US2560439A - Liquid explosive consisting of a nitroparaffin and n-dodecane - Google Patents
Liquid explosive consisting of a nitroparaffin and n-dodecane Download PDFInfo
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- US2560439A US2560439A US728712A US72871247A US2560439A US 2560439 A US2560439 A US 2560439A US 728712 A US728712 A US 728712A US 72871247 A US72871247 A US 72871247A US 2560439 A US2560439 A US 2560439A
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- United States
- Prior art keywords
- explosive
- tetranitromethane
- dodecane
- mixture
- nitroparaffin
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- 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.)
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
- C06B25/36—Compositions containing a nitrated organic compound the compound being a nitroparaffin
Definitions
- This invention relates to an explosive that is characterized by its great resistance to detona- I tion by mechanical shock and by its sensitivity to detonation when subjected to explosive shock.
- More particularly it relates to a powerful. explosive that is especially well adapted for military use and that is relatively safe to handle.
- a further object is to provide an explosive that is very sensitive to explosive shock and that may be detonated readily by a blasting cap or like detonator.
- Another object is to provide a powerful explosive that is well suited for military purposes and that may be handled and stored with a maximum of safety.
- An additional object is to provide an explosive with the characteristics indicated that is relatively simple and inexpensive to make.
- An explosive in accord with this invention and one that meets its objects may be made by mixing tetranitromethane C(NO2)4 or hexanitroethane C2(N'O2)s and one or more of those parafiin hydrocarbons with the formula CnH2n+2 preferably in stoichiometric proportions.
- I employ n-octane or n-dodecane from this series.
- the resistance to mechanical impact of an explosive prepared in accord-With this invention is illustrated by the following data.
- a mixture of .161 cc. consisting of equal volumes of tetranitromethane and toluene was exploded with a threshold mechanical impact energy of .57 foot pound when placed in a closed circular chamber one-half inch in diameter and exposed to the impact across one end.
- an explosive composed of equal volumes of tetranitromethane and n-octane required a threshold impact energy in excess of 52 foot pounds, or approximately times as much.
- the explosive power and the sensitivity to explosive impact of a reference mixture of toluene-tetranitromethane compared with mixtures embodying the present invention illustrates substantial similarity between them.
- the results of the data are given below in terms of grams of sand pulverized by explosion to finer than 50 mesh when .066 cc. of the various explosive mixtures are detonated by blasting cap charges of various weights in fractions of a gram. This information is summarized in the table below in which the column at the extreme left indicates the weight in fractions of a gram of each standard explosive cap charge used in the various tests.
- the column next to it indicates the number of grams of sand pulverized to 50 mesh fineness as a result of the explosion by these various charges of substantially stoichiometric mixtures of .066 cc. of tetranitromethane and toluene comprising 23 percent by volume of toluene and 77 per cent by volume of tetranitrm methane.
- Preferred forms of explosive embodying the present invention are either approximately stoichiometric mixtures of tetranitromethane and n-octane (M. P.,-56.90; B. R, 125.6 C.), or tetranitromethane and n-dodecane (M. P.,97; B. P., 216.2 0.).
- one or more parafiin hydrocarbons of the series CnH2n+2 may be used in an explosive, as for instance tetranitromethane and both normalootane and normal dodecane, to make up approximately' a stoichiometric mixture.
- a stoichiometr'ic mixture is one" 4 that results in a reaction whose end products are water, carbon dioxide and free nitrogen.
- the explosive described above is very powerful, highly resistant to mechanical shock, sensitive to explosive shock and is best suited for use as a high explosive for military and related uses.
- An explosive liquid mixture detonatable by means of ablasting cap consisting of between 13 and 10 percentby Weight of n-dodecane and between 87 and 90 percent by weight of .a compound selected from the group consisting of tetranitromethane and hexar'iitroethane, the mixture being sensitive to explosive shock, resistant to mechanical shock, and adapted for use as a high explosive for military purposes.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented July 10, 1951 LIQUID EXPLOSIVE CONSISTING OF A NITROPARAFFIN AND N-DODECANE John A. Hannum, Detroit, Mich., assignor, by
mesne assignments, to Borg-Warner Corporation, Chicago, 111., a corporation of Illinois No Drawing. Application February 14, 1947, Serial No. 728,712
1 Claim.
This invention relates to an explosive that is characterized by its great resistance to detona- I tion by mechanical shock and by its sensitivity to detonation when subjected to explosive shock.
More particularly it relates to a powerful. explosive that is especially well adapted for military use and that is relatively safe to handle.
Perhaps the most powerful and brisant chemical explosive now known is a stoichiometric mixture of toluene, CeHsCI-Ia,.and tetram'tromethane, C(NOz) abut the practical value of such a mixture is limited by the extreme caution with which it must be handled and by the sometimes unpredictable way in which it explodes prematurely because it is extremely sensitive to mechanical shock and any slight jar will cause it to detonate.
It is the general object of the present invention to provide an explosive of approximately the same power as a toluene-tetranitromethane mixture but one that is much safer to handle and that is highly resistant to detonation when subjected to mechanical impact. A further object is to provide an explosive that is very sensitive to explosive shock and that may be detonated readily by a blasting cap or like detonator. Another object is to provide a powerful explosive that is well suited for military purposes and that may be handled and stored with a maximum of safety. An additional object is to provide an explosive with the characteristics indicated that is relatively simple and inexpensive to make.
An explosive in accord with this invention and one that meets its objects may be made by mixing tetranitromethane C(NO2)4 or hexanitroethane C2(N'O2)s and one or more of those parafiin hydrocarbons with the formula CnH2n+2 preferably in stoichiometric proportions.
The range in percentage of either tetranitromethane of hexanitroethane required to make up an approximately stoichiometric mixture with a hydrocarbon of the above formula is narrow. For example when methane, the first member of the series, is used 89.09 per cent by weight of the whole should be tetranitromethane to make a stoichiometric mixture. n the other hand with the nth or highest possible member of the series, calculation shows that 87.5 per cent by weight of tetranitromethane is required in a stoichiometriq mixture. For stoichiometric mixtures all of the intermediate members of the series require percentages of tetranitromethane that lie between the two values just given. In each case the balance of the explosive is made up of hydrocarbons with the formula Chi-lawn.
Preferably I employ n-octane or n-dodecane from this series.
As a result of the data given above a satisfactory and approximately stoichiometric-mixture of tetranitromethane and one or more parafiin hydrocarbons with the formula CnHzn+z will lie within the following range:
Per cent by weight CnH2n+2 13-10 Tetranitromethane 87-90 I have found that somewhat greater latitude in percentages will produce an explosive with the tabulation above. sider mixtures falling Within the following range to lie within the scope of the present invention:
Per cent by weight C1LH21L+2 40-10 Tetranitromethane -90 When hexanitroethane is used instead of tetranitromethane the percentage ranges given above for the latter apply also to the former. The amount of either required for a stoichiometric mixture is substantially the same.
The resistance to mechanical impact of an explosive prepared in accord-With this invention is illustrated by the following data. A mixture of .161 cc. consisting of equal volumes of tetranitromethane and toluene was exploded with a threshold mechanical impact energy of .57 foot pound when placed in a closed circular chamber one-half inch in diameter and exposed to the impact across one end. Under the same conditions an explosive composed of equal volumes of tetranitromethane and n-octane required a threshold impact energy in excess of 52 foot pounds, or approximately times as much.
The explosive power and the sensitivity to explosive impact of a reference mixture of toluene-tetranitromethane compared with mixtures embodying the present invention illustrates substantial similarity between them. The results of the data are given below in terms of grams of sand pulverized by explosion to finer than 50 mesh when .066 cc. of the various explosive mixtures are detonated by blasting cap charges of various weights in fractions of a gram. This information is summarized in the table below in which the column at the extreme left indicates the weight in fractions of a gram of each standard explosive cap charge used in the various tests. The column next to it indicates the number of grams of sand pulverized to 50 mesh fineness as a result of the explosion by these various charges of substantially stoichiometric mixtures of .066 cc. of tetranitromethane and toluene comprising 23 percent by volume of toluene and 77 per cent by volume of tetranitrm methane.
The three columns at the right labeled A, B-
and C express the grams of sand pulverized to the same fineness by the explosion of .066 cc'. of a n-octane-tetranitromethane or n-dodecaiietetranitromethane mixture in the volumetric proportions indicated at the top of each column. The same amount of sand of the' same initial mesh was used in each of the test explosions and all the explosions were made under the sameconditions. While there is some disparity in the figures it will be evident from the similar amounts of sand pulverized that the paraffin hydrocarbon-tetranitromethane mixtures possess explosive properties very similar to those of the very powerful tetranitromethane toluene mixture when the two are subjected to identical explosive shocks.
Blasting Cap .23 Toluene, Charge, in Grams .77 'INM 3 nOctane, .214 n-Do- 21100133 805118 i .7 'lNM 7B TNM .s TNM s. 34 '7. 37 a. 74 9. 92 8.39 9.88 4. 3s 1: 36 9. 11. 9s 3. 47 10. 94 10. 25 11. 90 9.08 9. 52 9.- 58 8.79 t. 14 10. 84 7. 12 9.82 4. 45 9. 05 s. 24 s. 79 6. 43
Preferred forms of explosive embodying the present invention are either approximately stoichiometric mixtures of tetranitromethane and n-octane (M. P.,-56.90; B. R, 125.6 C.), or tetranitromethane and n-dodecane (M. P.,97; B. P., 216.2 0.). It will be evident thatone or more parafiin hydrocarbons of the series CnH2n+2 may be used in an explosive, as for instance tetranitromethane and both normalootane and normal dodecane, to make up approximately' a stoichiometric mixture. In the present application a stoichiometr'ic mixture is one" 4 that results in a reaction whose end products are water, carbon dioxide and free nitrogen.
The explosive described above is very powerful, highly resistant to mechanical shock, sensitive to explosive shock and is best suited for use as a high explosive for military and related uses.
An explosive liquid mixture detonatable by means of ablasting cap consisting of between 13 and 10 percentby Weight of n-dodecane and between 87 and 90 percent by weight of .a compound selected from the group consisting of tetranitromethane and hexar'iitroethane, the mixture being sensitive to explosive shock, resistant to mechanical shock, and adapted for use as a high explosive for military purposes.
JOHN A. HANNUM.
REFERENCES CITED The following" references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,597,343 Chandler Aug. 24, 1926 1,820,983 Loomis' Sept. 1, 1931 2,185,157 Nygaard' et a1 Dec. 26, 1939 2,355,817 Morrow s1 Aug. 15, 1944 PATENTS Number Country Date 248,548 Germany 1 June 25, 1912 277,594 Germany 1 Aug. 20, 1914 281,906 Germany 11=--- Feb. 5, 1915 26,261 Great Britain 1 1907 24,839 Great Britain 1913 OTHER REFERENCES Lemken, Bulletin of the American Interplanetary Society, article No. 16, February, 1932, pages 8 through 10. I
Roth, Spreng'stoifeigenschaften, Z. Ges. Schies's Und Sprengstoffiv, volume 36, No. 1 (1941), ages- 4 through 6.
Grus'e et "a1.-,- Chemical Technology of Petraleum, published in 1942, by McGraw Hill Corn-J pany, New Yjork City (p.66).
ComptesfiIendu's, volume 218, May 1, 1944, pages 718-720.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US728712A US2560439A (en) | 1947-02-14 | 1947-02-14 | Liquid explosive consisting of a nitroparaffin and n-dodecane |
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US728712A US2560439A (en) | 1947-02-14 | 1947-02-14 | Liquid explosive consisting of a nitroparaffin and n-dodecane |
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US2560439A true US2560439A (en) | 1951-07-10 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1167238B (en) * | 1961-05-16 | 1964-04-02 | Aerojet General Co | Sensitized nitro paraffin explosives |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE277594C (en) * | ||||
DE248548C (en) * | ||||
GB190726261A (en) * | 1906-12-06 | 1908-02-06 | Paul Winand | Improvements in the Manufacture of Explosives. |
GB191324839A (en) * | 1913-10-31 | 1914-05-21 | Conrad Claessen | Improvements in or relating to Explosive Substances. |
US1597343A (en) * | 1924-11-21 | 1926-08-24 | Edward F Chandler | Fuel for internal-combustion engines |
US1820983A (en) * | 1926-02-15 | 1931-09-01 | Standard Oil Dev Co | Heavy oil fuel |
US2185157A (en) * | 1938-11-30 | 1939-12-26 | Socony Vacuum Oil Co Inc | Improved diesel fuel |
US2355817A (en) * | 1940-12-03 | 1944-08-15 | Hercules Powder Co Ltd | Explosive compositions |
-
1947
- 1947-02-14 US US728712A patent/US2560439A/en not_active Expired - Lifetime
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE277594C (en) * | ||||
DE248548C (en) * | ||||
GB190726261A (en) * | 1906-12-06 | 1908-02-06 | Paul Winand | Improvements in the Manufacture of Explosives. |
GB191324839A (en) * | 1913-10-31 | 1914-05-21 | Conrad Claessen | Improvements in or relating to Explosive Substances. |
US1597343A (en) * | 1924-11-21 | 1926-08-24 | Edward F Chandler | Fuel for internal-combustion engines |
US1820983A (en) * | 1926-02-15 | 1931-09-01 | Standard Oil Dev Co | Heavy oil fuel |
US2185157A (en) * | 1938-11-30 | 1939-12-26 | Socony Vacuum Oil Co Inc | Improved diesel fuel |
US2355817A (en) * | 1940-12-03 | 1944-08-15 | Hercules Powder Co Ltd | Explosive compositions |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1167238B (en) * | 1961-05-16 | 1964-04-02 | Aerojet General Co | Sensitized nitro paraffin explosives |
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