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Activity solutions

Plenary 7(5. N I Koroteev et al, e-mail address Koroteev nik.phys.iusu.su (CARS/CSRS, CAHRS, BioCARS). A survey of the many applications of what we call the Class II spectroscopies from third order and beyond. 2D and 3D Raman imaging. Coherence as stored infonuation, quantum infonuation (the qubit ). Uses tenus CARS/CSRS regardless of order. BioCARS is fourtli order in optically active solutions. [Pg.1218]

Koroteev N I 1996 Optical rectification, circular photogalvanic effect and five-wave mixing in optically active solutions Proc. SPIE 2796 227-38... [Pg.1231]

Both the hquid and cured 2-cyanoacryhc esters support combustion. These adhesives should not be used near sparks, heat, or open flame, or ia areas of acute fire ha2ard. Highly exothermic polymerization can occur from direct addition of catalytic substances such as water, alcohols, and bases such as amines, ammonia, or caustics, or from contamination with any of the available surface activator solutions. [Pg.179]

The initiation of development in the activator solution is more rapid than in conventional processes because the developer molecules need not diffuse into the light-sensitive layers from the processing solution. In spite of the low activity of the coated developer, some unintentional reduction sensitization may occur, which produces unwanted fog. Therefore, coating the developer in a separate layer usually is preferred. Because of simplicity, rapid access, and solution stabihty, incorporated developer papers have been used for office copying appHcations. [Pg.456]

Product Quality. Under ideal plant operating conditions, the quahty of products derived from continuous SO film sulfonator units is unlikely to be significantly different (1). Typical LAB sulfonic acid composition is ca 96.6% active sulfonic acid, 1.2% free oil, 1.2% H2SO4, and 1.0% water, the last added for stabilization purposes to break sulfonic acid anhydrides and pyro-acids (279). Klett color for a 5% active solution is typically 15—25. [Pg.88]

Many benzenoid quaternary cationic surfactants possess germicidal, fungicidal, or algicidal activity. Solutions of such compounds, alone or in combination with nonionic surfactants, are used as detergent sanitizers in hospital maintenance. Classified as biocidal products, their labeling is regulated by the U.S. EPA. The 1993 U.S. shipments of cationic surfactants represented 16% of the total sales value of surfactant production. Some of this production is used for the preparation of more highly substituted derivatives (101). [Pg.255]

The first instant color photography system, introduced by the Polaroid Corp. in 1963 as Polacolor, used the transfer of subtractive dyes to a receiver sheet to produce a positive image. The incorporated dye-developers, containing a hydroquinone moiety, are soluble in the alkaline activator solution, except where silver development occurs, when they are immobilized as the quinone form. [Pg.470]

Foam Fractionation. An interesting experimental method that has been performed for wastewater treatment of disperse dyes is foam fractionation (88). This method is based on the phenomenon that surface-active solutes collect at gas—Hquid iaterfaces. The results were 86—96% color removal from a brown disperse dye solution and 75% color removal from a textile mill wastewater. Unfortunately, the necessary chemical costs make this method relatively expensive (see Foams). [Pg.382]

Catalysts for dielectric surfaces are more complex than the simple salts used on metals. The original catalysts were separate solutions of acidic staimous chloride [7772-99-8J, used to wet the surface and deposit an adherent reducing agent, and acidic palladium chloride [7647-10-17, which was reduced to metallic palladium by the tin. This two-step catalyst system is now essentially obsolete. One-step catalysts consist of a stabilized, pre-reacted solution of the palladium and staimous chlorides. The one-step catalyst is more stable, more active, and more economical than the two-step catalyst (21,23). A separate acceleration or activation solution removes loose palladium and excess tin before the catalyzed part is placed in the electroless bath, prolonging bath life and stability. [Pg.107]

The laser has revolutionized many aspects of science and other disciplines, as well as the daily lives of millions of people. When it was first invented, the laser was referred to by some as a solution looking for a problem because it came about mostly from basic research rather than the active solution to a particular concern. At the time, no one could have predicted the far-reaching effects it would have in the second half of the twentieth centuiy, or that it would come to be considered by many as one of the most inQuen-tial technological achievements of that time. [Pg.706]

The processes are dealt with fully in Chapters 11, 14 and 15. Because many paint systems include an initial surface pretreatment, e.g. chromated aluminium or phosphated steel, BS4479 1990, Part 3 deals with conversion coatings and should be consulted by designers. Whatever the method of treatment, liquids must be able to drain quickly and freely from the surfaces. Crevices where liquids can become entrapped are best avoided. The surface configuration needs to be such that active solutions can be washed away, leaving the surface to be painted completely free from unreacted pretreatment solution. Failure to achieve the requisite level of freedom from the surplus chemicals causes paint failure, e.g. osmotic blistering. [Pg.325]

When a polymer film is exposed to a gas or vapour at one side and to vacuum or low pressure at the other, the mechanism generally accepted for the penetrant transport is an activated solution-diffusion model. The gas dissolved in the film surface diffuses through the film by a series of activated steps and evaporates at the lower pressure side. It is clear that both solubility and diffusivity are involved and that the polymer molecular and morphological features will affect the penetrant transport behaviour. Some of the chemical and morphological modification that have been observed for some epoxy-water systems to induce changes of the solubility and diffusivity will be briefly reviewed. [Pg.191]

A number of chapters in this volume (especially Chapters 5 and 6) provide a more thorough discussion of osmotic adjustment by intact plants and tissues in response to environmental stress and the role of osmotically active solutes in this response. The following section focuses on the role of organic osmotica in the response of plant cells to salt stress. Cultured plant cells offer the opportunity to evaluate the effect of both internally synthesised and externally administered organic osmotica. [Pg.188]

Moderate soil salt concentration. These are external concentrations at which substantial osmotic adjustment in the plant is required, and could not be achieved with NaCl without compartmentation between cytoplasm and vacuole. Damage may still be attributable to excessive internal concentrations, but simply minimising salt uptake is not a sufficient answer. The concentration of osmotically active solutes within the cells has to be... [Pg.219]

The electrochemical mechanism was rejected by Salvago and Cavallotti [26] on the basis that it does not explain several features of electroless deposition of ferrous metals it does not account for the isotopic composition of the H2 gas evolved it does not explain the effect of the various solution components on reaction rate and it does not account for the homogeneous decomposition of very active solutions or the fact that they can give deposition on insulating surfaces. These authors put forward a chemical mechanism, involving various hydrolyzed nickel species, which they claim explains the observed behavior of the system ... [Pg.255]

Ashokkumar M, Hodnett M, Zeqiri B, Grieser F, Price G (2007) Acoustic emission spectra from 515 kHz cavitation in aqueous solutions containing surface-active solutes. J Am Chem Soc 129 2250-2258... [Pg.26]

Lee J, Tuziuti T, Yasui K, Kentish S, Grieser F, Ashokkumar M, Iida Y (2007) Influence of surface-active solutes on the coalescence, clustering, and fragmentation of acoustic bubbles confined in a microspace. J Phys Chem C 111 19015-19023... [Pg.26]

Tuziuti T, Yasui K, Lee J, Kozuka T, Towata A, Iida Y (2009) Influence of surface active solute on ultrasonic waveform distortion in liquid containing air bubbles. J Phys Chem A... [Pg.27]

Grieser F, Ashokkumar M (2001) The effect of surface active solutes on bubbles exposed to ultrasound. Adv Colloid Interface Sci 89-90 423 138... [Pg.354]

Candelaria L.M., Chang A.C. Cadmium activities, solution speciation, and solid phase distribution of Cd in cadmium nitrate and sewage sludge-treated soil systems. Soil Sci 1997 162 (10) 722-732. [Pg.333]

The basic idea of immobilising a catalytically active solution on a solid support to obtain a solid catalyst with homogeneous type selectivity and efficiency is not new. In the late seventies, Scholten [69] and Hjortkjaer [70] described supported liquid phase... [Pg.201]

The answer is b. (Hardman, pp 695-697.) A significant increase in the amount of any osmotically active solute in voided urine is usually accompanied by an increase in urine volume Osmotic diuretics affect diuresis through this principle. The osmotic diuretics (such as mannitol) are nonelectrolytes that are freely filtered at the glomerulus, undergo limited re absorption by the renal tubules, retain water in the renal tubule, and promote an osmotic diuresis, generally without significant Na excretion. Ln addition, these diuretics resist alteration by metabolic processes. [Pg.219]

Noyori et al. recently used ESI-MS to characterize species present in catalytically active solutions during the hydrogenation of aryl-alkyl ketones using their base-free catalyst precursors trans-[Ru((R)-tol-BINAP)((R, RJ-dpenJfHXf/ -BH ] (tol-BI-NAP = 2,2 -bis(ditolylphosphino) -1, T-binaphthyl dpen = 1,2-diphenylethylenedia-mine) in 2-propanol [9b]. Based upon ESI-MS observations, deuterium-labeling studies, kinetics, NMR observations, and other results, the authors proposed that the cationic dihydrogen complex trans-[Ru((R)-tol-BINAP)((R, R)-dpen)(H)( 2-H2)]+ is an intermediate in hydrogenations carried out in the absence of base. [Pg.367]

ESI represents a powerful method by which to transfer organometallic ions from catalytically active solutions into the gas phase. ESI-MS systems allow the characterization of the gas-phase ions using CID, reactivity, and isotope-labeling studies. The application of ESI-tandem-MS systems allows gas-phase preparations and isolation of desired organometallic ions in the first ESI-octopole-quad-rupole, followed by characterization or reactivity studies in the second octopole-quadrupole. [Pg.369]


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See also in sourсe #XX -- [ Pg.445 ]




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Activated Carbon Adsorption from Solutions

Activated Carbon Adsorption of Cobalt from Aqueous Solutions

Activated carbon aqueous solutions

Activation energy diffusion into solution

Activation free energy quantum mechanical solution

Active ingredient solution/suspension

Activities in Ideal Solutions

Activities in Real Solutions

Activities of Minor Components in Concentrated Solutions

Activity (Cont solute

Activity Coefficient Models for Electrolyte Solutions

Activity Coefficients of Some Ions in Aqueous Solution

Activity and Equilibrium in Nonelectrolyte Solutions

Activity aqueous solution

Activity calculation, solute

Activity cobalt catalyst solutions

Activity coefficient Flory-Huggins polymer solution

Activity coefficient fluctuation solution theory

Activity coefficient in electrolyte solutions

Activity coefficient in solution

Activity coefficient models regular solution

Activity coefficient of a solute

Activity coefficient of an electrolyte solute

Activity coefficient of electrolyte solutes

Activity coefficient of molecular solutes

Activity coefficient of solutions

Activity coefficient solute-free

Activity coefficient solution

Activity coefficient, decrease micelle solutions

Activity coefficients and solution standard states

Activity coefficients and spectroscopic properties of associated solutions

Activity coefficients aqueous solutes

Activity coefficients concentrated, mixed salt solutions

Activity coefficients in aqueous salt solutions

Activity coefficients in dilute solutions

Activity coefficients in ionic solutions

Activity coefficients in solid solutions

Activity coefficients solution phase

Activity coefficients symmetrical solutions

Activity electrolyte solution

Activity from solid solution composition

Activity in aqueous solutions

Activity in concentrated solutions

Activity in electrolyte solutions

Activity in electrolytic solutions

Activity measurements in solution

Activity of Real Electrolyte Solutions

Activity of a Solute from Distribution between Two Immiscible Solvents

Activity of a component in any solution Raoults and Henry s laws

Activity of a solute

Activity of electrolyte solutes

Activity of electrolyte solutions

Activity of ions in solution

Activity of nonvolatile solutes

Activity of solutes

Activity of solutions

Activity of species in solution

Activity of the solvent in a solution

Activity solid solution

Activity solutions and

Activity, 5.9, 5.11 ideal solution

Adhesion in Solutions of Surface-Active Substances

Aqueous solutions activity coefficients

Binary activity coefficients, regular solution approximation

Chemical Potentials of Real Solutions. Activity

Dilute solution activity coefficients

Electrolyte solutes activities

Electrolyte solutes activity coefficient

Electrolyte solutes mean ionic activity coefficients

Electrolyte solutions, activity coefficient

Electrolyte solutions, activity coefficient chemical potential

Electrolyte solutions, activity coefficient conventions

Electrolyte solutions, activity coefficient definition

Electrolyte solutions, activity coefficient weak electrolytes

Enzyme solution specific activity

Experimental Determination of Solution Activities

How to determine the specific activity of an experimental solution

Hydrogen-ion activity in solution

Ideal solutions calculating state-dependent activity

Interface active carbon-electrolyte solution

Ionic surface active solute

Liquid solutions activity coefficient

Liquid solutions activity-coefficient models

Liquid, fugacity solutions, activity

Modified Form of the Kohler Theory for a Surface-Active Solute

Molecular solutes, activity

Molecular solutes, activity coefficients

Multicomponent solutions activity coefficient

Nonvolatile solutes, activities

Osmotically active solute

Potassium hydroxide solutions activity coefficient

Preparing Accurate Activity Calibration Solutions

Pressures (Solvent Activities) for Binary Polymer Solutions

Reaction mechanisms in solution, entropies of activation and

Real solutions activities

Real solutions, activity coefficient

Regular solutions activity coefficients

Relation between the activity coefficients of a binary solution

Relationship of Solute Activity to Single Ion Activities

Solid solutions activity coefficients

Solute activity

Solute defining activity

Solute-activity coefficient

Solution activities and activity coefficients

Solution chemistry activity coefficients

Solution preparation activity

Solution-diffusion mechanism activated process

Solutions Containing Surface-active Solutes

Surface active solutes

Surface activity in aqueous solution

Surface-active solution

Surfactants (Soaps and Detergents) Aqueous Solutions (Surface-Active Substances)

The Activities of Nonvolatile Solutes

Water Activity Control Using Saturated Salt Solutions

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