GB1585083A - Method of treatment of cast high explosives - Google Patents
Method of treatment of cast high explosives Download PDFInfo
- Publication number
- GB1585083A GB1585083A GB443476A GB443476A GB1585083A GB 1585083 A GB1585083 A GB 1585083A GB 443476 A GB443476 A GB 443476A GB 443476 A GB443476 A GB 443476A GB 1585083 A GB1585083 A GB 1585083A
- Authority
- GB
- United Kingdom
- Prior art keywords
- explosive
- room temperature
- charge
- melted
- treatment
- 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.)
- Expired
Links
- 239000002360 explosive Substances 0.000 title claims description 43
- 238000000034 method Methods 0.000 title claims description 22
- 239000000470 constituent Substances 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 9
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical group [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 7
- 239000000155 melt Substances 0.000 claims description 7
- 238000002425 crystallisation Methods 0.000 claims description 5
- 230000008025 crystallization Effects 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 238000005336 cracking Methods 0.000 claims description 3
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- 239000000028 HMX Substances 0.000 claims description 2
- UATJOMSPNYCXIX-UHFFFAOYSA-N Trinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 UATJOMSPNYCXIX-UHFFFAOYSA-N 0.000 claims description 2
- 239000013078 crystal Substances 0.000 claims description 2
- 238000005474 detonation Methods 0.000 claims description 2
- UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 claims description 2
- 238000010583 slow cooling Methods 0.000 claims description 2
- 239000004429 Calibre Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B21/00—Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
- C06B21/0033—Shaping the mixture
- C06B21/005—By a process involving melting at least part of the ingredients
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heat Treatment Of Articles (AREA)
Description
(54) METHOD OF TREATMENT OF CAST HIGH EXPLOSIVES
We, MEssFRscHMlTT-BoLKow-BLoHM GESELLSCHAFT MIT BESCHRANKTER
HAFTUNG, of 8000 Munchen, German
Federal Republic, a company organised and existing under the laws of the German Federal
Republic do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:: This invention relates to a method treating cast high explosive substances which are prepared from a high proportion of at least one unmelted (solid) high explosive substance, particularly hexogen, in various grain sizes, and a smaller proportion of at least one melted explosive substance, particularly TNT, both explosive substances being heated and suspended and then poured into a mould, which may be an actual warhead casing. The solid explosive constituent can be compressed in the mould and the suspension subjected to pressure, after which the solid and the melted explosive constituent are cooled off to room temperature preferably in stages.
Reference is made to co-pending
Application 4433/76 (Serial No.1585082).
According to this invention there is provided a method of treating cast high explosives which have been prepared from a high proportion of at least one unmelted (solid) high explosive substance in various grain sizes, and a smaller proportion of at least one melted explosive substance both explosive constituents being heated and suspended and then immediately poured into a mould, which may be a warhead casing, after which the solid and the melted explosive constituent are cooled to room temperature, preferably in a number of stages, in which method the explosive mass, after the melt has solidified, that is after it has partly or completely cooled to room temperature, is re-heated to a temperature just above to the melting point of the explosive constituent melted in the production stage, the temperature being maintained for a time, after which the explosive mass is re-cooled to room temperature slowly to prevent cracking.
After solidification of the melt, therefore, the treatment of the explosive mass can be carried out either while the cooling process is in progress, so that the method of treatment according to the invention is integrated into the entire production process, or treatment may be effected after the moulded body has cooled down to room temperature, constituting an after-treatment. By after-treatment is meant that the treatment immediately follows the cooling but a complete warhead with charge can nevertheless undergo an after-treatment of this kind some considerable time after assembly, possibly even some years later and also repeatedly.
The following operations and times for the (after-) treatment according to the invention have been found preferable in the case of a 100 mm calibre warhead with a charge of hexagen and TNT. The explosive mass is heated from room temperature to 81 to 900 C, particularly to 850C with this heating period being 2 to 4 hours, particularly 3 hours; the constant after-treatment temperature is maintained for 0 to 1 hours, particularly lihour, the cooling period being 12 to 14 hours, particularly 13 hours, and the cooling can be carried out in stages and the temperature of 750C maintained for a certain period when reached, during which period the melt fully solidifies. This avoids stresses in the body of the charge.
This method of treatment ensures that the permissible heating temperature and the permissible time at this temperature which enables the maximum possible crystallization point to be obtained in the subsequent cooling of the melt can be maintained, that is the melt only needs to be liquified, immediately following which it can be slowly re-cooled.
The method of the invention can be applied in such a way that the explosive mass is melted a number of times in succession and as tests have shown in this the crystallization point is raised a few degrees centigrade each time. This is useful where, as a result of particularly unfavourable circumstances, the crystallization point has been very low at the actual production stage and has led to a very unfavourable finely crystalline structure.
The invention provides a means of subsequently increasing the crystallization point of an explosive melt as required, in order to obtain the desired structure with the necessary properties for the charge. The elongated
TNT crystals sought are intrinsically, and by reason of their firm adhesion to the adjacent hexogen grains, insensitive to the formation of further craks. The deliberate very slow cooling also enables internal stresses in the explosive moulded body to be avoided altogether.
Furthermore the method of treatment of the invention ensures that the explosive constituent to be melted will be more evenly distributed within the charge, so that homogeneity is once again increased. This improves the efficiency of the charge, owing to the evenness of the detonation wave front and the satisfactory formation of an armour piercing spike from a liner of a hollow charge. The mechanical strength of the charge is also increased by about 10%.
Octogen can be used in place of hexogen and trinitro-benzene in place of TNT.
WHAT WE CLAIM IS:
1. A method of treating cast high explosives which are prepared from a high proportion of at least one unmelted (solid) high explosive substance in various grain sizes and a smaller proportion of at least one melted explosive substance, both explosive constituents being heated and suspended and then immediately poured into a mould which may be a warhead casing, after which the solid and the melted explosive constituent are cooled to room temperature,preferably in a number of stages, in which method the explosive mass, after the melt has solidified, that is after it has partly or completely cooled to room temperature, is re-heated to a temperature just above the melting point of the explosive constituent melted in the production stage, the temperature being maintained for a time after which the explosive mass is re-cooled to room temperature slowly to avoid cracking.
2. A method in accordance with claim 1, wherein the explosive body comprises hexogen and TNT and is re-heRted from room temperature to 81 to 90 C, preferably to 850C, the heating period being 2 to 4 hours, preferably 3 hours, the constant after-treatment temperature being maintained for 0 to 1 hour, preferably 1E hour, while the period of cooling to room temperature amounts to 12 to 14 hours preferably 13 hours, the cooling being effected preferably in stages.
3. A method according to claim 1 comprising repeated applications of the treatment steps set forth in the preceding claims.
4. A method in accordance with claim 1 or 2 or 3, carried out substantially as herein described.
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (4)
1. A method of treating cast high explosives which are prepared from a high proportion of at least one unmelted (solid) high explosive substance in various grain sizes and a smaller proportion of at least one melted explosive substance, both explosive constituents being heated and suspended and then immediately poured into a mould which may be a warhead casing, after which the solid and the melted explosive constituent are cooled to room temperature,preferably in a number of stages, in which method the explosive mass, after the melt has solidified, that is after it has partly or completely cooled to room temperature, is re-heated to a temperature just above the melting point of the explosive constituent melted in the production stage, the temperature being maintained for a time after which the explosive mass is re-cooled to room temperature slowly to avoid cracking.
2. A method in accordance with claim 1, wherein the explosive body comprises hexogen and TNT and is re-heRted from room temperature to 81 to 90 C, preferably to 850C, the heating period being 2 to 4 hours, preferably 3 hours, the constant after-treatment temperature being maintained for 0 to 1 hour, preferably 1E hour, while the period of cooling to room temperature amounts to 12 to 14 hours preferably 13 hours, the cooling being effected preferably in stages.
3. A method according to claim 1 comprising repeated applications of the treatment steps set forth in the preceding claims.
4. A method in accordance with claim 1 or 2 or 3, carried out substantially as herein described.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19752506885 DE2506885C1 (en) | 1975-02-19 | 1975-02-19 | Treatment of high explosive molded molded parts |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1585083A true GB1585083A (en) | 1981-02-25 |
Family
ID=5939160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB443476A Expired GB1585083A (en) | 1975-02-19 | 1976-02-04 | Method of treatment of cast high explosives |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE2506885C1 (en) |
GB (1) | GB1585083A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2795967C1 (en) * | 2022-09-07 | 2023-05-15 | Российская Федерация, от имени которой выступает Государственная корпорация по атомной энергии "Росатом" (Госкорпорация "Росатом") | Method for reducing the detonation critical section of secondary explosives |
-
1975
- 1975-02-19 DE DE19752506885 patent/DE2506885C1/en not_active Expired
-
1976
- 1976-02-04 GB GB443476A patent/GB1585083A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2795967C1 (en) * | 2022-09-07 | 2023-05-15 | Российская Федерация, от имени которой выступает Государственная корпорация по атомной энергии "Росатом" (Госкорпорация "Росатом") | Method for reducing the detonation critical section of secondary explosives |
Also Published As
Publication number | Publication date |
---|---|
DE2506885C1 (en) | 1980-10-02 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
CSNS | Application of which complete specification have been accepted and published, but patent is not sealed |