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Element relative reactivities

It is hard to generalize about the chemical reactivities of a group of elements since reactivities depend upon two factors (A) the relative stability of the specific compounds formed compared with the reactants used up, and, (B) the rate at which the reaction occurs. In special cases there are other complications. For example, chromium metal (familiar in the form of chrome plate) is highly reactive toward oxygen. Still, a highly polished piece of chromium holds... [Pg.390]

This section is concerned with elements other than titanium however, it is sometimes difficult to treat this element separately from the others because several authors49,190 compared in the same work the relative reactivity of different catalysts. In most cases, a mechanism has not been suggested, nor has the effidency of the catalyst been characterized. The order with respect to catalyst is almost never given. [Pg.89]

Thus, the chemical reactivity of the elements in seawater is reflected by the residence time. It is important to note, however, that while residence times tell us something about the relative reactivities, they also tell us nothing about the nature of the reactions. The best source of clues for imderstanding these reactions is to study the shape of dissolved profiles of the different elements. When we do this we find that there are six main characteristic types of profiles as described in Table 10-8. Notice that most of these reactions occur at the phase discontinuities between the atmosphere, biosphere, hydrosphere, and lithosphere. [Pg.258]

The STEM Is Ideally suited for the characterization of these materials, because one Is normally measuring high atomic number elements In low atomic number metal oxide matrices, thus facilitating favorable contrast effects for observation of dispersed metal crystallites due to diffraction and elastic scattering of electrons as a function of Z number. The ability to observe and measure areas 2 nm In size In real time makes analysis of many metal particles relatively rapid and convenient. As with all techniques, limitations are encountered. Information such as metal surface areas, oxidation states of elements, chemical reactivity, etc., are often desired. Consequently, additional Input from other characterization techniques should be sought to complement the STEM data. [Pg.375]

Asymmetric diarylmethanes, hydrogenolytic behaviors, 29 229-270, 247-252 catalytic hydrogenolysis, 29 243-258 kinetics and scheme, 29 252-258 M0O3-AI2O3 catalyst, 29 259-269 relative reactivity, 29 255-257 schematic model, 29 254 Asymmetric hydrogenations, 42 490-491 Asymmetric synthesis, 25 82, 83 examples of, 25 82 Asymmetry factor, 42 123-124 Atom-by-species matrix, 32 302-303, 318-319 Atomic absorption, 27 317 Atomic catalytic activities of sites, 34 183 Atomic displacements, induced by adsorption, 21 212, 213 Atomic rate or reaction definition, 36 72-73 structure sensitivity and, 36 86-87 Atomic species, see also specific elements adsorbed... [Pg.51]

Thorium is a relatively reactive, metallic radioactive element. Because thorium is a radioactive element, evaluation of adverse health effects due to exposure to thorium requires a slightly different approach than with chemicals. Radiation is a health risk because radioactive elements can emit energetic particles or electromagnetic radiation that can damage cells. Radioactive elements are those that undergo spontaneous disintegration (decay) in which energy is released (emitted) either in... [Pg.26]

Look at Table 4.3 to find the relative reactivities of the elements. [Pg.134]

The vertical distributions of Be, Ba and Ra contrast sharply with those of Ca and Sr (Fig. 12.3). In the case of Be, low concentrations near the surface are likely to be attributable to the enhanced reactivity of this element relative to other Group 2 members. Due to a relatively large z2/r, Be11 is significantly hydrolysed in solution (BeOH+ and BeOH ) and should be much more reactive with biogenic particles than is the case for Mg2+, Ca2+ and Sr2+. [Pg.332]

This chapter presents a comprehensive review of the chemistry of organosilanes which have a nitrogen atom on the a-carbon in their structures. After presenting some elements relative to the structure, the synthesis, and the reactivity of SMAs in terms of making and cleaving bonds, their physicochemical and biological behaviors will be detailed. [Pg.178]

Carbon-14 content is measured by specially designed gas proportional counters (7. Aerosol samples are first converted to CO2 by combustion in a macroscale version of the thermal evolution technique. A clam shell oven was used to heat the sample for sequential evolution of organic and elemental carbon under equivalent conditions. Due to the possibility of thermal gradients, conditions in the macroscale apparatus were adjusted to produce the same recoveries of total carbon (yg C per cm of filter area) as for the microscale apparatus. Carbon-14 data are reported as % contemporary carbon based on the 1978 1 C02 content in the atmosphere. Aldehyde data referred to in this paper were obtained by impinger sampling in dinitrophenylhydrazine/acetonitrile solution and analysis of the derivatives by HPLC with UV detection (12). Olefin measurements were made by a specially designed ozone-chemiluminescence apparatus (13) difficulties in calibration accuracy and background drift with temperature limit its use to inferences of relative reactive hydrocarbon levels. [Pg.274]

Reactions. Sulfur is a relatively reactive element, with the majority of the reactions proceeding with cleavage of... [Pg.4614]

The reactions of tertiary phosphanes with elemental sulfur have been studied kinetically in detail. While trialkylphosphanes and, even more so, triaUcoxyphosphanes react with great vigor, certain arylphosphanes react slowly enough for kinetic data to be measured. It was found that diphenyl(2-tolyl)phosphane reacts with homocyclic sulfur molecules S (n = 6, 7, 8, 12) in CS2 at -12 to +35 °C in a second order reaction to give R2R PS. The activation energies (in klmol" ) see Activation) are 51 (Se), 40 (S7), 69 (Sg), and 46 (S12). At 20 °C, the relative reactivities (Sg = 1) are as follows ... [Pg.4691]

In the lower reaches of the Genesee River, the results of the extractions suggest that substances other than hydrous oxides are phosphorus sinks. This is evident where the amount of sediment phosphorus extracted by hydrochloric acid steadily increases down river, while the oxalate extractable phosphorus remains relatively constant. Schwertmann (2 ) emphasized that the results of such procedures are best considered as a measure of the relative amount of a phase or, more generally, a measure of an element s reactivity in a sediment under carefully controlled conditions. Laboratory experiments (Figure 8) show that phosphorus uptake by calcium carbonate, under simulated natural conditions, proceeds slowly. The large hydrochloric acid extractable component observed at Rochester may arise from slow uptake and subsequent mineralization of dissolved inorganic phosphorus by carbonate minerals. [Pg.754]

Uranium is a relatively reactive element. It combines with nonmetals such as oxygen, sulfur, chlorine, fluorine, phosphorus, and bromine. [Pg.643]

I) Nickel, Palladium, and Platinum. For the elements of group VIII, an assessment of the relative reactivity for the carbonyl insertion reaction is available in the literature. For reaction (a), koss (x s , 2.3°C) of the process was found to decrease in the... [Pg.605]

The relative reactivities of organometallics containing group 14 elements are closely associated with the electronegativity and dissociation energy of the M—C bonds of the elements. For example, some organotin compounds such as allylstannanes are easily decomposed to form radical species whereas homolysis of the carbon-silicon bond of allylsilanes is rarely achieved, which reflects the dissociation energy of the respective M—C bonds. [Pg.391]

An abbreviated relative reactivity table (Table 35) is given for the group VIA elements. The lack of fit for the selenium atoms is obvious, if the apparent trends are correct for the other elements. Yet, the care with which the selenium additions were studied certainly suggests that the rate coefficients are reasonably accurate. More research is desirable. [Pg.138]


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See also in sourсe #XX -- [ Pg.218 , Pg.219 ]




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