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method for producing an electrical lead acid accumulator accumulator and also available through the addition of electrolyte

机译:铅酸蓄电池蓄电池的制造方法,也可通过添加电解质获得

摘要

1474802 Lead-acid battery GOULD Inc 8 July 1974 [9 July 1973 (2)] 30217/74 Heading H1B Crystal growth between the formed negative and positive plates of a dry-charged lead-acid battery which may occur before activation of the battery by the addition of electolyte thereto, is prevented by treating the plates with a metal sulphate soluble in sulphuric acid or water. The preferred sulphate is of sodium, other suitable sulphates being of K, Li, Mg, Ca, Zn, and Al; additionally, the sulphates of Be, Ce, In, La, Sn, Tl, Zr and Rb, may be used. In one method of making the battery the metal sulphate is added to the formation electrolyte, viz. H 2 SO 4 solution of S.G. in the range 1À020- 1À100, the metal sulphate being present in an amount of about 2 per cent by wt. The electrolyte is subsequently removed by inverting the battery. In a preferred method, the formation electrolyte does not contain the metal sulphate and after removal of this electrolyte the battery is filled with a H 2 SO 4 rinse solution of S.G. in the range 1À200-1À400, this solution containing 0À05-5 per cent by wt. of the metal sulphate. The plates and separation are soaked for about 10 minutes in the rinse solution which may be stirred and the solution is then removed by inverting the battery. In another method the metal sulphate is dissolved in water in an amount 0À05-5 per cent by wt. and the battery is filled with this solution either after draining the formation electrolyte or after draining the rinse solution, the water being subsequently drained from the battery. Whatever method is used for adding the metal sulphate the battery is subsequently sealed in a manner such that gas-pressure build-up within the battery may be vented and slight ingress of air into the battery is permitted. The very small amount of oxygen permitted to enter the battery during its shelflife tends to equalize the self-discharge of the positive and negative plates and reduces the tendency for the initial battery performance to be positive plate limited. The vent aperture may be circular in shape and have a diameter of 0À0005-0À006 inch. A venting arrangment, Figs. 4, 5, comprises two groups 35 of three vent caps each having a main body 36 formed with normal labyrinth passages (not shown) for breathing of the battery after it has been made operational. During the battery shelf-life the cell apertures 34 in the battery lid 33 are sealed by plugs 38 each having a small vent aperture 40 (referred to above) and the caps 35 are retained by flanges 42 cooperating with upstanding portions 43 on the seal plugs 38. The battery is brought into operation by removing the plugs 38 by tabs 41, filling with electrolyte, and engaging the cap flanges 42 in the apertures 34. In a modified venting arrangement (Figs. 7-9, not shown) the small vent aperture is replaced by a small groove formed in the outer surface of the side wall of the seal plug.
机译:1474802铅酸电池GOULD Inc 1974年7月8日[1973年7月9日(2)] 30217/74标题H1B在干式铅酸电池的负极板和正极板之间形成的晶体生长,可能在通过以下方法激活电池之前发生通过用溶于硫酸或水的金属硫酸盐处理板,可以防止向其中添加电解质。优选的硫酸盐是钠,其他合适的硫酸盐是K,Li,Mg,Ca,Zn和Al。另外,可以使用Be,Ce,In,La,Sn,Tl,Zr和Rb的硫酸盐。在一种制造电池的方法中,将金属硫酸盐添加到地层电解质中。 S.G.的H 2 SO 4溶液的浓度范围为10-020-1-100,金属硫酸盐的含量约为2%(重量)。随后通过倒置电池除去电解质。在一种优选的方法中,地层电解质不包含金属硫酸盐,并且在除去该电解质之后,向电池填充SG的H 2 SO 4冲洗溶液,其范围为1-200-1-400,该溶液含有0-05-5%(按重量计)。重量金属硫酸盐。将板和分离物在漂洗溶液中浸泡约10分钟,然后将其搅拌,然后通过倒置电池除去溶液。在另一种方法中,金属硫酸盐以0-05-5重量%的量溶解在水中。并且在排空形成电解质或排空冲洗液后,用该溶液填充电池,随后从电池中排干水。不管使用哪种方法添加硫酸金属盐,随后都以某种方式密封电池,以使电池内的气体压力可以排出,并允许空气稍微进入电池。在保质期内允许进入电池的极少量氧气趋于使正极板和负极板的自放电相等,并减少了初始电池性能受到正极板限制的趋势。通风孔可以是圆形的,直径为0‑0005-0‑006英寸。排气装置如图4、5所示,包括两组35,每组三个通气帽,每个通气帽具有主体36,该主体36形成有正常的迷宫式通道(未示出),用于在电池工作之后进行呼吸。在电池的保质期内,电池盖33中的电池孔34被塞子38密封,每个塞子38都具有小的通风孔40(上面已经提到),并且盖35被凸缘42保持,该凸缘42与密封塞上的直立部分43配合。 38.通过以下方式使电池投入运行:通过凸片41取下塞子38,注满电解液,并使盖凸缘42啮合在孔口34中。在改进的排气装置(图7-9,未显示)中,小排气孔该孔被形成在密封塞侧壁的外表面上的小凹槽代替。

著录项

  • 公开/公告号IT1017659B

    专利类型

  • 公开/公告日1977-08-10

    原文格式PDF

  • 申请/专利权人 GOULD INC;

    申请/专利号IT19740024917

  • 发明设计人

    申请日1974-07-08

  • 分类号H01M;

  • 国家 IT

  • 入库时间 2022-08-23 00:37:20

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