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10.12      priMAry bATTerieS

                                                                                 2
                             420 mAh/g and >90% capacity retention after 50 1 mA (0.42 mA/cm  of cathode area) constant-
                             current discharge/charge cycles from 1 to 3 V.

                 10.7  ALUMINUM PRIMARY BATTERIES


                             experimental work on Al/MnO  primary or dry batteries was concentrated on the D-size cylindrical
                                                    2
                             battery using a construction similar to the one used for the Mg/MnO  battery (Fig. 10.3). The most
                                                                               2
                             successful anodes were made of a duplex metal sheet consisting of two different aluminum alloys.
                             The inner, thicker layer was more electrochemically active, leaving the outer layer intact in the event
                             of pitting of the inner layer. The cathode bobbin consisted of manganese dioxide and acetylene black,
                             wetted with the electrolyte. Aqueous solutions of aluminum or chromium chloride, containing a
                             chromate inhibitor, were the most satisfactory electrolytes.
                                Aluminum active primary batteries were never produced commercially. While the experimental
                             aluminum batteries delivered a higher energy output than conventional zinc batteries, anode corro-
                             sion, causing problems on intermittent and long-term discharges and irregularities in shelf life, and
                             the voltage-delay problem restrained commercial acceptance. Aluminum/air batteries are covered in
                             Chap. 33.


                 REFERENCES


                               1.  J. L. robinson, “Magnesium Cells,” in N. C. Cahoon and G. W. Heise (eds.), The Primary Battery, Vol. 2,
                                Wiley-interscience, New york, 1976, Chap. 2.
                               2.  G. r. Hoey and M. Cohen, “Corrosion of Anodically and Cathodically polarized Magnesium in Aqueous
                                Media,” J. Electrochem. Soc. 105:245 (1958).
                               3.  J. e. Oxley, r. J. ekern, K. L. Dittberner, p. J. Spellman, and D. M. Larsen, “Magnesium Dry Cells,” in Proc.
                                35th Power Sources Symp., ieee, New york, 1992, p. 18–21.
                               4.  b. V. ratnakumar and S. Sathyanarayana, “The Delayed Action of Magnesium Anodes in primary batteries.
                                part i: experimental Studies,” J. Power Sources 10:219 (1983).
                               5.  S. Sathyanarayana and b. V. ratnakumar, “The Delayed Action of Magnesium Anodes in primary batteries.
                                part ii: Theoretical Studies,” J. Power Sources 10:243 (1983).
                               6.  S. r. Narayanan and S. Sathyanarayana, “electrochemical Determination of the Anode Film resistance and
                                Double Layer Capacitance in Magnesium-Manganese Dioxide Cells,” J. Power Sources 15:27 (1985).
                               7.  b. V. ratnakumar, “passive Films on Magnesium Anodes in primary batteries,” J. Appl. Electrochem. 18:268
                                (1988).
                               8.  D. b. Wood, “Magnesium batteries,” in K. V. Kordesch (ed.), Batteries, Vol. 1: Manganese Dioxide, Marcel
                                Dekker, New york, 1974, Chap. 4.
                               9.  r. r. balaguer and F. p. Schiro, “New Magnesium Dry battery Structure,” in Proc. 20th Power Sources
                                Symp., Atlantic City, NJ, 1966, p. 90.
                               10.  r. r. balaguer, “Low Temperature battery (New Magnesium Anode Structure),” report: eCOM-03369-F, 1966.
                             11.  r. r. balaguer, “Method of Forming a battery Cup,” U.S. patent 3,405,013, 1968.
                             12.  D.  M.  Larsen,  K.  L.  Dittberner,  r.  J.  ekern,  p.  J.  Spellman,  and  J.  e.  Oxley,  “Magnesium  battery
                                Characterization,” in Proc. 35th Power Sources Symp., ieee, New york, 1992, p. 22.
                             13.  L. Jarvis, “Low Cost, improved Magnesium battery, in Proc. 35th Power Sources Symp., New york, 1992,
                                p. 26.
                             14.  p.  Novak,  r.  imhof,  and  O.  Haas,  “Magnesium  insertion  electrodes  for  rechargeable  Nonaqueous
                                batteries—a Competitive Alternative to Lithium?” Electrochimica Acta 45, (September 1999).
                             15.  D. Aurbach, y. Gofer, Z. Lu, A. Schechter, O. Chusid, H. Gizbar, y. Cohen, V. Ashkenazi, M. Moshkovich,
                                r.  Turgeman,  and  e.  Levi,  “A  Short  review  on  the  Comparison  between  Li  battery  Systems  and
                                rechargeable Magnesium battery Technology,” J. Power Sources 97–98:119 (July 2001).
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