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Monovalent

This means that the potential some distance away appears to follow Eq. V-13, but with an apparent value of AkTjze, which is independent of the actual value. For monovalent ions at room temperature this apparent would be 100 mV. [Pg.173]

The flow can be radial, that is, in or out through a hole in the center of one of the plates [75] the relationship between E and f (Eq. V-46) is independent of geometry. As an example, a streaming potential of 8 mV was measured for 2-cm-radius mica disks (one with a 3-mm exit hole) under an applied pressure of 20 cm H2 on QT M KCl at 21°C [75]. The i potentials of mica measured from the streaming potential correspond well to those obtained from force balance measurements (see Section V-6 and Chapter VI) for some univalent electrolytes however, important discrepancies arise for some monovalent and all multivalent ions. The streaming potential results generally support a single-site dissociation model for mica with Oo, Uff, and at defined by the surface site equilibrium [76]. [Pg.188]

Maroudas N G 1977 Sulphonated polystyrene as an optimal substratum for the adhesion and spreading of mesenohymal sells in monovalent and divalent saline solutions J. Cell. Physiol. 90 511-20... [Pg.2640]

The element before carbon in Period 2, boron, has one electron less than carbon, and forms many covalent compounds of type BX3 where X is a monovalent atom or group. In these, the boron uses three sp hybrid orbitals to form three trigonal planar bonds, like carbon in ethene, but the unhybridised 2p orbital is vacant, i.e. it contains no electrons. In the nitrogen atom (one more electron than carbon) one orbital must contain two electrons—the lone pair hence sp hybridisation will give four tetrahedral orbitals, one containing this lone pair. Oxygen similarly hybridised will have two orbitals occupied by lone pairs, and fluorine, three. Hence the hydrides of the elements from carbon to fluorine have the structures... [Pg.57]

Table 2. Predicted intrinsic and apparent pKa values for the Cys403 residue in Yersinia phosphatase for different models of the structure the data refer to a temperature of 293 K and an ionic strength corresponding to 150 mM of monovalent salt. See the text for the detailed description of the conditions under which each pK estimation was made. The experimentally determined value is 4.67 [39]... Table 2. Predicted intrinsic and apparent pKa values for the Cys403 residue in Yersinia phosphatase for different models of the structure the data refer to a temperature of 293 K and an ionic strength corresponding to 150 mM of monovalent salt. See the text for the detailed description of the conditions under which each pK estimation was made. The experimentally determined value is 4.67 [39]...
A halogen substituent Irke hydrogen rs monovalent and when present rn a molec ular formula rs treated as rf rt were hydrogen for counting purposes... [Pg.574]

The relative measurement error in concentration, therefore, is determined by the magnitude of the error in measuring the cell s potential and by the charge of the analyte. Representative values are shown in Table 11.7 for ions with charges of+1 and +2, at a temperature of 25 °C. Accuracies of 1-5% for monovalent ions and 2-10% for divalent ions are typical. Although equation 11.22 was developed for membrane electrodes, it also applies to metallic electrodes of the first and second kind when z is replaced by n. [Pg.495]

Precision The precision of a potentiometric measurement is limited by variations in temperature and the sensitivity of the potentiometer. Under most conditions, and with simple, general-purpose potentiometers, the potential can be measured with a repeatability of +0.1 mV. From Table 11.7 this result corresponds to an uncertainty of +0.4% for monovalent analytes, and +0.8% for divalent analytes. The reproducibility of potentiometric measurements is about a factor of 10 poorer. [Pg.495]

The ion-exchange reaction of a monovalent cation, M+, at a strong acid exchange site is... [Pg.592]

Oxygen Octahedra. An important group of ferroelectrics is that known as the perovskites. The perfect perovskite stmcture is a simple cubic one as shown in Figure 2, having the general formula ABO, where A is a monovalent or divalent metal such as Na, K, Rb, Ca, Sr, Ba, or Pb, and B is a tetra- or pentavalent cation such as Ti, Sn, Zr, Nb, Ta, or W. The first perovskite ferroelectric to be discovered was barium titanate [12047-27-7] and it is the most thoroughly investigated ferroelectric material (10). [Pg.203]

Only salts are salty however, not all salts are salty. Some are sweet, bitter, or tasteless. The salty taste is exhibited by ionized salts, and the greatest contribution to salty taste comes from the cations (29). The salt taste is produced by monovalent cations (15). [Pg.11]

Gallium compounds containing monovalent elements aie described in Reference 25. [Pg.162]

Departures from the ideal behavior expressed by equation 7 usually are found in alkaline solutions containing alkaH metal ions in appreciable concentration, and often in solutions of strong acids. The supposition that the alkaline error is associated with the development of an imperfect response to alkaH metal ions is substantiated by the successhil design of cation-sensitive electrodes that are used to determine sodium, silver, and other monovalent cations (3). [Pg.466]

In addition, most devices provide operator control of settings for temperature and/or response slope, isopotential point, zero or standardization, and function (pH, mV, or monovalent—bivalent cation—anion). Microprocessors are incorporated in advanced-design meters to faciHtate caHbration, calculation of measurement parameters, and automatic temperature compensation. Furthermore, pH meters are provided with output connectors for continuous readout via a strip-chart recorder and often with binary-coded decimal output for computer interconnections or connection to a printer. Although the accuracy of the measurement is not increased by the use of a recorder, the readabiHty of the displayed pH (on analogue models) can be expanded, and recording provides a permanent record and also information on response and equiHbrium times during measurement (5). [Pg.467]

The usual valence of indium is three, although monovalent and bivalent compounds of indium with oxygen, halogens, and Group 15 (VA) and 16 (VIA) elements ate well known. The lower valence compounds tend to disproportionate into the trivalent compound and indium metal the trivalent compounds ate stable. [Pg.81]

Mixed oxides of Fe(IV) can be prepared by heating iron(III) oxide with a metal oxide or hydroxide in oxygen at elevated temperatures. These black compounds have general formulas M FeO, M monovalent, or M2Fe04, M divalent, but do not contain discrete [FeOJ" ions. They are readily decomposed by mineral acids to iron(III) and oxygen. [Pg.437]

There are a number of complex chlorides of three general types M(MnCl2), M2(MnCl, and M4(MnClg). M is monovalent in each case. Fluorine forms only 9M(MnF.) and the only complex bromine compound reported is Ca(MnBt 4H2O. There are no iodide complexes. The anhydrous salt, MnCl2, forms cubic pink crystals, and three well-defined hydrates exist. Aqueous solubiUties of the tetrahydrate and dihydrate ate given in Table 7. [Pg.505]

Acetylene has a low solubiHty in Hquid oxygen. Excessive concentrations can lead to separation of soHd acetylene and produce accumulations that, once initiated, can decompose violently, detonating other oxidizable materials. Acetylene is monitored routinely when individual hydrocarbons are determined by gas chromatography, but one of the wet classical methods may be more convenient. These use the unique reaction of acetylene with Ilosvay s reagent (monovalent copper solution). The resulting brick-red copper acetyHde may be estimated colorimetricaHy or volumetricaHy with good sensitivity (30). [Pg.480]

Orthophosphate salts are generally prepared by the partial or total neutralization of orthophosphoric acid. Phase equiUbrium diagrams are particularly usehil in identifying conditions for the preparation of particular phosphate salts. The solution properties of orthophosphate salts of monovalent cations are distincdy different from those of the polyvalent cations, the latter exhibiting incongment solubiUty in most cases. The commercial phosphates include alkah metal, alkaline-earth, heavy metal, mixed metal, and ammonium salts of phosphoric acid. Sodium phosphates are the most important, followed by calcium, ammonium, and potassium salts. [Pg.331]

A third technique employs monovalent aluminum. By bringing vapors of aluminum fluoride or aluminum chloride into contact with carbothermicahy reduced aluminum ahoy at 1000—1400°C, the fohowing reaction occurs... [Pg.100]

The ground state distribution of electrons in the aluminum atom is lT2T2 3T3/). The oxidation state of aluminum is +3, except at high temperatures where monovalent species such as AIQ, AIF, and AI2 have been spectrally identified At lower temperatures, these compounds disproportionate... [Pg.135]


See other pages where Monovalent is mentioned: [Pg.2777]    [Pg.2784]    [Pg.115]    [Pg.1114]    [Pg.479]    [Pg.594]    [Pg.201]    [Pg.159]    [Pg.288]    [Pg.385]    [Pg.410]    [Pg.436]    [Pg.69]    [Pg.377]    [Pg.378]    [Pg.387]    [Pg.438]    [Pg.439]    [Pg.544]    [Pg.504]    [Pg.504]    [Pg.505]    [Pg.507]    [Pg.507]    [Pg.507]    [Pg.61]    [Pg.299]    [Pg.487]    [Pg.192]    [Pg.92]   
See also in sourсe #XX -- [ Pg.88 , Pg.131 , Pg.292 , Pg.310 ]

See also in sourсe #XX -- [ Pg.88 , Pg.131 , Pg.292 , Pg.310 ]

See also in sourсe #XX -- [ Pg.22 , Pg.46 ]

See also in sourсe #XX -- [ Pg.192 ]

See also in sourсe #XX -- [ Pg.88 , Pg.131 , Pg.292 , Pg.310 ]

See also in sourсe #XX -- [ Pg.88 , Pg.131 , Pg.292 , Pg.310 ]

See also in sourсe #XX -- [ Pg.88 , Pg.131 , Pg.292 , Pg.310 ]




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Agents, polymeric monovalent

Alkaline earth metals monovalent derivatives

Aluminum monovalent

Anions monovalent

Antigens monovalent

Biliary Excretion of Monovalent Bile Salts

Cation systems, monovalent

Cations, monovalent/divalent

Cobalt monovalent, complexes

Copper monovalent

Counterion monovalent

Counterions, monovalent

Designed Copolymers in the Presence of Monovalent Counterions

Display monovalent

Effect of monovalent

Effect of monovalent ions

Electrolyte monovalent

Group monovalent

Hydrogen bonds monovalent

Inorganic ions monovalent cations

Inorganic salts, monovalent

Iridium monovalent

Iridium monovalent, complexes

Iron carbonyl complexes with formally monovalent E substituents

Isotherms for monovalent-divalent exchange

Lewis acids monovalent

Metal monovalent

Monovalent Fluid Metals

Monovalent Gold

Monovalent M+ cations

Monovalent Polyether Antibiotics

Monovalent antibody

Monovalent atom

Monovalent atom bond exchange

Monovalent atoms reactions

Monovalent bile salts

Monovalent cation effects

Monovalent cations

Monovalent cations structure

Monovalent complexes

Monovalent compounds

Monovalent copper aqueous solutions

Monovalent elements

Monovalent halogen

Monovalent ions

Monovalent ions mercurous

Monovalent ions silver

Monovalent libraries

Monovalent metal cation

Monovalent metal cation complexes, stability

Monovalent metal clusters highest spin states

Monovalent metal clusters highest spin states bound triplet pairs

Monovalent peptide

Monovalent reaction centers

Monovalent reagent

Monovalent structures

Monovalent structures derivatives

Monovalent structures properties

Monovalent-divalent exchange model

Monovalent-divalent ion exchange

Nickel monovalent, complexes

Nitrates, monovalent metals

Phage monovalent display

Reactions Governed by Flux of Monovalent Ions

Reduction monovalent

Rhodium monovalent

Rhodium monovalent, complexes

Silver monovalent

Single association site monovalent

Solvation shell monovalent ions

Valency monovalent

With monovalent cations

Zirconium monovalent

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