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Solution stoichiometry diluting

The second difficulty, degradation, required the development of a two-step polyamidation process following salt formation (157). During salt formation, tetramethylenediammonium adipate salt is formed in water solution at approximately 50% concentration or at a higher concentration in a suspension. As in nylon-6,6 manufacture, this salt solution, when diluted, permits easy adjustment of the stoichiometry of the reactants by means of pH measurement. [Pg.235]

The relationship v/M XVj = MfX Vfis convenient for dilutions only. Students tend to use it for solution stoichiometry problems, which only works if file stoichiometry is 1 1. [Pg.93]

Now that we have discussed the concentration and dilution of solutions, we can examine the quantitative aspects of reactions in aqueous solution, or solution stoichiometry. Sections 4.6. 8 focus on two techniques for studying solution stoichiometry gravimetric analysis and titration. These techniques are important tools of quantitative analysis, which is the determination of the amount or concentration of a substance in a sample. [Pg.136]

Students often mistakenly try to use the relation V,M, = V2M2 to solve problems about solution stoichiometry. This equation is intended only tor dilution problems and should never be used for problems involving reactions. [Pg.379]

Amount-Mass-Number Conversions Involving Solutions 100 Diluting a Solution 100 Stoichiometry of Reactions in Solution 103... [Pg.896]

Another boron sulfide, of stoichiometry BS2, can be made by heating B2S3 and sulfur to 300°C under very carefully defined conditions. It is a colourless, moisture-sensitive material with a porphine-like molecular structure, BgSig, as shown in Fig. 6.29b. An alternative route to BgSie involves the reaction of dibromotrithiadiborolane with trithiocarbonic acid in an H2S generator in dilute CS2 solution ... [Pg.213]

The extent of the ionization produced by a Lewis acid is dependent on the nature of the more inert solvent component as well as on the Lewis acid. A trityl bromide-stannic bromide complex of one to one stoichiometry exists in the form of orange-red crystals, obviously ionic. But as is. always the case with crystalline substances, lattice energy is a very important factor in determining the stability and no quantitative predictions can be made about the behaviour of the same substance in solution. Thus the trityl bromide-stannic bromide system dilute in benzene solution seems to consist largely of free trityl bromide, free stannic bromide, and only a small amount of ion pairs.187 There is not even any very considerable fraction of covalent tfityl bromide-stannic bromide complex in solution. The extent of ion pair and ion formation roughly parallels the dielectric constant of the solvents used (Table V). The more polar solvent either provides a... [Pg.95]

Such an electrochemical arrangement can also be used to transport oxygen from one electrode to the other by the imposition of an externally applied potential. This technique, known as coulometric titration , has been used to prepare flowing gas mixtures of oxygen/argon with a controlled oxygen partial pressure, to vary the non-stoichiometry of oxides, to study the thermodynamics of dilute oxygen solutions in metals, and to measure the kinetics of metal oxidation, as examples. [Pg.242]

Kinetic studies in the physiological pH range (6.5 to 7.8) provided consistency with the above results in that the accumulation of H202 was also observed and the stoichiometry of the reaction depended on the conditions applied (66-69). However, a simple 2 1 stoichiometry was confirmed between cysteine consumed and hydrogen peroxide formed in dilute solution. The reaction followed Michaelis-Menten kinetics with... [Pg.428]

The intervention of a metal ion in the stoichiometry of a reaction has been illustrated several times previously. Reaction is forced to completion in ester hydrolysis since the carboxylate grouping forms a more stable complex than the ester moiety does. A similar driving force underlies the formation of macrocycles and the completion of transamination by formation of the metal-Schiff base complex. The latter is particularly relevant in dilute solution and at low pH. For example, the extent of aldimine formation between pyridoxal and alanine is undetectable at the physiological pH but occurs to the extent of = 10% in the presence of zinc... [Pg.323]

Using a dilute aqueous solution of the polymer in the absence of external salt, a molecular weight distribution was obtained, although it was perturbed by electrostatic exclusion. When CaCh was added, a salt exclusion corresponding to NaCl was formed, i.e., an exchange process occurred up to at least 40% of the stoichiometry, where in each case one Ca2+ expelled two Na+ (10). [Pg.326]

We have initiated a study of the photoreduction of a series of paramagnetic peroxy-bridged dicobalt ammines. All of these complexes, which are shown below, contain the (Co-O-O-Co)5 + group, which best present evidence indicates should be represented as (Co -O-O-Com)5+, although ESR studies indicate that the extra electron is to some extent delocalized over the cobalt centers.78,79,82 Our idea was derived from Sykes report in 196363 that solutions of l-p in sunlight in dilute acid were decomposed according to the stoichiometry shown in reaction (29). [Pg.179]

II. Rate Law and Stoichiometry for the Reduction of Dilute Solutions of Tris(diimine)iron(III)t -ruthenium(III), and -osmium(QI) in Base... [Pg.381]


See other pages where Solution stoichiometry diluting is mentioned: [Pg.111]    [Pg.111]    [Pg.5]    [Pg.58]    [Pg.5]    [Pg.6150]    [Pg.307]    [Pg.8]    [Pg.1384]    [Pg.107]    [Pg.307]    [Pg.242]    [Pg.339]    [Pg.151]    [Pg.156]    [Pg.216]    [Pg.52]    [Pg.234]    [Pg.790]    [Pg.867]    [Pg.182]    [Pg.108]    [Pg.118]    [Pg.270]    [Pg.61]    [Pg.213]    [Pg.868]    [Pg.131]    [Pg.1167]   
See also in sourсe #XX -- [ Pg.96 , Pg.97 ]

See also in sourсe #XX -- [ Pg.96 , Pg.97 ]




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