CA1077963A - Ammunition priming mixtures - Google Patents

Ammunition priming mixtures

Info

Publication number: CA1077963A
Authority: CA; Canada
Prior art keywords: lead; styphnate; styphnic acid; acid; styphnic
Prior art date: 1974-07-18
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

Application number

CA230,909A

Other languages

English (en)

French (fr)

Inventor

Joseph F. Kenney

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Remington Arms Co LLC

Original Assignee

Remington Arms Co LLC

Priority date (The priority date 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 date listed.)

1974-07-18

Filing date

1975-07-07

Publication date

1980-05-20

1975-07-07 Application filed by Remington Arms Co LLC filed Critical Remington Arms Co LLC

1980-05-20 Application granted granted Critical

1980-05-20 Publication of CA1077963A publication Critical patent/CA1077963A/en

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 88
230000037452 priming Effects 0.000 title claims abstract description 37
WETZJIOEDGMBMA-UHFFFAOYSA-L lead styphnate Chemical compound [Pb+2].[O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C([O-])=C1[N+]([O-])=O WETZJIOEDGMBMA-UHFFFAOYSA-L 0.000 claims abstract description 117
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 72
IXHMHWIBCIYOAZ-UHFFFAOYSA-N styphnic acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1[N+]([O-])=O IXHMHWIBCIYOAZ-UHFFFAOYSA-N 0.000 claims abstract description 70
238000000034 method Methods 0.000 claims abstract description 51
238000006243 chemical reaction Methods 0.000 claims abstract description 41
229910021514 lead(II) hydroxide Inorganic materials 0.000 claims abstract description 29
238000002156 mixing Methods 0.000 claims abstract description 29
150000002611 lead compounds Chemical class 0.000 claims abstract description 21
229910000004 White lead Inorganic materials 0.000 claims abstract description 16
229910000464 lead oxide Inorganic materials 0.000 claims abstract description 16
RYZCLUQMCYZBJQ-UHFFFAOYSA-H lead(2+);dicarbonate;dihydroxide Chemical compound [OH-].[OH-].[Pb+2].[Pb+2].[Pb+2].[O-]C([O-])=O.[O-]C([O-])=O RYZCLUQMCYZBJQ-UHFFFAOYSA-H 0.000 claims abstract description 16
229910000003 Lead carbonate Inorganic materials 0.000 claims abstract description 15
YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 claims abstract description 15
MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 claims abstract description 14
XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 claims abstract description 14
150000001875 compounds Chemical class 0.000 claims abstract description 14
IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 claims abstract description 14
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 10
239000000446 fuel Substances 0.000 claims abstract description 10
239000001301 oxygen Substances 0.000 claims abstract description 10
229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
239000004615 ingredient Substances 0.000 claims description 33
239000012535 impurity Substances 0.000 claims description 22
238000004519 manufacturing process Methods 0.000 claims description 19
150000002828 nitro derivatives Chemical class 0.000 claims description 18
239000003990 capacitor Substances 0.000 claims description 14
229920000084 Gum arabic Polymers 0.000 claims description 11
241000978776 Senegalia senegal Species 0.000 claims description 11
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 11
235000010489 acacia gum Nutrition 0.000 claims description 11
239000000205 acacia gum Substances 0.000 claims description 11
230000035939 shock Effects 0.000 claims description 8
RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical group [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 claims description 7
239000001117 sulphuric acid Substances 0.000 claims description 7
235000011149 sulphuric acid Nutrition 0.000 claims description 7
HTUMBQDCCIXGCV-UHFFFAOYSA-N lead oxide Chemical compound [O-2].[Pb+2] HTUMBQDCCIXGCV-UHFFFAOYSA-N 0.000 abstract description 21
IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 abstract description 20
238000002441 X-ray diffraction Methods 0.000 abstract description 16
230000035945 sensitivity Effects 0.000 abstract description 15
238000009527 percussion Methods 0.000 abstract description 12
238000011065 in-situ storage Methods 0.000 abstract description 8
RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 abstract description 7
239000005337 ground glass Substances 0.000 abstract description 5
239000002244 precipitate Substances 0.000 abstract description 4
239000002360 explosive Substances 0.000 description 32
239000013078 crystal Substances 0.000 description 22
239000000463 material Substances 0.000 description 19
239000000243 solution Substances 0.000 description 16
239000000047 product Substances 0.000 description 13
239000000843 powder Substances 0.000 description 12
230000000007 visual effect Effects 0.000 description 10
239000000080 wetting agent Substances 0.000 description 9
239000002253 acid Substances 0.000 description 8
239000007795 chemical reaction product Substances 0.000 description 8
238000004880 explosion Methods 0.000 description 8
238000012512 characterization method Methods 0.000 description 7
238000001035 drying Methods 0.000 description 7
238000001914 filtration Methods 0.000 description 7
239000004033 plastic Substances 0.000 description 7
239000000376 reactant Substances 0.000 description 7
238000003756 stirring Methods 0.000 description 7
230000003068 static effect Effects 0.000 description 6
238000004458 analytical method Methods 0.000 description 5
230000005611 electricity Effects 0.000 description 5
239000013067 intermediate product Substances 0.000 description 5
239000002245 particle Substances 0.000 description 5
238000012360 testing method Methods 0.000 description 5
238000005406 washing Methods 0.000 description 5
125000004429 atom Chemical group 0.000 description 4
229910021346 calcium silicide Inorganic materials 0.000 description 4
238000007689 inspection Methods 0.000 description 4
239000002994 raw material Substances 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
239000000126 substance Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
238000005422 blasting Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
230000008030 elimination Effects 0.000 description 3
238000003379 elimination reaction Methods 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
229940046892 lead acetate Drugs 0.000 description 3
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 3
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
150000001447 alkali salts Chemical class 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
239000002178 crystalline material Substances 0.000 description 2
238000010586 diagram Methods 0.000 description 2
239000000975 dye Substances 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
239000000284 extract Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
230000000977 initiatory effect Effects 0.000 description 2
DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 2
230000001788 irregular Effects 0.000 description 2
NVYSURDBVCQFBV-UHFFFAOYSA-L magnesium;2,4,6-trinitrobenzene-1,3-diolate Chemical compound [Mg+2].[O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C([O-])=C1[N+]([O-])=O NVYSURDBVCQFBV-UHFFFAOYSA-L 0.000 description 2
229910017604 nitric acid Inorganic materials 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
239000007800 oxidant agent Substances 0.000 description 2
229960003351 prussian blue Drugs 0.000 description 2
239000013225 prussian blue Substances 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 description 2
239000013589 supplement Substances 0.000 description 2
239000013598 vector Substances 0.000 description 2
239000002699 waste material Substances 0.000 description 2
QNRATNLHPGXHMA-XZHTYLCXSA-N (r)-(6-ethoxyquinolin-4-yl)-[(2s,4s,5r)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]methanol;hydrochloride Chemical compound Cl.C([C@H]([C@H](C1)CC)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OCC)C=C21 QNRATNLHPGXHMA-XZHTYLCXSA-N 0.000 description 1
QJRHVRNYDAXUNC-UHFFFAOYSA-N 2,4,6-trinitrobenzene-1,3-diol hydrate Chemical compound O.OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1[N+]([O-])=O QJRHVRNYDAXUNC-UHFFFAOYSA-N 0.000 description 1
JHLGIWLLGRJIEN-UHFFFAOYSA-L 2-hydroxypropanoate;lead(2+) Chemical compound [Pb+2].CC(O)C([O-])=O.CC(O)C([O-])=O JHLGIWLLGRJIEN-UHFFFAOYSA-L 0.000 description 1
XQMVBICWFFHDNN-UHFFFAOYSA-N 5-amino-4-chloro-2-phenylpyridazin-3-one;(2-ethoxy-3,3-dimethyl-2h-1-benzofuran-5-yl) methanesulfonate Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1.C1=C(OS(C)(=O)=O)C=C2C(C)(C)C(OCC)OC2=C1 XQMVBICWFFHDNN-UHFFFAOYSA-N 0.000 description 1
229910001369 Brass Inorganic materials 0.000 description 1
101100326341 Drosophila melanogaster brun gene Proteins 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
206010067482 No adverse event Diseases 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
PLXBWHJQWKZRKG-UHFFFAOYSA-N Resazurin Chemical compound C1=CC(=O)C=C2OC3=CC(O)=CC=C3[N+]([O-])=C21 PLXBWHJQWKZRKG-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
239000001045 blue dye Substances 0.000 description 1
239000010951 brass Substances 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
238000010961 commercial manufacture process Methods 0.000 description 1
238000010960 commercial process Methods 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000002447 crystallographic data Methods 0.000 description 1
238000005474 detonation Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000003912 environmental pollution Methods 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000036571 hydration Effects 0.000 description 1
238000006703 hydration reaction Methods 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
230000003993 interaction Effects 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
-1 lead oxide Chemical class 0.000 description 1
FYDIWJWWROEQCB-UHFFFAOYSA-L lead(2+);propanoate Chemical compound [Pb+2].CCC([O-])=O.CCC([O-])=O FYDIWJWWROEQCB-UHFFFAOYSA-L 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
MHWLNQBTOIYJJP-UHFFFAOYSA-N mercury difulminate Chemical compound [O-][N+]#C[Hg]C#[N+][O-] MHWLNQBTOIYJJP-UHFFFAOYSA-N 0.000 description 1
GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000002028 premature Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000011179 visual inspection Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/20—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C07C205/21—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to carbon atoms of six-membered aromatic rings having nitro groups and hydroxy groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
- C07C205/24—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to carbon atoms of six-membered aromatic rings having nitro groups and hydroxy groups bound to carbon atoms of the same non-condensed six-membered aromatic ring having three, and only three, nitro groups bound to the ring
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B41/00—Compositions containing a nitrated metallo-organic compound
- C06B41/02—Compositions containing a nitrated metallo-organic compound the compound containing lead
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C7/00—Non-electric detonators; Blasting caps; Primers
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/003—Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Air Bags (AREA)
Glanulating (AREA)
Inorganic Compounds Of Heavy Metals (AREA)

CA230,909A 1974-07-18 1975-07-07 Ammunition priming mixtures Expired CA1077963A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US48970474A	1974-07-18	1974-07-18
US05/572,829 US3983149A (en)	1974-07-18	1975-04-29	Ammunition priming mixtures and method of forming same

Publications (1)

Publication Number	Publication Date
CA1077963A true CA1077963A (en)	1980-05-20

Family

ID=27049801

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA230,909A Expired CA1077963A (en)	1974-07-18	1975-07-07	Ammunition priming mixtures

Country Status (10)

Country	Link
US (1)	US3983149A (2)
JP (1)	JPS5943478B2 (2)
AR (1)	AR211851A1 (2)
AU (1)	AU8287575A (2)
BR (1)	BR7504523A (2)
CA (1)	CA1077963A (2)
DE (1)	DE2531997A1 (2)
FR (1)	FR2284587A1 (2)
GB (1)	GB1479561A (2)
IT (1)	IT1039891B (2)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4405392A (en) *	1975-09-11	1983-09-20	Imperial Metal Industries (Kynoch) Limited	Method of making priming composition
US4247494A (en) *	1977-08-16	1981-01-27	Imi Kynoch Limited	Case priming
US4336084A (en) *	1980-08-29	1982-06-22	Olin Corporation	Method for making primer constituents
US4968364A (en) *	1988-12-05	1990-11-06	The Commonwealth Of Australia	Conducting primer compositions
US20050098248A1 (en) *	2003-06-26	2005-05-12	Vladimir Nikolaevich Khovonskov	Ammunition primer composition for small arms

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1443328A (en) *	1919-11-03	1923-01-23	Herz Edmund	Explosive and process of making same
US1999728A (en) *	1927-11-08	1935-04-30	Remington Arms Co Inc	Manufacture of lead styphnate
BE430296A (2) *	1937-09-22
US2239547A (en) *	1938-09-23	1941-04-22	Remington Arms Co Inc	Ammunition
US2295104A (en) *	1939-06-29	1942-09-08	Western Cartridge Co	Manufacture of normal lead trinitroresorcinate and double salts thereof
US2589703A (en) *	1950-08-17	1952-03-18	Remington Arms Co Inc	Lead styphnate and process of manufacturing same
US2702745A (en) *	1952-08-02	1955-02-22	Remington Arms Co Inc	Styphnate compound and priming composition thereof
US3002012A (en) *	1958-01-16	1961-09-26	Olin Mathieson	Method for the preparation of normal lead styphnate
GB1076981A (en) *	1963-01-07	1967-07-26	Mini Of Technology	Improvements in the manufacture of lead 2:4-dinitroresorcinate
DE1269555B (de) *	1964-02-28	1968-05-30	Dynamit Nobel Ag	Verfahren zur Herstellung leitfaehiger Zuendsaetze

1975
- 1975-03-07 AU AU82875/75A patent/AU8287575A/en not_active Expired
- 1975-04-29 US US05/572,829 patent/US3983149A/en not_active Expired - Lifetime
- 1975-07-07 CA CA230,909A patent/CA1077963A/en not_active Expired
- 1975-07-17 IT IT25506/75A patent/IT1039891B/it active
- 1975-07-17 FR FR7522419A patent/FR2284587A1/fr active Granted
- 1975-07-17 BR BR7504523*A patent/BR7504523A/pt unknown
- 1975-07-17 GB GB30119/75A patent/GB1479561A/en not_active Expired
- 1975-07-17 DE DE19752531997 patent/DE2531997A1/de not_active Withdrawn
- 1975-07-18 AR AR259650A patent/AR211851A1/es active
- 1975-07-18 JP JP50087438A patent/JPS5943478B2/ja not_active Expired

Also Published As

Publication number	Publication date
BR7504523A (pt)	1976-07-06
JPS5134131A (en)	1976-03-23
GB1479561A (en)	1977-07-13
DE2531997A1 (de)	1976-02-05
US3983149A (en)	1976-09-28
FR2284587A1 (fr)	1976-04-09
JPS5943478B2 (ja)	1984-10-22
IT1039891B (it)	1979-12-10
AR211851A1 (es)	1978-03-31
FR2284587B1 (2)	1980-05-23
AU8287575A (en)	1977-01-13

Legal Events

Date	Code	Title	Description
1997-05-20	MKEX	Expiry

Publication	Publication Date	Title
Chavez et al.	1999	High-nitrogen fuels for low-smoke pyrotechnics
US11814332B2 (en)	2023-11-14	Bismuth-based energetic materials
WO1997006099A1 (en)	1997-02-20	Method of preparing dinitramidic acid and salts thereof
CA1077963A (en)	1980-05-20	Ammunition priming mixtures
CN105481617A (zh)	2016-04-13	一种纳米复合含能材料及其制备方法
US2738369A (en)	1956-03-13	Method for making quaternary ammonium borohydrides
Huizing et al.	1977	Hydrates of manganese (II) oxalate
Singh et al.	1983	Hexanitrostilbene and its properties
CN115894453B (zh)	2024-04-02	一种吡唑类化合物及其含能离子盐和制备方法
US4029530A (en)	1977-06-14	Method of forming lead styphnate ammunition priming mixture
US3184286A (en)	1965-05-18	Cs2b12h12*csno3 product and process for making same
CN107602395A (zh)	2018-01-19	一种1,1‑二氨基‑2,2‑二硝基乙烯的合成方法
US2265230A (en)	1941-12-09	Basic lead styphnate and a process of making it
Nandi et al.	2014	Assay of the thermally stable, insensitive, high explosive 1, 3, 5-triamino-2, 4, 6-trinitrobenzene (TATB)
FI61469B (fi)	1982-04-30	Foerfarande foer framstaellning av ett knallsensitivt vattenhaltigt gelsuspensionsspraengaemne
US2989389A (en)	1961-06-20	Primer charge for detonators
Chikhradze et al.	2021	The improvement of picric acid synthesis methodology
Taylor et al.	1962	LEAD STYPHNATE: PART 4. THE MONOBASIC LEAD SALTS OF TRINITRORESORCINOL, POLYMORPHIC MODIFICATIONS AND THE DEVELOPMENT OF RD 1346 AND RD 1349
US1971030A (en)	1934-08-21	Chemical compound and priming mixture containing the same
WO2018209366A2 (en)	2018-11-15	Explosive compound and method of manufacturing same
US3009801A (en)	1961-11-21	Sensitized ammonium nitrate explosive and method of manufacture
Taylor	1923	Explosives, Their Materials, Constitution, and Analysis
Matyáš et al.	2012	Azides
Redman et al.	1983	Mercuric 5-Nitrotetrazole, a Possible Replacement for Lead Azide in Australian Ordnance. Part 1. An Assessment of Preparation Methods
Fairley	1877	III.—Study of hydrogen dioxide and of certain peroxides—(continued from page 24)