Zirconium determination

It is of interest to mention here the contribution of Baiulescu and Turcu14 for developing a tartrazine agent for zirconium determination ... 

This reagent reacts well with zirconium, obtaining a compound with a stoichiometric ratio Zr3Tz(OOH)3. It enables zirconium determination with good sensitivity and selectivity. Using this reagent, the authors demonstrated that it is possible to obtain stoichiometric compounds, with an ion that forms in solution hydrolysis, and polymeric compounds. 

The preparation and structure determination of ferrocene marked the beginning of metallocene chemistry Metallocenes are organometallic compounds that bear cyclo pentadiemde ligands A large number are known even some m which uranium is the metal Metallocenes are not only stucturally interesting but many of them have useful applications as catalysts for industrial processes Zirconium based metallocenes for example are the most widely used catalysts for Ziegler-Natta polymerization of alkenes We 11 have more to say about them m Section 14 15... 

The concentration of fluoride in drinking water may be determined indirectly by its ability to form a complex with zirconium. In the presence of the dye SPADNS, solutions of zirconium form a reddish colored compound, called a lake, that absorbs at 570 nm. When fluoride is added, the formation of the stable ZrFe complex causes a portion of the lake to dissociate, decreasing the absorbance. A plot of absorbance versus the concentration of fluoride, therefore, has a negative slope. 

Analyses of alloys or ores for hafnium by plasma emission atomic absorption spectroscopy, optical emission spectroscopy (qv), mass spectrometry (qv), x-ray spectroscopy (see X-ray technology), and neutron activation are possible without prior separation of hafnium (19). Alternatively, the combined hafnium and zirconium content can be separated from the sample by fusing the sample with sodium hydroxide, separating silica if present, and precipitating with mandelic acid from a dilute hydrochloric acid solution (20). The precipitate is ignited to oxide which is analy2ed by x-ray or emission spectroscopy to determine the relative proportion of each oxide. 

Zirconium is often deterniined gravimetrically. The most common procedure utilizes mandelic acid (81) which is fairly specific for zirconium plus hafnium. Other precipitants, including nine inorganic and 42 organic reagents, are Hsted in Reference 82. Volumetric procedures for zirconium, which also include hafnium as zirconium, are limited to either EDTA titrations (83) or indirect procedures (84). X-ray fluorescence spectroscopy gives quantitative results for zirconium, without including hafnium, for concentrations from 0.1 to 50% (85). Atomic absorption determines zirconium in aluminum in the presence of hafnium at concentrations of 0.1—3% (86). 

Linear dependence of current of additional peak 1 on concentration of Zr(IV) can be used for elaboration sensitive and selective determination of zirconium with detection limit of 1.7x10 mol/1. 

The chemical identities of the fission products determine their subsequent redistribution, those elements which are in the gaseous state at the temperature of the operation migrating to the cooler exterior of the fuel rods, and die less voltile elements undergoing incorporation in the fuel rod in solid solution. Thus caesium and iodine migrate to the gas fill which sunounds the fuel rod, and elements such as the rare earths and zirconium are accommodated in solid solution in UO2 without significant migration along the fuel rod radius. Strontium and barium oxidize to form separate islands which can be seen under the microscope. 

Polypropylenes produced by metallocene catalysis became available in the late 1990s. One such process adopts a standard gas phase process using a metallocene catalyst such as rac.-dimethylsilyleneto (2-methyl-l-benz(e)indenyl)zirconium dichloride in conjunction with methylaluminoxane (MAO) as cocatalyst. The exact choice of catalyst determines the direction by which the monomer approaches and attaches itself to the growing chain. Thus whereas the isotactic material is normally preferred, it is also possible to select catalysts which yield syndiotactic material. Yet another form is the so-called hemi-isotactic polypropylene in which an isotactic unit alternates with a random configuration. 

Determination of cerium as cerium(IV) iodate and subsequent ignition to cerium(IV) oxide Discussion. Cerium may be determined as cerium(IV) iodate, Ce(I03)4, which is ignited to and weighed as the oxide, Ce02. Thorium (also titanium and zirconium) must, however, be first removed (see Section 11.44) the method is then applicable in the presence of relatively large quantities of lanthanides. Titrimetric methods (see Section 10.104 to Section 10.109) are generally preferred. 

Determination of uranium with cupferron Discussion. Cupferron does not react with uranium(VI), but uranium(IV) is quantitatively precipitated. These facts are utilised in the separation of iron, vanadium, titanium, and zirconium from uranium(VI). After precipitation of these elements in acid solution with cupferron, the uranium in the filtrate is reduced to uranium(IV) by means of a Jones reductor and then precipitated with cupferron (thus separating it from aluminium, chromium, manganese, zinc, and phosphate). Ignition of the uranium(IV) cupferron complex affords U308. 

Determination of phosphate as ammonium molybdophosphate. This may be readily effected by precipitation with excess of ammonium molybdate in warm nitric acid solution arsenic, vanadium, titanium, zirconium, silica and excessive amounts of ammonium salts interfere. The yellow precipitate obtained may be weighed as either ammonium molybdophosphate, (NH4)3[PMo12O40], after drying at 200-400 °C, or as P205,24Mo03, after heating at 800-825 °C for about 30 minutes. 

Fluoride, in the absence of interfering anions (including phosphate, molybdate, citrate, and tartrate) and interfering cations (including cadmium, tin, strontium, iron, and particularly zirconium, cobalt, lead, nickel, zinc, copper, and aluminium), may be determined with thorium chloranilate in aqueous 2-methoxyethanol at pH 4.5 the absorbance is measured at 540 nm or, for small concentrations 0-2.0 mg L 1 at 330 nm. 

The crystal structures of Hf 2 (OH) 2 (S0O 3 (H2O) i, (14) and Ce2(0H)2(S0i,)3 (H20)it (14) also have been determined and found to be isomorphous to the zirconium compound. The cell constants for this series of four isomorphous compounds reflect the effect of the ionic radii on the dimensions of the unit cell. The values for these cell constants are in Table II. Thus, the cell constants for the zirconium and hafnium compounds are nearly identical and smaller than the cell constants for the cerium and plutonium compounds which are also nearly identical. This trend is exactly that followed by the ionic radii of these elements. 

With boron and an appropriate amount of some sort of alkaline metal halide present in the starting materials for the solid-state reactions, then we obtain zirconium cluster materials belonging to the 6-14 family. Single-crystal X-ray data of products from iodine-rich reactions were used to determine the crystal structures of Na[(Zr6B)Cl3.87(5)lio.i3], and Cs[(Zr6B)Cl2.i6(5)lii.84] [21]. Both phases... 

C02-0061. Determine the number of atoms present in 5.86 mg of each of the following elements (a) beryllium (b) phosphorus (c) zirconium and (d) uranium. 

C22-0034. Determine Z, A, and N for each of the following nuclides (a) the nuclide of neon that contains the same number of protons and neutrons (b) the nuclide of lead that contains 1.5 times as many neutrons as protons and (c) the nuclide of zirconium whose neutron-proton ratio is 1.25. 

In situ densitometry has been the most preferred method for quantitative analysis of substances. The important applications of densitometry in inorganic PLC include the determination of boron in water and soil samples [38], N03 and FefCNfg in molasses [56], Se in food and biological samples [28,30], rare earths in lanthanum, glass, and monazite sand [22], Mg in aluminum alloys [57], metallic complexes in ground water and electroplating waste water [58], and the bromate ion in bread [59]. TLC in combination with in situ fluorometry has been used for the isolation and determination of zirconium in bauxite and almnimun alloys [34]. The chromatographic system was silica gel as the stationary phase and butanol + methanol + HCl -H water -n HF (30 15 30 10 7) as the mobile phase. 

TLC spectrophotometry is used to determine zirconium in Mg-Al alloy. For this purpose, the alloy sample (2 g) is dissolved in HNO3 (20 ml, 6 M), and zirconium is extracted in 6 ml of 0.02-M diantipyrilmethane (DAM) solution in chloroform. The extract was concentrated to 0.4 ml and an aliquot (10 p,l) was chromatographed on silica gel LS plate using 4-M HCl -f dimethylformamide (1 2) as the mobile phase. After development, the portion of the sorbent layer containing the zirconium-DAM complex was removed, and the metal was extracted with 6-M HCl. The zirconium present in this solution was determined in the form of a xylenol orange complex (Amax, 540 nm) by spectrophotometry [22]. 

The concentration of a crosslinking agent containing zirconium in a gel is determined by first adding an acid to break the gel and converting the zirconium into the ionic (noncomplexed) form [340]. This is followed by the addition of... 

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