|United States Patent
, et al.
December 12, 2000
Process and compositions for nitration of n-nitric acid at elevated
temperatures to form HNIW and recovery of gamma HNIW with high yields
and purities and crystallizations to recover epsilon HNIW crystals
Processes and compositions for nitration of N-substituted isowurtzitane
compounds with concentrated nitric acid at elevated temperatures to form
HNIW and recovery thereof with high yields and purities. Polymorphic
conversions to the epsilon HNIW crystal form at quanititative yields are
Duddu; Raja (Budd Lake, NJ), Dave; Paritosh R. (Bridgewater, NJ) |
The United States of America as represented by the Secretary of the Army
April 28, 1999|
Related U.S. Patent Documents
||Application Number||Filing Date||Patent Number||Issue Date|
| ||071022||May 1, 1998||6015898||Jan 18, 2000|
|Current U.S. Class: ||540/554; 149/92; 540/556 |
|Current CPC Class:
||C07D 487/02 (20130101); C06B 25/34 (20130101)|
|Current International Class:
||C06B 25/34 (20060101); C06B 25/00 (20060101); C07D 487/02 (20060101); C07D 487/00 (20060101); C07D 255/04 (); C06B 025/34 ()|
|Field of Search:
References Cited [Referenced By]
U.S. Patent Documents
Foreign Patent Documents
| || |
Chemical Abstracts, vol. 128, No. 14, 1998, No. 167, 452 Kawabe et al. Prss and Preparation Etc..
Primary Examiner: Shah; Mukund J.
Assistant Examiner: Coleman; Brenda
Attorney, Agent or Firm: Moran; John F.
Sachs; Michael C.
Beam; Robert Charles
Parent Case Text
This application is a divisional of and claims the benefit of the filing
date of U.S. patent application Ser. No. 09/071,022, filed May 1, 1998,
now U.S. Pat. No. 6,015,898, issued Jan. 18, 2000, and titled: PROCESSES
AND COMPOSITIONS FOR NITRATION OF N-SUBSTITUTED ISOWURTZITANE COMPOUNDS
WITH CONCENTRATED NITRIC ACID AT ELEVATED TEMPERATURES TO FORM HNIW AND
RECOVERY OF GAMMA HNIW WITH HIGH YIELDS AND PURITIES.
1. A process for the polymorphic conversion of HNIW crystals having a form selected from alpha, beta, or gamma or mixtures thereof to the epsilon crystal form comprising preparing a
solution of the HNIW with acetic acid as a constituent of the solution, adding a very small amount of epsilon HNIW seed crystals to the solution, precipitating a solid product and recovering epsilon HNIW from the solid product.
BACKGROUND OF THE INVENTION
The invention is directed to the field of energetic materials known as poly(N-nitro) dodecane cage compounds and processes to prepare these materials. In particular this invention relates to hexa(N-Nitro),hexaazatetracyclic dodecane compounds
which are described in IUPAC nomenclature as 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazatetracyclo[126.96.36.199.sup.5,9.0. sup.3,11 ]dodecanes. The parent compounds and corresponding skeleton structures have the common name of isowurtzitane. The
skeletons are abbreviated as -HISW; the hexanitrohexaazaisowurtzitanes are abbreviated as HNIW; the compounds and the use of the nomenclature are described in U.S. Pat. No. 5,693,794.
The HNIW compounds have a density of about 2.0 g/cc and six nitro groups per molecule. The compounds are polymorphic with at least four crystal forms: alpha, beta, gamma and epsilon. Epsilon HNIW has the highest density. Typically the
processes of production will result in the alpha HNIW which is then converted to the epsilon HNIW, see CA, Vol 128, NO. 128, No. 14, p. 595, 167451w, Kawabe, et al, 1998. The product in the epsilon crystal form is preferred for use in energetic
compositions such as propellants and explosives. The energetic compositions with HNIWs are described as C1-20 containing compositions in U.S. Pat. Nos. 5,712,511, and 5,739,325. The preferred usage is to apply this term to the epsilon form of HNIW.
There are problems in developing compositions which utilize the epsilon HNIW as an energetic material. The intermediate HNIW crystal forms need to be available in high purity and yield. The processes for producing the intermediates need to be
simplified. The reactions and reaction media need to reduce or eliminate the presence of side reactions, shock-sensitive impurities, other impurities and oxygenated isowurtzitanes so that a high purity, shock insensitive epsilon HNIW crystal can be
obtained. It is to these ends that this invention is directed.
BRIEF SUMMARY OF THE INVENTION
This invention provides nitration of N-substituted isowurtzitanes (NHISW) with a nitrating agent consisting essentially of concentrated nitric acid. The reaction is conducted at an elevated temperature and a solid product is recovered that is
principally gamma HNIW. A novel process for converting the gamma HNIW to epsilon HNIW is also disclosed. Among the advantages of the invention are that the nitrating agent is highly concentrated nitric acid, a minimum molar excess of nitrating agent to
HNIW can be used, the reaction temperatures can be increased and the yield of product is increased and the reaction reaches substantially total completion in a relatively short time.
The nitration processes of this invention directly produces a solid product that can be recovered as essentially pure gamma HNIW and the levels of impurities and side products in the product are reduced or eliminated. The conditions of the
nitration can be controlled so that common impurities such as oxa-ISW and dioxa-ISWs and incompletely nitrolysed compounds such as PNAIW are present in only negligible amounts in the nitration media. Reaction promoters and solid proton donor resins can
also be used in carrying out the practice of the invention. The optimum reaction conditions are such that yields of gamma HNIW are above about 99%. The invention allows the minimization of costs of production and the costs of waste disposal.
BRIEF DESCRIPTION OF THE FIGURE
The FIGURE contains representative FTIR spectrum of the gamma HNIW product of Example 1 and the reported spectrum from technical publications for gamma HNIW.
DETAILED DESCRIPTION OF THE INVENTION
In the practice of the invention, the principal reactants are the NHISW compounds and the concentrated nitric acid which are reacted at an elevated temperature for a relatively short time. The temperature needs to be at or above the onset
temperature for the reaction to occur. As the reaction proceeds, an isolatable solid product will be formed. Significant amounts of HNIW crystals can be recovered from the product. They will be worked up so that a very pure form of gamma HNIW is
obtained. This is converted to the epsilon HNIW.
The NHISW has N-substituents which are known as facile leaving groups; these can withstand the rigorous nitration conditions without destruction of the isowurtzitane skeleton and allow the multiple nitrations at the N-sites which ultimately form
the hexanitro compound. In effect the NO.sub.2 groups replace the facile leaving groups. While there are many potential facile leaving groups for the NHISWs, the problems of cost and availability are such that only a relatively few compounds are
presently accessible. Generally, in terms of availability and efficacy, a preferred group of NHISWs are the compounds with skeletons whose N-substituents are selected from up to 6 hydrogen atoms, up to 6 alkyl groups, up to 6 acyl groups, up to 2
alkylaryl groups, up to 2 NO groups, and up to 2 NO.sub.2 groups. In terms of current availability, the particularly preferred substituents for the NHISW are hydrogen, acetyl, formyl, benzyl, NO, and NO.sub.2 groups. Exemplary compounds include
tetraacetyldiformyl isowurtzitane (TADF), tetraacetyldibenzyl isowurtzitane (TADB), tetraacetyldinitroso isowurtzitane and tetraacetyldinitro isowurtzitane (TADN).
The concentrated nitric acid reactant is historically considered to be HNO.sub.3 and H.sub.2 O. The exact mechanism of the reactant is still poorly understood in complex nitration systems such as the present invention. The reactant will have an
initial concentration of from about 90 to about 98% HNO.sub.3. As the reaction proceeds, the NO.sub.2 is consumed and the concentration of HNO.sub.3 becomes reduced. If the concentration falls to about 70%, the concurrent increase in the concentration
of water is sufficient for attacks and decompositions of the HNISW at elevated temperatures. This leads to the oxa and dioxa isowurtzitanes and other impurities in the reaction media. In this invention, the reaction condition variables of elevated
reaction temperature, choice of coreactant NHISW compounds, shortened reaction time and minimum molar excess of HNO.sub.3 can be selected to provide for high yields of gamma HNIW with minimum or undetectable impurities even though the concentration of
water is increasing. The concentrated nitric acid is preferably at least about 90% HNO.sub.3 and may be from about 95 to about 98% HNO.sub.3. Typically, the generally available 95% and 98% HNO.sub.3 grades are used.
Another advantage of this invention is that it employs simplified reaction procedures and advantageous ratios of reactants. The molar excess of HNO.sub.3 to NHISW is desirably kept to a minimum. This appears to reduce impurities; it reduces the
operating cost of the process and it reduces the waste disposal and clean up costs. The range of the molar excess can be from about 4 to about 6. This corresponds to about 24 to about 36 moles of HNO.sub.3 per mole of NHISW. It can also be appreciated
that the minimum molar excess of nitrating agent is an advantage whether the reaction is conducted under either batch or continuous operations.
It is preferred to put the concentrated HNO.sub.3 in the reactor and then to add the NHISW compound in small portions and mix until a clear solution is formed. The mixing temperature should be in the range of about 20 to 25 degrees Celsius. The
temperature of the solution is gradually increased until a temperature is reached where the nitration of the NHISW will begin; this is considered the onset temperature and will be about 75 degrees Celsius for the conditions set forth in the Examples. It
is the elevated temperature of the solution at which appreciable conversion to the NHISW occurs. In some cases, the onset temperature may be at about 80 degrees Celsius. The upper limit for the elevated temperature will in theory be the boiling point
of the reaction media. A lower temperature is practical. The Examples show that a temperature range of from about 100 to 115 degrees Celsius has given good results. A reaction temperature of about 115 degrees Celsius has been able to produce a gamma
HNIW at very high yields and of very high purity with short reaction times. The exact temperature range will also be affected by the presence of solid reaction promoters and solid proton donor resins. These can increase recoverable gamma HNIW, lower
onset temperature or decrease impurities.
The overall time of heating for the reaction to reach substantial completion varies within wide limits. The range is from about 3.5 to about 19 hours. It has been found that a short reaction time in the range of from about 3.5 to about 4 hours
is adequate to achieve substantial completion of the reaction. Reaction times in the range of 12 and 12.5 to 19 hours have also been used which allow for a margin of safety in reaction control. Under batch reaction conditions, the system can reach
about 100% completion.
The invention is also novel in the sense that it appears to be the first time that gamma HNIW is reported to be made by the use of concentrated nitric acid and elevated temperature. The presence of the gamma HNIW from the reaction is indicated
by the formation of a white, solid material in the reaction medium that may be worked up and identified as gamma HNIW from its FTIR spectrum. The work up and recovery of the HNIW follows the established practices in this field. When the reaction has
reached the target degree of completion, the reaction medium will have a suspended solid in the reaction liquid. The system will be cooled to room temperature. Then, the materials will be poured over crushed ice. The solids will be recovered by
filtration and examined with NMR. The solids represent the isolatable solid material of the reaction. The NMR will indicate the percentage of HNIW and the percentage of other materials. If oxa or dioxa isowurtzitanes are present, they can be
identified as such. Further purification steps such as washing can be performed as discussed in Example 1. The high yield and high purity of gamma HNIW of this invention is demonstrated by the FIGURE. The FTIR spectrum in the FIGURE for the product of
the process is substantially as is shown by the recognized technical literature publications for gamma HNIW.
The range of HNIW in the isolatable solid material from the reaction media is in the range of at least about 30% to about 99%. Intermediate contents of HNIW in the isolatable solids material were at least about 60%, 80%, 95%, 97%, and 98% are
noteworthy. This HNIW is usually recovered and worked up by aqueous procedures. By this stage, as well as in earlier stages, the HNIW can be principally in the gamma form. The gamma form can be converted to epsilon NHISW.
The practice of the invention is illustrated by the following Examples.
Preparation of Gamma HNIW by Nitration with 98% HNO.sub.3 at Elevated Temperature
Part A of Example 1 illustrates the nitration reaction of the invention in which the reaction is carried out with 98% HNO.sub.3 as the nitrating agent, TADF as the NHISW and where the reaction temperature is about 115 degrees Celsius. It
demonstrates that the isolated, solid HNIW material that is converted to a gamma HNIW that has an FTIR spectra substantially the same as that reported for the pure gamma NHISW. Part B describes the conversion of the gamma HNIW to the epsilon HNIW. The
yields and the purity of the gamma and epsilon HNIW are very high.
A three-necked, round-bottomed flask was fitted with a reflux condenser, a moisture-guard tube, a thermometer, and a stirrer. The equipment was placed in an oil bath. The nitrating agent was concentrated nitric acid in an amount of 15 ml at 98%
HNO.sub.3 which was placed in the flask. The TADF was added in small portions at such a rate that the temperature of the reaction stays between about 20 and 25 degrees Celsius. The media was stirred while the TADF went into solution. A total of 5.0 gm
was added and the solution was clear.
After the addition was completed, the temperature of the reaction mixture was gradually elevated by heating the flask until a reaction temperature of about 115 degrees Celsius was reached. This temperature corresponds to an external oil bath
temperature of 125 degrees Celsius. As the reaction continued, a white, solid material began to form. As the reaction was allowed to continue, additional white solid material was formed. The total heating time was 4.5 hours.
When the reaction approached 100% conversion, the reaction mixture was cooled to room temperature and poured over crushed ice. The white, solid material was recovered by filtration and washing three times with cold water. It was air dried and
formed a free-flowing powder. An FTIR spectrum of the product was taken and is shown in the FIGURE. There is a comparison with the published FTIR spectrum for pure HNIW. It can be seen that the product produced by this invention is gamma HNIW of very
high purity. The yield of gamma HNIW based on the amount of TADF was consistently in the range of from above about 90% to about 99%.
Polymorphic Transformation of Gamma HNIW to Epsilon HNIW
This is a novel process to convert either alpha, beta, or gamma HNIW to epsilon HNIW. Mixtures of the crystal forms may also be used. A 1.0 g. sample of gamma HNIW prepared as described above was mixed with 1 ml. Of acetic acid and 4.0 ml of
ethyl acetate; this formed a solution. 0.030 gm of seed crystals of epsilon HNIW were added to the solution. Then, 24 ml of hexane were added dropwise to the mixture. A solid material precipitated. The mixture of liquid and solids was stirred for
about 30 minutes and filtered. The solid filtrate was washed with hexane and dried to yield epsilon HNIW in quantitative yield. The epsilon HNIW crystals were free-flowing, white solids. If the acetic acid is not present, epsilon crystals are not
obtained even with extreme standing times. The acetic acid allows the crystallization media to produce fine quality epsilon HNIW.
In the following Examples 2-5, variations of the nitration conditions and the concentrated nitric acid reactant of Example 1 were used to demonstrate the effects of time, temperature (reported as internal reaction temperature), reaction promoters
and reactant ratios on product yield, product purity and production of side products, by-products, impurities, etc.
The general procedure follows Example 1. The specified amount and type of concentrated nitric acid is put into the flask. The NHISW is added in small portions at such a rate that the temperature of the reaction stays between about 20 and 25
degrees Celsius while stirring the solution. After the addition is completed, the temperature of the reaction mixture is gradually elevated by heating until the target temperature is attained. The reaction is continued for the desired period of time.
The reaction medium is separated into liquids and solid. The isolated solid material is examined by NMR. The approximate % of HNIW can be estimated from the NMR as well as the approximate % of other products. If oxa or dioxa isowurtzitanes were to be
present, this can be noted.
(a) 300 mg of TADF were used to form a solution in 1 ml of 98% HNO.sub.3. The elevated temperature was about 80 degrees Celsius and the total time of heating was 4 hours. A white solid product from the reaction was isolated. It was found to
contain about 30% of HNIW and about 70% other products.
(b) The same conditions as in 2(a) above were used except the elevated temperature was at about 115 degrees Celsius. The isolated material was found to contain at least about 98% HNIW and there was less than about 2% other products.
(c) The same conditions as in 2(a) above were used except the amount of TADF was 1,000 mg and the amount of 98% HNO.sub.3 was 1.5 ml. The elevated temperature was 115 degrees Celsius and the total time of heating was 4 hours. The isolated
material contained about 80% HNIW and about 20% side products. Oxa and dioxa isowurtzitane impurities were among the side products; this indicates decomposition of HNIWs by water.
(d) The same conditions as in 2(c) above were used except the amount of TADF was 1,000 mg and the amount of 98% HNO.sub.3 was 2.0 ml. The isolated material was about 80% HNIW and the side products were about 20%. Oxaisowurtzitane was present in
the side products; this indicates the decomposition of HNIWs by water.
(e) The same conditions as in 2(c) above were used except the amount of 98% HNO.sub.3 was 3 ml. The isolated material was about 98% HNIW and the side products were below about 2%.
(f) The same conditions as in Example 2(e) were used except the amount of materials were tripled. The isolated material was about 98% HNIW and the side products were below about 2%. This shows that the reaction conditions can be scaled up in a
predicable manner to produce suitable products.
95% HNO.sub.3 as Nitration Agent
This Example illustrates the use of 95% HNO.sub.3 as the concentrated nitric acid for the reactions of this invention. It also illustrates that the molar ratios of reactants can be varied to minimize the amount of excess concentrated nitric acid
required to drive the polynitration reaction and that the reaction conditions can be scaled up.
(a) 300 mg of TADF were used to form a solution with 1 ml of 95% HNO.sub.3. The elevated temperature was about 115 degrees Celsius and the total time of heating was 4 hours. The content of the isolated material was in the range of from about
95% HNIW to about 97% HNIW and the corresponding range for side products was from about 3% to below about 5%.
(b) 1,000 mg of TADF were used to form a solution with 3 ml of 95% HNO.sub.3. The elevated temperature was about 115 degrees Celsius and the total time of heating was 4 hours. The content of the isolated material was in the range of from above
about 95% HNIW to about 97% HNIW and the corresponding range for side products was from about 3% to about 5%.
(c) The conditions of 3(b) were duplicated except the amounts of material were tripled. The content of the isolated material was in the range of from above about 95% HNIW to about 97% HNIW and the corresponding range for side products was from
about 3% to about 5%. This illustrates that the conditions of the reaction can be scaled up.
Nitration with Concentrated Nitric Acid and Optionally Solid Reaction Promoters
This Example illustrates that the reaction temperature has a strong effect on the outset of nitration of the NHISWs with the concentrated nitric acid and that at suitable temperatures the nitration can be conducted either with or without solid
reaction promoters, such as solid proton donor resins.
(a) 300 mg of TADF were used to form a solution with 3 ml of 98% HNO.sub.3. 1300 mg of a solid resin having sulfonic acid groups in the proton form, available as Nafion-H, were also added to the solution. The elevated temperature was about 70
degrees Celsius. The range of heating times were from about 12 to 15 hours. No identifiable amount of HNIW was seen in the isolated material. The side products were not identified. This illustrates that nitration did not occur at this reaction
temperature even in the presence of the concentrated nitric acid and the reaction promoter.
(b) The same conditions as in 4(a) above were used except the elevated temperature was at about 75 degrees Celsius. The isolated material was about 60% HNIW and the side products were less than about 40%. The higher temperature reached the
onset of nitration to form the HNIW product. The successful production was very evident.
(c) The same conditions as in 4(a) above were used except the elevated temperature was at about 80 degrees Celsius. The isolated material was about 80% HNIW and the side products were less than about 20%. The higher temperature produced more
product. The successful production of solid white product was very evident.
(d) The same conditions as in 4(a) above were used except the elevated temperature was at about 100 degrees Celsius. The isolated material was at least about 95% HNIW and the side products were less than about 5%. Again, the higher temperature
produced even more product.
(e) The same conditions as in 4(a) above were used except the elevated temperature was at about 115 degrees Celsius. The isolated material was at least about 99% HNIW and the presence of other products can be described as nil.
Nitration with Varying Amounts of Solid Reaction Promoters at Same Reaction Temperature
This Example illustrates the combined benefits that can occur from the optimization of reaction conditions which use the preferred temperature, the type and amount of concentrated nitric acid and the presence of the reaction promoter.
(a) 300 mg of TADF were used to form a solution with 3 ml of 98% HNO.sub.3. No reaction promoter was used. The elevated temperature was about 115 degrees Celsius. The range of heating times were from about 12 to 15 hours. The isolated solid
material was at least about 98% HNIW and the other products were present in amounts of less than about 2%. This is substantially a repetition of Example 2(f).
(b) The same conditions as in 5(a) above were used except a solid reaction promoter in the form of solid sulfonic acid resin in the protonated form, Nafion-H, was also present. It was used in an amount of 25 mg. The isolated solid material was
at least about 98% HNIW and the other products were present in amounts of less than about 2%.
(c) The same conditions as in 5(b) above were used except the amount of Nafion-H was 100 mg. The isolated material was at least about 99% HNIW and there were no identifiable amounts of other products.
(d) The same conditions as in 5(b) above were used except the amount of Nafion-H was 300 mg. The isolated solid material was at least about 99% HNIW and there were no identifiable amounts of other products.
The detailed description and Examples are provided to illustrate specific modes of carrying out the invention.
The invention is intended to cover such equivalent practices, materials and supplementary techniques as would be evident to those skilled in the field and that the scope of the claims should be interpreted to that end.
* * * * *