Dissertation on Insensitive Highly Energetic Materials (Section 2.4)

Article Summary: This article contains Section: 2.4 (Ingredient Selection and Theory) of the “Dissertation on the Study of Insensitive Highly Energetic Materials” as part of the Doctoral requirements for Theodore S. Sumrall at The University of Tokyo, March of 1998. Theodore S. Sumrall was awarded a Doctorate Degree from the Department of Chemical Systems Engineering in April of 1998 as a result of his research, development testing and dissertation presentation.

2.4 Ingredient Selection and Theory

The overall logic for selection of raw materials is detailed in Figure 2.4-1. Once ingredients were selected, scale up to 450 gram mixes occurred. Ingredients were selected to help ensure that project objectives (Table 1-3) were achieved.

Binder Screening and Selection

Theoretical calculations for non AP containing PBX compositions which utilize an HTPB binder system revealed that significant amounts of un-reacted carbon was being generated in both the burn and detonation reactions. The code predicted that, while the majority of the aluminum was oxidized to Al2O3, the majority of the binder (a hydrocarbon) was un-oxidized.

Theoretical Calculation Logic Flow

Figure 2.3-1 Theoretical Calculation Logic Flow

It was postulated, and supported by thermochemical code output, that replacement of the non-oxygenated HTPB hydrocarbon binder with an oxygenated binder might allow the oxygen to enter into the detonation and/or deflagration reaction. This approach, if successful, would yield a dual benefit. First, oxygen from the binder could be utilized to burn the residual hydrocarbon and secondly, the more oxygenated (and more sensitive) ingredients (such as RDX) could be reduced in content. This would hopefully allow the PBX to pass tests which PBX-109 fails, namely Slow Cook-Off (SCO), Fragment Impact (FI) and Sympathetic Detonation (SD). In the process of oxygenated binder evaluation, binders were considered that not only had relatively high oxygen content, but which would also adequately wet the solids (to ensure low viscosity (Objective #4)) and which had a demonstrated capability of rapid cure (Objective #5). Both of these characteristics would be desirable from production cost standpoints.

Finally, only binder ingredients which were commercially available in large quantities and at a relatively low cost were chosen (Objective #8).

After a thorough evaluation of a number of potential binder candidates, three oxygenated, curable binders were selected for further evaluation, polyethyleneglycol (PEG), polypropyleneglycol (PPG), and ethyleneoxide-propyleneoxide (EOPO). The plasticizer chosen was triacetin (TA). In order to meet rapid cure goals, two types of cure catalysts were chosen for evaluation. The first cure catalyst evaluated was ferric-acetylacetonate (FeAA). The second cure catalyst evaluated was di-butyltin di-laurate (DBTDL) in conjunction with a cure delay/cure stimulation catalytic system consisting of minute concentrations of triphenyl bismuth (TPB) and maleic anhydride (MA) .

A comparison of the theoretical improvement which was predicted to occur by switching from an HTPB binder to a PPG binder for a well characterized explosive (PBX-109) is detailed in Table 2.4-1.

Table 2.4-1

Comparison of Theoretical Performance Improvement with Oxygenated Binders

Characteristic

HTPB Binder

PPG Binder

Density (g/cm3)

1.655

1.7071

Detonation Velocity (m/sec)

6721

7010

Detonation Pressure (MPa)

18435

21666

Percent Un-reacted Carbon

19.5

15.04

Temperature (K)

3682

4052

As shown later, PPG was down selected as the final polymer of choice due to superior processing, curing, and physical property characteristics.

Oxidizer Screening and Selection

Theoretical calculations showed a direct correlation between energetic material density and oxygen content with detonation velocity, detonation pressure and Impulse Density. It was predicted by the TIGER and NASA/Lewis codes that the inclusion of oxidizers such as Ammonium Nitrate (AN), Ammonium Perchlorate (AP), Potassium Nitrate (KN), etc., would improve detonation velocity, detonation pressure and blast pressure impulse.

The addition of oxidizers such as: Ammonium Nitrate (AN); Ammonium Perchlorate (AP); Potassium Nitrate (KN); and etc., have been proven beneficial to the more efficient combustion of fuels. A higher degree of fuel combustion will result in higher temperatures and therefore higher blast pressures. AP has long been the oxidizer of choice for solid rocket propulsion such as the Space Shuttle SRB and NASDA H-II Boosters. However, at the time that this project was initiated, AP availability had decreased (and cost had increased) due to an incident at one of only two major AP producers in the US. Also testing by other researchers revealed a correlation between AP content and Slow Cook-Off (SCO) test failure.

Criteria other than cost and availability which guided oxidizer selection were: high oxygen balance; non-hygroscopic character, and high-moderate density. Potassium Nitrate (KN), for example, met all of the screening criteria. At a crystal density of 2.1 g/cm3, and despite having 67% condensed products, KN reacts to form one half more mole of free O2 than AP as indicated by the following equations.

2KNO3 à K2O + N2 + 2 1/2 O2 Equation 2.4-1

2NH4ClO4 à N2 + 3H2O + 2HCl +2½ O2 Equation 2.4-2

Lead Nitrate (PbN) and Barium Nitrate (BaN) also have high densities (4.53 g/cm3 and 3.24 g/cm3 respectively) are non hygroscopic, and react to form three moles and 2.5 moles of excess O2 respectively according to Equations 2.4-3 and 2.4-4.

Pb(NO3)2 à 2Pb + N2 + 3O2 Equation 2.4-3

Ba(NO3)2à BaO + N2 + 2 1/2 O2 Equation 2.4-4

KN and PbN were selected as the oxidizers of choice during this phase of research. KN was eventually chosen over PbN due to superior sensitivity and environmental characteristics.

Molecular Explosive Screening and Selection

To achieve performance goals, it was determined that at least some molecular explosives would be required. Molecular explosives are defined as explosives which have the fuel and oxidizer segments linked via chemical bond. Common examples of molecular explosives are TNT, RDX, and HMX. The chemical structure of these three molecular explosives is found in Annex-A. Molecular explosives are therefore unlike other types of explosives, such as emulsion explosives or composite explosives where, although the fuel and oxidizer are in relatively close proximity to each other, they are not linked via chemical bond. Molecular explosive type was screened for incorporation into the insensitive energetic design matrix as outlined in Figure 2.3-1.

As a result of this analysis, from theoretical insensitivity, performance, and cost standpoints, it was determined that the only well characterized, economically attractive, insensitive, high performance explosive which was readily available at the time was nitroguanidine (NQ). Other low sensitivity, high performance explosives existed, but their cost and availability were not comparable to NQ. Tri-Amino Tri-Nitro Benzene (TATB), for example, while highly insensitive has a cost of » ¥7700/kg.

NQ Availability and Selection Rational

Four crystalline configurations of NQ were available at the time this research was being conducted from domestic and international producers. Figure 2.4-2 details the production differences of these four crystalline types. Low Bulk Density Nitroguanidine (LBDNQ), has a very high length to diameter (L/D) ratio. The typical diameter is approximately 5m however, the length can exceed 100m (Figure 2.4-3). The LBDNQ is very fibrous with a consistency of cotton and occasionally, the needles are hollow. The bulk density of the LBDNQ is » 0.17g/cm3. The LBDNQ, although inexpensive, is processable only in small quantities (<6%). Additionally, due to the potential of entrained air in the hollow needles, the potential for “hot spot” formation exists which could make the energetic material quite sensitive.

By dissolving LBDNQ in a solution of water and methyl cellulose, followed by re-crystallization, a much larger (»150m – 300m) and more processable crystalline form of NQ is produced. This material is referred to as “Cubical Nitroguanidine” (CNQ) or “Un-pulverized Nitroguanidine” with a bulk density of » 0.9g/c m3. (Figure 2.4-4)

CNQ is subsequently pulverized to a particle size of » 40m-120m and after this process is termed “High Bulk Density Nitroguanidine” (HBDNQ) or “Pulverized Nitroguanidine” (PNQ). This process increases the bulk density of the NQ to a bulk density of »0.4g/cm3 for HBDNQ. Depending on the manufacturer, the particle sizes of HBDNQ vary.

Figure 2.4-5 shows PNQ which was ground in plant and Figure 2.4-6 show PNQ which was ground at a facility in Md.

The fourth crystalline form of NQ is termed “Spherical Nitroguanidine” (SNQ) (Figure 2.4-7). This material is manufactured in a manner similar to CNQ, however, the re-crystallization solvent is an organic solvent rather than water.

~ Dr. Theodore Sheldon Sumrall

Theodore Sheldon Sumrall is the Owner, President and Chief Scientist of Institute for Energy Independence.

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