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Water nucleate

With continued heating, the local saturation temperature is reached and the steam bubbles move into the larger, bulk-water nucleate boiling region. Because the resulting steam bubble-water mixture close to the heated metal surface has a lower density than cooler water farther away from the heated surface, the steam bubble-water mixture rises. [Pg.6]

Kulmala, M., A. Laaksonen, and L. Pirjola, Parameterizations for Sulfuric Acid Water Nucleation Rates, J. Geophys. Res., 103, 8301-8307 (1998). [Pg.428]

Thus monomers such as styrene, isoprene and octyl acrylate, which have low solubilities in water, nucleate and grow very slowly during the early stages of an emulsion polymerization, whereas more soluble monomers such as methyl acrylate, vinyl acetate and acrylonitrile give rapid rates. In the presence of surfactant micelles the less soluble monomers are solubilized (11), so that they nucleate and grow more rapidly. [Pg.11]

Another application of quantum chemical methods is the investigation of the fundamental chemical behaviour of molecular systems potentially relevant to nu-cleation. Within the field of tropospheric nucleation mechanisms, two questions which have merited considerable study under the last decade are the modeling of the hydration of sulfuric acid, and the role of ammonia in sulfuric acid-water nucleation. [Pg.416]

Kim SW, Heckel A, McKeen SA, Frost GJ, Hsie EY, Trainer MK, Richter A, Burrows JP, Peckham SE, Grell GA (2006) Satellite-observed US power plant NOx emission reductions and their impact on air quality. Geophys Res Lett 33(L22812) 5 Kulmala M, Laaksonen A, Pirjola L (1998) Parametrization for sulphuric acid/water nucleation rates. J Geophys Res 103 8301-8307... [Pg.53]

Some similarity between the behavior of water close to C-phycocyanin protein and close to hydrophilic model systems can be stressed. In fact, for low-hydrated protein samples, no crystallization of water is detectable whereas for more than one monolayer coverage there is the appearance of the hexagonal crystalline ice. Moreover, the peak at 3.5 A is also detected. However, it should be noted that at the highest hydration level water nucleates into hexagonal ice at low temperature this is in contrast with hydrated Vycor where water nucleates into cubic ice. [Pg.64]

Kulrnala M, Kerminen VM, Laaksonen A (1995) Simrrlatiorts on the effect of sulphuric acid formation on atmospheric aerosol concentrations. Atmos Environ 29 377-382 Kulmala M, Laaksonen A, Piijola L (1998a) Parameterizatiorts for sulfuric acid/water nucleation rates. [Pg.343]

In practice, however, homogeneous nucleation is observed to occur at about 5°C, at a supersaturation In / 1.43. Inserting the latter value in Eq. (14.9), we derive rhom — 0.82 nm, which corresponds to a nucleus containing 75 water molecules, and which is far smaller than an ice nucleus. Equation (14.6) in fact shows that for a smaller value of y/AHy, rcr will be smaller at the same temperature ratio. For water nucleation to occur, this ratio is therefore much smaller than for ice nucleation (cf. the values in Table 14.2). It is likely that also the value of r om is smaller. Hence it is not allowed to take a fixed value for r om and to derive results from it. [Pg.578]

Nucleation plays a fundamental role whenever condensation, precipitation, crystallization, sublimation, boiling, or freezing occur. A transformation of a phase a, say, a vapor, to a phase p, say, a liquid, does not occur the instant the free energy of p is lower than that of a. Rather, small nuclei of p must form initially in the a phase. This first step in the phase transformation, the nucleation of clusters of the new phase, can actually be very slow. For example, at a relative humidity of 200% at 20°C (293 K), far above any relative humidity achieved in the ambient atmosphere, the rate at which water droplets nucleate homogeneously is about 10 54 droplets per cm3 per second. Stated differently, it would take about 1054 s (1 year is 3 x 107 s) for one droplet to appear in 1 cm3 of air. Yet, we know that droplets are readily formed in air at relative humidities only slightly over 100%. This is a result of the fact that water nucleates on foreign particles much more readily than it does on its own. Once the initial nucleation step has occurred, the nuclei of the new phase tend to grow rather rapidly. Nucleation theory attempts to describe the rate at which the first step in the phase transformation process occurs—the rate at which the initial very small nuclei appear. Whereas nucleation can occur from a liquid phase to a solid phase (crystallization) or from a liquid phase to a vapor phase (bubble formation), our interest will be in nucleation of trace substances and water from the vapor phase (air) to the liquid (droplet) or solid phase. [Pg.489]

The few observations of nucleation in the free troposphere are consistent with binary sulfuric acid-water nucleation. In the boundary layer a third nucleating component or a totally different nucleation mechanism is clearly needed. Gaydos et al. (2005) showed that ternary sulfuric acid-ammonia-water nucleation can explain the new particle formation events in the northeastern United States through the year. These authors were able to reproduce the presence or lack of nucleation in practically all the days both during summer and winter that they examined (Figure 11.16). Ion-induced nucleation is expected to make a small contribution to the major nucleation events in the boundary layer because it is probably limited by the availability of ions (Laakso et al. 2002). Homogeneous nucleation of iodine oxide is the most likely explanation for the rapid formation of particles in coastal areas (Hoffmann et al. 2001). It appears that different nucleation processes are responsible for new particle formation in different parts of the atmosphere. Sulfuric acid is a major component of the nucleation growth process in most cases. [Pg.530]

Noppel, M., Vehkamaki, H., and Kulmala, M. (2002) An improved model for hydrate formation in sulfuric acid-water nucleation, J. Chem. Phys. 116, 218-228. [Pg.535]

Lammel, G., and Novakov, T. (1995) Water nucleation properties of carbon black and diesel soot particles, Atmos. Environ. 29, 817-823. [Pg.825]

Sulfuric acid-water nucleation falls into the category where component B (H2SO4) is present at a very small concentration relative to that of A (H2O), yet the critical cluster is not dilute with respect to H2SO4. Thus the preexponential factor (10.94) applies. The rate... [Pg.576]

Reduced AA exists predominantly as the ascorbate anion in most body fluids. Molecules that are comparably water soluble diffuse rapidly through nonspecific pathways in cell membranes, especially through the lipid bilayer. In contrast, ascorbate, because of its size and charge, does not readily permeate the lipid bilayer. Simple diffusion of DHAA into cells is negligible probably due to the structure and water nucleation around the molecule. Weak organic acids can enter cells by simple diffusion of their undissociated forms. Once in the cytoplasm, these acids dissociate into organic ions and protons. However, it has been demonstrated that this process did not occur for AA (Wilson and Dixon, 1989). [Pg.260]

The pioneering work of Gershberg and Longfield [52] deals with the steady-state number of polystyrene particles per unit volume of water nucleated in a stirred tank reactor or a series of stirred tank reactors based on the conventional Smith-Ewart theory (see Chapter 3, Section 3.1.1), as shown by the following balance equation. [Pg.191]

FIGURE 7 The weighted mean annual a 0 values of precipitation compared with mean surface temperature. The correlation is best observed for stations where the mean annual temperature Is less than 15°C. The inset shows a schematic representation illustrating why there should be a correlation between surface temperature and precipitation when the primary fractionation step is occurring during liquid water nucleation in the clouds. This type of correlation (slightly less that r/1 per mil change in mean meteoric water) is the basis for proxy paleotemperature estimates e.g., ice cores). [Pg.224]

A trick to accelerate the simulation is to impose order parameters relevant to the description of the crystalline state to drive the system towards nucleation. This method was applied to the study of water nucleation and carbon dioxide hydrate formation using a conventional Monte Carlo method. ° ° Stein-hardt s bond-orientational order parameters Q and W , based on quadratic and third-order invariants formed from bond spherical harmonics (Y/ ,(0, (p)), were employed. These order parameters allow quantitative measures of the local symmetry in liquids and glasses. The rotationally invariant orientational order parameters are defined as ... [Pg.355]

In this context, cooperativity does not necessarily mean that different parts of the system depend on and need to interact with each other to change the macrostate (or the phase). Rather, local parts of the system can react individually in the same way upon a weak change of the environmental conditions. In the freezing transition of water, nucleation cores form independently and attract other molecules in the local environment of each nucleus to join. This leads to macroscopic crystalline structures which finally bind to each other in order to reduce instabilities due to surface effects. However, the individual growth of the nucleation centers also causes dislocations that typically appear at the boundaries of these crystalline substructures,... [Pg.53]


See other pages where Water nucleate is mentioned: [Pg.278]    [Pg.427]    [Pg.326]    [Pg.122]    [Pg.417]    [Pg.421]    [Pg.425]    [Pg.59]    [Pg.240]    [Pg.516]    [Pg.584]    [Pg.521]    [Pg.64]    [Pg.69]    [Pg.185]    [Pg.197]    [Pg.153]   
See also in sourсe #XX -- [ Pg.51 ]




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