Chloride ions determination

Figure 4, Structure of a series of alkyl bromides and the rate constants (1 O " cm s ) for the IM reaction of each compound with the chloride ion, determined by the photodetachment-modulated electron capture detector (PDM-ECD) in 10% argon-inmethane buffer gas at atmospheric pressure and 125 °C. ...

Specihc functional groups are also analyzed by chemical methods. For example, the various chlorosilanes can be hydrolyzed and the resulting chloride ions determined by... 

In all reactions involving X, Cl" as well as Br has been assumed. Because of the large quantities of chloride ions determined by aqueous extraction, its role in the wirebond degradation process is considered to be fairly important. From the above discussion, it seems very likely that elimination... 

A column of silver chloranilate was used for chloride ion determination in a FIA system. According to reaction 3, the column liberates into the solution violet chloranilate ions (38), that are measured with a spectrophotometric detector at 530 nm. The method is fast (30 samplesh-1) and was applied to the analysis of fresh and waste waters (1-20 ppm Cl-) with negligible interference of other anions107. 

Hence, we see that if we do not remove the silver chloride precipitate, an excess of thiocyanate ions is added and the chloride ions determination is endowed with a... 

Four different methods are applicable to an investigation of the kinetics of reaction (21). One approach is to determine the amount of chloride ion in solution as a function of time by any of the various analytical methods for chloride ion determination. Another is to follow the change in color of the reaction mixture over a period of time. In practice this is done spectro-photometrically at one or more wavelengths known to give the maximum difference in optical density between reactant and product. It is also apparent from Eq. (21) that the reaction results in an increase in the number of ions in solution. The rate of reaction can therefore be followed by intermittent conductivity measurements. The fourth method that can be applied is one taking advantage of the acidity of [Co(NH3)6H20] +(pKa 5.7). The amount of this acid product in solution can be determined at various... 

The development of scanning probe microscopies and x-ray reflectivity (see Chapter VIII) has allowed molecular-level characterization of the structure of the electrode surface after electrochemical reactions [145]. In particular, the important role of adsorbates in determining the state of an electrode surface is illustrated by scanning tunneling microscopic (STM) images of gold (III) surfaces in the presence and absence of chloride ions [153]. Electrodeposition of one metal on another can also be measured via x-ray diffraction [154]. 

Gravimetrically, silver nitrate is used to determine the chloride ion. 

Oxygen and nitrogen also are deterrnined by conductivity or chromatographic techniques following a hot vacuum extraction or inert-gas fusion of hafnium with a noble metal (25,26). Nitrogen also may be deterrnined by the Kjeldahl technique (19). Phosphoms is determined by phosphine evolution and flame-emission detection. Chloride is determined indirecdy by atomic absorption or x-ray spectroscopy, or at higher levels by a selective-ion electrode. Fluoride can be determined similarly (27,28). Uranium and U-235 have been determined by inductively coupled plasma mass spectroscopy (29). 

Qualitative. The classic method for the quaUtative determination of silver ia solution is precipitation as silver chloride with dilute nitric acid and chloride ion. The silver chloride can be differentiated from lead or mercurous chlorides, which also may precipitate, by the fact that lead chloride is soluble ia hot water but not ia ammonium hydroxide, whereas mercurous chloride turns black ia ammonium hydroxide. Silver chloride dissolves ia ammonium hydroxide because of the formation of soluble silver—ammonia complexes. A number of selective spot tests (24) iaclude reactions with /)-dimethy1amino-henz1idenerhodanine, ceric ammonium nitrate, or bromopyrogaHol red [16574-43-9]. Silver is detected by x-ray fluorescence and arc-emission spectrometry. Two sensitive arc-emission lines for silver occur at 328.1 and 338.3 nm. 

Chlorine dioxide gas is a strong oxidizer. The standard reversible potential is determined by the specific reaction chemistry. The standard potential for gaseous CIO2 in aqueous solution reactions where a chloride ion is the product is —1.511 V, but the potential can vary as a function of pH and concentration (26) ... 

Other ions, eg, ferrate, chloride, and formate, are determined by first removing the cyanide ion at ca pH 3.5 (methyl orange end point). Iron is titrated, using thioglycolic acid, and the optical density of the resulting pink solution is measured at 538 nm. Formate is oxidized by titration with mercuric chloride. The mercurous chloride produced is determined gravimetricaHy. Chloride ion is determined by a titration with 0.1 Ai silver nitrate. The end point is determined electrometricaHy. 

It was found that sorbed palladium might catalyse reaction of Mn(III) reduction by Cf not only after it s removing from coal, but AC with palladium, Pd/AC, has also his own catalytic effect. On the base of dependence between characteristics of AC, chemical state of palladium on AC surface and catalytic action of Pd/AC in indicator reaction it might establish, that catalytic action concerns only to non-reduced or partly reduced palladium ions connected with chloride ions on coal surface. The presence or absence of catalytic action of Pd/AC in above-mentioned reaction may be proposed for determination of chemical state of palladium on AC surface. Catalytic effect was also used for palladium micro-amounts determination by soi ption-catalytic method. 

IQ. To determine the concentration of chloride ion, - a 5-mL aliquot of the methyl lithium solution is cautiously added to 25 ml of water and the resulting solution is acidified with concentrated sulfuric acid and then treated with 2-3 ml of ferric ammonium sulfate [Fe(NH4)( 04)2 12 H2O] indicator solution and 2-3 ml of benzyl alcohol. The resulting mixture is treated with 10.0 mL of standard aqueous 0.100 M silver nitrate solution and then titrated with standard aqueous 0.100 H potassium thiocyanate solution to a brownish-red endpoint. 

A diagnosis of possible damage should be made before beginning repairs with other construction measures [48,49]. There should be a checklist [48] of the important corrosion parameters and the types of corrosion effects to be expected. Of special importance are investigations of the quality of the concrete (strength, type of cement, water/cement ratio, cement content), the depth of carbonization, concentration profile of chloride ions, moisture distribution, and the situation regarding cracks and displacements. The extent of corrosion attack is determined visually. Later the likelihood of corrosion can be assessed using the above data. 

Again, the chloride is almost exclusively the exo isomer. The distribution of deuterium in the product was determined by NMR spectroscopy. The fact that 1 and 2 are formed in unequal amoimts excludes the symmetrical bridged ion as the only intermediate. The excess of 1 over 2 indicates fliat some syn addition occurs by ion-pair collapse before the bridged ion achieves symmetry with respect to the chloride ion. If the amount of 2 is taken as an indication of the extent of bridged-ion involvement, one would conclude that 82% of the reaction proceeds through this intermediate, which must give equal amoimts of 1 and 2. 

During the next fifty years the interest in derivatives of divalent carbon was mainly confined to methylene (CHg) and substituted methylenes obtained by decomposition of the corresponding diazo compounds this phase has been fully reviewed by Huisgen. The first convincing evidence for the formation of dichlorocarbene from chloroform was presented by Hine in 1950. Kinetic studies of the basic hydrolysis of chloroform in aqueous dioxane led to the suggestion that the rate-determining step was loss of chloride ion from the tri-chloromethyl anion which is formed in a rapid pre-equilibrium with hydroxide ions ... 

The shape of a vessel determines how well it drains (Figure 53.7). If the outlet is not at the very lowest point process liquid may be left inside. This will concentrate by evaporation unless cleaned out, and it will probably become more corrosive. This also applies to horizontal pipe runs and steam or cooling coils attached to vessels. Steam heating coils that do not drain adequately collect condensate. This is very often contaminated by chloride ions, which are soon concentrated to high enough levels (10-100 ppm) to pose serious pitting and stress corrosion cracking risks for 300-series austenitic stainless steel vessels and steam coils. 

Suzuki, Yamake and Kitamura determined the pHs, chloride ion concentrations, metal ion concentrations and the potentials of artificial pits in Fe, Cr, Ni and Mo, and in three austenitic stainless steels during anodic polarisation in 0-5 N NaCl at 70°C. In the case of the pure metals the pH values were found to be lower than those calculated from the metal ion concentrations (Table 1.17), and the experimentally determined pHs were as follows ... 

The general approach illustrated by Example 18.7 is widely used to determine equilibrium constants for solution reactions. The pH meter in particular can be used to determine acid or base equilibrium constants by measuring the pH of solutions containing known concentrations of weak acids or bases. Specific ion electrodes are readily adapted to the determination of solubility product constants. For example, a chloride ion electrode can be used to find [Cl-] in equilibrium with AgCl(s) and a known [Ag+]. From that information, Ksp of AgCl can be calculated. 

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