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Conductance solvents

Mixing cellulose esters in nonpolar hydrocarbons, such as toluene or xylene, may result in static electricity buildup that can cause a flash fire or explosion. When adding cellulose esters to any flammable Hquid, an inert gas atmosphere should be maintained within the vessel (132). This risk may be reduced by the use of conductive solvents in combination with the hydrocarbon or by use of an antistatic additive. Protective clothing and devices should be provided. [Pg.259]

The discrepancies in the reported conductance data of Au-alkanedithiol-Au junctions attracted our attention, and we decided to carry out an in-depth experimental study of the charge transport properties of Au-a,oo-alkanedithiol-Au molecule junctions in a non-conducting solvent. The combination with quantum chemistry ab initio simulations yielded a detailed view of this archetype of molecular junctions, and helped to resolve the puzzle on the role of microscopic geometries at the contacts and in the molecular conformation. [Pg.146]

The influence can be either direct at the electrodes or indirect via the (electrically conducting) solvent lines connected to the instrument and via power supply or ground lines in common with other instruments. [Pg.41]

The fact that either the peak-to-peak separation, AEp, somewhat departs from the value of 59 mV or the current function ipJvl/2 is not rigorously constant seems to contrast with the diagnostic criteria (illustrated in Chapter 2, Section 1.1.1) for an electrochemically reversible one-electron process. This can be largely attributed to the non-compensated resistance given by the dichloromethane solution, which is a low conducting solvent. [Pg.162]

Sample dissolution in a low-conductivity solvent can induce sample stacking. This might also be achieved by injecting a low-conductivity solvent plug before or after the sample plug. [Pg.131]

Transition Region Considerations. The conductance of a binary system can be approached from the values of conductivity of the pure electrolyte one follows the variation of conductance as one adds water or other second component to the pure electrolyte. The same approach is useful for other electrochemical properties as well the e.m. f. and the anodic behaviour of light, active metals, for instance. The structure of water in this "transition region" (TR), and therefore its reactions, can be expected to be quite different from its structure and reactions, in dilute aqueous solutions. (The same is true in relation to other non-conducting solvents.) The molecular structure of any liquid can be assumed to be close to that of the crystals from which it is derived. The narrower is the temperature gap between the liquid and the solidus curve, the closer are the structures of liquid and solid. In the composition regions between the pure water and a eutectic point the structure of the liquid is basically like that of water between eutectic and the pure salt or its hydrates the structure is basically that of these compounds. At the eutectic point, the conductance-isotherm runs through a maximum and the viscosity-isotherm breaks. Examples are shown in (125). [Pg.283]

Increasing the concentration of 1,3-D in the reaction mixture leads to higher yields which are almost quantitative. With low-conducting solvents such as trichlorobenzene or o-dichlorobenzene, the synthesis of Pc without electrolytic conditions... [Pg.386]

As mentioned before the influence of the liquid on the signal decay behavior was also considered. For this purpose, we worked not only with ethanol but also with isopropanol and methoxy-nonafluorobutane (HFE-7100) because of their different thermal conductivities. Solvent... [Pg.264]

Steele, B.D., D. McIntosh, and E.H. Archibald. 1906. The halogen hydrides as conducting solvents. Part I - The vapour pressures, densities, surface energies and viscosities of the pure solvents. Phil. Trans. Roy. Soc. A205 99-167. [Pg.58]

The utilization of poorly conducting solvents is possible in electrochemistry,... [Pg.324]

The conductivity solvent enters through the solvent inlet and flows through the reference conductivity cell that is formed by the top and outer electrode assemblies. The solvent then flows into the gas-liquid contactor where it is mixed with the gaseous reaction products entering through the gas inlet. The heterogeneous gas-liquid mixture formed in the gas-liquid contactor is separated into gas and liquid phases in the gas-liquid separator. The gas phase exits... [Pg.236]

Detector response in the nitrogen mode is due to the formation of NHj by the catalytic reduction of organic nitrogen in the nickel tube. When ammonia is dissolved in the 50% -propanol/water solvent, it forms ammonium hydroxide, a weak base. The ammonium hydroxide dissociates to the electrolytically conducting species, NH/and OH". In order for the proper detector response to be obtained, the conductivity solvent must be slightly basic so that neutralization of the base does not occur. [Pg.237]

The processing equipment used to conduct solvent extraction of metals is the same as that used in conventional liquid-liquid extraction.1 1 The most common choices have been mixer-settlers, columns with agitated internals, and static mixers. Some advantages and disadvantages of several classes of equipment are summarized in Table 8.5-1. Many of the practical aspects of equipment selection are diicussed by Pratt and Hanson5 and by Ritcey and Ashbrook. ... [Pg.490]

Figure I. The limiting ionic conductance-solvent viscosity product plotted as a function of the reciprocal ionic radii for several ions in aqueous and acetonitrile solutions at 25 C,... Figure I. The limiting ionic conductance-solvent viscosity product plotted as a function of the reciprocal ionic radii for several ions in aqueous and acetonitrile solutions at 25 C,...
The primary advantage of such an approach is that it creates a flat flow profile, and thus allows definition of precise flow rates and narrow residence time distributions. Nevertheless, electroosmotic flow (EOF) pumps are severely limited in their widespread application to molecular synthesis due to a need for a conductive solvent and the fact that varying electrophoretic mobilities of reagents and products leads to time-dependent concentration gradients within the reactor that can degrade performance. [Pg.1190]

If method (3) or (4) is used there is a need for considerable ullage in the receiving tank at the end of unloading when a slug of gas will enter the base of the tank and carry some of the tank s contents out of the vent or overflow. The possibility of generating static electricity when air is blown through low electrical conductivity solvent mixtures is considerable. [Pg.135]

Ideal liquids are mutually soluble in all proportions, while the solubilities of ideal solids in ideal liquid solvents are limited by the energy required to liquify the solute. Real solutions of non-electrolytes in non-conducting solvents can be subdivided into regular solutions and solutions in which association occurs. The former have been the subject of extensive study by Hildebrand and Scott [43], who have developed methods of predicting regular solubilities from theoretical considerations. Tliey introduced the term solubility parameter (5), which is constant for a given solute or solvent, and dependent on intermolecular attraction and molar volume. Deviation from ideal solubility is calculated from an expression containing the term (Si-Sj), where the suffixes 1 and 2 represent solvent and solute respectively. When the solubility parameters of solvent and... [Pg.224]

This is at infinite dilution in a non-conductive solvent. In reality, it depends on both particle properties (size, charge, etc.) and liquid properties (pH, ionic strength, etc.) and is approximated by the Smulochowsld equation ... [Pg.351]


See other pages where Conductance solvents is mentioned: [Pg.39]    [Pg.162]    [Pg.173]    [Pg.154]    [Pg.667]    [Pg.668]    [Pg.248]    [Pg.121]    [Pg.264]    [Pg.220]    [Pg.322]    [Pg.401]    [Pg.180]    [Pg.185]    [Pg.562]    [Pg.187]    [Pg.212]    [Pg.111]    [Pg.29]    [Pg.441]    [Pg.796]    [Pg.796]    [Pg.796]    [Pg.3]    [Pg.227]    [Pg.173]    [Pg.1189]    [Pg.16]    [Pg.78]    [Pg.289]    [Pg.230]    [Pg.279]   
See also in sourсe #XX -- [ Pg.361 ]




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Binary solvent mixture conductivity

Chlorinated solvents conductivity

Conductance Data among Solvents

Conductance in non-aqueous solvents

Conductance in nonaqueous solvents

Conductance solvent viscosity

Conducting electrolytic polymerization, solvent

Conducting polymers solvent

Conducting polymers solvent dielectric constant differences

Conductive Electroactive Polymers solvent

Conductivities and Solvents

Conductivity solvent viscosity

Electric conductivity solvent effects

Hydrogen-bonded solvents, electrical conductivity

Nonaqueous solvents, conductance

Protic solvents, conductance

Protic solvents, conductance involving

Solvent conductivity

Solvent conductivity

Solvent dispersion process, conductive

Solvent-free polymer electrolytes conductivity

Solvents molar conductivities

Solvents, acceptor properties conductivity

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