IE34083L - Explosive compositions - Google Patents
Explosive compositionsInfo
- Publication number
- IE34083L IE34083L IE700419A IE41970A IE34083L IE 34083 L IE34083 L IE 34083L IE 700419 A IE700419 A IE 700419A IE 41970 A IE41970 A IE 41970A IE 34083 L IE34083 L IE 34083L
- Authority
- IE
- Ireland
- Prior art keywords
- cross
- ethylene glycol
- solution
- glycolic
- formamide
- Prior art date
Links
- 239000002360 explosive Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 11
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 abstract 4
- 239000000243 solution Substances 0.000 abstract 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 abstract 2
- 229930195725 Mannitol Natural products 0.000 abstract 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 abstract 2
- 239000003431 cross linking reagent Substances 0.000 abstract 2
- 239000000594 mannitol Substances 0.000 abstract 2
- 235000010355 mannitol Nutrition 0.000 abstract 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- IIQJBVZYLIIMND-UHFFFAOYSA-J potassium;antimony(3+);2,3-dihydroxybutanedioate Chemical compound [K+].[Sb+3].[O-]C(=O)C(O)C(O)C([O-])=O.[O-]C(=O)C(O)C(O)C([O-])=O IIQJBVZYLIIMND-UHFFFAOYSA-J 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 abstract 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 abstract 1
- 239000004971 Cross linker Substances 0.000 abstract 1
- 244000303965 Cyamopsis psoralioides Species 0.000 abstract 1
- 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 abstract 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- 229920000926 Galactomannan Polymers 0.000 abstract 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 abstract 1
- 229920002907 Guar gum Polymers 0.000 abstract 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 abstract 1
- 229920000161 Locust bean gum Polymers 0.000 abstract 1
- 229930006000 Sucrose Natural products 0.000 abstract 1
- 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 abstract 1
- -1 acrylate ester Chemical class 0.000 abstract 1
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 229910052787 antimony Inorganic materials 0.000 abstract 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 abstract 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 abstract 1
- 235000013312 flour Nutrition 0.000 abstract 1
- 229930182830 galactose Natural products 0.000 abstract 1
- 238000001879 gelation Methods 0.000 abstract 1
- 239000000665 guar gum Substances 0.000 abstract 1
- 235000010417 guar gum Nutrition 0.000 abstract 1
- 229960002154 guar gum Drugs 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008101 lactose Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000711 locust bean gum Substances 0.000 abstract 1
- 235000010420 locust bean gum Nutrition 0.000 abstract 1
- 230000003641 microbiacidal effect Effects 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 150000002772 monosaccharides Chemical class 0.000 abstract 1
- 229920001290 polyvinyl ester Polymers 0.000 abstract 1
- 239000011253 protective coating Substances 0.000 abstract 1
- 239000002002 slurry Substances 0.000 abstract 1
- 239000000600 sorbitol Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- 239000005720 sucrose Substances 0.000 abstract 1
- 150000005846 sugar alcohols Chemical class 0.000 abstract 1
- CIWAOCMKRKRDME-UHFFFAOYSA-N tetrasodium dioxido-oxo-stibonatooxy-lambda5-stibane Chemical compound [Na+].[Na+].[Na+].[Na+].[O-][Sb]([O-])(=O)O[Sb]([O-])([O-])=O CIWAOCMKRKRDME-UHFFFAOYSA-N 0.000 abstract 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Colloid Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
1,250,724. Protective coatings. CANADIAN INDUSTRIES Ltd. 26 March, 1970 [23 April, 1969], No. 14831/70. Heading B2E. [Also in Divisions C1 and C3] A cross-linking agent for the gelation of aqueous solutions prethickened by means of hydroxylated polymers containing vicinal cishydroxyl groups, comprises a solution of the product obtained by the admixture of soluble antimony and chromate compounds in a polar liquid comprising at least 10% by weight of a glycolic substance. The polymers are exemplified by galactomannans from guar gum and locust bean gum, though the acrylate ester of galactose and the polyvinyl ester of galacturonic acid are also mentioned. The cross-linking agent is composed of potassium antimony tartrate or sodium pyroantimonate, the chromate or dichromate of an alkali metal or ammonia, and a glycolic substance viz a monomeric or oligomeric glycol, a sugar alcohol or a monosaccharide containing free cis-hydroxyl groups exemplified by ethylene glycol, glycerol, mannitol, sorbitol and lactose, in association with water, formamide or dimethyl sulphoxide (also mannitol with sucrose). According to an Example, a viscous solution was prepared by blending 485g of water with a smooth slurry of 5g of high-viscosity guar flour and 0.05g of pentachlorophenol (microbiocide) in 10g of ethylene glycol. 2g of a cross-linker solution comprised of potassium antimony tartrate and sodium dichromate dissolved in ethylene glycol and formamide, were added with rapid stirring for 30 seconds and the resulting solution was very quickly poured on a flat counter and spread smoothly. A cross-linked film sheet formed in about 5 minutes and could be peeled from the smooth surface.
[GB1250724A]
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA49596 | 1969-04-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE34083L true IE34083L (en) | 1970-10-23 |
| IE34083B1 IE34083B1 (en) | 1975-01-22 |
Family
ID=4085177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE419/70A IE34083B1 (en) | 1969-04-23 | 1970-04-03 | Process for gelling water-bearing compositions containing thickeners |
Country Status (12)
| Country | Link |
|---|---|
| CA (1) | CA868421A (en) |
| CH (1) | CH527250A (en) |
| DE (1) | DE2019809C3 (en) |
| FR (1) | FR2046379A5 (en) |
| GB (1) | GB1250724A (en) |
| IE (1) | IE34083B1 (en) |
| IL (1) | IL34049A (en) |
| MY (1) | MY7300225A (en) |
| NO (1) | NO133194C (en) |
| OA (1) | OA03255A (en) |
| ZA (1) | ZA701903B (en) |
| ZM (1) | ZM3770A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1317327A (en) * | 1970-11-30 | 1973-05-16 | Ici Ltd | Slurry explosives |
-
1969
- 1969-04-23 CA CA868421A patent/CA868421A/en not_active Expired
-
1970
- 1970-03-10 IL IL34049A patent/IL34049A/en unknown
- 1970-03-20 ZA ZA701903A patent/ZA701903B/en unknown
- 1970-03-26 GB GB1250724D patent/GB1250724A/en not_active Expired
- 1970-03-31 ZM ZM37/70A patent/ZM3770A1/en unknown
- 1970-04-03 IE IE419/70A patent/IE34083B1/en unknown
- 1970-04-16 CH CH569470A patent/CH527250A/en not_active IP Right Cessation
- 1970-04-20 NO NO1491/70A patent/NO133194C/no unknown
- 1970-04-21 OA OA53904A patent/OA03255A/en unknown
- 1970-04-22 FR FR7014708A patent/FR2046379A5/fr not_active Expired
- 1970-04-23 DE DE2019809A patent/DE2019809C3/en not_active Expired
-
1973
- 1973-12-30 MY MY225/73A patent/MY7300225A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZM3770A1 (en) | 1972-02-21 |
| IL34049A (en) | 1973-07-30 |
| GB1250724A (en) | 1971-10-20 |
| MY7300225A (en) | 1973-12-31 |
| IE34083B1 (en) | 1975-01-22 |
| DE2019809A1 (en) | 1970-11-05 |
| IL34049A0 (en) | 1970-11-30 |
| CA868421A (en) | 1971-04-13 |
| DE2019809B2 (en) | 1973-11-22 |
| OA03255A (en) | 1970-12-15 |
| NO133194C (en) | 1976-03-24 |
| CH527250A (en) | 1972-08-31 |
| DE2019809C3 (en) | 1974-06-20 |
| FR2046379A5 (en) | 1971-03-05 |
| ZA701903B (en) | 1971-10-27 |
| NO133194B (en) | 1975-12-15 |
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