Daniell cell

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Daniell cells, 1836.

The Daniell cell was invented in 1836 by John Frederic Daniell, a British chemist and meteorologist, and consisted of a copper pot filled with a copper sulfate solution, in which was immersed an unglazed earthenware container filled with sulfuric acid and a zinc electrode. He was searching for a way to eliminate the hydrogen bubble problem found in the voltaic pile, and his solution was to use a second electrolyte to consume the hydrogen produced by the first. Zinc sulfate may be substituted for the sulfuric acid. The Daniell cell was a great improvement over the existing technology used in the early days of battery development. A later variant of the Daniell cell called the gravity cell or crowfoot cell was invented in the 1860s by a Frenchman named Callaud and became a popular choice for electrical telegraphy.

The Daniell cell is also the historical basis for the contemporary definition of the volt, which is the unit of electromotive force in the International System of Units. The definitions of electrical units that were proposed at the 1881 International Conference of Electricians were designed so that the electromotive force of the Daniell cell would be about 1.0 volts.[1][2] With contemporary definitions, the standard potential of the Daniell cell at 25 °C is actually 1.10 V.[3]

Chemistry[edit]

In the Daniell cell, copper and zinc electrodes are immersed in a solution of copper(II) sulfate and zinc sulfate respectively. At the anode, zinc is oxidized per the following half reaction:

The two half-cell form of the Daniell cell for classroom demonstrations
Zn(s) → Zn2+(aq) + 2e- .

At the cathode, copper is reduced per the following reaction:

Cu2+(aq) + 2e- → Cu(s) .

The total reaction being:

Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s).

In classroom demonstrations, a form of the Daniell cell known as two half cells is often used due to its simplicity. The two half cells each support one half of the reactions described above. A wire and light bulb may connect the two electrodes. Electrons that are “pulled” from the zinc anode travel through the wire, providing an electrical current that illuminates the bulb. In such a cell, the sulfate ions play an important role. Having a negative charge, these anions build up around the anode to maintain a neutral charge. Conversely, at the cathode the copper(II) cations accumulate to maintain this neutral charge. These two processes cause copper solid to accumulate at the cathode and the zinc electrode to "dissolve" into the solution.

Since neither half reaction will occur independently of the other, the two half cells must be connected in a way that will allow ions to move freely between them. A porous barrier or ceramic disk may be used to separate the two solutions while allowing ion flow. When the half cells are placed in two entirely different and separate containers, a salt bridge is often used to connect the two cells. In the above wet-cell during discharge, sulfate anions move from the cathode to the anode via the salt bridge and the Zn2+ cations move in the opposite direction to maintain neutrality. Recharge would have sulfate ions crossing with copper ions in the other direction. This cross-cell contamination reduces the reusability of the battery.

Development[edit]

Daniell's original construction[edit]

Diagram of early Daniell cell published by Daniell in 1839. In this design the original perforated disc has become a cylinder inside the upper part of the cell to hold copper sulfate crystals

Daniell first constructed his cell in 1836.[4] His original design consisted of a 3.5 inch diameter copper cylinder. A copper disc perforated with numerous holes was placed across the cylinder recessed down from the top. A tube of ox gullet hung from a large hole in the centre of the perforated copper disc. An 0.5 inch diameter zinc rod hung inside this ox-gullet tube suspended from wooden supports. The copper vessel was filled with sulfuric acid solution saturated with copper sulfate to above the level of the perforated disc. The ox-gullet tube was filled with sulfuric acid solution. Copper sulfate crystals were piled on the perforated copper disc to keep the solution saturated. The ox-gullet acts as a porous membrane allowing passage of ions. Daniell states that a porous earthenware tube may be used instead of the ox gullet for practical ease but this arrangement will produce less power. Another suggestion made by Daniell to improve the cell was to replace the copper with platinum and copper sulfate with platinum chloride, but he remarks "such an arrangement would be perfect, but too costly for ordinary applications".[5] It is the porous pot form of the cell that came to be widely used in telegraphy.

Porous pot cell[edit]

Porous pot cell

The porous pot cell consists of a central zinc anode dipped into a porous earthenware pot containing a zinc sulfate solution. The porous pot is, in turn, immersed in a solution of copper sulfate contained in a copper can, which acts as the cell's cathode. The use of a porous barrier allows ions to pass through but keeps the solutions from mixing. Without this barrier, when no current was drawn the copper ions would drift to the zinc anode and undergo reduction without producing a current, which would destroy the battery's life.[6]

Over time, copper buildup would block the pores in the earthenware barrier and cut short the battery's life. Nevertheless, the Daniell cell provided a longer and more reliable current than the Voltaic pile because the electrolyte deposited copper, which is a conductor, rather than hydrogen, which is an insulator, on the cathode. It was also safer and less corrosive. With an operating voltage of roughly 1.1 volts, it saw widespread use in telegraph networks until it was supplanted by the Leclanché cell in the late 1860s.[7]

Gravity cell[edit]

Early 20th-century engraving of a gravity cell. Note the distinctive crowfoot shape of the zinc anode.

Sometime during the 1860s, a Frenchman by the name of Callaud invented a variant of the Daniell cell which dispensed with the porous barrier.[7] Instead, a layer of zinc sulfate sat on top of a layer of copper sulfate, the two liquids kept separate by their differing densities, often with a layer of oil added on top to prevent evaporation. This reduced the internal resistance of the system and thus the battery yielded a stronger current.

This variant, called a gravity cell, consisted of a glass jar in which a copper cathode sat on the bottom and a zinc anode was suspended beneath the rim in the zinc sulfate layer. Copper sulfate crystals would be scattered around the cathode and the jar would then be filled with distilled water. As the current was drawn, a layer of zinc sulfate solution would form at the top around the anode. This top layer was kept separate from the bottom copper sulfate layer by its lower density and by the polarity of the cell. A disadvantage of the gravity cell was that a current had to be continually drawn to keep the two solutions from mixing by diffusion, so it was unsuitable for intermittent use. In addition, it was vulnerable to loss of integrity if too much electric current was drawn, which would also cause the layers to mix.

Sometimes called the crowfoot cell due to the distinctive shape of the electrodes, this arrangement was less costly for large multicell batteries and it quickly became the battery of choice for the American and British telegraph networks. Even after most telegraph lines started being powered by motor-generators the gravity battery continued to be used in way stations to power the local circuit at least into the 1950s.[8] In the telegraph industry, this battery was often assembled on site by the telegraph workers themselves, and when it ran down it could be renewed by replacing the consumed components.[9] The zinc sulfate layer was clear in contrast to the deep blue copper sulfate layer, which allowed a technician to measure the battery life with a glance. On the other hand, this setup meant the battery could only be used in a stationary appliance, otherwise the solutions would mix or spill.

Use in electrometallurgy[edit]

Bird's cell[edit]

A variant of the Daniell cell was invented in 1837 by the Guy's hospital physician Golding Bird who used a plaster of Paris barrier to keep the solutions separate. Bird's experiments with this cell were of some importance to the new discipline of electrometallurgy. A surprising result from Bird's experiments was the deposition of copper on the porous plaster and in veins running through it without any contact with the metal electrodes. So surprising, in fact, that it was at first disbelieved by electrochemical investigators, including Michael Faraday. Bird himself had to carefully examine his apparatus for inadvertent contact, perhaps through the growth of copper "whiskers", before he was convinced of the result. Deposition of copper, and other metals, had been previously noted, but always previously it had been metal on metal electrode.[10][11]

Electrotyping[edit]

John Dancer, a Liverpool instrument maker, in 1838 was the first to take commercial advantage of the unique features of the Daniell cell for copper plating. In a process now known as electrotyping he found he could make objects to any desired shape by using the porous barrier as a mould. Many others, however, had made the same discovery and in a patent dispute with Thomas Spencer it was pointed out that Bird had priority for the principle. Credit for invention of electrotyping is usually given to the Russian Moritz von Jacobi.[10]

See also[edit]

References[edit]

  1. ^ Borvon, Gérard (September 10, 2012). "History of the electrical units". Association S-EAU-S. 
  2. ^ Hamer, Walter J. (January 15, 1965). Standard Cells: Their Construction, Maintenance, and Characteristics. National Bureau of Standards Monograph #84. US National Bureau of Standards. 
  3. ^ Spencer, James N.; Bodner, George M.; Rickard, Lyman H. (2010). Chemistry: Structure and Dynamics (Fifth Edition). John Wiley & Sons. p. 564. ISBN 9780470587119. 
  4. ^ Elizabeth H. Oakes, A to Z of STS Scientists, p. 72, Infobase Publishing, 2009 ISBN 1438109253.
  5. ^ John Frederic Daniell, An Introduction to the Study of Chemical Philosophy, pp. 504-505, John W. Parker, 1843 OCLC 315534231 (pp. 438-439 in 1839 edition OCLC 7841489 in which the comments about platinum do not appear).
  6. ^ Giorgio Carboni, Experiments in Electrochemistry; Last accessed on Jul 30, 2010.
  7. ^ a b James B. Calvert. "The Electromagnetic Telegraph". Retrieved 2010-07-30. 
  8. ^ Tools of Telegraphy, Telegraph Lore; Last accessed Jul 30, 2010
  9. ^ Gregory S. Raven, Recollections of a Narrow Gauge Lightning Slinger; Last accessed on Jul 30, 2010.
  10. ^ a b Watt, Alexander; Philip, Arnold (2005). Electroplating and Electrorefining of Metals. Watchmaker Publishing. pp. 90–92. ISBN 1929148453.  Reprint of an 1889 volume.
  11. ^ Golding Bird, Report of the Seventh Meeting of the British Society for the Advancement of Science, vol.6 (1837), p.45, London: J. Murray, 1838.

Further reading[edit]

  • Saslow, Wayne M. (1999), "Voltaic cells for physicists: Two surface pumps and an internal resistance", American Journal of Physics 67 (7): 574, Bibcode:1999AmJPh..67..574S, doi:10.1119/1.19327 
  • Lester, James C.; Vicari, Rosa Maria; Paraguaçu, Fábio (2004), Lester, James C.; Vicari, Rosa Maria; Paraguaçu, Fábio, eds., A Qualitative Model of Daniell Cell for Chemical Education, Lecture Notes in Computer Science 3220, doi:10.1007/b100137, ISBN 978-3-540-22948-3 

External links[edit]