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Aqueous solutions Appearance

First we write the balanced chemical equation for the reaction. Then we write the equilibrium constant expressions, remembering that gases and solutes in aqueous solution appear in the Kc expression, but pure liquids and pure solids do not. [Pg.341]

Pressures of gases and molarities of solutes in aqueous solution appear in thermodynamic equilibrium constant expressions. Pure solids and liquids (including solvents) do not appear. [Pg.481]

Thus, the experimental rate constants for chain propagation and termination in the oxidation of methyl ethyl ketone in aqueous solutions appear to be effective and are... [Pg.170]

Oxidation of Mn2+ in aqueous solution appears to occur in a stepwise fashion to Mn02, with MnOOH (8) and Mn304 (9) as possible intermediates. The reaction exhibits the induction period and kinetics characteristic of an au-tocatalytic process (10). Mn(II) is strongly sorbed to the surfaces of the newly formed, insoluble oxides, where its oxidation is greatly facilitated. [Pg.495]

Icxlale ion in aqueous solution appears to be liOHi,. and the iodine atom in crystalline periodates always is coordinated to six oxygen atoms, three nearest neighbors on one side and three next nearest neighbors on ihe other side. Thus, potassium mdale. KlOt. has distorted perov kile structure... [Pg.859]

Thermal anomalies ( kinks ) in the properties of water and aqueous solutions appear to be manifestations of higher-order phase transitions in structured elements of water. Some concentration-dependent anomalies are also described and discussed in terms of (a) the occurrence of discrete structural units of water in the unaffected solvent, (b) the possible separate existence of somewhat similarly structured units in the ionic hydration atmospheres, and (c) overlapping of large (but not necessarily structured) hydration atmospheres. [Pg.76]

Complexation of poly(allylamine hydrochloride), — (CH—(CH2NH3C1)—CH2) —, with transition metal ions in aqueous solution appears to proceed in one step, in contrast to that of the corresponding low molecular weight metal complex. Interaction between polyallylamine and Cu2+, Ni2 +, Co2+, Zn2+, and Mg2+ has been reported 21). [Pg.109]

The standard potentials for some redox couples in aqueous solution appear in Table 1.2. More information about formal potentials of a great number of electrochemical systems can be found in [14, 15]. [Pg.13]

The reduction of hydrogen peroxide in aqueous solution appears to be analogous to that in CH3CN, with the mechanism represented by the reaction of Eq. (9.70) followed by the reactions of Eqs. (9.71) and (9.72). Thus, the reduction of HOOH yields H2 and HOO- initially, in a one-electron step. The final products are the result of the reaction of HOO- and HOOH, and are analogous to those for the base-induced decomposition of HOOH.43... [Pg.399]

The rate of formation of cisplatin-DNA adducts was found to be independent of superhelicity [59] and appears to be unaffected by the presence of histones in nucleosomes [29] and in chromatin [77], Therefore, isolated DNA in aqueous solution appears to be a relevant model for kinetic and mechanistic studies of cellular DNA-platination. It was early checked that the cisplatin-DNA adducts were stable for a least three days at 37 °C after their formation [78], There are now a few cases reported of unstable platinum adducts (vide supra) i) monoadducts with the diazapyrenium ligand [52], ii) a cisplatin intrastrand GG chelate rearranging into a GG interstrand crosslink [63], iii) cisplatin GG interstrand diadducts, slowly rearranging into intrastrand ones [65], tv) transplatin intrastrand GNG diadducts rearranging into interstrand crosslinks (J.-M. Malinge and M. Leng, Part 3). [Pg.231]

The decomposition of potassium ozonide in aqueous solution appears to involve a chain reaction whose rate is independent of solution pH. The rapid initial reaction is said to be ... [Pg.335]

As a final note concerning solvent effects, amphiphilic alcohols added to hydro-phobic electroactive n-alkanethiol SAMs in aqueous solution appear to aggregate on the monolayer surfaces, decreasing the capacitive envelope and enhancing the barrier properties [109, 110]. However, the formal potentials of the redox couples are shifted positively, and the electrochemical reversibility is decreased. This effect had previously been used by Becka and Miller to determine the pinhole current in the presence of a freely diffusing redox probe (see above) [96]. [Pg.2936]

Residual silicone oil is immiscible with water and disperses in aqueous solutions, appearing as a haze or a su.spension of fine particles. Therefore, excess silicone oil... [Pg.411]

Figure 13 shows the result of the reaction between KI and Pb(N03)2- The products are a yellow precipitate of Pbl2 and a colorless solution of KNO3. From the equation, it appears as though the parts of the compounds just change places. Early chemists called this a double-displacement reaction. It occurs when two compounds in aqueous solution appear to exchange ions and form two new compounds. For this to happen, one of the products must be a solid precipitate, a gas, or a molecular compound, such as water. Water is often written as HOH in these equations. [Pg.301]

Trans-[CrCl3en3]Cl consists of green crystals. A very thin layer of a cone, aqueous solution appears green, while thicker layers have a brown-red color. [Pg.1358]

Photo-reduction of [(phen)2(H20)Fe—O— Fe(H20)(phen)2] in aqueous solution appears to continue even after cessation of irradiation, and it has been suggested that the thermally labile peroxo-bridged dinuclear complex... [Pg.223]

Stern and Nobilione measured the heats of transfer of HCl and HCIO4 from water to aqueous acetic acid by determining enthalpies of dilution of aqueous HCl and HCIO4 with aqueous acetic acid. The resultant solvent composition range runs from pure water to 99.7 mol per cent acetic acid-water mixtures. The acid concentrations were around 0.003m. The correction to infinite dilution, for the highly aqueous solutions appears to be comparable to the experimental error. The limiting heat of dilution is not known for pure acetic acid. [Pg.59]

On the above basis, a critical review of the recent results of the more important coordination chemistry research into non-aqueous solutions appears absolutely justified. [Pg.19]

Residual silicone oil is immiscible with water and disperses in aqueous solutions, appearing as a haze or a suspension of fine particles. Therefore, excess silicone oil present on stoppers could contaminate a pharmaceutical product. In lyophilized products, only the prelyophilization and the reconstituted solutions are subject to contact with the stopper. However, components of the container closure system have been shown to create a residue in the container when water for injection only was lyophilized [3]. Silicone oil was one component of the residue. [Pg.331]

Nitrosyl halides, at least in aqueous solutions, appear to be more potent reagents than nitrous anhydride. Schmid and his coworkers have calculated actual rate coefficients for the reaction of unprotonated amine with both molecular nitrosyl chloride and nitrosyl bromide (i.e. from the equation. Rate = A[RNH2][NOHal]). These are listed in Table 6. The characteristic features of these rate... [Pg.162]

Carrott et al. (1997), in a study of the adsorption of zinc species from aqueous solution appear to have arrived at a quite unequivocal understanding of the phenomena involved. They used five carbons, derived from peat, lignin and pitch by activation with molten KOH (the Anderson process). Surface areas (BET, N2 at 77 K) were 644, 860, 1138, 1603 and 3085 m g , respectively, with PZC values of 8.3, 11.8, 7.5, 6.9 and 6.2, respectively. Attention was given to the speciation of the zinc in the pH range 0.0-14, and involving Zn (pH < 8) and Zn(OH), Zn(OH) and ZnfOH) . Zinc was adsorbed from solutions of zinc nitrate, the pH of which were adjusted by addition of nitric acid or sodium hydroxide. [Pg.397]


See other pages where Aqueous solutions Appearance is mentioned: [Pg.48]    [Pg.55]    [Pg.44]    [Pg.13]    [Pg.1210]    [Pg.163]    [Pg.119]    [Pg.107]    [Pg.149]    [Pg.76]    [Pg.48]    [Pg.55]    [Pg.165]    [Pg.13]    [Pg.264]    [Pg.166]    [Pg.48]    [Pg.172]    [Pg.337]    [Pg.3049]    [Pg.231]    [Pg.43]    [Pg.106]    [Pg.469]    [Pg.334]    [Pg.192]    [Pg.463]    [Pg.238]    [Pg.219]   
See also in sourсe #XX -- [ Pg.49 ]




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