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Charged Ions

Also used to describe the oppositely charged ion balancing charge, e.g. chloride is the counter-ion to Na in sodium chloride. [Pg.114]

Debye-Hiickel theory The activity coefficient of an electrolyte depends markedly upon concentration. Jn dilute solutions, due to the Coulombic forces of attraction and repulsion, the ions tend to surround themselves with an atmosphere of oppositely charged ions. Debye and Hiickel showed that it was possible to explain the abnormal activity coefficients at least for very dilute solutions of electrolytes. [Pg.125]

The electrovalent bond is formed by electrostatic attraction between oppositely charged ions. Thus Na, with one outer electron, loses this electron to achieve the noble gas Ne structure, while Cl with seven outer electrons, gains one electron to achieve the Ar structure. [Pg.415]

The Donnan effect acts to exclude like-charged substrate ions from a charged surface region, and this exclusion, as well as the concentration of oppositely charged ions, can be expressed in terms of a Donnan potential pD. Thus for a film of positively charged surfactant ions S one can write... [Pg.553]

Weak electrolytes in which dimerization (as opposed to ion pairing) is the result of chemical bonding between oppositely charged ions have been studied using a sticky electrolyte model (SEM). In this model, a delta fiinction interaction is introduced in the Mayer/-fiinction for the oppositely charged ions at a distance L = a, where a is the hard sphere diameter. The delta fiinction mimics bonding and tire Mayer /-function... [Pg.500]

At first sight, we would expect that the mobilities of more highly-charged ions would be larger, but it is... [Pg.573]

A third method for generating ions in mass spectrometers that has been used extensively in physical chemistry is chemical ionization (Cl) [2]. Chemical ionization can involve the transfer of an electron (charge transfer), proton (or otlier positively charged ion) or hydride anion (or other anion). [Pg.1330]

Energy is released on formation of the singly-charged ion but a greater amount of energy is required to add a second electron and... [Pg.33]

It will be noted that hydration enthalpy decreases with increasing ionic radius and increases very sharply with increase in ionic charge, these results being what we should expect for an electrostate interaction between a charged ion and the dipole of a water molecule (p, 44). [Pg.78]

FIGURE 1 4 An ionic bond IS the force of attrac tion between oppositely charged ions Each Na ion (yellow) in the crystal lattice of solid NaCI IS involved in ionic bonding to each of six surrounding Cl ions (green) and vice versa... [Pg.11]

Were we to simply add the ionization energy of sodium (496 kJ/mol) and the electron affin ity of chlorine (—349 kJ/mol) we would conclude that the overall process is endothermic with AH° = +147 kJ/mol The energy liberated by adding an electron to chlorine is msuf ficient to override the energy required to remove an electron from sodium This analysis however fails to consider the force of attraction between the oppositely charged ions Na" and Cl which exceeds 500 kJ/mol and is more than sufficient to make the overall process exothermic Attractive forces between oppositely charged particles are termed electrostatic, or coulombic, attractions and are what we mean by an ionic bond between two atoms... [Pg.12]

Section 1 2 An ionic bond is the force of electrostatic attraction between two oppo sitely charged ions Atoms at the upper right of the periodic table espe cially fluorine and oxygen tend to gam electrons to form anions Elements toward the left of the periodic table especially metals such as sodium tend to lose electrons to form cations Ionic bonds m which car bon IS the cation or anion are rare... [Pg.47]

Cation (Section 1 2) Positively charged ion Cellobiose (Section 25 14) A disacchande in which two glu cose units are joined by a 3(1 4) linkage Cellobiose is oh tamed by the hydrolysis of cellulose Cellulose (Section 25 15) A polysaccharide in which thou sands of glucose units are joined by 3(1 4) linkages Center of symmetry (Section 7 3) A point in the center of a structure located so that a line drawn from it to any element of the structure when extended an equal distance in the op posite direction encounters an identical element Benzene for example has a center of symmetry Cham reaction (Section 4 17) Reaction mechanism m which a sequence of individual steps repeats itself many times usu ally because a reactive intermediate consumed m one step is regenerated m a subsequent step The halogenation of alkanes is a chain reaction proceeding via free radical intermediates... [Pg.1278]

Quantum (Section 13 1) The energy associated with a photon Quaternary ammonium salt (Section 22 1) Salt of the type R4N X The positively charged ion contains a nitrogen with a total of four organic substituents (any combination of alkyl and aryl groups)... [Pg.1292]

Tabulate the probable groups that (a) give rise to the prominent charged ion peaks and (b) list the neutral fragments. [Pg.815]

A quantitative method for reporting the ionic composition of a solution that takes into account the greater effect of more highly charged ions (jr). [Pg.172]

Precipitate particles grow in size because of the electrostatic attraction between charged ions on the surface of the precipitate and oppositely charged ions in solution. Ions common to the precipitate are chemically adsorbed, extending the crystal lattice. Other ions may be physically adsorbed and, unless displaced, are incorporated into the crystal lattice as a coprecipitated impurity. Physically adsorbed ions are less strongly attracted to the surface and can be displaced by chemically adsorbed ions. [Pg.238]

Most ion sources produce singly charged ions, i.e., z = I and the ranges shown here apply to such ions. Matrix assisted methods may produce ions with r > 1. When = 1, m/z. = m, viz., mass can be measured directly. An ES ion source produces ions with z > 1 and this effectively extends the mass ranges that can be examined. For example, with z = 1 and m = 10,000, the m/z value is 10,000 and this would be beyond tbe capabilities of a quadrupole instrument. [Pg.282]


See other pages where Charged Ions is mentioned: [Pg.85]    [Pg.219]    [Pg.299]    [Pg.173]    [Pg.225]    [Pg.406]    [Pg.440]    [Pg.483]    [Pg.500]    [Pg.566]    [Pg.575]    [Pg.584]    [Pg.584]    [Pg.839]    [Pg.29]    [Pg.33]    [Pg.45]    [Pg.270]    [Pg.180]    [Pg.211]    [Pg.212]    [Pg.585]    [Pg.110]    [Pg.568]    [Pg.1276]    [Pg.416]    [Pg.592]    [Pg.597]    [Pg.603]    [Pg.774]    [Pg.47]    [Pg.93]    [Pg.189]   
See also in sourсe #XX -- [ Pg.9 ]

See also in sourсe #XX -- [ Pg.7 ]




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Ammonium ions formal charge

Anion A negatively charged ion

Anion A negatively charged ion that

Atomic complexities singly charged ions

Bimolecular reactions like-charge ions

Carbenium ions effects, positive charge interaction

Carbenium ions positive charge substituents

Cation A positively charged ion

Cation A positively charged ion that

Cationic structures like-charge ions

Charge Distribution around an Ion

Charge State of Ions

Charge density of ions

Charge density-N.M.R. chemical shift correlations in organic ions

Charge density-NMR chemical shift correlation in organic ions

Charge neutralization negative ions

Charge of ion

Charge of the ion

Charge on mercurous ion

Charge on monatomic ions

Charge on the ion

Charge potential) -determining ions

Charge separated ion pair

Charge separated ions

Charge transfer by ions

Charge transfer from singly charged ions

Charge transfer in neutral atom-multiply charged ion collisions

Charge transfer multiply charged ions

Charge transfer, and ion—molecule reactions

Charge, on ions

Charge-Transfer Coordination to Metallocomplex Ion-Radicals

Charge-balancing counter-ions

Charge-compensated ion

Charge-determining ions

Charge-transfer complexes and radical ion salts

Charged Catalysts Quaternary Ions

Charged Ions in Ionic Conductors

Charged Surface with Ion Adsorption

Charged ion-exchange membrane

Charged molecular ions

Charging lithium-ion batteries

Correction terms highly charged ions

Crystals of Molecules with Charge Transfer, Radical-ion Salts

Dealing with Multiply Charged Ions

Double charged ions

Doubly charged analyte ion

Doubly charged ion

Doubly charged ions, chemical reactions

Doubly charged negative ions

Effective Charges and Ion Softening

Electrical charges of ions

Electrical charges, ions

Electrically-charged particles (ion

Electrochemistry and electric field as origins of multiply charged ions

Electron ionization doubly charged ions

Electron transfer like charge radical ions

Electrospray ionization multiply charged ions produced

Excited ions charge transfer

Field ionization multiply charged ions

Fixed charge metallic ions

Fluoride ions, charge distribution

Formation of Ions from Charged Droplets

High-density charge clusters positive ions

Higher charge ion

Highly charged ions

Hydrophobic hydration for large charged ions

Interaction of Charged Surfaces with Ions and Molecules

Interferences double charged ions

Ion charge

Ion charge effects

Ion charge state

Ion charged species

Ion doubly charged ions

Ion pair charge transfer

Ion, charge ratio

Ionic bond The attraction between oppositely charged ions

Ionic bonding The attraction between oppositely charged ions

Ionization methods, mass multiply charged ions

Ions - simple charged particles or not

Ions, mass-to-charge ratios

Ions, negatively charged

Ions, organic, charge density-N.M.R. chemical shift correlations

Ions, organic, charge density-NMR

Ions, organic, charge density-NMR chemical shift correlations

James L., Electrides, Negatively Charged Metal Ions, and Related Phenomena

Lanthanide ions charge transfer

Large Analyte Ions such as Dendrimers and Proteins are Most Probably Produced by the Charged Residue Model (CRM)

Lasers multi-charged ions

Lithium ions, charge distribution

Lithium-ion batteries charge

Low charge-density ions

Mass doubly charged ions

Mass-to-charge ratio of ions

Metal ion charge

Metastable ions following charge exchange

Monatomic ions predicting charges

Multiply charged ions

Multiply charged ions isotopic patterns

Multiply charged ions resolving isotopic patterns

Multiply charged metal ions

Multiply charged negative ions

Multiply charged negative ions anions)

Multiply charged secondary ions

Multiply-Charged Ions in FI-MS

Multiply-charged molecular ions

Multiply-charged precursor ions

Multiply-charged reagent ions

Names and Charges of Polyatomic Ions

Negative ions charge transfer

Of single charged atomic ions

Organic Ion-Radicals with Several Unpaired Electrons or Charges

Peculiarities of multiply charged ions

Peptide, multiply charged ions

Permselectivity of Ions with the Same Charge

Polyatomic ions electrical charges

Positive ions charge transfer

Positively charged ions

Precursor ions, higher-charged

Probability of Finding Oppositely Charged Ions near Each Other

Product ions singly-charged

Proteins doubly charged ions

R-5 Names and Charges of Polyatomic Ions

Radical ions charges

Recombination energy doubly-charged ions

Relativistic and QED Effects in Highly Charged Ions

Resins types positively charged ions

Salt Ions Shield Charged Objects

Single charged ions

Singly charged ions

Singly-charged ions, large

Soil Readily Retains Positively Charged Ions

Spin-Charge Separation (Distonic Stabilization of Ion-Radicals)

Stable Electron Configurations and Charges on Ions

Surface charge adsorbed ions

Surface charge density metal ions

Surface charge: aluminosilicate ions

Tandem of multiply charged ions

The Heteropolar Linkage Between Oppositely Charged Ions

The distribution of ions in an electric field near a charged surface

The resonance charge exchange in ion-atom collisions

Transition metal ions charges

Triply charged ion

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