Enthalpies dioxides

Note the much larger enthalpy of formation of silieon dioxide as compared with carbon dioxide this arises in part because of greater strength in the Si—O bonds and also because the Si—Si bond in silieon is mueh weaker than the C—C bond (p. 162). 

Equations (1) and (2) are the heats of formation of carbon dioxide and water respectively Equation (3) is the reverse of the combustion of methane and so the heat of reaction is equal to the heat of combustion but opposite in sign The molar heat of formation of a substance is the enthalpy change for formation of one mole of the substance from the elements For methane AH = —75 kJ/mol... 

With all components in the ideal gas state, the standard enthalpy of the process is exothermic by —165 kJ (—39.4 kcal) per mole of methane formed. Biomass can serve as the original source of hydrogen, which then effectively acts as an energy carrier from the biomass to carbon dioxide, to produce substitute (or synthetic) natural gas (SNG) (see Euels, synthetic). 

Some values of physical properties of CO2 appear in Table 1. An excellent pressure—enthalpy diagram (a large Mohier diagram) over 260 to 773 K and 70—20,000 kPa (10—2,900 psi) is available (1). The thermodynamic properties of saturated carbon dioxide vapor and Hquid from 178 to the critical point,... 

Available data on the thermodynamic and transport properties of carbon dioxide have been reviewed and tables compiled giving specific volume, enthalpy, and entropy values for carbon dioxide at temperatures from 255 K to 1088 K and at pressures from atmospheric to 27,600 kPa (4,000 psia). Diagrams of compressibiHty factor, specific heat at constant pressure, specific heat at constant volume, specific heat ratio, velocity of sound in carbon dioxide, viscosity, and thermal conductivity have also been prepared (5). 

The following tables of properties of carbon dioxide are available enthalpy, entropy, and heat capacity at 0 and 5 MPa (0 and 50 atm, respectively) from 273 to 1273 K pressure—volume product (PV), enthalpy, and isobaric heat capacity (C from 373 to 1273 K at pressures from 5 to 140 MPa (50-1,400 atm) (14). 

Pressure enthalpy diagram ammonia, 497 carbon dioxide, 498... 

The sulfoxidation of normal Cl4-CI7 paraffins with sulfur dioxide, oxygen, and water is performed under UV radiation in parallel reactors (1 in Fig. 3). The reaction enthalpy is dissipated by cooling of the paraffin in heat exchangers. The 30- to 60-kW UV lamps are cooled by a temperature-controlled water cycle. The reaction mixture leaving the reactors separates spontaneously into two phases in 2. The lighter paraffin phase is recirculated to the reactors. The composition of the heavy raw acid phase is shown in Table 5. 

Sublimation is the direct conversion of a solid into its vapor. Frost disappears on a cold, dry morning as the ice sublimes directly into water vapor. Solid carbon dioxide also sublimes, which is why it is called dry ice. Each winter on Mars, solid carbon dioxide is deposited as polar frost, which sublimes when the feeble summer arrives (Fig. 6.24). The enthalpy of sublimation, AHsub, is the molar enthalpy change when a solid sublimes ... 

FIGURE 6.28 The enthalpy changes for the reactions in which 1 mol CH4(g) burns to give carbon dioxide and water in either the gaseous (left) or the liquid (right) state. The difference in enthalpy is equal to 88 k), the enthalpy of vaporization of 2 mol H20(l). 

FIGURE 6.29 The standard reaction enthalpy is the difference in enthalpy between the pure products and the pure reactants, each at I bar and the specified temperature (which is commonly but not necessarily 298 K). The scheme here is for the combustion of methane gas to carbon dioxide gas and liquid water. 

The standard enthalpy of combustion, AH°, is the change in enthalpy per mole of a substance that is burned in a combustion reaction under standard conditions. The products of the combustion of an organic compound are carbon dioxide... 

Amino acids are the building blocks of proteins, which have long chainlike molecules. They are oxidized in the body to urea, carbon dioxide, and liquid water. Is this reaction a source of heat for the body Use the information in Appendix 2A to predict the standard enthalpy of reaction for the oxidation of the simplest amino acid, glycine (NH2CH2COOH), a solid, to solid urea (H2NCONH2), carbon dioxide gas, and liquid water ... 

Elemental sulfur exists in several forms, with rhombic-sulfur the most stable under normal conditions and monoclinic sulfur slightly less stable. The standard enthalpies of combustion of the two forms (to sulfur dioxide) are —296.83 kj-mol 1 and —297.16 kj-mol, respectively. Calculate the enthalpy of the rhombic —> monoclinic transition. 

Two successive stages in the industrial manufacture of sulfuric acid are the combustion of sulfur and the oxidation of sulfur dioxide to sulfur trioxide. From the standard reaction enthalpies... 

In the manufacture of nitric acid by the oxidation of ammonia, the first product is nitric oxide, which is then oxidized to nitrogen dioxide. From the standard reaction enthalpies... 

The vapor pressure of chlorine dioxide, Cl02, is 155 Torr at —22.75°C and 485 Torr at ().()0°C. Calculate (a) the standard enthalpy of vaporization (b) the standard entropy of vaporization (c) the standard Gibbs free energy of vaporization (d) the normal boiling point of C102. 

Our analysis of the reaction of nitrogen dioxide molecules is not unique. The same type of path can be visualized for any chemical reaction, as Figure 6-20 shows. The reaction enthalpy for any chemical reaction can be found from the standard enthalpies of formation for all the reactants and products. Multiply each standard enthalpy of formation by the appropriate stoichiometric coefficient, add the values for the products, add the values for the reactants, and subtract the sum for reactants from the sum for products. Equation summarizes this procedure ... 

We could evaluate the enthalpy for this reaction step by step, first decomposing methane into its elemental constituents and then recombining the elements into carbon dioxide and liquid water. There is no need to do this, however, because Equation summarizes the step-by-step processes. The products are one mole of CO2 and two moles of H2 O, and the reactants are one mole of CH4 and two moles of O2 ... 

Heat management is of crucial importance for ethylene oxide synthesis (see original citahons in [4]). The reachon enthalpy of the total oxidation to carbon dioxide (AH = -1327 kj/mol) is more than 10 times larger than that of the partial oxidahon (AH = -105 kJ/mol), which induces locally very hot temperatures (hot spots) with corresponding negative consequences on the reaction course. 

More recently, a number of reports dealing with 1,3-sulfonyl shifts which proceed by other mechanisms have been published. For example, Baechler and coworkers suggested that the higher activation enthalpy observed for the isomerization of the deuterium labeled methallyl sulfone 72 in nitrobenzene at 150°C as compared to the corresponding sulfide, together with the positive entropy of activation may be taken as evidence for a homolytic dissociation mechanism (equation 44). A similar mechanism has also been suggested by Little and coworkers for the gas-phase thermal rearrangement of deuterium labelled allyl sec-butyl sulfone, which precedes its pyrolysis to alkene and sulfur dioxide. 

Hydrazine is an unstable substance because of its positive enthalpy of formation. It decomposes when heated. The decomposition can cause an inflammation even in the absence of air. It can also combust spontaneously in the presence of various materials from clothes to soil (see tables in Part Three the self-ignition temperatures vary according to the materials in contact with hydrazine). Also, violent decomposition of hydrazine in a steel reactor occurs when in a carbon dioxide atmosphere. 

The enthalpy of formation for this compound is positive. So it is hardly stable thermodynamically and it is to be expected that chlorine dioxide will give dangerous reactions, which are often linked to the catalysis of its decomposition. 

The enthalpy of absorption of 1- and 2-nitropropane on breathing mask cartridges made with carbon is such that the decomposition of the nitrated derivative can cause its ignition. This accident is aggravated when the cartridge also contains metal oxides such as copper (II) oxide or manganese dioxide. 

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