Big Chemical Encyclopedia

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

Articles Figures Tables About

Transient nuclei

Parameter "1 Transient nuclei 1. Accumulation 1 mode 1 Large particles 1... [Pg.373]

Atmospheric particles have spherical equivalent diameters (Dp) ranging from 1 nm to 100 pm. Plots of particle number concentration (as well as surface area and volume) as a function of particle size usually show that an atmospheric aerosol is composed of three or more modes, as illustrated in Figure 1. By convention, particles are classified into three approximate categories according to their size Aitken (or transient) nuclei mode (Dp <0.1 pm), accumulation mode (0.1 < Dp < 2.5 pm), and coarse mode (Dp > 2.5 pm) (Seinfeld and Pandis 1998). Particles smaller than 2.5 pm are generally classified as fine. The terms PM2.5 and PMio refer to particulate matter with aerodynamic equivalent diameters under 2.5 and 10 pm, respectively. These terms are often used to describe the total mass of particles with diameters smaller than the cutoff size. [Pg.294]

Transient Nuclei or I Accumulation Mechanically Generated Aitken Nuclei Range I Range Aerosol Range... [Pg.59]

Transient nuclei mode These particles are typically less than ca. 100 nm in diameter they are formed by the condensation of less volatile materials and subsequently grow by condensation processes. Their formation can occur both in hot combustion gases and within the atmosphere itself from chemical reactions of gases. [Pg.94]

Accumulation mode Particles in the transient nuclei mode can grow both by condensation of low-volatility materials and through coagulation, reaching the state of accumulation mode that consists of particles between ca. 100 nm and 2 pm in diameter. The accumulation mode is so called because particle removal mechanisms are the less efficient in this regime, causing particle to be accumulated. [Pg.94]

The analysis of steady-state and transient reactor behavior requires the calculation of reaction rates of neutrons with various materials. If the number density of neutrons at a point is n and their characteristic speed is v, a flux effective area of a nucleus as a cross section O, and a target atom number density N, a macroscopic cross section E = Na can be defined, and the reaction rate per unit volume is R = 0S. This relation may be appHed to the processes of neutron scattering, absorption, and fission in balance equations lea ding to predictions of or to the determination of flux distribution. The consumption of nuclear fuels is governed by time-dependent differential equations analogous to those of Bateman for radioactive decay chains. The rate of change in number of atoms N owing to absorption is as follows ... [Pg.211]

In several papers,Treibs argues that the effect of acid on the interaction of pyrroles with electrophilic reagents is to increase the susceptibility of the pyrrole nucleus to electrophilic attack the proton donor is believed to convert the pyrrole nucleus transiently and reversibly into what is described as a salt of an azacyclopentadienyl anion, the activation of the a-position, for example, occurring as follows, (23) being the activated species ... [Pg.298]

Fig. 2 RNAi inducers used in antiviral strategies. In general, RNAi is induced either by transfection of synthetic siRNAs into cells, or by stable or transient intracellular expression of double-stranded siRNA precursors (shRNA, e-shRNA, IhRNA, or pri-miRNAs). After transcription in the nucleus shRNAs, IhRNAs and e-shRNAs are exported to the cytoplasm and subsequently diced into mature siRNAs. Pri-miRNAs modified to encode antiviral siRNAs first undergo cleavage by Drosha before they are exported to the cytoplasm. Here the antiviral pre-miRNAs (also called shRNA-miRs) are processed by Dicer into the mature miRNAs. After loading of the antisense strand of the siRNAs/miRNAs into RISC, the complex will target and cleave viral transcripts bearing the complementary sequences... Fig. 2 RNAi inducers used in antiviral strategies. In general, RNAi is induced either by transfection of synthetic siRNAs into cells, or by stable or transient intracellular expression of double-stranded siRNA precursors (shRNA, e-shRNA, IhRNA, or pri-miRNAs). After transcription in the nucleus shRNAs, IhRNAs and e-shRNAs are exported to the cytoplasm and subsequently diced into mature siRNAs. Pri-miRNAs modified to encode antiviral siRNAs first undergo cleavage by Drosha before they are exported to the cytoplasm. Here the antiviral pre-miRNAs (also called shRNA-miRs) are processed by Dicer into the mature miRNAs. After loading of the antisense strand of the siRNAs/miRNAs into RISC, the complex will target and cleave viral transcripts bearing the complementary sequences...
The process as a whole is transient nucleation is predominant initially, and nucleus growth is predominant subsequently. Growth of the nuclei usually continues until they have reached a certain mean size. After some time a quasisteady state is attained, when the number of nuclei that cease to grow in unit time has become equal to the number of nuclei newly formed in unit time. [Pg.253]

When a gas bubble has tom away, usually the small nucleus of a new bubble is left behind in its place. Therefore, in gas evolution an appreciable supersaturation is needed only for creating an initial set of nuclei, and subsequent processes require less supersaturation. Hence, in a galvanostatic transient the electrode s polarization will initially be higher but will then fall to a lower, steady-state value (Fig. 14.10). Such a time dependence of polarization is typical for many processes involving formation of a new phase. [Pg.257]

Nowhere, perhaps, is this phenomenon better illustrated than in the phenothiazine class. The earlier volume devoted a full chapter to the discussion of this important structural class, which was represented by both major tranquilizers and antihistamines. The lone phenothiazine below, flutiazin (130), in fact fails to show the activities characteristic of its class. Instead, the ring system is used as the aromatic nucleus for a nonsteroidal antiinflammatory agent. Preparation of 130 starts with formylation of the rather complex aniline 123. Reaction with alcoholic sodium hydroxide results in net overall transformation to the phenothiazine by the Smiles rearrangement. The sequence begins with formation of the anion on the amide nitrogen addition to the carbon bearing sulfur affords the corresponding transient spiro intermediate 126. Rearomatization... [Pg.430]

This involves an aryl carbanion/enolate anion (64), and also eCQ3 derived from the action of strong bases on HCC13 (p. 267), though the latter has only a transient existence decomposing to CC12, a highly electron-deficient electrophile that attacks the aromatic nucleus ... [Pg.290]

The models incorporate two microscopic parameters, the site density and the critical nucleus size. A fit of experimental current transients to the models allows conclusions, for example, concerning the effect of additives on nucleation rate. Fabricus et al. found by analysis of current transients that thiourea increases the nucleation density of copper deposited on glassy carbon at low concentration, but decreases it at higher concentration [112], Schmidt et al. found that Gold nucleation on pyrolytic graphite is limited by the availability of nucleation sites [113], Nucleation density and rate were found to depend on applied potential as was the critical nucleus size. Depending on concentration, critical nuclei as small as one atom have been estimated from current transient measurements. Michailova et al. found a critical nucleus of 11 atoms for copper nucleation on platinum [114], These numbers are typical, and they are comparable to the thermodynamic critical radii [86],... [Pg.178]


See other pages where Transient nuclei is mentioned: [Pg.373]    [Pg.104]    [Pg.355]    [Pg.165]    [Pg.27]    [Pg.101]    [Pg.39]    [Pg.412]    [Pg.271]    [Pg.474]    [Pg.11]    [Pg.251]    [Pg.5]    [Pg.208]    [Pg.493]    [Pg.209]    [Pg.263]    [Pg.25]    [Pg.50]    [Pg.397]    [Pg.517]    [Pg.42]    [Pg.88]    [Pg.35]    [Pg.178]    [Pg.126]    [Pg.176]    [Pg.177]    [Pg.177]    [Pg.8]    [Pg.215]    [Pg.444]    [Pg.918]    [Pg.924]    [Pg.924]    [Pg.27]    [Pg.204]    [Pg.46]    [Pg.126]    [Pg.298]    [Pg.967]    [Pg.142]    [Pg.307]    [Pg.203]    [Pg.84]    [Pg.115]    [Pg.228]    [Pg.487]    [Pg.242]   


SEARCH



© 2024 chempedia.info