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Volume filling

Figure Bl.14.13. Derivation of the droplet size distribution in a cream layer of a decane/water emulsion from PGSE data. The inset shows the signal attenuation as a fiinction of the gradient strength for diflfiision weighting recorded at each position (top trace = bottom of cream). A Stokes-based velocity model (solid lines) was fitted to the experimental data (solid circles). The curious horizontal trace in the centre of the plot is due to partial volume filling at the water/cream interface. The droplet size distribution of the emulsion was calculated as a fiinction of height from these NMR data. The most intense narrowest distribution occurs at the base of the cream and the curves proceed logically up tlirough the cream in steps of 0.041 cm. It is concluded from these data that the biggest droplets are found at the top and the smallest at the bottom of tlie cream. Figure Bl.14.13. Derivation of the droplet size distribution in a cream layer of a decane/water emulsion from PGSE data. The inset shows the signal attenuation as a fiinction of the gradient strength for diflfiision weighting recorded at each position (top trace = bottom of cream). A Stokes-based velocity model (solid lines) was fitted to the experimental data (solid circles). The curious horizontal trace in the centre of the plot is due to partial volume filling at the water/cream interface. The droplet size distribution of the emulsion was calculated as a fiinction of height from these NMR data. The most intense narrowest distribution occurs at the base of the cream and the curves proceed logically up tlirough the cream in steps of 0.041 cm. It is concluded from these data that the biggest droplets are found at the top and the smallest at the bottom of tlie cream.
According to Dubinin s ideas, the process involved is volume filling of the micropores rather than layer-by-layer adsorption on the pore walls. A second parameter is therefore the degree of filling of the micropores, defined by... [Pg.220]

Eor the negative electrolyte, cadmium nitrate solution (density 1.8 g/mL) is used in the procedure described above. Because a small (3 —4 g/L) amount of free nitric acid is desirable in the impregnation solution, the addition of a corrosion inhibitor prevents excessive contamination of the solution with nickel from the sintered mass (see Corrosion and corrosion inhibitorsCorrosion and corrosion control). In most appHcations for sintered nickel electrodes the optimum positive electrode performance is achieved when one-third to one-half of the pore volume is filled with active material. The negative electrode optimum has one-half of its pore volume filled with active material. [Pg.548]

Rotary kilns are usually operated with between 3 and 12 percent of their volume filled with material 7 percent is considered normal. [Pg.1208]

To be able to control the PCM properties in the desired direction it is very important to know the relationships between the material composition and properties. Since melt viscosity is one of the most important characteristics of processability of PCM, there have naturally been a large number of equations proposed for describing the viscosity versus filler concentration relationship. For the purpose of this review it may be most interesting to discuss the numerous equations which have in common the use of the value < representing the maximum possible volume filling by filler particles packed in one way or another, as the principal constant. Here are a few examples of such equations. [Pg.7]

Of the three types, surface condensers using cooling water are by far the most common. When a volume filled with steam... [Pg.472]

This Second volume fills some of the gaps left by the earlier work and describes developments in the field up to the end of 1976. More specifically, we have included literature and patent preparations for... [Pg.538]

Introduction. After we have discussed examples of uncorrelated but polydisperse particle systems we now turn to materials in which there is more structure - discrete scattering indicates correlation among the domains. In order to establish such correlation, various structure evolution mechanisms are possible. They range from a stochastic volume-filling mechanism over spinodal decomposition, nucleation-and-growth mechanisms to more complex interplays that may become palpable as experimental and evaluation technique is advancing. [Pg.186]

V is the micropore volume filled with the adsorbed phase. [Pg.328]

After the product has been filled (and sealed) in its final product container. QC personnel then remove representative samples of the product and carry out tests to ensure conformance to final product specification. The most important specifications will relate to product potency, sterility and final volume fill, as well as the absence of endotoxin or other potentially toxic substances. Detection and quantification of excipients added will also be undertaken. Product analysis is considered in Chapter 7. [Pg.169]

Precipitation of the active component precursor starts when its concentration in the liquid phase reaches the saturation point Cs. At this point the degree of pore volume filling is Us. If the precursor is not volatile, one can determine Us as a ratio of Us=U0C0/CS. The redistribution of the precursor is minimal if Us< t/cr h. Aspiration of Us to U0 results in a predominant yield of the precursor at the external surface of a support grain. [Pg.271]

In a second series of experiments of type 1, the influence of the nature of the diamine on the rate of ZSM-48 crystallization has been examined (Table 2). Compared with the hydrogel involving 1,6 diaminohexane, ZSM-48 crystallizes more rapidly when 1,8 diaminooctane is present in the hydrogel. Probably the lenght of the diaminooctane chain is better accomodated into the channels of ZSM-48 zeolite as to achieve a more complete pore volume filling. Indeed, the channel length per unit cell of... [Pg.31]

The gel slices containing the protein of interest are minced in the presence of Soln. A (buffer volume nearly the same of gel volume), filled into a vessel of appropriate size and sonicated for 30 - 60 min. [Pg.66]


See other pages where Volume filling is mentioned: [Pg.124]    [Pg.266]    [Pg.520]    [Pg.1203]    [Pg.1497]    [Pg.40]    [Pg.100]    [Pg.179]    [Pg.307]    [Pg.747]    [Pg.7]    [Pg.31]    [Pg.254]    [Pg.493]    [Pg.184]    [Pg.406]    [Pg.408]    [Pg.190]    [Pg.33]    [Pg.35]    [Pg.578]    [Pg.193]    [Pg.5]    [Pg.296]    [Pg.81]    [Pg.84]    [Pg.227]    [Pg.114]    [Pg.144]    [Pg.167]    [Pg.178]    [Pg.201]    [Pg.29]    [Pg.90]    [Pg.542]    [Pg.34]   
See also in sourсe #XX -- [ Pg.150 ]

See also in sourсe #XX -- [ Pg.65 , Pg.66 , Pg.107 ]

See also in sourсe #XX -- [ Pg.140 ]




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Fill volume

Fill volume

Filling of Micropore Volume in Adsorption

Maximum Tensile Strength if the Pore Volume is Filled with a Liquid

Micropore volume filling

Micropores volume filling

Mold Filling Simulations Using the Control Volume Approach

Packaging fill volume

Parenteral preparations filling volume

Theory of the Volume Filling

Volume Filling diastolic

Volume Filling intercept

Volume filling factor

Volume filling of micropores

Volume filling, during adsorption

Volume resistivities silver-filled epoxies

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