Patent Application
20220259118
Pursuant to 37 C.F.R. § 1.78(a)(4), this application claims the benefit of and priority to prior filed co-pending Provisional Application Ser. No. 63/120,266, filed 2 Dec. 2020, which is expressly incorporated herein by reference.
The present invention relates generally to the manufacture of nano-scale nitramine particles and, more particularly, to the manufacture of nano-scale nitramine particles using a turbulent mixing technique.
Developing explosives with increased performance along with reduced sensitivity is a major objective in the energetic materials community. Reducing the particle size of energetic materials (EM) is one approach that can strongly influence the reactivity and sensitivity of the constituents.
For example, fine particles of ammonium perchlorate (AP) are more detonable than coarse particles. This disclosure is directed to nanometer-size high explosive (HE) particles which have gained increased attention due to their reduced sensitivity to ignition via friction, impact, and electrostatic discharge as compared to micrometer size particles. Many techniques have been used to reduce the particle size of HE including wet grinding, bidirectional grinding, sol-gel methods, supercritical fluid methods, ultrasonication, spray assisted precipitation, and solvent-antisolvent interaction. Many of these approaches are batch procedures that are labor intensive and cost prohibitive on an industrial scale.
The present invention overcomes the foregoing problems and other shortcomings, drawbacks, and challenges of manufacturing nanometer-size high explosive materials. While the invention will be described in connection with certain embodiments, it will be understood that the invention is not limited to these embodiments. To the contrary, this invention includes all alternatives, modifications, and equivalents as may be included within the spirit and scope of the present invention.
According to one embodiment of the present invention a method of making RDX nanoparticles comprises dissolving RDX in acetone; injecting the RDX/acetone through an inner tube of a turbulent mixer to form an inner flow; injecting an anti-solvent through an outer tube of a turbulent mixer to form an outer flow, wherein the inner tube is concentric with the outer tube, wherein turbulent mixing of the inner flow and outer flow precipitates nanoparticle of RDX.
The concentration of RDX in acetone may be 0.5-1.0 mg RDX/mL acetone.
The anti-solvent may be a mixture of hexane and cyclohexanone.
The ratio of hexane:cyclohexanone may be between 8:1-12:1.
The invention may be employed to produce nanoparticles of HMX, CL-20, PYX, and HNS using the same solvent/anti-solvent system described herein.
The solvent/anti-solvent systems are not restricted to those presented herein. Acetone may be replaced with other polar, aprotic solvents or solvent mixtures. Hexanes may be replaced with another non-polar or low polarity solvent or solvent mixtures. Cycicohexanone may be replaced with other known surfactants or surface stabilizing ligands to prevent agglomeration, control average particles size distributions, particle morphology and aspect ratio.
Additional objects, advantages, and novel features of the invention will be set forth in part in the description which follows, and in part will become apparent to those skilled in the art upon examination of the following or may be learned by practice of the invention. The objects and advantages of the invention may be realized and attained by means of the instrumentalities and combinations particularly pointed out in the appended claims.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the present invention and, together with a general description of the invention given above, and the detailed description of the embodiments given below, serve to explain the principles of the present invention.
It should be understood that the appended drawings are not necessarily to scale, presenting a somewhat simplified representation of various features illustrative of the basic principles of the invention. The specific design features of the sequence of operations as disclosed herein, including, for example, specific dimensions, orientations, locations, and shapes of various illustrated components, will be determined in part by the particular intended application and use environment. Certain features of the illustrated embodiments have been enlarged or distorted relative to others to facilitate visualization and clear understanding. In particular, thin features may be thickened, for example, for clarity or illustration.
This synthesis method creates nano-scale nitramine particles using a turbulent mixing technique. In this method, bulk nitramine high explosive (HE) particles are dissolved in a solvent and crash precipitated from solution into an anti-solvent mixture via a turbulent jet. The turbulent flow facilitates rapid mixing of solvent and anti-solvent streams. The rapid mixing and subsequent self-assembly of HE precursor forms homogeneous nanoscale nitramine particles.
Coaxial turbulent jet mixing technology was successfully adapted to facilitate production of nanometer scale RDX particles (RDX NPs), which is scalable for industrial applications.
RDX nanoparticles (NPs) with an average diameter of 123±28 nm were produced at a rate of 0.6 g/hour using a coaxial turbulent jet mixer. RDX was dissolved in acetone and precipitated into an anti-solvent mixture of 90% hexane and 10% cyclohexanone. Cyclohexanone was used as a surfactant to stabilize the NPs and prevent agglomeration; NPs of RDX were only observed when cyclohexane was added to Hexane in the anti-solvent solution. In the concentration range tested, 0.5, 0.75, 1, 1.5, and 2 mg RDX/mL acetone, only the lowest three concentrations formed NPs with very little difference in the average particle size. The two higher concentrations formed micron scale rod shaped particles. The coaxial turbulent jet mixer makes possible a scalable continuous flow solvent/antisolvent method for the production of NPs with a tunable size, morphology and aspect ratio and demonstrates industrial scale production of nano-RDX.
The coaxial turbulent jet mixer utilizes anti-solvent precipitation to rapidly reduce the solubility of a dissolved solid in a turbulent flow. Turbulent flow conditions result in rapid and efficient mixing with the anti-solvent yielding a dramatic reduction in solubility of the RDX causing precipitation the dissolved solid. Due to the near instantaneous precipitation and diffuse concentration of RDX in the anti-solvent the process yields precipitates of the dissolved solid with dimensions on the nano-scale.
Briefly, crystallization can be broken down into two steps, nucleation and growth. Increasing the number of nucleation points and reducing the growth time will lead to a reduction in particle size. Injecting the dissolved NP precursor into a turbulent flow of anti-solvent increases the number of nucleation points and decreases characteristic mixing time, leading to the formation of NPs.
The turbulent mixing apparatus 10 is shown in
The following examples illustrate particular properties and advantages of some of the embodiments of the present invention. Furthermore, these are examples of reduction to practice of the present invention and confirmation that the principles described in the present invention are therefore valid but should not be construed as in any way limiting the scope of the invention.
Class V RDX (BAE OSI-Holston) was dissolved into acetone (technical grade, Ashland Chemical Co.) at concentrations of 0.5, 0.75, 1, 1.5, and 2 mg/mL then these solutions were injected through the inner tube. Hexane (HPLC grade, >98.5% purity) was used as the anti-solvent and cyclohexanone (ReagentPlus grade, 99.8% purity from Sigma Aldrich) was added as a surfactant at a ratio of 9:1 hexane to cyclohexanone which was introduced to the system through the outer tube.
Particle size distributions were determined using images from a scanning electron microscope (SEM, Hitachi NX9000). After the samples were collected, a single drop of the resulting mixture was placed on a silicon wafer attached to an SEM stub and quickly (<1 min) dried in a fume hood. The SEM was calibrated using a 4000×4000 pixel range and a calibration grid. Images were obtained using the lower secondary electron detector with an accelerating voltage of 1 kV and emission current of 30 μA. The SEM images were analyzed using Image J software for particle size distributions.
There are many variables to consider when using a coaxial turbulent jet mixer for the synthesis of energetic NPs to include, but not limited to, RDX, HMX, CL-20, PYX, and HNS. First, the flow regime affects particle size and is primarily identified by the Reynolds Number (RE) and the Flow Velocity Ratio (R). In short, two turbulent flow regimes are seen at high RE numbers, defined as a turbulent jet and turbulent vortex. NPs are produced when the flow regime is a turbulent jet. The transition between turbulent jet and turbulent vortex is determined by the value of R. High R values (>2) with high RE (>500) produce a turbulent jet and low R (<2) values with high RE (>500) produce a turbulent vortex. Another important variable to consider is the solubility of the constituent of interest in the solvent and the amount of anti-solvent required to precipitate that material out of solution. Increasing the outer flow (anti-solvent solution) will increase both RE and the amount of anti-solvent in the system. For this study, the anti-solvent flow was set to the operating limit of the syringe pumps (2 pumps at 110 mL/min) to maximize the RE (˜2600) and maximize the amount of anti-solvent in the system. The inner flow was set to 10 mL/min which was the lowest setting that provided a high enough R value (2.2) for a turbulent jet. The lowest setting was used on the inner flow to be certain there was an adequate amount of hexane to precipitate the RDX out of solution.
Increasing the amount of solute in the solvent can potentially be employed to increase the production rate of RDX NPs. To determine the effect of solute concentration on particle diameter, the concentration of RDX in acetone in the inner flow was varied from 0.5 to 2 mg/mL.
In
The distribution in
the final solution (˜90 mg/L) which is well below the measurement threshold for the instrument (10 mg/mL).
To confirm that the nanoparticle formation was induced by the conditions generated by turbulent mixing, 0.75 mg/mL of RDX in acetone was mixed with the hexane/cyclohexanone solution in a beaker without utilizing the turbulent mixer and the formation of micron size rod shaped particles, similar to
At a concentration of 1 mg RDX/mL acetone with anti-solvent flow at 220 mL/min and inner solvent flow at 10 mL/min, RDX NPs can be produced at 0.6 g/hour. Increasing the concentration of the inner tube solvent or increasing inner tube flow rate while maintaining precipitation of NPs would increase the production rate of RDX NPs synthesis (shown in Table 1).
A major drawback to this method is the amount of anti-solvent needed as shown in Table 1 (˜20 liters of hexane for 1 g RDX). However, the values shown in Table 1 are at the operating limits of the pumps. The pumps were set to the operating limits to eliminate flow rate variables (i.e. RE and R) and isolate the effects of solute concentration on particle diameter. Since the pumps were set to their operating limits, future optimization of flow rate variables will reduce the amount of solvent needed and increase the production rate of RDX NPs. For example, increasing inner tube flow rate will increase RDX NPs production rate and decreasing anti-solvent flow rate will reduce the amount of anti-solvent per gram of RDX NPs. In addition to optimization, reclamation of the solvent/anti-solvent can be employed to minimize waste and production cost.
To produce RDX NPs on an industrial scale, the process must either be scalable or a continuous flow process. One of the major disadvantages of previous methods is the inability to scale up and to be a continuous flow process. The turbulent mixer can easily be scaled by parallelization of reactors and each reactor can be modified to be a continuous flow reactor. In the continuous flow reactor, each individual pump may be replaced with a pair of pumps with large reservoirs of solvent and anti-solvent. Each pair of pumps may have one pump continuously infusing into the reactor while the other pump withdraws solvent or anti-solvent from the reservoirs using check valves to control the direction of flow. When the infusing pump is empty (and the withdrawing pump is full), their directions will be reversed allowing for continuous flow into the reactor. The combination of process optimization and a continuous flow coaxial turbulent mixer will allow for faster and more efficient production of RDX NPs.
Using a coaxial turbulent mixer, RDX NPs was synthesized at a rate of 0.6 g/hour. The particle diameter of the RDX NPs was 123±28 nm when the RDX to acetone concentration is 0.5, 0.75 and 1 mg/mL. When the concentration exceeds 1 mg RDX/mL acetone, elongated particles with greater than micron sized lengths were observed. In this study, the flow rate variables were set to the operating limits to isolate the effects of solute concentration on particle size. Optimization of these variables (inner solvent flow rate, anti-solvent flow rate, and cyclohexanone/hexane ratio) will lead to higher production rates and less volume of solvent.
While the present invention has been illustrated by a description of one or more embodiments thereof and while these embodiments have been described in considerable detail, they are not intended to restrict or in any way limit the scope of the appended claims to such detail. Additional advantages and modifications will readily appear to those skilled in the art. The invention in its broader aspects is therefore not limited to the specific details, representative apparatus and method, and illustrative examples shown and described. Accordingly, departures may be made from such details without departing from the scope of the general inventive concept.
The invention described herein may be manufactured and used by or for the Government of the United States for all governmental purposes without the payment of any royalty.
| Number | Date | Country | |
|---|---|---|---|
| 63120266 | Dec 2020 | US |
