US2119050A - Liquid oxygen explosive - Google Patents
Liquid oxygen explosive Download PDFInfo
- Publication number
- US2119050A US2119050A US159914A US15991437A US2119050A US 2119050 A US2119050 A US 2119050A US 159914 A US159914 A US 159914A US 15991437 A US15991437 A US 15991437A US 2119050 A US2119050 A US 2119050A
- Authority
- US
- United States
- Prior art keywords
- liquid oxygen
- carbonaceous material
- proofing
- solution
- fire
- 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
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 title description 16
- 239000002360 explosive Substances 0.000 title description 10
- 239000003575 carbonaceous material Substances 0.000 description 20
- 239000000463 material Substances 0.000 description 18
- 238000004079 fireproofing Methods 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 230000035945 sensitivity Effects 0.000 description 5
- 238000004880 explosion Methods 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004254 Ammonium phosphate Substances 0.000 description 3
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 3
- 235000019289 ammonium phosphates Nutrition 0.000 description 3
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 3
- 229920005610 lignin Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 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
- 229910019142 PO4 Inorganic materials 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 2
- 239000004137 magnesium phosphate Substances 0.000 description 2
- 229960002261 magnesium phosphate Drugs 0.000 description 2
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 2
- 235000010994 magnesium phosphates Nutrition 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 239000004135 Bone phosphate Substances 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000001141 propulsive effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229940075581 sodium bromide Drugs 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B43/00—Compositions characterised by explosive or thermic constituents not provided for in groups C06B25/00 - C06B41/00
Definitions
- the carbonaceous material is first treated with. the fire-proofing material and then placed in the bags or casings in the usual way.
- a water soluble, fire-proofing material and as a specific 30 I example a solution of ammonium phosphate of desired strength may be first formed.
- the solution is then added to the carbonaceous material up to 20% by weight.
- the water and the fireproofingmaterial are allowed to remain in the 35 carbonaceous material and the carbonaceous material then placed in bags and liquid oxygen added thereto in the .usual manner.
- a material that is not water-soluble may 40 be empioyedand thoroughly mixed with the carbonaceous material before the liquid oxygen is added thereto.
- the addition of the fire-proofing material in the amounts stated reduces the sensitivity of the 4 completed cartridge to a point where it is'safer to handle but not enough to destroy its usefulmess.
- the cartridge so produced is thus capable of being detonated in the usual manner when desired but is less liable to premature explosions caused by stones 'or other objects falling on the cartridge as it is being lowered into drill holes and is also less liable to explosion by casual flames, such as cigarettes, sparks, etc.
- the carbonaceous material, treated as above 66 described, may be employed in the usual wrappers or bags of cotton fabric or the bag or wrapper may. also be treated with the fire-proofing agent.
- the solution is prepared as above described and containing about one gallon of water to one pound of the salt.
- Thebags or the material from which the bagsare to be made, are soaked in this solution and allowed to dry.
- the bag may be filled with a carbonaceo s material in the usual way and then treated 1 th the fire-proofing solution, either by spraying the finished bag or by coating it by placing it in a vessel or trough containing the solution. In this way the bag will become saturated with the fire-proofing solution and an outer layer of the carbonaceous material near the bag will also become saturated; If such outer layer of the carbonaceous material is saturated, it is not necessary to saturate the'carbonaceous material throughout as this treatment is eflective in stopping both flaming and glowing of the carbonaceous material;
- While the present invention may be practiced with any type of carbonaceous material capable of absorbing liquid 'oxygen I prefer to employ granular carbons having a high degree of absorption for liquid oxygen, or other explosives.
- a granular carbon of the type commercially known'as'Bugbird carbon, made in accordance with the Bugbird Patents Nos.'1,'706,871, 1,779,530 and 1,781,214, may be used. This material is obtained by carbonizing liquors rich in dissolved lignins, such as those derived from the manufacture of wood pulp by the alkali (soda) process.
- the carbonized lignin residues are leached to remove water soluble impurities and then sub-- mitted to a-slight grinding action to reduce the grains to a more or less-uniform size.
- This prograins are not more than about one-quarter inch in their longest dimension and sothat not more than about 25 percent of the material will pass through a 100 mesh screen.
- bonaceous material in granular form impregthe cartridge casing to. on it arid confine the.
- a liquid oxygen explosive comprising carbonaceous material ingranular form'impreg mated with a solution of ammonium phosphate.
- a liquid oxygen explosive comprising carbonaceous material in I granular form impreg nated with a solution of calcium chloride.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Respiratory Apparatuses And Protective Means (AREA)
Description
- Patented Ma 31, 1938 j s ArEs PATENT OFFlCE Q. Q fLIQUID ox l lmo m Y. v
No Drawing.- Application August 19, 1937.
Serial No. 159,914
6 Claims.
.In' the' -use of liquid oxygen explosives a suitable amount of carbon or carbonaceous material a v f is placedin a bag or wrapper or made into a cartridge',-,and liquid oxygen is added thereto. The
cartridges actually used in this manner may be i of considerable size and when they are to be used, theya'rei placed or dropped in a hole or bore to t 10 be blasted," tamped in place and then detonated. The most;fserious objection to the use of liquid oxygen explosives has been that they are sensitivefto'sparks'or flame. As a. result, premature explosions' have been caused by stones or other 1.; objects falling on" the saturated cartridges as they are being lowered into drill holes or such f explosions have been caused by shocksor sparks accidentally transmitted to the cartridges in transit. ,Many .attempts have been made to overcome -lthis fault. In the prior patent of GeorgeSt-JohnPerrott and me, No. 1,860,816, granted May 31, 1932 wehave disclosed and claimed a method of regulating the sensitivity of. explosives of this type whereinan incombustible :amaterial' in'a'finer state of division than the carbon is added to the carbon. Likewise in the Holderer and Clark Patent No. 1,865,104, granted June 28, 1932 we have-disclosed and claimed the use-of a binder in an amount sufficient to agglomerate thecarbonaceous material without appreciably" affecting its porosity, and in my prior Patent No.* 1,960,907, granted May 29, 1934, I have disclosed and claimed the use of carbonized lignin residues having a moisture content greater than 8 percent.
While each of these methods has resulted in the production-of liquid oxygen explosives which are sai'er' to handle than would otherwise be the case, I have now found that the sensitivity of 40 such cartridges. to outside spark or flame infiuence canbe greatly minimized by treating the carbonaceous mater l with a fire-proofing sub stance preierably in I or wrappersin whic 'the carbonaceous material 1S contained may be impregnated with fireproofing.material. Any of the ordinary fire proofing'salts. may be employed for this purpose. Oi. s'uchusalts I prt' to use either dibasic or monobasic' ammon .1 phosphate; My inven- 5 0 'tion; however-{is .n... limitedto theuse of this particular lsalt and cium ,chloride, magnesium sulphate, sodium silicate eborax,sodiumbromide, sodium tungstate,
magnesium phosphate, phosphoric acid, monolution. Likewisethe bags equivalents therefor cal- 'zinc chloride, tr'i-ba'sidzinc phosphate, tri-basic basic magnesium phosphate, boric acid, monobasic zinc phosphataaluminum sulphate, am--' monium bromide, ammonium chloride and ammonium sulphate. Combinations of these or similar chemicals may be desirable both from the 5 standpoint of efiectiveness and cost and the invention includes the use of two or more of these .materials together. Also wide latitude of the strength of solutions employed is within the scope of the invention and the strength employed is 10 based largely on the cost of the chemicals as all In practicing the invention the carbonaceous material is first treated with. the fire-proofing material and then placed in the bags or casings in the usual way. I preferably employ a water soluble, fire-proofing material and as a specific 30 I example a solution of ammonium phosphate of desired strength may be first formed. The solution is then added to the carbonaceous material up to 20% by weight. The water and the fireproofingmaterial are allowed to remain in the 35 carbonaceous material and the carbonaceous material then placed in bags and liquid oxygen added thereto in the .usual manner.
Instead of using a water-soluble, fire-proofing material, a material that is not water-soluble may 40 be empioyedand thoroughly mixed with the carbonaceous material before the liquid oxygen is added thereto.
The addition of the fire-proofing material in the amounts stated reduces the sensitivity of the 4 completed cartridge to a point where it is'safer to handle but not enough to destroy its usefulmess. The cartridge so produced is thus capable of being detonated in the usual manner when desired but is less liable to premature explosions caused by stones 'or other objects falling on the cartridge as it is being lowered into drill holes and is also less liable to explosion by casual flames, such as cigarettes, sparks, etc.
The carbonaceous material, treated as above 66 described, may be employed in the usual wrappers or bags of cotton fabric or the bag or wrapper may. also be treated with the fire-proofing agent. When the bag is to be treated, the solution is prepared as above described and containing about one gallon of water to one pound of the salt. Thebags or the material from which the bagsare to be made, are soaked in this solution and allowed to dry. a
As an alternative procedure, the bag may be filled with a carbonaceo s material in the usual way and then treated 1 th the fire-proofing solution, either by spraying the finished bag or by coating it by placing it in a vessel or trough containing the solution. In this way the bag will become saturated with the fire-proofing solution and an outer layer of the carbonaceous material near the bag will also become saturated; If such outer layer of the carbonaceous material is saturated, it is not necessary to saturate the'carbonaceous material throughout as this treatment is eflective in stopping both flaming and glowing of the carbonaceous material;
While the present invention may be practiced with any type of carbonaceous material capable of absorbing liquid 'oxygen I prefer to employ granular carbons having a high degree of absorption for liquid oxygen, or other explosives. A granular carbon of the type commercially known'as'Bugbird carbon, made in accordance with the Bugbird Patents Nos.'1,'706,871, 1,779,530 and 1,781,214, may be used. This material is obtained by carbonizing liquors rich in dissolved lignins, such as those derived from the manufacture of wood pulp by the alkali (soda) process.
The carbonized lignin residues are leached to remove water soluble impurities and then sub-- mitted to a-slight grinding action to reduce the grains to a more or less-uniform size. This prograins are not more than about one-quarter inch in their longest dimension and sothat not more than about 25 percent of the material will pass through a 100 mesh screen.
I am aware or prior patents disclosing -th etreatment of bags or casings of explosive cartridges with fire-proofing materials for the pur pose of making. them flre-damp-prooi. v damp-proofing is not to be confused with the treatment of the carbonaceous material itself forv the sensi-tivity'ot the' cartridge. This phrase means reducihg the flame the purpose of decreasing Firetemperature of theexplosive mixture to reduce of my invention the cartridge m" terial itself is treated to lower -its sensitivity casual flame without affecting its ability toy absorb liquid oxygen and without destroying its propulsive strength. I
I claim:
bonaceous material in granular form impregthe cartridge casing to. on it arid confine the.
nated with a solution of a fire-proofing material.
2. A liquid oxygen explosive comprising carbonaceous material ingranular form'impreg mated with a solution of ammonium phosphate.
3. A liquid oxygen explosive comprising carbonaceous material in I granular form impreg nated with a solution of calcium chloride.
4. The" herein described i'riethodfwhich com-" prises impregnating granular carbonaceous material with a solution of ii -proofing material,
ing liquid oxygen thereto;
5; The herein described-method which complacing the material in a bag or casing and addprises impregnating granular carbonaceous material with a solution of ammonium phosphate, placing thematerial infa bag or casingand vadd- I ing liquid oxygen thereto. duces a granular carbon in which the largest 6. The herein described method which comprises impregnating granular carbonaceous material with a solution of calcium chloride, placing the material in a bag or casingflandadding liquid oxygen theretm, f v
' GEORGE BURKLE HOLDERER.
v I 20 v 1. A liquid oxygen explosive frcomprising car-'- I
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US159914A US2119050A (en) | 1937-08-19 | 1937-08-19 | Liquid oxygen explosive |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US159914A US2119050A (en) | 1937-08-19 | 1937-08-19 | Liquid oxygen explosive |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2119050A true US2119050A (en) | 1938-05-31 |
Family
ID=22574651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US159914A Expired - Lifetime US2119050A (en) | 1937-08-19 | 1937-08-19 | Liquid oxygen explosive |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2119050A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2723188A (en) * | 1955-01-31 | 1955-11-08 | Glmite Corp | Liquid oxygen explosive and method of preparing same |
-
1937
- 1937-08-19 US US159914A patent/US2119050A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2723188A (en) * | 1955-01-31 | 1955-11-08 | Glmite Corp | Liquid oxygen explosive and method of preparing same |
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