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Complexes solution

As with safety, environmental considerations are usually left to a late stage in the design. However, like safety, early decisions often can lead to difficult environmental problems which later require complex solutions. Again, it is better to consider effluent problems as the design progresses in order to avoid complex waste treatment systems. [Pg.273]

Following this hierarchy, all to often safety, health and environmental considerations are left to the final stages of design. This approach leaves much to be desired, since early decisions made purely for process reasons often can lead to problems of safety, health, and environment that require complex solutions. It is better... [Pg.399]

Improved sensitivities can be attained by the use of longer collection times, more efficient mass transport or pulsed wavefomis to eliminate charging currents from the small faradic currents. Major problems with these methods are the toxicity of mercury, which makes the analysis less attractive from an eiivironmental point of view, and surface fouling, which coimnonly occurs during the analysis of a complex solution matrix. Several methods have been reported for the improvement of the pre-concentration step [17,18]. The latter is, in fact. [Pg.1932]

On the other hand, wet chlorination of refinery slimes has proven to be a rapid and simple method of obtaining high extractions of selenium from slimes. A simple wet chlorination flow sheet is shown in Figure 3. Slimes chlorination per se is not a simple deselenization operation, but rather a process wherein virtually all the constituents of slimes which form soluble chlorides report as a complex solution of mixed chlorides. Thus the use of wet chlorination requires a complete change in the process to recover the metal values in slimes. The first plant to use wet chlorination of slimes was started by Kennecott (Salt Lake City, Utah) in 1995. [Pg.330]

Flavin mononucleotide was first isolated from the yellow en2yme in yeast by Warburg and Christian in 1932 (4). The yellow en2yme was spHt into the protein and the yellow prosthetic group (coen2yme) by dialysis under acidic conditions. Flavin mononucleotide was isolated as its crystalline calcium salt and shown to be riboflavin-5Lphosphate its stmeture was confirmed by chemical synthesis by Kuhn and Rudy (94). It is commercially available as the monosodium salt dihydrate [6184-17 /, with a water solubiUty of more than 200 times that of riboflavin. It has wide appHcation in multivitamin and B-complex solutions, where it does not require the solubili2ers needed for riboflavin. [Pg.80]

The overhead temperatures of both the absorber and stripper are kept as low as possible to minimise solvent carryover. A temperature of about 311 K is typically used ia the high pressure absorber. The overhead temperature ia the stripper is set by the boiling poiat of the saturated complex solution and by the operating pressure of the stripper. At a stripping pressure of 0.166 MPa (1.7 atm), a temperature of 378 Kis used. The solvent-rich gas from the stripper is cooled to recover as much solvent as possible by condensation prior to the final aromatics-recovery section. Fiaal solvent recovery is accomphshed by adsorption on activated carbon (95). [Pg.58]

Definition the electronic tongue is an analytical instrarment including an array of low-selective chemical sensors and appropriate pattern recognition tool, capable to recognize quantitative and qualitative compositions of simple and complex solutions . [Pg.19]

Application of a modified sorbent is preferable, since in this case the intensity luminescence (/) of Ln, as well as the rate of its determination is higher about 6-7 times. The comparison of luminescence intensity of Ln -ligand complex solution before the soi ption with results of I after soi ption by both non-modified and modified PMMA showed that I increased in 30 and about 200 times, respectively. [Pg.82]

Evaluation of the corrosion potential from Eq. (2-53) is inadmissible when the metal ion, for example, reacts further in strongly complexing solutions ... [Pg.54]

However, with practical samples the way the (k ) values of the individual components for any given complex solute mixture are distributed is not predictable, and will vary very significantly from mixture to mixture, depending on the nature of the sample. Nevertheless, although the values for the theoretical peak capacity of a column given by equation (26) can be used as a reasonable practical guide for comparing different columns, the theoretical values that are obtained will always be in excess of the peak capacities that are actually realized in practice. [Pg.206]

A disaccharide is added to a pyridine SO3 complex solution, which is prepared by reacting 5 to 6 times the molar amount of liquid SO3 as much as that of disaccharide with 5 to 10 times the amount of pyridine as that of the disaccharide at 0°C to 5°C, for sulfation at 50°C to 70°C for 3 to 7 hours. After the completion of sulfation, the greater part of pyridine Is removed by decantation. The obtained solution exhibits an acidity that is so strong that it is improper to apply the reaction with aluminum ion and, therefore, sodium hydroxide is added for neutralization. After the remaining pyridine is removed by concentration, 100 unit volumes of water per unit volume of the residue is added thereto. To the solution is then added aluminum ion solution mainly containing aluminum dihydroxychloride, the pH of which is 1.0 to 1.2, in such an amount that the aluminum ion Is present in an amount of 4 to 6 molar parts of the amount of disaccharide to provide a pH of 4 to 4.5. The mixture is reacted under stirring at room temperature and the formed disaccharide poly sulfate-aluminum compound is allowed to precipitate. After filtration, the residue is washed with water and dried. [Pg.1396]

The preceding methods are the criteria in making a selection of the proper volume and choke-tube combination. A more complex solution is now in order. Here, the following relation is used ... [Pg.599]

Equation (11.61) has three roots three real, or one real and two complex, depending on the value of determinant D = q - -Pl (Korn and Korn 1968). Since our aim is to determine the complex frequency D, we will consider the complex solution of Eq. (11.61)only. [Pg.449]

This supramolecular approach has been used as a way to facilitate the crystallization of cuboidal aqua ions and to capture single intermediates present in complex solution mixtures. For example, [M3Q4Clx(H20)9.x] (Q = S, Se) supramolecular adducts have been isolated for x =1-5 from aqueous HCl solutions by varying the acid concentrations where the aggregates contain in each case only one of all possible isomers [46]. In addition to the hydrogen bonds, other kinds of interactions, namely C1---H20, C1---C1 and Q---Q contacts, are also involved in the network propagation. This supramolecular approach has also been efficiently employed for the crystallization of a large number of aqua complexes within the [M3M Q4] cubane-type family, where M is a transition or post-transition metal [47]. [Pg.118]

The deposition takes place from HTeOs and cadmium-EDTA complex solutions at a potential whereat, whilst Te is deposited from HTeOs under a diffusion-limited condition, the Cd-EDTA complex ion is not reduced to metallic Cd. The first step is the dark deposition of one monolayer of elemental Te on the p-Si substrate (Fig. 4.11a, i). After completion of this step, as specified by measuring the charge passed, the electrode is illuminated by light with energy higher than the band gap energy of silicon for a limited time. Then conduction band electrons are... [Pg.181]

Mourzina YG, Schubert J, Zander W, Legin A, Vlasov YG, Schdning MJ (2001) Development of multisensor systems based on chalcogenide thin film chemical sensors for the simultaneous multicomponent analysis of metal ions in complex solutions. Electrochim Acta 47 251-258... [Pg.348]

Beryllium(II) is the smallest metal ion, r = 27 pm (2), and as a consequence forms predominantly tetrahedral complexes. Solution NMR (nuclear magnetic resonance) (59-61) and x-ray diffraction studies (62) show [Be(H20)4]2+ to be the solvated species in water. In the solid state, x-ray diffraction studies show [Be(H20)4]2+ to be tetrahedral (63), as do neutron diffraction (64), infrared, and Raman scattering spectroscopic studies (65). Beryllium(II) is the only tetrahedral metal ion for which a significant quantity of both solvent-exchange and ligand-substitution data are available, and accordingly it occupies a... [Pg.17]

Modern TLC is thus an effective tool for separation of complex solutions into their components. Analysis can be qualitative or quantitative. When the composition or the analysed solution is known approximately, identification of the substance contained in a particular spot by its positional coordinates is frequently adequate. HPTLC provides the means not only for flexible screening procedures but also for demanding quantitative determinations. HPTLC features highly sensitive scanning densitometry and video technology for rapid chromatogram evaluation and documentation. [Pg.222]

In the study of effects of ultrasound on the aqueous reactions of nickel, we found some interesting results, for example, the colloidal formation of Ni-DMG complex and degassing of NH3 during different experiments. When 25 ml of 0.001 M NiSC>4 solution was complexed with 5 ml of 1% dimethyl glyoxime (DMG) in faintly alkaline ammonia medium and sonicated for 30 minutes and compared with another set of 25 ml of complexed solution which was stirred mechanically, a colloidal solution of Ni-DMG complex was formed in sonicated condition. Particles of Ni-DMG complex did not settle even after keeping 3 1 h because of their smaller size, in sonicated solution, whereas in the unsonicated condition large particles of Ni-DMG complex settled down immediately. [Pg.240]


See other pages where Complexes solution is mentioned: [Pg.132]    [Pg.53]    [Pg.481]    [Pg.52]    [Pg.2132]    [Pg.188]    [Pg.354]    [Pg.78]    [Pg.78]    [Pg.79]    [Pg.830]    [Pg.94]    [Pg.346]    [Pg.5]    [Pg.332]    [Pg.333]    [Pg.413]    [Pg.414]    [Pg.414]    [Pg.415]    [Pg.170]    [Pg.151]    [Pg.176]    [Pg.95]    [Pg.69]    [Pg.226]    [Pg.168]    [Pg.539]    [Pg.649]    [Pg.1207]   
See also in sourсe #XX -- [ Pg.328 ]




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2:3 lanthanide complexes aqueous solution

APPLICATIONS OF QUANTUM CHEMISTRY TO METAL COMPLEXES IN AQUEOUS SOLUTIONS

Absorbance complex solutions

Absorption spectra of lanthanide complexes in solutions

Adsorption from electrolyte solutions Surface complexation models

Algorithm for Solution of Complex Reactions

Aluminium to thallium salts of oxoacids, aqueous solution chemistry and complexes

Aluminum solute complexes, structure

Aqueous solution chemistry and complexes

Aqueous solution chemistry and macrocyclic complexes

Aqueous solution chemistry including macrocyclic complexes

Aqueous solution cyano complexes

Binding of Platinum Complexes in Solution

Borate complexes in aqueous solution

Carbonato Complexes in Acidic Solution

Cementation and Prevention of it by Deposition from the Complex Salt Solutions

Characterization of Inclusion Complexation in Solution State

Chlorine atom-solute complexes

Chloro complexes in solution

Chromium complexes aqueous solutions

Chromium complexes solution studies

Chromium complexes, absorption solutions

Competitive solution/surface complexation

Complex corresponding solutions

Complex equilibria in solution

Complex formation in aqueous solutions

Complex ideal solid solutions

Complex ions in aqueous solution

Complex ions in solution

Complex modulus concentrated solutions

Complex modulus dilute solutions

Complex oxides and their solid solution of irons

Complex salt solutions

Complex viscosity concentrated solutions

Complex viscosity dilute solutions

Complexation in dilute solutions

Complexation solutions

Complexes in aqueous solution

Complexes in neutral and alkaline solution

Complexes in non-aqueous solutions

Complexes in solutions

Complexes soil solution

Complexes solution-phase-based noncovalent

Complexing solution

Complexing solution

Composition of Complexes in Solution

Conjugated diene complexes NMR spectra of, in solution

Coordination complexes formation in aqueous solution

Copper complexes aqueous solution chemistry

Cyclodextrin solute inclusion complexation

Cyclodextrin-solute complexation

Cyclodextrin-solute complexation dependence

Cyclodextrin-solute complexes

DMSO solution complexes

Distribution of Complexes and Ligands in the Solution

Electrodeposited Films of Nickel -Complexes in Alkaline Solution

Equilibrium in the Solutions of Complex Compounds

Eu(III) Complex Speciation in Solution Number of Excitation Peaks

Exact solution for probabilities of complex particles

Experiments with Dihydrogen-Bonded Complexes in Solutions

Finding complex solutions

Glimmers of Complexity Three-Configuration Solutions

Group complex ions in aqueous solution

Hafnium complexes aqueous solutions

Halide complexes in aqueous solutions

Homoleptic complexes solution properties

Hydride complex, solutions

Hydroxo complexes in acidic or neutral solutions

Hydroxo complexes in alkaline solutions

Inorganic complexes aqueous solutions

Inorganic complexes solutions

Intermolecular complexations in solution

Kinetics of complexation in aqueous solution

Lanthanide complexes in aqueous solution

Lanthanide complexes in solutions

Lanthanum nitrate complexes aqueous solution

Macromolecular complex formation aqueous solution

Metal cation-carbohydrate complexes solution

Metal complexes in soil solution

Metallonitrosyls in aqueous solution, redox complexes with

Metals solution complexation reactions

Multiple complex formation with solutes

Nickel complexes in solution

Nonlinear algebraic systems complex solutions

Numerical solution surface complexation calculations

Numerical solution, of complex

Numerical solution, of complex flow models

Oxovanadium complexes aqueous solution

Photolysis of the Complex Salt Solution

Phthalocyanines Complexes in Solution

Platinum complexes in solution

Polymeric solutions complexity

Polynuclear complexes in solution

Porphyrins complexes in solution

Proton complexes solution chemistry

Reaction kinetics in complex solutions

Reactions of Excited Metal Complexes in Solid Matrices and Liquid Solutions

Soil solution inner sphere complexation Table

Soil solutions amino acid metal complexes

Solid—solution interface, surface complexation

Solute-CSP complexes

Solute-hydrogen complexes

Solute-solvent complex

Solute-solvent complex stability

Solute-solvent complexation

Solute-solvent hydrogen-bonded complexe

Solute-vacancy/-complexes

Solution Chemistry of Proton Complexes

Solution Chemistry of Rare Earth Complexes with Amino Acids

Solution Chemistry of Rare Earth Complexes with Polyaminopolycarboxylic Acids

Solution Complexes with Cations

Solution Complexes with Neutral Molecules

Solution complex formation, effect

Solution complexation 1197 --- cancer

Solution complexation reactions

Solution complexation, versus

Solution complexation, versus solvent water

Solution for complex eigenvalues

Solution of Complex Equations

Solution phase models complex’ model

Solution state complexes

Solution structures, chromium complexes

Solution-phase reactions, surface complexation models

Solutions and charge-transfer complexes

Solutions metal complexes

Solutions, aqueous halogeno complexes

Square-planar complexes, in solution

Stability of metal complexes in solution

Starch, complexes salt solutions

Starch, complexes solutions

Structure of Complexes in Solution

Structure of Complexes in Solution Derived from X-Ray Diffraction

Surface complexation models oxide-solution interface

Surface complexation models solid-solution interface

Tantalum and niobium complexes in fluoride solutions

The Carbonylation of Methanol Catalyzed by Rhodium Complexes in Solution

Transition-metal complexes solutions

Triazines solution complexes

Zirconium complexes aqueous solution

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