US1630578A - Nitroglucoside explosive - Google Patents
Nitroglucoside explosive Download PDFInfo
- Publication number
- US1630578A US1630578A US67208A US6720825A US1630578A US 1630578 A US1630578 A US 1630578A US 67208 A US67208 A US 67208A US 6720825 A US6720825 A US 6720825A US 1630578 A US1630578 A US 1630578A
- Authority
- US
- United States
- Prior art keywords
- nitrated
- glucoside
- glycol
- explosive
- ethylene glycol
- 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 30
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 114
- 229930182478 glucoside Natural products 0.000 description 37
- 150000008131 glucosides Chemical class 0.000 description 36
- 239000000203 mixture Substances 0.000 description 28
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 18
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 14
- 150000005846 sugar alcohols Polymers 0.000 description 13
- 239000002585 base Substances 0.000 description 11
- 235000000346 sugar Nutrition 0.000 description 10
- 150000002334 glycols Chemical class 0.000 description 9
- 235000011187 glycerol Nutrition 0.000 description 7
- 150000008163 sugars Chemical class 0.000 description 7
- -1 eta Natural products 0.000 description 6
- 238000006396 nitration reaction Methods 0.000 description 6
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 229960003711 glyceryl trinitrate Drugs 0.000 description 5
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- 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
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000008121 dextrose Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- UQXKXGWGFRWILX-UHFFFAOYSA-N ethylene glycol dinitrate Chemical compound O=N(=O)OCCON(=O)=O UQXKXGWGFRWILX-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 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 1
- SHZGCJCMOBCMKK-JFNONXLTSA-N L-rhamnopyranose Chemical compound C[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O SHZGCJCMOBCMKK-JFNONXLTSA-N 0.000 description 1
- PNNNRSAQSRJVSB-UHFFFAOYSA-N L-rhamnose Natural products CC(O)C(O)C(O)C(O)C=O PNNNRSAQSRJVSB-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001312 aldohexoses Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- 101150037671 hicd gene Proteins 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- 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
- C06B25/02—Compositions containing a nitrated organic compound the nitrated compound being starch or sugar
Definitions
- This invention relates to explosives, and particularly to high explosives such as dynamite, and comprises explosives of this type I which contain, as the main explosive constituent or explosive base, a nitrated glucoside of a glycol either alone or in conjunction with a nitrated polyhydric alcohol.
- glucoside is used herein in a generic sense to refer to the ethers formed by the condensation of hydroxy-hydrocarbons, and particularly glycols, with sugars (aldo-sugars) such as dextrose, mannosc, alactose, andother hexoses, rhamnose (a methyl-pentose), and various other sugars.
- glucosides are characterized by yieldmg upon hydrolysis a sugar and a glycol.
- chemical constitution of specific glucosides will be incheated by reference to both the sugar and the glycol components fromwhich the particular glucoside maybe assumed to have been derived.
- I designate the glucoside obtainable by the interaction of dextrose and ethylene glycol as the dextroseglucoside of ethylene glycol, the generally accepted structural formula of the glucoside be1ng:
- nitrated sugars have heretofore been used in the production of explosives for commercial purposes.
- the use of nitrated sugars possesses on the one hand the following advantages: first, it makes possible cheaper explosive bases due to the replacement in part of the nitratedpolyhydric alcohols by .the cheaper nitrated sugar; and, second, it permits the preparation of low-freezing explosive bases through the admixture of nitrated sugars with the nitrated polyhydric alcohols.
- the very great objection to the use of nitrated sugars in commercial explosives has been their instability.
- nitrated polymerized glycerine For the production of explosives of lowfreezing property, nitrated polymerized glycerine has been found advantageous. ,Such explosives are stable, but have the objection of relatively high cost, since nitrated polymerized glycerine is even more expensive than nitroglycerine or ethylene dinitratey' I have now discovered that nitrated g'hicd sides of the glycols may be used as explosives with essentially all the above-cited advantages associated with the use of.
- a stable explosive base with nitrated polyhydric alcohol is obtained; and, third, an explosive base with the nitrated polyhydrie alcohol can be obtained having a .degree of low-freezing property comparable to that imparted by nitrated polymerized glycerine, and at a decided saving.
- glucosides such as the dextrose, mannose, eta
- glucosides of tlie glycols such as ethylene glycol, propylene glycol, butylene glycol, trimethylene glycol,-etc.
- tlie glycols such as ethylene glycol, propylene glycol, butylene glycol, trimethylene glycol,-etc.
- Nitrated glucosides of the glycols' may be prepared from the corresponding glucosides by the general method described in the literature (Ber. 31, 68).
- such nitrated glucosides as for example the nitrated dextrose-glucoside of ethylene glycol
- a nitrated polyhydric alcohol as for example nitrated ethylene glycol
- proportions ranging from 80% to 20% nitrated dextroseglucoside of ethylene glycol to from 20% to 80% of nitrated ethylene glycol. While I have mentioned the above range of proportions of the nitrates as suitable, I Wish it to be understood that I do not limit myself to any specific proportions.
- nitrated glucosides of glycols and nitrated polyhydric alcohols I prefer to nitrate the corresponding mixtures of the glucosides of glycols with polyhydric alcohols, as for example, a mixture of dextrose-glucoside of ethylene glycol and ethylene glycol. This operation may be performed as follows:
- a glucoside such as the dextrose-glucoside of ethylene glycol
- a polyhydric alcohol such as ethylene glycol
- nitrated with 5 parts of a mixed acid of the approximate composition: Sulfuric acid 56%, nitric acid 44%.
- the temperature and time of nitration are approximately the same as for the glycol alone.
- the solution or mixture of ethylene dinitrate and nitrated glucoside of ethylene glycol is separated from the spent acid and stirred until neutral with a 6% solution of sodium carbonate, in water, at a temperature of aboutg7 0-100 F.
- alkali such as sodium hydroxide, as well as sodium bicarbonate
- the alkali solution is then drawn off and the nitrated mix ture is washed with pure water at a temperature of 7 O100 F.
- the mixture of ethylene dinitrate and nitrated glucoside is then pure, and ready for use.
- the mixed acid can be of various strengths, either anhydrous or containing up to several per cent (4 or 5%) of water. Different proportions of glycol, glucoside and mixed acid, different neutralizing agents of varying strength, and difi'erent temperatures of treatment are possible.
- desirable forms of dynamite may be made from explosive bases containing nitrated glucosides, as, for example, the nitrated dextrose-glucoside of ethylene glycol, by mixing such base with the usualingredients which make up nitroglycerine dynamites, such, for example, as sodium or potassium or ammonium nitrate, wood meal, etc. Moreover, it is possible by 'verted into a nitrate Ammo- Dyna- 3 223 nia mite. Igite dyna mite.
- the explosive base in the above examples may consist wholly of the nitrated glucoside of a glycol, such as, for instance, the nitrated dextrose-glucoside of butylene glycol, or the nitrated mannose-glucoside of ethylene glycol.
- the explosive base in the above dynamite formulas may be composed of a mixture of one of the nit-rated gluc-osides of glycol With one of the nitrated polyhydric alcohols, such as, ethylene, propylene, and butylene, dinitrates, trinitroglycerine, and nitrated polymerized glycerine.
- Suitable proportions of the two ingredients may be used such as equal parts of nitrated glucoside and nitrated alcohol, or instead of equal parts of the two constituents, the explosive base may consist, for example, of 30 parts nitrated glucoside to 7 0 parts nitrated polyhydric alcohol.
- nitrated glucosides which I prefer to use are derived from glucosides obtainable by condensing aldo-hexoses 'With glycols having from 2 to 9 carbon atoms, thus including such glycols as ethylene, butylene, and hexylene, glycols.
- nitrated glucoside-glycol mixtures are especially valuable, such mixtures gelatinizing more readily with nitrocotton than either nitrated sugar-glycol mixtures or nitrated polymerized glycerine.
- nitrated glucoside-glycol mixtures there may be mentioned the'mix tures of ethylene dinitrate with the dextrose-glucoside of ethylene glycol or of trim'ethylene glycol.
- nitrated glucosides and nitrated polyhydric alcohols mean, in general, glucosides and polyhydric alcohols which are completely nitrated, that is, in which each hydroxyl group has been con- (O-'-NO grou Partially nit-rated glucosides and alcoho s, however, also come within the scope'of my invention. e
- one or no I more of the hydroxyl groups may be converted to nitric esters, depending upon the amount of nitrating acid used.
- An' explosive mixture comprising a nitrated glucoside of a glycol.
- An explosive mixture comprising a nitrated glucoside of a glycol having from 2 to 9 carbon atoms.
- a dynamite containing a nitrated dexe trose-glucoside of a glycol 3.
- An explosive composition containing a nitrated dextroselucoside of a glycol and a nitrated polyhy ric alcohol.
- An explosive composition comprising a nitrated glucoside of a glycol and an alkylenedi'nitrate.
- a dynamite comprising a nitrated aldo-hexose-glucoside of a glycol.
- a dynamlte containing as the P 5 in completion is the penta-nitric ester of the dextrose glucoside of ethylene glycol; the probable structural formula of which is 14.
- An explosivecomposition comprising a nitrated hexose-glucoside of a glycol and an alkylene dinitrate.
- An explosive composition comprising a nitrated hexose-glucoside of ethylene glycol and nitrated ethylene glycol.
- An explosive composition comprising a. nitrated glucoside of ethylene glycol and nitroglycerine.
- An explosive mixture comprising a nitrated glucoside of ethylene glycol.
- I 19 An explosive composition comprising "a nitrated glucoside of ethylene glycol and 'nitrated ethylene glycol.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Saccharide Compounds (AREA)
Description
Patented May 31, 1927.
TES
mam
ROBERT C. MORAN, OF WOODBURY, NEW JERSEY, ASSIGNOR TO E. I. DU PONT DE NEMOURS & COMPANY, OF WILMINGTON, DELAWARE, A CORPORATION OF DELA- WARE,
No Drawing. Original application filed January 23, 1923, Serial No. 614,455. Divided and this application filed November 6, 1925. Serial No. 67,208.
This invention relates to explosives, and particularly to high explosives such as dynamite, and comprises explosives of this type I which contain, as the main explosive constituent or explosive base, a nitrated glucoside of a glycol either alone or in conjunction with a nitrated polyhydric alcohol.
The term glucoside is used herein in a generic sense to refer to the ethers formed by the condensation of hydroxy-hydrocarbons, and particularly glycols, with sugars (aldo-sugars) such as dextrose, mannosc, alactose, andother hexoses, rhamnose (a methyl-pentose), and various other sugars.
These glucosides are characterized by yieldmg upon hydrolysis a sugar and a glycol. In the following description the chemical constitution of specific glucosides will be incheated by reference to both the sugar and the glycol components fromwhich the particular glucoside maybe assumed to have been derived. Thus, I designate the glucoside obtainable by the interaction of dextrose and ethylene glycol as the dextroseglucoside of ethylene glycol, the generally accepted structural formula of the glucoside be1ng:
As set out in, co-periding application Serial No. 614,455, filed January 23, 1923, of which this application is a division, nitrated sugars have heretofore been used in the production of explosives for commercial purposes. The use of nitrated sugars possesses on the one hand the following advantages: first, it makes possible cheaper explosive bases due to the replacement in part of the nitratedpolyhydric alcohols by .the cheaper nitrated sugar; and, second, it permits the preparation of low-freezing explosive bases through the admixture of nitrated sugars with the nitrated polyhydric alcohols. On the other hand, the very great objection to the use of nitrated sugars in commercial explosives has been their instability.
For the production of explosives of lowfreezing property, nitrated polymerized glycerine has been found advantageous. ,Such explosives are stable, but have the objection of relatively high cost, since nitrated polymerized glycerine is even more expensive than nitroglycerine or ethylene dinitratey' I have now discovered that nitrated g'hicd sides of the glycols may be used as explosives with essentially all the above-cited advantages associated with the use of. both nitrated sugars and nitrated' polymerized glycerine and at the same time without the ond, a stable explosive base with nitrated polyhydric alcohol is obtained; and, third, an explosive base with the nitrated polyhydrie alcohol can be obtained having a .degree of low-freezing property comparable to that imparted by nitrated polymerized glycerine, and at a decided saving.
The glucosides, such as the dextrose, mannose, eta, glucosides of tlie glycols, such as ethylene glycol, propylene glycol, butylene glycol, trimethylene glycol,-etc., may be prepared by methods described in the literature (Ber. 26, 2411; 27, 2483; 28, 1145).
Nitrated glucosides of the glycols'may be prepared from the corresponding glucosides by the general method described in the literature (Ber. 31, 68). For use according to my invention such nitrated glucosides, as for example the nitrated dextrose-glucoside of ethylene glycol, may be mixed with a nitrated polyhydric alcohol, as for example nitrated ethylene glycol, in proportions ranging from 80% to 20% nitrated dextroseglucoside of ethylene glycol to from 20% to 80% of nitrated ethylene glycol. While I have mentioned the above range of proportions of the nitrates as suitable, I Wish it to be understood that I do not limit myself to any specific proportions.
Instead of mixing, as such, the nitrated glucosides of glycols and nitrated polyhydric alcohols, I prefer to nitrate the corresponding mixtures of the glucosides of glycols with polyhydric alcohols, as for example, a mixture of dextrose-glucoside of ethylene glycol and ethylene glycol. This operation may be performed as follows:
Thirty parts of a glucoside, such as the dextrose-glucoside of ethylene glycol, aredissolved in 7 0 parts of a polyhydric alcohol such as ethylene glycol, and one part of this mixture is nitrated with 5 parts of a mixed acid of the approximate composition: Sulfuric acid 56%, nitric acid 44%. The temperature and time of nitration are approximately the same as for the glycol alone. When the nitration is complete, the solution or mixture of ethylene dinitrate and nitrated glucoside of ethylene glycol is separated from the spent acid and stirred until neutral with a 6% solution of sodium carbonate, in water, at a temperature of aboutg7 0-100 F. Instead of sodium carbonate another alkali such as sodium hydroxide, as well as sodium bicarbonate, may be used. The alkali solution is then drawn off and the nitrated mix ture is washed with pure water at a temperature of 7 O100 F. The mixture of ethylene dinitrate and nitrated glucoside is then pure, and ready for use.
In regard to the above proportions, temperatures, etc., all these may be Varied just as they can in the manufacture of nitroglycerine. The mixed acid can be of various strengths, either anhydrous or containing up to several per cent (4 or 5%) of water. Different proportions of glycol, glucoside and mixed acid, different neutralizing agents of varying strength, and difi'erent temperatures of treatment are possible.
The same mixture proportions, nitration conditions, etc., hold for the other representative mixtures of a glucosideof a glycol and a polyhydric alcohol such as, for instance, a mixture of the/glucoside of ethylene glycol and glycerine.
According to my invention, desirable forms of dynamite may be made from explosive bases containing nitrated glucosides, as, for example, the nitrated dextrose-glucoside of ethylene glycol, by mixing such base with the usualingredients which make up nitroglycerine dynamites, such, for example, as sodium or potassium or ammonium nitrate, wood meal, etc. Moreover, it is possible by 'verted into a nitrate Ammo- Dyna- 3 223 nia mite. Igite dyna mite.
Per cent. Per cent. Per cent. Explosive base 40 33 10 Nitrocotton h k Absorbent 14 The explosive base in the above examples may consist wholly of the nitrated glucoside of a glycol, such as, for instance, the nitrated dextrose-glucoside of butylene glycol, or the nitrated mannose-glucoside of ethylene glycol. Or the explosive base in the above dynamite formulas may be composed of a mixture of one of the nit-rated gluc-osides of glycol With one of the nitrated polyhydric alcohols, such as, ethylene, propylene, and butylene, dinitrates, trinitroglycerine, and nitrated polymerized glycerine. Suitable proportions of the two ingredients may be used such as equal parts of nitrated glucoside and nitrated alcohol, or instead of equal parts of the two constituents, the explosive base may consist, for example, of 30 parts nitrated glucoside to 7 0 parts nitrated polyhydric alcohol.
The nitrated glucosides which I prefer to use are derived from glucosides obtainable by condensing aldo-hexoses 'With glycols having from 2 to 9 carbon atoms, thus including such glycols as ethylene, butylene, and hexylene, glycols.
For the production of gelatin dynamitcs the nitrated glucoside-glycol mixtures, are especially valuable, such mixtures gelatinizing more readily with nitrocotton than either nitrated sugar-glycol mixtures or nitrated polymerized glycerine. As examples of such nitrated glucoside-glycol mixtures there may be mentioned the'mix tures of ethylene dinitrate with the dextrose-glucoside of ethylene glycol or of trim'ethylene glycol. A By the expressions nitrated glucosides and nitrated polyhydric alcohols I mean, in general, glucosides and polyhydric alcohols which are completely nitrated, that is, in which each hydroxyl group has been con- (O-'-NO grou Partially nit-rated glucosides and alcoho s, however, also come within the scope'of my invention. e
In the nitration of the glucoside, one or no I more of the hydroxyl groups may be converted to nitric esters, depending upon the amount of nitrating acid used. The end product, when the nitration is carried to While the penta-nitric ester is given as a specific example, it is understood that the extent of the nitration may be varied, as
' has been pointed out.
While'I have described my new explosive compositions in detail, it will be understood that many changes may be made therein without departing from the spirit or scope of my invention.
' I claim:
1. An' explosive mixture comprising a nitrated glucoside of a glycol.
2. An explosive mixture comprising a nitrated glucoside of a glycol having from 2 to 9 carbon atoms.
3. A dynamite containing a nitrated dexe trose-glucoside of a glycol.
4. A dynamlte containing the nitrated dextrose-glucoside oi ethylene glycol.
5. An explosive composition containing a nitrated dextroselucoside of a glycol and a nitrated polyhy ric alcohol.
6. An ex losive composition containing the nitrate dextrose-glucoside of ethylene. glycol and a nitrated .polyhydric alcohol.
7. An explosive composition containing the nitrated dextrose-glucoside ofethylene glycol and ,nitrated ethylene glycol.
8. An explosive composition comprising a nitrated glucoside of a glycol and an alkylenedi'nitrate. P
9. A dynamite comprising a nitrated aldo-hexose-glucoside of a glycol.
10. A dynamlte containing as the P 5 in completion, is the penta-nitric ester of the dextrose glucoside of ethylene glycol; the probable structural formula of which is 14. An explosivecomposition comprising a nitrated hexose-glucoside of a glycol and an alkylene dinitrate. v
'15. An explosive composition comprising a nitrated hexose-glucoside of ethylene glycol and nitrated ethylene glycol.
16.-An ex losive-composition comprising a nitrated g ucoside of a glycol and nitroglycerine.
17. An explosive composition comprising a. nitrated glucoside of ethylene glycol and nitroglycerine.
18. An explosive mixture comprising a nitrated glucoside of ethylene glycol.
I 19. An explosive composition comprising "a nitrated glucoside of ethylene glycol and 'nitrated ethylene glycol.
In testimony whereof I aflix my signature.
ROBERT o; MORAN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67208A US1630578A (en) | 1923-01-23 | 1925-11-06 | Nitroglucoside explosive |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US614455A US1583895A (en) | 1923-01-23 | 1923-01-23 | Nitroglucoside explosive |
| US67208A US1630578A (en) | 1923-01-23 | 1925-11-06 | Nitroglucoside explosive |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1630578A true US1630578A (en) | 1927-05-31 |
Family
ID=26747606
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US67208A Expired - Lifetime US1630578A (en) | 1923-01-23 | 1925-11-06 | Nitroglucoside explosive |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1630578A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3203844A (en) * | 1963-06-26 | 1965-08-31 | Atlas Chem Ind | Explosive compositions containing sorbitan tetranitrate sensitizer |
-
1925
- 1925-11-06 US US67208A patent/US1630578A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3203844A (en) * | 1963-06-26 | 1965-08-31 | Atlas Chem Ind | Explosive compositions containing sorbitan tetranitrate sensitizer |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US1630578A (en) | Nitroglucoside explosive | |
| US1583895A (en) | Nitroglucoside explosive | |
| US1640712A (en) | Acceleration of gelatinization of cellulose nitrate | |
| US1691955A (en) | Explosive | |
| US1630577A (en) | Nitroglucoside explosive | |
| US2330112A (en) | Nitroethyl nitrate derivative | |
| US1962172A (en) | Process of nitrating quebrachitol | |
| US2389771A (en) | Explosive composition | |
| US1620714A (en) | Triazo-nitrate explosives and process of producing the same | |
| US2159973A (en) | Gelatinized high explosive composition and method of preparation | |
| US2340304A (en) | Blasting explosive | |
| US2194544A (en) | Gelatinized high explosive compositions | |
| US1883045A (en) | Explosive composition | |
| US1213369A (en) | Explosive and method of producing same. | |
| US1637726A (en) | bebgsiai | |
| US1686344A (en) | Diethylene glycol dinitrate and process of preparing same | |
| US1883044A (en) | Explosive composition | |
| US2716056A (en) | Blasting explosive and process of producing same | |
| US2683164A (en) | Preparation of 1, 2, 6-hexanetriol trinitrate | |
| US1307032A (en) | Jacob barab | |
| US1751437A (en) | Gelatinized explosive and process of manufacture | |
| US1301105A (en) | Explosive and process of producing the same. | |
| US1685771A (en) | Cyano nitrate explosive and process of producing the same | |
| US2012986A (en) | Process of producing a liquid explosive composition | |
| US2146026A (en) | Process of acceleration of gelatinization of cellulose nitric esters and liquid nitric esters and the product thereof |