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Mixed materials

Thus the weighted network area AJ itwork is 9546 m. Now calculate the network capital cost for mixed materials of construction by using AI t ork... [Pg.231]

Hall, S. G., Ahmad, S., and Smith, R., Capital Cost Target for Heat Exchanger Networks Comprising Mixed Materials of Construction, Pressure Ratings and Exchanger Types, Computers Chem. Eng., 14 319, 1990. [Pg.237]

Equation (F.l) shows that each stream makes a contribution to total heat transfer area defined only by its duty, position in the composite curves, and its h value. This contribution to area means also a contribution to capital cost. If, for example, a corrosive stream requires special materials of construction, it will have a greater contribution to capital cost than a similar noncorrosive stream. If only one cost law is to be used for a network comprising mixed materials of construction, the area contribution of streams requiring special materials must somehow increase. One way this may be done is by weighting the heat transfer coefficients to reflect the cost of the material the stream requires. [Pg.447]

For CW applieations of optieal-heterodyne eonversion, two laser fields are applied to the optoeleetronie material. The non-linear nature of the eleetro-optie effeet strongly suppresses eontimious emission relative to ultrashort pulse exeitation, and so most of the CW researeh earried out to date has used photoeonduetive anteimae. The CW mixing proeess is eharaeterized by the average drift veloeity t and earrier lifetime Xq of the mixing material, typieally... [Pg.1251]

Segregation. The problem of segregation occurs when a bulk soHd composed of different particle sizes or densities separates. The result can be quite serious if uniform density or mixed material is required for a process. [Pg.552]

Lost work, EW, is the irreversible loss in exergy that occurs because a process operates with driving forces or mixes material at different temperatures or compositions. [Pg.83]

AT the path length, and P (A) the mass absorption coefficient at wavelength A. Between absorption edges, P (A) is proportional to Z A and is nearly independent of physical or chemical state. An absorption measurement on each side of an absorption edge is required for each element analyzed. X-ray absorption is especially useful in determining heavy elements in mixed materials of lower Z, such as lead in gasoline and uranium in aqueous solution. [Pg.320]

Preparation and Addition of Materials To ensure maximum production of high-grade mixed material, the prehminary preparation... [Pg.1652]

Variations in measurable properties existing in the bulk material being sampled are the underlying basis for samphng theory. For samples that correctly lead to valid analysis results (of chemical composition, ash, or moisture as examples), a fundamental theoiy of sampling is applied. The fundamental theoiy as developed by Gy (see references) employs descriptive terms reflecting material properties to calculate a minimum quantity to achieve specified sampling error. Estimates of minimum quantity assumes completely mixed material. Each quantity of equal mass withdrawn provides equivalent representation of the bulk. [Pg.1757]

The muller is useful for mixing problems requiring certain types of aggregate breakdown, fricdional anchorage of particles to one another, and densification of the final mix. Materials which are excessively fluid or sticky should be avoided. The muller mixer is generally used for batch operations (Fig. 19-9g), although Fig. 19-9/j shows a continuous muller. [Pg.1766]

By incorporation of alkali metal halides in the reaction mix, materials of composition M4-[MfiXig] can be produced in which each MgXn unit has a further six X atoms attached to its apices, so forming discrete clusters. [Pg.992]

To a 2-liter flask were added 300 g of finely divided corn. The flask and its contents were then sterilized and after sterilization 150 ml of sterile deionized water wereadded. To the mixture in the flask were then added 45 ml of the inoculum prepared by the process and the material was thoroughly mixed. The mixed material was then incubated for about 20 days at 25°C in a dark room in a water-saturated atmosphere. The following illustrates the recovery of the anabolic substance from the fermentation medium. [Pg.1598]

Toward the end of the reaction, the mixture becomes quite viscous. Unless the stirring assembly is capable of mixing material at the flask walls, homogeneous temperature control cannot be guaranteed. [Pg.120]

Figure 4. Log intensity vs. potential plots (Tafel plots) obtained from the voltammograms of a platinum electrode submitted to a 2 mV s l potential sweep polarized in a 0.1 M LiC104 acetonitrile solution having different thiophene concentrations. (Reprinted from T. F. Otero and J. Rodriguez, Parallel kinetic studies of the electrogeneration of conducting polymers mixed materials, composition, and kinetic control. Electrochim, Acta 39, 245, 1994, Figs. 2, 7. Copyright 1997. Reprinted with permission from Elsevier Science.)... Figure 4. Log intensity vs. potential plots (Tafel plots) obtained from the voltammograms of a platinum electrode submitted to a 2 mV s l potential sweep polarized in a 0.1 M LiC104 acetonitrile solution having different thiophene concentrations. (Reprinted from T. F. Otero and J. Rodriguez, Parallel kinetic studies of the electrogeneration of conducting polymers mixed materials, composition, and kinetic control. Electrochim, Acta 39, 245, 1994, Figs. 2, 7. Copyright 1997. Reprinted with permission from Elsevier Science.)...
The final conclusion from the different kinetic studies that simultaneously followed productivity, consumed current, storage capacity of the obtained films, and the current efficiency in generating electroactive polymer in the final film is that any electropolymerization of conducting polymers occurs together a partial degradation of the electroactive polymer. The final film is a mixed material. From the kinetic studies we know the variables that increase or deplete the degradation reaction in relation to the polymerization reaction. [Pg.329]

The final conclusion of this short discussion is that electropolymerization is a fast method (a film of about 5 //mean be obtained by polarization in 1 rnin) that uses a complex mechanism (Fig. 12) in which electropolymerization, cross linking, degradation, and chemical polymerization can coexist to produce a mixed material with a cross-linked and electroactive part and a passive fraction.67-71 However, ifwe control the variables acting on the kinetics of the different simultaneous reactions, the complexity also provides flexibility, allowing us to obtain materials tailored for specific applications. [Pg.333]

Finally, other relevant treatment options for plastics waste include landfill and mechanical recycling. Since these options (unlike Vinyloop and cement kiln incineration) are not even similar to feedstock recycling we discuss them here only very briefly. Mechanical recycling of plastics (be it PVC or other plastics), needs dedicated collection of the plastic waste in question. This is only possible for selected plastic flows (high volumes, recognisable products, products consisting mainly of one plastic). Landfill can accept plastic waste in any waste context (pure plastic type, MPW, mixed materials). I will only address the costs of these alternative technologies. [Pg.22]

A fundamental criticism of the resin-modified glass polyalkenoate cements is that, to some extent, they go against the philosophy of the glass polyalkenoate cement namely, that the freshly mixed material should contain no monomer. Monomers are toxic, and HEMA is no exception. This disadvantage of composite resins is avoided in the glass polyalkenoate cement as the polyacid is pre-polymerized during manufacture, but the same cannot be said of these new materials. For this reason they may lack the biocompatibility of conventional glass polyalkenoate cements. These materials also absorb excessive amounts of water because of the hydrophilic nature of polyHEMA (Nicholson, Anstice McLean, 1992). [Pg.175]

Selection of the type of whole-body dosimeter is important. Inner whole-body dosimeters are usually white, 100% cotton, long underwear purchased from a variety of clothing outlets and stores. One- or two-piece inner whole-body dosimeters are common. Outer whole-body dosimeters can range from hand-made cotton coveralls to shirts and pants bought directly off the shelf at local retail stores. Outer whole-body dosimeters can also be purchased from wholesale clothing outlets. Outer whole-body dosimeters may be any color and may also be 100% cotton or mixed materials, depending on the purpose for which the outer whole-body dosimeter is to be used. For example, one may want to use a coverall as an outer whole-body dosimeter. This would be acceptable even if the coverall were not white and not 100% cotton provided that the fabric did not contain interfering analytical components. [Pg.1002]

Cost-weighing factor applied to film heat transfer coefficients to allow for mixed materials of construction, pressure rating, and equipment types in heat exchanger networks (-), or fugacity coefficient (-)... [Pg.711]

TYPE OF EQUIPMENT VERY HIGH UNIT COST EQUIPMENT MOSTLY ALLOY STEEL MIXED MATERIALS MOSTLY CARB. STEEL ... [Pg.251]

The results of the tests to determine the calorific power show satisfactory values for coprocessing, be it for mixed materials, otherwise unusable material from separation or plastics in general. As observed by [6], the level of chlorides is closely related to the quantity of plastics in the mixture, and also depends on the type of plastic. [Pg.397]

Free-living amebae Sigmoidoscopic material Fix films in Schaudinn fixative or mix material with PVA fixative. [Pg.34]


See other pages where Mixed materials is mentioned: [Pg.231]    [Pg.232]    [Pg.396]    [Pg.401]    [Pg.491]    [Pg.1645]    [Pg.295]    [Pg.391]    [Pg.412]    [Pg.406]    [Pg.216]    [Pg.372]    [Pg.218]    [Pg.181]    [Pg.324]    [Pg.325]    [Pg.330]    [Pg.198]    [Pg.945]    [Pg.394]    [Pg.394]    [Pg.419]    [Pg.650]   
See also in sourсe #XX -- [ Pg.209 , Pg.221 , Pg.226 ]




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Changes in material during mixing

Coating materials mixed layers

Materials mix-ups

Mixed (hybrid) processes and materials

Mixed Porous Materials

Mixed conducting materials

Mixed conductors as electrochromic materials

Mixed ionic and electronic conducting material

Mixed ionic electronic conductive material

Mixed ionic electronic conductive material MIEC)

Mixed matrix materials, membrane

Mixed matrix materials, membrane formation

Mixed oxide materials

Mixed protonic-electronic conducting materials

Mixed proton—electron conducting materials

Mixed-Material Erosion

Mixed-matrix technology material combination

Mixed-valence materials

Mixing electrode materials

Mixing pharmaceutical materials

Mixing pharmaceutical materials machines

Mixing pharmaceutical materials mechanism

Mixing pharmaceutical materials shear

Other Mixed-Valence Materials

Perovskite-type mixed-conducting materials

Retention in BeO and Mixed Be Materials

Shear mixing materials

Sputtering by Non-recycling Ions (Mixed Materials)

Viscous materials, mixing

Viscous materials, mixing planetary

Wet process for mixing materials

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