US2549005A - Large grain smokeless powder - Google Patents
Large grain smokeless powder Download PDFInfo
- Publication number
- US2549005A US2549005A US629709A US62970945A US2549005A US 2549005 A US2549005 A US 2549005A US 629709 A US629709 A US 629709A US 62970945 A US62970945 A US 62970945A US 2549005 A US2549005 A US 2549005A
- Authority
- US
- United States
- Prior art keywords
- powder
- cellulose acetate
- strip
- smokeless powder
- large grain
- 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
- 239000000843 powder Substances 0.000 title description 34
- 229920002301 cellulose acetate Polymers 0.000 description 21
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 15
- 239000000203 mixture Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 8
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 6
- 239000004014 plasticizer Substances 0.000 description 5
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000000020 Nitrocellulose Substances 0.000 description 4
- 229920001220 nitrocellulos Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 2
- 229960001826 dimethylphthalate Drugs 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000001087 glyceryl triacetate Substances 0.000 description 2
- 235000013773 glyceryl triacetate Nutrition 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 229960002622 triacetin Drugs 0.000 description 2
- NZDNCDGEHXHPCO-UHFFFAOYSA-N 2-[nitro(2-nitrooxyethyl)amino]ethyl nitrate Chemical compound [O-][N+](=O)OCCN([N+]([O-])=O)CCO[N+]([O-])=O NZDNCDGEHXHPCO-UHFFFAOYSA-N 0.000 description 1
- YJERZJLSXBRUDQ-UHFFFAOYSA-N 2-o-(3,4-dihydroxybutyl) 1-o-methyl benzene-1,2-dicarboxylate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OCCC(O)CO YJERZJLSXBRUDQ-UHFFFAOYSA-N 0.000 description 1
- MCNQUWLLXZZZAC-UHFFFAOYSA-N 4-cyano-1-(2,4-dichlorophenyl)-5-(4-methoxyphenyl)-n-piperidin-1-ylpyrazole-3-carboxamide Chemical compound C1=CC(OC)=CC=C1C1=C(C#N)C(C(=O)NN2CCCCC2)=NN1C1=CC=C(Cl)C=C1Cl MCNQUWLLXZZZAC-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 235000015842 Hesperis Nutrition 0.000 description 1
- 235000012633 Iberis amara Nutrition 0.000 description 1
- 235000003332 Ilex aquifolium Nutrition 0.000 description 1
- 241000209027 Ilex aquifolium Species 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- 239000000006 Nitroglycerin Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 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 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- PCYQQSKDZQTOQG-NXEZZACHSA-N dibutyl (2r,3r)-2,3-dihydroxybutanedioate Chemical compound CCCCOC(=O)[C@H](O)[C@@H](O)C(=O)OCCCC PCYQQSKDZQTOQG-NXEZZACHSA-N 0.000 description 1
- LYAGTVMJGHTIDH-UHFFFAOYSA-N diethylene glycol dinitrate Chemical compound [O-][N+](=O)OCCOCCO[N+]([O-])=O LYAGTVMJGHTIDH-UHFFFAOYSA-N 0.000 description 1
- 125000005594 diketone group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229960003711 glyceryl trinitrate Drugs 0.000 description 1
- XLSMFKSTNGKWQX-UHFFFAOYSA-N hydroxyacetone Chemical compound CC(=O)CO XLSMFKSTNGKWQX-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- -1 keto alcohols Chemical class 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000449 nitro group Chemical class [O-][N+](*)=O 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- YZWRNSARCRTXDS-UHFFFAOYSA-N tripropionin Chemical compound CCC(=O)OCC(OC(=O)CC)COC(=O)CC YZWRNSARCRTXDS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/12—Compositions or products which are defined by structure or arrangement of component of product having contiguous layers or zones
Definitions
- This invention relates to an improved large grain smokeless powder and, more particularly, to a large grain smokeless powder having cellulose acetate inhibitor strips bonded thereto by an improved adhesive.
- Plastic strips have been glued to the surface of large grain smokeless powder in order to control the burning area and also to act as spacers to prevent the powder from contact with the wall of the device in which it is .burned. These strips have been applied to the ends of the powder grains, to the sides of cylindrical sticks, and also to the arms of a cruciform stick of smokeless powder. improved ballistics have been obtained by reducing the initial surface of the powder by gluing inhibitor strips of cellulose acetate to the powder surface. The firmness with which the inhibitor strip is adhered to the powder is very important, since a single poorlyadhered strip may seriously affect the ballistics of the weapon or the behavior of the device in which the powder is burned. It has been found undesirable to have air bubbles between the strip and the powder or to have a crack along the edge of the strip which will permit access of the flame to a free surface of powder underneath the strip. Such defects tend to nullify the effect of the strip.
- the smokeless powder had the following composition:
- diacetone alcohol forms an excellent bondbetween cellulose acetate strips and smokeless powder grains.
- Substances which may be added to the diacetone alcohol include cellulose acetate. triacetin, methyl ethyl ketone, acetone, nitrocellulose, diethyl phthalate, dibutyl phthalate, acetol, acetonyl acetone, ethyl acetoacetate, and other diketones, keto esters and keto alcohols.
- cellulose acetate dissolved in diacetone alcohol When cellulose acetate dissolved in diacetone alcohol is used as an adhesive, a desirable bead is formed along the edges of the strip.
- the cellulose acetate may be added to diacetone alcohol up to its limit of solubility.
- the cellulose acetate inhibitor strips may be made from any cellulose acetate which is soluble in the usual organic solvent.
- the cellulose acetate should have an acetic acid content between 51 and 59%.
- the strips may contain between 60 and 90% of cellulose acetate and from 40 to 10% plasticizers.
- Suitable plasticizers include dimethyl phthalate, diethyl phthalate, dibutyl phthalate, methyl phthalyl ethyl glycolate, p-toluene sulfonamid, p-toluene sulfonate, triacetin, tripropionin, dibutyl tartrate and triphenylphosphate.
- the powder compositions for use in accordance with the present invention maybe varied considerably from the specific powder composition set forth in the examples.
- the content and type of nitrocellulose, the content and type of nonvolatile plasticizer and the content and type of other ingredients operable powders of considerable variety may be made.
- the present invention is primarily directed to compositions containing a substantial amount of nonvolatile plasticizer.
- the powder may contain from 35 to about 60% nitroglycerin and/ or similar organic nitrate, such as diethylene glycol dinitrate or diethanol nitramine dinitrate (di(2 nitroxyethyDnitra mine), as the nonvolatile plasticizer, from to about 5% inorganic salts, from about 0.5 to about stabilizer, from about 0.01 to about 2.0% opaquing agent, and from about 40 to about'65% of nitrocellulose.
- organic nitrate such as diethylene glycol dinitrate or diethanol nitramine dinitrate (di(2 nitroxyethyDnitra mine)
- inorganic salts from about 0.5 to about stabilizer, from about 0.01 to about 2.0% opaquing agent, and from about 40 to about'65% of nitrocellulose.
- the large grain smokeless powder grains formed in accordance with this invention are used in jet-propelled devices, such as rockets, airplane starters, assisted take-off devices, catapult devices, gas-producing devices, and the like, including any devices which derive translational o1 rotational energy at least partly from the action produced from the issuance at relatively high speed of fluid medium from an opening in the device.
- jet-propelled devices such as rockets, airplane starters, assisted take-off devices, catapult devices, gas-producing devices, and the like, including any devices which derive translational o1 rotational energy at least partly from the action produced from the issuance at relatively high speed of fluid medium from an opening in the device.
- the diacetone alcohol compositions described in accordance with this invention are excellent adhesives for applying cellulose acetate strips to smokeless powder grains. These compositions are quick-setting and form strong permanent bonds between cellulose acetate and the powder. They do not adversely afiect the stability of the powder and are easily applied without the formation of air bubbles between the strip and the powder; they are nontoxic, evaporate only relatively slowly on standing, and have excellent initial tackiness.
- the term large grain smokeless powder is used, it is meant a smokeless powder having a web thickness of more than 0.20 inch.
- the web thickness is defined as the least burning thickness from the edge of one surface to the edge of another surface, regardless of the configuration of the grain.
- a large smokeless powder grain having a cellulose acetate inhibitor strip tightly bound to the surface thereof by an adhesive region formed at the interface between the powder and the strip by means of a composition consisting essentially of a solution of about 5% cellulose acetate dissolved in diacetone alcohol acting as protect by Letters a plasticizing solvent for both the powder and the strip.
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
Patented Apr. 17, 1951 LARGE GRAIN SMOKELESS POWDER Ralph F. Preckel, Wilmington, DeL, assignor, by mesne assignments, to the United States of America as represented by the Secretary of War No Drawing. Application November 19, 1945, Serial No. 629,709
1 Claim. 1
This invention relates to an improved large grain smokeless powder and, more particularly, to a large grain smokeless powder having cellulose acetate inhibitor strips bonded thereto by an improved adhesive.
Plastic strips have been glued to the surface of large grain smokeless powder in order to control the burning area and also to act as spacers to prevent the powder from contact with the wall of the device in which it is .burned. These strips have been applied to the ends of the powder grains, to the sides of cylindrical sticks, and also to the arms of a cruciform stick of smokeless powder. improved ballistics have been obtained by reducing the initial surface of the powder by gluing inhibitor strips of cellulose acetate to the powder surface. The firmness with which the inhibitor strip is adhered to the powder is very important, since a single poorlyadhered strip may seriously affect the ballistics of the weapon or the behavior of the device in which the powder is burned. It has been found undesirable to have air bubbles between the strip and the powder or to have a crack along the edge of the strip which will permit access of the flame to a free surface of powder underneath the strip. Such defects tend to nullify the effect of the strip.
Many substances which are ordinarily used as 2. There follow some examples which illustrate specific embodiments of the'invention:
EXAMPLES 1 TO- 5 The adhesive compositions given in the table were applied to a cellulose acetate strip which wa then placed on an arm of a cruciform grain of double base smokeless powder. The cellulose acetate strips used had a thickness of 0.1 inch and had the following composition:
Per cent Cellulose acetate 74 Dibutyl phthalate 4 Diethyl phthalate 16 Dimethyl phthalate 6 Acetic acid content 56.557.5% viscosity 150-250 seconds i e., the time of fall of a 5/10-incl1 steel ball through 10 inches of a solution of cellulose acetate in a mixture of 9 parts of methylene chloride to 1 part of alcohol in a 1-inch tube at C.
The smokeless powder had the following composition:
Per cent Nitrocellulose 52.15 Nitro'glycerin 43.00 Diethyl phthalate 3.00 Diphenylamine 0.60 Potassium nitrate 1.25
The results are given in the following table:
Table A o t s r i fi Perm} R k dhesive omposition Time 0 et Up ac inency 0 Omar s amples ness Bond l Diacetcne Alcohol Less than two minutes Good Good. Pozivger pulled after ours. Cellulose Acetate 57 1 2 {lc)ialcetone Alcohol 957% Very good el ulose Acetate l5 3 {Dlacetone Alcohol }Less than three minutes. do Good.
Cellulose Acetate 20 4, Diacetone Alcohol 55% Less than five minutes" do do llr lethylEtlyl Ketone 25% riacetm 5 Diacetone Al ohol 50% mmutes 1 The cellulose acetate had an acetic acid content of 55% and a viscosity of 3 seconds.
It is noted that in each case the initial tackiness of the adhesive was good and the bond formed was strong. After the strip had been adhered to the grain for 24 hours, an attempt was made to pull the inhibitor strip away from the powder grain. When sufficient force was used, a line of separation was produced in the powder beneath the strip. This shows that the bond formed was stronger than the powder.
As illustrated in the above examples, diacetone alcohol, either alone or mixed with various other substances, forms an excellent bondbetween cellulose acetate strips and smokeless powder grains. Substances which may be added to the diacetone alcohol include cellulose acetate. triacetin, methyl ethyl ketone, acetone, nitrocellulose, diethyl phthalate, dibutyl phthalate, acetol, acetonyl acetone, ethyl acetoacetate, and other diketones, keto esters and keto alcohols.
When cellulose acetate dissolved in diacetone alcohol is used as an adhesive, a desirable bead is formed along the edges of the strip. The cellulose acetate may be added to diacetone alcohol up to its limit of solubility.
The cellulose acetate inhibitor strips may be made from any cellulose acetate which is soluble in the usual organic solvent. The cellulose acetate should have an acetic acid content between 51 and 59%. The strips may contain between 60 and 90% of cellulose acetate and from 40 to 10% plasticizers. Suitable plasticizers include dimethyl phthalate, diethyl phthalate, dibutyl phthalate, methyl phthalyl ethyl glycolate, p-toluene sulfonamid, p-toluene sulfonate, triacetin, tripropionin, dibutyl tartrate and triphenylphosphate.
The powder compositions for use in accordance with the present invention maybe varied considerably from the specific powder composition set forth in the examples. By proper variation of the content and type of nitrocellulose, the content and type of nonvolatile plasticizer and the content and type of other ingredients, operable powders of considerable variety may be made. However, the present invention is primarily directed to compositions containing a substantial amount of nonvolatile plasticizer. For example, the powder may contain from 35 to about 60% nitroglycerin and/ or similar organic nitrate, such as diethylene glycol dinitrate or diethanol nitramine dinitrate (di(2 nitroxyethyDnitra mine), as the nonvolatile plasticizer, from to about 5% inorganic salts, from about 0.5 to about stabilizer, from about 0.01 to about 2.0% opaquing agent, and from about 40 to about'65% of nitrocellulose.
The large grain smokeless powder grains formed in accordance with this invention are used in jet-propelled devices, such as rockets, airplane starters, assisted take-off devices, catapult devices, gas-producing devices, and the like, including any devices which derive translational o1 rotational energy at least partly from the action produced from the issuance at relatively high speed of fluid medium from an opening in the device.
The diacetone alcohol compositions described in accordance with this invention are excellent adhesives for applying cellulose acetate strips to smokeless powder grains. These compositions are quick-setting and form strong permanent bonds between cellulose acetate and the powder. They do not adversely afiect the stability of the powder and are easily applied without the formation of air bubbles between the strip and the powder; they are nontoxic, evaporate only relatively slowly on standing, and have excellent initial tackiness.
Where, in the specification and in the ap pended claims, the term large grain smokeless powder is used, it is meant a smokeless powder having a web thickness of more than 0.20 inch. The web thickness is defined as the least burning thickness from the edge of one surface to the edge of another surface, regardless of the configuration of the grain.
What I claim and desire to Patent is:
A large smokeless powder grain having a cellulose acetate inhibitor strip tightly bound to the surface thereof by an adhesive region formed at the interface between the powder and the strip by means of a composition consisting essentially of a solution of about 5% cellulose acetate dissolved in diacetone alcohol acting as protect by Letters a plasticizing solvent for both the powder and the strip.
RALPH F. PRECKEL.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 778,788 Maxim Dec. 27, 1904 1,354,442 Woodbridge et a1. Sept. 20, 1920 1,793,915 Dreyfus Feb. 24, 1931 2,044,356 Keeran June 16, 1936 2,229,208 Holm et a1. Jan. 21, 1941 FOREIGN PATENTS Number Country Date 27,197 Great Britain Nov. 30, 1897 of 1896 502,560 France Feb. 24, 1920 OTHER REFERENCES Brady: Materials Handbook, McGraw-Hill Book Company, 1944, pages 6, and 9 and 10. (Copy in Division 30.)
Hackhs Chemical Dictionary, by J. Grant, third edition, The Blakiston Company, Philadelphia, Pennsylvania, page 263, 1944. (Copy in Division 43, U. S. Patent Office.)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US629709A US2549005A (en) | 1945-11-19 | 1945-11-19 | Large grain smokeless powder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US629709A US2549005A (en) | 1945-11-19 | 1945-11-19 | Large grain smokeless powder |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2549005A true US2549005A (en) | 1951-04-17 |
Family
ID=24524159
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US629709A Expired - Lifetime US2549005A (en) | 1945-11-19 | 1945-11-19 | Large grain smokeless powder |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2549005A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2877709A (en) * | 1956-04-23 | 1959-03-17 | Olin Mathieson | Cartridge |
| US2939396A (en) * | 1954-09-02 | 1960-06-07 | Phillips Petroleum Co | Rocket grain |
| US3012508A (en) * | 1961-12-12 | Shaped ammonium nitrate propellant grain | ||
| US3012507A (en) * | 1961-12-12 | Shaped- ammonium nitrate propellant | ||
| US3077734A (en) * | 1956-12-10 | 1963-02-19 | Phillips Petroleum Co | Solid-propellant rocket motor |
| US3442744A (en) * | 1967-12-11 | 1969-05-06 | Robert M Teter Jr | Form wrapped with cellulose acetate strip material and method of wrapping said material |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US778788A (en) * | 1901-03-21 | 1904-12-27 | Hudson Maxim | Motive-power combustible for automobile torpedoes. |
| FR502560A (en) * | 1916-08-21 | 1920-05-19 | Procedes Westinghouse Leblanc | Aerial torpedo |
| US1354442A (en) * | 1920-02-25 | 1920-09-28 | Du Pont | Progressively-burning powder and proccess of making the same |
| US1793915A (en) * | 1927-07-15 | 1931-02-24 | Dreyfus Camille | Plaited fabric and process of producing the same |
| US2044356A (en) * | 1932-06-29 | 1936-06-16 | Du Pont Viscoloid Co | Method of making celluloid articles |
| US2229208A (en) * | 1936-10-22 | 1941-01-21 | Ici Ltd | Gas generating cartridge |
-
1945
- 1945-11-19 US US629709A patent/US2549005A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US778788A (en) * | 1901-03-21 | 1904-12-27 | Hudson Maxim | Motive-power combustible for automobile torpedoes. |
| FR502560A (en) * | 1916-08-21 | 1920-05-19 | Procedes Westinghouse Leblanc | Aerial torpedo |
| US1354442A (en) * | 1920-02-25 | 1920-09-28 | Du Pont | Progressively-burning powder and proccess of making the same |
| US1793915A (en) * | 1927-07-15 | 1931-02-24 | Dreyfus Camille | Plaited fabric and process of producing the same |
| US2044356A (en) * | 1932-06-29 | 1936-06-16 | Du Pont Viscoloid Co | Method of making celluloid articles |
| US2229208A (en) * | 1936-10-22 | 1941-01-21 | Ici Ltd | Gas generating cartridge |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3012508A (en) * | 1961-12-12 | Shaped ammonium nitrate propellant grain | ||
| US3012507A (en) * | 1961-12-12 | Shaped- ammonium nitrate propellant | ||
| US2939396A (en) * | 1954-09-02 | 1960-06-07 | Phillips Petroleum Co | Rocket grain |
| US2877709A (en) * | 1956-04-23 | 1959-03-17 | Olin Mathieson | Cartridge |
| US3077734A (en) * | 1956-12-10 | 1963-02-19 | Phillips Petroleum Co | Solid-propellant rocket motor |
| US3442744A (en) * | 1967-12-11 | 1969-05-06 | Robert M Teter Jr | Form wrapped with cellulose acetate strip material and method of wrapping said material |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2643611A (en) | Large grain smokeless powder | |
| US2549005A (en) | Large grain smokeless powder | |
| US2407209A (en) | Stabilization of nitrocellulose film base | |
| US1640712A (en) | Acceleration of gelatinization of cellulose nitrate | |
| US1969477A (en) | Nitrocellulose cement | |
| US2294228A (en) | Plasticized polyvinyl acetal resin | |
| US2471272A (en) | Water-soluble cellulose ether plasticized with a cyclomethylene sulfone | |
| US2371957A (en) | Plasticized polyvinyl acetal composition | |
| US1981141A (en) | Cementing foil and thin film | |
| US1924465A (en) | Process of producing propellent powder | |
| US2430424A (en) | Plastic compositions containing a fatty acid ester of styrene glycol | |
| US3418202A (en) | Hot metal adhesive composition | |
| US2218146A (en) | Chemical composition | |
| US2436116A (en) | Cellulose organic acid ester plastic containing resorcinol monobenzoate | |
| US2561315A (en) | Plasticized polyvinyl formal resin | |
| US2006182A (en) | Laminated safety glass | |
| US2375708A (en) | Plastic composition | |
| US2136436A (en) | Laminated article | |
| US2384538A (en) | Plasticized polyvinyl acetal resin | |
| US1958708A (en) | Protective covering including a dialkyl ester of phthalic acid | |
| US2399330A (en) | Plasticized compositions | |
| US2014403A (en) | Composition | |
| US1456782A (en) | Cellulose-ester composition | |
| US2393513A (en) | Polyvinyl acetal plasticized with a diglycerol ether | |
| US1647435A (en) | Actinismproof cellulose-ester composition |