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Elements alkaline earth metals

BeryUium reacts with fused alkaU haUdes releasing the alkaU metal until an equUibrium is estabUshed. It does not react with fused haUdes of the alkaline-earth metals to release the alkaline-earth metal. Water-insoluble fluoroberyUates, however, are formed in a fused-salt system whenever barium or calcium fluoride is present. BeryUium reduces haUdes of aluminum and heavier elements. Alkaline-earth metals can be used effectively to reduce beryUium from its haUdes, but the use of alkaline-earths other than magnesium [7439-95-4] is economically unattractive because of the formation of water-insoluble fluoroberyUates. Formation of these fluorides precludes efficient recovery of the unreduced beryUium from the reaction products in subsequent processing operations. [Pg.66]

Group-2 Elements Alkaline Earth Metals Increasing Decreasing Exceptions... [Pg.267]

Metals alkali metals (group 1 elements), alkaline earth metals (group 2 elements), transition metals (groups 3 to 11), post-transition metals (group 12 elements and Al, Ga, In, Tl, Sn, Pb, Bi), lanthanides and actinides... [Pg.24]

Group IIB and know that this means the group of elements zine. cadmium and mercury, whilst Group IIA refers to the alkaline earth metals beryllium, magnesium, calcium, barium and strontium. [Pg.13]

The elements in Group II of the Periodic Table (alkaline earth metals) are. in alphabetical order, barium (Ba). beryllium (Be), calcium (Ca). magnesium (Mg), radium (Ra) and strontium (Sr). [Pg.136]

The calculations indicate that the 8 subsheU should fiU at elements 119 and 120, thus making these an alkaH and alkaline earth metal, respectively. Next, the calculations point to the filling, after the addition of a 7t7 electron at element 121 of the inner 5 and (if subsheUs, 32 places in aU, which the author has termed the superactinide elements and which terminates at element 153. This is foUowed by the filling of the 7d subsheU (elements 154 through 162) and 8 subsheU (elements 163 through 168). [Pg.227]

Bina Selenides. Most biaary selenides are formed by beating selenium ia the presence of the element, reduction of selenites or selenates with carbon or hydrogen, and double decomposition of heavy-metal salts ia aqueous solution or suspension with a soluble selenide salt, eg, Na2Se or (NH 2S [66455-76-3]. Atmospheric oxygen oxidizes the selenides more rapidly than the corresponding sulfides and more slowly than the teUurides. Selenides of the alkah, alkaline-earth metals, and lanthanum elements are water soluble and readily hydrolyzed. Heavy-metal selenides are iasoluble ia water. Polyselenides form when selenium reacts with alkah metals dissolved ia hquid ammonia. Metal (M) hydrogen selenides of the M HSe type are known. Some heavy-metal selenides show important and useful electric, photoelectric, photo-optical, and semiconductor properties. Ferroselenium and nickel selenide are made by sintering a mixture of selenium and metal powder. [Pg.332]

Strontium [7440-24-6] Sr, is in Group 2 (IIA) of the Periodic Table, between calcium and barium. These three elements are called alkaline-earth metals because the chemical properties of the oxides fall between the hydroxides of alkaU metals, ie, sodium and potassium, and the oxides of earth metals, ie, magnesium, aluminum, and iron. Strontium was identified in the 1790s (1). The metal was first produced in 1808 in the form of a mercury amalgam. A few grams of the metal was produced in 1860—1861 by electrolysis of strontium chloride [10476-85-4]. [Pg.472]

Boron tnhahdes can be reduced to elemental boron by heating and presence of alkah metals, alkaline-earth metals, or (22—26) such reductions... [Pg.222]

Calcium [7440-70-2J, Ca, a member of Group 2 (IIA) of the Periodic Table between magnesium and strontium, is classified, together with barium and strontium, as an alkaline-earth metal and is the lightest of the three. Calcium metal does not occur free in nature however, in the form of numerous compounds, it is the fifth most abundant element constituting 3.63% of the earth s cmst. [Pg.399]

The carbides of the lanthanoids and actinoids can be prepared by heating M2O3 with C in an electric furnace or by arc-melting compressed pellets of the elements in an inert atmosphere. They contain the C2 unit and have a stoichiometry MC2 or M4(C2)3. MC2 have the CaC2 structure or a related one of lower symmetry in which the C2 units lie at right-angles to the c-axis of an orthogonal NaCl-type cell. They are more reactive than the alkaline-earth metal... [Pg.298]

Using tables of free energies of formation it is clear that most metals will react with most HX. Moreover, in many cases, e.g. with the alkali metals, alkaline earth metals, Zn, A1 and the lanthanide elements, such reactions are extremely exothermic. It is also clear that Ag should react with HCl, HBr and HI but not with HF, and... [Pg.813]

The three series of elements arising from the filling of the 3d, 4d and 5d shells, and situated in the periodic table following the alkaline earth metals, are commonly described as transition elements , though this term is sometimes also extended to include the lanthanide and actinide (or inner transition) elements. They exhibit a number of characteristic properties which together distinguish them from other groups of elements ... [Pg.905]

Electrons are not only charged, they also have a characteristic physicists call spin. Pairing two electrons by spin, which has two possible values, up or down, confers additional stability. Bei yllium (Be, atomic number 4) has two spin-paired electrons in its second shell that are easily given up in chemical reactions. Beryllium shares this characteristic with other elements in column two, the alkaline earth metals. These atoms also generally form ionic bonds. Boron... [Pg.806]

The person whose name is most closely associated with the periodic table is Dmitri Mendeleev (1836-1907), a Russian chemist. In writing a textbook of general chemistry, Mendeleev devoted separate chapters to families of elements with similar properties, including the alkali metals, the alkaline earth metals, and the halogens. Reflecting on the properties of these and other elements, he proposed in 1869 a primitive version of today s periodic table. Mendeleev shrewdly left empty spaces in his table for new elements yet to be discovered. Indeed, he predicted detailed properties for three such elements (scandium, gallium, and germanium). By 1886 all of these elements had been discovered and found to have properties very similar to those he had predicted. [Pg.33]

Heating with the following solids, their fusions, or vapours (a) oxides, peroxides, hydroxides, nitrates, nitrites, sulphides, cyanides, hexacyano-ferrate(III), and hexacyanoferrate(II) of the alkali and alkaline-earth metals (except oxides and hydroxides of calcium and strontium) (b) molten lead, silver, copper, zinc, bismuth, tin, or gold, or mixtures which form these metals upon reduction (c) phosphorus, arsenic, antimony, or silicon, or mixtures which form these elements upon reduction, particularly phosphates, arsenates,... [Pg.95]

A mercury cathode finds widespread application for separations by constant current electrolysis. The most important use is the separation of the alkali and alkaline-earth metals, Al, Be, Mg, Ta, V, Zr, W, U, and the lanthanides from such elements as Fe, Cr, Ni, Co, Zn, Mo, Cd, Cu, Sn, Bi, Ag, Ge, Pd, Pt, Au, Rh, Ir, and Tl, which can, under suitable conditions, be deposited on a mercury cathode. The method is therefore of particular value for the determination of Al, etc., in steels and alloys it is also applied in the separation of iron from such elements as titanium, vanadium, and uranium. In an uncontrolled constant-current electrolysis in an acid medium the cathode potential is limited by the potential at which hydrogen ion is reduced the overpotential of hydrogen on mercury is high (about 0.8 volt), and consequently more metals are deposited from an acid solution at a mercury cathode than with a platinum cathode.10... [Pg.513]

With all these advantages one might well wonder why the left-step table has not attracted more attention and indeed why it has not been widely adopted. The answer to this question lies in the placement of one crucial element, helium. In the left-step table, helium is placed among the alkaline earth metals as mentioned above. To most chemists this is completely abhorrent since helium is regarded as the noble gas par excellence. Meanwhile, to a physicist or somebody who emphasizes electronic properties, helium falls rather naturally into the alkaline earths since it has two outer-shell electrons. [Pg.9]

Laby21 demonstrated in 1930, with a photographic plate as detector, that copper or iron in zinc could be detected in concentrations approaching 1 part per million by weight. To be sure, he used electron excitation so that absorption effects were minimized (7.10). By contrast, attempts made in the authors laboratory to estimate alkaline-earth metals in brines were unsuccessful, primarily because of the high absorption effects that accompanied x-ray excitation. The use of dilution with a relatively transparent solvent can sometimes reduce or eliminate absorption effects (7.8), but this procedure will fail if the element to be determined is present at too low a concentration in the presence of another substance (the salt in brine in the example cited) primarily responsible for the absorption effect. A case in which dilution is helpful in connection with the absorption effect of the. element sought is that of tetraethyllead fluid in gasoline (7.13). [Pg.232]

The alkaline earth metals, by assuming the configuration nsnp, are able to form twice as many bonds as the alkalis. Similarly the succeeding elements in the periodic table can form bonds in increasing number. [Pg.345]


See other pages where Elements alkaline earth metals is mentioned: [Pg.20]    [Pg.198]    [Pg.201]    [Pg.546]    [Pg.27]    [Pg.129]    [Pg.174]    [Pg.327]    [Pg.412]    [Pg.946]    [Pg.949]    [Pg.1257]    [Pg.32]    [Pg.48]    [Pg.535]    [Pg.541]    [Pg.305]    [Pg.401]    [Pg.211]    [Pg.759]    [Pg.14]    [Pg.44]    [Pg.1012]    [Pg.377]   
See also in sourсe #XX -- [ Pg.65 ]




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