GB2181139A - Nitrated polybutadiene - Google Patents
Nitrated polybutadiene Download PDFInfo
- Publication number
- GB2181139A GB2181139A GB8520344A GB8520344A GB2181139A GB 2181139 A GB2181139 A GB 2181139A GB 8520344 A GB8520344 A GB 8520344A GB 8520344 A GB8520344 A GB 8520344A GB 2181139 A GB2181139 A GB 2181139A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polybutadiene
- reaction
- nitrated
- materials
- reacted
- 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.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C203/00—Esters of nitric or nitrous acid
- C07C203/02—Esters of nitric acid
- C07C203/04—Esters of nitric acid having nitrate groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/34—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups
- C08C19/40—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups with epoxy radicals
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (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
A nitrated derivative of polybutadiene has between 1% and 25% of the carbon atoms in the polymer substituted by nitrate (ONO2) groups. The materials are liquid rubbers with the initial polybutadiene having a molecular weight between 2000 and 10000. In an example, a hydroxy-terminated polybutadiene is epoxidised and then reacted with N2O5.
Description
SPECIFICATION
A process for the production of high energy materials
The present invention relates to a process for the production of high energy materials, to high energy materials produced thereby and to certain novel high energy materials.
At present the manufacture of the group of high energy materials which contain nitrate (0; nitro) substituents or the analogous materials which contain a mixture of Nitro substituents generally requires the use of strong acids (especially HNO3/H2SO4 mixtures) and high temperatures. These conditions present the manufacture of these materials with a number of problems which he must overcome if the method of production is to meet modern standards of safety. These problems include the control, containment and disposal of a highly dangerous and corrosive reaction mixture (hot mineral acids).
It is one object of the present invention to overcome at least some of the above problems by providing a process for the production of certain high energy materials (especially those which contain Nitro substituents) which proceeds effectively at ambient temperature (O-30 C), employs inert organic solvents, and does not require the disposal of strong mineral acids.
Other objects and advantages of the present invention will become apparent from the following description thereof.
According to the present invention a process for the production of a high energy material comprises reacting, in an inert organic solvent, a heterocyclic compound selected from the group oxirane (ethylene oxide) and oxetane with a nitrogen oxide selected from the group dinitrogen tetroxide (N204) and dinitrogen pentoxide (N2OS) and, when the nitrogen oxide is dinitrogen tetroxide, oxidising the nitrnso substituent or substituents in the product obtained to nitro substituent or substituents.
In the present specification each of the terms oxirane and oxetane encompasses both the unsubstituted compounds and the substituted derivatives of the compounds. In the latter case the heterocyclic ring may be substituted by any substituent group. Preferably however the substituent group is at least one of the following halogen, alkyl, alkenyl, nitro and epoxy (as in butadiene diepoxide or the epoxidised form of a polybutadiene), although other groups, such as aldehydo, amino, amido, acyl, carboxylate ester, carboxylic acid, hydroxy, alkoxy, aryl and alkyne, may either additionally or alternatively be present.
The reaction, between heterocyclic compound and nitrogen oxide, is conducted in an inert organic solvent. Any anhydrous organic solvent which does not react with either the starting materials or the reaction products of the present process may be employed. Preferably, however, it should also be possible to either dispose of or recycle the solvent, simply, safely and at little cost. The chlorinated alkanes, dichloromethane, chloroform and carbon tetrachloride, generally meet these criteria and are therefore preferred.
The present process may be conducted at high temperature (up to the boiling point of the solvent) and/or pressure. It is preferred, however, to allow the reaction to proceed at ambient temperature (0-300C, especially 10-20 C) and pressure.
When the present heterocyclic compounds are reacted with dinitrogen pentoxide the required highe energy materials are obtained without further treatment of the reaction mixture. However, when the present heterocyclic compounds are reacted with dinitrogen tetroxide the required high energy materials are only obtained after subsequent oxidation of the resultant O-nitroso compounds. This oxidation step may be performed by any oxidising agent that transforms an O-nitroso substituent into an nitro substituent provided that the agent has no effect on any other part of the nitroso compound (eg does not oxidise a double bond or hydrolyse a halo substituent). In many cases the preferred oxidising agent is ozone.
Generally the present process proceeds very quickly at ambient temperature and pressure.
In a few cases, however, the process, as described above, may be rather slow and it may be necessary to increase the rate of reaction.
This may be done by increasing the reaction temperature to above the ambient; alternatively the reaction may be controlled by the presence of a Lewis acid such as aluminium chloride or stannic chloride.
Although some of the products of the present process are known compounds, in a further aspect of the present invention there is provided a novel group of nitrated polymers.
More specifically there is provided a nitrated polybutadiene, especially a hydroxy-terminated polybutadiene, in which between 1% and 25%, especially between 5% and 20%, of the carbon atoms in the polymer are substituted by nitrate (ONO2) groups. These novel materials are liquid rubbers when the polybutadiene starting material (prior to nitration) has a molecular weight between 2000 and 10000.
The present process will now be described by way of example only.
Preparation of Dinitrogen Pentoxide (N2 05) N205 may be prepared by the oxidation of dinitrogen tetroxide (N2O4) with ozone. Because of the thermal instability of N2O5, during the preparation and subsequent use the temperature should not exceed 30"C and preferably operations are carried out between 0 C and 20"C. All operations must be carried out under anhydrous conditions since N205 is readily hydrolysed to nitric acid. For the reactions described here it is convenient to dissolve the N205 in an inert solvent, such as a chlorinated alkane.
An ozone/oxygen mixture, from a commercially available ozoniser was passed into a glass vessel containing N2O4. Oxidation occurs in the gas phase and the resulting N205 is carried in the oxygen stream and trapped in a series of cold traps kept at 200 to -30"C.
Any unreacted N204 is subsequently reacted by resubliming the initial trapped product in an ozonised oxygen stream. The pure, white crystals of N205 can be stored at --78"C for at least 7 days before use without any noticeable decomposition.
Dinitrogen Tetroxide (N2O,) N204 was obtained commercially as a compressed gas and was used in the following examples directly from a cylinder.
Reactions of Nitrogen Oxides with Heterocyclic
Compounds
General Procedures
A. Reaction with N205 A solution of N205 in an inert solvent was prepared. The heterocyclic compound, dissolved in the same solvent, was added to the stirred N205 solution in an equimolar amount.
The reaction was immediate and generally carried out at or below room temperature in order to minimise the thermal decomposition of N205 and in some cases to avoid losses of the reacting compound where it's volatility was high. Precautions were taken to avoid hydrolysis of the N205 by atmospheric water vapour. Any excess acidity was removed by stirring with solid sodium hydrogen carbonate and the product was isolated by vacuum distillation of the solvent.
B. Reaction with N204 and subsequent oxidation of the product
A solution of N204 was prepared by absorption of the gas into a dry inert solvent and the heterocyclic compound was added in an equi moiar amount to this stirred solution. The reaction mixture was stirred at room temperature for 30 mins and the resultant product (a nitrite-nitrate ester) was oxidised, in situ, with an anhydrous oxidising agent, for example ozone. After removal of any excess acidity with sodium hydrogen carbonate the product was isolated by vacuum distillation of the solvent.
Specific Examples 1. Ethylene Oxide
Ethylene oxide was reacted with N205 using the general procedure (A) described above.
The product was the dinitrate ester of ethylene glycol (O2NOH2C CH2ONO2). In some runs small amounts of ethylene glycol mononitrate were observed through the reaction of traces of nitric acid with ethylene oxide.
Ethylene oxide has also been reacted with N204 and subsequently oxidised with ozone, general procedure (B) above. The product of this reaction is also the dinitrate ester of ethylene glycol.
2. Propylene oxide
Propylene oxide was reacted with N205 as described in general procedure (A) to yield propylene glycol dinitrate (CH3CH(ONO2)CH20NO2) 3. Epichlorohydrin
Reaction of epichlorohydrin with N2O5, general procedure (A), gave 1-chloro-2, 3-propanediol dinitrate (ONO2CH2CH(ONO2)CH2Cl).
4. Butadiene Monoepoxide
Butadiene monoepoxide was reacted with N205 as described above in general procedure (A). The product was 3, 4-butenediol dinitrate, (CH =CHCH(ONO2)CH2ONO2).
5. Butadiene Diepoxide
Butadiene diepoxide was reacted with N205 as described in general procedure (A) except that the nitrogen oxide was added to the epoxide. This reaction gave mainly 1, 2epoxy-3, 4-butanediol dinitrate, although some polymeric products were also produced.
Reaction of 2 moles of N205 with 1 mole of butadiene diepoxide by the same procedure gave erythritol tetranitrate (O2NOCH2CH(ONO2)CH(ONO2)CH20NO2).
6. Epoxidised Polybutadiene
A commercially available hydroxy terminated polybutadiene was epoxidised by known procedures to give partially epoxidised materials where the degree of epoxidation ranged from 10 to 50% of the theoretical maximum. Solutions of these materials were reacted with an amount of N205 equivalent to the degree of epoxidation by the method of general procedure (A). The resulting polymers contained nitrate ester groups. The materials were liquid rubbers.
7. Oxetane
Reaction of oxetane with N2O5, as described in general procedure (A), gave 1, 3-propanediol dinitrate (O2NO(CH2)3ONO2).
8. 3, 3-Dimethyloxetane
Reaction of 3, 3-dimethyl oxetane with
N205, as described in general procedure (A), gave 2, 2-dimethyl-1, 3-propanediol dinitrate.
9. 3, 3-Pentamethylene oxetane
Reaction of 3, 3-pentamethyleneoxetane with N205, as described in general procedure (A), gave 2, 2-pentamethylene-1, 3-propanediol dinitrate.
Claims (4)
1. A novel nitrated polybutadiene wherein between 1% and 25% of the carbon atoms in the polybutadiene are substituted by nitrate groups.
2. A novel nitrated polybutadiene according to claim 1 wherein between 5% and 20% of the carbon atoms in the polybutadiene are substituted by nitrate groups.
3. A novel nitrated polybutadiene according to either claim 1 or claim 2 wherein the polybutadiene is hydroxy-terminated.
4. A novel nitrated polybutadiene according to claim 1 substantially as hereinbefore described with particular reference to Example 6.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8520344A GB2181139B (en) | 1982-07-15 | 1985-08-14 | Nitrated polybutadiene |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8220082 | 1982-07-15 | ||
GB8520344A GB2181139B (en) | 1982-07-15 | 1985-08-14 | Nitrated polybutadiene |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2181139A true GB2181139A (en) | 1987-04-15 |
GB2181139B GB2181139B (en) | 1987-10-21 |
Family
ID=26283313
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8520344A Expired GB2181139B (en) | 1982-07-15 | 1985-08-14 | Nitrated polybutadiene |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2181139B (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB899993A (en) * | 1960-01-12 | 1962-06-27 | Solvay | Improvements in or relating to the preparation of block or graft copolymers |
-
1985
- 1985-08-14 GB GB8520344A patent/GB2181139B/en not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB899993A (en) * | 1960-01-12 | 1962-06-27 | Solvay | Improvements in or relating to the preparation of block or graft copolymers |
Also Published As
Publication number | Publication date |
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GB2181139B (en) | 1987-10-21 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19960712 |