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Potassium valence

Is 2s 2p 3s 3p 3d 4s. If the 3d states were truly core states, then one might expect copper to resemble potassium as its atomic configuration is ls 2s 2p 3s 3p 4s The strong differences between copper and potassium in temis of their chemical properties suggest that the 3d states interact strongly with the valence electrons. This is reflected in the energy band structure of copper (figure Al.3.27). [Pg.129]

A typical absorption curve for vitreous siUca containing metallic impurities after x-ray irradiation is shown in Eigure 12. As shown, the primary absorption centers are at 550, 300, and between 220 and 215 nm. The 550-nm band results from a center consisting of an interstitial alkah cation associated with a network substituent of lower valency than siUcon, eg, aluminum (205). Only alkaUes contribute to the coloration at 550 nm. Lithium is more effective than sodium, and sodium more effective than potassium. Pure siUca doped with aluminum alone shows virtually no coloration after irradiation. The intensity of the band is deterrnined by the component that is present in lower concentration. The presence of hydrogen does not appear to contribute to the 550-nm color-center production (209). [Pg.510]

Examine electrostatic potential maps for potassium hydride and hydrogen chloride. How are they similar and how are they different (Focus on whether the molecules are polar or nonpolar (compare dipole moments), and on the electronic character of hydrogen.) Draw the ionic Lewis structure that is most consistent with each electrostatic potential map. Does each atom have a filled valence shell ... [Pg.123]

Electrodes and Galvanic Cells. In connection with Fig. 9 in See. 11 we discussed the removal of a positive atomic core from a metal. The same idea may be applied to any alloy that is a metallic conductor. When, for example, some potassium has been dissolved in liquid mercury, the valence electron from each potassium atom becomes a free electron, and we may discuss the removal of a K+ core from the surface of the amalgam. The work to remove the K+ into a vacuum may be denoted by Ycr When this amalgam is in contact with a solvent, we may consider the escape of a K+ into the solvent. The work Y to remove the positive core into the solvent is much smaller than Yvac. [Pg.217]

Potassium has one valence electron. It is the first member of the fourth row, the row based on the cluster of orbitals with about the same energy as the 45 orbital. There are nine such orbitals, tne 4s orbital, the three 4p orbitals, and the five 3d orbitals. Hence the fourth row of the periodic table will differ from the second and third rows. The fourth row, as seen in the periodic table, consists of eighteen elements. [Pg.271]

Potassium. K aw 39.102 at no 19 valence 1 soft, silvery metal, rapidly oxidized in moist air body-centered cubic structure mp 63° bp 770° d 0.862g/cc. Sol in liq ammonia, aniline, Hg and Na... [Pg.836]

In other crystals an octahedral metal atom is attached to six non-metal atoms, each of which forms one, two, or three, rather than four, bonds with other atoms. The interatomic distance in such a crystal should be equal to the sum of the octahedral radius of the metal atom and the normal-valence radius (Table VI) of the non-metal atom. This is found to be true for many crystals with the potassium chlorostannate (H 61) and cadmium iodide (C 6) structures (Table XIB). Data are included in Table XIC for crystals in which a tetrahedral atom is bonded to a non-metal atom with two or three covalent bonds. The values of dcalc are obtained by adding the tetrahedral radius for the former to the normal-valence radius for the latter atom. [Pg.177]

For a material to be a good conductor it must be possible to excite an electron from the valence band (the states below the Fermi level) to the conduction band (an empty state above the Fermi level) in which it can move freely through the solid. The Pauli principle forbids this in a state below the Fermi level, where all states are occupied. In the free-electron metal of Fig. 6.14 there will be plenty of electrons in the conduction band at any nonzero temperature - just as there will be holes in the valence band - that can undertake the transport necessary for conduction. This is the case for metals such as sodium, potassium, calcium, magnesium and aluminium. [Pg.232]

Sodium or potassium severely poisons Pt-Re catalysts but the manner in Which the alhali metal operates is not apparent. The present study was designed to use ESCA to determine the valence state of Re in Pt-Re bimetallic catalysts. The valence state would be determined in san les that had been reduced and transferred to the instrument without exposure to an oxidizing atmosphere. Catalysts with and without potassium would be examined. [Pg.58]

HEAVY ALKYNE ANION RADICALS The Only example of Compounds of this type, the anion radical of the valence isomer of distannyne 51-K, was recently synthesized by Power by the reduction of chlorostannylene 52 with potassium graphite in THF (Scheme 2.39). ... [Pg.85]

Apart from the two classifications described above, electrolytes may also be classified according to the number and valence of the ions produced. Thus, sodium chloride and copper sulfate may both be termed binary electrolytes since one molecule of each of these chemical substances is capable of producing two ions. In the case of sodium chloride, both the ions produced are univalent so that this substance may also be called a uni-univalent electrolyte. Copper sulfate, however, yields two bivalent ions and so may be called a bibivalent electrolyte. The valences of the ions are quoted in the positive-negative sequence. Calcium chloride and potassium sulfate are both ternary electrolytes since one molecule of each yields three ions the former is bi-univalent, whilst the latter is uni-bivalent. [Pg.612]

Redox titrants (mainly in acetic acid) are bromine, iodine monochloride, chlorine dioxide, iodine (for Karl Fischer reagent based on a methanolic solution of iodine and S02 with pyridine, and the alternatives, methyl-Cellosolve instead of methanol, or sodium acetate instead of pyridine (see pp. 204-205), and other oxidants, mostly compounds of metals of high valency such as potassium permanganate, chromic acid, lead(IV) or mercury(II) acetate or cerium(IV) salts reductants include sodium dithionate, pyrocatechol and oxalic acid, and compounds of metals at low valency such as iron(II) perchlorate, tin(II) chloride, vanadyl acetate, arsenic(IV) or titanium(III) chloride and chromium(II) chloride. [Pg.297]

Procedure 10% aqueous solution of potassium iodide, KI, when exposed to sunlight, liberated I2 due to the photolytic decomposition and gave blue colour with freshly prepared starch solution. The intensity of blue coloured complex with the starch increased many fold when the same solution was kept in the ultrasonic cleaning bath. As an extension of the experiment, the photochemical decomposition of KI could be seen to be increasing in the presence of a photocatalyst, Ti02, showing an additive effect of sonication and photocatalysis (sono-photocatalysis) However, the addition of different rare earth ions affect the process differently due to the different number of electrons in their valence shells. [Pg.391]

Group I sodium, potassium, etc + 1 Group VII fluorine, chlorine, etc. + 7), and a negative valency, such that the sum of the positive and negative numbers, neglecting signs, was always eight. [Pg.149]


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See also in sourсe #XX -- [ Pg.110 ]




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