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For volumetric flasks

Accuracy tolerances for volumetric flasks at 20°C are given by ASTM standard E288. [Pg.1179]

The United States Pharmacopoeia (USP) requirements for volumetric flasks calibrated to contain the indicated volume at 25°C are given in Table 2.7. [Pg.49]

Table 2.7 Designated Volume with Limit of Error for Volumetric Flasks... Table 2.7 Designated Volume with Limit of Error for Volumetric Flasks...
The British Standards Institution (BSI) and the National Physical Loaboratory (NPL) have laid down the tolerances in the capacity of volumetric flasks (i.e., measuring flask) at 20°C by two sets of tolerances viz., Grade A and Grade B respectively, evidently to indicate the class of accuracy to which the flask has been subjected to for graduation, followed by the manufacturer s name and finally the BS standard number. However, the permitted tolerances for volumetric flasks commonly used in analytical laboratories are depicted in Table 2.8. [Pg.49]

Small volume pipettes are avoided since they may lead to significant errors in the final results. Similarly, typical sizes for volumetric flasks should be between 25 and 500 ml if possible. [Pg.73]

Standards of Accuracy The capacity tolerances for volumetric flasks, transfer pipets, and burets are those accepted by the National Institute of Standards and Technology (Class A),1 as indicated in the accompanying tables. Use Class A volumetric apparatus unless otherwise specified in the individual monograph. For plastic volumetric apparatus, the accepted capacity tolerances are Class B.2... [Pg.832]

I) Dissolve 2.465 g Na3lrCIg in water and dilute to volume. (2) Transfer 1.000 g Ir sponge to a glass tube, add 20 ml of HCI and 1 ml of HCIO4. Seal the tube and place in an oven at 300°C for 24 hr. Cool, break open the tube, transfer the solution to a volumetric flask, and dilute to volume. Observe all safety precautions in opening the glass tube. [Pg.1185]

Pipets and volumetric flasks provide a more accurate means for measuring volume. When filled to its calibration mark, a volumetric flask is designed to contain a specified volume of solution at a stated temperature, usually 20 °C. The actual vol-... [Pg.26]

Three important precautions are needed when working with pipets and volumetric flasks. First, the volume delivered by a pipet or contained by a volumetric flask assumes that the glassware is clean. Dirt and grease on the inner glass surface prevents liquids from draining evenly, leaving droplets of the liquid on the container s walls. For a pipet this means that the delivered volume is less than the calibrated volume, whereas drops of liquid above the calibration mark mean that a volumetric flask contains more than its calibrated volume. Commercially available cleaning solutions can be used to clean pipets and volumetric flasks. [Pg.28]

Preparing a solution of known concentration is perhaps the most common activity in any analytical lab. The method for measuring out the solute and solvent depend on the desired concentration units, and how exact the solution s concentration needs to be known. Pipets and volumetric flasks are used when a solution s concentration must be exact graduated cylinders, beakers, and reagent bottles suffice when concentrations need only be approximate. Two methods for preparing solutions are described in this section. [Pg.30]

A sample of an ore was analyzed for Cu as follows. A 1.25-g sample of the ore was dissolved in acid and diluted to volume in a 250-mb volumetric flask. A 20-mb portion of the resulting solution was transferred by pipet to a 50-mb volumetric flask and diluted to volume. An analysis showed that the concentration of Cu in the final solution was 4.62 ppm. What is the weight percent of Cu in the original ore ... [Pg.31]

Substituting known volumes (with significant figures appropriate for pipets and volumetric flasks) into equation 2.4... [Pg.32]

Using the tolerance values for pipets and volumetric flasks given in Table 4.2, the overall uncertainties in Ma and Mb are... [Pg.70]

After adding p-rosaniline and formaldehyde, the colored solution was diluted to 25 ml in a volumetric flask. The absorbance was measured at 569 nm in a 1-cm cell, yielding a value of 0.485. A standard sample was prepared by substituting a 1.00-mL sample of a standard solution containing the equivalent of 15.00 ppm SO2 for the air sample. The absorbance of the standard was found to be 0.181. Report the concentration of SO2 in the air in parts per million. The density of air maybe taken as 1.18 g/L. [Pg.453]

Samples of analyte are dissolved in a suitable solvent and placed on the IR card. After the solvent evaporates, the sample s spectrum is obtained. Because the thickness of the PE or PTEE film is not uniform, the primary use for IR cards has been for qualitative analysis. Zhao and Malinowski showed how a quantitative analysis for polystyrene could be performed by adding an internal standard of KSCN to the sample. Polystyrene was monitored at 1494 cm- and KSCN at 2064 cm-. Standard solutions were prepared by placing weighed portions of polystyrene in a 10-mL volumetric flask and diluting to volume with a solution of 10 g/L KSCN in... [Pg.453]

A 0.3619-g sample of tetrachloropicolinic acid, C6HNO2CI4, is dissolved in distilled water, transferred to a 1000-mL volumetric flask, and diluted to volume. An exhaustive controlled-potential electrolysis of a 10.00-mL portion of this solution at a spongy silver cathode requires 5.374 C of charge. What is the value of n for this reduction reaction ... [Pg.506]

This analysis is an example of a concentration technique. Once the original sample is brought to volume in the 100-mL volumetric flask, any portion of the sample solution, even that obtained on filtering, may be used for the analysis. [Pg.527]

Determine the parts per million of F in the tap water, (b) For the analysis of toothpaste a 0.3619-g sample was transferred to a 100-mL volumetric flask along with 50.0 mL of TISAB and diluted to volume with distilled water. Three 20.0-mL aliquots were removed, and the potential was measured with an L ion-selective electrode using a saturated calomel electrode as a reference. Live separate 1.00-mL additions of a 100.0-ppm solution of L were added to each, measuring the potential following each addition. [Pg.537]

A sample was prepared for analysis by diluting a 0.246-g sample to volume in a 100-mb volumetric flask. The limiting current for the sample was found to be 444 pA. Report the purity of this sample of K3be(CN)6. [Pg.538]


See other pages where For volumetric flasks is mentioned: [Pg.20]    [Pg.20]    [Pg.20]    [Pg.20]    [Pg.102]    [Pg.27]    [Pg.27]    [Pg.58]    [Pg.69]    [Pg.69]    [Pg.130]    [Pg.131]    [Pg.365]    [Pg.365]    [Pg.399]    [Pg.421]    [Pg.439]    [Pg.451]    [Pg.451]    [Pg.451]    [Pg.452]    [Pg.456]    [Pg.456]    [Pg.490]    [Pg.526]    [Pg.538]    [Pg.538]    [Pg.540]    [Pg.576]   
See also in sourсe #XX -- [ Pg.11 , Pg.103 ]




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