USH272H - Poly(allyl azido nitrates) - Google Patents
Poly(allyl azido nitrates) Download PDFInfo
- Publication number
- USH272H USH272H US06/845,669 US84566986A USH272H US H272 H USH272 H US H272H US 84566986 A US84566986 A US 84566986A US H272 H USH272 H US H272H
- Authority
- US
- United States
- Prior art keywords
- poly
- allyl
- azide
- nitrate
- azido
- 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.)
- Abandoned
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C247/00—Compounds containing azido groups
- C07C247/02—Compounds containing azido groups with azido groups bound to acyclic carbon atoms of a carbon skeleton
- C07C247/04—Compounds containing azido groups with azido groups bound to acyclic carbon atoms of a carbon skeleton being saturated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F26/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F26/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
Definitions
- Vanderberg discloses linear poly (glycidyl azides) obtained by reacting a homo or copolymer of epichlorohydrin with a metal azide.
- Known polymeric azides such as the glycidyl azide polymers of the patent, are less energetic and more costly than the poly (vinyl azides) of the aforesaid patent application.
- the present invention relates to a novel class of poly (allyl azide) compositions and to a process for producing the same.
- novel poly (allyl azide) compositions of this invention are essentially linear allyl polymers having a molecular weight of at least about 300, wherein from about 1% to 100% of the repeating units are allyl azide monomer units of the formula ##STR1## and from about 0% to 99% of the repeating units are allyl nitrate monomer units of the formula ##STR2##
- the poly (allyl azide) compositions of this invention are energetic materials useful in gun, missile and rocket propellants and other purposes such as in detonation and igniter compositions for explosive charges.
- the allyl polymers of this invention contain the azide and nitrate groups attached to primary carbon atoms, viz. --CH 2 N 3 and --CH 2 ONO 2 respectively, whereas the poly (vinyl azide/nitrate) compounds of the aforesaid patent application contain the said groups attached to secondary carbon atoms, viz. --CHN 3 and --CHONO 2 respectively.
- the poly (allyl azide/nitrate) products of this invention are preferred, since the primary type of group is somewhat more chemically stable than the secondary type of group.
- the allyl azide polymers of the present invention can be prepared by reacting a poly(allyl nitrate) of molecular weight at least about 400 with a metal azide, preferably in the presence of a liquid solvent or diluent inert to the reaction.
- the chemical reaction involved therein can be represented essentially as follows: ##STR3##
- the reaction can be carried out at a temperature of from about 20° C. to 125° C. and prefereably from about 50° C. to 100° C.
- the reaction time, temperature, and amount of metal azide can be varied widely depending on the desired degree of replacement of the nitro groups in the poly (allyl nitrate). For example, the reaction time can vary from less than an hour to many hours and the amount of metal azide can vary from about 100% to about 200% of the stoichiometric amount required to react with the nitro groups of the poly (allyl nitrate).
- Liquid solvents or diluents which are suitable for use in the process of the present invention include dimethylformamide, dimethylsulfoxide, tetrahydrofuran, acetonitrile, hexamethylphosphoramide and water and 1-methyl-2 -pyrolidinone, acetone, and 2-methoxyethanol.
- the reaction is preferably carried out in a solvent in which at least one of the reactants (metal azide and polyallyl nitrate) is soluble.
- Alkali metal azides such as sodium, lithium and potassium azides, are preferably utilized for carrying out the present reaction, but any stable metal azide, particularly an alkaline earth metal azide, e.g. calcium azide, can be employed in a similar manner.
- the poly (allyl nitrate) employed in this example was prepared by nitration of poly(allyl alcohol) as described below. (General references to this preparation are given in Dutch Patent No. 66,784 (1950) per Chem. Abstracts 45,5452 (1951) and by Schulz et al. (Makromol. Chem. 67,192 (1963)).
- the product was dissolved in acetone and the solution was evaporated in dryness, yielding 0.8 g. (78%) of poly (allyl nitrate) product, a clear yellow, viscous semi-solid, which gave a positive match test.
- the IR spectrum of the material showed peaks for the nitrate group at 1620, 1280 and 860 cm -1 , and the absence of the hydroxyl peak at 3400 cm -1 which was present in the starting compound.
- Example 2 The procedure of Example 1 was repeated except that the reaction mixture was heated for 19 hours instead of 5 hours.
- the product weighed 0.4 g. and its infrared spectrum showed the strong azide peak and weak nitrate peaks. It analyzed 42.4% nitrogen, which corresponds to a ratio of 2 allyl nitrate monomer units to 9 allyl azide monomer units in the polymer (values of 2 and 9 for a and b respectively in the foregoing formula).
- the product gave an energetic match test.
- Poly(allyl alcohol) was prepared according to the method of Kargin et al., Ger. Offen. 1,907,612 (Chem. Abstracts 74,142661) by Cobalt 60 polymerization of allyl alcohol (30.1 g.) mixed with calcium chloride (32.5 g.) and water (48 ml.) using 9 ⁇ 10 4 rad/hr for 236 hours (21.2 megarads total).
- the resulting solution was processed by treatment with methanolic potassium hydroxide followed by thorough extraction of the precipitated Ca(OH) 2 with hot methanol. Evaporation to dryness yielded 22.0 g. (73% yield) of polyallyl alcohol.
- the poly (allyl alcohol) was nitrated by the procedure described in Example 1 and yielded a product which possessed an IR spectrum identical with that of the polyallyl nitrate material described in Example 1.
- the poly (allyl nitrate) thus obtained (1.6 g.) was reacted with sodium azide (1.6 g.) in dimethylformamide (40 ml.) at 75°-85° C. for 6 hours and the reaction mixture was worked up as described in Example 1.
- the product weighed 1.2 g. and was a viscous brown oil, which gave a positive match test and an IR curve showing strong azide absorption and residual nitrate groups.
- Poly (allyl alcohol) was prepared by heating allyl alcohol in the presence of hydrogen perioxide as described in Example 9 of U.S. Pat. No. 2,541,155.
- the poly (allyl alcohol) thus obtained (mol. wt. about 280) was nitrated by the method described in Example 1 above.
- the IR spectrum of the resulting product showed the presence of nitrate groups and the absence of hydroxyl groups. Analysis: Calculated for C 3 H 5 NO 3 : C, 35.0; H, 4.9; found: C, 34.7; H, 4.5.
- the poly(allyl nitrate) thus obtained (1.8 g.) was reacted with sodium azide (2.0 g.) in dimethylformamide (50 ml.) at 75°-85° C. for 6 hours by the method described in Example 1.
- the product (1.1 g.) gave an IR spectrum showing the presence of azide and nitrate groups, and produced a positive match test.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Novel poly (allyl azide) compositions are produced by reacting a poly (al nitrate) of molecular weight at least about 400 with a metal azide in the presence of an inert liquid solvent or diluent. The poly (allyl azides), which may contain residual nitro groups, are energetic materials, which are useful in propellants for guns, missiles and rockets and in detonator and igniter compositions for explosive charges.
Description
The invention described herein may be manufactured, used and licensed by or for the Government for Governmental purposes without payment to me of any royalties thereon.
In the past azidonitrate polymers have been prepared by copolymerizing azido monomers and nitrate monomers, which is a relatively costly and cumbersome procedure. U.S. patent application Ser. No. 600,869, filed Apr. 16, 1984, pending, Everett E. Gilbert, inventor, describes the preparation of novel polyvinyl azido nitrates by reaction of poly (vinyl nitrates) with metal azides. The poly(vinyl azides) and azido nitrates thus obtained are energetic compositions useful in propellants, detonators, etc. U.S. Pat. No. 3,654,917, E. J. Vanderberg, discloses linear poly (glycidyl azides) obtained by reacting a homo or copolymer of epichlorohydrin with a metal azide. Known polymeric azides, such as the glycidyl azide polymers of the patent, are less energetic and more costly than the poly (vinyl azides) of the aforesaid patent application.
The present invention relates to a novel class of poly (allyl azide) compositions and to a process for producing the same.
The novel poly (allyl azide) compositions of this invention are essentially linear allyl polymers having a molecular weight of at least about 300, wherein from about 1% to 100% of the repeating units are allyl azide monomer units of the formula ##STR1## and from about 0% to 99% of the repeating units are allyl nitrate monomer units of the formula ##STR2## The poly (allyl azide) compositions of this invention are energetic materials useful in gun, missile and rocket propellants and other purposes such as in detonation and igniter compositions for explosive charges.
The allyl polymers of this invention contain the azide and nitrate groups attached to primary carbon atoms, viz. --CH2 N3 and --CH2 ONO2 respectively, whereas the poly (vinyl azide/nitrate) compounds of the aforesaid patent application contain the said groups attached to secondary carbon atoms, viz. --CHN3 and --CHONO2 respectively. The poly (allyl azide/nitrate) products of this invention are preferred, since the primary type of group is somewhat more chemically stable than the secondary type of group.
The allyl azide polymers of the present invention can be prepared by reacting a poly(allyl nitrate) of molecular weight at least about 400 with a metal azide, preferably in the presence of a liquid solvent or diluent inert to the reaction. The chemical reaction involved therein can be represented essentially as follows: ##STR3##
The reaction can be carried out at a temperature of from about 20° C. to 125° C. and prefereably from about 50° C. to 100° C. The reaction time, temperature, and amount of metal azide can be varied widely depending on the desired degree of replacement of the nitro groups in the poly (allyl nitrate). For example, the reaction time can vary from less than an hour to many hours and the amount of metal azide can vary from about 100% to about 200% of the stoichiometric amount required to react with the nitro groups of the poly (allyl nitrate).
Liquid solvents or diluents which are suitable for use in the process of the present invention include dimethylformamide, dimethylsulfoxide, tetrahydrofuran, acetonitrile, hexamethylphosphoramide and water and 1-methyl-2 -pyrolidinone, acetone, and 2-methoxyethanol. The reaction is preferably carried out in a solvent in which at least one of the reactants (metal azide and polyallyl nitrate) is soluble.
Alkali metal azides, such as sodium, lithium and potassium azides, are preferably utilized for carrying out the present reaction, but any stable metal azide, particularly an alkaline earth metal azide, e.g. calcium azide, can be employed in a similar manner.
The following examples illustrate the invention.
Poly (allyl nitrate) (0.6 g), sodium azide (0.6 g) and dimethylformamide (25 ml) were mixed and heated with agitation for 5 hours at 80° C. The reaction mixture was poured into about 100 ml. water and acidified with hydrochloric acid to precipitate the product as a gum. The precipitate was separated by filtration and dried under a heat lamp, yielding 0.35 g. of material, whose infrared spectrum showed the strong azide peak 2100 cm-1 and weak peaks for nitrate 1620, 1280 and 860 cm-1.
Match Test. A small quantity of the product thus obtained, when heated on a spatula over a low Bunsen flame, produced a strong flash, showing the highly energetic nature of the material.
The poly (allyl nitrate) employed in this example was prepared by nitration of poly(allyl alcohol) as described below. (General references to this preparation are given in Dutch Patent No. 66,784 (1950) per Chem. Abstracts 45,5452 (1951) and by Schulz et al. (Makromol. Chem. 67,192 (1963)).
0.5 g Poly (allyl alcohol) (no. ave. mol. wt. 4000; wt. ave. mol. wt. 20,000; hydroxyl value 30%; analysis: Theory C, 62.0; H, 10.4; found: C, 62.9; H, 10.5; ash 1%; Cl, 0.4%; Zn 0.12%) was added to a mixture of 10 ml. 100% nitric acid and 20 ml. methylene chloride with agitation at 5° C. The reaction mixture was stirred for 30 minutes at 5° C. and then drowned in ice water, whereupon the product separated as a viscous grease. The product was dissolved in acetone and the solution was evaporated in dryness, yielding 0.8 g. (78%) of poly (allyl nitrate) product, a clear yellow, viscous semi-solid, which gave a positive match test. The IR spectrum of the material showed peaks for the nitrate group at 1620, 1280 and 860 cm-1, and the absence of the hydroxyl peak at 3400 cm-1 which was present in the starting compound.
The procedure of Example 1 was repeated except that the reaction mixture was heated for 19 hours instead of 5 hours. The product weighed 0.4 g. and its infrared spectrum showed the strong azide peak and weak nitrate peaks. It analyzed 42.4% nitrogen, which corresponds to a ratio of 2 allyl nitrate monomer units to 9 allyl azide monomer units in the polymer (values of 2 and 9 for a and b respectively in the foregoing formula). The product gave an energetic match test.
Poly(allyl alcohol) was prepared according to the method of Kargin et al., Ger. Offen. 1,907,612 (Chem. Abstracts 74,142661) by Cobalt 60 polymerization of allyl alcohol (30.1 g.) mixed with calcium chloride (32.5 g.) and water (48 ml.) using 9×104 rad/hr for 236 hours (21.2 megarads total). The resulting solution was processed by treatment with methanolic potassium hydroxide followed by thorough extraction of the precipitated Ca(OH)2 with hot methanol. Evaporation to dryness yielded 22.0 g. (73% yield) of polyallyl alcohol.
The poly (allyl alcohol) was nitrated by the procedure described in Example 1 and yielded a product which possessed an IR spectrum identical with that of the polyallyl nitrate material described in Example 1.
The poly (allyl nitrate) thus obtained (1.6 g.) was reacted with sodium azide (1.6 g.) in dimethylformamide (40 ml.) at 75°-85° C. for 6 hours and the reaction mixture was worked up as described in Example 1. The product weighed 1.2 g. and was a viscous brown oil, which gave a positive match test and an IR curve showing strong azide absorption and residual nitrate groups.
Poly (allyl alcohol) was prepared by heating allyl alcohol in the presence of hydrogen perioxide as described in Example 9 of U.S. Pat. No. 2,541,155. The poly (allyl alcohol) thus obtained (mol. wt. about 280) was nitrated by the method described in Example 1 above. The IR spectrum of the resulting product showed the presence of nitrate groups and the absence of hydroxyl groups. Analysis: Calculated for C3 H5 NO3 : C, 35.0; H, 4.9; found: C, 34.7; H, 4.5.
The poly(allyl nitrate) thus obtained (1.8 g.) was reacted with sodium azide (2.0 g.) in dimethylformamide (50 ml.) at 75°-85° C. for 6 hours by the method described in Example 1. The product (1.1 g.) gave an IR spectrum showing the presence of azide and nitrate groups, and produced a positive match test.
Claims (1)
1. An essentially linear allyl azide polymer having a molecular weight of at least about 300, wherein from about 1% to 100% of the repeating units are allyl azide monomer units of the formula ##STR4## and from 0% to about 99% of the repeating units are allyl nitrate monomer units of the formula ##STR5##
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/845,669 USH272H (en) | 1986-03-26 | 1986-03-26 | Poly(allyl azido nitrates) |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/845,669 USH272H (en) | 1986-03-26 | 1986-03-26 | Poly(allyl azido nitrates) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH272H true USH272H (en) | 1987-05-05 |
Family
ID=25295791
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/845,669 Abandoned USH272H (en) | 1986-03-26 | 1986-03-26 | Poly(allyl azido nitrates) |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH272H (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4839420A (en) | 1984-04-16 | 1989-06-13 | The United States Of America As Represented By The Secretary Of The Army | Preparation of polyvinylazides from polyvinylnitrate |
| US4843121A (en) | 1984-04-16 | 1989-06-27 | The United States Of America As Represented By The Secretary Of The Army | Polyvinylazidonitrate |
| US5214110A (en) * | 1989-10-02 | 1993-05-25 | Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of National Defence Of Her Majesty's Canadian Government | Branched azido copolymers |
| EP0594523A1 (en) * | 1992-07-31 | 1994-04-27 | Union Espanola De Explosivos S.A. | A process for producing energetic polymers starting with hydroxy-terminated polyglycidil nitrate |
| US20070272107A1 (en) * | 2003-04-30 | 2007-11-29 | Twarog Joseph W Jr | Energetic Linear Timing Element |
-
1986
- 1986-03-26 US US06/845,669 patent/USH272H/en not_active Abandoned
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4839420A (en) | 1984-04-16 | 1989-06-13 | The United States Of America As Represented By The Secretary Of The Army | Preparation of polyvinylazides from polyvinylnitrate |
| US4843121A (en) | 1984-04-16 | 1989-06-27 | The United States Of America As Represented By The Secretary Of The Army | Polyvinylazidonitrate |
| US5214110A (en) * | 1989-10-02 | 1993-05-25 | Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of National Defence Of Her Majesty's Canadian Government | Branched azido copolymers |
| EP0594523A1 (en) * | 1992-07-31 | 1994-04-27 | Union Espanola De Explosivos S.A. | A process for producing energetic polymers starting with hydroxy-terminated polyglycidil nitrate |
| US20070272107A1 (en) * | 2003-04-30 | 2007-11-29 | Twarog Joseph W Jr | Energetic Linear Timing Element |
| US8327766B2 (en) * | 2003-04-30 | 2012-12-11 | Dyno Nobel Inc. | Energetic linear timing element |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
| AS | Assignment |
Owner name: UNITED STATES OF AMERICA, AS REPRESENTED BY THE SE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:GILBERT, EVERETT E.;REEL/FRAME:004756/0540 Effective date: 19860320 |