Big Chemical Encyclopedia

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

Articles Figures Tables About

Partial estimation

Under these conditions, a study of the antioxidant potential of pure compounds could be carried out. Table 1 shows the values of antioxidant activity (expressed as TEAC) of different compounds of interest, determined by the on-hne method (HPLC-ARTS method) and compared with the values obtained by our conventional photometric end-point method. As can be observed, the two most important standard antioxidants, trolox and ascorbic acid, presented similar TEAC using either method. Thus, either can be used as reference to express antioxidant activity, except that trolox has the advantage because it can be used in both hydrophilic and lipophilic assays. The TEAC values of phenolic compounds were underestimated by approximately half when the HPLC-ARTS method was used as compared to the end-point method. This was due to the different reactivities of antioxidants with ARTS, and because, unfortunately, the time dependence of online scavenging activity determinations made it very difficult to obtain the total reaction for the slowest antioxidants, resulting in a partial estimation of this activity. Nevertheless, the HPLC-ARTS method provided important additional information in the form of correlation between the different peaks of a sample and their antioxidant activities. [Pg.171]

Uncertainties were partially estimated (ro and r ) in the original paper. ... [Pg.123]

Uncertainties were partially estimated in the original paper. [Pg.133]

Number of deaths Absolute figure indicating the number of people who die as a result of a road traffic crash. Gives a partial estimate of magnitude of the road traffic problem, in terms of deaths. Useful for planning at the local level for emergency medical services. Not useful for making comparisons. [Pg.8]

To illustrate the criterion for parameter estimation, let 1, 2, and 3 represent the three components in a mixture. Components 1 and 2 are only partially miscible components 1 and 3, as well as components 2 and 3 are totally miscible. The two binary parameters for the 1-2 binary are determined from mutual-solubility data and remain fixed. Initial estimates of the four binary parameters for the two completely miscible binaries, 1-3 and 2-3, are determined from sets of binary vapor-liquid equilibrium (VLE) data. The final values of these parameters are then obtained by fitting both sets of binary vapor-liquid equilibrium data simultaneously with the limited ternary tie-line data. [Pg.67]

VSTR is useful for estimating partial molar volumes at infinite dilution but is not used here because of Equation (4-17)... [Pg.143]

As P is increased, the partial cancellation between the kinetic part and the spring part may worsen the statistics on E. This has led to suggestions of alternative ways of estimating E [198]. As P goes up, the springs become stronger, the interactions in become (individually) weaker, and this leads to sampling problems. In... [Pg.2274]

The concentration at which micellization commences is called the critical micelle concentration, erne. Any experimental teclmique sensitive to a solution property modified by micellization or sensitive to some probe (molecule or ion) property modified by micellization is generally adequate to quantitatively estimate the onset of micellization. The detennination of erne is usually done by plotting the experimentally measured property or response as a hmction of the logarithm of the surfactant concentration. The intersection of asymptotes fitted to the experimental data or as a breakpoint in the experimental data denotes the erne. A partial listing of experimental... [Pg.2580]

Many phenomena ask for local, site-specific properties of a molecule such as the partial charge on a specific atom in a molecule or the hydrogen bond donor ability of a certain OH group. It would be highly desirable to have methods as simple as an additivity model to estimate such site-specific molecular properties. [Pg.327]

When Che diameter of the Cube is small compared with molecular mean free path lengths in che gas mixture at Che pressure and temperature of interest, molecule-wall collisions are much more frequent Chan molecule-molecule collisions, and the partial pressure gradient of each species is entirely determined by momentum transfer to Che wall by mechanism (i). As shown by Knudsen [3] it is not difficult to estimate the rate of momentum transfer in this case, and hence deduce the flux relations. [Pg.8]

The first quantitative studies of the nitration of quinoline, isoquinoline, and cinnoline were made by Dewar and Maitlis, who measured isomer proportions and also, by competition, the relative rates of nitration of quinoline and isoquinoline (1 24-5). Subsequently, extensive kinetic studies were reported for all three of these heterocycles and their methyl quaternary derivatives (table 10.3). The usual criteria established that over the range 77-99 % sulphuric acid at 25 °C quinoline reacts as its cation (i), and the same is true for isoquinoline in 71-84% sulphuric acid at 25 °C and 67-73 % sulphuric acid at 80 °C ( 8.2 tables 8.1, 8.3). Cinnoline reacts as the 2-cinnolinium cation (nia) in 76-83% sulphuric acid at 80 °C (see table 8.1). All of these cations are strongly deactivated. Approximate partial rate factors of /j = 9-ox io and /g = i-o X io have been estimated for isoquinolinium. The unproto-nated nitrogen atom of the 2-cinnolinium (ina) and 2-methylcinno-linium (iiiA) cations causes them to react 287 and 200 more slowly than the related 2-isoquinolinium (iia) and 2-methylisoquinolinium (iii)... [Pg.208]

A more detailed study of the nitration of quinolinium (l) in 80-05 % sulphuric acid at 25 °C, using isotopic dilution analysis, has shown that 3-) 5-) 6-, 7- and 8-nitroquinoline are formed (table 10.3). Combining these results with the kinetic ones, and assuming that no 2- and 4-nitration occurs, gives the partial rate factors listed in table 10.4. Isoquinolinium is 14 times more reactive than quinolinium. The strong deactivation of the 3-position is in accord with an estimated partial rate factor of io for hydrogen isotope exchange at the 3-position in the pyridinium ion. It has been estimated that the reactivity of this ion is at least 10 less than that of the quinolinium ion. Based on this estimate, the partial rate factor for 3-nitration of the pyridinium ion would be less than 5 x io . [Pg.212]

Partial rate factors may be used to estimate product distributions in disubstituted benzene derivatives The reactivity of a particular position in o bromotoluene for example is given by the product of the partial rate factors for the corresponding position in toluene and bromobenzene On the basis of the partial rate factor data given here for Fnedel-Crafts acylation predict the major product of the reaction of o bromotoluene with acetyl chlonde and aluminum chloride... [Pg.517]

The drop in pressure when a stream of gas or liquid flows over a surface can be estimated from the given approximate formula if viscosity effects are ignored. The example calculation reveals that, with the sorts of gas flows common in a concentric-tube nebulizer, the liquid (the sample solution) at the end of the innermost tube is subjected to a partial vacuum of about 0.3 atm. This vacuum causes the liquid to lift out of the capillary, where it meets the flowing gas stream and is broken into an aerosol. For cross-flow nebulizers, the vacuum created depends critically on the alignment of the gas and liquid flows but, as a maximum, it can be estimated from the given formula. [Pg.141]

Acetaldehyde, first used extensively during World War I as a starting material for making acetone [67-64-1] from acetic acid [64-19-7] is currendy an important intermediate in the production of acetic acid, acetic anhydride [108-24-7] ethyl acetate [141-78-6] peracetic acid [79-21 -0] pentaerythritol [115-77-5] chloral [302-17-0], glyoxal [107-22-2], aLkylamines, and pyridines. Commercial processes for acetaldehyde production include the oxidation or dehydrogenation of ethanol, the addition of water to acetylene, the partial oxidation of hydrocarbons, and the direct oxidation of ethylene [74-85-1]. In 1989, it was estimated that 28 companies having more than 98% of the wodd s 2.5 megaton per year plant capacity used the Wacker-Hoechst processes for the direct oxidation of ethylene. [Pg.48]

When a sound wave comes in contact with a soHd stmcture, such as a wall between two spaces, some of the sound energy is transmitted from the vibrating air particles into the stmcture causing it to vibrate. The vibrating stmcture, in turn, transmits some of its vibrational energy into the air particles immediately adjacent on the opposite side, thereby radiating sound to the adjacent space. For an incomplete barrier, such as a fence or open-plan office screen, sound also diffracts over the top and around the ends of the barrier. The subject of this section is confined to complete barriers that provide complete physical separation of two adjacent spaces. Procedures for estimating the acoustical performance of partial barriers can be found in References 5 and 7. [Pg.315]

An estimation of the amount of amino acid production and the production methods are shown ia Table 11. About 340,000 t/yr of L-glutamic acid, principally as its monosodium salt, are manufactured ia the world, about 85% ia the Asian area. The demand for DL-methionine and L-lysiae as feed supplements varies considerably depending on such factors as the soybean harvest ia the United States and the anchovy catch ia Pern. Because of the actions of D-amiao acid oxidase and i.-amino acid transamiaase ia the animal body (156), the D-form of methionine is as equally nutritive as the L-form, so that DL-methionine which is iaexpensively produced by chemical synthesis is primarily used as a feed supplement. In the United States the methionine hydroxy analogue is partially used ia place of methionine. The consumption of L-lysiae has iacreased ia recent years. The world consumption tripled from 35,000 t ia 1982 to 100,000 t ia 1987 (214). Current world consumption of L-tryptophan and i.-threonine are several tens to hundreds of tons. The demand for L-phenylalanine as the raw material for the synthesis of aspartame has been increasing markedly. [Pg.291]

Alkali sihcates are used as components, rather than reactants, in many appHcations. In many cases they only contribute partially to overall performance. Utility factors are generally not as easy to identify. Their benefit usually depends on the surface and solution chemical properties of the wide range of highly hydrophilic polymeric siUcate ions deUverable from soluble sihcate products or their proprietary modifications. In most cases, however, one or two of the many possible induences of these complex anions cleady express themselves in final product performance at a level sufficient to justify their use (102). Estimates of the 1995 U.S. consumption of sodium sihcates are shown in Table 6. [Pg.12]

The edible oilseed protein industry is comparatively small and is restricted to peanut and soybean proteins. One company manufactures partially defatted peanut flours made by hydraulic pressing. The products contain 40—42% protein. Production estimates for edible soybean proteins in the United States in 1993—1994 (56) and wholesale prices as of November 1995 are given in Table 15. [Pg.300]

Uses. High fmctose symp is used as a partial or complete replacement for sucrose or invert sugar in food appHcations to provide sweetness, flavor enhancement, fermentables, or humectant properties. It is used in beverages, baking, confections, processed foods, dairy products, and other apphcations. Worldwide HES production in the 1994—1995 fiscal year was estimated at about 8.6 x 10 t (dry basis) (18). About 75% of total world production is in the United States. [Pg.294]


See other pages where Partial estimation is mentioned: [Pg.356]    [Pg.2346]    [Pg.292]    [Pg.16]    [Pg.48]    [Pg.421]    [Pg.428]    [Pg.3154]    [Pg.356]    [Pg.2346]    [Pg.292]    [Pg.16]    [Pg.48]    [Pg.421]    [Pg.428]    [Pg.3154]    [Pg.861]    [Pg.2587]    [Pg.215]    [Pg.79]    [Pg.191]    [Pg.71]    [Pg.108]    [Pg.254]    [Pg.65]    [Pg.234]    [Pg.272]    [Pg.543]    [Pg.394]    [Pg.482]    [Pg.435]    [Pg.470]    [Pg.222]   
See also in sourсe #XX -- [ Pg.43 ]




SEARCH



Estimation of partial excess properties

© 2024 chempedia.info