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Reactants masses

Am = change in mass = mass products — mass reactants AE = energy products — energy reactants c = speed of light... [Pg.520]

Note 1 The easy separation of low-molar-mass reactants or products from the polymer-supported species is a great advantage of polymer-supported reactions. [Pg.240]

The term reactive diluents denotes low molecular mass reactants that act as solvents with an extremely low volatility and participate in the cross-linking reaction. Reactive diluents have become especially important in one-pack systems because they can partially or wholly replace the solvent in high-solvent paints. Reactive diluents participate in the cross-linking reaction because their functional groups are identical or similar to those of the principal binder. They are completely incorporated into the polymer network during curing. Good compatibility with the principal... [Pg.106]

Several stochastic models have been developed to reconstract the GDL microstructure. With a reconstracted GDL, Wang etal [34] further presented a detailed DNS study to investigate the transport phenomena of mass, reactant, electron, and heat inside a GDL. In this approach, the Navier-Stokes equation was apphed directly to the void space with no slip boundary condition at the sohd matrix surface. The oxygen and water transport can be expressed in a similar way to that in the DNS of CLs. Figure 30.8 shows the mass flow through the microstructure of the GDL. The results were used to evaluate the GDL properties, such as the permeabihty and tortuosity. They found that the tortuosity of the considered pore structure is 1.2 whereas the permeability fC is 3.1 x 10 m [34]. [Pg.850]

A bimoleciilar reaction can be regarded as a reactive collision with a reaction cross section a that depends on the relative translational energy of the reactant molecules A and B (masses and m ). The specific rate constant k(E ) can thus fonnally be written in tenns of an effective reaction cross section o, multiplied by the relative centre of mass velocity... [Pg.776]

Several reactivity trends are worth noting. Reactions that are rapid frequently stay rapid as the temperature or centre-of-mass kinetic energy of the reactants is varied. Slow exothenuic reactions almost always show behaviour such tliat... [Pg.806]

To detemiine k E) from equation (A3.12.9) it is assumed that transition states with positivefomi products. Notmg that / f = p dqf/dt, where p is the reduced mass of the separating fragments, all transition states that lie within and + dq with positive will cross the transition state toward products in the time interval dt = pj dqf p. Inserting this expression into equation (A3.12.9), one finds that the reactant-to-product rate (i.e. flux) through the transition state for momenPim p is... [Pg.1012]

Of course, in order to vary the mass transport of the reactant to the electrode surface, the radius of the electrode must be varied, and this unplies the need for microelectrodes of different sizes. Spherical electrodes are difficult to constnict, and therefore other geometries are ohen employed. Microdiscs are conunonly used in the laboratory, as diey are easily constnicted by sealing very fine wires into glass epoxy resins, cutting... [Pg.1939]

Reactive scattering or a chemical reaction is characterized by a rearrangement of the component particles within the collision system, thereby resulting in a change of the physical and chemical identity of the original collision reactants A + B into different collision products C + D. Total mass is conserved. The reaction is exothemiic when rel(CD) > (AB) and is endothermic when rel(CD) < (AB). A threshold energy is required for the endothemiic reaction. [Pg.2007]

Instead of shifting the detector position, as indicated in figure B2.5.1 one often varies the location of the reactant mixing region using moveable injectors. This allows complex, possibly slow, but powerfril, analytical teclmiques to be used for monitoring gas-phase reactions. In combination with mass-spectrometric detection. [Pg.2116]

The reactivity of size-selected transition-metal cluster ions has been studied witli various types of mass spectrometric teclmiques [1 ]. Fourier-transfonn ion cyclotron resonance (FT-ICR) is a particularly powerful teclmique in which a cluster ion can be stored and cooled before experimentation. Thus, multiple reaction steps can be followed in FT-ICR, in addition to its high sensitivity and mass resolution. Many chemical reaction studies of transition-metal clusters witli simple reactants and hydrocarbons have been carried out using FT-ICR [49, 58]. [Pg.2394]

A solution containing botli reactants and a catalyst may be mixed mechanically to bring tire constituents into efficient contact—otlierwise, tire rate of tire catalytic reaction would be affected by mass transport (e.g., diffusion)... [Pg.2700]

H at m energy of 1.2 eV in the center-of-mass frame. By using an atomic orbital basis and a representation of the electronic state of the system in terms of a Thouless determinant and the protons as classical particles, the leading term of the electronic state of the reactants is... [Pg.231]

The flux of material to and from the electrode surface is a complex function of all three modes of mass transport. In the limit in which diffusion is the only significant means for the mass transport of the reactants and products, the current in a voltammetric cell is given by... [Pg.512]

Influence of the Kinetics of Electron Transfer on the Faradaic Current The rate of mass transport is one factor influencing the current in a voltammetric experiment. The ease with which electrons are transferred between the electrode and the reactants and products in solution also affects the current. When electron transfer kinetics are fast, the redox reaction is at equilibrium, and the concentrations of reactants and products at the electrode are those specified by the Nernst equation. Such systems are considered electrochemically reversible. In other systems, when electron transfer kinetics are sufficiently slow, the concentration of reactants and products at the electrode surface, and thus the current, differ from that predicted by the Nernst equation. In this case the system is electrochemically irreversible. [Pg.512]

Among the complications that can interfere with this conclusion is the possibility that the polymer becomes insoluble beyond a critical molecular weight or that the low molecular weight by-product molecules accumulate as the viscosity of the mixture increases and thereby shift some equilibrium to favor reactants. Note that we do not express reservations about the effect of increasing viscosity on the mobility of the polymer molecules themselves. Apparently it is not the migration of the center of mass of the molecule as a whole that determines the reactivity but, rather, the mobility of the chain ends which carry the reactive groups. [Pg.279]

Mass-Transfer Coefficients with Chemical Reaction. Chemical reaction can occur ia any of the five regions shown ia Figure 3, ie, the bulk of each phase, the film ia each phase adjacent to the iaterface, and at the iaterface itself. Irreversible homogeneous reaction between the consolute component C and a reactant D ia phase B can be described as... [Pg.64]

The enhanced rate expressions for regimes 3 and 4 have been presented (48) and can be appHed (49,50) when one phase consists of a pure reactant, for example in the saponification of an ester. However, it should be noted that in the more general case where component C in equation 19 is transferred from one inert solvent (A) to another (B), an enhancement of the mass-transfer coefficient in the B-rich phase has the effect of moving the controlling mass-transfer resistance to the A-rich phase, in accordance with equation 17. Resistance in both Hquid phases is taken into account in a detailed model (51) which is apphcable to the reversible reactions involved in metal extraction. This model, which can accommodate the case of interfacial reaction, has been successfully compared with rate data from the Hterature (51). [Pg.64]

M ass Transfer. Mass transfer in a fluidized bed can occur in several ways. Bed-to-surface mass transfer is important in plating appHcations. Transfer from the soHd surface to the gas phase is important in drying, sublimation, and desorption processes. Mass transfer can be the limiting step in a chemical reaction system. In most instances, gas from bubbles, gas voids, or the conveying gas reacts with a soHd reactant or catalyst. In catalytic systems, the surface area of a catalyst can be enormous. Eor Group A particles, surface areas of 5 to over 1000 m /g are possible. [Pg.76]


See other pages where Reactants masses is mentioned: [Pg.230]    [Pg.204]    [Pg.110]    [Pg.212]    [Pg.992]    [Pg.65]    [Pg.2148]    [Pg.300]    [Pg.932]    [Pg.933]    [Pg.230]    [Pg.204]    [Pg.110]    [Pg.212]    [Pg.992]    [Pg.65]    [Pg.2148]    [Pg.300]    [Pg.932]    [Pg.933]    [Pg.251]    [Pg.181]    [Pg.692]    [Pg.693]    [Pg.779]    [Pg.806]    [Pg.811]    [Pg.812]    [Pg.813]    [Pg.872]    [Pg.1351]    [Pg.1925]    [Pg.1939]    [Pg.2293]    [Pg.2702]    [Pg.237]    [Pg.696]    [Pg.511]    [Pg.512]    [Pg.34]    [Pg.581]   
See also in sourсe #XX -- [ Pg.100 , Pg.103 , Pg.105 ]




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Inhomogeneities within reactant mass

Mass Balance for Reactant

Masses of reactants and products

Reactant mass transfers, representation

Reactants calculating mass

Reactants limiting from initial masses

Relating masses of reactants and products

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