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Volume ranges

A typical arrangement for a voltammetric electrochemical cell is shown in Figure 11.28. Besides the working, reference, and auxiliary electrodes, the cell also includes a N2 purge line for removing dissolved O2 and an optional stir bar. Electrochemical cells are available in a variety of sizes, allowing for the analysis of solution volumes ranging from more than 100 mL to as small as 50 )+L. [Pg.510]

AH forms and compositions of reinforcements, ie, mats, woven roving, glass, carbon, and aramid, are commonly used with these processes. Special continuous glass strand mats with a thermoplastic binder aHow preforms to be made using thermoforming techniques. These processes are used for tmck and autobody components, medical equipment cabinets, transportation seating, and other parts needed in the intermediate volume range (1,000—10,000 parts/yr). [Pg.95]

Fluidized-bed opposed-jet mills Hosokawa Micron Powder Systems Div.) differ from the Majac mill in that powder is not fed into the jets, but the jets impinge into a chamber mich contains suspended powder. The powder is entrained into the jets. This ehminates wear on the nozzles, and reduces contamination. Otherwise, construction and appheations are similar to the Majac mill. The fluidized-bed level is maintained a few inches above the jets. The Fluidized-bed mill is available in 13 sizes with air volumes ranging from. 50 to 11,000 mVh. One application is for toner grinding. [Pg.1866]

The sliding-vane compressor is widely used as a vacuum pump as well as a compressor, with the largest volume approximately 6,000 cfm. The lower end of the volume range is 50 cfm. A single-stage compressor with atmospheric inlet pressure is limited to a 50 psi discharge pressure. In booster service, the smaller units can be used to approximately 400 psi. [Pg.8]

The volume range of the axial starts at approximately 30,000 cfm. One of the largest sizes built is 1,000,000 cfm, though this size is certainly not common. The common upper range is 300,000 cfm. The axial compressor, because of a low pressure rise per stage, is exclusively manufacturetl as a multistage machine. [Pg.226]

It is seen that the maximum sample volume ranges from a fraction of a microliter when (a=1.01) to several ml when (a) = 1.2. The small sample volume results from... [Pg.406]

Fay and Lewis (1977) used spherical gas samples inside soap bubbles whose volumes ranged from 20 to 190 cm. Typically, a sphere was ignited with resistance wire, and the combustion process was then filmed with a high-speed camera. The fireball s maximum height and diameter, as well as the time needed to complete combustion, were evaluated. The fireball s thermal radiation was sensed by a radiation detector. Figure 6.3 relates fireball burning time and size to initial propane... [Pg.161]

Lihou and Maund (1982) carried out two series of experiments (Figure 6.4). One series involved butane-filled bubbles whose masses ranged from 1.5 to 6 g. The second series was performed with methane and butane in volumes ranging from 100 to 800 ml. (For methane, this corresponds to a mass range from 0.07 to 0.6 g, and for butane, from 0.24 to 1.9 g.) Measured temperatures ranged from 1000 K to 1400 K for butane fireballs, and from 1100 K to 1700 K for methane fireballs. [Pg.162]

The resolution required in any analytical SEC procedure, e.g., to detect sample impurities, is primarily based on the nature of the sample components with respect to their shape, the relative size differences of species contained in the sample, and the minimal size difference to be resolved. These sample attributes, in addition to the range of sizes to be examined, determine the required selectivity. Earlier work has shown that the limit of resolvability in SEC of molecules [i.e., the ability to completely resolve solutes of different sizes as a function of (1) plate number, (2) different solute shapes, and (3) media pore volumes] ranges from close to 20% for the molecular mass difference required to resolve spherical solutes down to near a 10% difference in molecular mass required for the separation of rod-shaped molecules (Hagel, 1993). To approach these limits, a SEC medium and a system with appropriate selectivity and efficiency must be employed. [Pg.30]

No. stages per case max. 7 Nominal overall eff, % 77 Intake volume range 3,500-12,000 Nominal head per stage, ft 8,500 Nominal speed, rpm 8,100 Max. case pressure 250 psi cast iron... [Pg.501]

Figure 12-99. Stable volume range extended by stator blade control. (Used by permission Claude, R. E. Chemical Engineering, V. 63, No. 6, 1956. McGraw-Hill, Inc. All rights reserved.)... Figure 12-99. Stable volume range extended by stator blade control. (Used by permission Claude, R. E. Chemical Engineering, V. 63, No. 6, 1956. McGraw-Hill, Inc. All rights reserved.)...
There are basically two types of LC sample valve, those with an internal loop and those with an external loop. Valves with an internal loop are normally designed to deliver sample volumes of less than one microliters. Valves with external loops can deliver sample volumes ranging from a few microliters to several milliliters or more. In general, LC sample valves must be able to sustain pressures up to 10,000 p.s.i., although they are likely to operate on a continuous basis, at pressures of 3,000 p.s.i. or less. [Pg.138]

In Fig. 3.4d the relative molecular mass of the solute, Mr, is plotted on a log scale against the retention volume. The interstitial volume, which represents the volume range within which separations occur, and the size range of solutes that are eluted in this volume range, depend on the sort of material that is used for the stationary phase. Because for a given separation, F0 and V are constant, we can reliably predict the total volume of solvent or the time taken for a particular analysis. The calibration curve is established by determining the retention volume for standards of known Mr. [Pg.127]

The chapters cover the following areas (i) use of coordination complexes in all types of catalysis (Chapters 1-11) (ii) applications related to the optical properties of coordination complexes, which covers fields as diverse as solar cells, nonlinear optics, display devices, pigments and dyes, and optical data storage (Chapters 12-16) (iii) hydrometallurgical extraction (Chapter 17) (iv) medicinal and biomedical applications of coordination complexes, including both imaging and therapy (Chapters 18-22) and (v) use of coordination complexes as precursors to semiconductor films and nanoparticles (Chapter 23). As such, the material in this volume ranges from solid-state physics to biochemistry. [Pg.1066]

For these volumes in the Springer book review series Topics in Current Chemistry, it seemed natural to blend a mix of theory and experiment in chemistry, materials science, and physics. The content of this volume ranges from conducting polymers and charge-transfer conductors and superconductors, to single-molecule behavior and the more recent understanding in single-molecule electronic properties at the metal-molecule interface. [Pg.282]

In the region of a first-order transition ip has equal minima at volumes V and V2, in line with the Maxwell construction. The mixed phase is the preferred state in the volume range between V and V2. It follows that the transition from vapour to liquid does not occur by an unlikely fluctuation in which the system contracts from vapour to liquid at uniform density, as would be required by the maximum in the Van der Waals function. Maxwell construction allows the nudeation of a liquid droplet by local fluctuation within the vapour, and subsequent growth of the liquid phase. [Pg.511]

Applications of GC-MS or LC-MS techniques to forensic toxicology considerably reduced the volume of specimens necessary for analytical procedure. Recently, the volumes range from 0.2 to 1.0 mL. [Pg.312]

The case of PEO as a crystallizable component within block copolymers, as well as isolated droplets, is atypical in the sense that it has been studied in a wide variety of block copolymers and in the widest possible volume range if micron-size droplets are also considered (Figs. 4, 5, Tables 2, 3). Nevertheless, the observed change in crystallization temperature is particularly large, not only in comparison with low molecular weight materials, as previously mentioned, but also with other polymers. [Pg.40]

The 5-mm tube held in the sample probe is indicative of the sample size used in an NMR instrument— typically some fraction of a milliliter. Typical analyte quantities dissolved in this volume range from 10... [Pg.287]

Many buffers, such as phosphate, carbonate, and borate, have ionization volumes ranging from -24 to -32 cm3 mol-1. These buffers should be used only for reactions that are independent of pH to at least 0.5 unit below the pH at 1 bar. Very pH-sensitive reactions should be carried out in Tris buffer, which has an ionization volume of 1 cm3 mol-1. [Pg.143]


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See also in sourсe #XX -- [ Pg.17 ]

See also in sourсe #XX -- [ Pg.17 ]




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Long-Range Excluded-Volume Effects in Solutions

Mean corpuscular volume normal range

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