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Alpha elements

Laha, T., McManus, D.P., Loukas, A. and Brindley, P.J. (2000) Sj-alpha elements, short interspersed elementlike retroposons bearing a hammerhead ribozyme motif from the genome of the oriental blood fluke Schistosoma japonicum. Biochimica et Biophysica Acta 1492, 477 182. [Pg.74]

Secondary nuclei tend to be neutron-rich isotopes of the alpha elements (O, Ne, Mg, Si, S, Ar, and Ca). To make neutron-rich isotopes in stars requires a source of neutrons, and this in turn requires that the gas in bulk contain more neutrons than protons by a small amount. This requires that the star contain an abundant... [Pg.308]

Introduction and commercial application Safety and the environment have become important elements of all parts of the field life cycle, and involve all of the technical and support functions in an oil company. The Piper Alpha disaster in the North Sea in 1988 has resulted in a major change in the approach to management of safety of world-wide oil and gas exploration and production activities. Companies recognise that good safety and environmental management make economic sense and are essential to guaranteeing long term presence in the industry. [Pg.65]

Electron density represents the probability of finding an electron at a poin t in space. It is calcii lated from th e elements of th e den sity matrix. The total electron density is the sum of the densities for alpha and beta electrons. In a closed-shell RUE calculation, electron densities are the same for alpha and beta electrons. [Pg.52]

Gr. helios, the sun). Janssen obtained the first evidence of helium during the solar eclipse of 1868 when he detected a new line in the solar spectrum. Lockyer and Frankland suggested the name helium for the new element. In 1895 Ramsay discovered helium in the uranium mineral clevite while it was independently discovered in cleveite by the Swedish chemists Cleve and Langlet at about the same time. Rutherford and Royds in 1907 demonstrated that alpha particles are helium nuclei. [Pg.6]

Element 259-104 is formed by the merging of a 13C nuclei with 249Cf, followed by emission of three neutrons. This isotope has a half-life of 3 to 4 s, and decays by emitting an alpha particle into 255No, which has a half-life of 185 s. [Pg.159]

Element 106 was created by the reaction 249Gf(180,4N)263X, which decayed by alpha emission to rutherfordium, and then by alpha emission to nobelium, which in turn further decayed by alpha between daughter and granddaughter. The element so identified had alpha energies of 9.06 and 9.25 MeV with a half-life of 0.9 +/- 0.2 s. [Pg.162]

The acceptance of the name was premature because both Russian and American efforts now completely rule out the possibility of any isotope of Element 102 having a half-life of 10 min in the vicinity of 8.5 MeV. Early work in 1957 on the search for this element, in Russia at the Kurchatov Institute, was marred by the assignment of 8.9 +/- 0.4 MeV alpha radiation with a half-life of 2 to 40 sec, which was too indefinite to support discovery claims. [Pg.163]

Because of the high rate of emission of alpha particles and the element being specifically absorbed on bone the surface and collected in the liver, plutonium, as well as all of the other transuranium elements except neptunium, are radiological poisons and must be handled with very special equipment and precautions. Plutonium is a very dangerous radiological hazard. Precautions must also be taken to prevent the unintentional formulation of a critical mass. Plutonium in liquid solution is more likely to become critical than solid plutonium. The shape of the mass must also be considered where criticality is concerned. [Pg.205]

The isotope produced was the 20-hour 255Fm. During 1953 and early 1954, while discovery of elements 99 and 100 was withheld from publication for security reasons, a group from the Nobel Institute of Physics in Stockholm bombarded 238U with 160 ions, and isolated a 30-min alpha-emitter, which they ascribed to 250-100, without claiming discovery of the element. This isotope has since been identified positively, and the 30-min half-life confirmed. [Pg.212]

Ernest O. Lawrence, inventor of the cyclotron) This member of the 5f transition elements (actinide series) was discovered in March 1961 by A. Ghiorso, T. Sikkeland, A.E. Larsh, and R.M. Latimer. A 3-Mg californium target, consisting of a mixture of isotopes of mass number 249, 250, 251, and 252, was bombarded with either lOB or IIB. The electrically charged transmutation nuclei recoiled with an atmosphere of helium and were collected on a thin copper conveyor tape which was then moved to place collected atoms in front of a series of solid-state detectors. The isotope of element 103 produced in this way decayed by emitting an 8.6 MeV alpha particle with a half-life of 8 s. [Pg.215]

Natural radioactive processes in themselves give rise to changes of one element into another. Emission of an alpha particle reduces the atomic number of an element by two units, and emission of a beta particle increases the atomic number by one unit. Thus, for isotopes of elements near... [Pg.364]

The effects of a rather distinct deformed shell at = 152 were clearly seen as early as 1954 in the alpha-decay energies of isotopes of californium, einsteinium, and fermium. In fact, a number of authors have suggested that the entire transuranium region is stabilized by shell effects with an influence that increases markedly with atomic number. Thus the effects of shell substmcture lead to an increase in spontaneous fission half-Hves of up to about 15 orders of magnitude for the heavy transuranium elements, the heaviest of which would otherwise have half-Hves of the order of those for a compound nucleus (lO " s or less) and not of milliseconds or longer, as found experimentally. This gives hope for the synthesis and identification of several elements beyond the present heaviest (element 109) and suggest that the peninsula of nuclei with measurable half-Hves may extend up to the island of stabiHty at Z = 114 andA = 184. [Pg.227]

The electromagnetic separation plant built during World War 11 at Oak Ridge, involved two types of calutrons, alpha and beta. The larger alpha calutrons were used for the enrichment of natural uranium, and the beta calutrons were used for the final separation of U from the pre-enriched alpha product. For the electromagnetic separation process, UO was converted into UCl [10026-10-5] with CCl. The UCl was fed into the calutron for separation. The calutron technique has been used to separate pure samples of and stable isotopes of many other elements. The Y-12 calutron... [Pg.322]

Boron [7440-42-8] B, is unique in that it is the only nonmetal in Group 13 (IIIA) of the Periodic Table. Boron, at wt 10.81, at no. 5, has more similarity to carbon and siUcon than to the other elements in Group 13. There are two stable boron isotopes, B and B, which are naturally present at 19.10—20.31% and 79.69—80.90%, respectively. The range of the isotopic abundancies reflects a variabiUty in naturally occurring deposits such as high B ore from Turkey and low °B ore from California. Other boron isotopes, B, B, and B, have half-Hves of less than a second. The B isotope has a very high cross-section for absorption of thermal neutrons, 3.835 x 10 (3835 bams). This neutron absorption produces alpha particles. [Pg.183]

Uranium and thorium are the first members of natural radioactive chain which makes their determination in natural materials interesting from geochemical and radioecological aspect. They are quantitatively determined as elements by spectrophotometric method and/or their radioisotopes by alpha spectrometry. It is necessary to develop inexpensive, rapid and sensitive methods for the routine researches because of continuous monitoring of the radioactivity level. [Pg.214]

Figure 1.1 The amino acid sequence of a protein s polypeptide chain is called Its primary structure. Different regions of the sequence form local regular secondary structures, such as alpha (a) helices or beta (P) strands. The tertiary structure is formed by packing such structural elements into one or several compact globular units called domains. The final protein may contain several polypeptide chains arranged in a quaternary structure. By formation of such tertiary and quaternary structure amino acids far apart In the sequence are brought close together in three dimensions to form a functional region, an active site. Figure 1.1 The amino acid sequence of a protein s polypeptide chain is called Its primary structure. Different regions of the sequence form local regular secondary structures, such as alpha (a) helices or beta (P) strands. The tertiary structure is formed by packing such structural elements into one or several compact globular units called domains. The final protein may contain several polypeptide chains arranged in a quaternary structure. By formation of such tertiary and quaternary structure amino acids far apart In the sequence are brought close together in three dimensions to form a functional region, an active site.
The alpha (a) helix is an important element of secondary structure... [Pg.14]


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See also in sourсe #XX -- [ Pg.176 , Pg.184 ]




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