of the salt do not interfere with the required depth of color, while the desirable depth of color or intense blackness is interfered with more or less when some of the ordinary antacid substances-like magnesium carbonate, for instance are used.
As to proportions, for explosive compounds I would recommend two per cent. by weight,
of the salt to the amount of pyroxylin pres ent in the compound. For manufacturing compounds made with solvents I have obtained the best results by the use of one per cent.
Although I have only spoken of lead acetate thus far, yet lead acetate is only one member of a class of substances known as the lead salts of the volatile monatomic fatty acids. These acids are formic, acetic, propionic, butyric, and Valerie acids. Ihave found that all of these salts are equivalents as preserving agents for pyroxylin, although they vary in intensity of effect. The lead acetate is to be preferred, both on account of its gen eral properties and low price.
The butyrate and valerate of lead are equal to the acetate as preservers and can be used in the same proportions; but they have an ofiensive odor. The propionate of lead is a powerful antacid and also yields transparent products. The formate of lead is more feeble in preserving power than the acetate and other members of this class, and 1t does not give good transparency.
Eflicient antacid or preserving agents to be used with pyroxylin are scarce. Many substances have been proposed and used, but with more or less failure. I have found in practice that some of the proposed antacids really aid decomposition and seem to either invite the nitro elements to leave the pyroxylin or else by their presence or reducing action change the pyroxylin to a more easily decomposable condition.
.In general I advise using the lead acetate and lead propionate in a proportion of one per cent, by weight, of the salt to the pyroxylin for transparent products and in non-ex plosive compounds and would recommend the use of both of these salts and the formate in a two-per-cent. proportion for explosive compounds. I would confine the butyrate and valerate of lead to explosives or to compounds in which the offensive odor they impart would be unobj ectionable. I do not confine myself to definite proportions; but the proportions suggested are the best to use.
I am unable to explain why the lead salts 'act as a preserving agent when the lead is already saturated with an acid and in neutral condition, as is the case with lead acetate. I can only saythat my experiments show this to be a fact.
I have found that in the case of salts containing two or more dissimilar acid radicals the preserving power depends largely on the nature of the acid radicals present. Thus a compound lead salt containing the radical of acetic acid would have some preserving power even though the other acid radical present possessed no power to form an antacid of pyroxylin and a lead salt of a volatile monatomic fatty acid.
2. A new composition of matter consisting of pyroxylin, a solvent of the same, and a lead salt of a volatile monatomic fatty acid.
3. A new transparent composition of matter containing pyroxylin and acetate of lead.
JOHN H. STEVENS.
Witnesses ABRAHAM MANNERS, J. W. FAITONTE.
Publications (1)
Publication Number | Publication Date |
---|---|
US608726A true US608726A (en) | 1898-08-09 |
Family
ID=2677345
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US608726D Expired - Lifetime US608726A (en) | Pyroxylin compound |
Country Status (1)
Country | Link |
---|---|
US (1) | US608726A (en) |
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0
- US US608726D patent/US608726A/en not_active Expired - Lifetime
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