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Kinetics problems associated with

The Kinetic Problems Associated with Proton Abstraction from Carbon... [Pg.1108]

Lanthanide chelate-dyed polystyrene particles containing carboxylic acid groups have been covalently coated with antibodies, streptavidin [95], and nucleic acids [96] for different biomolecular-binding assays. Particulate labels can be coated with antibodies and used as such, but the obvious steric and kinetic problems associated with the large molecular size can be particularly avoided by indirect detection of the bound antibodies using, e.g., biotin-streptavidin interaction [97,... [Pg.97]

Effects of Impurities nd Solvent. The presence of impurities usually decreases the growth rates of crystalline materials, and problems associated with the production of crystals smaller than desired are commonly attributed to contamination of feed solutions. Strict protocols should be followed in operating units upstream from a crystallizer to minimize the possibiUty of such occurrences. Equally important is monitoring the composition of recycle streams so as to detect possible accumulation of impurities. Furthermore, crystalliza tion kinetics used in scaleup should be obtained from experiments on solutions as similar as possible to those expected in the full-scale process. [Pg.345]

Several of the problems associated with whole cell bioprocesses are related to the highly effective metabolic control of microbial cells. Because cells are so well regulated, substrate or product inhibition often limits the concentration of desired product that can be achieved. This problem is often difficult to solve because of a poor understanding of the kinetic characteristics of the metabolic pathway leading to the desired product. [Pg.23]

The Instantaneous values for the initiator efficiencies and the rate constants associated with the suspension polymerization of styrene using benzoyl peroxide have been determined from explicit equations based on the instantaneous polymer properties. The explicit equations for the rate parameters have been derived based on accepted reaction schemes and the standard kinetic assumptions (SSH and LCA). The instantaneous polymer properties have been obtained from the cummulative experimental values by proposing empirical models for the instantaneous properties and then fitting them to the cummulative experimental values. This has circumvented some of the problems associated with differenciating experimental data. The results obtained show that ... [Pg.217]

The detailed kinetics of the FTS have been studied extensively over several catalysts since the 1950s, and many attempts have been reported in the literature to derive rate equations describing the FT reacting system. A major problem associated with the development of such kinetics, however, is the complexity of the related catalytic mechanism, which results in a very large number of species (more than two hundred) with different chemical natures involved in a highly interconnected reaction network as reaction intermediates or products. [Pg.294]

Technically, there is no reason to limit consideration to homogeneous flows. However, since the micromixing time and location-conditioned expected values will be independent of particle position, we do so here in order to simplify the notation and to isolate the problems associated with the chemical kinetics. [Pg.327]

Most problems associated with approximate kinetics are avoided when Michaelis Menten-type rate equations are utilized. Though this choice sacrifices the possibility of analytical treatment, reversible Michaelis Menten-type equations are straightforwardly consistent with fundamental thermodynamic constraints, have intuitively interpretable parameters, are computationally no more demanding than logarithmic functions, and are well known to give an excellent account of biochemical kinetics. Consequently, Michaelis Menten-type kinetics are an obvious choice to translate large-scale metabolic networks into (approximate) dynamic models. It should also be emphasized that simplified Michaelis Menten kinetics are common in biochemical practice almost all rate equations discussed in Section III.C are simplified instances of more complicated rate functions. [Pg.186]

The design of crystallization processes for the manufacture of Active Pharmaceutical Ingredients is a significant technical challenge to Process Research and Development groups throughout the Pharmaceutical and related industries. It requires an understanding of both the thermodynamic and kinetic aspects of crystallization, to ensure that the physical properties of the product will consistently meet specification. Failure to address these issues may lead to production problems associated with crystal size, shape and solubility, and to dissolution and bioavailability effects in the formulated product. [Pg.77]

Terrestrial BMOs have also been widely used for monitoring environmental contaminants. In particular, the lipid-like waxy cuticle layer of various types of plant leaves has been used to monitor residues of HOCs in the atmosphere. However, some of the problems associated with aquatic BMOs apply to terrestrial BMOs as well. For example, Bohme et al. (1999) found that the concentrations of HOCs with log KoaS < 9 (i.e., those compounds that should have attained equilibrium) varied by as much as 37-fold in plant species, after normalization of residue concentrations to levels in ryegrass (Lolium spp.). These authors suggested that differences in cuticular wax composition (quality) were responsible for this deviation from equilibrium partition theory. Other characteristics of plant leaves may affect the amount of kinetically-limited and particle-bound HOCs sampled by plant leaves but to a lesser extent (i.e., <4-fold), these include age, surface area, topography of the surface, and leaf orientation. [Pg.7]

Figure 4.1S Representation of the three primary steps for the generic inverse problem in chemical kinetics including homogeneous catalysis. In situ spectroscopic data is represented by 4kexv Tbe inverse spectroscopic problem (Eq. (2)), which is the focus of this chapter, is represented by S [,s, Ojxv The inverse problem associated with stoichiometries and reaction topology is represented by r rxs moles, reactions, extents of reaction and reaction stoi-... Figure 4.1S Representation of the three primary steps for the generic inverse problem in chemical kinetics including homogeneous catalysis. In situ spectroscopic data is represented by 4kexv Tbe inverse spectroscopic problem (Eq. (2)), which is the focus of this chapter, is represented by S [,s, Ojxv The inverse problem associated with stoichiometries and reaction topology is represented by r rxs moles, reactions, extents of reaction and reaction stoi-...
Restrictions which may exist for the choice of a commercial reactor need not be imposed at the development stage. In some cases, a reactor of one type may be best for acquiring data in model characterisation, whereas a reactor of another type might be more suitable for full-scale production. (The cautions expressed in Sect. 4 must be taken into account.) Continuous flow back-mixed reactors can be very useful for kinetic studies because the absence of concentration gradients can reduce uncertainties in concentration measurements. When these reactors have attained a steady state, many of the problems associated with stiffness (see above) can be avoided. [Pg.140]

Chapter 1 reviews the concepts necessary for treating the problems associated with the design of industrial reactions. These include the essentials of kinetics, thermodynamics, and basic mass, heat and momentum transfer. Ideal reactor types are treated in Chapter 2 and the most important of these are the batch reactor, the tubular reactor and the continuous stirred tank. Reactor stability is considered. Chapter 3 describes the effect of complex homogeneous kinetics on reactor performance. The special case of gas—solid reactions is discussed in Chapter 4 and Chapter 5 deals with other heterogeneous systems namely those involving gas—liquid, liquid—solid and liquid—liquid interfaces. Finally, Chapter 6 considers how real reactors may differ from the ideal reactors considered in earlier chapters. [Pg.300]


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