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Total anions/cations

The stoichiometry between two reactants in a precipitation reaction is governed by a conservation of charge, requiring that the total cation charge and the total anion charge in the precipitate be equal. The reaction units in a precipitation reaction, therefore, are the absolute values of the charges on the cation and anion that make up the precipitate. Applying equation 2.3 to a precipitate of Ca3(P04)2 formed from the reaction of Ca and P04 , we write... [Pg.22]

A solution s ionic balance is defined as the ratio of the total cation charge to the total anion charge. Determine the ion balance for this sample of water, and comment on whether the result is reasonable. [Pg.618]

Studies carried out on anionic, cationic, and nonionic surfactants bave shown tbat tbe aromatic and bydropbilic portions of molecules are easily oxidi2ed, wbereas tbe long hydrocarbon chains are converted at slower rates. Surfactant activity does, however, disappear upon loss of the aromatic portion, thereby reducing the nuisance of the reactants (32). Total mineraLi2ation to CO2 has been demonstrated for nonionic polyethoxylated 4-nonylphenols having average numbers of 2,5, and 12 ethoxy units (33). [Pg.402]

Electroneutrality requires that the total cation concentration must equal total anion concentration and hence, taking account of charge numbers,... [Pg.34]

The Gibbs energy AG°d depends on the electrode potential . This dependence will be different for anions, cations, and neutral species. The simplest possible case is the adsorption and total discharge of an ion according to the equation ... [Pg.36]

A concept of anion mobility may be considered a useful paradigm for explaining the net retention and loss of cations from soils, and thus exposure pathways. This paradigm relies on the simple fact that total cations must balance total anions in soil solution (or any other solution), and, therefore, total cation leaching can be thought of as a function of total anion leaching. The net production of anions within the soil (e.g., by oxidation or hydrolysis reactions) must result in the net production of cations (normally H+), whereas the net retention of anions (by either absorption or biological uptake) must result in the net retention of cations. [Pg.160]

The ionic strength is a measure of erther the total anionic or cationic charge of a solution. m... [Pg.133]

The classification of surfactants in common usage depends on their electrolytic dissociation, which allows the determination of the nature of the hydrophilic polar group, for example, anionic, cationic, nonionic, and amphoteric. As reported by Greek [18], the total 1988 U.S. production of surfactants consisted of 62% anionic, 10% cationic, 27% nonionic, and 1% amphoteric. [Pg.308]

Below the CMC, the surfactant mixing in monolayers composed of similarly structured surfactants approximately obeys ideal solution theory. This means that the total surfactant concentration required to attain a specified surface tension for a mixture is intermediate between those concentrations for the pure surfactants involved. For mixtures of ionic/nonionic or anionic/cationic surfactants, below the CMC, the surfactant mixing in the monolayer exhibits negative deviation from ideality (i.e., the surfactant concentration required to attain a specified surface tension is less than that predicted from ideal solution theory). The same guidelines already discussed to select surfactant mixtures which have low monomer concentrations when micelles are present would also apply to the selection of surfactants which would reduce surface tension below the CMC. [Pg.16]

The incremental acidification of LRL over a 6-year period resulted in a gradual change in the lake s major ion chemistry such that the composition at pH 4.7 was substantially different from the pH 6.1 conditions. Sulfate increased by a factor of 2.8 and replaced bicarbonate as the major anion. Base cations increased in the water column at each treatment pH such that at pH 4.7 total base-cation concentration increased 56% over preacidification values. Increases in Ca2+ accounted for about 75% of the increase in total base-cation concentration. [Pg.161]

Perfluoroalkyl compounds have been manufactured since the 1950s.The total production of fluorinated surfactants (anionic, cationic and neutral) was 2001 in 1979, whereas in 2000 the total production of PFOS (perfluorooctane sulfonate) alone was nearly 3000t (Shoeib et al., 2004). Together with PFOA (perfluoroocta-noic acid), PFOS is used in refrigerants, surfactants, fire retardants, stain-resistant coatings for fabrics, carpets and paper and insecticides. Surface treatments, such as protection of clothing and carpets constitute the largest volume of PFOS production (Moriwaki, Takata and Arakawa, 2003). PFOA as well is present in several... [Pg.246]

Figure 9.3 The variation in cation species (as % of the total cation concentration) with the total soluble cation anion ratio of the components of a 1 1 complex in the presence of a competing anion (concentration = 5molm-3 pK of complex = 1.98) at pH 4 when the pK of formation of the 1 1 complex is (a) 2, (b) 4 and (c) 6. Figure 9.3 The variation in cation species (as % of the total cation concentration) with the total soluble cation anion ratio of the components of a 1 1 complex in the presence of a competing anion (concentration = 5molm-3 pK of complex = 1.98) at pH 4 when the pK of formation of the 1 1 complex is (a) 2, (b) 4 and (c) 6.
It will be assumed that the pH value was attained by adding an acid (or a base) with the same anion (cation) as the electrolyte. The salt and the acid or base will be assumed totally dissociated. The surface charge is therefore screened by monovalent ions with a total bulk concentration c = cE+cA + cB, where cA(cB) is the concentration of the added acid (base). [Pg.407]

A. Chatterjee, Determination of total cationic and total anionic arsenic species in oyster tissue using microwave-assisted extraction followed by HPLC-ICP-MS,... [Pg.591]

The reaction error (section 5.8) is the difference between total cations and total anions, expressed as a percentage of the TDI. For sample 1 of Table 5.4 this would be... [Pg.110]

The data of Table 5.4 have been reworked again in Table 5.6, which includes the total cations, total anions, total ions, and reaction errors. The data in Table 5.4 have been expressed in meq/1. However, most people are used to the mg/1 units for assessment of the degree of salinity of water. The conversion of meq/1 data into mg/1 was discussed in section 5.6, and is here demonstrated on the Wisdom Spring data (Table 5.7) ... [Pg.111]

Sample K+ Na+ ca2+ Mg2+ cr hco3 so42 Total cations Total anions Total ions Reaction error... [Pg.111]

The reaction errors in repeated measurements are expected to be random, that is, in part of the measurements the total cations will exceed the total anions and in the rest of the cases the total cations will exceed the total anions. However, occasionally a systematic pattern is seen. In Table 5.6 all the measurements reveal total cations to be higher than total anions (check it). Possible explanations are ... [Pg.112]

Sample no. Li Sr K Na Mg Ca Br Cl so4 hco3 Total anions Total cations Total ions Reaction error (%)... [Pg.133]

One characteristic of Friedel-Crafts reactions in ionic liquids is their pronounced solvent dependence in that different anion-cation combinations can determine complete and fast conversion and total inactivity of a given catalyst. It is somewhat striking that the catalytic activity is often lowest in hydrophilic ionic liquids from which halide impurities are harder to remove. In any case, screening of a selection of cations and anions appears to be necessary in order to evaluate the suitability of any potential catalyst. [Pg.203]

Based on data from field campaigns in the Arabian Sea and tropical North Atlantic Ocean, Johansen et al. (1999, 2000) also suggest evidence for chlorine release processes other than acid displacement. This conclusion was made based on discrepancies in measured total anion and cation charges. Release of chlorine in the form of a reactive species may not be replaced by a detectable ion (e.g., 003 ) and this charge difference might, therefore, be used as a measirre for nonacid displacement release processes for chlorine. [Pg.1951]

Na-Ca-Cl-type water. In this classification scheme, the cations followed by the anions are listed in order of decreasing concentrations. The concentration, commonly in mgL , of any ion listed must be 5% of the concentration of TDS. This is equivalent to 10% of the total of cations or anions (Kharaka and Thordsen, 1992). [Pg.2751]

Ct is the total anionic and cationic molar concentration R is the ideal gas constant (8,312 PJM—K)... [Pg.1104]

Abbreviations TH = total hardness, TC = total cations, TA = total anions, ALK = total alkalinity, EMA = equivalent mineral acidity, TOC total organic carbon... [Pg.184]


See other pages where Total anions/cations is mentioned: [Pg.2853]    [Pg.2853]    [Pg.388]    [Pg.363]    [Pg.142]    [Pg.11]    [Pg.388]    [Pg.121]    [Pg.299]    [Pg.53]    [Pg.266]    [Pg.323]    [Pg.363]    [Pg.266]    [Pg.1142]    [Pg.274]    [Pg.185]    [Pg.304]    [Pg.110]    [Pg.989]    [Pg.228]    [Pg.200]    [Pg.174]    [Pg.142]    [Pg.51]   
See also in sourсe #XX -- [ Pg.184 , Pg.185 , Pg.206 , Pg.207 ]




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Anionic cationic

Cation anion

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