Primary cell

A primary cell is a battery that is designed to be used once and discarded, and not recharged with electricity and reused like a secondary cell (rechargeable battery). In general, the electrochemical reaction occurring in the cell is not reversible, rendering the cell unrechargeable. As a primary cell is used, chemical reactions in the battery use up the chemicals that generate the power; when they are gone, the battery stops producing electricity and is useless. In contrast, in a secondary cell, the reaction can be reversed by running a current into the cell with a battery charger to recharge it, regenerating the chemical reactants. Primary cells are made in a range of standard sizes to power small household appliances.

A variety of standard sizes of primary cells. From left:4.5V multicell battery, D, C, AA, AAA, AAAA, A23, 9V multicell battery, (top) LR44, (bottom) CR2032

Usage trend

In the twenty-first century, primary cells began losing market share to secondary cells, as relative costs declined for the latter. Flashlight power demands were reduced by the switch from incandescent bulbs to light-emitting diodes.^[1]

The remaining market experienced increased competition from private- or no-label versions. The market share of the two leading US manufacturers, Energizer and Duracell, declined to 37% in 2012. Along with Rayovac, these three are trying to move consumers from zinc-carbon to more expensive, long-lasting and safer alkaline batteries.^[1]

Western battery manufacturers shifted production offshore and no longer make zinc-carbon batteries in the United States.^[1]

China became the largest battery market, with demand projected to climb faster than anywhere else, and has also shifted to alkaline cells. In other developing countries disposable batteries must compete with cheap wind-up, solar-powered and rechargeable devices that have proliferated.^[1]

Comparison between primary and secondary cells

Secondary cells (Rechargeable batteries) are in general more economical to use than primary cells. Their initially higher cost and the purchase cost of a charging system can be spread out over many use cycles (between 100 and 1000 cycles); for example, in hand-held power tools, it would be very costly to replace a high-capacity primary battery pack every few hours of use.

Primary batteries are useful where long periods of storage are required; a primary battery can be constructed to have a lower self-discharge rate than a rechargeable battery, so all its capacity is available for useful purposes. Applications that require a small current for a long time, for example a smoke detector, also use primary batteries since the self-discharge current of a rechargeable battery would exceed the load current and limit service time to a few days or weeks. For example, a flashlight used for emergencies must work when needed, even if it has sat on a shelf for a long time. Primary cells are also more cost-efficient in this case, as rechargeable batteries would use only a small fraction of available recharge cycles. Reserve batteries achieve very long storage time (on the order of 10 years or more) without loss of capacity, by physically separating the components of the battery and only assembling them at the time of use. Such constructions are expensive but are found in applications like munitions, which may be stored for years before use.

Recharging primary cells

Attempts to extend the life of primary cells, for example by recharging alkaline batteries, meet with variable results. Third-party devices are manufactured and represented as being able to recharge primary cells. The internal chemical reactions of a primary cell are not easily reversed by externally applied currents, so reactants do not entirely return to their initial state and location. Recharged primary cells will not have the life or performance of secondary cells. Manufacturers of primary cells usually warn against recharging.

Polarization

A major factor reducing the lifetime of primary cells is that they become polarized during use. This means that hydrogen accumulates at the cathode and reduces the effectiveness of the cell.

To reduce the effects of polarization in commercial cells and to extend their lives, chemical depolarization is used; that is, an oxidizing agent is added to the cell, to oxidize the hydrogen to water. Manganese dioxide is used in the Leclanché cell and zinc–carbon cell, and nitric acid is used in the Bunsen cell and Grove cell.

Attempts have been made to make simple cells self-depolarizing by roughening the surface of the copper plate to facilitate the detachment of hydrogen bubbles with little success. Electrochemical depolarization exchanges the hydrogen for a metal, such as copper (e.g., Daniell cell), or silver (e.g., Silver-oxide cell).

Terminology

Anode and cathode

The plate that has the negative terminal (usually carbon) is termed the cathode and the plate that has the positive terminal (usually zinc) is termed the anode. (This is the reverse of the terminology used in an electrolytic cell). The reason is that these terms are related to the direction of passage of electric charges (ions) through the electrolyte, not in the external circuit.

Inside the cell the anode is the electrode where chemical oxidation occurs, as it donates electrons to the circuit. The cathode is defined as the electrode where chemical reduction occurs, as it accepts electrons from the circuit.

Outside the cell, different terminology is used. As the anode donates positive charge to the electrolyte, it becomes negatively charged and is therefore connected to the terminal marked "−" on the outside of the cell. The cathode, meanwhile, donates negative charge to the electrolyte, so it becomes positively charged and is therefore connected to the terminal marked "+" on the outside of the cell.^[2]

Old textbooks sometimes contain different terminology that can cause confusion to modern readers. For example, a 1911 textbook by Ayrton and Mather^[3] describes the electrodes as the "positive plate" and "negative plate" .

References

1 2 3 4 Stay informed today and every day (2014-01-18). "Batteries: Out of juice". The Economist. Retrieved 2014-02-10.
↑ John S. Newman, Karen E. Thomas-Alyea, Electrochemical systems, Wiley-IEEE, 3rd ed. 2004, ISBN 0-471-47756-7
↑ W. E. Ayrton and T. Mather, Practical Electricity, Cassell and Company, London, 1911, page 170

External links

Nonrechargeable batteries

Galvanic cells

Types	Voltaic pile Battery Flow battery Trough battery Concentration cell Fuel cell Thermogalvanic cell

Primary cell (non-rechargable)	Alkaline Aluminium–air Bunsen Chromic acid Clark Daniell Dry Edison-Lalande Grove Leclanché Lithium Mercury Nickel oxyhydroxide Silicon–air Silver oxide Weston Zamboni Zinc–air Zinc–carbon

Secondary cell (rechargeable)	Automotive Lead–acid gel / VRLA Lithium–air Lithium–ion Lithium polymer Lithium iron phosphate Lithium titanate Lithium–sulfur Dual carbon battery Molten salt Nanopore Nanowire Nickel–cadmium Nickel–hydrogen Nickel–iron Nickel–lithium Nickel–metal hydride Nickel–zinc Polysulfide bromide Potassium-ion Rechargeable alkaline Sodium-ion Sodium–sulfur Vanadium redox Zinc–bromine Zinc–cerium

Cell parts	Anode Binder Catalyst Cathode Electrode Electrolyte Half-cell Ions Salt bridge Semipermeable membrane

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