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Mixed formation

File 4-7. TINKER Input File for Propene in Mixed Format. Mixed format can be used when one is modifying or editing an output file from a previous calculation. [Pg.111]

Movement of raw and transformed materials can take place within the soil and results in zones of accumulation, depletion, or mixing. Formation, migration, and accumulation of different elements, clays, oxides, and organic matter can occur in different parts of the soil. These different zones or layers in soil that are approximately parallel to the surface are called soil horizons. Depleted or enriched soil horizons result in different depths in the soil having different chemical and physical properties. Translocations are caused by a combination of physical, chemical, and biological processes. [Pg.169]

More recently, 1 2 complexes of the chromium(III) ion with 5-sulphosalicylic [84,85], salicylic and citric acids have been compared with the lactate complex [85]. Like the latter, the citrate (5.79) and 5-sulphosalicylate (5.80 X = S03H) complexes are readily water-soluble but the unsubstituted salicylate (5.80 X = H) is not. If formic acid is added, however, the mixed formate-salicylate complex (5.81) shows moderate solubility. The pH value for maximum uptake of the complexes varied slightly but was always within the range of pH 2-4. Compared with conventional dichromate treatment, the lactate complex sometimes gave inferior wet fastness. Fastness ratings equal to conventional aftertreatment were given by the two salicylate mordant complexes (5.80) without the drawbacks characteristic of the dichromate process [85]. [Pg.273]

Coastal all Controls by the mixed layer are modified by seasonality of winds causing coastal upwelling, tidal mixing, formation of fronts and river discharge. Includes marginal seas. [Pg.683]

The same group also showed that mono(cyclopentadienyl) mixed hydride/ aryloxide dimer complexes of several lanthanide elements (Y, Dy, Lu) could be synthesized easily by the acid-base reaction between the mixed hydride/alkyl complexes and an aryl alcohol [144]. These complexes reacted with C02 to generate mixed formate/carboxylate derivatives, which were moderately active initiators for the copolymerization of C02 and cyclohexene oxide, without requiring a co-catalyst. The lutetium derivative 21 was the most active (at 110°C, TOF = 9.4 h ), yet despite a good selectivity (99% carbonate linkages), the molecular weight distribution remained broad (6.15) (Table 6). [Pg.207]

Fig. 5 NRL Array Biosensor mixed format immunoassays (modified from [119]). Schematic of (a) the sandwich and (b) the competitive immunoassay fonnats used in the detection of the Campylobacter jejuni and aflatoxin Bi (AFBi), respectively, (a) Sandwich format antigen captured by the immobilized antibody then quantified by passing a second, fluorescently labeled, antibody over the surface, (b) Competitive format competition for binding sites on the fluorescently labeled antibody occurs between the unlabeled antigen in solution and the surface-bound antigen analog, (c) Final charge-coupled devices image taken with the NRL Array Biosensor of a waveguide exposed simultaneously to the C. jejuni (5 x 10" cfu/mL) sandwich assay (SAND) and the aflatoxin Bj (AFBi-1 ng/mL) competitive assay (COMP) in various combinations... Fig. 5 NRL Array Biosensor mixed format immunoassays (modified from [119]). Schematic of (a) the sandwich and (b) the competitive immunoassay fonnats used in the detection of the Campylobacter jejuni and aflatoxin Bi (AFBi), respectively, (a) Sandwich format antigen captured by the immobilized antibody then quantified by passing a second, fluorescently labeled, antibody over the surface, (b) Competitive format competition for binding sites on the fluorescently labeled antibody occurs between the unlabeled antigen in solution and the surface-bound antigen analog, (c) Final charge-coupled devices image taken with the NRL Array Biosensor of a waveguide exposed simultaneously to the C. jejuni (5 x 10" cfu/mL) sandwich assay (SAND) and the aflatoxin Bj (AFBi-1 ng/mL) competitive assay (COMP) in various combinations...
Figure 6 Combinatorial synthesis using a split-mix format. Building blocks are added separately in different vials, but the beads with reaction products are pooled before being distributed again before the next reaction step. Each vial contains all combined products of the previous reaction steps, but each bead contains only a single compound. Figure 6 Combinatorial synthesis using a split-mix format. Building blocks are added separately in different vials, but the beads with reaction products are pooled before being distributed again before the next reaction step. Each vial contains all combined products of the previous reaction steps, but each bead contains only a single compound.
Behaviour depends on the cation present. Studies of the decompositions of some mixed formates, e.g. Ni - Mg [22], Zn - Ba [23] and Cu - Ba [23], have been reported. Sodium and potassium formates melt prior to anion decomposition and reaction is believed [24] to proceed through the intermediate COj". In the absence of oxygen, this entity dimerizes to yield the oxalate, whereas in the presence of oxygen the dismutation reaction, which produces carbon monoxide and carbonate, is preferred. [Pg.447]

To achieve homogeneity with these relatively solublecompounds, which, however, have different solubilities, the mixed formates must be prepared by a special spray-drying technique [31]. The mixed oxalates, which are precipitated with oxalic acid and ammonium oxalate rather than with alkali oxalates (this tends to give more active catalysts), yield, as a rule, homogeneous materials via a simple precipitation. Complex oxalates are just as usable as the mixed oxalates [33]. [Pg.1618]

Rate differences have been monitored in the reaction of formic acid with various Cr species, and in the presence of an oxalic acid-formic acid mixture simultaneous oxidation occurs at a rate much greater than with either of the substrates under identical conditions. This has been observed previously by Rocek and his co-workers (see previous Reports) and is consistent with a three-electron oxidation of a mixed formate-oxalate ester. The oxidation of methyl phenyl sulphoxides in aqueous acetic acid is first order with respect both to substrate and to [Cr ], the suggested mechanism involving a one-electron... [Pg.84]

Ruta J, Ravelet C, Baussane 1 et al (2008) Competitive affinity capillary electrophoresis assay based on a hybrid pre-incubation/on-capillary mixing format using an enantioselective aptamer as affinity ligand. J Sep Sci 31 2239-2243... [Pg.288]

The molar heats of vaporization of ammonia, carbon dioxide, and water from a typical copper-ammonium-salt solution (mixed formate and carbonate) have been calculated by Zhavoronkov (1939) using the Clausius-Clapeyron equation and the slopes of the log p versus 1/T lines as plotted in Figure 16-23. For the solution illustrated in this figure, he obtained the results in Table 16-19. [Pg.1350]

Source Mixed formate and carbonate solution, data of Zhavoronkov (1939) ... [Pg.1351]

Heat Calorimetry Reaction, adsorption, absorption, hydration, mixing, formation, catalysis, thermodynamics, heat capacity, kinetics,... [Pg.53]

Even if the reactor temperature is controlled within acceptable limits, the reactor effluent may need to be cooled rapidly, or quenched, to stop the reaction quickly to prevent excessive byproduct formation. This quench can be accomplished by indirect heat transfer using conventional heat transfer equipment or by direct heat transfer by mixing with another fluid. A commonly encountered situation is... [Pg.42]

Flares. Flares are used for the combustion of waste hydrocarbon gases in which the rates may vary over a wide range and for emergency releases. Steam injection is usually used to enhance mixing and the formation of a clean flame. [Pg.305]

Still another manifestation of mixed-film formation is the absorption of organic vapors by films. Stearic acid monolayers strongly absorb hexane up to a limiting ratio of 1 1 [272], and data reminiscent of adsorption isotherms for gases on solids are obtained, with the surface density of the monolayer constituting an added variable. [Pg.145]

Other properties of association colloids that have been studied include calorimetric measurements of the heat of micelle formation (about 6 kcal/mol for a nonionic species, see Ref. 188) and the effect of high pressure (which decreases the aggregation number [189], but may raise the CMC [190]). Fast relaxation methods (rapid flow mixing, pressure-jump, temperature-jump) tend to reveal two relaxation times t and f2, the interpretation of which has been subject to much disagreement—see Ref. 191. A fast process of fi - 1 msec may represent the rate of addition to or dissociation from a micelle of individual monomer units, and a slow process of ti < 100 msec may represent the rate of total dissociation of a micelle (192 see also Refs. 193-195). [Pg.483]

The energetics and kinetics of film formation appear to be especially important when two or more solutes are present, since now the matter of monolayer penetration or complex formation enters the picture (see Section IV-7). Schul-man and co-workers [77, 78], in particular, noted that especially stable emulsions result when the adsorbed film of surfactant material forms strong penetration complexes with a species present in the oil phase. The stabilizing effect of such mixed films may lie in their slow desorption or elevated viscosity. The dynamic effects of surfactant transport have been investigated by Shah and coworkers [22] who show the correlation between micellar lifetime and droplet size. More stable micelles are unable to rapidly transport surfactant from the bulk to the surface, and hence they support emulsions containing larger droplets. [Pg.505]

Sagiv J 1980 Organized monolayers by adsorption. 1. Formation and struoture of oleophobio mixed monolayers on solid surfaoes J. Am. Chem. Soc. 102 92-8... [Pg.2635]

Only thallium of the Group III elements is affected by air at room temperature and thalliumflll) oxide is slowly formed. All the elements, however, burn in air when strongly heated and, with the exception of gallium, form the oxide M2O3 gallium forms a mixed oxide of composition GaO. In addition to oxide formation, boron and aluminium react at high temperature with the nitrogen in the air to form nitrides (BN and AIN). [Pg.144]

Toluene however sulphonates readily, and the following preparation illustrates the rapid formation of toluene-p ulphonic acid mixed with a small proportion of the deliquescent o-sulphonic acid, and the isolation of the pure crystalline /lara-isomer. [Pg.178]

When an aqueous solution of a diazonium salt is added to an alkaline solution of a phenol, coupling occurs with formation of an azo-compound (p. 188). If ho vc cr the ntiueous solution of the diazonium salt, t. . ., />-bromohenzene diazonium chloride, is mixed with an excess of an aromatic hydrocarbon, and aqueous sodium hydroxide then added to the vigorously stirred mixture, the diazotate which is formed, e.g., BrC,H N OH, dissolves in the hydrocarbon and there undergoes decomposition with the formation of nitrogen and two free radicals. The aryl free radical then reacts with the hydrocarbon to give a... [Pg.201]

Phenylhydrazine is usually dissolved in acetic acid for hydrazone formation if a salt of phenylhydrazine with an inorganic acid is used, it must be mixed with an excess of sodium acetate (see preparation of osazones, p. 137). [Pg.229]

At the end of 30 minutes treat the mixture in A as follows Dissolve 8 ml. of glacial acetic acid in 10 ml. of water, add 4 ml. of phenylhydra-zine and mix well in order to obtain a clear solution. Add this to the solution in A and mix thoroughly a slightly cloudy solution may be obtained, but this will clear on heating. Place the mixture in a boiling water-bath and note the formation of j ellow crystals of glucosazone after about 15 minutes. At the end of about i hour, cool, filter off the precipitate and identify as directed on p. 139. [Pg.515]

Some liquids are practically immiscible e.g., water and mercury), whilst others e.g., water and ethyl alcohol or acetone) mix with one another in all proportions. Many examples are known, however, in which the liquids are partially miscible with one another. If, for example, water be added to ether or if ether be added to water and the mixture shaken, solution will take place up to a certain point beyond this point further addition of water on the one hand, or of ether on the other, will result in the formation of two liquid layers, one consisting of a saturated solution of water in ether and the other a saturated solution of ether in water. Two such mutually saturated solutions in equilibrium at a particular temperature are called conjugate solutions. It must be mentioned that there is no essential theoretical difference between liquids of partial and complete miscibility for, as wdll be shown below, the one may pass into the other with change of experimental conditions, such as temperature and, less frequently, of pressure. [Pg.17]

Higher alcohols (> C3) react comparatively slowly with sodium because of the slight solubility of the sodium alkoxide in the alcohol a large excess (say, 8 mols) is therefore employed. The mixed ether is distilled off, and the process (formation of alkoxide and its reaction with the alkyl halide) may be repeated several times. The excess of alcohol can be recovered. cj/cloAliphatic alcohols form sodio compounds with difficulty if small pieces... [Pg.309]


See other pages where Mixed formation is mentioned: [Pg.243]    [Pg.160]    [Pg.263]    [Pg.251]    [Pg.144]    [Pg.1719]    [Pg.263]    [Pg.142]    [Pg.184]    [Pg.1618]    [Pg.184]    [Pg.243]    [Pg.160]    [Pg.263]    [Pg.251]    [Pg.144]    [Pg.1719]    [Pg.263]    [Pg.142]    [Pg.184]    [Pg.1618]    [Pg.184]    [Pg.26]    [Pg.307]    [Pg.221]    [Pg.257]    [Pg.337]    [Pg.545]    [Pg.546]    [Pg.376]    [Pg.142]    [Pg.48]    [Pg.76]    [Pg.173]    [Pg.32]   
See also in sourсe #XX -- [ Pg.70 ]




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