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Membrane data

Fig. 18.8 Plot of power consumption of the BiChlor electrolyser for different membranes. Data breakdown is given in Table 18.1. Fig. 18.8 Plot of power consumption of the BiChlor electrolyser for different membranes. Data breakdown is given in Table 18.1.
Au nanotubule membranes with the following approximate nanotubule diameters were used to obtain the majority of the data reported here i.d. = 28 1, 7.0 0.1, 1.9 0.1, and 1.5 0.2 nm. Figure 19 shows permeation data for transport of pyridine through these various membranes. Data for membranes derivatized with both the R = -C2H4-OH (upper solid curve) and the R = -C16H33 (lower dashed curve) thiols are shown. The corresponding flux data are shown in Table 3. As would be expected [114], the flux of pyridine decreases with decreasing tubule diameter for both the... [Pg.43]

Figure 6.1. Permeability of several gases through a silica based hollow fiber membrane data taken from Shindo et al. (1983). Figure 6.1. Permeability of several gases through a silica based hollow fiber membrane data taken from Shindo et al. (1983).
The practical differences between centroid and maximum entropy maps can be seen with reference to membrane data in [7],... [Pg.345]

Gilmore, C.J., Shatikland, K. and Fryer, J.R. (1993), Phase extension in electron crystallography using the maximum entropy method and its application to two-dimensional purple membrane data fromHalobacterium halobium. Ultramicroscopy, 49, 147-178. [Pg.354]

Figure 10.7 Permeance of various components with an eight component mixture feed (at 1 atm) for MFl-type zeolite membrane (data from ref [41]). Figure 10.7 Permeance of various components with an eight component mixture feed (at 1 atm) for MFl-type zeolite membrane (data from ref [41]).
Fig. 3.6. Percentage of retention of proteins by ultrafiltration membranes. (Data according to Millipore/Amicon application note)... Fig. 3.6. Percentage of retention of proteins by ultrafiltration membranes. (Data according to Millipore/Amicon application note)...
Improved organic rejections result from the chemical nature of the newer polymeric materials in the nylon and thin-film composite membranes. Data by Chian and Fang (6) represented in Figure 2 illustrate different membrane rejections for a variety of organic com-... [Pg.429]

Fig. 22. Catalytic activities of Mo03, Bi203, and bismuth molybdates for the oxidation of propylene to acrolein. ( ) Under usual catalytic conditions. (O) In the absence of gaseous oxygen. Active oxygen is supplied through an oxygen transfer membrane. Data were taken from (118). Fig. 22. Catalytic activities of Mo03, Bi203, and bismuth molybdates for the oxidation of propylene to acrolein. ( ) Under usual catalytic conditions. (O) In the absence of gaseous oxygen. Active oxygen is supplied through an oxygen transfer membrane. Data were taken from (118).
Figure 2.17 Flux of n-hexane through a rubbery membrane as a function of the hexane concentration difference in the membrane. Data taken from both reverse osmosis ( ) and pervaporation (O) experiments. Feed-side and permeate-side membrane concentrations, Ci0 m) and Cie m), calculated from the operating conditions through Equations (2.26), (2.36) and (2.76). Maximum flux is obtained at the maximum concentration difference, when the permeate-side membrane concentration cit(m)), equals zero [19]. Reprinted from Driving Force for Hydraulic and Pervaporation Transport in Homogeneous Membranes, D.R. Paul and D.J. Paciotti, J. Polym. Sci., Polym. Phys. Ed. 13, 1201 Copyright 1975. This material is used by permission of John Wiley Sons, Inc. Figure 2.17 Flux of n-hexane through a rubbery membrane as a function of the hexane concentration difference in the membrane. Data taken from both reverse osmosis ( ) and pervaporation (O) experiments. Feed-side and permeate-side membrane concentrations, Ci0 m) and Cie m), calculated from the operating conditions through Equations (2.26), (2.36) and (2.76). Maximum flux is obtained at the maximum concentration difference, when the permeate-side membrane concentration cit(m)), equals zero [19]. Reprinted from Driving Force for Hydraulic and Pervaporation Transport in Homogeneous Membranes, D.R. Paul and D.J. Paciotti, J. Polym. Sci., Polym. Phys. Ed. 13, 1201 Copyright 1975. This material is used by permission of John Wiley Sons, Inc.
When the intrinsic PAMPA data (P0) are corrected for the appropriate unstirred water layer permeability (P "), the unified relationship between the biological barrier data (Papp) and the artificial membrane data is ... [Pg.106]

Sequencing was done in ABI protein sequencer models 470,477, or 473 using Blott Cartridges and using standard cycles and conditions for sequencing from PVDF membranes. Data acquisition and analysis was done using ABI 610 software. [Pg.194]

PAM analysis indicated that salt treatment in the light irreversibly damaged the photosynthetic activity of thylakoid membranes (data not shown). [Pg.252]

The roule (raveled by a Ca channel blocker, such as verapamil, (o its receptor site parallels (hat observed with many local aneslhetic-like antiarrhythmic agents. It i.s believed that verapamil, like mo.sl of (he Ca channel blockers. crosses the cell membrane in an uncharged form to gain access to its site of action on the intracellular side of the membrane. Data show a greater affinity of verapamil and other Ca- channel hlockers to the inactivated. state of the channel. ... [Pg.630]

Figure 5. Room temperature proton conductivities of several membranes. Data compiled from [97-99]. Figure 5. Room temperature proton conductivities of several membranes. Data compiled from [97-99].
Figure 6 Total white cell count (A) and arterial C3a concentration (B) as a function of time on dialysis for a dialyzer containing cellulose membranes. Data are shown as mean + SEM, n=14. See reference 44 for methodology. Figure 6 Total white cell count (A) and arterial C3a concentration (B) as a function of time on dialysis for a dialyzer containing cellulose membranes. Data are shown as mean + SEM, n=14. See reference 44 for methodology.
Notes aDisplacement of [3H]cytisine from rat brain membranes data from ref. 10 unless otherwise indicated. bData from ref. 15. [Pg.94]

Semibalch, Membrane Data Analysis Regression tCh. S) Multiple Reactions (Ch. 6)... [Pg.1104]

A) Concentration-effect curves of 5-HT and 5-CT on stimulation of AC activity in guinea-pig hippocampal membranes (data from [2]). [Pg.262]

Fig. 6. Partition coefficients and permeability coefficients of amides as a function of carbon chain length. Dashed hues partition coefficients for (oUve oil + fatty acid)/water system (OOFA) or ether. Solid lines permeabihties across red cell membranes of dog or man, as indicated data from (11 ] or across artificial lipid bilayer membranes, data from Poznansky et al. [25]. Fig. 6. Partition coefficients and permeability coefficients of amides as a function of carbon chain length. Dashed hues partition coefficients for (oUve oil + fatty acid)/water system (OOFA) or ether. Solid lines permeabihties across red cell membranes of dog or man, as indicated data from (11 ] or across artificial lipid bilayer membranes, data from Poznansky et al. [25].
Figure 8.9 Binding of [ HJiloprost to NCB-20 membranes. A, equilibrium binding of selected concentrations of pHJiloprost to NCB-20 membranes. Data are means SEM of triplicate determinations of specific binding, and are represented as a Scatchard plot (B). F is the free ligand concentration (nmolL ), and B is the pH]iloprost bound (fmol (mg protein) (Reproduced from reference 28 with permission)... Figure 8.9 Binding of [ HJiloprost to NCB-20 membranes. A, equilibrium binding of selected concentrations of pHJiloprost to NCB-20 membranes. Data are means SEM of triplicate determinations of specific binding, and are represented as a Scatchard plot (B). F is the free ligand concentration (nmolL ), and B is the pH]iloprost bound (fmol (mg protein) (Reproduced from reference 28 with permission)...
Roofing membrane. [Data from Stevenson, D. R. Harr, M. E. Jakupca, M. R., US Patent... [Pg.112]

Impact resistant roofing membrane. [Data from Mehta, NR,FiathJC,Pettey, da. World Patent WO2009143432, Nov. 26,2009, Cooley Group Holdings Inc.]... [Pg.112]

Figure 8.10 Correlation times vs reciprocal of temperature for DMPC membranes. Data is obtained from relaxation time measurements (Dufourc et ai, 1992). Dravirings in inserts picture intramolecular (ti,2,3), molecular and collective motions, the latter only occurring in the... Figure 8.10 Correlation times vs reciprocal of temperature for DMPC membranes. Data is obtained from relaxation time measurements (Dufourc et ai, 1992). Dravirings in inserts picture intramolecular (ti,2,3), molecular and collective motions, the latter only occurring in the...
Membrane permeance and selectivity data are based on those of polymeric membranes obtained from Faiz and Li (2012). This is due to a lack of studies on CMS membranes for the separation of olefins/parafifins. The assumption of the use of polymeric membrane data is conservative since CMS membranes have been shown to give better permeance and selectivity than polymeric membranes for olefln/paraffin separation (Xu et al., 2012)... [Pg.291]


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Data Oxygen Permeability of Solid Oxide Membranes

Membranes Methane data

Membranes Methanol data

Membranes Naphthalene data

Membranes Nitrogen data

Membranes Octane data

Membranes Octanol data

Membranes Oxygen data

Membranes Poly data

Membranes Potassium chloride data

Membranes Propane data

Membranes Propanol data

Membranes Propylene data

Membranes Pyridine data

Membranes selectivity data

Typical Permeation and Separation Data for Porous Membranes

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