US608316A - George jseneke - Google Patents
George jseneke Download PDFInfo
- Publication number
- US608316A US608316A US608316DA US608316A US 608316 A US608316 A US 608316A US 608316D A US608316D A US 608316DA US 608316 A US608316 A US 608316A
- Authority
- US
- United States
- Prior art keywords
- resin
- carbonate
- ammonium nitrate
- potassium
- explosive
- 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
- 239000011347 resin Substances 0.000 description 30
- 229920005989 resin Polymers 0.000 description 30
- 239000002360 explosive Substances 0.000 description 24
- 239000000203 mixture Substances 0.000 description 24
- DVARTQFDIMZBAA-UHFFFAOYSA-O Ammonium nitrate Chemical compound [NH4+].[O-][N+]([O-])=O DVARTQFDIMZBAA-UHFFFAOYSA-O 0.000 description 22
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 20
- 150000001875 compounds Chemical class 0.000 description 18
- 239000000843 powder Substances 0.000 description 18
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 16
- 239000000463 material Substances 0.000 description 10
- 230000001590 oxidative Effects 0.000 description 10
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 8
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 239000001187 sodium carbonate Substances 0.000 description 8
- 229910000029 sodium carbonate Inorganic materials 0.000 description 8
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 6
- XMXNVYPJWBTAHN-UHFFFAOYSA-N Potassium chromate Chemical compound [K+].[K+].[O-][Cr]([O-])(=O)=O XMXNVYPJWBTAHN-UHFFFAOYSA-N 0.000 description 6
- PXLIDIMHPNPGMH-UHFFFAOYSA-N Sodium chromate Chemical compound [Na+].[Na+].[O-][Cr]([O-])(=O)=O PXLIDIMHPNPGMH-UHFFFAOYSA-N 0.000 description 6
- 238000010348 incorporation Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 6
- 229910052700 potassium Inorganic materials 0.000 description 6
- 239000011591 potassium Substances 0.000 description 6
- 235000015497 potassium bicarbonate Nutrition 0.000 description 6
- 229940094025 potassium bicarbonate Drugs 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- TYJJADVDDVDEDZ-UHFFFAOYSA-M Potassium bicarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 4
- 239000011736 potassium bicarbonate Substances 0.000 description 4
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 4
- 239000001184 potassium carbonate Substances 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N Potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- KIEOKOFEPABQKJ-UHFFFAOYSA-N Sodium dichromate Chemical compound [Na+].[Na+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KIEOKOFEPABQKJ-UHFFFAOYSA-N 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000005422 blasting Methods 0.000 description 2
- 239000002817 coal dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
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
Definitions
- nitrate of ammonium and bodies of a resinous or hydrocarbon nature have been employed, sometimes with the addition of oxidizing materials, such as chromate or bichromate of sodium or potassium.
- my invention consists in the incorporation with nitrate of ammonium and a resinous body, with or without an oxidizing material, such as an alkaline ehromate or bichromate, of sodium or potassium carbonate or bicarbonate.
- My invention also includes a particular method of incorporating the alkaline carbonate or bicarbonate into the mixture in order to prevent increase in the hygroscopicity of the mixture, which would otherwise be liable to become hygroscopic to such an extent as to liquefy and become unfit for use.
- the novel method of incorporating the alkaline carbonate or bicarbonate is to mix it with the resin when the latter is in a melted or liquid or semiliquid state, prior to the incorporation of the resin with the ammonium nitrate.
- sodium or potassium chromate or bichromatc is to constitute one of the ingredients of the explosive compound, it is also similarly incorporated with the resin prior to the incorporation of the resin with the ammonium nitrate.
- I melt five parts of resin, taking care that the temperature is not raised much above the meltingpoint of the resin, and when reduced to a fluid state I stir into it two and one-half parts of potassium'fbiehromate (or its equivalent quantity of potassium chromate or sodium chromate or bichromate) and three-fourths part of sodium carbonate (or the equivalent weight of sodium bicarbonate, potassium earbonate, or potassium bicarbonate.) I do not confine myself to these proportions and may increase the proportion of potassium bichromate to about three and three-fourths parts and the proportion of the sodium carbonate Serial No. 663,433. (No specimens.)
- the mixture is maintained just above the melting-point of the resin and constantly stirred until the ingredients have been uniformly mixed, when the melt will present a dull-yellow color aeeording to the quality of resin employed.
- the mixture should not, however, become green and dark, which is a sign of overheating.
- the mixture is then allowed to cool and ground to an extremely-fine powder,
- the explosive manufactured as described above should be hermetically closed in eartridges or otherwise. It is specially suitable for blasting rock and stone in coal-mines,v
- coal-dust and pit-gas abound where coal-dust and pit-gas abound. I It will not ignite them and is a most powerful explosive and quick in its action.
- the sodium or potassium chromate or bichromate is not to constitute one of the ingredients of the explosive compound, I may carry the invention into eflect as follows: I melt one to one and one-half parts ofresimand then I stir into it one to one and' one-half parts of finely-powdered icaronate, (or an equivalent quanti't sodium carbonate or of potassium carbonate or bicarbonate.) I let the mixture cool and then grind it into a fine powder. I mix this intimately with five or four parts of resin ground to an extremely-fine powder. I add this mixturein a 'of finely-powdered ammonium nitrate, the
- ⁇ Vhencver hereinafter the expression chromate is used, it will be understood to include either chromate or a bichromate, and whenever the term carbonate is hereinafter used it will be understood to signify either a carbonate or a bicarbonate.
- An explosive compound consisting of the following substances incorporated together in approximately the proportions stated, namely ammonium nitrate, aresin, an oxidizing material and an alkaline carbonate.
- An explosive compound consisting of the following substances incorporated together in approximately the proportions stated, namely ammonium nitrate; a resin and an alkaline carbonate 7 In' witness whereof I have hereunto signed my name in the presence of two subscribing witnesses.
Description
FIPTQOQ UNITED STATES PATENT OFFICE.
GEORGE BENEKE, OF SOUTIIIOIt'l, ENGLAND.
PECIFICATI N forming part of Letters Patent No. 608,316, dated August 2, 1898.
Applicationfiled December 24, 1897- T0 all whom it may concern.-
Be it known that I, Gnonen llnxlnu'a, of Southport, England, have invented certain new and useful Improvements in the Mannfaetu re of Explosive Compounds, of which the following is a specification.
Various explosive compounds have already been invented in which nitrate of ammonium and bodies of a resinous or hydrocarbon nature have been employed, sometimes with the addition of oxidizing materials, such as chromate or bichromate of sodium or potassium. Now my invention consists in the incorporation with nitrate of ammonium and a resinous body, with or without an oxidizing material, such as an alkaline ehromate or bichromate, of sodium or potassium carbonate or bicarbonate.
My invention also includes a particular method of incorporating the alkaline carbonate or bicarbonate into the mixture in order to prevent increase in the hygroscopicity of the mixture, which would otherwise be liable to become hygroscopic to such an extent as to liquefy and become unfit for use. The novel method of incorporating the alkaline carbonate or bicarbonate is to mix it with the resin when the latter is in a melted or liquid or semiliquid state, prior to the incorporation of the resin with the ammonium nitrate. When sodium or potassium chromate or bichromatc is to constitute one of the ingredients of the explosive compound, it is also similarly incorporated with the resin prior to the incorporation of the resin with the ammonium nitrate.
The manner in which I may carry the invention into effect is as follows: I melt five parts of resin, taking care that the temperature is not raised much above the meltingpoint of the resin, and when reduced to a fluid state I stir into it two and one-half parts of potassium'fbiehromate (or its equivalent quantity of potassium chromate or sodium chromate or bichromate) and three-fourths part of sodium carbonate (or the equivalent weight of sodium bicarbonate, potassium earbonate, or potassium bicarbonate.) I do not confine myself to these proportions and may increase the proportion of potassium bichromate to about three and three-fourths parts and the proportion of the sodium carbonate Serial No. 663,433. (No specimens.)
to one and one-half parts; but I prefer to keep within these limits. The mixture is maintained just above the melting-point of the resin and constantly stirred until the ingredients have been uniformly mixed, when the melt will present a dull-yellow color aeeording to the quality of resin employed. The mixture should not, however, become green and dark, which is a sign of overheating. The mixture is then allowed to cool and ground to an extremely-fine powder,
which its extremely-brittle character and absence of hygroscopic properties renders very easy. To eight or ten parts of this powder I then add about ninety or ninety-two partsjof ammonium nitrate, which must have been previously dried, ground to an extremely fine powder, and again heated for about two hours at a temperature of 109 eentigrade to drive off the last traces of moisture. The mixture of the resinous powder should be made in a revolving drum with the ammonium nitrate direct as it comes from the drying-oven and while still hot. In this waya more uniform mixture and better aggregation of the particles of the ingredients is eifeeted, while in order to insure the absence of moisture it is preferable before packing the explosive or making up into cartridges to again heat the powder in a steam-jacket to centigrade, a temperature insuiliciently high to melt the resin or render it sticky. I q The explosive manufactured as described above should be hermetically closed in eartridges or otherwise. It is specially suitable for blasting rock and stone in coal-mines,v
where coal-dust and pit-gas abound. I It will not ignite them and is a most powerful explosive and quick in its action.
Then the sodium or potassium chromate or bichromate is not to constitute one of the ingredients of the explosive compound, I may carry the invention into eflect as follows: I melt one to one and one-half parts ofresimand then I stir into it one to one and' one-half parts of finely-powdered icaronate, (or an equivalent quanti't sodium carbonate or of potassium carbonate or bicarbonate.) I let the mixture cool and then grind it into a fine powder. I mix this intimately with five or four parts of resin ground to an extremely-fine powder. I add this mixturein a 'of finely-powdered ammonium nitrate, the
latter having been previously heated to about 100 'centigrade, and while still hot I intimately mix. The explosive compound thus made is slower in action than that in which the chromate or bichromatc is present.
\Vhencver hereinafter the expression chromate is used, it will be understood to include either chromate or a bichromate, and whenever the term carbonate is hereinafter used it will be understood to signify either a carbonate or a bicarbonate.
What I claim, and desire to secure by Letters Patent, is
l. The process of manufacture of explosive compounds in which ammonium nitrate, resin, an oxidizing material (such as alkaline cllr'amatel n ml an alkaline carbonate, are employed, which consists in incorporating the alkaline carbonate and the oxidizing material with the resin when the latter is in a liquid state,then allowing the thereby-obtained mixture to cool, then reducing it to powder, and then incorporating it with the ammonium nitrate.
:2. The process of manufacture of explosive compounds in which ammonium nitrate, resin and an alkaline carbonate are employed, which consists in incorporating the alkaline carbonate with the resin when the latter is in a liquid state, then' allowing the thereby-obtained mixture to cool, then reducing it-to powder and then incorporating it with the ammonium nitrate.
3. An explosive compound consisting of the following substances incorporated together in approximately the proportions stated, namely ammonium nitrate, aresin, an oxidizing material and an alkaline carbonate.
4. An explosive compound consisting of the following substances incorporated together in approximately the proportions stated, namely ammonium nitrate; a resin and an alkaline carbonate 7 In' witness whereof I have hereunto signed my name in the presence of two subscribing witnesses.
GEORGE llENEKF.
Witnesses:
WILLIAM PIERCE, SAMUEL MOCREADY.
Publications (1)
Publication Number | Publication Date |
---|---|
US608316A true US608316A (en) | 1898-08-02 |
Family
ID=2676937
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US608316D Expired - Lifetime US608316A (en) | George jseneke |
Country Status (1)
Country | Link |
---|---|
US (1) | US608316A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2997377A (en) * | 1952-04-01 | 1961-08-22 | Standard Oil Co | Polyamine chromate catalysts for inorganic nitrate explosives |
-
0
- US US608316D patent/US608316A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2997377A (en) * | 1952-04-01 | 1961-08-22 | Standard Oil Co | Polyamine chromate catalysts for inorganic nitrate explosives |
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