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Influence of System Composition

If we consider this reaction in terms of flavor formation, the type of carbohydrate tends to play a larger role in determining the rate of the reaction than influencing the flavor character. The rate of reaction largely follows that of the loss of reactants and/or color formation. Sugar type may have some influence on flavor character but the amino acid selection generally plays a much greater role in this respect. [Pg.108]

This observation is obvious to those who create process flavors (Chapter 9). When one makes a process flavor, the choice of sugar type is of minimal importance in determining flavor character while the choice of amino acid is aU important. As [Pg.108]

There has been substantial research on how fipids influence the Maillard reaction. This topic will be discussed later in this chapter (Section 5.3). [Pg.109]


Figure 14-12 illustrates the influence of system composition and degree of reaetant eonversion upon the numerical values of for the absorption of CO9 into sodium hydroxide solutions at constant conditions of temperature, pressure, and type of packing. An excellent experimental study of the influence of operating variables upon overall values is that of Field et al. (Pilot-Plant Studie.s of the Hot Carbonate Proce.s.s for Removing Carbon Dioxide and Hydrogen Sulfide, U.S. Bureau of Mines Bulletin 597, 1962). [Pg.1365]

Dimethylformamide is also a suitable solvent [50], it has, however, the disadvantage of being oxidized at fairly low potentials to A-acyloxy-iV-methyl formamide [51]. The influence of the composition of the ternary system water/methanol/dimethyl-formamide on the material and current yield has been systematically studied in the electrolysis of co-acetoxy or -acetamido substituted carboxylates [32]. Acetonitrile can also be used, when some water is.added [52]. The influence of various solvents on the ratio of Kolbe to non-Kolbe products is shown in Table 1 [53]. [Pg.94]

The changes that occur after the heat processing of food systems are often monitored by different parameters, such as total carotenoid content (and therefore isomerization and oxidation are underestimated), individual carotenoids (overall changes may be missed), and CIELAB color parameters (no information on carotenoid degradation mechanism). The data given in Table 12.3 reflects the influence of matrix composition, food state (liquid or solid), and measured parameter on the carotenoid degradation kinetics. [Pg.235]

In the mixtures of water with organic solvents of lower than water donicity such as water-methanol [56, 57] and water-ethanol [58], the rate constant of the Zn(II)/Zn(Hg) system changes nonmono-tonically with solvent composition and exhibits a minimum for such concentration of organic component in the mixture, at which the Zn(II) ions are solvated by water molecules but the electrode is already solvated by the organic solvent. The influence of the composition of such mixtures on the rate of the Zn(II)/Zn(Hg) electrode processes was described by the equation [56, 57, 59]... [Pg.732]

There is currently little understanding of the influence of interfacial composition and (nano)structure on the kinetics of enzymatic hydrolysis of biopolymers and lipids. However, a few preliminary studies are beginning to emerge (McClements et al., 2008 Dickinson, 2008). Thus, for example, Jourdain et al. (2009) have shown recently that, in a mixed5 sodium caseinate + dextran sulfate system, the measured interfacial viscosity increased from qs = 220 mN s m 1 without enzyme to qs = 950 mN s m 1 with trypsin present. At the same time, the interfacial elasticity was initially slightly reduced from (7S = 1.6 mN m 1 to (h = 0.7 mN m, although it later returned to close to its original value. Conversely, in the... [Pg.342]

The most appropriate method of mimicking partition into biological membranes is by using artificial membranes composed of various phospholipids as model systems [37, 38]. The influence of phospholipid composition on drug partitioning can easily be studied (Table 2.2). [Pg.39]

Additional experiments related to the influence of the composition of the surface layer in mixed solvents on electrode kinetics were carried out [281] with the V(III)/V(II) system. The electrode kinetics of this system in water-f-butanol mixtures were studied in parallel with the kinetics of the homogeneous electron exchange... [Pg.277]

Influence of the composition of the system on the velocity of reaction.—Is it possible to further specify the fundamental principle of chemical dynamics and formulate the law which, for a system, joins the velocity of combination to the conditions in which this s3Tstem is placed There may be stated, in a general and certain manner only, some very simple propositions. [Pg.415]

Acceleration of a reaction, 418.—308. Comparison of the fundamental principle of chemical dynamics and the principle of dynamics properly so called, 418.—309. Influence of the composition of the system on the velodty of reaction, 416.—310. Every isothermal reaction is a moderated reaction, 416.— 3x1. The acceleration of a mod- erated reaction is negative, 416. 31 a. Influence of temperature on the velocity of reaction, 416.-—3x3. Example Phenomena of etherlfl-cation, 416.-3x4. Variation of the velocity due to a small change of composition and temperature, 418.-3x5. Return to isothermal reactions, 418.— 3x6. Adiabatic reactions, 418.—3x7. An adiabatic reaction may have a positive acceleration, 430.-3x8. Reactions with positive acceleration and explosive reactions, 430.-3x9. Conditions In order that an adiabatic reaction be explosive, 421.—320. Indetermination of the temperature which renders a reaction explosive, 421.—3ax. Stability and instability of limiting false equilibria, 421.—32a. Eveiy state of false equilibrium which is not limited is indifferent, 428.—... [Pg.490]

The chemistry of the carbonic acid system in seawater has been one of the more intensely studied areas of carbonate geochemistry. This is because a very precise and detailed knowledge of this system is necessary to understand carbon dioxide cycling and the deposition of carbonate sediments in the marine environment. A major concept applicable to problems dealing with the behavior of carbonic acid and carbonate minerals in seawater is the idea of a constant ionic medium. This concept is based on the observation that the salt in seawater has almost constant composition, i.e., the ratios of the major ions are the same from place to place in the ocean (Marcet s principle). Possible exceptions can include seawater in evaporative lagoons, pores of marine sediments, and near river mouths. Consequently, the major ion composition of seawater can generally be determined from its salinity. It has been possible, therefore, to develop equations in which the influence of seawater composition on carbonate equilibria is described simply in terms of salinity. [Pg.3535]

When using, however, two-component catalysts alcohols also react with inactive metal-polymer (aluminium-polymer) bonds which are formed in the chain transfer reactions with a cocatalyst. It is expedient to use the alcohol method only for catalytic systems and polymerization conditions for which the number of inactive metal-polymer bonds is low. Such a case is the polymerization of 4-methyl-1-pentene on vanadium trichloride activated with various organoaluminium compounds. For this system the influence of catalyst composition and polymerization conditions on Cp and kp was determined by quenching the polymerization with tritiated alcohol. [Pg.64]

Raveendran, K, "Studies on Influence of Biomass Composition on Pyrolysis", Ph. D. Thesis, 1995, Interdisciplinary Program in Energy Systems Engineering, Indian Institute of Technology, Bombay, India. [Pg.1033]

It is demonstrated that besides ionic interactions, covalent interactions can be important in zeolitic systems. Then, besides acid strength, the concept of acid softness-hardness in zeolites needs to be considered and its importance to explain selectivity effects in orbital controlled reactions is discussed. The influence of zeolite composition and pore structure (electronic confinement) on acid softness-hardness, and orbital control, and their effects on para/ortho selectivity during alkylation of toluene by methanol in large pore zeolites is presented. [Pg.736]

The influence of atmospheric composition (and other factors) on climate can be studied by determining physical principles governing the climate and by constructing appopriate mathematical equations on the basis of these principles. As we have seen, the climate (radiation balance, temperature, circulation, etc.) is determined by the interaction of several processes. The parameters controlling these processes can be included in statistical or physico-mathematical equation systems which are called climate models. The solutions of these model equations provide the so-called climate theories. With the aid of these models, if they are formulated correctly, we can calculate theoretically the consequence of a given change in the parameters (e.g. an increase of COz level). Furthermore, it is also possible to include the effects of human activity in the models as supplementary mathematical relations. [Pg.166]

The framework types discussed in the last section describe only the connectivities of the frameworks. While these characterize the basic framework structure in terms of approximate pore opening, cage arrangement and channel system, and facilitate comparison of related materials, they do not describe real materials. That is, the influence of framework composition, extra-framework cations, organic species, sorbed molecules, or structural defects, is not considered. These aspects are addressed in the following sections. [Pg.57]

Cole DR (1992) Influence of solution composition and pressure on the rates of oxygen isotope exchange in the system calcite-H20-NaCl at elevated temperatures. Chem Geol 102 199-216 Cole DR (1994) Evidence for oxygen isotope disequilibrium in selected geothermal and hydrothermal ore deposit systems. Chem Geol 111 283-296... [Pg.175]

The acid or base catalyzed hydrolysis of polyacrylamide (PAM) or Its partially hydrolyzed counterpart (HPAM) In aqueous solutions has been the subject of numerous studies. In part because this system provides an opportunity for evaluating the influence of polymer composition, and steric and electrostatic effects on the course of a simple organic reaction In a convenient solvent medium. [Pg.261]

Majumdar, P. Webster, D. C., Influence of Solvent Composition and Degree of Reaction on the Formation of Surface Microtopography in a Thermoset Silox-ane-Urethane System. Polymer 2006, 46, 4172-4181. [Pg.138]

The influence of the composition on the internal structure of lyotropic LCNP has already been studied intensively but many aspects related to their pharmaceutical use, for example stability issues, their interaction with biological systems as well as drug incorporation and release remain to be studied in more detail. Moreover, there is hitherto no experimental information whether a certain structure type of these particles (cubosome, hexosome etc.) may have specific advantages with respect to pharmaceutical applications. [Pg.488]

Trejo Hernandez, M.R. and Lonsane, B.K. (1993) Spectra of ergot alkaloids produced by Claviceps purpurea 1029c in solid-state fermentation system Influence of the composition of liquid medium used for impregnating sugar-cane pith bagasse. Process Biochem., 28, 23-27. [Pg.369]


See other pages where Influence of System Composition is mentioned: [Pg.108]    [Pg.108]    [Pg.158]    [Pg.277]    [Pg.71]    [Pg.122]    [Pg.204]    [Pg.391]    [Pg.64]    [Pg.136]    [Pg.1106]    [Pg.168]    [Pg.219]    [Pg.60]    [Pg.1851]    [Pg.384]    [Pg.204]    [Pg.819]    [Pg.128]    [Pg.185]    [Pg.50]    [Pg.272]    [Pg.610]    [Pg.94]   


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Composition of systems

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