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Distribution activity

Fission product distribution Radioactive waste activity distribution... [Pg.602]

Galactan synthase activity distribution using two centrifugation protocols. Post-lOOOg supernatants were centrifuged as indicated. Centrifugations were at 4°C. [Pg.129]

In any catalyst selection procedure the first step will be the search for an active phase, be it a. solid or complexes in a. solution. For heterogeneous catalysis the. second step is also deeisive for the success of process development the choice of the optimal particle morphology. The choice of catalyst morphology (size, shape, porous texture, activity distribution, etc.) depends on intrinsic reaction kinetics as well as on diffusion rates of reactants and products. The catalyst cannot be cho.sen independently of the reactor type, because different reactor types place different demands on the catalyst. For instance, fixed-bed reactors require relatively large particles to minimize the pressure drop, while in fluidized-bed reactors relatively small particles must be used. However, an optimal choice is possible within the limits set by the reactor type. [Pg.84]

From the above dependence, and from the definition of the limiting or activity distribution coefficient of electrolyte, i.e., from the equation ... [Pg.24]

Several biochemical events occur posttranscriptionally that define the response of cells to stimuli. For instance, alternative splicing, posttrans-lational modifications, regulation of enzyme activities, distribution of metabolites between cellular compartments, necessitate analysis at the level of the proteome and the metabolome. [Pg.233]

Fig. 2.10 Classification of different types of techniques for understanding cavitational activity distribution... Fig. 2.10 Classification of different types of techniques for understanding cavitational activity distribution...
Cavitation medium gets disturbed due to the presence of external instrument such as thermocouple, hydrophone, aluminum foil, test tube etc. and hence we may not get a realistic picture of the cavitational activity distribution... [Pg.46]

Prediction of cavitational activity distribution based on theoretical analysis of the bubble dynamics equations can be used to identify the regions with maximum pressure fields in a large scale reactor and then may be small reactors can... [Pg.48]

The reactor design in terms of ratio of the diameter of the immersion transducer to reactor diameter, liquid height, position of the transducers and characteristics of the cell plays a important role in deciding the cavitational activity distribution and hence the efficacy of sonochemical reactors for the specific application. Based on a critical analysis of the existing literature, following important design related information can be recommended ... [Pg.53]

The position of the transducers in reactors based on the multiple frequency arrangement should be done in such a way that maximum and uniform cavita-tional activity is obtained. Theoretical analysis of the cavitational activity distribution as discussed earlier aids in arriving at an optimum location of the transducers. Similar argument holds true for the geometry of the reactor. [Pg.54]

Design of sonochemical reactors is a very important parameter in deciding the net cavitational effects. Use of multiple transducers and multiple frequencies with possibility of variable power dissipation is recommended. Theoretical analysis for predicting the cavitational activity distribution is recommended for optimization of the geometry of the reactor including the transducer locations in the case of multiple transducer reactors. Use of process intensifying parameters at zones with minimum cavitational intensity should help in enhancing the net cavitational effects. [Pg.63]

Chu et al. (1987) present results of laboratory studies of the formation of an ultrafine aerosol by converting SO- to sulfuric acid using measurement methods described by Holub and Knutson (1987) and Kulju et al. (1987). It was found that the size of the resulting activity distributions is dependent on the S02 concentration. The role of humidity is still unclear and more studies are needed, but it appears that both future theoretical models and laboratory studies will be extremely fruitful in elucidating the behavior of Po-218 from shortly after its formation until its incorporation into the existing accumulation mode aerosol. [Pg.10]

Khan, A., F. Bandi, C.R. Phillips and P. Duport, Underground Measurements of Aerosol and Radon and Thoron Progeny Activity Distributions, to be published in Proc. 191st American Chemical Society National Meeting, New York, April 13-18 (1986). [Pg.162]

Underground Measurements of Aerosol and Activity Distributions of Radon and Thoron Progeny... [Pg.223]

The radon progeny Working Levels for calculation of activity distributions were calculated using the equation ... [Pg.227]

All our measurements i/ere carried out in rooms with i < 1 hr1 and the radon concentration outdoors (c 5 Bq nr 3) i/as always much smaller than indoors (cj > 100 Bq m 3). Assuming a constant radon emanation, a homogeneous activity distribution and 100 % prefiltering of the free fractions of the incoming air, the radon, the free and attached radon daughter activity concentrations indoors (cj cjf cja) and outdoors (eg c f c a) under steady conditions are ... [Pg.294]

Pb-210, Be-7, P-32, S-35 (as So ), and stable so - were measured using cascade impactors. The activity distribution of Pb-212 and Pb-214 was largely associated with aerosols smaller than 0.52 pm. [Pg.380]

The mean measured activity per unit surface area are shown for airways and bifurcations separately in Table II. These data are for those segments which contained only airway lengths bifurcations. The results are given as the number of particles which deposit per cm2 for 10 particles which enter the trachea. This assumes that the particle and activity distributions are equivalent. For the 0.2 and 0.15 ym particles the surface density at the bifurcations is greater than that along the airway lengths at p <. 01 when the paired data are compared by a one tailed t-test. [Pg.481]

For both ethanol and 1-propanol, co-feeding of methylene- and methyl-labeled alcohols shows nearly the same activity distribution of formed hydrocarbons, indicating that C-C bonds of incorporated alcohols are not cleaved. Accordingly, the formation of methane is very small.1,3... [Pg.206]

Figure 2.6 Compound target activity distribution ( promiscuity ) for 1388 drugs profiled in BioPrint assay panel (with 50% inhibition at 10pM taken as active), shown as a histogram. The number of active compounds is shown along the y-axis and the number of targets along the x-axis (adapted from ref. [6]). Figure 2.6 Compound target activity distribution ( promiscuity ) for 1388 drugs profiled in BioPrint assay panel (with 50% inhibition at 10pM taken as active), shown as a histogram. The number of active compounds is shown along the y-axis and the number of targets along the x-axis (adapted from ref. [6]).
Figure 11. Current and water activity distributions in a low humidity 50 cm fuel cell with serpentine flow field at 0.6 V or average current density of 0.71 A/cm. The membrane is 18/rmthick (EW < 1000). The anode/cathode feed conditions are pressure = 3/3 atm, relative humidity = 75%/dry, stoichiometry = 1.2/2, and cell temperature = 80 °C. Figure 11. Current and water activity distributions in a low humidity 50 cm fuel cell with serpentine flow field at 0.6 V or average current density of 0.71 A/cm. The membrane is 18/rmthick (EW < 1000). The anode/cathode feed conditions are pressure = 3/3 atm, relative humidity = 75%/dry, stoichiometry = 1.2/2, and cell temperature = 80 °C.
This type of analysis has, for the first time, provided us with a model that predicts what the addition of specific classes of compounds actually offers in a proactive or design sense. There are many related issues that we are also exploring using these concepts. One is how is biological activity distributed over this GaP space This gives us clues as to the relative importance of some of the partitions in the GaP space. With this type of information, decisions can be made as to whether to concentrate more specifically on some partitions that may be well represented already but provide excellent returns against some targets. [Pg.47]

Important limitations of the PBPK approach are realized for class 3 and 4 compounds with significant active distribution/absorption processes, where biliary elimination is a major component of the elimination process or where the assumptions of flow-limited distribution and well mixed compartments are not valid and permeability-limited distribution is apparent. These drawbacks could be addressed by the addition of permeability barriers for some tissues and by the incorporation of a more complex liver model which addresses active uptake into the liver, active efflux into the bile, biliary elimination and enterohepatic recirculation. However, this improvement to current methodologies requires the availability of the appropriate input data for quantification of the various processes involved as well as validation of the corresponding in vitro to in vivo scaling approaches. [Pg.237]

Figure 3 illustrates the distributions found for Pu and Am when a mixed sample of these tracers was infiltrated into a large (30 cm x 30 cm) block of Bandolier tuff (6). The nuclide activities were determined simultaneously by coring sections of the tuff and represent the activity distributions in the rock. It is obvious that although the activities are both normalized at 100% at the surface the increased dispersion of the plutonium concentration during elution leads to an increase of almost an order of magnitude in its activity relative to Am at the 5-6 cm depth. It is highly unlikely that abnormal flow paths or movement of colloidal clay particles would discriminate between americium and plutonium therefore this experimental result tends to discount these possible types of mechanisms. However, a pure Pu polymer could carry the Pu more rapidly downstream. [Pg.192]


See other pages where Distribution activity is mentioned: [Pg.65]    [Pg.58]    [Pg.73]    [Pg.31]    [Pg.44]    [Pg.45]    [Pg.45]    [Pg.47]    [Pg.223]    [Pg.223]    [Pg.225]    [Pg.227]    [Pg.229]    [Pg.231]    [Pg.233]    [Pg.235]    [Pg.237]    [Pg.239]    [Pg.241]    [Pg.278]    [Pg.499]    [Pg.7]   
See also in sourсe #XX -- [ Pg.73 ]




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Activated alumina pore size distribution

Activated carbon fibers pore distribution characterization

Activated carbon particle size distribution

Activated carbon pore volume distribution

Activated carbons pore size distributions

Activated carbons with narrow micropore size distributions

Activated pore size distribution

Activation energies distribution

Activation energies product distribution

Activation energy distribution function

Activator distribution

Active pharmaceutical ingredient Particle size distribution

Active protection systems water distribution

Active reactivity distribution

Active sites, nonuniform distribution

Active-site distributions

Activity functions, catalysts with distributed

Activity median diameter distribution

Activity of a Solute from Distribution between Two Immiscible Solvents

Activity size distribution

Activity size distribution measurements

Activity size distribution of radioactive aerosol particles

Activity size distribution radon daughters

Activity size distributions of the radon product decay aerosols

Biological activity distribution

Branch distribution lower activation temperature

Capital cost activity distribution

Catalysts activity site distribution

Catalytic activity distribution

Catalytic activity product distribution

Cavitation activity distribution

Chemical activation narrow micropore size distributions

Coefficient, activity distribution

Concentration Distribution in the Active Reaction Layer

Continuous distribution of activation

Delta function distribution, catalyst activity

Discharge activity probability distribution

Distributed active vibration absorbers

Distribution of activation energies

Distribution of active centers

Distribution of activities

Distribution of cavitational activity

Drug distribution active transport

Enzymic activities, distribution

Exponential distribution of activation

Isoprene polymerization active site distributions over kinetic

Kinetic product distribution activation energy

Microbial distribution and activity at vents

Nonuniform Activity Distributions

Pore size distribution for activated

Pore size distribution for activated carbons

Probability distribution resonant activation

Protein activities, distribution

QSAR (Quantitative structure-activity distribution coefficients

Radon progeny activity distributions

Spatial Distribution of the Active Ingredients in a Pharmaceutical Drug Formulation

Structure-activity relationships distribution

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