One disadvantage of deep cycle flooded lead-acid batteries is increasing water loss caused by use of (+) Pb-Sb / () Pb-Sb alloy grid. Water loss is generated by the emission of hydrogen gas from the () electrode during battery charging. In this paper, we maintain cycle life aspect through the development of hybrid flooded lead-acid batteries to which a (+) Pb- Sb / () Pb-Ca grid is applied and deal with the improvement of water loss. The amount of water loss compared to that of the () Pb-Sb grid decreased when Ca was added to the () Pb grid. For the () Pb-Ca grid, it was confirmed that the time to reach 0.0 V, at which water decomposition occurs, was increased compared to that of the () Pb-Sb grid at the NPV (Negative Potential Voltage). In the cycle life test conducted with the BCI (Battery Council International) standard, compared to the (+) Pb-Ca grid, the (+) Pb-Sb grid increased the life cycle of the batteries and the (+) Pb-Ca grid showed an early end of life due to PbO corrosion layer generation, as determined through SEM / EDS and Tear Down analysis. In conclusion, by addition of Sb to (+) Pb grid and Ca to () Pb grid, we developed a hybrid flooded lead-acid battery that meets user requirements to improve water loss characteristics and preserve cycle life characteristics.

To cope with automobile exhaust gas regulations, ISG and charging control systems are applied to HEV vehicles for the purpose of improving fuel economy. These systems require quick charge-discharge performance of high current. Therefore, a Module of the AGM battery with high energy density and EDLC(Electric Double Layer Capacitor) with high power density are constructed to study the charging and discharging behavior. In CCA, which evaluates the starting performance at -18 oC & 30 oC with high current, EDLC contributed for about 8 sec at the beginning. At 0 oC CA (Charge Acceptance), the initial Charging current of the AGM/EDLC Module, is twice that of the AGM lead acid battery. To play the role of EDLC during high-current rapid charging and discharging, the condition of the AGM lead-acid battery is optimally maintained. As a result of a Standard of Battery Association of Japan (SBA) S0101 test, the service life of the Module of the AGM Lead Acid Battery/EDLC is found to improve by 2 times compared to that of the AGM Lead Acid Battery.

To cope with automobile exhaust gas regulations, ISG (Idling Stop & Go) and charging control systems are applied to HEVs (Hybrid Electric Vehicle) for the purpose of improving fuel economy. These systems require quick charge/discharge performance at high current. To satisfy this characteristic, improvement of the positive electrode plate is studied to improve the charge/discharge process and performance of AGM(Absorbent Glass Mat) lead-acid batteries applied to ISG automotive systems. The bonding between grid and A.M (Active Material) can be improved by applying the Sand-Blasting method to provide roughness to the surface of the positive grid. When the Sand-Blasting method is applied with conditions of ball speed 1,000 rpm and conveyor speed 5 M/min, ideal bonding is achieved between grid and A.M. The positive plate of each condition is applied to the AGM LAB (Absorbent Glass Mat Lead Acid Battery); then, the performance and ISG life characteristics are tested by the vehicle battery test method. In CCA, which evaluates the starting performance at -18 oC and 30 oC with high current, the advanced AGM LAB improves about 25 %. At 0 oC CA (Charge Acceptance), the initial charging current of the advanced AGM LAB increases about 25 %. Improving the bonding between the grid and A.M. by roughening the grid surface improves the flow of current and lowers the resistance, which is considered to have a significant effect on the high current charging/discharging area. In a Standard of Battery Association of Japan (SBA) S0101 test, after 300 A discharge, the voltage of the advanced AGM LAB with the Sand-Blasting method grid was 0.059 V higher than that of untreated grid. As the cycle progresses, the gap widens to 0.13 V at the point of 10,800 cycles. As the bonding between grid and A.M. increases through the Sand Blasting method, the slope of the discharge voltage declines gradually as the cycle progresses, showing excellent battery life characteristics. It is believed that system will exhibit excellent characteristics in the vehicle environment of the ISG system, in which charge/discharge occurs over a short time.

Positive plate was composed of lead hydroxide via reaction between lead oxide and H2O and lead sulfate was formed of the reaction of lead hydroxide with sulfuric acid. And its density is 3.8 g/cm3, 4.0 g/cm3, 4.2 g/cm3 and 4.4 g/cm3 by controlling volume of refined water. Curing of positive plate is done for low (45℃, 40hr, over 95% of relative humidity) & high (80℃, 40hr, over 95% of relative humidity) temperature, which created 3BS & 4BS active materials. Experimental result of DOD with 100% life cycle test shows that it was not related to the density of active materials but to the low & high temperature aging of active materials. The test makes us to understand that the crystallization which is made by curing of active materials is a more of a main factor than density of active materials under the deep cycle using circumstances. The active materials which were from the high temperature curing are better for deep cycle performance.

본 연구는 온실 운영에 필요한 전력량을 확보함으로서 온실경영비 절감을 목적으로 태양광발전시스템을 온실에 인접한 건물의 옥상에 설치하여 일사량에 따른 발전량을 실험적으로 검토하였다. 연구결과를 요약하면 다음과 같다. 실험기간 동안 수평면 일사량의 최대, 평균 및 최소 값은 각각 26.1MJ · m−2, 14.0MJ · m−2 및 0.6MJ · m−2 정도였고, 일일 전력량은 각각 약 6.1kWh, 3.7kWh 및 0.01kWh 이었다. 그리고 누계 일사량과 전력량은 각각 약 4,378.2MJ · m−2 및 1,163.2kWh 정도이었다. 그리고 부하에 의해 소비된 적산전력량의 최대, 평균 및 최소값은 각각 4.5kWh, 2.4kWh 및 0.0kWh 정도이었고, 누계 전력량은 739.2kWh 정도로서 발생 전력량의 약 63.5% 에 해당하였다. 본 실험에 사용된 시스템의 평균 소비전 력량을 기준으로 보면, 온풍기의 용량 및 작동시간이 작은 경우는 충분하지만 큰 경우는 부족한 것으로 나타났다. 어레이 표면온도가 상대적으로 높아지면 일사량에 비례해서 발생 전력이 증가하지 않은 것으로 나타났지만, 두 인자 간에 상관계수는 0.851 정도로서 상관관계가 높은 것으로 나타났다.

충전과 방전이 빈번히 발생하는 축전지의 사용수명을 늘리고 안정적인 사용을 위해서는 과 방전을 방지하는 것이 가장 중요한 요인중 하나이다. 축전지의 건강상태를 파악하는 방법에는 여러 가지로 연구가 진행되고 있으며, 그 중에서도 본 논문에서는 가장 간단하게 축전지의 상태를 파악할 수 있는 단자전압을 이용하는 방법을 활용하여 축전지의 잔존용량을 파악하였다. 일정 전압 이하로 축전지의 전압이 떨어지지 못하도록 간단하게 비교기를 이용하여 과 방전이 되지 못하도록 설계 제작하였다. 상수도 시설이 없는 장소의 저수조탱크의 물 소독을 목적으로 제작된 태양광발전을 응용한 소독약 자동 주입장치의 축전지에 설계한 회로를 제작 설치하여 그 동작실험을 하고 그 유용함을 확인하였다.

The influence of red lead(Pb3O4) to curing and formation reaction properties when it was added in positive material of lead acid battery for vehicle use has been investigated. At the results, it was confirmed that the addition of red lead led 4BS crystal size to be smaller and increased the rates of 4BS formation and Pb consumption. Consequently the curing time was shortened to half compared with that of red lead-free one. In addition to this, the lead acid battery prepared by adding red lead showed 14% higher efficiency at the life cycle test than that without red lead.

This study investigates the paste mixing of positive active materials which, affect the life cycle of batteries in Pb-Ca-Sn grids, and generation of 4BS in a curing process and considers the effects of these things on the initial charge characteristics and life cycle. In the results of the experiments applied in this study, it was possible to reduce the curing time in which the fine 4BS was formed by the mixing of the positive active materials of lead acid battery applied at high temperature compared to that of the existing coarse 4BS and that represented some improvements in the life cycle performance.

This study was conducted to made a grid alloy (Pb-Ca-Sn-Al) which has a temporary composition ratio in order to improve the efficiency of lead acid batteries. The positive activity material made a 3BS(tri-basic lead sulfate; 3PbO·PbSO4·H2O) by a low temperature curing and it evaluates the plate efficiency through the life cycle testing. The initial current capacity of low temperature curing plate was excellent but the life cycle was not good (S1). As for the S2 plate, however, the initial current capacity and the life cycle were superior.

Generally, it has been known that positive plate efficiency is the most influential effect on the initial current capacity of lead acid battery. Thus, in this study, we have investigated the curing effect of the positive plate, which is one of the important lead acid battery processes. The curing process of the positive plate is performed either with the separation of each plate with 1mm gap or with no gap of plate. As a result, when there is no interval between each plate, the higher temperature current happened than expected, resulting in the changes in the initial current efficiency of the lead acid battery. The chemical composition and crystal structure of a material coated on the positive plate were identified with XRD and SEM. It was resulted that were only there not a lot of 4BS (tetrabasic-lead sulfate, 4PbO·PbSO4) on the plate in case of curing of plates without interval, but a large quantity of Pb3O4 also formed on the surface. On the other hand, it was observed that 3BS (tribasic-lead sulface, 3PbO·PbSO4·H2O) was the main product on the plate in case of typical curing process with some interval. From the initial current capacity test, the positive plate having 3BS was approximately 40% higher in initial current capacity than that having 4BS. It was concluded that 4BS and Pb3O4 on the plate surface were harmful to the initial current capacity of lead acid battery.

Lead-acid battery is being most widely used with secondary battery because of its low price, and long life cycles. But According to using for a long time, its voltage, capacity, and recovery ability is decreased gradually. Therefore there are many papers about improving the property of a lead-acid battery. One of them is to slow down sulfation due to formation of inner PbSO sub(4) by adding inhibitor to electrolyte, however it was not well known what is inhibitor's composition and its role acting on both cathodic and anodic electrode because of its know-how of every country and companies. The purpose of this paper is to study about improvement of property of lead-acid battery by adding one of the inhibitor to H sub(2) SO sub(4) electrolyte.