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Lead solution

Other uses of ethylene dichloride include its formulation with tetraethyl and tetramethyl lead solutions as a lead scavenger, as a degreasing agent, and as an intermediate in the synthesis of many ethylene derivatives. [Pg.201]

These results imply that at the specified pH the magnesium complex is appreciably dissociated, whereas the lead complex is stable, and clearly titration of an Mg( II) solution with EDTA at this pH will be unsatisfactory, but titration of the lead solution under the same conditions will be quite feasible. In practice, for a metal ion to be titrated with EDTA at a stipulated pH the value of log K H should be greater than 8 when a metallochromic indicator is used. [Pg.59]

A mixture of tin(IV) and lead(II) ions may be complexed by adding an excess of standard EDTA solution, the excess EDTA being determined by titration with a standard solution of lead nitrate the total lead-plus-tin content of the solution is thus determined. Sodium fluoride is then added and this displaces the EDTA from the tin(IV)-EDTA complex the liberated EDTA is determined by titration with a standard lead solution. [Pg.337]

Procedure. Prepare a standard EDTA solution (0.2M), a standard lead solution (0.01 M), a 30 per cent aqueous solution of hexamine, and a 0.2 per cent aqueous solution of xylenol orange. [Pg.337]

Reagents. Standard lead solution. Dissolve 0.160 g of analytical grade lead nitrate in 1 L of distilled water 10.0 mL of this solution, diluted to 250 mL gives a working solution containing 4 pg of lead mL"1. [Pg.692]

Procedure. Place 10.0 mL of the working lead solution in a 250 mL separatory funnel, add 75 mL of the ammonia-cyanide-sulphite solution and then by the cautious addition of dilute hydrochloric acid adjust the pH of the solution to 9.5 (pH-meter). This operation must be carried out slowly if the pH of the solution falls even temporarily below 9.5, HCN may be liberated and so use of a fume cupboard is necessary. Now add 7.5 mL of the dithizone reagent to the separatory funnel, followed by a further 17.5 mL of chloroform. Shake for 1 minute, allow the layers to separate, then remove the chloroform layer. Measure the absorbance of this against a blank solution, using a 1 cm cell and a wavelength of 510 nm (green filter). [Pg.692]

Repeat the procedure with 5.0 mL, 7.5 mL and 15.0 mL portions of the working lead solution and then with 10 mL of the test solution. [Pg.692]

Note. If lead caprate is not available, standard lead solutions can be prepared from aqueous solutions containing known weights of lead nitrate and following through the extraction procedure as detailed for the final extraction of lead into methyl isobutyl ketone for the alloy. It should also be noted that steps should be taken to avoid excessive inhalation of the vapour of the methyl isobutyl ketone, which can cause a headache. [Pg.810]

A cyclic-voltammetric peak current of 12.5 pA was observed for the reversible reduction of a 1.5 mM lead solution using a 1.2 mm-diameter disk electrode and a 50 mV s 1 scan rate. Calculate the lead concentration that yields a peak current of 20.2 pA at 250 mV s 1. [Pg.58]

Heywood RR, James RQ, Pulsford AH, et al. 1979. Chronic oral administration of alkyl lead solution to the Rhesus monkey. Toxicol Lett 4 119-125. [Pg.533]

Zhan and Mao [60] used a simple, fast, and selective alternating current oscilloscop-ic polarographic titration method for the determination of primaquine and other alkaloid phosphate in pharmaceutical preparation. The titration was carried out with a standard lead solution in hexamethylene tetramine buffer containing 1 M sodium chlorate (pH 5.5). The results obtained by this method are comparable to those obtained by pharmacopoeial method. [Pg.184]

Standard Lead Solution On the day of use, dilute 10.0 ml of lead nitrate stock solution with DW to 100.0 ml. Each ml of standard lead solution contains the equivalent of 10 microgrammes of lead. A control comparison solution prepared with 2.0 ml of standard lead solution contains, when compared to a solution representing 1.0 g of the substance being tested, the equivalent of 20 parts per million of lead. [Pg.25]

Standard Solution Into a 50 ml Nessler Cylinder, pipette 2 ml of standard lead solution and dilute with DW to 25 ml. Adjust with dilute acetic acid Sp. (IP) or dilute ammonia solution Sp. (IP) to a pH between 3.0 and 4.0, dilute with DW to about 35 ml and mix. [Pg.26]

Weigh accurately a sample of Pb-salt to give a 0.01 to 0.02 M lead solution,... [Pg.261]

HTC materials have been used and structurally improved as electrodes in Li-ion batteries [30-32], Rechargeable lithium-ion batteries are the technical leading solution and essential to portable electronic devices. Owing to the rapid development of such equipment there is an increasing demand for lithium-ion batteries with higher energy density and a longer lifetime. [Pg.210]

Add a volume of standard lead solution containing each of the following three levels of lead to samples of the drug substance the content equal to the expected specification limit and those higher and lower than the... [Pg.97]

A typical example of accuracy (recovery rate) is shown in Table 7.2. The samples were prepared by adding a standard lead solution corresponding to 2, 5, 10, and 15 ppm to 2.0 g of a compound. Results of the recovery were determined from the absorbance at 400 nm. [Pg.98]

Place an appropriate volume of standard lead solution which corresponds to each of five concentration levels in a Nessler tube, and add water to make up to 40 mL. Add 2 mL of dilute acetic acid and water to make up to 50 mL, and designate it as the test solution. Three tubes of test solution at each concentration level are prepared for separate runs. [Pg.99]

Detection Limit. The detection limit of heavy metals limit test method is obtained from the test solutions and the control solution. These solutions are prepared using one of methods 1 to 4 of the control solution preparation method. The detection limit is determined by visual inspection of a series of diluted standard lead solutions. [Pg.101]

The control solution is prepared as follows Evaporate a mixture of 2 mL of nitric acid, 5 drops of sulfuric acid, and 2 mL of hydrochloric acid on a water bath, further evaporate to dryness on a sand bath, and moisten the residue with 3 drops of hydrochloric acid. Proceed as directed in the test solution, then add the volume of standard lead solution directed in the monograph and water to make 50 mL. [Pg.102]

Another secret-ink system used by the Germans during the war involved the chemical reactions between lead nitrate and sodium sulfide. As any high school student should know, solutions of these compounds are colorless, but form a black precipitate of lead sulfide when mixed. A spy can inscribe a message with the lead solution, and its recipient can read the missive by spraying it with the sodium sulfide solution. [Pg.163]

A simple flow-through system that permits the constant flow of lead solution in 0.1 M HC1 was also used. The electrochemical cell used permitted the integration of the same three-electrode configuration as in the batch measurements. The detection limit was similar to batch measurements. The stability of the system for 16 runs of a 500 ppb lead solution showed a 4% RSD. [Pg.151]

The concentration of 210Po in seawater is generally close to what would be expected from radiochemical equilibrium with its grandparent, 210Pb. Below 400 m, Po activities are very similar to those of Pb. At shallower depths, the concentrations of Po and Pb are somewhat decoupled. Po is more readily adsorbed by particles than is Pb in the surface ocean (Bernat and Church, 1989) and, due to the short residence times of particles in the upper ocean, the relative concentrations of Po and Pb are controlled, in part, by particle fluxes and differences in polonium and lead solution and surface chemistries. The chemistry of... [Pg.345]

Standard Lead Solution On the day of use, dilute stepwise and quantitatively an accurately measured volume of Lead Nitrate Stock Solution with water to obtain the Standard Lead Solution, which contains 0.25 xg/mL of lead (Pb) ion. [Pg.81]

Procedure Set a suitable atomic absorption spectrophotometer to a wavelength of 217 nm. Adjust the instrument to zero absorbance against water. Read the absorbance of the Standard Lead Solution. [Pg.82]


See other pages where Lead solution is mentioned: [Pg.50]    [Pg.131]    [Pg.131]    [Pg.132]    [Pg.625]    [Pg.626]    [Pg.811]    [Pg.412]    [Pg.185]    [Pg.30]    [Pg.152]    [Pg.96]    [Pg.198]    [Pg.30]    [Pg.275]    [Pg.100]    [Pg.484]    [Pg.339]    [Pg.225]   
See also in sourсe #XX -- [ Pg.158 ]

See also in sourсe #XX -- [ Pg.158 ]




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Alkaline solutions, lead corrosion

Aqueous solution, protonation-lead binding

Aqueous solutions, lead polymers

Determination of lead with standard potassium dichromate solution

Determination of sulphate with standard lead nitrate solution

Lead Acetate Subacetate Solution

Lead acetate solution

Lead chloride solutions

Lead fluoroborate solution

Lead-free piezoelectrics solutions

Leading order solution

Leading order terms, asymptotic solutions

PZT) and lead-lanthane zirconate-titanate (PLZT) solid solutions

The Photocatalysed Removal of Lead Ions from Solution

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