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Heat distribution, distillation

ARS minimizes refrigeration energy by using distributed distillation and simultaneous heat and mass transfer in the dephlegmator (exclusive arrangement with Air Products) or HRS system. Two C2 streams of varying composition are produced. Hydrogen and methane are separated overhead. [Pg.77]

Complete thermodynamic analysis, based on reversible distillation, takes into account the effects of finite temperature and composition driving forces as well as nonuniform heat distribution and hydraulic resistance (Fonyo, 1974a,b). The effect of nonuniform heat distribution (i.e., adiabatic distillation) can be mitigated by the introduction of intercoolers/interheaters (Terranova and Westerberg, 1989 Dhole and Linnhoff. 1992). [Pg.176]

As a residual solid or viscous liquid is concentrated to dryness, stirring becomes difficult, especially in an immobile vessel. Due to the small surface area-to-volume ratio of large equipment, heat transfer and distillation take longer than similar operations in the laboratory. Decomposition may occur with extended heating, especially if there is uneven heat distribution. Complete removal of residual solids and viscous liquids is difficult from vessels with access limited through manways. Residual solvents may be removed ( stripped ) from liquids using specialized stills, e.g., wiped film evaporators, in which the mobile liquid flows over a heated zone. Only rarely are extracts concentrated to dryness. [Pg.12]

The ARS minimizes refrigeration energy by using distributed distillation and simultaneous heat and mass transfer in the HRS system. [Pg.129]

Figure 9 - Influence of the Heat Distribution on the Flow Rate of the Distillate... Figure 9 - Influence of the Heat Distribution on the Flow Rate of the Distillate...
Kayihan, F., Optimum Distribution of Heat Load in Distillation Columns Using Intermediate Condensers and Reboilers, AfC/iS Symp. Ser., 192(76) 1, 1980. [Pg.354]

Manganese is the third most abundant transition metal, and is widely distributed in the earth s crust. The most important ore is pyrolusite, manganese(IV) oxide. Reduction of this ore by heating with aluminium gives an explosive reaction, and the oxide Mn304 must be used to obtain the metal. The latter is purified by distillation in vacuo just above its melting point (1517 K) the pure metal can also he obtained by electrolysis of aqueous manganese(II) sulphate. [Pg.384]

The use of V-notches in a trough wall for overflow is more sensitive to leveling problems than the other designs, and for the same %- to Me-in. level tolerance produces a more severe non-uniform flow distribution. The quality of distribution from a V-notch is poor compared to the other types of trough distributor, but does have advantages in slurry systems [131]. It should not be used for critical distillation applications, but is good for heat transfer and where solids are in the system. [Pg.265]

Acid anhydrides have been employed with, and without the use of a base catalyst. For example, acetates, propionates, butyrates, and their mixed esters, DS of 1 to ca. 3, have been obtained by reaction of activated cellulose with the corresponding anhydride, or two anhydrides, starting with the one with the smaller volume. In all cases, the distribution of both ester groups was almost statistic. Activation has been carried out by partial solvent distillation, and later by heat activation, under reduced pressure, of the native cellulose (bagasse, sisal), or the mercerized one (cotton linters). No catalyst has been employed the anhydride/AGU ratio was stoichiometric for microcrystalhne cellulose. Alternatively, 50% excess of anhydride (relative to targeted DS) has been employed for fibrous celluloses. In all cases, polymer degradation was minimum, and functionalization occurs preferentially at Ce ( C NMR spectroscopic analysis [52,56,57]). [Pg.129]

It can be detonated on impact, but is normally considered a stable intermediate (m.p. 288° C), suitable for purification of pyridine [1]. Occasionally explosions have occurred when the salt was disturbed [2], which have been variously attributed to presence of ethyl perchlorate, ammonium perchlorate, or chlorates. A sample was being dried in a glass vacuum desiccator. Over-enthusiastic release of vacuum distributed some of the salt onto the lid. The grinding action as the lid was slid off initiated explosion of this, shattering the lid [6], A safer preparative modification is described [3], It explodes on heating to above 335°C, or at a lower temperature if ammonium perchlorate is present [4], A violent explosion which occurred during the final distillation according to the preferred method [3] was recorded [5],... [Pg.612]

Continuous Multicomponent Distillation Column 501 Gas Separation by Membrane Permeation 475 Transport of Heavy Metals in Water and Sediment 565 Residence Time Distribution Studies 381 Nitrification in a Fluidised Bed Reactor 547 Conversion of Nitrobenzene to Aniline 329 Non-Ideal Stirred-Tank Reactor 374 Oscillating Tank Reactor Behaviour 290 Oxidation Reaction in an Aerated Tank 250 Classic Streeter-Phelps Oxygen Sag Curves 569 Auto-Refrigerated Reactor 295 Batch Reactor of Luyben 253 Reversible Reaction with Temperature Effects 305 Reversible Reaction with Variable Heat Capacities 299 Reaction with Integrated Extraction of Inhibitory Product 280... [Pg.607]

Solute equilibrium between the mobile and stationary phases is never achieved in the chromatographic column except possibly (as Giddings points out) at the maximum of a peak (1). As stated before, to circumvent this non equilibrium condition and allow a simple mathematical treatment of the chromatographic process, Martin and Synge (2) borrowed the plate concept from distillation theory and considered the column consisted of a series of theoretical plates in which equilibrium could be assumed to occur. In fact each plate represented a dwell time for the solute to achieve equilibrium at that point in the column and the process of distribution could be considered as incremental. It has been shown that employing this concept an equation for the elution curve can be easily obtained and, from that basic equation, others can be developed that describe the various properties of a chromatogram. Such equations will permit the calculation of efficiency, the calculation of the number of theoretical plates required to achieve a specific separation and among many applications, elucidate the function of the heat of absorption detector. [Pg.93]


See other pages where Heat distribution, distillation is mentioned: [Pg.223]    [Pg.1111]    [Pg.168]    [Pg.19]    [Pg.19]    [Pg.894]    [Pg.425]    [Pg.899]    [Pg.391]    [Pg.280]    [Pg.235]    [Pg.887]    [Pg.163]    [Pg.308]    [Pg.350]    [Pg.478]    [Pg.482]    [Pg.525]    [Pg.728]    [Pg.47]    [Pg.214]    [Pg.73]    [Pg.112]    [Pg.132]    [Pg.226]    [Pg.887]    [Pg.626]    [Pg.218]    [Pg.225]    [Pg.317]    [Pg.441]    [Pg.154]    [Pg.30]   
See also in sourсe #XX -- [ Pg.481 ]




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