US2004505A - Priming mixture - Google Patents
Priming mixture Download PDFInfo
- Publication number
- US2004505A US2004505A US631102A US63110232A US2004505A US 2004505 A US2004505 A US 2004505A US 631102 A US631102 A US 631102A US 63110232 A US63110232 A US 63110232A US 2004505 A US2004505 A US 2004505A
- Authority
- US
- United States
- Prior art keywords
- lead
- priming
- mixture
- priming mixture
- tetrazene
- 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
- 239000000203 mixture Substances 0.000 title description 20
- 230000037452 priming Effects 0.000 title description 15
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 14
- 150000001540 azides Chemical class 0.000 description 9
- 150000004655 tetrazenes Chemical class 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 8
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 description 6
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 5
- 229910021346 calcium silicide Inorganic materials 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- 229910052788 barium Inorganic materials 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- MHWLNQBTOIYJJP-UHFFFAOYSA-N mercury difulminate Chemical compound [O-][N+]#C[Hg]C#[N+][O-] MHWLNQBTOIYJJP-UHFFFAOYSA-N 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 229910021332 silicide Inorganic materials 0.000 description 3
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 3
- BZWKPZBXAMTXNQ-UHFFFAOYSA-N sulfurocyanidic acid Chemical compound OS(=O)(=O)C#N BZWKPZBXAMTXNQ-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
- ATWZAQSVECJGON-UHFFFAOYSA-N 2-(aminodiazenyl)-1-(2-oxohydrazinyl)guanidine Chemical compound N(=O)NNC(=N)N=NNN ATWZAQSVECJGON-UHFFFAOYSA-N 0.000 description 1
- 101100367123 Caenorhabditis elegans sul-1 gene Proteins 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000005267 amalgamation Methods 0.000 description 1
- HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical compound NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000005337 ground glass Substances 0.000 description 1
- 239000003721 gunpowder Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B35/00—Compositions containing a metal azide
Definitions
- I employ an initiat0l,i00IlSiStiIlg 0f normal lead azide, a-sensitizer, as hereinafter defined more at length, afuel' in-' gredient preferably consisting of antimony sul- 1 phide, 'lea'd sulphocyanide 'and cal'cium' silicide,
- an oxidizing ingredient preferably consisting of lead' peroxide" and barium nitrate, :ortheir'equivalents, either with Y or without minor additions of components here'- tofore used in priming compounds to control or vary thezicharacteris'tics thereof :5.
- Heretofore.mercury fulmina'te hasbeen' generally used as the initiator in priming mixtures "for smallarms ammunition. It possesses many composition of the mercury fulminate when the cartridge is exploded prevents reloading of center fire cartridges. By employing an initiator in which no mercury fulminate is present, this amalgamation is eliminated, which permits reloading and re-use of center fire cartridge cases.
- the priming mixture of my invention also possesses advantage for use in rim fire primers. It has greater stability on storing and therefore permits the ammunition to be used and better results obtained after it has been stored forlong periods of time.
- a suitable priming mixture for center fire cartridges may be formed by mixing the following ingredients in substantially the following proportions, by weight:
- these ingredients are first thoroughly and homogeneously mixed. The mixture is then poured into individual pellets of the proper size for the individual charges, all in a customcartridge, the magnitude of the gun powder 0 aryway.
- the priming mixture forming the subject matter o? the present ginvefi'tion'; may fals'o be employed in rim fire cartridges and Without substantial change in the illustrative proportions above set forth, excepting for the addition of say 20% of ground glass, the latter being -a common constituent of rim fire mixtureswhere'" serves as an abrasive in :a manner WeIl un derstood in the art.
- the priming mixture then fl-creed to distributeitselfintofihe'ihollow rim of "the cartri'dge'shell byfspinr'iing'the shell in the customary machine.
- the shells are then loaded with powder and "bullets in'the 'custor'n-
- the "oxygen supplying elements and fills mentioned above? are referred to; ample?Knownequivalentsmay ,7 I foranyor all of them without departingfrom the spirit crthe'invention.
- jle'a'd nitrate may be .employedin place ,.of bariumjnltrata'the quantity of'lead nitrateto be employed varying slightly "from 'the'i quantity o fjfbarium nitrate given above .to obtainsubstantially the same qualitiesinthe resulting mixture.
- a priming mixture for small arms ammunition comprising normal lead azide, barium nitrate, lead peroxide, calcium silicide, antimony sulphide and tetrazene.
- a priming mixture for small arms ammunitidn comprisingfwrmalflead azide; tetrazene, barium nitrate; lead peroxide, antimony sulphide, calcium silicide and lead sulphocyanide. 5.
- a priming mixture for small arms ammuniti-omeorn prising 10% to 20% normal lead azide, 20% to30'% barium nitrate, 15% to lead perox-lde, "ll5% ito25% antimony sulphide, 5%
- I I 'to 15% 'calciumsilicide, 10% to 20% lead sulwith center fire mixtures, changesma'ybe'made' -niti'on- -consisting essentially of about 12% normal lead azide, 3% tetrazene, 23% barium nitrate,20%'- lead peroxide, 20% antimony sulphide calcium.;,silicide and .-12.% lead sulh cramd y, a J.
- a priming-mixture for small arms ammunition consisting essentially of normalxleadazide, tetraaene, barium nitrate, lead peroxide, antimony sulphide, calcium, silicide, lead sulphocyanide; andzground glass. l; ,7 :8, All "improved 1D.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Air Bags (AREA)
Description
Patented June 11, 1935 This invention rel'ates' ts improvements in: pr ming mixtures for small arms ammunition, and 'more' particularly 'to priming mixtures in' which the oxidizing' agents are o'f a non-wrrosive type Itis one of the objects'of the pres"- ent:inven'tion to provide apriming mixture having an initiator, a sensitiz'er, a'fuel ingredient, and an oxidizing ingredient, none of which will produce a corrosive residue in the g'unl- It is a-lfurther' object' of the presentinventionto avoid the use of mercury fulminate. To attain these and other objects I employ an initiat0l,i00IlSiStiIlg 0f normal lead azide, a-sensitizer, as hereinafter defined more at length, afuel' in-' gredient preferably consisting of antimony sul- 1 phide, 'lea'd sulphocyanide 'and cal'cium' silicide,
or their equivalents; and an oxidizing ingredient preferably consisting of lead' peroxide" and barium nitrate, :ortheir'equivalents, either with Y or without minor additions of components here'- tofore used in priming compounds to control or vary thezicharacteris'tics thereof :5.Heretofore.mercury =fulmina'te hasbeen' generally used as the initiator in priming mixtures "for smallarms ammunition. It possesses many composition of the mercury fulminate when the cartridge is exploded prevents reloading of center fire cartridges. By employing an initiator in which no mercury fulminate is present, this amalgamation is eliminated, which permits reloading and re-use of center fire cartridge cases. The priming mixture of my invention also possesses advantage for use in rim fire primers. It has greater stability on storing and therefore permits the ammunition to be used and better results obtained after it has been stored forlong periods of time. A suitable priming mixture for center fire cartridges may be formed by mixing the following ingredients in substantially the following proportions, by weight:
Tetrazene 1 to 5% preferably 3% Normal lead azide to 20% preferably 12% Barium nitrate 1 20 to 30% preferably 23% Lead peroxide to 25% preferably ,qJosephlD McNutt,-,l lew (lo nu v1. 1:0Hillinche ster RepeatingArms. Company, New- ,Ha-vemfionm, a, corporation of -Maryland;
N6 Application Augusttil, 1932 assignor Serial No. 531,102
(dye-4 t k Antimony sulphide' 15m preferably 20% Calcium silicide 5 to"-15% preferably 10% lie'ad -sulphocyahide 10 to20% preferably 12% Proportions of thes'e ingredients may be varied depending onithestr ength or purity of the ingredients; as, obtainable commercially. Also the proportions maybe varied to'correlate the characteristics of the priming mixture to the size of thefl'art. I
he terms.tetrazene and ftetrazole derivatives have been 'variously defined by earlier workers in the'explosives art and there is much confusion in nomenclature; Likewise, structural formulae for these materials as heretofore published arenot easily reconcilable. The material whichll employ may be obtained by treating aminoguan'idine in the form I of its bicarbonate saltto convert it to the sulphate or soluble form of that salti- Thus the dry bicarbonate is treat- 2 ed with a slight excess of 6% sulphuric acid. To a 15% water solution of this sulphate of aminoguanidine, while still acid from the excess of sulphuric acid, I add a aqueous solution of sodium nitrite and allow the two solutions to react at a temperature between 30 and C. for a period of 1 to 2 hours, when the reaction is complete. The solid residue is then washed with water and then with alcohol and dried at room temperature, or somewhat higher, from 5 to 10 hours, depending on operating conditions. The chemical structure of the resultant product is complex. Throughout this specification I designate it as tetrazene. The material is apparently one species of the generic class of compounds sometimes called tetrazenes and has been designated by the term guanylnitroso-aminoguanyltetrazene. Thus in French Patent No. 671,800 to Rathsburg et all, dated September 9, 1929, the name tetrazene is used as synonymous with guanylnitroso amino guanyltetrazene, though it must be recognized that tetrazene is the genus of which the alleged synonym is but one of scores of species.
To make primers from the ingredients above tabulated, these ingredients are first thoroughly and homogeneously mixed. The mixture is then poured into individual pellets of the proper size for the individual charges, all in a customcartridge, the magnitude of the gun powder 0 aryway.
The priming mixture forming the subject matter o? the present ginvefi'tion'; may fals'o be employed in rim fire cartridges and Without substantial change in the illustrative proportions above set forth, excepting for the addition of say 20% of ground glass, the latter being -a common constituent of rim fire mixtureswhere'" serves as an abrasive in :a manner WeIl un derstood in the art. Withrlm 'firelmi-xtures'as in the relative percentages of theinitiator, the sensitizer, the oxidizer, and the fuel, to correlate the priming mixture to the size of the shelland to the nature and amount of powder usedthereof a charge plate and then transferred to empty rim fire cartridge shells. The priming mixture then fl-creed to distributeitselfintofihe'ihollow rim of "the cartri'dge'shell byfspinr'iing'the shell in the customary machine. The shells are then loaded with powder and "bullets in'the 'custor'n- The "oxygen supplying elements and fills mentioned above? are referred to; ample?Knownequivalentsmay ,7 I foranyor all of them without departingfrom the spirit crthe'invention. Asan examplejle'a'd nitrate may be .employedin place ,.of bariumjnltrata'the quantity of'lead nitrateto be employed varying slightly "from 'the'i quantity o fjfbarium nitrate given above .to obtainsubstantially the same qualitiesinthe resulting mixture.
I claim:
1. A priming "for small arms ammu nition, comprisingnormal lead 'az'i'de, suitable oxidizers and 'fuels and tetra'zene. 3
' nitresa mi u l 'W YQ IQ X-Yi substituted tion comprising normal lead azide, barium ni trate, lead peroxide and tetrazen 3. A priming mixture for small arms ammunition comprising normal lead azide, barium nitrate, lead peroxide, calcium silicide, antimony sulphide and tetrazene.
l. A priming mixture for small arms ammunitidn comprisingfwrmalflead azide; tetrazene, barium nitrate; lead peroxide, antimony sulphide, calcium silicide and lead sulphocyanide. 5. A priming mixture for small arms ammuniti-omeornprising 10% to 20% normal lead azide, 20% to30'% barium nitrate, 15% to lead perox-lde, "ll5% ito25% antimony sulphide, 5%
I I 'to 15% 'calciumsilicide, 10% to 20% lead sulwith center fire mixtures, changesma'ybe'made' -niti'on- -consisting essentially of about 12% normal lead azide, 3% tetrazene, 23% barium nitrate,20%'- lead peroxide, 20% antimony sulphide =calcium.;,silicide and .-12.% lead sulh cramd y, a J. A priming-mixture=for small arms ammunition consisting essentially of normalxleadazide, tetraaene, barium nitrate, lead peroxide, antimony sulphide, calcium, silicide, lead sulphocyanide; andzground glass. l; ,7 :8, All "improved 1D. H vg, Emixture ,ifor :small arms ammunitioncccmprising lead'azide, guanylnoguanyltetrazene,ibarium nitrateiand .9, ;;imp ;oyed-, priming, mixture 'forxsmall rm ammu ti n comprisin -l ad azidet euanr v nitrosoaminoguanyltetrazene, ,.;:barium'..,.nitrat.e, and ;calciumz si-lieide. -1, z
.;10 :-A :pri-mingmixture, "or ammunition primers comprising -gguanylnitrosoaminoguanyltetrazenej and-leadzazida- 1.;An pproyed-primingicomposition roomprising ,leadrazide,1guanylnitrosoaminoguanyltetrazene, g-barium mitrateiandi-a :fuel in which the lead azide contentzisefromiltlitoizll:pereent andv the,guanylnitrosoaminoguanyltetrazenecontentis from]; pr ming'mixtureforsmall ar f
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US631102A US2004505A (en) | 1932-08-30 | 1932-08-30 | Priming mixture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US631102A US2004505A (en) | 1932-08-30 | 1932-08-30 | Priming mixture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2004505A true US2004505A (en) | 1935-06-11 |
Family
ID=24529776
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US631102A Expired - Lifetime US2004505A (en) | 1932-08-30 | 1932-08-30 | Priming mixture |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2004505A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2981616A (en) * | 1956-10-01 | 1961-04-25 | North American Aviation Inc | Gas generator grain |
-
1932
- 1932-08-30 US US631102A patent/US2004505A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2981616A (en) * | 1956-10-01 | 1961-04-25 | North American Aviation Inc | Gas generator grain |
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