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Byproducts physical properties

Mixtures that are already 99% (S,S)-diol (a7 )-a-chloro boronic ester on reaction with methylmagnesium bromide or other simple alkylmetallic compounds must undergo destruction of the 1 % (. >,.SJ-diol (o S)-a-chloro boronic ester to byproducts that have very different physical properties from the major product. Thus, this chemistry accounts for the very high diastereomeric ratios noted in Table 1 (Section 1.1.2.1.2.1.). [Pg.1079]

Some physical properties of the main species are listed in Table 5.2. Bringing phenol in reaction conditions implies vaporization at low partial pressure. Vacuum is necessary for carrying out separations by distillation. Phenol forms azeotropes with both cyclohexanol and cyclohexanone. If unconverted phenol should be recycled this could affect the global yield by recycling desired product too. If water appears as a byproduct, it gives azeotropes with both cyclohexanone and cyclohexanol. Because these azeotropes are low boilers they can be removed easily by distillation. [Pg.131]

The reactor/separator/recycle structure is decided by considering the physical properties of the species found in the reactor effluent (Table 9.1). The catalyst and the organic phase are immiscible. Therefore, they can be separated by liquid-liquid splitting. The separation of the organic components by distillation seems easy. In a direct sequence, the inert and any light byproduct will be removed in the first column. The second column will separate the reactants, which have adjacent volatilities. Therefore, there will be only one recycle for both reactants. The third column will separate the product from the heavies. The reactor/separation/ recycle structure of the flowsheet is presented in Figure 9.2. [Pg.268]

In addition to agitation, the interfacial areas are significantly affected by the following acid/hydrocarbon ratio, acid composition (and especially the amounts of dissolved conjunct polymers), and temperature. Conjunct polymers are surfactants that collect in appreciable concentrations at the interface. Here, they act as a reservoir of H s in the transfer steps from isobutane or other isoparaffins to the i-Cs to i-Cie cations. Conjunct polymers also have a major effect on the viscosity and other physical properties of the acid phase. In the alkylation reactor, the preferred sulfuric acid and HF phases contain appreciable amounts of conjunct polymers optimum amounts result in higher RON values, higher yields, less byproducts, etc. [Pg.59]

Of the relevant time scales that drive the frequency effects of the polymer pads, many of them have their origin in the physical structure of the polishing pad. The largest scale of these is represented by the groove. But the basic nature of many of the typical polymer pads includes a somewhat random interruption of the polymer material in the form of pores. The pores have three major impacts (a) they modulate the abrasive surface presented to the wafer (b) they break up the homogenous nature of the pad material itself, causing modification of the physical properties of the material and (c) they provide microreservoirs for both slurry distribution and byproduct... [Pg.123]

The byproducts of rice-bran oil refining include waxes, lecithin, soap-stock (containing high-value oryzanol), and deodoriser distillate containing sterols, tocopherols, tocotrienols and squalene. The characteristics and physical properties of purified rice wax are similar to camauba wax (Sayre and Saunders... [Pg.312]

Several groups reported the use of ion exchange resins for the parallel purification of small-molecular-weight compound libraries. Reaction conditions for the synthesis of the library are chosen such that the product of interest has distinctly different physical properties than the byproducts or the excess reagents. [Pg.224]

If Na is present in the precursor, it usually reacts with HCN in the furnace to form NaCN, so it is most beneficial to use a precursor with a low Na content or better, with none. If Na is present, it will be released from the fiber and at working temperature, will vaporize and form NaCN, Na2C03, or could possibly remain as elemental Na. Table 10.7 lists the physical properties of these byproducts. [Pg.400]


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See also in sourсe #XX -- [ Pg.205 ]




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