Generation secondary mechanisms

Cold-roUed alloys of lead with 0.06 wt % teUurium often attain ultimate tensile strengths of 25—30 MPa (3625—5350 psi). High mechanical strength, excellent creep resistance, and low levels of alloying elements have made lead—teUurium aUoys the primary material for nuclear shielding for smaU reactors such as those aboard submarines. The aUoy is self-supporting and does not generate secondary radiation. 

In addition to nitric oxide, superoxide, and peroxynitrite, NO synthases are able to generate secondary free radicals because similar to cytochrome P-450 reductase, the reductase domain can transfer an electron from the heme to a xenobiotic. Thus it has been found [158,159] that neuronal NO synthase NOS I catalyzed the formation of CH3CH(OH) radical from ethanol. It was suggested that the perferryl complex of NOS I is responsible for the formation of such secondary radicals. Miller [160] also demonstrated that 1,3-dinitrobenzene mediated the formation of superoxide by nNOS. It was proposed that the enhancement of superoxide production in the presence of 1,3-dinitrobenzene converted nNOS into peroxynitrite-produced synthase and may be a mechanism of neurotoxicity of certain nitro compounds. 

It has been argued [235] by analogy with the case of molecules adsorbed on glassy n-hexane [232] that this enhancement is due to the electron transfer to CF2CI2 of an electron previously captured in a precursor state of the solvated electron in the water layer, which lies at and just below the vacuum level [300,301] and the subsequent. Similar results have been reported for HCl adsorbed on water ice [236]. It has been proposed that enhanced DEA to CF2CI2 via electron transfer from precursor-solvated states in ice [235] may explain an apparent correlation between cosmic ray activity (which would generate secondary LEE in ice crystals) and atmospheric ozone loss [11]. The same electron transfer mechanism may contribute to the marked enhancement in electron, and x-ray-induced dissociation for halo-uracil molecules is deposited inside water ice matrices [39]. 

In the case of addiction, we know a great deal about the neurobiological substrate of the core cases. Some of the borderline cases are likely to prove very different. Yet there are some causal mechanisms common to chemical and behavioral addictions, notably those that are linked to the axvareness of being addicted. These mechanisms generate secondary features of phenomena that are linked by analogy rather than by common causal mechanisms. 

The sources and chemical compositions of the fine and coarse urban particles are different. Coarse particles are generated by mechanical processes and consist of soil dust, seasalt, fly ash, tire wear particles, and so on. Aitken and accumulation mode particles contain primary particles from combustion sources and secondary aerosol material (sulfate, nitrate, ammonium, secondary organics) formed by chemical reactions resulting in gas-to-particle conversion (see Chapters 10 and 14). 

This computer program generates detailed primary mechanisms of oxidation and combustion reactions of alkanes and lumped secondary mechanisms of the primary products formed. It is interfaced with the KERGAS reaction database and the THERGAS, KINBEN and KINCOR computer programs. It produces reaction models (mechanisms, thermodynamic and kinetic data) which can be used directly in the CHEMKIN computer programs. 

In addition to resonant conversion. Auger cascades, and shake-off electrons, there are other secondary mechanisms that can lead to the generation of resonant electrons. Thus, electrons coming from the photoionization of an atom hit by resonant gamma or X-rays originated during the nuclear or atomic relaxation of the Mossbauer isotope (and usually denoted as GPE and XPE, respectively) are also electrons carrying resonant information and, consequently, contribute to the Mossbauer spectrum [4]. 

Chromium compounds decompose primary and secondary hydroperoxides to the corresponding carbonyl compounds, both homogeneously and heterogeneously (187—191). The mechanism of chromium catalyst interaction with hydroperoxides may involve generation of hexavalent chromium in the form of an alkyl chromate, which decomposes heterolyticaHy to give ketone (192). The oxidation of alcohol intermediates may also proceed through chromate ester intermediates (193). Therefore, chromium catalysis tends to increase the ketone alcohol ratio in the product (194,195). 

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