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Section 2.6 Solids

Belt conveyors belt speed 1 m/s handling solids of density 1.6 Mg/m with steel welded frame, head and tail pulley, troughing idlers, roller bearings, cold rolled steel shafters, four ply, 28 oz belt excluding motor, drive and supports. FOB cost = 21000 for the product of (solids capacity, Mg/h) X (length, m) = 10 with n = 0.20 for the range 5000-5 X 10. L+M = 1.7-2.7. L/M = 0.3. [Pg.385]

Hoists for medium lift, heavy duty with push trolley, multiple disc brakes including motor and drive. FOB cost = 16000 for lifting capacity = 2.6 Mg with n = 0.36 for the range 4.5-26 and n = 1.48 for the range 26-45. For motor driven trolley X 1.6. [Pg.386]

Hoists for long hft with motor driven trolley, cab or floor controlled, variable speed, mechanical or electric load braking, double reeving, single or twin load hooks, overload relays, AC current. FOB cost = 40000 for lifting capacity = 3 Mg with n = 0.82 for the range 2-20. For DC current X 1.05. L-tM = 1.5. L/M = 0.22. [Pg.386]


Depending on the process requirements catalysts are produced in a variety of ways. Fig. 3.12 shows some typical processes used in catalyst manufacture. In all cases the process starts from a solution. The various process steps used arc explained in subsequent sections. Solid catalysts can be subdivided in bulk catalysts and supports and catalysts prepared by impregnation of shaped supports. [Pg.69]

Fig. 25. Comparison between the experimental abstraction reaction H + H2O(00)(0) cross-section (solid point with error bars), and the 5D QM calculations (solid line). The 6D QM cross-sections with the CS approximation (dotted line), and the QCT data using normal (o) and Gaussian (A) binning procedures are shown. Fig. 25. Comparison between the experimental abstraction reaction H + H2O(00)(0) cross-section (solid point with error bars), and the 5D QM calculations (solid line). The 6D QM cross-sections with the CS approximation (dotted line), and the QCT data using normal (o) and Gaussian (A) binning procedures are shown.
The data of Fig. 20 also point out an interesting phenomenon—while the heat transfer coefficients at bed wall and bed centerline both correlate with suspension density, their correlations are quantitatively different. This strongly suggests that the cross-sectional solid concentration is an important, but not primary parameter. Dou et al. speculated that the difference may be attributed to variations in the local solid concentration across the diameter of the fast fluidized bed. They show that when the cross-sectional averaged density is modified by an empirical radial distribution to obtain local suspension densities, the heat transfer coefficient indeed than correlates as a single function with local suspension density. This is shown in Fig. 21 where the two sets of data for different radial positions now correlate as a single function with local mixture density. The conclusion is That the convective heat transfer coefficient for surfaces in a fast fluidized bed is determined primarily by the local two-phase mixture density (solid concentration) at the location of that surface, for any given type of particle. The early observed parametric effects of elevation, gas velocity, solid mass flux, and radial position are all secondary to this primary functional dependence. [Pg.185]

Solid Particulates These contaminants can originate from a variety of sources, and their presence is a major concern because they can block gas passages and/or the anode surface. Carbon deposition and conditions that can be used to control its formation have been discussed earlier in this section. Solid particles such as ZnO, which is used for sulfur removal, can be entrained in the fuel gas leaving the desulfurizer. The results by Pigeaud (72) indicate that the tolerance limit of MCFCs to particulates larger than 3 pm diameter is <0.1 g/1. [Pg.157]

Solid state chemistry of potentially important waste forms is covered in the fifth section. Solid state reactions can determine the oxidation state and physical and chemical stability of radionuclides in various host waste forms. This information can be used to evaluate the utility of crystalline materials as potential hosts for radioactive wastes. [Pg.6]

Fig. 1.12. Maximum temperature (a) and ethylbenzene conversion (b) during one production cycle for a fixed bed of uniform heat capacity (dotted line), fora structured fixed-bed with inert end sections of higher heat capacity (dashed line), and for latent heat storage inside the catalytic section (solid line) [9]. Fig. 1.12. Maximum temperature (a) and ethylbenzene conversion (b) during one production cycle for a fixed bed of uniform heat capacity (dotted line), fora structured fixed-bed with inert end sections of higher heat capacity (dashed line), and for latent heat storage inside the catalytic section (solid line) [9].
As described in the previous section, solid particles can be broken up if the applied shear stresses are sufficiently large. In contrast, however, liquid droplets cannot be dispersed under certain conditions, even in shear fields with very large shear stresses. The Weber number We is often used to characterize the dispersion of droplets (another notation often used instead... [Pg.169]

In this section solids represent a partitioning or adsorption phase such as soil, asphalt pavement, or granular activated carbon. In contrast to air, water, and octanol, solid phases are typically very complex and poorly characterized. For example, many studies have shown that soils and sediments are characterized by many different types and amounts of organic matter and minerals, and that these different environments have various affinities for an organic chemical. The fugacity for the solid or sorbed phase is expressed as follows ... [Pg.10]

FIGURE 8.3 Calculated and observed SO2 mixing ratios for the April-May period between 26°N to 32°N latitude. 2D model calculations incorporate our calculated vibrational transitions in the visible region and three values for the Lyman-a cross section no Lyman-a cross section (solid), the Lyman-a cross section of 6.4 x 10 cm molecule (dot dash) and Lyman-a cross section of 6.3 x 10 cm molecule (dashed). Observations from Spacelab 3 (circles with horizontal lines) from 1985 [12]. [Pg.154]

The current, I, in a PEVD process can be recorded simultaneously by an ammeter in the external circuit to reveal the kinetics of the PEVD reactions. As discussed in the last section, solid-state reactant (A) needs to be transported as a combination of ionic and electronic species from the source to the sink side through the solid electrochemical cell to participate in a PEVD reaction with vapor phase reactant (B). The PEVD reaction rate, and subsequent product (D) formation rate, v(t), can be expressed as... [Pg.114]

Protein A, a structural component of certain strains of staphylococci, has been used successfully in the place of the second antibody in radioimmunoassay techniques, as well as the solid phase adsorbent of antibody (mentioned in the section Solid Phase Materials). This protein can be heavily labeled with and is, therefore, a reasonable alternative for the use of labeled antiglobulins in immunoassays. [Pg.408]

The Hildebrandt extractor consists of a U-shaped screw conveyer with a separated helix in each of the downward, horizontal, and upward sections. Solids are fed to one leg and fresh solvent is fed to the other to give countercurrent flow. In a Dorr classifier, soUd is introduced near the bottom of a sloping tank and is gradually moved up by means of a rake. The solvent enters at the top and flows in the opposite direction of the sohd and passes under a baffle before finally being discharged over a weir. A number of these units can be connected in series to give countercurrent flow. [Pg.598]

Chapter 8 provides practical guidance on the use of widely used extraction and isolation techniques from the sample preparation perspective. The first two sections, solid-phase extraction and liquid-liquid extraction deal with liquid samples. The sections on supercritical fluid extraction and accelerated solvent extraction focus mainly on solid samples while the centrifugation and filtration sections handle suspensions. A successful sample preparation protocol accounts for specificity and homogeneity as well as recovery and final physical state of the targeted material. The ultimate aim is to produce a sample that is compatible with the desired analytical technique to assure generation of maximum information. [Pg.18]

In this section, solid-state NMR of fibrous proteins is reviewed. For solid-state NMR studies of oriented samples, orientation-dependent nuclear spin interaction tensors serve as probes with which the relative orientations of specific bond vectors can be determined as described in Chapter 8. [Pg.853]

In the next sections, solid catalysts are classified on the basis of their type of material, the most important types comprising metals, metal oxides, and metal sulfides. It is emphasized, however, that a more fundamental classification is also possible, although it can be developed to only a small degree because the science of catalysis is so complex. The next few paragraphs summarize this alternative classification based on the reactions catalyzed and the structures of intermediates this classification also is a start toward unifying homogeneous and heterogeneous catalysis, which have traditionally been considered separately. [Pg.57]

Strain and stress in a specimen are largely defined by the three dimensions of the specimen, by location of the load application, and by the specimen s profile, that is, a confignration of its cross section. Solid composite deck boards are typically represented by jnst one, flat, rectangnlar section. Hollow boards, having ribs, can be... [Pg.226]

NOx (NO and NO2) gas is known to be very harmful to humans and is one of the main causes of acid rain. They are typical noxious gases released from combustion facilities and automobiles. The lower exposure limits (LEE) have been provided in the previous section. Solid-state NOx sensors are widely demanded for monitoring NOx ID the environmental atmosphere as well as in combustion exhausts. Particularly, NOx monitoring is indispensable for the feedback control of combustion systems or de-NOx systems. The NO and NOx have quite different properties from each other. [Pg.23]

LEIS measurements result in an energy spectrum of the backscattered ions from the sample surface. The energy of scattered ions provides information on the mass of the surface atoms, which is directly related to their chemical identity. The cross-section, solid angle and transmission factor (the analyser acts as an energy filter, with transmission characteristics that depend on the mode of operation) are used for these calculations. [Pg.542]

Because polymer NMR papers tend to be published in a number of different journals, we thought it would be beneficial to assemble the symposium papers into one book. This symposium volume is the result. Hopefully this book will be a useful reference work for students and practitioners of polymer NMR, as well as a practical handbook for many state-of-the-art NMR techniques. A total of 31 chapters are included herein, including an overview chapter (Chapter 1). For convenience, this book is organized into five sections solid-state NMR of polymers, solution NMR of synthetic polymers, solution NMR of natural polymers, combined NMR-separation techniques, and dynamics of polymers in solution. [Pg.1]

A partial isothermal section at 325°C determined in the monosulfide region is presented in Fig. 10 from [2002Far] as quoted by [2004Rag]. It shows the X phase of the NiAs type (1C) and its superstructure (3C), see section Solid Phases . [Pg.686]

Elastomer nanocomposites can better be characterized with the help of NMR studies as illustrated in the introduction section. Solid-state NMR is the best choice as the sample is in the solid state, but the same information is obtained from the liquid state NMR as well, in fact this latter method is rather simple and has better sensitivity and resolution. Both these methods determine the crosslink density of composites from the differences in chemical shift values between the bulk solvent and trapped molecules. Prior to the NMR spectral... [Pg.713]

The technique of liquid-liquid extraction was described in Sections 12.1-12.8. In this section, solid-liquid extraction is described. Solid-liquid extraction is often used to extract a solid natural product from a natural source, such as a plant. A solvent is chosen that selectively dissolves the desired compound but that leaves behind the undesired insoluble solid. A continuous solid-liquid extraction apparatus, called a Soxhlet extractor, is commonly used in a research laboratory. [Pg.720]

Square section hollow rod Square section solid rod Z-profile... [Pg.218]


See other pages where Section 2.6 Solids is mentioned: [Pg.385]    [Pg.161]    [Pg.228]    [Pg.12]    [Pg.189]    [Pg.560]    [Pg.596]    [Pg.342]    [Pg.190]    [Pg.48]    [Pg.536]    [Pg.253]    [Pg.1046]    [Pg.2138]    [Pg.855]    [Pg.207]    [Pg.2124]    [Pg.1227]    [Pg.145]    [Pg.372]    [Pg.42]    [Pg.708]    [Pg.1908]    [Pg.293]    [Pg.253]    [Pg.317]    [Pg.357]   


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Feed and Solid Conveying Section

Scattering cross section solid angle

Section 2.5 Pumping Slurries Liquid-Solid Systems

Section 5.2 Gas-Solid

Section 5.5 Liquid-Solid General Selection

Section 7.3 Liquid-Solid

Section 7.3.1 Solids Suspension

Section 7.3.2 Solids Dispersion

Section 7.3.3 Solids Dissolving

Section 7.3.4 Solids Flocculating

Section 7.4 Dry Solids

Solid conveying section

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