US2548688A - Nitrocellulose-containing composition and process of preparing same - Google Patents

Nitrocellulose-containing composition and process of preparing same Download PDF

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US2548688A
US2548688A US7529A US752948A US2548688A US 2548688 A US2548688 A US 2548688A US 7529 A US7529 A US 7529A US 752948 A US752948 A US 752948A US 2548688 A US2548688 A US 2548688A
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nitrocellulose
water
weight
solution
preparation
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US7529A
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Taylor James
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Imperial Chemical Industries Ltd
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Imperial Chemical Industries Ltd
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B21/00Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
    • C06B21/0008Compounding the ingredient

Definitions

  • ammonium nitrate is present as an ingredient of the explosive, the presence of the water may also accelerate the tendency 'of the 'cornposition to-"set. It is also known: to employ' spirit wet nitrocellulose, which isiobtained “bydisplaeing the water from water wetnitrocellulo'se with somewhat dilutedialcohol; but the; use of. spirit Wet'nitrocellulose causes the liquid: nitric ester to dissolve the. nitrocellulose with the formation of a solution characterised at least when freshly made by excessive capacity for extension: andadhesiveness;properties which. in-.
  • the im'-' proved nitrocellulose preparation consists of nitrocellulose of the kind soluble in liquid explosive nitric esters,.in uncolloided condition and moist with a solution comprising at least 30% by weight-of a mixture of: ammoniumnitrate and urea-in binary eutectic proportion inan aqueous alcoholic solvent substantially richer'in alcohol thaniin water,. the amount of'water being not more than 20% on. weight of the nitrocellulose;
  • amixture ofxammonium nitrate and urea in: binary eutectic proportion includes mixtures in which the .proportionpf ammonium nitrate and urea is only: approximatelya binary eutectic one.
  • the :weight 10f the-said :solution may be: for
  • the binary eutectic composition preferably amounts to approximately 35 to
  • the binary eutectic composition is ammonium nitrate, 53% urea 47%; and this composition melts at 44.7 C. and requires the addition of about 10% waterjto bringit into the'form of a 'viscid solution at 'room temperature.
  • Nitrocellulose moistened with the resulting solution dissolves too slowly in explosive liquid nitric esters to be useful for the manufacture'of explosive compositions.
  • the manufacture may be carried out, for instance, by spraying spirit wet nitrocellulose with the substantially eutectic mixtures dissolved in a suitably limited amount of water, or by washing the spirit wet nitrocellulose ina centrifuge with a solution of the substantially eutectic mixture in i an alcohol-water mixture of say 60-70% alcoholic strength and centrifuging away a predetermined quantity of the liquor.
  • the spraying of the aqueous solution can be carried out by passing the said solution through the rose of a watering can.
  • the nitrocellulose equivalent to 32.5 parts wet weight, is uniformly spread in a pan of area 10 square feet thereby permitting uniform spraying of an appreciable area of the nitrocellulose.
  • the mass is turned over intermittently by hand during the spraying operation to eifect approximate uniformity of wetting throughout the mass.
  • nitrocellulose preparation thus formed, 2.? parts waxed woodmeal, 0.5 part woodmeal, 28 parts of an 80:20 mixture of nitroglycerinc and ethylene glycol dinitrate and 1.8 part of a liquid dinitrotoluene-trinitrotoluene mixture are mixed together in a Talley mixer for about 3 minutes by which time the nitrocellulose is dissolved to give a solution of somewhat gelatinous character. 42 parts ammonium nitrate, 19 parts sodium nitrate, 3-parts sulphur, 1 part starch and 0.5 parts chalk are worked into the mixture while running the mixer for about another 5 minutes.
  • the resulting non-tacky gelatine explosive composition is removed from the mixer, and is extruded and cartridged in known manner without difficulty. It is satisfactorily sensitive to a No. 6 commercial detonator. cartridge gap test, in which two diameter cartridges are arranged end to end separated by a gap, the maximum gap over which detonation of the receptor cartridge can be induced was 3 -to4 inches when the cartridges are freshly made In a double 4 and 3 to 4 inches after 3 months dry storage at 35 C.
  • Example 2 An improved preparation containing:
  • Example 2 is prepared as in Example 1, except that 6.5 parts of the aqueous solution of ammonium nitrate and urea is uniformly sprayed on to 20 parts (dry weight) of the uncolloided nitrocelluloses of an alcohol-water content of 38%, in which alcoholwater mixture the quantity of alcohol is 86%.
  • the maximum gap over which detonation of the receptor cartridge can be induced is 11 to 12 inches when the cartridges are freshly made and 8 to 9 inches after 1 months atmospheric temperature storage.
  • An improved nitrocellulose containing preparation for the manufacture of explosives comprising uncolloided liquid nitric ester-soluble nitrocellulose moistened with a solution comprising at least 30% by weight of a substantially binary eutectic mixture of ammonium nitrate and urea in an aqueous alcoholic solvent, the said solvent being substantially richer in alcohol than in'water and the amount of water present in the preparation being less than 20% by weight'of the nitrocellulose.
  • a process for the preparation of an improved nitrocellulose containing composition for the manufacture of explosives comprising moistening spirit wet uncolloided liquid nitric ester-soluble nitrocellulose with atleast 30 by Weight of a solution comprising a substantially binary eutectic mixture of ammonium nitrate and urea dissolved in a solution comprising water, the amount of water present in the resulting preparation being less than 20% by weight of the nitrocellulose.
  • a process for the preparation of :an improved nitrocellulose containing composition for the manufacture of explosives comprising moistening water wet uncolloided liquid nitric ester-soluble nitrocellulose with at least 30% by weight of a solution comprising a substantially binary eutectic mixture of ammonium nitrate and urea dissolved in a solution comprising water and alcohol, the amount of water present in the resulting preparation being less than 20% by weight of the nitrocellulose, and the preparation being substantially richer in alcohol than in water.

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  • Organic Chemistry (AREA)
  • Medicinal Preparation (AREA)

Description

Patented Apr. 10, 1951 UNITED STATES NITROCELLULOSEaCONTAINING COMPOSL- TION AND PROCESS OF PREPARING SAME James Taylor, Saltcoats, Scotland, assignor to Imperial Chemical Industries Limited, a corporation of- Great Britain No Drawing. Application February 10, 1948, Serial N 0. 7,529. In Great Britain April 18, 1947 While nitrocellulose in a wat'er'wet form containing aproportion of the water resulting from the nature of the manufacture of nitrocellulose is often used in limited amounts in the manufacture of'blasting explosives for the purpose of thickening-the liquid nitric ester, the presence of the water, which'amounts to about 25 to 33 per cent of the weight of the water wet nitrocellulose, has a desensitising effect on the resulting explosive, and may' render it necessary to work the mixture for a longer time than usual in order to bring about the solution of the nitrocellulose in the liquid explosive nitric ester. If ammonium nitrate is present as an ingredient of the explosive, the presence of the water may also accelerate the tendency 'of the 'cornposition to-"set. It is also known: to employ' spirit wet nitrocellulose, which isiobtained "bydisplaeing the water from water wetnitrocellulo'se with somewhat dilutedialcohol; but the; use of. spirit Wet'nitrocellulose causes the liquid: nitric ester to dissolve the. nitrocellulose with the formation of a solution characterised at least when freshly made by excessive capacity for extension: andadhesiveness;properties which. in-.
troduce diificulties in: the conduct" of thej mixing operation and in the subsequent extrusion: op eration I According tothe. present invention; the im'-' proved nitrocellulose preparation consists of nitrocellulose of the kind soluble in liquid explosive nitric esters,.in uncolloided condition and moist with a solution comprising at least 30% by weight-of a mixture of: ammoniumnitrate and urea-in binary eutectic proportion inan aqueous alcoholic solvent substantially richer'in alcohol thaniin water,. the amount of'water being not more than 20% on. weight of the nitrocellulose;
It is to be understood that the phrase amixture ofxammonium nitrate and urea in: binary eutectic proportion includes mixtures in which the .proportionpf ammonium nitrate and urea is only: approximatelya binary eutectic one.
' The :weight 10f the-said :solution may be: for
. difliculties.
2 instance from about 0.9 to 1.3 times the weight of the uncolloided nitrocellulose, and of this solution the mixture of ammonium nitrate andurea of .substantiallythe binary eutectic composition preferably amounts to approximately 35 to The binary eutectic composition is ammonium nitrate, 53% urea 47%; and this composition melts at 44.7 C. and requires the addition of about 10% waterjto bringit into the'form of a 'viscid solution at 'room temperature. Nitrocellulose moistened with the resulting solution dissolves too slowly in explosive liquid nitric esters to be useful for the manufacture'of explosive compositions. further dilutedwith industrial spirit'without precipitating eitherof the solids; and uncolloided nitrocellulose moist with a damping solutionas herein beforespecifiedidissolves rapidly in :liquid explosive nitric esters without forming tacky solutions su'chas would. lead to mixing and extrusion The desensiti'sing and settling difiiculties experienced When water is'used as damping medium for nitrocellulose are also'minimised. It is possible-to make the improved: nitrocellulose preparation' directly from water wet nitrocellulose by treating the latter with strongly alcoholic aqueous solution of ammonium nitrate and urea under such conditions that the displacement of the water is'nearly complete. This usually necessitates the introduction as the displacing liquor of an alcoholic solution of ammonium nitrate and urea of suchlow water content asonly to be free from crystallisation at temperatures substantially above atmospheric' It is however, more convenient to make the product from the water Wet nitrocellulose indirectly, that is to'say from spiritwet' nitrocellulose, since it is then unnecessary toachieve a high degree of displacement of the spirit to attain in the product the required low water content. It is even possible to attain'the required. composition by treatment of the spirit wet nitrocellulose with a strong aqueous solution. ofthe ammonium nitrate and urea, which need in this case contain no alcohol, without rejection of any of the liquors at all, that is to say by a process wherein the whole of v the spirit of the spirit wet nitrocellulose is retained and mixes with the incoming liquor. Whether the final composition is attained by dilution alone or bya combination of dilution and displacement of the spirit in the spirit wet nitrocellulose it is easy to arrange that the liquor that is added will contain sufiicient Water to maintain it free from crystallisation at ordinary temperature while also containing suflicient ammonium nitrate and urea The solution" can however, be
3 to allow its dilution by the retained spirit of the spirit wet nitrocellulose.
The manufacture may be carried out, for instance, by spraying spirit wet nitrocellulose with the substantially eutectic mixtures dissolved in a suitably limited amount of water, or by washing the spirit wet nitrocellulose ina centrifuge with a solution of the substantially eutectic mixture in i an alcohol-water mixture of say 60-70% alcoholic strength and centrifuging away a predetermined quantity of the liquor.
The following examples illustrate a method of producing improved nitrocellulose preparations in accordance with the invention and their application to the production of explosives. The percentages and parts are by weight.
Example .1
A nitrocellulose preparation containing:
Per cent Uncolloided nitrocellulose of 12.1% nitrogen content 48 Alcohol 25 Water 6.5 Ammonium nitrate 10.7 Urea 9.8
is produced in the following manner.
An aqueous solution containing:
Parts Ammonium nitrate l2 Urea i 10.5 Water 2.5
is first formed by adding the ammonium nitrate and urea to water in said proportions and'efiecting dissolution in a hot water bath at about 90 C. 9.5 parts of this aqueous solution is sprayed uniformly on to parts (dry weight) of uncolloided nitrocellulose of 12.1% nitrogen content, previously dehydrated in a centrifugal to an alcohol-water content of 38%, in which alcoholwater mixture the quantity of alcohol is 86%.
The spraying of the aqueous solution can be carried out by passing the said solution through the rose of a watering can. The nitrocellulose, equivalent to 32.5 parts wet weight, is uniformly spread in a pan of area 10 square feet thereby permitting uniform spraying of an appreciable area of the nitrocellulose. The mass is turned over intermittently by hand during the spraying operation to eifect approximate uniformity of wetting throughout the mass.
parts of the nitrocellulose preparation thus formed, 2.? parts waxed woodmeal, 0.5 part woodmeal, 28 parts of an 80:20 mixture of nitroglycerinc and ethylene glycol dinitrate and 1.8 part of a liquid dinitrotoluene-trinitrotoluene mixture are mixed together in a Talley mixer for about 3 minutes by which time the nitrocellulose is dissolved to give a solution of somewhat gelatinous character. 42 parts ammonium nitrate, 19 parts sodium nitrate, 3-parts sulphur, 1 part starch and 0.5 parts chalk are worked into the mixture while running the mixer for about another 5 minutes. The resulting non-tacky gelatine explosive composition is removed from the mixer, and is extruded and cartridged in known manner without difficulty. It is satisfactorily sensitive to a No. 6 commercial detonator. cartridge gap test, in which two diameter cartridges are arranged end to end separated by a gap, the maximum gap over which detonation of the receptor cartridge can be induced was 3 -to4 inches when the cartridges are freshly made In a double 4 and 3 to 4 inches after 3 months dry storage at 35 C.
Example 2 An improved preparation containing:
is prepared as in Example 1, except that 6.5 parts of the aqueous solution of ammonium nitrate and urea is uniformly sprayed on to 20 parts (dry weight) of the uncolloided nitrocelluloses of an alcohol-water content of 38%, in which alcoholwater mixture the quantity of alcohol is 86%.
6 parts of the above nitrocellulose preparation and 61 parts of an 80.20 mixture of nitroglycerine and ethylene glycol dinitrate are mixed together in a Talley mixer for about 5 to 10 minutes, thus forming a fairly stiff jelly. Into this jelly are worked in the course of another 5 minutes 6.5 parts woodmeal, 26.2 parts sodium nitrate and 0.3 part chalk. The resulting non-tacky explosive composition is removed, extruded and cartridged without difficulty, in known manner. It is satisfactorily sensitive to a No. 6 commercial detonator. In a double cartridge gap test, in which two '7 diameter cartridges are arranged end to end separated by a gap, the maximum gap over which detonation of the receptor cartridge can be induced is 11 to 12 inches when the cartridges are freshly made and 8 to 9 inches after 1 months atmospheric temperature storage.
An explosive not in accordance with the in-' vention similar in composition to' that of Example 2, except that 5.5 parts water wet nitrocellulose (containing 3.5 parts dry nitrocellulose) are used instead of 6 parts of the above nitrocellulose preparation and the amount of ammonium nitrate is increased by 0.5 parts, gives a gap test of only 3 to 4 inches when the cartridges are freshly made and 2 to 3 inches after 1 months atmospheric storage.
I claim:
1. An improved nitrocellulose containing preparation for the manufacture of explosives comprising uncolloided liquid nitric ester-soluble nitrocellulose moistened with a solution comprising at least 30% by weight of a substantially binary eutectic mixture of ammonium nitrate and urea in an aqueous alcoholic solvent, the said solvent being substantially richer in alcohol than in'water and the amount of water present in the preparation being less than 20% by weight'of the nitrocellulose.
2. An improved nitrocellulose containing preparation as claimed in claim 1 wherein the weight of the said solution is from 0.9 to 1.3 times the weight of theuncolloided nitrocellulose.
- 3. An improved nitrocellulose containing preparation as claimed in claim 1 wherein the said solution contains up to 50% of the substantially binary eutectic mixture of ammonium nitrate and urea.
4. A process for the preparation of an improved nitrocellulose containing composition for the manufacture of explosives comprising moistening spirit wet uncolloided liquid nitric ester-soluble nitrocellulose with atleast 30 by Weight of a solution comprising a substantially binary eutectic mixture of ammonium nitrate and urea dissolved in a solution comprising water, the amount of water present in the resulting preparation being less than 20% by weight of the nitrocellulose.
5. A process for the preparation of :an improved nitrocellulose containing composition for the manufacture of explosives comprising moistening water wet uncolloided liquid nitric ester-soluble nitrocellulose with at least 30% by weight of a solution comprising a substantially binary eutectic mixture of ammonium nitrate and urea dissolved in a solution comprising water and alcohol, the amount of water present in the resulting preparation being less than 20% by weight of the nitrocellulose, and the preparation being substantially richer in alcohol than in water.
JAMIES TAYLOR.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,510,348 Snelling Sept. 30. 1924 1,819,458 Dehn Aug. 18, 1931 1,966,806 Spurlin Aug. 17, 1934 2,063,572 Woodbury et al Dec. 8, 1936 FOREIGN PATENTS Number Country Date 552,645 Great Britain Apr. 19, 1943 43,911 Switzerland June 29, 1908

Claims (2)

1. AN IMPROVED NITROCELLULOSE CONTAINING PREPARATION FOR THE MANUFACTURE OF EXPLOSIVES COMPRISING UNCOLLOIDED LIQUID NITRIC ESTER-SOLUBLE NITROCELLULOSE MOISTENED WITH A SOLUTION COMPRISING AT LEAST 30% BY WEIGHT OF A SUBSTANTIALLY BINARY EUTECTIC MIXTURE OF AMMONIUM NITRATE AND UREA IN AN AQUEOUS ALCOHOLIC SOLVENT, THE SAID SOLVENT BEING SUBSTANTIALLY RICHER IN ALCOHOL THAN IN WATER AND THE AMOUNT OF WATER PRESENT IN THE PREPARATION BEING LESS THAN 20% BY WEIGHT OF THE NITROCELLULOSE.
4. A PROCESS FOR THE PREPARATION OF AN IMPROVED NITROCELLULOSE CONTAINING COMPOSITION FOR THE MANUFACTURE OF EXPLOSIVES COMPRISING MOISTENING SPIRIT WET UNCOLLOIDED LIQUID NITRIC ESTER-SOLUBLE NITROCELLULOSE WITH AT LEAST 30% BY WEIGHT OF A SOLUTION COMPRISING A SUBSTANTIALLY BINARY EUTECTIC MIXTURE OF AMMONIUM NITRATE AND UREA DISSOLVED IN A SOLUTION COMPRISING WATER, THE AMOUNT OF WATER PRESENT IN THE RESULTING PREPARATION BEING LESS THAN 20% BY WEIGHT OF THE NITROCELLULOSE.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2817581A (en) * 1955-05-18 1957-12-24 Trojan Powder Co Cast ammonium nitrate and urea explosive
WO2003055829A1 (en) * 2002-01-03 2003-07-10 Nxco International Limited Explosive for rock breaking
WO2016128148A1 (en) * 2015-02-15 2016-08-18 Avocet Solutions Inc. Enhanced fuels, methods of producing enhanced fuels, and additives for mitigating corrision

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH43911A (en) * 1908-06-29 1909-06-16 Friedrich Lehmann Julius Process for the manufacture of ammonium nitrate explosive cartridges
US1510348A (en) * 1920-12-14 1924-09-30 Trojan Powder Co Explosive and its manufacture
US1819458A (en) * 1929-10-28 1931-08-18 William M Dehn Propellent explosive
US1966806A (en) * 1929-09-17 1934-07-17 Hercules Powder Co Ltd Method of producing smokeless powder
US2063572A (en) * 1934-08-08 1936-12-08 Du Pont Process of preparing explosive charges
GB552645A (en) * 1941-09-15 1943-04-19 John Whetstone Improvements in or relating to granular or powder explosives and their manufacture

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH43911A (en) * 1908-06-29 1909-06-16 Friedrich Lehmann Julius Process for the manufacture of ammonium nitrate explosive cartridges
US1510348A (en) * 1920-12-14 1924-09-30 Trojan Powder Co Explosive and its manufacture
US1966806A (en) * 1929-09-17 1934-07-17 Hercules Powder Co Ltd Method of producing smokeless powder
US1819458A (en) * 1929-10-28 1931-08-18 William M Dehn Propellent explosive
US2063572A (en) * 1934-08-08 1936-12-08 Du Pont Process of preparing explosive charges
GB552645A (en) * 1941-09-15 1943-04-19 John Whetstone Improvements in or relating to granular or powder explosives and their manufacture

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2817581A (en) * 1955-05-18 1957-12-24 Trojan Powder Co Cast ammonium nitrate and urea explosive
WO2003055829A1 (en) * 2002-01-03 2003-07-10 Nxco International Limited Explosive for rock breaking
WO2016128148A1 (en) * 2015-02-15 2016-08-18 Avocet Solutions Inc. Enhanced fuels, methods of producing enhanced fuels, and additives for mitigating corrision
GB2535235B (en) * 2015-02-15 2018-05-16 Avocet Infinite Plc Enhanced fuels, methods of producing enhanced fuels, and additives for mitigating corrosion

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