CA1110074A - Explosif detonant resistant a l'eau - Google Patents

Explosif detonant resistant a l'eau

Info

Publication number: CA1110074A
Authority: CA; Canada
Prior art keywords: composition according; acid; ester; high explosive; agent
Prior art date: 1977-05-13
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

CA303,187A

Other languages

English (en)

Inventor

Nicholas J. Strolla

Francis Gilmour

Peter Macrae

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.)

Orica Ltd

Original Assignee

ICI Australia Ltd

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.)

1977-05-13

Filing date

1978-05-12

Publication date

1981-10-06

1978-05-12 Application filed by ICI Australia Ltd filed Critical ICI Australia Ltd

1981-10-06 Application granted granted Critical

1981-10-06 Publication of CA1110074A publication Critical patent/CA1110074A/fr

Status Expired legal-status Critical Current

Links

239000002360 explosive Substances 0.000 title claims abstract description 42
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 26
239000000463 material Substances 0.000 claims abstract description 38
150000002148 esters Chemical class 0.000 claims abstract description 20
238000002844 melting Methods 0.000 claims abstract description 14
230000008018 melting Effects 0.000 claims abstract description 14
239000002253 acid Substances 0.000 claims abstract description 12
125000005907 alkyl ester group Chemical group 0.000 claims abstract description 8
125000001931 aliphatic group Chemical group 0.000 claims abstract 3
239000000203 mixture Substances 0.000 claims description 51
239000003795 chemical substances by application Substances 0.000 claims description 40
TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 claims description 26
239000000306 component Substances 0.000 claims description 18
-1 aromatic dicarboxylic acids Chemical class 0.000 claims description 15
238000000034 method Methods 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
239000002245 particle Substances 0.000 claims description 9
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 9
238000004519 manufacturing process Methods 0.000 claims description 7
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
239000008358 core component Substances 0.000 claims description 6
239000000026 Pentaerythritol tetranitrate Substances 0.000 claims description 5
229960004321 pentaerithrityl tetranitrate Drugs 0.000 claims description 5
IJFPVINAQGWBRJ-UHFFFAOYSA-N Diisooctyl phthalate Chemical group CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C IJFPVINAQGWBRJ-UHFFFAOYSA-N 0.000 claims description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 4
239000001361 adipic acid Substances 0.000 claims description 3
235000011037 adipic acid Nutrition 0.000 claims description 3
159000000032 aromatic acids Chemical class 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 3
239000007788 liquid Substances 0.000 claims description 3
239000012736 aqueous medium Substances 0.000 claims description 2
238000000586 desensitisation Methods 0.000 claims description 2
150000002823 nitrates Chemical class 0.000 claims description 2
229960003656 ricinoleic acid Drugs 0.000 claims description 2
FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 claims description 2
239000001384 succinic acid Substances 0.000 claims description 2
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims 2
235000021122 unsaturated fatty acids Nutrition 0.000 claims 2
150000004670 unsaturated fatty acids Chemical class 0.000 claims 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims 1
239000005642 Oleic acid Substances 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
239000011248 coating agent Substances 0.000 claims 1
238000000576 coating method Methods 0.000 claims 1
238000013016 damping Methods 0.000 claims 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 1
239000011976 maleic acid Substances 0.000 claims 1
239000002609 medium Substances 0.000 claims 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
235000006408 oxalic acid Nutrition 0.000 claims 1
WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 claims 1
150000005846 sugar alcohols Polymers 0.000 claims 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
125000003118 aryl group Chemical group 0.000 abstract description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 22
239000011162 core material Substances 0.000 description 20
SIXWIUJQBBANGK-UHFFFAOYSA-N 4-(4-fluorophenyl)-1h-pyrazol-5-amine Chemical compound N1N=CC(C=2C=CC(F)=CC=2)=C1N SIXWIUJQBBANGK-UHFFFAOYSA-N 0.000 description 16
239000007787 solid Substances 0.000 description 8
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 6
238000005474 detonation Methods 0.000 description 6
238000007654 immersion Methods 0.000 description 6
229920000139 polyethylene terephthalate Polymers 0.000 description 6
239000005020 polyethylene terephthalate Substances 0.000 description 6
239000012452 mother liquor Substances 0.000 description 5
XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 4
239000004698 Polyethylene Substances 0.000 description 4
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 4
235000013539 calcium stearate Nutrition 0.000 description 4
239000008116 calcium stearate Substances 0.000 description 4
239000013078 crystal Substances 0.000 description 4
239000012065 filter cake Substances 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000000243 solution Substances 0.000 description 4
229920001169 thermoplastic Polymers 0.000 description 4
239000004416 thermosoftening plastic Substances 0.000 description 4
ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
238000005422 blasting Methods 0.000 description 3
238000011065 in-situ storage Methods 0.000 description 3
JQCXWCOOWVGKMT-UHFFFAOYSA-N phthalic acid diheptyl ester Natural products CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
239000011343 solid material Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000004753 textile Substances 0.000 description 3
SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 2
239000004677 Nylon Substances 0.000 description 2
238000005299 abrasion Methods 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
230000005540 biological transmission Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
SNFOERUNNSHUGP-ZXZARUISSA-N erythrityl tetranitrate Chemical compound [O-][N+](=O)OC[C@@H](O[N+]([O-])=O)[C@@H](O[N+]([O-])=O)CO[N+]([O-])=O SNFOERUNNSHUGP-ZXZARUISSA-N 0.000 description 2
125000004356 hydroxy functional group Chemical group O* 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000005065 mining Methods 0.000 description 2
229920001778 nylon Polymers 0.000 description 2
230000035515 penetration Effects 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
239000002002 slurry Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000000015 trinitrotoluene Substances 0.000 description 2
QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
HTKIMWYSDZQQBP-UHFFFAOYSA-N 2-hydroxyethyl nitrate Chemical compound OCCO[N+]([O-])=O HTKIMWYSDZQQBP-UHFFFAOYSA-N 0.000 description 1
QVTZGGQGWAKDNU-UHFFFAOYSA-N 6-(2,2-dimethoxyethoxy)-6-oxohexanoic acid Chemical compound COC(COC(=O)CCCCC(=O)O)OC QVTZGGQGWAKDNU-UHFFFAOYSA-N 0.000 description 1
229920003319 Araldite® Polymers 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
229920008712 Copo Polymers 0.000 description 1
101150105088 Dele1 gene Proteins 0.000 description 1
101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
ODUIXUGXPFKQLG-QWRGUYRKSA-N [2-(4-chloro-2-fluoroanilino)-5-methyl-1,3-thiazol-4-yl]-[(2s,3s)-2,3-dimethylpiperidin-1-yl]methanone Chemical compound C[C@H]1[C@@H](C)CCCN1C(=O)C1=C(C)SC(NC=2C(=CC(Cl)=CC=2)F)=N1 ODUIXUGXPFKQLG-QWRGUYRKSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
239000000956 alloy Substances 0.000 description 1
229910045601 alloy Inorganic materials 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
WXZOXVVKILCOPG-UHFFFAOYSA-N bis(2-ethylhexyl) benzene-1,3-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC(C(=O)OCC(CC)CCCC)=C1 WXZOXVVKILCOPG-UHFFFAOYSA-N 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
238000009954 braiding Methods 0.000 description 1
BEWFIPLBFJGWSR-UHFFFAOYSA-N butyl 12-acetyloxyoctadec-9-enoate Chemical compound CCCCCCC(OC(C)=O)CC=CCCCCCCCC(=O)OCCCC BEWFIPLBFJGWSR-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000010276 construction Methods 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
229960002380 dibutyl phthalate Drugs 0.000 description 1
125000001142 dicarboxylic acid group Chemical group 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 1
MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000000578 dry spinning Methods 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
229960005450 eritrityl tetranitrate Drugs 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
238000010304 firing Methods 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
DGMJZELBSFOPHH-KVTDHHQDSA-N mannite hexanitrate Chemical compound [O-][N+](=O)OC[C@@H](O[N+]([O-])=O)[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)CO[N+]([O-])=O DGMJZELBSFOPHH-KVTDHHQDSA-N 0.000 description 1
229960001765 mannitol hexanitrate Drugs 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
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 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 description 1
229940059574 pentaerithrityl Drugs 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000012466 permeate Substances 0.000 description 1
HCTVWSOKIJULET-LQDWTQKMSA-M phenoxymethylpenicillin potassium Chemical compound [K+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)COC1=CC=CC=C1 HCTVWSOKIJULET-LQDWTQKMSA-M 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
239000012815 thermoplastic material Substances 0.000 description 1
238000004078 waterproofing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C5/00—Fuses, e.g. fuse cords
- C06C5/06—Fuse igniting means; Fuse connectors
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/009—Wetting agents, hydrophobing agents, dehydrating agents, antistatic additives, viscosity improvers, antiagglomerating agents, grinding agents and other additives for working up
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
- 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
- C06B45/18—Compositions or products which are defined by structure or arrangement of component of product comprising a coated component
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C5/00—Fuses, e.g. fuse cords
- C06C5/04—Detonating fuses

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Crystallography & Structural Chemistry (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Compositions Of Macromolecular Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

CA303,187A 1977-05-13 1978-05-12 Explosif detonant resistant a l'eau Expired CA1110074A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
AUPD008777		1977-05-13
AUPD.0087		1977-05-13

Publications (1)

Publication Number	Publication Date
CA1110074A true CA1110074A (fr)	1981-10-06

Family

ID=3766988

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA303,187A Expired CA1110074A (fr)	1977-05-13	1978-05-12	Explosif detonant resistant a l'eau

Country Status (9)

Country	Link
BR (1)	BR7802945A (fr)
CA (1)	CA1110074A (fr)
DE (1)	DE2821244C2 (fr)
FR (1)	FR2390407A1 (fr)
GB (1)	GB1584931A (fr)
IT (1)	IT1158711B (fr)
NZ (1)	NZ186989A (fr)
SE (1)	SE445993B (fr)
ZA (1)	ZA782374B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4490196A (en) *	1984-04-05	1984-12-25	Hercules Incorporated	Low detonation velocity explosive composition
US4555279A (en) *	1984-04-05	1985-11-26	Hercules Incorporated	Low detonation velocity explosive composition
US4595430A (en) *	1984-05-07	1986-06-17	Atlas Powder Company	Desensitized dynamites

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3884735A (en) *	1956-07-19	1975-05-20	Du Pont	Explosive composition
US3401215A (en) *	1965-08-19	1968-09-10	Du Pont	Making flexible detonating fuse

1978
- 1978-04-17 NZ NZ186989A patent/NZ186989A/xx unknown
- 1978-04-21 GB GB15864/78A patent/GB1584931A/en not_active Expired
- 1978-04-26 ZA ZA00782374A patent/ZA782374B/xx unknown
- 1978-05-10 BR BR7802945A patent/BR7802945A/pt unknown
- 1978-05-11 SE SE7805403A patent/SE445993B/sv not_active IP Right Cessation
- 1978-05-12 FR FR7814204A patent/FR2390407A1/fr active Granted
- 1978-05-12 CA CA303,187A patent/CA1110074A/fr not_active Expired
- 1978-05-15 IT IT23414/78A patent/IT1158711B/it active
- 1978-05-16 DE DE2821244A patent/DE2821244C2/de not_active Expired

Also Published As

Publication number	Publication date
DE2821244C2 (de)	1986-10-16
NZ186989A (en)	1980-11-14
SE7805403L (sv)	1978-11-14
IT7823414A0 (it)	1978-05-15
BR7802945A (pt)	1979-01-02
ZA782374B (en)	1979-09-26
FR2390407B1 (fr)	1985-05-24
FR2390407A1 (fr)	1978-12-08
SE445993B (sv)	1986-08-04
DE2821244A1 (de)	1978-11-16
GB1584931A (en)	1981-02-18
IT1158711B (it)	1987-02-25

Legal Events

Date	Code	Title	Description
1998-10-06	MKEX	Expiry

Publication	Publication Date	Title
CA1146807A (fr)	1983-05-24	Dispositif transmetteur d'un signal de detonation par la voie d'un tube renfermant une matiere auto-oxydante
CA1115959A (fr)	1982-01-12	Composition de sautage
DE2350200A1 (de)	1974-04-18	Explosivmaterialien
CA1110073A (fr)	1981-10-06	Composition detonante
US4218272A (en)	1980-08-19	Water-in-oil NCN emulsion blasting agent
US4149917A (en)	1979-04-17	Cap sensitive emulsions without any sensitizer other than occluded air
US4414044A (en)	1983-11-08	Water-in-oil emulsion explosive composition
US4149916A (en)	1979-04-17	Cap sensitive emulsions containing perchlorates and occluded air and method
US2349048A (en)	1944-05-16	Smokeless powder
US2775200A (en)	1956-12-25	Priming device
CA1110074A (fr)	1981-10-06	Explosif detonant resistant a l'eau
US4453989A (en)	1984-06-12	Solid sensitizers for water-in-oil emulsion explosives
EP0968983B1 (fr)	2003-07-02	Composition d' hexanitrohexaazaisowurtzitane et composition explosive la contenant
US3731625A (en)	1973-05-08	Packaged explosive
JPH0319196B2 (fr)	1991-03-14
US4523967A (en)	1985-06-18	Invert emulsion explosives containing a one-component oil phase
US3764419A (en)	1973-10-09	Method of making a blasting agent having variable density
US3293056A (en)	1966-12-20	Composition for a combustible cartridge case
US3985593A (en)	1976-10-12	Water gel explosives
US4023996A (en)	1977-05-17	Moldable compositions comprising polyvinyl nitrate
US4428784A (en)	1984-01-31	Blasting compositions containing sodium nitrate
US4664729A (en)	1987-05-12	Water-in-oil explosive emulsion composition
RU2033989C1 (ru)	1995-04-30	Способ получения взрывчатых составов, содержащих аммиачную селитру, углеводородное горючее и поверхностно-активное вещество
US4933028A (en)	1990-06-12	High emulsifier content explosives
WO1999021809A1 (fr)	1999-05-06	Composition d'explosifs a emulsion