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Relative acidity index

To estimate the positions of melts within the general oxoacidity scale, it is necessary to determine parameters reflecting the oxoacidic properties of a given melt. This requires to choose the reference melt which acidity will serve as reference point and to develop methods of acidity estimation. The relative acidity index of this melt shoitld be equal 0. [Pg.520]

The exact electromagnetic scattering theory of the concentric shell model was first solved by Aden and Kerker (1.) and shortly thereafter by Guttler (2). The problem has been extensively studied both theoretically and experimentally for aerosols by Kerker and co-workers and is reviewed in Kerker s book (3 ). The aerosol system had a core of relative refractive index m =2.105 and a shell of m2=1.482 corresponding to silver chloride coated with linolenic acid. The results indicated that for a smooth variation in the refractive index of the shell, the refractive index might not be sensitive to the form of the variation. [Pg.279]

Independent of the model used, it is quite clear that the core diameter is 0.44 to 0.45 ym and the relative refractive index of the core is 1.22+0.02. The evidence for a shell structure is again very tenuous. The "shell" thickness is unrealistically large, constant in extent, and little different from the results for the no-acid latex. If a shell structure was present it was at best marginally observable in the wide-angle light scattering. [Pg.287]

All known investigations of the relative acidic properties of ionic melts are based just on the determination of the equilibrium constants of reaction (1.3.6) in these media. Since the applicability of these data for estimating the equilibrium parameters and conditions was not checked experimentally, there was no reason to doubt the correctness of the use of equilibrium (1.3.6) as an indicator one for f estimations. Indeed, we shall now consider the data presented in Ref. [169], where the acidic properties of the KCl-LiCl eutectic at 600 °C were investigated using equilibrium (1.3.6). The shift of the oxoacidity scale as compared with the KCl-NaCl equimolar mixture was found to be close to 8. Such a considerable difference in acidities for KCl-NaCl and KCl-LiCl melts is unexpected, since the index of the Li20 dissociation constant (pK) ... [Pg.110]

The solubility product index of MgO in the molten KCl-LiCl exceeds the corresponding values in the low-acidic chloride melts by approximately 3.5pP units. This is in good agreement with the data obtained at 600 and 700 °C. Moreover, this difference shows that the relative acidic properties of ionic melts do not undergo a sharp change with elevation of the melt s temperature. [Pg.321]

Intoxication. This indicates that the absorbed lead is having adverse metabolic effects upon a body tissue. The toxicity is proportional to the concentration of lead at the site. Defining minimal manifestations of toxicity has extended with our increasing ability to develop sensitive indices of toxicity. Inhibition of delta-amino levulinic add dehydratase with an increase in urinary amino-levulinic acid is a relatively sensitive index of toxidty in intoxication, indicating that the lead is having an adverse effect on porphyrin metabolism... [Pg.496]

Another interesting use of empirical AN and DN indexes obtained by the method of refs.30,35 is exemplified in Table 3. This reports the temperature dependence of acid/base interactions in two commodity polymers, PVC and PC. The relevant AN and DN parameters for these polymers were evaluated by IGC at temperatures ranging from 30 - 130 C. As expected, at room temperature PVC again classifies as acid, and the relative acidity of the polymer surface increases steadily from 30 to about 70 C. Above 80 -90 C, however, the trend is reversed and acid/base interaction forces diminish. PC behaves as an amphoteric solid, its AN and DN finite and roughly equal at room temperatures. Above about 60 C however, the relative behavior of the polymer is that of a Lewis base. The results may be rationalized as follows ... [Pg.33]

Amino acid Three- letter code One- letter code Mass of residue in. b proteins Accessible surface area, 2 nm Hydrophobicity index ionizable side chain Occurrence in n/ proteins, /o Relative mutabihty... [Pg.195]

The mineral talc is extremely soft (Mohs hardness = 1), has good sHp, a density of 2.7 to 2.8 g/cm, and a refractive index of 1.58. It is relatively inert and nonreactive with conventional acids and bases. It is soluble in hydroduoric acid. Although it has a pH in water of 9.0 to 9.5, talc has Lewis acid sites on its surface and at elevated temperatures is a mild catalyst for oxidation, depolymerization, and cross-linking of polymers. [Pg.301]

APPENDIX 1 RELATIVE ATOMIC MASSES. 1985 819 APPENDIX 2 INDEX OF ORGANIC CHEMICAL REAGENTS 820 APPENDIX 3 CONCENTRATIONS OF AQUEOUS SOLUTIONS OF THE COMMON ACIDS AND OF AQUEOUS AMMONIA 829... [Pg.899]

When testing for a tannin reserve or tannin index, the presence of natural color aids detection. Testing for tannin is simple and relatively accurate using either a permanganate reduction test (development of permanent purple color) or lignin/tannic acid polymer test (tungstate blue color). [Pg.409]

Well A.. This oil producer was to be converted into a water injector. Though its production period had been relatively smooth, with no sign of production damage build-up, the operator wanted to be sure to obtain a maximum injectivity index before initiating water injection. The well data and acid job main parameters are summarized in Table I. [Pg.612]

Relative humidity changes were measured with a nano-scale HRI-coated LPG in a wide range from 38.9% to 100% RH with a sensitivity of 0.2 nm/%RH, and an accuracy of 2.3% RH59. The material used was a hydro-gel layer composed by, among other chemicals, acrylic acid and vinyl pyridine. Fine adjust of the components proportion made possible to obtain a refractive index of the gel of about 1.55. The overlay thickness was estimated to be in that case 600 nm. [Pg.71]

We have developed a common residue numbering scheme that facilitates comparison of the sequences of different NTs. The numbering scheme is informative of the relative position of each amino acid, the amino acid present at that position, and the actual amino acid number in a particular transporter. Each index number starts with the number of the transmembrane segment (TM), e.g., 1 for TM1, and is followed by a number indicating the position relative to a reference residue that is the most conserved position in that TM. That reference residue is arbitrarily assigned the number 50. For exam-... [Pg.213]

The vat dyes section of the Colour Index incorporates a subgroup called solubilised vat dyes. These are sodium salts of sulphuric acid esters of the parent leuco vat dyes, such as Cl Solubilised Vat Blue 6 (1.50). In contrast to the leuco compounds, the vat leuco esters dissolve readily in water at neutral pH. They have relatively low substantivity for cellulose and thus have been used mainly in continuous dyeing and printing. In the presence of an oxidant in mineral acid solution (sodium nitrite and sulphuric acid, for example) the leuco ester is rapidly decomposed and the insoluble vat dye regenerated. Thus application of a vat leuco ester represents a simpler (but more costly and less versatile) alternative to conventional dyeing methods via the alkaline leuco compound. [Pg.19]

Another example of the use of transition state pKa values has been provided by Pollack (1978). From the rate constants for the decarboxylation of substituted a,a-dimethylbenzoylacetic acids ([37] — [38]) and their anions, he calculated pK for reaction of the acids (Table A6.2). The values vary significantly with the phenyl substituent (p = +1.7), much more so than the p/(a values of the substrate acids (p = +0.2). This difference is consistent with the proton being much closer to the phenyl group in the transition state than in the initial state, and it may even denote a relatively late transition state (Pollack, 1978). However, from the pKa values of the reactant acids (approximately 3.4), the transition states (approximately 4.4), and the enol product (11.8) (Pruszynski et al., 1986), the Leffler index... [Pg.49]


See other pages where Relative acidity index is mentioned: [Pg.61]    [Pg.61]    [Pg.306]    [Pg.306]    [Pg.333]    [Pg.115]    [Pg.338]    [Pg.423]    [Pg.210]    [Pg.2658]    [Pg.61]    [Pg.635]    [Pg.1110]    [Pg.365]    [Pg.143]    [Pg.478]    [Pg.21]    [Pg.184]    [Pg.217]    [Pg.450]    [Pg.404]    [Pg.188]    [Pg.533]    [Pg.138]    [Pg.56]    [Pg.136]    [Pg.136]    [Pg.567]    [Pg.35]    [Pg.229]    [Pg.38]    [Pg.199]    [Pg.48]    [Pg.1043]   
See also in sourсe #XX -- [ Pg.61 ]

See also in sourсe #XX -- [ Pg.520 ]




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