US1464667A - Walter - Google Patents
Walter Download PDFInfo
- Publication number
- US1464667A US1464667A US1464667DA US1464667A US 1464667 A US1464667 A US 1464667A US 1464667D A US1464667D A US 1464667DA US 1464667 A US1464667 A US 1464667A
- Authority
- US
- United States
- Prior art keywords
- water
- explosive
- explosives
- crystallization
- walter
- 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
- 239000002360 explosive Substances 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 239000000463 material Substances 0.000 description 14
- 238000002425 crystallisation Methods 0.000 description 9
- 230000008025 crystallization Effects 0.000 description 9
- 150000002823 nitrates Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 239000003245 coal Substances 0.000 description 5
- 229910002651 NO3 Inorganic materials 0.000 description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 238000005065 mining Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 229910052602 gypsum Inorganic materials 0.000 description 3
- 239000010440 gypsum Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 229910052599 brucite Inorganic materials 0.000 description 2
- 229910021540 colemanite Inorganic materials 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910021539 ulexite Inorganic materials 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910000329 aluminium sulfate Inorganic materials 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000011128 aluminium sulphate Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 229910001679 gibbsite Inorganic materials 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- VLCLHFYFMCKBRP-UHFFFAOYSA-N tricalcium;diborate Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]B([O-])[O-].[O-]B([O-])[O-] VLCLHFYFMCKBRP-UHFFFAOYSA-N 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Classifications
-
- 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
- C06B23/04—Compositions characterised by non-explosive or non-thermic constituents for cooling the explosion gases including antifouling and flash suppressing agents
Definitions
- My invention relates to explosives for use in coal mining operations, and its object is to provide an explosive possessing the characteristics requisite for safe use in the presence of the inflammable gases prevalent in coal mines, and possessing also the property of stability which is an essential of all practical commercial explosives.
- these materials should contain suitable amounts of water of crystallization or of constitution, and must be relatively insoluble in water: but also they should be relatively chemically inert, since there are many materials possessing the first named properties which are nevertheless unsuitable for incorporation in an explosive because of their strongly acid or basic properties, or for other reasons.
- I may mention gypsum and ulcxite, and hydrous water insoluble minerals, cit-her natural or artificial, such as Brucite, Colemanite, Gibbsite, and Evansite.
- a suitable amountol the temperature reducing agent is mixed with the explosive material, the proportion in which these materials are present depending upon the amount of water of crystallization contained by the temperature reducing material. and upon the extent of the reduction desired.
- the amount of the temperature redueing agent present in the explosive may be roughly 3% to 25%, while with ma- 'ter1als holding small'amounts of Water of crystallization the amount of the reducing material pres-nt may be to 40%.
- I may form my explosive of 80% explosive base if gypsum is employed l may have 30% of this material with i()% of explosive base.
- cooling agent and ulexi't/e; 01'' should be added to insure the presence in -the explosive of 3% to 20% of available water. and for coal mining purposes sufficient material should be added to bring the flame temperature of the explosive below 2200 C. and preferably below 2000 C.
- I refer to water contained or held in such a form as to be a vailahle for the purpose described, such as water of crystallization, or water of constitution.
- An explosive mixture comprising a nitrate explosive base associated with a water-containing water-insoluble borate.
- An explosive mixture comprising a nitrate explosive base associated with a hydrous calcium borate.
- An explosive mixture comprising a nitrate explosive base associated with ulexite,
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Description
Patented Aug. 14, 1923.
UNITED STATES PATENT OFFICE.
WALTER O. SNELLING, OF ALLENTOWN, PENNSYLVANIA, ASSIGNOR TO TROJAN POWDEBCOMPANY, OF NEW YORK, N. Y., A CORPORATION OF NEW YORK.
EXPLOSIVE.
No Drawing.
To all whom it may concern:
Be it known that I, WALTER O. SNELLING, a citizen of the United States, and resident of Allentown, Lehigh County, Pennsylvania, have invented certain Improvements in Explosives, of ,Which the following is a specitication.
My invention relates to explosives for use in coal mining operations, and its object is to provide an explosive possessing the characteristics requisite for safe use in the presence of the inflammable gases prevalent in coal mines, and possessing also the property of stability which is an essential of all practical commercial explosives.
Exhaustive experiments have shown that the flame temperature of explosives must be close to 2000 C. or lower to insure safety when the explosives are employed in the presence of inflammable mine. gases. It has been one of the practices in attempting to reduce the normal flame temperatures of explosives to the safety point, to add to the explosive material salts such as sodium sulfate, magnesium sulfate, aluminium sulfate and zinc sulfate, containing large amounts of Water of crystallization, the theory of the use of such salts being that a cooling effect is produced upon the flame of explosion through the utilization of a portion of the heat energy in vaporizing the Water of crystallization and through the distribution of a further portion of the heat energy through the water vapor thus produced. This method has proved successful to the extent that lower flame temperatures have been obtained, but the product has proved unpractical as a commercial explosive because of an inherent instability. These explosives have been found to be extremely liable to deterioration on storage. and particularly so if they become somewhat wet.
I have discovered that the lack of stability of these explosives is due to the fact that the temperature reducing agents hitherto employed have the property of entering into chemical reaction with the nitrates, such as the nitrates of ammonium, sodium, potassium. and barium, which form a constituent of all commercial coal mining explosives.
I have further discovered that this tendency of thc temperature reducing agents to enter readily into reaction with the solublc alkali nitrate and alkali earth nitrates which are Application filed August 6, 1919. Serial N0. 315,674.
present in coal mining explosives, is due to z certain salts containing relatively high percentages of water of crystallization which salts I have found will not react with the nitrates of sodium, ammonium, potassium and barium, and which accordingly may remain in admixture with an explosive for an indefinite period With no resultant deterioration. These salts are for practical purposes substantially insoluble in water, requiring fifty or more times their own weight of water to bring about solution, and it is due to this property that they are able to withstand admixture with alkali nitrates and alkali earth nitrates, without undergting reaction.
There are many materials adapted to the purposes of my invention. As already indicated, these materials should contain suitable amounts of water of crystallization or of constitution, and must be relatively insoluble in water: but also they should be relatively chemically inert, since there are many materials possessing the first named properties which are nevertheless unsuitable for incorporation in an explosive because of their strongly acid or basic properties, or for other reasons. As examples of some of the materials which I have found adapted t my purpose, I may mention gypsum and ulcxite, and hydrous water insoluble minerals, cit-her natural or artificial, such as Brucite, Colemanite, Gibbsite, and Evansite. I have found also that in general all chemically inert and water insoluble borates, sulfates, carbonates and silicates, if they contain a suitable amount of water of crystallization, ma be applied to the purpose of mv invention, as well as certain phosphates and arsenatcs of iron and other metals. I prefer to use the borates of calcium and magnesium such as Colemanite and ulexite, and such minerals as Brucite and gypsum, because of their relative availability; but in general, any material which is relatively chemically inert. which holds 10% or more of water of crystallization, and which rcquires for its solution not less than titty times its own weight of water at a temperature of 20 is suitable.
in the formation of my explosive, a suitable amountol the temperature reducing agent is mixed with the explosive material, the proportion in which these materials are present depending upon the amount of water of crystallization contained by the temperature reducing material. and upon the extent of the reduction desired. \Yilh materials holding large amounts of water of ervstallization, the amount of the temperature redueing agent present in the explosive may be roughly 3% to 25%, while with ma- 'ter1als holding small'amounts of Water of crystallization the amount of the reducing material pres-nt may be to 40%. As specitie examples. I may form my explosive of 80% explosive base if gypsum is employed l may have 30% of this material with i()% of explosive base. In any event, enough of the cooling agent and ulexi't/e; 01'' should be added to insure the presence in -the explosive of 3% to 20% of available water. and for coal mining purposes sufficient material should be added to bring the flame temperature of the explosive below 2200 C. and preferably below 2000 C.
Where in the claims I employ the terms materials or salts containing water, I refer to water contained or held in such a form as to be a vailahle for the purpose described, such as water of crystallization, or water of constitution.
1. An explosive mixture comprising a nitrate explosive base associated with a water-containing water-insoluble borate.
2. An explosive mixture comprising a nitrate explosive base associated with a hydrous calcium borate.
3. An explosive mixture comprising a nitrate explosive base associated with ulexite,
said ulexit-e constituting 3% to of the mixture.
WALTER O. SNELLIHG.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1464667A true US1464667A (en) | 1923-08-14 |
Family
ID=3404757
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US1464667D Expired - Lifetime US1464667A (en) | Walter |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1464667A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2711366A (en) * | 1951-07-03 | 1955-06-21 | Ici Ltd | Blasting explosives |
| US2769701A (en) * | 1952-12-05 | 1956-11-06 | Ici Ltd | Compositions for use in re-utilisable blasting apparatus |
-
0
- US US1464667D patent/US1464667A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2711366A (en) * | 1951-07-03 | 1955-06-21 | Ici Ltd | Blasting explosives |
| US2769701A (en) * | 1952-12-05 | 1956-11-06 | Ici Ltd | Compositions for use in re-utilisable blasting apparatus |
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