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Formula atomic ratio from

We could calculate the number of atoms of the remaining elements in the same maimer, or we can use the atom ratios from the molecular formula. The carbon atom to nitrogen atom ratio in a urea molecule is 1 2, the oxygen atom to nitrogen atom ratio is 1 2, and the hydrogen atom to nitrogen atom ration is 4 2. [Pg.43]

To this point, our study of chemistry has been largely qualitative, involving very few calculations. However, chemistry is a quantitative science. Atoms of elements differ from one another not only in composition (number of protons, electrons, neutrons), but also in mass. Chemical formulas of compounds tell us not only the atom ratios in which elements are present but also the mass ratios. [Pg.51]

Colour centres are formed if a crystal of NaCl is heated in sodium vapour sodium is taken into the crystal, and the formula becomes Nai+/fl. The sodium atoms occupy cation sites, creating an equivalent number of anion vacancies they subsequently ionize to form a sodium cation with an electron trapped at the anion vacancy. The solid so formed is a non-stoichiometric compound because the ratio of the atomic components is no longer the simple integer that we have come to expect for well-characterized compounds. A careful analysis of many substances, particularly inorganic solids, demonstrates that it is common for the atomic ratios to be non-integral. Uranium dioxide, for instance, can range in composition from UOi 05 to UO2.25, certainly not the perfect UO2 that we might expect Many other examples exist, some of which we discuss in some detail. [Pg.246]

Tables 3.1, 3.2 and 3.3 compiled by Povarennykh (1963) specify the initial data accepted for the calculation of hardness from formulae (3.5) and (3.6). As the ratio WJWa increases, the coefficient a decreases (Table 3.1). For compounds with ratios inverse to those given in the table, i.e., for compounds having a so-called antistructure, the coefficient a will be exactly the same, e.g., 1/2 and 2/1. In both cases, x — 80. The link attenuation coefficient / varies over a relatively narrow range, usually between 0.7 and 1.0 (Table 3.2). This coefficient requires the state of lattice linkage to be considered in each case, and like coefficient a it depends on the type of compound involved. For various types of compounds, the values of the coefficient / may be lower taking as an example minerals in the pyrite and skutterudite group, they are as follows for compounds 2/2—0.60, for 3/3—0.48 and for 4/4—0.39. The values of the coefficient y grow proportionally with coordination number (Table 3.3). The constancy of the coefficient y depends on the constancy of the coordination number which is influenced by the valence ratio of electropositive and electronegative atoms. Lattice spacings, state of chemical bonds and electron-shell structure, and for complex compounds, also the degree of action of the remain-... Tables 3.1, 3.2 and 3.3 compiled by Povarennykh (1963) specify the initial data accepted for the calculation of hardness from formulae (3.5) and (3.6). As the ratio WJWa increases, the coefficient a decreases (Table 3.1). For compounds with ratios inverse to those given in the table, i.e., for compounds having a so-called antistructure, the coefficient a will be exactly the same, e.g., 1/2 and 2/1. In both cases, x — 80. The link attenuation coefficient / varies over a relatively narrow range, usually between 0.7 and 1.0 (Table 3.2). This coefficient requires the state of lattice linkage to be considered in each case, and like coefficient a it depends on the type of compound involved. For various types of compounds, the values of the coefficient / may be lower taking as an example minerals in the pyrite and skutterudite group, they are as follows for compounds 2/2—0.60, for 3/3—0.48 and for 4/4—0.39. The values of the coefficient y grow proportionally with coordination number (Table 3.3). The constancy of the coefficient y depends on the constancy of the coordination number which is influenced by the valence ratio of electropositive and electronegative atoms. Lattice spacings, state of chemical bonds and electron-shell structure, and for complex compounds, also the degree of action of the remain-...
Elemental analysis is a common tool used for the characterization and differentiation of HS isolated from organic amendments and unamended and amended soils. It provides information on the distribution of major elements, typically C, H, N, S, and O, in HS, thus setting limits for HS possible molecular composition. The atomic ratios C/N, C/H, and O/C are also useful in identifying types of HS, monitoring their structural changes, and devising HS structural formulas (Stevenson, 1994 Senesi and Loffredo, 1999). [Pg.152]

This approach has also been attempted by Koch et al. (2005), who used FTTCR-MS (positive ion mode) to analyze samples that were isolated by Ci8 SPE from the Weddell Sea in Antarctica. For six samples from depths of 30-4600 m, an average of 1064 245 molecular formulae could be assigned for each sample by assuming that the compounds contained only C, H, and O. Those molecular formulae were used, in turn, to calculate an intensity-weighted average elemental composition for each sample. If the tabulated average elemental compositions and atomic ratios of Koch et al. (2005) for the six samples of marine DOM are themselves averaged, the... [Pg.435]

In addition to using the absolute intensities of the atomic emission lines, the peak intensity ratios of these lines have been used to analyze samples. Tran et al. [77] analyzed the atomic intensity ratios of several organic compounds with the hope to determine the empirical formula of a compound based on the ratios from several elements. Calibration curves were built based on C H, C 0, and C N atomic emission ratios from various compounds that covered a wide range of stoichiometries. Then, four compounds with known stoichiometries were tested against the calibration curves. The ratios determined from the calibration curves were compared with the actual stoichiometries and showed accuracy of 3% on average. In the study of nitroaromatic and polycyclic aromatic hydrocarbon samples, the ratios between C2 and CN and between O and N of different samples were shown to correlate with the molecular formula [75], Anzano et al. [71] also attribute success of their correlation of plastics to differences in the C/H atomic emission intensity ratio of each sample. [Pg.294]

The nomenclature for molecular compounds is much less complicated than for ionic compounds. Molecular compounds are formed from covalently bonded nonmetallic elements. The formula for a molecule represents a stable unit of atoms, unlike a formula for an ionic compound, which only represents the simplest whole number ratio of ions. As a result, molecular formulas cannot be simplified like formulas for ionic compounds. An example would... [Pg.232]

The chemical formula for a compound gives the ratio of atoms of each element in the compound to atoms of every other element in the compound. It also gives the ratio of dozens of atoms of each element in the compound to dozens of atoms of every other element in the compound. Moreover, it gives the ratio of moles of atoms of each element in the compound to moles of atoms of every other element in the compound. For example, a given quantity of H2O has 2 mol of H atoms for every mole of O atoms, and a given quantity of CH4 has 1 mol of C atoms for every 4 mol of H atoms. The mole ratio from the formula can be used as a factor to convert from moles of any element in the formula to moles of any other element or to moles of the formula unit as a whole. In Figure 7.2, these additional conversions have been added to those already presented in Figure 7.1. [Pg.202]

All of these glasses were made with the Type 3 Fe-Mn sludge at 1150°G. Mix 5 is based on the English-Italian model. All atom ratios are in the range for a good glass. Mix 6 is based on the Hahn-Meitner formula. Mix 7 is from Jiilich, and Mix 8 is the Karlsruhe formula which... [Pg.21]

A striking feature of this table is the variety of formulae of alloys with a particular structure. Hume-Rothery first pointed out that these formulae could be accounted for if we assume that the appearance of a particular structure is determined by the ratio of valence electrons to atoms. Thus for all the formulae in the first two columns we have an electron atom ratio of 3 2, for the third column 21 13, and for the fourth 7 4, if we assume the normal numbers of valence electrons for all the atoms except the triads in Group VIII of the Periodic Table. These fit into the scheme only if we assume that they contribute no valence electrons, as may be seen from the following examples ... [Pg.1044]

If the chemical composition of the tar is known, the procedure to compute its chemical availability is entirely parallel to that used for coals and chars. After estimating the tar s lower heating value and determining its atomic ratios, the corresponding formula from table II is applied. [Pg.55]

These mole quantities represent numbers of atoms (remember that a mole of atoms is 6.022 x 10 atoms). It is clear from the moles of atoms that the compound contains an equal number of Ni and O atoms, so the formula is NiO. This is the empirical formula it expresses the smallest whole-number ratio of atoms ... [Pg.199]

Boranes and carboranes have structures in which their skeletal B- or C-atoms form triangular-faced polyhedra. There are basically three structural types, namely the closo- (an euphonious modification of the Greek clovo = cage, i. e., a complete or closed polyhedron), the nido (from Latin nest-like ) and the arachno- (from Greek cob-web ) structure. Each of these three types is adopted by cluster compounds of specific atomic ratios. c/o o-Structures occur in borane dianions B H , in car-borane anions (CB iH ) , and carboranes (C2B 2H ). Each skeletal atom has a single H-atom terminally attached by a bond directed outwards, away from the polyhedron center (see the example of BioHio in Fig. 3-1 below). Wo-Structures are adopted by boranes B H +4 and their related carboranes CB iH +3, C2H 2H +2 etc., and amc/z/2o-structures by boranes B H +6 and related carboranes CB iH +5, C2B 2H +4 etc. In other words, carboranes have the general formula [(CH) (BH) Hc] , where the sum a + c + x) is equal to 2 for a closo-structure, 4 for a /do-structure, and 6 for an amc/z o-structure. [Pg.102]


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See also in sourсe #XX -- [ Pg.68 ]




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