NO157449B - Emulsjonssprengstoffblanding. - Google Patents
Emulsjonssprengstoffblanding. Download PDFInfo
- Publication number
- NO157449B NO157449B NO833503A NO833503A NO157449B NO 157449 B NO157449 B NO 157449B NO 833503 A NO833503 A NO 833503A NO 833503 A NO833503 A NO 833503A NO 157449 B NO157449 B NO 157449B
- Authority
- NO
- Norway
- Prior art keywords
- acid
- oxide
- phosphorus
- sugar
- reaction
- Prior art date
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- 239000000839 emulsion Substances 0.000 title 1
- 239000002360 explosive Substances 0.000 title 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 64
- 239000000203 mixture Substances 0.000 claims description 37
- 238000006243 chemical reaction Methods 0.000 claims description 36
- 235000011007 phosphoric acid Nutrition 0.000 claims description 34
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 32
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 30
- 235000000346 sugar Nutrition 0.000 claims description 30
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 24
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 23
- 125000002947 alkylene group Chemical group 0.000 claims description 22
- 229910052698 phosphorus Inorganic materials 0.000 claims description 20
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 19
- 150000002148 esters Chemical class 0.000 claims description 19
- 239000011574 phosphorus Substances 0.000 claims description 19
- 229920001228 polyisocyanate Polymers 0.000 claims description 19
- 239000005056 polyisocyanate Substances 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 16
- -1 glycol ethers Chemical class 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 15
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- 229940005657 pyrophosphoric acid Drugs 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 12
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 10
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 10
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- 235000021317 phosphate Nutrition 0.000 claims description 7
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 6
- 229930006000 Sucrose Natural products 0.000 claims description 6
- 239000005720 sucrose Substances 0.000 claims description 6
- YDHWWBZFRZWVHO-UHFFFAOYSA-N [hydroxy(phosphonooxy)phosphoryl] phosphono hydrogen phosphate Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(=O)OP(O)(O)=O YDHWWBZFRZWVHO-UHFFFAOYSA-N 0.000 claims description 5
- 239000008121 dextrose Substances 0.000 claims description 5
- HOVAGTYPODGVJG-ZFYZTMLRSA-N methyl alpha-D-glucopyranoside Chemical compound CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HOVAGTYPODGVJG-ZFYZTMLRSA-N 0.000 claims description 5
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 239000011496 polyurethane foam Substances 0.000 claims description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 3
- 239000008103 glucose Substances 0.000 claims description 3
- 150000002440 hydroxy compounds Chemical class 0.000 claims description 3
- 229910001392 phosphorus oxide Inorganic materials 0.000 claims description 3
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 2
- 229930091371 Fructose Natural products 0.000 claims description 2
- 239000005715 Fructose Substances 0.000 claims description 2
- 239000002798 polar solvent Substances 0.000 claims description 2
- VSAISIQCTGDGPU-UHFFFAOYSA-N tetraphosphorus hexaoxide Chemical compound O1P(O2)OP3OP1OP2O3 VSAISIQCTGDGPU-UHFFFAOYSA-N 0.000 claims description 2
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims 1
- 239000006260 foam Substances 0.000 description 46
- 239000000047 product Substances 0.000 description 42
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical group O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 25
- 230000001413 cellular effect Effects 0.000 description 19
- 239000000243 solution Substances 0.000 description 19
- 238000003756 stirring Methods 0.000 description 14
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 14
- 229940029284 trichlorofluoromethane Drugs 0.000 description 14
- 238000007792 addition Methods 0.000 description 13
- 239000000376 reactant Substances 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 11
- 229920000570 polyether Polymers 0.000 description 11
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 10
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 9
- 239000004721 Polyphenylene oxide Substances 0.000 description 9
- 238000009835 boiling Methods 0.000 description 9
- 239000012948 isocyanate Substances 0.000 description 9
- 150000002513 isocyanates Chemical class 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- 229960001031 glucose Drugs 0.000 description 8
- 238000005292 vacuum distillation Methods 0.000 description 8
- 238000001816 cooling Methods 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 239000004604 Blowing Agent Substances 0.000 description 6
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 229940089206 anhydrous dextrose Drugs 0.000 description 6
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 6
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 6
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 6
- 150000004682 monohydrates Chemical class 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000001569 carbon dioxide Substances 0.000 description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
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- SPFMQWBKVUQXJV-BTVCFUMJSA-N (2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanal;hydrate Chemical compound O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O SPFMQWBKVUQXJV-BTVCFUMJSA-N 0.000 description 4
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 4
- 229910015900 BF3 Inorganic materials 0.000 description 4
- YYQRGCZGSFRBAM-UHFFFAOYSA-N Triclofos Chemical compound OP(O)(=O)OCC(Cl)(Cl)Cl YYQRGCZGSFRBAM-UHFFFAOYSA-N 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
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- 238000000354 decomposition reaction Methods 0.000 description 4
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- 239000012975 dibutyltin dilaurate Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- 229920002545 silicone oil Polymers 0.000 description 4
- 150000003512 tertiary amines Chemical class 0.000 description 4
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- QVCUKHQDEZNNOC-UHFFFAOYSA-N 1,2-diazabicyclo[2.2.2]octane Chemical compound C1CC2CCN1NC2 QVCUKHQDEZNNOC-UHFFFAOYSA-N 0.000 description 3
- NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 3
- AWBIJARKDOFDAN-UHFFFAOYSA-N 2,5-dimethyl-1,4-dioxane Chemical compound CC1COC(C)CO1 AWBIJARKDOFDAN-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000004292 cyclic ethers Chemical class 0.000 description 3
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- 238000009826 distribution Methods 0.000 description 3
- 239000012456 homogeneous solution Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229920000137 polyphosphoric acid Polymers 0.000 description 3
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- 238000004448 titration Methods 0.000 description 3
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical group N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
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- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
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- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
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- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- RXYPXQSKLGGKOL-UHFFFAOYSA-N 1,4-dimethylpiperazine Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 1
- QDLQFWNOQPOPHV-UHFFFAOYSA-N 1-[bis(2-chloroethoxy)phosphoryl]-1-[2-chloroethoxy-[1-[2-chloroethoxy(2-chloroethyl)phosphoryl]oxyethyl]phosphoryl]oxyethane Chemical compound ClCCOP(=O)(OCCCl)C(C)OP(=O)(OCCCl)C(C)OP(=O)(CCCl)OCCCl QDLQFWNOQPOPHV-UHFFFAOYSA-N 0.000 description 1
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- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical class [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 239000002984 plastic foam Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 239000008259 solid foam Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000012970 tertiary amine catalyst Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- 229940113165 trimethylolpropane Drugs 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B47/00—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase
- C06B47/14—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase comprising a solid component and an aqueous phase
- C06B47/145—Water in oil emulsion type explosives in which a carbonaceous fuel forms the continuous phase
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Cosmetics (AREA)
- Colloid Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/427,495 US4404050A (en) | 1982-09-29 | 1982-09-29 | Water-in-oil emulsion blasting agents containing unrefined or partly refined petroleum product as fuel component |
Publications (2)
Publication Number | Publication Date |
---|---|
NO833503L NO833503L (no) | 1984-03-30 |
NO157449B true NO157449B (no) | 1987-12-14 |
Family
ID=23695109
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO833503A NO157449B (no) | 1982-09-29 | 1983-09-28 | Emulsjonssprengstoffblanding. |
Country Status (18)
Country | Link |
---|---|
US (1) | US4404050A (en, 2012) |
EP (1) | EP0107891B1 (en, 2012) |
JP (1) | JPS5983992A (en, 2012) |
AU (1) | AU559714B2 (en, 2012) |
CA (1) | CA1166017A (en, 2012) |
CH (1) | CH661266A5 (en, 2012) |
DE (1) | DE3373895D1 (en, 2012) |
GB (1) | GB2128601B (en, 2012) |
HK (1) | HK97188A (en, 2012) |
IE (1) | IE55671B1 (en, 2012) |
IN (1) | IN163275B (en, 2012) |
NO (1) | NO157449B (en, 2012) |
NZ (1) | NZ204539A (en, 2012) |
OA (1) | OA07483A (en, 2012) |
PH (1) | PH18427A (en, 2012) |
SG (1) | SG107987G (en, 2012) |
ZA (1) | ZA834665B (en, 2012) |
ZW (1) | ZW13783A1 (en, 2012) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59156991A (ja) * | 1983-02-24 | 1984-09-06 | 日本化薬株式会社 | 油中水滴型エマルジヨン爆薬 |
CA1188898A (en) * | 1983-04-21 | 1985-06-18 | Howard A. Bampfield | Water-in-wax emulsion blasting agents |
ES8703394A1 (es) * | 1983-05-12 | 1987-02-16 | Du Pont | Un metodo para la preparacion de una composicion explosiva a base de nitrato amonico. |
US4555278A (en) * | 1984-02-03 | 1985-11-26 | E. I. Du Pont De Nemours And Company | Stable nitrate/emulsion explosives and emulsion for use therein |
US4548659A (en) * | 1984-04-05 | 1985-10-22 | Ireco Incorporated | Cast emulsion explosive composition |
US4844756A (en) * | 1985-12-06 | 1989-07-04 | The Lubrizol Corporation | Water-in-oil emulsions |
US4708753A (en) * | 1985-12-06 | 1987-11-24 | The Lubrizol Corporation | Water-in-oil emulsions |
US4863534A (en) * | 1987-12-23 | 1989-09-05 | The Lubrizol Corporation | Explosive compositions using a combination of emulsifying salts |
US5047175A (en) * | 1987-12-23 | 1991-09-10 | The Lubrizol Corporation | Salt composition and explosives using same |
US5527491A (en) * | 1986-11-14 | 1996-06-18 | The Lubrizol Corporation | Emulsifiers and explosive emulsions containing same |
US4840687A (en) * | 1986-11-14 | 1989-06-20 | The Lubrizol Corporation | Explosive compositions |
US4828633A (en) * | 1987-12-23 | 1989-05-09 | The Lubrizol Corporation | Salt compositions for explosives |
CA1299371C (en) * | 1987-06-10 | 1992-04-28 | Kevin Hunter Waldock | Dry mix explosive composition |
JP2669836B2 (ja) * | 1987-12-03 | 1997-10-29 | 日本工機株式会社 | 油中水型エマルジョン爆薬組成物 |
US4790890A (en) * | 1987-12-03 | 1988-12-13 | Ireco Incorporated | Packaged emulsion explosives and methods of manufacture thereof |
US5129972A (en) * | 1987-12-23 | 1992-07-14 | The Lubrizol Corporation | Emulsifiers and explosive emulsions containing same |
US5028284A (en) * | 1990-04-24 | 1991-07-02 | Chemfx, Ltd. | Explosion effects enhancer for fireworks |
US5920031A (en) * | 1992-03-17 | 1999-07-06 | The Lubrizol Corporation | Water-in-oil emulsions |
DE19649763A1 (de) * | 1996-11-30 | 1998-06-04 | Appenzeller Albert | Sprengstoff für zivile, insbesondere bergmännische Zwecke |
US6451920B1 (en) | 1999-11-09 | 2002-09-17 | Chevron Chemical Company Llc | Process for making polyalkylene/maleic anhydride copolymer |
US6955731B2 (en) * | 2003-01-28 | 2005-10-18 | Waldock Kevin H | Explosive composition, method of making an explosive composition, and method of using an explosive composition |
ES2436189T3 (es) * | 2009-09-23 | 2013-12-27 | Ael Mining Services Limited | Procedimiento para la producción de un explosivo |
WO2016100160A1 (en) | 2014-12-15 | 2016-06-23 | Dyno Nobel Inc. | Explosive compositions and related methods |
CA3093129A1 (en) | 2018-03-08 | 2019-10-03 | Orica International Pte Ltd | Systems, apparatuses, devices, and methods for initiating or detonating tertiary explosive media by way of photonic energy |
RU2710426C1 (ru) * | 2019-01-21 | 2019-12-26 | Михаил Николаевич Оверченко | Эмульсионный взрывчатый состав |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4181546A (en) * | 1977-09-19 | 1980-01-01 | Clay Robert B | Water resistant blasting agent and method of use |
US4149917A (en) * | 1977-11-03 | 1979-04-17 | Atlas Powder Company | Cap sensitive emulsions without any sensitizer other than occluded air |
JPS55160057A (en) * | 1979-04-09 | 1980-12-12 | Nippon Oil & Fats Co Ltd | Water-in-oil emulsion type explosive composition |
US4322258A (en) * | 1979-11-09 | 1982-03-30 | Ireco Chemicals | Thermally stable emulsion explosive composition |
-
1982
- 1982-09-29 US US06/427,495 patent/US4404050A/en not_active Expired - Lifetime
-
1983
- 1983-01-28 CA CA000420496A patent/CA1166017A/en not_active Expired
- 1983-06-13 NZ NZ204539A patent/NZ204539A/en unknown
- 1983-06-15 ZW ZW137/83A patent/ZW13783A1/xx unknown
- 1983-06-16 AU AU15825/83A patent/AU559714B2/en not_active Ceased
- 1983-06-27 ZA ZA834665A patent/ZA834665B/xx unknown
- 1983-07-01 OA OA58050A patent/OA07483A/xx unknown
- 1983-08-24 DE DE8383304895T patent/DE3373895D1/de not_active Expired
- 1983-08-24 GB GB08322792A patent/GB2128601B/en not_active Expired
- 1983-08-24 EP EP83304895A patent/EP0107891B1/en not_active Expired
- 1983-08-29 IE IE2021/83A patent/IE55671B1/en unknown
- 1983-08-30 IN IN593/DEL/83A patent/IN163275B/en unknown
- 1983-09-26 PH PH29589A patent/PH18427A/en unknown
- 1983-09-28 NO NO833503A patent/NO157449B/no unknown
- 1983-09-29 JP JP58179489A patent/JPS5983992A/ja active Pending
-
1984
- 1984-02-07 CH CH574/84A patent/CH661266A5/de not_active IP Right Cessation
-
1987
- 1987-12-09 SG SG1079/87A patent/SG107987G/en unknown
-
1988
- 1988-12-01 HK HK971/88A patent/HK97188A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
ZW13783A1 (en) | 1985-01-23 |
NO833503L (no) | 1984-03-30 |
IE55671B1 (en) | 1990-12-19 |
ZA834665B (en) | 1984-03-28 |
SG107987G (en) | 1988-05-20 |
PH18427A (en) | 1985-07-08 |
AU1582583A (en) | 1984-04-05 |
DE3373895D1 (en) | 1987-11-05 |
JPS5983992A (ja) | 1984-05-15 |
AU559714B2 (en) | 1987-03-19 |
GB8322792D0 (en) | 1983-09-28 |
CA1166017A (en) | 1984-04-24 |
EP0107891A2 (en) | 1984-05-09 |
EP0107891B1 (en) | 1987-09-30 |
IE832021L (en) | 1984-03-29 |
OA07483A (en) | 1984-12-31 |
EP0107891A3 (en) | 1985-04-03 |
HK97188A (en) | 1988-12-09 |
GB2128601A (en) | 1984-05-02 |
CH661266A5 (de) | 1987-07-15 |
NZ204539A (en) | 1986-05-09 |
GB2128601B (en) | 1985-12-11 |
US4404050A (en) | 1983-09-13 |
IN163275B (en, 2012) | 1988-09-03 |
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