Chemistry » Nuclear Chemistry » Transmutation and Nuclear Energy

# Synthesis of Nuclides

## Transmutation and Nuclear Energy

After the discovery of radioactivity, the field of nuclear chemistry was created and developed rapidly during the early twentieth century. A slew of new discoveries in the 1930s and 1940s, along with World War II, combined to usher in the Nuclear Age in the mid-twentieth century. Scientists learned how to create new substances, and certain isotopes of certain elements were found to possess the capacity to produce unprecedented amounts of energy, with the potential to cause tremendous damage during war, as well as produce enormous amounts of power for society’s needs during peace.

## Synthesis of Nuclides

Nuclear transmutation is the conversion of one nuclide into another. It can occur by the radioactive decay of a nucleus, or the reaction of a nucleus with another particle. The first manmade nucleus was produced in Ernest Rutherford’s laboratory in 1919 by a transmutation reaction, the bombardment of one type of nuclei with other nuclei or with neutrons. Rutherford bombarded nitrogen atoms with high-speed α particles from a natural radioactive isotope of radium and observed protons resulting from the reaction:

$${}_{\phantom{\rule{0.5em}{0ex}}7}^{14}\text{N}+{}_{2}^{4}\text{He}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}8}^{17}\text{O}+{}_{1}^{1}\text{H}$$

The $${}_{\phantom{\rule{0.5em}{0ex}}8}^{17}\text{O}$$ and $${}_{1}^{1}\text{H}$$ nuclei that are produced are stable, so no further (nuclear) changes occur.

To reach the kinetic energies necessary to produce transmutation reactions, devices called particle accelerators are used. These devices use magnetic and electric fields to increase the speeds of nuclear particles. In all accelerators, the particles move in a vacuum to avoid collisions with gas molecules. When neutrons are required for transmutation reactions, they are usually obtained from radioactive decay reactions or from various nuclear reactions occurring in nuclear reactors. The Chemistry in Everyday Life feature that follows discusses a famous particle accelerator that made worldwide news.

Prior to 1940, the heaviest-known element was uranium, whose atomic number is 92. Now, many artificial elements have been synthesized and isolated, including several on such a large scale that they have had a profound effect on society. One of these—element 93, neptunium (Np)—was first made in 1940 by McMillan and Abelson by bombarding uranium-238 with neutrons. The reaction creates unstable uranium-239, with a half-life of 23.5 minutes, which then decays into neptunium-239. Neptunium-239 is also radioactive, with a half-life of 2.36 days, and it decays into plutonium-239. The nuclear reactions are:

$$\begin{array}{l}{}_{\phantom{\rule{0.5em}{0ex}}92}^{238}\text{U}+{}_{0}^{1}\text{n}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}92}^{239}\text{U}\\ \\ \\ \phantom{\rule{2.2em}{0ex}}{}_{\phantom{\rule{0.5em}{0ex}}92}^{239}\text{U}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}93}^{239}\text{Np}+{}_{-1}^{\phantom{\rule{0.5em}{0ex}}0}\text{e}\phantom{\rule{4.9em}{0ex}}\text{half-life}=\text{23.5 min}\\ \phantom{\rule{1.7em}{0ex}}{}_{\phantom{\rule{0.5em}{0ex}}93}^{239}\text{Np}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}94}^{239}\text{Pu}+{}_{-1}^{\phantom{\rule{0.5em}{0ex}}0}\text{e}\phantom{\rule{5em}{0ex}}\text{half-life}=\text{2.36 days}\end{array}$$

Plutonium is now mostly formed in nuclear reactors as a byproduct during the decay of uranium. Some of the neutrons that are released during U-235 decay combine with U-238 nuclei to form uranium-239; this undergoes β decay to form neptunium-239, which in turn undergoes β decay to form plutonium-239 as illustrated in the preceding three equations. It is possible to summarize these equations as:

$${}_{\phantom{\rule{0.5em}{0ex}}92}^{238}\text{U}+{}_{0}^{1}\text{n}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}92}^{239}\text{U}\;\stackrel{\phantom{\rule{0.4em}{0ex}}{\text{β}}^{\text{−}}\phantom{\rule{0.4em}{0ex}}}{\to }\;{}_{\phantom{\rule{0.5em}{0ex}}93}^{239}\text{Np}\;\stackrel{\phantom{\rule{0.4em}{0ex}}{\text{β}}^{\text{−}}\phantom{\rule{0.4em}{0ex}}}{\to }\;{}_{\phantom{\rule{0.5em}{0ex}}94}^{239}\text{Pu}$$

Heavier isotopes of plutonium—Pu-240, Pu-241, and Pu-242—are also produced when lighter plutonium nuclei capture neutrons. Some of this highly radioactive plutonium is used to produce military weapons, and the rest presents a serious storage problem because they have half-lives from thousands to hundreds of thousands of years.

Although they have not been prepared in the same quantity as plutonium, many other synthetic nuclei have been produced. Nuclear medicine has developed from the ability to convert atoms of one type into other types of atoms. Radioactive isotopes of several dozen elements are currently used for medical applications. The radiation produced by their decay is used to image or treat various organs or portions of the body, among other uses.

The elements beyond element 92 (uranium) are called transuranium elements. As of this writing, 22 transuranium elements have been produced and officially recognized by IUPAC; several other elements have formation claims that are waiting for approval. Some of these elements are shown in the table below.

Preparation of Some of the Transuranium Elements
NameSymbolAtomic NumberReaction
americiumAm95$${}_{\phantom{\rule{0.5em}{0ex}}94}^{239}\text{Pu}+{}_{0}^{1}\text{n}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}95}^{240}\text{Am}+{}_{-1}^{\phantom{\rule{0.5em}{0ex}}0}\text{e}$$
curiumCm96$${}_{\phantom{\rule{0.5em}{0ex}}94}^{239}\text{Pu}+{}_{2}^{4}\text{He}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}96}^{242}\text{Cm}+{}_{0}^{1}\text{n}$$
californiumCf98$${}_{\phantom{\rule{0.5em}{0ex}}96}^{242}\text{Cm}+{}_{2}^{4}\text{He}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}98}^{245}\text{Cf}+{}_{0}^{1}\text{n}$$
einsteiniumEs99$${}_{\phantom{\rule{0.5em}{0ex}}92}^{238}\text{U}+15{}_{0}^{1}\text{n}\;⟶\;{}_{\phantom{\rule{0.5em}{0ex}}99}^{253}\text{Es}+7{}_{-1}^{\phantom{\rule{0.5em}{0ex}}0}\text{e}$$
mendeleviumMd101$${}_{\phantom{\rule{0.5em}{0ex}}99}^{253}\text{Es}+{}_{2}^{4}\text{He}\;⟶\;{}_{101}^{256}\text{Md}+{}_{0}^{1}\text{n}$$
nobeliumNo102$${}_{\phantom{\rule{0.5em}{0ex}}96}^{246}\text{Cm}+{}_{\phantom{\rule{0.5em}{0ex}}6}^{12}\text{C}\;⟶\;{}_{102}^{254}\text{No}+4{}_{0}^{1}\text{n}$$
rutherfordiumRf104$${}_{\phantom{\rule{0.5em}{0ex}}98}^{249}\text{Cf}+{}_{\phantom{\rule{0.5em}{0ex}}6}^{12}\text{C}\;⟶\;{}_{104}^{257}\text{Rf}+4{}_{0}^{1}\text{n}$$
seaborgiumSg106$$\begin{array}{l}{}_{\phantom{\rule{0.5em}{0ex}}82}^{206}\text{Pb}+{}_{24}^{54}\text{Cr}\;⟶\;{}_{106}^{257}\text{Sg}+3{}_{0}^{1}\text{n}\\ {}_{\phantom{\rule{0.5em}{0ex}}98}^{249}\text{Cf}+{}_{\phantom{\rule{0.5em}{0ex}}8}^{18}\text{O}\;⟶\;{}_{106}^{263}\text{Sg}+4{}_{0}^{1}\text{n}\end{array}$$
meitneriumMt107$${}_{\phantom{\rule{0.5em}{0ex}}83}^{209}\text{Bi}+{}_{26}^{58}\text{Fe}\;⟶\;{}_{109}^{266}\text{Mt}+{}_{0}^{1}\text{n}$$