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Condensation on ions

Example 14.6 Determine the saturation ratio that corresponds to the diameter in Example 14.5. Hence, predict the minimum saturation ratio at which spontaneous condensation on ions will occur. Assume T = 0°C. From Eq. 14.13... [Pg.132]

The cloud chamber experiments of Wilson (summarized in his 1927 Nobel Lecture) qualitatively demonstrated two nudeation mechanisms (1) condensation on ions at relatively low saturation ratios and (2) condensation on uncharged molecular dusters at much higher saturation ratios. Wilson s studies of condensation on ions are discussed briefly in this chapter. His resulLs on nudeation by molecular dusters which served as a starting point for development of the theory of homogeneous nudeation are discussed in the next chapter. Wil.son .s principal interest was in condensation on ions and its application to the measurement of high-energy nuclear particles,... [Pg.251]

The goal of an experiment is to set up a critical chamber state—that is, a state that just produces nucleation at some height in the chamber where the vapor is critically supersaturated and droplets are visible. This occurs when the temperature difference across the chamber has been increased to the point where a rain of drops forms at an approximately constant height. Drop formation in this way must be distinguished from condensation on ions generated by cosmic rays passing through the chamber. An electrical field is applied to sweep out such ions which appear as a trail of drops. [Pg.281]

Metallization layers are generally deposited either by CVD or by physical vapor deposition methods such as evaporation (qv) or sputtering. In recent years sputter deposition has become the predominant technique for aluminum metallization. Energetic ions are used to bombard a target such as soHd aluminum to release atoms that subsequentiy condense on the desired substrate surface. The quaUty of the deposited layers depends on the cleanliness and efficiency of the vacuum systems used in the process. The mass deposited per unit area can be calculated using the cosine law of deposition ... [Pg.348]

Polytungsta.tes, An important and characteristic feature of the tungstate ion is its abiUty to form condensed complex ions of isopolytungstates in acid solution (38). As the acidity increases, the molecular weight of the isopolyanions increases until tungstic acid precipitates. However, the extensive investigations on these systems have been hampered by lack of weU-defined soHd derivatives. [Pg.289]

Figure 1 Schematic of DC glow-discharge atomization and ionization processes. The sample is the cathode for a DC discharge in 1 Torr Ar. Ions accelerated across the cathode dark space onto the sample sputter surface atoms into the plasma (a). Atoms are ionized in collisions with metastable plasma atoms and with energetic plasma electrons. Atoms sputtered from the sample (cathode) diffuse through the plasma (b). Atoms ionized in the region of the cell exit aperture and passing through are taken into the mass spectrometer for analysis. The largest fraction condenses on the discharge cell (anode) wall. Figure 1 Schematic of DC glow-discharge atomization and ionization processes. The sample is the cathode for a DC discharge in 1 Torr Ar. Ions accelerated across the cathode dark space onto the sample sputter surface atoms into the plasma (a). Atoms are ionized in collisions with metastable plasma atoms and with energetic plasma electrons. Atoms sputtered from the sample (cathode) diffuse through the plasma (b). Atoms ionized in the region of the cell exit aperture and passing through are taken into the mass spectrometer for analysis. The largest fraction condenses on the discharge cell (anode) wall.
The most widely deposition technique is the ion assisted deposition (lAD). A material in a melting-pot is vaporized by heating either with an electron beam, or by Joule effect, or with a laser beam, or with microwaves, or whatever else. The vapor flow condensates on the substrate. In the same time, an ion... [Pg.335]

Figure 19. Schematic view of the ion assisted deposition technique. As the vapor condenses on the substrate, ions hammer the coating in formation to compress it. Figure 19. Schematic view of the ion assisted deposition technique. As the vapor condenses on the substrate, ions hammer the coating in formation to compress it.
In ion beam deposition, hydrocarbon gas such as methane or ethyene is ionized into plasma by an ion source such as the Kaufman source [3]. The hydrocarbon ions are then extracted from the ion source and accelerated to form an ion beam. The ions and the unionized molecules condense on the substrate surface to form DEC coating. However, in this method, ionized ratio of precursor gases could hardly exceed 10 %. In order to obtain a better quality of DEC coatings. [Pg.147]

The Manning theory(16,17) predicts a critical value c above which counterions are condensated on polyion. In the case of monovalent ions, =1 and for > c, the chain expansion... [Pg.122]

In most cases the symmetric boron-capped clathrochelates have been synthesized by template condensation on a metal ion matrix as, for instance, is shown in Scheme 68 <2005MI3>. [Pg.625]

Cloud Chambers A chamber containing air saturated with vapor is used. Radioactive particles ionize air molecules in the chamber. Cooling the chamber causes droplets of liquid to condense on these ions, giving observable fog-like tracks. [Pg.378]

This chapter is designed to show how coordination chemistry may be studied in the gas phase and give some examples from the literature. The examples will mainly be from the past decade. This chapter will concentrate on ions studied by MS and cannot be comprehensive since the literature is too extensive. The literature involving coordination chemistry of gas-phase ions is very extensive and in many cases the quoted sources were often not aware of, or did not consider, the processes being observed as coordination chemistry. This chapter will concentrate on the reactions of transition metal systems and changes in coordination behavior. There will inevitably be similarities of gas- and condensed-phase behavior, but these instances may only be occasionally highlighted. [Pg.345]

In order to find out what R+ is, we consider first the common experience that when a tert- mty halide is treated with an aluminium halide under ordinary conditions, there is a brisk evolution of hydrogen halide and a coloured solution containing oligo-isobutylenes and condensed allylic ions is formed. In the present experiments the solutions were colourless, no hydrogen halide was evolved, and the conductivity was stable and behaved reversibly. Further, the rectilinearity of the k-[A1X3] plots in Figures 9 and 10, and the smallness of the intercepts on the K-axis, showed that ions generated by reactions other than those of type (viii) must have been very scarce, and for the experiment with tert-butyl bromide this was borne out by the absence of any byproducts. [Pg.320]

As mentioned above, a substantial part of the electrical charge of the micelle surface has been shown to be neutralized by the association of the counter ions with the micelle. In the calculation based on Equation 12, however, the loss in entropy arising from this counter ion association is not taken into account. This is by no means insignificant in comparison to of Equation 12 (4). A major part of the counter ions are condensed on the ionic micelle surface and counteract the electrical energy assigned to the amphiphilic ions on the micellar surface. The minor part of the counter ions,in the diffuse double layer, are also restricted to the vicinity of the micellar surface. [Pg.81]

Another important technology in the national security and homeland defense arena is ion trap secondary ion mass spectrometry. Many chemical warfare agents are not volatile and tend to condense on particle surfaces. Research at Idaho National Engineering and Environmental Laboratories has used this technology to analyze mustard agent on the surface of soil particles down to a surface coverage of 0.07 monolayers. [Pg.85]

Cations and anions with a strong solvation shell retain their solvation shell and thus interact with the electrode surface only through electrostatic forces. Since the interaction is exclusively electrostatic, the amount of these ions at the interface is defined by the electrostatic bias between the sample and the counter electrodes and independent from the chemical properties of the electrode surface non-specific adsorption. Considering the size effect of their hydration shell, these ions are able to approach the electrode to a distance limited by the size of the solvation shell of the ion. The center of these ions at a distance of closest approach defined by the size of the solvation shell is called the outer Helmholtz layer. The electrode surface and the outer Helmholtz layer have charges of equal magnitude but opposite sign, resulting in the formation of an equivalent of a plate condenser on a scale of a molecular layer. Helmholtz proposed such a plate condenser on such a molecular scale for the first time in the middle of the nineteenth century. [Pg.405]

A three-carbon unit can be introduced on ketosugars under Reformatsky conditions, as recently demonstrated by several groups [33,34], The analogous Dreiding-Schmidt procedure has also been applied in this case with successful double stereodifferentiation [35]. This is exemplified on ketone 18 which yields lactone 20 as a single isomer (see Scheme 10). The condensation on ketosugars of trimethylsilylacetate [36] or acrylate [33], in the presence of fluoride ion, has also been used with success for the synthesis of P-hydroxy acids or ra-methylene-y-lactones, respectively. [Pg.214]

Attention may be called, in conclusion, to the observation of Brunei 55 that cyclohexene oxide fails to condense with hydrogen cyanide ThiB is again compatible with the weakly nuoleopliilii-obaracter of the ON ion and the low dissociation constant of its conjugate acid. [Pg.199]


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See also in sourсe #XX -- [ Pg.263 ]




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