This image shows what appears to be a fighter jet firing a missile at Malaysia Airlines Flight MH17 from a distance of about 700 meters (2,300 feet). The Boeing aircraft is about 209 feet long with a wingspan of 200 feet. The fighter jet is about 11 times the length of the Boeing away.

http://www.bollyn.com/

ACID TRIP - Binaural beats - DIGITAL DRUGS: EXTREME BRAIN WAVE EFFECTS

PRISON BREAK

MELT IRON : hydrofluoric acid (DO NOT SMELL OR TOUCH THE LIQUID WITHOUT PROTECTION) 

BATERRIES AND SALT TO MAKE HIDROGENE GAS

EASY NAPALM

Materials that you will need:
Empty jar (I used a pickle jar, I also already have a little bit left from my last batch)
Stick (spoon, straw, etc.)
Citronella oil (Lighter's fluid will also work)  oil is "Lemon scented"

Combustible base

  

• Fuel and oxidizer mixtures: Charcoal or wood powder forms the fuel for the combustion. Gums such as Gum Arabic or Gum Tragacanth are used to bind the mixture together while an oxidizer such as sodium nitrate or potassium nitrate sustains the burning of the incense. Fragrant materials are combined into the base prior to formation as in the case of powdered incense materials or after formation as in the case of essential oils. The formula for the charcoal-based incense is superficially similar to black powder, though it lacks the sulfur. (SULFUR : ON CLEANING CELLS OF QUIMIOTERAPHY PILLS)

Chronic Haze Lemon Incense 500mgs 

Powdered Sugar

.1. Take the powdered sugar and pour about a cup into the jar. 

2. Now take the oil and pour about a 3/4 cup into the jar. 

3. Mix them together, add more oil or sugar as needed until you get a mixture that resembles whipped cream or butter. 

That's all there is to it

http://www.instructables.com/id/Easy-to-make-and-safer-to-breathe-Napalm/

How to Make napalm with gas and Styrofoam

Before you can make napalm, you first need a container for it, so get a nice metal container since the napalm will eat through plastic. See how to make this fun flammable substance.

You'll need a can opener, napalm container (soda can), gas, and Styrofoam. Note: this is a substance known as napalm-B, but its lacking benzene.

Warning: Napalm is very dangerous! Water boils at 100 degrees Celsius, napalm will burn anywhere from 800 to 1200 degrees Celsius.

http://explosives.wonderhowto.com/how-to/make-napalm-with-gas-and-styrofoam-271333/

Transmutations of Mercury to Gold

Transmutations of Mercury to Gold

(1) H. Nagaoka ~ A. Miethe ~ H. Stammreich ~ (2) F. Tausend ~ (3) References

(1) H. Nagaoka~ A. Miethe ~ H. Stammreich

In March 1924, Prof. Hantaro Nagaoka, et al.(Tokyo Imperial University), described their studies "on the isotopes of mercury and bismuth revealed in the satellites of their spectral lines" ¾ gold in particular. In May 1925, they reported some of the technical details: Nagaoka and his co-workers discharged about 15 x 10⁴ volts/cm for 4 hours between tungsten and mercury terminal under a dielectric layer of paraffin oil. They used the Purple of Cassius test to detect Au in the viscous residue of C, Hg, etc. The black mass was purified in vacuo, then by combustion with oxygen and extraction with HCl to yield Au, either in aqua regia solution or as ruby-red spots in the glassware. Microscopic films of Au were found on occasion. (19, 22)

Nagaoka stated that when a discharge was passed through drops of Hg falling between iron electrodes, the formation of silver and other elements was observed. Another run of a Hg lamp for more than 200 hours at 226 volts produced a milligram of gold, plus some platinum. He noted that, "In order to be sure of transmutation, repeated purification of Hg by distilling in vacuum at temperatures below 200^o C is essential."

Considerations of the satellites of the spectral lines of Hg led Nagaoka to the conclusion that a proton is "slightly detached" from the nucleus of Hg, and it can be removed:

If the above assumption as to the Hg nucleus is valid, we can perhaps realize the dream of alchemists by striking out a hydrogen-proton from the nucleus by a -rays, or by some other powerful methods of disruption [to produce Au from Hg]. (21, 26)

At about the same time, Professor Adolf Miethe of the Photochemical Department at the Berlin Technical High School found that the mercury vapor lamps used as a source for ultra-violet rays ceased to work after a time because of a sooty deposit which formed in the quartz tubes. Miethe tested these deposits and detected gold. Subsequently, Dr. Miethe and Dr. Hans Stammreich were issued German Patent Specification #233,715 (8 May 1924) for "Improvements in or Relating to the Extraction of Precious Metals":

An electric arc is formed between mercury poles, in the same way as is done in mercury quartz lamps. With sufficient difference in potential, gold is then produced in the mercury. It is advisable to condense again the evaporated mercury. The quantity of gold produced depends, all other conditions being equal, on the quantity of current and also, among others, on the vapor pressure of the mercury or on the difference of potential in the arc. The difference of potential in the arc must therefore be sufficiently great. If it drops to excessively small amounts, the efficiency will be greatly reduced. If the difference of potential is increased, the quantity of gold formed will be considerably increased, beginning with a certain difference of potential. (12)

In July of 1924, Drs. Miethe and Stammreich announced that they had changed mercury into gold in a high-tension mercury vapor lamp. The experiment produced $1 of gold at a cost of $60,000, equivalent to over $2 million (gold then sold for $330/lb). Miethe used a potential of 170 volts applied for 20-200 hours. The lamp consumed 400-2,000 watts. A minimum potential difference is necessary. The yield of gold was minute: 0.1-0.01 mg. The mercury and the electrodes were analyzed and determined to be free of gold before the experiments. Miethe was not able to attempt to prove the production of a or b rays, hydrogen or helium. (22)

O. Honigschmid and E. Zintl determined the atomic weight of Miethe's mercuric Au, using potentiometric titration of auric salt with TiCl₂. It was found to be 197.26, which is heavier than ordinary Au (197.2). They emphasized the need for a mass spectrographic analysis. (10)

Frederick Soddy suggested that such a change might be effected by attaching an electron to the mercury nucleus:

Consider the collision of high-speed electrons with mercury atoms. A small proportion of these electrons must be directed upon the nucleus. If they possess sufficient energy to penetrate the external levels of electrons in the mercury atom, they must reach the positively charged nucleus and be captured by it. Since the loss of an electron (as a b -ray) by the nucleus of an element results in the atomic number of the element in question being increased by one, the gain of an electron by an atomic nucleus must result in the diminution of the atomic number by one. This is quite general. In the case of an isotope of mercury of atomic number 80, the product will be an isotope of gold of atomic number 79. Upon existing knowledge it is simply a question of (1) the potential sufficient to drive the electron through the outer levels of electrons surrounding the mercury nucleus until it comes within the sphere of attraction of the powerfully charged nucleus; (2) whether the exceedingly small fraction of direct collisions with the nucleus that is to be anticipated will be sufficient to enable the gold produced to be detected.
As regards the first, it may be expected that the repulsion of the external shell of mercury electrons will diminish rather than prevent altogether the chance of the radiant electron reaching the nucleus; for once the shell is penetrated, the resultant force on the radiant electron must be on the average an attraction... The chemical detection of the gold produced would probably be the more formidable experimental difficulty. (30)

A.S. Russell offered this opinion:

The experiments on the transformation of Hg into Au suggest the possibility of the transformation of a nucleus into that of the element next below it by the absorption of one electron when both nuclei are stable. This occurs most obviously as an isobare. The possibility of the existence of two isobares of odd mass-number, Tl 205 and Au 199, among non-radioactive elements may be inferred from experimental work... Aston has shown the existence of the Hg isotope 199... This type of transformation may occur in the two pairs of elements Pb and Tl, Hg and Au... The masses of the Tl and Au produced are 205 and 199 respectively.

Aston advanced strong arguments against the probability of the alleged Hg-Au transmutation. Conceivably it could be effected by the addition of an electron to the nucleus of Hg, or by removing a proton from it, but the chance of an electron hitting a nucleus is extremely remote, and its weight would not make a significant contribution. Theoretically, a Hg isotope of atomic weight 197 could absorb an electron and produce common Au, but none of the six Hg isotopes (198, 199, 201, 202, 204, 209) identified by Aston have that weight. According to Aston, the removal of a proton from the nucleus by Miethe's method is untenable: "The forces employed are ludicruously inadequate." (1, 22)

The process can be shown as:

Hg - a - q = Au

At. wt. 201 - 4 = 197

80 - 2 + 1 = 79 , or:

Hg - 4H - 3q = Au

At. wt. 201 - 4 = 197

80 - 4 + 3 = 79

In December 1924, the journal Scientific American announced that it would arrange for a comprehensive and exact test of the Miethe experiment. It was conducted at New York University by Prof. H.H. Sheldon and Roger Estey. They used a quartz lamp which contained no gold, and pure tungsten wires were sealed into the quartz to provide electrical contacts. The mercury was tested for purity. Three runs were made lasting from 30-50 hours each, at about 170 volts/13 amperes. The mercury was removed and tested:

In no instance was any trace of gold detected... According to Prof. Miethe's reports, taken in connection with the theoretical interpretation of Prof. Soddy, this experiment should have produced a substantial quantity of gold; at least ten times as much as could easily have been detected by the analytical methods used. The negative result of the three experiments established, therefore, a strong probability that the transmutation announced by Prof. Miethe could not be confirmed. (27)

The researchers procured from the manufacturers in Germany an replica of the lamp used by Miethe, and repeated the exact technique described by him. The final run lasted 172 hours, at 165-174 volts/12 amps, depending upon the temperature of the lamp:

After the run the most careful analytical tests failed to show any trace whatsoever of the precious metal. It is necessary to conclude, therefore, that the experiment described by Prof. Miethe does not always result in the transmutation of mercury atoms into gold atoms. The experiments recorded by Prof. Miethe and our on experiments, conducted as far as humanly possible in exactly the method described by Prof. Miethe, are entirely discordant with each other.
It would be improper to assert on the basis of these results alone, that Prof. Miethe's experiments have been proved to be definitely wrong. All that is proper to say is that a careful, competent, and long continued effort to confirm the German results has resulted in an entire failure to do so.

The Scientific American offered a suggestion:

One very vital possibility of mistake in experiments of this character lies in the accidental presence of a small impurity of gold in the mercury employed... It is at least possible that such was the case... Perhaps it will be discovered that some minor and unnoticed detail in the arrangements or in the conduct of the experiment was really responsible for a successful transmutation in Prof. Miethe's case... We must confess, however, that we do not believe that this will prove to be the case. On the basis of all the evidence now available, including the experiments of Dr. Sheldon and Mr. Estey... it is our belief that a transmutation of mercury atoms into gold atoms does not occur and will not occur under the conditions which have been described by Prof. Miethe.
It is to be freely admitted, of course, that a transmutation of mercury atoms into gold atoms is a theoretical possibility. The internal structures of the two atoms are similar. The removal of one unit of positive electric charge from the nucleus of a mercury atom, or the insertion of one additional electron into this atomic nucleus would result, it is believed, in the conversion of the mercury atom into an atom indistinguishable from the ordinary atoms of gold. Quite aside from the failure to confirm the results of Prof. Miethe, it remains entirely possible that one of these changes of atomic structure can be accomplished by some physical or chemical method yet to be discovered...
Gold can be extracted from mercury, but mercury cannot be transmuted into gold.

Sheldon and Estey also commented:

The suggested explanation of a change of the number of electrons in the nucleus changing mercury to gold seems good in theory, but incredible in fact, for the potential drop per mean free path of a Hg molecule is only about 0.1 volt in these arcs. (28)

Scientific American published another report of "More Mercuric Gold from Germany" in April 1926, announcing that a 10,000-fold increase in yield had been obtained in the production of mercuric-gold process. In his first experiments, Miethe found 1 part Au per 100 million parts Hg. The Siemens Works in Berlin bombarded Hg with electrons in extremely high vacuum, and obtained 100 mg Au from 1 kg of Hg. (27)

Siemens & Halske Akt.-Ges. registered their German Patent Specification (#243,670) in June 1925 for "Treating Mercury" with spark discharges, cathode rays, and canal rays. The difference of potential could be between 100-150,000 volts; capacitance was adjustable. Paraffin, ether, or carbon tetrachloride were used as dielectrics. (29)

Other researchers were not so optimistic. Erich Tiede, et al., reported "The transmutation of Hg into Au is considered theoretically possible but all experiments carried out under strict control of the original Hg proved to be failures. When the Hg, which was purified according to Miethe and Stammreich, was distilled in an all-glass apparatus similar to the one used by Bronsted and von Hevesey to separate the isotopes of Hg, it showed still up to 10^-9% Au. Optical detection is not sufficiently accurate, so they considered it necessary to melt the Au granule, which still held Hg, and weigh it on a microbalance. (32)

Milan Garrett (Clarendon Lab, Oxford) published completely negative results of his repeated attempts to reproduce the Hg-Au transmutation experiment by several methods. Garrett also attempted to prepare indium from tin, and scandium from titanium by X-ray bombardment, also without success. (5)

Erich Tiede, et al., reported the negative results of their experiments:

Mercury distilled according to Miethe still had 0.3 mg Au per kg Hg. After two high-vacuum distillations, no more Au could be detected. With this preparation the experiments of Miethe were repeated in several forms; no resultant Au formation was observed in any case.

E. Duhme and A. Lotz confirmed this negative finding. Duhme and Lotz also conducted numerous experiments with the initial cooperation of Miethe and Stammreich. They used very large arcs carrying 10 kw at 40 kv/800 A/cm² through Hg vapor. Gold was found in some instances, such as when a sufficiently powerful current was passed between electrodes dipped in mercury, but those experiments were rejected because there had been too much contact with foreign metals. They found that Au will escape detection if certain impurities are present, producing an inhomogenous distribution of Au which becomes detectable only after the arc treatment has coagulated it. (3, 4, 31)

Prof. Fritz Haber, et al., made careful attempts to repeat the work of Nagaoka and Miethe. Mercury in which no Au could be detected was subjected to six different treatments, but no Au was formed. In some cases, Au was found, but only in amounts smaller than what could have come from the materials, or from contamination. Nor could the yield be increased at will. The applied treatments were made with liquid and solid dielectrics with high-tension discharges, arcs in low, normal and high pressures, and high-vacuum electron bombardments.

The extraordinary sensitivity of their detection methods was exemplified by the instance of a co-worker who suddenly found traces of gold in some material he was analyzing. No one else could detect Au in the other samples. It was found that the chemist habitually removed his gold frame eyeglasses before making an observation; on this occasion, he had removed the glasses and then picked up a strip of ultra-pure lead to perform an analysis. Another incident occurred when a lab worker was melting some Au; soon afterwards, another worker in the next room found Au in material which previously had none in it. The authors proved "merely that no method has yet been published whereby analytically detectable amounts of Au can be formed in Hg." (8)

Scientific American (April 1926) reported on a recent meeting of the German Chemical Society, at which positive results were announced:

Prof. Haber, who previously cherished the greatest doubt as to the accuracy of the experiments, congratulated Prof. Miethe and related... that he himself could confirm the results by repetition of the experiment.

Haber apparently, however, made the comment before he had completed his analyses of the electrodes, etc, and determined them to be the source of the Au.

Most of the criticism of Miethe, Stammreich, and Nagaoka's experimental work focused on the questionable purity of the mercury they used. Their Hg had been purified by distillation and by dissolving it in nitric acid (1:4) and fusing the residue with borax (0.1 gr). The resulting bead of Au, if any, was examined under the microscope. Usually they distilled the Hg twice, but in some cases as many as 15 times. Other researchers showed that no matter how carefully or often Hg was distilled, Au could be detected.

Miethe and Stammreich showed that the formation of Au from Hg depends on the application of intermittent electrical discharges. No gold forms when Hg is exposed to direct current. They also described a Hg-turbine which allowed 2,000 breaks/minute with a potential of 110 volts; the current varied from 1-12 amps. The experiments showed a linear proportionality between the yield of Au and the product of wattage and time. The average yield of gold was 0.0004 mg/amp/hour. The production of Au was facilitated by high-pressure. When the discharge was passed between Hg poles in a paraffin dielectric, the gold was found dispersed along the line of discharge, but not in the Hg poles. (15)

A. Gaschler attempted to reverse the Miethe-Nagaoka experiment by treating gold with high-speed hydrogen nuclei. He assumed that one of them might penetrate deeply into the electron shells of Au, be held by the innermost shells as a "paranucleus", and form a "Tiefenverbindung". After 30 hours bombardment, the spectrum of the tube began to show Hg lines which steadily increased in intensity. Gaschler postulated that Hg is a gold hydrogen compound, similar to Manley's "Hg-Helide". (6, 7, 13)

The scientific community gave a fair and thorough review of the claims of Miethe, Stammreich and Nagaoka, who also skillfully managed the criticism. However, the entire issue was never definitively resolved. Therefore, these experiments ought to be repeated with modern equipment and analytical techniques.

(2) Franz Tausend

The German alchemist Franz Tausend began to produce gold from mercury in the 1920s. He began to work in association with General Ludendorff in 1925, and eventually produced artificial gold for the Nazis. He based his work on Quabbalistic principles, and developed a circular table of periodic elements based on musical frequencies. His life was documented inDer Goldmacher Franz Tausend (1929) by Dr. H. Schleff..

The ingredients of Tausend's formula are known to be: (Part 1) ¾ PbCl₂ (111 gr), KOH (60 gr) and (Part 2) ¾ K (76 gr), Na (55 gr) amalgamated with Hg (131 and 365 gr) melted under paraffin. Reaction of Part 1 (17.4 gr) with Part 2 (5.4 gr) yielded 5.4 gr Au.

Dr Schleff also listed other reagents used by Tausend, but their use is not clear: ammonium carbonate, lime, potassium nitrate, soda, borax, sulfuric acid, and potassium cyanide, oxalic acid, uranyl nitrate, aluminum chloride, potassium arsenide, lead sulfate, tin oxide, silica, and asbestos.

(3) References

1. Aston: Nature (19 December 1925)
2. Davies, A.C., & Horton, Frank: Nature 117: 152 (1926); "The Transmutation of Elements"
3. Duhme, E. & Lotz, A.: Wissenschaft Veroffentlich Siemens Konzern 5: 128-151 (1926
4. Duhme, E. & Lotz, A.: Chem. Ber. Deutsch. Ges. 59: 1649-1651 (1926);Chem. Abstr 20: 3264 (1926)
5. Garrett, Milan W.: Nature 118 (#2959), 17 July 1926; "Transmutation Experiments"
6. Gaschler, A.: Zeit. Elektrochem. 32: 186-187 (1926): "Transmutation of Au into Hg"
7. Gaschler, A.: Scientific American (August 1926)
8. Haber, Fritz, et al.: Z. Anorg Allg. Chem. 153: 153-183 (1926); Chem. Abstr. 20: 2614; ibid., 19: 3443
9. Haber. F.: Nature (29 May 1926).
10. Honigschmid, O. & Zintl, E.: Naturwissenschaften 13: 644 (1925); "The Atomic Weight of Au..."
11. Honigschmid, O.: Zeit. Anorg. Allgem. Chem. 147: 262-264 (1925).
12. Literary Digest (14 March 1925); "Attempts at Artificial Au"; ibid., (12 December 1925); "Negative Evidence in the Hg-Au Case"; ibid., (6 February 1926).
13. Manley, J.J.: Nature 114: 861 91924); ibid., 115: 337 (1925)
14. Miethe, Adolf: Naturwiss. (July 18, 1924) ; ibid., 13: 635-637 (1925); "Transmutation of Hg into Au"
15. Miethe, A. & Stammreich, H.: Zeit. Anorg. Allgem. Chem. 150: 350-354 (1926)
16. Miethe, A. & Stammreich, H. German Patent Specification #233,715 [Class 82 (i).], (8 May 1924).
17. Miethe, A. & Stammreich, H.: French Patent 598,140 (1925)
18. Nagaoka, H.: Chem. Abstracts 19: 3209 (1925)
19. Nagaoka, H.: Naturwiss. 13: 682-684 (1925); "Transmutation of Hg into Au"; ibid., 14: 85 (1926)
20. Nagaoka, H.: Nature (July 1925).
21. Nagaoka, H.: Journal de Physique et la Radium 6: 209 (1925)
22. Nature 114: 197 ( 9 August 1924); ibid., 117 (#2952): 758-760 (29 May 1926
23. Piutti, Arnaldo, & Boggio-Lera, Enrico: Giorn. chim. ind. applicata 8: 59-61 (1925
24. Reisenfeld, E.H., & Haase, W.: Chem. Ber. Deutsch. Ges. 59: 1625-1629 (1926)
25. Russell, A.S.: Nature 116: 312 (1925); "Transformation of Hg into Au"
26. Science 61 (#1581), 17 April 1925; "The Transmutation of Hg"
27. Sci. Amer. (Dec. 1924); ibid., p. 256 (Nov. 1925); ibid., p. 90 (17 April 1926); ibid., 138: 208 (1928)
28. Sheldon, Horton & Estey, Roger S.: Phys. Review 27 (2): 515 (1926)
29. Siemens & Halske Akt.-Ges.: German Patent Spec. #243,670 [Cl. 39(i) & 82 (i)]; "Treating Hg"
30. Soddy, Frederick: Nature 114: 244 (16 August 1924); "The Reported Transmutation of Hg into Au"
31. Tiede, Erich, et al.: Naturwiss. 13: 745-746 (1925); "Formation of Au from Hg"

32. Tiede, E., et al.: Chem. Ber. Deutsch. Ges. 59: 1629-1641 (1926); "The Formation of Au from Hg...

http://www.levity.com/alchemy/nelson2_7.html

Gold was synthesized from mercury by neutron bombardment in 1941, but the isotopes of gold produced were all radioactive.[3] In 1924, a Japanese physicist, Hantaro Nagaoka, accomplished the same feat.[4] 

Gold can currently be manufactured in a nuclear reactor by irradiation either of platinum or mercury. 

Only the mercury isotope 196Hg, which occurs with a frequency of 0.15% in natural mercury, can be converted to gold by neutron capture, and following electron capture-decay into 197Au with slow neutrons. Other mercury isotopes are converted when irradiated with slow neutrons into one another or formed mercury isotopes, which beta decay into thallium. 

Using fast neutrons, the mercury isotope 198Hg, which composes 9.97% of natural mercury, can be converted by splitting off a neutron and becoming 197Hg, which then disintegrates to stable gold. This reaction, however, possesses a smaller activation cross-section and is feasible only with un-moderated reactors. 

It is also possible to eject several neutrons with very high energy into the other mercury isotopes in order to form 197Hg. However such high-energy neutrons can be produced only by particle accelerators

How to get hydrogen gas from water THE MOST BIG NIGHTMARE OF THE "SYSTEM"

When a mixture of calcium carbonate and magnesium is heated in a
current of hydrogen, a violent explosion occurs...
1. magnesium carbonate : chalk
2. calcium carbonate: tea leafs for diet tea

film-base photographic explosive + charcoal pills ´+ sulphur pills

so, let's make another BUM! mix! smile emoticon 
Cellulose nitrate is the plastic commonly used for film-base photographic...--- and ----The primary ingredient in nail polish is nitrocellulose (cellulose nitrate) cotton, a flammable and explosive ingredient also used in making dynamite.
Os rolos de filmes da Kodak deterioram-se e ficam com uma espécie de ferrugem e manchas transparentes e é assim que se torna um explosivo, ficando igualmente pegajosos, criando assim o nitrato de celulose; acontece que este material é incompatível, com as seguintes mix's : carvão e sulfur!!! ambos em comprimidos para a saúde, o carvão para tratar dos peidos das condensas e o sulfur orgâncio para limpar as células dos tratamentos da quimioterapia.

how to make a fully working papercraft gun

~


MAKE THE BULLET OUT OFF SOLDERING WIRE, BUT IT WILL HEAT THE CANNON AND ONLY ONE SHOT IS AVAILABLE

Homemade Single Shot pistol #1