Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Chemicals react

Figure A2.1.9. Chemically reacting systems, (a) The entropy. S as a fiinction of the degree of advancement of the reaction at constant U and V. (b) The affinity Aas a fiinction of for the same reacting system. Equilibrium is reached at 0.623 where tiis a maxuniim and A= 0. Figure A2.1.9. Chemically reacting systems, (a) The entropy. S as a fiinction of the degree of advancement of the reaction at constant U and V. (b) The affinity Aas a fiinction of for the same reacting system. Equilibrium is reached at 0.623 where tiis a maxuniim and A= 0.
The Onsager regression hypothesis, stated mathematically for the chemically reacting system just described, is given in the classical limit by... [Pg.884]

Most chemically reacting systems tliat we encounter are not tliennodynamically controlled since reactions are often carried out under non-equilibrium conditions where flows of matter or energy prevent tire system from relaxing to equilibrium. Almost all biochemical reactions in living systems are of tliis type as are industrial processes carried out in open chemical reactors. In addition, tire transient dynamics of closed systems may occur on long time scales and resemble tire sustained behaviour of systems in non-equilibrium conditions. A reacting system may behave in unusual ways tliere may be more tlian one stable steady state, tire system may oscillate, sometimes witli a complicated pattern of oscillations, or even show chaotic variations of chemical concentrations. [Pg.3054]

In spite of these limitations it is hoped that this chapter will provide an introduction to the unusual phenomena that chemically reacting systems exlribit when driven far from equilibrium and an indication of how these phenomena may be analysed. Although such systems were often regarded as curiosities in the past, it is now clear that they are the mle rather than the exception in nature and deserve our full attention. [Pg.3072]

It appears that a loose interpretation of this type may be the origin of a discrenancy found by Otanl and Smith [59] in attempting to apply effective diffusivities from Wakao and Smith s [32] isobaric diffusion data to measurements on a chemically reacting system. This was pointed out by Steisel and Butt [60], and further pursued to the point of detailed computer modeling of a particular pore network by Wakao and Nardse [61]. [Pg.104]

Metal organic decomposition (MOD) is a synthesis technique in which metal-containing organic chemicals react with water in a nonaqueous solvent to produce a metal hydroxide or hydrous oxide, or in special cases, an anhydrous metal oxide (7). MOD techniques can also be used to prepare nonoxide powders (8,9). Powders may require calcination to obtain the desired phase. A major advantage of the MOD method is the control over purity and stoichiometry that can be achieved. Two limitations are atmosphere control (if required) and expense of the chemicals. However, the cost of metal organic chemicals is decreasing with greater use of MOD techniques. [Pg.310]

Taste-active chemicals react with receptors on the surface of sensory cells in the papillae causing electrical depolarization, ie, drop in the voltage across the sensory cell membrane. The collection of biochemical events that are involved in this process is called transduction (15,16). Not all the chemical steps involved in transduction are known however, it is clear that different transduction mechanisms are involved in different taste quaUties different transduction mechanisms exist for the same chemical in different species (15). Thus the specificity of chemosensory processes, ie, taste and smell, to different chemicals is caused by differences in the sensory cell membrane, the transduction mechanisms, and the central nervous system (14). [Pg.10]

Figure 12 shows an optional step at the end of the process ia which the siUca is chemically reacted with a siUcone oil, typically polydimethyl siloxane, to render the product hydrophobic. Other aftertreatments are also commonly employed, such as wax coatings that enhance the performance of precipitated siUcas used as flatting agents ia paints (78). [Pg.479]

Precipitation softening processes are used to reduce raw water hardness, alkalinity, siHca, and other constituents. This helps prepare water for direct use as cooling tower makeup or as a first-stage treatment followed by ion exchange for boiler makeup or process use. The water is treated with lime or a combination of lime and soda ash (carbonate ion). These chemicals react with the hardness and natural alkalinity in the water to form insoluble compounds. The compounds precipitate and are removed from the water by sedimentation and, usually, filtration. Waters with moderate to high hardness and alkalinity concentrations (150—500 ppm as CaCO ) are often treated in this fashion. [Pg.259]

An important use of bromine compounds is in the production of flame retardants (qv). These are of the additive-type, which is physically blended into polymers, and the reactive-type, which chemically reacts during the formation of the polymer. Bromine compounds are also used in fire extinguishers. Brominated polymers are used in flame retardant appHcations and bromine-containing epoxy sealants are used in semiconductor devices (see... [Pg.289]

Table 14-3 presents a typical range of values for chemically reacting systems. The first two entries in the table represent systems that can be designed by the use of purely physical design methods, for they are completely gas-phase mass-transfer limited. To ensure a negligible liquid-phase resistance in these two tests, the HCl was absorbed into a solution maintained at less than 8 percent weight HCl and the NH3 was absorbed into a water solution maintained below pH 7 by the addition of acid. The last two entries in Table 14-3 represent liquid-phase mass-transfer hmited systems. [Pg.1365]

TABLE 14-2 Typical Effects of Packing Type, Size, and Liquid Rate on K o in a Chemically Reacting System, KgO, kmol/(h m )... [Pg.1365]

Danckwerts and Gillham did not investigate the influence of the gas-phase resistance in their study (for some processes gas-phase resistance may be neglected). However, in 1975 Danckwerts and Alper [Trans. Tn.st. Chem. Eng., 53, 34 (1975)] showed that by placing a stirrer in the gas space of the stirred-cell laboratoiy absorber, the gas-phase mass-transfer coefficient fcc in the laboratoiy unit could be made identical to that in a packed-tower absorber. When this was done, laboratoiy data obtained for chemically reacting systems having a significant gas-side resistance coiild successfully be sc ed up to predict the performance of a commercial packed-tower absorber. [Pg.1366]

There are a number of different types of experimental laboratory units that could be used to develop design data for chemically reacting systems. Charpentier [ACS Symp. Sen, 72, 223-261 (1978)] has summarized the state of the art with respect to methods of scaUng up lab-oratoiy data and tabulated typical values of the mass-transfer coefficients, interfacial areas, and contact times to be found in various commercial gas absorbers as well as in currently available laboratoiy units. [Pg.1366]

Most ion exchangers in large-scale use are based on synthetic resins—either preformed and then chemically reacted, as for polystyrene, or formed from active monomers (olefinic acids, amines, or phenols). Natural zeolites were the first ion exchangers, and both natural and synthetic zeolites are in use today. [Pg.1496]

Chemical compatibility chart (How do the chemicals involved react with each other if one is added m excess or the addition of one is limited how do these chemicals react with common metals and chemicals )... [Pg.17]

How the chemicals react with one another if added in wrong amounts... [Pg.61]

Although much as been done, much work remains. Improved material models for anisotropic materials, brittle materials, and chemically reacting materials challenge the numerical methods to provide greater accuracy and challenge the computer manufacturers to provide more memory and speed. Phenomena with different time and length scales need to be coupled so shock waves, structural motions, electromagnetic, and thermal effects can be analyzed in a consistent manner. Smarter codes must be developed to adapt the mesh and solution techniques to optimize the accuracy without human intervention. [Pg.349]

Smitz, R.A., 1975, Multiplicity, Stability, and Sensitivity of States in Chemically Reacting Systems, a review m Advances in Chem. Series, 148. [Pg.216]

Chemical Reactivity - Reactivity with Water. Forms solution of hydrogen peroxide. The reaction is nonhazardous Reactivity with Common Materials There are no significant reactions under ordinary conditions and temperatures. At 50 °C (122 of) the chemical reacts with dust and rubbish Stability During Transport Stable below 60 °C (140 of) Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Not pertinent Inhibitor of Polymerization Not pertinent. [Pg.388]

According to Eq. (8.7), the total concentration of H2S in the aqueous caustic soda (physically dissolved and chemically reacted) can be expressed as follows... [Pg.198]

Chemisorption An adsorption process in which the solute chemically reacts with the adsorbent to form a new compound. [Pg.1421]

Coated/treated filters Filters that have been coated with a chemical specific for the contaminant to be collected. The coatings enhance the collection by chemically reacting with the contaminant as the air is drawn through the filter. [Pg.1422]

This book will take the reader from the simplest condition of shock-compressed matter—the large elastic strain—through the complications introduced by rapid plastic deformation, to perhaps the most complex conditions—chemically reacting solids. Even in the simplest case, unexpected complexities are observed. The full complexity of shock-induced solid state chemistry is yet to be determined. [Pg.11]


See other pages where Chemicals react is mentioned: [Pg.49]    [Pg.302]    [Pg.362]    [Pg.731]    [Pg.341]    [Pg.69]    [Pg.70]    [Pg.75]    [Pg.79]    [Pg.31]    [Pg.23]    [Pg.624]    [Pg.673]    [Pg.1369]    [Pg.209]    [Pg.54]    [Pg.437]    [Pg.453]    [Pg.290]    [Pg.140]    [Pg.297]    [Pg.383]    [Pg.430]    [Pg.430]    [Pg.5]   
See also in sourсe #XX -- [ Pg.298 ]




SEARCH



REACT

© 2019 chempedia.info