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Relative concentrations

Measurements of mechanical and chemical parameters (time, dimensions, force, pressure, mass, concentration, relative molecular mass) + + + + + + -H -h... [Pg.916]

Dimer formation, which is favored by increasing temperature, generally does not reduce the quaHty of acryhc acid for most applications. The term dimer includes higher oligomers formed by further addition reactions and present in low concentrations relative to the amount of dimer (3-acryloxypropionic acid). Glacial acrylic acid should be stored at 16—29°C to maintain high quaHty. [Pg.157]

The onset of action is fast (within 60 seconds) for the intravenous anesthetic agents and somewhat slower for inhalation and local anesthetics. The induction time for inhalation agents is a function of the equiUbrium estabUshed between the alveolar concentration relative to the inspired concentration of the gas. Onset of anesthesia can be enhanced by increasing the inspired concentration to approximately twice the desired alveolar concentration, then reducing the concentration once induction is achieved (3). The onset of local anesthetic action is influenced by the site, route, dosage (volume and concentration), and pH at the injection site. [Pg.407]

Fig. 6. Breakthrough curves for aqueous acetone (10 mg 1" in feed) flowing through exnutshell granular active carbon, GAC, and PAN-based active carbon fibers, ACF, in a continuous flow reactor (see Fig. 5) at 10 ml min" and 293 K [64]. C/Cq is the outlet concentration relative to the feed concentration. Reprinted from Ind. Eng. Chem. Res., Volume 34, Lin, S. H. and Hsu, F. M., Liquid phase adsorption of organic compounds by granular activated carbon and activated carbon fibers, pp. 2110-2116, Copyright 1995, with permission from the American Chemical Society. Fig. 6. Breakthrough curves for aqueous acetone (10 mg 1" in feed) flowing through exnutshell granular active carbon, GAC, and PAN-based active carbon fibers, ACF, in a continuous flow reactor (see Fig. 5) at 10 ml min" and 293 K [64]. C/Cq is the outlet concentration relative to the feed concentration. Reprinted from Ind. Eng. Chem. Res., Volume 34, Lin, S. H. and Hsu, F. M., Liquid phase adsorption of organic compounds by granular activated carbon and activated carbon fibers, pp. 2110-2116, Copyright 1995, with permission from the American Chemical Society.
Sulfuric acid concentration [%] Relative humidity Manufacture [%] ml cone, sulfuric acid + ml water ... [Pg.130]

Thermal decomposition of oxyfluoroniobates yields two main compounds containing higher and lower oxygen concentrations relative to the initial compound ... [Pg.216]

For the reaction scheme A - I — P the time profiles of concentration (relative to [A]0) are shown. The following are the conditions displayed and some characteristic values ... [Pg.72]

As we saw in Section 9.2, the activity of a solute J in a dilute solution is approximately equal to the molar concentration relative to the standard molar concentration, [JJ/c°, with c° = 1 mol-L, and so a practical form of this expression is... [Pg.521]

One can see the M procedure has a parallel to either g (s) vs. s or c(s) vs. s in sedimentation velocity where the data are transformed from radial displacement space [concentration, c(r) versus r] to sedimentation coefficient space [g s) or c(s) versus s]. Here we are transforming the data from concentration space [concentration relative to the meniscus j(r) versus r] to molecular weight space [M r) versus r]. [Pg.230]

EL = emissions level ERA = Environmental Protection Agency HSDB = Hazardous Substances Data Bank lARC = International Agency for Research on Cancer IRIS = Integrated Risk Information System NIOSH = National Institute of Occupational Safety and Health OEL = occupational exposure limit OSHA = Occupational Safety and Health Administration PEL = permissible exposure limit RAC = reference air concentration REL = recommended exposure limit RCRA = Resource Conservation and Recovery Act RfD = reference dose TLV = threshold limit value TWA = time-weighted average WHO = World Health Organization... [Pg.190]

Moderate Reactor Productivity. The rhodium catalyst is continuously recycled, but the catalyst is inherently unstable at low CO partial pressures, for example in the post-reactor flash tank. Under these conditions the catalyst may lose CO and eventually form insoluble Rhl3 resulting in an unacceptable loss of expensive catalyst. This reaction is also more likely to occur at low water concentrations, hence in order to run the process satisfactorily catalyst concentrations are kept low and water concentrations relatively high. Hence through a combination of lower than optimum reaction rate (because of low catalyst concentrations) and water taking up valuable reactor volume the overall reactor utilization is less than optimum. [Pg.265]

Sun et al. [41] synthesized a series of benzimidazoles (II) and evaluated their topo I-mediated cleavage as well as cytotoxicity against four cancer cell fines. Topo I cleavage values are reported as REC, the relative effective concentration (i.e., concentrations relative to that of Hoechst 33342, whose value... [Pg.48]

This is an inverted parabolic relation in terms of ttx (calculated hydrophobic parameter of the substituents), which suggests that activity of these compounds first decreases as the hydrophobicity of substituents increases and after a certain point (inversion point ttx = 0.67), activity begins to increase. This may correspond to an allosteric reaction [54]. The indicator variable I is assigned the value of 1 and 0 for the presence and absence of N(CH3)2 substituent at the X position. Its positive coefficient suggests that the presence of a N(CH3)2 substituent at X position, increases the activity. REC is the relative effective concentration i.e., concentration relative to topotecan, whose value is arbitrarily assumed as 1, that is able to produce the same cleavage on the plasmid DNA in the presence of human topo I. [Pg.56]

This is the first example of a reaction for which the presence of a chelating ligand was observed to facilitate rather than retard metal-catalysed epoxidation (Gao et al., 1987). It was found that the use of molecular sieves greatly improves this process by removing minute amounts of water present in the reaction medium. Water was found to deactivate the catalyst. All these developments led to an improved catalytic version that allows a five-fold increased substrate concentration relative to the stoichiometric method. Sensitive water-soluble, optically active glycidols can be prepared in an efficient manner by an in situ derivatisation. This epoxidation method appears to be competitive with enzyme-catalysed processes and was applied in 1981 for the commercial production of the gypsy moth pheromone, (-1-) disparlure, used for insect control (Eqn. (25)). [Pg.178]

For a receptor concentration of approximately the dissociation constant and a 10-fold excess of ligand Pbomid" 1. he- essentially all receptor molecules are complexed with maximum intensity of the desired NMR interactions. Lower receptor concentrations relative to Ku can be compensated by a higher ligand excess and might be pushed up to a 1000-fold ligand excess [95], but experiments are easiest appUcable with the mentioned 10-20 fold excess. [Pg.231]

PVA can be crosslinked with a crosslinker present in a molar concentration, relative to monomer residues, of 0.01% to 1.0%. The crosslinker may be formaldehyde, acetaldehyde, glyoxal, glutaraldehyde, maleic acid, oxalic acid, dimethylurea, polyacrolein, diisocyanate, divinyl sulfonate, or a chloride of a diacid [89-91]. [Pg.48]

The predictable flux of °Thxs to the seafloor means that the flux of other components into marine sediments can be assessed by simply measuring their concentration relative to that of °Th (Fig. 5). This approach, termed °Thxs profiling, has seen widespread use in the last decade and has become a standard technique for measuring accumulation rates of many chemical species and sedimentary components. °Thxs provides possibly the best constraint on such accumulation rates for late Pleistocene sediments and is therefore an important tool. It is the best constrained of the constant flux proxies which include ofher chemical species such as Ti (Murray et al. 2000) and He (Marcantonio ef al. 1995). As wifh these other proxies, °Thxs is not mobilized during sediment dissolution because of its extreme insolubility so that °Thxs profiling assesses the final sedimentary burial flux, rather than the flux that initially arrives at the seafloor. [Pg.505]

Most UV/VIS applications concern single-component quantification, which normally requires only relative measurements (e.g. the absorbance of an unknown concentration relative to the absorbance of a standard). Absorption and return to ground state are fast processes, and equilibrium is reached very quickly. Thus, absorption of UV/VIS light is quantitatively highly accurate. Method development involves selecting the wave-length(s) that yield the best results for the particular... [Pg.304]

Figure 6.9 Effect of substrate concentration (relative to KM) on the value of kAs at a fixed concentration of a slow binding inhibitor that is competitive (closed circles), uncompetitive (open circles), or noncompetitive (a = 1, closed squares) with respect to the varied substrate. Figure 6.9 Effect of substrate concentration (relative to KM) on the value of kAs at a fixed concentration of a slow binding inhibitor that is competitive (closed circles), uncompetitive (open circles), or noncompetitive (a = 1, closed squares) with respect to the varied substrate.
Solution To achieve the target in practice requires that the starting concentrations relative to the pinch be first identified. The pinch is at 100 ppm and Stream 1 starts above the pinch. Stream 2 starts at the pinch and Stream 3 starts below the pinch. Thus, Stream 1 must be completely treated, Stream 2 partially treated and partially bypassed and Stream 3 totally... [Pg.612]

The solids flux depends on the local concentration of solids, the settling velocity of the solids at this concentration relative to the liquid, and the net velocity of the liquid. Thus the local solids flux will vary within the thickener because the concentration of solids increases with depth and the amount of liquid that is displaced (upward) by the solids decreases as the solids concentration increases, thus affecting the upward drag on the particles. As these two effects act in opposite directions, there will be some point in the thickener at which the actual solids flux is a minimum. This point determines the conditions for stable steady-state operation, as explained below. [Pg.433]


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See also in sourсe #XX -- [ Pg.31 ]




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Overlap factor and relative concentration

Plasma drug concentrations relative bioavailability

Relative aquatic concentrations (RAC

Relative change in concentration

Relative concentrations of proteins

Relative concentrations, relaxed error

Relative efficiency of catalysts and the kinetic order in catalyst concentration

Relative surface concentrations

Relative surface excess concentration

Relative viscosity concentration

Relative viscosity, effect concentration

Sulfuric acid relative concentrations

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