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P production

The procedure for the Clemmensen reduction is somewhat different from that previously described (Sections III,9, and IV,6) the chief modification of moment is the use of toluene. The concentration of organic material in the aqueous layer is considerably reduced this results in less high b.p. products being formed, thus leading to a better yield of a purer product,... [Pg.738]

Fig. 16. Two-hquid flotation flow sheet (39). The original ROM is kaolin (white clay) that contains 11% impurity in the form of mica, anatase, and siUca. Treatment produces high purity kaolin and a Ti02-rich fraction. A, Kaolin stockpile D, dispersant (sodium siUcate plus alkah) W, water K, kerosene C, collector (sodium oleate) RK, recycled kerosene S, screen M, inline mixer SPR, separator CFG, centrifuge P, product and T, to waste. Fig. 16. Two-hquid flotation flow sheet (39). The original ROM is kaolin (white clay) that contains 11% impurity in the form of mica, anatase, and siUca. Treatment produces high purity kaolin and a Ti02-rich fraction. A, Kaolin stockpile D, dispersant (sodium siUcate plus alkah) W, water K, kerosene C, collector (sodium oleate) RK, recycled kerosene S, screen M, inline mixer SPR, separator CFG, centrifuge P, product and T, to waste.
Fig. 1. Natural ckculation evaporators where C = condensate, E = entrainment return, F = feed, N = noncondensibles vent, P = product or concentrate, S = steam, V = vapor, and M = knitmesh separator (a) horizontal-tube, (b) short-tube vertical, (c) propeUer calandria, and (d) long-tube reckculating. Fig. 1. Natural ckculation evaporators where C = condensate, E = entrainment return, F = feed, N = noncondensibles vent, P = product or concentrate, S = steam, V = vapor, and M = knitmesh separator (a) horizontal-tube, (b) short-tube vertical, (c) propeUer calandria, and (d) long-tube reckculating.
Experimental confirmations of the relative independence of kc with respecl to total pressure have been widely reported. Deviations do occur at extreme conditions. For example, Bretsznajder (Pi ediction of Ti anspoii and Othei Physical Piopeiiies of fluids, Pergamon Press, Oxford, 1971, p. 343) discusses the effects of pressure on the D bPt product and presents experimental data on the self-diffusion of CO9 which show tnat the D-p product begins to decrease at a pressure of... [Pg.607]

FIG. 11-122 Evaporator types, a) Forced circulation, (h) Siibmerged-tiihe forced circulation, (c) Oslo-type crystallizer, (d) Short-tube vertical, (e) Propeller calandria. (f) Long-tube vertical, (g) Recirculating long-tube vertical, (h) Falling film, (ij) Horizontal-tube evaporators. G = condensate F = feed G = vent P = product S = steam V = vapor ENT T = separated entrainment outlet. [Pg.1138]

Mechanisms of decomposition reactions at interfaces are conveniently considered with reference to the diagrammatic representations in Fig. 8 (R = reactant, 1,1 = intermediates and P = product) and classified under the following headings. [Pg.111]

Fig. 8. Mechanisms of decomposition reactions occurring at interfaces. R = reactant I, I = intermediates and P = product. A more detailed account of these phenomena is given in the text. Fig. 8. Mechanisms of decomposition reactions occurring at interfaces. R = reactant I, I = intermediates and P = product. A more detailed account of these phenomena is given in the text.
Bentley P. Product Formulation Expert System (PEES). In Rowe RC, Roberts RJ, Intelligent software for product formulation. London Taylor and Erancis, 1998. pp. 27-41. [Pg.697]

S] + K )] for the hexokinase-catalyzed phosphorylation reactions of 2DG and D-glucose, respectively [S (substrate) + E (enzyme) — ES— -I- P (product)]. This constant (LC) accounts for the ratio of the arteriovenous extraction fraction (by transport and phosphorylation) of 2DG to that of D-glucose (LC= 1) under steady-state conditions. This concept can be directly applied to the case of 2DFG by employing the LC (-0.5) for 2DFG. [Pg.187]

Fig. 22 a and b. Schematic representation of the potential energy curves for a M +. L ion pair, (a) the excited pair M. L returns nonradiatively to the ground state. L. (b) in competition with the process in (a) a photochemical reaction (P products) is possible (modified from Ref. [1])... [Pg.182]

FIG. 2 Localization of the biocatalyst with different phase distributions of substrate and product in two-phase medium. S substrate P product B biocatalyst. [Pg.559]

The increased serum phosphorus binds to calcium in the serum, which leads to deposition of hydroxyapatite crystals throughout the body. The calcium-phosphorus (Ca-P) product reflects serum solubility. A Ca-P product greater than 75 mg2/dL2 promotes crystal deposition in the joints and eye, leading to arthritis and conjunctivitis, respectively. Soft tissue deposition primarily affects the coronary arteries of the heart, lungs, and vascular tissue and is associated with a Ca-P product greater than 55 mg2/dL2.36 The Ca-P product has been associated with increased mortality37 and is a risk factor for calcification of vascular and soft tissues.35... [Pg.387]

Increased serum phosphorus levels Low to normal serum calcium levels Increased Ca-P product Increased PTH levels Decreased vitamin D levels... [Pg.388]

Ca-P product Less than 55 mg2/dL2 Less than 55 mg2/dL2 Less than 55 mg2/dL2... [Pg.389]

Cinacalcet is a calcimimetic that increases the sensitivity of receptors on the parathyroid gland to serum calcium levels to reduce PTH secretion. Cinacalcet maybe beneficial in patients with an increased Ca-P product who have elevated PTH levels and cannot use vitamin D therapy. Because the effects of cinacalcet on PTH can reduce serum calcium levels and result in hypocalcemia, cinacalcet should not be used if serum calcium levels are below normal. [Pg.391]

The first step of a free radical aromatic substitution, the formation of the a-com-plex, is also an addition step. The o,m,p-product ratio therefore also responds to steric effects. This is shown for the free radical phenylation and dimethylamination of toluene and r.-butylbenzene in Table 8. The larger the substituent on the aromatic system and the bulkier the attacking radical, the more p-substitution product is obtained at the expense of o-substitution. In the phenylation reaction the yield of m-product also increases in contrast to the dimethylamination reaction. The substitution pattern of this latter reaction is, in addition to the steric effect, governed heavily by polar effects because a radical cation is the attacking species113. ... [Pg.25]

The NHCOR group is not protonated in acid solution, and nitration of aniline to yield o-/p-products can thus be carried out by using, for example, COMe as a protecting group which is subsequently removed. [Pg.155]


See other pages where P production is mentioned: [Pg.964]    [Pg.801]    [Pg.1838]    [Pg.2149]    [Pg.286]    [Pg.67]    [Pg.964]    [Pg.230]    [Pg.239]    [Pg.241]    [Pg.208]    [Pg.31]    [Pg.34]    [Pg.4]    [Pg.304]    [Pg.645]    [Pg.298]    [Pg.358]    [Pg.389]    [Pg.391]    [Pg.391]    [Pg.391]    [Pg.392]    [Pg.307]    [Pg.44]    [Pg.247]    [Pg.283]    [Pg.46]    [Pg.659]    [Pg.53]    [Pg.129]    [Pg.150]    [Pg.157]   
See also in sourсe #XX -- [ Pg.161 , Pg.162 , Pg.163 , Pg.164 , Pg.165 , Pg.166 , Pg.167 , Pg.168 , Pg.169 , Pg.170 , Pg.171 , Pg.172 , Pg.173 ]




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