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Tin -ONE

Fig. 3.6. (a) The copper-nickel diagram is a good deal simpler than the lead-tin one, largely because copper and nickel are completely soluble in one another in the solid state. (b) The copper-zinc diagram is much more involved than the lead-tin one, largely because there are extra (intermediate) phases in between the end (terminal] phases. However, it is still an assembly of single-phase and two-phase fields. [Pg.31]

There are two allotropes of tin. One is known as gray or alpha (a) tin, which is not very stable. The other is known as white tin or beta ((3), which is the most common allotrope. The two forms (allotropes) of tin are dependent on temperature and crystalline structure. White tin is stable at about 13.2°C. Below this temperature, it turns into the unstable gray alpha form. There is also a lesser-known third allotrope of tin called brittle tin, which exists above 161°C. Its name is derived from its main property. [Pg.201]

Cream (eight examples) Four had iron (trace-small amounts) and no tin one had tin (large amount) and no iron three had neither iron nor tin. [Pg.416]

In most types of IC s, the contacts can end on n+ or p+ mono-crystalline silicon, poly-silicon, various types of silicides, and other materials such as TiN. One of the most important properties of the contact and the via is the contact resistance (Rc) ... [Pg.4]

The reduction of iodate with aqueous sulfiir dioxide would be far cheaper than reduction with because sulfur dioxide costs less than tin. One reason this is so is because sulfuric acid, for which SOj is an mtermediate, is prepared worldwide on an enormous scale. [Pg.159]

Good Soft Solder, —Good soft solder is composed of equal parts of pme tin and good soft lead. The lead from old tea-choats is excellent. Plumbers" solder ia often made of lead three parts and tin one part. [Pg.387]

There is no subject Concerning which more different opinions have been expressed that tins one of milk control. Nevertheless a sound science and practice of safe milk production has been built up. The following testing and inspection has been found to result in satisfactory milk control ... [Pg.372]

Figure 8 is depicting the resist insensitivity to TiN substrates. The resist based on a partially crosslinked acetal protected PHS as binder resin was processed on TiN, one of the most critical substrates in this respect (48-50). In contrast to the t-BOC protected polymer based formulations no footing was observed. [Pg.88]

Data on the formation of the chemical composition of the waters of the Far East deposits (including tin ones) are given in the works (Kisileva et al., 1979 Kolotov et al., 1979 Zvereva, 2007, 2008 Zvereva, Krupskaya, 2012). They show that the Sn content can reach 0.030 mg/1 that is 40 times higher than the background values, and Cu, Pb, Zn, and Mn contents are 15—40 times higher than the background ones. The lengtti of the dispersion current is about 1.5 km. [Pg.262]

Take, for example, the dissolution of tin from a plated wire. This determination could be made non-electrochemically, the final result being obtained by a volumetric titration. On the other hand, the dissolution can be carried out electrochemically in one cell, with a second cell, connected in series, in which silver is dissolved from a silver anode. The amoxint of tin oxidized in the first cell becomes directly related to the amount of silver dissolved in the second, and this can be determined volumetrically. The result is that instead of titrating the tin, one titrates the silver. If silver can be quantified with greater accuracy and convenience than tin, then this becomes a useful procedure, but not otherwise. [Pg.405]

Tin, element 50, has 14 electrons outside of the krypton shell, and nine stable orbitals Ad, 5s, 5p). The five Ad orbitals, which are more stable than the 55 and 5p orbitals, are occupied by five unshared electron pairs. The remaining four electrons may separately occupy the four tetrahedral 5s5p - orbitals, and be used in forming four bonds, tetrahedrally directed. In fact, gray tin, one of the two allotropic forms of the element, has the diamond structure. The tin atoms in gray tin are quadrivalent, as are the carbon atoms in diamond. They have no metallic orbital, and gray tin is not a metal, but is a metalloid. [Pg.570]

Since the Sn — Sn potential is only—0.15 v. tin is easily oxidized to its highest oxidation state and most radiochemical tin procedures deal almost-exclusively with stannic tin. With a single oxidation state predoininating, one would expect the chemistry of tin to be relatively simple. Tin salts may be fairly easily volatilized, however, and stannic tin in aqueous solution has a notable tendency to hydrolyze at the slightest provocation. This behavior, plus the fact that there are very few chemical separation steps which are at all selective for tin, makes tin one of the more difficult elements to obtain radiochemically pure. A more detailed description of the chemical behavior of stannic tin will be presented in subsequent sections. [Pg.6]

Tin.—One of the major uses of stannanes is as precursors to difficultly available lithium derivatives, as discussed above. Scheme 16 represents a further example leading to an a-alkoxyorganolithium reagent, and where the critical intermediate results from addition of RaSn". The new reagent PhS(MeaSn)CuLi efficiently replaces the halogen of )3-iodo-a,/3-enones by McaSn, in contrast to MeaSnLi. " However, the relative ease of Michael addition of the two reagents to simple a,/3-enones is reversed. [Pg.219]

Figures 5 and 6 show the band structures of ZrC and ZrN, respectively. The band structures are similar to those of TiC and TiN. One can recognize the s band (originating from the state Fi), the p bands (originating from the state Fis), and the d bands (originating from the states r 25 and Fi2). The M-s band, which lies above the d bands in the 3d compounds, is found to lie in ZrC and ZrN at much lower energies. The states of the bands at higher energies are highly delocalized and represent a mixture of different symmetries. Figures 5 and 6 show the band structures of ZrC and ZrN, respectively. The band structures are similar to those of TiC and TiN. One can recognize the s band (originating from the state Fi), the p bands (originating from the state Fis), and the d bands (originating from the states r 25 and Fi2). The M-s band, which lies above the d bands in the 3d compounds, is found to lie in ZrC and ZrN at much lower energies. The states of the bands at higher energies are highly delocalized and represent a mixture of different symmetries.
Figure Cl.4.5. Population modulation as the atom moves through the standing wave in the Tin-periD-lin one dimensional optical molasses. The population lags the light shift such that kinetic is converted to potential energy then dissipated into the empty modes of the radiation field by spontaneous emission (after 1171). Figure Cl.4.5. Population modulation as the atom moves through the standing wave in the Tin-periD-lin one dimensional optical molasses. The population lags the light shift such that kinetic is converted to potential energy then dissipated into the empty modes of the radiation field by spontaneous emission (after 1171).
Lead has only one form, a cubic metallic lattice. Thus we can see the change from non-metal to metal in the physical structure of these elements, occurring with increasing atomic weight of the elements carbon, silicon, germanium, tin and lead. [Pg.168]

The greater metallic nature of tin is clearly indicated here for tin forms only one hydride, stannane, SnH4. It is best prepared by the... [Pg.176]

Lead, like tin, forms only one hydride, plumbane. This hydride is very unstable, dissociating into lead and hydrogen with great rapidity. It has not been possible to analyse it rigorously or determine any of its physical properties, but it is probably PbH4. Although this hydride is unstable, some of its derivatives are stable thus, for example, tetraethyllead, Pb(C2Hj)4, is one of the most stable compounds with lead in a formal oxidation state of + 4. It is used as an antiknock in petrol. [Pg.177]

Coordin ates of atom s can he set by n orm al translation orrotation of HyperCh cm molecules, fo set initial velocities, however, it is necessary to edit th e H l. file explicitly. The tin it o f velocity in the HIN file is. An gstrom s/picosecon d.. Areact.hin file and a script react.scr are in eluded with HyperChem to illustrate one simple reacting trajectory. In order to have these initial velocities used in a trajectory the Restart check box of the Molecular Dynamics Option s dialog box must he checked. If it is n ot, the in itial velocities in the HIN file will be ignored and a re-equilibration to the tern peratiire f of th e Molecular Dyn am ics Option s dialog box will occur. This destroys any imposed initial conditions on the molecular dynamics trajectory. [Pg.329]

Secondary and tertiary amines are not generally prepared in the laboratory. On the technical scale methylaniline is prepared by heating a mixture of aniline hydrochloride (55 parts) and methyl alcohol (16 parts) at 120° in an autoclave. For dimethylaniline, aniline and methyl alcohol are mixed in the proportion of 80 78, 8 parts of concentrated sulphuric acid are added and the mixture heated in an autoclave at 230-235° and a pressure of 25-30 atmospheres. Ethyl- and diethyl-anihne are prepared similarly. One method of isolating pure methyl- or ethyl-aniline from the commercial product consists in converting it into the Y-nitroso derivative with nitrous acid, followed by reduction of the nitroso compound with tin and hydrochloric acid ... [Pg.562]


See other pages where Tin -ONE is mentioned: [Pg.162]    [Pg.571]    [Pg.416]    [Pg.416]    [Pg.2839]    [Pg.354]    [Pg.2579]    [Pg.211]    [Pg.2838]    [Pg.242]    [Pg.433]    [Pg.162]    [Pg.571]    [Pg.416]    [Pg.416]    [Pg.2839]    [Pg.354]    [Pg.2579]    [Pg.211]    [Pg.2838]    [Pg.242]    [Pg.433]    [Pg.256]    [Pg.214]    [Pg.607]    [Pg.564]    [Pg.1208]    [Pg.2562]    [Pg.345]    [Pg.21]    [Pg.114]    [Pg.202]    [Pg.206]    [Pg.206]    [Pg.231]    [Pg.324]    [Pg.324]    [Pg.634]    [Pg.499]    [Pg.500]    [Pg.80]    [Pg.628]   


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