Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nuclear-Chemical Initiation

An entirely new approach to initiation in cationic polymerisation was recently rqxM t-ed in a short communication by Akulow et al. These authors used low concentrations of tritium to induce the polymerisation of liquid isobutene and styrene at low temperature. The 4ecay of tritium [Pg.223]


Several classes of compounds initiate cationic polymerizations of alkenes, including protonic acids, Lewis acids (usually in combination with a cation or proton source), stable carbenium ions, oxidizing reagents, and other strong electrophiles. This section attempts to explain the mechanism of initiation with quantitative information when available physical means of initiation (electric current, y-rays, field ionization and emission, nuclear chemical initiation) will not be discussed. [Pg.166]

The cation is more reactive than the free radical, thereby dominating the initiation reaction. Radical cations can also he formed by high energy electrons, vacuum UV radiation, high intensity electric fields, or anodic oxidation of the monomer. Nuclear chemical initiation involves the use of tritium this method produced very high molecular weight polyisobutylenes and polystyrenes (65). [Pg.934]

Our initial expectations were that we would interview far more FDA officials than we did. However, we ended up interviewing more DoD officials, at all levels of policy and operations. Officials were interviewed in the following DoD offices Anthrax Vaccine Immunization Program (AVIP) J-4 Eogistics Directorate Office of the ASD(HA) JPO-BD the Defense Supply Center in Philadelphia Office of the Assistant to the Secretary of Defense for Nuclear, Chemical, and Biological Defense Programs U.S. Army Soldier Biological and Chemical Command U.S. Army Medical Materiel Development Activity and U.S. Army Medical Research Institute of Infectious Diseases... [Pg.30]

The chemical nature of photosynthesis had intrigued chemists for decades but little was learned about the details until radioactive 14C became available. Discovered in 1940 by Ruben and Kamen, the isotope was available in quantity by 1946 as a product of nuclear reactors. Initial studies of photosynthesis had been conducted by Ruben and Kamen using nC but 14C made rapid progress possible. In 1946 Melvin Calvin and Andrew A. Benson began their studies that elucidated the mechanism of incorporation of C02 into organic materials. [Pg.985]

Nuclear Explosions Although conventional explosives have become the weapons of choice of terrorist groups, a joint report issued in 2008 by Harvard s Kennedy School of Government and the Nuclear Threat Initiative reminds us that there is a real danger that terrorists could get and use a nuclear weapon.16 In order to understand what this would mean, we return to the atomic nucleus. A nuclear fission reaction releases far more energy than any ordinary chemical process. The Oklahoma City bomb was equivalent to the explosion of approximately 40001b of TNT.17 In contrast, the atomic bomb dropped on... [Pg.78]

One of the primary concerns that precipitated the creation of the Department of Energy/National Nuclear Security Administration (DOE/NNSA) Nuclear Cities Initiative (NCI) and Initiatives for Proliferation Prevention (IPP) was that destitute individuals in the nuclear weapons research and production complex would feel compelled to sell their knowledge to obtain funds to enable their families to survive." Similar concerns contributed to the creation of programs to support individuals involved in research and production of biological and chemical weapons. Since the assessment in this report runs counter to commonly held impressions of the Russian economy, the evidence behind our conclusions is laid out in some detail. [Pg.9]

The Nuclear Threat Initiative, Syria Profile Chemical Chronology, 1993-2003, http //www.nti.org/e research/profiles/Syria/2976 3281.html (as of April 30, 2004). [Pg.53]

Chawla, S. Ghosh, A.K. Avasthi, D.K. Knlriya, P.K. Ahmad, S. 2009. Functional polymers synthesized by grafting of glycidyl methacrylate onto swift heavy ions irradiated BOPP films using chemical initiator. Nuclear Instruments and Methods in Physics Research Section B, 267(14) 2416—2422. [Pg.21]

With the exception of nuclear reactions, explosives are chemical compounds that are not individually prone to detonation. When combined with other elements, however, the reaction between the chemicals, initiated by an outside promotion, causes the materials to break down their molecular bonds and release their stored potential energy in the form of blast and heat. Nuclear explosions are again an exception in that, besides heat and blast, they also release a large amount of radioactive particles not present in conventional explosions. [Pg.737]

While event trees are not so common in chemical plant PSA they are extensively used to analyze nuclear accidents, but before beginning the analysis, preliminaries that are needed are plant tamiliarity and initiator selection... [Pg.228]

There had been small-scale probabilistic risk studies, but the first in-depth study v, as initiated by the U.S, Atomic Energy Commission in September 1972 and completed by the Nuclear Regulatory Commission (NRC). This was known as the Reactor Safety Study, W. SH-(400, Ociuher 1975) that set the pattern for subsequent PSAs not only nuclear, but chemical md tniii portation, PSA had it beginnings in nuclear power because of the unknown risk and the large amounts of funds for the investigation. [Pg.540]

The maximum explosion pressure is a function of and is directly proportioiuil to die initial pressure. Blast waves are pressure waves of finite amplitude tliat are generated in air by a rapid release in energy and an instantaneous rise in pressure. The most conunon plant explosion types eiicomitered in iiidustiy are chemical, nuclear, expanding vapors, and pressurized gas. [Pg.246]

Nuclear and non-nuclear munitions (to include mines, grenades, demolition devices, explosives, explosive devices and initiators) except chemical and smoke munitions assigned to Edgewood Arsenal... [Pg.744]

Half-lives span a very wide range (Table 17.5). Consider strontium-90, for which the half-life is 28 a. This nuclide is present in nuclear fallout, the fine dust that settles from clouds of airborne particles after the explosion of a nuclear bomb, and may also be present in the accidental release of radioactive materials into the air. Because it is chemically very similar to calcium, strontium may accompany that element through the environment and become incorporated into bones once there, it continues to emit radiation for many years. About 10 half-lives (for strontium-90, 280 a) must pass before the activity of a sample has fallen to 1/1000 of its initial value. Iodine-131, which was released in the accidental fire at the Chernobyl nuclear power plant, has a half-life of only 8.05 d, but it accumulates in the thyroid gland. Several cases of thyroid cancer have been linked to iodine-131 exposure from the accident. Plutonium-239 has a half-life of 24 ka (24000 years). Consequently, very long term storage facilities are required for plutonium waste, and land contaminated with plutonium cannot be inhabited again for thousands of years without expensive remediation efforts. [Pg.832]

The first example of chemically induced multiplet polarization was observed on treatment of a solution of n-butyl bromide and n-butyl lithium in hexane with a little ether to initiate reaction by depolymerizing the organometallic compound (Ward and Lawler, 1967). Polarization (E/A) of the protons on carbon atoms 1 and 2 in the 1-butene produced was observed and taken as evidence of the correctness of an earlier suggestion (Bryce-Smith, 1956) that radical intermediates are involved in this elimination. Similar observations were made in the reaction of t-butyl lithium with n-butyl bromide when both 1-butene and isobutene were found to be polarized. The observations were particularly significant because multiplet polarization could not be explained by the electron-nuclear cross-relaxation theory of CIDNP then being advanced to explain net polarization (Lawler, 1967 Bargon and Fischer, 1967). [Pg.110]

It is particularly important to study process phenomena under dynamic (rather than static) conditions. Most current analytical techniques are designed to determine the initial and final states of a material or process. Instmments must be designed for the analysis of materials processing in real time, so that the cmcial chemical reactions in materials synthesis and processing can be monitored as they occur. Recent advances in nuclear magnetic resonance and laser probes indicate valuable lines of development for new techniques and comparable instmmentation for the study of interfaces, complex hquids, microstmctures, and hierarchical assemblies of materials. Instmmentation needs for the study of microstmctured materials are discussed in Chapter 9. [Pg.88]

The spin-echo experiment therefore leads to the refocusing not only of the individual nuclear resonances but also of the field inhomogeneity components lying in front or behind those resonances, a maximum negative amplitude being observed at time 2t after the initial 90° pulse. The frequency of rotation of each signal in the rotating frame will depend on its chemical shift and after the vector has been flipped by the 180° pulse, it... [Pg.93]

The radioactive element is a silvery, shiny, soft metal that is chemically similar to calcium and barium. It is found in tiny amounts in uranium ores. Its radioactivity is a million times stronger that that of uranium. Famous history of discovery (in a shed). Initially used in cancer therapy. Fatal side effects. Small amounts are used in luminous dyes. Radium was of utmost importance for research into the atom. Today its reputation is rather shaky as its decay gives rise to the unpleasant radon (see earlier). In nuclear reactors, tiny amounts of actinium are formed from radium. [Pg.80]


See other pages where Nuclear-Chemical Initiation is mentioned: [Pg.223]    [Pg.223]    [Pg.79]    [Pg.397]    [Pg.284]    [Pg.250]    [Pg.24]    [Pg.392]    [Pg.313]    [Pg.1437]    [Pg.2304]    [Pg.121]    [Pg.227]    [Pg.327]    [Pg.53]    [Pg.123]    [Pg.555]    [Pg.232]    [Pg.307]    [Pg.93]    [Pg.388]    [Pg.591]    [Pg.1097]    [Pg.188]    [Pg.841]    [Pg.17]    [Pg.71]    [Pg.881]    [Pg.410]    [Pg.739]    [Pg.81]   


SEARCH



Chemical Initiator

Chemical initiation

Chemical nuclear

© 2024 chempedia.info