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Alkaline battery

Type of electrical cell

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A selection of alkaline batteries in various form factors
Aney · CC BY-SA 3.0

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Through Electrolyte, Alkali and Amalgam (chemistry)

Compared with zinc–carbon batteries, alkaline batteries have a higher energy density and longer shelf life yet provide the same voltage.

The alkaline battery gets its name because it has an alkaline electrolyte of potassium hydroxide (KOH) instead of the acidic ammonium chloride (NH4Cl) or zinc chloride (ZnCl2) electrolyte of the zinc–carbon batteries. Other battery systems also use alkaline electrolytes, but they use different active materials for the electrodes.

As of 2011, alkaline batteries accounted for 80% of manufactured batteries in the US and over 10 billion individual units produced worldwide. In Japan, alkaline batteries accounted for 46% of all primary battery sales. In Switzerland, alkaline batteries accounted for 68%, in the UK 60% and in the EU 47% of all battery sales including secondary types.

Alkaline batteries contain zinc (Zn) and manganese dioxide (MnO2), which is a cumulative neurotoxin and can be toxic in higher concentrations. However, compared to other battery types, the toxicity of alkaline batteries is moderate.

Alkaline batteries are used in many household items such as portable media players, digital cameras, toys, flashlights, and radios.

History

Batteries with alkaline (rather than acid) electrolyte were first developed by Waldemar Jungner in 1899, and, working independently, Thomas Edison in 1901. The modern alkaline dry battery, using the zinc/manganese dioxide chemistry, was invented by the Canadian engineer Lewis Urry in the 1950s before he started working for Union Carbide's Eveready Battery division in Cleveland, Ohio, building on earlier work by Edison. On October 9, 1957, Urry, Karl Kordesch, and P. A. Marsal filed US patent (2,960,558) for the alkaline battery. It was granted in 1960 and was assigned to Union Carbide.

When alkaline batteries were introduced in the late 1960s, their zinc electrodes (in common with the then ubiquitous carbon-zinc cells) had a surface film of mercury amalgam. Its purpose was to control electrolytic action on impurities in the zinc; that unwanted electrolytic action would reduce shelf life and promote leakage. When reductions in mercury content were mandated by various legislatures, it became necessary to greatly improve the purity and consistency of the zinc.

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