Dry cell

1890 Many experimenters tried to immobilize the electrolyte of an electrochemical cell to make it more convenient to use. The Zamboni pile of 1812 is a high-voltage dry battery but capable of delivering only minute currents. Various experiments were made with cellulose, sawdust, spun glass, asbestos fibers, and gelatine. In 1886, Carl Gassner obtained a German patent (No. 37,758) on a variant of the (wet) Leclanché cell, which came to be known as the dry cell because it did not have a free liquid electrolyte. Instead, the ammonium chloride was mixed with Plaster of Paris to create a paste, with a small amount of zinc chloride added in to extend the shelf life. The manganese dioxide cathode was dipped in this paste, and both were sealed in a zinc shell, which also acts as the anode. In November 1887, he obtained for the same device. A dry-battery was also invented in Japan during the Meiji Era in 1887. The inventor was Sakizō Yai. However, as Yai didn't have enough money to file the patent, the first patent holder of a battery in Japan was not Yai, but Takahashi Ichisaburo. Wilhelm Hellesen also invented a dry-battery in 1887 and obtained in 1890. The NCC improved Gassner's model by replacing the plaster of Paris with coiled cardboard, an innovation that leaves more space for the cathode and makes the battery easier to assemble. It was the first convenient battery for the masses and made portable electrical devices practical. The zinc–carbon cell (as it came to be known) is still manufactured today. == Design ==

A dry cell uses a paste electrolyte, with only enough moisture to allow current to flow. Unlike a wet cell, a dry cell can operate in any orientation without spilling, as it contains no free liquid, making it suitable for portable equipment. By comparison, the first wet cells were typically fragile glass containers with lead rods hanging from the open top and needed careful handling to avoid spillage. Lead–acid batteries did not achieve the safety and portability of the dry cell until the development of the gel battery. Wet cells have continued to be used for high-drain applications, such as starting internal combustion engines, because inhibiting the electrolyte flow tends to reduce the current capability. A common dry cell is the zinc–carbon cell, sometimes called the dry Leclanché cell, with a nominal voltage of 1.5 volts, the same as the alkaline cell (since both use the same zinc–manganese dioxide combination). A standard dry cell comprises a zinc anode, usually in the form of a cylindrical pot, with a carbon cathode in the form of a central rod. The electrolyte is ammonium chloride in the form of a paste next to the zinc anode. The remaining space between the electrolyte and carbon cathode is taken up by a second paste consisting of ammonium chloride and manganese dioxide, the latter acting as a depolariser. In some designs, often marketed as "heavy duty", the ammonium chloride is replaced with zinc chloride. == Types ==

Primary cells are not rechargeable and are generally disposed of after the cell's internal reaction has consumed the reactive starting chemicals. Secondary cells are rechargeable, and may be reused multiple times. • Primary cell • Zinc–carbon cell • Alkaline cell • Lithium cell • Mercury cell • Silver-oxide cell • Secondary cell • Nickel–cadmium cell • Lithium-ion cell • Nickel–metal hydride cell == See also ==