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Initiation processes, possible

Chemical Exposure Index (CEI) Chemical Exposure Index, 1994). The CEI provides a method of rating the relative potential of acute health hazard to people from possible chemical release incidents. It may be used for conducting the initial process hazard analysis and it establishes the degree of mrther analysis needed. The CEI also may be used as part of the site review process. [Pg.2273]

When considering the possibility of using internal combustion drivers, evaluate process requirements and costs. If a low-cost, gaseous fuel is available, gas engines and gas turbines may surpass other drivers in economical installation and operation. In the initial process design stage, a method of establishing the cost of purchase, installation, and operation for drivers is needed. [Pg.292]

The availability of organic ligands in the surface complexes obtained by the reaction of organometallic compounds with supports allows us to consider two possibilities of the initiation process (1) the monomer insertion into the organic ligand-metal bond (bensyl, allyl, etc.) (9a) ... [Pg.190]

The reaction of MnC03 is of particular interest because of the possibility of the formation and interconversion of the various oxides of manganese [733,1276], Westerdahl and Leader [762] identify the initial process as... [Pg.173]

It is possible to observe that U increases with the utility flow rate and initial process fluid temperature. This corresponds to a classical evolution of the Nusselt number function of Reynolds and Prandtl numbers. [Pg.276]

Dialkylindolines and 1,3-dialkylindoles are formed in poor yield (<10%) from the reaction of ethyl- or phenymagnesium bromide with 2-chloro-N-methyl-N-allylaniline in the presence of catalytic quantities of (bistriphenylphosphine)nickel dichloride.72 In a modification of this procedure, the allyl derivatives can be converted by stoichiometric amounts of tetrakis(triphenylphosphine)nickel into 1,3-dialkylindoles in moderate yield72 (Scheme 43) an initial process of oxidative addition and ensuing cyclization of arylnickel intermediates is thought to occur. In contrast to the nickel system,72 it has proved possible to achieve the indole synthesis by means of catalytic quantities of palladium acetate.73 It is preferable to use... [Pg.340]

In 1988 Bast and Haenen [201] reported that both LA and DHLA did not affect iron-stimulated microsomal lipid peroxidation. However, Scholich et al. [202] found that DHLA inhibited NADPH-stimulated microsomal lipid peroxidation in the presence of iron-ADP complex. Inhibitory effect was observed only in the presence of a-tocopherol, suggesting that some interaction takes place between these two antioxidants. Stimulatory and inhibitory effects of DHLA have also been shown in other transition metal-stimulated lipid peroxidation systems [203,204]. Later on, the ability of DHLA (but not LA) to react with water-soluble and lipid-soluble peroxyl radicals has been proven [205], But it is possible that the double (stimulatory and inhibitory) effect of DHLA on lipid peroxidation originates from subsequent reactions of the DHLA free radical, capable of participating in new initiating processes. [Pg.874]

Chemical Exposure Index (CEI) (Chemical Exposure Index, 1994 Mannan, 2005, pp. 8/22-8/26.) The CEI provides a method of rating the relative potential of acute health hazard to people from possible chemical release incidents. It may be used for prioritizing initial process hazard analysis and establishing the degree of further analysis needed. The CEI also may be used as part of the site review process. The system provides a method of ranking one risk relative to another. It is not intended to define a particular containment system as safe or unsafe, but provides a way of comparing toxic hazards. It deals with acute, not chronic, releases. Flammability and explosion hazards are not included in this index. To develop a CEI, information needs include... [Pg.47]

The assessment begins with an assessment of the reactants. The question is whether all initial process reactants can be regarded as thermally stable within the intended temperature range and time domain. Possible interactions with non-reacting materials need to be considered as part of this assessment. [Pg.235]

Up to now it has not been possible to prove a mechanism which is able to explain all these effects. Neither intramolecular termination alone, nor a combination of intramolecular termination and monomer termination fit the data. However, they can be fitted by a hypothetical kinetic scheme which assumes that a slow reaction takes place between the living end and a deactivating species which is produced in the initial stage of the reaction. The dependence of the rate of termination on the initial monomer concentration can only be explained on the basis of a side reaction occuring in the initiation process. To verify this model, however, the deactivating species has to be identified by analyzing the oligomers produced in the initiation step. [Pg.458]

The insight of photoinitiation is complicated. Even when CT absorption is observed, the initiation process may not start from a charge transferred state or form ion-radicals. An alternative mechanism is triplet excitation via charge transfer absorption. Namely, when the CT excited level is higher than the triplet level, a considerable amount of the CT excitation would be converted to the triplet state. The TMPD+-naphthalene pair fits in this case (20). Conversely, the contribution of CT might be predominant even when the CT interaction in the ground state is not observed. As shown in Eqs. (14) and (16), charge transfer interaction will not take part in photoexcitation but occurs in the excited state. Possible reaction mechanismus may be explained as follows. [Pg.337]

So far as vinyl monomers are concerned, ionic propagation proceeds with carbonium ions (cationic polymerization) or carbanions (anionic polymerization) at the chain ends. The study of the initiation process of radiation-induced ionic polymerization seeks to elucidate how these ions are formed from the primary ionic intermediates. Possible reactions... [Pg.402]

When 14C-benzoin (19) or its methyl ether (20) is used as photosensitizer for polymerizations, more of the sensitizer is incorporated in polymer than can possibly be accounted for by the initiation process. The reactions have the characteristics of mono-radical polymerizations and separate experiments with thermal initiators have shown that transfer to the carbonyl compound is of little importance. It appears that photo-excited states of these compounds, but not the ground states, can engage... [Pg.7]

The thickness of UV-cured samples is generally less than 100 /am. To cure sample thicknesses up to 1 cm or more, it is possible to use a dual initiation process. The heat of reaction developed during the UV cure of the material located close to the surface is used to decompose a peroxide that initiates the polymerization in the bulk. [Pg.63]

This is a highly simplified mechanism, but it does contain the essentials of the main chain process. This mechanism involves a three stage initiation process, something not uncommon in chain mechanisms. Only one of the possible propagation chains is given, and only one termination step is quoted. [Pg.230]


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See also in sourсe #XX -- [ Pg.354 ]

See also in sourсe #XX -- [ Pg.354 ]




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