Ionising radiation was discovered by Wilhelm Rontgen in 1895, by passing an electric current through an evacuated glass tube and producing continuous X-rays. Then in 1896 Henri Becquerel found that pitchblende (an ore containing radium and uranium) caused a photographic plate to darken. He went on to demonstrate that this was due to beta radiation (electrons) and alpha particles (helium nuclei) being emitted. Villard found a third type of radiation from pitchblende: gamma rays, which were much the same as X-rays. Then in 1896 Pierre and Marie Curie gave the name 'radioactivity' to this phenomenon, and in 1898 isolated polonium and radium from the pitchblende. Radium was later used in medical treatment. In 1898 Samuel Prescott showed that radiation destroyed bacteria in food.
In 1902 Ernest Rutherford showed that radioactivity, as a spontaneous event emitting an alpha or beta particle from the nucleus, created a different element. He went on to develop a fuller understanding of atoms and in 1919 he fired alpha particles from a radium source into nitrogen and found that nuclear rearrangement was occurring, with formation of oxygen. Niels Bohr was another scientist who advanced our understanding of the atom and the way electrons were arranged around its nucleus through to the 1940s.
By 1911 Frederick Soddy discovered that naturally-radioactive elements had a number of different isotopes (radionuclides), with the same chemistry. Also in 1911, George de Hevesy showed that such radionuclides were invaluable as tracers, because minute amounts could readily be detected with simple instruments.
In 1932 James Chadwick discovered the neutron. Also in 1932 Cockcroft and Walton produced nuclear transformations by bombarding atoms with accelerated protons, then in 1934 Irene Curie and Frederic Joliot found that some such transformations created artificial radionuclides. The next year Enrico Fermi found that a much greater variety of artificial radionuclides could be formed when neutrons were used instead of protons.
Fermi continued his experiments, mostly producing heavier elements from his targets, but also, with uranium, some much lighter ones. At the end of 1938 Otto Hahn and Fritz Strassmann in Berlin showed that the new lighter elements were barium and others which were about half the mass of uranium, thereby demonstrating that atomic fission had occurred. Lise Meitner and her nephew Otto Frisch, working under Niels Bohr, then explained this by suggesting that the neutron was captured by the nucleus, causing severe vibration leading to the nucleus splitting into two not quite equal parts. They calculated the energy release from this fission as about 200 million electron volts. Frisch then confirmed this figure experimentally in January 1939.
These 1939 developments sparked activity in many laboratories. Hahn and Strassmann showed that fission not only released a lot of energy, but that it also released additional neutrons which could cause fission in other uranium nuclei and possibly a self-sustaining chain reaction leading to an enormous release of energy. This suggestion was soon confirmed experimentally by Joliot and his co-workers in Paris, and Leo Szilard working with Fermi in New York.
Bohr soon proposed that fission was much more likely to occur in the uranium-235 isotope than in U-238 and that fission would occur more effectively with slow-moving neutrons than with fast neutrons. The latter point was confirmed by Szilard and Fermi, who proposed using a 'moderator' to slow down the emitted neutrons. Bohr and Wheeler extended these ideas into what became the classical analysis of the fission process, and their paper was published only two days before war broke out in 1939.
Another important factor was that U-235 was then known to comprise only 0.7% of natural uranium, with the other 99.3% being U-238, with similar chemical properties. Hence the separation of the two to obtain pure U-235 would be difficult and would require the use of their very slightly different physical properties. This increase in the proportion of the U-235 isotope became known as 'enrichment'.
The remaining piece of the fission/atomic bomb concept was provided in 1939 by Francis Perrin who introduced the concept of the critical mass of uranium required to produce a self-sustaining release of energy. His theories were extended by Rudolf Peierls at Birmingham University and the resulting calculations were of considerable importance in the development of the atomic bomb. Perrin's group in Paris continued their studies and demonstrated that a chain reaction could be sustained in a uranium-water mixture (the water being used to slow down the neutrons) provided external neutrons were injected into the system. They also demonstrated the idea of introducing neutron-absorbing material to limit the multiplication of neutrons and thus control the nuclear reaction (which is the basis for the operation of a nuclear power station).
Peierls had been a student of Werner Heisenberg, who from April 1939 presided over the German nuclear energy project under the German Ordnance Office. Initially this was directed towards military applications, and by the end of 1939 Heisenberg had calculated that nuclear fission chain reactions might be possible. When slowed down and controlled in a 'uranium machine' (nuclear reactor), these chain reactions could generate energy; when uncontrolled, they would lead to a nuclear explosion many times more powerful than a conventional explosion. It was suggested that natural uranium could be used in a uranium machine, with heavy water moderator (from Norway), but it appears that researchers were unaware of delayed neutrons which would enable a nuclear reactor to be controlled. Heisenberg noted that they could use pure uranium-235, a rare isotope, as an explosive, but he apparently believed that the critical mass required was higher than was practical.
In the summer of 1940, Carl Friedrich von Weizsäcker, a younger colleague and friend of Heisenberg's, drew upon publications by scholars working in Britain, Denmark, France, and the USA to conclude that if a uranium machine could sustain a chain reaction, then some of the more common uranium-238 would be transmuted into 'element 94', now called plutonium. Like uranium-235, element 94 would be an incredibly powerful explosive. In 1941, von Weizsäcker went so far as to submit a patent application for using a uranium machine to manufacture this new radioactive element.
By 1942 the military objective was wound down as impractical, requiring more resources than available. The priority became building rockets. However, the existence of the German Uranverein project provided the main incentive for wartime development of the atomic bomb by Britain and the USA.
Russian nuclear physics predates the Bolshevik Revolution by more than a decade. Work on radioactive minerals found in central Asia began in 1900 and the St Petersburg Academy of Sciences began a large-scale investigation in 1909. The 1917 Revolution gave a boost to scientific research and over 10 physics institutes were established in major Russian towns, particularly St Petersburg, in the years which followed. In the 1920s and early 1930s many prominent Russian physicists worked abroad, encouraged by the new regime initially as the best way to raise the level of expertise quickly. These included Kirill Sinelnikov, Pyotr Kapitsa and Vladimir Vernadsky.
By the early 1930s there were several research centres specialising in nuclear physics. Kirill Sinelnikov returned from Cambridge in 1931 to organise a department at the Ukrainian Institute of Physics and Technology (later renamed Kharkov Institute of Physics and Technology, KIPT) in Kharkov, which had been set up in 1928. Academician Abram Ioffe formed another group at the Leningrad Physics and Technical Institute (FTI), later becoming independent as the Ioffe Institute, including the young Igor Kurchatov. Ioffe was its first director, through to 1950.
British scientists had kept pressure on their government. The refugee physicists Peierls and Frisch (who had stayed in England with Peierls after the outbreak of war), gave a major impetus to the concept of the atomic bomb in a three-page document known as the Frisch-Peierls Memorandum. In this they predicted that an amount of about 5kg of pure U-235 could make a very powerful atomic bomb equivalent to several thousand tonnes of dynamite. They also suggested how such a bomb could be detonated, how the U-235 could be produced, and what the radiation effects might be in addition to the explosive effects. They proposed thermal diffusion as a suitable method for separating the U-235 from the natural uranium. This memorandum stimulated a considerable response in Britain at a time when there was little interest in the USA.
A group of eminent scientists known as the MAUD Committee was set up in Britain and supervised research at the Universities of Birmingham, Bristol, Cambridge, Liverpool and Oxford. The chemical problems of producing gaseous compounds of uranium and pure uranium metal were studied at Birmingham University and Imperial Chemical Industries (ICI). Dr Philip Baxter at ICI made the first small batch of gaseous uranium hexafluoride for Professor James Chadwick in 1940. ICI received a formal contract later in 1940 to make 3kg of this vital material for the future work. Most of the other research was funded by the universities themselves.
Two important developments came from the work at Cambridge. The first was experimental proof that a chain reaction could be sustained with slow neutrons in a mixture of uranium oxide and heavy water, ie. the output of neutrons was greater than the input. The second was by Bretscher and Feather based on earlier work by Halban and Kowarski soon after they arrived in Britain from Paris. When U-235 and U-238 absorb slow neutrons, the probability of fission in U-235 is much greater than in U-238. The U-238 is more likely to form a new isotope U-239, and this isotope rapidly emits an electron to become a new element with a mass of 239 and an Atomic Number of 93. This element also emits an electron and becomes a new element of mass 239 and Atomic Number 94, which has a much greater half-life. Bretscher and Feather argued on theoretical grounds that element 94 would be readily fissionable by slow and fast neutrons, and had the added advantages that it was chemically different to uranium and therefore could easily be separated from it.
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