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Ionic color

Iron is associated with silica sand, usually as a light surface stain on the grains. Amber glass develops ionic color centers or complexes of Fe-S-C added to the batch as iron sulfide and powdered anthracite. Although the Fe content be four or five times that shown in the example in Table I, it appears to be bound in the complex so that no greater extraction occurs with the S and C. Titanium is associated with sand as... [Pg.25]

Acid Wool (hair) Acetic add Affinity by ionic Color... [Pg.284]

Most of the qualitative relationships between color and structure of methine dyes based on the resonance theory were established independently during the 1940 s by Brooker and coworkers (16, 72-74) and by Kiprianov (75-78), and specific application to thiazolo dyes appeared later with the studies of Knott (79) and Rout (80-84). In this approach, the absorptions of dyes belonging to amidinium ionic system are conveyed by a group of contributing structures resulting from the different ways of localization of the 2n rr electrons on the 2n l atoms of the chromophoric cationic chain, rather than by a single formula ... [Pg.68]

A great number of monoaza or polyaza. either symmetrica] or unsym-metrical, mono trimethine thiazolocyainines have been synthesized in order to verify or to obtain semiempirical rules, more or less based on the resonance theory, concerning the relation between the color of a thiazolo dye and the number and place of nitrogen atoms in the chromophoric chain. For example. Forster s rule applies to ionic dyes and stipulates that the will increase with the decreasing tendency of chromophoric atoms lying between the two auxochromes to take up the characteristic charges (90). [Pg.78]

The actinide elements exhibit uniformity in ionic types. In acidic aqueous solution, there are four types of cations, and these and their colors are hsted in Table 5 (12—14,17). The open spaces indicate that the corresponding oxidation states do not exist in aqueous solution. The wide variety of colors exhibited by actinide ions is characteristic of transition series of elements. In general, protactinium(V) polymerizes and precipitates readily in aqueous solution and it seems unlikely that ionic forms ate present in such solutions. [Pg.218]

Maleic acid and fumaric acid can also be, and are often, incorporated in alkyd resins in the form of the Diels-Alder adduct of rosin. The adducts are tribasic acids which provide pendent carboxyl groups in the resin molecules, which can be saponified to give ionic, and, in turn, water-soluble characteristics to the resin. However, the resultant alkyds often have poorer color retention, toughness, gloss retention, and exterior durabiUty. [Pg.33]

Silver bromide crystals, formed from stoichiometric amounts of silver nitrate and potassium bromide, are characterized by a cubic stmcture having interionic distances of 0.29 nm. If, however, an excess of either ion is present, octahedral crystals tend to form. The yellow color of silver bromide has been attributed to ionic deformation, an indication of its partially covalent character. Silver bromide melts at 434°C and dissociates when heated above 500°C. [Pg.89]

Color from Transition-Metal Compounds and Impurities. The energy levels of the excited states of the unpaked electrons of transition-metal ions in crystals are controlled by the field of the surrounding cations or cationic groups. Erom a purely ionic point of view, this is explained by the electrostatic interactions of crystal field theory ligand field theory is a more advanced approach also incorporating molecular orbital concepts. [Pg.418]

Another desirable property for a ceramic color is a high refractive index. For example, valuable pigments are based on spinels [1302-67-6] ( 2jj = 1.8) and on zircon ( 2j = 1.9), but no valuable pigments are based on apatite ( 2j = 1.6), even though the lattice of apatite is as versatile for making ionic substitutions as that of spinel. [Pg.426]

Table 3 is arranged by crystal class (14). The crystal class of a given pigment is determined almost solely by the ratio of the ionic sizes of the cation and the anion and thek respective valences. Hence, for any given stoichiometry and ionic size ratio, only one or two stmctures will be possible. In some classes (spkiel, zkcon), a wide range of colors is possible within the confines of that class. Pigments within a given class usually have excellent chemical and... [Pg.427]

Wool—Acrylic Fibers. This blend is being used for iadustrial and hand knitting yams. The acryHc fiber is aesthetically similar to wool, iacreases the strength of the yam, and adds bulk to the goods. Special precautions are necessary siace the two fibers are colored with dyes of opposite ionic type. Coprecipitation is prevented with the use of an antiprecipitant. Usually, level dyeing acid dyes are used for the wool portion in combination with the cationic dyes for acryHc fiber. [Pg.366]

In accordance with these data, ionic associates (lA) can be precipitated at phosphate concentrations more than 10 M. Below this concentration stabile supersaturated solutions of lA are formed. Colour of lA appeal s immediately after mixing of the solutions and remains constant during several hours. There is a new band in spectmm at 570-590 nm. Appearance of color is caused by formation of stable solid phase in the solution. [Pg.87]

Section 2.1 excellently describes methods used to produce colorless ionic liquids. From this it has become obvious that freshly distilled starting materials and low-temperature processing during the synthesis and drying steps are key aspects for avoidance of coloration of the ionic liquid. [Pg.23]

A compromise between coloration and economics in commercial ionic liquid production is therefore necessary. Since chromatographic decoloration steps are known and relatively easy to perform (see Section 2.2.3), we would not expect there to be a market for a colorless ionic liquid, if the same substance can be made in a slightly colored state, but at a much lower price. [Pg.24]

A number of different methods to monitor the amount of methylimidazole left in a final ionic liquid are known. NMR spectroscopy is used by most academic groups, but may have a detection limit of about 1 mol%. The photometric analysis described by Holbrey, Seddon, and Wareing has the advantage of being a relatively quick method that can be performed with standard laboratory equipment [13]. This makes it particularly suitable for monitoring of the methylimidazole content during commercial ionic liquid synthesis. The method is based on the formation and colorimetric analysis of the intensely colored complex of l-methylimidazole with cop-per(II) chloride. [Pg.25]

For all research carried out with commercial ionic liquids we recommend a serious quality check of the product prior to work. As already mentioned, a good commercial ionic liquid may be colored and may contain some traces of water. However, it should be free of organic volatiles, halides (if not an halide ionic liquid), and all ionic impurities. [Pg.27]

Regarding the color, we only see a need for colorless ionic liquids in very specific applications (see above). One easy treatment that often reduces coloration quite impressively, especially of imidazolium ionic liquids, is purification by column chromatography/filtration over silica 60. For this purification method, the ionic liquid is dissolved in a volatile solvent such as CFF2C12. Usually, most of the colored impurities stick to the silica, while the ionic liquid is eluted with the solvent. By repetition of the process several times, a seriously colored ionic liquid can be converted into an almost completely colorless material. [Pg.28]

Polycyclic aromatic hydrocarbons dissolve in chloroaluminate(III) ionic liquids to give brightly colored solutions (due to the protonated aromatic compound [31]). The... [Pg.179]

Flowever, ionic liquids acting as transition metal catalysts are not necessarily based on classical Lewis acids. Dyson et al. recently reported the ionic liquid [BMIM][Co(CO)4] [38]. The system was obtained as an intense blue-green colored liquid by metathesis between [BMIM]C1 and Na[Co(CO)4]. The liquid was used as a catalyst in the debromination of 2-bromoketones to their corresponding ketones. [Pg.225]

The precipitation diagram shown in Figure 4.3 enables you to determine whether or not a precipitate will form when dilute solutions of two ionic solutes are mixed. If a cation in solution 1 mixes with an anion in solution 2 to form an insoluble compound (colored squares), that compound will precipitate. Cation-anion combinations that lead to the formation of a soluble compound (white squares) will not give a precipitate. For example, if solutions of NiCl2 (Ni2+, Cl- ions) and NaOH (Na+, OH- ions) are mixed (Figure 4.4)—... [Pg.78]

A solution of potassium dichromate is made basic with sodium hydroxide the color changes from red to yellow. Addition of silver nitrate to the yellow solution gives a precipitate. This precipitate dissolves in concentrated ammonia but re-forms when nitric acid is added. Write balanced net ionic equations for all the reactions in this sequence. [Pg.553]


See other pages where Ionic color is mentioned: [Pg.516]    [Pg.226]    [Pg.27]    [Pg.567]    [Pg.567]    [Pg.516]    [Pg.226]    [Pg.27]    [Pg.567]    [Pg.567]    [Pg.943]    [Pg.1170]    [Pg.197]    [Pg.545]    [Pg.214]    [Pg.492]    [Pg.347]    [Pg.251]    [Pg.13]    [Pg.171]    [Pg.350]    [Pg.495]    [Pg.276]    [Pg.122]    [Pg.17]    [Pg.23]    [Pg.24]    [Pg.24]    [Pg.26]    [Pg.37]    [Pg.227]    [Pg.154]    [Pg.684]    [Pg.684]   
See also in sourсe #XX -- [ Pg.28 , Pg.682 ]




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