Sunday, December 17, 2017

so, talking about patents and not referring machinery, is a little bit useless


Nano bead mill for repeatable dispersions with high power input

The nano bead mill DISPERMAT® SL-nano is a closed, horizontally operating nano bead mill with a high power input and extremely low clearance volume for circulation and pass procedure. The nano bead mill can be used for wet grinding in laboratory, techniques and the production.


Distinguishing marks of the nano bead mill:

  • High grinding stock production due to pneumatic press out system
  • Extremely small milling beads from 0.1 – 0.3 mm

again to surgical assassinations , and MEMs explosive : "According to the present invention, a micro-capsulated explosive composition can be easily obtained by micro-capsulating and fixing a dangerous explosive, and therefore the micro-capsulated explosive composition is an epoch-making explosive composition.."

As the explosive liquid compounds to be used for the production of micro-capsules of the present invention, mention may be made of glycerine trinitrate, glycerine dinitrate, ethylene glycol dinitrate, diethylene glycol dinitrate, triethylene glycol dinitrate, trimethylene glycol dinitrate, diglycerine tetranitrate, monochlorohydrin dinitrate, acetylglycerine dinitrate, 1,2,3-butanetriol trinitrate, 2-nitro-2-oxymethyl-1,3-propanediol trinitrate, 2-methyl-2-oxymethyl-1,3-propanediol trinitrate, nitrobenzene, tetranitromethane and the like, and mixtures thereof.
Further, gelatinized products of the above described explosive liquid compounds with gelatinizing agents, such as nitrocellulose and the like, for example, gelatinized products obtained by absorbing glycerine trinitrate, glycerine dinitrate, ethylene glycol dinitrate and the like in nitrocellulose can be used for the production of micro-capsules of the present invention.
As the high molecular weight compounds to be used for the production of micro-capsules of the present invention, mention may be made of thermosetting resins, such as polyurethane, polyurea, epoxy resin and the like, and thermoplastic resins, such as polystyrene, polyvinyl alcohol and the like.
The micro-capsules of the present invention are produced in the following manner. An explosive liquid compound is dispersed in water together with methylcellulose, a surfactant and the like, monomer of a high molecular weight compound, which forms the capsule wall, is added to the dispersed system, and, if necessary, a polymerization initiator or a reactive monomer is added thereto, and the resulting mixture is subjected to a polymerization reaction.
According to the above described method, it is possible to produce micro-capsules containing an explosive liquid compound in an amount as large as about 80-95% by weight.

Saturday, December 16, 2017

wlcome ! making a highly impact insensi- tive form of HMX called Alpha HMX - having an average particle size of 5 microns "HMX, which is known as l,3,5,7-tetranitro-l,3,5,7- tetraazacyclooctane, is the most powerful non-atomic 25 explosive in military use...The special insensitivity of this HMX is due to several factors, each of which must be held in tight tolerance. The particle size must be kept to about 1 to about 5 micron in range, the polymorph must be alpha, and the purity must be very high. To obtain the right poly- morph the amount of nitric acid used must be carefully controlled as too high or too low a dilution could cause the formation of gamma HMX..."

SUMMARY OF INVENTION 

65 

It is an object of this invention to provide an im- 
proved process of making HMX which provides both 
high power, and extreme insensitivity, at a price which 



The special insensitivity of this HMX is due to several 
factors, each of which must be held in tight tolerance. 
The particle size must be kept to about 1 to about 5 
micron in range, the polymorph must be alpha, and the 
purity must be very high. To obtain the right poly- 
morph the amount of nitric acid used must be carefully 
controlled as too high or too low a dilution could cause 
the formation of gamma HMX. Further, the tempera- 
ture of the reaction must be kept as close to room tem- 
perature as possible because if the temperature rises 
above 45 degrees Centigrade, the product again ob- 
tained is gamma HMX, instead of alpha HMX, the de- 
sired product. To obtain the right size, the product must 
be precipitated with great agitation in the manner de- 
scribed with a high speed mixing turbine at about 15,000 
RPM. The purity of the product must be upgraded 
using the solid phase up-grading techniques hereinafter 
described. Failure to follow any and all of the steps in 
the procedure, may seriously compromise, if not pre- 
vent the establishment of the special property of insensi- 
tivity to this alpha HMX material. 

EXAMPLE 1 

Nitration of TAT with a mixture of nitric acid and 
phosphorous pentoxide. 

250 grams, within the effective range of 200 to 300 
grams, of 98% nitric acid were introduced into a 500 ml. 
beaker, provided with a thermometer, and a magnetic 
stirring bar. 70 grams of phosphorous pentoxide were 
then added in portions over a 30 minute period. The 
addition was made with stirring via the magnetic stir- 
ring bar and the rate of addition of the phosphorous 
pentoxide was dictated by the temperature of the reac- 
tion mixture, which was not permitted to rise above 35 
degrees Centigrade. The reaction mixture was allowed 
to stir covered by a piece of aluminum foil until the 
temperature fell to room temperature. 50 grams of TAT 
were then added in about 4 equal portions at such a rate 
that the temperature was prevented from rising above 
40 degrees Centigrade. The reaction mixture was al- 
lowed to fall to room temperature, and the stirring bar 
was removed when all signs of any exothermic action 
had subsided. The beaker was covered by aluminum foil 
and allowed to set undisturbed for 16 hours at room 
temperature. During this time the entire reaction mix- 
ture sets-up to a cream cheese like consistency. 

The reaction mixture is discharged directly into the 
vortex of a room temperature water bath stirred by an 
L-TEC air turbine mixed, (see U.S. Pat. No. 4,424,677), 
specifically designed for very high speed mixing and 





dispersing. The water acts to brake the reaction com- 



4 



plex, and precipitates the alpha HMX, guaranteeing the 
formation of extremely small particles (crystals). The 
solid crude alpha is filtered, and washed with as much 
cold water as necessary to reach a constant of 7 ph. 
(This water should be maintained between 10 to 35 
degrees Centigrade to prevent any digestion of the size 
of the crystals. The filtered but damp cake is then dis- 
persed in 6 to 8 times its mass of agitated boiling water. 
The total washing time should not exceed 2 minutes in 
order to prevent size enhancement via digestion. The 
washed crude HMX, which should have no odor, is 



METHOD B 

The quantities and methods as in Example 1 above, 
however, a water proof container is employed and the 
mixture is placed in a constant temperature bath at 40 
degrees centigrade. The thickness of the paste in the 
container is limited so as to permit attainment of bath 
temperature throughout the mixture in a reasonable 
period of time. If necessary the mixture may be stirred 
mechanically. Under these conditions the upgrading 
time is reduced to approximately 4 hours. 



then filtered hot, and rinsed with cold water. This cur- 



METHOD C 



tails crystal digestion before being thoroughly dried. 
The drying may be simple air drying, or vacuum drying 
at a temperature near 50 degrees Centigrade. 

The still crude HMX must now be up-graded in pu- 
rity before use. This is accomplished by anyone of the 
following methods. 

PART 2 



The same quantities were used as set forth in Example 
1 however, the mixture is fed through a heated screw 
mixer or feeder for rapid mixing and temperature equili- 
bration. The temperature may be adjusted upwards to 
the 70 degree region reducing the reaction time to a 
matter of minutes. 

RESULTS 



METHOD A 

Purification of the contaminated HMX produced above 
by trituration with a nitric acid/phosphorous pentoxide 
mixture. 

100 grams of the contaminated HMX are added por- 
tion wise to 100 grams of nitric acid (about 70 ml.), 
within the effective range 80 to 120 grams, containing 
12.5 grams, which is within effective range 10 to 14 30 
grams, of phosphorous pentoxide. The container may 
be a simple beaker which may be covered with alumi- 
num foil. The quantity of nitric acid used here may be 
increased (not above 1 30 grams) for easier mixing of the 
mixture. The quantity used here has been found to be 35 
given about as thick a mixture as is practical. The quan- 
tity of phosphorous pentoxide may be reduced or in- 
creased depending for the greater part upon the amount 
of water originally present in the nitric acid and the 
amount of SEX present in the sample. The quantities 40 
used here have been found to work well over a very 
wide range of sample purities with initial melting points 
as low as 230 degrees centigrade. The phosphorous 
pentoxide should be fully dissolved and contain no solid 
particles. The nitric acid may be prepared ahead of time 45 
and kept as a stock solution. The HMX must be free of 
DANNO (l,5-diacetyloctahydro-3-nitro-7-nitroso- 
1,3,5,7-tetraazocine), since contamination with this 



The impact values obtained via the “ERL, Type 12 
Impact Tester” using a 2 and one half kilogram mass, 
demonstrated values 5 to 10 times greater than normally 
achievable with “Class 5 Beta HMX”, and kinetic en- 
ergy values 10 to 20 times greater than normal, As the 
following actual data indicates 



DROP 


Initiation y = yes, n = no 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


100 cm drop 


n 


150 cm drop 


n 


150 cm drop 


n 


150 cm drop 


y 


150 cm drop 


n 


150 cm drop 


n 


150 cm drop 


y 


150 cm drop 


n 


150 cm drop 


y 


150 cm drop 


n 


1 50 cm drop 


y 



compound can cause dangerous fume-offs. The gradual 

addition of the HMX to the nitric acid solution is to 50 Do t0 tbe dam age being caused to the test apparatus 
facilitate the mixing as no exothermic action should by the lar 8 e amount of kinetic energy released from 

occur. The paste is left for about 16 hours at room tern- sucb S reat dro P heights it was decided to accept the 

perature, samples may be taken to determine comple- 50% initiation value as being somewhere above 150 cm. 

tion of the reaction. Reactions have been intentionally ANAT Y

Friday, December 15, 2017

Let's begin with what's beeing worrying nuclear non proliferation people

Magnetized Cylindrial Targets for Heavy Ion Fusion

Cylindrical targets are promising as an alternative approach to heavy ion fusion (HIF)[1], as well as for basic science-oriented experiments in the near future [2]. In my PhD thesis (available as download), I have investigated basic properties of such targets. In difference to spherical heavy ion fusion targets, the cylindrical targets can be driven directly by a single ion beam, while axial magnetic fields (for heat insulation) can be applied to the targets prior to  implosions. In cylindrical targets,  the magnetic field geometry is consistent with the target; this is the main difference to other approaches to magnetized target fusion [3].

 Magnetized Cylindrical Target 

Figure: Schematic view of a magnetized cylindrical target. The target consists of a metallic tube filled with fuel plasma at low density. An axial magnetic field ( indicated by B) is applied externally before the implosion. The driving ion beam then heats the outer part of of the hollow cylinder; it expands radially and drives the inner part of the tube (pusher) towards the axis, as indicated by arrows. A typical size of the targets is approximately 1-3mm in radius and 10-30mm in length.

The most prominent features of magnetized cylindrical fusion targets are:
  • ignition at reduced fuel \rhor, 
  • relaxed demands on the driver pulse duration and power,  
  • total energies comparable to standard ICF
Targets operate in the hot-spot ignition mode: a fuel reservoir is ignited from a small spark, high gain relies on the propagation of a burn wave along the cylinder axis. Due to the absence of shock heating during implosions, one has to start from high fuel temperatures (T\simeq100 eV) brought into the target from outside; this is essentially the scheme of injected  entropy as suggested by Caruso et al. [4]Heavy ion beams planned for the near future at GSI and  ITEP may allow implosion experiments at pulse energies below 100kJ. Magnetization effects would manifest in enhanced peak fuel temperatures and corresponding DD fusion neutron yields. To prevent rapid diffusive loss of the magnetic flux, one has to fulfill certain conditions on the initial fuel temperature and the product of implosion velocity and fuel radius. Detailed results can be found in MPQ Report 261. 

References:

[1] R.Ramis, J.Honrubia and J.Meyer-ter-Vehn, Hohlraum targets for HIDIF. In  C.Labaune, W.Hogan and K.Tanaka (Eds)
Inertial Fusion Sciences and Applications, p.88, Elsevier, Paris (1988)
[2] M.M. Basko, Magnetized implosions driven by intense ion beams, Physics of Plasmas 7, 4579 (2000)
[3] Kirkpatrick et al, Magnetized Target Fusion: An Overview, Fusion Technology 27, 201 (1995)
[4] A.Caruso and C.Strangio, The injected entropy approach for the ignition and high targets by heavy ion beams or incoherent x-ray pulses, in C.Labaune, WHogan and K.Tanaka (Eds) ibid.


 --> go back to Andreas Kemp's home page

-->go back to the MPQ Theory home page

Thursday, December 14, 2017

And ....ops....I love this. Process and apparatus for producing ultrafine explosive particles

Process and apparatus for producing ultrafine explosive particles 
EP 0600881 B1
SAMENVATTING  (tekst uit WO1993004018A1)
A method and an improved eductor apparatus for producing ultrafine explosive particles is disclosed. The explosive particles, which when incorporated into a binder system, have the ability to propagate in thin sheets, and have very low impact sensitivity and very high propagation sensitivity. A stream of a solution of the explosive dissolved in a solvent is thoroughly mixed with a stream of an inert nonsolvent so as to obtain nonlaminar flow of the streams by applying pressure against the flow of the nonsolvent stream, to thereby diverge the stream as it contacts the explosive solution, and violently agitating the combined stream to rapidly precipitate the explosive particles from the solution in the form of generally spheroidal, ultrafine particles. The two streams are injected coaxially through continuous, concentric orifices of a nozzle into a mixing chamber. Preferably, the nonsolvent stream is injected centrally of the explosive solution stream. The explosive solution stream is injected downstream of and surrounds the nonsolvent solution stream for a substantial distance prior to being ejected into the mixing chamber.

Talking about , octahydro-1,3,5,7-tetranitro-1,3,5,7 tetrazocine, HMX, organic nitrate explosives, (the importance of organic...here) and the preparation of nano particles, for MEMS explosive...starts here

GIN-PFA Bidirectional Two-way Punch Pin Grinder Grinding Machine Punch Former Lathe Turning Tool




mark 21 nuclear bomb...can I carry this ? :)


Ordnance that will end major wars. Thank Israel Last night I found the patent for the new munitions that are winning the war in Syria. This ordnance combines a thermobaric or fuel-air explosive and a warhead for generating non-nuclear electromagnetic pulses (EMPs).


http://www.thomaswictor.com/ordnance-that-will-end-major-wars-thank-israel/

Launchable unit 
US 8434412 B2
RESUMO
A launchable unit including a warhead for generating non-nuclear electro magnetic pulses and a thermobaric warhead without dangerous fragments. The warheads in combination are arranged to operate in different modes dependent on target types and/or objectives with engagement controlled by the aiming and setting of the weapon by a gunner.

So, let's move on...you already understand that when they refer to "energetic" they are referring "fusion" , which means the detonation, provokes, a nucleic reaction as discovered on the atomic bomb. One of the most important explosives, is the consistent properties of nitrogen. Nitrogen-Rich High Explosives

The possibility of new high explosives based on nitrogen-rich tetrazole building blocks is discussed. The expected advantages include gaseous products, high heats of formation, high propulsive/expolosive power, high specific impulse, and high flame temperatures. In addition, these new explosives do not have the toxicity and environmental activity of currently used organo-nitro explosives. The synthesis and characteristics of a series of neutral tetrazole compounds are looked at as well as the neutral nitramine, dinitrobiuret.

of course, no se pasa nada compadres. So, what do I have here, another "energetic" explosive? Do I mean, a fantastic replacement of the nuclear bomb?

Explosive laser
US 3904985 A
RESUMO
A laser system wherein reaction products from the detonation of a condensed explosive expand to form a gaseous medium with low translational temperature but high vibration population. Thermal pumping of the upper laser level and de-excitation of the lower laser level occur during the expansion, resulting in a population inversion. The expansion may be free or through a nozzle as in a gas-dynamic configuration. In one preferred embodiment, the explosive is such that its reaction products are CO2 and other species that are beneficial or at least benign to CO2 lasing.

Portugal Ukraine Russia (mercenaires killed)

  https://sicnoticias.pt/especiais/guerra-russia-ucrania/2025-04-03-video-russia-diz-ter-abatido-mercenarios-portugueses-na-ucrania-755f2fec