US1882190A - Explosive - Google Patents
Explosive Download PDFInfo
- Publication number
- US1882190A US1882190A US589704A US58970432A US1882190A US 1882190 A US1882190 A US 1882190A US 589704 A US589704 A US 589704A US 58970432 A US58970432 A US 58970432A US 1882190 A US1882190 A US 1882190A
- Authority
- US
- United States
- Prior art keywords
- nitrate
- explosive
- dnt
- formula
- mesh
- 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 title description 28
- 235000013339 cereals Nutrition 0.000 description 31
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 28
- 229910002651 NO3 Inorganic materials 0.000 description 21
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 21
- 230000008014 freezing Effects 0.000 description 17
- 238000007710 freezing Methods 0.000 description 17
- 235000010344 sodium nitrate Nutrition 0.000 description 14
- 239000004317 sodium nitrate Substances 0.000 description 14
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- DYSXLQBUUOPLBB-UHFFFAOYSA-N 2,3-dinitrotoluene Chemical compound CC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O DYSXLQBUUOPLBB-UHFFFAOYSA-N 0.000 description 5
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- 239000004571 lime Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- ZPTVNYMJQHSSEA-UHFFFAOYSA-N 4-nitrotoluene Chemical compound CC1=CC=C([N+]([O-])=O)C=C1 ZPTVNYMJQHSSEA-UHFFFAOYSA-N 0.000 description 3
- 229920001131 Pulp (paper) Polymers 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 241000609240 Ambelania acida Species 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000010905 bagasse Substances 0.000 description 2
- 238000005422 blasting Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
- C06B31/02—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate
- C06B31/12—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate with a nitrated organic compound
- C06B31/14—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate with a nitrated organic compound the compound being an aromatic
- C06B31/16—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate with a nitrated organic compound the compound being an aromatic the compound being a nitrated toluene
Definitions
- Patented Get. H 1932 STTE GLENN ALBERT PRITCHETT, OF RENO, NEVADA.
- My invention relates to explosives, and contemplates the production of a series of explosive mixtures or compounds of mutually difierent characteristics and uses. all of which however possess in common certain novel features and properties.
- the invention also contemplates a novel method of compounding explosives.
- Principal objects of the invention are to provide a superior and inexpensive explosive product which will be free from certain serious disadvantages of explosives of the prior art hereinafter briefly indicated.
- the invention includes the use of dinitrotoluene of approximately a freezing point which has not been used in the manufacture of explosives prior to my present invention.
- the novelty of my invention also resides principally in the elimination of certain ingredients heretofore regarded as necessary to the production of explosives of comparable grade. and in certain novel features of the processing of the ingredients. all of which will hereinafter be more particularly described and claimed.
- the invention contemplates several varying formulae. each formula providing an explosive of differentgrade and influence. Dinitrotoluene is used in each formula. Th s material is commercially obtainable in various grades characterized b difi'erentfreezing points ranging from about C. to 65 C. I have found it necessary to use DYT having a freezing point not lower than C. in order that the material may exist in a crystalline condition in the product.
- the lowest grade explosive contemnlated by mv invention contains the following ingredients:
- Formula A Per cent Dmitrotoluene 10 Sodium nitrate 90
- the sodium nitrate is sized between 8 and 18 mesh and thus introduced into the composition in relatively granular form. as distinguished from the pulverulent state in which this material has been used heretofore.
- the nitrate grains used in Formula A are such as pass an 8 mesh sieve and are retained on an 18 mesh sieve. Consequently, none of the grains are larger than S mesh and none are smaller than 18 mesh.
- the curve on the accompanying raph, hereinafter referred to, indicates the average size. I consider the proper sizing of the nitrate important and conducive to the improved efficiency of the resulting product.
- the DXT is warmed to a temperature above its melting point, say C. for average material. and mixed with the nit-rate. The mixture is maintained above the melting temperature of the DXT during the mixing operation to prevent crystallization of the liquid until an intimate mixture is obtained.
- the D'ST adheres as an oily coating to the nitrate grains, protecting the nitrate from moisture. and minimizing friction.
- Each grain of the product is an independent explosive agent, combustion being transmitted from one grain to another when the mixture is set off.
- the relatively coarse character of the granular product prevents the explosive becoming dense and insensitive to the influence of detonators when packed tightly in machine loaded cartridges or tamped in blast holes.
- the explosive product is solid at ordinary atmospheric temperatures. Disintegration and separation of constituents cannot therefore occur, and the efficacy and safety of the productare not affected by ordinary climatic changes.
- the explosive composition is superior in strength to ordinary black blasting powder and is comparable thereto in cost of production and safety in handling.
- My product is equal in all respects to prior art explosives including relatively expensive sodium chlorate, which it has heretofore been thought' 'ne'cessary to use in an amount equal to atleast 25% of the total weight of all ingredients in order to produce complete combustion when even the best detonator is employed.
- An important object of the invention 15 produce an explosive compound which will not pack densely, and to this end DNT is selected having a freezing point directly related to the size of the nitrate grains.
- the ratio of DNT freezing point and nitrate grain size given for Formula A by way of example may be more or less departed from, especially by using DNT of a higher freezing point, since the nitrate grains in Formula A are large enough to prevent density of pack in the product. It may, however, be stated that with nitrate grains of the size prescribed for Formula A, the freezing point of. the DNT should not be lower than 40 C. It is important that the DNT be in the frozen state in the product, and the smaller the grains the less solidly frozen must be the DNT. Otherwise the product packs densely and becomes relatively insensitive to the action of ordinary fuse caps or electric exploders.
- ⁇ Vhen substantially the ratio prescribed is followed a satisfactory low grade explosive compound is produced which is slightly higher in percentage of strength than ordinary black blasting powder, which will detonate consistently with No. 6 fuse caps or electric exploders, and which possesses resistance to friction, fire and impact superior to any other comparable explosive of which I am aware.
- Formula B Per cent Dinitrotoluene 10 Sodium nitrate 73 Sodium chlorate 15 Lime 5 pulp provides carbon and serves to absorb and retain any excess oil.
- a still stronger explosive is provided by further increasing the proportion of chlorate, as follows:
- Formula C I prefer to use smaller sized nitrate grains e. g.. such as sieve between 10 and 20 mesh.
- the DXT may be of the same freezing point as that prescribed for Formula A, since in Formula C the nitrate grains are still large enough to prevent density of pack in tlie product.
- the nitrate grains are sized at not larger than 20 mesh. Such reduction in grain size necessitates usin DNT of a lower freezing point, to prevent ensity of pack, and to this end a small proportion of mononitrotoluene is added to the DNT.
- the freezing point of the mixture of the two toluenes in Formulae D and E should be not higher than 37 C.
- the moisture content is less than 1%.
- An explosive including DNT and'sodium nitrate in which the DNT has a freez- 5 ing point not lower than 40 6., and the grains of nitrate are sized between Sand 18 mesh. and in which the DNT is carried as a coating on the nitrate grains.
- S.- An explosive as claimed in claim 1 which contains substantially 10 parts of BN1, 7 3 parts of sodium nitrate and 15 parts of sodium chlorate.
- An explosive as claimed in claim 1 which contains substantially 10 parts of DNT, 41 parts of sodium nitrate and 39.5 parts of sodium chlorate.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Thermotherapy And Cooling Therapy Devices (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Patented Get. H, 1932 STTE GLENN ALBERT PRITCHETT, OF RENO, NEVADA.
EXPLOSIVE Application filed January 29, 1932. Serial No. 589,704.
My invention relates to explosives, and contemplates the production of a series of explosive mixtures or compounds of mutually difierent characteristics and uses. all of which however possess in common certain novel features and properties. The invention also contemplates a novel method of compounding explosives.
Principal objects of the invention are to provide a superior and inexpensive explosive product which will be free from certain serious disadvantages of explosives of the prior art hereinafter briefly indicated.
The invention includes the use of dinitrotoluene of approximately a freezing point which has not been used in the manufacture of explosives prior to my present invention. The novelty of my invention also resides principally in the elimination of certain ingredients heretofore regarded as necessary to the production of explosives of comparable grade. and in certain novel features of the processing of the ingredients. all of which will hereinafter be more particularly described and claimed.
The invention contemplates several varying formulae. each formula providing an explosive of differentgrade and influence. Dinitrotoluene is used in each formula. Th s material is commercially obtainable in various grades characterized b difi'erentfreezing points ranging from about C. to 65 C. I have found it necessary to use DYT having a freezing point not lower than C. in order that the material may exist in a crystalline condition in the product.
The lowest grade explosive contemnlated by mv invention contains the following ingredients:
Formula A Per cent Dmitrotoluene 10 Sodium nitrate 90 The sodium nitrate is sized between 8 and 18 mesh and thus introduced into the composition in relatively granular form. as distinguished from the pulverulent state in which this material has been used heretofore. The nitrate grains used in Formula A are such as pass an 8 mesh sieve and are retained on an 18 mesh sieve. Consequently, none of the grains are larger than S mesh and none are smaller than 18 mesh. The curve on the accompanying raph, hereinafter referred to, indicates the average size. I consider the proper sizing of the nitrate important and conducive to the improved efficiency of the resulting product.
The DXT is warmed to a temperature above its melting point, say C. for average material. and mixed with the nit-rate. The mixture is maintained above the melting temperature of the DXT during the mixing operation to prevent crystallization of the liquid until an intimate mixture is obtained.
Upon cooling. the D'ST adheres as an oily coating to the nitrate grains, protecting the nitrate from moisture. and minimizing friction. Each grain of the product is an independent explosive agent, combustion being transmitted from one grain to another when the mixture is set off. The relatively coarse character of the granular product prevents the explosive becoming dense and insensitive to the influence of detonators when packed tightly in machine loaded cartridges or tamped in blast holes.
The explosive product is solid at ordinary atmospheric temperatures. Disintegration and separation of constituents cannot therefore occur, and the efficacy and safety of the productare not affected by ordinary climatic changes. The explosive composition is superior in strength to ordinary black blasting powder and is comparable thereto in cost of production and safety in handling.
My product is equal in all respects to prior art explosives including relatively expensive sodium chlorate, which it has heretofore been thought' 'ne'cessary to use in an amount equal to atleast 25% of the total weight of all ingredients in order to produce complete combustion when even the best detonator is employed.
An important object of the invention 15 produce an explosive compound which will not pack densely, and to this end DNT is selected having a freezing point directly related to the size of the nitrate grains. The larger the annexed drawing, which formsv part of this application for Letters Patent, there is plotted a curve showing the ratio of grain size to DNT freezing points between 8 and 50 mesh and 65 and 25 C. The thickness of the curve indicates the amount of variation in the ratio of grain size and freezing point which may be practiced without materially sacrificing the benefits obtained by strictly observing the ideal ratios. -Thus, it will be noted that the ratio of DNT freezing point and nitrate grain size given for Formula A by way of example may be more or less departed from, especially by using DNT of a higher freezing point, since the nitrate grains in Formula A are large enough to prevent density of pack in the product. It may, however, be stated that with nitrate grains of the size prescribed for Formula A, the freezing point of. the DNT should not be lower than 40 C. It is important that the DNT be in the frozen state in the product, and the smaller the grains the less solidly frozen must be the DNT. Otherwise the product packs densely and becomes relatively insensitive to the action of ordinary fuse caps or electric exploders.
\Vhen substantially the ratio prescribed is followed a satisfactory low grade explosive compound is produced which is slightly higher in percentage of strength than ordinary black blasting powder, which will detonate consistently with No. 6 fuse caps or electric exploders, and which possesses resistance to friction, fire and impact superior to any other comparable explosive of which I am aware.
To provide a more quickly burning and stronger explosive, having otherwise all the advantages of the physical property of Formula A, I replace some of the nitrates of the formula with other ingredients, including a. chlorate, as follows:
Formula B Per cent Dinitrotoluene 10 Sodium nitrate 73 Sodium chlorate 15 Lime 5 pulp provides carbon and serves to absorb and retain any excess oil.
A still stronger explosive is provided by further increasing the proportion of chlorate, as follows:
Formula 6' Per cent Dinitrotoluene 11 Sodium nitrate 56. 5 Sodium chlorate 30 Lime .5 Wood pulp 2 In Formula C I prefer to use smaller sized nitrate grains e. g.. such as sieve between 10 and 20 mesh. To illustrate the latitude permissible in the ratio of DNT freezing point and nitrate grain size, it may be stated that with nitrate grains so slightly reduced in size compared with those of Formula A. the DXT may be of the same freezing point as that prescribed for Formula A, since in Formula C the nitrate grains are still large enough to prevent density of pack in tlie product.
A still stronger product is given by the following formulae:
Fm'mula D Percent Dmitrotoluene 10 Sodium nitrate 41 Sodium chlorate 39.5 Lime .5 Wood pulp -Q. 8 Mononitrotoluene 1 v Formula)? Percent Dinitrotoluene 10 Sodium nitrate 44 Sodium chlorate 39. Lime .5 Bagasse. flour 5 Mononitrotoluene 1 These two formulae produce products substantially equal in strength, Formula E being desirable where it is necessary to consider oxygen balance in the product and a lower carbon contentis required. Bagasse flour has almost twice the absorbent qualities of wood pulp. so that a smaller quantity may be used.
In Formulae D and E the nitrate grains are sized at not larger than 20 mesh. Such reduction in grain size necessitates usin DNT of a lower freezing point, to prevent ensity of pack, and to this end a small proportion of mononitrotoluene is added to the DNT. The freezing point of the mixture of the two toluenes in Formulae D and E should be not higher than 37 C.
In each formula the moisture content is less than 1%.
It is to be understood that the five formula set out hereinabove are 'ven merely by way of example of several em iments of the 1nvention. It will be understood of course that an indefinite number of other formulas are contemplated by the invention, when explosives of varying strengths are desired, all ex emplifying the characteristic ratio of toluene freezing pointand nitrate grain size; Furthermore. slight departures from the proportions of ingredients. temperatures, and grain sizes specifically set out in the specification and appended claims are considered within the spirit of the invention and within the scope of the claims.
I claim :7
1. An explosive including DNT and'sodium nitrate in which the DNT has a freez- 5 ing point not lower than 40 6., and the grains of nitrate are sized between Sand 18 mesh. and in which the DNT is carried as a coating on the nitrate grains.
2. An explosive as claimed in claim 1,
20 which contains substantially 10 parts of DNT and 90 parts of sodium nitrate.
S.- An explosive as claimed in claim 1 which contains substantially 10 parts of BN1, 7 3 parts of sodium nitrate and 15 parts of sodium chlorate.
4. An explosive as claimed in claim 1 which contains substantially 10 parts of DNT, 41 parts of sodium nitrate and 39.5 parts of sodium chlorate.
5. An explosive including DNT and sodium nitrate in which the freezing point of the DNT and the grain size of the sodium nitrate are related as follows: for nitrate grain sizes above 50 mesh to approximately 14 mesh the freezing point of the DNT varies directly with the grain size between substantially 25 C. and substantially 41 C., and for nitrate grain sizes above 14 mesh to approximately 8 mesh the freezing point of the DNT varies directly with the grain size between substantially 41 C. and substantially 65 C.
6. The method of compounding an explosive containing DNT and sodium nitrate in- 45 cluding the step of admixing DNT and sodium nitrate having the following relation: for nitrate grain sizes above mesh to approximately 14' mesh the freezing point of the DST varies directly with the grain size 59 between substantially 25 C. and substantially 41 C. and for nitrate grain sizes above 14 mesh to approximately 8 mesh the freez= ing point of the DNT varies directly with the grain size between substantially 41 C. and substantially 65C.
In testimony whereof I aflix my signature.
GLENN ALBERT PBITCHETT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US589704A US1882190A (en) | 1932-01-29 | 1932-01-29 | Explosive |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US589704A US1882190A (en) | 1932-01-29 | 1932-01-29 | Explosive |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1882190A true US1882190A (en) | 1932-10-11 |
Family
ID=24359129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US589704A Expired - Lifetime US1882190A (en) | 1932-01-29 | 1932-01-29 | Explosive |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1882190A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6345577B1 (en) | 2000-09-27 | 2002-02-12 | The United States Of America As Represented By The Secretary Of The Navy | Energetic deterrent coating for gun propellant |
-
1932
- 1932-01-29 US US589704A patent/US1882190A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6345577B1 (en) | 2000-09-27 | 2002-02-12 | The United States Of America As Represented By The Secretary Of The Navy | Energetic deterrent coating for gun propellant |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2220891A (en) | Ammonium nitrate explosive composition | |
| US3279965A (en) | Ammonium nitrate explosive compositions | |
| US2124201A (en) | Explosive composition and process of production | |
| US3247033A (en) | Hexamethylenetetramine-ammonium nitrate explosive compositions and methods of making the same | |
| US1882190A (en) | Explosive | |
| US3994756A (en) | Castable composite explosive compositions containing a mixture of trinitrobenzene and trinitroxylene | |
| NO128576B (en) | ||
| US3210160A (en) | Apparatus for forming an explosive component from a melt | |
| US2647047A (en) | Explosive composition | |
| US2839374A (en) | Explosive compositions | |
| US2126401A (en) | Explosive | |
| US3044912A (en) | Ammonium nitrate-cyanide explosive | |
| US1833573A (en) | Black powder and method of manufacturing the same | |
| US2235060A (en) | Manufacture of explosive compositions or blasting charges | |
| US2481795A (en) | Explosives suitable for safety blasting explosives | |
| US4431468A (en) | TL-170 Blasting agent | |
| US751751A (en) | Explosive and process of making sarse | |
| US2344840A (en) | Explosive composition and method of producing same | |
| US2324363A (en) | Ammonium nitrate explosive | |
| US3303072A (en) | Low density, nitrate-based explosive compositions | |
| US2314809A (en) | Explosive composition | |
| US1658816A (en) | Casl d | |
| US2999014A (en) | Explosive composition | |
| US1357764A (en) | Ammonium-perchlorate explosives | |
| US1334303A (en) | Explosive mixture |