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Fluoride masking

The absorbance of the Co(III) complex solution may be measured with higher sensitivity at 415-425 nm, or with lower sensitivity at 500-520 nm (a reagent blank, or water as reference). The reaction of cobalt with nitroso-R salt is usually done in a hot weakly acidic medium buffered with sodium acetate. The solution is then made sufficiently acidic with hydrochloric or nitric acid to decompose the nitroso-R salt complexes of other metals (e.g., Cu, Ni, Fe, and Mn), which are less stable than the cobalt(III) complex. Phosphate or fluoride masks iron (III), which has a yellow colour in hydrochloric acid medium. [Pg.170]

Most interfering cations are masked with EDTA. Tartrate masks milligram quantities of Ta, Ti, W, Mo, Sb(V), and Sn(IV) U(VI) and Zr can be masked with phosphate fluoride masks A1 and Th cyanide masks any silver present. The interfering effect of Ce(IV) and V(V) can be eliminated by addition of ascorbic acid which reduces them to Ce(III) and V(IV), respectively. Thus, the BPR method can be regarded as specific, provided that... [Pg.295]

Masking can be achieved by precipitation, complex formation, oxidation-reduction, and kinetically. A combination of these techniques may be employed. For example, Cu " can be masked by reduction to Cu(I) with ascorbic acid and by complexation with I . Lead can be precipitated with sulfate when bismuth is to be titrated. Most masking is accomplished by selectively forming a stable, soluble complex. Hydroxide ion complexes aluminum ion [Al(OH)4 or AlOa"] so calcium can be titrated. Fluoride masks Sn(IV) in the titration of Sn(II). Ammonia complexes copper so it cannot be titrated with EDTA using murexide indicator. Metals can be titrated in the presence of Cr(III) because its EDTA chelate, although very stable, forms only slowly. [Pg.305]

Another type of demasking involves formation of new complexes or other compounds that are more stable than the masked species. For example, boric acid is used to demask fluoride complexes of tin(IV) and molybdenum(VI). Formaldehyde is often used to remove the masking action of cyanide ions by converting the masking agent to a nonreacting species through the reaction ... [Pg.1170]

Show that F is an effective masking agent in preventing a reaction of AP+ with EDTA. Assume that the only significant forms of fluoride and EDTA are F and Y. ... [Pg.229]

The ACGIH adopted TLV/TWA for 1992—1993 for fluorides as F is TWA 2.5 mg/m, and for cobalt as Co metal dust TWA 0.05 mg/m. Dust masks should be used while handling both the cobalt fluorides and all other cobalt compounds. CoF is shipped as an oxidizer and a corrosive material. [Pg.178]

Highly irritating and poisonous Very soluble in water. Liquid liberates heat as it dissolves in water. The entrapment of water in an anhydrous hydrogen fluoride cylinder can cause rapid generation of heat and pressure which can lead to an explosion. Containers should never be heated to >52°C. A liquid hydrogen fluoride spill area should not be entered unless protective clothing (impervious to the compound) and a self-contained gas mask are worn Fumes in air... [Pg.134]

Because of the hazardous nature of anhydrous hydrogen fluoride, adequate precautions should he taken to protect the head, eyes, and skin. Rubber gloves, an apron, and a plastic face mask are strongly recommended. All operations should be carried out in a hood. If hydrogen fluoride comes in contact with the skin, the contacted area should be thoroughly washed with water and then immersed in ice water while the patient is taken to a physi-... [Pg.58]

It is therefore possible to determine cations such as Ca2+, Mg2+, Pb2+, and Mn2+ in the presence of the above-mentioned metals by masking with an excess of potassium or sodium cyanide. A small amount of iron may be masked by cyanide if it is first reduced to the iron(II) state by the addition of ascorbic acid. Titanium(IV), iron(III), and aluminium can be masked with triethanolamine mercury with iodide ions and aluminium, iron(III), titanium(lV), and tin(II) with ammonium fluoride (the cations of the alkaline-earth metals yield slightly soluble fluorides). [Pg.313]

The effect of different ions upon the titration is similar to that given under iron(III) (Section 17.57). Iron(III) interferes (small amounts may be precipitated with sodium fluoride solution) tin(IV) should be masked with 20 per cent aqueous tartaric acid solution. The procedure may be employed for the determination of copper in brass, bronze, and bell metal without any previous separations except the removal of insoluble lead sulphate when present. [Pg.724]

The procedure utilises eriochrome blue black RC (also called pontachrome blue black R Colour Index No. 15705) at a pH of 4,8 in a buffer solution. Beryllium gives no fluorescence and does not interfere iron, chromium, copper, nickel, and cobalt mask the fluorescence fluoride must be removed if present. The method may be adapted for the determination of aluminium in steel. [Pg.737]

Sakurai reactions proceed regiospecifically with a large variety of electrophiles due to the so-called /1-effect5-9. However, allylsilanes are also known as masked allyl carbanions, which may be activated by the presence of fluoride ion10-12. [Pg.937]

P 55] Before synthesis, a micro-mixing tee chip micro reactor (Figure 4.85) (with two mixing tees and four reservoirs) was primed with anhydrous tetrahydrofuran (THF). A 40 gl volume of a 0.1 M solution of tetrabutylammonium fluoride trihydrate in anhydrous THF is filled into one reservoir of a micro-mixing tee chip reactor [15], 40 gl of a 0.1 M solution of 4-bromobenzaldehyde in anhydrous THF is added to a second reservoir, 40 gl of a 0.1 M solution of the silyl enol ether (masking the enolate of a carbonyl compound such as cyclohexanone) in anhydrous THF is added to a third reservoir and anhydrous TH F is filled into the fourth collection reservoir. Electrical fields of417,455,476 and 0 V cm are applied to transport the reaction species from the respective reservoirs. The reaction is carried out at room temperature. [Pg.529]

The isopropenyl side chain may derive by elimination of a tertiary alcohol or ether as in 202. Such a masking of the olefin avoids a possible competing vinylcyclopropane rearrangement. The correspondence of the cyclopentene of 202 with the vinylcyclopropane in 203 now becomes obvious. The presence of the dimethylcarbinol side chain now also offers the opportunity for its introduction by addition of a cyclopropyl anion to acetone. The feasibility of creating such an anion by fluoride initiated desilylation... [Pg.78]

In addition to metal ions, detection of halides such as fluoride is important, as the latter is often present in nerve gases and nuclear weapons manufacture. Our group utilized the unique reactivities of F with Si to specifically sense for fluoride ions [30]. PArE 35 was constructed with a masked precursor to a flu-... [Pg.165]

The preparation of ethynylpurines was achieved through the use of protected acetylenes. Hocek and co-workers coupled halopurines with trimethysilylacetylene to introduced the masked ethyne function, which was efficiently released on treatment with fluorides or base (8.26.).35 The same compounds were also prepared by Hayashi and Kotschy, who used 2-methyl-3-butyn-2-ol as acetylene source and a strong base to remove the protecting group from the acetyl moiety.36... [Pg.186]


See other pages where Fluoride masking is mentioned: [Pg.245]    [Pg.288]    [Pg.245]    [Pg.288]    [Pg.671]    [Pg.1169]    [Pg.10]    [Pg.190]    [Pg.155]    [Pg.265]    [Pg.17]    [Pg.84]    [Pg.184]    [Pg.41]    [Pg.671]    [Pg.150]    [Pg.380]    [Pg.192]    [Pg.1438]    [Pg.403]    [Pg.355]    [Pg.75]    [Pg.98]    [Pg.154]    [Pg.167]    [Pg.322]    [Pg.161]    [Pg.288]    [Pg.293]    [Pg.417]    [Pg.69]    [Pg.81]    [Pg.323]   
See also in sourсe #XX -- [ Pg.9 , Pg.288 ]




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