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Solid forming component, carbon

Using the proposed procedure in conjunction with literature values for the density (11) and vapor pressure (12) of solid carbon dioxide, the solid-formation conditions have been determined for a number of mixtures containing carbon dioxide as the solid-forming component. The binary interaction parameters used in Equation 14 were the same as those used previously for two-phase vapor-liquid equilibrium systems (6). The value for methane-carbon dioxide was 0.110 and that for ethane-carbon dioxide was 0.130. Excellent agreement has been obtained between the calculated results and the experimental data found in the literature. As shown in Figure 2, the predicted SLV locus for the methane-carbon... [Pg.197]

Adsorption. Adsorption involves the transfer of a component onto a solid surface. An example is the adsorption of organic vapors by activated carbon. Activated carbon is a highly porous form of carbon manufactured from a variety of carbonaceous raw materials such as coal or wood. The adsorbent may need to be... [Pg.108]

Step 4. The steam-volatile neutral compounds. The solution (containing water-soluble neutral compounds obtained in Step 1 is usually very dilute. It is advisable to concentrate it by distillation until about one-third to one-half of the original volume is collected as distillate the process may be repeated if necessary and the progress of the concentration may be followed by determination of the densities of the distillates. It is frequently possible to salt out the neutral components from the concentrated distillate by saturating it with solid potassium carbonate. If a layer of neutral compound makes its appearance, remove it. Treat this upper layer (which usually contains much water) with solid anhydrous potassium carbonate if another aqueous layer forms, separate the upper organic layer and add more anhydrous potassium carbonate to it. Identify the neutral compound. [Pg.1099]

The bioavailability of trace elements in soil-water-plant ecosystems of arid zones is largely determined by their partitioning between solution and solid-phase components. The redistribution and transformation of trace elements among solid-phase components under various biogeochemical conditions strongly adjust their lability and bioavailability. Soluble, exchangeable and organically bound forms are bioavailable to plants. The carbonate bound fraction represents a reservoir of potentially bio-available trace elements to plants. In paddy soils, the amorphous Fe/Al oxide fraction contributes to trace element availability as well. [Pg.236]

To a flame-dried, three-neck, 1-1 flask were added, in order, p-xylene (107 g, 1.0 mol), phosphorus trichloride (412 g, 3.0 mol), and anhydrous aluminum chloride (160 g, 1.2 mol). The reaction mixture was slowly heated to reflux with stirring. After 2.5 h at reflux, the reaction was allowed to cool to room temperature and the volatile components distilled at reduced pressure. The residual oil was slowly added to cold water (1 1) with stirring, and a white solid formed. The solid was removed by filtration, washed with water, and air dried. The solid was suspended in water (1 1) to which was added 50% sodium hydroxide solution (90 ml) to cause dissolution. The solution was saturated with carbon dioxide and filtered through Celite . The basic solution was washed with methylene chloride (200 ml) and acidified with concentrated hydrochloric acid (200 ml). The white solid that separated was isolated by extraction with methylene chloride (3 x 250 ml). The extracts were dried over magnesium sulfate, filtered, and evaporated under reduced pressure to give the pure 2,5-dimethylbenzenephosphinic acid (99 g, 60%) as an oil, which slowly crystallized to a solid of mp 77-79°C. [Pg.137]

Several comments need to be made concerning the state of aggregation of the substances. For gases, the standard state is the ideal gas at a pressure of 1 bar this definition is consistent with the standard state developed in Chapter 7. When a substance may exist in two allotropic solid states, one state must be chosen as the standard state for example, graphite is usually chosen as the standard form of carbon, rather than diamond. If the chemical reaction takes place in a solution, there is no added complication when the standard state of the components of the solution can be taken as the pure components, because the change of enthalpy on the formation of a compound in its standard state is identical whether we are concerned with the pure... [Pg.225]

If the element exists in the solid state, information about the crystal form is also necessary. Carbon, for example, often exists as graphite. Other forms of carbon do not yield zero values of Ag°j and A/j°In general, the states of aggregation of the components specified in the reactions of interest and fisted in the tables for A °, and A/ °, may not be the same. [Pg.377]

As an example of this, we may first consider the system formed by the two components CaO and CO2, which can combine to form the compound CaCO. This substance, on being heated, dissociates into calcium oxide and carbon dioxide, and gives rise to the equilibrium CaCOa CaO + COg, In accordance with the definition given on p. 6, there are present here two solid phases, the carbonate and the quicklime, and one vapour phase the system is therefore univariant. To each temperature, therefore, there will correspond a certain definite maximum pressure of carbon dioxide (dissociation pressure) and this... [Pg.74]

In the smelting chamber the coal does not react completely. This applies in particular to the solid carbon and the ash-forming components, while the so-called volatile fuel components (H, N, O, S) are completely oxidized. To simulate this fact, the degrees of conversion of the input materials or their components are restricted. For simplification it is first assumed that the unreacted portion of the coal leaves the reactor at the process temperature. [Pg.1990]

Fig. 19.5 Two-component ILs composite film formed on Si substrate solid-like (long carbon chain) and liquid-like (short carbon chain)... Fig. 19.5 Two-component ILs composite film formed on Si substrate solid-like (long carbon chain) and liquid-like (short carbon chain)...
A phase transition occurs when a pure component changes from one phase to another. Table 6.1 lists the different types of phase transitions, most of which should already be familiar to you. There are also phase transitions between different solid forms of a chemical component, which is a characteristic called polymorphism. For example, elemental carbon exists as graphite or diamond, and the conditions for phase transitions between the two forms are well known. Solid H2O can actually exist as at least six structurally different solids, depending on the temperature and pressure. We say that water has at least six polymorphs. (In application to elements, we use the word allotrope instead of polymorph. Graphite and diamond are two allotropes of the element carbon.) In mineral form, calcium carbonate exists either as aragonite or calcite, depending on the crystalline form of the solid. [Pg.157]


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Carbon forms

Carbonate components

Solid carbon

Solid forms

Solider component

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