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Neutral solutions, from

EL pyridine-phenylene copolymers 564 [666] and 565 [667] have been synthesized and studied by Bryce and coworkers. Although a rather low el(<0.1%) was reported for the devices, an interesting phenomenon was found for polymers 565. When the PLED (ITO/PEDOT/565/Ca/Al) was fabricated using acidic solutions, a strong red shift in the EL band compared to that obtained with the neutral solution (from 510 to 575 nm) was observed. The authors explained this concept by planarization of the protonated polymer chain as a result of intramolecular hydrogen bonding N H- O. Variation of pyridine linkage in copolymers 565, 566, and 567 affects the PL and EL emissions (AEL = 444, 432,... [Pg.233]

Chloro-6-desoxy-3,5-benzylidene-l,4-anhydro-D-sorbitol (XVI) possesses an unusual property in that the benzylidene group is removed by distillation in alkaline or neutral solution. From the neutral solution it was possible to isolate 6-chloro-6-desoxy-l,4-anhydro-D-sorbitol as its triacetyl derivative. At the same time diacetyl-1,4 3,6-dianhydro-D-sorbitol was also formed. This removal of an acetal residue from a... [Pg.210]

Ionization of phenolic hydroxyl groups in lignin with alkali causes a batho-chromic shift and a hyperchromic effect in the absorption spectrum. An alkaline ionization difference spectrum is obtained by subtracting the spectrum of the solute in a neutral solution from the corresponding spectrum measured in an alkaline medium. The difference spectrum may be measured directly with a spectrophotometer according to the following procedure ... [Pg.221]

Test with iron(III) chloride solution Treat the other portion of the neutral solution from test 5 with aqueous iron(III) chloride solution. [Pg.556]

In a 25-ml standard flask place 5 ml of a 1 1 mixture of ammonium molybdate solution and 1 M sulphuric acid, and add 3 ml of acetone and an aliquot of sample solution e.g., neutralized solution from sodium carbonate fusion) containing not more than 0.2 mg of Si. Dilute to the mark with water, mix well, let stand for 15 min, and measure the absorbance at... [Pg.387]

Strategy The aim is to find the values of and v corresponding to the reaction, for then we can use a modified form of eqn 5.16 to calculate the value of K in neutral solution from fd. To do so, we express the equation as the difference of two reduction half-reactions. The stoichiometric number of the electron in these matching half-reactions is the value of v we require. We then look up the biological standard potentials for the couples corresponding to the half-reactions and calculate their difference to find... [Pg.204]

Reduced chalcogens. Sulfane, H2S, does not precipitate Al fium acidic or neutral solution from alkaline Al(OH)4 H2S precipitates Al203-aq if enough is used to neutralize the alkali (distinction from Zn, which is rapidly precipitated as ZnS from solutions not too alkaline). [Pg.313]

Solutes bound to micellar and microemulsion aggregates are in rapid equilibrium with free solute and aggregates. Rate constants for the exit of neutral solutes from ionic micelles are estimated at 10 -10 s ". Rates for recapture are near or at diffusion control. Rates of these processes are similar to equilibration rates between micelles and surfactant momomers. Solutes in micelles and microemulsions are most probably solubilized near the Stern layer or in the interfacial region. Hydrophilic or hydrophobic environments will be preferred depending on the properties of the particular solutie. There is little evidence for deep solute penetration into the core of the aggregate. Vesicles have much slower dynamics of solute equilibria. [Pg.566]

Step 4. The steam-volatile neutral compounds. The solution (containing water-soluble neutral compounds obtained in Step 1 is usually very dilute. It is advisable to concentrate it by distillation until about one-third to one-half of the original volume is collected as distillate the process may be repeated if necessary and the progress of the concentration may be followed by determination of the densities of the distillates. It is frequently possible to salt out the neutral components from the concentrated distillate by saturating it with solid potassium carbonate. If a layer of neutral compound makes its appearance, remove it. Treat this upper layer (which usually contains much water) with solid anhydrous potassium carbonate if another aqueous layer forms, separate the upper organic layer and add more anhydrous potassium carbonate to it. Identify the neutral compound. [Pg.1099]

The urea produced is normally either prilled or granulated. In some countries there is a market for Hquid urea—ammonium nitrate solutions (32% N). In this case, a partial-recycle stripping process is the best and cheapest system. The unconverted NH coming from the stripped urea solution and the reactor off-gas is neutralized with nitric acid. The ammonium nitrate solution formed and the urea solution from the stripper bottom are mixed, resulting in a 32—35 wt % solution. This system drastically reduces investment costs as evaporation, finishing (priQ or granulation), and wastewater treatment are not required. [Pg.300]

L-Glutamic acid does not racemize in neutral solution, even at 100°C. Deviation of pH from neutral to greater than 8.5 results in thermal racemization with loss of taste characteristics. Racemization in neutral solution occurs at 190 °C after formation of the lactam, 5-oxo-L-proline, pyroglutamic acid [98-79-3]. [Pg.303]

Arsenates are oxidizing agents and are reduced by concentrated hydrochloric acid or sulfur dioxide. Treatment of a solution of orthoarsenate with silver nitrate in neutral solution results in the formation of a chocolate-brown precipitate of silver orthoarsenate, Ag AsO, which may be used as a test to distinguish arsenates from phosphates. With hydrofluoric acid, orthoarsenate solutions yield hexafluoroarsenates, eg, potassium hexafluoroarsenate [17029-22-0] (KAsFg)2 H2O. Arsenates of calcium or lead are used as insecticides sodium arsenate is used in printing inks and as a mordant. [Pg.334]

After being removed from the neutralizing solution, the ware is transferred to a dryer maintained at about 110—120°C that has good air circulation. This ensures quick and complete drying without msting of the metal. After being dried, the sheet ware is ready for apphcation of enamel. [Pg.212]

Thiazolidines have been prepared from /3-aminothiols—for example, cysteine—to protect the —SH and — NH groups during syntheses of peptides, including glu-tathione. Thiazolidines are oxidized to symmetrical disulfides with iodine they do not react with thiocyanogen in a neutral solution. [Pg.292]

Lead (II) bromide [10031-22-8] M 367.0, m 373°. Crystallised from water containing a few drops of HBr (25mL of water per gram PbBr2) between 100° and 0°. A neutral solution was evaporated at 110° and the crystals that separated were collected by rapid filtration at 70°, and dried at 105° (to give the monohydrate). To prepare the anhydrous bromide, the hydrate is heated for several hours at 170° and then in a Pt boat at 200° in a stream of HBr and H2. Finally fused [Clayton et al. J Chem Soc, Faraday Trans 1 76 2362 1980]. [Pg.434]

H2O). Crystallise from a small volume of H2O (sol 59g/100mL at 25°), or dissolve in H2O and add EtOH since it is sparingly soluble in EtOH. Insoluble in Et20. It forms a Cu comples in alkaline soln and a complex with Fe in neutral solution. [J Am Chem Soc 81 5302 7959.]... [Pg.471]

Data exist for die endialpy of chemical reactions, formation of substances from dieir constituent elements, combustion, fusion, neutralization, solution, vaporization, etc. [Pg.42]

Anionic and neutral polymers are usually analyzed successfully on Syn-Chropak GPC columns because they have minimal interaction with the appropriate mobile-phase selection however, cationic polymers adsorb to these columns, often irreversibly. Mobile-phase selection for hydrophilic polymers is similar to that for proteins but the solubilities are of primary importance. Organic solvents can be added to the mobile phase to increase solubility. In polymer analysis, ionic strength and pH can change the shape of the solute from mostly linear to globular therefore, it is very important to use the same conditions during calibration and analysis of unknowns (8). Many mobile phases have been used, but 0.05-0.2 M sodium sulfate or sodium nitrate is common. [Pg.316]

Separation of Se and Te can also be achieved by neutralizing the alkaline selenite and tellurite leach with H2SO4 this precipitates the tellurium as a hydrous dioxide and leaves the more acidic selenous acid, H2Se03, in solution from which 99.5% pure Se can be precipitated by S02 ... [Pg.749]


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