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Slowing Down in Hydrogen

A typical history of a neutron slowing down in a medium which contains both absorbing and scattering materials was described in Sec. 2.1a. An important feature of this process was that at every collision between a neutron and a nucleus there was a finite probability that the neutron could be absorbed. The probability that a neutron is absorbed upon making a collision is 2o(iJ)/2t( ), and that it be scattered, [Pg.99]

The appropriate neutron-balance condition for a medium of hydrogen is seen to be [cf. Eq. (4.75)] [Pg.99]

Equation (4.94) may be solved by reducing it to a differential equation. Thus, if we differentiate (4.94), we obtain [Pg.100]

The identity follows from (4.94). This result may be written in terms of F(E) given in (4.96) thus [Pg.100]

This function may also be written in terms of the lethargy, define u s In EofE, then it follows from (4.99) that [Pg.101]


Slow neutrons cannot play an essential role in an explosion process since they require about a microsecond to be slowed down in hydrogenic materials and the explosion is all over before they are slowed down. [Pg.353]

The reaction of peroxidase (metmyoglobin) with hydrogen peroxide leads to the generation of a green-blue radical from a colorless compound 2,2 -azino-(u s(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). It is slowed down in the presence of an antioxidant, an effect that is used for its quantitation in the Total Antioxidant Status Kit (manufacturer Randox, UK) [10]. Problems associated with this method are due to potential interference of the reaction compound H202 with components of the sample to be investigated. No investigation of fat-soluble compounds is possible. [Pg.502]

Hydrogenation of some basic nitriles such as 2-methyl-4-aminopyrimidine-5-carboni-trile was not successful in acidic solvents or in the presence of acetic anhydride with palladium or platinum catalysts, because formation of considerably less soluble salt or acetylated product slowed down the hydrogenation.64 The hydrogenation, however, could be performed smoothly and with an excellent yield over Raney Ni in organic solvents and in the presence of ammonia (eq. 7.51). [Pg.275]

As a consequence of the scavenging of the long-lived HO2 radicals by cloud droplets, oxidation of organics and the production of O3 are slowed down in the gas phase. The hydrogen peroxide formed by reaction 2a or reaction 2b reacts with Fe(II) ions yielding hydroxyl radicals... [Pg.60]

Slowing down the hydrogen transfer favors the production of olefins. Heavy naphtenic compounds are converted into aromatic gas oil components under fast hydrogen transfer, but into aromatic gasoline components when the hydrogen transfer is slowed down relative to the rate of cracking. These catalysts therefore contribute in two ways to increased gasoline octane. [Pg.32]

If there are no particular species in the environment (such as sulfur compounds, thiocyanates, cyanates, or compounds of arsenic, or antimony) recombination of atomic hydrogen occurs rapidly, so that the amount of hydrogen adsorbed in the metal lattice is modest. On the contrary, if these substances are present, recombination slows down, and hydrogen accumulates on the surface. Also in the presence of oxygen the concentration of atomic hydrogen on the metallic surface may be reduced because of the reaction ... [Pg.157]

The process of setting in resin-modified glass-ionomers is complicated because of the variety of reactions involved [6]. In principle it consists of two distinct parts, namely an acid-base reaction as in conventional glass-ionomers, and a free radial polymerization reaction. However, the two reactions influence each other in various ways. The acid-base reaction is slowed down in these materials for two reasons. One is that, as we have seen, the presence of HEMA causes the molecules to adopt a more coiled configuration and this reduces the ease with which they donate protons and behave as acids. The other reason is that the reduced polarity of the HEMA/water mixture compared with pure water inhibits the activation step of the acid-base reaction. This step involves electronically charged species, namely hydrogen ions from the acid and... [Pg.141]

Abstract. The resonance escape probability, p, in a lattice is expressed in terms of the resonance absorption integral (f era dEjE)efi and the spatial distribution of resonance neutrons. It is shown that the dependence on the spatial distribution is very nearly the same whether the slowing down in the moderator is Gaussian or exponential. The dependence on (f a a dEjE)ef( is rigorous only for a hydrogen moderator for a heavy moderator the formula overestimates the resonance escape. [Pg.475]

That this is the correct description for neutron slowing down in zirconium hydride has been experimentally verified [5 21], and the quantum hv has been measured to be 0.13 ev. Due to the finite mass of the zirconium atoms, it is not quite correct to treat the motion of the hydrogen atom as if it were in a fixed potential well. It is necessary to include the motion of the zirconium atoms in the ordinary vibrations of the crystal lattice. This introduces a Doppler broadening of the energy-transfer cross section so that energy transfers with a certain spread in the neighborhood of multiples of hv are allowed. To treat this broadening in detail, it is necessary to treat... [Pg.38]

Aptamer based biosensors, for example for recombinant human erythropoietin (as model analyte), can be made more sensitive by amplification with a boronic acid tethered gold nanoparticle that is then associated with an alkaline phosphatase to produce a redox active probe molecule. A similar re-usable bio-immuno-sensor has been suggested for carcinoembryonic antigen. A phenylboronic acid is assembled on gold to (reversibly) bind the antibody horseradish peroxidase conjugate. Interaction with the antigen slows down the hydrogen peroxide reduction. An HIV-1 immunoassay based on electroluminescence has been proposed by Zhou etaV In this process the... [Pg.249]

A. Simon, Neutron Slowing Down by Hydrogen in the Consistent Pi Approximation, Oak Ridge National Laboratory, ORNL-2098, July 19, 1956. [Pg.759]

It is seen that the obtained dependence is not a linear combination of known values. For 0 < Xh2 < 0.5 H2 added to CH4 has a weak effect on the flame velocity and the methane dominates the flame propagation. For hydrogen content 0.9 < Xh2 < 1 in the mixture, the CH4 additive noticeably slows down the hydrogen combustion. When the binary fuel is diluted with CH4 and in the range 0.5 < X 2 < 0.9 transient variations of hydrogen combustion with moderate difficulties for flame propagation, have been observed. [Pg.46]

Deuterium is used as a moderator to slow down neutrons. Tritium atoms are also present but in much smaller proportions. Tritium is readily produced in nuclear reactors and is used in the production of the hydrogen (fusion) bomb. It is also used as a radioactive agent in making luminous paints, and as a tracer. [Pg.5]

These effects can be attributed mainly to the inductive nature of the chlorine atoms, which reduces the electron density at position 4 and increases polarization of the 3,4-double bond. The dual reactivity of the chloropteridines has been further confirmed by the preparation of new adducts and substitution products. The addition reaction competes successfully, in a preparative sense, with the substitution reaction, if the latter is slowed down by a low temperature and a non-polar solvent. Compounds (12) and (13) react with dry ammonia in benzene at 5 °C to yield the 3,4-adducts (IS), which were shown by IR spectroscopy to contain little or none of the corresponding substitution product. The adducts decompose slowly in air and almost instantaneously in water or ethanol to give the original chloropteridine and ammonia. Certain other amines behave similarly, forming adducts which can be stored for a few days at -20 °C. Treatment of (12) and (13) in acetone with hydrogen sulfide or toluene-a-thiol gives adducts of the same type. [Pg.267]


See other pages where Slowing Down in Hydrogen is mentioned: [Pg.8]    [Pg.98]    [Pg.751]    [Pg.451]    [Pg.8]    [Pg.98]    [Pg.751]    [Pg.451]    [Pg.137]    [Pg.76]    [Pg.216]    [Pg.213]    [Pg.528]    [Pg.441]    [Pg.1101]    [Pg.190]    [Pg.236]    [Pg.229]    [Pg.552]    [Pg.213]    [Pg.201]    [Pg.296]    [Pg.241]    [Pg.32]    [Pg.57]    [Pg.13]    [Pg.1213]    [Pg.110]    [Pg.448]    [Pg.93]    [Pg.146]    [Pg.883]    [Pg.347]    [Pg.302]    [Pg.386]    [Pg.171]    [Pg.98]    [Pg.254]    [Pg.393]   


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