Gravimetric analysis

Gravimetric analysis
Analytical balance mettler ae-260.jpg
Analytical balance
Classification Gravimetric
Analytes Solids
Liquids
Other Techniques
Related Precipitation
Titration


Gravimetric analysis describes a set of methods in analytical chemistry for the quantitative determination of an analyte based on the mass of a solid.

In most cases, the analyte in solution is first converted to a solid by precipitation with an appropriate reagent.[1] The precipitate can then be collected by filtration, washed to remove impurities, dried to remove traces of moisture from the solution, and weighed. The amount of analyte in the original sample can then be calculated from the mass of the precipitate and its chemical composition. This approach has been used to determine the atomic weights of many chemical elements.

Contents

In other cases, it may be easier to remove the analyte by vaporization. The analyte may be collected—perhaps in a cryogenic trap or on some absorbent material such as activated carbon—and measured directly. Alternatively, the sample may be weighed before and after it is dried; the difference between the two masses gives the mass of analyte lost. This approach has been especially useful in determining the water content of complex materials such as foodstuffs.

General procedure

A general procedure for gravimetric analysis is outlined below.

  1. The sample is dissolved, if it is not already in solution.
  2. The solution may be treated to adjust the pH (so that the proper precipitate is formed, or to suppress the formation of other precipitates). If it is known that species are present which interfere (by also forming precipitates under the same conditions as the analyte), the sample might require treatment with a different reagent to remove these interferents.
  3. The precipitating reagent is added at a concentration that favors the formation of a "good" precipitate. This may require low concentration, extensive heating (often described as "digestion"), or careful control of the pH. Digestion can help reduce the amount of coprecipitation.
  4. After the precipitate has formed and been allowed to "digest," the solution is carefully filtered. The filter needs to be appropriately chosen to trap the precipitate; smaller particles are more difficult to filter.
  5. Depending on the procedure followed, the filter might be a piece of ashless filter paper in a fluted funnel, or a filter crucible. Filter paper is convenient because it does not typically require cleaning before use; however, filter paper can be chemically attacked by some solutions (such as concentrated acid or base), and may tear during the filtration of large volumes of solution.
  6. The alternative is a crucible that has a bottom made of some porous material, such as sintered glass, porcelain, or sometimes a metal. These materials are chemically inert and mechanically stable, even at elevated temperatures. However, they must be carefully cleaned to minimize contamination or carryover (cross-contamination). Crucibles are often used with a mat of glass or asbestos fibers to trap small particles.
  7. After the solution has been filtered, it should be tested to make sure that the analyte has been completely precipitated. This is easily done by adding a few drops of the precipitating reagent; if a precipitate is observed, the precipitation is incomplete.
  8. After filtration, the precipitate, along with the filter paper or crucible, is heated. This achieves three purposes:
  9. The remaining moisture is removed (drying).
  10. Secondly, the precipitate is converted to a more chemically stable form. For instance, calcium ion might be precipitated using oxalate ion, to produce calcium oxalate (CaC2O4); it might then be heated to convert it into the oxide (CaO). It is vital that the empirical formula of the weighed precipitate be known, and that the precipitate be pure; if two forms are present, the results will be inaccurate.
  11. The precipitate cannot be weighed with the necessary accuracy in place on the filter paper; nor can the precipitate be completely removed from the filter paper in order to weigh it. The precipitate can be carefully heated in a crucible until the filter paper has burned away; this leaves only the precipitate. (As the name suggests, "ashless" paper is used so that the precipitate is not contaminated with ash.)
  12. After the precipitate is allowed to cool (preferably in a desiccator to keep it from absorbing moisture), it is weighed (in the crucible). The mass of the crucible is subtracted from the combined mass, giving the mass of the precipitated analyte. Since the composition of the precipitate is known, it is simple to calculate the mass of analyte in the original sample.

Washing and filtering

The precipitate is often washed to remove impurities adsorbed onto the surface of the particles. Washing may be done with a solution of the precipitating agent, to avoid redissolving a slightly soluble salt. With many precipitates, a process known as "peptization" may occur during washing. In this case, part of the precipitate reverts to the colloidal form. (For example, AgCl(colloidal) converts reversibly to AgCl(s).) This results in the loss of part of the precipitate because the colloidal form may pass through the filter. Peptization can be reduced with careful technique and washing with a solution of appropriate pH and ionic strength.

Example

A simple example of gravimetric analysis is the measurement of solids suspended in a water sample. A known volume of the suspension is filtered and the collected solids are weighed.

A chunk of ore is treated with concentrated nitric acid and potassium chlorate to convert all of the sulfur content to sulfate (SO42-). The nitrate and chlorate are removed by treating the solution with concentrated hydrochloric acid (HCl). The sulfate is precipitated with barium ions (Ba2+) and weighed as BaSO4.

Advantages

Gravimetric analysis, if methods are followed carefully, provides for exceedingly precise analysis. In fact, gravimetric analysis was used to determine the atomic masses of many elements to six-figure accuracy. Gravimetry provides very little room for instrumental error and does not require a series of standards for the calculation of an unknown. Usually, the methods also do not require expensive equipment. In light of its high degree of accuracy, when gravimetric analysis is performed correctly, it can also be used to calibrate other instruments in lieu of reference standards.

Disadvantages

Gravimetric analysis usually provides for the analysis of only a single element, or a limited group of elements, at a time. Comparing modern dynamic flash combustion coupled with gas chromatography with traditional combustion analysis, one finds that the former is both faster and allows for the simultaneous determination of multiple elements, while traditional determination allowed only for the determination of carbon and hydrogen. Methods are often convoluted and a slight mis-step in a procedure can often mean disaster for the analysis. (For example, a colloid may be formed during precipitation gravimetry.) By comparison, hardy methods such as spectrophotometry provide much more efficient analyses.

Notes

  1. www.chem.tamu.edu, Gravimetric Analysis. Retrieved July 24, 2008.

References

  • Earnest, Charles M., and Larry Wilson. 2000. Quantitative Analysis: Gravimetric, Volumetric & Instrumental Analysis, 4th edition. Loudonville, OH: Mohican Textbook Pub. Co. ISBN 0923231390.
  • Harris, Daniel C. 2007. Quantitative Chemical Analysis. New York: W.H. Freeman and Co. ISBN 978-0716770411.
  • Hawkins, M.D. 1970. Calculations in Volumetric and Gravimetric Analysis. London: Butterworths.
  • Jones, Loretta, and Peter Atkins. 2000. Chemistry: Molecules, Matter and Change. Gordonsville, VA: W. H. Freeman. ISBN 0716735954.

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